chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	62193047	62193048	C	T	35	GENIC	homozygous	116939609
10	62194548	62194549	G	T	34	GENIC	homozygous	116939611
10	62195979	62195980	A	G	25	GENIC	homozygous	116613498
10	62196407	62196408	G	A	20	GENIC	homozygous	116939613
10	62196783	62196784	T	C	32	GENIC	homozygous	116939615
10	62199332	62199333	G	C	22	GENIC	homozygous	116939617
10	62200410	62200411	T	A	16	GENIC	homozygous	116613508
10	62201688	62201689	G	A	19	GENIC	homozygous	116939619
10	62202814	62202815	A	G	18	GENIC	homozygous	116613510
10	62208062	62208063	A	G	37	GENIC	homozygous	116939621
10	62208867	62208868	T	C	22	GENIC	homozygous	116613514
10	62209517	62209518	C	T	19	GENIC	homozygous	116939623
10	62210720	62210721	C	T	19	GENIC	homozygous	116613516
10	62210759	62210760	G	A	23	GENIC	homozygous	116939625
10	62212586	62212587	A	G	24	GENIC	homozygous	116613518
10	62214260	62214261	G	T	8	GENIC	homozygous	117061915
10	62220425	62220426	A	G	13	GENIC	possibly homozygous	116613526
10	62226470	62226471	A	G	25	GENIC	homozygous	116613542
10	62231897	62231898	T	A	30	GENIC	homozygous	116613548
10	62232746	62232747	T	C	23	GENIC	homozygous	116613556
10	62235933	62235934	G	A	31	GENIC	possibly homozygous	116939627
10	62237622	62237623	G	A	24	GENIC	homozygous	116939629