| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:67373586-67373869 | Rare:53 | ||||
| chr11:67374096-67374099 | |||||
| chr11:67401783-67402075 | Common:3; Rare:109 | ||||
| chr11:67428323-67428531 | Rare:72 | ||||
| chr11:67443451-67443599 | Common:1; Rare:52 | ||||
| chr11:67482936-67483157 | Rare:52; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr11:67508615-67508761 | Common:2; Rare:48 | ||||
| chr11:68038915-68039101 | Rare:54; Clinvar:1 | ||||
| chr11:68061959-68062261 | Rare:58 | ||||
| chr11:68271891-68272108 | Common:2; Rare:93 | ||||
| chr11:68460223-68460507 | Common:3; Rare:92 | ||||
| chr11:68903795-68903954 | Common:5; Rare:73; Clinvar:1; Clinvar (benign):7 | ||||
| chr11:69013158-69013478 | Common:4; Rare:95 | ||||
| chr11:69048757-69048996 | Common:6; Rare:90 | ||||
| chr11:69641030-69641287 | Common:1; Rare:53 |