| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:65638035-65638140 | Common:3; Rare:48 | ||||
| chr11:65662664-65663012 | Common:1; Rare:88 | ||||
| chr11:65711915-65712271 | Common:1; Rare:125 | ||||
| chr11:65720474-65720578 | Common:1; Rare:61 | ||||
| chr11:65856982-65857319 | Common:4; Rare:103 | ||||
| chr11:65860171-65860828 | Common:3; Rare:216 | ||||
| chr11:65861252-65861275 | Common:1; Rare:6 | ||||
| chr11:65869857-65870224 | Rare:124; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr11:65888361-65888686 | Common:1; Rare:107 | ||||
| chr11:65900241-65900491 | Common:4; Rare:53 | ||||
| chr11:65918989-65919540 | Common:2; Rare:205 | ||||
| chr11:65976375-65976763 | Rare:112 | ||||
| chr11:66002081-66002397 | Common:3; Rare:94; Clinvar:7; Clinvar (benign):3 | ||||
| chr11:66002414-66002855 | Common:2; Rare:125; Clinvar:1 | ||||
| chr11:66011903-66012008 | Rare:27 |