Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:95526701-95526798 | Common:1; Rare:29 | ||||
chr2:96842643-96842867 | Rare:33 | ||||
chr2:99404827-99404841 | Rare:1 | ||||
chr2:99404874-99404971 | Rare:15 | ||||
chr2:104853187-104853291 | Rare:20 | ||||
chr2:105361301-105361568 | Common:3; Rare:59; Clinvar:2; Clinvar (benign):4 | ||||
chr2:113584044-113584117 | Rare:17 | ||||
chr2:113818627-113818741 | Rare:25 | ||||
chr2:131682408-131682550 | Common:3; Rare:47 | ||||
chr2:133674825-133675035 | Rare:39 | ||||
chr2:134441371-134441545 | Common:2; Rare:27 | ||||
chr2:168644127-168644275 | Common:2; Rare:22 | ||||
chr2:170770736-170771101 | Common:2; Rare:66 | ||||
chr2:178527444-178528005 | Rare:123; Clinvar:11; Clinvar (benign):7; Clinvar (pathogenic):3 | ||||
chr2:178529038-178529520 | Common:1; Rare:111; Clinvar:7; Clinvar (benign):3 |