chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	41720130	41720130		CCTT	12	GENIC	possibly homozygous	135403132
1	41726762	41726763	T	G	12	GENIC	heterozygous	146340581
1	41726766	41726767	G	A	12	GENIC	heterozygous	146340582
1	41769060	41769061	A		16	GENIC	heterozygous	143734788
1	41795251	41795252	A	G	23	GENIC	homozygous	135535667
1	41868024	41868026	GA		9	GENIC	heterozygous	140957319
1	41868025	41868026	A		9	GENIC	heterozygous	402944585
1	41868025	41868026	A	T	9	GENIC	heterozygous	402944586
1	41868031	41868032	G	T	16	GENIC	homozygous	402944587
1	41868031	41868032	G		16	GENIC	heterozygous	402944588
1	41929734	41929735	T		12	GENIC	heterozygous	404602519
1	41929734	41929735	T	C	12	GENIC	heterozygous	404602520
1	41929736	41929737	T	C	12	GENIC	heterozygous	135535671
1	41929736	41929737	T		12	GENIC	heterozygous	403968649