Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:19485439-19485738 | Common:1; Rare:100 | ||||
chr1:19596858-19597096 | Common:2; Rare:106 | ||||
chr1:19645337-19645415 | Rare:18 | ||||
chr1:19799676-19800012 | Common:5; Rare:105 | ||||
chr1:19814799-19814952 | Common:1; Rare:52 | ||||
chr1:19815068-19815445 | Common:5; Rare:78 | ||||
chr1:20186008-20186143 | Rare:44 | ||||
chr1:20486179-20486390 | Rare:52 | ||||
chr1:20507978-20508194 | Common:2; Rare:76 | ||||
chr1:20588816-20589126 | Common:7; Rare:71 | ||||
chr1:20645382-20645716 | Common:7; Rare:119; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr1:20660948-20661025 | Common:1; Rare:28; Clinvar:1; Clinvar (benign):1 | ||||
chr1:20661340-20661692 | Common:3; Rare:126; Clinvar:4; Clinvar (benign):6 | ||||
chr1:20786594-20786786 | Rare:70 | ||||
chr1:21176848-21177174 | Common:1; Rare:98 |