| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:197736838-197737193 | Common:3; Rare:119 | ||||
| chr3:197749742-197750031 | Common:1; Rare:103 | ||||
| chr3:197912852-197913370 | Common:16; Rare:141 | ||||
| chr3:197949871-197950250 | Common:4; Rare:114; Clinvar (benign):2 | ||||
| chr3:197959979-197960248 | Common:1; Rare:93 | ||||
| chr4:337411-337888 | Common:5; Rare:137 | ||||
| chr4:499123-499324 | Common:3; Rare:79 | ||||
| chr4:663657-663727 | Rare:21 | ||||
| chr4:674212-674585 | Common:4; Rare:171 | ||||
| chr4:705684-705953 | Common:1; Rare:90 | ||||
| chr4:730927-730975 | Rare:10 | ||||
| chr4:932254-932487 | Common:2; Rare:90 | ||||
| chr4:986919-987177 | Common:3; Rare:89; Clinvar:3; Clinvar (benign):2 | ||||
| chr4:1113524-1113629 | Common:2; Rare:38 | ||||
| chr4:1172767-1173022 | Common:4; Rare:37 |