geneid | 10290 |
---|---|
ensemblid | ENSG00000072195.15 |
hgncid | 16901 |
symbol | SPEG |
name | striated muscle enriched protein kinase |
refseq_nuc | NM_005876.5 |
refseq_prot | NP_005867.3 |
ensembl_nuc | ENST00000312358.12 |
ensembl_prot | ENSP00000311684.7 |
mane_status | MANE Select |
chr | chr2 |
start | 219434843 |
end | 219493629 |
strand | + |
ver | v1.2 |
region | chr2:219434843-219493629 |
region5000 | chr2:219429843-219498629 |
regionname0 | SPEG_chr2_219434843_219493629 |
regionname5000 | SPEG_chr2_219429843_219498629 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 3267 | 116 | 27 | 25 | 46 | 6 | 11 | 36 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0002 | 0/0 | 3267 | 72 | 16 | 14 | 22 | 1 | 19 | 18 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0003 | 0/0 | 3267 | 21 | 0 | 10 | 5 | 2 | 4 | 2 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0004 | 0/0 | 3267 | 13 | 0 | 2 | 11 | 0 | 0 | 8 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0005 | 0/0 | 3267 | 13 | 13 | 0 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0006 | 0/1 | 3267 | 11 | 2 | 4 | 3 | 1 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0007 | 0/0 | 3267 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0008 | 0/0 | 3267 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0009 | 0/0 | 3267 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0010 | 0/0 | 3267 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0011 | 0/0 | 3267 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0012 | 0/0 | 3267 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0013 | 0/0 | 3267 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0014 | 0/0 | 3267 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0015 | 0/0 | 3267 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0016 | 0/0 | 3267 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0017 | 0/0 | 3267 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0018 | 0/0 | 3267 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0019 | 0/0 | 3267 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0020 | 0/0 | 3267 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0021 | 0/0 | 3267 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0022 | 0/0 | 3267 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0023 | 0/0 | 3267 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0024 | 0/0 | 3267 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0025 | 0/0 | 3267 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0026 | 0/0 | 3267 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0027 | 0/0 | 3267 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0028 | 0/0 | 3267 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0029 | 0/0 | 3267 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0030 | 0/0 | 3267 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0031 | 0/0 | 3267 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0032 | 0/0 | 3267 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0033 | 0/0 | 3267 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0034 | 0/0 | 3267 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0035 | 0/0 | 3267 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0036 | 0/0 | 3267 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0037 | 0/0 | 3267 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0038 | 0/0 | 3267 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0039 | 0/0 | 3267 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0040 | 0/0 | 3267 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0041 | 0/0 | 3267 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0042 | 0/0 | 3267 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0043 | 0/0 | 3267 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0044 | 0/0 | 3267 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0045 | 0/0 | 3267 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0046 | 0/0 | 3267 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0047 | 0/0 | 3267 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0048 | 0/0 | 3267 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0049 | 0/0 | 3267 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0050 | 0/0 | 3267 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 9804 | 62 | 1 | 20 | 32 | 6 | 3 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
c0002 | 0/0 | 9804 | 39 | 17 | 3 | 12 | 0 | 7 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
c0003 | 0/0 | 9804 | 31 | 6 | 7 | 11 | 1 | 6 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
c0004 | 0/0 | 9804 | 23 | 1 | 4 | 7 | 0 | 11 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
c0005 | 0/0 | 9804 | 15 | 0 | 8 | 4 | 0 | 3 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
c0006 | 0/0 | 9804 | 12 | 12 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
c0007 | 0/1 | 9804 | 9 | 0 | 4 | 3 | 1 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
c0008 | 0/0 | 9804 | 8 | 5 | 2 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
c0009 | 0/0 | 9804 | 6 | 0 | 2 | 4 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
c0010 | 1/0 | 9804 | 6 | 5 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
c0011 | 0/0 | 9804 | 4 | 0 | 1 | 1 | 2 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
c0012 | 0/0 | 9804 | 4 | 0 | 0 | 4 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
c0013 | 0/0 | 9804 | 4 | 4 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
c0014 | 0/0 | 9804 | 3 | 3 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
c0015 | 0/0 | 9804 | 2 | 2 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
c0016 | 0/0 | 9804 | 2 | 0 | 0 | 2 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
c0017 | 0/0 | 9804 | 2 | 2 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
c0018 | 0/0 | 9804 | 2 | 0 | 0 | 2 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
c0019 | 0/0 | 9804 | 2 | 2 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
c0020 | 0/0 | 9804 | 2 | 2 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
c0021 | 0/0 | 9804 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
c0022 | 0/0 | 9804 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
c0023 | 0/0 | 9804 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
c0024 | 0/0 | 9804 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
c0025 | 0/0 | 9804 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
c0026 | 0/0 | 9804 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
c0027 | 0/0 | 9804 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
c0028 | 0/0 | 9804 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
c0029 | 0/0 | 9804 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
c0030 | 0/0 | 9804 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
c0031 | 0/0 | 9804 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
c0032 | 0/0 | 9804 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
c0033 | 0/0 | 9804 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
c0034 | 0/0 | 9804 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
c0035 | 0/0 | 9804 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
c0036 | 0/0 | 9804 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
c0037 | 0/0 | 9804 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
c0038 | 0/0 | 9804 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
c0039 | 0/0 | 9804 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
c0040 | 0/0 | 9804 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
c0041 | 0/0 | 9804 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
c0042 | 0/0 | 9804 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
c0043 | 0/0 | 9804 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
c0044 | 0/0 | 9804 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
c0045 | 0/0 | 9804 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
c0046 | 0/0 | 9804 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
c0047 | 0/0 | 9804 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
c0048 | 0/0 | 9804 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
c0049 | 0/0 | 9804 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
c0050 | 0/0 | 9804 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
c0051 | 0/0 | 9804 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
c0052 | 0/0 | 9804 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
c0053 | 0/0 | 9804 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
c0054 | 0/0 | 9804 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
c0055 | 0/0 | 9804 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
c0056 | 0/0 | 9804 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
c0057 | 0/0 | 9804 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
c0058 | 0/0 | 9804 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
c0059 | 0/0 | 9804 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
c0060 | 0/0 | 9804 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
c0061 | 0/0 | 9804 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
c0062 | 0/0 | 9804 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
c0063 | 0/0 | 9804 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
c0064 | 0/0 | 9804 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
c0065 | 0/0 | 9804 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
c0066 | 0/0 | 9804 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
c0067 | 0/0 | 9804 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
c0068 | 0/0 | 9804 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
c0069 | 0/0 | 9804 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
c0070 | 0/0 | 9804 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
c0071 | 0/0 | 9804 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
c0072 | 0/0 | 9804 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
c0073 | 0/0 | 9804 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
c0074 | 0/0 | 9804 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
c0075 | 0/0 | 9804 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
c0076 | 0/0 | 9804 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
c0077 | 0/0 | 9804 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
c0078 | 0/0 | 9804 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
c0079 | 0/0 | 9804 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
c0080 | 0/0 | 9804 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
c0081 | 0/0 | 9804 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
c0082 | 0/0 | 9804 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
c0083 | 0/0 | 9804 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
c0084 | 0/0 | 9804 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
c0085 | 0/0 | 9804 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
c0086 | 0/0 | 9804 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 979 | 163 | 46 | 38 | 54 | 8 | 16 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
t0002 | 0/1 | 979 | 118 | 36 | 23 | 37 | 2 | 19 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
t0003 | 0/0 | 979 | 9 | 9 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
t0004 | 0/0 | 979 | 4 | 0 | 0 | 0 | 0 | 4 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
t0005 | 0/0 | 979 | 4 | 3 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
t0006 | 0/0 | 979 | 2 | 2 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
t0007 | 0/0 | 979 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
t0008 | 0/0 | 979 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
t0009 | 0/0 | 979 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
t0010 | 0/0 | 979 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0002 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0004 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0007 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0010 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0011 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0012 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0140 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 9804 | 62 | 1 | 20 | 32 | 6 | 3 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0001c0002 | 0/0 | 9804 | 39 | 17 | 3 | 12 | 0 | 7 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0001c0010 | 1/0 | 9804 | 6 | 5 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0001c0019 | 0/0 | 9804 | 2 | 2 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0001c0037 | 0/0 | 9804 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0001c0039 | 0/0 | 9804 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0001c0057 | 0/0 | 9804 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0001c0066 | 0/0 | 9804 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0001c0069 | 0/0 | 9804 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0001c0076 | 0/0 | 9804 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0001c0077 | 0/0 | 9804 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0002c0003 | 0/0 | 9804 | 31 | 6 | 7 | 11 | 1 | 6 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0002c0004 | 0/0 | 9804 | 23 | 1 | 4 | 7 | 0 | 11 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0002c0008 | 0/0 | 9804 | 8 | 5 | 2 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0002c0017 | 0/0 | 9804 | 2 | 2 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0002c0045 | 0/0 | 9804 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0002c0048 | 0/0 | 9804 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0002c0054 | 0/0 | 9804 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0002c0064 | 0/0 | 9804 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0002c0065 | 0/0 | 9804 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0002c0068 | 0/0 | 9804 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0002c0074 | 0/0 | 9804 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0002c0085 | 0/0 | 9804 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0003c0005 | 0/0 | 9804 | 15 | 0 | 8 | 4 | 0 | 3 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0003c0011 | 0/0 | 9804 | 4 | 0 | 1 | 1 | 2 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0003c0038 | 0/0 | 9804 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0003c0075 | 0/0 | 9804 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0004c0009 | 0/0 | 9804 | 6 | 0 | 2 | 4 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0004c0012 | 0/0 | 9804 | 4 | 0 | 0 | 4 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0004c0016 | 0/0 | 9804 | 2 | 0 | 0 | 2 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0004c0080 | 0/0 | 9804 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0005c0006 | 0/0 | 9804 | 12 | 12 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0005c0081 | 0/0 | 9804 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0006c0007 | 0/1 | 9804 | 9 | 0 | 4 | 3 | 1 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0006c0053 | 0/0 | 9804 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0006c0058 | 0/0 | 9804 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0007c0013 | 0/0 | 9804 | 4 | 4 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0007c0020 | 0/0 | 9804 | 2 | 2 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0008c0014 | 0/0 | 9804 | 3 | 3 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0008c0041 | 0/0 | 9804 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0008c0061 | 0/0 | 9804 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0008c0078 | 0/0 | 9804 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0009c0015 | 0/0 | 9804 | 2 | 2 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0010c0051 | 0/0 | 9804 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0010c0052 | 0/0 | 9804 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0011c0036 | 0/0 | 9804 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0011c0055 | 0/0 | 9804 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0012c0018 | 0/0 | 9804 | 2 | 0 | 0 | 2 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0013c0021 | 0/0 | 9804 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0014c0022 | 0/0 | 9804 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0015c0024 | 0/0 | 9804 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0016c0026 | 0/0 | 9804 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0017c0027 | 0/0 | 9804 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0018c0028 | 0/0 | 9804 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0019c0032 | 0/0 | 9804 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0020c0050 | 0/0 | 9804 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0021c0034 | 0/0 | 9804 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0022c0033 | 0/0 | 9804 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0023c0072 | 0/0 | 9804 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0024c0047 | 0/0 | 9804 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0025c0071 | 0/0 | 9804 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0026c0070 | 0/0 | 9804 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0027c0035 | 0/0 | 9804 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0028c0063 | 0/0 | 9804 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0029c0044 | 0/0 | 9804 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0030c0031 | 0/0 | 9804 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0031c0030 | 0/0 | 9804 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0032c0042 | 0/0 | 9804 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0033c0062 | 0/0 | 9804 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0034c0056 | 0/0 | 9804 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0035c0060 | 0/0 | 9804 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0036c0059 | 0/0 | 9804 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0037c0040 | 0/0 | 9804 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0038c0043 | 0/0 | 9804 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0039c0067 | 0/0 | 9804 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0040c0046 | 0/0 | 9804 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0041c0073 | 0/0 | 9804 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0042c0049 | 0/0 | 9804 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0043c0029 | 0/0 | 9804 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0044c0079 | 0/0 | 9804 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0045c0084 | 0/0 | 9804 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0046c0083 | 0/0 | 9804 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0047c0082 | 0/0 | 9804 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0048c0025 | 0/0 | 9804 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0049c0023 | 0/0 | 9804 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0050c0086 | 0/0 | 9804 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 10782 | 60 | 1 | 19 | 31 | 6 | 3 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0001c0001t0007 | 0/0 | 10782 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0001c0001t0008 | 0/0 | 10782 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0001c0002t0001 | 0/0 | 10782 | 36 | 15 | 3 | 11 | 0 | 7 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0001c0002t0002 | 0/0 | 10782 | 2 | 2 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0001c0002t0010 | 0/0 | 10782 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0001c0010t0001 | 1/0 | 10782 | 6 | 5 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0001c0019t0001 | 0/0 | 10782 | 2 | 2 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0001c0037t0001 | 0/0 | 10782 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0001c0039t0001 | 0/0 | 10782 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0001c0057t0002 | 0/0 | 10782 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0001c0066t0001 | 0/0 | 10782 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0001c0069t0001 | 0/0 | 10782 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0001c0076t0001 | 0/0 | 10782 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0001c0077t0001 | 0/0 | 10782 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0002c0003t0002 | 0/0 | 10782 | 30 | 6 | 7 | 11 | 1 | 5 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0002c0003t0005 | 0/0 | 10782 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0002c0004t0001 | 0/0 | 10782 | 2 | 1 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0002c0004t0002 | 0/0 | 10782 | 18 | 0 | 4 | 6 | 0 | 8 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0002c0004t0004 | 0/0 | 10782 | 3 | 0 | 0 | 0 | 0 | 3 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0002c0008t0002 | 0/0 | 10782 | 8 | 5 | 2 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0002c0017t0001 | 0/0 | 10782 | 2 | 2 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0002c0045t0002 | 0/0 | 10782 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0002c0048t0004 | 0/0 | 10782 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0002c0054t0001 | 0/0 | 10782 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0002c0064t0002 | 0/0 | 10782 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0002c0065t0002 | 0/0 | 10782 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0002c0068t0002 | 0/0 | 10782 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0002c0074t0002 | 0/0 | 10782 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0002c0085t0002 | 0/0 | 10782 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0003c0005t0001 | 0/0 | 10782 | 15 | 0 | 8 | 4 | 0 | 3 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0003c0011t0001 | 0/0 | 10782 | 4 | 0 | 1 | 1 | 2 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0003c0038t0001 | 0/0 | 10782 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0003c0075t0001 | 0/0 | 10782 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0004c0009t0002 | 0/0 | 10782 | 6 | 0 | 2 | 4 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0004c0012t0002 | 0/0 | 10782 | 4 | 0 | 0 | 4 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0004c0016t0002 | 0/0 | 10782 | 2 | 0 | 0 | 2 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0004c0080t0002 | 0/0 | 10782 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0005c0006t0001 | 0/0 | 10782 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0005c0006t0002 | 0/0 | 10782 | 11 | 11 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0005c0081t0002 | 0/0 | 10782 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0006c0007t0002 | 0/1 | 10782 | 9 | 0 | 4 | 3 | 1 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0006c0053t0002 | 0/0 | 10782 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0006c0058t0002 | 0/0 | 10782 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0007c0013t0001 | 0/0 | 10782 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0007c0013t0005 | 0/0 | 10782 | 2 | 2 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0007c0013t0006 | 0/0 | 10782 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0007c0020t0002 | 0/0 | 10782 | 2 | 2 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0008c0014t0003 | 0/0 | 10782 | 3 | 3 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0008c0041t0001 | 0/0 | 10782 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0008c0061t0003 | 0/0 | 10782 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0008c0078t0003 | 0/0 | 10782 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0009c0015t0002 | 0/0 | 10782 | 2 | 2 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0010c0051t0002 | 0/0 | 10782 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0010c0052t0002 | 0/0 | 10782 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0011c0036t0003 | 0/0 | 10782 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0011c0055t0003 | 0/0 | 10782 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0012c0018t0001 | 0/0 | 10782 | 2 | 0 | 0 | 2 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0013c0021t0002 | 0/0 | 10782 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0014c0022t0002 | 0/0 | 10782 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0015c0024t0001 | 0/0 | 10782 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0016c0026t0002 | 0/0 | 10782 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0017c0027t0001 | 0/0 | 10782 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0018c0028t0001 | 0/0 | 10782 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0019c0032t0001 | 0/0 | 10782 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0020c0050t0002 | 0/0 | 10782 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0021c0034t0001 | 0/0 | 10782 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0022c0033t0002 | 0/0 | 10782 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0023c0072t0006 | 0/0 | 10782 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0024c0047t0001 | 0/0 | 10782 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0025c0071t0001 | 0/0 | 10782 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0026c0070t0003 | 0/0 | 10782 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0027c0035t0001 | 0/0 | 10782 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0028c0063t0009 | 0/0 | 10782 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0029c0044t0002 | 0/0 | 10782 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0030c0031t0003 | 0/0 | 10782 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0031c0030t0002 | 0/0 | 10782 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0032c0042t0001 | 0/0 | 10782 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0033c0062t0001 | 0/0 | 10782 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0034c0056t0001 | 0/0 | 10782 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0035c0060t0001 | 0/0 | 10782 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0036c0059t0001 | 0/0 | 10782 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0037c0040t0001 | 0/0 | 10782 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0038c0043t0001 | 0/0 | 10782 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0039c0067t0001 | 0/0 | 10782 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0040c0046t0001 | 0/0 | 10782 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0041c0073t0001 | 0/0 | 10782 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0042c0049t0002 | 0/0 | 10782 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0043c0029t0002 | 0/0 | 10782 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0044c0079t0002 | 0/0 | 10782 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0045c0084t0001 | 0/0 | 10782 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0046c0083t0005 | 0/0 | 10782 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0047c0082t0002 | 0/0 | 10782 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0048c0025t0001 | 0/0 | 10782 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0049c0023t0001 | 0/0 | 10782 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
