Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:181712562-181712807 | Rare:47; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):3 | ||||
chr3:183447427-183447674 | Common:2; Rare:63 | ||||
chr3:185418816-185418974 | Rare:17 | ||||
chr3:187862867-187863113 | Rare:82 | ||||
chr3:194583897-194584026 | Common:6; Rare:43 | ||||
chr3:195657901-195658110 | Common:11; Rare:35 | ||||
chr3:195990233-195990470 | Common:1; Rare:31 | ||||
chr3:197627823-197628017 | Common:6; Rare:74 | ||||
chr3:197850988-197851204 | Rare:39 | ||||
chr4:781817-782153 | Common:2; Rare:110 | ||||
chr4:9152219-9152369 | Rare:59 | ||||
chr4:11149018-11149274 | Common:8; Rare:83 | ||||
chr4:52712223-52712517 | Common:4; Rare:75 | ||||
chr4:75127182-75127320 | Rare:29 | ||||
chr4:84965633-84965652 | Rare:4 |