chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	5175336	5175337	C	G	9	GENIC	homozygous	109077614
20	5175432	5175433	C	T	18	GENIC	possibly homozygous	109077616
20	5175746	5175747	C	A	11	GENIC	homozygous	109077618
20	5175896	5175897	A	G	11	GENIC	homozygous	109077622
20	5175904	5175905	A	G	11	GENIC	homozygous	109329690
20	5177040	5177041	A	G	5	GENIC	homozygous	109077628
20	5177337	5177338	G	C	9	GENIC	homozygous	109077634
20	5177342	5177343	C	T	9	GENIC	homozygous	109077636
20	5177346	5177347	T	C	9	GENIC	homozygous	109077638
20	5177565	5177566	A	T	3	GENIC	homozygous	109077640
20	5177610	5177611	G	C	7	GENIC	homozygous	109077642
20	5177654	5177655	T	G	8	GENIC	homozygous	109077644
20	5177664	5177665	G	A	8	GENIC	homozygous	109077646
20	5177675	5177676	G	A	7	GENIC	homozygous	109077648
20	5177800	5177801	G	C	10	GENIC	homozygous	109077650
20	5177830	5177831	T	C	12	GENIC	homozygous	109077652
20	5178096	5178097	T	C	25	GENIC	homozygous	109077654
20	5178134	5178135	T	A	19	GENIC	homozygous	109077656
20	5178216	5178217	G	A	30	GENIC	homozygous	109077658
20	5178239	5178240	T	C	29	GENIC	homozygous	109077660
20	5178354	5178355	G	C	29	GENIC	homozygous	109077662
20	5178364	5178365	A	G	32	GENIC	homozygous	109077664
20	5178504	5178505	G	A	15	GENIC	homozygous	109077666
20	5178523	5178524	A	G	13	GENIC	homozygous	109077668
20	5178575	5178576	A	G	20	GENIC	homozygous	109077670
20	5178639	5178640	T	C	17	GENIC	homozygous	109233919
20	5178647	5178648	A	G	15	GENIC	homozygous	109233920
20	5178675	5178676	T	A	10	GENIC	homozygous	109077672
20	5178876	5178877	G	A	18	GENIC	homozygous	109077674
20	5178883	5178884	T	G	18	GENIC	homozygous	109077676
20	5178912	5178913	A	G	15	GENIC	homozygous	109077678
20	5179100	5179101	C	T	20	GENIC	homozygous	109077680
20	5179248	5179249	G	A	13	GENIC	homozygous	109077682