chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	4167979	4167980	A	G	16	GENIC	homozygous	125199251
20	4168249	4168250	C	T	8	GENIC	homozygous	125199252
20	4168721	4168722	C	G	9	GENIC	homozygous	125199253
20	4169027	4169028	G	A	9	GENIC	homozygous	125199257
20	4169028	4169029	T	C	9	GENIC	homozygous	125199258
20	4169060	4169061	T	G	6	GENIC	heterozygous	125199259
20	4169078	4169079	G	A	12	GENIC	homozygous	125199260
20	4169122	4169123	T	G	13	GENIC	homozygous	125209590
20	4169173	4169174	A	G	9	GENIC	homozygous	125209591
20	4169188	4169189	A	G	9	GENIC	homozygous	125209592
20	4169210	4169211	G	T	7	GENIC	homozygous	125209593
20	4169215	4169216	C	A	8	GENIC	homozygous	125209594
20	4169325	4169326	C	T	14	GENIC	homozygous	125209595
20	4169333	4169334	G	A	13	GENIC	homozygous	125209596
20	4169346	4169347	G	A	12	GENIC	homozygous	125199261
20	4169929	4169930	T	C	4	GENIC	homozygous	125209597
20	4170107	4170108	T	A	9	GENIC	homozygous	125209598
20	4170264	4170265	G	A	9	GENIC	homozygous	125209599
20	4170277	4170278	A	G	8	GENIC	homozygous	125209600
20	4170279	4170280	G	T	7	GENIC	homozygous	125209601
20	4170303	4170304	G	C	18	GENIC	homozygous	125209602
20	4170332	4170333	T	C	14	GENIC	homozygous	125209603
20	4170411	4170412	T	C	12	GENIC	homozygous	125209604