| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:136868422-136868475 | Rare:13 | ||||
| chr7:136868531-136868587 | Rare:11 | ||||
| chr7:136868591-136868900 | Common:1; Rare:63 | ||||
| chr7:136868964-136869288 | Common:2; Rare:67; Clinvar (benign):3 | ||||
| chr7:137454945-137455262 | Common:1; Rare:74 | ||||
| chr7:137513688-137513833 | Rare:24 | ||||
| chr7:138002021-138002175 | Common:1; Rare:39 | ||||
| chr7:139109324-139109482 | Common:1; Rare:48 | ||||
| chr7:139133654-139133830 | Rare:45 | ||||
| chr7:139231026-139231274 | Common:2; Rare:92 | ||||
| chr7:139341245-139341380 | Rare:30 | ||||
| chr7:139359456-139359519 | Rare:19 | ||||
| chr7:139359654-139359968 | Common:2; Rare:134 | ||||
| chr7:140696648-140696838 | Common:1; Rare:72 | ||||
| chr7:140924674-140925059 | Common:3; Rare:136; Clinvar:2; Clinvar (benign):5 |