Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:15732371-15732675 | Rare:93; Clinvar:5; Clinvar (benign):2 | ||||
chr1:15834846-15835133 | Common:2; Rare:130 | ||||
chr1:15835794-15836134 | Common:6; Rare:164 | ||||
chr1:15910939-15911145 | Common:1; Rare:40 | ||||
chr1:16499232-16499373 | Rare:67 | ||||
chr1:16644644-16644789 | Common:1; Rare:2 | ||||
chr1:16913904-16914121 | Common:7; Rare:45 | ||||
chr1:20643796-20644077 | Common:5; Rare:54 | ||||
chr1:21857125-21857325 | Common:1; Rare:56; Clinvar:2; Clinvar (benign):2 | ||||
chr1:21860178-21860476 | Rare:71; Clinvar:1 | ||||
chr1:22025185-22025522 | Common:7; Rare:83 | ||||
chr1:25875508-25875780 | Rare:73 | ||||
chr1:28648308-28648640 | Common:6; Rare:125 | ||||
chr1:31696265-31696499 | Common:2; Rare:47 | ||||
chr1:32228996-32229185 | Rare:42 |