Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:42017593-42017643 | Rare:15 | ||||
chr17:42423163-42423422 | Common:1; Rare:67; Clinvar:1 | ||||
chr17:42458738-42458914 | Common:1; Rare:70 | ||||
chr17:42566929-42567116 | Common:3; Rare:65 | ||||
chr17:42577631-42577844 | Rare:101 | ||||
chr17:42609330-42609723 | Common:8; Rare:164; Clinvar (benign):2 | ||||
chr17:42773362-42773488 | Rare:38 | ||||
chr17:42833346-42833461 | Rare:42 | ||||
chr17:43125321-43125590 | Rare:61; Clinvar:3; Clinvar (benign):3 | ||||
chr17:43170279-43170446 | Common:1; Rare:35 | ||||
chr17:43170966-43171245 | Rare:91 | ||||
chr17:43778917-43779062 | Rare:31 | ||||
chr17:44070612-44070935 | Common:3; Rare:110; Clinvar:4; Clinvar (benign):2 | ||||
chr17:44111237-44111447 | Rare:55 | ||||
chr17:44186658-44186998 | Common:1; Rare:126 |