chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	70349872	70349873	G	A	24	GENIC	homozygous	116627614
10	70349935	70349936	G	A	29	GENIC	homozygous	116627616
10	70350206	70350207	T	C	27	GENIC	homozygous	116627618
10	70351787	70351788	G	A	30	GENIC	homozygous	116627620
10	70352274	70352275	A	G	35	GENIC	homozygous	116627622
10	70353156	70353157	G	A	44	GENIC	homozygous	116627624
10	70353714	70353715	A	G	37	GENIC	homozygous	116627626
10	70357063	70357064	C	T	27	GENIC	homozygous	116627628
10	70357775	70357776	G	A	28	GENIC	homozygous	116627630
10	70357924	70357925	G	A	18	GENIC	homozygous	116627632
10	70358143	70358144	C	T	17	GENIC	homozygous	116627634
10	70358151	70358152	G	A	23	GENIC	homozygous	116627636
10	70358155	70358156	A	G	23	GENIC	homozygous	116627638
10	70358190	70358191	C	G	23	GENIC	homozygous	116627640
10	70358511	70358512	G	T	25	GENIC	homozygous	116627642
10	70358885	70358886	C	T	24	GENIC	homozygous	116799100
10	70359156	70359157	A	G	11	GENIC	homozygous	116627644
10	70359177	70359178	G	C	14	GENIC	homozygous	116799104
10	70359391	70359392	C	T	31	GENIC	homozygous	116627646
10	70359451	70359452	T	A	18	GENIC	homozygous	116627648
10	70359463	70359464	A	G	20	GENIC	homozygous	116627650
10	70366461	70366462	T	C	19	GENIC	homozygous	116627664
10	70366654	70366655	C	G	33	GENIC	homozygous	116627666
10	70366660	70366661	G	C	33	GENIC	homozygous	116627668
10	70366697	70366698	G	A	31	GENIC	homozygous	116627670
10	70366711	70366712	C	T	28	GENIC	homozygous	116627672