| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:112790355-112790492 | Common:1; Rare:38 | ||||
| chr7:112939622-112940120 | Common:4; Rare:167 | ||||
| chr7:113918811-113919186 | Common:2; Rare:102; Clinvar (benign):1 | ||||
| chr7:114086188-114086506 | Common:2; Rare:120 | ||||
| chr7:116210402-116210693 | Common:4; Rare:70 | ||||
| chr7:116499421-116499827 | Common:3; Rare:136 | ||||
| chr7:116499926-116500445 | Common:3; Rare:127 | ||||
| chr7:116524503-116525205 | Common:5; Rare:195; Clinvar (benign):2 | ||||
| chr7:116525653-116525814 | Rare:35 | ||||
| chr7:116526133-116526683 | Common:3; Rare:156; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr7:116672201-116672509 | Common:1; Rare:73; Clinvar:2 | ||||
| chr7:118183964-118184217 | Common:2; Rare:100 | ||||
| chr7:118214547-118214664 | Common:2; Rare:37 | ||||
| chr7:120856764-120856954 | Common:1; Rare:47; Clinvar:1 | ||||
| chr7:120857038-120857141 | Rare:22 |