| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:179652685-179653313 | Common:7; Rare:285 | ||||
| chr3:179653333-179653674 | Common:5; Rare:90 | ||||
| chr3:180601984-180602610 | Common:4; Rare:394 | ||||
| chr3:180679340-180679720 | Common:1; Rare:139; Clinvar:5 | ||||
| chr3:180912341-180912519 | Common:3; Rare:48 | ||||
| chr3:180912475-180912737 | Common:2; Rare:212 | ||||
| chr3:180989514-180989987 | Rare:370; Clinvar:5; Clinvar (benign):5 | ||||
| chr3:181711260-181711560 | Common:1; Rare:53 | ||||
| chr3:181711670-181712048 | Rare:258 | ||||
| chr3:182793264-182793812 | Common:11; Rare:319 | ||||
| chr3:182980004-182980277 | Common:1; Rare:71 | ||||
| chr3:182980354-182980681 | Rare:278 | ||||
| chr3:182980767-182980894 | Common:2; Rare:36 | ||||
| chr3:183099314-183099833 | Common:4; Rare:288; Clinvar:6; Clinvar (benign):11; Clinvar (pathogenic):2 | ||||
| chr3:183116020-183116350 | Common:9; Rare:177 |