| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:113314422-113314595 | Rare:63 | ||||
| chr11:114296235-114296638 | Rare:85 | ||||
| chr11:114400444-114400748 | Common:2; Rare:123 | ||||
| chr11:115504402-115504673 | Common:1; Rare:77 | ||||
| chr11:117232515-117232749 | Common:2; Rare:78 | ||||
| chr11:118790910-118791255 | Rare:98 | ||||
| chr11:118997977-118998185 | Common:4; Rare:62 | ||||
| chr11:119018297-119018809 | Common:13; Rare:193 | ||||
| chr11:119057040-119057446 | Common:3; Rare:153 | ||||
| chr11:119067626-119067821 | Common:3; Rare:65 | ||||
| chr11:119101381-119101623 | Rare:72; Clinvar:3; Clinvar (pathogenic):2 | ||||
| chr11:119206175-119206424 | Common:5; Rare:108; Clinvar:8; Clinvar (benign):5 | ||||
| chr11:119381569-119381810 | Common:1; Rare:60 | ||||
| chr11:120210843-120211032 | Rare:49 | ||||
| chr11:124673696-124673944 | Common:4; Rare:79 |