| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:196318184-196318352 | Common:1; Rare:68 | ||||
| chr3:196639604-196639799 | Common:2; Rare:47 | ||||
| chr3:196942399-196942659 | Common:1; Rare:103 | ||||
| chr3:197749756-197749962 | Common:1; Rare:77 | ||||
| chr3:197949875-197950250 | Common:4; Rare:112; Clinvar (benign):2 | ||||
| chr3:197959971-197960245 | Common:1; Rare:96 | ||||
| chr4:337759-337857 | Rare:36 | ||||
| chr4:499136-499307 | Common:3; Rare:64 | ||||
| chr4:663611-663753 | Rare:48 | ||||
| chr4:674253-674588 | Common:3; Rare:155 | ||||
| chr4:932300-932487 | Common:2; Rare:76 | ||||
| chr4:1113544-1113627 | Common:1; Rare:30 | ||||
| chr4:2468920-2469154 | Common:2; Rare:72 | ||||
| chr4:2843687-2844009 | Common:3; Rare:119 | ||||
| chr4:2934767-2934903 | Common:1; Rare:62 |