chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	144901166	144901167	C	T	18	GENIC	homozygous	116378351
7	144901920	144901921	G	T	26	GENIC	homozygous	116378353
7	144905408	144905409	G	A	21	GENIC	homozygous	115946037
7	144907491	144907492	A	G	21	GENIC	homozygous	116378354
7	144908617	144908618	C	T	23	GENIC	possibly homozygous	116378356
7	144910779	144910780	G	T	13	GENIC	heterozygous	116378358
7	144913521	144913522	C	T	29	GENIC	homozygous	116378360
7	144913789	144913790	A	C	19	GENIC	homozygous	115946080
7	144916617	144916618	A	G	37	GENIC	homozygous	115946101
7	144917115	144917116	G	A	25	GENIC	homozygous	115946103
7	144917242	144917243	T	C	19	GENIC	homozygous	115946105
7	144917497	144917498	C	T	17	GENIC	homozygous	115946107
7	144918705	144918706	C	T	8	GENIC	heterozygous	116397032
7	144918908	144918909	T	C	35	GENIC	homozygous	115946113
7	144919091	144919092	A	G	29	GENIC	homozygous	116378364
7	144919480	144919481	T	G	43	GENIC	homozygous	116378366
7	144919611	144919612	G	A	27	GENIC	homozygous	116378368
7	144920007	144920008	C	A	39	GENIC	homozygous	116378369
7	144920174	144920175	C	T	31	GENIC	homozygous	116378371
7	144920468	144920469	T	C	31	GENIC	possibly homozygous	116378373
7	144921400	144921401	G	A	30	GENIC	homozygous	116378374
7	144922182	144922183	T	C	39	GENIC	homozygous	115946119
7	144922417	144922418	T	C	25	GENIC	homozygous	116378376
7	144922476	144922477	A	G	31	GENIC	homozygous	115946123
7	144922737	144922738	G	T	34	GENIC	homozygous	116378378
7	144923269	144923270	G	A	29	GENIC	homozygous	116378380
7	144923455	144923456	G	A	20	GENIC	homozygous	116378382
7	144923642	144923643	A	G	23	GENIC	homozygous	115946129
7	144925893	144925894	G	A	27	GENIC	homozygous	116378384