| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:114296251-114296602 | Rare:65 | ||||
| chr11:114400032-114400133 | Rare:47 | ||||
| chr11:114400421-114400723 | Common:2; Rare:124 | ||||
| chr11:116772949-116773069 | Rare:46 | ||||
| chr11:117232043-117232177 | Rare:33 | ||||
| chr11:117232555-117232758 | Common:2; Rare:72 | ||||
| chr11:117986274-117986441 | Common:4; Rare:61; Clinvar:2 | ||||
| chr11:118790894-118791263 | Rare:107 | ||||
| chr11:118997973-118998186 | Common:4; Rare:66 | ||||
| chr11:119017925-119018170 | Common:2; Rare:89 | ||||
| chr11:119018280-119018795 | Common:13; Rare:199 | ||||
| chr11:119057068-119057448 | Common:3; Rare:149 | ||||
| chr11:119067630-119067821 | Common:3; Rare:65 | ||||
| chr11:119206180-119206367 | Common:5; Rare:84; Clinvar:7; Clinvar (benign):4 | ||||
| chr11:119381597-119381721 | Rare:36 |