| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:33736400-33736596 | Common:1; Rare:62 | ||||
| chr11:34052138-34052440 | Common:4; Rare:142 | ||||
| chr11:34916318-34916657 | Common:10; Rare:136; Clinvar:4; Clinvar (benign):11; Clinvar (pathogenic):1 | ||||
| chr11:36510240-36510361 | Rare:34 | ||||
| chr11:43358790-43359011 | Rare:105 | ||||
| chr11:44066174-44066346 | Common:2; Rare:44 | ||||
| chr11:45917833-45918180 | Common:1; Rare:86; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:46617210-46617611 | Common:5; Rare:113 | ||||
| chr11:46700562-46700753 | Common:1; Rare:47 | ||||
| chr11:46846235-46846412 | Common:1; Rare:49 | ||||
| chr11:47426420-47426632 | Rare:52 | ||||
| chr11:47553065-47553341 | Common:2; Rare:101 | ||||
| chr11:47565490-47565625 | Common:3; Rare:27 | ||||
| chr11:47578959-47579089 | Rare:66; Clinvar:2 | ||||
| chr11:47848331-47848406 | Rare:36 |