| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:99504910-99505000 | Rare:28 | ||||
| chr7:99558491-99558907 | Common:5; Rare:125 | ||||
| chr7:99919428-99919635 | Rare:72 | ||||
| chr7:100089125-100089176 | Rare:8 | ||||
| chr7:100100468-100100845 | Common:2; Rare:158 | ||||
| chr7:100101319-100101748 | Common:1; Rare:171; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr7:100119328-100119762 | Rare:130; Clinvar:1 | ||||
| chr7:100428678-100428862 | Common:3; Rare:80 | ||||
| chr7:100586119-100586456 | Common:3; Rare:107 | ||||
| chr7:100602994-100603262 | Common:2; Rare:40 | ||||
| chr7:100604154-100604449 | Common:1; Rare:80 | ||||
| chr7:100827474-100827780 | Rare:107 | ||||
| chr7:100852609-100852762 | Rare:39 | ||||
| chr7:100883794-100884459 | Common:7; Rare:215 | ||||
| chr7:101127072-101127221 | Rare:41; Clinvar:2 |