| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:131327736-131327902 | Rare:57 | ||||
| chr7:131478451-131478654 | Common:1; Rare:59 | ||||
| chr7:131507347-131507577 | Common:1; Rare:38 | ||||
| chr7:134646566-134646925 | Common:9; Rare:115 | ||||
| chr7:134779547-134779732 | Rare:36 | ||||
| chr7:134891364-134891649 | Common:3; Rare:80 | ||||
| chr7:134986340-134986568 | Common:5; Rare:84 | ||||
| chr7:135147998-135148149 | Rare:38 | ||||
| chr7:135170677-135170827 | Common:2; Rare:60 | ||||
| chr7:135211463-135211782 | Common:2; Rare:149 | ||||
| chr7:135662398-135662520 | Common:2; Rare:52 | ||||
| chr7:136869150-136869281 | Common:2; Rare:24; Clinvar (benign):3 | ||||
| chr7:138460397-138460439 | Common:1; Rare:14 | ||||
| chr7:138797815-138797942 | Common:2; Rare:23 | ||||
| chr7:138797977-138798089 | Common:1; Rare:43; Clinvar:1; Clinvar (benign):2 |