chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	16153505	16153506	T	C	33	GENIC	homozygous	45448863
20	16154156	16154157	A	G	25	GENIC	homozygous	45448865
20	16154618	16154619	G	A	34	GENIC	possibly homozygous	45448867
20	16154736	16154737	A	G	30	GENIC	homozygous	45448869
20	16155077	16155078	C	T	28	GENIC	homozygous	45448871
20	16155477	16155478	G	A	49	GENIC	homozygous	45448873
20	16155667	16155668	T	A	21	GENIC	homozygous	45448875
20	16155847	16155848	G	A	31	GENIC	homozygous	45448877
20	16156378	16156379	G	A	33	GENIC	homozygous	45448879
20	16156602	16156603	A	G	31	GENIC	homozygous	45448881
20	16156996	16156997	A	AG	35	GENIC	homozygous	45448883
20	16157929	16157930	A	G	35	GENIC	homozygous	45448885
20	16158124	16158125	C	T	41	GENIC	homozygous	45448887
20	16158431	16158432	G	GAA	19	GENIC	homozygous	45448889
20	16158593	16158594	C	T	34	GENIC	homozygous	45448891
20	16158740	16158741	T	C	36	GENIC	homozygous	45448893
20	16159090	16159091	A	G	38	GENIC	homozygous	45448895
20	16159108	16159109	C	T	38	GENIC	homozygous	45448897
20	16159666	16159667	T	C	4	GENIC	heterozygous	45781054
20	16159669	16159670	G	T	5	GENIC	heterozygous	45781055
20	16159848	16159849	A	G	23	GENIC	homozygous	45448899
20	16159860	16159861	G	T	24	GENIC	homozygous	45448901
20	16159896	16159897	C	-	26	GENIC	homozygous	45448903
20	16160479	16160480	C	-	27	GENIC	homozygous	45448905
20	16160481	16160482	G	-	27	GENIC	homozygous	45448907
20	16160508	16160509	C	T	39	GENIC	homozygous	45448909