chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	102620799	102620801	GA	--	12	GENIC	homozygous	61486673
1	102620804	102620809	AATCT	-----	12	GENIC	homozygous	61486674
1	102620812	102620813	G	-	15	GENIC	possibly homozygous	61486675
1	102620848	102620849	T	G	21	GENIC	heterozygous	61486676
1	102621757	102621758	C	T	28	GENIC	homozygous	61486677
1	102622244	102622245	C	CCTAT	14	GENIC	homozygous	60780066
1	102622310	102622314	TCTA	----	20	GENIC	homozygous	61486678
1	102622588	102622589	A	ATG	24	GENIC	possibly homozygous	61486679
1	102622706	102622707	A	G	22	GENIC	homozygous	61486680
1	102623322	102623323	A	G	27	GENIC	homozygous	61486681
1	102623766	102623767	T	C	29	GENIC	possibly homozygous	61486682
1	102624134	102624135	T	C	16	GENIC	homozygous	61486683
1	102624441	102624442	A	G	29	GENIC	homozygous	61486684
1	102624576	102624577	C	T	12	GENIC	homozygous	61486685
1	102624603	102624604	A	G	22	GENIC	homozygous	61486686
1	102624662	102624663	T	TG	22	GENIC	homozygous	61486687
1	102625102	102625103	G	C	21	GENIC	homozygous	61486688
1	102625215	102625216	T	G	19	GENIC	heterozygous	61486689
1	102625484	102625485	C	CAGA	18	GENIC	homozygous	61486690
1	102626578	102626579	A	G	31	GENIC	homozygous	61486691
1	102626676	102626677	T	C	28	GENIC	homozygous	61486692
1	102627655	102627656	C	CTT	10	GENIC	homozygous	61486693
1	102629216	102629217	C	CTGTGTG	9	GENIC	heterozygous	61486694
1	102629216	102629217	C	CTGTG	9	GENIC	heterozygous	61486695