| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:159790244-159790550 | Common:8; Rare:105 | ||||
| chr6:166999095-166999397 | Common:1; Rare:102 | ||||
| chr6:169751593-169751644 | Rare:21; Clinvar (benign):1 | ||||
| chr7:727249-727281 | Rare:10; Clinvar:1 | ||||
| chr7:727291-727304 | Rare:2 | ||||
| chr7:975519-975674 | Common:1; Rare:60 | ||||
| chr7:1028315-1028525 | Common:1; Rare:71 | ||||
| chr7:1138196-1138461 | Common:2; Rare:82 | ||||
| chr7:1570020-1570142 | Common:1; Rare:41 | ||||
| chr7:2242178-2242247 | Common:2; Rare:42 | ||||
| chr7:4775471-4775634 | Common:6; Rare:69 | ||||
| chr7:5513746-5513886 | Common:1; Rare:61 | ||||
| chr7:6009030-6009377 | Common:4; Rare:142; Clinvar:4; Clinvar (benign):14 | ||||
| chr7:6447952-6448049 | Rare:31 | ||||
| chr7:10940055-10940213 | Common:1; Rare:77; Clinvar (benign):3 |