| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:112584346-112584633 | Common:1; Rare:79 | ||||
| chr2:112584801-112584885 | Rare:18 | ||||
| chr2:112645701-112645962 | Common:1; Rare:99 | ||||
| chr2:112646253-112646434 | Common:1; Rare:65 | ||||
| chr2:112764584-112764773 | Common:1; Rare:62; Clinvar (pathogenic):1 | ||||
| chr2:112836774-112836869 | Common:1; Rare:17; Clinvar:1 | ||||
| chr2:113157241-113157511 | Common:3; Rare:69 | ||||
| chr2:113627041-113627312 | Common:4; Rare:79 | ||||
| chr2:113756507-113756745 | Common:2; Rare:73 | ||||
| chr2:113889765-113890286 | Common:9; Rare:162 | ||||
| chr2:113891013-113891109 | Rare:24 | ||||
| chr2:118014037-118014251 | Common:2; Rare:116 | ||||
| chr2:118088171-118088550 | Common:2; Rare:95 | ||||
| chr2:118088810-118088919 | Common:1; Rare:23 | ||||
| chr2:119223624-119223875 | Common:1; Rare:77 |