chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	51457822	51457823	T	C	39	GENIC	homozygous	140473486
19	51462978	51462979	C	T	40	GENIC	homozygous	147381439
19	51459553	51459554	C	T	47	GENIC	homozygous	147381436
19	51462096	51462097	G	A	68	GENIC	homozygous	147381437
19	51462647	51462648	C	G	52	GENIC	homozygous	147381438
19	51463378	51463379	A	T	43	GENIC	possibly homozygous	147381440
19	51463727	51463730	ACT		24	GENIC	homozygous	140928794
19	51463789	51463800	CCTCCTCCTCC		24	GENIC	homozygous	147442464
19	51463803	51463824	TCCTCCTCTTCCTCTTCCTCC		23	GENIC	homozygous	147442465
19	51463838	51463841	TCC		23	GENIC	homozygous	147442466
19	51463865	51463874	TCCTCCTCT		23	GENIC	homozygous	147442467
19	51463932	51463933	C	T	21	GENIC	homozygous	147442743
19	51464114	51464115	C	A	32	GENIC	homozygous	147381441
19	51464124	51464125	A	G	30	GENIC	homozygous	140473489
19	51464571	51464572	A	G	41	GENIC	homozygous	140473490