| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:16738183-16738245 | Rare:14 | ||||
| chr11:16738392-16738733 | Common:4; Rare:89 | ||||
| chr11:16738803-16738947 | Rare:43 | ||||
| chr11:16739400-16739735 | Common:3; Rare:66 | ||||
| chr11:17014046-17014330 | Common:1; Rare:111 | ||||
| chr11:17014386-17014566 | Common:2; Rare:87 | ||||
| chr11:17077388-17077463 | Rare:12 | ||||
| chr11:17077535-17077983 | Common:3; Rare:186 | ||||
| chr11:17078063-17078128 | Common:1; Rare:18 | ||||
| chr11:17078153-17078238 | Rare:21 | ||||
| chr11:17207606-17207720 | Rare:29 | ||||
| chr11:17207837-17208199 | Common:2; Rare:127 | ||||
| chr11:17208324-17208546 | Rare:41 | ||||
| chr11:17276242-17276389 | Common:1; Rare:38 | ||||
| chr11:17276392-17277056 | Common:6; Rare:169; Clinvar:4; Clinvar (pathogenic):1 |