a0050c0086t0001 | 0/0 | 10782 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | copy fasta | chr2 | 219429843 | 219498629 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0001t0001g0002 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0001t0001g0004 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0001t0007g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0001t0008g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0002t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0002t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0002t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0002t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0002t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0002t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0002t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0002t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0002t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0002t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0002t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0002t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0002t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0002t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0002t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0002t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0002t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0002t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0002t0002g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0002t0010g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0010t0001g0011 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0010t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0010t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0010t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0010t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0019t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0019t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0037t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0039t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0057t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0066t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0069t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0076t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0001c0077t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0002c0003t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0002c0003t0002g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0002c0003t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0002c0003t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0002c0003t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0002c0003t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0002c0003t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0002c0003t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0002c0003t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0002c0003t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0002c0003t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0002c0003t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0002c0003t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0002c0003t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0002c0003t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0002c0003t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0002c0003t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0002c0003t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0002c0003t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0002c0003t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0002c0003t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0002c0003t0002g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0002c0003t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0002c0003t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0002c0003t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0002c0003t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0002c0003t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0002c0003t0002g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0002c0003t0002g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0002c0003t0005g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0002c0004t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0002c0004t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0002c0004t0002g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0002c0004t0002g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0002c0004t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0002c0004t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0002c0004t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0002c0004t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0002c0004t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0002c0004t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0002c0004t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0002c0004t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0002c0004t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0002c0004t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0002c0004t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0002c0004t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0002c0004t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0002c0004t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0002c0004t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0002c0004t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0002c0004t0004g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0002c0004t0004g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0002c0004t0004g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0002c0008t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0002c0008t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0002c0008t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0002c0008t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0002c0008t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0002c0008t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0002c0008t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0002c0008t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0002c0017t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0002c0017t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0002c0045t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0002c0048t0004g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0002c0054t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0002c0064t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0002c0065t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0002c0068t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0002c0074t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0002c0085t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0003c0005t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0003c0005t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0003c0005t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0003c0005t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0003c0005t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0003c0005t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0003c0005t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0003c0005t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0003c0005t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0003c0005t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0003c0005t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0003c0005t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0003c0005t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0003c0005t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0003c0005t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0003c0011t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0003c0011t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0003c0011t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0003c0011t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0003c0038t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0003c0075t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0004c0009t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0004c0009t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0004c0009t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0004c0009t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0004c0009t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0004c0009t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0004c0012t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0004c0012t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0004c0012t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0004c0012t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0004c0016t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0004c0016t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0004c0080t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0005c0006t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0005c0006t0002g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0005c0006t0002g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0005c0006t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0005c0006t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0005c0006t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0005c0006t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0005c0006t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0005c0006t0002g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0005c0081t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0006c0007t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0006c0007t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0006c0007t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0006c0007t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0006c0007t0002g0140 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0006c0007t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0006c0007t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0006c0007t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0006c0007t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0006c0053t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0006c0058t0002g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0007c0013t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0007c0013t0005g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0007c0013t0005g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0007c0013t0006g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0007c0020t0002g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0007c0020t0002g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0008c0014t0003g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0008c0014t0003g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0008c0014t0003g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0008c0041t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0008c0061t0003g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0008c0078t0003g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0009c0015t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0009c0015t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0010c0051t0002g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0010c0052t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0011c0036t0003g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0011c0055t0003g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0012c0018t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0013c0021t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0014c0022t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0015c0024t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0016c0026t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0017c0027t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0018c0028t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0019c0032t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0020c0050t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0021c0034t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0022c0033t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0023c0072t0006g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0024c0047t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0025c0071t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0026c0070t0003g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0027c0035t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0028c0063t0009g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0029c0044t0002g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0030c0031t0003g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0031c0030t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0032c0042t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0033c0062t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0034c0056t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0035c0060t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0036c0059t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0037c0040t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0038c0043t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0039c0067t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0040c0046t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0041c0073t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0042c0049t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0043c0029t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0044c0079t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0045c0084t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0046c0083t0005g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0047c0082t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0048c0025t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0049c0023t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
a0050c0086t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00280 | hp1 | a0006 | c0007 | t0002 | g0050 | EUR | FIN | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0010 | EUR | FIN | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG00323 | hp1 | a0003 | c0011 | t0001 | g0130 | EUR | FIN | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG00438 | hp1 | a0006 | c0007 | t0002 | g0047 | EAS | CHS | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | CHS | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG00609 | hp1 | a0002 | c0003 | t0002 | g0261 | EAS | CHS | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG00639 | hp1 | a0002 | c0003 | t0002 | g0248 | AMR | PUR | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG00642 | hp1 | a0002 | c0008 | t0002 | g0100 | AMR | PUR | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG00673 | hp1 | a0006 | c0007 | t0002 | g0191 | EAS | CHS | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG00673 | hp2 | a0003 | c0011 | t0001 | g0157 | EAS | CHS | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG00733 | hp1 | a0002 | c0008 | t0002 | g0107 | AMR | PUR | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG00738 | hp1 | a0006 | c0007 | t0002 | g0040 | AMR | PUR | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG00738 | hp2 | a0003 | c0005 | t0001 | g0087 | AMR | PUR | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG00741 | hp1 | a0015 | c0024 | t0001 | g0268 | AMR | PUR | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG00741 | hp2 | a0002 | c0004 | t0002 | g0171 | AMR | PUR | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG01069 | hp1 | a0002 | c0004 | t0002 | g0029 | AMR | PUR | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG01071 | hp1 | a0001 | c0002 | t0001 | g0080 | AMR | PUR | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG01074 | hp1 | a0037 | c0040 | t0001 | g0037 | AMR | PUR | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG01074 | hp2 | a0001 | c0002 | t0001 | g0250 | AMR | PUR | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG01099 | hp1 | a0013 | c0021 | t0002 | g0090 | AMR | PUR | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG01109 | hp1 | a0002 | c0085 | t0002 | g0170 | AMR | PUR | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG01109 | hp2 | a0002 | c0004 | t0002 | g0190 | AMR | PUR | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG01167 | hp1 | a0002 | c0004 | t0002 | g0046 | AMR | PUR | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG01168 | hp1 | a0001 | c0037 | t0001 | g0143 | AMR | PUR | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG01168 | hp2 | a0003 | c0005 | t0001 | g0256 | AMR | PUR | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG01243 | hp1 | a0001 | c0077 | t0001 | g0241 | AMR | PUR | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG01255 | hp1 | a0002 | c0003 | t0002 | g0251 | AMR | CLM | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG01255 | hp2 | a0002 | c0003 | t0002 | g0121 | AMR | CLM | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG01256 | hp2 | a0010 | c0052 | t0002 | g0093 | AMR | CLM | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG01257 | hp1 | a0001 | c0002 | t0001 | g0060 | AMR | CLM | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG01257 | hp2 | a0006 | c0007 | t0002 | g0169 | AMR | CLM | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG01346 | hp1 | a0003 | c0038 | t0001 | g0172 | AMR | CLM | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG01346 | hp2 | a0003 | c0005 | t0001 | g0075 | AMR | CLM | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG01433 | hp2 | a0043 | c0029 | t0002 | g0136 | AMR | CLM | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG01496 | hp1 | a0001 | c0001 | t0007 | g0123 | AMR | CLM | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG01496 | hp2 | a0003 | c0005 | t0001 | g0083 | AMR | CLM | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG01517 | hp1 | a0002 | c0003 | t0002 | g0258 | EUR | IBS | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG01884 | hp1 | a0001 | c0002 | t0001 | g0188 | AFR | ACB | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG01884 | hp2 | a0025 | c0071 | t0001 | g0023 | AFR | ACB | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG01891 | hp1 | a0006 | c0053 | t0002 | g0133 | AFR | ACB | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG01891 | hp2 | a0008 | c0014 | t0003 | g0220 | AFR | ACB | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG01934 | hp1 | a0002 | c0003 | t0002 | g0014 | AMR | PEL | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PEL | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | PEL | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG01952 | hp2 | a0002 | c0003 | t0002 | g0262 | AMR | PEL | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG01975 | hp1 | a0040 | c0046 | t0001 | g0041 | AMR | PEL | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG01975 | hp2 | a0048 | c0025 | t0001 | g0012 | AMR | PEL | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG01978 | hp1 | a0002 | c0003 | t0002 | g0077 | AMR | PEL | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PEL | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG01981 | hp1 | a0003 | c0005 | t0001 | g0091 | AMR | PEL | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG01981 | hp2 | a0004 | c0009 | t0002 | g0229 | AMR | PEL | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PEL | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG01993 | hp2 | a0003 | c0005 | t0001 | g0086 | AMR | PEL | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG02004 | hp2 | a0003 | c0005 | t0001 | g0078 | AMR | PEL | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG02015 | hp1 | a0002 | c0003 | t0002 | g0065 | EAS | KHV | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG02015 | hp2 | a0012 | c0018 | t0001 | g0008 | EAS | KHV | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG02027 | hp1 | a0004 | c0016 | t0002 | g0181 | EAS | KHV | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG02027 | hp2 | a0001 | c0002 | t0010 | g0127 | EAS | KHV | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG02055 | hp1 | a0002 | c0008 | t0002 | g0212 | AFR | ACB | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG02055 | hp2 | a0049 | c0023 | t0001 | g0226 | AFR | ACB | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG02056 | hp1 | a0001 | c0002 | t0001 | g0084 | EAS | KHV | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG02056 | hp2 | a0002 | c0068 | t0002 | g0068 | EAS | KHV | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG02071 | hp1 | a0012 | c0018 | t0001 | g0008 | EAS | KHV | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG02071 | hp2 | a0001 | c0002 | t0001 | g0249 | EAS | KHV | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG02083 | hp1 | a0002 | c0045 | t0002 | g0049 | EAS | KHV | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG02083 | hp2 | a0004 | c0009 | t0002 | g0228 | EAS | KHV | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG02129 | hp1 | a0003 | c0005 | t0001 | g0187 | EAS | KHV | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG02129 | hp2 | a0001 | c0002 | t0001 | g0274 | EAS | KHV | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG02145 | hp1 | a0035 | c0060 | t0001 | g0193 | AFR | ACB | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG02145 | hp2 | a0002 | c0074 | t0002 | g0211 | AFR | ACB | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG02148 | hp1 | a0002 | c0003 | t0002 | g0081 | AMR | PEL | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG02148 | hp2 | a0003 | c0011 | t0001 | g0057 | AMR | PEL | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG02257 | hp1 | a0001 | c0076 | t0001 | g0103 | AFR | ACB | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG02257 | hp2 | a0033 | c0062 | t0001 | g0252 | AFR | ACB | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG02258 | hp1 | a0009 | c0015 | t0002 | g0223 | AFR | ACB | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG02258 | hp2 | a0002 | c0008 | t0002 | g0217 | AFR | ACB | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG02280 | hp1 | a0005 | c0006 | t0002 | g0119 | AFR | ACB | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG02280 | hp2 | a0001 | c0002 | t0001 | g0254 | AFR | ACB | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG02293 | hp1 | a0006 | c0007 | t0002 | g0178 | AMR | PEL | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0260 | AMR | PEL | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG02300 | hp1 | a0006 | c0007 | t0002 | g0176 | AMR | PEL | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG02300 | hp2 | a0003 | c0005 | t0001 | g0079 | AMR | PEL | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG02451 | hp1 | a0005 | c0006 | t0002 | g0259 | AFR | ACB | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG02451 | hp2 | a0001 | c0069 | t0001 | g0021 | AFR | ACB | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG02523 | hp1 | a0001 | c0002 | t0001 | g0066 | EAS | KHV | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG02572 | hp1 | a0007 | c0013 | t0005 | g0074 | AFR | GWD | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG02572 | hp2 | a0002 | c0003 | t0002 | g0101 | AFR | GWD | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG02602 | hp2 | a0002 | c0003 | t0002 | g0085 | SAS | PJL | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG02622 | hp1 | a0022 | c0033 | t0002 | g0025 | AFR | GWD | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG02622 | hp2 | a0001 | c0010 | t0001 | g0204 | AFR | GWD | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG02630 | hp1 | a0009 | c0015 | t0002 | g0221 | AFR | GWD | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG02630 | hp2 | a0039 | c0067 | t0001 | g0122 | AFR | GWD | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG02647 | hp1 | a0005 | c0081 | t0002 | g0115 | AFR | GWD | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG02647 | hp2 | a0006 | c0058 | t0002 | g0285 | AFR | GWD | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG02683 | hp1 | a0002 | c0004 | t0002 | g0145 | SAS | PJL | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG02683 | hp2 | a0020 | c0050 | t0002 | g0098 | SAS | PJL | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG02698 | hp1 | a0029 | c0044 | t0002 | g0035 | SAS | PJL | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG02698 | hp2 | a0036 | c0059 | t0001 | g0245 | SAS | PJL | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG02717 | hp1 | a0030 | c0031 | t0003 | g0216 | AFR | GWD | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG02717 | hp2 | a0002 | c0003 | t0002 | g0210 | AFR | GWD | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG02723 | hp1 | a0046 | c0083 | t0005 | g0111 | AFR | GWD | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG02723 | hp2 | a0002 | c0008 | t0002 | g0214 | AFR | GWD | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG02735 | hp1 | a0002 | c0008 | t0002 | g0105 | SAS | PJL | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG02735 | hp2 | a0002 | c0003 | t0002 | g0064 | SAS | PJL | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG02738 | hp1 | a0002 | c0003 | t0002 | g0273 | SAS | PJL | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG02738 | hp2 | a0001 | c0002 | t0001 | g0113 | SAS | PJL | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG02809 | hp1 | a0001 | c0002 | t0001 | g0120 | AFR | GWD | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG02809 | hp2 | a0014 | c0022 | t0002 | g0222 | AFR | GWD | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG02818 | hp1 | a0021 | c0034 | t0001 | g0026 | AFR | GWD | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG02818 | hp2 | a0001 | c0002 | t0001 | g0284 | AFR | GWD | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG02886 | hp1 | a0011 | c0055 | t0003 | g0281 | AFR | GWD | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG02886 | hp2 | a0008 | c0014 | t0003 | g0109 | AFR | GWD | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG02895 | hp1 | a0019 | c0032 | t0001 | g0020 | AFR | GWD | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG02895 | hp2 | a0007 | c0020 | t0002 | g0278 | AFR | GWD | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG02896 | hp1 | a0001 | c0002 | t0001 | g0207 | AFR | GWD | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG02896 | hp2 | a0002 | c0003 | t0002 | g0208 | AFR | GWD | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG02897 | hp1 | a0002 | c0003 | t0002 | g0209 | AFR | GWD | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG02897 | hp2 | a0007 | c0020 | t0002 | g0279 | AFR | GWD | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG02922 | hp1 | a0005 | c0006 | t0002 | g0006 | AFR | ESN | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG02922 | hp2 | a0050 | c0086 | t0001 | g0168 | AFR | ESN | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG02965 | hp1 | a0027 | c0035 | t0001 | g0167 | AFR | ESN | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG02965 | hp2 | a0017 | c0027 | t0001 | g0018 | AFR | ESN | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG02970 | hp1 | a0031 | c0030 | t0002 | g0218 | AFR | ESN | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG02970 | hp2 | a0002 | c0054 | t0001 | g0198 | AFR | ESN | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG02976 | hp1 | a0001 | c0002 | t0001 | g0013 | AFR | ESN | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG02976 | hp2 | a0047 | c0082 | t0002 | g0117 | AFR | ESN | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG03017 | hp1 | a0002 | c0048 | t0004 | g0139 | SAS | PJL | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG03017 | hp2 | a0002 | c0004 | t0002 | g0137 | SAS | PJL | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG03041 | hp1 | a0005 | c0006 | t0002 | g0006 | AFR | GWD | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG03041 | hp2 | a0002 | c0003 | t0002 | g0206 | AFR | GWD | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG03098 | hp1 | a0024 | c0047 | t0001 | g0017 | AFR | MSL | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG03098 | hp2 | a0001 | c0002 | t0001 | g0231 | AFR | MSL | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG03130 | hp1 | a0002 | c0008 | t0002 | g0215 | AFR | ESN | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG03130 | hp2 | a0001 | c0010 | t0001 | g0205 | AFR | ESN | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG03139 | hp1 | a0001 | c0002 | t0001 | g0129 | AFR | ESN | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG03139 | hp2 | a0005 | c0006 | t0002 | g0003 | AFR | ESN | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG03195 | hp1 | a0002 | c0017 | t0001 | g0126 | AFR | ESN | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG03195 | hp2 | a0001 | c0010 | t0001 | g0202 | AFR | ESN | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG03225 | hp1 | a0026 | c0070 | t0003 | g0265 | AFR | MSL | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG03225 | hp2 | a0005 | c0006 | t0001 | g0114 | AFR | MSL | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG03239 | hp1 | a0001 | c0002 | t0001 | g0269 | SAS | PJL | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG03239 | hp2 | a0002 | c0004 | t0004 | g0024 | SAS | PJL | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG03453 | hp1 | a0001 | c0002 | t0001 | g0232 | AFR | MSL | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG03453 | hp2 | a0011 | c0036 | t0003 | g0138 | AFR | MSL | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG03486 | hp1 | a0005 | c0006 | t0002 | g0118 | AFR | MSL | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG03486 | hp2 | a0018 | c0028 | t0001 | g0240 | AFR | MSL | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG03492 | hp1 | a0002 | c0004 | t0002 | g0048 | SAS | PJL | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG03492 | hp2 | a0003 | c0005 | t0001 | g0076 | SAS | PJL | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG03516 | hp1 | a0008 | c0061 | t0003 | g0238 | AFR | ESN | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG03516 | hp2 | a0005 | c0006 | t0002 | g0003 | AFR | ESN | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG03540 | hp1 | a0001 | c0010 | t0001 | g0203 | AFR | GWD | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG03540 | hp2 | a0032 | c0042 | t0001 | g0019 | AFR | GWD | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG03579 | hp1 | a0001 | c0002 | t0001 | g0239 | AFR | MSL | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG03579 | hp2 | a0007 | c0013 | t0005 | g0200 | AFR | MSL | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG03654 | hp1 | a0001 | c0002 | t0001 | g0247 | SAS | PJL | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG03654 | hp2 | a0016 | c0026 | t0002 | g0034 | SAS | PJL | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG03688 | hp1 | a0001 | c0002 | t0001 | g0257 | SAS | STU | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG03688 | hp2 | a0002 | c0004 | t0002 | g0142 | SAS | STU | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG03704 | hp1 | a0041 | c0073 | t0001 | g0071 | SAS | PJL | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG03704 | hp2 | a0002 | c0003 | t0002 | g0097 | SAS | PJL | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG03710 | hp1 | a0010 | c0051 | t0002 | g0271 | SAS | PJL | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG03710 | hp2 | a0002 | c0004 | t0004 | g0160 | SAS | PJL | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG03831 | hp1 | a0001 | c0057 | t0002 | g0069 | SAS | BEB | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG03831 | hp2 | a0002 | c0003 | t0005 | g0099 | SAS | BEB | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | BEB | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG03834 | hp2 | a0001 | c0002 | t0001 | g0246 | SAS | BEB | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG03927 | hp1 | a0002 | c0003 | t0002 | g0275 | SAS | BEB | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG03927 | hp2 | a0003 | c0005 | t0001 | g0070 | SAS | BEB | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG03942 | hp1 | a0003 | c0075 | t0001 | g0094 | SAS | BEB | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG03942 | hp2 | a0002 | c0004 | t0002 | g0149 | SAS | BEB | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG04115 | hp1 | a0002 | c0004 | t0002 | g0102 | SAS | STU | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0044 | SAS | STU | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG04199 | hp1 | a0002 | c0004 | t0002 | g0162 | SAS | STU | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG04199 | hp2 | a0003 | c0005 | t0001 | g0244 | SAS | STU | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG04204 | hp1 | a0002 | c0004 | t0004 | g0159 | SAS | STU | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG04204 | hp2 | a0001 | c0002 | t0001 | g0192 | SAS | STU | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG04228 | hp1 | a0001 | c0002 | t0001 | g0104 | SAS | STU | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG04228 | hp2 | a0002 | c0004 | t0002 | g0161 | SAS | STU | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
NA18522 | hp1 | a0007 | c0013 | t0006 | g0195 | AFR | YRI | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
NA18522 | hp2 | a0005 | c0006 | t0002 | g0110 | AFR | YRI | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
NA18612 | hp1 | a0001 | c0001 | t0008 | g0164 | EAS | CHB | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
NA18612 | hp2 | a0003 | c0005 | t0001 | g0088 | EAS | CHB | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
NA18747 | hp1 | a0004 | c0016 | t0002 | g0165 | EAS | CHB | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | CHB | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
NA18906 | hp1 | a0008 | c0041 | t0001 | g0183 | AFR | YRI | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
NA18906 | hp2 | a0002 | c0003 | t0002 | g0194 | AFR | YRI | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
NA18943 | hp1 | a0003 | c0005 | t0001 | g0092 | EAS | JPT | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
NA18944 | hp1 | a0002 | c0003 | t0002 | g0267 | EAS | JPT | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
NA18944 | hp2 | a0034 | c0056 | t0001 | g0067 | EAS | JPT | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
NA18945 | hp2 | a0004 | c0009 | t0002 | g0061 | EAS | JPT | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
NA18950 | hp1 | a0004 | c0009 | t0002 | g0063 | EAS | JPT | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
NA18952 | hp1 | a0003 | c0005 | t0001 | g0237 | EAS | JPT | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
NA18956 | hp1 | a0002 | c0004 | t0002 | g0270 | EAS | JPT | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
NA18957 | hp2 | a0002 | c0065 | t0002 | g0073 | EAS | JPT | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
NA18959 | hp2 | a0002 | c0004 | t0002 | g0185 | EAS | JPT | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
NA18960 | hp2 | a0002 | c0064 | t0002 | g0082 | EAS | JPT | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
NA18962 | hp2 | a0004 | c0012 | t0002 | g0234 | EAS | JPT | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
NA18964 | hp1 | a0002 | c0003 | t0002 | g0134 | EAS | JPT | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
NA18966 | hp1 | a0004 | c0080 | t0002 | g0036 | EAS | JPT | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
NA18967 | hp1 | a0001 | c0002 | t0001 | g0096 | EAS | JPT | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
NA18967 | hp2 | a0002 | c0004 | t0002 | g0055 | EAS | JPT | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
NA18969 | hp2 | a0038 | c0043 | t0001 | g0182 | EAS | JPT | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
NA18970 | hp2 | a0001 | c0002 | t0001 | g0263 | EAS | JPT | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
NA18971 | hp1 | a0002 | c0004 | t0001 | g0009 | EAS | JPT | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
NA18971 | hp2 | a0001 | c0002 | t0001 | g0072 | EAS | JPT | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
NA18973 | hp2 | a0002 | c0003 | t0002 | g0028 | EAS | JPT | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
NA18980 | hp1 | a0004 | c0012 | t0002 | g0236 | EAS | JPT | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
NA18982 | hp2 | a0004 | c0009 | t0002 | g0062 | EAS | JPT | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
NA18983 | hp2 | a0001 | c0066 | t0001 | g0089 | EAS | JPT | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
NA18986 | hp1 | a0002 | c0004 | t0002 | g0009 | EAS | JPT | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
NA18986 | hp2 | a0002 | c0003 | t0002 | g0266 | EAS | JPT | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
NA18992 | hp2 | a0004 | c0012 | t0002 | g0233 | EAS | JPT | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
NA18995 | hp1 | a0002 | c0003 | t0002 | g0005 | EAS | JPT | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
NA19003 | hp2 | a0001 | c0002 | t0001 | g0095 | EAS | JPT | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
NA19007 | hp1 | a0001 | c0039 | t0001 | g0141 | EAS | JPT | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
NA19007 | hp2 | a0002 | c0004 | t0002 | g0052 | EAS | JPT | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
NA19011 | hp1 | a0006 | c0007 | t0002 | g0059 | EAS | JPT | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
NA19011 | hp2 | a0002 | c0003 | t0002 | g0264 | EAS | JPT | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
NA19030 | hp1 | a0001 | c0019 | t0001 | g0225 | AFR | LWK | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
NA19030 | hp2 | a0005 | c0006 | t0002 | g0116 | AFR | LWK | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
NA19043 | hp1 | a0001 | c0002 | t0001 | g0219 | AFR | LWK | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
NA19043 | hp2 | a0001 | c0019 | t0001 | g0224 | AFR | LWK | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
NA19054 | hp2 | a0001 | c0002 | t0001 | g0135 | EAS | JPT | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
NA19057 | hp2 | a0042 | c0049 | t0002 | g0230 | EAS | JPT | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
NA19060 | hp1 | a0004 | c0012 | t0002 | g0235 | EAS | JPT | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
NA19060 | hp2 | a0002 | c0004 | t0002 | g0189 | EAS | JPT | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
NA19063 | hp2 | a0001 | c0002 | t0001 | g0272 | EAS | JPT | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
NA19065 | hp1 | a0002 | c0003 | t0002 | g0243 | EAS | JPT | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
NA19074 | hp1 | a0002 | c0003 | t0002 | g0255 | EAS | JPT | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
NA19082 | hp1 | a0001 | c0002 | t0001 | g0242 | EAS | JPT | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
NA19082 | hp2 | a0028 | c0063 | t0009 | g0128 | EAS | JPT | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
NA19086 | hp1 | a0002 | c0003 | t0002 | g0005 | EAS | JPT | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
NA19240 | hp1 | a0001 | c0002 | t0002 | g0201 | AFR | YRI | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
NA19240 | hp2 | a0008 | c0014 | t0003 | g0108 | AFR | YRI | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
NA20129 | hp1 | a0001 | c0002 | t0001 | g0106 | AFR | ASW | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
NA20129 | hp2 | a0023 | c0072 | t0006 | g0196 | AFR | ASW | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | TSI | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0030 | EUR | TSI | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
NA20805 | hp1 | a0003 | c0011 | t0001 | g0124 | EUR | TSI | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0144 | EUR | TSI | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | CLM | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG01123 | hp2 | a0004 | c0009 | t0002 | g0227 | AMR | CLM | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG02109 | hp1 | a0001 | c0002 | t0001 | g0013 | AFR | ACB | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG02109 | hp2 | a0001 | c0002 | t0002 | g0282 | AFR | ACB | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG02486 | hp1 | a0002 | c0008 | t0002 | g0213 | AFR | ACB | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG02486 | hp2 | a0007 | c0013 | t0001 | g0197 | AFR | ACB | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG02559 | hp1 | a0005 | c0006 | t0002 | g0003 | AFR | ACB | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG02559 | hp2 | a0002 | c0004 | t0001 | g0016 | AFR | ACB | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG03471 | hp1 | a0002 | c0017 | t0001 | g0184 | AFR | MSL | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG03471 | hp2 | a0001 | c0002 | t0001 | g0012 | AFR | MSL | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG06807 | hp1 | a0001 | c0010 | t0001 | g0011 | AFR | USA | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
HG06807 | hp2 | a0008 | c0078 | t0003 | g0253 | AFR | USA | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
NA18955 | hp1 | a0044 | c0079 | t0002 | g0276 | EAS | JPT | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
NA20300 | hp1 | a0005 | c0006 | t0002 | g0112 | AFR | USA | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | USA | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
NA21309 | hp1 | a0001 | c0002 | t0001 | g0283 | AFR | LWK | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
NA21309 | hp2 | a0045 | c0084 | t0001 | g0022 | AFR | LWK | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
homoSapiens_chm13v2 | hp1 | a0006 | c0007 | t0002 | g0140 | REF | REF | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
homoSapiens_grch38 | hp1 | a0001 | c0010 | t0001 | g0011 | REF | REF | SPEG_chr2_219429843_219498629 | SPEG | chr2 | 219429843 | 219498629 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:219434991
|
G | A | 1 | a0013 | 1 | HG01099.hp1 | missense_variant | MODERATE | c.14G>A | p.Arg5Gln | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 1/41 | 149/10782 | 14/9804 | 5/3267 | chr2 | 219434991 | ||
chr2:219435093
|
T | C | 2 | a0009a0014 | 3 | HG02258.hp1 HG02630.hp1 HG02809.hp2 |
missense_variant | MODERATE | c.116T>C | p.Val39Ala | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 1/41 | 251/10782 | 116/9804 | 39/3267 | chr2 | 219435093 | ||
chr2:219435164
|
C | T | 1 | a0050 | 1 | HG02922.hp2 | missense_variant | MODERATE | c.187C>T | p.Arg63Trp | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 1/41 | 322/10782 | 187/9804 | 63/3267 | chr2 | 219435164 | ||
chr2:219444677
|
T | A | 1 | a0049 | 1 | HG02055.hp2 | missense_variant | MODERATE | c.413T>A | p.Ile138Asn | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 2/41 | 548/10782 | 413/9804 | 138/3267 | chr2 | 219444677 | ||
chr2:219444963
|
G | A | 1 | a0015 | 1 | HG00741.hp1 | missense_variant | MODERATE | c.617G>A | p.Arg206His | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 3/41 | 752/10782 | 617/9804 | 206/3267 | chr2 | 219444963 | ||
chr2:219445067
|
G | A | 1 | a0048 | 1 | HG01975.hp2 | missense_variant | MODERATE | c.721G>A | p.Ala241Thr | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 3/41 | 856/10782 | 721/9804 | 241/3267 | chr2 | 219445067 | ||
chr2:219448306
|
G | C | 1 | a0016 | 1 | HG03654.hp2 | missense_variant | MODERATE | c.1148G>C | p.Arg383Pro | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 4/41 | 1283/10782 | 1148/9804 | 383/3267 | chr2 | 219448306 | ||
chr2:219448459
|
G | A | 1 | a0017 | 1 | HG02965.hp2 | missense_variant | MODERATE | c.1301G>A | p.Arg434His | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 4/41 | 1436/10782 | 1301/9804 | 434/3267 | chr2 | 219448459 | ||
chr2:219448648
|
A | T | 4 | a0005a0045a0046others(1): Show | 16 | HG02280.hp1 HG02451.hp1 HG02559.hp1 others(13): Show |
missense_variant | MODERATE | c.1490A>T | p.Glu497Val | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 4/41 | 1625/10782 | 1490/9804 | 497/3267 | chr2 | 219448648 | ||
chr2:219448795
|
G | A | 1 | a0018 | 1 | HG03486.hp2 | missense_variant | MODERATE | c.1637G>A | p.Arg546Gln | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 4/41 | 1772/10782 | 1637/9804 | 546/3267 | chr2 | 219448795 | ||
chr2:219448872
|
A | T | 1 | a0044 | 1 | NA18955.hp1 | missense_variant | MODERATE | c.1714A>T | p.Arg572Trp | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 4/41 | 1849/10782 | 1714/9804 | 572/3267 | chr2 | 219448872 | ||
chr2:219448911
|
G | A | 1 | a0043 | 1 | HG01433.hp2 | missense_variant | MODERATE | c.1753G>A | p.Gly585Ser | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 4/41 | 1888/10782 | 1753/9804 | 585/3267 | chr2 | 219448911 | ||
chr2:219462013
|
C | T | 1 | a0019 | 1 | HG02895.hp1 | missense_variant | MODERATE | c.2572C>T | p.Arg858Cys | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 7/41 | 2707/10782 | 2572/9804 | 858/3267 | chr2 | 219462013 | ||
chr2:219462353
|
G | A | 1 | a0020 | 1 | HG02683.hp2 | missense_variant | MODERATE | c.2672G>A | p.Arg891His | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 8/41 | 2807/10782 | 2672/9804 | 891/3267 | chr2 | 219462353 | ||
chr2:219468599
|
G | A | 1 | a0010 | 2 | HG01256.hp2 HG03710.hp1 |
missense_variant | MODERATE | c.3164G>A | p.Arg1055Gln | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 11/41 | 3299/10782 | 3164/9804 | 1055/3267 | chr2 | 219468599 | ||
chr2:219472319
|
G | A | 2 | a0004a0042 | 14 | HG01123.hp2 HG01981.hp2 HG02027.hp1 others(11): Show |
missense_variant | MODERATE | c.3928G>A | p.Asp1310Asn | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 15/41 | 4063/10782 | 3928/9804 | 1310/3267 | chr2 | 219472319 | ||
chr2:219472947
|
C | T | 1 | a0021 | 1 | HG02818.hp1 | missense_variant | MODERATE | c.3998C>T | p.Thr1333Met | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 16/41 | 4133/10782 | 3998/9804 | 1333/3267 | chr2 | 219472947 | ||
chr2:219472968
|
G | A | 2 | a0021a0022 | 2 | HG02622.hp1 HG02818.hp1 |
missense_variant | MODERATE | c.4019G>A | p.Arg1340Gln | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 16/41 | 4154/10782 | 4019/9804 | 1340/3267 | chr2 | 219472968 | ||
chr2:219477404
|
C | T | 1 | a0041 | 1 | HG03704.hp1 | missense_variant | MODERATE | c.4688C>T | p.Ala1563Val | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 20/41 | 4823/10782 | 4688/9804 | 1563/3267 | chr2 | 219477404 | ||
chr2:219477927
|
C | T | 1 | a0023 | 1 | NA20129.hp2 | missense_variant | MODERATE | c.4849C>T | p.Arg1617Cys | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 22/41 | 4984/10782 | 4849/9804 | 1617/3267 | chr2 | 219477927 | ||
chr2:219478006
|
G | T | 1 | a0024 | 1 | HG03098.hp1 | missense_variant | MODERATE | c.4928G>T | p.Arg1643Leu | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 22/41 | 5063/10782 | 4928/9804 | 1643/3267 | chr2 | 219478006 | ||
chr2:219478077
|
C | G | 1 | a0026 | 1 | HG03225.hp1 | missense_variant | MODERATE | c.4999C>G | p.Arg1667Gly | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 22/41 | 5134/10782 | 4999/9804 | 1667/3267 | chr2 | 219478077 | ||
chr2:219478077
|
C | T | 1 | a0025 | 1 | HG01884.hp2 | missense_variant | MODERATE | c.4999C>T | p.Arg1667Cys | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 22/41 | 5134/10782 | 4999/9804 | 1667/3267 | chr2 | 219478077 | ||
chr2:219478080
|
C | T | 1 | a0040 | 1 | HG01975.hp1 | missense_variant | MODERATE | c.5002C>T | p.Arg1668Trp | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 22/41 | 5137/10782 | 5002/9804 | 1668/3267 | chr2 | 219478080 | ||
chr2:219483185
|
A | G | 1 | a0039 | 1 | HG02630.hp2 | missense_variant | MODERATE | c.5722A>G | p.Met1908Val | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 30/41 | 5857/10782 | 5722/9804 | 1908/3267 | chr2 | 219483185 | ||
chr2:219484029
|
C | T | 13 | a0002a0005a0009others(10): Show | 98 | HG00609.hp1 HG00639.hp1 HG00642.hp1 others(95): Show |
missense_variant | MODERATE | c.6566C>T | p.Pro2189Leu | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 30/41 | 6701/10782 | 6566/9804 | 2189/3267 | chr2 | 219484029 | ||
chr2:219484155
|
C | A | 1 | a0031 | 1 | HG02970.hp1 | missense_variant | MODERATE | c.6692C>A | p.Pro2231His | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 30/41 | 6827/10782 | 6692/9804 | 2231/3267 | chr2 | 219484155 | ||
chr2:219484157
|
C | A | 1 | a0030 | 1 | HG02717.hp1 | missense_variant | MODERATE | c.6694C>A | p.Pro2232Thr | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 30/41 | 6829/10782 | 6694/9804 | 2232/3267 | chr2 | 219484157 | ||
chr2:219484158
|
C | A | 1 | a0011 | 2 | HG02886.hp1 HG03453.hp2 |
missense_variant | MODERATE | c.6695C>A | p.Pro2232His | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 30/41 | 6830/10782 | 6695/9804 | 2232/3267 | chr2 | 219484158 | ||
chr2:219484158
|
C | G | 1 | a0029 | 1 | HG02698.hp1 | missense_variant | MODERATE | c.6695C>G | p.Pro2232Arg | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 30/41 | 6830/10782 | 6695/9804 | 2232/3267 | chr2 | 219484158 | ||
chr2:219484232
|
C | T | 1 | a0038 | 1 | NA18969.hp2 | missense_variant | MODERATE | c.6769C>T | p.His2257Tyr | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 30/41 | 6904/10782 | 6769/9804 | 2257/3267 | chr2 | 219484232 | ||
chr2:219484245
|
C | T | 5 | a0017a0024a0032others(2): Show | 5 | HG02257.hp2 HG02965.hp2 HG03098.hp1 others(2): Show |
missense_variant | MODERATE | c.6782C>T | p.Pro2261Leu | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 30/41 | 6917/10782 | 6782/9804 | 2261/3267 | chr2 | 219484245 | ||
chr2:219484367
|
G | C | 1 | a0034 | 1 | NA18944.hp2 | missense_variant | MODERATE | c.6904G>C | p.Val2302Leu | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 30/41 | 7039/10782 | 6904/9804 | 2302/3267 | chr2 | 219484367 | ||
chr2:219488262
|
C | T | 3 | a0021a0022a0035 | 3 | HG02145.hp1 HG02622.hp1 HG02818.hp1 |
missense_variant | MODERATE | c.7810C>T | p.Leu2604Phe | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 32/41 | 7945/10782 | 7810/9804 | 2604/3267 | chr2 | 219488262 | ||
chr2:219488593
|
G | A | 1 | a0028 | 1 | NA19082.hp2 | missense_variant | MODERATE | c.7954G>A | p.Ala2652Thr | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 33/41 | 8089/10782 | 7954/9804 | 2652/3267 | chr2 | 219488593 | ||
chr2:219488810
|
C | A | 2 | a0003a0015 | 22 | HG00323.hp1 HG00673.hp2 HG00738.hp2 others(19): Show |
missense_variant | MODERATE | c.8059C>A | p.Pro2687Thr | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 34/41 | 8194/10782 | 8059/9804 | 2687/3267 | chr2 | 219488810 | ||
chr2:219489218
|
C | G | 1 | a0036 | 1 | HG02698.hp2 | missense_variant | MODERATE | c.8314C>G | p.Gln2772Glu | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 35/41 | 8449/10782 | 8314/9804 | 2772/3267 | chr2 | 219489218 | ||
chr2:219489386
|
A | G | 28 | a0002a0004a0005others(25): Show | 140 | HG00280.hp1 HG00438.hp1 HG00609.hp1 others(137): Show |
missense_variant | MODERATE | c.8368A>G | p.Arg2790Gly | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 36/41 | 8503/10782 | 8368/9804 | 2790/3267 | chr2 | 219489386 | ||
chr2:219489644
|
G | A | 1 | a0042 | 1 | NA19057.hp2 | missense_variant | MODERATE | c.8626G>A | p.Val2876Ile | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 36/41 | 8761/10782 | 8626/9804 | 2876/3267 | chr2 | 219489644 | ||
