Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:6444111-6444455 | Common:2; Rare:97 | ||||
chr17:6640415-6641090 | Common:9; Rare:190 | ||||
chr17:6651517-6651672 | Common:1; Rare:53 | ||||
chr17:7012278-7012865 | Rare:189 | ||||
chr17:7035778-7036026 | Rare:59 | ||||
chr17:7176884-7177000 | Common:2; Rare:40 | ||||
chr17:7191995-7192084 | Rare:32 | ||||
chr17:7204878-7204982 | Rare:24 | ||||
chr17:7205091-7205304 | Common:2; Rare:45 | ||||
chr17:7213857-7214181 | Common:1; Rare:69 | ||||
chr17:7217046-7217125 | Common:1; Rare:15 | ||||
chr17:7219700-7219944 | Common:3; Rare:89; Clinvar:5; Clinvar (benign):1 | ||||
chr17:7224577-7224830 | Common:1; Rare:82; Clinvar:5; Clinvar (benign):11; Clinvar (pathogenic):2 | ||||
chr17:7234201-7234337 | Rare:55 | ||||
chr17:7234456-7234648 | Common:2; Rare:102 |