chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	103638773	103638774	A	AT	25	GENIC	possibly homozygous	53158321
8	103640560	103640561	T	C	29	GENIC	homozygous	53158323
8	103640702	103640703	T	A	23	GENIC	homozygous	53158325
8	103640832	103640833	C	T	25	GENIC	homozygous	53158327
8	103641007	103641038	GTGTGTACACACAATAGTAAACAGTGACAGT	-------------------------------	3	GENIC	homozygous	53652693
8	103642131	103642132	C	CCACAGTCCTGCTGCCTCTGCTTTGCCCA	20	GENIC	homozygous	53652694
8	103642233	103642242	CTGATGGCA	---------	28	GENIC	homozygous	53158331
8	103642324	103642325	T	C	24	GENIC	homozygous	52779352
8	103643661	103643662	C	CAAAA	9	GENIC	heterozygous	53579083
8	103643662	103643666	AAAA	----	9	GENIC	possibly homozygous	53406400
8	103643923	103643924	A	AGCGTGCGT	17	GENIC	homozygous	53630508
8	103645158	103645159	G	C	18	GENIC	homozygous	52779363
8	103646566	103646567	C	CCAT	12	GENIC	heterozygous	53652695
8	103646580	103646581	T	TTCCA	15	GENIC	possibly homozygous	53652696
8	103647563	103647564	C	T	18	GENIC	homozygous	52779372
8	103648546	103648552	AAAAAA	------	10	GENIC	homozygous	53158343
8	103649109	103649110	A	-	21	GENIC	homozygous	53023222
8	103649126	103649127	T	C	23	GENIC	homozygous	52779376
8	103650934	103650935	T	TAAA	20	GENIC	homozygous	53158345
8	103656654	103656659	ACAAA	-----	9	GENIC	homozygous	53158347
8	103656939	103656940	A	T	24	GENIC	homozygous	52779384
8	103657307	103657308	A	G	21	GENIC	homozygous	52779387
8	103657336	103657337	C	T	24	GENIC	homozygous	53158349
8	103657571	103657572	C	CAA	13	GENIC	possibly homozygous	53158353
8	103657571	103657572	C	CA	13	GENIC	heterozygous	53652697
8	103658507	103658508	C	T	36	GENIC	homozygous	53367103
8	103658508	103658509	T	G	36	GENIC	homozygous	52779393
8	103661198	103661199	T	C	28	GENIC	homozygous	52779399
8	103661755	103661756	A	-	9	GENIC	homozygous	53158355