Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:188993310-188993479 | Rare:32; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):7 | ||||
chr2:188994224-188994831 | Common:3; Rare:151; Clinvar:5; Clinvar (benign):8; Clinvar (pathogenic):11 | ||||
chr2:188997162-188997389 | Common:5; Rare:59; Clinvar:6; Clinvar (benign):9; Clinvar (pathogenic):5 | ||||
chr2:188999362-188999577 | Rare:61; Clinvar:3; Clinvar (benign):5; Clinvar (pathogenic):16 | ||||
chr2:189003979-189004364 | Rare:115; Clinvar:10; Clinvar (benign):8; Clinvar (pathogenic):23 | ||||
chr2:189006203-189006457 | Rare:68; Clinvar:7; Clinvar (benign):5; Clinvar (pathogenic):10 | ||||
chr2:202376115-202376205 | Rare:49 | ||||
chr2:231514362-231514603 | Common:5; Rare:97 | ||||
chr2:240456692-240456920 | Rare:56 | ||||
chr2:242088467-242088669 | Common:6; Rare:62 | ||||
chr20:13220107-13220228 | Rare:44 | ||||
chr20:19757929-19758266 | Common:5; Rare:116 | ||||
chr20:35557115-35557249 | Rare:44 | ||||
chr20:36049976-36050164 | Common:1; Rare:41 | ||||
chr20:36050389-36050729 | Common:1; Rare:126 |