chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	23907667	23907668	C	G	179	GENIC	heterozygous	50130362
12	23907829	23907830	G	T	232	GENIC	heterozygous	51141712
12	23907831	23907832	A	T	230	GENIC	heterozygous	51141713
12	23907832	23907833	C	T	230	GENIC	heterozygous	51141714
12	23907847	23907848	C	A	241	GENIC	heterozygous	51141715
12	23907863	23907864	C	T	231	GENIC	heterozygous	50130368
12	23907884	23907885	C	G	189	GENIC	heterozygous	50130370
12	23909272	23909273	G	A	59	GENIC	heterozygous	50130386
12	23909613	23909614	C	A	64	GENIC	heterozygous	50130388
12	23911892	23911893	T	G	182	GENIC	heterozygous	50130396
12	23912411	23912412	G	T	161	GENIC	heterozygous	50130400
12	23912433	23912434	G	A	164	GENIC	heterozygous	50130402
12	23912665	23912666	C	A	132	GENIC	heterozygous	50130406
12	23912851	23912852	C	T	210	GENIC	heterozygous	50130408
12	23912877	23912878	G	A	195	GENIC	heterozygous	50130410
12	23912992	23912993	G	T	128	GENIC	heterozygous	51141718
12	23939454	23939455	T	C	96	GENIC	heterozygous	51141720
12	23939462	23939463	C	A	97	GENIC	heterozygous	51141721
12	23939464	23939465	C	A	99	GENIC	heterozygous	51141722
12	23939466	23939467	A	C	99	GENIC	heterozygous	51141723
12	23939482	23939483	G	T	106	GENIC	heterozygous	51141724
12	23939526	23939527	C	T	123	GENIC	heterozygous	51141727