chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	42620619	42620620	G	C	23	GENIC	homozygous	146545370
13	42620773	42620774	C	A	10	GENIC	heterozygous	145152767
13	42620814	42620815	G	A	14	GENIC	homozygous	146545371
13	42621874	42621875	G	C	14	GENIC	homozygous	404468879
13	42621872	42621873	G		15	GENIC	possibly homozygous	404468876
13	42621872	42621873	G	C	15	GENIC	heterozygous	404468877
13	42621874	42621875	G		14	GENIC	heterozygous	404468878
13	42621876	42621877	G		15	GENIC	heterozygous	404468880
13	42621876	42621877	G	C	15	GENIC	possibly homozygous	404468881
13	42622548	42622549	A	G	16	GENIC	homozygous	143578708
13	42623353	42623354	C	T	28	GENIC	homozygous	146545372
13	42627209	42627210	T	A	34	GENIC	homozygous	146545373
13	42628274	42628275	G	A	27	GENIC	homozygous	143578714
13	42629039	42629040	C	T	24	GENIC	homozygous	146545374
13	42629760	42629761	T	C	23	GENIC	homozygous	143578715
13	42630397	42630398	T	C	29	GENIC	homozygous	143578716
13	42630853	42630854	T	C	12	GENIC	homozygous	143578717
13	42631276	42631277	A	C	30	GENIC	homozygous	143578718
13	42631789	42631790	A	G	22	GENIC	homozygous	143578719
13	42632215	42632216	C	T	25	GENIC	homozygous	146545375
13	42632354	42632355	C	T	16	GENIC	homozygous	143578720
13	42633200	42633201	G	A	27	GENIC	homozygous	144929446
13	42634306	42634307	A	G	24	GENIC	homozygous	143578721
13	42634484	42634485	A	G	28	GENIC	homozygous	143578722
13	42634952	42634953	C	G	18	GENIC	homozygous	143578723
13	42635749	42635750	A	G	8	GENIC	homozygous	154805094
13	42635886	42635887	A	G	26	GENIC	homozygous	146545376
13	42635749	42635750	A		8	GENIC	heterozygous	403337477
13	42623628	42623628		AGAT	21	GENIC	possibly homozygous	143549457
13	42631545	42631545		CTTAT	19	GENIC	homozygous	143549459