| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:106284885-106285480 | Common:6; Rare:218 | ||||
| chr7:107563840-107564032 | Common:2; Rare:111; Clinvar:1; Clinvar (benign):5 | ||||
| chr7:107580174-107580333 | Common:2; Rare:52 | ||||
| chr7:107743593-107743884 | Common:5; Rare:111 | ||||
| chr7:107744016-107744175 | Rare:50 | ||||
| chr7:108526099-108526396 | Common:5; Rare:99 | ||||
| chr7:108569576-108570059 | Common:2; Rare:171 | ||||
| chr7:112206372-112206766 | Common:1; Rare:137 | ||||
| chr7:112450176-112450465 | Common:6; Rare:85 | ||||
| chr7:116499435-116500078 | Common:4; Rare:208 | ||||
| chr7:116525685-116525792 | Rare:27 | ||||
| chr7:116526146-116526436 | Common:2; Rare:82 | ||||
| chr7:116672093-116672428 | Common:1; Rare:72; Clinvar:2 | ||||
| chr7:118184002-118184199 | Common:1; Rare:75 | ||||
| chr7:121396263-121396594 | Common:1; Rare:113 |