| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:140924666-140925116 | Common:6; Rare:320; Clinvar:4; Clinvar (benign):11 | ||||
| chr7:141014900-141015111 | Rare:92 | ||||
| chr7:141551302-141551443 | Rare:69; Clinvar:8; Clinvar (benign):4 | ||||
| chr7:141737949-141738470 | Common:9; Rare:283 | ||||
| chr7:143263370-143263528 | Rare:93 | ||||
| chr7:143284794-143284984 | Rare:69 | ||||
| chr7:143288005-143288493 | Common:4; Rare:309 | ||||
| chr7:143380884-143381556 | Common:3; Rare:353 | ||||
| chr7:143381910-143382550 | Common:2; Rare:350 | ||||
| chr7:143902098-143902292 | Common:11; Rare:117 | ||||
| chr7:144835891-144836191 | Common:3; Rare:157; Clinvar (benign):4 | ||||
| chr7:148698697-148699012 | Common:3; Rare:195 | ||||
| chr7:148884151-148884521 | Common:3; Rare:281; Clinvar:4; Clinvar (benign):2 | ||||
| chr7:148884570-148884900 | Common:4; Rare:145 | ||||
| chr7:149028341-149028606 | Common:3; Rare:101 |