chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	37616970	37616970		ATT	12	GENIC	homozygous	128808220
10	37619258	37619259	G	A	17	GENIC	homozygous	116562572
10	37622039	37622040	T		25	GENIC	homozygous	128808221
10	37622176	37622177	C	A	19	GENIC	homozygous	116562574
10	37622396	37622397	A	G	23	GENIC	homozygous	116562576
10	37623388	37623389	G	A	30	GENIC	homozygous	116562578
10	37624774	37624775	T	C	17	GENIC	homozygous	116562580
10	37627471	37627472	C	T	32	GENIC	homozygous	116562582
10	37628329	37628329		A	6	GENIC	homozygous	128808222
10	37630046	37630047	T	C	24	GENIC	homozygous	116562584
10	37631235	37631236	T	C	20	GENIC	homozygous	116562586
10	37631860	37631861	T	C	20	GENIC	homozygous	116562588
10	37634380	37634381	C	G	20	GENIC	homozygous	116562590
10	37637818	37637819	A	T	23	GENIC	possibly homozygous	116562592
10	37638947	37638948	C	T	24	GENIC	homozygous	116562594
10	37639148	37639149	T	C	19	GENIC	homozygous	116562596
10	37640222	37640223	A	G	23	GENIC	homozygous	116760253
10	37641834	37641835	A	G	26	GENIC	homozygous	116562598
10	37642219	37642220	A	C	24	GENIC	homozygous	116562600