chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	87127117	87127118	G	A	23	GENIC	possibly homozygous	52700486
8	87127593	87127597	TGTG	----	1	GENIC	homozygous	52700488
8	87127630	87127631	A	G	8	GENIC	heterozygous	52700495
8	87129054	87129055	A	AAAG	3	GENIC	heterozygous	53364862
8	87133909	87133910	A	ACACT	7	GENIC	possibly homozygous	52700535
8	87145208	87145209	G	A	3	GENIC	heterozygous	53325131
8	87146995	87146996	A	G	14	GENIC	possibly homozygous	52700591
8	87158964	87158965	T	G	19	GENIC	homozygous	52700631
8	87161248	87161249	C	-	15	GENIC	possibly homozygous	52700653
8	87180537	87180538	A	-	5	GENIC	heterozygous	52700712
8	87182606	87182607	G	A	16	GENIC	homozygous	53325134
8	87182647	87182648	C	T	3	GENIC	heterozygous	53364863
8	87182648	87182649	C	G	3	GENIC	heterozygous	53364864
8	87187760	87187761	A	AGTAC	2	GENIC	homozygous	53402700
8	87187914	87187915	C	T	3	GENIC	homozygous	52700809
8	87187916	87187917	C	A	3	GENIC	homozygous	52700811
8	87211890	87211891	C	T	10	GENIC	possibly homozygous	53325136
8	87215367	87215368	G	A	13	GENIC	homozygous	52700999
8	87221174	87221175	A	G	27	GENIC	possibly homozygous	52701013
8	87226579	87226580	G	A	7	GENIC	possibly homozygous	53325137
8	87236177	87236178	C	T	32	GENIC	homozygous	53325138
8	87245664	87245668	CATA	----	1	GENIC	homozygous	53182776
8	87247188	87247189	C	T	25	GENIC	homozygous	53325139
8	87250307	87250308	A	C	10	GENIC	homozygous	52701155
8	87254193	87254194	G	A	11	GENIC	possibly homozygous	52701167
8	87255951	87255952	T	C	3	GENIC	heterozygous	53325140
8	87262560	87262561	C	A	17	GENIC	homozygous	53325141
8	87267345	87267346	T	C	22	GENIC	homozygous	52701304