| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:87628165-87628514 | Common:1; Rare:100 | ||||
| chr7:87876224-87876685 | Common:3; Rare:196 | ||||
| chr7:90245083-90245214 | Rare:37 | ||||
| chr7:90346573-90346744 | Common:4; Rare:75 | ||||
| chr7:90595887-90596031 | Common:6; Rare:55 | ||||
| chr7:90596272-90596622 | Common:2; Rare:113 | ||||
| chr7:90709606-90709884 | Common:2; Rare:49 | ||||
| chr7:91880668-91880801 | Common:1; Rare:36 | ||||
| chr7:91940839-91941102 | Common:3; Rare:87; Clinvar:4; Clinvar (benign):1 | ||||
| chr7:92134291-92134891 | Common:5; Rare:181 | ||||
| chr7:92245842-92246482 | Common:6; Rare:206; Clinvar:4; Clinvar (benign):5 | ||||
| chr7:92528352-92528838 | Common:4; Rare:154; Clinvar:5; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr7:92590042-92590132 | Rare:37 | ||||
| chr7:93232201-93232444 | Common:3; Rare:52 | ||||
| chr7:94509713-94510084 | Rare:126 |