chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	6168221	6168222	C	A	31	GENIC	heterozygous	63643784
20	6168392	6168393	G	A	23	GENIC	homozygous	63643785
20	6169358	6169359	C	T	35	GENIC	homozygous	63643786
20	6169844	6169845	G	T	26	GENIC	homozygous	63345679
20	6170283	6170284	C	T	21	GENIC	homozygous	63345681
20	6170338	6170339	A	G	23	GENIC	homozygous	63345682
20	6170274	6170275	G	A	22	GENIC	homozygous	63574994
20	6170530	6170531	G	T	26	GENIC	heterozygous	63345686
20	6170636	6170637	C	T	22	GENIC	possibly homozygous	63643787
20	6170872	6170873	T	G	28	GENIC	homozygous	63345689
20	6171269	6171270	A	G	36	GENIC	homozygous	63345692
20	6172134	6172135	G	A	27	GENIC	homozygous	63643788
20	6175005	6175006	T	C	28	GENIC	homozygous	63575012
20	6175965	6175966	C	T	31	GENIC	homozygous	63643789
20	6176093	6176094	T	C	35	GENIC	homozygous	63345704
20	6176264	6176265	T	C	49	GENIC	homozygous	63345706
20	6176346	6176347	G	A	32	GENIC	possibly homozygous	63643790
20	6177295	6177296	T	G	30	GENIC	homozygous	63643791