chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	6123450	6123451	A	G	19	GENIC	homozygous	63345499
20	6123531	6123532	T	C	22	GENIC	homozygous	63345501
20	6123973	6123974	G	T	11	GENIC	homozygous	63345502
20	6124013	6124014	C	T	12	GENIC	homozygous	63345504
20	6124108	6124109	A	G	17	GENIC	homozygous	63345506
20	6124365	6124366	T	G	24	GENIC	homozygous	63345507
20	6124569	6124570	A	G	9	GENIC	homozygous	63345509
20	6125256	6125257	A	G	16	GENIC	homozygous	63345510
20	6125588	6125589	A	C	20	GENIC	homozygous	63345511
20	6125946	6125947	C	T	16	GENIC	homozygous	63345513
20	6126529	6126530	A	G	16	GENIC	homozygous	63345514
20	6126761	6126762	C	T	23	GENIC	homozygous	63345516
20	6127355	6127356	T	C	10	GENIC	homozygous	63345517
20	6127357	6127358	A	G	9	GENIC	homozygous	63345519
20	6127639	6127640	A	C	7	GENIC	homozygous	63345520
20	6127647	6127648	T	C	6	GENIC	homozygous	63345522
20	6127796	6127797	T	C	15	GENIC	homozygous	63345524
20	6127889	6127890	T	C	19	GENIC	homozygous	63345525
20	6128326	6128327	C	T	20	GENIC	homozygous	63345529
20	6128343	6128344	C	A	23	GENIC	homozygous	63345530
20	6128492	6128493	T	C	11	GENIC	homozygous	63345535
20	6128655	6128656	A	G	18	GENIC	homozygous	63345537
20	6127601	6127601		ACTTCT	8	GENIC	heterozygous	64114776