Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:160270311-160270476 | Common:1; Rare:46 | ||||
chr2:178413921-178413982 | Rare:21 | ||||
chr2:188994780-188995099 | Rare:67; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):3 | ||||
chr2:188996176-188996496 | Common:12; Rare:71; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
chr2:189008864-189008978 | Rare:31; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):5 | ||||
chr2:202376074-202376219 | Rare:80 | ||||
chr2:207163530-207163703 | Rare:27 | ||||
chr2:207239392-207239666 | Rare:42 | ||||
chr2:207310309-207310519 | Common:1; Rare:43 | ||||
chr2:218402615-218402714 | Rare:37 | ||||
chr2:219685033-219685327 | Common:1; Rare:81 | ||||
chr2:226652448-226652711 | Rare:54 | ||||
chr2:226796097-226796258 | Rare:60 | ||||
chr2:226796793-226797000 | Rare:61; Clinvar (pathogenic):1 | ||||
chr2:226797309-226797446 | Rare:50 |