chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	37616343	37616343		TG	14	GENIC	homozygous	131091147
10	37616968	37616969	G	A	15	GENIC	homozygous	117004021
10	37624774	37624775	T	C	9	GENIC	homozygous	116562580
10	37619258	37619259	G	A	28	GENIC	homozygous	116562572
10	37622176	37622177	C	A	18	GENIC	homozygous	116562574
10	37622396	37622397	A	G	14	GENIC	homozygous	116562576
10	37631235	37631236	T	C	10	GENIC	homozygous	116562586
10	37631860	37631861	T	C	15	GENIC	homozygous	116562588
10	37634053	37634053		CCTGTGCCT	11	GENIC	homozygous	131091148
10	37637818	37637819	A	T	15	GENIC	homozygous	116562592
10	37639148	37639149	T	C	28	GENIC	homozygous	116562596
10	37641834	37641835	A	G	10	GENIC	homozygous	116562598
10	37642219	37642220	A	C	18	GENIC	homozygous	116562600
10	37616970	37616970		ATT	15	GENIC	homozygous	128808220
10	37617616	37617617	C	T	14	GENIC	homozygous	116760249
10	37636981	37636982	G	A	11	GENIC	homozygous	116760251
10	37640222	37640223	A	G	15	GENIC	homozygous	116760253
10	37644780	37644781	C	A	10	GENIC	homozygous	116760255