Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:2470691-2471087 | Common:4; Rare:134 | ||||
chr20:2652415-2652644 | Common:7; Rare:81 | ||||
chr20:2664190-2664265 | Common:2; Rare:33 | ||||
chr20:2840410-2840755 | Common:3; Rare:106 | ||||
chr20:3071783-3071972 | Common:4; Rare:50 | ||||
chr20:3084514-3084551 | Rare:11 | ||||
chr20:3159826-3159907 | Rare:28 | ||||
chr20:3209433-3209552 | Common:1; Rare:41 | ||||
chr20:3820486-3820576 | Rare:39 | ||||
chr20:3846741-3846886 | Rare:42 | ||||
chr20:3889034-3889396 | Common:2; Rare:203; Clinvar:8; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr20:4015465-4015715 | Common:4; Rare:85 | ||||
chr20:4686212-4686473 | Common:1; Rare:61; Clinvar (benign):1 | ||||
chr20:5112866-5113168 | Common:1; Rare:114 | ||||
chr20:5119369-5119537 | Rare:52 |