chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	96111922	96111923	G	A	7	GENIC	homozygous	114904400
13	96112404	96112405	T	A	11	GENIC	homozygous	114904402
13	96123848	96123849	T	A	23	GENIC	homozygous	114904404
13	96125815	96125816	T	A	25	GENIC	homozygous	114790710
13	96127241	96127242	T	C	20	GENIC	homozygous	114790716
13	96129779	96129780	G	A	17	GENIC	homozygous	114790724
13	96132961	96132962	T	C	16	GENIC	homozygous	114790742
13	96133832	96133833	T	A	10	GENIC	homozygous	114790744
13	96134776	96134777	A	G	17	GENIC	homozygous	114904406
13	96138803	96138804	T	C	25	GENIC	homozygous	114790760
13	96145825	96145826	T	A	15	GENIC	homozygous	114904408
13	96145839	96145840	T	A	17	GENIC	homozygous	114904410
13	96145960	96145961	G	A	28	GENIC	homozygous	114904412
13	96146891	96146892	A	T	29	GENIC	homozygous	114790782
13	96146932	96146933	G	T	34	GENIC	homozygous	114790784
13	96147468	96147469	C	T	14	GENIC	homozygous	114904414
13	96147818	96147819	T	C	15	GENIC	homozygous	114790790
13	96147856	96147857	T	C	13	GENIC	homozygous	114904416
13	96148365	96148366	G	C	18	GENIC	homozygous	114790792
13	96149422	96149423	T	C	23	GENIC	homozygous	114790794
13	96150167	96150168	T	C	27	GENIC	homozygous	114790800
13	96150203	96150204	G	A	30	GENIC	homozygous	114904418
13	96150356	96150357	C	T	20	GENIC	homozygous	114904420
13	96151425	96151426	A	G	32	GENIC	homozygous	114790802
13	96151955	96151956	A	C	35	GENIC	homozygous	114790806
13	96153035	96153036	T	C	23	GENIC	homozygous	114790808
13	96154747	96154748	A	G	29	GENIC	homozygous	114790812
13	96155253	96155254	T	G	22	GENIC	homozygous	114790814
13	96141508	96141509	T	G	27	GENIC	homozygous	114431224