chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	39654340	39654341	A	T	21	GENIC	homozygous	115494454
12	39655459	39655460	G	A	31	GENIC	homozygous	115494458
12	39656564	39656565	G	A	17	GENIC	homozygous	115494462
12	39656622	39656623	T	C	18	GENIC	homozygous	115326419
12	39656677	39656678	C	G	25	GENIC	homozygous	115326423
12	39656767	39656768	G	A	28	GENIC	homozygous	115494464
12	39657329	39657330	C	T	27	GENIC	homozygous	115326427
12	39657635	39657636	A	G	36	GENIC	homozygous	115326429
12	39658377	39658378	G	A	29	GENIC	homozygous	115494466
12	39658541	39658542	A	C	25	GENIC	homozygous	115326431
12	39658918	39658919	C	T	23	GENIC	homozygous	115326433
12	39659443	39659444	A	G	19	GENIC	homozygous	115326435
12	39661171	39661172	C	T	30	GENIC	homozygous	115494468
12	39661341	39661342	G	A	23	GENIC	homozygous	115326439
12	39661833	39661834	C	T	24	GENIC	homozygous	115494470
12	39662949	39662950	G	A	19	GENIC	homozygous	115326441
12	39663418	39663419	C	T	26	GENIC	homozygous	115494474
12	39663789	39663790	G	A	19	GENIC	homozygous	115494476
12	39663822	39663823	C	A	20	GENIC	homozygous	115494478
12	39663840	39663841	G	A	15	GENIC	homozygous	115326443
12	39665500	39665501	C	T	21	GENIC	homozygous	115494480
12	39667436	39667437	G	T	22	GENIC	homozygous	115494482
12	39667542	39667543	A	G	28	GENIC	homozygous	115326447
12	39667800	39667801	A	G	27	GENIC	homozygous	115326449