Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:7885213-7885331 | Rare:35 | ||||
chr17:7931906-7932268 | Common:5; Rare:103 | ||||
chr17:8087783-8088100 | Rare:63 | ||||
chr17:8147536-8147774 | Common:1; Rare:88 | ||||
chr17:8151929-8151988 | Rare:11 | ||||
chr17:8152378-8152695 | Common:4; Rare:77 | ||||
chr17:8248040-8248119 | Common:2; Rare:41; Clinvar:2; Clinvar (benign):2 | ||||
chr17:8435705-8436034 | Common:4; Rare:125 | ||||
chr17:8867661-8867775 | Common:1; Rare:19 | ||||
chr17:8965667-8965789 | Common:1; Rare:36 | ||||
chr17:10697505-10697654 | Common:3; Rare:57; Clinvar:2; Clinvar (benign):2 | ||||
chr17:10729754-10729801 | Rare:25 | ||||
chr17:14069323-14069546 | Common:2; Rare:69; Clinvar:1; Clinvar (benign):2 | ||||
chr17:15999590-16000028 | Common:3; Rare:185; Clinvar:6; Clinvar (benign):12; Clinvar (pathogenic):2 | ||||
chr17:17591604-17591926 | Common:1; Rare:92 |