chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	10369996	10369997	C	T	17	GENIC	possibly homozygous	111524770
17	10370469	10370470	C	T	15	GENIC	homozygous	110953949
17	10375407	10375408	G	A	13	GENIC	possibly homozygous	111524778
17	10375435	10375436	C	T	9	GENIC	possibly homozygous	111637345
17	10376405	10376406	T	C	36	GENIC	possibly homozygous	111524780
17	10377097	10377098	G	A	30	GENIC	homozygous	111524782
17	10377172	10377173	C	T	23	GENIC	homozygous	111524784
17	10380301	10380302	T	C	27	GENIC	homozygous	111524786
17	10380404	10380405	T	C	30	GENIC	possibly homozygous	111524788
17	10380508	10380509	T	G	7	GENIC	heterozygous	111637347
17	10381151	10381152	G	A	26	GENIC	possibly homozygous	111524792
17	10381433	10381434	A	G	29	GENIC	homozygous	110953964
17	10381724	10381725	T	C	35	GENIC	possibly homozygous	111524794
17	10382124	10382125	A	G	30	GENIC	possibly homozygous	111524796
17	10382185	10382186	C	A	30	GENIC	homozygous	111524798
17	10382376	10382377	C	A	27	GENIC	homozygous	111524800
17	10382606	10382607	A	T	27	GENIC	homozygous	111524802
17	10382652	10382653	T	C	22	GENIC	homozygous	111524804
17	10382962	10382963	C	T	40	GENIC	possibly homozygous	111524806
17	10383034	10383035	C	T	32	GENIC	possibly homozygous	111524808
17	10383409	10383410	T	C	28	GENIC	homozygous	111524810
17	10383692	10383693	G	T	25	GENIC	homozygous	111524812
17	10384178	10384179	C	T	41	GENIC	homozygous	111524814
17	10384934	10384935	T	C	11	GENIC	possibly homozygous	111637350
17	10387353	10387354	A	G	26	GENIC	homozygous	111524816
17	10387531	10387532	C	T	25	GENIC	possibly homozygous	111524818
17	10388400	10388401	C	T	29	GENIC	possibly homozygous	111524820
17	10389098	10389099	G	A	16	GENIC	possibly homozygous	111637352
17	10390831	10390832	C	T	33	GENIC	possibly homozygous	111524822