chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	10495650	10495650		ACCTGGCCCAG	41	GENIC	homozygous	129583521
19	10495701	10495702	G		44	GENIC	homozygous	129583522
19	10495709	10495710	G		47	GENIC	homozygous	129583523
19	10495717	10495718	T	C	50	GENIC	homozygous	110169046
19	10495727	10495728	G	T	49	GENIC	homozygous	110058358
19	10495732	10495733	T		50	GENIC	homozygous	129583524
19	10495738	10495739	T	C	51	GENIC	homozygous	110169048
19	10495751	10495752	G	A	52	GENIC	homozygous	110169050
19	10495756	10495757	G		52	GENIC	homozygous	129583525
19	10495766	10495767	T		56	GENIC	homozygous	129583526
19	10495770	10495771	T	G	56	GENIC	homozygous	109634044
19	10495772	10495773	A	C	56	GENIC	homozygous	109634046
19	10495790	10495791	C		54	GENIC	homozygous	129583527
19	10495805	10495806	A		58	GENIC	homozygous	129583528
19	10495814	10495815	T		63	GENIC	homozygous	129583529
19	10495827	10495828	C		61	GENIC	homozygous	129583530
19	10495763	10495764	C	A	54	GENIC	homozygous	119596328
19	10501015	10501016	G	T	26	GENIC	homozygous	119656103
19	10509958	10509959	G	T	18	GENIC	homozygous	129632148