chr2:219489669
|
C | T | 3 | a0007a0023a0046 | 8 | HG02486.hp2 HG02572.hp1 HG02723.hp1 others(5): Show |
missense_variant | MODERATE | c.8651C>T | p.Pro2884Leu | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 36/41 | 8786/10782 | 8651/9804 | 2884/3267 | chr2 | 219489669 | ||
chr2:219489713
|
C | T | 3 | a0024a0033a0045 | 3 | HG02257.hp2 HG03098.hp1 NA21309.hp2 |
missense_variant | MODERATE | c.8695C>T | p.Pro2899Ser | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 36/41 | 8830/10782 | 8695/9804 | 2899/3267 | chr2 | 219489713 | ||
chr2:219489728
|
A | G | 1 | a0012 | 2 | HG02015.hp2 HG02071.hp1 |
missense_variant | MODERATE | c.8710A>G | p.Thr2904Ala | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 36/41 | 8845/10782 | 8710/9804 | 2904/3267 | chr2 | 219489728 | ||
chr2:219490807
|
A | G | 24 | a0002a0005a0006others(21): Show | 130 | HG00280.hp1 HG00438.hp1 HG00609.hp1 others(127): Show |
missense_variant | MODERATE | c.9236A>G | p.His3079Arg | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 38/41 | 9371/10782 | 9236/9804 | 3079/3267 | chr2 | 219490807 | ||
chr2:219492155
|
C | T | 1 | a0014 | 1 | HG02809.hp2 | missense_variant | MODERATE | c.9506C>T | p.Thr3169Met | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 40/41 | 9641/10782 | 9506/9804 | 3169/3267 | chr2 | 219492155 | ||
chr2:219492179
|
G | A | 1 | a0027 | 1 | HG02965.hp1 | missense_variant | MODERATE | c.9530G>A | p.Arg3177His | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 40/41 | 9665/10782 | 9530/9804 | 3177/3267 | chr2 | 219492179 | ||
chr2:219492746
|
G | A | 1 | a0037 | 1 | HG01074.hp1 | missense_variant | MODERATE | c.9764G>A | p.Arg3255His | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 41/41 | 9899/10782 | 9764/9804 | 3255/3267 | chr2 | 219492746 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:219448142
|
C | T | 2 | a0009c0015a0014c0022 | 3 | HG02258.hp1 HG02630.hp1 HG02809.hp2 |
synonymous_variant | LOW | c.984C>T | p.Pro328Pro | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 4/41 | 1119/10782 | 984/9804 | 328/3267 | chr2 | 219448142 | ||
chr2:219448496
|
G | T | 1 | a0002c0085 | 1 | HG01109.hp1 | synonymous_variant | LOW | c.1338G>T | p.Pro446Pro | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 4/41 | 1473/10782 | 1338/9804 | 446/3267 | chr2 | 219448496 | ||
chr2:219448778
|
C | G | 1 | a0004c0080 | 1 | NA18966.hp1 | synonymous_variant | LOW | c.1620C>G | p.Ser540Ser | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 4/41 | 1755/10782 | 1620/9804 | 540/3267 | chr2 | 219448778 | ||
chr2:219448958
|
G | C | 5 | a0002c0008a0008c0014a0019c0032others(2): Show | 14 | HG00642.hp1 HG00733.hp1 HG01891.hp2 others(11): Show |
synonymous_variant | LOW | c.1800G>C | p.Arg600Arg | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 4/41 | 1935/10782 | 1800/9804 | 600/3267 | chr2 | 219448958 | ||
chr2:219449045
|
G | A | 2 | a0021c0034a0022c0033 | 2 | HG02622.hp1 HG02818.hp1 |
synonymous_variant | LOW | c.1887G>A | p.Arg629Arg | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 4/41 | 2022/10782 | 1887/9804 | 629/3267 | chr2 | 219449045 | ||
chr2:219451248
|
G | A | 26 | a0001c0001a0001c0037a0001c0039others(23): Show | 123 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(120): Show |
synonymous_variant | LOW | c.2226G>A | p.Lys742Lys | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 5/41 | 2361/10782 | 2226/9804 | 742/3267 | chr2 | 219451248 | ||
chr2:219451272
|
G | A | 2 | a0004c0009a0042c0049 | 7 | HG01123.hp2 HG01981.hp2 HG02083.hp2 others(4): Show |
synonymous_variant | LOW | c.2250G>A | p.Pro750Pro | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 5/41 | 2385/10782 | 2250/9804 | 750/3267 | chr2 | 219451272 | ||
chr2:219451737
|
G | A | 1 | a0005c0081 | 1 | HG02647.hp1 | synonymous_variant | LOW | c.2370G>A | p.Gly790Gly | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/41 | 2505/10782 | 2370/9804 | 790/3267 | chr2 | 219451737 | ||
chr2:219467296
|
C | T | 2 | a0001c0077a0008c0078 | 2 | HG01243.hp1 HG06807.hp2 |
synonymous_variant | LOW | c.3004C>T | p.Leu1002Leu | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 10/41 | 3139/10782 | 3004/9804 | 1002/3267 | chr2 | 219467296 | ||
chr2:219467334
|
A | G | 2 | a0009c0015a0014c0022 | 3 | HG02258.hp1 HG02630.hp1 HG02809.hp2 |
synonymous_variant | LOW | c.3042A>G | p.Lys1014Lys | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 10/41 | 3177/10782 | 3042/9804 | 1014/3267 | chr2 | 219467334 | ||
chr2:219467352
|
T | C | 2 | a0009c0015a0014c0022 | 3 | HG02258.hp1 HG02630.hp1 HG02809.hp2 |
synonymous_variant | LOW | c.3060T>C | p.Asp1020Asp | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 10/41 | 3195/10782 | 3060/9804 | 1020/3267 | chr2 | 219467352 | ||
chr2:219468902
|
C | T | 1 | a0001c0076 | 1 | HG02257.hp1 | synonymous_variant | LOW | c.3345C>T | p.Asp1115Asp | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 12/41 | 3480/10782 | 3345/9804 | 1115/3267 | chr2 | 219468902 | ||
chr2:219469228
|
T | C | 85 | a0001c0001a0001c0002a0001c0019others(82): Show | 298 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(295): Show |
synonymous_variant | LOW | c.3564T>C | p.Pro1188Pro | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 13/41 | 3699/10782 | 3564/9804 | 1188/3267 | chr2 | 219469228 | ||
chr2:219469357
|
C | T | 1 | a0003c0075 | 1 | HG03942.hp1 | synonymous_variant | LOW | c.3693C>T | p.Ser1231Ser | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 13/41 | 3828/10782 | 3693/9804 | 1231/3267 | chr2 | 219469357 | ||
chr2:219471914
|
C | T | 1 | a0002c0074 | 1 | HG02145.hp2 | synonymous_variant | LOW | c.3762C>T | p.His1254His | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 14/41 | 3897/10782 | 3762/9804 | 1254/3267 | chr2 | 219471914 | ||
chr2:219476952
|
A | G | 1 | a0002c0048 | 1 | HG03017.hp1 | synonymous_variant | LOW | c.4530A>G | p.Gly1510Gly | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 19/41 | 4665/10782 | 4530/9804 | 1510/3267 | chr2 | 219476952 | ||
chr2:219477282
|
G | A | 2 | a0006c0007a0006c0053 | 10 | HG00280.hp1 HG00438.hp1 HG00673.hp1 others(7): Show |
synonymous_variant | LOW | c.4566G>A | p.Glu1522Glu | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 20/41 | 4701/10782 | 4566/9804 | 1522/3267 | chr2 | 219477282 | ||
chr2:219479994
|
G | A | 1 | a0001c0019 | 2 | NA19030.hp1 NA19043.hp2 |
synonymous_variant | LOW | c.5196G>A | p.Ala1732Ala | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 25/41 | 5331/10782 | 5196/9804 | 1732/3267 | chr2 | 219479994 | ||
chr2:219480040
|
C | T | 1 | a0001c0069 | 1 | HG02451.hp2 | synonymous_variant | LOW | c.5242C>T | p.Leu1748Leu | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 25/41 | 5377/10782 | 5242/9804 | 1748/3267 | chr2 | 219480040 | ||
chr2:219483145
|
C | T | 2 | a0002c0045a0002c0068 | 2 | HG02056.hp2 HG02083.hp1 |
synonymous_variant | LOW | c.5682C>T | p.Pro1894Pro | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 30/41 | 5817/10782 | 5682/9804 | 1894/3267 | chr2 | 219483145 | ||
chr2:219483214
|
G | A | 3 | a0002c0017a0002c0054a0027c0035 | 4 | HG02965.hp1 HG02970.hp2 HG03195.hp1 others(1): Show |
synonymous_variant | LOW | c.5751G>A | p.Gly1917Gly | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 30/41 | 5886/10782 | 5751/9804 | 1917/3267 | chr2 | 219483214 | ||
chr2:219483877
|
C | T | 1 | a0001c0066 | 1 | NA18983.hp2 | synonymous_variant | LOW | c.6414C>T | p.Pro2138Pro | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 30/41 | 6549/10782 | 6414/9804 | 2138/3267 | chr2 | 219483877 | ||
chr2:219484054
|
C | T | 1 | a0044c0079 | 1 | NA18955.hp1 | synonymous_variant | LOW | c.6591C>T | p.Thr2197Thr | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 30/41 | 6726/10782 | 6591/9804 | 2197/3267 | chr2 | 219484054 | ||
chr2:219484633
|
C | T | 6 | a0008c0014a0008c0061a0008c0078others(3): Show | 8 | HG01891.hp2 HG02886.hp1 HG02886.hp2 others(5): Show |
synonymous_variant | LOW | c.7170C>T | p.Arg2390Arg | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 30/41 | 7305/10782 | 7170/9804 | 2390/3267 | chr2 | 219484633 | ||
chr2:219484663
|
C | A | 1 | a0001c0037 | 1 | HG01168.hp1 | synonymous_variant | LOW | c.7200C>A | p.Val2400Val | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 30/41 | 7335/10782 | 7200/9804 | 2400/3267 | chr2 | 219484663 | ||
chr2:219484765
|
G | A | 1 | a0025c0071 | 1 | HG01884.hp2 | synonymous_variant | LOW | c.7302G>A | p.Gly2434Gly | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 30/41 | 7437/10782 | 7302/9804 | 2434/3267 | chr2 | 219484765 | ||
chr2:219488291
|
G | A | 26 | a0002c0003a0002c0004a0002c0008others(23): Show | 98 | HG00609.hp1 HG00639.hp1 HG00642.hp1 others(95): Show |
synonymous_variant | LOW | c.7839G>A | p.Pro2613Pro | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 32/41 | 7974/10782 | 7839/9804 | 2613/3267 | chr2 | 219488291 | ||
chr2:219489520
|
G | A | 1 | a0001c0039 | 1 | NA19007.hp1 | synonymous_variant | LOW | c.8502G>A | p.Ser2834Ser | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 36/41 | 8637/10782 | 8502/9804 | 2834/3267 | chr2 | 219489520 | ||
chr2:219489526
|
G | A | 1 | a0010c0051 | 1 | HG03710.hp1 | synonymous_variant | LOW | c.8508G>A | p.Lys2836Lys | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 36/41 | 8643/10782 | 8508/9804 | 2836/3267 | chr2 | 219489526 | ||
chr2:219489553
|
T | C | 1 | a0002c0064 | 1 | NA18960.hp2 | synonymous_variant | LOW | c.8535T>C | p.Pro2845Pro | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 36/41 | 8670/10782 | 8535/9804 | 2845/3267 | chr2 | 219489553 | ||
chr2:219489637
|
G | A | 1 | a0001c0019 | 2 | NA19030.hp1 NA19043.hp2 |
synonymous_variant | LOW | c.8619G>A | p.Lys2873Lys | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 36/41 | 8754/10782 | 8619/9804 | 2873/3267 | chr2 | 219489637 | ||
chr2:219489643
|
C | T | 26 | a0002c0003a0002c0004a0002c0008others(23): Show | 98 | HG00609.hp1 HG00639.hp1 HG00642.hp1 others(95): Show |
synonymous_variant | LOW | c.8625C>T | p.Phe2875Phe | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 36/41 | 8760/10782 | 8625/9804 | 2875/3267 | chr2 | 219489643 | ||
chr2:219489820
|
G | A | 7 | a0004c0009a0004c0012a0004c0016others(4): Show | 24 | HG00280.hp1 HG00438.hp1 HG00673.hp1 others(21): Show |
synonymous_variant | LOW | c.8802G>A | p.Pro2934Pro | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 36/41 | 8937/10782 | 8802/9804 | 2934/3267 | chr2 | 219489820 | ||
chr2:219490424
|
T | C | 1 | a0007c0020 | 2 | HG02895.hp2 HG02897.hp2 |
synonymous_variant | LOW | c.8937T>C | p.Val2979Val | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 37/41 | 9072/10782 | 8937/9804 | 2979/3267 | chr2 | 219490424 | ||
chr2:219490754
|
C | T | 1 | a0003c0038 | 1 | HG01346.hp1 | synonymous_variant | LOW | c.9183C>T | p.Asp3061Asp | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 38/41 | 9318/10782 | 9183/9804 | 3061/3267 | chr2 | 219490754 | ||
chr2:219490760
|
C | A | 1 | a0002c0065 | 1 | NA18957.hp2 | synonymous_variant | LOW | c.9189C>A | p.Ala3063Ala | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 38/41 | 9324/10782 | 9189/9804 | 3063/3267 | chr2 | 219490760 | ||
chr2:219490901
|
C | T | 1 | a0008c0061 | 1 | HG03516.hp1 | synonymous_variant | LOW | c.9330C>T | p.Tyr3110Tyr | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 38/41 | 9465/10782 | 9330/9804 | 3110/3267 | chr2 | 219490901 | ||
chr2:219491798
|
G | T | 24 | a0001c0057a0002c0003a0002c0004others(21): Show | 95 | HG00609.hp1 HG00639.hp1 HG00642.hp1 others(92): Show |
synonymous_variant | LOW | c.9390G>T | p.Pro3130Pro | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 39/41 | 9525/10782 | 9390/9804 | 3130/3267 | chr2 | 219491798 | ||
chr2:219492219
|
C | T | 1 | a0028c0063 | 1 | NA19082.hp2 | synonymous_variant | LOW | c.9570C>T | p.Ser3190Ser | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 40/41 | 9705/10782 | 9570/9804 | 3190/3267 | chr2 | 219492219 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:219434929
|
C | T | 2 | a0001c0002t0010a0028c0063t0009 | 2 | HG02027.hp2 NA19082.hp2 |
5_prime_UTR_variant | MODIFIER | c.-49C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 1/41 | 49 | chr2 | 219434929 | |||||
chr2:219492872
|
C | A | 45 | a0001c0002t0002a0001c0057t0002a0002c0003t0002others(42): Show | 132 | HG00280.hp1 HG00438.hp1 HG00609.hp1 others(129): Show |
3_prime_UTR_variant | MODIFIER | c.*86C>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 41/41 | 86 | chr2 | 219492872 | |||||
chr2:219492936
|
C | A | 1 | a0001c0001t0007 | 1 | HG01496.hp1 | 3_prime_UTR_variant | MODIFIER | c.*150C>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 41/41 | 150 | chr2 | 219492936 | |||||
chr2:219493270
|
A | T | 2 | a0002c0004t0004a0002c0048t0004 | 4 | HG03017.hp1 HG03239.hp2 HG03710.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*484A>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 41/41 | 484 | chr2 | 219493270 | |||||
chr2:219493396
|
C | T | 2 | a0007c0013t0006a0023c0072t0006 | 2 | NA18522.hp1 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*610C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 41/41 | 610 | chr2 | 219493396 | |||||
chr2:219493432
|
C | T | 1 | a0001c0001t0008 | 1 | NA18612.hp1 | 3_prime_UTR_variant | MODIFIER | c.*646C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 41/41 | 646 | chr2 | 219493432 | |||||
chr2:219493450
|
A | T | 1 | a0001c0001t0007 | 1 | HG01496.hp1 | 3_prime_UTR_variant | MODIFIER | c.*664A>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 41/41 | 664 | chr2 | 219493450 | |||||
chr2:219493476
|
C | T | 48 | a0001c0002t0002a0001c0057t0002a0002c0003t0002others(45): Show | 136 | HG00280.hp1 HG00438.hp1 HG00609.hp1 others(133): Show |
3_prime_UTR_variant | MODIFIER | c.*690C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 41/41 | 690 | chr2 | 219493476 | |||||
chr2:219493543
|
C | T | 7 | a0008c0014t0003a0008c0061t0003a0008c0078t0003others(4): Show | 9 | HG01891.hp2 HG02717.hp1 HG02886.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*757C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 41/41 | 757 | chr2 | 219493543 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:219435380
|
G | A | 1 | a0002c0003t0002g0014 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.388+15G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 1/40 | chr2 | 219435380 | ||||||
chr2:219435382
|
G | C | 1 | a0001c0001t0001g0015 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.388+17G>C | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 1/40 | chr2 | 219435382 | ||||||
chr2:219435490
|
CT | C | 8 | a0001c0069t0001g0021a0002c0004t0001g0016a0017c0027t0001g0018others(5): Show | 8 | HG01884.hp2 HG02451.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.388+127delT | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr2 | 219435490 | |||||
chr2:219435649
|
G | A | 81 | a0001c0001t0001g0002a0001c0001t0001g0027a0001c0001t0001g0030others(78): Show | 84 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.388+284G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 1/40 | chr2 | 219435649 | ||||||
chr2:219435673
|
G | A | 29 | a0001c0002t0001g0104a0001c0002t0001g0106a0001c0002t0001g0113others(26): Show | 32 | HG00733.hp1 HG01884.hp2 HG02257.hp1 others(29): Show |
intron_variant | MODIFIER | c.388+308G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 1/40 | chr2 | 219435673 | ||||||
chr2:219435675
|
A | G | 1 | a0006c0058t0002g0285 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.388+310A>G | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 1/40 | chr2 | 219435675 | ||||||
chr2:219435920
|
C | G | 5 | a0001c0002t0001g0013a0001c0002t0001g0283a0001c0002t0001g0284others(2): Show | 6 | HG02109.hp1 HG02109.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.388+555C>G | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 1/40 | chr2 | 219435920 | ||||||
chr2:219436083
|
A | G | 1 | a0001c0002t0001g0120 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.388+718A>G | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 1/40 | chr2 | 219436083 | ||||||
chr2:219436176
|
G | A | 1 | a0002c0004t0004g0024 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.388+811G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 1/40 | chr2 | 219436176 | ||||||
chr2:219436243
|
G | A | 1 | a0002c0003t0002g0121 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.388+878G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 1/40 | chr2 | 219436243 | ||||||
chr2:219436246
|
TGGGCCCA others(4): Show |
T | 1 | a0001c0001t0001g0280 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.388+882_388+892del others(11): Show |
SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 1/40 | chr2 | 219436246 | ||||||
chr2:219436481
|
C | T | 1 | a0025c0071t0001g0023 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.388+1116C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 1/40 | chr2 | 219436481 | ||||||
chr2:219436486
|
C | T | 25 | a0001c0002t0001g0104a0001c0002t0001g0106a0001c0002t0001g0113others(22): Show | 28 | HG00733.hp1 HG02280.hp1 HG02451.hp2 others(25): Show |
intron_variant | MODIFIER | c.388+1121C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 1/40 | chr2 | 219436486 | ||||||
chr2:219436535
|
C | G | 2 | a0007c0020t0002g0278a0007c0020t0002g0279 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.388+1170C>G | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 1/40 | chr2 | 219436535 | ||||||
chr2:219436554
|
G | A | 1 | a0039c0067t0001g0122 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.388+1189G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 1/40 | chr2 | 219436554 | ||||||
chr2:219436654
|
C | T | 1 | a0001c0001t0001g0277 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.388+1289C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 1/40 | chr2 | 219436654 | ||||||
chr2:219436829
|
G | A | 1 | a0001c0001t0007g0123 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.388+1464G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 1/40 | chr2 | 219436829 | ||||||
chr2:219437344
|
G | A | 1 | a0003c0011t0001g0124 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.388+1979G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 1/40 | chr2 | 219437344 | ||||||
chr2:219437405
|
G | A | 2 | a0007c0020t0002g0278a0007c0020t0002g0279 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.388+2040G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 1/40 | chr2 | 219437405 | ||||||
chr2:219437419
|
G | A | 3 | a0001c0002t0001g0104a0021c0034t0001g0026a0022c0033t0002g0025 | 3 | HG02622.hp1 HG02818.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.388+2054G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 1/40 | chr2 | 219437419 | ||||||
chr2:219437429
|
A | G | 1 | a0002c0003t0002g0101 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.388+2064A>G | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 1/40 | chr2 | 219437429 | ||||||
chr2:219437491
|
T | A | 1 | a0002c0003t0002g0101 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.388+2126T>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 1/40 | chr2 | 219437491 | ||||||
chr2:219437540
|
T | C | 137 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(134): Show | 149 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.388+2175T>C | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 1/40 | chr2 | 219437540 | ||||||
chr2:219437563
|
A | G | 94 | a0001c0001t0001g0199a0001c0001t0001g0260a0001c0002t0001g0066others(91): Show | 98 | HG00609.hp1 HG00639.hp1 HG00642.hp1 others(95): Show |
intron_variant | MODIFIER | c.388+2198A>G | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 1/40 | chr2 | 219437563 | ||||||
chr2:219437827
|
C | T | 134 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(131): Show | 146 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.388+2462C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 1/40 | chr2 | 219437827 | ||||||
chr2:219438020
|
CGGATATG others(8): Show |
C | 1 | a0001c0077t0001g0241 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.388+2656_388+2670d others(17): Show |
SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 1/40 | chr2 | 219438020 | ||||||
chr2:219438021
|
G | A | 2 | a0001c0002t0002g0201a0007c0013t0005g0200 | 2 | HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.388+2656G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 1/40 | chr2 | 219438021 | ||||||
chr2:219438034
|
C | T | 1 | a0002c0054t0001g0198 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.388+2669C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 1/40 | chr2 | 219438034 | ||||||
chr2:219439022
|
A | C | 1 | a0002c0003t0002g0121 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.388+3657A>C | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 1/40 | chr2 | 219439022 | ||||||
chr2:219439049
|
G | C | 2 | a0001c0002t0001g0242a0002c0003t0002g0243 | 2 | NA19065.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.388+3684G>C | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 1/40 | chr2 | 219439049 | ||||||
chr2:219439157
|
A | G | 36 | a0001c0002t0001g0012a0001c0002t0001g0060a0001c0002t0001g0106others(33): Show | 36 | HG00642.hp1 HG00733.hp1 HG01123.hp2 others(33): Show |
intron_variant | MODIFIER | c.388+3792A>G | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 1/40 | chr2 | 219439157 | ||||||
chr2:219439270
|
C | T | 12 | a0001c0002t0001g0013a0001c0002t0001g0104a0001c0002t0001g0192others(9): Show | 13 | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.388+3905C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 1/40 | chr2 | 219439270 | ||||||
chr2:219439558
|
A | C | 22 | a0001c0002t0001g0012a0001c0002t0001g0231a0001c0002t0001g0232others(19): Show | 22 | HG01123.hp2 HG01975.hp2 HG01981.hp2 others(19): Show |
intron_variant | MODIFIER | c.388+4193A>C | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 1/40 | chr2 | 219439558 | ||||||
chr2:219439562
|
G | A | 7 | a0004c0009t0002g0061a0004c0009t0002g0062a0004c0009t0002g0063others(4): Show | 7 | HG01123.hp2 HG01981.hp2 HG02083.hp2 others(4): Show |
intron_variant | MODIFIER | c.388+4197G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 1/40 | chr2 | 219439562 | ||||||
chr2:219439570
|
T | G | 1 | a0002c0008t0002g0105 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.388+4205T>G | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 1/40 | chr2 | 219439570 | ||||||
chr2:219439758
|
G | A | 1 | a0003c0005t0001g0244 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.388+4393G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 1/40 | chr2 | 219439758 | ||||||
chr2:219439809
|
G | A | 3 | a0001c0001t0001g0277a0001c0002t0010g0127a0028c0063t0009g0128 | 3 | HG02027.hp2 NA18995.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.388+4444G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 1/40 | chr2 | 219439809 | ||||||
chr2:219440241
|
G | A | 1 | a0001c0076t0001g0103 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.389-4412G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 1/40 | chr2 | 219440241 | ||||||
chr2:219440310
|
C | T | 1 | a0008c0014t0003g0220 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.389-4343C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 1/40 | chr2 | 219440310 | ||||||
chr2:219440354
|
C | A | 1 | a0001c0001t0001g0027 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.389-4299C>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 1/40 | chr2 | 219440354 | ||||||
chr2:219440362
|
T | G | 92 | a0001c0001t0001g0260a0001c0002t0001g0066a0001c0002t0001g0072others(89): Show | 96 | HG00609.hp1 HG00639.hp1 HG00738.hp2 others(93): Show |
intron_variant | MODIFIER | c.389-4291T>G | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 1/40 | chr2 | 219440362 | ||||||
chr2:219440561
|
T | TTTTA | 37 | a0001c0002t0001g0095a0001c0002t0001g0096a0001c0002t0001g0269others(34): Show | 38 | HG00673.hp1 HG00738.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.389-4051_389-4048d others(6): Show |
SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr2 | 219440561 | |||||
chr2:219440561
|
T | TTTTATTT others(1): Show |
5 | a0001c0002t0001g0219a0002c0003t0002g0101a0002c0003t0002g0275others(2): Show | 5 | HG02572.hp2 HG03831.hp2 HG03927.hp1 others(2): Show |
intron_variant | MODIFIER | c.389-4055_389-4048d others(10): Show |
SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr2 | 219440561 | |||||
chr2:219440561
|
TTTTA | T | 96 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(93): Show | 106 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.389-4051_389-4048d others(6): Show |
SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr2 | 219440561 | |||||
chr2:219440561
|
TTTTATTT others(1): Show |
T | 29 | a0001c0002t0001g0066a0001c0002t0001g0129a0001c0002t0001g0231others(26): Show | 29 | HG00639.hp1 HG01074.hp2 HG01123.hp2 others(26): Show |
intron_variant | MODIFIER | c.389-4055_389-4048d others(10): Show |
SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr2 | 219440561 | |||||
chr2:219440561
|
TTTTATTT others(13): Show |
T | 12 | a0001c0002t0001g0013a0001c0002t0001g0104a0001c0002t0001g0192others(9): Show | 13 | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.389-4067_389-4048d others(22): Show |
SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr2 | 219440561 | |||||
chr2:219441056
|
G | T | 1 | a0002c0004t0002g0046 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.389-3597G>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 1/40 | chr2 | 219441056 | ||||||
chr2:219441103
|
A | T | 1 | a0002c0004t0002g0189 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.389-3550A>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 1/40 | chr2 | 219441103 | ||||||
chr2:219441311
|
G | T | 3 | a0001c0002t0001g0106a0001c0069t0001g0021a0049c0023t0001g0226 | 3 | HG02055.hp2 HG02451.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.389-3342G>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 1/40 | chr2 | 219441311 | ||||||
chr2:219441364
|
G | T | 5 | a0001c0002t0001g0129a0001c0002t0001g0188a0025c0071t0001g0023others(2): Show | 5 | HG01884.hp1 HG01884.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.389-3289G>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 1/40 | chr2 | 219441364 | ||||||
