| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:118997973-118998193 | Common:4; Rare:71 | ||||
| chr11:119018280-119018798 | Common:13; Rare:201 | ||||
| chr11:119057068-119057438 | Common:3; Rare:142 | ||||
| chr11:119067730-119067822 | Rare:35 | ||||
| chr11:119084826-119084908 | Rare:19 | ||||
| chr11:119101777-119101846 | Rare:19; Clinvar:1 | ||||
| chr11:119206180-119206378 | Common:5; Rare:90; Clinvar:8; Clinvar (benign):4 | ||||
| chr11:119317087-119317270 | Rare:61 | ||||
| chr11:119340589-119340693 | Rare:22 | ||||
| chr11:119381578-119381839 | Common:1; Rare:66 | ||||
| chr11:119423111-119423336 | Common:3; Rare:65 | ||||
| chr11:121292569-121292889 | Rare:106; Clinvar:3 | ||||
| chr11:123062042-123062311 | Common:5; Rare:116 | ||||
| chr11:123062373-123062677 | Common:4; Rare:142 | ||||
| chr11:123560163-123560321 | Common:1; Rare:33 |