chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	15325031	15325032	C	T	3	GENIC	heterozygous	50072230
12	15325109	15325110	T	TC	4	GENIC	heterozygous	50072232
12	15325159	15325160	T	C	6	GENIC	heterozygous	50072234
12	15325303	15325304	C	T	14	GENIC	homozygous	50072236
12	15325345	15325346	A	G	9	GENIC	possibly homozygous	50072238
12	15325713	15325714	C	T	8	GENIC	homozygous	50072240
12	15325824	15325825	T	TTTTTTCTTTCCTTTTTTCTTTTTTTCGGAGCTGGGGACTGAACCCAGGGCCTTATGCTTGCTAGGCAAGCGCTCTACCACTGAGCTAAATCCCCAACCCCTGTTAATAGTTTCTA	7	GENIC	homozygous	50504030
12	15326882	15326892	GAGAATGAAT	----------	5	GENIC	heterozygous	50504031
12	15327773	15327774	A	G	3	GENIC	homozygous	50072254
12	15329116	15329117	T	G	5	GENIC	heterozygous	50072260
12	15329644	15329645	T	C	7	GENIC	possibly homozygous	50072262
12	15330320	15330321	A	G	6	GENIC	heterozygous	50436027
12	15330375	15330376	A	G	13	GENIC	possibly homozygous	50072264
12	15331308	15331309	G	A	13	GENIC	heterozygous	50072266
12	15331382	15331383	A	ATT	1	GENIC	homozygous	50072270
12	15331484	15331485	C	T	6	GENIC	homozygous	50072272
12	15332049	15332050	A	G	13	GENIC	homozygous	50072278
12	15332058	15332059	T	C	8	GENIC	homozygous	50072280
12	15332309	15332310	G	A	10	GENIC	possibly homozygous	50072282
12	15332451	15332452	A	T	18	GENIC	homozygous	50568397
12	15332679	15332680	A	AGT	7	GENIC	homozygous	50072284
12	15337155	15337156	T	C	18	GENIC	homozygous	50072361
12	15338173	15338174	G	A	8	GENIC	homozygous	50568398