| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:177197129-177197392 | Rare:87 | ||||
| chr3:179148028-179148213 | Common:3; Rare:64 | ||||
| chr3:179347600-179347942 | Common:1; Rare:87 | ||||
| chr3:179562669-179563066 | Rare:123 | ||||
| chr3:179604591-179604939 | Common:4; Rare:141 | ||||
| chr3:180602054-180602407 | Common:1; Rare:123 | ||||
| chr3:180679446-180679568 | Rare:25; Clinvar:3 | ||||
| chr3:180912336-180912722 | Common:4; Rare:127 | ||||
| chr3:180989610-180989804 | Rare:84; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:180989805-180989843 | Rare:13 | ||||
| chr3:182793366-182793706 | Common:3; Rare:91 | ||||
| chr3:183099397-183099690 | Common:2; Rare:103; Clinvar:3; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr3:183162687-183162851 | Common:4; Rare:33 | ||||
| chr3:183253039-183253293 | Common:3; Rare:75 | ||||
| chr3:183555603-183555770 | Rare:47 |