| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:179562610-179562995 | Rare:131 | ||||
| chr3:179604614-179604857 | Common:2; Rare:91 | ||||
| chr3:180602050-180602235 | Common:1; Rare:62 | ||||
| chr3:180679439-180679568 | Rare:27; Clinvar:3 | ||||
| chr3:180912442-180912505 | Rare:22 | ||||
| chr3:180912557-180912700 | Rare:55 | ||||
| chr3:180989618-180989803 | Rare:79; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:181711735-181711996 | Rare:78 | ||||
| chr3:183099462-183099755 | Common:2; Rare:88; Clinvar:2; Clinvar (benign):5 | ||||
| chr3:183884850-183884987 | Rare:51 | ||||
| chr3:184017864-184018034 | Rare:44 | ||||
| chr3:184135344-184135396 | Rare:20 | ||||
| chr3:184185861-184186203 | Common:5; Rare:127 | ||||
| chr3:184249495-184249777 | Common:1; Rare:88 | ||||
| chr3:184298944-184299269 | Common:3; Rare:100 |