chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	116086581	116086582	A	G	8	GENIC	homozygous	52827369
8	116086987	116086988	T	-	8	GENIC	heterozygous	53168130
8	116087103	116087105	TT	--	10	GENIC	heterozygous	53051088
8	116087104	116087105	T	-	10	GENIC	heterozygous	53051090
8	116087917	116087918	G	C	13	GENIC	possibly homozygous	53982627
8	116088536	116088537	A	G	27	GENIC	homozygous	52827376
8	116090053	116090054	A	G	10	GENIC	homozygous	52827378
8	116091185	116091186	A	G	19	GENIC	homozygous	52827385
8	116092163	116092164	C	T	27	GENIC	possibly homozygous	53305570
8	116092698	116092699	T	TG	22	GENIC	homozygous	52827391
8	116094517	116094518	G	GA	6	GENIC	homozygous	53367989
8	116094636	116094637	A	G	18	GENIC	homozygous	52827396
8	116098198	116098199	T	TGTGC	3	GENIC	homozygous	53634389
8	116101091	116101092	C	T	28	GENIC	homozygous	52827414
8	116101378	116101379	C	T	31	GENIC	homozygous	53305571
8	116101693	116101694	T	TC	24	GENIC	heterozygous	52827416
8	116101763	116101765	AC	--	16	GENIC	heterozygous	53612712
8	116101768	116101770	AG	--	17	GENIC	heterozygous	53634390
8	116102035	116102036	C	G	28	GENIC	possibly homozygous	53305572
8	116102209	116102210	G	A	27	GENIC	homozygous	52827417
8	116102467	116102468	C	G	29	GENIC	possibly homozygous	53305573
8	116102988	116102989	G	C	35	GENIC	homozygous	53305574
8	116103438	116103439	G	GAA	15	GENIC	heterozygous	52827420
8	116103438	116103439	G	GAAA	15	GENIC	possibly homozygous	53051100
8	116103538	116103539	A	G	32	GENIC	homozygous	53305575
8	116103723	116103724	A	G	20	GENIC	possibly homozygous	53305576
8	116103738	116103739	C	T	22	GENIC	possibly homozygous	53305577
8	116104285	116104286	G	GTCCCCTC	22	GENIC	homozygous	53305578
8	116104318	116104319	A	G	21	GENIC	homozygous	52827423
8	116104662	116104663	A	T	36	GENIC	homozygous	52827424