chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	10885457	10885458	T	G	22	GENIC	homozygous	109091584
20	10887085	10887086	T	C	47	GENIC	homozygous	109091586
20	10887825	10887826	A	C	38	GENIC	homozygous	109091588
20	10889906	10889907	G	A	36	GENIC	homozygous	109091590
20	10891666	10891667	G	A	50	GENIC	homozygous	109091592
20	10897215	10897216	T	C	46	GENIC	homozygous	109091594
20	10897303	10897304	T	C	49	GENIC	homozygous	109091596
20	10897688	10897689	T	A	35	GENIC	homozygous	109091598
20	10898073	10898074	G	C	40	GENIC	homozygous	109091600
20	10898402	10898403	T	G	39	GENIC	homozygous	109091602
20	10898582	10898583	G	A	56	GENIC	homozygous	109091604
20	10906054	10906055	G	A	45	GENIC	homozygous	109091606
20	10906698	10906699	C	T	49	GENIC	homozygous	109091608
20	10907020	10907021	C	T	31	GENIC	homozygous	109091610
20	10907186	10907187	C	T	37	GENIC	homozygous	109091612
20	10909311	10909312	A	G	38	GENIC	homozygous	109091614
20	10909522	10909523	G	A	34	GENIC	homozygous	109091616
20	10909762	10909763	T	G	43	GENIC	homozygous	109091618
20	10909766	10909767	T	C	43	GENIC	homozygous	109091620
20	10910604	10910605	C	T	40	GENIC	homozygous	109091622
20	10910684	10910685	G	A	40	GENIC	homozygous	109091624
20	10911903	10911904	C	T	31	GENIC	homozygous	109091626
20	10911983	10911984	C	T	26	GENIC	homozygous	109091628
20	10912267	10912268	A	G	60	GENIC	homozygous	109091630