chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	143171792	143171793	C	T	22	GENIC	homozygous	109518104
1	143171862	143171863	T	A	20	GENIC	homozygous	109518105
1	143189888	143189892	TTGT		18	GENIC	homozygous	127440355
1	143196324	143196325	T	C	22	GENIC	homozygous	109518107
1	143196581	143196581		T	16	GENIC	homozygous	127440357
1	143197319	143197320	T	C	15	GENIC	homozygous	108264886
1	143197405	143197406	A	G	9	GENIC	heterozygous	120761571
1	143197408	143197409	A	T	8	GENIC	heterozygous	120761573
1	143219896	143219897	A	G	25	GENIC	homozygous	108264930
1	143230206	143230207	C		10	GENIC	homozygous	127440369
1	143230220	143230221	T	C	9	GENIC	homozygous	108264950
1	143230274	143230275	C	A	6	GENIC	homozygous	108264952
1	143249067	143249067		T	18	GENIC	homozygous	127440375
1	143251243	143251244	T	C	8	GENIC	homozygous	108264987
1	143251244	143251245	T	C	8	GENIC	homozygous	108264989
1	143255073	143255074	T	C	20	GENIC	homozygous	108264997
1	143258633	143258634	A	T	18	GENIC	homozygous	109518109
1	143269503	143269504	T	C	14	GENIC	homozygous	108265009
1	143278259	143278259		C	19	GENIC	homozygous	127440388
1	143232152	143232153	T	C	12	GENIC	heterozygous	134323687
1	143232156	143232157	C	T	12	GENIC	heterozygous	134323688