chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	38030803	38030804	T	C	25	GENIC	homozygous	115322345
12	38031100	38031101	T	C	28	GENIC	homozygous	115322347
12	38031570	38031571	C	T	42	GENIC	homozygous	115322349
12	38038078	38038079	T	C	50	GENIC	homozygous	115322353
12	38039262	38039263	C	T	44	GENIC	homozygous	115322355
12	38040499	38040500	T	C	34	GENIC	homozygous	115322357
12	38043676	38043677	C	A	45	GENIC	possibly homozygous	115322359
12	38044405	38044406	G	A	45	GENIC	homozygous	115322365
12	38044567	38044568	C	T	41	GENIC	homozygous	115322367
12	38045298	38045299	G	C	45	GENIC	homozygous	115322369
12	38045325	38045326	G	A	57	GENIC	homozygous	115322371
12	38046545	38046546	C	A	40	GENIC	homozygous	115322373
12	38046938	38046939	C	T	41	GENIC	homozygous	115322375
12	38047325	38047326	G	T	53	GENIC	homozygous	115322377
12	38048974	38048975	C	T	52	GENIC	homozygous	115322379
12	38049265	38049266	G	A	42	GENIC	possibly homozygous	115322381