| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:112584362-112584639 | Common:1; Rare:75 | ||||
| chr2:112584794-112584892 | Rare:20 | ||||
| chr2:112645701-112645944 | Common:1; Rare:89 | ||||
| chr2:112764584-112764859 | Common:2; Rare:92; Clinvar (pathogenic):1 | ||||
| chr2:113437621-113437924 | Common:4; Rare:121 | ||||
| chr2:113627047-113627341 | Common:4; Rare:83 | ||||
| chr2:113756556-113756792 | Common:3; Rare:82 | ||||
| chr2:113889709-113890272 | Common:9; Rare:182 | ||||
| chr2:113890532-113890706 | Rare:42 | ||||
| chr2:113891013-113891157 | Rare:33 | ||||
| chr2:118014020-118014221 | Common:2; Rare:110 | ||||
| chr2:118088112-118088541 | Common:2; Rare:113 | ||||
| chr2:119366591-119367059 | Common:4; Rare:115 | ||||
| chr2:119431709-119431862 | Common:4; Rare:37 | ||||
| chr2:119679072-119679219 | Common:3; Rare:46 |