Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:44186705-44187050 | Rare:106 | ||||
chr17:44187153-44187296 | Rare:35 | ||||
chr17:44324780-44324963 | Common:2; Rare:62 | ||||
chr17:44351127-44351434 | Common:1; Rare:83; Clinvar:5; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
chr17:44708531-44708665 | Rare:32 | ||||
chr17:44899391-44899468 | Rare:30 | ||||
chr17:45051406-45051680 | Common:1; Rare:89 | ||||
chr17:45060939-45061341 | Common:3; Rare:103 | ||||
chr17:45132331-45132631 | Common:2; Rare:89 | ||||
chr17:45148244-45148478 | Rare:77 | ||||
chr17:47649414-47649471 | Rare:12 | ||||
chr17:47649504-47650009 | Common:1; Rare:179 | ||||
chr17:47831462-47831690 | Rare:75 | ||||
chr17:47941382-47941635 | Rare:56; Clinvar:1 | ||||
chr17:48048051-48048377 | Rare:88 |