| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:102748696-102749010 | Common:2; Rare:66 | ||||
| chr7:102973257-102973343 | Rare:19 | ||||
| chr7:103074773-103075053 | Common:5; Rare:122 | ||||
| chr7:103297322-103297483 | Common:1; Rare:60 | ||||
| chr7:104207943-104208123 | Common:3; Rare:90 | ||||
| chr7:105013572-105013709 | Common:1; Rare:47 | ||||
| chr7:105014097-105014309 | Common:1; Rare:76 | ||||
| chr7:105532082-105532250 | Common:1; Rare:42 | ||||
| chr7:105876477-105876816 | Common:6; Rare:100 | ||||
| chr7:106284890-106285529 | Common:6; Rare:228 | ||||
| chr7:106285537-106285569 | Rare:9 | ||||
| chr7:106285627-106285739 | Rare:20 | ||||
| chr7:107168720-107169015 | Rare:98 | ||||
| chr7:107563855-107564028 | Common:2; Rare:102; Clinvar:1; Clinvar (benign):4 | ||||
| chr7:107580174-107580284 | Common:2; Rare:39 |