| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:196867738-196867954 | Rare:74 | ||||
| chr3:196928027-196928337 | Common:1; Rare:48 | ||||
| chr3:196942368-196942686 | Common:1; Rare:134 | ||||
| chr3:197736784-197737221 | Common:3; Rare:140 | ||||
| chr3:197749742-197749978 | Common:1; Rare:88 | ||||
| chr3:197791074-197791357 | Common:3; Rare:108 | ||||
| chr3:197791401-197791495 | Rare:29 | ||||
| chr3:197949890-197950250 | Common:4; Rare:111; Clinvar (benign):2 | ||||
| chr3:197950692-197950978 | Common:1; Rare:68; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:197959969-197960248 | Common:1; Rare:97 | ||||
| chr4:337605-337918 | Common:4; Rare:87 | ||||
| chr4:499124-499340 | Common:3; Rare:89 | ||||
| chr4:663593-663753 | Rare:54 | ||||
| chr4:673842-673948 | Rare:45 | ||||
| chr4:674228-674588 | Common:3; Rare:168 |