chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	101872038	101872039	A	G	66	GENIC	homozygous	109953214
2	101873264	101873265	T	A	66	GENIC	homozygous	109953215
2	101874372	101874373	G	A	87	GENIC	homozygous	109953216
2	101874683	101874684	A	G	59	GENIC	homozygous	109953217
2	101875397	101875398	G	T	71	GENIC	homozygous	109953218
2	101875768	101875769	C	G	64	GENIC	homozygous	109953219
2	101875780	101875781	G	A	72	GENIC	possibly homozygous	109953220
2	101875934	101875935	A	T	50	GENIC	homozygous	109953221
2	101876016	101876017	C	A	105	GENIC	heterozygous	109953222
2	101876084	101876085	A	G	152	GENIC	heterozygous	109953223
2	101876102	101876103	C	G	147	GENIC	heterozygous	109953224
2	101876129	101876130	A	G	132	GENIC	heterozygous	109953225
2	101876346	101876347	A	G	170	GENIC	heterozygous	109953226
2	101876355	101876356	C	A	175	GENIC	heterozygous	109953227
2	101876423	101876424	A	G	144	GENIC	heterozygous	110577904
2	101876432	101876433	G	A	141	GENIC	heterozygous	110577906
2	101876459	101876460	T	C	118	GENIC	heterozygous	110577908
2	101876491	101876492	T	A	97	GENIC	heterozygous	110577910
2	101876500	101876501	G	C	95	GENIC	heterozygous	110577912
2	101877654	101877655	C	T	61	GENIC	possibly homozygous	109953228