geneid | 64167 |
---|---|
ensemblid | ENSG00000164308.17 |
hgncid | 29499 |
symbol | ERAP2 |
name | endoplasmic reticulum aminopeptidase 2 |
refseq_nuc | NM_022350.5 |
refseq_prot | NP_071745.1 |
ensembl_nuc | ENST00000437043.8 |
ensembl_prot | ENSP00000400376.3 |
mane_status | MANE Select |
chr | chr5 |
start | 96876500 |
end | 96919703 |
strand | + |
ver | v1.2 |
region | chr5:96876500-96919703 |
region5000 | chr5:96871500-96924703 |
regionname0 | ERAP2_chr5_96876500_96919703 |
regionname5000 | ERAP2_chr5_96871500_96924703 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0000 | 0/0 | 0 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0001 | 0/1 | 960 | 193 | 56 | 39 | 69 | 9 | 19 | 54 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0002 | 1/0 | 960 | 127 | 27 | 25 | 58 | 2 | 14 | 46 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0003 | 0/0 | 960 | 30 | 0 | 2 | 26 | 0 | 2 | 24 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0004 | 0/0 | 960 | 15 | 0 | 1 | 14 | 0 | 0 | 12 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0005 | 0/0 | 960 | 13 | 0 | 6 | 0 | 3 | 4 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0006 | 0/0 | 960 | 4 | 0 | 0 | 1 | 0 | 3 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0007 | 0/0 | 960 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0008 | 0/0 | 960 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0009 | 0/0 | 960 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0010 | 0/0 | 960 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0011 | 0/0 | 960 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0012 | 0/0 | 960 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0013 | 0/0 | 960 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0014 | 0/0 | 960 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0015 | 0/0 | 960 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0016 | 0/0 | 960 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0017 | 0/0 | 960 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0018 | 0/0 | 960 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 2883 | 152 | 34 | 29 | 67 | 6 | 16 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
c0002 | 1/0 | 2883 | 126 | 27 | 25 | 58 | 2 | 13 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
c0003 | 0/0 | 2883 | 30 | 0 | 2 | 26 | 0 | 2 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
c0004 | 0/0 | 2883 | 26 | 21 | 3 | 0 | 0 | 2 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
c0005 | 0/0 | 2883 | 14 | 0 | 1 | 13 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
c0006 | 0/0 | 2883 | 13 | 0 | 6 | 0 | 3 | 4 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
c0007 | 0/1 | 2883 | 11 | 0 | 6 | 0 | 3 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
c0008 | 0/0 | 2883 | 4 | 0 | 0 | 1 | 0 | 3 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
c0009 | 0/0 | 2883 | 2 | 2 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
c0010 | 0/0 | 2354 | 2 | 0 | 0 | 2 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
c0011 | 0/0 | 2883 | 2 | 0 | 0 | 2 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
c0012 | 0/0 | 2883 | 2 | 1 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
c0013 | 0/0 | 2883 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
c0014 | 0/0 | 2883 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
c0015 | 0/0 | 2883 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
c0016 | 0/0 | 2883 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
c0017 | 0/0 | 2883 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
c0018 | 0/0 | 2883 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
c0019 | 0/0 | 2883 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
c0020 | 0/0 | 2883 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
c0021 | 0/0 | 2883 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
c0022 | 0/0 | 2883 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
c0023 | 0/0 | 2883 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
c0024 | 0/0 | 2883 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
c0025 | 0/0 | 2883 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
c0026 | 0/0 | 2883 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 2249 | 167 | 37 | 35 | 67 | 9 | 17 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
t0002 | 0/0 | 2249 | 99 | 21 | 20 | 45 | 2 | 11 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
t0003 | 0/0 | 2250 | 29 | 2 | 1 | 24 | 0 | 2 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
t0004 | 0/0 | 2252 | 24 | 0 | 2 | 20 | 0 | 2 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
t0005 | 0/0 | 2251 | 10 | 0 | 5 | 0 | 3 | 2 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
t0006 | 0/0 | 2250 | 9 | 8 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
t0007 | 0/0 | 2250 | 7 | 7 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
t0008 | 0/0 | 2250 | 7 | 2 | 0 | 3 | 0 | 2 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
t0009 | 0/0 | 2253 | 7 | 2 | 1 | 4 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
t0010 | 0/0 | 2248 | 5 | 0 | 4 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
t0011 | 0/0 | 2250 | 5 | 3 | 2 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
t0012 | 0/0 | 2252 | 4 | 4 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
t0013 | 0/0 | 2252 | 3 | 0 | 1 | 0 | 0 | 2 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
t0014 | 0/0 | 151 | 2 | 0 | 0 | 2 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
t0015 | 0/0 | 2251 | 2 | 2 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
t0016 | 0/0 | 2251 | 2 | 0 | 0 | 2 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
t0017 | 0/0 | 2237 | 2 | 0 | 0 | 2 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
t0018 | 0/0 | 2251 | 2 | 0 | 0 | 2 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
t0019 | 0/0 | 2249 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
t0020 | 0/0 | 2249 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
t0021 | 0/0 | 2251 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
t0022 | 0/0 | 2250 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
t0023 | 0/0 | 2249 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
t0024 | 0/0 | 2249 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
t0025 | 0/0 | 2249 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
t0026 | 0/0 | 2249 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
t0027 | 0/0 | 2249 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
t0028 | 0/0 | 2249 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
t0029 | 0/0 | 2249 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
t0030 | 0/0 | 2249 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 7 | 0 | 0 | 4 | 0 | 3 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0003 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0004 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0005 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0009 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0010 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0016 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0017 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0019 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0020 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0023 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0036 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0038 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0123 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0260 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0327 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0328 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0329 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0000c0010 | 0/0 | 2354 | 2 | 0 | 0 | 2 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0001c0001 | 0/0 | 2883 | 152 | 34 | 29 | 67 | 6 | 16 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0001c0004 | 0/0 | 2883 | 26 | 21 | 3 | 0 | 0 | 2 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0001c0007 | 0/1 | 2883 | 11 | 0 | 6 | 0 | 3 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0001c0011 | 0/0 | 2883 | 2 | 0 | 0 | 2 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0001c0021 | 0/0 | 2883 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0001c0022 | 0/0 | 2883 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0002c0002 | 1/0 | 2883 | 126 | 27 | 25 | 58 | 2 | 13 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0002c0024 | 0/0 | 2883 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0003c0003 | 0/0 | 2883 | 30 | 0 | 2 | 26 | 0 | 2 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0004c0005 | 0/0 | 2883 | 14 | 0 | 1 | 13 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0004c0016 | 0/0 | 2883 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0005c0006 | 0/0 | 2883 | 13 | 0 | 6 | 0 | 3 | 4 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0006c0008 | 0/0 | 2883 | 4 | 0 | 0 | 1 | 0 | 3 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0007c0012 | 0/0 | 2883 | 2 | 1 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0008c0009 | 0/0 | 2883 | 2 | 2 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0009c0014 | 0/0 | 2883 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0010c0015 | 0/0 | 2883 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0011c0017 | 0/0 | 2883 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0012c0020 | 0/0 | 2883 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0013c0019 | 0/0 | 2883 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0014c0023 | 0/0 | 2883 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0015c0018 | 0/0 | 2883 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0016c0013 | 0/0 | 2883 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0017c0025 | 0/0 | 2883 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0018c0026 | 0/0 | 2883 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0000c0010t0014 | 0/0 | 2504 | 2 | 0 | 0 | 2 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0001c0001t0001 | 0/0 | 5131 | 144 | 31 | 27 | 64 | 6 | 16 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0001c0001t0008 | 0/0 | 5132 | 4 | 2 | 0 | 2 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0001c0001t0020 | 0/0 | 5131 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0001c0001t0023 | 0/0 | 5131 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0001c0001t0027 | 0/0 | 5131 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0001c0001t0028 | 0/0 | 5131 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0001c0004t0006 | 0/0 | 5132 | 9 | 8 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0001c0004t0007 | 0/0 | 5132 | 7 | 7 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0001c0004t0011 | 0/0 | 5132 | 5 | 3 | 2 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0001c0004t0015 | 0/0 | 5133 | 2 | 2 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0001c0004t0022 | 0/0 | 5132 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0001c0004t0024 | 0/0 | 5131 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0001c0004t0030 | 0/0 | 5131 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0001c0007t0001 | 0/1 | 5131 | 11 | 0 | 6 | 0 | 3 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0001c0011t0001 | 0/0 | 5131 | 2 | 0 | 0 | 2 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0001c0021t0001 | 0/0 | 5131 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0001c0022t0001 | 0/0 | 5131 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0002c0002t0001 | 1/0 | 5131 | 1 | 0 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0002c0002t0002 | 0/0 | 5131 | 92 | 19 | 19 | 42 | 2 | 10 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0002c0002t0003 | 0/0 | 5132 | 16 | 1 | 1 | 12 | 0 | 2 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0002c0002t0009 | 0/0 | 5135 | 3 | 2 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0002c0002t0010 | 0/0 | 5130 | 4 | 0 | 4 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0002c0002t0012 | 0/0 | 5134 | 4 | 4 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0002c0002t0016 | 0/0 | 5133 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0002c0002t0017 | 0/0 | 5119 | 2 | 0 | 0 | 2 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0002c0002t0019 | 0/0 | 5131 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0002c0002t0026 | 0/0 | 5131 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0002c0002t0029 | 0/0 | 5131 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0002c0024t0002 | 0/0 | 5131 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0003c0003t0004 | 0/0 | 5134 | 24 | 0 | 2 | 20 | 0 | 2 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0003c0003t0009 | 0/0 | 5135 | 4 | 0 | 0 | 4 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0003c0003t0018 | 0/0 | 5133 | 2 | 0 | 0 | 2 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0004c0005t0002 | 0/0 | 5131 | 2 | 0 | 1 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0004c0005t0003 | 0/0 | 5132 | 11 | 0 | 0 | 11 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0004c0005t0016 | 0/0 | 5133 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0004c0016t0002 | 0/0 | 5131 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0005c0006t0005 | 0/0 | 5133 | 10 | 0 | 5 | 0 | 3 | 2 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0005c0006t0013 | 0/0 | 5134 | 3 | 0 | 1 | 0 | 0 | 2 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0006c0008t0008 | 0/0 | 5132 | 3 | 0 | 0 | 1 | 0 | 2 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0006c0008t0021 | 0/0 | 5133 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0007c0012t0001 | 0/0 | 5131 | 2 | 1 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0008c0009t0002 | 0/0 | 5131 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0008c0009t0025 | 0/0 | 5131 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0009c0014t0001 | 0/0 | 5131 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0010c0015t0001 | 0/0 | 5131 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0011c0017t0001 | 0/0 | 5131 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0012c0020t0010 | 0/0 | 5130 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0013c0019t0002 | 0/0 | 5131 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0014c0023t0001 | 0/0 | 5131 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0015c0018t0001 | 0/0 | 5131 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0016c0013t0002 | 0/0 | 5131 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0017c0025t0003 | 0/0 | 5132 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
a0018c0026t0003 | 0/0 | 5132 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | copy fasta | chr5 | 96871500 | 96924703 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0000c0010t0014g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0005 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0008g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0008g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0008g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0008g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0020g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0023g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0027g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0001t0028g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0004t0006g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0004t0006g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0004t0006g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0004t0006g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0004t0006g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0004t0006g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0004t0006g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0004t0006g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0004t0006g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0004t0007g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0004t0007g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0004t0007g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0004t0007g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0004t0007g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0004t0007g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0004t0007g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0004t0011g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0004t0011g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0004t0011g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0004t0011g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0004t0011g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0004t0015g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0004t0015g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0004t0022g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0004t0024g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0004t0030g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0007t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0007t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0007t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0007t0001g0260 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0007t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0007t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0007t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0007t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0007t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0007t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0011t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0011t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0021t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0001c0022t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0001g0123 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0002g0001 | 0/0 | 6 | 0 | 0 | 4 | 0 | 2 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0002g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0002g0003 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0002g0004 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0002g0009 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0002g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0002g0016 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0002g0017 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0002g0019 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0002g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0002g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0003g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0003g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0003g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0003g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0003g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0009g0023 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0009g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0010g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0010g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0010g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0012g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0012g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0012g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0012g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0016g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0017g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0017g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0019g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0026g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0002t0029g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0002c0024t0002g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0003c0003t0004g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0003c0003t0004g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0003c0003t0004g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0003c0003t0004g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0003c0003t0004g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0003c0003t0004g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0003c0003t0004g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0003c0003t0004g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0003c0003t0004g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0003c0003t0004g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0003c0003t0004g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0003c0003t0004g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0003c0003t0004g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0003c0003t0004g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0003c0003t0004g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0003c0003t0004g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0003c0003t0004g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0003c0003t0004g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0003c0003t0004g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0003c0003t0004g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0003c0003t0004g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0003c0003t0004g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0003c0003t0009g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0003c0003t0009g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0003c0003t0009g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0003c0003t0018g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0003c0003t0018g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0004c0005t0002g0036 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0004c0005t0003g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0004c0005t0003g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0004c0005t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0004c0005t0003g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0004c0005t0003g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0004c0005t0003g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0004c0005t0003g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0004c0005t0003g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0004c0005t0003g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0004c0005t0016g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0004c0016t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0005c0006t0005g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0005c0006t0005g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0005c0006t0005g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0005c0006t0005g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0005c0006t0005g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0005c0006t0005g0327 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0005c0006t0005g0328 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0005c0006t0005g0329 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0005c0006t0005g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0005c0006t0005g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0005c0006t0013g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0005c0006t0013g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0005c0006t0013g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0006c0008t0008g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0006c0008t0008g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0006c0008t0008g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0006c0008t0021g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0007c0012t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0007c0012t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0008c0009t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0008c0009t0025g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0009c0014t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0010c0015t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0011c0017t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0012c0020t0010g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0013c0019t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0014c0023t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0015c0018t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0016c0013t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0017c0025t0003g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
