Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:43013042-43013327 | Common:1; Rare:84 | ||||
chr17:43125351-43125612 | Rare:50; Clinvar:3; Clinvar (benign):2 | ||||
chr17:43170978-43171233 | Rare:79 | ||||
chr17:44070612-44070951 | Common:3; Rare:120; Clinvar:4; Clinvar (benign):2 | ||||
chr17:44186701-44187038 | Rare:105 | ||||
chr17:44187161-44187310 | Common:1; Rare:39 | ||||
chr17:44324780-44324989 | Common:2; Rare:74 | ||||
chr17:44503374-44503713 | Rare:133 | ||||
chr17:44899378-44899735 | Common:2; Rare:111; Clinvar:1; Clinvar (benign):1 | ||||
chr17:45051406-45051662 | Common:1; Rare:85 | ||||
chr17:45060939-45061405 | Common:3; Rare:132 | ||||
chr17:47649420-47650007 | Common:2; Rare:201 | ||||
chr17:47831464-47831656 | Rare:61 | ||||
chr17:47941382-47941619 | Rare:48; Clinvar:1 | ||||
chr17:48048049-48048384 | Rare:92 |