chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	153733082	153733083	T	A	22	GENIC	homozygous	108314039
1	153733575	153733576	A	G	12	GENIC	homozygous	108946998
1	153733896	153733897	A	G	13	GENIC	homozygous	109150393
1	153734011	153734012	C	A	11	GENIC	homozygous	109150395
1	153734788	153734789	G	A	25	GENIC	homozygous	109150397
1	153734802	153734803	A	T	28	GENIC	homozygous	109150399
1	153735449	153735450	T	C	25	GENIC	homozygous	108947001
1	153735543	153735544	T	C	27	GENIC	homozygous	108314045
1	153736357	153736358	A	G	32	GENIC	homozygous	108314047
1	153736727	153736728	C	T	33	GENIC	homozygous	108314053
1	153736730	153736731	G	A	33	GENIC	homozygous	108947002
1	153736810	153736811	A	G	21	GENIC	homozygous	108314055
1	153737290	153737291	C	T	22	GENIC	homozygous	108947004
1	153737441	153737442	A	G	25	GENIC	homozygous	108314059
1	153737513	153737514	A	G	27	GENIC	homozygous	108314061
1	153737835	153737836	G	A	24	GENIC	possibly homozygous	109150403
1	153737900	153737901	T	C	26	GENIC	homozygous	108314065
1	153737952	153737953	G	A	31	GENIC	homozygous	109150405
1	153737993	153737994	C	G	22	GENIC	homozygous	108314067
1	153738229	153738230	G	A	22	GENIC	homozygous	109150407
1	153738646	153738647	G	A	23	GENIC	homozygous	120486830
1	153738659	153738660	C	T	25	GENIC	homozygous	108947006
1	153738697	153738698	C	T	20	GENIC	homozygous	109150409
1	153739476	153739477	A	T	31	GENIC	homozygous	109150411
1	153740013	153740014	T	A	20	GENIC	homozygous	108314073
1	153740094	153740095	T	C	17	GENIC	homozygous	108947007
1	153740675	153740676	A	G	3	GENIC	homozygous	108314079
1	153741196	153741197	C	T	8	GENIC	homozygous	109150415
1	153741458	153741459	T	C	10	GENIC	homozygous	108314081
1	153742026	153742027	T	A	23	GENIC	homozygous	109150419