chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	52564445	52564445		A	11	GENIC	homozygous	129003529
12	52564584	52564585	C	T	23	GENIC	homozygous	115356630
12	52574150	52574151	C		17	GENIC	homozygous	129003539
12	52574259	52574259		T	20	GENIC	homozygous	129003540
12	52574262	52574263	G		20	GENIC	homozygous	129003541
12	52574268	52574270	TT		20	GENIC	homozygous	129003542
12	52574294	52574295	T	G	20	GENIC	homozygous	123655043
12	52574296	52574296		ATATGAATATAC	20	GENIC	homozygous	129003543
12	52574300	52574301	G	T	16	GENIC	homozygous	123655045
12	52574302	52574302		TTTAT	16	GENIC	homozygous	129003544
12	52574303	52574304	G	T	15	GENIC	homozygous	123655047
12	52574305	52574306	G		15	GENIC	homozygous	129003545
12	52574306	52574307	C	T	14	GENIC	homozygous	123655049
12	52574308	52574309	C	T	14	GENIC	homozygous	123655050
12	52587919	52587920	T		6	GENIC	homozygous	129003553
12	52587982	52587983	C		4	GENIC	homozygous	129003557
12	52587986	52587987	A		4	GENIC	homozygous	129003558
12	52587992	52587993	C		4	GENIC	homozygous	129003559
12	52587997	52587998	C		5	GENIC	homozygous	129003560
12	52588004	52588006	CC		4	GENIC	homozygous	129003561
12	52588012	52588013	T		6	GENIC	homozygous	129003562