Skip to main content
. 2013 May;195(10):2389–2399. doi: 10.1128/JB.02112-12

Table 1.

Undermethylated intergenic sites identified by methyl HTM-seq

Chromosome Positiona Intergenic locusa Frequencyb Fold overrepresentionc
Dam data
    chrI 1306007 VC1231-VC1232 6.96E−04 26.2
    chrI 1306010 VC1231-VC1232 5.74E−04 21.6
    chrI 1933145 VC1783-VC1784 3.28E−04 12.4
    chrI 1933148 VC1783-VC1784 4.60E−04 17.3
    chrI 2364224 K139p05-K139p04 2.02E−04 7.6
    chrI 2364255 K139p05-K139p04 1.22E−04 4.6
    chrII 68810 VCA0062-VCA0063 3.11E−04 11.7
    chrII 68813 VCA0062-VCA0063 1.07E−03 40.3
VchM data
    chrI 296268 VC0286-VC0287 1.10E−02 47.0
    chrI 296271 VC0286-VC0287 9.66E−03 41.4
    chrI 1356851 VC1280-VC1281 5.55E−03 23.8
    chrI 1356854 VC1280-VC1281 2.72E−03 11.6
    chrI 1670727 VC1558-VC1559 5.27E−03 22.6
    chrI 1670730 VC1558-VC1559 3.80E−03 16.3
a

The position and locus are based on the annotated N16961 genome containing the K139 prophage genome in chromosome I. The unmethylated site is located in the intergenic region between the indicated loci.

b

Indicates the frequency of reads mapping to the indicated site relative to the total number of reads mapped.

c

Indicates the degree of overrepresentation of the reads at the indicated site relative to the mean number of reads obtained for all sites.