chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
15	35760005	35760006	G	A	21	GENIC	homozygous	139715515
15	35760061	35760062	C	T	21	GENIC	homozygous	139715516
15	35762532	35762533	T	A	22	GENIC	possibly homozygous	139715517
15	35762535	35762535		CTAATTGTTAGCAAAG	22	GENIC	possibly homozygous	139627935
15	35762683	35762684	A	T	16	GENIC	homozygous	139715518
15	35762838	35762839	G	A	17	GENIC	possibly homozygous	139715519
15	35762890	35762891	G	C	17	GENIC	homozygous	139715520
15	35763216	35763217	C	T	20	GENIC	homozygous	139715521
15	35763230	35763231	G	A	18	GENIC	homozygous	139715522
15	35763406	35763407	C	T	22	GENIC	homozygous	139715523
15	35764019	35764020	T	C	15	GENIC	homozygous	139715524
15	35764072	35764073	T	C	15	GENIC	homozygous	139715525
15	35765865	35765869	TCTA		14	GENIC	homozygous	139627936
15	35766677	35766678	A	T	11	GENIC	homozygous	139715529
15	35765450	35765451	T	C	15	GENIC	homozygous	139715526
15	35766191	35766192	G	T	21	GENIC	homozygous	139715527
15	35766272	35766273	A	G	20	GENIC	homozygous	139715528
15	35766678	35766679	T	C	11	GENIC	homozygous	139715530
15	35766720	35766721	G	A	15	GENIC	homozygous	139715531
15	35766834	35766835	C	T	20	GENIC	homozygous	139715532
15	35766869	35766870	C	T	19	GENIC	homozygous	139715533
15	35766935	35766936	A	G	18	GENIC	homozygous	139715534
15	35767788	35767789	G	A	20	GENIC	homozygous	139715535
15	35769909	35769910	T	C	25	GENIC	homozygous	139715536
15	35769994	35769995	A	G	16	GENIC	homozygous	139715537
15	35770301	35770302	G	A	19	GENIC	homozygous	139715538
15	35770479	35770480	G	A	21	GENIC	homozygous	139715539
15	35770505	35770506	T	C	18	GENIC	homozygous	139715540
15	35770940	35770941	T	C	30	GENIC	homozygous	139715541