Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:105278860-105279059 | Common:4; Rare:31 | ||||
chr6:108562692-108562740 | Common:1; Rare:14 | ||||
chr6:108589366-108589709 | Rare:72 | ||||
chr6:108654085-108654135 | Rare:9 | ||||
chr6:117999195-117999330 | Common:3; Rare:35 | ||||
chr6:118506158-118506392 | Common:2; Rare:53 | ||||
chr6:122453807-122454162 | Common:2; Rare:80 | ||||
chr6:123105663-123105938 | Rare:47 | ||||
chr6:125214110-125214439 | Common:1; Rare:62 | ||||
chr6:129452809-129453085 | Rare:75; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr6:129460122-129460311 | Rare:54; Clinvar:3; Clinvar (pathogenic):2 | ||||
chr6:129486236-129486609 | Common:4; Rare:83; Clinvar:1; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
chr6:129512181-129512493 | Rare:85; Clinvar:5; Clinvar (benign):3 | ||||
chr6:133242256-133242496 | Common:3; Rare:45 | ||||
chr6:139289390-139289420 | Rare:3 |