| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:100586116-100586456 | Common:3; Rare:109 | ||||
| chr7:100627575-100627973 | Rare:125; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr7:100633002-100633551 | Common:1; Rare:191; Clinvar:7; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr7:100852596-100852788 | Common:2; Rare:49 | ||||
| chr7:100868243-100868329 | Rare:24 | ||||
| chr7:100874942-100875223 | Common:2; Rare:98 | ||||
| chr7:100896079-100896116 | Common:1; Rare:8 | ||||
| chr7:101126836-101127139 | Common:1; Rare:66 | ||||
| chr7:101127319-101127651 | Common:4; Rare:60 | ||||
| chr7:101200993-101201120 | Rare:20 | ||||
| chr7:101217847-101218207 | Common:4; Rare:117 | ||||
| chr7:101245000-101245172 | Common:1; Rare:73 | ||||
| chr7:101252286-101252511 | Common:1; Rare:48 | ||||
| chr7:101321729-101321861 | Common:2; Rare:48 | ||||
| chr7:101815592-101815937 | Common:2; Rare:93 |