chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	38782648	38782649	C	G	37	GENIC	homozygous	116762496
10	38783095	38783096	A	G	41	GENIC	homozygous	116925226
10	38783213	38783214	G	A	38	GENIC	homozygous	116762498
10	38783407	38783408	T	A	43	GENIC	homozygous	116762500
10	38783418	38783419	A	C	45	GENIC	homozygous	116762502
10	38783419	38783420	G	A	44	GENIC	homozygous	116762504
10	38783430	38783431	A	G	41	GENIC	possibly homozygous	116762506
10	38784448	38784449	T	C	42	GENIC	homozygous	117004390
10	38784522	38784523	A	G	36	GENIC	homozygous	117312372
10	38784956	38784957	A	G	54	GENIC	homozygous	117194058
10	38785168	38785169	T	C	19	GENIC	homozygous	118065737
10	38785648	38785649	T	C	4	GENIC	homozygous	132332865
10	38786195	38786196	C	T	5	GENIC	heterozygous	131100897
10	38787112	38787113	G	A	12	GENIC	heterozygous	131100899
10	38787682	38787683	C	T	12	GENIC	homozygous	131100900
10	38787916	38787917	C	T	43	GENIC	homozygous	117194059
10	38787937	38787937		TAAAA	33	GENIC	homozygous	131091467
10	38784949	38784950	C	A	53	GENIC	possibly homozygous	117409782
10	38787304	38787305	T		12	GENIC	possibly homozygous	131091463
10	38787306	38787308	AT		12	GENIC	possibly homozygous	131091464
10	38787690	38787691	T		13	GENIC	homozygous	131091465
10	38787693	38787695	AT		13	GENIC	homozygous	131091466
10	38788499	38788500	A	G	42	GENIC	homozygous	116762510
10	38788577	38788577		AAAC	34	GENIC	homozygous	131091468
10	38789656	38789657	T		40	GENIC	homozygous	131091469
10	38790257	38790258	G	T	46	GENIC	homozygous	116762512
10	38791516	38791517	A	T	45	GENIC	homozygous	116762514
10	38791566	38791567	C	T	46	GENIC	homozygous	116762516
10	38791835	38791835		TATGG	49	GENIC	homozygous	131091470
10	38791840	38791841	G	A	50	GENIC	homozygous	116762518
10	38791205	38791206	T	C	42	GENIC	homozygous	117150864