Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr12:122975133-122975240 | Common:1; Rare:24 | ||||
chr12:123233078-123233509 | Common:3; Rare:146; Clinvar:1 | ||||
chr12:123584351-123584627 | Common:5; Rare:102 | ||||
chr12:123584655-123584801 | Common:3; Rare:43 | ||||
chr12:123633549-123633868 | Common:2; Rare:155; Clinvar:8; Clinvar (benign):1 | ||||
chr12:123972575-123972930 | Common:6; Rare:122 | ||||
chr12:128823404-128823512 | Rare:36 | ||||
chr12:131828261-131828426 | Common:3; Rare:59 | ||||
chr12:132144309-132144480 | Rare:69 | ||||
chr12:132687322-132687654 | Common:2; Rare:120; Clinvar:2; Clinvar (benign):8 | ||||
chr12:132956260-132956370 | Common:1; Rare:26 | ||||
chr12:133130289-133130611 | Common:7; Rare:101 | ||||
chr13:19863456-19863626 | Common:2; Rare:52 | ||||
chr13:20525756-20525972 | Common:1; Rare:78 | ||||
chr13:20567020-20567201 | Common:1; Rare:63 |