| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:156816975-156817050 | Rare:33 | ||||
| chr3:157476831-157477073 | Common:3; Rare:31 | ||||
| chr3:159732251-159732375 | Rare:22 | ||||
| chr3:160419510-160419566 | Common:1; Rare:14 | ||||
| chr3:160515187-160515482 | Common:1; Rare:64 | ||||
| chr3:160566266-160566631 | Common:1; Rare:64 | ||||
| chr3:169765032-169765189 | Rare:70; Clinvar:2; Clinvar (pathogenic):2 | ||||
| chr3:170726664-170726862 | Rare:35 | ||||
| chr3:171056464-171056708 | Common:4; Rare:50 | ||||
| chr3:171066289-171066443 | Rare:30 | ||||
| chr3:171190783-171190790 | Rare:1 | ||||
| chr3:172085112-172085191 | Common:1; Rare:9 | ||||
| chr3:172163349-172163646 | Common:1; Rare:59 | ||||
| chr3:177026362-177026602 | Rare:42; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:179163527-179163732 | Common:3; Rare:38 |