chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	31023678	31023679	C	T	54	GENIC	homozygous	116545422
10	31024251	31024252	T	G	46	GENIC	homozygous	116545424
10	31025161	31025162	A	T	58	GENIC	homozygous	116545426
10	31025427	31025428	G	T	42	GENIC	homozygous	116545428
10	31026336	31026337	C	T	39	GENIC	homozygous	116545430
10	31029018	31029019	T	G	46	GENIC	homozygous	116545432
10	31031552	31031553	A	C	35	GENIC	homozygous	116545434
10	31031741	31031742	A	G	24	GENIC	possibly homozygous	116545436
10	31032225	31032226	G	T	30	GENIC	homozygous	116545438
10	31033460	31033461	A	G	42	GENIC	homozygous	116545440
10	31034288	31034289	C	T	51	GENIC	heterozygous	117986600
10	31034290	31034291	G	A	51	GENIC	heterozygous	117986601
10	31036213	31036214	T	A	50	GENIC	heterozygous	117986602
10	31036233	31036234	C	A	12	GENIC	heterozygous	117986603
10	31036759	31036760	T	G	55	GENIC	homozygous	116545442
10	31037969	31037970	G	C	53	GENIC	homozygous	116545444
10	31038447	31038448	G	A	37	GENIC	homozygous	116545446