chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	129652598	129652599	T	C	31	GENIC	homozygous	57670469
3	129652599	129652600	G	A	31	GENIC	homozygous	57670471
3	129653298	129653299	G	A	32	GENIC	homozygous	57670473
3	129653987	129653988	C	T	39	GENIC	homozygous	57670475
3	129654504	129654505	T	TGTATGTTTCTC	24	GENIC	homozygous	58623726
3	129654838	129654839	G	A	30	GENIC	homozygous	57670479
3	129656308	129656325	CAGGTCCCCCGGAAAGG	-----------------	27	GENIC	homozygous	57670481
3	129656985	129656986	G	A	36	GENIC	homozygous	57670483
3	129657111	129657112	C	T	32	GENIC	homozygous	57670485
3	129657568	129657569	G	GA	15	GENIC	heterozygous	58623727
3	129657568	129657569	G	GAA	15	GENIC	heterozygous	58623728
3	129658097	129658098	A	AT	27	GENIC	homozygous	57670487
3	129658262	129658263	C	CTT	15	GENIC	heterozygous	58695705
3	129659438	129659439	C	T	23	GENIC	homozygous	57670491
3	129659588	129659589	G	C	29	GENIC	homozygous	58560480
3	129660226	129660227	T	-	30	GENIC	homozygous	57670495
3	129661042	129661043	C	T	27	GENIC	homozygous	57670497
3	129663140	129663141	G	A	38	GENIC	homozygous	57670499
3	129664167	129664168	G	GA	18	GENIC	possibly homozygous	57670501
3	129665319	129665320	A	AT	5	GENIC	heterozygous	58623729
3	129665363	129665364	T	TGTGCTTGCTAGGCAA	11	GENIC	homozygous	58623730
3	129665366	129665367	G	GCTCT	11	GENIC	homozygous	58623731
3	129665367	129665368	A	AC	11	GENIC	homozygous	58623732
3	129665369	129665370	A	ACTGAGC	11	GENIC	homozygous	58623733
3	129665374	129665375	T	TCCC	16	GENIC	homozygous	58623734
3	129665568	129665569	C	G	19	GENIC	homozygous	57670503
3	129666506	129666507	A	T	22	GENIC	homozygous	57670505
3	129667397	129667407	TTTTTTTTTT	----------	16	GENIC	heterozygous	58037304
3	129668229	129668230	C	T	19	GENIC	homozygous	57670509
3	129668628	129668629	A	-	20	GENIC	homozygous	57670511
3	129668632	129668633	A	C	23	GENIC	homozygous	58560481
3	129669216	129669217	G	A	20	GENIC	homozygous	57670517
3	129669784	129669785	C	T	34	GENIC	homozygous	57670519