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. 2017 Feb 6;7:41845. doi: 10.1038/srep41845

Table 2. Marker distributions of SNP markers associated with the swede vs. non-swede morphotype split in B. napus, along with the most closely associated markers from deep sequencing for the swede vs. non-swede split.

Marker name Chromosome Position non-swede allele swede allele located in gene clear non-swede clear swede mixed deletions
non-swede pop swede pop non-swede pop swede pop −log(p)
split markers nn ss sn 00
chrA03_4639027 chrA03 4639027 260 0 0 11 57.7 Bna.VIN3.A03 260 11 na 0
chrA04_12696607 chrA04 12696607 0 8 260 3 55.8   263 8 na 0
chrA06_5607262 chrA06 5607262 2 11 258 0 56.0 Bna.CCR1.A06 257 6 8 0
chrA06_5607744 chrA06 5607744 0 9 260 2 56.3 Bna.CCR1.A06
chrA06_5608016 chrA06 5608016 1 11 259 0 56.9 Bna.CCR1.A06
chrA06_5608089 chrA06 5608089 1 11 259 0 56.9 Bna.CCR1.A06
chrA06_5614815 chrA06 5614815 0 8 260 3 55.8  
chrA08_14983629 chrA08 14983629 260 3 0 8 55.8 Bna.TEM1.A08 263 8 na 0
chrA09_11993194 chrA09 11993194 0 8 260 3 55.8 BnaA09g19070D 263 8 0 0
chrA09_11993662 chrA09 11993662 0 8 260 3 55.8 BnaA09g19070D
chrA09_11995810 chrA09 11995810 260 3 0 8 55.8
Bn-A09-p21922383 chrA09 19312044 0 8 260 3 55.8 263 8 na 0
chrA09_32435440 chrA09 32435440 2 11 258 0 56.0 Bna.PHYA.A09 258 9 4 0
chrA09_32435455 chrA09 32435455 2 11 258 0 56.0 Bna.PHYA.A09
chrA09_32437048 chrA09 32437048 0 10 260 1 56.9 Bna.PHYA.A09
chrA09_32441986 chrA09 32441986 260 2 0 9 56.3 BnaA09g48430D
chrA10_17106726 chrA10 17106726 0 8 260 3 55.8 Bna.ELF7.A10 263 8 0 0
chrA10_17106744 chrA10 17106744 0 8 260 3 55.8 Bna.ELF7.A10
chrA10_17108533 chrA10 17108533 260 3 0 8 55.8 Bna.ELF7.A10
chrC01_1447013 chrC01 1447013 0 8 260 3 55.8   262 8 1 0
chrC01_1447235 chrC01 1447235 0 9 260 2 56.3 Bna.FD.C01
chrC01_1447273 chrC01 1447273 260 2 0 9 56.3 Bna.FD.C01
chrC01_1447516 chrC01 1447516 0 9 260 2 56.3 Bna.FD.C01
chrC01_1447693 chrC01 1447693 260 2 0 9 56.3 Bna.FD.C01
chrC01_1447972 chrC01 1447972 0 9 260 2 56.3 Bna.FD.C01
Bn-scaff_16770_1-p1357882 chrC08 24087909 0 8 260 3 55.8   263 8 na 0
chrC08_36752901 chrC08 36752901 260 1 0 10 56.9 BnaC08g42670D 259 9 3 0
chrC08_36752954 chrC08 36752954 0 10 260 1 56.9 BnaC08g42670D
chrC08_36753586 chrC08 36753586 1 10 259 1 56.1
chrC08_36754224 chrC08 36754224 0 9 260 2 56.3 BnaC08g42680D
chrC08_36755379 chrC08 36755379 1 10 259 1 56.1
chrC08_36755562 chrC08 36755562 0 9 260 2 56.3
Bn-scaff_16389_1-p12505 chrC08 38113567 0 8 260 0 56.8 260 8 na 3
chrC09_43739821 chrC09 43739821 0 8 260 3 55.8 Bna.CO-li.C09 263 8 na 0
Regions from deep sequencing
chrA01_random_477115 chrA01_random 477115 5 8 255 3 51.6 mads-box protein        
chrA03_6053137 chrA03 6053137 8 9 252 2 49.6 Bna.FRI.A03
chrA03_6243410 chrA03 6243410 12 8 248 2 46.2 Bna.FLC.A03
chrA04_12695445 chrA04 12695445 3 8 257 3 53.3 Bna.ELF3.A04
chrA05_5425314 chrA05 5425314 1 8 259 3 55.0 Bna.SPL3.A05
chrA05_9211460 chrA05 9211460 4 9 256 2 52.9 ubiquitin-conjugating enzyme family protein
chrA07_23775522 chrA07 23775522 3 8 257 3 53.3 cinnamoyl- reductase 2-2
chrA10_1357187 chrA10 1357187 1 8 259 3 55.0 Bna.CRY2.A10
chrA10_13359226 chrA10 13359226 1 9 259 2 55.4 Bna.CO.A10
chrA10_14998679 chrA10 14998679 3 10 257 1 54.4 Bna.FLC.A10
chrAnn_random_610372 chrAnn_random 610372 10 11 250 0 49.4 Bna.TFL1.Ann.random
chrAnn_random_20504534 chrAnn_random 20504534 253 3 7 8 49.9 Bna.VRN2.Ann.random
chrC03_8403949 chrC03 8403949 12 8 248 3 45.9 Bna.FLC.C03
chrC03_random_5400150 chrC03_random 5400150 259 2 1 9 55.4 Bna.FD.C03.random

The table shows the marker name, chromosomal position and the number of lines carrying either a non-swede or a swede allele in the respective non-swede and swede populations. The table also gives the −log(p-value) which used to determine the split markers, along with the gene ID or the name of the gene where the marker is located. If empty, the marker is non-genic. The markers with the highest −log(p-value) in each split region are shown in bold letters. The last four columns of the table show how many clear non-swede or swede haplotypes were counted, along with the number of mixed haplotypes and deletions. For regions only containing one marker, mixed haplotypes do not apply (na).