chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	38193908	38193909	T	G	22	GENIC	homozygous	109814248
19	38194198	38194199	G	A	17	GENIC	homozygous	109814250
19	38195009	38195010	T	G	10	GENIC	homozygous	109814252
19	38196241	38196242	A	G	22	GENIC	homozygous	109814254
19	38197007	38197008	A	T	20	GENIC	homozygous	109814256
19	38197607	38197608	C	T	10	GENIC	homozygous	109814258
19	38201050	38201051	A	C	16	GENIC	heterozygous	125259684
19	38201906	38201907	T	C	22	GENIC	homozygous	109814260
19	38215561	38215562	G	A	21	GENIC	homozygous	109814262
19	38215847	38215848	C	A	24	GENIC	homozygous	109814264
19	38216164	38216165	C	T	7	GENIC	homozygous	109814266
19	38216520	38216521	T	A	9	GENIC	homozygous	109814268
19	38217417	38217418	G	A	17	GENIC	homozygous	109814270
19	38223170	38223171	A	G	7	GENIC	homozygous	110035806
19	38232961	38232962	C	T	13	GENIC	homozygous	109814276
19	38235442	38235443	G	T	17	GENIC	homozygous	109814278
19	38235637	38235638	C	T	21	GENIC	homozygous	109814280
19	38236689	38236690	T	G	22	GENIC	homozygous	109814282