Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:41688676-41688894 | Common:1; Rare:75 | ||||
chr17:42609346-42609732 | Common:7; Rare:158; Clinvar (benign):2 | ||||
chr17:42773371-42773470 | Rare:27 | ||||
chr17:42833388-42833479 | Rare:39 | ||||
chr17:43125351-43125621 | Rare:54; Clinvar:3; Clinvar (benign):2 | ||||
chr17:43171063-43171245 | Rare:52 | ||||
chr17:44070619-44070911 | Common:3; Rare:98; Clinvar:4; Clinvar (benign):2 | ||||
chr17:44503377-44503710 | Rare:132 | ||||
chr17:44899375-44899707 | Common:2; Rare:103; Clinvar (benign):1 | ||||
chr17:45061080-45061339 | Common:1; Rare:75 | ||||
chr17:47323868-47323962 | Rare:35 | ||||
chr17:48048045-48048384 | Common:1; Rare:92 | ||||
chr17:48048653-48048813 | Common:3; Rare:23 | ||||
chr17:49788546-49788704 | Rare:44 | ||||
chr17:50345950-50346135 | Common:4; Rare:58 |