chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	50966383	50966384	A	C	13	GENIC	heterozygous	58817781
2	50966567	50966568	T	G	13	GENIC	heterozygous	58817783
2	50966920	50966921	C	A	11	GENIC	homozygous	59689472
2	50969784	50969785	A	G	10	GENIC	homozygous	58817791
2	50969916	50969917	A	G	8	GENIC	homozygous	58817792
2	50970068	50970069	G	-	2	GENIC	homozygous	58817793
2	50971789	50971790	G	T	7	GENIC	homozygous	60209672
2	50966767	50966768	C	A	13	GENIC	heterozygous	60209667
2	50966998	50966999	A	-	6	GENIC	homozygous	60209668
2	50969644	50969645	T	A	13	GENIC	possibly homozygous	60209669
2	50971146	50971147	C	T	12	GENIC	homozygous	60209671
2	50969965	50969966	A	-	4	GENIC	homozygous	60112351
2	50972177	50972178	A	T	9	GENIC	possibly homozygous	60209673
2	50974199	50974200	T	C	12	GENIC	homozygous	60209674
2	50974225	50974226	A	G	11	GENIC	homozygous	58817809