chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	39688826	39688827	G	A	45	GENIC	possibly homozygous	52963101
8	39690555	39690556	G	A	41	GENIC	homozygous	52591421
8	39690934	39690935	A	G	57	GENIC	homozygous	52591422
8	39691255	39691256	G	GTA	30	GENIC	heterozygous	52591426
8	39691257	39691258	G	A	29	GENIC	heterozygous	53203380
8	39691382	39691383	G	-	18	GENIC	homozygous	52963103
8	39691385	39691393	TTGTTTTG	--------	16	GENIC	homozygous	52963104
8	39691392	39691393	G	-	19	GENIC	homozygous	52963105
8	39691393	39691394	T	-	19	GENIC	homozygous	52591428
8	39691742	39691743	C	T	46	GENIC	possibly homozygous	52963106
8	39692640	39692641	A	G	34	GENIC	homozygous	52591430
8	39693527	39693528	C	CTT	7	GENIC	heterozygous	52963107
8	39694346	39694347	T	A	77	GENIC	heterozygous	53316604
8	39694463	39694464	A	ATAGACTGAC	5	GENIC	homozygous	52591439
8	39694487	39694488	A	T	23	GENIC	heterozygous	52591440
8	39694496	39694497	C	T	35	GENIC	heterozygous	52591441
8	39694522	39694523	C	T	47	GENIC	heterozygous	52591442
8	39694527	39694528	C	-	38	GENIC	heterozygous	52591443
8	39695029	39695030	C	CTT	18	GENIC	homozygous	52963109
8	39695049	39695050	G	T	35	GENIC	heterozygous	52963110
8	39695107	39695108	T	C	33	GENIC	homozygous	52591447
8	39695400	39695401	G	A	46	GENIC	homozygous	52963111
8	39695727	39695728	A	T	37	GENIC	homozygous	52963112
8	39695729	39695730	C	G	38	GENIC	homozygous	52963113
8	39695767	39695768	T	C	56	GENIC	homozygous	52591450
8	39696400	39696401	G	GT	14	GENIC	possibly homozygous	52591452
8	39696568	39696569	A	G	53	GENIC	homozygous	52591453
8	39696961	39696962	C	T	68	GENIC	homozygous	52591454
8	39697481	39697482	A	G	49	GENIC	homozygous	52591455
8	39697811	39697812	C	T	46	GENIC	homozygous	52591456
8	39697844	39697845	C	T	53	GENIC	homozygous	52963115
8	39699119	39699120	A	G	54	GENIC	possibly homozygous	52963116
8	39703868	39703869	C	-	14	GENIC	homozygous	52963117