chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	116671258	116671259	A	G	39	GENIC	possibly homozygous	144317747
2	116676213	116676214	C	A	34	GENIC	homozygous	136266436
2	116679918	116679919	T	G	30	GENIC	homozygous	136266443
2	116681228	116681229	C	T	37	GENIC	homozygous	144317748
2	116685892	116685893	C	T	48	GENIC	homozygous	136266453
2	116694268	116694269	C	A	40	GENIC	homozygous	144317749
2	116694365	116694366	C	T	23	GENIC	homozygous	144317750
2	116694434	116694435	C	T	56	GENIC	homozygous	144317751
2	116694491	116694492	G	A	54	GENIC	homozygous	136266464
2	116694714	116694715	A	C	46	GENIC	homozygous	144317752
2	116695773	116695774	A	G	56	GENIC	homozygous	136266465
2	116697082	116697083	T	G	42	GENIC	homozygous	144317753
2	116697162	116697163	T	C	47	GENIC	homozygous	136266467
2	116699048	116699049	G	A	41	GENIC	homozygous	136266469
2	116700646	116700647	G	A	37	GENIC	homozygous	136266470
2	116700741	116700742	G	A	39	GENIC	homozygous	144317754
2	116701047	116701048	A	C	43	GENIC	homozygous	136266472
2	116701101	116701102	A	G	51	GENIC	homozygous	136266475
2	116701174	116701175	T	G	51	GENIC	homozygous	136266476
2	116701279	116701280	G	A	47	GENIC	homozygous	144317755
2	116701785	116701786	C	T	41	GENIC	homozygous	144317756
2	116701950	116701951	A		47	GENIC	homozygous	135938393
2	116702126	116702127	T	C	44	GENIC	homozygous	136266480
2	116702410	116702411	G	A	37	GENIC	homozygous	136266481
2	116702487	116702487		A	32	GENIC	homozygous	135938394
2	116702655	116702656	G	A	48	GENIC	homozygous	144317757
2	116702681	116702682	T	A	48	GENIC	homozygous	136266482
2	116702692	116702693	C	A	46	GENIC	homozygous	144317758
2	116702693	116702694	A	G	46	GENIC	homozygous	136266483
2	116696107	116696107		T	53	GENIC	homozygous	144276277