chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	96143875	96143876	G	C	14	GENIC	homozygous	109933282
2	96143927	96143928	A	G	13	GENIC	homozygous	109933284
2	96143963	96143964	A	G	9	GENIC	homozygous	109933286
2	96144108	96144109	T	C	21	GENIC	homozygous	109933288
2	96144433	96144434	C	T	5	GENIC	homozygous	109933290
2	96144575	96144576	G	A	15	GENIC	homozygous	109933292
2	96144654	96144655	A	G	5	GENIC	homozygous	109933294
2	96144700	96144701	G	A	9	GENIC	homozygous	109933296
2	96144713	96144714	T	G	8	GENIC	homozygous	109933298
2	96144842	96144843	C	T	11	GENIC	homozygous	109933300
2	96145218	96145219	C	T	12	GENIC	homozygous	125576919
2	96145408	96145409	C	G	24	GENIC	homozygous	109933302
2	96145502	96145503	G	A	6	GENIC	homozygous	109933304
2	96145530	96145531	T	A	9	GENIC	homozygous	109933306
2	96145717	96145718	C	T	10	GENIC	homozygous	109933308
2	96145736	96145737	C	T	4	GENIC	homozygous	109933310
2	96145874	96145875	A	T	6	GENIC	homozygous	109933312
2	96145875	96145876	G	T	6	GENIC	homozygous	109933314
2	96145978	96145979	G	C	22	GENIC	homozygous	109933316
2	96146012	96146013	G	A	10	GENIC	homozygous	109933318
2	96146260	96146261	T	C	28	GENIC	homozygous	109933320
2	96146823	96146824	C	T	16	GENIC	homozygous	109933322
2	96146898	96146899	G	A	12	GENIC	homozygous	109933324
2	96146904	96146905	G	A	11	GENIC	homozygous	109933326