| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:103149063-103149386 | Common:4; Rare:94 | ||||
| chr7:104207956-104208112 | Common:3; Rare:72 | ||||
| chr7:105013581-105013719 | Common:1; Rare:46 | ||||
| chr7:105014091-105014268 | Common:1; Rare:70 | ||||
| chr7:105108698-105108961 | Rare:47 | ||||
| chr7:105522207-105522330 | Common:1; Rare:48 | ||||
| chr7:105532077-105532256 | Common:1; Rare:45 | ||||
| chr7:105876477-105876833 | Common:6; Rare:105 | ||||
| chr7:106112204-106112611 | Common:3; Rare:147 | ||||
| chr7:106284867-106285268 | Common:2; Rare:160 | ||||
| chr7:106285539-106285668 | Rare:30 | ||||
| chr7:106661152-106661192 | Common:1; Rare:8 | ||||
| chr7:107563861-107564047 | Common:2; Rare:110; Clinvar:2; Clinvar (benign):5 | ||||
| chr7:107580126-107580285 | Common:2; Rare:62 | ||||
| chr7:107743589-107743802 | Common:3; Rare:81 |