| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:103149043-103149386 | Common:5; Rare:99 | ||||
| chr7:104207962-104208112 | Common:3; Rare:68 | ||||
| chr7:105014087-105014427 | Common:1; Rare:116 | ||||
| chr7:105522207-105522330 | Common:1; Rare:48 | ||||
| chr7:105532082-105532263 | Common:1; Rare:47 | ||||
| chr7:105876470-105876833 | Common:6; Rare:105 | ||||
| chr7:105877398-105877520 | Common:2; Rare:21 | ||||
| chr7:106284883-106285529 | Common:6; Rare:234 | ||||
| chr7:106285537-106285592 | Rare:14 | ||||
| chr7:106285764-106286091 | Common:2; Rare:67 | ||||
| chr7:106661152-106661428 | Common:1; Rare:45 | ||||
| chr7:107563848-107564028 | Common:2; Rare:106; Clinvar:1; Clinvar (benign):4 | ||||
| chr7:107580168-107580316 | Common:2; Rare:53 | ||||
| chr7:107743582-107743865 | Common:5; Rare:110 | ||||
| chr7:107744007-107744198 | Common:1; Rare:63 |