chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	10369986	10369987	C	T	38	GENIC	homozygous	110953947
17	10370469	10370470	C	T	25	GENIC	homozygous	110953949
17	10370877	10370878	T	C	24	GENIC	possibly homozygous	110953952
17	10371072	10371073	C	T	38	GENIC	homozygous	110953954
17	10372137	10372138	A	C	39	GENIC	homozygous	110953956
17	10372212	10372213	C	T	27	GENIC	homozygous	110953958
17	10373905	10373906	G	A	26	GENIC	possibly homozygous	119263951
17	10373916	10373917	T	A	25	GENIC	possibly homozygous	119263952
17	10373944	10373945	C	T	30	GENIC	heterozygous	119263953
17	10375645	10375646	C	A	30	GENIC	homozygous	110953959
17	10375648	10375649	C	G	30	GENIC	homozygous	110953961
17	10381433	10381434	A	G	40	GENIC	possibly homozygous	110953964