chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	56055087	56055088	T	A	25	GENIC	homozygous	109737736
19	56055184	56055185	T	C	8	GENIC	homozygous	109737738
19	56055493	56055494	G	A	30	GENIC	homozygous	109737740
19	56055494	56055495	A	C	30	GENIC	homozygous	109737742
19	56055496	56055497	C	T	30	GENIC	homozygous	109737744
19	56055498	56055499	A	G	31	GENIC	homozygous	109737746
19	56055595	56055596	G	T	32	GENIC	homozygous	109737748
19	56056384	56056385	A	G	25	GENIC	homozygous	109737750
19	56056978	56056979	C	A	24	GENIC	homozygous	109737752
19	56057526	56057527	G	A	15	GENIC	homozygous	109737754
19	56058526	56058527	G	C	21	GENIC	homozygous	109737756
19	56059302	56059303	T	C	24	GENIC	homozygous	109737758
19	56060566	56060567	A	T	24	GENIC	homozygous	109737760
19	56060598	56060599	A	G	16	GENIC	homozygous	109737762
19	56060765	56060766	T	C	24	GENIC	homozygous	109737764
19	56061380	56061381	T	G	21	GENIC	homozygous	109737766
19	56062172	56062173	G	A	14	GENIC	homozygous	109737768
19	56063029	56063030	C	T	27	GENIC	homozygous	109737770
19	56066333	56066334	T	C	22	GENIC	homozygous	109737772
19	56067372	56067373	C	T	23	GENIC	homozygous	109737774
19	56067437	56067438	C	A	23	GENIC	homozygous	109737776
19	56060987	56060988	T	G	19	GENIC	homozygous	109825772