chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	71086708	71086709	T	C	30	GENIC	homozygous	111606162
3	71087652	71087653	A	G	29	GENIC	homozygous	119974730
3	71089118	71089119	G	A	34	GENIC	homozygous	111606164
3	71089808	71089809	A	G	23	GENIC	homozygous	111606165
3	71090222	71090223	A	G	23	GENIC	homozygous	119796578
3	71090532	71090533	G	A	22	GENIC	homozygous	111606166
3	71091514	71091515	C	T	39	GENIC	homozygous	119796582
3	71091897	71091898	C	T	40	GENIC	homozygous	119796584
3	71092651	71092652	G	A	12	GENIC	homozygous	111606167
3	71092676	71092677	A	G	4	GENIC	homozygous	119974731
3	71092780	71092781	G	A	12	GENIC	homozygous	119974732
3	71092907	71092908	A	G	3	GENIC	homozygous	111606172
3	71092915	71092916	C	T	3	GENIC	homozygous	119796586
3	71093057	71093058	T	C	17	GENIC	homozygous	111920916
3	71093164	71093165	C	T	30	GENIC	homozygous	119796588
3	71093300	71093301	G	A	27	GENIC	homozygous	111606173
3	71093448	71093449	G	A	29	GENIC	homozygous	119796590
3	71093926	71093927	C	G	4	GENIC	homozygous	111920922
3	71094463	71094464	T	C	9	GENIC	homozygous	119796592
3	71097534	71097535	A	C	19	GENIC	homozygous	111606194
3	71098074	71098075	G	T	33	GENIC	homozygous	111606199
3	71098226	71098227	A	G	11	GENIC	homozygous	111606200
3	71100479	71100480	A	G	31	GENIC	homozygous	119974733
3	71101914	71101915	A	G	28	GENIC	homozygous	111606210
3	71103000	71103001	C	G	6	GENIC	homozygous	111606215
3	71103839	71103840	G	A	23	GENIC	homozygous	119974734
3	71104722	71104723	A	T	24	GENIC	homozygous	111606221