chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	96143875	96143876	G	C	18	GENIC	homozygous	109933282
2	96143927	96143928	A	G	12	GENIC	homozygous	109933284
2	96144108	96144109	T	C	16	GENIC	homozygous	109933288
2	96144241	96144242	T	C	16	GENIC	homozygous	110723226
2	96144396	96144397	C	T	21	GENIC	homozygous	110723228
2	96144433	96144434	C	T	20	GENIC	homozygous	109933290
2	96144455	96144456	T	C	18	GENIC	homozygous	110723230
2	96144575	96144576	G	A	25	GENIC	homozygous	109933292
2	96144654	96144655	A	G	11	GENIC	homozygous	109933294
2	96144700	96144701	G	A	13	GENIC	homozygous	109933296
2	96144713	96144714	T	G	14	GENIC	homozygous	109933298
2	96144780	96144781	C	A	21	GENIC	homozygous	110723232
2	96144798	96144799	C	T	14	GENIC	homozygous	110723234
2	96145066	96145067	T	C	19	GENIC	homozygous	110723236
2	96145126	96145127	A	G	15	GENIC	homozygous	110723238
2	96145177	96145178	T	A	18	GENIC	homozygous	110723239
2	96145408	96145409	C	G	28	GENIC	homozygous	109933302
2	96145530	96145531	T	A	25	GENIC	homozygous	109933306
2	96145671	96145672	C	T	14	GENIC	homozygous	110723241
2	96145736	96145737	C	T	25	GENIC	homozygous	109933310
2	96145874	96145875	A	T	23	GENIC	homozygous	109933312
2	96145875	96145876	G	T	23	GENIC	homozygous	109933314
2	96145923	96145924	C	T	23	GENIC	homozygous	110723243
2	96145978	96145979	G	C	19	GENIC	homozygous	109933316
2	96146012	96146013	G	A	26	GENIC	homozygous	109933318
2	96146090	96146091	C	T	30	GENIC	homozygous	110723245
2	96146260	96146261	T	C	29	GENIC	homozygous	109933320
2	96146829	96146830	T	C	25	GENIC	homozygous	110723247
2	96146876	96146877	A	G	25	GENIC	homozygous	110723249
2	96146904	96146905	G	A	25	GENIC	homozygous	109933326
2	96146156	96146157	C	T	29	GENIC	homozygous	110957991
2	96146157	96146158	T	A	29	GENIC	homozygous	110957993