chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	60537758	60537759	T	C	21	GENIC	homozygous	111072842
17	60538167	60538168	A	C	30	GENIC	homozygous	111072844
17	60538358	60538359	C	T	35	GENIC	possibly homozygous	111209345
17	60539512	60539513	A	G	24	GENIC	possibly homozygous	111072845
17	60539797	60539798	T	C	9	GENIC	homozygous	111072846
17	60540574	60540575	G	C	17	GENIC	homozygous	111209347
17	60541092	60541093	A	G	26	GENIC	homozygous	111072850
17	60541214	60541215	G	A	39	GENIC	homozygous	111072851
17	60541452	60541453	G	A	30	GENIC	homozygous	111072852
17	60541607	60541608	T	C	30	GENIC	homozygous	111072853
17	60541628	60541629	C	G	30	GENIC	homozygous	111209350
17	60542301	60542302	C	G	24	GENIC	homozygous	111209351
17	60542573	60542574	T	C	28	GENIC	homozygous	111209352
17	60542822	60542823	A	T	22	GENIC	homozygous	111072855
17	60543359	60543360	C	T	13	GENIC	homozygous	111209353
17	60543523	60543524	A	G	14	GENIC	homozygous	111072856
17	60545648	60545649	C	T	15	GENIC	homozygous	111209354
17	60547055	60547056	C	G	19	GENIC	homozygous	111072858
17	60548127	60548128	A	C	28	GENIC	homozygous	111072859
17	60549524	60549525	T	C	27	GENIC	homozygous	111072861
17	60550029	60550030	C	A	22	GENIC	homozygous	111072862
17	60550080	60550081	G	A	27	GENIC	possibly homozygous	111209355
17	60550322	60550323	C	A	24	GENIC	homozygous	111072863
17	60550769	60550770	T	C	23	GENIC	homozygous	111072864
17	60552840	60552841	G	T	21	GENIC	homozygous	111072865