chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	123706579	123706580	T	C	39	GENIC	homozygous	113156038
4	123707481	123707482	G	A	21	GENIC	heterozygous	113241128
4	123708656	123708657	C	T	5	GENIC	homozygous	113156039
4	123709103	123709104	T	C	22	GENIC	homozygous	113156040
4	123710195	123710196	A	T	32	GENIC	homozygous	113156041
4	123713099	123713100	C	T	39	GENIC	homozygous	113156042
4	123713757	123713758	G	A	33	GENIC	homozygous	113156043
4	123715955	123715956	G	T	4	GENIC	homozygous	113156044
4	123716739	123716740	T	C	25	GENIC	homozygous	113156045
4	123717580	123717581	A	T	30	GENIC	homozygous	113156046
4	123718309	123718310	T	C	35	GENIC	homozygous	113156047
4	123719507	123719508	G	A	21	GENIC	homozygous	113156048
4	123722552	123722553	C	T	27	GENIC	homozygous	113156049
4	123722927	123722928	A	G	25	GENIC	homozygous	113156050
4	123723482	123723483	T	C	31	GENIC	homozygous	113156051
4	123725061	123725062	A	G	26	GENIC	homozygous	113156052
4	123725352	123725353	G	C	24	GENIC	homozygous	113156053
4	123725731	123725732	A	G	41	GENIC	homozygous	113156054
4	123725926	123725927	C	G	20	GENIC	homozygous	113156055
4	123727924	123727925	G	A	33	GENIC	homozygous	113156058
4	123728872	123728873	T	A	27	GENIC	homozygous	113156059
4	123729364	123729365	T	A	29	GENIC	homozygous	113156060
4	123729407	123729408	A	G	25	GENIC	homozygous	113156061
4	123732137	123732138	G	A	27	GENIC	homozygous	113156062
4	123732214	123732215	C	T	31	GENIC	homozygous	113156063
4	123732964	123732965	G	A	28	GENIC	homozygous	113156064
4	123733151	123733152	T	G	34	GENIC	homozygous	113156065
4	123733165	123733166	A	G	31	GENIC	homozygous	113156066
4	123733523	123733524	T	G	29	GENIC	homozygous	113156067
4	123733599	123733600	C	A	15	GENIC	possibly homozygous	113156068
4	123737592	123737593	T	C	26	GENIC	homozygous	113156069
4	123737635	123737636	C	T	34	GENIC	homozygous	113156070
4	123737732	123737733	G	A	30	GENIC	homozygous	113156071