Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:41688848-41689045 | Common:2; Rare:103 | ||||
chr17:41812604-41813032 | Common:3; Rare:94; Clinvar:5 | ||||
chr17:42017367-42017576 | Common:1; Rare:79 | ||||
chr17:42423149-42423422 | Common:1; Rare:71; Clinvar:1 | ||||
chr17:42536124-42536275 | Common:1; Rare:51; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
chr17:42577667-42577844 | Rare:86 | ||||
chr17:42609320-42609730 | Common:8; Rare:172; Clinvar (benign):2 | ||||
chr17:42682388-42682710 | Common:3; Rare:67 | ||||
chr17:42798661-42798792 | Rare:44 | ||||
chr17:42833309-42833623 | Common:1; Rare:103 | ||||
chr17:42964430-42964579 | Common:1; Rare:62 | ||||
chr17:42980444-42980582 | Common:1; Rare:49 | ||||
chr17:43125338-43125708 | Rare:92; Clinvar:3; Clinvar (benign):2 | ||||
chr17:43170204-43170418 | Common:1; Rare:47 | ||||
chr17:43171002-43171295 | Common:1; Rare:102 |