| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:50783592-50783851 | Common:2; Rare:86 | ||||
| chr3:197011-197314 | Common:3; Rare:105 | ||||
| chr3:2098654-2098962 | Common:4; Rare:121 | ||||
| chr3:3126786-3126981 | Common:4; Rare:80; Clinvar (benign):1 | ||||
| chr3:4303279-4303405 | Common:1; Rare:54 | ||||
| chr3:4493177-4493353 | Rare:63 | ||||
| chr3:5187299-5187657 | Common:5; Rare:135 | ||||
| chr3:8501644-8501947 | Common:2; Rare:110 | ||||
| chr3:9362997-9363109 | Rare:40 | ||||
| chr3:9397436-9397721 | Common:1; Rare:102 | ||||
| chr3:9397817-9397896 | Rare:13 | ||||
| chr3:9749789-9749991 | Rare:63 | ||||
| chr3:9769886-9769954 | Rare:23 | ||||
| chr3:9792414-9792591 | Rare:45 | ||||
| chr3:9792696-9793139 | Common:3; Rare:156 |