Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:43006708-43006916 | Common:2; Rare:45 | ||||
chr17:43125351-43125664 | Rare:69; Clinvar:3; Clinvar (benign):2 | ||||
chr17:43170176-43170460 | Common:1; Rare:68 | ||||
chr17:43170969-43171228 | Rare:83 | ||||
chr17:43211773-43211903 | Common:1; Rare:28 | ||||
chr17:43491246-43491467 | Rare:44 | ||||
chr17:43778943-43779140 | Common:2; Rare:55 | ||||
chr17:44066290-44066365 | Rare:28 | ||||
chr17:44070636-44070911 | Common:3; Rare:93; Clinvar:4; Clinvar (benign):2 | ||||
chr17:44186699-44187050 | Rare:111 | ||||
chr17:44187153-44187307 | Rare:38 | ||||
chr17:44198371-44198551 | Common:2; Rare:43 | ||||
chr17:44219664-44219904 | Rare:82 | ||||
chr17:44324781-44324989 | Common:2; Rare:74 | ||||
chr17:44345145-44345324 | Rare:36; Clinvar:4; Clinvar (benign):3 |