| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:179347592-179347768 | Common:1; Rare:40 | ||||
| chr3:179604610-179604873 | Common:2; Rare:103 | ||||
| chr3:180602100-180602235 | Common:1; Rare:44 | ||||
| chr3:180912442-180912711 | Rare:102 | ||||
| chr3:180989618-180989803 | Rare:79; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:183635569-183635670 | Common:1; Rare:33 | ||||
| chr3:183884841-183885086 | Common:2; Rare:81 | ||||
| chr3:184017870-184018092 | Common:1; Rare:70 | ||||
| chr3:184135248-184135385 | Common:2; Rare:35; Clinvar:2 | ||||
| chr3:184186039-184186204 | Common:2; Rare:66 | ||||
| chr3:184248885-184249006 | Rare:65; Clinvar:5; Clinvar (benign):2 | ||||
| chr3:184249481-184249777 | Common:1; Rare:92 | ||||
| chr3:184298944-184299276 | Common:3; Rare:101 | ||||
| chr3:184314460-184314661 | Common:3; Rare:57 | ||||
| chr3:184711953-184712202 | Common:1; Rare:91 |