chr2:219441412
|
C | G | 2 | a0002c0003t0002g0085a0020c0050t0002g0098 | 2 | HG02602.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.389-3241C>G | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 1/40 | chr2 | 219441412 | ||||||
chr2:219441415
|
T | C | 1 | a0006c0007t0002g0169 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.389-3238T>C | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 1/40 | chr2 | 219441415 | ||||||
chr2:219441691
|
G | T | 232 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(229): Show | 247 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(244): Show |
intron_variant | MODIFIER | c.389-2962G>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 1/40 | chr2 | 219441691 | ||||||
chr2:219441735
|
G | T | 8 | a0001c0002t0001g0013a0001c0002t0002g0282a0002c0003t0002g0194others(5): Show | 9 | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.389-2918G>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 1/40 | chr2 | 219441735 | ||||||
chr2:219441746
|
A | G | 3 | a0009c0015t0002g0221a0009c0015t0002g0223a0014c0022t0002g0222 | 3 | HG02258.hp1 HG02630.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.389-2907A>G | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 1/40 | chr2 | 219441746 | ||||||
chr2:219441933
|
C | T | 1 | a0044c0079t0002g0276 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.389-2720C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 1/40 | chr2 | 219441933 | ||||||
chr2:219442435
|
G | T | 1 | a0001c0002t0001g0263 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.389-2218G>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 1/40 | chr2 | 219442435 | ||||||
chr2:219442440
|
C | G | 1 | a0001c0001t0001g0058 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.389-2213C>G | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 1/40 | chr2 | 219442440 | ||||||
chr2:219442777
|
TCGGGCTG others(12): Show |
T | 4 | a0001c0002t0001g0060a0001c0002t0001g0283a0001c0002t0001g0284others(1): Show | 4 | HG01257.hp1 HG02257.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.389-1848_389-1830d others(21): Show |
SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr2 | 219442777 | |||||
chr2:219442911
|
G | A | 1 | a0003c0011t0001g0130 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.389-1742G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 1/40 | chr2 | 219442911 | ||||||
chr2:219443032
|
A | T | 1 | a0001c0002t0001g0084 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.389-1621A>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 1/40 | chr2 | 219443032 | ||||||
chr2:219443171
|
C | T | 1 | a0031c0030t0002g0218 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.389-1482C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 1/40 | chr2 | 219443171 | ||||||
chr2:219443177
|
C | G | 1 | a0003c0005t0001g0070 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.389-1476C>G | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 1/40 | chr2 | 219443177 | ||||||
chr2:219443349
|
C | T | 1 | a0003c0005t0001g0083 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.389-1304C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 1/40 | chr2 | 219443349 | ||||||
chr2:219443415
|
A | G | 14 | a0001c0002t0001g0080a0001c0002t0001g0242a0001c0002t0001g0263others(11): Show | 14 | HG00609.hp1 HG01071.hp1 HG01952.hp2 others(11): Show |
intron_variant | MODIFIER | c.389-1238A>G | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 1/40 | chr2 | 219443415 | ||||||
chr2:219443532
|
C | G | 1 | a0019c0032t0001g0020 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.389-1121C>G | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 1/40 | chr2 | 219443532 | ||||||
chr2:219443569
|
C | T | 2 | a0002c0004t0001g0016a0024c0047t0001g0017 | 2 | HG02559.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.389-1084C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 1/40 | chr2 | 219443569 | ||||||
chr2:219443743
|
G | GGT | 32 | a0001c0002t0001g0013a0001c0002t0001g0104a0001c0002t0001g0192others(29): Show | 33 | HG00642.hp1 HG00733.hp1 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.389-892_389-891dup others(2): Show |
SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr2 | 219443743 | |||||
chr2:219443859
|
A | C | 245 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(242): Show | 261 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(258): Show |
intron_variant | MODIFIER | c.389-794A>C | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 1/40 | chr2 | 219443859 | ||||||
chr2:219443976
|
G | A | 1 | a0036c0059t0001g0245 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.389-677G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 1/40 | chr2 | 219443976 | ||||||
chr2:219444067
|
A | G | 11 | a0001c0001t0001g0045a0001c0001t0001g0051a0001c0001t0001g0053others(8): Show | 11 | HG01123.hp1 HG01934.hp2 HG01978.hp2 others(8): Show |
intron_variant | MODIFIER | c.389-586A>G | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 1/40 | chr2 | 219444067 | ||||||
chr2:219444124
|
C | T | 1 | a0002c0003t0002g0121 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.389-529C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 1/40 | chr2 | 219444124 | ||||||
chr2:219444227
|
T | C | 3 | a0002c0003t0002g0121a0002c0004t0002g0171a0002c0004t0002g0190 | 3 | HG00741.hp2 HG01109.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.389-426T>C | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 1/40 | chr2 | 219444227 | ||||||
chr2:219444280
|
C | A | 1 | a0006c0007t0002g0191 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.389-373C>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 1/40 | chr2 | 219444280 | ||||||
chr2:219444385
|
C | T | 5 | a0002c0017t0001g0126a0002c0017t0001g0184a0002c0054t0001g0198others(2): Show | 5 | HG02965.hp1 HG02970.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.389-268C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 1/40 | chr2 | 219444385 | ||||||
chr2:219444409
|
G | A | 7 | a0001c0002t0001g0012a0001c0002t0001g0231a0001c0002t0001g0232others(4): Show | 7 | HG01975.hp2 HG03098.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.389-244G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 1/40 | chr2 | 219444409 | ||||||
chr2:219444553
|
T | G | 1 | a0002c0008t0002g0107 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.389-100T>G | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 1/40 | chr2 | 219444553 | ||||||
chr2:219445201
|
C | A | 4 | a0001c0002t0001g0060a0001c0002t0001g0283a0001c0002t0001g0284others(1): Show | 4 | HG01257.hp1 HG02257.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.815+40C>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 3/40 | chr2 | 219445201 | ||||||
chr2:219445217
|
G | A | 1 | a0005c0006t0002g0110 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.815+56G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 3/40 | chr2 | 219445217 | ||||||
chr2:219445390
|
C | T | 14 | a0002c0008t0002g0100a0002c0008t0002g0105a0002c0008t0002g0107others(11): Show | 14 | HG00642.hp1 HG00733.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.815+229C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 3/40 | chr2 | 219445390 | ||||||
chr2:219445556
|
ATC | A | 8 | a0001c0002t0001g0013a0001c0002t0002g0282a0002c0003t0002g0194others(5): Show | 9 | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.815+401_815+402del others(2): Show |
SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 3/40 | INFO_REALIGN_3_PRIME | chr2 | 219445556 | |||||
chr2:219445802
|
G | A | 1 | a0002c0003t0002g0264 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.815+641G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 3/40 | chr2 | 219445802 | ||||||
chr2:219445821
|
G | A | 2 | a0005c0006t0002g0112a0046c0083t0005g0111 | 2 | HG02723.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.815+660G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 3/40 | chr2 | 219445821 | ||||||
chr2:219445905
|
G | A | 2 | a0002c0003t0002g0064a0041c0073t0001g0071 | 2 | HG02735.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.815+744G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 3/40 | chr2 | 219445905 | ||||||
chr2:219446010
|
A | G | 282 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(279): Show | 298 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(295): Show |
intron_variant | MODIFIER | c.815+849A>G | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 3/40 | chr2 | 219446010 | ||||||
chr2:219446050
|
G | A | 10 | a0001c0002t0001g0207a0001c0002t0001g0219a0002c0003t0002g0206others(7): Show | 10 | HG02145.hp2 HG02258.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.815+889G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 3/40 | chr2 | 219446050 | ||||||
chr2:219446242
|
T | C | 1 | a0001c0001t0001g0131 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.815+1081T>C | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 3/40 | chr2 | 219446242 | ||||||
chr2:219446317
|
C | A | 95 | a0001c0001t0001g0260a0001c0002t0001g0066a0001c0002t0001g0072others(92): Show | 99 | HG00609.hp1 HG00639.hp1 HG00738.hp2 others(96): Show |
intron_variant | MODIFIER | c.815+1156C>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 3/40 | chr2 | 219446317 | ||||||
chr2:219446664
|
T | A | 4 | a0001c0002t0001g0060a0001c0002t0001g0283a0001c0002t0001g0284others(1): Show | 4 | HG01257.hp1 HG02257.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.816-1310T>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 3/40 | chr2 | 219446664 | ||||||
chr2:219446714
|
TG | T | 3 | a0009c0015t0002g0221a0009c0015t0002g0223a0014c0022t0002g0222 | 3 | HG02258.hp1 HG02630.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.816-1257delG | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 3/40 | INFO_REALIGN_3_PRIME | chr2 | 219446714 | |||||
chr2:219446865
|
A | G | 3 | a0001c0002t0001g0060a0001c0002t0001g0283a0001c0002t0001g0284 | 3 | HG01257.hp1 HG02818.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.816-1109A>G | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 3/40 | chr2 | 219446865 | ||||||
chr2:219446975
|
C | CT | 14 | a0001c0001t0001g0125a0001c0001t0001g0132a0001c0002t0001g0060others(11): Show | 14 | HG01071.hp1 HG01257.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.816-983dupT | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 3/40 | INFO_REALIGN_3_PRIME | chr2 | 219446975 | |||||
chr2:219446975
|
C | CTT | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(207): Show | 226 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.816-984_816-983dup others(2): Show |
SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 3/40 | INFO_REALIGN_3_PRIME | chr2 | 219446975 | |||||
chr2:219446975
|
C | CTTT | 30 | a0001c0001t0001g0166a0001c0001t0001g0280a0001c0001t0008g0164others(27): Show | 30 | HG00733.hp1 HG00741.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.816-985_816-983dup others(3): Show |
SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 3/40 | INFO_REALIGN_3_PRIME | chr2 | 219446975 | |||||
chr2:219446975
|
CT | C | 7 | a0001c0002t0001g0012a0001c0002t0001g0239a0004c0012t0002g0233others(4): Show | 7 | HG01975.hp2 HG03471.hp2 HG03579.hp1 others(4): Show |
intron_variant | MODIFIER | c.816-983delT | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 3/40 | INFO_REALIGN_3_PRIME | chr2 | 219446975 | |||||
chr2:219446995
|
T | A | 26 | a0001c0002t0001g0207a0001c0002t0001g0219a0001c0077t0001g0241others(23): Show | 26 | HG00733.hp1 HG01243.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.816-979T>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 3/40 | chr2 | 219446995 | ||||||
chr2:219447211
|
T | C | 8 | a0001c0002t0001g0013a0001c0002t0002g0282a0002c0003t0002g0194others(5): Show | 9 | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.816-763T>C | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 3/40 | chr2 | 219447211 | ||||||
chr2:219447213
|
TG | T | 260 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(257): Show | 276 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(273): Show |
intron_variant | MODIFIER | c.816-752delG | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 3/40 | INFO_REALIGN_3_PRIME | chr2 | 219447213 | |||||
chr2:219447254
|
G | A | 2 | a0002c0004t0002g0171a0002c0004t0002g0190 | 2 | HG00741.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.816-720G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 3/40 | chr2 | 219447254 | ||||||
chr2:219447375
|
G | A | 1 | a0001c0002t0001g0272 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.816-599G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 3/40 | chr2 | 219447375 | ||||||
chr2:219447930
|
G | A | 2 | a0003c0005t0001g0086a0003c0005t0001g0087 | 2 | HG00738.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.816-44G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 3/40 | chr2 | 219447930 | ||||||
chr2:219449355
|
G | A | 2 | a0002c0004t0001g0016a0024c0047t0001g0017 | 2 | HG02559.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2113+84G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 4/40 | chr2 | 219449355 | ||||||
chr2:219449488
|
A | G | 25 | a0001c0002t0001g0013a0001c0002t0002g0282a0002c0003t0002g0194others(22): Show | 26 | HG00642.hp1 HG00733.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.2113+217A>G | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 4/40 | chr2 | 219449488 | ||||||
chr2:219449644
|
C | A | 1 | a0008c0014t0003g0220 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2113+373C>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 4/40 | chr2 | 219449644 | ||||||
chr2:219449657
|
C | T | 2 | a0010c0051t0002g0271a0010c0052t0002g0093 | 2 | HG01256.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.2113+386C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 4/40 | chr2 | 219449657 | ||||||
chr2:219449840
|
A | G | 14 | a0002c0008t0002g0100a0002c0008t0002g0105a0002c0008t0002g0107others(11): Show | 14 | HG00642.hp1 HG00733.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.2113+569A>G | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 4/40 | chr2 | 219449840 | ||||||
chr2:219449981
|
T | A | 1 | a0001c0002t0001g0272 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.2113+710T>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 4/40 | chr2 | 219449981 | ||||||
chr2:219450172
|
C | T | 5 | a0002c0003t0002g0206a0002c0003t0002g0208a0002c0003t0002g0209others(2): Show | 5 | HG02145.hp2 HG02717.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.2113+901C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 4/40 | chr2 | 219450172 | ||||||
chr2:219450291
|
G | A | 10 | a0001c0002t0001g0104a0001c0002t0001g0192a0001c0002t0002g0282others(7): Show | 10 | HG02109.hp2 HG02145.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.2114-845G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 4/40 | chr2 | 219450291 | ||||||
chr2:219450492
|
A | G | 1 | a0038c0043t0001g0182 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.2114-644A>G | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 4/40 | chr2 | 219450492 | ||||||
chr2:219450647
|
C | T | 2 | a0007c0020t0002g0278a0007c0020t0002g0279 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2114-489C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 4/40 | chr2 | 219450647 | ||||||
chr2:219450710
|
G | A | 1 | a0001c0001t0008g0164 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2114-426G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 4/40 | chr2 | 219450710 | ||||||
chr2:219450792
|
G | A | 261 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(258): Show | 276 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(273): Show |
intron_variant | MODIFIER | c.2114-344G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 4/40 | chr2 | 219450792 | ||||||
chr2:219450803
|
C | T | 112 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(109): Show | 123 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.2114-333C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 4/40 | chr2 | 219450803 | ||||||
chr2:219451307
|
G | A | 1 | a0001c0002t0001g0219 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2257+28G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 5/40 | chr2 | 219451307 | ||||||
chr2:219451317
|
G | A | 5 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(2): Show | 5 | HG00733.hp2 HG01069.hp1 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.2257+38G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 5/40 | chr2 | 219451317 | ||||||
chr2:219451501
|
T | G | 2 | a0002c0003t0002g0085a0020c0050t0002g0098 | 2 | HG02602.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.2258-124T>G | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 5/40 | chr2 | 219451501 | ||||||
chr2:219451592
|
C | T | 4 | a0001c0002t0001g0104a0001c0002t0001g0192a0021c0034t0001g0026others(1): Show | 4 | HG02622.hp1 HG02818.hp1 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.2258-33C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 5/40 | chr2 | 219451592 | ||||||
chr2:219451857
|
C | T | 261 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(258): Show | 276 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(273): Show |
intron_variant | MODIFIER | c.2440+50C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/40 | chr2 | 219451857 | ||||||
chr2:219451973
|
C | T | 1 | a0001c0001t0001g0163 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2440+166C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/40 | chr2 | 219451973 | ||||||
chr2:219452019
|
C | T | 1 | a0001c0076t0001g0103 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2440+212C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/40 | chr2 | 219452019 | ||||||
chr2:219452116
|
G | A | 257 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(254): Show | 272 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(269): Show |
intron_variant | MODIFIER | c.2440+309G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/40 | chr2 | 219452116 | ||||||
chr2:219452205
|
T | C | 1 | a0002c0085t0002g0170 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2440+398T>C | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/40 | chr2 | 219452205 | ||||||
chr2:219452401
|
T | C | 1 | a0001c0001t0001g0033 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2440+594T>C | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/40 | chr2 | 219452401 | ||||||
chr2:219452630
|
G | A | 3 | a0001c0019t0001g0224a0001c0019t0001g0225a0039c0067t0001g0122 | 3 | HG02630.hp2 NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2440+823G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/40 | chr2 | 219452630 | ||||||
chr2:219452650
|
C | T | 3 | a0001c0002t0001g0129a0001c0002t0001g0188a0050c0086t0001g0168 | 3 | HG01884.hp1 HG02922.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2440+843C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/40 | chr2 | 219452650 | ||||||
chr2:219452662
|
A | C | 1 | a0002c0004t0002g0162 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2440+855A>C | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/40 | chr2 | 219452662 | ||||||
chr2:219452736
|
G | A | 1 | a0002c0003t0002g0121 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2440+929G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/40 | chr2 | 219452736 | ||||||
chr2:219452865
|
C | G | 1 | a0001c0002t0001g0219 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2440+1058C>G | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/40 | chr2 | 219452865 | ||||||
chr2:219452886
|
A | G | 1 | a0003c0005t0001g0070 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2440+1079A>G | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/40 | chr2 | 219452886 | ||||||
chr2:219452908
|
C | T | 4 | a0001c0002t0001g0104a0001c0002t0001g0192a0021c0034t0001g0026others(1): Show | 4 | HG02622.hp1 HG02818.hp1 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.2440+1101C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/40 | chr2 | 219452908 | ||||||
chr2:219452928
|
C | T | 1 | a0001c0001t0001g0199 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2440+1121C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/40 | chr2 | 219452928 | ||||||
chr2:219453143
|
C | T | 285 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(282): Show | 301 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(298): Show |
intron_variant | MODIFIER | c.2440+1336C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/40 | chr2 | 219453143 | ||||||
chr2:219453220
|
T | G | 1 | a0003c0011t0001g0124 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2440+1413T>G | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/40 | chr2 | 219453220 | ||||||
chr2:219453295
|
C | T | 1 | a0001c0001t0001g0280 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.2440+1488C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/40 | chr2 | 219453295 | ||||||
chr2:219453589
|
C | T | 17 | a0002c0008t0002g0100a0002c0008t0002g0105a0002c0008t0002g0107others(14): Show | 17 | HG00642.hp1 HG00733.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.2440+1782C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/40 | chr2 | 219453589 | ||||||
chr2:219453720
|
G | A | 2 | a0001c0019t0001g0224a0001c0019t0001g0225 | 2 | NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2440+1913G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/40 | chr2 | 219453720 | ||||||
chr2:219453899
|
G | A | 1 | a0003c0011t0001g0124 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2440+2092G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/40 | chr2 | 219453899 | ||||||
chr2:219454082
|
T | C | 257 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(254): Show | 272 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(269): Show |
intron_variant | MODIFIER | c.2440+2275T>C | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/40 | chr2 | 219454082 | ||||||
chr2:219454157
|
T | G | 1 | a0044c0079t0002g0276 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2440+2350T>G | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/40 | chr2 | 219454157 | ||||||
chr2:219454269
|
G | C | 1 | a0001c0001t0001g0051 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.2440+2462G>C | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/40 | chr2 | 219454269 | ||||||
chr2:219454271
|
A | G | 1 | a0001c0001t0001g0051 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.2440+2464A>G | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/40 | chr2 | 219454271 | ||||||
chr2:219454549
|
G | A | 1 | a0008c0014t0003g0220 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2440+2742G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/40 | chr2 | 219454549 | ||||||
chr2:219454607
|
G | A | 1 | a0002c0004t0002g0185 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2440+2800G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/40 | chr2 | 219454607 | ||||||
chr2:219454759
|
G | A | 3 | a0002c0008t0002g0100a0002c0008t0002g0105a0002c0008t0002g0107 | 3 | HG00642.hp1 HG00733.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.2440+2952G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/40 | chr2 | 219454759 | ||||||
chr2:219455079
|
G | A | 1 | a0002c0004t0004g0024 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2440+3272G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/40 | chr2 | 219455079 | ||||||
chr2:219455140
|
C | G | 8 | a0001c0001t0001g0051a0001c0001t0001g0053a0001c0001t0001g0054others(5): Show | 8 | HG01123.hp1 HG01934.hp2 HG01978.hp2 others(5): Show |
intron_variant | MODIFIER | c.2440+3333C>G | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/40 | chr2 | 219455140 | ||||||
chr2:219455240
|
G | A | 1 | a0008c0014t0003g0220 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2440+3433G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/40 | chr2 | 219455240 | ||||||
chr2:219455259
|
T | G | 1 | a0001c0001t0001g0051 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.2440+3452T>G | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/40 | chr2 | 219455259 | ||||||
chr2:219455322
|
G | A | 113 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(110): Show | 124 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.2440+3515G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/40 | chr2 | 219455322 | ||||||
chr2:219455363
|
G | C | 8 | a0001c0001t0001g0051a0001c0001t0001g0053a0001c0001t0001g0054others(5): Show | 8 | HG01123.hp1 HG01934.hp2 HG01978.hp2 others(5): Show |
intron_variant | MODIFIER | c.2440+3556G>C | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/40 | chr2 | 219455363 | ||||||
chr2:219455461
|
T | A | 3 | a0001c0019t0001g0224a0001c0019t0001g0225a0039c0067t0001g0122 | 3 | HG02630.hp2 NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2440+3654T>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/40 | chr2 | 219455461 | ||||||
chr2:219455478
|
T | A | 3 | a0001c0019t0001g0224a0001c0019t0001g0225a0039c0067t0001g0122 | 3 | HG02630.hp2 NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2440+3671T>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/40 | chr2 | 219455478 | ||||||
chr2:219455627
|
C | T | 1 | a0003c0011t0001g0057 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.2440+3820C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/40 | chr2 | 219455627 | ||||||
chr2:219455676
|
C | T | 1 | a0001c0002t0001g0219 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2440+3869C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/40 | chr2 | 219455676 | ||||||
chr2:219455757
|
A | G | 5 | a0001c0002t0001g0104a0001c0002t0001g0192a0006c0007t0002g0050others(2): Show | 5 | HG00280.hp1 HG02622.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.2440+3950A>G | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/40 | chr2 | 219455757 | ||||||
chr2:219455845
|
C | A | 1 | a0043c0029t0002g0136 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2440+4038C>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/40 | chr2 | 219455845 | ||||||
chr2:219455968
|
