chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	11627396	11627397	A	C	17	GENIC	possibly homozygous	53788708
7	11627487	11627488	G	A	18	GENIC	possibly homozygous	53788709
7	11628523	11628524	T	C	13	GENIC	homozygous	53788710
7	11629634	11629635	A	G	13	GENIC	heterozygous	53788711
7	11630788	11630789	C	T	15	GENIC	possibly homozygous	53788715
7	11632588	11632589	G	A	28	GENIC	possibly homozygous	53788718
7	11633416	11633417	T	C	24	GENIC	possibly homozygous	53788719
7	11633519	11633520	C	A	17	GENIC	homozygous	53788720
7	11633525	11633526	A	G	13	GENIC	homozygous	53788721
7	11633538	11633539	A	C	17	GENIC	homozygous	53788722
7	11634931	11634932	T	C	15	GENIC	homozygous	53788723
7	11635815	11635816	A	T	18	GENIC	homozygous	53788724
7	11637249	11637250	T	-	7	GENIC	possibly homozygous	54181611
7	11637433	11637434	A	G	12	GENIC	possibly homozygous	53788725
7	11639232	11639233	T	C	8	GENIC	possibly homozygous	53788726
7	11639499	11639500	C	T	15	GENIC	possibly homozygous	53788727
7	11639689	11639690	G	A	18	GENIC	heterozygous	53788728
7	11639873	11639874	A	AT	24	GENIC	homozygous	53788729
7	11640906	11640907	T	C	10	GENIC	heterozygous	54884856
7	11640907	11640908	C	A	10	GENIC	heterozygous	54181612
7	11642750	11642751	A	G	9	GENIC	homozygous	53788731
7	11643494	11643495	A	G	22	GENIC	homozygous	53788732
7	11643826	11643827	T	TCTGG	8	GENIC	homozygous	53788733
7	11643835	11643836	C	T	14	GENIC	homozygous	53788734
7	11644484	11644485	T	G	19	GENIC	possibly homozygous	53788736
7	11644524	11644525	T	C	22	GENIC	homozygous	53788737
7	11644756	11644757	T	C	26	GENIC	possibly homozygous	53788738
7	11645636	11645637	C	T	6	GENIC	heterozygous	53788739