chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	145118052	145118053	G	A	23	GENIC	homozygous	115946569
7	145119351	145119352	A	G	22	GENIC	homozygous	115946571
7	145120078	145120079	T	G	23	GENIC	homozygous	115946573
7	145120692	145120693	C	A	25	GENIC	homozygous	115946575
7	145120839	145120840	C	T	18	GENIC	homozygous	115946577
7	145121171	145121172	T	C	14	GENIC	homozygous	115946580
7	145121810	145121811	T	G	16	GENIC	homozygous	115946582
7	145121814	145121815	T	C	16	GENIC	homozygous	115946584
7	145121834	145121835	C	G	16	GENIC	homozygous	115946586
7	145121967	145121968	G	T	14	GENIC	homozygous	115946588
7	145122094	145122095	G	A	15	GENIC	homozygous	115946590
7	145123742	145123743	A	T	11	GENIC	homozygous	115946591
7	145124175	145124176	A	G	17	GENIC	homozygous	115946593
7	145124844	145124845	G	A	13	GENIC	homozygous	115946595
7	145125788	145125789	A	G	16	GENIC	homozygous	115946597
7	145125874	145125875	G	A	19	GENIC	homozygous	115946599
7	145126437	145126438	G	A	17	GENIC	homozygous	115946601
7	145128606	145128607	T	C	10	GENIC	homozygous	115946603
7	145129024	145129029	TTTTG		10	GENIC	homozygous	128532339
7	145129161	145129162	A	G	14	GENIC	homozygous	115946605
7	145121876	145121876		TCTC	10	GENIC	heterozygous	129940208
7	145130460	145130461	T		14	GENIC	homozygous	128532340
7	145130955	145130956	G	A	15	GENIC	homozygous	115946607
7	145131424	145131425	G	A	17	GENIC	homozygous	115946609
7	145134037	145134038	G	T	13	GENIC	homozygous	115946611
7	145134845	145134845		AG	18	GENIC	homozygous	128532342
7	145135727	145135728	G	A	10	GENIC	homozygous	115946613
7	145136230	145136231	G	A	18	GENIC	homozygous	115946614
7	145132646	145132646		TTTG	2	GENIC	homozygous	132407469
7	145132651	145132651		CAGGT	2	GENIC	homozygous	132407470
7	145132648	145132649	G	T	2	GENIC	homozygous	118261264
7	145145016	145145017	C	T	12	GENIC	homozygous	115946616