chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	52125186	52125186		CTTAAAAGTTTGTGCTACACTATAGCTGTAGTCTCAGTTTCTT	30	GENIC	homozygous	129053766
13	52126039	52126040	G	A	22	GENIC	homozygous	114345465
13	52127275	52127276	C	T	11	GENIC	homozygous	114345467
13	52127277	52127278	G	A	10	GENIC	homozygous	114345469
13	52127603	52127604	T	C	25	GENIC	homozygous	114672475
13	52128147	52128148	G	A	23	GENIC	homozygous	114345471
13	52128499	52128499		A	20	GENIC	homozygous	129053768
13	52128827	52128828	C	A	16	GENIC	homozygous	114345473
13	52129299	52129300	G	A	13	GENIC	homozygous	114345475
13	52129311	52129312	G	A	13	GENIC	homozygous	114345477
13	52129415	52129416	G	A	17	GENIC	homozygous	114720455
13	52131567	52131568	G	T	27	GENIC	possibly homozygous	115152185
13	52131633	52131634	G	A	27	GENIC	homozygous	118450961
13	52131641	52131642	C	T	28	GENIC	homozygous	123734669
13	52131642	52131643	A	G	28	GENIC	homozygous	123734670
13	52131643	52131644	G	A	27	GENIC	homozygous	123734671
13	52131681	52131682	C	T	22	GENIC	homozygous	114672478
13	52131792	52131793	T	C	27	GENIC	homozygous	114345479
13	52131981	52131982	G	A	29	GENIC	homozygous	114345481
13	52132378	52132379	A		17	GENIC	homozygous	129053769
13	52132650	52132651	A	C	13	GENIC	homozygous	114345483
13	52132740	52132741	A	G	22	GENIC	homozygous	114857687
13	52132994	52132995	C	T	23	GENIC	homozygous	114345485
13	52133138	52133142	ACTT		21	GENIC	homozygous	129053770
13	52134365	52134366	C	T	27	GENIC	homozygous	114345487
13	52134808	52134808		TTA	21	GENIC	homozygous	129053771
13	52135947	52135948	T	C	20	GENIC	homozygous	114345489