chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	37813435	37813436	C	T	36	GENIC	possibly homozygous	109694445
19	37813573	37813574	G	A	31	GENIC	possibly homozygous	109694447
19	37814045	37814046	T	C	15	GENIC	possibly homozygous	109694449
19	37815315	37815316	G	T	18	GENIC	possibly homozygous	109694453
19	37815316	37815317	C	G	18	GENIC	possibly homozygous	109694455
19	37815382	37815383	T	C	20	GENIC	possibly homozygous	109694457
19	37815440	37815441	C	T	25	GENIC	possibly homozygous	109694459
19	37815809	37815810	C	T	28	GENIC	possibly homozygous	109694461
19	37816528	37816529	C	T	28	GENIC	homozygous	109694463
19	37816580	37816581	T	C	31	GENIC	possibly homozygous	109694465
19	37816595	37816596	C	G	31	GENIC	possibly homozygous	109694467
19	37818702	37818703	A	T	32	GENIC	homozygous	109694469