chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	36763448	36763449	G	GGGCTGTGTAGAGACCCTGTCTCAAAAACAAACAACCAACAAACCCCCAAACCAACCAACCAACAGCCAACCCCAACTCCATCCATCTGTC	23	GENIC	homozygous	46461330
19	36766882	36766883	C	T	33	GENIC	homozygous	46109418
19	36767132	36767133	C	T	38	GENIC	homozygous	46109420
19	36767582	36767583	A	G	10	GENIC	homozygous	46109422
19	36767752	36767754	TT	--	15	GENIC	possibly homozygous	46109424
19	36767753	36767754	T	-	15	GENIC	heterozygous	46109426
19	36768471	36768472	C	CT	10	GENIC	homozygous	46109428
19	36768636	36768637	C	CACACACACACACACACACACAT	10	GENIC	homozygous	46380045
19	36769408	36769409	G	GA	11	GENIC	heterozygous	46109432
19	36769483	36769484	G	GA	21	GENIC	homozygous	46109434
19	36769503	36769504	A	AG	19	GENIC	homozygous	46109436
19	36769540	36769541	C	A	11	GENIC	homozygous	46380047
19	36769541	36769542	A	C	11	GENIC	homozygous	46380049
19	36769553	36769554	A	G	12	GENIC	homozygous	46109438
19	36769583	36769584	C	-	15	GENIC	homozygous	46109440
19	36769611	36769612	T	A	19	GENIC	homozygous	46109442
19	36769615	36769616	G	GC	19	GENIC	homozygous	46109444
19	36772540	36772541	C	CTA	22	GENIC	homozygous	46109445
19	36773746	36773747	A	-	14	GENIC	heterozygous	46429696
19	36775220	36775221	T	TCACACACACACA	11	GENIC	heterozygous	46461332
19	36775220	36775221	T	TCACACACACACACA	11	GENIC	possibly homozygous	46461334
19	36776224	36776225	T	TCA	7	GENIC	homozygous	46109449