Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:42422733-42423290 | Common:1; Rare:195; Clinvar:6; Clinvar (pathogenic):1 | ||||
chr17:42458806-42458914 | Rare:32 | ||||
chr17:42566994-42567127 | Common:3; Rare:40 | ||||
chr17:42577682-42577802 | Rare:57 | ||||
chr17:42609333-42609705 | Common:8; Rare:150; Clinvar (benign):1 | ||||
chr17:42761075-42761264 | Rare:52 | ||||
chr17:42798678-42798785 | Rare:32 | ||||
chr17:42852605-42852922 | Common:2; Rare:117 | ||||
chr17:42964428-42964493 | Rare:27 | ||||
chr17:43125344-43125662 | Rare:74; Clinvar:3; Clinvar (benign):2 | ||||
chr17:43170292-43170491 | Common:2; Rare:41 | ||||
chr17:43171043-43171245 | Rare:61 | ||||
chr17:44186691-44187002 | Rare:104 | ||||
chr17:44324760-44324963 | Common:2; Rare:71 | ||||
chr17:44503341-44503713 | Rare:143 |