chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	10049313	10049314	C	A	48	GENIC	homozygous	140052149
17	10050597	10050598	T	G	35	GENIC	homozygous	140052150
17	10050986	10050987	G	T	41	GENIC	homozygous	140052151
17	10051640	10051641	C	T	16	GENIC	homozygous	140052152
17	10051075	10051075		CTGCCT	34	GENIC	homozygous	140008753
17	10052140	10052141	A	G	51	GENIC	homozygous	140052153
17	10052275	10052276	G	A	62	GENIC	homozygous	140052154
17	10052911	10052915	TGCC		46	GENIC	heterozygous	140008754
17	10054326	10054327	A	G	33	GENIC	homozygous	140052155
17	10056298	10056299	A	G	54	GENIC	homozygous	140052156
17	10056510	10056511	C	T	56	GENIC	homozygous	140052157
17	10056553	10056554	G	A	52	GENIC	homozygous	140052158
17	10056587	10056588	C	T	44	GENIC	homozygous	140052159
17	10056812	10056813	C	T	45	GENIC	homozygous	140052160
17	10056965	10056966	C	A	38	GENIC	homozygous	140052161
17	10057471	10057472	G	C	57	GENIC	homozygous	140052162
17	10057892	10057893	A	T	61	GENIC	homozygous	140052163
17	10058070	10058071	T	A	46	GENIC	homozygous	140052164
17	10058116	10058117	C	T	48	GENIC	homozygous	140052165
17	10058350	10058351	A	G	58	GENIC	homozygous	140052166
17	10058440	10058441	A	T	53	GENIC	homozygous	140052167
17	10058598	10058599	A	G	51	GENIC	homozygous	140052168
17	10058646	10058647	C	A	51	GENIC	homozygous	140052169
17	10058676	10058677	T	G	53	GENIC	homozygous	140052170
17	10059530	10059531	C	G	57	GENIC	homozygous	140052171
17	10059682	10059683	T	C	34	GENIC	homozygous	140052172
17	10060088	10060089	C	T	42	GENIC	homozygous	140052173
17	10061244	10061245	C	T	35	GENIC	homozygous	140052176
17	10061091	10061091		CCT	13	GENIC	homozygous	145221464
17	10061002	10061003	T	G	26	GENIC	homozygous	140052174
17	10061010	10061011	C	T	23	GENIC	homozygous	140052175
17	10061396	10061415	CTCACTTTGTAGCCGTGGC		41	GENIC	homozygous	140008755
17	10061504	10061505	C	A	39	GENIC	homozygous	140052177