chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	183733749	183733750	A	G	28	GENIC	homozygous	108442933
1	183734692	183734693	T	C	26	GENIC	homozygous	108442937
1	183734739	183734740	T	C	26	GENIC	homozygous	108442939
1	183735051	183735052	T	G	19	GENIC	homozygous	109358702
1	183735704	183735705	G	A	19	GENIC	homozygous	108442941
1	183736851	183736852	T	C	28	GENIC	homozygous	108442943
1	183736969	183736970	A	G	20	GENIC	possibly homozygous	108442945
1	183737389	183737390	A	G	27	GENIC	homozygous	108442947
1	183738671	183738672	T	C	34	GENIC	homozygous	108442949
1	183738782	183738783	A	G	36	GENIC	homozygous	109358704
1	183739507	183739508	T	C	29	GENIC	homozygous	109358706
1	183739776	183739777	A	G	31	GENIC	homozygous	108442953
1	183740454	183740455	G	A	24	GENIC	homozygous	109358708
1	183741995	183741996	T	C	17	GENIC	homozygous	108442957
1	183739090	183739091	A		22	GENIC	possibly homozygous	127462097
1	183740767	183740772	TTTTC		31	GENIC	homozygous	134262341
1	183742219	183742220	G	A	32	GENIC	homozygous	108971660
1	183742233	183742234	A	C	30	GENIC	homozygous	108442959
1	183743163	183743164	T	C	36	GENIC	homozygous	108442961
1	183743752	183743753	T	C	20	GENIC	homozygous	108442963
1	183743929	183743930	C	G	22	GENIC	homozygous	108442965
1	183744306	183744307	C	A	22	GENIC	homozygous	108442967