Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:169751593-169751645 | Rare:22; Clinvar (benign):1 | ||||
chr6:170554221-170554420 | Common:1; Rare:64 | ||||
chr7:727235-727281 | Rare:17; Clinvar:1 | ||||
chr7:727283-727325 | Rare:11 | ||||
chr7:1138203-1138511 | Common:2; Rare:89 | ||||
chr7:1537274-1537450 | Rare:58 | ||||
chr7:1570012-1570134 | Common:1; Rare:37 | ||||
chr7:2242166-2242262 | Common:2; Rare:59 | ||||
chr7:2403288-2403599 | Common:1; Rare:119 | ||||
chr7:2688083-2688242 | Rare:46 | ||||
chr7:4775532-4775652 | Common:3; Rare:53; Clinvar:1 | ||||
chr7:6009026-6009355 | Common:4; Rare:139; Clinvar:4; Clinvar (benign):15 | ||||
chr7:6104627-6105002 | Common:5; Rare:134 | ||||
chr7:6447925-6448049 | Rare:45 | ||||
chr7:6483976-6484418 | Common:3; Rare:168 |