chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	93716963	93716964	G	A	21	GENIC	homozygous	49965839
13	93717849	93717850	A	AG	16	GENIC	homozygous	49965840
13	93718600	93718601	T	C	12	GENIC	homozygous	49965841
13	93718970	93718971	C	T	19	GENIC	homozygous	49965842
13	93719396	93719397	A	C	15	GENIC	homozygous	49965843
13	93719538	93719539	G	A	10	GENIC	homozygous	49965844
13	93719878	93719879	G	GC	10	GENIC	homozygous	49965845
13	93719879	93719880	T	C	10	GENIC	homozygous	50497465
13	93719991	93719992	T	C	13	GENIC	homozygous	49965846
13	93721604	93721605	T	A	19	GENIC	homozygous	49965847
13	93723379	93723380	A	C	24	GENIC	homozygous	49965848
13	93723624	93723625	G	A	11	GENIC	homozygous	49965849
13	93723625	93723626	C	A	11	GENIC	homozygous	49965850
13	93723642	93723643	A	C	15	GENIC	homozygous	49965851
13	93723872	93723873	G	C	14	GENIC	homozygous	49965852
13	93724070	93724071	A	G	9	GENIC	homozygous	49965853
13	93724105	93724106	G	C	10	GENIC	homozygous	49965854
13	93728756	93728757	T	TA	9	GENIC	homozygous	49965863
13	93729483	93729484	G	A	14	GENIC	homozygous	49965865
13	93730110	93730111	A	T	15	GENIC	homozygous	49965867
13	93730652	93730653	T	C	22	GENIC	homozygous	49965868
13	93730989	93730990	G	C	16	GENIC	homozygous	49965869
13	93731761	93731765	AAAC	----	19	GENIC	homozygous	49965871
13	93734393	93734394	C	T	22	GENIC	homozygous	49965872
13	93734659	93734660	T	C	21	GENIC	homozygous	49965873
13	93735724	93735725	T	TCTGG	9	GENIC	homozygous	49965875
13	93724812	93724813	G	A	7	GENIC	heterozygous	51268777
13	93736412	93736413	A	G	10	GENIC	homozygous	50497466
13	93736926	93736927	C	T	21	GENIC	homozygous	49965876
13	93737415	93737417	AA	--	14	GENIC	homozygous	49965877
13	93737733	93737734	T	C	17	GENIC	homozygous	49965878