chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	14003513	14003514	G	A	26	GENIC	homozygous	111452140
3	14003578	14003579	G	C	23	GENIC	homozygous	111452141
3	14003937	14003938	G	T	41	GENIC	homozygous	111452142
3	14004169	14004170	T	C	30	GENIC	homozygous	111452143
3	14004184	14004185	G	T	32	GENIC	homozygous	111452144
3	14004517	14004518	T	A	19	GENIC	homozygous	111452145
3	14004616	14004617	C	T	23	GENIC	homozygous	111452146
3	14008220	14008221	G	A	37	GENIC	homozygous	111452147
3	14009120	14009121	T	G	26	GENIC	homozygous	111452148
3	14010210	14010211	C	A	33	GENIC	homozygous	111452149
3	14010788	14010789	T	C	29	GENIC	homozygous	111452150
3	14010848	14010849	T	C	9	GENIC	homozygous	111452151
3	14019514	14019515	A	C	26	GENIC	homozygous	111452152
3	14019522	14019523	G	C	27	GENIC	homozygous	111452153
3	14019523	14019524	T	C	27	GENIC	homozygous	111452154
3	14019779	14019780	A	G	41	GENIC	homozygous	111452155
3	14020453	14020454	A	G	31	GENIC	homozygous	111452156
3	14021084	14021085	G	A	39	GENIC	homozygous	111452157
3	14021098	14021099	G	A	41	GENIC	homozygous	111452158
3	14021476	14021477	T	A	31	GENIC	homozygous	111452159
3	14021525	14021526	C	T	37	GENIC	homozygous	111452160
3	14021782	14021783	C	T	31	GENIC	homozygous	111452161