| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:99408555-99408661 | Common:2; Rare:36 | ||||
| chr7:99408820-99409009 | Common:1; Rare:63 | ||||
| chr7:99438744-99438998 | Common:1; Rare:75 | ||||
| chr7:99505160-99505307 | Common:5; Rare:49 | ||||
| chr7:99558541-99558701 | Common:2; Rare:54 | ||||
| chr7:100088859-100089036 | Common:1; Rare:65 | ||||
| chr7:100101344-100101677 | Common:1; Rare:124 | ||||
| chr7:100119335-100119688 | Rare:99 | ||||
| chr7:100874946-100875202 | Common:1; Rare:87 | ||||
| chr7:101217850-101218198 | Common:4; Rare:111 | ||||
| chr7:101321718-101321881 | Common:3; Rare:58 | ||||
| chr7:104207979-104208112 | Common:2; Rare:54 | ||||
| chr7:105014097-105014220 | Common:1; Rare:55 | ||||
| chr7:106285149-106285437 | Common:5; Rare:98 | ||||
| chr7:107563892-107563988 | Common:1; Rare:58; Clinvar (benign):1 |