chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	110620512	110620513	G	A	36	GENIC	possibly homozygous	112292341
3	110620795	110620796	C	T	49	GENIC	homozygous	112292343
3	110621260	110621261	C	T	44	GENIC	homozygous	112292345
3	110622393	110622394	C	T	42	GENIC	homozygous	112292347
3	110622982	110622983	A	C	66	GENIC	homozygous	112003887
3	110623216	110623217	C	T	42	GENIC	homozygous	112138962
3	110624496	110624497	G	A	45	GENIC	homozygous	112003889
3	110625631	110625632	T	C	42	GENIC	homozygous	112003891
3	110626881	110626881		ACCTGGT	42	GENIC	homozygous	130907821
3	110626964	110626965	C	T	35	GENIC	homozygous	112292349
3	110628152	110628153	T	C	47	GENIC	homozygous	112003899
3	110630082	110630083	G	A	45	GENIC	homozygous	112292353
3	110631947	110631948	G	A	49	GENIC	homozygous	112292355
3	110633139	110633140	C	T	61	GENIC	homozygous	112292357
3	110633253	110633254	G	C	52	GENIC	homozygous	111673098
3	110631298	110631299	G		50	GENIC	homozygous	127918172
3	110632367	110632368	A	T	53	GENIC	homozygous	111673093
3	110632368	110632369	G	C	53	GENIC	homozygous	111673095
3	110633583	110633583		ACA	45	GENIC	possibly homozygous	127918173
3	110634584	110634585	G	A	48	GENIC	homozygous	111673102
3	110636109	110636110	T	C	56	GENIC	homozygous	111673105
3	110636137	110636138	G	C	50	GENIC	homozygous	111673107
3	110636553	110636554	T	C	41	GENIC	homozygous	111673109
3	110636841	110636842	A	G	47	GENIC	homozygous	111673112
3	110636918	110636919	A	G	46	GENIC	homozygous	111673114
3	110637465	110637466	A	G	63	GENIC	homozygous	112138975
3	110637822	110637823	G	A	58	GENIC	homozygous	112292359