| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:114400344-114400784 | Common:2; Rare:161 | ||||
| chr11:116772896-116773069 | Common:1; Rare:66 | ||||
| chr11:116787963-116788070 | Rare:33 | ||||
| chr11:117144197-117144418 | Common:2; Rare:100 | ||||
| chr11:117181182-117181452 | Common:2; Rare:59 | ||||
| chr11:117199018-117199458 | Common:6; Rare:134 | ||||
| chr11:117200568-117200824 | Common:3; Rare:62 | ||||
| chr11:117203160-117203484 | Common:2; Rare:103 | ||||
| chr11:117219111-117219286 | Common:1; Rare:40 | ||||
| chr11:117232036-117232177 | Rare:36 | ||||
| chr11:117232493-117232731 | Common:2; Rare:75 | ||||
| chr11:117986260-117986494 | Common:5; Rare:86; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:117987038-117987181 | Rare:24 | ||||
| chr11:117989751-117990035 | Common:1; Rare:42 | ||||
| chr11:118252275-118252378 | Rare:37 |