chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	63656591	63656592	G	T	51	GENIC	possibly homozygous	115694590
7	63656639	63656640	T	C	28	GENIC	possibly homozygous	115694591
7	63658132	63658133	A	G	30	GENIC	homozygous	115694592
7	63659566	63659567	G	A	35	GENIC	homozygous	115694593
7	63660398	63660399	A	G	28	GENIC	homozygous	115694594
7	63660399	63660400	T	G	29	GENIC	homozygous	115694595
7	63660652	63660653	G	C	48	GENIC	homozygous	115694596
7	63661076	63661077	A	G	37	GENIC	homozygous	115694597
7	63662358	63662359	T	A	25	GENIC	homozygous	115694598
7	63665002	63665003	C	T	30	GENIC	homozygous	115694599
7	63665401	63665402	T	C	49	GENIC	homozygous	115694600
7	63667576	63667577	G	A	58	GENIC	homozygous	115694601
7	63668125	63668126	T	C	29	GENIC	homozygous	115694602
7	63668181	63668182	T	C	35	GENIC	homozygous	115694603
7	63670265	63670266	C	T	35	GENIC	homozygous	115694604
7	63670377	63670378	T	C	22	GENIC	homozygous	115694605
7	63670910	63670911	C	T	40	GENIC	heterozygous	115694606
7	63672357	63672358	C	T	25	GENIC	homozygous	115694607
7	63673389	63673390	C	T	41	GENIC	homozygous	115694608
7	63674039	63674040	G	T	13	GENIC	heterozygous	115694609
7	63674078	63674079	C	T	14	GENIC	heterozygous	115694610
7	63675834	63675835	G	A	31	GENIC	homozygous	115694611
7	63678395	63678396	C	T	46	GENIC	homozygous	115694612
7	63678544	63678545	T	C	38	GENIC	possibly homozygous	115694613
7	63682001	63682002	T	C	35	GENIC	homozygous	115694614
7	63683575	63683576	A	G	45	GENIC	homozygous	115694615
7	63684750	63684751	A	G	51	GENIC	homozygous	115694616
7	63685553	63685554	A	G	42	GENIC	homozygous	115694617
7	63686051	63686052	T	C	39	GENIC	possibly homozygous	115694618
7	63687094	63687095	C	T	58	GENIC	homozygous	115694619