Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:244864384-244864691 | Rare:120 | ||||
chr1:244969660-244969801 | Rare:41 | ||||
chr1:246566204-246566612 | Common:2; Rare:130 | ||||
chr1:246724264-246724436 | Common:2; Rare:67 | ||||
chr1:247416351-247416426 | Common:2; Rare:16 | ||||
chr1:247417841-247418229 | Common:1; Rare:66; Clinvar:2; Clinvar (benign):1 | ||||
chr1:248838053-248838451 | Common:3; Rare:126 | ||||
chr1:248859033-248859154 | Rare:45 | ||||
chr1:248906094-248906275 | Rare:71 | ||||
chr10:988344-988492 | Common:1; Rare:60 | ||||
chr10:1048872-1049119 | Common:2; Rare:123 | ||||
chr10:1056779-1056856 | Rare:31 | ||||
chr10:3782454-3782692 | Rare:51 | ||||
chr10:3784972-3785557 | Common:5; Rare:231 | ||||
chr10:5813220-5813520 | Common:3; Rare:103 |