chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	101878988	101878989	C	T	9	GENIC	heterozygous	52074632
10	101879014	101879015	T	C	16	GENIC	heterozygous	52074634
10	101879090	101879091	C	G	14	GENIC	heterozygous	52074636
10	101879973	101879974	A	G	12	GENIC	heterozygous	52074638
10	101880548	101880549	A	T	10	GENIC	homozygous	51585835
10	101882280	101882281	A	AG	20	GENIC	heterozygous	52074646
10	101882741	101882742	G	T	14	GENIC	heterozygous	52074648
10	101882742	101882743	C	T	13	GENIC	heterozygous	52074650
10	101883001	101883002	C	T	14	GENIC	heterozygous	52074656
10	101883354	101883355	G	A	12	GENIC	heterozygous	52074662
10	101884361	101884362	A	G	21	GENIC	homozygous	51585837
10	101884738	101884739	C	CTAGGACAGGCTG	10	GENIC	heterozygous	52074666
10	101885165	101885166	T	A	12	GENIC	heterozygous	52074668
10	101886184	101886186	TC	--	9	GENIC	homozygous	51585839
10	101886207	101886208	C	G	14	GENIC	heterozygous	52074674
10	101886462	101886463	G	A	16	GENIC	heterozygous	52074676
10	101887268	101887269	A	AAG	11	GENIC	heterozygous	52074678
10	101887687	101887688	G	GA	11	GENIC	heterozygous	52074680
10	101887688	101887689	T	A	11	GENIC	heterozygous	52936773
10	101887777	101887778	C	T	10	GENIC	heterozygous	52074682
10	101888576	101888577	G	A	13	GENIC	heterozygous	52074684
10	101889090	101889091	T	C	14	GENIC	heterozygous	52074686
10	101889687	101889688	A	G	17	GENIC	heterozygous	52074690
10	101890040	101890041	G	A	7	GENIC	heterozygous	52074692