chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	102915069	102915070	T	C	58	GENIC	possibly homozygous	109115375
1	102915393	102915394	T	C	60	GENIC	possibly homozygous	109115377
1	102915949	102915950	A	G	57	GENIC	possibly homozygous	109115379
1	102916994	102916995	T	A	45	GENIC	possibly homozygous	109115381
1	102917876	102917877	G	A	48	GENIC	homozygous	109115383
1	102918313	102918314	G	A	46	GENIC	homozygous	109115387
1	102920051	102920052	T	G	40	GENIC	homozygous	109115389
1	102921573	102921574	C	T	53	GENIC	homozygous	109115391
1	102922641	102922642	A	C	59	GENIC	homozygous	109115393
1	102923364	102923365	C	T	46	GENIC	homozygous	109115395
1	102923491	102923492	G	A	41	GENIC	homozygous	109115397
1	102925081	102925082	C	T	48	GENIC	homozygous	109115399
1	102925086	102925087	A	G	49	GENIC	homozygous	109115401
1	102925549	102925550	G	A	45	GENIC	homozygous	109115403
1	102925703	102925704	T	C	40	GENIC	homozygous	109115405
1	102926657	102926658	A	G	57	GENIC	homozygous	109115407
1	102926705	102926706	T	C	55	GENIC	homozygous	109115409
1	102926848	102926849	T	C	45	GENIC	homozygous	109115411
1	102926877	102926878	C	T	53	GENIC	homozygous	109115413
1	102927694	102927695	G	A	42	GENIC	homozygous	109115419
1	102928187	102928188	G	T	36	GENIC	homozygous	109115421
1	102929262	102929263	G	A	50	GENIC	homozygous	109115423
1	102918034	102918035	C		8	GENIC	homozygous	130818472
1	102918040	102918044	TTTC		7	GENIC	homozygous	130818473
1	102921192	102921307	CTGACTCTTTTTTTTTTTTTTTTTTTTTGGTTCTTTTTTTCGGAGCTGGGGACCGAACCCAGGGCCTTGCGCTTCCTAGGTAAGCGCTCTACCACTGAGCTAAATCCCCAGCCCC		28	GENIC	homozygous	130818474
1	102922013	102922013		C	28	GENIC	homozygous	130818475
1	102925356	102925457	AAAAAAATGTTGGTTCGGGGTTGGGGATTTAGCTCAGTGGTAGAGCGCTTGCCTAGGAAGCGCAAGGCCCTGGGTTCGGTCCCCAGCTCCGGAAAAAAGAA		31	GENIC	homozygous	130818476