| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:66616356-66616661 | Common:1; Rare:96 | ||||
| chr11:66638417-66638762 | Common:4; Rare:143 | ||||
| chr11:66677845-66678080 | Rare:84 | ||||
| chr11:66744656-66744859 | Common:3; Rare:83 | ||||
| chr11:67056792-67056901 | Rare:35 | ||||
| chr11:67353254-67353316 | Rare:27 | ||||
| chr11:67353459-67353614 | Rare:36 | ||||
| chr11:67374051-67374098 | Rare:6 | ||||
| chr11:67401742-67402075 | Common:3; Rare:122 | ||||
| chr11:67428307-67428537 | Rare:79 | ||||
| chr11:67443458-67443604 | Common:1; Rare:55 | ||||
| chr11:67469201-67469410 | Common:3; Rare:69 | ||||
| chr11:67488994-67489343 | Rare:83; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr11:68010132-68010354 | Common:1; Rare:58 | ||||
| chr11:68030393-68030742 | Common:3; Rare:96; Clinvar:1; Clinvar (benign):2 |