chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	37429023	37429024	G	A	73	GENIC	possibly homozygous	109924780
19	37429586	37429587	C	T	50	GENIC	homozygous	109924782
19	37430377	37430378	C	T	53	GENIC	homozygous	109924784
19	37430575	37430576	C	T	49	GENIC	homozygous	109693745
19	37431674	37431675	C	T	62	GENIC	homozygous	109924786
19	37431979	37431980	A	G	52	GENIC	homozygous	109693749
19	37431982	37431983	G	A	53	GENIC	homozygous	109924788
19	37433425	37433426	T	C	53	GENIC	homozygous	109693751
19	37434580	37434581	A	G	61	GENIC	homozygous	109693757
19	37437117	37437118	A	G	47	GENIC	homozygous	109924790
19	37437486	37437487	G	A	40	GENIC	homozygous	109924792
19	37437978	37437979	G	A	34	GENIC	homozygous	109693769
19	37443757	37443758	C	T	46	GENIC	homozygous	109693781
19	37446234	37446235	A		30	GENIC	possibly homozygous	133330188
19	37433632	37433632		C	36	GENIC	homozygous	133330186
19	37446169	37446170	A		36	GENIC	homozygous	133330187
19	37439469	37439469		C	8	GENIC	homozygous	129605620
19	37444637	37444638	G	C	7	GENIC	heterozygous	119629191
19	37448967	37448968	G	T	43	GENIC	homozygous	109693796
19	37446120	37446121	T	G	54	GENIC	homozygous	119629192
19	37446510	37446511	G	A	42	GENIC	homozygous	109693790
19	37447595	37447596	T	G	48	GENIC	homozygous	109693794
19	37449469	37449470	A	T	60	GENIC	homozygous	109924794
19	37449482	37449483	A	T	60	GENIC	homozygous	109693798
19	37450764	37450764		AGG	16	GENIC	possibly homozygous	129605623
19	37451362	37451363	A	G	37	GENIC	homozygous	109924796
19	37451882	37451883	G	A	40	GENIC	homozygous	109924798
19	37452160	37452161	T	A	54	GENIC	homozygous	109924800
19	37452799	37452800	C	G	39	GENIC	homozygous	109924802
19	37450795	37450796	A	G	17	GENIC	homozygous	110065517