chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	91253234	91253235	A	C	13	GENIC	homozygous	111653719
3	91253252	91253253	C	A	13	GENIC	homozygous	111653720
3	91253494	91253495	G	T	14	GENIC	homozygous	111653721
3	91253947	91253947		T	20	GENIC	homozygous	127908488
3	91254292	91254293	T	G	19	GENIC	homozygous	111653722
3	91254314	91254315	T		17	GENIC	homozygous	127908489
3	91254738	91254739	A	G	20	GENIC	homozygous	111653723
3	91255402	91255403	G	A	20	GENIC	homozygous	111653724
3	91255512	91255512		A	18	GENIC	possibly homozygous	127908490
3	91255778	91255779	A	G	25	GENIC	homozygous	111653725
3	91256267	91256268	A	G	12	GENIC	homozygous	111653726
3	91257906	91257907	A	C	27	GENIC	homozygous	111653727
3	91258456	91258457	T	C	15	GENIC	homozygous	111653728
3	91258826	91258827	T	A	15	GENIC	homozygous	111653729
3	91259624	91259625	A	G	14	GENIC	homozygous	111653730
3	91259998	91259999	C	G	18	GENIC	homozygous	111653731
3	91260178	91260179	T	C	25	GENIC	homozygous	111653732
3	91260308	91260309	G	A	15	GENIC	homozygous	112253790
3	91261502	91261503	G	A	20	GENIC	homozygous	111653733
3	91261698	91261699	A	C	28	GENIC	homozygous	111653734
3	91262005	91262006	G	A	25	GENIC	homozygous	111653735
3	91262637	91262638	T	C	11	GENIC	homozygous	111653736
3	91263643	91263644	C	T	29	GENIC	homozygous	111653737
3	91264081	91264082	A		16	GENIC	homozygous	127908491
3	91264597	91264598	C	T	7	GENIC	homozygous	111653738
3	91266680	91266681	C	A	15	GENIC	homozygous	111653740
3	91266720	91266721	G	A	16	GENIC	homozygous	111653741
3	91267100	91267101	G	A	17	GENIC	homozygous	111653742
3	91268107	91268108	G	A	26	GENIC	homozygous	111653743
3	91268326	91268327	G	T	25	GENIC	homozygous	111653744
3	91268694	91268695	C	T	16	GENIC	homozygous	111653745
3	91270811	91270812	A	C	31	GENIC	homozygous	111653746