| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:3558247-3558481 | Common:5; Rare:105 | ||||
| chr2:3575120-3575447 | Common:2; Rare:94; Clinvar:3; Clinvar (benign):6 | ||||
| chr2:9003955-9004054 | Rare:29 | ||||
| chr2:9423108-9423299 | Common:2; Rare:38 | ||||
| chr2:9423398-9423707 | Rare:96 | ||||
| chr2:9474502-9474594 | Common:6; Rare:51 | ||||
| chr2:9555621-9555994 | Common:2; Rare:124 | ||||
| chr2:9630816-9631344 | Common:3; Rare:164 | ||||
| chr2:9843061-9843414 | Common:6; Rare:102 | ||||
| chr2:9843416-9843541 | Common:3; Rare:36 | ||||
| chr2:9843662-9843803 | Common:3; Rare:47 | ||||
| chr2:10043326-10043756 | Common:4; Rare:186; Clinvar:4; Clinvar (benign):2 | ||||
| chr2:10689886-10689997 | Common:2; Rare:46 | ||||
| chr2:10778491-10778551 | Rare:17 | ||||
| chr2:12716750-12717051 | Common:1; Rare:87 |