| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:159852997-159853288 | Rare:50 | ||||
| chr3:160399171-160399307 | Rare:35; Clinvar:2 | ||||
| chr3:160399500-160399697 | Rare:52; Clinvar:1 | ||||
| chr3:160414206-160414452 | Common:3; Rare:65 | ||||
| chr3:160449710-160449993 | Common:2; Rare:93 | ||||
| chr3:160565271-160565831 | Common:3; Rare:189 | ||||
| chr3:160676988-160677285 | Common:3; Rare:38 | ||||
| chr3:160755455-160755752 | Common:2; Rare:95 | ||||
| chr3:160756042-160756265 | Rare:53 | ||||
| chr3:161105025-161105110 | Common:1; Rare:26 | ||||
| chr3:161105239-161105386 | Common:2; Rare:50 | ||||
| chr3:161221429-161221582 | Common:2; Rare:39 | ||||
| chr3:161371466-161371660 | Common:2; Rare:34 | ||||
| chr3:167734811-167735237 | Common:3; Rare:140; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:167735577-167735752 | Rare:44 |