chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	23956027	23956028	A	G	28	GENIC	homozygous	115286245
12	23956663	23956664	T	C	32	GENIC	possibly homozygous	115286247
12	23958508	23958509	G	A	24	GENIC	homozygous	115286249
12	23959056	23959057	G	A	26	GENIC	homozygous	115286251
12	23960295	23960296	A	C	23	GENIC	homozygous	115286253
12	23961678	23961679	T	A	33	GENIC	homozygous	115510216
12	23961880	23961881	G	T	16	GENIC	homozygous	115469778
12	23964126	23964127	G	A	43	GENIC	homozygous	115286255
12	23965489	23965490	C	T	42	GENIC	homozygous	115286259
12	23968549	23968550	C	A	41	GENIC	homozygous	115286261
12	23969437	23969438	C	T	35	GENIC	homozygous	115446259
12	23971190	23971191	T	G	41	GENIC	heterozygous	118301179
12	23973275	23973276	C	T	23	GENIC	homozygous	115286265
12	23975336	23975337	A	G	27	GENIC	homozygous	115469780
12	23976538	23976539	C	T	39	GENIC	homozygous	115422070
12	23979405	23979406	G	A	64	GENIC	heterozygous	118301180
12	23979641	23979642	C	T	33	GENIC	heterozygous	118364948
12	23982041	23982042	C	G	30	GENIC	homozygous	115286281
12	23983262	23983263	C	T	31	GENIC	possibly homozygous	115469782
12	23984708	23984709	G	C	14	GENIC	possibly homozygous	115703399
12	23985256	23985257	C	A	51	GENIC	heterozygous	118364949
12	23986274	23986275	A	C	2	GENIC	homozygous	118331601
12	23986279	23986280	G	C	4	GENIC	homozygous	118301185
12	23986286	23986287	G	C	13	GENIC	homozygous	118301186
12	23986307	23986308	G	C	19	GENIC	homozygous	118301187
12	23986359	23986360	T	C	37	GENIC	homozygous	115469784
12	23986312	23986313	G	C	20	GENIC	homozygous	118261922
12	23964530	23964531	C	A	41	GENIC	possibly homozygous	115632718
12	23971194	23971195	T	G	38	GENIC	possibly homozygous	118261921