Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:8310712-8310849 | Rare:40 | ||||
chr17:10697417-10697654 | Common:3; Rare:105; Clinvar:5; Clinvar (benign):5 | ||||
chr17:10729964-10730094 | Common:3; Rare:30 | ||||
chr17:11997450-11997600 | Rare:51 | ||||
chr17:13018012-13018284 | Common:5; Rare:71 | ||||
chr17:14069440-14069546 | Common:2; Rare:36; Clinvar:1; Clinvar (benign):2 | ||||
chr17:15260748-15260996 | Common:2; Rare:84; Clinvar (benign):4 | ||||
chr17:15262460-15262656 | Rare:44 | ||||
chr17:15563441-15563754 | Common:1; Rare:101 | ||||
chr17:15699515-15699797 | Common:3; Rare:76 | ||||
chr17:15999545-16000003 | Common:3; Rare:199; Clinvar:5; Clinvar (benign):12; Clinvar (pathogenic):2 | ||||
chr17:17281137-17281318 | Rare:73 | ||||
chr17:17496388-17496503 | Rare:28 | ||||
chr17:17591589-17591926 | Common:2; Rare:96 | ||||
chr17:18087803-18088015 | Rare:60 |