Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:161153057-161153457 | Common:5; Rare:63 | ||||
chr1:161153402-161154788 | Common:16; Rare:1236; Clinvar (pathogenic):6 | ||||
chr1:161158938-161159574 | Common:9; Rare:351 | ||||
chr1:161159999-161160699 | Common:1; Rare:145 | ||||
chr1:161160875-161161275 | Common:1; Rare:221 | ||||
chr1:161161951-161162540 | Common:4; Rare:403 | ||||
chr1:161165602-161166813 | Common:34; Rare:1123; Clinvar:35; Clinvar (benign):14 | ||||
chr1:161166828-161167228 | Common:1; Rare:162; Clinvar:5; Clinvar (pathogenic):4 | ||||
chr1:161176664-161177667 | Common:5; Rare:540 | ||||
chr1:161177640-161177940 | Rare:91 | ||||
chr1:161197175-161197673 | Common:10; Rare:164 | ||||
chr1:161198890-161199378 | Common:1; Rare:215; Clinvar (benign):1 | ||||
chr1:161201406-161201674 | Common:1; Rare:48 | ||||
chr1:161201851-161202563 | Common:16; Rare:683; Clinvar:22; Clinvar (benign):43 | ||||
chr1:161202620-161202759 | Common:2; Rare:25 |