chr start stop reference nuc variant nuc depth genic status zygosity variant ID 17 10741444 10741445 T C 29 GENIC homozygous 942383682 17 10741502 10741503 A G 35 GENIC homozygous 942383683 17 10742269 10742270 A G 27 GENIC homozygous 942383684 17 10742613 10742614 C T 28 GENIC homozygous 942383685 17 10743548 10743549 A T 23 GENIC homozygous 942383686 17 10743592 10743593 A T 21 GENIC homozygous 942383687 17 10743593 10743594 A T 23 GENIC homozygous 942383688 17 10743594 10743595 A T 23 GENIC homozygous 942383689 17 10743861 10743862 C T 34 GENIC homozygous 942383690 17 10743946 10743947 A G 27 GENIC homozygous 942383691 17 10744694 10744695 T G 41 GENIC homozygous 942383692 17 10744844 10744845 T A 31 GENIC homozygous 942383693 17 10745781 10745782 T G 35 GENIC homozygous 942383694 17 10746039 10746040 G C 26 GENIC homozygous 942383695 17 10746047 10746048 G A 25 GENIC homozygous 942383696 17 10760680 10760681 T C 16 GENIC homozygous 942383697 17 10761275 10761276 A T 20 GENIC homozygous 942383698 17 10768419 10768420 C G 17 GENIC homozygous 942383699