chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	40374033	40374034	C	T	20	GENIC	homozygous	125568293
2	40374393	40374394	C	T	5	GENIC	heterozygous	125568294
2	40375206	40375207	A	C	23	GENIC	homozygous	125568295
2	40375378	40375379	C	T	17	GENIC	homozygous	125568296
2	40375584	40375585	A	G	24	GENIC	homozygous	125568297
2	40376279	40376280	T	C	7	GENIC	homozygous	125568298
2	40376875	40376876	A	C	4	GENIC	homozygous	125568299
2	40377066	40377067	A	T	9	GENIC	homozygous	125568300
2	40379198	40379199	G	A	9	GENIC	homozygous	125568301
2	40379439	40379440	T	C	12	GENIC	homozygous	125568302
2	40379901	40379902	A	G	20	GENIC	homozygous	125568303
2	40381118	40381119	G	A	14	GENIC	homozygous	125568304
2	40381140	40381141	G	A	17	GENIC	homozygous	125568305
2	40381332	40381333	C	T	26	GENIC	homozygous	125568306
2	40381590	40381591	G	T	15	GENIC	homozygous	125568307
2	40381735	40381736	C	T	11	GENIC	homozygous	125568308
2	40382422	40382423	A	C	19	GENIC	homozygous	125568309
2	40382485	40382486	A	G	19	GENIC	homozygous	125568310
2	40382670	40382671	T	C	17	GENIC	homozygous	125568311
2	40383175	40383176	T	A	5	GENIC	homozygous	125568312
2	40383225	40383226	G	A	15	GENIC	homozygous	125568313
2	40383730	40383731	G	T	9	GENIC	homozygous	125568314
2	40383784	40383785	T	G	11	GENIC	homozygous	125568315
2	40383921	40383922	A	G	22	GENIC	homozygous	125568316
2	40385098	40385099	C	T	27	GENIC	homozygous	125568317