chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	95390495	95390496	G	GA	5	GENIC	homozygous	51141204
13	95390496	95390497	G	GAGAGAGAGAGAGA	5	GENIC	homozygous	51141205
13	95390591	95390592	A	G	23	GENIC	possibly homozygous	50367456
13	95392130	95392131	T	C	21	GENIC	homozygous	50141341
13	95392212	95392213	C	-	23	GENIC	homozygous	50367467
13	95392668	95392669	T	C	37	GENIC	homozygous	51141206
13	95393777	95393778	C	T	23	GENIC	homozygous	50367469
13	95393913	95393914	G	GT	15	GENIC	homozygous	50367473
13	95393930	95393931	C	T	10	GENIC	homozygous	51141207
13	95394537	95394538	T	C	29	GENIC	homozygous	50141343
13	95394798	95394799	C	A	22	GENIC	homozygous	51141208
13	95395171	95395172	A	G	25	GENIC	homozygous	50141345
13	95395630	95395631	G	A	32	GENIC	homozygous	50141353
13	95395656	95395657	T	TG	28	GENIC	homozygous	50141355
13	95395690	95395691	C	T	20	GENIC	homozygous	51141209
13	95395923	95395924	T	C	34	GENIC	possibly homozygous	50141357
13	95396618	95396619	C	A	20	GENIC	homozygous	50367481
13	95396657	95396664	TTTTTTT	-------	12	GENIC	homozygous	51141210
13	95396678	95396679	T	A	21	GENIC	homozygous	51141211
13	95399578	95399579	C	CT	20	GENIC	homozygous	51141212
13	95399929	95399930	C	T	25	GENIC	homozygous	51141213
13	95402988	95402989	C	T	34	GENIC	homozygous	51141214
13	95404646	95404647	T	C	17	GENIC	homozygous	50141368
13	95397768	95397769	A	AAAAG	9	GENIC	heterozygous	50585188
13	95405541	95405542	C	CTGTGTGTGTGTGTGTG	5	GENIC	homozygous	50860568