| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:188994709-188994955 | Rare:42; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr2:188996122-188996501 | Common:12; Rare:81; Clinvar:6; Clinvar (benign):5; Clinvar (pathogenic):4 | ||||
| chr2:188997162-188997389 | Common:5; Rare:59; Clinvar:6; Clinvar (benign):9; Clinvar (pathogenic):5 | ||||
| chr2:188997660-188997754 | Rare:34; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):4 | ||||
| chr2:188998617-188998902 | Common:1; Rare:72; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):3 | ||||
| chr2:189002217-189002368 | Rare:39; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr2:189003935-189004371 | Rare:122; Clinvar:10; Clinvar (benign):8; Clinvar (pathogenic):24 | ||||
| chr2:189005279-189005465 | Rare:58; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):12 | ||||
| chr2:189179167-189179194 | Rare:6 | ||||
| chr2:189771854-189772043 | Rare:41 | ||||
| chr2:190912490-190912794 | Common:1; Rare:52 | ||||
| chr2:190919400-190919437 | Rare:8 | ||||
| chr2:190932519-190932831 | Common:1; Rare:64 | ||||
| chr2:191846508-191846571 | Common:2; Rare:26 | ||||
| chr2:197487172-197487390 | Common:1; Rare:47 |