chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	13078567	13078568	C	T	13	GENIC	homozygous	111295544
17	13079357	13079358	G	A	22	GENIC	homozygous	111295545
17	13079852	13079853	G	A	15	GENIC	possibly homozygous	111462198
17	13080129	13080130	A	T	15	GENIC	homozygous	111462200
17	13080323	13080324	G	A	30	GENIC	possibly homozygous	111295546
17	13081261	13081262	A	T	33	GENIC	homozygous	111295548
17	13081289	13081290	A	G	31	GENIC	homozygous	110962313
17	13081329	13081330	G	A	28	GENIC	homozygous	111295549
17	13081453	13081454	A	G	20	GENIC	homozygous	111295550
17	13081729	13081730	G	A	31	GENIC	homozygous	111462202
17	13082128	13082129	A	G	30	GENIC	homozygous	111462204
17	13082181	13082182	C	T	24	GENIC	homozygous	111462206
17	13082594	13082595	G	T	24	GENIC	possibly homozygous	111462208
17	13083676	13083677	G	A	33	GENIC	homozygous	111295552
17	13084791	13084792	T	C	39	GENIC	homozygous	110962323
17	13084949	13084950	T	C	22	GENIC	homozygous	110962325
17	13085081	13085082	C	T	15	GENIC	homozygous	110962327
17	13085103	13085104	T	C	15	GENIC	homozygous	110962329
17	13085618	13085619	G	A	23	GENIC	homozygous	110962331
17	13086817	13086818	C	G	33	GENIC	homozygous	110962341
17	13086040	13086041	T	G	31	GENIC	homozygous	110962333
17	13086619	13086620	A	G	22	GENIC	homozygous	110962337
17	13086724	13086725	C	G	26	GENIC	homozygous	110962339
17	13087158	13087159	C	T	28	GENIC	possibly homozygous	110962343
17	13087197	13087198	C	T	26	GENIC	homozygous	110962345
17	13087505	13087506	T	C	26	GENIC	homozygous	110962347
17	13087556	13087557	T	C	31	GENIC	homozygous	110962349