C | T | 4 | a0001c0002t0001g0104a0001c0002t0001g0192a0021c0034t0001g0026others(1): Show | 4 | HG02622.hp1 HG02818.hp1 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.2440+4161C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/40 | chr2 | 219455968 | ||||||
chr2:219456051
|
G | A | 6 | a0001c0002t0002g0282a0002c0003t0002g0194a0007c0013t0001g0197others(3): Show | 6 | HG02109.hp2 HG02145.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.2440+4244G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/40 | chr2 | 219456051 | ||||||
chr2:219456163
|
C | T | 1 | a0002c0003t0002g0264 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.2440+4356C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/40 | chr2 | 219456163 | ||||||
chr2:219456378
|
C | T | 4 | a0001c0019t0001g0224a0001c0019t0001g0225a0002c0003t0002g0264others(1): Show | 4 | HG02630.hp2 NA19011.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.2440+4571C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/40 | chr2 | 219456378 | ||||||
chr2:219456514
|
C | T | 2 | a0007c0020t0002g0278a0007c0020t0002g0279 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2440+4707C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/40 | chr2 | 219456514 | ||||||
chr2:219456533
|
C | G | 2 | a0007c0020t0002g0278a0007c0020t0002g0279 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2440+4726C>G | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/40 | chr2 | 219456533 | ||||||
chr2:219456612
|
A | G | 18 | a0002c0008t0002g0100a0002c0008t0002g0105a0002c0008t0002g0107others(15): Show | 18 | HG00642.hp1 HG00733.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.2440+4805A>G | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/40 | chr2 | 219456612 | ||||||
chr2:219456656
|
T | C | 2 | a0006c0007t0002g0047a0006c0007t0002g0191 | 2 | HG00438.hp1 HG00673.hp1 |
intron_variant | MODIFIER | c.2440+4849T>C | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/40 | chr2 | 219456656 | ||||||
chr2:219456765
|
C | T | 1 | a0004c0016t0002g0181 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2440+4958C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/40 | chr2 | 219456765 | ||||||
chr2:219456864
|
A | G | 120 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(117): Show | 131 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.2441-5018A>G | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/40 | chr2 | 219456864 | ||||||
chr2:219456893
|
TGCGAGAC others(61): Show |
T | 113 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(110): Show | 124 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.2441-4988_2441-492 others(72): Show |
SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/40 | chr2 | 219456893 | ||||||
chr2:219456908
|
C | CA | 7 | a0002c0008t0002g0100a0002c0008t0002g0105a0002c0008t0002g0107others(4): Show | 7 | HG00642.hp1 HG00733.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.2441-4958dupA | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/40 | INFO_REALIGN_3_PRIME | chr2 | 219456908 | |||||
chr2:219456908
|
CA | C | 55 | a0001c0002t0001g0012a0001c0002t0001g0013a0001c0002t0001g0060others(52): Show | 59 | HG01109.hp1 HG01123.hp2 HG01257.hp1 others(56): Show |
intron_variant | MODIFIER | c.2441-4958delA | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/40 | INFO_REALIGN_3_PRIME | chr2 | 219456908 | |||||
chr2:219456936
|
G | GA | 17 | a0001c0002t0001g0231a0001c0002t0001g0246a0001c0002t0001g0247others(14): Show | 17 | HG01123.hp2 HG02145.hp1 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.2441-4938dupA | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/40 | INFO_REALIGN_3_PRIME | chr2 | 219456936 | |||||
chr2:219457041
|
C | T | 1 | a0002c0004t0002g0161 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2441-4841C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/40 | chr2 | 219457041 | ||||||
chr2:219457061
|
A | G | 1 | a0003c0005t0001g0070 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2441-4821A>G | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/40 | chr2 | 219457061 | ||||||
chr2:219457106
|
C | T | 3 | a0009c0015t0002g0221a0009c0015t0002g0223a0014c0022t0002g0222 | 3 | HG02258.hp1 HG02630.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.2441-4776C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/40 | chr2 | 219457106 | ||||||
chr2:219457702
|
G | C | 1 | a0016c0026t0002g0034 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2441-4180G>C | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/40 | chr2 | 219457702 | ||||||
chr2:219457736
|
G | A | 3 | a0002c0004t0002g0102a0002c0004t0002g0137a0029c0044t0002g0035 | 3 | HG02698.hp1 HG03017.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.2441-4146G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/40 | chr2 | 219457736 | ||||||
chr2:219457846
|
G | A | 1 | a0038c0043t0001g0182 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.2441-4036G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/40 | chr2 | 219457846 | ||||||
chr2:219457941
|
G | T | 3 | a0009c0015t0002g0221a0009c0015t0002g0223a0014c0022t0002g0222 | 3 | HG02258.hp1 HG02630.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.2441-3941G>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/40 | chr2 | 219457941 | ||||||
chr2:219457975
|
GC | G | 3 | a0001c0002t0001g0012a0001c0002t0001g0239a0048c0025t0001g0012 | 3 | HG01975.hp2 HG03471.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2441-3903delC | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/40 | INFO_REALIGN_3_PRIME | chr2 | 219457975 | |||||
chr2:219458010
|
T | C | 2 | a0001c0002t0001g0254a0026c0070t0003g0265 | 2 | HG02280.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2441-3872T>C | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/40 | chr2 | 219458010 | ||||||
chr2:219458018
|
G | A | 4 | a0001c0002t0001g0060a0001c0002t0001g0283a0001c0002t0001g0284others(1): Show | 4 | HG01257.hp1 HG02257.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.2441-3864G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/40 | chr2 | 219458018 | ||||||
chr2:219458198
|
C | T | 6 | a0001c0002t0001g0106a0001c0002t0002g0201a0001c0069t0001g0021others(3): Show | 6 | HG02055.hp2 HG02451.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.2441-3684C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/40 | chr2 | 219458198 | ||||||
chr2:219458376
|
A | T | 3 | a0001c0019t0001g0224a0001c0019t0001g0225a0039c0067t0001g0122 | 3 | HG02630.hp2 NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2441-3506A>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/40 | chr2 | 219458376 | ||||||
chr2:219458396
|
C | A | 1 | a0045c0084t0001g0022 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2441-3486C>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/40 | chr2 | 219458396 | ||||||
chr2:219458396
|
C | CT | 6 | a0001c0001t0001g0044a0003c0005t0001g0070a0009c0015t0002g0221others(3): Show | 6 | HG02258.hp1 HG02630.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.2441-3473dupT | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/40 | INFO_REALIGN_3_PRIME | chr2 | 219458396 | |||||
chr2:219458396
|
CT | C | 7 | a0002c0003t0002g0255a0005c0006t0002g0003a0005c0006t0002g0110others(4): Show | 9 | HG02451.hp1 HG02559.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.2441-3473delT | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/40 | INFO_REALIGN_3_PRIME | chr2 | 219458396 | |||||
chr2:219458760
|
C | T | 1 | a0001c0002t0001g0219 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2441-3122C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/40 | chr2 | 219458760 | ||||||
chr2:219459077
|
C | T | 4 | a0001c0002t0002g0201a0004c0009t0002g0227a0007c0013t0005g0074others(1): Show | 4 | HG01123.hp2 HG02572.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.2441-2805C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/40 | chr2 | 219459077 | ||||||
chr2:219459106
|
C | G | 9 | a0002c0008t0002g0212a0002c0008t0002g0213a0002c0008t0002g0214others(6): Show | 9 | HG01891.hp2 HG02055.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.2441-2776C>G | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/40 | chr2 | 219459106 | ||||||
chr2:219459430
|
C | A | 3 | a0009c0015t0002g0221a0009c0015t0002g0223a0014c0022t0002g0222 | 3 | HG02258.hp1 HG02630.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.2441-2452C>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/40 | chr2 | 219459430 | ||||||
chr2:219459503
|
C | G | 9 | a0002c0008t0002g0212a0002c0008t0002g0213a0002c0008t0002g0214others(6): Show | 9 | HG01891.hp2 HG02055.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.2441-2379C>G | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/40 | chr2 | 219459503 | ||||||
chr2:219459859
|
C | T | 1 | a0003c0005t0001g0187 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2441-2023C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/40 | chr2 | 219459859 | ||||||
chr2:219459927
|
C | T | 3 | a0001c0019t0001g0224a0001c0019t0001g0225a0039c0067t0001g0122 | 3 | HG02630.hp2 NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2441-1955C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/40 | chr2 | 219459927 | ||||||
chr2:219459934
|
C | T | 1 | a0001c0057t0002g0069 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2441-1948C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/40 | chr2 | 219459934 | ||||||
chr2:219460018
|
T | C | 1 | a0006c0058t0002g0285 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2441-1864T>C | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/40 | chr2 | 219460018 | ||||||
chr2:219460080
|
G | T | 7 | a0001c0002t0001g0104a0001c0002t0001g0192a0009c0015t0002g0221others(4): Show | 7 | HG02258.hp1 HG02622.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.2441-1802G>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/40 | chr2 | 219460080 | ||||||
chr2:219460136
|
T | C | 9 | a0001c0002t0001g0104a0001c0002t0001g0192a0007c0020t0002g0278others(6): Show | 9 | HG02258.hp1 HG02622.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.2441-1746T>C | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/40 | chr2 | 219460136 | ||||||
chr2:219460295
|
C | T | 1 | a0001c0002t0001g0120 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2441-1587C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/40 | chr2 | 219460295 | ||||||
chr2:219460357
|
G | A | 1 | a0002c0004t0002g0102 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2441-1525G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/40 | chr2 | 219460357 | ||||||
chr2:219460437
|
G | A | 4 | a0001c0002t0001g0104a0001c0002t0001g0192a0021c0034t0001g0026others(1): Show | 4 | HG02622.hp1 HG02818.hp1 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.2441-1445G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/40 | chr2 | 219460437 | ||||||
chr2:219460460
|
G | A | 2 | a0007c0013t0005g0074a0007c0013t0005g0200 | 2 | HG02572.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2441-1422G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/40 | chr2 | 219460460 | ||||||
chr2:219460523
|
G | A | 3 | a0001c0002t0001g0106a0001c0069t0001g0021a0049c0023t0001g0226 | 3 | HG02055.hp2 HG02451.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2441-1359G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/40 | chr2 | 219460523 | ||||||
chr2:219460653
|
C | T | 9 | a0002c0008t0002g0212a0002c0008t0002g0213a0002c0008t0002g0214others(6): Show | 9 | HG01891.hp2 HG02055.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.2441-1229C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/40 | chr2 | 219460653 | ||||||
chr2:219460687
|
C | T | 114 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(111): Show | 125 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.2441-1195C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/40 | chr2 | 219460687 | ||||||
chr2:219460806
|
C | G | 1 | a0001c0002t0001g0247 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2441-1076C>G | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/40 | chr2 | 219460806 | ||||||
chr2:219460916
|
G | A | 5 | a0002c0017t0001g0126a0002c0017t0001g0184a0002c0054t0001g0198others(2): Show | 5 | HG02965.hp1 HG02970.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.2441-966G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/40 | chr2 | 219460916 | ||||||
chr2:219461106
|
C | T | 1 | a0004c0009t0002g0229 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.2441-776C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/40 | chr2 | 219461106 | ||||||
chr2:219461146
|
G | C | 6 | a0001c0002t0002g0282a0002c0003t0002g0194a0007c0013t0001g0197others(3): Show | 6 | HG02109.hp2 HG02145.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.2441-736G>C | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/40 | chr2 | 219461146 | ||||||
chr2:219461325
|
G | A | 1 | a0004c0009t0002g0062 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.2441-557G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/40 | chr2 | 219461325 | ||||||
chr2:219461433
|
G | C | 1 | a0001c0002t0001g0013 | 2 | HG02109.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2441-449G>C | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/40 | chr2 | 219461433 | ||||||
chr2:219461456
|
C | T | 3 | a0009c0015t0002g0221a0009c0015t0002g0223a0014c0022t0002g0222 | 3 | HG02258.hp1 HG02630.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.2441-426C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/40 | chr2 | 219461456 | ||||||
chr2:219461773
|
G | A | 1 | a0003c0005t0001g0187 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2441-109G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 6/40 | chr2 | 219461773 | ||||||
chr2:219462223
|
G | A | 1 | a0019c0032t0001g0020 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2617-75G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 7/40 | chr2 | 219462223 | ||||||
chr2:219462396
|
C | T | 1 | a0001c0069t0001g0021 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2705+10C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 8/40 | chr2 | 219462396 | ||||||
chr2:219462420
|
A | G | 4 | a0001c0002t0001g0104a0001c0002t0001g0192a0021c0034t0001g0026others(1): Show | 4 | HG02622.hp1 HG02818.hp1 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.2705+34A>G | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 8/40 | chr2 | 219462420 | ||||||
chr2:219462426
|
T | C | 2 | a0007c0020t0002g0278a0007c0020t0002g0279 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2705+40T>C | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 8/40 | chr2 | 219462426 | ||||||
chr2:219462479
|
G | A | 1 | a0001c0002t0001g0060 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.2705+93G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 8/40 | chr2 | 219462479 | ||||||
chr2:219462494
|
G | A | 4 | a0001c0002t0001g0104a0001c0002t0001g0192a0021c0034t0001g0026others(1): Show | 4 | HG02622.hp1 HG02818.hp1 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.2705+108G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 8/40 | chr2 | 219462494 | ||||||
chr2:219462540
|
C | T | 102 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(99): Show | 113 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.2705+154C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 8/40 | chr2 | 219462540 | ||||||
chr2:219462596
|
G | C | 1 | a0004c0080t0002g0036 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2705+210G>C | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 8/40 | chr2 | 219462596 | ||||||
chr2:219462598
|
G | A | 1 | a0001c0057t0002g0069 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2705+212G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 8/40 | chr2 | 219462598 | ||||||
chr2:219462613
|
T | G | 3 | a0001c0002t0001g0106a0001c0069t0001g0021a0049c0023t0001g0226 | 3 | HG02055.hp2 HG02451.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2705+227T>G | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 8/40 | chr2 | 219462613 | ||||||
chr2:219462712
|
T | C | 2 | a0007c0020t0002g0278a0007c0020t0002g0279 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2705+326T>C | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 8/40 | chr2 | 219462712 | ||||||
chr2:219463392
|
A | AT | 46 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0001g0042others(43): Show | 46 | HG00438.hp1 HG00438.hp2 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.2706-1003dupT | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 8/40 | INFO_REALIGN_3_PRIME | chr2 | 219463392 | |||||
chr2:219463392
|
A | ATT | 28 | a0001c0001t0001g0004a0001c0001t0001g0031a0001c0001t0001g0044others(25): Show | 31 | HG00609.hp2 HG00673.hp1 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.2706-1004_2706-100 others(6): Show |
SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 8/40 | INFO_REALIGN_3_PRIME | chr2 | 219463392 | |||||
chr2:219463392
|
A | ATTT | 12 | a0001c0001t0001g0032a0001c0001t0001g0158a0002c0004t0002g0102others(9): Show | 12 | HG00673.hp2 HG00733.hp2 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.2706-1005_2706-100 others(7): Show |
SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 8/40 | INFO_REALIGN_3_PRIME | chr2 | 219463392 | |||||
chr2:219463392
|
A | ATTTT | 9 | a0001c0001t0001g0125a0001c0001t0001g0163a0001c0001t0001g0166others(6): Show | 9 | HG02896.hp1 HG02896.hp2 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.2706-1006_2706-100 others(8): Show |
SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 8/40 | INFO_REALIGN_3_PRIME | chr2 | 219463392 | |||||
chr2:219463392
|
A | ATTTTT | 7 | a0001c0001t0001g0180a0002c0003t0002g0210a0002c0004t0002g0052others(4): Show | 7 | HG01952.hp1 HG02145.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.2706-1007_2706-100 others(9): Show |
SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 8/40 | INFO_REALIGN_3_PRIME | chr2 | 219463392 | |||||
chr2:219463392
|
A | ATTTTTTT others(3): Show |
5 | a0002c0004t0004g0159a0002c0004t0004g0160a0006c0007t0002g0059others(2): Show | 5 | HG02895.hp2 HG03654.hp2 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.2706-1012_2706-100 others(14): Show |
SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 8/40 | INFO_REALIGN_3_PRIME | chr2 | 219463392 | |||||
chr2:219463392
|
A | ATTTTTTT others(4): Show |
2 | a0001c0001t0001g0058a0007c0020t0002g0279 | 2 | HG02897.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.2706-1013_2706-100 others(15): Show |
SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 8/40 | INFO_REALIGN_3_PRIME | chr2 | 219463392 | |||||
chr2:219463392
|
AT | A | 44 | a0001c0001t0001g0033a0001c0001t0001g0173a0001c0002t0001g0072others(41): Show | 47 | HG00280.hp1 HG00642.hp1 HG00738.hp1 others(44): Show |
intron_variant | MODIFIER | c.2706-1003delT | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 8/40 | INFO_REALIGN_3_PRIME | chr2 | 219463392 | |||||
chr2:219463392
|
ATT | A | 48 | a0001c0002t0001g0066a0001c0002t0001g0084a0001c0002t0001g0113others(45): Show | 49 | HG00639.hp1 HG00733.hp1 HG00738.hp2 others(46): Show |
intron_variant | MODIFIER | c.2706-1004_2706-100 others(6): Show |
SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 8/40 | INFO_REALIGN_3_PRIME | chr2 | 219463392 | |||||
chr2:219463392
|
ATTT | A | 8 | a0001c0002t0001g0257a0002c0003t0002g0266a0003c0005t0001g0086others(5): Show | 8 | HG01168.hp2 HG01993.hp2 HG02129.hp1 others(5): Show |
intron_variant | MODIFIER | c.2706-1005_2706-100 others(7): Show |
SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 8/40 | INFO_REALIGN_3_PRIME | chr2 | 219463392 | |||||
chr2:219463392
|
ATTTTTTT others(3): Show |
A | 8 | a0001c0001t0001g0007a0001c0001t0001g0039a0001c0002t0001g0104others(5): Show | 9 | HG00741.hp2 HG01069.hp2 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.2706-1012_2706-100 others(14): Show |
SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 8/40 | INFO_REALIGN_3_PRIME | chr2 | 219463392 | |||||
chr2:219463392
|
ATTTTTTT others(4): Show |
A | 6 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0010others(3): Show | 13 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(10): Show |
intron_variant | MODIFIER | c.2706-1013_2706-100 others(15): Show |
SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 8/40 | INFO_REALIGN_3_PRIME | chr2 | 219463392 | |||||
chr2:219463392
|
ATTTTTTT others(5): Show |
A | 1 | a0003c0005t0001g0076 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.2706-1014_2706-100 others(16): Show |
SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 8/40 | INFO_REALIGN_3_PRIME | chr2 | 219463392 | |||||
chr2:219463392
|
ATTTTTTT others(6): Show |
A | 1 | a0001c0002t0001g0080 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.2706-1015_2706-100 others(17): Show |
SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 8/40 | INFO_REALIGN_3_PRIME | chr2 | 219463392 | |||||
chr2:219463392
|
ATTTTTTT others(7): Show |
A | 4 | a0001c0002t0001g0012a0001c0002t0001g0239a0002c0003t0002g0097others(1): Show | 4 | HG01975.hp2 HG03471.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2706-1016_2706-100 others(18): Show |
SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 8/40 | INFO_REALIGN_3_PRIME | chr2 | 219463392 | |||||
chr2:219463392
|
ATTTTTTT others(8): Show |
A | 1 | a0002c0048t0004g0139 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2706-1017_2706-100 others(19): Show |
SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 8/40 | INFO_REALIGN_3_PRIME | chr2 | 219463392 | |||||
chr2:219463392
|
ATTTTTTT others(12): Show |
A | 1 | a0003c0005t0001g0075 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2706-1021_2706-100 others(23): Show |
SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 8/40 | INFO_REALIGN_3_PRIME | chr2 | 219463392 | |||||
chr2:219463430
|
T | A | 6 | a0001c0002t0002g0282a0002c0003t0002g0194a0007c0013t0001g0197others(3): Show | 6 | HG02109.hp2 HG02145.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.2706-1003T>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 8/40 | chr2 | 219463430 | ||||||
chr2:219463480
|
C | G | 1 | a0001c0076t0001g0103 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2706-953C>G | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 8/40 | chr2 | 219463480 | ||||||
chr2:219463604
|
G | A | 3 | a0001c0002t0001g0106a0001c0069t0001g0021a0049c0023t0001g0226 | 3 | HG02055.hp2 HG02451.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2706-829G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 8/40 | chr2 | 219463604 | ||||||
chr2:219463612
|
G | A | 1 | a0001c0002t0001g0219 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2706-821G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 8/40 | chr2 | 219463612 | ||||||
chr2:219463658
|
G | A | 5 | a0001c0002t0001g0129a0001c0002t0001g0188a0025c0071t0001g0023others(2): Show | 5 | HG01884.hp1 HG01884.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.2706-775G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 8/40 | chr2 | 219463658 | ||||||
chr2:219463919
|
C | T | 9 | a0002c0008t0002g0212a0002c0008t0002g0213a0002c0008t0002g0214others(6): Show | 9 | HG01891.hp2 HG02055.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.2706-514C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 8/40 | chr2 | 219463919 | ||||||
chr2:219463940
|
G | A | 3 | a0009c0015t0002g0221a0009c0015t0002g0223a0014c0022t0002g0222 | 3 | HG02258.hp1 HG02630.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.2706-493G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 8/40 | chr2 | 219463940 | ||||||
chr2:219464037
|
G | A | 1 | a0003c0005t0001g0088 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2706-396G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 8/40 | chr2 | 219464037 | ||||||
chr2:219464121
|
T | TA | 10 | a0001c0019t0001g0224a0001c0019t0001g0225a0001c0066t0001g0089others(7): Show | 10 | HG02148.hp2 HG02559.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.2706-296dupA | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 8/40 | INFO_REALIGN_3_PRIME | chr2 | 219464121 | |||||
chr2:219464121
|
TA | T | 12 | a0001c0001t0001g0156a0001c0002t0001g0250a0002c0004t0002g0137others(9): Show | 12 | HG01074.hp2 HG01109.hp1 HG01993.hp2 others(9): Show |
intron_variant | MODIFIER | c.2706-296delA | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 8/40 | INFO_REALIGN_3_PRIME | chr2 | 219464121 | |||||
chr2:219464155
|
A | C | 1 | a0002c0003t0002g0275 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2706-278A>C | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 8/40 | chr2 | 219464155 | ||||||
chr2:219464366
|
G | A | 3 | a0009c0015t0002g0221a0009c0015t0002g0223a0014c0022t0002g0222 | 3 | HG02258.hp1 HG02630.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.2706-67G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 8/40 | chr2 | 219464366 | ||||||
chr2:219464384
|
G | A | 4 | a0001c0002t0001g0104a0001c0002t0001g0192a0021c0034t0001g0026others(1): Show | 4 | HG02622.hp1 HG02818.hp1 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.2706-49G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 8/40 | chr2 | 219464384 | ||||||
chr2:219464851
|
G | T | 1 | a0001c0002t0001g0219 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2881+243G>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 9/40 | chr2 | 219464851 | ||||||
chr2:219464975
|
C | A | 4 | a0001c0002t0001g0104a0001c0002t0001g0192a0021c0034t0001g0026others(1): Show | 4 | HG02622.hp1 HG02818.hp1 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.2881+367C>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 9/40 | chr2 | 219464975 | ||||||
chr2:219464975
|
C | T | 120 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(117): Show | 131 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.2881+367C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 9/40 | chr2 | 219464975 | ||||||
chr2:219464979
|
C | T | 4 | a0001c0002t0001g0060a0001c0002t0001g0283a0001c0002t0001g0284others(1): Show | 4 | HG01257.hp1 HG02257.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.2881+371C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 9/40 | chr2 | 219464979 | ||||||
chr2:219465109
|
A | G | 4 | a0002c0004t0001g0016a0017c0027t0001g0018a0024c0047t0001g0017others(1): Show | 4 | HG02559.hp2 HG02965.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2881+501A>G | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 9/40 | chr2 | 219465109 | ||||||
