Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:61471214-61471399 | Common:4; Rare:67 | ||||
chr2:61538008-61538140 | Common:2; Rare:23 | ||||
chr2:61854023-61854180 | Common:2; Rare:66; Clinvar:1; Clinvar (benign):1 | ||||
chr2:61888405-61888695 | Common:1; Rare:135 | ||||
chr2:63588618-63589016 | Common:1; Rare:120; Clinvar (benign):1 | ||||
chr2:63840822-63841134 | Common:1; Rare:86 | ||||
chr2:64019319-64019540 | Rare:75 | ||||
chr2:64524508-64524588 | Rare:22 | ||||
chr2:64653831-64654079 | Common:1; Rare:100 | ||||
chr2:64988316-64988497 | Common:1; Rare:36 | ||||
chr2:65056130-65056381 | Rare:77 | ||||
chr2:65129921-65130077 | Common:1; Rare:52 | ||||
chr2:65227591-65227906 | Rare:92 | ||||
chr2:65432474-65432575 | Rare:20 | ||||
chr2:66435067-66435397 | Common:1; Rare:80 |