chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	55706280	55706281	A	T	39	GENIC	homozygous	109737066
19	55707333	55707334	T	C	29	GENIC	homozygous	109737068
19	55708126	55708127	T	C	35	GENIC	homozygous	109737070
19	55710362	55710363	G	A	24	GENIC	homozygous	110066341
19	55710776	55710777	G	A	37	GENIC	homozygous	109737072
19	55714226	55714227	T	C	42	GENIC	homozygous	109737074
19	55714448	55714449	C	T	26	GENIC	possibly homozygous	109737076
19	55717078	55717079	A	G	24	GENIC	homozygous	109737078
19	55719614	55719615	T	C	25	GENIC	homozygous	109737080
19	55722613	55722614	G	C	25	GENIC	homozygous	109737082
19	55738389	55738390	T	C	34	GENIC	homozygous	109737084
19	55749482	55749483	C	A	24	GENIC	homozygous	109737086
19	55753955	55753956	A	G	96	GENIC	heterozygous	119646472
19	55753959	55753960	C	T	99	GENIC	heterozygous	119683450
19	55771260	55771261	T	A	15	GENIC	heterozygous	119633594
19	55720010	55720011	C	A	22	GENIC	homozygous	110036179
19	55720012	55720013	C	A	22	GENIC	homozygous	110036181
19	55764600	55764601	T	C	39	GENIC	homozygous	119633593
19	55780593	55780594	C	T	28	GENIC	homozygous	109737088
19	55781108	55781109	A	C	34	GENIC	homozygous	109737090
19	55793278	55793279	C	T	26	GENIC	heterozygous	119714566
19	55853123	55853124	A	T	18	GENIC	possibly homozygous	109789048
19	55858539	55858540	G	T	14	GENIC	homozygous	109890309