chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	5955901	5955902	A	G	24	GENIC	homozygous	130036583
20	5956872	5956873	C	T	19	GENIC	homozygous	130036584
20	5956969	5956970	G	A	18	GENIC	homozygous	130036585
20	5959150	5959151	C	T	23	GENIC	homozygous	130036588
20	5957733	5957734	G	A	13	GENIC	homozygous	130036586
20	5958865	5958866	C	G	8	GENIC	homozygous	130036587
20	5959572	5959573	T	C	26	GENIC	homozygous	130036589
20	5960742	5960743	T	C	37	GENIC	homozygous	130036590
20	5961023	5961024	G	C	1	GENIC	homozygous	130036591
20	5961025	5961026	G	C	1	GENIC	homozygous	130036592
20	5961027	5961028	G	C	1	GENIC	homozygous	130036593
20	5960043	5960045	CT		23	GENIC	homozygous	129980426
20	5961365	5961366	A	G	24	GENIC	homozygous	130036595
20	5961602	5961603	C	T	19	GENIC	homozygous	130036596
20	5962169	5962169		T	10	GENIC	homozygous	129980429
20	5962298	5962299	A	G	23	GENIC	homozygous	130036597
20	5963537	5963538	C	T	18	GENIC	homozygous	130036598