chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	16153505	16153506	T	C	46	GENIC	homozygous	45448863
20	16154156	16154157	A	G	39	GENIC	homozygous	45448865
20	16154618	16154619	G	A	39	GENIC	possibly homozygous	45448867
20	16154736	16154737	A	G	36	GENIC	homozygous	45448869
20	16155077	16155078	C	T	42	GENIC	homozygous	45448871
20	16155477	16155478	G	A	40	GENIC	homozygous	45448873
20	16155667	16155668	T	A	57	GENIC	homozygous	45448875
20	16155847	16155848	G	A	26	GENIC	homozygous	45448877
20	16156378	16156379	G	A	54	GENIC	homozygous	45448879
20	16156602	16156603	A	G	34	GENIC	homozygous	45448881
20	16156996	16156997	A	AG	28	GENIC	homozygous	45448883
20	16157929	16157930	A	G	34	GENIC	homozygous	45448885
20	16158124	16158125	C	T	41	GENIC	homozygous	45448887
20	16158431	16158432	G	GAA	16	GENIC	possibly homozygous	45448889
20	16158593	16158594	C	T	44	GENIC	homozygous	45448891
20	16158740	16158741	T	C	36	GENIC	homozygous	45448893
20	16159090	16159091	A	G	36	GENIC	homozygous	45448895
20	16159108	16159109	C	T	43	GENIC	homozygous	45448897
20	16159848	16159849	A	G	31	GENIC	homozygous	45448899
20	16159860	16159861	G	T	23	GENIC	homozygous	45448901
20	16159896	16159897	C	-	19	GENIC	homozygous	45448903
20	16160479	16160480	C	-	30	GENIC	homozygous	45448905
20	16160481	16160482	G	T	30	GENIC	homozygous	45864403
20	16160508	16160509	C	T	43	GENIC	homozygous	45448909
20	16158431	16158432	G	GAAAA	16	GENIC	heterozygous	45900904
20	16159657	16159658	G	GCCCACCGCCCCT	8	GENIC	homozygous	45843720