chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	9892140	9892140		A	20	GENIC	homozygous	129657794
20	9892418	9892419	G	A	22	GENIC	homozygous	109089301
20	9892894	9892895	A	G	16	GENIC	homozygous	109089315
20	9892997	9892998	C	A	20	GENIC	homozygous	109089317
20	9893136	9893137	T	C	17	GENIC	homozygous	109089319
20	9892429	9892430	A	G	23	GENIC	homozygous	109421401
20	9893430	9893431	G	T	21	GENIC	homozygous	109089321
20	9893639	9893640	C		13	GENIC	homozygous	129657797
20	9893654	9893655	C	T	15	GENIC	homozygous	109301296
20	9893667	9893668	T	C	17	GENIC	homozygous	109089323
20	9893960	9893961	T	C	17	GENIC	homozygous	109089325
20	9894026	9894027	A	G	14	GENIC	homozygous	109089327
20	9895669	9895670	T	C	17	GENIC	homozygous	109089336
20	9893670	9893671	A		17	GENIC	homozygous	131229148
20	9893707	9893707		CTGGCACT	16	GENIC	homozygous	129657798