chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	75876031	75876032	C	A	25	GENIC	homozygous	61441907
1	75876116	75876117	T	C	32	GENIC	possibly homozygous	61441908
1	75877661	75877662	G	A	33	GENIC	homozygous	61879493
1	75877826	75877827	T	TAA	11	GENIC	possibly homozygous	61441909
1	75877826	75877827	T	TA	11	GENIC	heterozygous	61441910
1	75880160	75880162	CA	--	21	GENIC	homozygous	60740246
1	75881778	75881779	G	T	21	GENIC	homozygous	61441911
1	75882182	75882184	AA	--	7	GENIC	heterozygous	61441913
1	75882870	75882871	A	C	50	GENIC	homozygous	61441914
1	75883190	75883191	G	A	49	GENIC	heterozygous	60740247
1	75883197	75883198	G	A	43	GENIC	heterozygous	60740248
1	75883248	75883249	A	G	15	GENIC	heterozygous	60740249
1	75883252	75883253	A	G	11	GENIC	heterozygous	60740250
1	75883273	75883274	G	A	13	GENIC	heterozygous	60740251
1	75883292	75883293	T	C	12	GENIC	heterozygous	60740252
1	75885210	75885211	G	T	30	GENIC	heterozygous	61879494
1	75885640	75885641	A	G	38	GENIC	heterozygous	61296445
1	75885643	75885644	C	A	38	GENIC	heterozygous	61296446
1	75885725	75885726	G	T	26	GENIC	heterozygous	60740255
1	75885735	75885736	G	C	24	GENIC	heterozygous	61296447
1	75887586	75887587	T	-	32	GENIC	homozygous	61441916
1	75888611	75888612	C	T	21	GENIC	homozygous	61441917