chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
18	15757520	15757521	A	T	12	GENIC	homozygous	46368279
18	15757636	15757637	T	C	16	GENIC	homozygous	46368280
18	15758367	15758368	G	A	20	GENIC	heterozygous	46368281
18	15759605	15759606	A	G	20	GENIC	heterozygous	46368282
18	15759645	15759646	G	A	12	GENIC	heterozygous	46368283
18	15760426	15760427	C	T	23	GENIC	possibly homozygous	46368284
18	15764586	15764587	A	G	20	GENIC	possibly homozygous	46368288
18	15765235	15765237	AA	--	1	GENIC	homozygous	46368289
18	15765356	15765357	A	G	8	GENIC	homozygous	46368290
18	15765540	15765541	T	C	3	GENIC	homozygous	46368291
18	15765615	15765617	GA	--	2	GENIC	heterozygous	46368292
18	15766493	15766494	A	G	19	GENIC	homozygous	46368294
18	15768585	15768586	T	C	5	GENIC	heterozygous	46368297
18	15769057	15769058	C	G	21	GENIC	possibly homozygous	46368298
18	15769294	15769295	G	T	9	GENIC	heterozygous	46368299
18	15770429	15770430	C	-	1	GENIC	homozygous	46368300
18	15770438	15770440	AA	--	2	GENIC	heterozygous	46368301
18	15770888	15770889	A	C	18	GENIC	possibly homozygous	46368302
18	15771202	15771203	G	A	18	GENIC	possibly homozygous	46368303
18	15771409	15771410	C	T	18	GENIC	heterozygous	46368304