Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:41310142-41310303 | Rare:71 | ||||
chr19:41364105-41364185 | Rare:25; Clinvar:1 | ||||
chr19:41397318-41397604 | Common:4; Rare:77 | ||||
chr19:41860051-41860524 | Common:5; Rare:175; Clinvar:4; Clinvar (benign):3 | ||||
chr19:42075840-42076210 | Rare:102 | ||||
chr19:42132416-42132629 | Rare:45 | ||||
chr19:42220128-42220354 | Common:2; Rare:62 | ||||
chr19:42302427-42302534 | Rare:21 | ||||
chr19:42423543-42423753 | Common:4; Rare:74 | ||||
chr19:42528422-42528580 | Common:2; Rare:38 | ||||
chr19:43596647-43596688 | Rare:10 | ||||
chr19:43670129-43670324 | Common:2; Rare:51 | ||||
chr19:43754839-43755094 | Common:3; Rare:103 | ||||
chr19:43827204-43827424 | Common:2; Rare:46 | ||||
chr19:43901782-43901873 | Rare:18 |