Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:3900182-3900406 | Common:12; Rare:114 | ||||
chr1:5992358-5992711 | Common:4; Rare:119; Clinvar:6 | ||||
chr1:6026166-6026377 | Common:1; Rare:47 | ||||
chr1:6199526-6199822 | Common:2; Rare:99 | ||||
chr1:6208680-6208820 | Common:1; Rare:38 | ||||
chr1:6358916-6359132 | Rare:39 | ||||
chr1:6385737-6385911 | Common:1; Rare:48 | ||||
chr1:6393755-6393918 | Rare:57 | ||||
chr1:6490525-6490696 | Rare:43 | ||||
chr1:6491567-6491793 | Common:2; Rare:30; Clinvar (benign):1 | ||||
chr1:6579803-6580056 | Common:3; Rare:84 | ||||
chr1:6701780-6701976 | Rare:62 | ||||
chr1:7771116-7771363 | Common:4; Rare:99 | ||||
chr1:7961455-7961785 | Common:4; Rare:110; Clinvar:2; Clinvar (benign):3 | ||||
chr1:8026241-8026493 | Common:3; Rare:125 |