chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	104135844	104135845	A	C	43	GENIC	possibly homozygous	50268549
13	104136106	104136107	T	C	37	GENIC	homozygous	50268550
13	104136719	104136720	G	T	36	GENIC	homozygous	50268551
13	104136823	104136825	AA	--	5	GENIC	homozygous	50268552
13	104137409	104137410	G	T	31	GENIC	possibly homozygous	49873126
13	104137846	104137847	T	TCTG	34	GENIC	homozygous	50268553
13	104137978	104137979	T	G	53	GENIC	possibly homozygous	50268554
13	104138938	104138939	T	C	34	GENIC	homozygous	50268555
13	104139246	104139247	G	GT	26	GENIC	homozygous	50268556
13	104139288	104139289	G	T	28	GENIC	homozygous	49873127
13	104139507	104139508	T	-	5	GENIC	homozygous	49873128
13	104140437	104140438	T	G	32	GENIC	homozygous	50268557
13	104140950	104140951	A	G	43	GENIC	homozygous	50268558
13	104141271	104141272	A	G	43	GENIC	homozygous	50268559
13	104142068	104142069	C	CT	40	GENIC	homozygous	50268560
13	104143661	104143663	TT	--	23	GENIC	homozygous	50268561
13	104144205	104144206	C	T	19	GENIC	possibly homozygous	50268562
13	104144273	104144274	G	C	18	GENIC	homozygous	49873129
13	104145569	104145570	C	G	33	GENIC	homozygous	50268563
13	104146955	104146956	T	-	21	GENIC	possibly homozygous	50268564
13	104147096	104147098	TG	--	9	GENIC	heterozygous	49873130
13	104147138	104147139	T	C	24	GENIC	heterozygous	50268565
13	104147277	104147278	C	G	27	GENIC	homozygous	50268566
13	104147491	104147492	C	G	18	GENIC	possibly homozygous	50268567
13	104147495	104147496	C	G	17	GENIC	possibly homozygous	50268568
13	104147503	104147504	C	G	23	GENIC	heterozygous	50268569
13	104147790	104147791	T	C	53	GENIC	heterozygous	50268570
13	104148185	104148186	C	T	20	GENIC	heterozygous	50268571
13	104148187	104148188	C	T	20	GENIC	heterozygous	50268572
13	104150671	104150672	G	A	29	GENIC	heterozygous	50268573
13	104147140	104147150	CGCGCGCGCT	----------	19	GENIC	heterozygous	49974165
13	104139267	104139268	T	-	25	GENIC	homozygous	49974163
13	104146307	104146308	C	CG	6	GENIC	heterozygous	49974164