chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	27406716	27406717	A	G	24	GENIC	homozygous	110047548
19	27407219	27407220	A	G	21	GENIC	homozygous	109673826
19	27411744	27411745	T	C	24	GENIC	homozygous	109673828
19	27412356	27412357	A	G	34	GENIC	homozygous	109673830
19	27420911	27420912	A	G	40	GENIC	homozygous	109673832
19	27421662	27421663	T	C	33	GENIC	homozygous	109673834
19	27421840	27421841	C	T	30	GENIC	homozygous	109673836
19	27423597	27423598	C	T	40	GENIC	heterozygous	119708369
19	27423611	27423612	T	A	46	GENIC	heterozygous	119708370
19	27425809	27425810	G	A	38	GENIC	homozygous	109673838
19	27425835	27425836	C	T	41	GENIC	homozygous	109673840
19	27427078	27427079	T	C	39	GENIC	homozygous	109673842
19	27427836	27427837	T	C	30	GENIC	homozygous	109673844
19	27429475	27429476	C	G	29	GENIC	homozygous	109673846
19	27417226	27417227	G	C	37	GENIC	heterozygous	119609803
19	27433409	27433410	G	T	28	GENIC	heterozygous	119609804
19	27434463	27434464	C	T	36	GENIC	heterozygous	119609806
19	27434734	27434735	C	T	49	GENIC	homozygous	109673848
19	27436172	27436173	C	T	23	GENIC	homozygous	109673850
19	27440765	27440766	T	G	24	GENIC	homozygous	109673852
19	27441987	27441988	G	A	29	GENIC	homozygous	109673854