| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:178558701-178558947 | Rare:48 | ||||
| chr3:179148088-179148196 | Common:3; Rare:44 | ||||
| chr3:179604620-179604925 | Common:3; Rare:121 | ||||
| chr3:180602054-180602381 | Common:1; Rare:114 | ||||
| chr3:180679457-180679552 | Rare:18; Clinvar:3 | ||||
| chr3:180989610-180989795 | Rare:82; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:183099443-183099707 | Common:2; Rare:87; Clinvar:3; Clinvar (benign):5 | ||||
| chr3:183253063-183253293 | Common:2; Rare:68 | ||||
| chr3:183884837-183884969 | Rare:53 | ||||
| chr3:184017876-184018103 | Common:1; Rare:70 | ||||
| chr3:184135248-184135385 | Common:2; Rare:35; Clinvar:2 | ||||
| chr3:184156612-184156630 | Rare:3 | ||||
| chr3:184249515-184249682 | Rare:42 | ||||
| chr3:184298947-184299290 | Common:3; Rare:110 | ||||
| chr3:184305566-184305895 | Common:2; Rare:66 |