| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:179652882-179653193 | Common:4; Rare:166 | ||||
| chr3:180601960-180602356 | Common:2; Rare:239 | ||||
| chr3:180912515-180912711 | Rare:75 | ||||
| chr3:180913085-180913374 | Rare:77 | ||||
| chr3:180989561-180989789 | Rare:155; Clinvar:3; Clinvar (benign):2 | ||||
| chr3:182793360-182793660 | Common:6; Rare:143 | ||||
| chr3:182980460-182980617 | Rare:106 | ||||
| chr3:183099441-183099742 | Common:4; Rare:188; Clinvar:6; Clinvar (benign):10 | ||||
| chr3:183635447-183635702 | Common:6; Rare:139 | ||||
| chr3:184017840-184018084 | Common:3; Rare:142 | ||||
| chr3:184134810-184135070 | Common:2; Rare:94 | ||||
| chr3:184135212-184135434 | Common:4; Rare:125; Clinvar:11 | ||||
| chr3:184155266-184155574 | Common:2; Rare:153 | ||||
| chr3:184156220-184156406 | Rare:89 | ||||
| chr3:184164107-184165001 | Common:5; Rare:515 |