chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	23956027	23956028	A	G	13	GENIC	homozygous	115286245
12	23956663	23956664	T	C	22	GENIC	homozygous	115286247
12	23958508	23958509	G	A	23	GENIC	homozygous	115286249
12	23959056	23959057	G	A	21	GENIC	homozygous	115286251
12	23960295	23960296	A	C	17	GENIC	homozygous	115286253
12	23961678	23961679	T	A	13	GENIC	heterozygous	115510216
12	23964126	23964127	G	A	15	GENIC	homozygous	115286255
12	23964530	23964531	C	A	7	GENIC	heterozygous	115632718
12	23965489	23965490	C	T	10	GENIC	homozygous	115286259
12	23968549	23968550	C	A	10	GENIC	homozygous	115286261
12	23969437	23969438	C	T	14	GENIC	homozygous	115446259
12	23973275	23973276	C	T	19	GENIC	homozygous	115286265
12	23961880	23961881	G	T	15	GENIC	homozygous	115469778
12	23975336	23975337	A	G	6	GENIC	homozygous	115469780
12	23971194	23971195	T	G	11	GENIC	heterozygous	118261921
12	23976538	23976539	C	T	16	GENIC	homozygous	115422070
12	23982041	23982042	C	G	4	GENIC	homozygous	115286281
12	23983262	23983263	C	T	12	GENIC	homozygous	115469782
12	23986359	23986360	T	C	7	GENIC	homozygous	115469784