| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:11849046-11849270 | Common:3; Rare:112 | ||||
| chr8:11849778-11850001 | Common:1; Rare:80 | ||||
| chr8:11854113-11854429 | Common:2; Rare:107 | ||||
| chr8:11867981-11868303 | Common:1; Rare:147 | ||||
| chr8:12194077-12194274 | Common:3; Rare:44 | ||||
| chr8:12436346-12436569 | Common:4; Rare:39 | ||||
| chr8:12951378-12951407 | Rare:12 | ||||
| chr8:12951446-12951633 | Common:4; Rare:68 | ||||
| chr8:12951957-12952451 | Common:4; Rare:205 | ||||
| chr8:13133237-13133614 | Common:13; Rare:108 | ||||
| chr8:13514624-13514857 | Common:1; Rare:51 | ||||
| chr8:13514859-13515018 | Rare:43 | ||||
| chr8:15540139-15540386 | Common:5; Rare:85; Clinvar:11; Clinvar (benign):1 | ||||
| chr8:17157111-17157234 | Common:1; Rare:48 | ||||
| chr8:17234830-17234938 | Rare:35 |