chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	59509961	59509962	C	A	32	GENIC	homozygous	117942774
8	59511649	59511650	G	A	27	GENIC	homozygous	117942775
8	59511797	59511798	C	T	33	GENIC	homozygous	117942776
8	59516680	59516681	T	A	41	GENIC	homozygous	116512382
8	59517501	59517502	C	T	29	GENIC	homozygous	117942777
8	59518417	59518418	T	C	23	GENIC	homozygous	116512384
8	59520098	59520099	T	G	32	GENIC	homozygous	117942778
8	59521018	59521019	A	C	23	GENIC	homozygous	116512388
8	59521247	59521248	T	C	31	GENIC	homozygous	116512390
8	59521602	59521603	C	T	30	GENIC	homozygous	117942779
8	59522874	59522875	C	T	20	GENIC	homozygous	117942780
8	59523604	59523605	C	T	26	GENIC	homozygous	117942781
8	59524982	59524983	C	T	38	GENIC	homozygous	117942782
8	59526056	59526057	C	G	33	GENIC	homozygous	117942783
8	59527135	59527136	T	C	31	GENIC	homozygous	116512396
8	59527998	59527999	G	A	33	GENIC	homozygous	116512402
8	59528631	59528632	T	C	39	GENIC	homozygous	116512404
8	59528672	59528673	G	A	30	GENIC	homozygous	117942784
8	59529596	59529597	T	C	33	GENIC	homozygous	116512410
8	59529781	59529782	T	C	33	GENIC	homozygous	116512412
8	59531528	59531529	A	G	25	GENIC	homozygous	116512414