chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	109727493	109727494	T	C	21	GENIC	homozygous	60789712
1	109727761	109727762	T	TTG	4	GENIC	homozygous	62554163
1	109727818	109727819	T	C	13	GENIC	homozygous	60789713
1	109728936	109728937	A	-	31	GENIC	homozygous	60789714
1	109729045	109729046	T	G	27	GENIC	homozygous	60789715
1	109729455	109729456	T	C	32	GENIC	homozygous	60789716
1	109730351	109730352	C	CT	23	GENIC	homozygous	60789718
1	109730361	109730362	C	A	24	GENIC	homozygous	60789719
1	109730562	109730563	A	G	24	GENIC	homozygous	60789722
1	109730587	109730588	C	T	26	GENIC	homozygous	62570897
1	109730648	109730649	G	GA	22	GENIC	possibly homozygous	60789723
1	109727954	109727955	A	AT	18	GENIC	possibly homozygous	61500180
1	109729642	109729643	T	C	21	GENIC	possibly homozygous	61500181
1	109730421	109730422	T	C	23	GENIC	possibly homozygous	61500182
1	109729826	109729827	G	A	30	GENIC	homozygous	62690757
1	109730262	109730268	ACACAC	------	3	GENIC	heterozygous	62690758
1	109731470	109731471	A	T	25	GENIC	homozygous	60789725
1	109731617	109731618	T	C	31	GENIC	homozygous	60789726
1	109731920	109731921	T	A	39	GENIC	homozygous	60789727
1	109732178	109732179	A	G	27	GENIC	homozygous	60789728
1	109732279	109732280	C	G	17	GENIC	homozygous	60789729
1	109733299	109733301	TA	--	25	GENIC	heterozygous	62150263
1	109733302	109733303	T	TCC	28	GENIC	heterozygous	62150265
1	109733501	109733502	T	TA	30	GENIC	heterozygous	62085829
1	109733504	109733505	T	TA	32	GENIC	heterozygous	62085830
1	109733509	109733510	C	CA	31	GENIC	heterozygous	62085831
1	109733531	109733532	T	C	32	GENIC	heterozygous	60789731
1	109733563	109733567	GTTT	----	34	GENIC	heterozygous	60789732
1	109733664	109733666	AC	--	29	GENIC	heterozygous	62150267
1	109733671	109733672	A	ACATG	29	GENIC	heterozygous	62150269
1	109733677	109733681	GCGA	----	31	GENIC	heterozygous	62229989