Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:7931906-7932248 | Common:5; Rare:94 | ||||
chr17:8162893-8163093 | Rare:69 | ||||
chr17:8176336-8176422 | Rare:29 | ||||
chr17:8248042-8248139 | Common:2; Rare:46; Clinvar:2; Clinvar (benign):2 | ||||
chr17:8249221-8249317 | Common:1; Rare:28 | ||||
chr17:8435689-8436034 | Common:4; Rare:131 | ||||
chr17:10059761-10059916 | Rare:29 | ||||
chr17:10697485-10697654 | Common:3; Rare:75; Clinvar:5; Clinvar (benign):2 | ||||
chr17:14069375-14069580 | Common:2; Rare:78; Clinvar:3; Clinvar (benign):3 | ||||
chr17:15260734-15261015 | Common:2; Rare:93; Clinvar (benign):4 | ||||
chr17:15699491-15699785 | Common:3; Rare:78 | ||||
chr17:15999590-16000032 | Common:3; Rare:187; Clinvar:6; Clinvar (benign):12; Clinvar (pathogenic):2 | ||||
chr17:16217094-16217235 | Rare:39; Clinvar:1 | ||||
chr17:17281194-17281379 | Rare:76 | ||||
chr17:17496390-17496513 | Rare:30 |