chr start stop reference nuc variant nuc depth genic status zygosity variant ID 8 40944157 40944158 A - 27 GENIC heterozygous 710393684 8 40944179 40944183 TCGT ---- 55 GENIC heterozygous 710393685 8 40944463 40944464 A AT 183 GENIC heterozygous 710393686 8 40944715 40944716 G - 154 GENIC heterozygous 710393687 8 40944835 40944836 C - 52 GENIC heterozygous 710393688 8 40945377 40945378 T TG 104 GENIC heterozygous 710393689 8 40946726 40946727 A - 81 GENIC heterozygous 710393690 8 40948264 40948265 T - 99 GENIC heterozygous 710393691 8 40949767 40949769 AG -- 97 GENIC heterozygous 710393692 8 40949849 40949851 AA -- 50 GENIC heterozygous 710393693 8 40949850 40949851 A - 50 GENIC heterozygous 710393694 8 40950436 40950437 A - 10 GENIC heterozygous 710393695 8 40957949 40957950 G GCTT 20 GENIC possibly homozygous 710393696 8 40958441 40958442 T - 29 GENIC possibly homozygous 710393697 8 40962585 40962586 C - 17 GENIC heterozygous 710393698 8 40963282 40963283 T - 22 GENIC heterozygous 710393699 8 40963477 40963478 C CT 20 GENIC heterozygous 710393700 8 40963805 40963806 C CTTT 20 GENIC heterozygous 710393703 8 40963806 40963808 TT -- 20 GENIC heterozygous 710393701 8 40965397 40965398 C CA 14 GENIC heterozygous 710393705 8 40965398 40965400 AA -- 14 GENIC heterozygous 710393704 8 40967667 40967668 A - 73 GENIC heterozygous 710393707 8 40968323 40968324 A ACATAGC 26 GENIC heterozygous 710393708 8 40968404 40968405 A - 15 GENIC possibly homozygous 710393709 8 40968672 40968673 C - 35 GENIC heterozygous 710393710 8 40969021 40969022 C - 15 GENIC heterozygous 710393711 8 40969556 40969557 T - 201 GENIC heterozygous 710393712 8 40969985 40969986 G - 102 GENIC heterozygous 710393713 8 40970260 40970261 G GCAAGGA 13 GENIC homozygous 710393714 8 40976084 40976085 T - 94 GENIC heterozygous 710393715