chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	62070745	62070746	T	G	9	GENIC	homozygous	118894588
5	62071545	62071546	G	C	10	GENIC	homozygous	113830611
5	62071684	62071685	G	A	7	GENIC	homozygous	118843063
5	62071686	62071687	A	G	7	GENIC	homozygous	114118954
5	62074373	62074374	T	C	20	GENIC	homozygous	113830621
5	62074664	62074665	G	A	22	GENIC	possibly homozygous	114593101
5	62075145	62075146	C	T	25	GENIC	possibly homozygous	118894590
5	62076523	62076524	T	C	25	GENIC	homozygous	113830623
5	62077985	62077986	C	G	12	GENIC	possibly homozygous	119165638
5	62080069	62080070	G	A	27	GENIC	homozygous	118894594
5	62080631	62080632	T	C	24	GENIC	homozygous	114593107
5	62080760	62080761	G	A	23	GENIC	possibly homozygous	114593109
5	62081254	62081255	A	T	30	GENIC	possibly homozygous	118894596
5	62081928	62081929	G	A	28	GENIC	possibly homozygous	118894598
5	62082812	62082813	T	G	17	GENIC	possibly homozygous	118894600
5	62082969	62082970	C	T	34	GENIC	possibly homozygous	118894602
5	62087227	62087228	G	T	19	GENIC	homozygous	118894604
5	62088561	62088562	A	C	29	GENIC	possibly homozygous	114593121
5	62088827	62088828	T	A	38	GENIC	homozygous	113830635
5	62090683	62090684	A	T	26	GENIC	homozygous	114593133
5	62090857	62090858	A	G	33	GENIC	possibly homozygous	118894606
5	62091029	62091030	T	C	34	GENIC	possibly homozygous	114593135
5	62091349	62091350	A	G	25	GENIC	possibly homozygous	114593137
5	62091563	62091564	T	C	28	GENIC	homozygous	113830639
5	62091639	62091640	C	A	29	GENIC	homozygous	114593141
5	62091813	62091814	C	T	26	GENIC	homozygous	118894608
5	62092326	62092327	A	T	15	GENIC	homozygous	114593147