chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	131413368	131413369	G	A	20	GENIC	homozygous	137622924
5	131414203	131414204	C	T	15	GENIC	homozygous	137622925
5	131415136	131415137	T	C	17	GENIC	homozygous	137622926
5	131415458	131415458		G	13	GENIC	homozygous	137342141
5	131415460	131415462	CA		13	GENIC	homozygous	137342142
5	131415827	131415828	C	T	23	GENIC	homozygous	137622927
5	131415976	131415977	T	C	19	GENIC	homozygous	137622928
5	131416339	131416340	T	G	12	GENIC	homozygous	137622929
5	131417442	131417443	C	T	13	GENIC	homozygous	137622930
5	131418041	131418042	G	C	14	GENIC	homozygous	137622931
5	131418798	131418799	C	T	17	GENIC	homozygous	137622932
5	131418808	131418809	A	G	17	GENIC	homozygous	137622933
5	131418826	131418827	A		14	GENIC	heterozygous	403158134
5	131418824	131418825	A	T	14	GENIC	homozygous	154337120
5	131418824	131418825	A		14	GENIC	heterozygous	403158133
5	131418826	131418827	A	T	14	GENIC	homozygous	154337121
5	131418828	131418829	A		14	GENIC	heterozygous	403158135
5	131418828	131418829	A	T	14	GENIC	homozygous	403158136
5	131418870	131418871	T	A	22	GENIC	homozygous	154337126
5	131418870	131418871	T		22	GENIC	heterozygous	403158139
5	131419166	131419166		AGC	22	GENIC	homozygous	137342143
5	131419456	131419457	T	A	17	GENIC	homozygous	137622934
5	131419875	131419876	T	A	20	GENIC	homozygous	137622935