chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	44138817	44138818	C	T	27	GENIC	homozygous	116949113
8	44138832	44138833	T	C	30	GENIC	homozygous	116949115
8	44140525	44140526	G	A	25	GENIC	homozygous	116949117
8	44140923	44140924	A	G	39	GENIC	homozygous	116949119
8	44141838	44141839	T	A	40	GENIC	homozygous	116949123
8	44143307	44143308	A	G	10	GENIC	homozygous	116949125
8	44144118	44144119	T	C	21	GENIC	homozygous	116949127
8	44144338	44144339	C	T	28	GENIC	homozygous	116949129
8	44144386	44144387	C	G	23	GENIC	homozygous	116949131
8	44145028	44145029	A	G	24	GENIC	homozygous	116949133
8	44145450	44145451	A	G	24	GENIC	homozygous	116949135
8	44145477	44145478	T	C	28	GENIC	homozygous	116949137
8	44145640	44145641	A	G	33	GENIC	homozygous	116949139
8	44145765	44145766	A	G	33	GENIC	homozygous	116949141
8	44146734	44146735	G	A	18	GENIC	homozygous	117927752
8	44149957	44149958	C	T	26	GENIC	homozygous	116949143
8	44150201	44150202	A	G	20	GENIC	homozygous	116949145
8	44157539	44157540	A	C	30	GENIC	homozygous	116949147