| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:68841773-68841934 | Common:1; Rare:55; Clinvar (benign):3 | ||||
| chr11:68844014-68844143 | Common:1; Rare:29 | ||||
| chr11:68903760-68904041 | Common:6; Rare:117; Clinvar:6; Clinvar (benign):8 | ||||
| chr11:68904314-68904384 | Common:1; Rare:20 | ||||
| chr11:69048695-69048998 | Common:6; Rare:108 | ||||
| chr11:69049129-69049217 | Rare:28 | ||||
| chr11:69049401-69049530 | Common:2; Rare:28 | ||||
| chr11:69640411-69640709 | Common:3; Rare:56 | ||||
| chr11:69640913-69641324 | Common:1; Rare:94 | ||||
| chr11:69641428-69641836 | Rare:101 | ||||
| chr11:69643339-69643621 | Rare:85 | ||||
| chr11:69674517-69674698 | Common:4; Rare:41 | ||||
| chr11:69674877-69674978 | Common:1; Rare:36 | ||||
| chr11:69674980-69675194 | Common:1; Rare:87 | ||||
| chr11:69675207-69675604 | Common:3; Rare:113 |