| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:161308334-161308566 | Common:2; Rare:56 | ||||
| chr2:163735995-163736113 | Rare:22 | ||||
| chr2:165469538-165469701 | Rare:27 | ||||
| chr2:165953809-165954118 | Common:4; Rare:84; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:166375896-166376104 | Common:4; Rare:62; Clinvar:1; Clinvar (benign):5 | ||||
| chr2:168890344-168890613 | Common:2; Rare:64 | ||||
| chr2:169509512-169509774 | Rare:45 | ||||
| chr2:169584325-169584415 | Rare:44 | ||||
| chr2:169584709-169584809 | Rare:26 | ||||
| chr2:169694369-169694529 | Common:4; Rare:51 | ||||
| chr2:169798778-169798965 | Rare:47 | ||||
| chr2:170928949-170929324 | Common:4; Rare:114 | ||||
| chr2:171433945-171434248 | Common:2; Rare:77 | ||||
| chr2:171434726-171434886 | Common:1; Rare:33 | ||||
| chr2:171522260-171522525 | Common:3; Rare:64 |