Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:53220550-53220672 | Common:1; Rare:66 | ||||
chr1:53238464-53238592 | Rare:58 | ||||
chr1:53946262-53946385 | Rare:47 | ||||
chr1:54053161-54053308 | Rare:57 | ||||
chr1:54053384-54053616 | Common:3; Rare:72 | ||||
chr1:54199985-54200241 | Rare:69 | ||||
chr1:54887177-54887386 | Rare:67; Clinvar:1 | ||||
chr1:59296520-59296833 | Common:12; Rare:81 | ||||
chr1:62688292-62688526 | Rare:72 | ||||
chr1:62784067-62784180 | Rare:44 | ||||
chr1:63367432-63367678 | Rare:74; Clinvar (benign):1 | ||||
chr1:63523165-63523548 | Common:3; Rare:101 | ||||
chr1:66924845-66925013 | Rare:72 | ||||
chr1:67430160-67430267 | Rare:34 | ||||
chr1:67430297-67430584 | Rare:114 |