a0018c0026t0003g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | GBR | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG00140 | hp2 | a0002 | c0002 | t0002 | g0046 | EUR | GBR | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0110 | EUR | FIN | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0267 | EUR | FIN | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0047 | EUR | FIN | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG00323 | hp2 | a0002 | c0002 | t0002 | g0017 | EUR | FIN | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG00423 | hp1 | a0002 | c0002 | t0026 | g0041 | EAS | CHS | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | CHS | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG00544 | hp1 | a0002 | c0002 | t0003 | g0082 | EAS | CHS | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG00544 | hp2 | a0002 | c0002 | t0002 | g0074 | EAS | CHS | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | CHS | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG00558 | hp2 | a0003 | c0003 | t0004 | g0288 | EAS | CHS | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG00597 | hp1 | a0004 | c0005 | t0003 | g0316 | EAS | CHS | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | CHS | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG00609 | hp1 | a0003 | c0003 | t0004 | g0286 | EAS | CHS | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG00609 | hp2 | a0002 | c0002 | t0002 | g0077 | EAS | CHS | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG00621 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | CHS | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | CHS | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG00642 | hp1 | a0005 | c0006 | t0005 | g0212 | AMR | PUR | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG00735 | hp1 | a0005 | c0006 | t0013 | g0326 | AMR | PUR | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG00738 | hp2 | a0002 | c0002 | t0010 | g0039 | AMR | PUR | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG00741 | hp2 | a0002 | c0002 | t0002 | g0056 | AMR | PUR | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG01069 | hp1 | a0002 | c0002 | t0002 | g0081 | AMR | PUR | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | PUR | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG01070 | hp1 | a0002 | c0002 | t0002 | g0106 | AMR | PUR | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0263 | AMR | PUR | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0262 | AMR | PUR | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | PUR | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG01074 | hp1 | a0007 | c0012 | t0001 | g0152 | AMR | PUR | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG01074 | hp2 | a0002 | c0002 | t0002 | g0096 | AMR | PUR | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG01081 | hp1 | a0002 | c0002 | t0002 | g0009 | AMR | PUR | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0253 | AMR | PUR | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG01099 | hp2 | a0002 | c0002 | t0002 | g0101 | AMR | PUR | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | PUR | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG01109 | hp1 | a0001 | c0004 | t0011 | g0134 | AMR | PUR | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG01109 | hp2 | a0002 | c0002 | t0002 | g0202 | AMR | PUR | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG01167 | hp1 | a0001 | c0007 | t0001 | g0261 | AMR | PUR | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG01167 | hp2 | a0002 | c0002 | t0010 | g0335 | AMR | PUR | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG01168 | hp1 | a0001 | c0007 | t0001 | g0031 | AMR | PUR | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG01168 | hp2 | a0005 | c0006 | t0005 | g0330 | AMR | PUR | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG01175 | hp1 | a0001 | c0001 | t0020 | g0151 | AMR | PUR | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG01175 | hp2 | a0002 | c0002 | t0002 | g0017 | AMR | PUR | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG01192 | hp1 | a0002 | c0002 | t0003 | g0239 | AMR | PUR | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG01192 | hp2 | a0001 | c0001 | t0027 | g0333 | AMR | PUR | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG01243 | hp1 | a0001 | c0004 | t0006 | g0139 | AMR | PUR | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG01243 | hp2 | a0002 | c0002 | t0009 | g0023 | AMR | PUR | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG01255 | hp2 | a0002 | c0002 | t0002 | g0204 | AMR | CLM | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG01256 | hp1 | a0001 | c0007 | t0001 | g0271 | AMR | CLM | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG01257 | hp1 | a0003 | c0003 | t0004 | g0032 | AMR | CLM | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | CLM | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG01258 | hp2 | a0003 | c0003 | t0004 | g0032 | AMR | CLM | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG01261 | hp1 | a0002 | c0002 | t0002 | g0009 | AMR | CLM | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG01261 | hp2 | a0001 | c0007 | t0001 | g0031 | AMR | CLM | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | CLM | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG01358 | hp2 | a0001 | c0007 | t0001 | g0258 | AMR | CLM | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG01361 | hp1 | a0005 | c0006 | t0005 | g0264 | AMR | CLM | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG01361 | hp2 | a0002 | c0002 | t0002 | g0091 | AMR | CLM | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG01433 | hp2 | a0002 | c0002 | t0002 | g0059 | AMR | CLM | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG01496 | hp1 | a0001 | c0004 | t0011 | g0136 | AMR | CLM | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG01496 | hp2 | a0002 | c0002 | t0002 | g0119 | AMR | CLM | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG01516 | hp1 | a0005 | c0006 | t0005 | g0329 | EUR | IBS | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG01516 | hp2 | a0001 | c0007 | t0001 | g0270 | EUR | IBS | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG01517 | hp1 | a0005 | c0006 | t0005 | g0328 | EUR | IBS | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0088 | EUR | IBS | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG01884 | hp1 | a0001 | c0001 | t0023 | g0216 | AFR | ACB | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG01884 | hp2 | a0001 | c0004 | t0011 | g0135 | AFR | ACB | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG01934 | hp1 | a0005 | c0006 | t0005 | g0038 | AMR | PEL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG01934 | hp2 | a0002 | c0002 | t0002 | g0075 | AMR | PEL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PEL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG01943 | hp2 | a0002 | c0002 | t0002 | g0087 | AMR | PEL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG01975 | hp1 | a0002 | c0002 | t0010 | g0039 | AMR | PEL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG01975 | hp2 | a0001 | c0021 | t0001 | g0214 | AMR | PEL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PEL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | PEL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG01981 | hp1 | a0002 | c0002 | t0010 | g0336 | AMR | PEL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | PEL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | PEL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG01993 | hp2 | a0002 | c0002 | t0002 | g0086 | AMR | PEL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0247 | AMR | PEL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG02004 | hp2 | a0001 | c0007 | t0001 | g0266 | AMR | PEL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | KHV | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG02027 | hp2 | a0002 | c0002 | t0003 | g0097 | EAS | KHV | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG02040 | hp1 | a0006 | c0008 | t0008 | g0171 | EAS | KHV | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | KHV | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG02055 | hp1 | a0016 | c0013 | t0002 | g0067 | AFR | ACB | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG02055 | hp2 | a0001 | c0004 | t0015 | g0129 | AFR | ACB | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG02056 | hp2 | a0002 | c0002 | t0002 | g0099 | EAS | KHV | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG02071 | hp2 | a0002 | c0002 | t0002 | g0057 | EAS | KHV | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG02083 | hp1 | a0002 | c0002 | t0002 | g0060 | EAS | KHV | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG02083 | hp2 | a0002 | c0002 | t0003 | g0068 | EAS | KHV | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG02129 | hp2 | a0002 | c0002 | t0002 | g0092 | EAS | KHV | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG02135 | hp1 | a0002 | c0002 | t0002 | g0085 | EAS | KHV | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | KHV | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | ACB | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG02145 | hp2 | a0001 | c0001 | t0008 | g0045 | AFR | ACB | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG02148 | hp1 | a0004 | c0005 | t0002 | g0036 | AMR | PEL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | PEL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | CDX | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG02155 | hp2 | a0001 | c0001 | t0028 | g0189 | EAS | CDX | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | ACB | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG02257 | hp2 | a0002 | c0002 | t0003 | g0240 | AFR | ACB | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | ACB | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | ACB | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | ACB | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG02293 | hp1 | a0002 | c0002 | t0002 | g0009 | AMR | PEL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | PEL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG02300 | hp1 | a0002 | c0002 | t0002 | g0084 | AMR | PEL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0246 | AMR | PEL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG02451 | hp1 | a0001 | c0004 | t0007 | g0298 | AFR | ACB | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG02451 | hp2 | a0001 | c0004 | t0006 | g0130 | AFR | ACB | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG02572 | hp1 | a0008 | c0009 | t0025 | g0022 | AFR | GWD | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | GWD | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG02602 | hp1 | a0003 | c0003 | t0004 | g0274 | SAS | PJL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG02602 | hp2 | a0002 | c0002 | t0002 | g0055 | SAS | PJL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG02615 | hp1 | a0002 | c0002 | t0002 | g0073 | AFR | GWD | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG02615 | hp2 | a0010 | c0015 | t0001 | g0144 | AFR | GWD | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG02622 | hp1 | a0001 | c0004 | t0011 | g0133 | AFR | GWD | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG02622 | hp2 | a0001 | c0004 | t0007 | g0115 | AFR | GWD | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | GWD | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG02630 | hp2 | a0001 | c0004 | t0006 | g0131 | AFR | GWD | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG02647 | hp1 | a0002 | c0002 | t0009 | g0138 | AFR | GWD | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0236 | SAS | PJL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG02683 | hp2 | a0002 | c0002 | t0002 | g0102 | SAS | PJL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG02698 | hp1 | a0002 | c0002 | t0019 | g0001 | SAS | PJL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG02698 | hp2 | a0006 | c0008 | t0008 | g0238 | SAS | PJL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG02717 | hp1 | a0002 | c0002 | t0002 | g0019 | AFR | GWD | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | GWD | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG02738 | hp1 | a0001 | c0004 | t0030 | g0226 | SAS | PJL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0237 | SAS | PJL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG02809 | hp1 | a0001 | c0004 | t0007 | g0114 | AFR | GWD | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG02818 | hp1 | a0001 | c0001 | t0008 | g0024 | AFR | GWD | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG02818 | hp2 | a0002 | c0002 | t0002 | g0122 | AFR | GWD | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG02886 | hp1 | a0001 | c0004 | t0007 | g0116 | AFR | GWD | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG02895 | hp1 | a0001 | c0004 | t0006 | g0150 | AFR | GWD | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG02895 | hp2 | a0002 | c0002 | t0002 | g0125 | AFR | GWD | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG02896 | hp2 | a0002 | c0002 | t0012 | g0244 | AFR | GWD | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG02897 | hp1 | a0001 | c0004 | t0006 | g0149 | AFR | GWD | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | GWD | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | ESN | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ESN | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG02965 | hp1 | a0002 | c0002 | t0002 | g0004 | AFR | ESN | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG02965 | hp2 | a0015 | c0018 | t0001 | g0210 | AFR | ESN | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0300 | AFR | ESN | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG02970 | hp2 | a0002 | c0002 | t0002 | g0126 | AFR | ESN | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG02976 | hp1 | a0002 | c0002 | t0012 | g0241 | AFR | ESN | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG02976 | hp2 | a0002 | c0002 | t0002 | g0004 | AFR | ESN | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG03017 | hp1 | a0002 | c0002 | t0002 | g0003 | SAS | PJL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG03017 | hp2 | a0002 | c0024 | t0002 | g0295 | SAS | PJL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG03041 | hp1 | a0002 | c0002 | t0002 | g0028 | AFR | GWD | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG03041 | hp2 | a0002 | c0002 | t0002 | g0071 | AFR | GWD | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG03098 | hp1 | a0008 | c0009 | t0002 | g0022 | AFR | MSL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG03098 | hp2 | a0001 | c0004 | t0024 | g0148 | AFR | MSL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG03130 | hp1 | a0002 | c0002 | t0009 | g0023 | AFR | ESN | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG03130 | hp2 | a0002 | c0002 | t0002 | g0113 | AFR | ESN | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0301 | AFR | ESN | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG03195 | hp1 | a0002 | c0002 | t0002 | g0028 | AFR | ESN | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | ESN | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | MSL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | MSL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG03225 | hp2 | a0001 | c0004 | t0015 | g0146 | AFR | MSL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG03239 | hp2 | a0005 | c0006 | t0005 | g0265 | SAS | PJL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | MSL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG03453 | hp2 | a0002 | c0002 | t0002 | g0004 | AFR | MSL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG03486 | hp1 | a0001 | c0004 | t0011 | g0137 | AFR | MSL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG03486 | hp2 | a0002 | c0002 | t0002 | g0118 | AFR | MSL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0195 | SAS | PJL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | PJL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG03491 | hp2 | a0002 | c0002 | t0002 | g0016 | SAS | PJL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG03492 | hp2 | a0002 | c0002 | t0002 | g0016 | SAS | PJL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ESN | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG03516 | hp2 | a0002 | c0002 | t0002 | g0004 | AFR | ESN | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG03540 | hp1 | a0001 | c0004 | t0007 | g0303 | AFR | GWD | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG03540 | hp2 | a0001 | c0004 | t0006 | g0147 | AFR | GWD | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | MSL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG03579 | hp2 | a0002 | c0002 | t0012 | g0243 | AFR | MSL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG03654 | hp2 | a0002 | c0002 | t0002 | g0001 | SAS | PJL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG03688 | hp1 | a0002 | c0002 | t0002 | g0107 | SAS | STU | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG03688 | hp2 | a0003 | c0003 | t0004 | g0278 | SAS | STU | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG03710 | hp1 | a0002 | c0002 | t0002 | g0093 | SAS | PJL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG03710 | hp2 | a0005 | c0006 | t0005 | g0268 | SAS | PJL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG03831 | hp1 | a0001 | c0004 | t0022 | g0225 | SAS | BEB | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG03831 | hp2 | a0001 | c0007 | t0001 | g0269 | SAS | BEB | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0228 | SAS | BEB | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG03834 | hp2 | a0002 | c0002 | t0003 | g0083 | SAS | BEB | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG03927 | hp1 | a0006 | c0008 | t0021 | g0159 | SAS | BEB | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG03927 | hp2 | a0005 | c0006 | t0013 | g0038 | SAS | BEB | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | BEB | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0257 | SAS | BEB | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0229 | SAS | STU | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0167 | SAS | STU | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG04184 | hp1 | a0002 | c0002 | t0003 | g0058 | SAS | BEB | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0220 | SAS | BEB | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG04199 | hp1 | a0002 | c0002 | t0002 | g0001 | SAS | STU | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | STU | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG04204 | hp1 | a0005 | c0006 | t0013 | g0331 | SAS | STU | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0179 | SAS | STU | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG04228 | hp1 | a0002 | c0002 | t0002 | g0098 | SAS | STU | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG04228 | hp2 | a0006 | c0008 | t0008 | g0172 | SAS | STU | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | YRI | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA18522 | hp2 | a0001 | c0004 | t0007 | g0299 | AFR | YRI | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | CHB | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | CHB | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | CHB | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA18747 | hp2 | a0004 | c0016 | t0002 | g0318 | EAS | CHB | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | YRI | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA18906 | hp2 | a0001 | c0004 | t0006 | g0132 | AFR | YRI | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA18939 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA18942 | hp2 | a0004 | c0005 | t0003 | g0037 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA18943 | hp2 | a0002 | c0002 | t0002 | g0042 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA18945 | hp2 | a0002 | c0002 | t0002 | g0080 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA18946 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA18947 | hp2 | a0002 | c0002 | t0002 | g0064 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA18948 | hp1 | a0004 | c0005 | t0002 | g0036 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA18948 | hp2 | a0002 | c0002 | t0002 | g0018 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA18949 | hp2 | a0002 | c0002 | t0017 | g0070 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA18950 | hp1 | a0003 | c0003 | t0004 | g0033 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA18953 | hp2 | a0002 | c0002 | t0002 | g0013 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA18959 | hp1 | a0012 | c0020 | t0010 | g0334 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA18960 | hp2 | a0002 | c0002 | t0002 | g0015 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA18961 | hp2 | a0004 | c0005 | t0003 | g0323 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA18962 | hp1 | a0003 | c0003 | t0004 | g0282 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA18964 | hp2 | a0003 | c0003 | t0004 | g0280 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA18967 | hp1 | a0002 | c0002 | t0003 | g0066 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA18968 | hp1 | a0003 | c0003 | t0009 | g0287 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA18968 | hp2 | a0002 | c0002 | t0003 | g0044 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA18970 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA18971 | hp1 | a0002 | c0002 | t0002 | g0013 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA18972 | hp1 | a0002 | c0002 | t0002 | g0105 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA18973 | hp2 | a0003 | c0003 | t0009 | g0034 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA18975 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA18975 | hp2 | a0001 | c0001 | t0008 | g0307 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA18977 | hp1 | a0002 | c0002 | t0002 | g0201 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA18977 | hp2 | a0002 | c0002 | t0003 | g0104 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA18978 | hp2 | a0004 | c0005 | t0003 | g0037 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA18979 | hp2 | a0013 | c0019 | t0002 | g0072 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA18980 | hp1 | a0001 | c0001 | t0008 | g0197 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA18980 | hp2 | a0002 | c0002 | t0002 | g0054 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA18981 | hp2 | a0003 | c0003 | t0004 | g0277 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA18982 | hp1 | a0004 | c0005 | t0003 | g0021 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA18983 | hp2 | a0000 | c0010 | t0014 | g0026 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA18984 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA18984 | hp2 | a0003 | c0003 | t0018 | g0275 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA18985 | hp1 | a0001 | c0011 | t0001 | g0010 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA18985 | hp2 | a0003 | c0003 | t0004 | g0294 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA18986 | hp1 | a0003 | c0003 | t0004 | g0292 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA18987 | hp1 | a0004 | c0005 | t0003 | g0321 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA18988 | hp1 | a0002 | c0002 | t0002 | g0090 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA18990 | hp1 | a0002 | c0002 | t0003 | g0076 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA18990 | hp2 | a0003 | c0003 | t0004 | g0033 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA18991 | hp1 | a0003 | c0003 | t0004 | g0281 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA18991 | hp2 | a0004 | c0005 | t0016 | g0304 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA18992 | hp2 | a0003 | c0003 | t0004 | g0285 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA18993 | hp2 | a0002 | c0002 | t0002 | g0019 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA18994 | hp1 | a0002 | c0002 | t0003 | g0108 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA18994 | hp2 | a0003 | c0003 | t0009 | g0034 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA19001 | hp1 | a0003 | c0003 | t0009 | g0279 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA19001 | hp2 | a0002 | c0002 | t0002 | g0223 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA19002 | hp1 | a0018 | c0026 | t0003 | g0317 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA19002 | hp2 | a0003 | c0003 | t0018 | g0290 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA19003 | hp1 | a0003 | c0003 | t0004 | g0276 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA19003 | hp2 | a0002 | c0002 | t0002 | g0109 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA19005 | hp1 | a0002 | c0002 | t0002 | g0015 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA19005 | hp2 | a0011 | c0017 | t0001 | g0319 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA19006 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA19006 | hp2 | a0004 | c0005 | t0003 | g0320 