Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:70411063-70411344 | Common:2; Rare:74; Clinvar:1; Clinvar (benign):1 | ||||
chr1:71080956-71081400 | Rare:123 | ||||
chr1:72282841-72283367 | Common:7; Rare:169 | ||||
chr1:74198079-74198298 | Common:2; Rare:109 | ||||
chr1:74732988-74733370 | Common:6; Rare:132 | ||||
chr1:75724305-75724790 | Common:6; Rare:169; Clinvar:7; Clinvar (benign):5 | ||||
chr1:76074570-76074833 | Common:2; Rare:85 | ||||
chr1:76867350-76867543 | Rare:48 | ||||
chr1:77219384-77219521 | Rare:64 | ||||
chr1:77682641-77682688 | Rare:11 | ||||
chr1:77683322-77683583 | Common:1; Rare:85 | ||||
chr1:77759660-77759919 | Common:2; Rare:100 | ||||
chr1:77779536-77779690 | Rare:51 | ||||
chr1:77979000-77979326 | Common:3; Rare:113 | ||||
chr1:77979458-77979559 | Common:1; Rare:29 |