chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
18	60995606	60995607	T	C	37	GENIC	homozygous	110370337
18	60995728	60995729	A	G	33	GENIC	homozygous	110370339
18	60997077	60997078	C	T	22	GENIC	homozygous	110370341
18	60997243	60997244	T	C	31	GENIC	homozygous	119496536
18	60997258	60997259	A	G	32	GENIC	homozygous	119496537
18	60997281	60997282	C	T	34	GENIC	possibly homozygous	119496538
18	60997436	60997437	A	T	39	GENIC	homozygous	110370343
18	60998225	60998226	A	G	32	GENIC	heterozygous	110886297
18	60998371	60998372	T	A	15	GENIC	homozygous	110775706
18	60999160	60999161	C	T	27	GENIC	homozygous	110370345
18	60999474	60999475	C	T	19	GENIC	homozygous	110370347
18	60999767	60999768	G	A	39	GENIC	homozygous	110370349
18	61001218	61001219	C	T	27	GENIC	possibly homozygous	110370351