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA19007 | hp1 | a0002 | c0002 | t0017 | g0069 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA19009 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA19010 | hp1 | a0002 | c0002 | t0003 | g0014 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA19010 | hp2 | a0003 | c0003 | t0004 | g0273 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA19030 | hp1 | a0001 | c0004 | t0006 | g0128 | AFR | LWK | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA19030 | hp2 | a0002 | c0002 | t0002 | g0120 | AFR | LWK | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA19043 | hp1 | a0002 | c0002 | t0002 | g0121 | AFR | LWK | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA19043 | hp2 | a0002 | c0002 | t0029 | g0117 | AFR | LWK | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA19054 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA19056 | hp2 | a0002 | c0002 | t0016 | g0018 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA19057 | hp1 | a0003 | c0003 | t0004 | g0289 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA19057 | hp2 | a0002 | c0002 | t0002 | g0053 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA19058 | hp1 | a0004 | c0005 | t0003 | g0205 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA19058 | hp2 | a0002 | c0002 | t0002 | g0078 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA19060 | hp1 | a0004 | c0005 | t0003 | g0322 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA19063 | hp1 | a0001 | c0011 | t0001 | g0184 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA19063 | hp2 | a0002 | c0002 | t0002 | g0061 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA19064 | hp1 | a0003 | c0003 | t0004 | g0284 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA19066 | hp2 | a0002 | c0002 | t0002 | g0063 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA19067 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA19068 | hp1 | a0002 | c0002 | t0003 | g0014 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA19068 | hp2 | a0000 | c0010 | t0014 | g0026 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA19072 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA19074 | hp1 | a0003 | c0003 | t0004 | g0250 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA19076 | hp2 | a0002 | c0002 | t0002 | g0052 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA19077 | hp1 | a0003 | c0003 | t0004 | g0283 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA19080 | hp2 | a0002 | c0002 | t0002 | g0062 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA19081 | hp2 | a0002 | c0002 | t0002 | g0051 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA19083 | hp1 | a0002 | c0002 | t0003 | g0170 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA19083 | hp2 | a0004 | c0005 | t0003 | g0324 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA19086 | hp2 | a0002 | c0002 | t0002 | g0095 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA19087 | hp2 | a0003 | c0003 | t0004 | g0291 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA19088 | hp1 | a0002 | c0002 | t0002 | g0094 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA19088 | hp2 | a0003 | c0003 | t0004 | g0272 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA19089 | hp1 | a0002 | c0002 | t0003 | g0079 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA19090 | hp1 | a0003 | c0003 | t0004 | g0293 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA19240 | hp1 | a0001 | c0004 | t0006 | g0224 | AFR | YRI | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA19240 | hp2 | a0009 | c0014 | t0001 | g0302 | AFR | YRI | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA20752 | hp1 | a0001 | c0007 | t0001 | g0259 | EUR | TSI | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA20752 | hp2 | a0005 | c0006 | t0005 | g0327 | EUR | TSI | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA20805 | hp1 | a0001 | c0007 | t0001 | g0296 | EUR | TSI | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0111 | EUR | TSI | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG01123 | hp1 | a0005 | c0006 | t0005 | g0332 | AMR | CLM | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG01123 | hp2 | a0002 | c0002 | t0002 | g0100 | AMR | CLM | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG02109 | hp1 | a0014 | c0023 | t0001 | g0217 | AFR | ACB | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | ACB | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | ACB | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG02559 | hp2 | a0002 | c0002 | t0012 | g0242 | AFR | ACB | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG03471 | hp1 | a0001 | c0022 | t0001 | g0145 | AFR | MSL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG03471 | hp2 | a0017 | c0025 | t0003 | g0203 | AFR | MSL | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG06807 | hp1 | a0007 | c0012 | t0001 | g0154 | AFR | USA | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
HG06807 | hp2 | a0002 | c0002 | t0002 | g0124 | AFR | USA | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA18955 | hp2 | a0004 | c0005 | t0003 | g0021 | EAS | JPT | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | USA | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA20300 | hp2 | a0001 | c0004 | t0007 | g0297 | AFR | USA | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA21309 | hp1 | a0002 | c0002 | t0002 | g0103 | AFR | LWK | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
NA21309 | hp2 | a0002 | c0002 | t0002 | g0325 | AFR | LWK | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
homoSapiens_chm13v2 | hp1 | a0001 | c0007 | t0001 | g0260 | REF | REF | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
homoSapiens_grch38 | hp1 | a0002 | c0002 | t0001 | g0123 | REF | REF | ERAP2_chr5_96871500_96924703 | ERAP2 | chr5 | 96871500 | 96924703 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:96879693
|
A | C | 1 | a0018 | 1 | NA19002.hp1 | missense_variant | MODERATE | c.8A>C | p.His3Pro | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 2/19 | 158/5131 | 8/2883 | 3/960 | chr5 | 96879693 | ||
chr5:96879773
|
C | T | 1 | a0017 | 1 | HG03471.hp2 | missense_variant | MODERATE | c.88C>T | p.Pro30Ser | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 2/19 | 238/5131 | 88/2883 | 30/960 | chr5 | 96879773 | ||
chr5:96880043
|
G | C | 1 | a0016 | 1 | HG02055.hp1 | missense_variant | MODERATE | c.358G>C | p.Ala120Pro | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 2/19 | 508/5131 | 358/2883 | 120/960 | chr5 | 96880043 | ||
chr5:96883830
|
G | A | 1 | a0009 | 1 | NA19240.hp2 | missense_variant | MODERATE | c.614G>A | p.Arg205His | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 3/19 | 764/5131 | 614/2883 | 205/960 | chr5 | 96883830 | ||
chr5:96883857
|
C | T | 1 | a0003 | 30 | HG00558.hp2 HG00609.hp1 HG01257.hp1 others(27): Show |
missense_variant | MODERATE | c.641C>T | p.Pro214Leu | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 3/19 | 791/5131 | 641/2883 | 214/960 | chr5 | 96883857 | ||
chr5:96886656
|
T | C | 1 | a0010 | 1 | HG02615.hp2 | missense_variant&splice_region_variant | MODERATE | c.716T>C | p.Val239Ala | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/19 | 866/5131 | 716/2883 | 239/960 | chr5 | 96886656 | ||
chr5:96889200
|
T | G | 3 | a0004a0011a0018 | 17 | HG00597.hp1 HG02148.hp1 NA18747.hp2 others(14): Show |
missense_variant | MODERATE | c.865T>G | p.Ser289Ala | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/19 | 1015/5131 | 865/2883 | 289/960 | chr5 | 96889200 | ||
chr5:96892368
|
C | T | 1 | a0007 | 2 | HG01074.hp1 HG06807.hp1 |
missense_variant | MODERATE | c.1040C>T | p.Thr347Met | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 6/19 | 1190/5131 | 1040/2883 | 347/960 | chr5 | 96892368 | ||
chr5:96892446
|
C | A | 1 | a0015 | 1 | HG02965.hp2 | missense_variant | MODERATE | c.1118C>A | p.Ala373Glu | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 6/19 | 1268/5131 | 1118/2883 | 373/960 | chr5 | 96892446 | ||
chr5:96895296
|
G | T | 9 | a0000a0001a0006others(6): Show | 206 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(203): Show |
missense_variant | MODERATE | c.1176G>T | p.Lys392Asn | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 7/19 | 1326/5131 | 1176/2883 | 392/960 | chr5 | 96895296 | ||
chr5:96895339
|
A | G | 1 | a0012 | 1 | NA18959.hp1 | missense_variant | MODERATE | c.1219A>G | p.Thr407Ala | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 7/19 | 1369/5131 | 1219/2883 | 407/960 | chr5 | 96895339 | ||
chr5:96901626
|
C | T | 1 | a0014 | 1 | HG02109.hp1 | missense_variant | MODERATE | c.1693C>T | p.Arg565Cys | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 11/19 | 1843/5131 | 1693/2883 | 565/960 | chr5 | 96901626 | ||
chr5:96903530
|
G | T | 2 | a0008a0016 | 3 | HG02055.hp1 HG02572.hp1 HG03098.hp1 |
missense_variant | MODERATE | c.1982G>T | p.Gly661Val | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/19 | 2132/5131 | 1982/2883 | 661/960 | chr5 | 96903530 | ||
chr5:96903554
|
T | A | 1 | a0005 | 13 | HG00642.hp1 HG00735.hp1 HG01123.hp1 others(10): Show |
missense_variant | MODERATE | c.2006T>A | p.Leu669Gln | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/19 | 2156/5131 | 2006/2883 | 669/960 | chr5 | 96903554 | ||
chr5:96909661
|
C | T | 1 | a0006 | 4 | HG02040.hp1 HG02698.hp2 HG03927.hp1 others(1): Show |
missense_variant | MODERATE | c.2251C>T | p.Arg751Cys | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/19 | 2401/5131 | 2251/2883 | 751/960 | chr5 | 96909661 | ||
chr5:96912223
|
TGCCTTCA others(9786): Show |
T | 1 | a0000 | 2 | NA18983.hp2 NA19068.hp2 |
exon_loss_variant | HIGH | c.2355-413_*4411del | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 16/19 | chr5 | 96912223 | ||||||
chr5:96912792
|
T | C | 1 | a0013 | 1 | NA18979.hp2 | missense_variant | MODERATE | c.2510T>C | p.Leu837Ser | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 16/19 | 2660/5131 | 2510/2883 | 837/960 | chr5 | 96912792 | ||
chr5:96917577
|
T | C | 1 | a0009 | 1 | NA19240.hp2 | missense_variant | MODERATE | c.2855T>C | p.Leu952Pro | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 19/19 | 3005/5131 | 2855/2883 | 952/960 | chr5 | 96917577 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:96879976
|
C | T | 2 | a0001c0007a0002c0024 | 12 | HG01167.hp1 HG01168.hp1 HG01256.hp1 others(9): Show |
synonymous_variant | LOW | c.291C>T | p.Ile97Ile | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 2/19 | 441/5131 | 291/2883 | 97/960 | chr5 | 96879976 | ||
chr5:96896438
|
T | A | 14 | a0000c0010a0001c0001a0001c0004others(11): Show | 206 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(203): Show |
synonymous_variant | LOW | c.1305T>A | p.Pro435Pro | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 8/19 | 1455/5131 | 1305/2883 | 435/960 | chr5 | 96896438 | ||
chr5:96901622
|
G | A | 14 | a0000c0010a0001c0001a0001c0004others(11): Show | 206 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(203): Show |
synonymous_variant | LOW | c.1689G>A | p.Gln563Gln | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 11/19 | 1839/5131 | 1689/2883 | 563/960 | chr5 | 96901622 | ||
chr5:96909015
|
T | C | 1 | a0005c0006 | 13 | HG00642.hp1 HG00735.hp1 HG01123.hp1 others(10): Show |
synonymous_variant | LOW | c.2067T>C | p.His689His | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 14/19 | 2217/5131 | 2067/2883 | 689/960 | chr5 | 96909015 | ||
chr5:96909030
|
C | T | 1 | a0001c0022 | 1 | HG03471.hp1 | synonymous_variant | LOW | c.2082C>T | p.Pro694Pro | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 14/19 | 2232/5131 | 2082/2883 | 694/960 | chr5 | 96909030 | ||
chr5:96909639
|
C | T | 13 | a0000c0010a0001c0001a0001c0007others(10): Show | 180 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(177): Show |
synonymous_variant | LOW | c.2229C>T | p.Gly743Gly | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/19 | 2379/5131 | 2229/2883 | 743/960 | chr5 | 96909639 | ||
chr5:96909735
|
C | T | 14 | a0000c0010a0001c0001a0001c0004others(11): Show | 206 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(203): Show |
synonymous_variant | LOW | c.2325C>T | p.Ser775Ser | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/19 | 2475/5131 | 2325/2883 | 775/960 | chr5 | 96909735 | ||
chr5:96913411
|
C | T | 13 | a0001c0001a0001c0004a0001c0007others(10): Show | 204 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(201): Show |
