| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:197554713-197555179 | Common:5; Rare:125 | ||||
| chr3:197555350-197555488 | Rare:29 | ||||
| chr3:197555920-197556116 | Rare:50 | ||||
| chr3:197736043-197736368 | Rare:58 | ||||
| chr3:197736370-197736400 | Rare:2 | ||||
| chr3:197736792-197737251 | Common:3; Rare:143 | ||||
| chr3:197749661-197749988 | Common:1; Rare:109 | ||||
| chr3:197750576-197750763 | Common:4; Rare:55 | ||||
| chr3:197790996-197791542 | Common:3; Rare:188 | ||||
| chr3:197949860-197950296 | Common:4; Rare:126; Clinvar (benign):2 | ||||
| chr3:197959971-197960311 | Common:1; Rare:139 | ||||
| chr4:124269-124584 | Common:8; Rare:87 | ||||
| chr4:124669-124828 | Common:2; Rare:48 | ||||
| chr4:124926-125172 | Common:1; Rare:64 | ||||
| chr4:337605-337915 | Common:4; Rare:87 |