chr start stop reference nuc variant nuc depth genic status zygosity variant ID 2 111835770 111835771 T C 24 GENIC homozygous 59021738 2 111835791 111835792 G T 22 GENIC homozygous 59021739 2 111835826 111835827 A AC 23 GENIC homozygous 59021740 2 111835908 111835909 C T 18 GENIC homozygous 59021741 2 111836059 111836060 T C 10 GENIC homozygous 59021742 2 111836218 111836219 T G 20 GENIC homozygous 59021743 2 111836860 111836861 T A 19 GENIC homozygous 59021744 2 111837033 111837034 C T 20 GENIC homozygous 59021745 2 111837055 111837056 T C 16 GENIC homozygous 59021746 2 111837056 111837057 C T 16 GENIC homozygous 59021747 2 111837531 111837532 A C 23 GENIC homozygous 59021748 2 111837554 111837555 T C 21 GENIC homozygous 59021749 2 111837855 111837856 G A 25 GENIC homozygous 59021750 2 111838008 111838009 T G 13 GENIC homozygous 59021751 2 111838338 111838339 T C 18 GENIC homozygous 59021752 2 111838463 111838464 T C 19 GENIC homozygous 59021753 2 111838660 111838661 C A 14 GENIC homozygous 59021754 2 111839273 111839274 G T 15 GENIC homozygous 59021755 2 111839692 111839693 T C 12 GENIC homozygous 59021756 2 111839973 111839974 C T 10 GENIC homozygous 59021757 2 111840740 111840741 T C 15 GENIC homozygous 59021758 2 111841130 111841131 C T 8 GENIC homozygous 59021759 2 111841151 111841152 T G 10 GENIC homozygous 59021760 2 111841673 111841674 G A 13 GENIC homozygous 59021761 2 111841706 111841707 T C 13 GENIC homozygous 59021762 2 111841936 111841937 C T 16 GENIC homozygous 59021763 2 111842216 111842217 C A 19 GENIC homozygous 59021764