Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:18314898-18315372 | Common:1; Rare:137 | ||||
chr17:18682211-18682521 | Common:10; Rare:30 | ||||
chr17:18697971-18698034 | Common:1; Rare:16 | ||||
chr17:18781091-18781318 | Common:5; Rare:64 | ||||
chr17:18856178-18856375 | Common:1; Rare:33 | ||||
chr17:18857929-18858221 | Common:6; Rare:74 | ||||
chr17:19004707-19004867 | Rare:52 | ||||
chr17:19362549-19362773 | Common:2; Rare:99; Clinvar:1; Clinvar (benign):2 | ||||
chr17:19377726-19377773 | Common:1; Rare:8 | ||||
chr17:19377887-19378035 | Common:1; Rare:37 | ||||
chr17:19378120-19378570 | Common:2; Rare:109 | ||||
chr17:19387148-19387512 | Common:2; Rare:88 | ||||
chr17:19648010-19648209 | Rare:45 | ||||
chr17:19648585-19649139 | Common:4; Rare:204; Clinvar:1; Clinvar (benign):1 | ||||
chr17:19977789-19977928 | Common:1; Rare:48 |