chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	154520833	154520834	A	G	76	GENIC	possibly homozygous	110768550
2	154521257	154521258	C	T	27	GENIC	homozygous	110768552
2	154521832	154521833	G	A	47	GENIC	homozygous	110065339
2	154523478	154523479	G	A	44	GENIC	homozygous	110065341
2	154524350	154524351	G	T	79	GENIC	heterozygous	110977559
2	154524636	154524637	C	G	40	GENIC	homozygous	110768554
2	154524703	154524704	C	T	43	GENIC	possibly homozygous	110768556
2	154525945	154525946	A	C	35	GENIC	homozygous	110768557
2	154526379	154526380	T	C	33	GENIC	homozygous	110768559
2	154527269	154527270	C	T	36	GENIC	homozygous	110768561
2	154527527	154527528	A	G	34	GENIC	possibly homozygous	110768563
2	154530652	154530653	A	G	49	GENIC	homozygous	110768565
2	154530754	154530755	C	A	47	GENIC	homozygous	110768566
2	154534203	154534204	C	G	55	GENIC	homozygous	110065352
2	154534830	154534831	C	T	65	GENIC	homozygous	110768568
2	154535023	154535024	G	A	40	GENIC	possibly homozygous	110768570
2	154535066	154535067	G	A	26	GENIC	possibly homozygous	110768572
2	154535779	154535780	C	T	33	GENIC	homozygous	110768574
2	154535813	154535814	C	T	45	GENIC	homozygous	110768576
2	154536206	154536207	G	A	46	GENIC	homozygous	110768578
2	154536260	154536261	G	A	47	GENIC	possibly homozygous	110768580
2	154537477	154537478	G	C	55	GENIC	homozygous	110768582
2	154538184	154538185	T	C	38	GENIC	homozygous	110065359