chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	175495466	175495467	G	T	43	GENIC	homozygous	142965493
2	175496541	175496542	G	A	54	GENIC	homozygous	142965494
2	175498305	175498306	A	C	56	GENIC	homozygous	136374441
2	175498612	175498613	T	C	49	GENIC	homozygous	136374442
2	175498881	175498882	A	G	42	GENIC	homozygous	142965495
2	175499344	175499345	A	G	43	GENIC	homozygous	136374443
2	175500598	175500599	G	T	50	GENIC	homozygous	142965496
2	175501404	175501405	C	T	45	GENIC	homozygous	142965497
2	175501545	175501546	C	A	66	GENIC	possibly homozygous	142965498
2	175502217	175502218	C	T	41	GENIC	homozygous	142965499
2	175502971	175502972	G	A	50	GENIC	homozygous	142965500
2	175503964	175503965	C	A	46	GENIC	homozygous	136374444
2	175504746	175504747	T	C	35	GENIC	homozygous	142965501
2	175504753	175504754	A	G	35	GENIC	homozygous	142965502
2	175504872	175504873	T		9	GENIC	possibly homozygous	403028231
2	175504872	175504873	T	C	9	GENIC	heterozygous	403028232
2	175504872	175504873	T	G	9	GENIC	heterozygous	403028233
2	175505620	175505621	A	G	41	GENIC	homozygous	136374446
2	175504860	175504861	T		9	GENIC	possibly homozygous	404058022
2	175505515	175505518	CTC		31	GENIC	homozygous	135961525
2	175504860	175504861	T	G	9	GENIC	heterozygous	404058021