chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	88098135	88098136	A	G	24	GENIC	homozygous	109898700
2	88098937	88098938	T	G	17	GENIC	homozygous	109898702
2	88102649	88102650	T	C	19	GENIC	homozygous	109898704
2	88102667	88102668	G	T	20	GENIC	homozygous	109898706
2	88102778	88102779	G	A	16	GENIC	homozygous	109898708
2	88103107	88103108	C	T	30	GENIC	homozygous	109898710
2	88103556	88103557	A	G	15	GENIC	homozygous	109898712
2	88104411	88104412	T	C	16	GENIC	homozygous	109898714
2	88105285	88105286	G	A	21	GENIC	homozygous	109898716
2	88105579	88105580	T	C	23	GENIC	homozygous	109898718
2	88106281	88106282	G	A	30	GENIC	homozygous	109898719
2	88106359	88106360	T	A	32	GENIC	homozygous	109898721
2	88106367	88106368	G	A	32	GENIC	homozygous	109898723
2	88106408	88106409	C	T	38	GENIC	homozygous	109898725
2	88106775	88106776	A	G	30	GENIC	homozygous	109898727
2	88106779	88106780	T	C	30	GENIC	homozygous	109898729
2	88106963	88106964	C	T	12	GENIC	homozygous	109898731
2	88107189	88107190	T	G	18	GENIC	homozygous	109898733
2	88107248	88107249	A	G	18	GENIC	homozygous	109898735
2	88107582	88107583	A	G	33	GENIC	homozygous	109898737
2	88108169	88108170	T	C	37	GENIC	homozygous	109898739
2	88108368	88108369	A	C	22	GENIC	possibly homozygous	109898741
2	88109180	88109181	T	C	20	GENIC	homozygous	109898742
2	88110585	88110586	T	C	34	GENIC	homozygous	109898744
2	88111090	88111091	C	T	24	GENIC	homozygous	109898746
2	88112310	88112311	G	T	24	GENIC	homozygous	109898748