Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:112674417-112674787 | Common:2; Rare:75 | ||||
chr1:112707080-112707252 | Rare:62 | ||||
chr1:112956111-112956644 | Common:6; Rare:172; Clinvar:10; Clinvar (benign):3 | ||||
chr1:113073081-113073257 | Common:1; Rare:70 | ||||
chr1:113759446-113759630 | Common:2; Rare:58 | ||||
chr1:113812233-113812653 | Common:3; Rare:164 | ||||
chr1:113904824-113905428 | Common:7; Rare:178; Clinvar (benign):1 | ||||
chr1:113979297-113979502 | Rare:51 | ||||
chr1:114152901-114153074 | Common:3; Rare:53 | ||||
chr1:114153810-114154024 | Rare:55 | ||||
chr1:114581569-114581818 | Common:1; Rare:115 | ||||
chr1:114716674-114716891 | Common:1; Rare:94; Clinvar:5; Clinvar (benign):2 | ||||
chr1:114757925-114758134 | Common:3; Rare:68 | ||||
chr1:114780539-114780809 | Common:1; Rare:103 | ||||
chr1:116373066-116373362 | Rare:96 |