Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:86499096-86499259 | Common:2; Rare:47 | ||||
chr16:86508669-86509153 | Common:3; Rare:123 | ||||
chr16:86509559-86509699 | Rare:32 | ||||
chr16:86511067-86511346 | Common:1; Rare:104; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr16:87345150-87345445 | Common:3; Rare:88 | ||||
chr16:88769704-88769869 | Common:1; Rare:50 | ||||
chr16:90047741-90048054 | Common:8; Rare:29 | ||||
chr17:1681950-1682256 | Common:3; Rare:82; Clinvar:1; Clinvar (benign):1 | ||||
chr17:1712485-1712573 | Rare:12 | ||||
chr17:3921655-3921895 | Common:1; Rare:66 | ||||
chr17:4189383-4189593 | Rare:44 | ||||
chr17:7311034-7311481 | Rare:106 | ||||
chr17:7556841-7557119 | Rare:77; Clinvar (benign):2 | ||||
chr17:7834149-7834256 | Rare:41 | ||||
chr17:7841686-7841946 | Rare:74 |