Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:44899383-44899746 | Common:2; Rare:114; Clinvar:2; Clinvar (benign):1 | ||||
chr17:45060993-45061339 | Common:2; Rare:91 | ||||
chr17:45148247-45148476 | Rare:75 | ||||
chr17:46922856-46923174 | Common:3; Rare:82; Clinvar (benign):6 | ||||
chr17:47189268-47189568 | Rare:77 | ||||
chr17:47831501-47831641 | Rare:38 | ||||
chr17:47957822-47958023 | Rare:37 | ||||
chr17:48048061-48048384 | Rare:86 | ||||
chr17:48048649-48048812 | Common:3; Rare:22 | ||||
chr17:48590239-48590451 | Common:1; Rare:45 | ||||
chr17:48944773-48944928 | Common:2; Rare:50 | ||||
chr17:48997125-48997449 | Rare:61 | ||||
chr17:48997452-48997498 | Rare:10 | ||||
chr17:49708152-49708371 | Common:1; Rare:64 | ||||
chr17:49788410-49788704 | Rare:86 |