synonymous_variant | LOW | c.2611C>T | p.Leu871Leu | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/19 | 2761/5131 | 2611/2883 | 871/960 | chr5 | 96913411 | ||
chr5:96915724
|
C | T | 1 | a0001c0011 | 2 | NA18985.hp1 NA19063.hp1 |
synonymous_variant | LOW | c.2694C>T | p.Ile898Ile | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 18/19 | 2844/5131 | 2694/2883 | 898/960 | chr5 | 96915724 | ||
chr5:96917527
|
G | A | 1 | a0004c0016 | 1 | NA18747.hp2 | synonymous_variant | LOW | c.2805G>A | p.Leu935Leu | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 19/19 | 2955/5131 | 2805/2883 | 935/960 | chr5 | 96917527 | ||
chr5:96917572
|
G | A | 1 | a0001c0021 | 1 | HG01975.hp2 | synonymous_variant | LOW | c.2850G>A | p.Pro950Pro | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 19/19 | 3000/5131 | 2850/2883 | 950/960 | chr5 | 96917572 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:96879641
|
C | T | 1 | a0001c0004t0011 | 5 | HG01109.hp1 HG01496.hp1 HG01884.hp2 others(2): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-45C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 2/19 | chr5 | 96879641 | ||||||
chr5:96917679
|
G | A | 1 | a0002c0002t0019 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*74G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 19/19 | 74 | chr5 | 96917679 | |||||
chr5:96917681
|
C | T | 1 | a0001c0004t0030 | 1 | HG02738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*76C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 19/19 | 76 | chr5 | 96917681 | |||||
chr5:96917744
|
A | G | 8 | a0002c0002t0009a0002c0002t0012a0002c0002t0029others(5): Show | 51 | HG00558.hp2 HG00609.hp1 HG00642.hp1 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*139A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 19/19 | 139 | chr5 | 96917744 | |||||
chr5:96917859
|
T | C | 1 | a0001c0001t0020 | 1 | HG01175.hp1 | 3_prime_UTR_variant | MODIFIER | c.*254T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 19/19 | 254 | chr5 | 96917859 | |||||
chr5:96917905
|
C | CA | 10 | a0001c0001t0008a0001c0004t0006a0001c0004t0007others(7): Show | 58 | HG00544.hp1 HG00597.hp1 HG01109.hp1 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*323dupA | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 19/19 | 324 | INFO_REALIGN_3_PRIME | chr5 | 96917905 | ||||
chr5:96917905
|
C | CAA | 7 | a0001c0004t0015a0001c0004t0022a0002c0002t0016others(4): Show | 18 | HG00642.hp1 HG01123.hp1 HG01168.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*322_*323dupAA | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 19/19 | 324 | INFO_REALIGN_3_PRIME | chr5 | 96917905 | ||||
chr5:96917905
|
C | CAAA | 3 | a0002c0002t0012a0003c0003t0004a0005c0006t0013 | 31 | HG00558.hp2 HG00609.hp1 HG00735.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*321_*323dupAAA | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 19/19 | 324 | INFO_REALIGN_3_PRIME | chr5 | 96917905 | ||||
chr5:96917905
|
C | CAAAA | 2 | a0002c0002t0009a0003c0003t0009 | 7 | HG01243.hp2 HG02647.hp1 HG03130.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*320_*323dupAAAA | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 19/19 | 324 | INFO_REALIGN_3_PRIME | chr5 | 96917905 | ||||
chr5:96917905
|
CAAAAAAA others(5): Show |
C | 1 | a0002c0002t0017 | 2 | NA18949.hp2 NA19007.hp1 |
3_prime_UTR_variant | MODIFIER | c.*312_*323delAAAAAA others(6): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 19/19 | 312 | INFO_REALIGN_3_PRIME | chr5 | 96917905 | ||||
chr5:96917922
|
A | G | 1 | a0001c0001t0028 | 1 | HG02155.hp2 | 3_prime_UTR_variant | MODIFIER | c.*317A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 19/19 | 317 | chr5 | 96917922 | |||||
chr5:96917923
|
A | G | 1 | a0001c0001t0027 | 1 | HG01192.hp2 | 3_prime_UTR_variant | MODIFIER | c.*318A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 19/19 | 318 | chr5 | 96917923 | |||||
chr5:96918486
|
T | C | 1 | a0001c0004t0007 | 7 | HG02451.hp1 HG02622.hp2 HG02809.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*881T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 19/19 | 881 | chr5 | 96918486 | |||||
chr5:96918505
|
A | G | 34 | a0001c0004t0006a0001c0004t0007a0001c0004t0011others(31): Show | 217 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(214): Show |
3_prime_UTR_variant | MODIFIER | c.*900A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 19/19 | 900 | chr5 | 96918505 | |||||
chr5:96918597
|
A | G | 8 | a0002c0002t0009a0002c0002t0012a0002c0002t0029others(5): Show | 51 | HG00558.hp2 HG00609.hp1 HG00642.hp1 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*992A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 19/19 | 992 | chr5 | 96918597 | |||||
chr5:96918650
|
T | A | 34 | a0001c0004t0006a0001c0004t0007a0001c0004t0011others(31): Show | 217 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(214): Show |
3_prime_UTR_variant | MODIFIER | c.*1045T>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 19/19 | 1045 | chr5 | 96918650 | |||||
chr5:96918795
|
C | T | 1 | a0002c0002t0026 | 1 | HG00423.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1190C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 19/19 | 1190 | chr5 | 96918795 | |||||
chr5:96918881
|
AC | A | 4 | a0001c0004t0022a0001c0004t0030a0002c0002t0010others(1): Show | 7 | HG00738.hp2 HG01167.hp2 HG01975.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1282delC | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 19/19 | 1282 | INFO_REALIGN_3_PRIME | chr5 | 96918881 | ||||
chr5:96918945
|
T | A | 4 | a0001c0004t0006a0001c0004t0011a0001c0004t0015others(1): Show | 17 | HG01109.hp1 HG01243.hp1 HG01496.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1340T>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 19/19 | 1340 | chr5 | 96918945 | |||||
chr5:96919025
|
C | T | 2 | a0002c0002t0012a0002c0002t0029 | 5 | HG02559.hp2 HG02896.hp2 HG02976.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1420C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 19/19 | 1420 | chr5 | 96919025 | |||||
chr5:96919113
|
G | A | 34 | a0001c0004t0006a0001c0004t0007a0001c0004t0011others(31): Show | 217 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(214): Show |
3_prime_UTR_variant | MODIFIER | c.*1508G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 19/19 | 1508 | chr5 | 96919113 | |||||
chr5:96919175
|
A | C | 1 | a0008c0009t0025 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1570A>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 19/19 | 1570 | chr5 | 96919175 | |||||
chr5:96919290
|
T | A | 2 | a0005c0006t0005a0005c0006t0013 | 13 | HG00642.hp1 HG00735.hp1 HG01123.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1685T>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 19/19 | 1685 | chr5 | 96919290 | |||||
chr5:96919313
|
T | C | 8 | a0002c0002t0009a0002c0002t0012a0002c0002t0029others(5): Show | 51 | HG00558.hp2 HG00609.hp1 HG00642.hp1 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*1708T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 19/19 | 1708 | chr5 | 96919313 | |||||
chr5:96919548
|
T | C | 2 | a0001c0004t0022a0001c0004t0030 | 2 | HG02738.hp1 HG03831.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1943T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 19/19 | 1943 | chr5 | 96919548 | |||||
chr5:96919627
|
A | G | 1 | a0001c0001t0023 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2022A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 19/19 | 2022 | chr5 | 96919627 | |||||
chr5:96919649
|
T | C | 1 | a0002c0002t0012 | 4 | HG02559.hp2 HG02896.hp2 HG02976.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2044T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 19/19 | 2044 | chr5 | 96919649 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:96876861
|
C | T | 4 | a0002c0002t0010g0039a0002c0002t0010g0335a0002c0002t0010g0336others(1): Show | 5 | HG00738.hp2 HG01167.hp2 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.-123+334C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 1/18 | chr5 | 96876861 | ||||||
chr5:96876933
|
A | G | 10 | a0001c0001t0027g0333a0005c0006t0005g0038a0005c0006t0005g0327others(7): Show | 10 | HG00735.hp1 HG01123.hp1 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.-123+406A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 1/18 | chr5 | 96876933 | ||||||
chr5:96876999
|
G | C | 1 | a0001c0001t0001g0040 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-123+472G>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 1/18 | chr5 | 96876999 | ||||||
chr5:96877006
|
G | A | 2 | a0002c0002t0002g0042a0002c0002t0026g0041 | 2 | HG00423.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.-123+479G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 1/18 | chr5 | 96877006 | ||||||
chr5:96877013
|
C | T | 1 | a0002c0002t0002g0325 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-123+486C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 1/18 | chr5 | 96877013 | ||||||
chr5:96877037
|
C | T | 24 | a0001c0001t0001g0012a0001c0001t0001g0305a0001c0001t0001g0306others(21): Show | 28 | HG00597.hp1 HG00597.hp2 HG02148.hp1 others(25): Show |
intron_variant | MODIFIER | c.-123+510C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 1/18 | chr5 | 96877037 | ||||||
chr5:96877077
|
C | T | 189 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(186): Show | 216 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(213): Show |
intron_variant | MODIFIER | c.-123+550C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 1/18 | chr5 | 96877077 | ||||||
chr5:96877136
|
G | A | 16 | a0001c0001t0001g0024a0001c0001t0001g0140a0001c0001t0001g0141others(13): Show | 17 | HG00738.hp1 HG01243.hp1 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.-123+609G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 1/18 | chr5 | 96877136 | ||||||
chr5:96877191
|
T | C | 188 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(185): Show | 215 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(212): Show |
intron_variant | MODIFIER | c.-123+664T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 1/18 | chr5 | 96877191 | ||||||
chr5:96877241
|
C | G | 9 | a0001c0001t0001g0035a0001c0001t0001g0300a0001c0001t0001g0301others(6): Show | 10 | HG02451.hp1 HG02559.hp1 HG02970.hp1 others(7): Show |
intron_variant | MODIFIER | c.-123+714C>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 1/18 | chr5 | 96877241 | ||||||
chr5:96877355
|
G | T | 1 | a0001c0004t0007g0303 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-123+828G>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 1/18 | chr5 | 96877355 | ||||||
chr5:96877423
|
C | CA | 189 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(186): Show | 216 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(213): Show |
intron_variant | MODIFIER | c.-123+896_-123+897i others(3): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 1/18 | chr5 | 96877423 | ||||||
chr5:96877426
|
G | T | 7 | a0001c0004t0006g0131a0001c0004t0006g0132a0001c0004t0011g0133others(4): Show | 7 | HG01109.hp1 HG01496.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.-123+899G>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 1/18 | chr5 | 96877426 | ||||||
chr5:96877467
|
C | A | 189 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(186): Show | 216 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(213): Show |
intron_variant | MODIFIER | c.-123+940C>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 1/18 | chr5 | 96877467 | ||||||
chr5:96877536
|
C | T | 1 | a0001c0004t0007g0303 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-123+1009C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 1/18 | chr5 | 96877536 | ||||||
chr5:96877629
|
A | C | 189 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(186): Show | 216 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(213): Show |
intron_variant | MODIFIER | c.-123+1102A>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 1/18 | chr5 | 96877629 | ||||||
chr5:96877682
|
T | A | 1 | a0001c0001t0001g0043 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-123+1155T>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 1/18 | chr5 | 96877682 | ||||||
chr5:96877683
|
C | A | 1 | a0001c0001t0001g0043 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-123+1156C>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 1/18 | chr5 | 96877683 | ||||||
