chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	143111656	143111657	G	A	34	GENIC	homozygous	114151058
5	143111826	143111827	A	G	35	GENIC	homozygous	114034270
5	143111845	143111846	T	A	30	GENIC	homozygous	114034271
5	143112759	143112760	C	T	19	GENIC	homozygous	114034272
5	143112970	143112971	T	C	32	GENIC	homozygous	114034273
5	143113027	143113028	A	G	24	GENIC	homozygous	114034274
5	143113032	143113033	C	T	24	GENIC	homozygous	114034275
5	143115410	143115411	T	C	10	GENIC	homozygous	114034276
5	143115558	143115559	G	C	7	GENIC	possibly homozygous	114151059
5	143115569	143115570	C	A	10	GENIC	possibly homozygous	114034277
5	143115595	143115596	C	A	18	GENIC	homozygous	114034278
5	143115666	143115667	C	G	22	GENIC	homozygous	114034281
5	143115672	143115673	C	G	22	GENIC	homozygous	114034282
5	143115688	143115689	C	A	31	GENIC	homozygous	114034283
5	143115706	143115707	C	G	27	GENIC	homozygous	114034284
5	143116014	143116015	G	A	33	GENIC	homozygous	114151060
5	143116613	143116614	T	C	30	GENIC	homozygous	114151061
5	143116651	143116652	C	A	30	GENIC	homozygous	114034287
5	143116675	143116676	T	C	35	GENIC	homozygous	114034288
5	143116699	143116700	G	A	31	GENIC	homozygous	114151062
5	143116751	143116752	T	G	31	GENIC	homozygous	114034289
5	143119414	143119415	T	A	24	GENIC	homozygous	114034292
5	143118803	143118804	C	T	24	GENIC	homozygous	114344213
5	143117437	143117438	G	A	36	GENIC	homozygous	114344209
5	143118300	143118301	C	T	29	GENIC	homozygous	114344211