chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	101878988	101878989	C	T	11	GENIC	homozygous	52074632
10	101879014	101879015	T	C	10	GENIC	homozygous	52074634
10	101879973	101879974	A	G	12	GENIC	homozygous	52074638
10	101880362	101880363	T	A	18	GENIC	homozygous	53173655
10	101880548	101880549	A	T	30	GENIC	homozygous	51585835
10	101881019	101881020	A	-	17	GENIC	possibly homozygous	52074640
10	101881142	101881143	C	G	19	GENIC	homozygous	52074642
10	101881184	101881185	T	A	19	GENIC	homozygous	52074644
10	101882280	101882281	A	AG	17	GENIC	homozygous	52074646
10	101882907	101882909	TT	--	18	GENIC	homozygous	52074652
10	101882948	101882949	G	GTT	9	GENIC	homozygous	52074654
10	101883030	101883031	A	AGTCCTTGTTTTGTTTTTTAACAATTTGATTAAACTCAATGAAGTCAAATAAATAAATAATG	18	GENIC	heterozygous	53173656
10	101883354	101883355	G	A	17	GENIC	homozygous	52074662
10	101883664	101883665	T	C	21	GENIC	possibly homozygous	52074664
10	101884361	101884362	A	G	12	GENIC	homozygous	51585837
10	101884738	101884739	C	CTAGGACAGGCTG	23	GENIC	homozygous	52074666
10	101885165	101885166	T	A	27	GENIC	homozygous	52074668
10	101885686	101885687	A	C	13	GENIC	homozygous	53173657
10	101886184	101886186	TC	--	18	GENIC	homozygous	51585839
10	101886207	101886208	C	G	23	GENIC	homozygous	52074674
10	101886217	101886218	G	A	23	GENIC	homozygous	53173658
10	101886462	101886463	G	A	29	GENIC	homozygous	52074676
10	101887268	101887269	A	AAG	18	GENIC	homozygous	52074678
10	101887687	101887688	G	GA	20	GENIC	homozygous	52074680
10	101887777	101887778	C	T	21	GENIC	homozygous	52074682
10	101887883	101887885	GA	--	11	GENIC	homozygous	53173659
10	101889090	101889091	T	C	27	GENIC	homozygous	52074686
10	101889530	101889531	G	A	5	GENIC	homozygous	52074688
10	101889687	101889688	A	G	26	GENIC	homozygous	52074690
10	101890040	101890041	G	A	15	GENIC	homozygous	52074692
10	101887688	101887689	T	A	21	GENIC	homozygous	52936773
10	101882949	101882950	G	T	9	GENIC	homozygous	52936771