chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	80998126	80998127	C	T	21	GENIC	homozygous	138832720
10	80998702	80998703	G	A	26	GENIC	homozygous	143459374
10	81000068	81000069	T	C	13	GENIC	homozygous	143459375
10	81000209	81000210	T	C	12	GENIC	homozygous	143459376
10	81004116	81004117	A		13	GENIC	homozygous	138693943
10	81005674	81005675	G	A	21	GENIC	homozygous	143459377
10	81007028	81007029	A		17	GENIC	homozygous	138693944
10	81007415	81007416	G	A	23	GENIC	homozygous	143459379
10	81009139	81009140	A	G	26	GENIC	homozygous	138832723
10	81010419	81010420	G	A	23	GENIC	homozygous	143459380
10	81011237	81011237		AGAC	18	GENIC	homozygous	143433926
10	81006544	81006544		AAAACAAAAC	16	GENIC	homozygous	143433925
10	81011303	81011304	T	C	20	GENIC	homozygous	143459381
10	81011905	81011906	A	G	23	GENIC	homozygous	143459382
10	81012420	81012421	A	G	36	GENIC	homozygous	143459383
10	81014152	81014153	A	T	13	GENIC	homozygous	143459384
10	81014154	81014170	AAAAAAAAAAAGAACC		12	GENIC	homozygous	143433927
10	81014178	81014179	A	T	15	GENIC	homozygous	143459385
10	81014317	81014318	G	A	27	GENIC	homozygous	143459386
10	81014782	81014783	T	C	6	GENIC	homozygous	143459387
10	81015939	81015940	G	A	26	GENIC	homozygous	143459388
10	81016483	81016484	G	A	26	GENIC	possibly homozygous	143459389
10	81016518	81016519	T	C	28	GENIC	possibly homozygous	143459390
10	81014081	81014082	C	T	12	GENIC	homozygous	403901502
10	81014165	81014166	G		12	GENIC	homozygous	404016129
10	81014165	81014166	G	C	12	GENIC	heterozygous	404016130
10	81014165	81014166	G	A	12	GENIC	heterozygous	404016131