| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:157160134-157160334 | Rare:81 | ||||
| chr3:158110017-158110154 | Rare:30 | ||||
| chr3:158571020-158571254 | Common:2; Rare:75 | ||||
| chr3:158801825-158802111 | Common:3; Rare:99 | ||||
| chr3:160399185-160399290 | Rare:25; Clinvar:2 | ||||
| chr3:160399495-160399669 | Rare:45; Clinvar:1 | ||||
| chr3:160565435-160565845 | Common:2; Rare:150 | ||||
| chr3:161221210-161221331 | Rare:35 | ||||
| chr3:167734830-167735232 | Common:3; Rare:128; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:167735577-167735809 | Rare:63; Clinvar:1 | ||||
| chr3:169772766-169772875 | Rare:23 | ||||
| chr3:169773270-169773459 | Common:1; Rare:69 | ||||
| chr3:169966732-169966852 | Rare:52 | ||||
| chr3:169975394-169975701 | Common:2; Rare:47 | ||||
| chr3:170358510-170358599 | Rare:33 |