| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:196942347-196942682 | Common:1; Rare:144 | ||||
| chr3:197029778-197029928 | Common:1; Rare:48 | ||||
| chr3:197736745-197737128 | Common:3; Rare:114 | ||||
| chr3:197749742-197750073 | Common:1; Rare:113 | ||||
| chr3:197949894-197950250 | Common:4; Rare:110; Clinvar (benign):2 | ||||
| chr3:197950825-197950978 | Rare:37; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:197959989-197960248 | Common:1; Rare:91 | ||||
| chr4:337462-337858 | Common:1; Rare:112 | ||||
| chr4:499120-499340 | Common:3; Rare:93 | ||||
| chr4:663529-663714 | Common:1; Rare:59 | ||||
| chr4:674210-674577 | Common:3; Rare:171 | ||||
| chr4:675018-675070 | Rare:12 | ||||
| chr4:689111-689449 | Common:3; Rare:86 | ||||
| chr4:932093-932492 | Common:2; Rare:150 | ||||
| chr4:1113524-1113632 | Common:2; Rare:39 |