| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:181711735-181712052 | Rare:87 | ||||
| chr3:183099460-183099800 | Common:2; Rare:95; Clinvar:3; Clinvar (benign):5 | ||||
| chr3:183635375-183635655 | Common:3; Rare:71 | ||||
| chr3:183884833-183885204 | Common:3; Rare:112 | ||||
| chr3:184017856-184018078 | Common:1; Rare:67 | ||||
| chr3:184135215-184135395 | Common:2; Rare:53; Clinvar:5 | ||||
| chr3:184142576-184142869 | Rare:76; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:184155218-184155500 | Rare:83 | ||||
| chr3:184185931-184186256 | Common:4; Rare:127 | ||||
| chr3:184243582-184243823 | Common:1; Rare:66; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:184245195-184245498 | Common:2; Rare:94; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):3 | ||||
| chr3:184248754-184248815 | Rare:16; Clinvar (pathogenic):1 | ||||
| chr3:184248886-184249008 | Rare:64; Clinvar:5; Clinvar (benign):2 | ||||
| chr3:184249445-184249771 | Common:1; Rare:95 | ||||
| chr3:184303946-184304390 | Rare:101 |