chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	10495548	10495549	T	C	28	GENIC	homozygous	109634042
19	10495751	10495752	G	A	23	GENIC	homozygous	110169050
19	10495650	10495650		ACCTGGCCCAG	25	GENIC	homozygous	129583521
19	10495701	10495702	G		21	GENIC	homozygous	129583522
19	10495709	10495710	G		20	GENIC	homozygous	129583523
19	10495732	10495733	T		24	GENIC	homozygous	129583524
19	10495717	10495718	T	C	23	GENIC	homozygous	110169046
19	10495738	10495739	T	C	24	GENIC	homozygous	110169048
19	10495727	10495728	G	T	23	GENIC	homozygous	110058358
19	10495756	10495757	G		23	GENIC	homozygous	129583525
19	10495766	10495767	T		23	GENIC	homozygous	129583526
19	10495770	10495771	T	G	23	GENIC	homozygous	109634044
19	10495772	10495773	A	C	23	GENIC	homozygous	109634046
19	10495790	10495791	C		24	GENIC	homozygous	129583527
19	10495805	10495806	A		25	GENIC	homozygous	129583528
19	10495814	10495815	T		29	GENIC	homozygous	129583529
19	10495827	10495828	C		29	GENIC	homozygous	129583530
19	10496300	10496301	G	T	14	GENIC	possibly homozygous	109634048
19	10496905	10496906	G	C	22	GENIC	homozygous	109634050
19	10498387	10498388	C	T	21	GENIC	homozygous	109634052
19	10499679	10499680	G	A	24	GENIC	homozygous	109634054
19	10500386	10500387	G	T	17	GENIC	homozygous	109634056
19	10505751	10505752	G	A	23	GENIC	homozygous	109634058
19	10506143	10506143		AGAC	24	GENIC	homozygous	129583531
19	10495763	10495764	C	A	24	GENIC	homozygous	119596328
19	10514076	10514077	C	G	12	GENIC	homozygous	109634060
19	10514078	10514079	A	G	14	GENIC	homozygous	109634062
19	10514542	10514543	C	T	31	GENIC	homozygous	109634064
19	10514593	10514594	A	G	27	GENIC	homozygous	109634066
19	10514636	10514637	G	A	32	GENIC	homozygous	109634068
19	10514028	10514029	G	A	14	GENIC	homozygous	109799513
19	10509958	10509959	G	T	15	GENIC	homozygous	129632148