| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:105819477-105819515 | Rare:7 | ||||
| chr7:106657197-106657444 | Common:2; Rare:41 | ||||
| chr7:106770162-106770558 | Common:2; Rare:62 | ||||
| chr7:106775773-106775931 | Rare:23 | ||||
| chr7:107260810-107261165 | Common:4; Rare:81 | ||||
| chr7:107916601-107916950 | Common:1; Rare:82 | ||||
| chr7:107917104-107917461 | Rare:65; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):3 | ||||
| chr7:107933617-107933953 | Common:3; Rare:87 | ||||
| chr7:107944000-107944097 | Rare:20 | ||||
| chr7:111214998-111215161 | Common:1; Rare:31 | ||||
| chr7:112463719-112464023 | Common:24; Rare:62 | ||||
| chr7:112472275-112472447 | Rare:36 | ||||
| chr7:112787168-112787427 | Common:1; Rare:46 | ||||
| chr7:112788452-112788671 | Common:1; Rare:48 | ||||
| chr7:112956571-112956705 | Common:1; Rare:25 |