Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:41966529-41966836 | Common:3; Rare:96 | ||||
chr17:42017144-42017474 | Rare:110 | ||||
chr17:42458541-42458914 | Common:3; Rare:131 | ||||
chr17:42566911-42567130 | Common:3; Rare:76 | ||||
chr17:42577664-42577869 | Common:1; Rare:104 | ||||
chr17:42609333-42609705 | Common:8; Rare:150; Clinvar (benign):1 | ||||
chr17:42773375-42773491 | Rare:37 | ||||
chr17:42833378-42833454 | Rare:30 | ||||
chr17:42998361-42998486 | Common:3; Rare:42 | ||||
chr17:43125345-43125654 | Rare:74; Clinvar:3; Clinvar (benign):2 | ||||
chr17:43170292-43170511 | Common:2; Rare:43 | ||||
chr17:43170972-43171255 | Rare:94 | ||||
chr17:43211773-43211895 | Common:1; Rare:28 | ||||
chr17:43483659-43484024 | Rare:97 | ||||
chr17:44070620-44070935 | Common:3; Rare:109; Clinvar:4; Clinvar (benign):2 |