chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	49514381	49514382	C	CCT	13	GENIC	heterozygous	49755234
13	49514382	49514384	CT	--	13	GENIC	heterozygous	50517509
13	49524616	49524621	TGCTT	-----	12	GENIC	homozygous	49755236
13	49524665	49524666	A	AT	6	GENIC	homozygous	49755237
13	49524666	49524667	G	GTGACGGGAGGTGTTT	6	GENIC	homozygous	49755238
13	49524786	49524787	G	A	7	GENIC	homozygous	49755240
13	49528868	49528869	C	CTTAGAATGATACACAGGA	24	GENIC	homozygous	50495083
13	49530431	49530432	C	CTCTTTCTTTCTT	6	GENIC	heterozygous	50517511
13	49533023	49533025	AC	--	11	GENIC	heterozygous	50550924
13	49537887	49537889	CA	--	15	GENIC	heterozygous	50550925
13	49538523	49538524	A	G	1	GENIC	homozygous	49755247
13	49538740	49538741	T	-	12	GENIC	possibly homozygous	49755248
13	49543012	49543016	CTCT	----	18	GENIC	heterozygous	50517513
13	49543014	49543016	CT	--	18	GENIC	heterozygous	50517514
13	49546734	49546735	A	AT	12	GENIC	homozygous	49755249
13	49547302	49547304	TG	--	10	GENIC	heterozygous	50580288
13	49550970	49550972	GT	--	10	GENIC	heterozygous	50562903