chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	39343508	39343509	A	G	20	GENIC	heterozygous	50198384
12	39343710	39343711	A	G	18	GENIC	heterozygous	50198386
12	39343714	39343715	A	G	16	GENIC	heterozygous	50592090
12	39344196	39344197	G	A	12	GENIC	heterozygous	50511625
12	39344326	39344327	C	T	10	GENIC	heterozygous	50198392
12	39344705	39344706	C	T	8	GENIC	homozygous	50511627
12	39345009	39345010	A	T	18	GENIC	heterozygous	50198400
12	39345019	39345020	G	GT	20	GENIC	heterozygous	50198402
12	39345422	39345423	T	C	9	GENIC	homozygous	50198406
12	39345425	39345426	C	G	8	GENIC	heterozygous	50198408
12	39346111	39346112	C	T	12	GENIC	homozygous	50198410
12	39346126	39346127	G	C	13	GENIC	heterozygous	50198412
12	39346287	39346288	A	G	17	GENIC	heterozygous	50198414
12	39346571	39346572	T	C	13	GENIC	heterozygous	50198416
12	39346800	39346801	C	CT	18	GENIC	heterozygous	50198418
12	39346918	39346919	T	C	12	GENIC	heterozygous	50198420
12	39347181	39347182	C	T	13	GENIC	heterozygous	50198424
12	39347230	39347231	T	G	8	GENIC	heterozygous	50198426
12	39347719	39347720	A	G	11	GENIC	heterozygous	50198431
12	39348150	39348151	A	G	19	GENIC	heterozygous	50198435
12	39348477	39348478	C	A	23	GENIC	heterozygous	50198439
12	39348884	39348885	G	C	21	GENIC	heterozygous	50198441
12	39348940	39348941	C	G	14	GENIC	heterozygous	50198443
12	39349254	39349255	C	G	15	GENIC	heterozygous	50198444
12	39349447	39349448	G	GC	12	GENIC	homozygous	50198446
12	39349468	39349469	A	G	17	GENIC	heterozygous	50198448
12	39350307	39350308	G	C	12	GENIC	heterozygous	50511629
12	39350842	39350843	A	AC	12	GENIC	homozygous	50198452
12	39351115	39351116	G	A	8	GENIC	heterozygous	51099065
12	39344697	39344698	A	ATT	8	GENIC	homozygous	50571261