Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:43344343-43344530 | Rare:25 | ||||
chr1:43349023-43349261 | Common:2; Rare:76; Clinvar (benign):1 | ||||
chr1:44780743-44780930 | Rare:33 | ||||
chr1:50977707-50977761 | Common:1; Rare:14 | ||||
chr1:50977940-50978186 | Common:1; Rare:85 | ||||
chr1:51421005-51421051 | Rare:10 | ||||
chr1:51423418-51423712 | Common:1; Rare:44 | ||||
chr1:51518119-51518308 | Rare:39 | ||||
chr1:51787442-51787862 | Common:1; Rare:116 | ||||
chr1:53524843-53525040 | Common:1; Rare:69 | ||||
chr1:54927533-54927685 | Rare:21 | ||||
chr1:56439625-56439857 | Common:4; Rare:35 | ||||
chr1:56645920-56646168 | Common:8; Rare:43 | ||||
chr1:57722389-57722693 | Common:2; Rare:47 | ||||
chr1:58785046-58785163 | Rare:36 |