| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:188994036-188994358 | Common:2; Rare:88; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):7 | ||||
| chr2:188997160-188997389 | Common:5; Rare:60; Clinvar:6; Clinvar (benign):9; Clinvar (pathogenic):6 | ||||
| chr2:188998642-188998722 | Common:1; Rare:22; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr2:189001394-189001588 | Common:1; Rare:62; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):7 | ||||
| chr2:189003948-189004393 | Rare:123; Clinvar:10; Clinvar (benign):9; Clinvar (pathogenic):24 | ||||
| chr2:190970600-190970798 | Rare:29 | ||||
| chr2:191846417-191846719 | Common:5; Rare:110 | ||||
| chr2:191847890-191848024 | Common:1; Rare:24 | ||||
| chr2:195612789-195613055 | Rare:53 | ||||
| chr2:197489170-197489320 | Rare:39; Clinvar (benign):1 | ||||
| chr2:197498801-197498917 | Common:1; Rare:32; Clinvar (benign):3 | ||||
| chr2:199459312-199459497 | Common:1; Rare:49 | ||||
| chr2:201644161-201644284 | Common:1; Rare:19 | ||||
| chr2:202376074-202376219 | Rare:80 | ||||
| chr2:203454437-203454748 | Rare:76 |