chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
14	15723025	15723026	A	G	14	GENIC	homozygous	139459017
14	15723338	15723339	A	T	19	GENIC	homozygous	139459020
14	15723355	15723356	C	T	16	GENIC	homozygous	146552459
14	15723518	15723519	C	T	19	GENIC	homozygous	146552460
14	15723897	15723898	C	G	3	GENIC	homozygous	146552463
14	15723899	15723900	C	G	3	GENIC	homozygous	146552464
14	15723901	15723902	C	G	3	GENIC	homozygous	146552465
14	15723919	15723920	C	G	6	GENIC	homozygous	154826186
14	15724022	15724023	G	A	14	GENIC	homozygous	146552466
14	15724097	15724098	A	G	13	GENIC	homozygous	146552467
14	15724315	15724316	T	C	8	GENIC	homozygous	154826187
14	15724390	15724391	T	C	8	GENIC	homozygous	403851083
14	15723919	15723920	C		6	GENIC	heterozygous	403851079
14	15723923	15723924	C		6	GENIC	heterozygous	403851080
14	15723923	15723924	C	G	6	GENIC	homozygous	403851081
14	15724375	15724376	T	C	7	GENIC	homozygous	403851082
14	15724391	15724392	C	G	9	GENIC	homozygous	403851084
14	15724638	15724639	C	T	8	GENIC	homozygous	403851085
14	15724643	15724644	G	A	8	GENIC	homozygous	146552468
14	15724783	15724784	T	C	10	GENIC	homozygous	139459021
14	15724851	15724852	A	T	16	GENIC	homozygous	146552469
14	15725041	15725042	C	T	11	GENIC	homozygous	146552470
14	15725194	15725195	T	A	23	GENIC	homozygous	139459022
14	15725496	15725497	T	C	13	GENIC	homozygous	139459023
14	15725653	15725654	T	G	14	GENIC	homozygous	139459024
14	15725767	15725768	T	G	16	GENIC	possibly homozygous	146552471
14	15726439	15726440	A	T	10	GENIC	homozygous	146552472
14	15724338	15724338		TC	7	GENIC	homozygous	146546702
14	15724478	15724478		T	17	GENIC	homozygous	146546703
14	15724684	15724684		AA	3	GENIC	homozygous	146546704
14	15726281	15726282	G	A	11	GENIC	homozygous	154826191
14	15726293	15726294	G	A	11	GENIC	homozygous	154826192