chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	115345026	115345027	T	G	45	GENIC	homozygous	116666312
8	115346931	115346932	A	G	41	GENIC	homozygous	116666314
8	115347657	115347658	A	G	35	GENIC	homozygous	116666330
8	115347694	115347695	G	A	38	GENIC	homozygous	116666332
8	115347985	115347986	C	T	36	GENIC	possibly homozygous	116666334
8	115348784	115348785	T	C	43	GENIC	homozygous	116666344
8	115348807	115348808	T	C	38	GENIC	homozygous	116666346
8	115349094	115349095	T	A	49	GENIC	homozygous	116666348
8	115351181	115351182	A	G	40	GENIC	homozygous	116666350
8	115348628	115348628		CACCCATGACTGACACCCGGCAC	37	GENIC	homozygous	128634402
8	115351572	115351573	G		31	GENIC	homozygous	128634404
8	115346133	115346133		C	41	GENIC	homozygous	128634400
8	115347259	115347259		GGAGGTCAAGGGAGGTCAAG	18	GENIC	homozygous	128634401
8	115350530	115350530		CTTTTCTTTT	33	GENIC	homozygous	128634403
8	115351596	115351596		T	32	GENIC	homozygous	128634405
8	115352925	115352926	C	G	53	GENIC	homozygous	116666352
8	115353766	115353766		C	10	GENIC	heterozygous	128634406
8	115356380	115356381	G	A	56	GENIC	homozygous	116666356
8	115357653	115357659	AGTCCA		35	GENIC	homozygous	128634407
8	115358118	115358119	G	A	28	GENIC	homozygous	116666358
8	115358136	115358137	T	C	29	GENIC	homozygous	116666360
8	115358094	115358095	G	C	25	GENIC	heterozygous	132130786