chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	48118172	48118173	T	C	25	GENIC	homozygous	50622672
12	48118241	48118242	A	G	25	GENIC	homozygous	50622673
12	48118322	48118323	G	A	28	GENIC	homozygous	50622674
12	48118336	48118338	CT	--	23	GENIC	homozygous	50622675
12	48119357	48119358	A	G	30	GENIC	homozygous	50622676
12	48119395	48119396	A	T	30	GENIC	homozygous	50225662
12	48119893	48119894	C	T	25	GENIC	homozygous	50622677
12	48120055	48120061	GTGAAC	------	19	GENIC	homozygous	50622678
12	48120930	48120931	T	C	24	GENIC	homozygous	50225666
12	48121348	48121349	A	G	26	GENIC	homozygous	50225668
12	48121960	48121961	G	A	13	GENIC	homozygous	50622679
12	48122269	48122270	A	G	28	GENIC	homozygous	50622680
12	48122364	48122365	A	G	11	GENIC	homozygous	50622681
12	48122398	48122399	C	T	12	GENIC	homozygous	50622682
12	48122652	48122653	G	A	23	GENIC	homozygous	50622683
12	48122763	48122764	T	C	21	GENIC	homozygous	50225672
12	48122821	48122822	G	A	24	GENIC	homozygous	50622684
12	48124366	48124367	G	C	29	GENIC	homozygous	50225674
12	48125214	48125215	C	T	21	GENIC	homozygous	50225680
12	48125306	48125316	CGCACACACA	----------	14	GENIC	possibly homozygous	50593122
12	48127079	48127080	G	A	20	GENIC	homozygous	50622685
12	48127680	48127681	T	C	29	GENIC	homozygous	50225690