| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:62621915-62622273 | Common:2; Rare:112 | ||||
| chr11:62646577-62646778 | Common:1; Rare:79; Clinvar (pathogenic):1 | ||||
| chr11:62665061-62665418 | Common:5; Rare:163 | ||||
| chr11:62679006-62679201 | Rare:64 | ||||
| chr11:62706257-62706445 | Common:2; Rare:89; Clinvar (benign):3 | ||||
| chr11:62707110-62707931 | Common:8; Rare:178; Clinvar:1; Clinvar (benign):1 | ||||
| chr11:62727455-62727707 | Rare:93 | ||||
| chr11:62727913-62728138 | Common:5; Rare:44 | ||||
| chr11:62753850-62753936 | Rare:30 | ||||
| chr11:62754136-62754406 | Common:1; Rare:64 | ||||
| chr11:62761371-62761663 | Common:1; Rare:86 | ||||
| chr11:62771229-62771465 | Rare:64 | ||||
| chr11:62787245-62787425 | Common:1; Rare:130 | ||||
| chr11:62791954-62792270 | Common:1; Rare:122 | ||||
| chr11:62832015-62832223 | Rare:78 |