| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:119055289-119055567 | Rare:83 | ||||
| chr11:119056890-119057025 | Rare:39 | ||||
| chr11:119057028-119057481 | Common:3; Rare:168 | ||||
| chr11:119067624-119067824 | Common:3; Rare:65 | ||||
| chr11:119084795-119084949 | Common:1; Rare:45; Clinvar (benign):1 | ||||
| chr11:119095404-119095765 | Common:3; Rare:125 | ||||
| chr11:119101380-119101533 | Rare:45; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr11:119101788-119101895 | Rare:32; Clinvar:1 | ||||
| chr11:119121244-119121631 | Common:1; Rare:100 | ||||
| chr11:119206180-119206367 | Common:5; Rare:84; Clinvar:7; Clinvar (benign):4 | ||||
| chr11:119317034-119317275 | Rare:74 | ||||
| chr11:119334252-119334546 | Rare:79 | ||||
| chr11:119381653-119381843 | Common:1; Rare:37 | ||||
| chr11:119423914-119423917 | Rare:1 | ||||
| chr11:121024016-121024154 | Rare:47 |