chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	128399816	128399817	A	G	7	GENIC	possibly homozygous	53234251
8	128405576	128405577	C	T	11	GENIC	homozygous	53234255
8	128407253	128407254	A	G	5	GENIC	homozygous	53234259
8	128412027	128412028	T	TA	13	GENIC	homozygous	53234264
8	128412529	128412530	A	G	15	GENIC	possibly homozygous	53234266
8	128412905	128412906	A	G	29	GENIC	homozygous	53234268
8	128413560	128413561	C	G	10	GENIC	homozygous	53234270
8	128413595	128413596	C	T	9	GENIC	homozygous	53234272
8	128413598	128413599	A	C	9	GENIC	homozygous	53234274
8	128413627	128413628	T	C	2	GENIC	homozygous	53234275
8	128413631	128413632	C	T	3	GENIC	homozygous	53234277
8	128413648	128413649	A	G	5	GENIC	homozygous	53234279
8	128413664	128413665	G	A	4	GENIC	homozygous	53234281
8	128413694	128413695	A	T	4	GENIC	heterozygous	53234282
8	128415192	128415193	T	C	21	GENIC	homozygous	53234284
8	128415622	128415623	C	CTT	2	GENIC	heterozygous	53539922
8	128417257	128417258	A	G	15	GENIC	heterozygous	53234288
8	128417336	128417337	T	C	30	GENIC	homozygous	53234290
8	128418085	128418086	T	TC	3	GENIC	homozygous	53539923
8	128419689	128419690	G	A	7	GENIC	heterozygous	53234292
8	128423893	128423894	T	C	21	GENIC	possibly homozygous	53234296
8	128424105	128424111	GTGTGT	------	1	GENIC	homozygous	53539924
8	128426511	128426512	C	T	16	GENIC	possibly homozygous	53234298
8	128426538	128426539	C	T	9	GENIC	homozygous	53234299
8	128426977	128426978	T	G	17	GENIC	possibly homozygous	53234301
8	128427035	128427036	G	GGA	2	GENIC	heterozygous	53539925
8	128427050	128427051	G	GTT	2	GENIC	heterozygous	53234303
8	128427064	128427065	T	G	1	GENIC	homozygous	53234305
8	128427084	128427085	T	A	10	GENIC	homozygous	53234307
8	128427884	128427885	A	AC	3	GENIC	heterozygous	53234309
8	128428355	128428357	AT	--	3	GENIC	homozygous	53234311