Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr15:34101840-34102083 | Common:1; Rare:50 | ||||
chr15:34795504-34795866 | Common:1; Rare:80; Clinvar:4; Clinvar (benign):4 | ||||
chr15:35546128-35546252 | Common:1; Rare:47 | ||||
chr15:36579410-36579731 | Common:4; Rare:84 | ||||
chr15:37100484-37100776 | Common:1; Rare:99 | ||||
chr15:39933883-39934211 | Common:4; Rare:102 | ||||
chr15:40039081-40039350 | Rare:105 | ||||
chr15:40695076-40695202 | Rare:34 | ||||
chr15:40807444-40807767 | Common:4; Rare:106 | ||||
chr15:41115987-41116260 | Common:2; Rare:76 | ||||
chr15:41402450-41402573 | Common:2; Rare:40 | ||||
chr15:41416982-41417182 | Common:3; Rare:87 | ||||
chr15:41621463-41621553 | Common:1; Rare:19 | ||||
chr15:41827930-41828127 | Common:3; Rare:64 | ||||
chr15:42273126-42273272 | Common:1; Rare:71 |