chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	82184942	82184943	C	T	8	GENIC	homozygous	120481754
1	82185177	82185178	C	T	17	GENIC	homozygous	108877564
1	82192007	82192008	C	T	20	GENIC	homozygous	108877569
1	82193014	82193015	A	C	23	GENIC	possibly homozygous	120481756
1	82199036	82199037	T	C	27	GENIC	homozygous	108877575
1	82199378	82199379	G	A	33	GENIC	homozygous	120481757
1	82199695	82199696	A	T	19	GENIC	homozygous	120481758
1	82200518	82200519	C	G	22	GENIC	homozygous	120820207
1	82201018	82201019	A	G	25	GENIC	homozygous	108877579
1	82201121	82201122	A	G	24	GENIC	possibly homozygous	108877580
1	82201530	82201531	C	T	18	GENIC	homozygous	108877581
1	82201639	82201640	A	G	13	GENIC	homozygous	108877582
1	82201825	82201826	T	C	15	GENIC	homozygous	108877583
1	82202052	82202053	A	G	15	GENIC	homozygous	108877585
1	82206750	82206751	G	A	24	GENIC	homozygous	120481759
1	82206937	82206938	G	A	27	GENIC	homozygous	120481760
1	82216395	82216396	T	C	17	GENIC	homozygous	108877608
1	82216717	82216718	C	A	25	GENIC	homozygous	120481761
1	82217019	82217020	A	G	14	GENIC	homozygous	108877609
1	82217229	82217230	A	G	18	GENIC	homozygous	108877611
1	82220094	82220095	C	T	28	GENIC	homozygous	120481762
1	82223102	82223103	T	C	20	GENIC	homozygous	120820208
1	82226426	82226427	A	G	20	GENIC	homozygous	108877616
1	82227963	82227964	G	A	19	GENIC	homozygous	108877617
1	82228672	82228673	A	G	14	GENIC	homozygous	108877618
1	82228860	82228861	T	A	14	GENIC	homozygous	120839563
1	82228867	82228868	A	C	14	GENIC	homozygous	120839564
1	82228875	82228876	A	T	13	GENIC	homozygous	120481763
1	82233305	82233306	G	A	37	GENIC	possibly homozygous	120481764