chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	77728878	77728879	A	G	68	GENIC	homozygous	139349814
13	77730118	77730119	T	C	58	GENIC	homozygous	139349815
13	77733745	77733746	C	T	63	GENIC	homozygous	139349816
13	77735665	77735666	T	G	54	GENIC	homozygous	154788422
13	77735665	77735666	T		54	GENIC	heterozygous	403344242
13	77735693	77735694	T	G	53	GENIC	homozygous	139349817
13	77735697	77735698	T	G	53	GENIC	homozygous	139349818
13	77738247	77738248	C	T	50	GENIC	possibly homozygous	139349819
13	77739350	77739351	A	C	37	GENIC	homozygous	139349820
13	77740149	77740150	G	A	57	GENIC	homozygous	139349821
13	77740918	77740919	G	C	46	GENIC	homozygous	139349822
13	77744418	77744419	C	T	52	GENIC	homozygous	139349823
13	77745158	77745159	T	G	77	GENIC	homozygous	139349824
13	77745468	77745469	G	A	45	GENIC	homozygous	139349825
13	77745577	77745578	T	C	58	GENIC	homozygous	139349826
13	77746234	77746235	C	T	30	GENIC	homozygous	139349827
13	77746341	77746342	G	C	7	GENIC	heterozygous	403344253
13	77746341	77746342	G		7	GENIC	heterozygous	403344254
13	77746529	77746530	G	A	14	GENIC	homozygous	140912319
13	77744403	77744403		TA	46	GENIC	homozygous	139185757
13	77736217	77736220	TTG		62	GENIC	possibly homozygous	139185755
13	77742845	77742845		C	41	GENIC	homozygous	139185756