| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:112784459-112784585 | Rare:30 | ||||
| chr2:113058500-113058672 | Common:1; Rare:35 | ||||
| chr2:113117583-113118028 | Common:6; Rare:110; Clinvar:2; Clinvar (benign):3 | ||||
| chr2:113627041-113627277 | Common:1; Rare:69 | ||||
| chr2:113756489-113756792 | Common:4; Rare:99 | ||||
| chr2:113889765-113890165 | Common:8; Rare:129 | ||||
| chr2:118014056-118014249 | Common:2; Rare:104 | ||||
| chr2:118088123-118088523 | Common:2; Rare:109 | ||||
| chr2:119223601-119223845 | Common:1; Rare:70 | ||||
| chr2:119366776-119367080 | Common:1; Rare:95 | ||||
| chr2:119679072-119679216 | Common:3; Rare:46 | ||||
| chr2:120012756-120013091 | Common:3; Rare:115 | ||||
| chr2:120252580-120252967 | Common:3; Rare:127 | ||||
| chr2:121285194-121285340 | Rare:50 | ||||
| chr2:121530340-121530413 | Rare:22 |