Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:36573284-36573418 | Common:3; Rare:35 | ||||
chr19:36916289-36916392 | Common:1; Rare:25 | ||||
chr19:38849875-38850171 | Common:2; Rare:115 | ||||
chr19:38899531-38899993 | Rare:136 | ||||
chr19:38930742-38930992 | Common:3; Rare:65; Clinvar:2; Clinvar (benign):3 | ||||
chr19:39391115-39391418 | Common:1; Rare:129 | ||||
chr19:39406710-39406847 | Rare:52 | ||||
chr19:40348377-40348739 | Common:4; Rare:121 | ||||
chr19:41262326-41262571 | Rare:45 | ||||
chr19:41353860-41354244 | Common:2; Rare:108 | ||||
chr19:42075813-42076220 | Rare:114 | ||||
chr19:42132409-42132618 | Rare:44 | ||||
chr19:42220132-42220312 | Common:1; Rare:46 | ||||
chr19:42302332-42302480 | Rare:48 | ||||
chr19:43595973-43596392 | Common:5; Rare:129 |