Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:40120629-40120902 | Common:2; Rare:57 | ||||
chr17:40444793-40444847 | Common:1; Rare:10 | ||||
chr17:40539379-40539511 | Rare:24 | ||||
chr17:40542769-40542883 | Rare:27 | ||||
chr17:41515562-41516007 | Rare:128 | ||||
chr17:41516556-41517012 | Common:2; Rare:127 | ||||
chr17:41517018-41517282 | Rare:93 | ||||
chr17:41582204-41582369 | Rare:34 | ||||
chr17:41619808-41619836 | Rare:4 | ||||
chr17:41655619-41655921 | Common:2; Rare:63 | ||||
chr17:42050599-42050778 | Common:1; Rare:45 | ||||
chr17:42315773-42315905 | Rare:26; Clinvar (benign):1 | ||||
chr17:42422631-42422816 | Rare:77; Clinvar:2; Clinvar (pathogenic):1 | ||||
chr17:43315650-43315920 | Common:7; Rare:116 | ||||
chr17:43388310-43388391 | Rare:15 |