chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	19593226	19593227	T	C	10	GENIC	homozygous	115279443
12	19593374	19593375	C	T	14	GENIC	homozygous	115279445
12	19593533	19593534	G	C	20	GENIC	homozygous	115279447
12	19593749	19593750	C	G	31	GENIC	homozygous	115279449
12	19593971	19593972	T	G	17	GENIC	homozygous	115279451
12	19594722	19594723	T	C	32	GENIC	homozygous	115366026
12	19595820	19595821	C	A	28	GENIC	homozygous	115279453
12	19596398	19596399	T	C	16	GENIC	homozygous	115279455
12	19596512	19596513	A	G	16	GENIC	homozygous	115279457
12	19597116	19597117	C	T	22	GENIC	homozygous	115279459
12	19597145	19597146	A	G	20	GENIC	homozygous	115279461
12	19597536	19597537	T	C	18	GENIC	homozygous	115279463
12	19597554	19597555	C	G	20	GENIC	homozygous	115279465
12	19597695	19597696	G	A	26	GENIC	homozygous	115279467
12	19598015	19598016	A	G	19	GENIC	homozygous	115279469
12	19598215	19598216	A	G	28	GENIC	possibly homozygous	115279471
12	19598331	19598332	A	G	24	GENIC	homozygous	115279473
12	19598487	19598488	A	T	26	GENIC	homozygous	115279475
12	19598817	19598818	T	A	24	GENIC	homozygous	115279477
12	19598837	19598838	C	T	21	GENIC	homozygous	115279479
12	19598912	19598913	C	A	23	GENIC	homozygous	115279481
12	19599152	19599153	C	T	19	GENIC	homozygous	115279483