chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	96364863	96364867	AAAT	----	6	GENIC	homozygous	51554296
10	96366119	96366120	T	C	9	GENIC	possibly homozygous	51554298
10	96366523	96366524	A	G	11	GENIC	possibly homozygous	51554299
10	96366987	96366988	A	G	16	GENIC	homozygous	51554300
10	96367234	96367235	G	A	10	GENIC	heterozygous	51554301
10	96367629	96367630	A	C	10	GENIC	homozygous	51554302
10	96369485	96369486	T	C	10	GENIC	heterozygous	51554311
10	96369862	96369863	T	C	9	GENIC	possibly homozygous	51554312
10	96371384	96371385	G	C	7	GENIC	heterozygous	51554313
10	96371691	96371692	G	C	13	GENIC	possibly homozygous	51554315
10	96372375	96372376	A	G	10	GENIC	possibly homozygous	51554316
10	96373090	96373094	TTTG	----	3	GENIC	homozygous	51554317
10	96373098	96373099	T	G	3	GENIC	homozygous	52766953
10	96373126	96373127	A	-	3	GENIC	homozygous	51554319
10	96373182	96373183	T	A	11	GENIC	homozygous	51554320
10	96374018	96374019	A	ATT	1	GENIC	homozygous	51554322
10	96374574	96374575	T	C	2	GENIC	homozygous	51554326
10	96375173	96375175	TG	--	3	GENIC	heterozygous	51554327
10	96375249	96375250	T	C	6	GENIC	heterozygous	52934905
10	96375354	96375355	G	A	5	GENIC	heterozygous	51554328
10	96375479	96375480	C	T	11	GENIC	possibly homozygous	51554329
10	96375792	96375793	C	T	10	GENIC	homozygous	51554331
10	96375850	96375851	A	G	20	GENIC	possibly homozygous	51554332
10	96375905	96375906	C	T	8	GENIC	homozygous	51554333
10	96376106	96376107	C	A	7	GENIC	homozygous	51554334
10	96376406	96376407	G	A	4	GENIC	heterozygous	51554335
10	96376600	96376601	C	T	15	GENIC	homozygous	51554336
10	96377398	96377399	C	T	14	GENIC	possibly homozygous	51554337
10	96377472	96377473	G	A	7	GENIC	homozygous	51554338
10	96377801	96377802	T	-	5	GENIC	homozygous	51554339