chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	43084980	43084981	A	G	26	GENIC	homozygous	109270288
20	43085575	43085576	G	A	21	GENIC	homozygous	109402637
20	43087612	43087613	T	C	23	GENIC	homozygous	109270292
20	43090781	43090782	C	A	24	GENIC	possibly homozygous	109402638
20	43092611	43092612	T	G	24	GENIC	homozygous	109270300
20	43097143	43097144	T	C	36	GENIC	homozygous	109270310
20	43098343	43098344	C	T	32	GENIC	homozygous	109270312
20	43098856	43098857	C	T	23	GENIC	possibly homozygous	109402639
20	43099094	43099095	A	G	18	GENIC	homozygous	109402640
20	43099163	43099164	C	G	16	GENIC	possibly homozygous	109402641
20	43099409	43099410	C	T	23	GENIC	homozygous	109270318
20	43099579	43099580	G	A	18	GENIC	homozygous	109270320
20	43100919	43100920	A	G	35	GENIC	possibly homozygous	109402642
20	43102636	43102637	A	G	20	GENIC	homozygous	109270328
20	43103367	43103368	G	A	22	GENIC	possibly homozygous	109402643
20	43107043	43107044	C	T	31	GENIC	homozygous	109402644
20	43107349	43107350	C	T	24	GENIC	homozygous	109270334
20	43104213	43104214	T	C	16	GENIC	homozygous	109550658
20	43104704	43104705	T	C	19	GENIC	homozygous	109316143