chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	19574352	19574353	T	C	45	GENIC	homozygous	115279380
12	19575393	19575394	T	A	49	GENIC	homozygous	115279382
12	19575632	19575633	C	T	49	GENIC	homozygous	115279384
12	19575673	19575674	A	C	48	GENIC	homozygous	115279386
12	19575953	19575954	A	G	54	GENIC	homozygous	115279388
12	19576172	19576173	G	A	54	GENIC	possibly homozygous	115279390
12	19576437	19576438	C	T	37	GENIC	possibly homozygous	115279392
12	19576440	19576441	G	T	37	GENIC	possibly homozygous	118248745
12	19576483	19576484	G	A	29	GENIC	homozygous	118248746
12	19576488	19576489	G	A	29	GENIC	homozygous	118248748
12	19576506	19576507	C	G	24	GENIC	homozygous	118248750
12	19576768	19576769	G	A	48	GENIC	homozygous	115279394
12	19576819	19576820	C	T	44	GENIC	homozygous	115279396
12	19576864	19576865	C	T	40	GENIC	homozygous	115279397
12	19576873	19576874	C	T	42	GENIC	homozygous	115279399
12	19576932	19576933	A	G	44	GENIC	homozygous	115279401
12	19577491	19577492	T	C	50	GENIC	homozygous	115279403
12	19576442	19576443	C	T	36	GENIC	homozygous	115581168
12	19576780	19576780		GTGTAAAG	43	GENIC	homozygous	128968818