chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	149537728	149537729	A	G	25	GENIC	homozygous	110051784
2	149539664	149539665	C	T	29	GENIC	homozygous	120373402
2	149542277	149542278	A	G	23	GENIC	homozygous	110051785
2	149542491	149542492	C	T	24	GENIC	possibly homozygous	110051786
2	149542513	149542514	C	A	27	GENIC	homozygous	110051787
2	149542523	149542524	A	G	30	GENIC	homozygous	110051788
2	149543626	149543627	G	A	23	GENIC	homozygous	110051790
2	149543811	149543812	T	C	22	GENIC	homozygous	110051791
2	149543974	149543975	C	A	38	GENIC	homozygous	110051792
2	149544214	149544215	T	C	26	GENIC	homozygous	110051793
2	149544812	149544813	T	C	26	GENIC	homozygous	120373403
2	149544857	149544858	G	A	25	GENIC	homozygous	120373404
2	149544975	149544976	A	G	21	GENIC	homozygous	110051795
2	149545004	149545005	C	A	20	GENIC	homozygous	120373405
2	149545601	149545602	A	G	23	GENIC	homozygous	110051796
2	149552863	149552864	C	T	29	GENIC	homozygous	110051811
2	149552954	149552955	G	T	35	GENIC	homozygous	110051812
2	149553320	149553321	A	G	33	GENIC	homozygous	110051813
2	149555489	149555490	T	C	31	GENIC	homozygous	110051817
2	149556069	149556070	T	C	34	GENIC	homozygous	110051819
2	149556136	149556137	G	A	27	GENIC	homozygous	120373406
2	149556511	149556512	A	G	35	GENIC	homozygous	110051820
2	149556578	149556579	C	T	22	GENIC	homozygous	110051821
2	149556669	149556670	G	T	29	GENIC	homozygous	110051822
2	149557476	149557477	G	T	25	GENIC	homozygous	120373407
2	149559100	149559101	T	G	20	GENIC	homozygous	110051829
2	149559281	149559282	C	A	34	GENIC	homozygous	110051830
2	149559389	149559390	C	G	25	GENIC	homozygous	120373408
2	149559478	149559479	A	G	28	GENIC	homozygous	120150061
2	149559757	149559758	T	G	18	GENIC	homozygous	120373409
2	149563586	149563587	C	T	29	GENIC	homozygous	110051833