chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	397743	397823	GAGAGGGAGAGGGGGAGGGGGAGGGGAGTGGGAGAGGGAGGAGGAGAGAGGAGAGGGAGAGAGAGGAAGACGGGAGAGGA		7	GENIC	possibly homozygous	135016094
17	397853	397854	A		12	GENIC	homozygous	129414349
17	397863	397863		A	16	GENIC	homozygous	129414350
17	397892	397893	T		22	GENIC	homozygous	129414351
17	398230	398231	A		36	GENIC	homozygous	129414352
17	398296	398297	T		37	GENIC	homozygous	129414353
17	398351	398351		G	35	GENIC	homozygous	129414354
17	398382	398383	C		38	GENIC	homozygous	129414355
17	398421	398421		C	39	GENIC	homozygous	129414356
17	398455	398456	A		38	GENIC	homozygous	129414357
17	398533	398534	T		45	GENIC	homozygous	129414358
17	398580	398581	C		44	GENIC	homozygous	129414359
17	398609	398610	G		46	GENIC	homozygous	129414360
17	398615	398615		C	50	GENIC	homozygous	129414361
17	398632	398633	A		52	GENIC	homozygous	129414362
17	398648	398649	C		49	GENIC	homozygous	129414363
17	398638	398639	C	A	50	GENIC	homozygous	110936920
17	398642	398643	T	G	51	GENIC	homozygous	110936924
17	401085	401085		G	33	GENIC	homozygous	129414364
17	401098	401099	C		38	GENIC	homozygous	129414365
17	401130	401131	C		36	GENIC	homozygous	129414366
17	401144	401144		T	33	GENIC	homozygous	129414367
17	401166	401166		T	32	GENIC	homozygous	129414368
17	401176	401176		T	32	GENIC	homozygous	129414369
17	401195	401197	TC		26	GENIC	homozygous	129414370
17	401539	401539		C	18	GENIC	homozygous	129414371
17	405377	405377		GTACCTGAGCCAGGGAT	32	GENIC	possibly homozygous	129414372
17	405564	405565	A		52	GENIC	homozygous	129414374
17	401332	401336	CCTC		2	GENIC	homozygous	130599439
17	416599	416600	C		49	GENIC	homozygous	129414375
17	416605	416606	T		49	GENIC	homozygous	129414376
17	416632	416633	G	A	55	GENIC	homozygous	110936927
17	416635	416636	G		55	GENIC	homozygous	129414377