Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:21345467-21345678 | Common:2; Rare:80 | ||||
chr1:21782900-21783291 | Common:2; Rare:127 | ||||
chr1:21838824-21839349 | Rare:156; Clinvar:7; Clinvar (benign):2 | ||||
chr1:21874601-21875011 | Common:2; Rare:127; Clinvar:1; Clinvar (benign):3 | ||||
chr1:21878431-21878684 | Common:1; Rare:88; Clinvar:5; Clinvar (benign):1 | ||||
chr1:22451644-22451952 | Common:1; Rare:87 | ||||
chr1:22636411-22636743 | Common:1; Rare:65 | ||||
chr1:22652912-22653297 | Common:1; Rare:83 | ||||
chr1:23019327-23019517 | Rare:61 | ||||
chr1:23050184-23050507 | Rare:69 | ||||
chr1:23344233-23344521 | Common:2; Rare:93 | ||||
chr1:23368207-23368534 | Common:1; Rare:95 | ||||
chr1:23368643-23369243 | Common:4; Rare:164 | ||||
chr1:23369807-23369938 | Rare:25 | ||||
chr1:23424450-23424528 | Rare:21 |