Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:43367961-43368216 | Rare:68 | ||||
chr1:43389752-43389937 | Common:3; Rare:82 | ||||
chr1:44674411-44674724 | Common:3; Rare:84 | ||||
chr1:44775459-44775615 | Common:1; Rare:62 | ||||
chr1:45339978-45340236 | Rare:91; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
chr1:45500065-45500350 | Common:1; Rare:71; Clinvar:4; Clinvar (pathogenic):3 | ||||
chr1:45521864-45522077 | Common:1; Rare:84 | ||||
chr1:45550689-45551097 | Common:3; Rare:105 | ||||
chr1:45687059-45687312 | Common:1; Rare:69 | ||||
chr1:45688019-45688211 | Common:1; Rare:42 | ||||
chr1:46132626-46132755 | Rare:46 | ||||
chr1:46198399-46198525 | Common:1; Rare:50; Clinvar:1 | ||||
chr1:46303301-46303740 | Common:2; Rare:119 | ||||
chr1:46393620-46393789 | Rare:31 | ||||
chr1:47333703-47333984 | Common:3; Rare:92 |