chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	48626453	48626454	T	C	18	GENIC	homozygous	117002501
8	48626499	48626500	G	A	20	GENIC	homozygous	117002503
8	48626614	48626615	A	T	12	GENIC	homozygous	117002505
8	48626697	48626698	G	A	20	GENIC	homozygous	117002507
8	48627249	48627250	C	A	20	GENIC	homozygous	117002509
8	48628492	48628493	G	A	15	GENIC	homozygous	117002511
8	48629217	48629218	C	T	23	GENIC	homozygous	117002513
8	48629748	48629749	G	A	19	GENIC	homozygous	117002515
8	48632030	48632031	T	C	27	GENIC	homozygous	117002517
8	48632475	48632476	T	G	21	GENIC	homozygous	117002519
8	48632781	48632782	G	A	20	GENIC	homozygous	116957250
8	48632874	48632875	C	T	15	GENIC	homozygous	117002521
8	48633554	48633555	C	A	13	GENIC	possibly homozygous	116957252
8	48634362	48634363	A	G	10	GENIC	homozygous	116957254
8	48634716	48634717	T	C	19	GENIC	homozygous	116957258
8	48634866	48634867	A	G	22	GENIC	homozygous	116957260
8	48635688	48635689	T	C	18	GENIC	homozygous	116957262
8	48636227	48636228	C	G	16	GENIC	homozygous	117002523
8	48635824	48635827	TCC		20	GENIC	homozygous	132122116