chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	90780556	90780557	A	T	10	GENIC	heterozygous	154786347
13	90780556	90780557	A		10	GENIC	heterozygous	403346025
13	90808570	90808571	A		16	GENIC	heterozygous	403346029
13	90808570	90808571	A	T	16	GENIC	possibly homozygous	403346030
13	90838245	90838246	C	T	14	GENIC	possibly homozygous	403346031
13	90838245	90838246	C		14	GENIC	heterozygous	403346032
13	90848566	90848567	A	T	8	GENIC	heterozygous	141143927
13	90848571	90848572	A	G	8	GENIC	heterozygous	141143928
13	90848572	90848573	C	T	8	GENIC	heterozygous	141143929
13	90992703	90992704	G		12	GENIC	heterozygous	403346039
13	90992703	90992704	G	C	12	GENIC	heterozygous	403346040
13	90992705	90992706	G		12	GENIC	heterozygous	403346041
13	90992705	90992706	G	C	12	GENIC	heterozygous	403346042
13	91077584	91077585	T	G	20	GENIC	heterozygous	154788377
13	91077584	91077585	T		20	GENIC	heterozygous	403740075
13	91201312	91201313	A		9	GENIC	heterozygous	139188799
13	91201312	91201313	A	G	9	GENIC	homozygous	403346049
13	91229963	91229964	G		12	GENIC	heterozygous	403346050
13	91229963	91229964	G	C	12	GENIC	heterozygous	403346051
13	91252252	91252253	G		11	GENIC	heterozygous	403346052
13	91252252	91252253	G	T	11	GENIC	homozygous	403346053
13	91252256	91252257	G	T	12	GENIC	homozygous	403346054
13	91252256	91252257	G		12	GENIC	heterozygous	403346055
13	91252270	91252271	A	T	12	GENIC	homozygous	403346056
13	91252270	91252271	A		12	GENIC	heterozygous	403346057
13	91008153	91008155	CA		19	GENIC	heterozygous	141143618
13	90946741	90946742	T		17	GENIC	possibly homozygous	141041760
13	91093241	91093242	A		25	GENIC	heterozygous	141143619
13	91217849	91217851	GT		14	GENIC	heterozygous	141143620