chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	10495572	10495573	G	A	25	GENIC	homozygous	110143438
19	10495900	10495901	C	T	13	GENIC	possibly homozygous	110143440
19	10496905	10496906	G	C	23	GENIC	possibly homozygous	109634050
19	10497960	10497961	A	G	46	GENIC	possibly homozygous	110143442
19	10500386	10500387	G	T	37	GENIC	homozygous	109634056
19	10501546	10501547	A	G	17	GENIC	possibly homozygous	109993710
19	10504532	10504533	T	C	15	GENIC	homozygous	109993715
19	10505353	10505354	A	G	24	GENIC	possibly homozygous	109993717
19	10507965	10507966	G	A	24	GENIC	possibly homozygous	110143445
19	10508739	10508740	C	T	28	GENIC	possibly homozygous	110143447
19	10508968	10508969	C	T	32	GENIC	possibly homozygous	110143449
19	10510496	10510497	C	G	33	GENIC	possibly homozygous	110143452
19	10511265	10511266	G	A	40	GENIC	possibly homozygous	110143454
19	10512135	10512136	C	T	26	GENIC	possibly homozygous	110143456
19	10512681	10512682	G	C	23	GENIC	possibly homozygous	110143459
19	10513321	10513322	C	T	23	GENIC	homozygous	110130778
19	10513329	10513330	C	T	23	GENIC	homozygous	110143461
19	10513599	10513600	G	A	3	GENIC	homozygous	110143463
19	10513723	10513724	C	T	4	GENIC	homozygous	110143466
19	10513792	10513793	C	T	13	GENIC	homozygous	109993730
19	10513829	10513830	G	A	7	GENIC	homozygous	110143468
19	10513853	10513854	A	G	6	GENIC	homozygous	110143470
19	10513937	10513938	C	T	8	GENIC	homozygous	110130781
19	10514028	10514029	G	A	8	GENIC	homozygous	109799513
19	10514078	10514079	A	G	6	GENIC	homozygous	109634062
19	10514542	10514543	C	T	15	GENIC	homozygous	109634064
19	10514593	10514594	A	G	14	GENIC	homozygous	109634066