| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:102464837-102465153 | Common:3; Rare:127 | ||||
| chr7:102912477-102913124 | Common:9; Rare:124 | ||||
| chr7:103074763-103075178 | Common:6; Rare:165 | ||||
| chr7:103149043-103149385 | Common:5; Rare:99 | ||||
| chr7:103344578-103344847 | Common:1; Rare:98 | ||||
| chr7:103348055-103348261 | Rare:36 | ||||
| chr7:104207905-104208112 | Common:4; Rare:103 | ||||
| chr7:105014014-105014510 | Common:3; Rare:164 | ||||
| chr7:105532055-105532335 | Common:3; Rare:72 | ||||
| chr7:105876461-105876833 | Common:6; Rare:106 | ||||
| chr7:106284525-106284557 | Rare:14 | ||||
| chr7:106284844-106285384 | Common:4; Rare:204 | ||||
| chr7:106285540-106285813 | Rare:60 | ||||
| chr7:106660937-106661269 | Common:2; Rare:98 | ||||
| chr7:107563852-107564047 | Common:2; Rare:115; Clinvar:2; Clinvar (benign):5 |