| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:112086721-112086921 | Rare:84; Clinvar:3; Clinvar (pathogenic):2 | ||||
| chr11:112150687-112150912 | Common:2; Rare:33 | ||||
| chr11:112163935-112164160 | Common:2; Rare:49 | ||||
| chr11:113314457-113314602 | Rare:48 | ||||
| chr11:114059400-114059897 | Common:1; Rare:99 | ||||
| chr11:114400428-114400714 | Common:2; Rare:120 | ||||
| chr11:117199025-117199406 | Common:6; Rare:120 | ||||
| chr11:117232526-117232717 | Common:2; Rare:66 | ||||
| chr11:117929363-117929576 | Common:5; Rare:44 | ||||
| chr11:117986270-117986415 | Common:4; Rare:49; Clinvar:2 | ||||
| chr11:118264252-118264602 | Common:1; Rare:53 | ||||
| chr11:118790904-118791255 | Rare:100 | ||||
| chr11:118997980-118998193 | Common:4; Rare:66 | ||||
| chr11:119018280-119018792 | Common:13; Rare:199 | ||||
| chr11:119057110-119057421 | Common:3; Rare:117 |