chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	72772100	72772101	T		44	GENIC	homozygous	129071812
13	72772101	72772102	T	A	44	GENIC	homozygous	123761863
13	72772251	72772252	G	A	44	GENIC	homozygous	114387274
13	72772360	72772360		CGCAT	44	GENIC	homozygous	129071813
13	72772542	72772543	C	T	39	GENIC	homozygous	114387276
13	72773609	72773610	C	T	37	GENIC	homozygous	114387280
13	72772837	72772838	A	C	44	GENIC	homozygous	114926121
13	72773142	72773143	C	T	53	GENIC	homozygous	114926123
13	72773871	72773872	A	G	36	GENIC	homozygous	114926125
13	72774167	72774168	C	G	25	GENIC	homozygous	114926127
13	72774185	72774186	A	C	7	GENIC	homozygous	115137505
13	72774218	72774218		TA	7	GENIC	homozygous	131504098
13	72775112	72775113	T	A	52	GENIC	homozygous	114949767
13	72780142	72780143	G	C	40	GENIC	homozygous	114387284
13	72780391	72780392	C	T	10	GENIC	homozygous	123761865
13	72780393	72780393		GGGA	10	GENIC	homozygous	129071814
13	72780396	72780396		AG	11	GENIC	homozygous	129071815
13	72780398	72780398		CAGTGGTAGAGCGCTTGCCTAGCAAGCA	11	GENIC	homozygous	129071816
13	72781971	72781972	G	C	35	GENIC	possibly homozygous	114926129
13	72783218	72783222	TATC		25	GENIC	possibly homozygous	131504101