Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:3068966-3069228 | Common:1; Rare:61 | ||||
chr1:3796482-3796630 | Common:2; Rare:51 | ||||
chr1:3857203-3857521 | Common:1; Rare:80 | ||||
chr1:3900180-3900390 | Common:12; Rare:110 | ||||
chr1:5992376-5992772 | Common:4; Rare:128; Clinvar:6 | ||||
chr1:6199478-6199762 | Common:2; Rare:113 | ||||
chr1:6208680-6208903 | Common:1; Rare:65 | ||||
chr1:6393266-6393586 | Common:4; Rare:113 | ||||
chr1:6579781-6580069 | Common:5; Rare:96 | ||||
chr1:6613542-6613768 | Common:2; Rare:72 | ||||
chr1:6625060-6625270 | Rare:89 | ||||
chr1:7771092-7771337 | Common:4; Rare:89 | ||||
chr1:7961449-7961767 | Common:4; Rare:112; Clinvar:2; Clinvar (benign):3 | ||||
chr1:8026169-8026529 | Common:3; Rare:160 | ||||
chr1:8423616-8424007 | Common:2; Rare:147 |