Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:133674774-133674944 | Rare:35 | ||||
chr2:135135266-135135780 | Rare:121; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr2:157258142-157258443 | Common:1; Rare:85 | ||||
chr2:157258504-157258582 | Common:1; Rare:29 | ||||
chr2:166222666-166222941 | Common:4; Rare:30 | ||||
chr2:188990092-188990360 | Rare:78; Clinvar:3; Clinvar (benign):5; Clinvar (pathogenic):5 | ||||
chr2:188999297-188999551 | Common:1; Rare:74; Clinvar:6; Clinvar (benign):8; Clinvar (pathogenic):18 | ||||
chr2:189004029-189004365 | Rare:101; Clinvar:7; Clinvar (benign):6; Clinvar (pathogenic):20 | ||||
chr2:190954419-190954658 | Rare:41 | ||||
chr2:197401469-197401788 | Rare:66 | ||||
chr2:202033521-202033868 | Common:11; Rare:117 | ||||
chr2:202035538-202035980 | Rare:141 | ||||
chr2:202036953-202037099 | Rare:25 | ||||
chr2:202376110-202376381 | Rare:111 | ||||
chr2:215408110-215408423 | Common:1; Rare:87 |