| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:47979507-47979772 | Common:1; Rare:101 | ||||
| chr7:48088902-48088922 | Rare:1 | ||||
| chr7:50450311-50450453 | Common:1; Rare:58 | ||||
| chr7:56051416-56051915 | Common:1; Rare:186; Clinvar:5; Clinvar (benign):1 | ||||
| chr7:56106429-56106681 | Common:6; Rare:85 | ||||
| chr7:66114768-66114895 | Common:1; Rare:64 | ||||
| chr7:66115179-66115353 | Rare:40 | ||||
| chr7:66682039-66682172 | Common:5; Rare:63 | ||||
| chr7:72828138-72828463 | Common:1; Rare:94 | ||||
| chr7:73683429-73683622 | Common:3; Rare:77 | ||||
| chr7:73738798-73739051 | Common:1; Rare:77 | ||||
| chr7:74254379-74254497 | Rare:50 | ||||
| chr7:74658003-74658067 | Common:1; Rare:10 | ||||
| chr7:75878832-75879076 | Common:12; Rare:88 | ||||
| chr7:75914923-75915189 | Common:3; Rare:94; Clinvar:3; Clinvar (benign):1 |