| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:50450345-50450456 | Rare:46 | ||||
| chr7:56051396-56051857 | Common:1; Rare:175; Clinvar:5; Clinvar (benign):1 | ||||
| chr7:66114764-66114862 | Common:1; Rare:48 | ||||
| chr7:66115186-66115353 | Rare:38 | ||||
| chr7:66682028-66682210 | Common:6; Rare:85 | ||||
| chr7:66921060-66921456 | Common:1; Rare:115 | ||||
| chr7:73683396-73683624 | Common:3; Rare:95 | ||||
| chr7:74254335-74254517 | Rare:83 | ||||
| chr7:75073826-75073921 | Common:1; Rare:33 | ||||
| chr7:75994498-75994773 | Common:4; Rare:136 | ||||
| chr7:76047748-76048220 | Common:3; Rare:139 | ||||
| chr7:77696232-77696468 | Rare:97 | ||||
| chr7:77798304-77798885 | Common:1; Rare:136 | ||||
| chr7:87152325-87152458 | Common:1; Rare:43 | ||||
| chr7:87345412-87345753 | Common:6; Rare:102 |