chr start stop reference nuc variant nuc depth genic status zygosity variant ID 17 10741444 10741445 T C 26 GENIC homozygous 814141769 17 10741502 10741503 A G 40 GENIC homozygous 814141770 17 10742269 10742270 A G 32 GENIC homozygous 814141771 17 10742613 10742614 C T 22 GENIC homozygous 814141772 17 10743548 10743549 A T 17 GENIC homozygous 814141773 17 10743861 10743862 C T 54 GENIC homozygous 814141774 17 10743946 10743947 A G 39 GENIC homozygous 814141775 17 10744694 10744695 T G 30 GENIC homozygous 814141776 17 10744844 10744845 T A 36 GENIC homozygous 814141777 17 10745781 10745782 T G 29 GENIC homozygous 814141778 17 10746039 10746040 G C 35 GENIC homozygous 814141779 17 10746047 10746048 G A 32 GENIC homozygous 814141780 17 10760680 10760681 T C 24 GENIC homozygous 814141781 17 10761275 10761276 A T 34 GENIC homozygous 814141782 17 10768419 10768420 C G 32 GENIC homozygous 814141783 17 10769187 10769188 T G 38 GENIC homozygous 814141784