chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	104692854	104692855	G	A	28	GENIC	possibly homozygous	118087589
10	104693589	104693590	T	C	46	GENIC	homozygous	116836143
10	104694014	104694015	C	G	35	GENIC	homozygous	118087590
10	104694045	104694046	T	C	39	GENIC	homozygous	116836145
10	104694350	104694351	A	G	44	GENIC	homozygous	116836149
10	104694668	104694669	A	G	40	GENIC	possibly homozygous	116836151
10	104695859	104695860	A	G	35	GENIC	possibly homozygous	116836157
10	104695878	104695879	T	G	34	GENIC	possibly homozygous	116836159
10	104696772	104696773	A	G	28	GENIC	homozygous	116836161
10	104698143	104698144	C	T	34	GENIC	homozygous	118087591
10	104698367	104698368	A	C	40	GENIC	homozygous	118087592
10	104698532	104698533	T	C	31	GENIC	homozygous	116836169
10	104699058	104699059	G	C	37	GENIC	homozygous	118087593
10	104699099	104699100	A	C	19	GENIC	homozygous	116836171
10	104699422	104699423	C	T	25	GENIC	homozygous	118087594
10	104699947	104699948	C	T	38	GENIC	homozygous	118087595
10	104701432	104701433	A	G	38	GENIC	homozygous	118087596
10	104704636	104704637	G	A	29	GENIC	possibly homozygous	118087597
10	104705531	104705532	T	G	32	GENIC	homozygous	118087598
10	104705656	104705657	G	C	7	GENIC	homozygous	118087599
10	104705662	104705663	A	T	9	GENIC	homozygous	118087600
10	104706720	104706721	T	C	30	GENIC	homozygous	116836185
10	104706775	104706776	G	A	38	GENIC	homozygous	118087601
10	104707347	104707348	A	G	45	GENIC	homozygous	116836187
10	104708013	104708014	C	T	69	GENIC	homozygous	118087602
10	104708785	104708786	A	G	35	GENIC	homozygous	116836189
10	104710612	104710613	G	A	34	GENIC	homozygous	118087603
10	104710665	104710666	G	A	14	GENIC	possibly homozygous	118087604
10	104712280	104712281	G	T	21	GENIC	homozygous	118087605
10	104712423	104712424	G	A	36	GENIC	homozygous	118087606
10	104713030	104713031	G	A	58	GENIC	possibly homozygous	118087607
10	104713971	104713972	A	C	48	GENIC	homozygous	118087608
10	104714472	104714473	A	T	42	GENIC	possibly homozygous	118087609
10	104715311	104715312	C	T	39	GENIC	homozygous	118087610
10	104715387	104715388	G	A	38	GENIC	homozygous	118087611
10	104716921	104716922	G	A	50	GENIC	homozygous	118087612
10	104717182	104717183	G	A	45	GENIC	homozygous	116836203