chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	54972137	54972138	A	C	8	GENIC	homozygous	46166474
19	54972980	54972981	T	TG	15	GENIC	homozygous	46166475
19	54974525	54974526	A	G	27	GENIC	homozygous	46263644
19	54975389	54975390	T	C	14	GENIC	homozygous	46166485
19	54975429	54975430	A	T	6	GENIC	homozygous	46166487
19	54975444	54975445	T	C	10	GENIC	homozygous	46166488
19	54975567	54975568	A	T	23	GENIC	homozygous	46166489
19	54976783	54976784	G	A	35	GENIC	homozygous	46166491
19	54976928	54976929	T	C	35	GENIC	homozygous	46166492
19	54977357	54977358	T	TTC	17	GENIC	homozygous	46166494
19	54978086	54978092	GAAGTG	------	23	GENIC	homozygous	46166496
19	54979381	54979382	C	T	23	GENIC	homozygous	46166497
19	54979723	54979724	C	T	29	GENIC	homozygous	46166498
19	54980778	54980779	C	T	31	GENIC	homozygous	46166499
19	54980799	54980800	T	C	30	GENIC	homozygous	46166500
19	54981054	54981055	T	A	21	GENIC	homozygous	46718717
19	54978361	54978362	G	T	19	GENIC	homozygous	46718711
19	54979947	54979948	C	T	22	GENIC	homozygous	46718713
19	54980980	54980981	G	A	18	GENIC	homozygous	46718715
19	54981068	54981069	A	G	20	GENIC	homozygous	46166502
19	54981247	54981248	C	A	22	GENIC	homozygous	46166503
19	54981345	54981346	C	T	25	GENIC	homozygous	46166504
19	54982463	54982464	A	AAT	13	GENIC	homozygous	46263652
19	54982504	54982505	T	C	27	GENIC	homozygous	46166506