chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	38030803	38030804	T	C	70	GENIC	homozygous	115322345
12	38031089	38031089		G	51	GENIC	homozygous	128986354
12	38031100	38031101	T	C	55	GENIC	homozygous	115322347
12	38031570	38031571	C	T	57	GENIC	homozygous	115322349
12	38032498	38032498		CCCC	20	GENIC	homozygous	128986355
12	38032499	38032500	G	C	21	GENIC	homozygous	115322351
12	38037817	38037818	G		54	GENIC	homozygous	128986356
12	38037841	38037849	TGGAGGCA		58	GENIC	homozygous	128986357
12	38038078	38038079	T	C	46	GENIC	homozygous	115322353
12	38039262	38039263	C	T	62	GENIC	homozygous	115322355
12	38040499	38040500	T	C	51	GENIC	homozygous	115322357
12	38041048	38041049	A		43	GENIC	homozygous	128986358
12	38041202	38041202		T	39	GENIC	homozygous	128986359
12	38042147	38042147		CCATCAA	52	GENIC	homozygous	128986360
12	38043676	38043677	C	A	55	GENIC	homozygous	115322359
12	38043970	38043971	G	T	71	GENIC	homozygous	115322361
12	38047325	38047326	G	T	69	GENIC	homozygous	115322377
12	38043971	38043972	T	C	72	GENIC	homozygous	115322363
12	38044405	38044406	G	A	56	GENIC	homozygous	115322365
12	38044567	38044568	C	T	59	GENIC	homozygous	115322367
12	38045298	38045299	G	C	31	GENIC	homozygous	115322369
12	38045325	38045326	G	A	36	GENIC	homozygous	115322371
12	38046545	38046546	C	A	67	GENIC	homozygous	115322373
12	38046938	38046939	C	T	64	GENIC	homozygous	115322375
12	38034437	38034438	A	C	3	GENIC	heterozygous	132170051
12	38048974	38048975	C	T	58	GENIC	homozygous	115322379
12	38049265	38049266	G	A	49	GENIC	possibly homozygous	115322381
12	38052896	38052896		GCCGCC	9	GENIC	homozygous	128986361
12	38052945	38052951	GCCCGC		7	GENIC	homozygous	128986362