Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:42817213-42817616 | Rare:126 | ||||
chr1:42846387-42846648 | Common:1; Rare:77 | ||||
chr1:42958754-42959066 | Common:3; Rare:83; Clinvar:5; Clinvar (benign):4 | ||||
chr1:43172214-43172359 | Common:1; Rare:68 | ||||
chr1:43270933-43271049 | Rare:26 | ||||
chr1:43285519-43285660 | Common:1; Rare:30 | ||||
chr1:43300817-43301060 | Common:3; Rare:45 | ||||
chr1:43358660-43359006 | Common:7; Rare:111 | ||||
chr1:43367917-43368208 | Rare:76 | ||||
chr1:43389752-43389955 | Common:3; Rare:94 | ||||
chr1:43946553-43946983 | Rare:115 | ||||
chr1:43974788-43975068 | Common:3; Rare:74 | ||||
chr1:44031420-44031668 | Common:2; Rare:50 | ||||
chr1:44631922-44632106 | Common:1; Rare:63 | ||||
chr1:44674406-44674749 | Common:3; Rare:92 |