| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:726154-726419 | Common:2; Rare:114 | ||||
| chr11:747290-747514 | Rare:93; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:763222-763501 | Common:19; Rare:142; Clinvar:2; Clinvar (pathogenic):3 | ||||
| chr11:777451-777598 | Common:1; Rare:66 | ||||
| chr11:809751-810038 | Common:2; Rare:126 | ||||
| chr11:827239-827344 | Common:3; Rare:27 | ||||
| chr11:832833-833022 | Common:7; Rare:64 | ||||
| chr11:834380-834533 | Common:2; Rare:37 | ||||
| chr11:842500-842895 | Common:7; Rare:159 | ||||
| chr11:910781-910968 | Common:4; Rare:79 | ||||
| chr11:1222939-1223067 | Common:2; Rare:24 | ||||
| chr11:1309566-1309780 | Common:1; Rare:94 | ||||
| chr11:1834212-1834495 | Rare:63 | ||||
| chr11:1871279-1871369 | Common:3; Rare:27 | ||||
| chr11:2400275-2400538 | Common:3; Rare:94 |