Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:45490708-45490896 | Rare:62 | ||||
chr17:46923093-46923187 | Common:2; Rare:42; Clinvar:1; Clinvar (benign):7 | ||||
chr17:47188799-47188942 | Rare:22 | ||||
chr17:47189165-47189229 | Common:1; Rare:24 | ||||
chr17:47189242-47189342 | Rare:27 | ||||
chr17:47323861-47324026 | Common:2; Rare:62 | ||||
chr17:47649498-47649872 | Common:1; Rare:114 | ||||
chr17:47941354-47941708 | Rare:95; Clinvar:5; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
chr17:48048092-48048400 | Rare:72 | ||||
chr17:48048653-48048857 | Common:3; Rare:33 | ||||
chr17:48107464-48107764 | Common:5; Rare:68 | ||||
chr17:48597165-48597276 | Rare:18 | ||||
chr17:48604220-48604459 | Common:2; Rare:36 | ||||
chr17:48604947-48605130 | Common:1; Rare:32 | ||||
chr17:48610707-48611078 | Common:4; Rare:112 |