chr2:219465137
|
A | C | 1 | a0002c0004t0002g0185 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2881+529A>C | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 9/40 | chr2 | 219465137 | ||||||
chr2:219465219
|
C | T | 6 | a0001c0002t0001g0207a0002c0003t0002g0206a0002c0003t0002g0208others(3): Show | 6 | HG02145.hp2 HG02717.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.2881+611C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 9/40 | chr2 | 219465219 | ||||||
chr2:219465308
|
A | G | 3 | a0001c0019t0001g0224a0001c0019t0001g0225a0039c0067t0001g0122 | 3 | HG02630.hp2 NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2881+700A>G | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 9/40 | chr2 | 219465308 | ||||||
chr2:219465317
|
C | T | 1 | a0001c0001t0001g0131 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.2881+709C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 9/40 | chr2 | 219465317 | ||||||
chr2:219465469
|
G | C | 6 | a0001c0002t0001g0207a0002c0003t0002g0206a0002c0003t0002g0208others(3): Show | 6 | HG02145.hp2 HG02717.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.2881+861G>C | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 9/40 | chr2 | 219465469 | ||||||
chr2:219465596
|
G | C | 6 | a0001c0002t0001g0207a0002c0003t0002g0206a0002c0003t0002g0208others(3): Show | 6 | HG02145.hp2 HG02717.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.2881+988G>C | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 9/40 | chr2 | 219465596 | ||||||
chr2:219465688
|
G | A | 1 | a0001c0002t0001g0106 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2881+1080G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 9/40 | chr2 | 219465688 | ||||||
chr2:219465810
|
T | C | 104 | a0001c0002t0001g0066a0001c0002t0001g0072a0001c0002t0001g0080others(101): Show | 108 | HG00609.hp1 HG00639.hp1 HG00642.hp1 others(105): Show |
intron_variant | MODIFIER | c.2881+1202T>C | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 9/40 | chr2 | 219465810 | ||||||
chr2:219465860
|
TGTGTGTG others(1): Show |
T | 6 | a0001c0002t0001g0207a0002c0003t0002g0206a0002c0003t0002g0208others(3): Show | 6 | HG02145.hp2 HG02717.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.2881+1264_2881+127 others(12): Show |
SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 9/40 | INFO_REALIGN_3_PRIME | chr2 | 219465860 | |||||
chr2:219465894
|
C | T | 97 | a0001c0002t0001g0066a0001c0002t0001g0072a0001c0002t0001g0080others(94): Show | 101 | HG00609.hp1 HG00639.hp1 HG00738.hp2 others(98): Show |
intron_variant | MODIFIER | c.2882-1280C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 9/40 | chr2 | 219465894 | ||||||
chr2:219465900
|
GGTGTGTG others(5): Show |
G | 1 | a0002c0004t0004g0024 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2882-1266_2882-125 others(16): Show |
SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 9/40 | INFO_REALIGN_3_PRIME | chr2 | 219465900 | |||||
chr2:219465922
|
TGCGCGCG others(5): Show |
T | 96 | a0001c0002t0001g0066a0001c0002t0001g0072a0001c0002t0001g0080others(93): Show | 100 | HG00609.hp1 HG00639.hp1 HG00642.hp1 others(97): Show |
intron_variant | MODIFIER | c.2882-1250_2882-123 others(16): Show |
SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 9/40 | INFO_REALIGN_3_PRIME | chr2 | 219465922 | |||||
chr2:219465924
|
C | T | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(135): Show | 149 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.2882-1250C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 9/40 | chr2 | 219465924 | ||||||
chr2:219465925
|
GCGCGTGT others(7): Show |
G | 6 | a0001c0077t0001g0241a0003c0005t0001g0086a0003c0005t0001g0087others(3): Show | 6 | HG00738.hp2 HG01243.hp1 HG01993.hp2 others(3): Show |
intron_variant | MODIFIER | c.2882-1246_2882-123 others(18): Show |
SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 9/40 | INFO_REALIGN_3_PRIME | chr2 | 219465925 | |||||
chr2:219465927
|
GCGTGTGC others(5): Show |
G | 2 | a0001c0002t0001g0106a0018c0028t0001g0240 | 2 | HG03486.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2882-1234_2882-122 others(16): Show |
SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 9/40 | INFO_REALIGN_3_PRIME | chr2 | 219465927 | |||||
chr2:219465928
|
C | CGTGTGCG others(17): Show |
1 | a0002c0004t0002g0137 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2882-1236_2882-123 others(28): Show |
SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 9/40 | INFO_REALIGN_3_PRIME | chr2 | 219465928 | |||||
chr2:219465928
|
CGTGTGCG others(17): Show |
C | 2 | a0021c0034t0001g0026a0022c0033t0002g0025 | 2 | HG02622.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.2882-1236_2882-121 others(28): Show |
SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 9/40 | INFO_REALIGN_3_PRIME | chr2 | 219465928 | |||||
chr2:219465929
|
G | A | 1 | a0001c0010t0001g0203 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2882-1245G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 9/40 | chr2 | 219465929 | ||||||
chr2:219465939
|
A | G | 247 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(244): Show | 262 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(259): Show |
intron_variant | MODIFIER | c.2882-1235A>G | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 9/40 | chr2 | 219465939 | ||||||
chr2:219465940
|
C | T | 1 | a0001c0019t0001g0224 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2882-1234C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 9/40 | chr2 | 219465940 | ||||||
chr2:219465941
|
G | A | 3 | a0001c0002t0001g0135a0001c0002t0001g0242a0001c0002t0010g0127 | 3 | HG02027.hp2 NA19054.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.2882-1233G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 9/40 | chr2 | 219465941 | ||||||
chr2:219465993
|
G | A | 1 | a0001c0002t0001g0283 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2882-1181G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 9/40 | chr2 | 219465993 | ||||||
chr2:219466002
|
C | T | 110 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(107): Show | 121 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.2882-1172C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 9/40 | chr2 | 219466002 | ||||||
chr2:219466082
|
T | C | 127 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(124): Show | 138 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.2882-1092T>C | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 9/40 | chr2 | 219466082 | ||||||
chr2:219466109
|
G | A | 1 | a0037c0040t0001g0037 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2882-1065G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 9/40 | chr2 | 219466109 | ||||||
chr2:219466183
|
C | G | 1 | a0002c0074t0002g0211 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2882-991C>G | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 9/40 | chr2 | 219466183 | ||||||
chr2:219466254
|
C | A | 109 | a0001c0002t0001g0066a0001c0002t0001g0072a0001c0002t0001g0080others(106): Show | 113 | HG00609.hp1 HG00639.hp1 HG00642.hp1 others(110): Show |
intron_variant | MODIFIER | c.2882-920C>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 9/40 | chr2 | 219466254 | ||||||
chr2:219466295
|
G | A | 2 | a0002c0004t0001g0016a0024c0047t0001g0017 | 2 | HG02559.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2882-879G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 9/40 | chr2 | 219466295 | ||||||
chr2:219466646
|
T | C | 1 | a0001c0001t0001g0174 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.2882-528T>C | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 9/40 | chr2 | 219466646 | ||||||
chr2:219466776
|
G | A | 2 | a0007c0020t0002g0278a0007c0020t0002g0279 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2882-398G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 9/40 | chr2 | 219466776 | ||||||
chr2:219466805
|
C | T | 4 | a0001c0002t0001g0104a0001c0002t0001g0192a0021c0034t0001g0026others(1): Show | 4 | HG02622.hp1 HG02818.hp1 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.2882-369C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 9/40 | chr2 | 219466805 | ||||||
chr2:219466876
|
G | GT | 242 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(239): Show | 257 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(254): Show |
intron_variant | MODIFIER | c.2882-289dupT | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 9/40 | INFO_REALIGN_3_PRIME | chr2 | 219466876 | |||||
chr2:219466876
|
G | GTT | 6 | a0001c0001t0001g0043a0001c0002t0001g0135a0002c0008t0002g0100others(3): Show | 6 | HG00642.hp1 HG02970.hp2 HG03927.hp2 others(3): Show |
intron_variant | MODIFIER | c.2882-290_2882-289d others(4): Show |
SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 9/40 | INFO_REALIGN_3_PRIME | chr2 | 219466876 | |||||
chr2:219466975
|
A | C | 1 | a0002c0003t0002g0266 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.2882-199A>C | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 9/40 | chr2 | 219466975 | ||||||
chr2:219467548
|
G | A | 1 | a0001c0001t0001g0045 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.3142+114G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 10/40 | chr2 | 219467548 | ||||||
chr2:219467580
|
C | A | 4 | a0001c0002t0001g0104a0001c0002t0001g0192a0021c0034t0001g0026others(1): Show | 4 | HG02622.hp1 HG02818.hp1 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.3142+146C>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 10/40 | chr2 | 219467580 | ||||||
chr2:219467733
|
C | G | 116 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(113): Show | 127 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.3142+299C>G | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 10/40 | chr2 | 219467733 | ||||||
chr2:219467812
|
G | T | 1 | a0001c0002t0001g0219 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3142+378G>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 10/40 | chr2 | 219467812 | ||||||
chr2:219468017
|
C | T | 1 | a0001c0001t0001g0152 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.3143-561C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 10/40 | chr2 | 219468017 | ||||||
chr2:219468425
|
A | G | 1 | a0001c0002t0001g0269 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.3143-153A>G | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 10/40 | chr2 | 219468425 | ||||||
chr2:219468427
|
C | T | 3 | a0001c0019t0001g0224a0001c0019t0001g0225a0039c0067t0001g0122 | 3 | HG02630.hp2 NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.3143-151C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 10/40 | chr2 | 219468427 | ||||||
chr2:219468740
|
C | T | 6 | a0001c0002t0001g0207a0002c0003t0002g0206a0002c0003t0002g0208others(3): Show | 6 | HG02145.hp2 HG02717.hp2 HG02896.hp1 others(3): Show |
splice_region_variant&intron_variant | LOW | c.3301+4C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 11/40 | chr2 | 219468740 | ||||||
chr2:219469383
|
C | T | 1 | a0021c0034t0001g0026 | 1 | HG02818.hp1 | splice_region_variant&intron_variant | LOW | c.3715+4C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 13/40 | chr2 | 219469383 | ||||||
chr2:219469744
|
G | C | 1 | a0008c0014t0003g0220 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3715+365G>C | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 13/40 | chr2 | 219469744 | ||||||
chr2:219469916
|
C | T | 1 | a0031c0030t0002g0218 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.3715+537C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 13/40 | chr2 | 219469916 | ||||||
chr2:219470099
|
G | A | 115 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(112): Show | 119 | HG00609.hp1 HG00639.hp1 HG00642.hp1 others(116): Show |
intron_variant | MODIFIER | c.3715+720G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 13/40 | chr2 | 219470099 | ||||||
chr2:219470122
|
T | C | 276 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(273): Show | 292 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(289): Show |
intron_variant | MODIFIER | c.3715+743T>C | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 13/40 | chr2 | 219470122 | ||||||
chr2:219470300
|
TGCCCA | T | 70 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0150others(67): Show | 71 | HG00438.hp1 HG00733.hp1 HG00738.hp2 others(68): Show |
intron_variant | MODIFIER | c.3715+924_3715+928d others(7): Show |
SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 13/40 | INFO_REALIGN_3_PRIME | chr2 | 219470300 | |||||
chr2:219470303
|
CCAGCT | C | 20 | a0001c0002t0001g0012a0001c0002t0001g0188a0001c0002t0001g0231others(17): Show | 23 | HG01884.hp1 HG01975.hp2 HG02280.hp1 others(20): Show |
intron_variant | MODIFIER | c.3715+926_3715+930d others(7): Show |
SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 13/40 | INFO_REALIGN_3_PRIME | chr2 | 219470303 | |||||
chr2:219470339
|
G | A | 143 | a0001c0001t0001g0004a0001c0001t0001g0031a0001c0001t0001g0032others(140): Show | 148 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(145): Show |
intron_variant | MODIFIER | c.3715+960G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 13/40 | chr2 | 219470339 | ||||||
chr2:219470378
|
G | A | 5 | a0001c0001t0001g0153a0001c0002t0001g0113a0002c0003t0002g0275others(2): Show | 5 | HG01891.hp1 HG02738.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.3715+999G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 13/40 | chr2 | 219470378 | ||||||
chr2:219470472
|
T | TG | 16 | a0001c0002t0001g0219a0001c0002t0002g0282a0002c0017t0001g0126others(13): Show | 16 | HG02109.hp2 HG02145.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.3715+1094dupG | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 13/40 | INFO_REALIGN_3_PRIME | chr2 | 219470472 | |||||
chr2:219470487
|
G | A | 1 | a0004c0009t0002g0061 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.3715+1108G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 13/40 | chr2 | 219470487 | ||||||
chr2:219470491
|
C | A | 1 | a0002c0003t0005g0099 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3715+1112C>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 13/40 | chr2 | 219470491 | ||||||
chr2:219470526
|
G | A | 1 | a0001c0001t0001g0153 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.3715+1147G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 13/40 | chr2 | 219470526 | ||||||
chr2:219470749
|
C | T | 1 | a0025c0071t0001g0023 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3716-1119C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 13/40 | chr2 | 219470749 | ||||||
chr2:219470823
|
A | T | 2 | a0001c0001t0001g0174a0001c0001t0001g0180 | 2 | HG01952.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.3716-1045A>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 13/40 | chr2 | 219470823 | ||||||
chr2:219470825
|
A | T | 2 | a0001c0001t0001g0174a0001c0001t0001g0180 | 2 | HG01952.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.3716-1043A>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 13/40 | chr2 | 219470825 | ||||||
chr2:219470828
|
G | T | 2 | a0001c0001t0001g0174a0001c0001t0001g0180 | 2 | HG01952.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.3716-1040G>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 13/40 | chr2 | 219470828 | ||||||
chr2:219470931
|
T | G | 1 | a0001c0002t0002g0201 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3716-937T>G | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 13/40 | chr2 | 219470931 | ||||||
chr2:219470948
|
T | TTACTGTG others(9): Show |
97 | a0001c0001t0001g0166a0001c0077t0001g0241a0002c0003t0002g0005others(94): Show | 101 | HG00609.hp1 HG00639.hp1 HG00642.hp1 others(98): Show |
intron_variant | MODIFIER | c.3716-910_3716-909i others(18): Show |
SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 13/40 | INFO_REALIGN_3_PRIME | chr2 | 219470948 | |||||
chr2:219470997
|
G | A | 4 | a0002c0004t0004g0024a0002c0004t0004g0159a0002c0004t0004g0160others(1): Show | 4 | HG03017.hp1 HG03239.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.3716-871G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 13/40 | chr2 | 219470997 | ||||||
chr2:219471067
|
G | A | 102 | a0001c0077t0001g0241a0002c0003t0002g0005a0002c0003t0002g0014others(99): Show | 106 | HG00609.hp1 HG00639.hp1 HG00642.hp1 others(103): Show |
intron_variant | MODIFIER | c.3716-801G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 13/40 | chr2 | 219471067 | ||||||
chr2:219471117
|
G | T | 2 | a0002c0004t0002g0171a0002c0004t0002g0190 | 2 | HG00741.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.3716-751G>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 13/40 | chr2 | 219471117 | ||||||
chr2:219471143
|
A | G | 1 | a0019c0032t0001g0020 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.3716-725A>G | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 13/40 | chr2 | 219471143 | ||||||
chr2:219471692
|
C | T | 1 | a0006c0058t0002g0285 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3716-176C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 13/40 | chr2 | 219471692 | ||||||
chr2:219471736
|
T | C | 3 | a0006c0058t0002g0285a0031c0030t0002g0218a0047c0082t0002g0117 | 3 | HG02647.hp2 HG02970.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.3716-132T>C | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 13/40 | chr2 | 219471736 | ||||||
chr2:219471795
|
C | T | 101 | a0001c0077t0001g0241a0002c0003t0002g0005a0002c0003t0002g0014others(98): Show | 105 | HG00609.hp1 HG00639.hp1 HG00642.hp1 others(102): Show |
intron_variant | MODIFIER | c.3716-73C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 13/40 | chr2 | 219471795 | ||||||
chr2:219472001
|
C | T | 66 | a0001c0077t0001g0241a0002c0003t0002g0005a0002c0003t0002g0014others(63): Show | 70 | HG00609.hp1 HG00642.hp1 HG00733.hp1 others(67): Show |
intron_variant | MODIFIER | c.3835+14C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 14/40 | chr2 | 219472001 | ||||||
chr2:219472042
|
C | T | 1 | a0003c0011t0001g0157 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.3835+55C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 14/40 | chr2 | 219472042 | ||||||
chr2:219472118
|
T | A | 1 | a0001c0001t0001g0125 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.3836-109T>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 14/40 | chr2 | 219472118 | ||||||
chr2:219472141
|
G | A | 14 | a0004c0009t0002g0061a0004c0009t0002g0062a0004c0009t0002g0063others(11): Show | 14 | HG01123.hp2 HG01981.hp2 HG02027.hp1 others(11): Show |
intron_variant | MODIFIER | c.3836-86G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 14/40 | chr2 | 219472141 | ||||||
chr2:219472189
|
C | G | 1 | a0026c0070t0003g0265 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3836-38C>G | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 14/40 | chr2 | 219472189 | ||||||
chr2:219472423
|
G | A | 1 | a0008c0061t0003g0238 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3940+92G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 15/40 | chr2 | 219472423 | ||||||
chr2:219472474
|
G | A | 126 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(123): Show | 137 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.3940+143G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 15/40 | chr2 | 219472474 | ||||||
chr2:219472616
|
C | A | 1 | a0001c0001t0001g0044 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.3941-274C>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 15/40 | chr2 | 219472616 | ||||||
chr2:219472620
|
C | T | 1 | a0004c0012t0002g0236 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.3941-270C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 15/40 | chr2 | 219472620 | ||||||
chr2:219472756
|
G | A | 2 | a0008c0014t0003g0108a0008c0014t0003g0109 | 2 | HG02886.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.3941-134G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 15/40 | chr2 | 219472756 | ||||||
chr2:219472885
|
G | A | 1 | a0012c0018t0001g0008 | 2 | HG02015.hp2 HG02071.hp1 |
splice_region_variant&intron_variant | LOW | c.3941-5G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 15/40 | chr2 | 219472885 | ||||||
chr2:219473214
|
C | T | 2 | a0001c0002t0001g0231a0001c0002t0001g0232 | 2 | HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.4147+118C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 16/40 | chr2 | 219473214 | ||||||
chr2:219473343
|
T | C | 114 | a0001c0077t0001g0241a0002c0003t0002g0005a0002c0003t0002g0014others(111): Show | 118 | HG00280.hp1 HG00438.hp1 HG00609.hp1 others(115): Show |
intron_variant | MODIFIER | c.4148-161T>C | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 16/40 | chr2 | 219473343 | ||||||
chr2:219473355
|
C | A | 5 | a0001c0002t0002g0282a0007c0013t0001g0197a0007c0013t0006g0195others(2): Show | 5 | HG02109.hp2 HG02145.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.4148-149C>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 16/40 | chr2 | 219473355 | ||||||
chr2:219473367
|
C | T | 1 | a0002c0008t0002g0212 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.4148-137C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 16/40 | chr2 | 219473367 | ||||||
chr2:219473691
|
C | T | 1 | a0019c0032t0001g0020 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.4272-37C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 17/40 | chr2 | 219473691 | ||||||
chr2:219474170
|
G | T | 14 | a0004c0009t0002g0061a0004c0009t0002g0062a0004c0009t0002g0063others(11): Show | 14 | HG01123.hp2 HG01981.hp2 HG02027.hp1 others(11): Show |
intron_variant | MODIFIER | c.4447+267G>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 18/40 | chr2 | 219474170 | ||||||
chr2:219474195
|
T | C | 1 | a0002c0003t0002g0077 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.4447+292T>C | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 18/40 | chr2 | 219474195 | ||||||
chr2:219474207
|
A | G | 12 | a0006c0007t0002g0040a0006c0007t0002g0047a0006c0007t0002g0050others(9): Show | 12 | HG00280.hp1 HG00438.hp1 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.4447+304A>G | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 18/40 | chr2 | 219474207 | ||||||
chr2:219474345
|
G | A | 2 | a0002c0004t0002g0162a0016c0026t0002g0034 | 2 | HG03654.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.4447+442G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 18/40 | chr2 | 219474345 | ||||||
chr2:219474378
|
CA | C | 112 | a0001c0001t0001g0280a0001c0077t0001g0241a0002c0003t0002g0005others(109): Show | 116 | HG00609.hp1 HG00639.hp1 HG00642.hp1 others(113): Show |
intron_variant | MODIFIER | c.4447+494delA | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 18/40 | INFO_REALIGN_3_PRIME | chr2 | 219474378 | |||||
chr2:219474378
|
CAAA | C | 13 | a0004c0009t0002g0061a0004c0009t0002g0062a0004c0009t0002g0227others(10): Show | 13 | HG01123.hp2 HG01981.hp2 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.4447+492_4447+494d others(5): Show |
SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 18/40 | INFO_REALIGN_3_PRIME | chr2 | 219474378 | |||||
chr2:219474744
|
C | T | 126 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(123): Show | 137 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.4447+841C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 18/40 | chr2 | 219474744 | ||||||
chr2:219474795
|
CT | C | 19 | a0001c0001t0001g0038a0001c0001t0001g0054a0001c0002t0001g0135others(16): Show | 19 | HG00741.hp1 HG01123.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.4447+912delT | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 18/40 | INFO_REALIGN_3_PRIME | chr2 | 219474795 | |||||
chr2:219474795
|
CTT | C | 209 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(206): Show | 224 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(221): Show |
intron_variant | MODIFIER | c.4447+911_4447+912d others(4): Show |
SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 18/40 | INFO_REALIGN_3_PRIME | chr2 | 219474795 | |||||
chr2:219474881
|
C | T | 1 | a0001c0002t0001g0188 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.4447+978C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 18/40 | chr2 | 219474881 | ||||||
chr2:219475037
|
G | A | 1 | a0024c0047t0001g0017 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.4447+1134G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 18/40 | chr2 | 219475037 | ||||||
chr2:219475074
|
C | T | 2 | a0001c0002t0001g0188a0001c0002t0001g0239 | 2 | HG01884.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.4447+1171C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 18/40 | chr2 | 219475074 | ||||||
chr2:219475081
|
G | T | 1 | a0002c0008t0002g0212 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.4447+1178G>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 18/40 | chr2 | 219475081 | ||||||
chr2:219475292
|
C | T | 38 | a0001c0002t0001g0013a0001c0002t0001g0106a0001c0002t0001g0207others(35): Show | 39 | HG01123.hp2 HG01981.hp2 HG02027.hp1 others(36): Show |
intron_variant | MODIFIER | c.4447+1389C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 18/40 | chr2 | 219475292 | ||||||
chr2:219475514
|
G | A | 1 | a0001c0001t0001g0146 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.4448-1356G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 18/40 | chr2 | 219475514 | ||||||
chr2:219475576
|
T | C | 1 | a0001c0002t0001g0106 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.4448-1294T>C | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 18/40 | chr2 | 219475576 | ||||||
chr2:219475631
|
C | A | 1 | a0002c0003t0002g0262 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.4448-1239C>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 18/40 | chr2 | 219475631 | ||||||
chr2:219475802
|
C | A | 119 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(116): Show | 130 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.4448-1068C>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 18/40 | chr2 | 219475802 | ||||||
chr2:219475818
|
C | T | 126 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(123): Show | 137 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.4448-1052C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 18/40 | chr2 | 219475818 | ||||||
