| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:14643631-14643756 | Common:1; Rare:58 | ||||
| chr11:14891652-14891839 | Rare:45 | ||||
| chr11:16738466-16738725 | Common:3; Rare:56 | ||||
| chr11:17077595-17077880 | Common:2; Rare:119 | ||||
| chr11:17207920-17208111 | Common:1; Rare:72 | ||||
| chr11:17276472-17276813 | Common:4; Rare:100; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr11:18012909-18013241 | Common:6; Rare:110 | ||||
| chr11:18106037-18106308 | Common:2; Rare:83 | ||||
| chr11:18322131-18322332 | Common:5; Rare:75; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:18322512-18322613 | Common:2; Rare:48 | ||||
| chr11:18394411-18394634 | Common:1; Rare:87; Clinvar (benign):1 | ||||
| chr11:18526840-18526993 | Rare:75 | ||||
| chr11:18588672-18588860 | Common:2; Rare:63 | ||||
| chr11:18634289-18634580 | Common:3; Rare:99 | ||||
| chr11:20363689-20363776 | Rare:18 |