chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	53631020	53631021	T	G	21	GENIC	homozygous	115685774
7	53632967	53632968	A	G	30	GENIC	homozygous	115685776
7	53633695	53633696	T	C	32	GENIC	homozygous	115685777
7	53634222	53634223	A	G	22	GENIC	homozygous	115685778
7	53635845	53635846	T	A	23	GENIC	possibly homozygous	115685779
7	53635893	53635894	T	C	28	GENIC	homozygous	115685780
7	53635902	53635903	A	G	27	GENIC	homozygous	115685781
7	53635914	53635915	C	T	23	GENIC	homozygous	115685782
7	53636050	53636051	C	T	32	GENIC	homozygous	115685783
7	53636317	53636318	T	G	20	GENIC	homozygous	115685784
7	53636700	53636701	A	G	31	GENIC	homozygous	115685785
7	53636803	53636804	T	A	34	GENIC	homozygous	115685786
7	53637893	53637894	T	A	26	GENIC	homozygous	115685789
7	53638857	53638858	A	G	28	GENIC	homozygous	115685790
7	53638873	53638874	G	A	26	GENIC	homozygous	115685791
7	53638996	53638997	G	A	26	GENIC	homozygous	115685792
7	53639294	53639295	G	T	25	GENIC	homozygous	115685793
7	53639339	53639340	A	G	22	GENIC	homozygous	115685794
7	53639520	53639521	G	A	18	GENIC	homozygous	115685795
7	53639915	53639916	T	C	24	GENIC	homozygous	115685796
7	53640397	53640398	T	A	25	GENIC	homozygous	115685797
7	53640596	53640597	T	C	41	GENIC	homozygous	115685798
7	53640727	53640728	G	A	34	GENIC	homozygous	115685799
7	53640992	53640993	C	A	29	GENIC	homozygous	115685800
7	53642478	53642479	C	T	18	GENIC	homozygous	115685801
7	53642861	53642862	G	T	30	GENIC	homozygous	115685802
7	53644832	53644833	G	C	27	GENIC	homozygous	116290118
7	53645844	53645845	A	G	28	GENIC	homozygous	115685803
7	53646692	53646693	A	T	18	GENIC	homozygous	115685804
7	53647912	53647913	G	T	32	GENIC	homozygous	116290119
7	53648284	53648285	A	G	24	GENIC	homozygous	115685806
7	53648681	53648682	C	T	54	GENIC	homozygous	116290121