| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:176150291-176150392 | Rare:24 | ||||
| chr2:176637591-176637749 | Common:2; Rare:57 | ||||
| chr2:177117467-177117526 | Rare:10 | ||||
| chr2:188606036-188606313 | Common:1; Rare:74 | ||||
| chr2:188990093-188990352 | Rare:75; Clinvar:2; Clinvar (benign):5; Clinvar (pathogenic):4 | ||||
| chr2:188994035-188994330 | Common:1; Rare:81; Clinvar:5; Clinvar (benign):4; Clinvar (pathogenic):7 | ||||
| chr2:188994537-188994672 | Rare:37; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr2:188996121-188996494 | Common:12; Rare:80; Clinvar:6; Clinvar (benign):5; Clinvar (pathogenic):4 | ||||
| chr2:188997170-188997389 | Common:5; Rare:56; Clinvar:6; Clinvar (benign):9; Clinvar (pathogenic):4 | ||||
| chr2:189001394-189001590 | Common:1; Rare:62; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):7 | ||||
| chr2:189004025-189004364 | Rare:103; Clinvar:7; Clinvar (benign):7; Clinvar (pathogenic):20 | ||||
| chr2:197450922-197451178 | Common:1; Rare:55 | ||||
| chr2:217920909-217921027 | Common:3; Rare:19 | ||||
| chr2:217980035-217980278 | Common:1; Rare:44 | ||||
| chr2:218272429-218272624 | Common:1; Rare:61 |