Table 4.
Name | CTCF bs (count) | CTCF bs (%) | CTCF bs/kbp | H3K27ac | 99-way cons. score |
---|---|---|---|---|---|
FRA1E | 97 | 0.002 | 0.261 | 1.32 | 0.133 |
FRA1H | 17,338 | 0.372 | 1.631 | 3.07 | – |
FRA2Ctel | 700 | 0.015 | 0.938 | 2.53 | 0.071 |
FRA2Ccen | 1,108 | 0.024 | 1.486 | 1.56 | 0.111 |
FRA2G | 1,501 | 0.032 | 1.698 | 4.22 | 0.114 |
FRA2H | 132 | 0.003 | 0.255 | 1.44 | 0.103 |
FRA3B | 4,156 | 0.089 | 0.982 | 1.57 | 0.105 |
FRA4F | 4,765 | 0.102 | 0.671 | 1.63 | 0.085 |
FRA6H | 33,735 | 0.724 | 3.607 | 8.14 | 0.12 |
FRA6F | 2,104 | 0.045 | 2.123 | 2.93 | 0.126 |
FRA6E | 6,274 | 0.135 | 1.081 | 2.47 | 0.062 |
FRA7B | 23,331 | 0.5 | 1.907 | 3.13 | – |
FRA7E | 4,253 | 0.091 | 0.961 | 1.6 | 0.082 |
FRA7K | 265 | 0.006 | 0.709 | 2.56 | 0.097 |
FRA7G | 265 | 0.006 | 1.489 | 2.46 | 0.098 |
FRA7H | 1,458 | 0.031 | 3.283 | 4.38 | 0.089 |
FRA7I | 435 | 0.009 | 0.3 | 1.98 | 0.065 |
FRA8C | 8,599 | 0.184 | 2.079 | 3.26 | 0.082 |
FRA9G | 168 | 0.004 | 0.455 | 1.2 | 0.142 |
FRA10F | 5,878 | 0.126 | 2.051 | 2.57 | 0.071 |
FRA11E | 4,494 | 0.096 | 2.314 | 4.05 | 0.123 |
FRA11G | 9,545 | 0.205 | 2.136 | 2.57 | 0.126 |
FRA13A | 193 | 0.004 | 0.302 | 1.23 | 0.108 |
FRA13E | 2,950 | 0.063 | 0.951 | 1.78 | 0.104 |
FRA16D | 378 | 0.008 | 1.215 | 1.87 | 0.118 |
FRAXB | 718 | 0.015 | 0.753 | 1.54 | 0.056 |
CTCF binding sites, studied in 89 cell lines, are shown respectively as absolute counts, with respect to the total number of CTCF binding sites in the whole genome and as a frequency per kb. Average H3k27 acetylation scores from ChIP-seq analysis of the K562 cell line have been calculated for each fragile site. Average conservation score between human and 99 vertebrates was obtained from the UCSC browser (http://genome.ucsc.edu/cgi-bin/hgTrackUi?db=hg19&g=cons100way). We compiled a list of molecularly mapped CFSs by performing a systematic search of the literature for each one of the known cytogenetically mapped CFSs (n = 125). Twenty-six CFSs with a precise mapping were identified (see Table 3), and their coordinates were then mapped to the reference genome version GRC37. Whenever the precise location of BACs was unknown, it was verified by alignment with NCBI Megablast (default settings). The annotation of the reference human genome was obtained from UCSC (URL: hgdownload.cse.ucsc.edu/goldenPath/hg19/) in December 2013. The utility “bigWigSummary” was used to extract mean scores for molecularly mapped fragile regions and randomly selected non-fragile control regions