chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	38130466	38130467	G	T	32	GENIC	homozygous	109814147
19	38131601	38131602	G	A	23	GENIC	homozygous	109814149
19	38131762	38131763	G	T	22	GENIC	homozygous	109814151
19	38133603	38133604	G	A	27	GENIC	homozygous	109814153
19	38135005	38135006	C	A	9	GENIC	homozygous	109814155
19	38135784	38135785	C	T	42	GENIC	homozygous	109814157
19	38136038	38136039	T	C	45	GENIC	possibly homozygous	109814159
19	38138602	38138603	T	C	28	GENIC	homozygous	109814161
19	38139730	38139731	G	A	24	GENIC	homozygous	109814163
19	38140257	38140258	T	C	42	GENIC	homozygous	109814165
19	38140581	38140582	G	A	24	GENIC	homozygous	109814167
19	38140975	38140976	T	C	25	GENIC	homozygous	109814169
19	38141111	38141112	G	A	44	GENIC	homozygous	109814171
19	38141190	38141191	A	G	33	GENIC	homozygous	109814174
19	38142427	38142428	T	C	28	GENIC	homozygous	109814176
19	38142707	38142708	C	T	32	GENIC	homozygous	109814178
19	38144031	38144032	T	G	27	GENIC	possibly homozygous	119665319
19	38144337	38144338	C	T	33	GENIC	homozygous	109814180
19	38144463	38144464	T	C	27	GENIC	homozygous	109814182