| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:6484077-6484363 | Common:1; Rare:123 | ||||
| chr7:7566804-7567047 | Common:4; Rare:98 | ||||
| chr7:10940117-10940465 | Common:3; Rare:121 | ||||
| chr7:17298454-17298652 | Common:3; Rare:46 | ||||
| chr7:19117633-19117934 | Common:1; Rare:68 | ||||
| chr7:23105678-23105839 | Common:2; Rare:87; Clinvar:2; Clinvar (benign):3 | ||||
| chr7:25125251-25125438 | Rare:72; Clinvar:3 | ||||
| chr7:26201384-26201823 | Common:2; Rare:205 | ||||
| chr7:27143648-27143701 | Rare:10 | ||||
| chr7:27156232-27156364 | Common:1; Rare:50 | ||||
| chr7:27185050-27185436 | Common:1; Rare:120 | ||||
| chr7:27740085-27740212 | Common:3; Rare:35 | ||||
| chr7:29563679-29563833 | Rare:42 | ||||
| chr7:30028245-30028434 | Common:1; Rare:61 | ||||
| chr7:30594706-30595116 | Common:7; Rare:183; Clinvar:10; Clinvar (benign):15 |