Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:13017957-13018333 | Common:7; Rare:121; Clinvar (benign):2 | ||||
chr17:14069349-14069642 | Common:3; Rare:112; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
chr17:15260787-15260961 | Common:1; Rare:57 | ||||
chr17:15262455-15262668 | Rare:49 | ||||
chr17:15999590-15999999 | Common:3; Rare:182; Clinvar:5; Clinvar (benign):12; Clinvar (pathogenic):2 | ||||
chr17:16040440-16040709 | Common:2; Rare:46 | ||||
chr17:17281130-17281583 | Common:1; Rare:137 | ||||
chr17:17495978-17496043 | Rare:22 | ||||
chr17:17496388-17496532 | Rare:35 | ||||
chr17:17507016-17507267 | Common:4; Rare:75 | ||||
chr17:17591589-17591911 | Common:2; Rare:91 | ||||
chr17:18039095-18039416 | Common:3; Rare:82; Clinvar:1; Clinvar (benign):1 | ||||
chr17:18183035-18183152 | Rare:38 | ||||
chr17:18183282-18183511 | Rare:58 | ||||
chr17:18183683-18183931 | Rare:114 |