Mapping	Reference Position	Consensus Position	Variation Type	Length	Reference	Variants	Allele Variations	Frequencies	Counts	Coverage	Variant #1	Frequency of #1	Count of #1	Variant #2	Frequency of #2	Count of #2	Overlapping Annotations	Amino Acid Change
chr1	62138	1289	SNP	1	T	2	T/C	72.7/27.3	8/3	11	T	72.73	8	C	27.27	3		
chr1	136398	4069	SNP	1	G	1	T	66.7	2	3	T	66.67	2					
chr1	631246	11970	SNP	1	G	1	A	80	4	5	A	80.00	4					
chr1	1238847	23571	SNP	1	G	1	A	100	2	2	A	100.00	2					
chr1	1238854	23578	SNP	1	G	1	T	100	2	2	T	100.00	2					
chr1	1654641	32002	SNP	1	A	2	A/G	50.0/50.0	2/2	4	A	50.00	2	G	50.00	2		
chr1	1699458	34167	SNP	1	T	1	A	66.7	2	3	A	66.67	2					
chr1	1711362	34822	SNP	1	A	2	A/G	62.5/37.5	5/3	8	A	62.50	5	G	37.50	3		
chr1	1911517	39277	SNP	1	T	2	T/A	60.0/40.0	3/2	5	T	60.00	3	A	40.00	2		
chr1	1922921	39917	SNP	1	G	1	C	100	6	6	C	100.00	6					
chr1	2249518	48051	SNP	1	G	1	T	80	4	5	T	80.00	4					
chr1	2988795	66247	SNP	1	T	1	C	75	3	4	C	75.00	3					
chr1	3176306	70162	SNP	1	C	2	C/G	83.3/16.7	10/2	12	C	83.33	10	G	16.67	2		
chr1	3176389	70228	SNP	1	A	2	C/A	66.7/33.3	4/2	6	C	66.67	4	A	33.33	2		
chr1	3429804	77073	SNP	1	T	1	G	75	3	4	G	75.00	3					
chr1	3545597	80804	SNP	1	C	1	T	100	2	2	T	100.00	2					
chr1	3562769	81296	SNP	1	G	2	G/A	57.1/42.9	4/3	7	G	57.14	4	A	42.86	3		
chr1	3734375	85429	SNP	1	C	1	G	100	4	4	G	100.00	4					
chr1	3958934	91815	SNP	1	G	1	T	100	6	6	T	100.00	6					
chr1	4076830	95557	SNP	1	G	1	T	75	3	4	T	75.00	3					
chr1	4076837	95564	SNP	1	G	1	C	100	4	4	C	100.00	4					
chr1	4762634	113806	SNP	1	G	1	A	100	2	2	A	100.00	2					
chr1	4808856	115296	SNP	1	G	2	G/T	50.0/50.0	3/3	6	G	50.00	3	T	50.00	3		
chr1	4911746	118512	SNP	1	T	1	C	100	8	8	C	100.00	8					
chr1	4933448	119603	SNP	1	T	1	G	100	5	5	G	100.00	5