chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	41649672	41649673	T	C	17	GENIC	homozygous	52598918
8	41650813	41650814	A	AT	18	GENIC	heterozygous	52599008
8	41651149	41651150	A	AG	15	GENIC	heterozygous	52599019
8	41651150	41651151	G	-	15	GENIC	heterozygous	52599024
8	41651223	41651224	A	AG	5	GENIC	heterozygous	52599029
8	41651223	41651224	A	AC	5	GENIC	heterozygous	52599031
8	41651281	41651282	C	CA	2	GENIC	heterozygous	52599037
8	41651284	41651285	A	AG	3	GENIC	heterozygous	52599043
8	41651368	41651369	A	AG	4	GENIC	heterozygous	52599046
8	41651446	41651447	G	GT	18	GENIC	heterozygous	52599054
8	41651451	41651454	TTT	---	23	GENIC	heterozygous	52599056
8	41652819	41652820	G	GT	66	GENIC	heterozygous	52599112
8	41653863	41653867	AGAG	----	30	GENIC	heterozygous	52599213
8	41657078	41657079	C	CCTCCCCG	5	GENIC	heterozygous	53379022
8	41657218	41657219	A	-	26	GENIC	heterozygous	52599388
8	41657221	41657222	C	-	27	GENIC	heterozygous	52599391
8	41657707	41657708	G	GT	2	GENIC	homozygous	53363285
8	41658733	41658734	G	T	14	GENIC	heterozygous	52599421
8	41660543	41660551	TCTTTCAA	--------	24	GENIC	heterozygous	52599477
8	41660620	41660621	G	T	26	GENIC	possibly homozygous	52599482
8	41661270	41661271	A	-	26	GENIC	heterozygous	52599524