chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	30295625	30295626	G	A	34	GENIC	homozygous	115634055
7	30314684	30314685	A	G	29	GENIC	homozygous	116133972
7	30314904	30314905	C	A	21	GENIC	homozygous	116133974
7	30318047	30318048	T	A	32	GENIC	homozygous	116133976
7	30318245	30318246	A	G	24	GENIC	homozygous	115634081
7	30318599	30318600	C	T	29	GENIC	homozygous	115634082
7	30319600	30319601	G	C	25	GENIC	homozygous	115634083
7	30323247	30323248	T	G	32	GENIC	homozygous	115634087
7	30324285	30324286	C	A	25	GENIC	homozygous	118276682
7	30325538	30325539	T	C	33	GENIC	homozygous	116133978
7	30325891	30325892	G	A	36	GENIC	homozygous	116133980
7	30325959	30325960	A	G	36	GENIC	homozygous	115634089
7	30328154	30328155	A	G	30	GENIC	homozygous	116133982
7	30331216	30331217	T	A	35	GENIC	homozygous	115634094
7	30332395	30332396	G	A	32	GENIC	homozygous	116133984
7	30333687	30333688	G	A	31	GENIC	homozygous	116133986
7	30336131	30336132	T	A	33	GENIC	homozygous	115634095
7	30338016	30338017	T	C	35	GENIC	homozygous	115634096
7	30341861	30341862	C	T	21	GENIC	homozygous	116133990
7	30342055	30342056	G	C	24	GENIC	homozygous	116133992
7	30342088	30342089	T	C	38	GENIC	homozygous	115634099
7	30342498	30342499	G	A	32	GENIC	homozygous	115634101
7	30342543	30342544	C	G	39	GENIC	homozygous	116133994
7	30344138	30344139	T	C	10	GENIC	homozygous	116326212