chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	15557449	15557450	G	GA	19	GENIC	homozygous	51625430
10	15557451	15557452	C	CCTGTAA	19	GENIC	homozygous	51625431
10	15557453	15557454	G	C	20	GENIC	homozygous	52313280
10	15557608	15557609	T	C	22	GENIC	homozygous	51625432
10	15557647	15557652	TTTTT	-----	12	GENIC	heterozygous	53023483
10	15557648	15557652	TTTT	----	12	GENIC	possibly homozygous	52796145
10	15557665	15557666	T	TAA	17	GENIC	homozygous	52554255
10	15557739	15557740	T	C	19	GENIC	homozygous	51625433
10	15558122	15558123	A	C	16	GENIC	homozygous	51625434
10	15558506	15558507	C	T	24	GENIC	homozygous	51625435
10	15559161	15559162	G	A	28	GENIC	homozygous	51812614
10	15559425	15559426	C	T	23	GENIC	homozygous	51625436
10	15560732	15560733	G	GGGAT	32	GENIC	homozygous	51625437
10	15561655	15561656	T	C	16	GENIC	homozygous	51812616
10	15561930	15561931	T	C	24	GENIC	homozygous	51625438
10	15562700	15562701	A	-	31	GENIC	homozygous	51331259
10	15562723	15562724	C	CA	25	GENIC	homozygous	51625439