| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:14520318-14520593 | Rare:86 | ||||
| chr11:14643596-14643810 | Common:2; Rare:82 | ||||
| chr11:14891561-14891779 | Common:1; Rare:67 | ||||
| chr11:16607288-16607541 | Rare:46 | ||||
| chr11:16738456-16738722 | Common:3; Rare:56 | ||||
| chr11:17013050-17013155 | Common:3; Rare:15 | ||||
| chr11:17013838-17013994 | Common:6; Rare:64 | ||||
| chr11:17014131-17014346 | Common:1; Rare:81 | ||||
| chr11:17014385-17014530 | Common:1; Rare:77 | ||||
| chr11:17077608-17077796 | Common:2; Rare:79 | ||||
| chr11:17207905-17208102 | Common:2; Rare:77 | ||||
| chr11:17276484-17276809 | Common:4; Rare:96; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr11:17544320-17544499 | Common:3; Rare:46; Clinvar:2 | ||||
| chr11:18012913-18013251 | Common:6; Rare:113 | ||||
| chr11:18322075-18322321 | Common:4; Rare:90; Clinvar:2; Clinvar (benign):2 |