Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:161166279-161166544 | Common:3; Rare:64; Clinvar:5; Clinvar (benign):1 | ||||
chr1:161196945-161197072 | Rare:23 | ||||
chr1:161197190-161197428 | Common:2; Rare:40 | ||||
chr1:161199022-161199298 | Rare:41 | ||||
chr1:161209763-161209934 | Rare:43; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
chr1:161314264-161314412 | Common:3; Rare:55; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr1:161749541-161749841 | Common:1; Rare:93 | ||||
chr1:161766217-161766601 | Common:6; Rare:114; Clinvar (pathogenic):1 | ||||
chr1:162498012-162498243 | Rare:90 | ||||
chr1:162561346-162561626 | Common:3; Rare:106 | ||||
chr1:162632292-162632576 | Rare:54 | ||||
chr1:163070895-163070942 | Rare:7 | ||||
chr1:163202910-163203210 | Common:1; Rare:58 | ||||
chr1:163321713-163322194 | Common:1; Rare:127 | ||||
chr1:165631914-165632209 | Common:3; Rare:60 |