chr5:96877731
|
A | AT | 189 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(186): Show | 216 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(213): Show |
intron_variant | MODIFIER | c.-123+1212dupT | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 96877731 | |||||
chr5:96877766
|
A | G | 14 | a0001c0001t0027g0333a0002c0002t0010g0039a0002c0002t0010g0335others(11): Show | 15 | HG00735.hp1 HG00738.hp2 HG01123.hp1 others(12): Show |
intron_variant | MODIFIER | c.-123+1239A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 1/18 | chr5 | 96877766 | ||||||
chr5:96877812
|
T | C | 1 | a0001c0001t0020g0151 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-123+1285T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 1/18 | chr5 | 96877812 | ||||||
chr5:96877857
|
C | CTTTA | 189 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(186): Show | 216 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(213): Show |
intron_variant | MODIFIER | c.-123+1331_-123+133 others(8): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 96877857 | |||||
chr5:96877903
|
G | T | 52 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253others(49): Show | 56 | HG00280.hp2 HG00558.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.-123+1376G>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 1/18 | chr5 | 96877903 | ||||||
chr5:96878111
|
G | A | 1 | a0002c0002t0003g0044 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-122-1453G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 1/18 | chr5 | 96878111 | ||||||
chr5:96878222
|
G | A | 189 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(186): Show | 216 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(213): Show |
intron_variant | MODIFIER | c.-122-1342G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 1/18 | chr5 | 96878222 | ||||||
chr5:96878228
|
T | TA | 189 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(186): Show | 216 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(213): Show |
intron_variant | MODIFIER | c.-122-1329dupA | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 96878228 | |||||
chr5:96878311
|
C | T | 5 | a0001c0001t0001g0245a0001c0001t0001g0246a0001c0001t0001g0247others(2): Show | 5 | HG01069.hp2 HG01071.hp2 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.-122-1253C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 1/18 | chr5 | 96878311 | ||||||
chr5:96878404
|
G | GTAA | 301 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(298): Show | 350 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(347): Show |
intron_variant | MODIFIER | c.-122-1151_-122-114 others(7): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr5 | 96878404 | |||||
chr5:96878432
|
T | C | 8 | a0001c0001t0001g0035a0001c0001t0001g0300a0001c0001t0001g0301others(5): Show | 9 | HG02451.hp1 HG02559.hp1 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.-122-1132T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 1/18 | chr5 | 96878432 | ||||||
chr5:96878478
|
A | G | 4 | a0001c0001t0001g0127a0001c0004t0006g0128a0001c0004t0006g0130others(1): Show | 4 | HG02055.hp2 HG02258.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.-122-1086A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 1/18 | chr5 | 96878478 | ||||||
chr5:96878513
|
C | T | 19 | a0001c0001t0001g0040a0001c0001t0001g0227a0001c0001t0001g0228others(16): Show | 19 | HG01192.hp1 HG01358.hp1 HG01993.hp1 others(16): Show |
intron_variant | MODIFIER | c.-122-1051C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 1/18 | chr5 | 96878513 | ||||||
chr5:96878536
|
G | A | 134 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(131): Show | 157 | HG00140.hp1 HG00423.hp2 HG00558.hp1 others(154): Show |
intron_variant | MODIFIER | c.-122-1028G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 1/18 | chr5 | 96878536 | ||||||
chr5:96878621
|
T | C | 3 | a0001c0004t0006g0139a0002c0002t0009g0023a0002c0002t0009g0138 | 4 | HG01243.hp1 HG01243.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.-122-943T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 1/18 | chr5 | 96878621 | ||||||
chr5:96878803
|
C | T | 189 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(186): Show | 216 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(213): Show |
intron_variant | MODIFIER | c.-122-761C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 1/18 | chr5 | 96878803 | ||||||
chr5:96878877
|
A | G | 189 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(186): Show | 216 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(213): Show |
intron_variant | MODIFIER | c.-122-687A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 1/18 | chr5 | 96878877 | ||||||
chr5:96878955
|
G | A | 210 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(207): Show | 238 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(235): Show |
intron_variant | MODIFIER | c.-122-609G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 1/18 | chr5 | 96878955 | ||||||
chr5:96879084
|
C | T | 8 | a0001c0001t0001g0043a0001c0001t0001g0110a0001c0001t0001g0111others(5): Show | 8 | HG00280.hp1 HG02622.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.-122-480C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 1/18 | chr5 | 96879084 | ||||||
chr5:96879107
|
T | C | 7 | a0001c0004t0006g0131a0001c0004t0006g0132a0001c0004t0011g0133others(4): Show | 7 | HG01109.hp1 HG01496.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.-122-457T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 1/18 | chr5 | 96879107 | ||||||
chr5:96879227
|
C | T | 1 | a0002c0002t0002g0126 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-122-337C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 1/18 | chr5 | 96879227 | ||||||
chr5:96879382
|
A | G | 2 | a0001c0004t0022g0225a0001c0004t0030g0226 | 2 | HG02738.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.-122-182A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 1/18 | chr5 | 96879382 | ||||||
chr5:96880372
|
T | C | 7 | a0001c0004t0006g0131a0001c0004t0006g0132a0001c0004t0011g0133others(4): Show | 7 | HG01109.hp1 HG01496.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.575+112T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 2/18 | chr5 | 96880372 | ||||||
chr5:96880469
|
A | G | 51 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253others(48): Show | 55 | HG00280.hp2 HG00558.hp2 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.575+209A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 2/18 | chr5 | 96880469 | ||||||
chr5:96880513
|
T | C | 16 | a0001c0001t0001g0040a0001c0001t0001g0227a0001c0001t0001g0228others(13): Show | 16 | HG01175.hp1 HG01192.hp1 HG01358.hp1 others(13): Show |
intron_variant | MODIFIER | c.575+253T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 2/18 | chr5 | 96880513 | ||||||
chr5:96880609
|
A | T | 3 | a0001c0004t0007g0114a0001c0004t0007g0115a0001c0004t0007g0116 | 3 | HG02622.hp2 HG02809.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.575+349A>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 2/18 | chr5 | 96880609 | ||||||
chr5:96880683
|
A | G | 189 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(186): Show | 216 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(213): Show |
intron_variant | MODIFIER | c.575+423A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 2/18 | chr5 | 96880683 | ||||||
chr5:96880695
|
GA | G | 106 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(103): Show | 128 | HG00140.hp1 HG00423.hp2 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.575+438delA | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr5 | 96880695 | |||||
chr5:96880705
|
A | T | 1 | a0002c0002t0002g0325 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.575+445A>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 2/18 | chr5 | 96880705 | ||||||
chr5:96880920
|
T | C | 1 | a0001c0001t0008g0045 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.575+660T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 2/18 | chr5 | 96880920 | ||||||
chr5:96881043
|
A | C | 5 | a0001c0004t0011g0133a0001c0004t0011g0134a0001c0004t0011g0135others(2): Show | 5 | HG01109.hp1 HG01496.hp1 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.575+783A>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 2/18 | chr5 | 96881043 | ||||||
chr5:96881080
|
G | A | 170 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(167): Show | 195 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(192): Show |
intron_variant | MODIFIER | c.575+820G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 2/18 | chr5 | 96881080 | ||||||
chr5:96881189
|
GCT | G | 30 | a0001c0001t0001g0012a0001c0001t0001g0127a0001c0001t0001g0305others(27): Show | 34 | HG00597.hp1 HG00597.hp2 HG02055.hp2 others(31): Show |
intron_variant | MODIFIER | c.575+932_575+933del others(2): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr5 | 96881189 | |||||
chr5:96881200
|
T | C | 1 | a0003c0003t0004g0250 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.575+940T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 2/18 | chr5 | 96881200 | ||||||
chr5:96881337
|
C | T | 1 | a0001c0007t0001g0296 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.575+1077C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 2/18 | chr5 | 96881337 | ||||||
chr5:96881445
|
C | T | 2 | a0002c0002t0002g0109a0002c0002t0003g0108 | 2 | NA18994.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.575+1185C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 2/18 | chr5 | 96881445 | ||||||
chr5:96881591
|
T | G | 1 | a0002c0002t0002g0046 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.575+1331T>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 2/18 | chr5 | 96881591 | ||||||
chr5:96881642
|
A | G | 8 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0206others(5): Show | 13 | HG02258.hp1 HG02280.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.575+1382A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 2/18 | chr5 | 96881642 | ||||||
chr5:96881686
|
A | G | 26 | a0001c0001t0001g0012a0001c0001t0001g0305a0001c0001t0001g0306others(23): Show | 30 | HG00597.hp1 HG00597.hp2 HG02148.hp1 others(27): Show |
intron_variant | MODIFIER | c.575+1426A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 2/18 | chr5 | 96881686 | ||||||
chr5:96881988
|
G | GA | 245 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(242): Show | 276 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.575+1730dupA | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr5 | 96881988 | |||||
chr5:96882068
|
C | G | 1 | a0004c0005t0003g0324 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.576-1724C>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 2/18 | chr5 | 96882068 | ||||||
chr5:96882087
|
G | A | 1 | a0007c0012t0001g0152 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.576-1705G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 2/18 | chr5 | 96882087 | ||||||
chr5:96882346
|
G | T | 2 | a0004c0005t0003g0322a0004c0005t0003g0323 | 2 | NA18961.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.576-1446G>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 2/18 | chr5 | 96882346 | ||||||
chr5:96882389
|
G | T | 1 | a0002c0002t0002g0107 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.576-1403G>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 2/18 | chr5 | 96882389 | ||||||
chr5:96882429
|
A | G | 16 | a0001c0004t0006g0128a0001c0004t0006g0130a0001c0004t0006g0131others(13): Show | 16 | HG01109.hp1 HG01243.hp1 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.576-1363A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 2/18 | chr5 | 96882429 | ||||||
chr5:96882464
|
C | T | 4 | a0002c0002t0010g0039a0002c0002t0010g0335a0002c0002t0010g0336others(1): Show | 5 | HG00738.hp2 HG01167.hp2 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.576-1328C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 2/18 | chr5 | 96882464 | ||||||
chr5:96882660
|
C | T | 1 | a0002c0002t0002g0204 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.576-1132C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 2/18 | chr5 | 96882660 | ||||||
chr5:96882787
|
TC | T | 14 | a0002c0002t0010g0039a0002c0002t0010g0335a0002c0002t0010g0336others(11): Show | 15 | HG00642.hp1 HG00735.hp1 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.576-1002delC | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr5 | 96882787 | |||||
chr5:96882844
