chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	37668418	37668419	G	A	24	GENIC	heterozygous	118304591
12	37668424	37668425	A	C	23	GENIC	heterozygous	118269786
12	37668425	37668426	T	C	22	GENIC	heterozygous	118269787
12	37668433	37668434	C	T	25	GENIC	heterozygous	118269788
12	37668440	37668441	C	A	28	GENIC	heterozygous	118269789
12	37668445	37668446	C	T	26	GENIC	heterozygous	118269790
12	37668449	37668450	G	A	25	GENIC	heterozygous	118269791
12	37668472	37668473	C	T	23	GENIC	heterozygous	118269792
12	37668473	37668474	C	G	23	GENIC	heterozygous	118269793
12	37668485	37668486	G	C	18	GENIC	heterozygous	118269794
12	37668489	37668490	G	C	18	GENIC	heterozygous	118269795
12	37668491	37668492	G	A	18	GENIC	heterozygous	118269796
12	37668498	37668499	G	T	17	GENIC	heterozygous	118304592
12	37668500	37668501	C	G	17	GENIC	heterozygous	118304593
12	37668512	37668513	C	T	11	GENIC	heterozygous	118304594
12	37668749	37668750	A	G	13	GENIC	homozygous	115321201
12	37668751	37668752	A	G	13	GENIC	homozygous	115321203
12	37668850	37668851	G	C	11	GENIC	homozygous	115525352
12	37669045	37669046	T	C	23	GENIC	homozygous	115321205
12	37673499	37673500	T	C	31	GENIC	homozygous	115321211
12	37676688	37676689	T	C	32	GENIC	heterozygous	118343010