chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	38193908	38193909	T	G	29	GENIC	homozygous	109814248
19	38194198	38194199	G	A	19	GENIC	homozygous	109814250
19	38195009	38195010	T	G	26	GENIC	homozygous	109814252
19	38196241	38196242	A	G	28	GENIC	homozygous	109814254
19	38197007	38197008	A	T	16	GENIC	homozygous	109814256
19	38197607	38197608	C	T	15	GENIC	homozygous	109814258
19	38201906	38201907	T	C	23	GENIC	homozygous	109814260
19	38215561	38215562	G	A	29	GENIC	homozygous	109814262
19	38216164	38216165	C	T	41	GENIC	homozygous	109814266
19	38216520	38216521	T	A	15	GENIC	homozygous	109814268
19	38217417	38217418	G	A	22	GENIC	homozygous	109814270
19	38218165	38218166	C	T	6	GENIC	homozygous	109814272
19	38232961	38232962	C	T	32	GENIC	homozygous	109814276
19	38235442	38235443	G	T	34	GENIC	homozygous	109814278
19	38235637	38235638	C	T	40	GENIC	homozygous	109814280
19	38236689	38236690	T	G	32	GENIC	homozygous	109814282