| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:763185-763519 | Common:23; Rare:164; Clinvar:2; Clinvar (pathogenic):3 | ||||
| chr11:777458-777598 | Common:1; Rare:61 | ||||
| chr11:809201-809307 | Common:1; Rare:27 | ||||
| chr11:809492-809655 | Common:2; Rare:46 | ||||
| chr11:809767-810038 | Common:2; Rare:120 | ||||
| chr11:821829-821964 | Rare:61; Clinvar:2 | ||||
| chr11:832819-833022 | Common:7; Rare:68 | ||||
| chr11:842464-842978 | Common:8; Rare:212 | ||||
| chr11:843965-844159 | Common:1; Rare:47 | ||||
| chr11:910781-911135 | Common:4; Rare:141 | ||||
| chr11:914996-915268 | Common:2; Rare:64 | ||||
| chr11:925701-926010 | Common:3; Rare:131 | ||||
| chr11:933401-933561 | Common:1; Rare:29 | ||||
| chr11:1309547-1309785 | Common:2; Rare:106 | ||||
| chr11:1750564-1750757 | Common:3; Rare:36 |