chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	10576424	10576425	T	C	60	GENIC	homozygous	110076256
19	10577291	10577292	T	C	65	GENIC	homozygous	109634266
19	10577350	10577353	CTG		67	GENIC	homozygous	133510503
19	10577548	10577549	C	T	59	GENIC	homozygous	109634268
19	10577895	10577896	G	A	79	GENIC	homozygous	109993855
19	10578495	10578496	G	C	64	GENIC	homozygous	109634272
19	10579285	10579286	T	C	48	GENIC	homozygous	109634278
19	10579485	10579486	G	T	37	GENIC	homozygous	109634280
19	10580268	10580269	C	T	52	GENIC	possibly homozygous	110076258
19	10579097	10579098	A		60	GENIC	homozygous	129583623
19	10580380	10580380		A	52	GENIC	homozygous	129583624
19	10580217	10580218	G	A	49	GENIC	homozygous	109764606
19	10581558	10581559	C	G	56	GENIC	homozygous	109634284