chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	55706280	55706281	A	T	22	GENIC	homozygous	109737066
19	55707333	55707334	T	C	22	GENIC	homozygous	109737068
19	55708126	55708127	T	C	22	GENIC	homozygous	109737070
19	55710776	55710777	G	A	13	GENIC	possibly homozygous	109737072
19	55714226	55714227	T	C	20	GENIC	homozygous	109737074
19	55714448	55714449	C	T	25	GENIC	homozygous	109737076
19	55717078	55717079	A	G	21	GENIC	homozygous	109737078
19	55719614	55719615	T	C	28	GENIC	homozygous	109737080
19	55722613	55722614	G	C	38	GENIC	homozygous	109737082
19	55738389	55738390	T	C	20	GENIC	homozygous	109737084
19	55780593	55780594	C	T	25	GENIC	homozygous	109737088
19	55720010	55720011	C	A	14	GENIC	homozygous	110036179
19	55720012	55720013	C	A	14	GENIC	homozygous	110036181
19	55749482	55749483	C	A	23	GENIC	homozygous	109737086
19	55764600	55764601	T	C	33	GENIC	homozygous	119633593
19	55754021	55754022	T	C	70	GENIC	heterozygous	119666429
19	55754022	55754023	G	A	70	GENIC	heterozygous	119666430
19	55754031	55754032	A	C	66	GENIC	heterozygous	119666431
19	55781108	55781109	A	C	18	GENIC	homozygous	109737090
19	55787666	55787667	G	A	18	GENIC	heterozygous	119633595
19	55852852	55852853	G	A	25	GENIC	heterozygous	119646475
19	55853123	55853124	A	T	15	GENIC	possibly homozygous	109789048
19	55858539	55858540	G	T	19	GENIC	homozygous	109890309