chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	122158811	122158812	G	C	24	GENIC	homozygous	115860288
7	122163780	122163781	C	T	48	GENIC	heterozygous	116225842
7	122163909	122163910	A	G	51	GENIC	heterozygous	116225843
7	122164788	122164789	A	G	30	GENIC	homozygous	116225844
7	122173567	122173568	C	A	3	GENIC	homozygous	118259198
7	122173675	122173676	A	G	26	GENIC	homozygous	115860318
7	122175376	122175377	A	G	25	GENIC	homozygous	116225846
7	122175524	122175525	A	G	32	GENIC	possibly homozygous	116225847
7	122178140	122178141	C	A	31	GENIC	possibly homozygous	118418319
7	122174957	122174958	G	C	23	GENIC	possibly homozygous	118418315
7	122176508	122176509	T	A	20	GENIC	possibly homozygous	118418316
7	122176647	122176648	T	G	28	GENIC	possibly homozygous	118418317
7	122177611	122177612	G	A	26	GENIC	possibly homozygous	118418318
7	122179320	122179321	G	A	29	GENIC	homozygous	118418320
7	122179521	122179522	C	A	21	GENIC	homozygous	116225857
7	122180123	122180124	A	T	32	GENIC	possibly homozygous	116225858
7	122181092	122181093	T	C	19	GENIC	possibly homozygous	116225859
7	122182155	122182156	T	A	37	GENIC	possibly homozygous	116225862
7	122182736	122182737	G	A	26	GENIC	possibly homozygous	118418321
7	122183152	122183153	T	C	31	GENIC	possibly homozygous	116225865
7	122185265	122185266	A	G	28	GENIC	possibly homozygous	116225869
7	122185452	122185453	G	A	6	GENIC	heterozygous	118433228
7	122186409	122186410	G	A	33	GENIC	homozygous	118418322
7	122187667	122187668	G	A	29	GENIC	homozygous	118418324
7	122187669	122187670	T	G	28	GENIC	homozygous	118418325
7	122188163	122188164	C	T	28	GENIC	possibly homozygous	118418326
7	122188540	122188541	T	C	33	GENIC	homozygous	116225877
7	122190529	122190530	G	A	33	GENIC	possibly homozygous	116225882
7	122191893	122191894	A	G	29	GENIC	possibly homozygous	116225889
7	122192144	122192145	G	A	28	GENIC	possibly homozygous	118418327