chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	37528284	37528285	T	C	29	GENIC	possibly homozygous	109693874
19	37528664	37528665	A	G	16	GENIC	homozygous	109693876
19	37532185	37532186	C	T	15	GENIC	homozygous	109693878
19	37536304	37536305	T	C	21	GENIC	homozygous	109693880
19	37538575	37538576	G	A	20	GENIC	homozygous	109924806
19	37538736	37538737	G	A	24	GENIC	homozygous	109961688
19	37546875	37546876	T	C	27	GENIC	homozygous	109693884
19	37552195	37552196	C	A	17	GENIC	homozygous	109693886
19	37555177	37555178	G	C	27	GENIC	homozygous	109693888
19	37555872	37555873	G	T	20	GENIC	homozygous	109693890
19	37561818	37561819	C	A	24	GENIC	homozygous	109693892
19	37564151	37564152	G	A	19	GENIC	homozygous	109693894
19	37567102	37567103	A	G	19	GENIC	homozygous	109693896
19	37567113	37567114	A	T	19	GENIC	homozygous	109693898
19	37567280	37567281	A	C	29	GENIC	homozygous	109693900
19	37571689	37571690	C	T	18	GENIC	homozygous	109693902
19	37572370	37572371	C	G	12	GENIC	homozygous	109693904
19	37572792	37572793	G	A	14	GENIC	homozygous	109693906
19	37572864	37572865	A	G	13	GENIC	homozygous	109693908
19	37575723	37575724	T	A	32	GENIC	homozygous	109693910
19	37576706	37576707	G	C	18	GENIC	homozygous	109693912
19	37576783	37576784	A	C	25	GENIC	homozygous	109693914
19	37576791	37576792	A	T	25	GENIC	homozygous	109693916
19	37576796	37576797	G	A	27	GENIC	homozygous	109693918
19	37576808	37576809	T	A	26	GENIC	homozygous	109693920
19	37576855	37576856	T	G	28	GENIC	homozygous	109693922
19	37581659	37581660	A	G	17	GENIC	homozygous	109693924
19	37581717	37581718	C	T	18	GENIC	homozygous	109693926
19	37582375	37582376	C	G	35	GENIC	homozygous	109693928
19	37582524	37582525	T	C	17	GENIC	homozygous	109693930
19	37571896	37571897	G	C	21	GENIC	homozygous	110065519