Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:7583542-7583858 | Common:1; Rare:130; Clinvar:3; Clinvar (benign):3 | ||||
chr17:7931898-7932216 | Common:5; Rare:88 | ||||
chr17:8162898-8163093 | Rare:66 | ||||
chr17:8248042-8248136 | Common:2; Rare:45; Clinvar:2; Clinvar (benign):2 | ||||
chr17:8249180-8249317 | Common:1; Rare:40 | ||||
chr17:8965709-8965802 | Common:1; Rare:28 | ||||
chr17:10421857-10422095 | Common:2; Rare:43 | ||||
chr17:10629852-10630201 | Rare:104; Clinvar:3 | ||||
chr17:10657184-10657585 | Common:4; Rare:115 | ||||
chr17:10697481-10697654 | Common:3; Rare:78; Clinvar:5; Clinvar (benign):2 | ||||
chr17:10729980-10730121 | Common:3; Rare:30 | ||||
chr17:14069440-14069549 | Common:2; Rare:37; Clinvar:1; Clinvar (benign):2 | ||||
chr17:15260756-15260961 | Common:1; Rare:72; Clinvar (benign):2 | ||||
chr17:15262455-15262658 | Rare:47 | ||||
chr17:15651844-15652017 | Rare:28 |