chr2:219475956
|
G | A | 1 | a0002c0003t0002g0064 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.4448-914G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 18/40 | chr2 | 219475956 | ||||||
chr2:219475960
|
G | A | 2 | a0007c0020t0002g0278a0007c0020t0002g0279 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.4448-910G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 18/40 | chr2 | 219475960 | ||||||
chr2:219476029
|
G | C | 1 | a0005c0006t0002g0119 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.4448-841G>C | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 18/40 | chr2 | 219476029 | ||||||
chr2:219476044
|
G | A | 2 | a0001c0002t0001g0080a0041c0073t0001g0071 | 2 | HG01071.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.4448-826G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 18/40 | chr2 | 219476044 | ||||||
chr2:219476143
|
T | C | 1 | a0015c0024t0001g0268 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.4448-727T>C | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 18/40 | chr2 | 219476143 | ||||||
chr2:219476158
|
TG | T | 126 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(123): Show | 137 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.4448-711delG | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 18/40 | chr2 | 219476158 | ||||||
chr2:219476175
|
C | A | 2 | a0001c0001t0001g0051a0001c0002t0001g0263 | 2 | NA18970.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.4448-695C>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 18/40 | chr2 | 219476175 | ||||||
chr2:219476236
|
G | GTTAC | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(179): Show | 194 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.4448-632_4448-631i others(6): Show |
SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 18/40 | INFO_REALIGN_3_PRIME | chr2 | 219476236 | |||||
chr2:219476343
|
G | T | 12 | a0001c0002t0001g0013a0001c0002t0001g0106a0001c0002t0001g0207others(9): Show | 13 | HG02055.hp2 HG02109.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.4448-527G>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 18/40 | chr2 | 219476343 | ||||||
chr2:219476345
|
G | A | 12 | a0001c0002t0001g0013a0001c0002t0001g0106a0001c0002t0001g0207others(9): Show | 13 | HG02055.hp2 HG02109.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.4448-525G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 18/40 | chr2 | 219476345 | ||||||
chr2:219476443
|
G | C | 1 | a0003c0075t0001g0094 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.4448-427G>C | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 18/40 | chr2 | 219476443 | ||||||
chr2:219476553
|
G | T | 1 | a0001c0001t0001g0015 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.4448-317G>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 18/40 | chr2 | 219476553 | ||||||
chr2:219476607
|
A | T | 1 | a0001c0001t0001g0174 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.4448-263A>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 18/40 | chr2 | 219476607 | ||||||
chr2:219476746
|
A | AG | 3 | a0004c0009t0002g0229a0004c0012t0002g0233a0004c0016t0002g0181 | 3 | HG01981.hp2 HG02027.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.4448-122dupG | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 18/40 | INFO_REALIGN_3_PRIME | chr2 | 219476746 | |||||
chr2:219476749
|
C | G | 14 | a0004c0009t0002g0061a0004c0009t0002g0062a0004c0009t0002g0063others(11): Show | 14 | HG01123.hp2 HG01981.hp2 HG02027.hp1 others(11): Show |
intron_variant | MODIFIER | c.4448-121C>G | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 18/40 | chr2 | 219476749 | ||||||
chr2:219476854
|
T | C | 1 | a0002c0003t0002g0251 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.4448-16T>C | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 18/40 | chr2 | 219476854 | ||||||
chr2:219477014
|
A | C | 1 | a0019c0032t0001g0020 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.4560+32A>C | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 19/40 | chr2 | 219477014 | ||||||
chr2:219477042
|
G | C | 2 | a0019c0032t0001g0020a0039c0067t0001g0122 | 2 | HG02630.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.4560+60G>C | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 19/40 | chr2 | 219477042 | ||||||
chr2:219477059
|
T | G | 1 | a0002c0004t0002g0270 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.4560+77T>G | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 19/40 | chr2 | 219477059 | ||||||
chr2:219477137
|
A | G | 5 | a0001c0001t0001g0015a0001c0001t0001g0173a0001c0001t0001g0179others(2): Show | 5 | NA18943.hp2 NA18962.hp1 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.4561-140A>G | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 19/40 | chr2 | 219477137 | ||||||
chr2:219477192
|
C | T | 1 | a0003c0038t0001g0172 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.4561-85C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 19/40 | chr2 | 219477192 | ||||||
chr2:219477215
|
G | GGCGGGGC others(13): Show |
138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(135): Show | 149 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.4561-62_4561-61ins others(20): Show |
SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 19/40 | chr2 | 219477215 | ||||||
chr2:219477216
|
C | T | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(135): Show | 149 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.4561-61C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 19/40 | chr2 | 219477216 | ||||||
chr2:219477232
|
G | T | 9 | a0004c0009t0002g0061a0004c0009t0002g0062a0004c0009t0002g0063others(6): Show | 9 | HG01123.hp2 HG01981.hp2 HG02083.hp2 others(6): Show |
intron_variant | MODIFIER | c.4561-45G>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 19/40 | chr2 | 219477232 | ||||||
chr2:219477685
|
C | T | 2 | a0021c0034t0001g0026a0022c0033t0002g0025 | 2 | HG02622.hp1 HG02818.hp1 |
splice_region_variant&intron_variant | LOW | c.4730-4C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 20/40 | chr2 | 219477685 | ||||||
chr2:219478310
|
C | T | 1 | a0001c0077t0001g0241 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.5027+205C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 22/40 | chr2 | 219478310 | ||||||
chr2:219478363
|
T | G | 1 | a0001c0001t0001g0280 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.5027+258T>G | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 22/40 | chr2 | 219478363 | ||||||
chr2:219478634
|
G | T | 1 | a0015c0024t0001g0268 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.5028-510G>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 22/40 | chr2 | 219478634 | ||||||
chr2:219479086
|
C | T | 2 | a0001c0001t0001g0152a0001c0066t0001g0089 | 2 | NA18983.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.5028-58C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 22/40 | chr2 | 219479086 | ||||||
chr2:219479087
|
G | A | 1 | a0019c0032t0001g0020 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.5028-57G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 22/40 | chr2 | 219479087 | ||||||
chr2:219479115
|
G | A | 1 | a0002c0003t0002g0266 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.5028-29G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 22/40 | chr2 | 219479115 | ||||||
chr2:219479282
|
G | C | 1 | a0014c0022t0002g0222 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.5085+81G>C | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 23/40 | chr2 | 219479282 | ||||||
chr2:219479423
|
C | T | 1 | a0001c0076t0001g0103 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.5085+222C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 23/40 | chr2 | 219479423 | ||||||
chr2:219479533
|
C | T | 1 | a0026c0070t0003g0265 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.5086-250C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 23/40 | chr2 | 219479533 | ||||||
chr2:219479672
|
C | T | 1 | a0039c0067t0001g0122 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.5086-111C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 23/40 | chr2 | 219479672 | ||||||
chr2:219480204
|
C | T | 1 | a0040c0046t0001g0041 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.5342+64C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 25/40 | chr2 | 219480204 | ||||||
chr2:219480306
|
G | A | 1 | a0001c0002t0002g0201 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.5342+166G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 25/40 | chr2 | 219480306 | ||||||
chr2:219480328
|
T | C | 1 | a0001c0002t0002g0282 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.5342+188T>C | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 25/40 | chr2 | 219480328 | ||||||
chr2:219480395
|
T | G | 147 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(144): Show | 158 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.5342+255T>G | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 25/40 | chr2 | 219480395 | ||||||
chr2:219480396
|
T | C | 147 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(144): Show | 158 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.5342+256T>C | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 25/40 | chr2 | 219480396 | ||||||
chr2:219480752
|
T | A | 8 | a0008c0014t0003g0108a0008c0014t0003g0109a0008c0014t0003g0220others(5): Show | 8 | HG01891.hp2 HG02886.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.5369+55T>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 26/40 | chr2 | 219480752 | ||||||
chr2:219480920
|
G | A | 1 | a0003c0011t0001g0124 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.5369+223G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 26/40 | chr2 | 219480920 | ||||||
chr2:219480940
|
G | A | 5 | a0017c0027t0001g0018a0024c0047t0001g0017a0032c0042t0001g0019others(2): Show | 5 | HG02257.hp2 HG02965.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.5369+243G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 26/40 | chr2 | 219480940 | ||||||
chr2:219481604
|
G | A | 1 | a0001c0076t0001g0103 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.5523-34G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 27/40 | chr2 | 219481604 | ||||||
chr2:219481803
|
C | T | 2 | a0001c0002t0001g0219a0002c0004t0004g0160 | 2 | HG03710.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.5565+123C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 28/40 | chr2 | 219481803 | ||||||
chr2:219481874
|
C | T | 117 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(114): Show | 128 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.5565+194C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 28/40 | chr2 | 219481874 | ||||||
chr2:219481906
|
T | C | 1 | a0001c0001t0001g0030 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.5565+226T>C | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 28/40 | chr2 | 219481906 | ||||||
chr2:219481916
|
G | A | 1 | a0001c0001t0001g0054 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.5565+236G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 28/40 | chr2 | 219481916 | ||||||
chr2:219481923
|
G | C | 14 | a0004c0009t0002g0061a0004c0009t0002g0062a0004c0009t0002g0063others(11): Show | 14 | HG01123.hp2 HG01981.hp2 HG02027.hp1 others(11): Show |
intron_variant | MODIFIER | c.5565+243G>C | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 28/40 | chr2 | 219481923 | ||||||
chr2:219482092
|
A | G | 141 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(138): Show | 152 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.5565+412A>G | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 28/40 | chr2 | 219482092 | ||||||
chr2:219482102
|
C | T | 1 | a0012c0018t0001g0008 | 2 | HG02015.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.5565+422C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 28/40 | chr2 | 219482102 | ||||||
chr2:219482214
|
G | T | 4 | a0006c0058t0002g0285a0014c0022t0002g0222a0031c0030t0002g0218others(1): Show | 4 | HG02647.hp2 HG02809.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.5565+534G>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 28/40 | chr2 | 219482214 | ||||||
chr2:219482311
|
C | T | 1 | a0001c0066t0001g0089 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.5566-473C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 28/40 | chr2 | 219482311 | ||||||
chr2:219482954
|
C | A | 3 | a0021c0034t0001g0026a0022c0033t0002g0025a0035c0060t0001g0193 | 3 | HG02145.hp1 HG02622.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.5634+102C>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 29/40 | chr2 | 219482954 | ||||||
chr2:219485166
|
C | T | 1 | a0001c0002t0001g0219 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.7609+94C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 30/40 | chr2 | 219485166 | ||||||
chr2:219485201
|
C | T | 1 | a0001c0001t0001g0153 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.7609+129C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 30/40 | chr2 | 219485201 | ||||||
chr2:219485327
|
C | A | 5 | a0004c0012t0002g0233a0004c0012t0002g0234a0004c0012t0002g0235others(2): Show | 5 | HG02027.hp1 NA18962.hp2 NA18980.hp1 others(2): Show |
intron_variant | MODIFIER | c.7610-19C>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 30/40 | chr2 | 219485327 | ||||||
chr2:219485529
|
A | G | 3 | a0007c0013t0005g0074a0007c0013t0005g0200a0046c0083t0005g0111 | 3 | HG02572.hp1 HG02723.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.7741+52A>G | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 31/40 | chr2 | 219485529 | ||||||
chr2:219485545
|
A | G | 2 | a0001c0077t0001g0241a0039c0067t0001g0122 | 2 | HG01243.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.7741+68A>G | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 31/40 | chr2 | 219485545 | ||||||
chr2:219485602
|
A | G | 2 | a0007c0020t0002g0278a0007c0020t0002g0279 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.7741+125A>G | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 31/40 | chr2 | 219485602 | ||||||
chr2:219485730
|
C | T | 144 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(141): Show | 155 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.7741+253C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 31/40 | chr2 | 219485730 | ||||||
chr2:219485780
|
A | G | 127 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(124): Show | 138 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.7741+303A>G | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 31/40 | chr2 | 219485780 | ||||||
chr2:219485865
|
C | T | 118 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(115): Show | 129 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.7741+388C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 31/40 | chr2 | 219485865 | ||||||
chr2:219485901
|
C | A | 1 | a0001c0001t0001g0045 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.7741+424C>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 31/40 | chr2 | 219485901 | ||||||
chr2:219485942
|
A | G | 1 | a0001c0002t0001g0284 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.7741+465A>G | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 31/40 | chr2 | 219485942 | ||||||
chr2:219486309
|
G | A | 1 | a0002c0004t0002g0145 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.7741+832G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 31/40 | chr2 | 219486309 | ||||||
chr2:219486355
|
G | A | 264 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(261): Show | 279 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(276): Show |
intron_variant | MODIFIER | c.7741+878G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 31/40 | chr2 | 219486355 | ||||||
chr2:219486414
|
G | A | 3 | a0007c0013t0001g0197a0007c0013t0006g0195a0023c0072t0006g0196 | 3 | HG02486.hp2 NA18522.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.7741+937G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 31/40 | chr2 | 219486414 | ||||||
chr2:219486520
|
G | A | 6 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0131others(3): Show | 6 | HG02523.hp2 NA18964.hp2 NA18973.hp1 others(3): Show |
intron_variant | MODIFIER | c.7741+1043G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 31/40 | chr2 | 219486520 | ||||||
chr2:219486546
|
A | G | 1 | a0041c0073t0001g0071 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.7741+1069A>G | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 31/40 | chr2 | 219486546 | ||||||
chr2:219486609
|
C | T | 1 | a0002c0003t0002g0065 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.7741+1132C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 31/40 | chr2 | 219486609 | ||||||
chr2:219486657
|
C | T | 94 | a0002c0003t0002g0005a0002c0003t0002g0014a0002c0003t0002g0028others(91): Show | 98 | HG00609.hp1 HG00639.hp1 HG00642.hp1 others(95): Show |
intron_variant | MODIFIER | c.7741+1180C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 31/40 | chr2 | 219486657 | ||||||
chr2:219486749
|
T | C | 3 | a0001c0002t0001g0269a0003c0005t0001g0256a0003c0011t0001g0130 | 3 | HG00323.hp1 HG01168.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.7741+1272T>C | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 31/40 | chr2 | 219486749 | ||||||
chr2:219486802
|
CCT | C | 5 | a0001c0002t0001g0060a0001c0002t0001g0283a0001c0002t0001g0284others(2): Show | 5 | HG01257.hp1 HG01884.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.7741+1339_7741+134 others(6): Show |
SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 31/40 | INFO_REALIGN_3_PRIME | chr2 | 219486802 | |||||
chr2:219486867
|
G | A | 1 | a0010c0052t0002g0093 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.7742-1327G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 31/40 | chr2 | 219486867 | ||||||
chr2:219487053
|
G | T | 1 | a0001c0002t0002g0282 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.7742-1141G>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 31/40 | chr2 | 219487053 | ||||||
chr2:219487129
|
C | T | 1 | a0019c0032t0001g0020 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.7742-1065C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 31/40 | chr2 | 219487129 | ||||||
chr2:219487240
|
G | T | 2 | a0001c0002t0001g0095a0001c0002t0001g0096 | 2 | NA18967.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.7742-954G>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 31/40 | chr2 | 219487240 | ||||||
chr2:219487308
|
G | A | 140 | a0001c0076t0001g0103a0001c0077t0001g0241a0002c0003t0002g0005others(137): Show | 144 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(141): Show |
intron_variant | MODIFIER | c.7742-886G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 31/40 | chr2 | 219487308 | ||||||
chr2:219487369
|
A | T | 141 | a0001c0076t0001g0103a0001c0077t0001g0241a0002c0003t0002g0005others(138): Show | 145 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(142): Show |
intron_variant | MODIFIER | c.7742-825A>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 31/40 | chr2 | 219487369 | ||||||
chr2:219487444
|
T | C | 1 | a0001c0002t0001g0219 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.7742-750T>C | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 31/40 | chr2 | 219487444 | ||||||
chr2:219487505
|
C | T | 1 | a0001c0001t0001g0125 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.7742-689C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 31/40 | chr2 | 219487505 | ||||||
chr2:219487601
|
A | G | 5 | a0017c0027t0001g0018a0024c0047t0001g0017a0032c0042t0001g0019others(2): Show | 5 | HG02257.hp2 HG02965.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.7742-593A>G | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 31/40 | chr2 | 219487601 | ||||||
chr2:219488176
|
T | C | 1 | a0002c0004t0002g0137 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.7742-18T>C | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 31/40 | chr2 | 219488176 | ||||||
chr2:219488189
|
T | C | 1 | a0003c0005t0001g0076 | 1 | HG03492.hp2 | splice_region_variant&intron_variant | LOW | c.7742-5T>C | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 31/40 | chr2 | 219488189 | ||||||
chr2:219488382
|
A | G | 116 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(113): Show | 127 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.7858+72A>G | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 32/40 | chr2 | 219488382 | ||||||
chr2:219488408
|
TA | T | 4 | a0001c0001t0001g0033a0001c0001t0001g0038a0001c0001t0001g0144others(1): Show | 4 | HG01074.hp1 HG01167.hp2 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.7859-89delA | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 32/40 | chr2 | 219488408 | ||||||
chr2:219488439
|
G | C | 29 | a0004c0009t0002g0061a0004c0009t0002g0062a0004c0009t0002g0063others(26): Show | 29 | HG00280.hp1 HG00438.hp1 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.7859-59G>C | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 32/40 | chr2 | 219488439 | ||||||
chr2:219488718
|
G | T | 123 | a0002c0003t0002g0005a0002c0003t0002g0014a0002c0003t0002g0028others(120): Show | 127 | HG00280.hp1 HG00438.hp1 HG00609.hp1 others(124): Show |
intron_variant | MODIFIER | c.8026+53G>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 33/40 | chr2 | 219488718 | ||||||
chr2:219489286
|
C | T | 1 | a0002c0004t0002g0048 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.8318-50C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 35/40 | chr2 | 219489286 | ||||||
chr2:219490035
|
G | C | 132 | a0002c0003t0002g0005a0002c0003t0002g0014a0002c0003t0002g0028others(129): Show | 136 | HG00280.hp1 HG00438.hp1 HG00609.hp1 others(133): Show |
intron_variant | MODIFIER | c.8921+96G>C | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 36/40 | chr2 | 219490035 | ||||||
chr2:219490236
|
G | A | 3 | a0007c0013t0005g0074a0007c0013t0005g0200a0046c0083t0005g0111 | 3 | HG02572.hp1 HG02723.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.8922-173G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 36/40 | chr2 | 219490236 | ||||||
chr2:219490243
|
G | A | 1 | a0001c0001t0001g0039 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.8922-166G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 36/40 | chr2 | 219490243 | ||||||
chr2:219490349
|
C | T | 8 | a0007c0013t0001g0197a0007c0013t0005g0074a0007c0013t0005g0200others(5): Show | 8 | HG02486.hp2 HG02572.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.8922-60C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 36/40 | chr2 | 219490349 | ||||||
chr2:219490721
|
C | T | 4 | a0002c0003t0002g0206a0002c0003t0002g0208a0002c0003t0002g0209others(1): Show | 4 | HG02145.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.9162-12C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 37/40 | chr2 | 219490721 | ||||||
chr2:219491167
|
C | T | 3 | a0001c0002t0001g0135a0001c0002t0001g0242a0001c0002t0010g0127 | 3 | HG02027.hp2 NA19054.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.9385+211C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 38/40 | chr2 | 219491167 | ||||||
chr2:219491238
|
A | G | 2 | a0006c0007t0002g0169a0006c0053t0002g0133 | 2 | HG01257.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.9385+282A>G | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 38/40 | chr2 | 219491238 | ||||||
chr2:219491357
|
G | A | 94 | a0002c0003t0002g0005a0002c0003t0002g0014a0002c0003t0002g0028others(91): Show | 98 | HG00609.hp1 HG00639.hp1 HG00642.hp1 others(95): Show |
intron_variant | MODIFIER | c.9385+401G>A | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 38/40 | chr2 | 219491357 | ||||||
chr2:219491413
|
A | G | 1 | a0001c0002t0001g0120 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.9386-381A>G | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 38/40 | chr2 | 219491413 | ||||||
chr2:219491479
|
C | T | 3 | a0002c0003t0002g0266a0002c0004t0002g0052a0002c0065t0002g0073 | 3 | NA18957.hp2 NA18986.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.9386-315C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 38/40 | chr2 | 219491479 | ||||||
chr2:219491645
|
C | T | 1 | a0002c0004t0002g0270 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.9386-149C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 38/40 | chr2 | 219491645 | ||||||
chr2:219491701
|
A | G | 1 | a0014c0022t0002g0222 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.9386-93A>G | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 38/40 | chr2 | 219491701 | ||||||
chr2:219491727
|
G | C | 131 | a0001c0057t0002g0069a0002c0003t0002g0005a0002c0003t0002g0014others(128): Show | 135 | HG00280.hp1 HG00438.hp1 HG00609.hp1 others(132): Show |
intron_variant | MODIFIER | c.9386-67G>C | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 38/40 | chr2 | 219491727 | ||||||
chr2:219491910
|
C | T | 10 | a0006c0007t0002g0040a0006c0007t0002g0047a0006c0007t0002g0050others(7): Show | 10 | HG00280.hp1 HG00438.hp1 HG00673.hp1 others(7): Show |
intron_variant | MODIFIER | c.9461+41C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 39/40 | chr2 | 219491910 | ||||||
chr2:219491952
|
C | T | 2 | a0011c0036t0003g0138a0011c0055t0003g0281 | 2 | HG02886.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.9461+83C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 39/40 | chr2 | 219491952 | ||||||
chr2:219491984
|
C | T | 1 | a0023c0072t0006g0196 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.9461+115C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 39/40 | chr2 | 219491984 | ||||||
chr2:219492084
|
C | T | 273 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(270): Show | 288 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(285): Show |
intron_variant | MODIFIER | c.9462-27C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 39/40 | chr2 | 219492084 | ||||||
chr2:219492321
|
A | G | 1 | a0013c0021t0002g0090 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.9611+61A>G | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 40/40 | chr2 | 219492321 | ||||||
chr2:219492524
|
C | T | 1 | a0001c0002t0001g0246 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.9612-70C>T | SPEG | ENSG00000072195.15 | transcript | ENST00000312358.12 | protein_coding | 40/40 | chr2 | 219492524 |