Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:179882183-179882324 | Rare:28 | ||||
chr1:179882474-179882841 | Rare:171; Clinvar:7; Clinvar (benign):2 | ||||
chr1:179882843-179882884 | Rare:24; Clinvar:2 | ||||
chr1:179954697-179954822 | Rare:28 | ||||
chr1:180631849-180632135 | Common:5; Rare:105 | ||||
chr1:181088494-181088701 | Rare:67 | ||||
chr1:182391286-182391427 | Rare:29 | ||||
chr1:182391744-182391948 | Common:2; Rare:68; Clinvar:2; Clinvar (benign):2 | ||||
chr1:182789634-182789778 | Common:2; Rare:48 | ||||
chr1:182839213-182839376 | Common:1; Rare:69 | ||||
chr1:183472255-183472552 | Common:2; Rare:105 | ||||
chr1:183635666-183636094 | Common:4; Rare:123 | ||||
chr1:184386907-184387158 | Rare:69 | ||||
chr1:184387344-184387367 | Rare:7 | ||||
chr1:184754812-184755209 | Common:1; Rare:103 |