| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:65505430-65505892 | Rare:221 | ||||
| chr11:65744508-65744631 | Common:3; Rare:26 | ||||
| chr11:66062884-66063116 | Rare:45 | ||||
| chr11:66211022-66211253 | Rare:52; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr11:66259148-66259289 | Common:1; Rare:16 | ||||
| chr11:66263854-66264102 | Common:2; Rare:58 | ||||
| chr11:66280410-66280656 | Common:1; Rare:68 | ||||
| chr11:66316019-66316112 | Rare:21 | ||||
| chr11:66623961-66624287 | Rare:64 | ||||
| chr11:66639473-66639774 | Common:1; Rare:88 | ||||
| chr11:66715055-66715147 | Rare:13 | ||||
| chr11:66951221-66951350 | Rare:21 | ||||
| chr11:67731996-67732305 | Common:2; Rare:86 | ||||
| chr11:67805291-67805575 | Common:3; Rare:113 | ||||
| chr11:68546544-68546746 | Common:1; Rare:29 |