chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	88098135	88098136	A	G	47	GENIC	homozygous	109898700
2	88098632	88098633	G	A	26	GENIC	homozygous	110951678
2	88098937	88098938	T	G	63	GENIC	homozygous	109898702
2	88101093	88101094	G	A	34	GENIC	homozygous	110951680
2	88102649	88102650	T	C	39	GENIC	homozygous	109898704
2	88102667	88102668	G	T	44	GENIC	homozygous	109898706
2	88102778	88102779	G	A	32	GENIC	homozygous	109898708
2	88104411	88104412	T	C	32	GENIC	homozygous	109898714
2	88105579	88105580	T	C	57	GENIC	homozygous	109898718
2	88106281	88106282	G	A	47	GENIC	homozygous	109898719
2	88106359	88106360	T	A	39	GENIC	possibly homozygous	109898721
2	88106775	88106776	A	G	44	GENIC	homozygous	109898727
2	88106779	88106780	T	C	40	GENIC	homozygous	109898729
2	88107189	88107190	T	G	57	GENIC	homozygous	109898733
2	88107248	88107249	A	G	48	GENIC	homozygous	109898735
2	88107582	88107583	A	G	53	GENIC	possibly homozygous	109898737
2	88108702	88108703	G	T	30	GENIC	heterozygous	110951682
2	88108799	88108800	G	A	43	GENIC	homozygous	110951684
2	88109180	88109181	T	C	56	GENIC	possibly homozygous	109898742
2	88109224	88109225	C	A	61	GENIC	homozygous	110951686
2	88110585	88110586	T	C	48	GENIC	homozygous	109898744
2	88110903	88110904	G	A	50	GENIC	homozygous	110951688
2	88112310	88112311	G	T	52	GENIC	homozygous	109898748