| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:149143-149274 | Common:2; Rare:48 | ||||
| chr7:149401-149761 | Common:8; Rare:126 | ||||
| chr7:522539-522607 | Common:1; Rare:23 | ||||
| chr7:604505-604702 | Common:4; Rare:61 | ||||
| chr7:1483791-1484107 | Common:4; Rare:131 | ||||
| chr7:2020100-2020437 | Common:5; Rare:100 | ||||
| chr7:2312444-2312558 | Rare:22 | ||||
| chr7:2541745-2541943 | Rare:83; Clinvar:5; Clinvar (benign):2 | ||||
| chr7:2632865-2633175 | Common:1; Rare:61 | ||||
| chr7:2633434-2633583 | Common:2; Rare:44 | ||||
| chr7:2637336-2637425 | Rare:16 | ||||
| chr7:2709590-2709675 | Rare:57 | ||||
| chr7:2978566-2978746 | Common:1; Rare:42 | ||||
| chr7:3118012-3118073 | Common:1; Rare:14 | ||||
| chr7:4011341-4011532 | Common:2; Rare:60 |