chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	55210174	55210175	G	A	46	GENIC	homozygous	114618038
13	55210427	55210428	T	A	49	GENIC	homozygous	114618040
13	55212639	55212640	C	T	48	GENIC	homozygous	114552772
13	55213309	55213310	G	A	48	GENIC	homozygous	114618042
13	55213555	55213556	T	A	61	GENIC	homozygous	114353322
13	55213646	55213647	A	G	88	GENIC	heterozygous	118592199
13	55213683	55213684	C	T	91	GENIC	heterozygous	118592200
13	55213708	55213709	G	A	61	GENIC	homozygous	115100827
13	55213809	55213810	C	T	55	GENIC	homozygous	114353324
13	55214186	55214187	T	C	49	GENIC	homozygous	114353332
13	55214274	55214275	A	T	54	GENIC	homozygous	114552773
13	55214522	55214523	C	A	40	GENIC	possibly homozygous	114353336
13	55214795	55214796	A	G	60	GENIC	homozygous	114552774
13	55215462	55215463	G	C	57	GENIC	homozygous	114353338
13	55215607	55215608	G	A	47	GENIC	homozygous	114353340
13	55216630	55216631	T	G	38	GENIC	homozygous	114618044
13	55217401	55217402	A	G	47	GENIC	homozygous	114618046
13	55218151	55218152	T	C	45	GENIC	homozygous	114618048
13	55218379	55218380	C	T	39	GENIC	possibly homozygous	114618052
13	55218593	55218594	A	C	50	GENIC	homozygous	114618054