chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	71700089	71700091	GT	--	3	GENIC	heterozygous	52673688
8	71711227	71711228	G	A	37	GENIC	heterozygous	52673689
8	71711273	71711274	C	T	54	GENIC	heterozygous	52673690
8	71711282	71711283	A	G	56	GENIC	heterozygous	52673691
8	71711285	71711286	C	A	59	GENIC	heterozygous	52673692
8	71711636	71711637	T	-	16	GENIC	heterozygous	52673693
8	71713253	71713254	G	A	16	GENIC	heterozygous	52673694
8	71715133	71715134	A	AT	10	GENIC	heterozygous	52673695
8	71717294	71717295	A	-	29	GENIC	heterozygous	52673696
8	71720629	71720630	T	-	19	GENIC	heterozygous	52673697
8	71720654	71720655	C	T	34	GENIC	heterozygous	52673698
8	71721837	71721843	GTGTGT	------	7	GENIC	homozygous	52673699
8	71732079	71732082	CCC	---	9	GENIC	heterozygous	52673700
8	71778411	71778412	T	C	26	GENIC	heterozygous	52673701
8	71780978	71780979	A	-	6	GENIC	homozygous	52673702
8	71782233	71782234	G	GT	22	GENIC	homozygous	52673703
8	71786487	71786488	C	T	18	GENIC	heterozygous	52673704
8	71789595	71789596	G	-	4	GENIC	homozygous	52673705
8	71789595	71789596	G	GT	4	GENIC	homozygous	52673706
8	71796071	71796072	C	CA	5	GENIC	homozygous	52673707
8	71802037	71802038	T	-	16	GENIC	heterozygous	52673708
8	71822772	71822773	A	C	20	GENIC	heterozygous	52673709
8	71843591	71843593	GT	--	13	GENIC	heterozygous	52673710
8	71845019	71845020	C	-	11	GENIC	homozygous	52673711
8	71845042	71845043	C	CA	1	GENIC	homozygous	52673712