| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:116787935-116788077 | Rare:52 | ||||
| chr11:117199025-117199435 | Common:6; Rare:129 | ||||
| chr11:117200006-117200263 | Common:6; Rare:54 | ||||
| chr11:117232590-117232714 | Common:2; Rare:50 | ||||
| chr11:118565052-118565337 | Common:1; Rare:42 | ||||
| chr11:118572721-118572842 | Common:1; Rare:23 | ||||
| chr11:118790900-118791259 | Rare:103 | ||||
| chr11:118997977-118998185 | Common:4; Rare:62 | ||||
| chr11:119018285-119018795 | Common:13; Rare:197 | ||||
| chr11:119057070-119057438 | Common:3; Rare:142 | ||||
| chr11:119067660-119067822 | Common:2; Rare:59 | ||||
| chr11:119206178-119206318 | Common:4; Rare:63; Clinvar:5; Clinvar (benign):3 | ||||
| chr11:120210845-120211032 | Rare:48 | ||||
| chr11:124673706-124673949 | Common:5; Rare:73 | ||||
| chr11:125625873-125625976 | Rare:35 |