chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	124461251	124461252	G	A	22	GENIC	possibly homozygous	116082990
7	124461914	124461915	A	G	25	GENIC	homozygous	115865938
7	124462214	124462215	C	T	22	GENIC	homozygous	115865940
7	124463066	124463067	A	C	21	GENIC	possibly homozygous	116082991
7	124463386	124463387	G	A	31	GENIC	possibly homozygous	116082992
7	124463577	124463578	G	T	35	GENIC	homozygous	116082993
7	124463601	124463602	A	G	35	GENIC	homozygous	115865944
7	124464535	124464536	T	C	15	GENIC	homozygous	115865948
7	124464632	124464633	C	T	27	GENIC	possibly homozygous	116082996
7	124465205	124465206	A	G	14	GENIC	homozygous	115865954
7	124465578	124465579	C	G	31	GENIC	homozygous	115865958
7	124466531	124466532	T	G	12	GENIC	homozygous	118332365
7	124466535	124466536	C	A	12	GENIC	homozygous	118259348
7	124466536	124466537	C	G	13	GENIC	homozygous	118259350
7	124467387	124467388	C	G	26	GENIC	possibly homozygous	116082998
7	124466643	124466644	C	G	8	GENIC	homozygous	118286505
7	124466660	124466661	C	G	5	GENIC	homozygous	118286507
7	124468082	124468083	G	T	23	GENIC	possibly homozygous	116082999
7	124468283	124468284	G	A	24	GENIC	possibly homozygous	116083000
7	124468627	124468628	A	G	33	GENIC	homozygous	116083001
7	124468816	124468817	A	G	29	GENIC	homozygous	116083002
7	124469104	124469105	T	C	29	GENIC	possibly homozygous	116083003
7	124469105	124469106	T	A	30	GENIC	possibly homozygous	116083004
7	124469282	124469283	A	G	21	GENIC	possibly homozygous	116083005
7	124469490	124469491	C	T	24	GENIC	homozygous	116083006
7	124469787	124469788	C	T	47	GENIC	possibly homozygous	116083007
7	124469887	124469888	A	T	27	GENIC	homozygous	115865976
7	124470030	124470031	G	A	37	GENIC	homozygous	116083008
7	124470511	124470512	T	C	30	GENIC	possibly homozygous	116083009
7	124470523	124470524	G	A	34	GENIC	possibly homozygous	116083010
7	124468282	124468283	A	T	24	GENIC	possibly homozygous	118433616