| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:107743588-107743861 | Common:4; Rare:106 | ||||
| chr7:107744003-107744173 | Common:1; Rare:53 | ||||
| chr7:107940254-107940493 | Common:2; Rare:81; Clinvar:1; Clinvar (benign):2 | ||||
| chr7:107940976-107941203 | Common:2; Rare:40 | ||||
| chr7:108003110-108003422 | Common:3; Rare:96 | ||||
| chr7:108130304-108130670 | Common:2; Rare:72 | ||||
| chr7:108526039-108526383 | Common:4; Rare:109 | ||||
| chr7:108569592-108570013 | Common:2; Rare:149 | ||||
| chr7:111090962-111091129 | Rare:34 | ||||
| chr7:111561900-111562133 | Rare:61 | ||||
| chr7:112206384-112206762 | Common:1; Rare:133 | ||||
| chr7:112790177-112790460 | Common:1; Rare:77 | ||||
| chr7:116499521-116499827 | Common:3; Rare:106 | ||||
| chr7:116524729-116525092 | Rare:96 | ||||
| chr7:116525197-116525627 | Common:3; Rare:114 |