chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	80006892	80006893	T	C	29	GENIC	homozygous	125526628
1	80007264	80007265	T	G	21	GENIC	homozygous	125526629
1	80007869	80007869		TGGGTGGGTGTCCCATGTTTTA	12	GENIC	homozygous	131258258
1	80008999	80009000	A	G	13	GENIC	homozygous	109297994
1	80009016	80009017	T	C	12	GENIC	homozygous	109297996
1	80009778	80009779	C	T	29	GENIC	possibly homozygous	120481128
1	80010252	80010253	A		20	GENIC	homozygous	131258259
1	80011015	80011016	T	C	17	GENIC	homozygous	120481129
1	80011131	80011132	A	G	18	GENIC	homozygous	109298002
1	80011453	80011454	G	A	20	GENIC	homozygous	120481130
1	80011657	80011657		AAAAT	14	GENIC	homozygous	131778807
1	80011800	80011801	G	A	24	GENIC	homozygous	120481131
1	80013065	80013066	T		11	GENIC	homozygous	131258260
1	80013161	80013162	T	C	19	GENIC	homozygous	109298004
1	80013534	80013535	T	C	17	GENIC	homozygous	109298006
1	80014009	80014009		TGGTT	18	GENIC	homozygous	131258261
1	80014428	80014429	G	A	8	GENIC	homozygous	121260881
1	80015797	80015798	G	A	25	GENIC	homozygous	125526632
1	80017747	80017748	T	A	23	GENIC	homozygous	125526633
1	80018607	80018608	C	G	18	GENIC	possibly homozygous	109298014
1	80019588	80019589	T	C	20	GENIC	homozygous	120779151
1	80019741	80019742	T	C	24	GENIC	homozygous	120481132
1	80019840	80019841	C	G	12	GENIC	homozygous	109298016
1	80022798	80022799	A	G	13	GENIC	homozygous	120779152
1	80024679	80024680	G	C	29	GENIC	homozygous	109298038
1	80025077	80025078	T	C	21	GENIC	homozygous	109298040
1	80026532	80026533	C	T	29	GENIC	homozygous	109298042
1	80027917	80027917		GGAAAAGGATGGGACAG	32	GENIC	possibly homozygous	131258265
1	80028724	80028725	C	T	31	GENIC	homozygous	125526634
1	80020712	80020712		A	12	GENIC	homozygous	135285995
1	80020720	80020721	T	A	12	GENIC	homozygous	131789871