Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:73385670-73385869 | Common:2; Rare:79; Clinvar:8; Clinvar (benign):3 | ||||
chr2:73828804-73829005 | Common:1; Rare:45 | ||||
chr2:74147862-74148111 | Common:1; Rare:70; Clinvar:2; Clinvar (benign):1 | ||||
chr2:74440515-74440694 | Rare:51 | ||||
chr2:74465343-74465446 | Rare:29; Clinvar:1 | ||||
chr2:74482904-74483095 | Common:1; Rare:61 | ||||
chr2:74507377-74507548 | Rare:50 | ||||
chr2:74507669-74507790 | Rare:25 | ||||
chr2:74529653-74530009 | Rare:110; Clinvar:3; Clinvar (benign):1 | ||||
chr2:74654112-74654285 | Rare:43 | ||||
chr2:74958876-74959076 | Rare:71 | ||||
chr2:75560880-75561051 | Rare:35 | ||||
chr2:79087840-79088223 | Common:1; Rare:85 | ||||
chr2:79120234-79120730 | Common:7; Rare:100 | ||||
chr2:84459192-84459604 | Common:3; Rare:109; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 |