chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	76278691	76278692	G	A	34	GENIC	homozygous	52257241
10	76279501	76279502	T	-	34	GENIC	homozygous	51500487
10	76280380	76280381	C	T	38	GENIC	homozygous	52257243
10	76280399	76280400	C	G	44	GENIC	homozygous	51500488
10	76280760	76280761	A	G	41	GENIC	homozygous	51500489
10	76281790	76281791	C	T	54	GENIC	homozygous	52257244
10	76282740	76282741	T	G	49	GENIC	homozygous	51500490
10	76282826	76282827	A	G	36	GENIC	homozygous	52257246
10	76283387	76283388	A	-	25	GENIC	heterozygous	51697853
10	76283840	76283841	A	G	45	GENIC	homozygous	51500492
10	76283882	76283883	T	C	32	GENIC	homozygous	51500494
10	76283911	76283912	C	CCCAAGCA	35	GENIC	homozygous	51500495
10	76283915	76283916	G	-	33	GENIC	heterozygous	51500496
10	76283953	76283954	T	C	42	GENIC	homozygous	51500497
10	76283970	76283971	C	G	37	GENIC	homozygous	51500498
10	76283996	76283997	T	C	41	GENIC	homozygous	52257248
10	76282255	76282256	A	C	40	GENIC	heterozygous	51912590
10	76284786	76284787	C	CCA	45	GENIC	homozygous	52257250
10	76285346	76285347	A	G	53	GENIC	homozygous	52257252
10	76286846	76286847	C	T	42	GENIC	homozygous	52257254
10	76286871	76286872	T	C	39	GENIC	homozygous	52257256
10	76287574	76287575	T	-	7	GENIC	homozygous	51500501
10	76287577	76287578	T	A	9	GENIC	homozygous	51500502
10	76287677	76287678	C	CA	17	GENIC	possibly homozygous	51500503
10	76287693	76287694	G	A	27	GENIC	possibly homozygous	52257258
10	76288327	76288328	G	GA	30	GENIC	homozygous	52257260
10	76288862	76288863	G	A	41	GENIC	homozygous	52257262
10	76289228	76289229	C	CT	33	GENIC	homozygous	51500504
10	76289471	76289472	C	T	43	GENIC	homozygous	51500505
10	76289906	76289907	A	-	24	GENIC	homozygous	51697867
10	76290867	76290870	AAG	---	37	GENIC	homozygous	52257264
10	76290968	76290969	C	T	46	GENIC	heterozygous	52257266
10	76291198	76291199	T	-	17	GENIC	possibly homozygous	51500506