chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	115345026	115345027	T	G	31	GENIC	homozygous	116666312
8	115346931	115346932	A	G	37	GENIC	homozygous	116666314
8	115347657	115347658	A	G	42	GENIC	homozygous	116666330
8	115347694	115347695	G	A	42	GENIC	homozygous	116666332
8	115347985	115347986	C	T	53	GENIC	homozygous	116666334
8	115348784	115348785	T	C	35	GENIC	homozygous	116666344
8	115348807	115348808	T	C	38	GENIC	homozygous	116666346
8	115349094	115349095	T	A	56	GENIC	homozygous	116666348
8	115351181	115351182	A	G	47	GENIC	homozygous	116666350
8	115351572	115351573	G		56	GENIC	homozygous	128634404
8	115346133	115346133		C	52	GENIC	homozygous	128634400
8	115347259	115347259		GGAGGTCAAGGGAGGTCAAG	23	GENIC	possibly homozygous	128634401
8	115348628	115348628		CACCCATGACTGACACCCGGCAC	28	GENIC	homozygous	128634402
8	115350530	115350530		CTTTTCTTTT	31	GENIC	possibly homozygous	128634403
8	115351596	115351596		T	58	GENIC	homozygous	128634405
8	115352925	115352926	C	G	50	GENIC	homozygous	116666352
8	115353766	115353766		C	13	GENIC	heterozygous	128634406
8	115356380	115356381	G	A	62	GENIC	homozygous	116666356
8	115357653	115357659	AGTCCA		47	GENIC	homozygous	128634407
8	115358118	115358119	G	A	27	GENIC	homozygous	116666358
8	115358136	115358137	T	C	32	GENIC	homozygous	116666360