chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	80094102	80094103	G	GCTCATATGGTTTGTTTTAGACAGTTTTGAAAACCATAGTTGCTCTTTTCACAGAATCTCATCAAC	15	GENIC	heterozygous	50496501
13	80097459	80097460	A	G	15	GENIC	homozygous	49833323
13	80097461	80097462	A	G	16	GENIC	homozygous	49833324
13	80101608	80101610	TG	--	7	GENIC	heterozygous	50612972
13	80105828	80105830	CA	--	13	GENIC	heterozygous	50761597
13	80109197	80109198	G	GTGTGTGTGTGT	1	GENIC	homozygous	50582863
13	80119190	80119191	G	GGGAGGGAGGGAGGGAGAAAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAAAGAGA	5	GENIC	homozygous	50582865
13	80129545	80129546	A	AGAGAGG	1	GENIC	homozygous	50524708
13	80130564	80130565	G	A	15	GENIC	homozygous	49833463
13	80131268	80131269	A	ATGCAAG	22	GENIC	homozygous	49833465
13	80131354	80131358	TCTA	----	11	GENIC	homozygous	50761599
13	80131436	80131437	C	CTCTA	18	GENIC	homozygous	50617982
13	80131543	80131544	C	CATCT	9	GENIC	homozygous	50108382