chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	53102982	53102983	G	A	21	GENIC	homozygous	50255574
12	53103100	53103101	G	A	17	GENIC	homozygous	50255576
12	53103878	53103879	G	A	27	GENIC	homozygous	50255578
12	53104289	53104290	C	T	27	GENIC	homozygous	50255580
12	53104811	53104812	T	C	25	GENIC	homozygous	50255582
12	53105340	53105341	T	C	33	GENIC	homozygous	50255584
12	53105563	53105564	G	GT	15	GENIC	homozygous	50255586
12	53105935	53105936	G	A	15	GENIC	homozygous	50255588
12	53106163	53106164	T	TTG	17	GENIC	homozygous	50255590
12	53106291	53106292	G	A	24	GENIC	homozygous	50255592
12	53106588	53106589	G	A	17	GENIC	homozygous	50255594
12	53106951	53106952	T	A	28	GENIC	heterozygous	50255596
12	53106951	53106952	T	TGA	23	GENIC	homozygous	50255598
12	53106953	53106954	T	A	28	GENIC	possibly homozygous	50255600
12	53106958	53106959	C	T	21	GENIC	possibly homozygous	50255602
12	53107399	53107400	T	A	30	GENIC	homozygous	50255604
12	53107599	53107600	T	A	20	GENIC	homozygous	50255606
12	53107624	53107625	T	TA	18	GENIC	possibly homozygous	50255608
12	53107741	53107742	C	G	32	GENIC	homozygous	50255610
12	53107842	53107843	T	C	19	GENIC	heterozygous	50255612
12	53107844	53107845	A	G	20	GENIC	heterozygous	50255614
12	53108018	53108019	A	G	17	GENIC	heterozygous	50255616
12	53108032	53108033	C	T	17	GENIC	heterozygous	50255618
12	53108034	53108035	G	A	17	GENIC	heterozygous	50255620
12	53108056	53108057	A	G	15	GENIC	heterozygous	50255622
12	53108198	53108199	A	ATC	17	GENIC	homozygous	50255628
12	53108207	53108208	T	C	18	GENIC	homozygous	50255630
12	53108514	53108515	T	C	26	GENIC	homozygous	50255632
12	53108517	53108518	C	CT	27	GENIC	homozygous	50255634