Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:75724277-75724634 | Common:4; Rare:103; Clinvar:3; Clinvar (benign):3 | ||||
chr1:75724637-75724816 | Common:2; Rare:86; Clinvar:4; Clinvar (benign):2 | ||||
chr1:75786784-75787076 | Common:2; Rare:63 | ||||
chr1:76074570-76074848 | Common:2; Rare:90 | ||||
chr1:77219389-77219545 | Rare:67 | ||||
chr1:77683303-77683556 | Common:1; Rare:83 | ||||
chr1:77759668-77759973 | Common:4; Rare:126 | ||||
chr1:77779536-77779686 | Rare:50 | ||||
chr1:77888073-77888219 | Rare:44 | ||||
chr1:77888373-77888741 | Common:2; Rare:84; Clinvar:2 | ||||
chr1:77978961-77979336 | Common:3; Rare:131 | ||||
chr1:77979443-77979537 | Common:1; Rare:27 | ||||
chr1:78004547-78005001 | Common:4; Rare:99 | ||||
chr1:81800422-81800621 | Rare:59 | ||||
chr1:81800666-81801004 | Common:3; Rare:112 |