chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	116109030	116109031	A	G	12	GENIC	possibly homozygous	52827433
8	116109321	116109322	A	G	20	GENIC	homozygous	52827434
8	116109374	116109375	G	A	5	GENIC	homozygous	52827435
8	116109529	116109530	C	CCCTT	7	GENIC	homozygous	52827436
8	116109837	116109838	T	C	15	GENIC	possibly homozygous	52827437
8	116110752	116110753	G	A	14	GENIC	homozygous	52827438
8	116111384	116111385	G	A	14	GENIC	possibly homozygous	52827439
8	116112150	116112151	A	G	21	GENIC	possibly homozygous	52827440
8	116112345	116112346	C	CA	2	GENIC	homozygous	52827441
8	116112472	116112473	C	A	12	GENIC	heterozygous	52827442
8	116112564	116112565	C	T	19	GENIC	homozygous	52827443
8	116112717	116112718	A	G	22	GENIC	possibly homozygous	52827444
8	116113650	116113651	T	-	2	GENIC	homozygous	53051102
8	116114055	116114056	T	C	18	GENIC	possibly homozygous	52827446
8	116114778	116114779	C	A	19	GENIC	homozygous	52827447
8	116115028	116115029	C	T	12	GENIC	homozygous	52827448
8	116115800	116115801	C	G	3	GENIC	homozygous	52827450
8	116115860	116115861	G	A	8	GENIC	homozygous	52827451
8	116117009	116117010	C	-	1	GENIC	homozygous	52827452
8	116117011	116117012	A	G	2	GENIC	homozygous	53367992
8	116117013	116117014	A	T	3	GENIC	homozygous	52827453
8	116117161	116117162	C	T	21	GENIC	heterozygous	52827454
8	116119030	116119031	C	G	5	GENIC	homozygous	52827455
8	116119374	116119375	C	T	13	GENIC	homozygous	52827456
8	116119916	116120036	AAGAGATAGGACTCTTAAGGGGCTGGGGATTTAGCTCAGTGGTAGAGCGCTTACCTAGGAAGCGCAAGGCCCTGGGTTCGGTCCCCAGCTCCGGAAAAAAAAAAAAAAAAAAAAAAAAAA	------------------------------------------------------------------------------------------------------------------------	11	GENIC	homozygous	53367993
8	116120150	116120151	A	-	1	GENIC	homozygous	52827459