Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:75647634-75647785 | Common:1; Rare:73; Clinvar:3 | ||||
chr16:81006834-81007265 | Common:3; Rare:143 | ||||
chr16:88856932-88857156 | Common:4; Rare:99; Clinvar (benign):2 | ||||
chr17:1516628-1516949 | Rare:111 | ||||
chr17:2303783-2303980 | Common:2; Rare:73 | ||||
chr17:3668571-3668824 | Common:1; Rare:98 | ||||
chr17:3723789-3723917 | Common:1; Rare:68 | ||||
chr17:4939914-4940081 | Common:1; Rare:56 | ||||
chr17:4967806-4967909 | Rare:42 | ||||
chr17:5419674-5419869 | Common:3; Rare:48 | ||||
chr17:5486166-5486385 | Common:4; Rare:97 | ||||
chr17:6640657-6641066 | Common:7; Rare:122 | ||||
chr17:6651574-6651767 | Common:1; Rare:62 | ||||
chr17:7012326-7012667 | Rare:115 | ||||
chr17:7484203-7484370 | Common:1; Rare:66 |