| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:117144197-117144418 | Common:2; Rare:100 | ||||
| chr11:117179030-117179159 | Rare:24 | ||||
| chr11:117199037-117199389 | Common:6; Rare:113 | ||||
| chr11:117232036-117232190 | Rare:41 | ||||
| chr11:117232504-117232761 | Common:2; Rare:83 | ||||
| chr11:117299666-117299813 | Common:1; Rare:25 | ||||
| chr11:117316284-117316418 | Common:1; Rare:29 | ||||
| chr11:117824686-117824818 | Common:2; Rare:29; Clinvar (benign):2 | ||||
| chr11:117986277-117986507 | Common:5; Rare:84; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:118359451-118359667 | Common:3; Rare:92 | ||||
| chr11:118401332-118401672 | Rare:112 | ||||
| chr11:118790869-118791259 | Rare:113 | ||||
| chr11:118791261-118791316 | Rare:37 | ||||
| chr11:118997977-118998193 | Common:4; Rare:68 | ||||
| chr11:119018280-119018481 | Common:7; Rare:81 |