Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:40443853-40444065 | Common:1; Rare:43 | ||||
chr17:41688858-41689039 | Common:2; Rare:96 | ||||
chr17:41812604-41813028 | Common:3; Rare:93; Clinvar:5 | ||||
chr17:41930569-41930661 | Rare:19 | ||||
chr17:42017367-42017492 | Rare:55 | ||||
chr17:42423133-42423423 | Common:1; Rare:75; Clinvar:2 | ||||
chr17:42609308-42609744 | Common:8; Rare:185; Clinvar (benign):2 | ||||
chr17:42682429-42682592 | Rare:38 | ||||
chr17:42798661-42798813 | Rare:50 | ||||
chr17:42964423-42964508 | Rare:38 | ||||
chr17:42980444-42980586 | Common:1; Rare:53 | ||||
chr17:43125297-43125716 | Rare:112; Clinvar:5; Clinvar (benign):4 | ||||
chr17:43170204-43170397 | Rare:42 | ||||
chr17:43171003-43171294 | Common:1; Rare:102 | ||||
chr17:44070620-44070936 | Common:3; Rare:109; Clinvar:4; Clinvar (benign):2 |