chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	37539840	37539841	C	T	58	GENIC	homozygous	145079205
19	37540763	37540764	A	G	36	GENIC	homozygous	145079206
19	37541049	37541050	T	C	48	GENIC	homozygous	145079207
19	37541757	37541758	C	T	50	GENIC	homozygous	145079208
19	37542213	37542214	G	A	66	GENIC	homozygous	145079209
19	37542718	37542724	GCCTCT		39	GENIC	homozygous	140388547
19	37542756	37542757	C	T	49	GENIC	homozygous	145079210
19	37542801	37542802	T	A	60	GENIC	homozygous	145079211
19	37542829	37542830	C	T	59	GENIC	homozygous	145079212
19	37543074	37543075	C	T	39	GENIC	homozygous	145079213
19	37543321	37543322	A	T	40	GENIC	homozygous	145079214
19	37543365	37543366	C	T	40	GENIC	homozygous	145079215
19	37543376	37543377	T	A	42	GENIC	homozygous	145079216
19	37543698	37543699	C	T	45	GENIC	homozygous	145079217
19	37544057	37544058	G	A	49	GENIC	homozygous	140452353
19	37543431	37543431		T	40	GENIC	homozygous	145068790