chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	62387032	62387033	C	A	34	GENIC	homozygous	117109785
8	62387269	62387270	C	T	26	GENIC	homozygous	117109786
8	62387307	62387308	C	T	20	GENIC	homozygous	117109787
8	62387790	62387791	C	A	38	GENIC	homozygous	117109788
8	62388307	62388308	A	G	23	GENIC	homozygous	117109789
8	62388675	62388676	G	T	26	GENIC	homozygous	116836400
8	62388896	62388897	C	T	29	GENIC	homozygous	117109790
8	62390636	62390637	G	T	24	GENIC	homozygous	117158194
8	62391283	62391284	T	C	33	GENIC	homozygous	116836428
8	62391539	62391540	A	T	36	GENIC	homozygous	117109791
8	62392327	62392328	C	T	33	GENIC	homozygous	116836444
8	62392708	62392709	A	G	39	GENIC	homozygous	116836450
8	62392867	62392868	A	G	24	GENIC	homozygous	116836454
8	62393645	62393646	T	G	23	GENIC	homozygous	116836458
8	62393877	62393878	G	C	38	GENIC	homozygous	116836460
8	62394113	62394114	T	C	28	GENIC	homozygous	116836462
8	62394382	62394383	C	T	33	GENIC	homozygous	116836464
8	62395121	62395122	T	C	28	GENIC	homozygous	116836468
8	62395707	62395708	C	T	21	GENIC	homozygous	117158196
8	62396074	62396075	C	T	35	GENIC	homozygous	117158197
8	62396224	62396225	G	A	28	GENIC	homozygous	117158198
8	62397446	62397447	G	C	19	GENIC	homozygous	116836482
8	62397476	62397477	G	A	16	GENIC	homozygous	117158199
8	62398688	62398689	A	C	35	GENIC	homozygous	117109800
8	62398826	62398827	C	T	25	GENIC	homozygous	117109801
8	62399214	62399215	G	A	35	GENIC	homozygous	117109802
8	62399560	62399561	T	C	34	GENIC	homozygous	117109803
8	62399989	62399990	T	G	23	GENIC	homozygous	117158200