| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:118925871-118926051 | Common:1; Rare:51 | ||||
| chr11:118997960-118998252 | Common:4; Rare:104 | ||||
| chr11:119017955-119018876 | Common:15; Rare:331 | ||||
| chr11:119019009-119019226 | Common:3; Rare:86 | ||||
| chr11:119057010-119057470 | Common:3; Rare:169 | ||||
| chr11:119067632-119067826 | Common:3; Rare:64 | ||||
| chr11:119091369-119091416 | Rare:18; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr11:119095076-119095322 | Common:1; Rare:61 | ||||
| chr11:119095398-119095737 | Common:3; Rare:124 | ||||
| chr11:119101015-119101467 | Rare:115; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr11:119101750-119101956 | Rare:53; Clinvar:3 | ||||
| chr11:119121262-119121647 | Common:1; Rare:97 | ||||
| chr11:119206226-119206396 | Common:4; Rare:74; Clinvar:8; Clinvar (benign):4 | ||||
| chr11:119334252-119334607 | Common:1; Rare:99 | ||||
| chr11:119364172-119364311 | Common:2; Rare:58 |