chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	11905061	11905062	T	G	3	GENIC	homozygous	53789654
7	11905571	11905572	C	T	31	GENIC	homozygous	53789655
7	11905648	11905649	G	A	29	GENIC	homozygous	53789656
7	11905784	11905785	G	A	25	GENIC	homozygous	53789657
7	11906186	11906187	T	A	7	GENIC	homozygous	53789658
7	11906189	11906190	A	AGG	5	GENIC	homozygous	53789659
7	11907537	11907538	A	G	30	GENIC	homozygous	53789660
7	11908069	11908070	A	G	29	GENIC	homozygous	53789661
7	11908712	11908713	G	A	7	GENIC	homozygous	53789662
7	11909017	11909018	A	T	17	GENIC	homozygous	53789663
7	11909228	11909229	T	-	11	GENIC	possibly homozygous	53789665
7	11910476	11910477	A	G	33	GENIC	homozygous	53789668
7	11910508	11910509	C	T	35	GENIC	homozygous	53789669
7	11910519	11910520	C	T	31	GENIC	homozygous	53789670
7	11910617	11910618	G	T	29	GENIC	homozygous	53789671
7	11910938	11910939	A	G	23	GENIC	homozygous	53789672
7	11911345	11911346	T	A	31	GENIC	homozygous	53789673
7	11912951	11912952	C	T	30	GENIC	homozygous	53789674
7	11913107	11913108	G	C	30	GENIC	homozygous	53789675
7	11913791	11913792	C	T	17	GENIC	homozygous	53789676
7	11913995	11913996	G	C	16	GENIC	homozygous	53789677