Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:3767730-3768058 | Common:5; Rare:104 | ||||
chr20:3796160-3796479 | Common:2; Rare:73 | ||||
chr20:4015509-4015793 | Common:4; Rare:103 | ||||
chr20:4686225-4686475 | Common:1; Rare:56; Clinvar (benign):1 | ||||
chr20:5112862-5113168 | Common:1; Rare:114 | ||||
chr20:5119913-5120168 | Common:1; Rare:86 | ||||
chr20:5950410-5950684 | Common:8; Rare:82 | ||||
chr20:10218732-10218857 | Rare:28 | ||||
chr20:13638904-13639029 | Common:1; Rare:35 | ||||
chr20:13784894-13785080 | Common:2; Rare:82; Clinvar (benign):3 | ||||
chr20:16573321-16573540 | Common:1; Rare:59 | ||||
chr20:16729922-16730073 | Rare:44 | ||||
chr20:17569949-17570211 | Common:3; Rare:116 | ||||
chr20:17682193-17682616 | Common:5; Rare:138 | ||||
chr20:17968388-17968548 | Common:4; Rare:62 |