| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:158801976-158802155 | Common:2; Rare:82 | ||||
| chr3:159763184-159763347 | Rare:29 | ||||
| chr3:159763632-159763751 | Rare:33 | ||||
| chr3:159764323-159764571 | Common:1; Rare:70 | ||||
| chr3:160399185-160399290 | Rare:25; Clinvar:2 | ||||
| chr3:160399518-160399656 | Rare:26 | ||||
| chr3:160565271-160565836 | Common:3; Rare:190 | ||||
| chr3:160755300-160755664 | Common:1; Rare:113 | ||||
| chr3:160756191-160756265 | Rare:21 | ||||
| chr3:161105075-161105383 | Common:4; Rare:87 | ||||
| chr3:165196714-165196982 | Common:5; Rare:95 | ||||
| chr3:167734825-167735210 | Common:3; Rare:120; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:167735617-167735741 | Rare:30 | ||||
| chr3:169146280-169146419 | Rare:34 | ||||
| chr3:169147281-169147483 | Common:2; Rare:47 |