chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	142869847	142869848	T	C	19	GENIC	homozygous	59643056
4	142870177	142870178	C	T	23	GENIC	homozygous	59643058
4	142870320	142870321	A	G	18	GENIC	homozygous	59643060
4	142870594	142870595	C	T	28	GENIC	homozygous	59643062
4	142870769	142870770	A	G	22	GENIC	homozygous	59643064
4	142870890	142870891	C	CCATG	4	GENIC	homozygous	59643066
4	142870925	142870926	T	TGC	7	GENIC	homozygous	59643068
4	142870929	142870930	T	TGTGTGTGTGTGC	9	GENIC	homozygous	59643070
4	142870967	142870968	T	TATGTGTGC	5	GENIC	homozygous	58567658
4	142871009	142871010	C	T	8	GENIC	homozygous	59643072
4	142871508	142871509	T	C	32	GENIC	homozygous	59643074
4	142871777	142871778	C	T	23	GENIC	homozygous	59643076
4	142871974	142871975	G	A	10	GENIC	homozygous	59643078
4	142872126	142872127	C	T	12	GENIC	homozygous	59643080
4	142872142	142872143	A	G	11	GENIC	homozygous	59643082
4	142872619	142872620	G	A	15	GENIC	homozygous	59643085
4	142871644	142871645	T	C	35	GENIC	homozygous	57505389