| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:96265968-96266348 | Common:2; Rare:114; Clinvar:1 | ||||
| chr2:96305394-96305662 | Common:2; Rare:96; Clinvar:3; Clinvar (benign):2 | ||||
| chr2:96325216-96325412 | Rare:54 | ||||
| chr2:96335670-96335848 | Common:2; Rare:66 | ||||
| chr2:96536569-96536760 | Common:1; Rare:51 | ||||
| chr2:96637184-96637427 | Rare:42 | ||||
| chr2:96638282-96638459 | Common:1; Rare:45 | ||||
| chr2:96642626-96642794 | Rare:34 | ||||
| chr2:96740039-96740268 | Common:5; Rare:60 | ||||
| chr2:96857887-96858232 | Common:2; Rare:124 | ||||
| chr2:96868522-96868800 | Rare:70 | ||||
| chr2:97094820-97094966 | Common:1; Rare:30 | ||||
| chr2:97112889-97113247 | Common:1; Rare:82 | ||||
| chr2:97113381-97113770 | Common:4; Rare:109 | ||||
| chr2:97589689-97589995 | Common:7; Rare:78 |