chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	61150525	61150526	T	C	10	GENIC	homozygous	54429576
7	61151303	61151304	A	G	12	GENIC	possibly homozygous	54429578
7	61151669	61151670	A	AG	8	GENIC	homozygous	53931173
7	61151677	61151678	G	GT	9	GENIC	homozygous	53931174
7	61152435	61152436	C	CCACCG	2	GENIC	homozygous	54429582
7	61152459	61152460	T	TG	7	GENIC	possibly homozygous	54429584
7	61152497	61152498	G	T	8	GENIC	heterozygous	54429586
7	61152625	61152626	G	T	8	GENIC	homozygous	54429588
7	61152631	61152632	A	G	8	GENIC	homozygous	54429590
7	61152803	61152804	A	T	1	GENIC	homozygous	54429596
7	61152844	61152845	A	ATAT	5	GENIC	homozygous	54429598
7	61152967	61152968	C	A	14	GENIC	homozygous	54429600
7	61153424	61153425	G	A	9	GENIC	homozygous	54429602
7	61153523	61153524	C	CTACT	2	GENIC	heterozygous	54429613
7	61153744	61153745	C	CACT	1	GENIC	homozygous	55355596
7	61154003	61154004	A	G	9	GENIC	homozygous	54429631
7	61154044	61154045	A	C	6	GENIC	homozygous	54429633
7	61154789	61154790	C	T	15	GENIC	possibly homozygous	54429637
7	61155115	61155116	A	G	14	GENIC	possibly homozygous	54429639
7	61155364	61155365	C	G	16	GENIC	homozygous	54429641
7	61156324	61156325	T	-	2	GENIC	homozygous	54429643
7	61156583	61156584	G	-	16	GENIC	homozygous	54429645
7	61156665	61156666	T	C	13	GENIC	homozygous	54429647
7	61156739	61156740	A	G	12	GENIC	possibly homozygous	54429649
7	61157322	61157323	T	TA	5	GENIC	heterozygous	54429659
7	61157371	61157372	C	T	7	GENIC	homozygous	54429661
7	61157430	61157431	A	G	16	GENIC	possibly homozygous	54429663
7	61157522	61157523	C	G	15	GENIC	homozygous	54429665
7	61157543	61157544	A	C	10	GENIC	homozygous	54429667
7	61158124	61158125	A	G	7	GENIC	homozygous	54429683
7	61158147	61158148	C	-	11	GENIC	homozygous	54429685
7	61159201	61159202	T	C	18	GENIC	possibly homozygous	54429687
7	61159833	61159839	ATGAAG	------	2	GENIC	homozygous	54429689
7	61160210	61160211	T	C	10	GENIC	homozygous	54429691
7	61155066	61155067	A	T	15	GENIC	homozygous	55569726