| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:119107086-119107717 | Common:6; Rare:151 | ||||
| chr11:119107800-119107964 | Rare:45 | ||||
| chr11:119108273-119108603 | Common:1; Rare:56 | ||||
| chr11:119121188-119121661 | Common:1; Rare:122 | ||||
| chr11:119121755-119121857 | Common:1; Rare:22 | ||||
| chr11:119168681-119169280 | Rare:131 | ||||
| chr11:119169300-119169629 | Rare:56 | ||||
| chr11:119205785-119206112 | Common:2; Rare:98 | ||||
| chr11:119206125-119206462 | Common:5; Rare:138; Clinvar:10; Clinvar (benign):6 | ||||
| chr11:119317087-119317290 | Rare:67 | ||||
| chr11:119318815-119318981 | Common:1; Rare:31 | ||||
| chr11:119320970-119321225 | Common:3; Rare:52 | ||||
| chr11:119321325-119321456 | Common:1; Rare:21 | ||||
| chr11:119334344-119334583 | Rare:66 | ||||
| chr11:119334745-119334820 | Common:2; Rare:16 |