chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	106338802	106338803	T	C	20	GENIC	homozygous	51765361
10	106339208	106339209	T	C	21	GENIC	homozygous	51765365
10	106341067	106341068	C	T	9	GENIC	homozygous	53546572
10	106341732	106341733	A	G	17	GENIC	homozygous	51765369
10	106343499	106343500	C	CTT	7	GENIC	homozygous	53546573
10	106343933	106343934	T	C	12	GENIC	homozygous	51765375
10	106346481	106346482	G	A	8	GENIC	homozygous	53546574
10	106349378	106349379	T	A	10	GENIC	homozygous	51765383
10	106351703	106351705	AC	--	7	GENIC	homozygous	51765385
10	106351968	106351969	A	G	16	GENIC	homozygous	51765387
10	106353336	106353337	A	G	13	GENIC	homozygous	51765392
10	106354938	106354939	G	A	17	GENIC	homozygous	51765394
10	106355595	106355596	T	-	10	GENIC	homozygous	52734168
10	106356241	106356242	T	G	13	GENIC	homozygous	51765400
10	106358324	106358325	C	T	8	GENIC	homozygous	51765402
10	106360601	106360602	G	A	12	GENIC	homozygous	53546575
10	106361268	106361269	C	T	22	GENIC	homozygous	53546576
10	106361607	106361608	T	G	19	GENIC	homozygous	51765406
10	106363981	106363982	T	C	11	GENIC	homozygous	51765410
10	106376988	106376989	T	TA	9	GENIC	homozygous	53546577
10	106378745	106378746	G	-	9	GENIC	homozygous	53546578
10	106378750	106378751	G	T	10	GENIC	homozygous	53546579
10	106379951	106379952	A	G	7	GENIC	homozygous	51765434
10	106380534	106380535	C	T	7	GENIC	homozygous	53546580
10	106383446	106383447	G	A	25	GENIC	possibly homozygous	53546581
10	106384898	106384899	T	C	13	GENIC	homozygous	51765440
10	106388270	106388271	A	G	19	GENIC	homozygous	51765444
10	106388322	106388323	T	A	19	GENIC	homozygous	51765446
10	106389303	106389304	A	C	22	GENIC	homozygous	51765448
10	106389762	106389763	A	T	12	GENIC	homozygous	53546582
10	106391724	106391725	A	AAT	12	GENIC	homozygous	53546583
10	106391725	106391726	G	GATGA	12	GENIC	homozygous	53546584
10	106396787	106396788	C	-	9	GENIC	homozygous	51765454
10	106398091	106398092	T	C	18	GENIC	homozygous	51765458