chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	49435801	49435802	T	C	35	GENIC	homozygous	109723632
19	49438794	49438795	A	C	24	GENIC	homozygous	109723634
19	49440433	49440434	G	A	34	GENIC	heterozygous	110085062
19	49445153	49445154	A	G	16	GENIC	homozygous	109723636
19	49439201	49439202	G	A	32	GENIC	homozygous	109820865
19	49441232	49441233	A	G	208	GENIC	heterozygous	119714387
19	49441236	49441237	A	G	212	GENIC	heterozygous	119632142
19	49441237	49441238	C	T	214	GENIC	heterozygous	119632143
19	49441241	49441242	T	C	237	GENIC	heterozygous	119632144
19	49448865	49448866	A	G	17	GENIC	homozygous	109820867
19	49451578	49451579	T	C	11	GENIC	homozygous	109723638
19	49452640	49452641	G	A	23	GENIC	homozygous	109723640
19	49456143	49456144	C	T	42	GENIC	possibly homozygous	109820869
19	49457551	49457552	A	C	19	GENIC	homozygous	109723642
19	49447079	49447080	C	A	11	GENIC	homozygous	109977576
19	49447118	49447119	C	T	13	GENIC	homozygous	110049849
19	49447119	49447120	C	A	13	GENIC	homozygous	110049851
19	49456206	49456207	A	G	39	GENIC	heterozygous	119666132