Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:161021012-161021260 | Common:5; Rare:80 | ||||
chr1:161041774-161041996 | Common:2; Rare:52 | ||||
chr1:161044974-161045264 | Common:1; Rare:55 | ||||
chr1:161045867-161046075 | Common:1; Rare:53 | ||||
chr1:161069786-161070117 | Rare:46 | ||||
chr1:161098207-161098381 | Common:1; Rare:26 | ||||
chr1:161118012-161118141 | Rare:64 | ||||
chr1:161131690-161131792 | Rare:18 | ||||
chr1:161132389-161132667 | Common:1; Rare:91 | ||||
chr1:161166268-161166689 | Common:4; Rare:102; Clinvar:5; Clinvar (benign):2 | ||||
chr1:161176245-161176416 | Rare:29 | ||||
chr1:161199051-161199321 | Rare:43 | ||||
chr1:161215155-161215370 | Common:2; Rare:74 | ||||
chr1:161225768-161226069 | Common:10; Rare:44 | ||||
chr1:161314262-161314433 | Common:3; Rare:68; Clinvar:10; Clinvar (benign):3; Clinvar (pathogenic):1 |