| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:174025295-174025352 | Rare:14 | ||||
| chr2:174026604-174026766 | Common:2; Rare:30 | ||||
| chr2:174787793-174788054 | Rare:55 | ||||
| chr2:174788576-174788788 | Common:3; Rare:55 | ||||
| chr2:175627512-175627837 | Common:1; Rare:48 | ||||
| chr2:178413910-178413982 | Rare:24 | ||||
| chr2:186544474-186544622 | Rare:21 | ||||
| chr2:188785680-188785846 | Rare:34 | ||||
| chr2:188811568-188811725 | Rare:20 | ||||
| chr2:188969390-188969507 | Rare:16 | ||||
| chr2:188990093-188990365 | Rare:80; Clinvar:3; Clinvar (benign):5; Clinvar (pathogenic):6 | ||||
| chr2:188994443-188994593 | Rare:29; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr2:188996121-188996494 | Common:12; Rare:80; Clinvar:6; Clinvar (benign):5; Clinvar (pathogenic):4 | ||||
| chr2:188997162-188997390 | Common:5; Rare:59; Clinvar:6; Clinvar (benign):9; Clinvar (pathogenic):5 | ||||
| chr2:189004025-189004364 | Rare:103; Clinvar:7; Clinvar (benign):7; Clinvar (pathogenic):20 |