| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:99472646-99472979 | Common:4; Rare:99 | ||||
| chr7:99500229-99500431 | Common:2; Rare:55 | ||||
| chr7:99552075-99552203 | Rare:44 | ||||
| chr7:99558514-99558716 | Common:2; Rare:67 | ||||
| chr7:99919518-99919640 | Rare:41 | ||||
| chr7:100101338-100101725 | Common:1; Rare:148; Clinvar (benign):1 | ||||
| chr7:100119335-100119730 | Rare:120; Clinvar:1 | ||||
| chr7:100428635-100428865 | Common:4; Rare:100 | ||||
| chr7:100677352-100677654 | Common:1; Rare:92 | ||||
| chr7:100852598-100852719 | Common:1; Rare:33 | ||||
| chr7:101217849-101218203 | Common:4; Rare:114 | ||||
| chr7:101244698-101244990 | Common:1; Rare:116 | ||||
| chr7:102464829-102465040 | Common:1; Rare:87 | ||||
| chr7:102748674-102748992 | Common:3; Rare:64 | ||||
| chr7:103074863-103075187 | Common:7; Rare:124 |