| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:67398419-67398805 | Rare:157 | ||||
| chr11:67613936-67614052 | Common:1; Rare:25 | ||||
| chr11:68045011-68045317 | Rare:80; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr11:71994651-71994733 | Rare:18 | ||||
| chr11:72018198-72018497 | Common:2; Rare:80 | ||||
| chr11:72712240-72712446 | Common:1; Rare:68 | ||||
| chr11:72738171-72738415 | Common:1; Rare:44 | ||||
| chr11:72738974-72739110 | Common:1; Rare:21 | ||||
| chr11:72953728-72953932 | Common:2; Rare:30 | ||||
| chr11:73386160-73386340 | Rare:36 | ||||
| chr11:73981536-73981923 | Common:1; Rare:62 | ||||
| chr11:73995250-73995468 | Rare:33 | ||||
| chr11:74011863-74012097 | Common:1; Rare:36 | ||||
| chr11:76629556-76629836 | Common:5; Rare:54 | ||||
| chr11:82689796-82689872 | Rare:12 |