chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	116086581	116086582	A	G	10	GENIC	possibly homozygous	52827369
8	116086987	116086988	T	-	2	GENIC	heterozygous	53168130
8	116088536	116088537	A	G	10	GENIC	homozygous	52827376
8	116091185	116091186	A	G	13	GENIC	possibly homozygous	52827385
8	116092163	116092164	C	T	4	GENIC	heterozygous	53305570
8	116094517	116094518	G	GA	2	GENIC	heterozygous	53367989
8	116094636	116094637	A	G	12	GENIC	homozygous	52827396
8	116101091	116101092	C	T	15	GENIC	homozygous	52827414
8	116101378	116101379	C	T	17	GENIC	possibly homozygous	53305571
8	116102035	116102036	C	G	8	GENIC	possibly homozygous	53305572
8	116102209	116102210	G	A	6	GENIC	homozygous	52827417
8	116102467	116102468	C	G	9	GENIC	homozygous	53305573
8	116102988	116102989	G	C	14	GENIC	homozygous	53305574
8	116103538	116103539	A	G	2	GENIC	heterozygous	53305575
8	116103723	116103724	A	G	9	GENIC	homozygous	53305576
8	116103738	116103739	C	T	7	GENIC	homozygous	53305577
8	116104285	116104286	G	GTCCCCTC	4	GENIC	heterozygous	53305578
8	116104318	116104319	A	G	15	GENIC	possibly homozygous	52827423
8	116104662	116104663	A	T	15	GENIC	homozygous	52827424