chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	42107688	42107689	A	AG	25	GENIC	homozygous	58782411
2	42107701	42107702	A	AG	26	GENIC	homozygous	58782413
2	42121594	42121595	C	A	29	GENIC	homozygous	58782439
2	42125426	42125427	A	C	44	GENIC	heterozygous	58782442
2	42127461	42127462	G	GTT	21	GENIC	heterozygous	58782445
2	42112474	42112475	C	-	5	GENIC	heterozygous	60322651
2	42132284	42132285	T	TTA	9	GENIC	possibly homozygous	58782453
2	42145829	42145834	TTAAA	-----	26	GENIC	homozygous	60322653
2	42150045	42150046	C	CTATCTATG	50	GENIC	heterozygous	58782480
2	42153699	42153701	GT	--	13	GENIC	heterozygous	60322655
2	42156838	42156840	CA	--	33	GENIC	heterozygous	58782500
2	42173161	42173162	G	T	55	GENIC	heterozygous	58782553
2	42183275	42183276	T	TG	31	GENIC	homozygous	58782561
2	42183277	42183278	T	TCA	28	GENIC	homozygous	58782562
2	42183341	42183342	T	A	18	GENIC	heterozygous	58782563
2	42183346	42183349	CTC	---	13	GENIC	heterozygous	58782564
2	42183351	42183352	C	CA	17	GENIC	heterozygous	58782565
2	42184736	42184737	A	-	37	GENIC	heterozygous	58782576
2	42195725	42195726	C	-	25	GENIC	homozygous	58782586
2	42195731	42195732	C	-	28	GENIC	homozygous	58782587
2	42195741	42195742	G	-	26	GENIC	homozygous	58782588
2	42198149	42198150	T	G	42	GENIC	heterozygous	60322657
2	42206793	42206794	T	G	48	GENIC	heterozygous	60047337
2	42206812	42206813	T	C	41	GENIC	heterozygous	59669094