chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	25029125	25029125		C	10	GENIC	homozygous	129595696
19	25029141	25029142	G		11	GENIC	homozygous	129595697
19	25029163	25029163		GGC	9	GENIC	homozygous	129595698
19	25029173	25029174	G		7	GENIC	homozygous	129595699
19	25029178	25029179	C		7	GENIC	homozygous	129595700
19	25029182	25029183	G	C	7	GENIC	homozygous	109672124
19	25029204	25029204		C	11	GENIC	homozygous	129595701
19	25029268	25029269	G		9	GENIC	homozygous	129595702
19	25029287	25029288	A	G	8	GENIC	homozygous	109672126
19	25029313	25029313		G	9	GENIC	homozygous	129595703
19	25029324	25029326	GT		9	GENIC	homozygous	129595704
19	25029347	25029347		G	12	GENIC	homozygous	129595705
19	25029380	25029380		C	9	GENIC	homozygous	129595706
19	25029401	25029402	G		10	GENIC	homozygous	129595707
19	25029411	25029411		G	10	GENIC	homozygous	129595708
19	25029422	25029422		G	12	GENIC	homozygous	129595709
19	25029445	25029445		C	16	GENIC	homozygous	129595710
19	25029457	25029457		C	15	GENIC	homozygous	129595711
19	25029459	25029460	G		16	GENIC	homozygous	129595712
19	25066488	25066489	G		16	GENIC	homozygous	129595717
19	25034990	25034991	C	A	15	GENIC	heterozygous	131763913
19	25035021	25035022	C	T	13	GENIC	heterozygous	131763914