chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	61172442	61172443	T		21	GENIC	heterozygous	131017207
7	61192210	61192210		GTGA	21	GENIC	homozygous	128469585
7	61192924	61192926	AC		7	GENIC	heterozygous	130665908
7	61194175	61194175		G	8	GENIC	possibly homozygous	133674454
7	61194195	61194211	AGAGGACGGGAAGAGG		9	GENIC	homozygous	133674455
7	61194230	61194243	AGGAGGGAAGAGA		9	GENIC	homozygous	133674456
7	61194249	61194314	GAGGGGAGAGAGAAAAGGAGGGGAGGAGAAAGTGAGGGAGGAGGAGGAGAAGGAGAGGAGGGAAA		10	GENIC	homozygous	133674457
7	61194353	61194354	C		7	GENIC	homozygous	129937180
7	61194178	61194179	A	G	8	GENIC	homozygous	115688777
7	61194343	61194344	C		8	GENIC	homozygous	129937178
7	61194346	61194347	C		9	GENIC	homozygous	129937179
7	61194356	61194357	C		7	GENIC	homozygous	129937181
7	61194371	61194371		G	9	GENIC	homozygous	129937182
7	61194377	61194378	T	G	11	GENIC	homozygous	115688779
7	61194578	61194578		A	26	GENIC	homozygous	128469589
7	61194480	61194480		C	24	GENIC	homozygous	128469586
7	61194526	61194527	A		28	GENIC	homozygous	128469587
7	61194569	61194571	GT		26	GENIC	homozygous	128469588
7	61194580	61194581	A		26	GENIC	homozygous	128469590
7	61194656	61194657	A		29	GENIC	homozygous	128469591
7	61194584	61194585	A	G	25	GENIC	homozygous	118254671