Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:42112689-42112809 | Common:1; Rare:31 | ||||
chr17:42154904-42155234 | Common:3; Rare:85 | ||||
chr17:42423064-42423455 | Common:1; Rare:110; Clinvar:2 | ||||
chr17:42458738-42458945 | Common:3; Rare:79 | ||||
chr17:42566883-42567149 | Common:3; Rare:91 | ||||
chr17:42577645-42577869 | Common:1; Rare:113 | ||||
chr17:42609333-42609775 | Common:8; Rare:178; Clinvar (benign):2 | ||||
chr17:42682417-42682609 | Rare:45 | ||||
chr17:42760959-42761350 | Common:2; Rare:105 | ||||
chr17:42773362-42773501 | Rare:43 | ||||
chr17:42833351-42833497 | Rare:56 | ||||
chr17:42964419-42964552 | Common:1; Rare:60 | ||||
chr17:42998322-42998572 | Common:4; Rare:75 | ||||
chr17:43020165-43020387 | Rare:46 | ||||
chr17:43125288-43125597 | Rare:80; Clinvar:7; Clinvar (benign):5 |