|
C | A | 6 | a0001c0001t0001g0213a0001c0001t0001g0215a0001c0001t0001g0245others(3): Show | 6 | HG01975.hp2 HG01981.hp2 HG02004.hp1 others(3): Show |
intron_variant | MODIFIER | c.576-948C>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 2/18 | chr5 | 96882844 | ||||||
chr5:96882894
|
C | T | 67 | a0001c0004t0007g0114a0001c0004t0007g0115a0001c0004t0007g0116others(64): Show | 75 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(72): Show |
intron_variant | MODIFIER | c.576-898C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 2/18 | chr5 | 96882894 | ||||||
chr5:96882913
|
A | T | 1 | a0002c0002t0029g0117 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.576-879A>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 2/18 | chr5 | 96882913 | ||||||
chr5:96882962
|
G | C | 2 | a0002c0002t0009g0023a0002c0002t0009g0138 | 3 | HG01243.hp2 HG02647.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.576-830G>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 2/18 | chr5 | 96882962 | ||||||
chr5:96883034
|
A | G | 1 | a0001c0001t0001g0200 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.576-758A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 2/18 | chr5 | 96883034 | ||||||
chr5:96883173
|
G | T | 40 | a0001c0004t0007g0114a0001c0004t0007g0115a0001c0004t0007g0116others(37): Show | 45 | HG00597.hp1 HG00642.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.576-619G>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 2/18 | chr5 | 96883173 | ||||||
chr5:96883464
|
A | G | 1 | a0002c0002t0002g0106 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.576-328A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 2/18 | chr5 | 96883464 | ||||||
chr5:96883469
|
T | G | 14 | a0002c0002t0010g0039a0002c0002t0010g0335a0002c0002t0010g0336others(11): Show | 15 | HG00642.hp1 HG00735.hp1 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.576-323T>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 2/18 | chr5 | 96883469 | ||||||
chr5:96883569
|
G | A | 1 | a0002c0002t0002g0051 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.576-223G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 2/18 | chr5 | 96883569 | ||||||
chr5:96883691
|
C | A | 2 | a0003c0003t0004g0272a0003c0003t0004g0273 | 2 | NA19010.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.576-101C>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 2/18 | chr5 | 96883691 | ||||||
chr5:96884034
|
T | TTATC | 65 | a0000c0010t0014g0026a0001c0001t0001g0007a0001c0001t0001g0020others(62): Show | 73 | HG00558.hp2 HG00609.hp1 HG01074.hp2 others(70): Show |
intron_variant | MODIFIER | c.714+149_714+152dup others(4): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr5 | 96884034 | |||||
chr5:96884034
|
TTATC | T | 102 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(99): Show | 123 | HG00423.hp1 HG00558.hp1 HG00642.hp1 others(120): Show |
intron_variant | MODIFIER | c.714+149_714+152del others(4): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr5 | 96884034 | |||||
chr5:96884034
|
TTATCTAT others(1): Show |
T | 29 | a0001c0001t0001g0030a0001c0001t0001g0043a0001c0001t0001g0047others(26): Show | 33 | HG00280.hp2 HG00323.hp1 HG01099.hp1 others(30): Show |
intron_variant | MODIFIER | c.714+145_714+152del others(8): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr5 | 96884034 | |||||
chr5:96884034
|
TTATCTAT others(5): Show |
T | 44 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0110others(41): Show | 46 | HG00280.hp1 HG00597.hp1 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.714+141_714+152del others(12): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr5 | 96884034 | |||||
chr5:96884034
|
TTATCTAT others(13): Show |
T | 1 | a0001c0001t0001g0005 | 4 | HG00140.hp1 HG00735.hp2 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.714+133_714+152del others(20): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr5 | 96884034 | |||||
chr5:96884075
|
T | A | 4 | a0001c0004t0007g0114a0001c0004t0007g0115a0001c0004t0007g0116others(1): Show | 4 | HG02622.hp2 HG02809.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.714+145T>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 3/18 | chr5 | 96884075 | ||||||
chr5:96884079
|
T | A | 4 | a0001c0004t0007g0114a0001c0004t0007g0115a0001c0004t0007g0116others(1): Show | 4 | HG02622.hp2 HG02809.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.714+149T>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 3/18 | chr5 | 96884079 | ||||||
chr5:96884146
|
CT | C | 178 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(175): Show | 202 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.714+225delT | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr5 | 96884146 | |||||
chr5:96884383
|
C | T | 244 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(241): Show | 276 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.714+453C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 3/18 | chr5 | 96884383 | ||||||
chr5:96884555
|
T | TTTTGTTT others(1): Show |
174 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(171): Show | 198 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.714+637_714+644dup others(8): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr5 | 96884555 | |||||
chr5:96884555
|
T | TTTTGTTT others(5): Show |
4 | a0001c0001t0001g0300a0001c0004t0022g0225a0001c0004t0030g0226others(1): Show | 4 | HG02738.hp1 HG02970.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.714+633_714+644dup others(12): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr5 | 96884555 | |||||
chr5:96884566
|
T | C | 1 | a0002c0002t0002g0325 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.714+636T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 3/18 | chr5 | 96884566 | ||||||
chr5:96884667
|
C | G | 2 | a0001c0001t0001g0188a0001c0001t0001g0199 | 2 | NA18939.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.714+737C>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 3/18 | chr5 | 96884667 | ||||||
chr5:96884764
|
T | A | 4 | a0002c0002t0010g0039a0002c0002t0010g0335a0002c0002t0010g0336others(1): Show | 5 | HG00738.hp2 HG01167.hp2 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.714+834T>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 3/18 | chr5 | 96884764 | ||||||
chr5:96884825
|
T | C | 1 | a0004c0005t0003g0205 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.714+895T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 3/18 | chr5 | 96884825 | ||||||
chr5:96884962
|
T | TG | 230 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(227): Show | 259 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(256): Show |
intron_variant | MODIFIER | c.714+1033dupG | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr5 | 96884962 | |||||
chr5:96885133
|
C | T | 1 | a0001c0001t0001g0187 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.714+1203C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 3/18 | chr5 | 96885133 | ||||||
chr5:96885307
|
C | T | 185 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(182): Show | 210 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.715-1348C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 3/18 | chr5 | 96885307 | ||||||
chr5:96885371
|
G | A | 10 | a0005c0006t0005g0038a0005c0006t0005g0212a0005c0006t0005g0327others(7): Show | 10 | HG00642.hp1 HG00735.hp1 HG01123.hp1 others(7): Show |
intron_variant | MODIFIER | c.715-1284G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 3/18 | chr5 | 96885371 | ||||||
chr5:96885637
|
C | A | 178 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(175): Show | 202 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.715-1018C>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 3/18 | chr5 | 96885637 | ||||||
chr5:96885721
|
AGGAGTTG others(9): Show |
A | 3 | a0001c0001t0001g0030a0001c0001t0001g0219a0014c0023t0001g0217 | 4 | HG01106.hp2 HG01257.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.715-933_715-918del others(16): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 3/18 | chr5 | 96885721 | ||||||
chr5:96885722
|
G | A | 175 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(172): Show | 198 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.715-933G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 3/18 | chr5 | 96885722 | ||||||
chr5:96885738
|
T | A | 3 | a0001c0001t0001g0030a0001c0001t0001g0219a0014c0023t0001g0217 | 4 | HG01106.hp2 HG01257.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.715-917T>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 3/18 | chr5 | 96885738 | ||||||
chr5:96885763
|
G | T | 4 | a0001c0001t0001g0309a0001c0001t0001g0310a0001c0001t0001g0314others(1): Show | 4 | NA18946.hp2 NA18961.hp1 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.715-892G>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 3/18 | chr5 | 96885763 | ||||||
chr5:96885832
|
G | A | 4 | a0002c0002t0012g0241a0002c0002t0012g0242a0002c0002t0012g0243others(1): Show | 4 | HG02559.hp2 HG02896.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.715-823G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 3/18 | chr5 | 96885832 | ||||||
chr5:96885861
|
C | G | 178 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(175): Show | 202 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.715-794C>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 3/18 | chr5 | 96885861 | ||||||
chr5:96886049
|
A | G | 1 | a0002c0002t0002g0325 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.715-606A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 3/18 | chr5 | 96886049 | ||||||
chr5:96886109
|
T | C | 1 | a0001c0001t0023g0216 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.715-546T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 3/18 | chr5 | 96886109 | ||||||
chr5:96886180
|
C | T | 1 | a0001c0004t0007g0303 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.715-475C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 3/18 | chr5 | 96886180 | ||||||
chr5:96886185
|
A | G | 178 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(175): Show | 202 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.715-470A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 3/18 | chr5 | 96886185 | ||||||
chr5:96886281
|
G | A | 3 | a0001c0004t0007g0114a0001c0004t0007g0115a0001c0004t0007g0116 | 3 | HG02622.hp2 HG02809.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.715-374G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 3/18 | chr5 | 96886281 | ||||||
chr5:96886316
|
A | C | 178 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(175): Show | 202 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.715-339A>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 3/18 | chr5 | 96886316 | ||||||
chr5:96886316
|
A | G | 27 | a0003c0003t0004g0032a0003c0003t0004g0033a0003c0003t0004g0250others(24): Show | 30 | HG00558.hp2 HG00609.hp1 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.715-339A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 3/18 | chr5 | 96886316 | ||||||
chr5:96886479
|
A | G | 178 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(175): Show | 202 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.715-176A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 3/18 | chr5 | 96886479 | ||||||
chr5:96886481
|
C | T | 154 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(151): Show | 178 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.715-174C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 3/18 | chr5 | 96886481 | ||||||
chr5:96886808
|
G | A | 4 | a0001c0004t0007g0297a0001c0004t0007g0298a0001c0004t0007g0299others(1): Show | 4 | HG02451.hp1 HG03540.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.849+19G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96886808 | ||||||
chr5:96886815
|
G | A | 2 | a0001c0001t0001g0047a0001c0001t0008g0045 | 2 | HG00323.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.849+26G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96886815 | ||||||
chr5:96886849
|
TTTG | T | 14 | a0002c0002t0010g0039a0002c0002t0010g0335a0002c0002t0010g0336others(11): Show | 15 | HG00642.hp1 HG00735.hp1 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.849+63_849+65delGT others(1): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr5 | 96886849 | |||||
chr5:96886920
|
T | G | 4 | a0002c0002t0010g0039a0002c0002t0010g0335a0002c0002t0010g0336others(1): Show | 5 | HG00738.hp2 HG01167.hp2 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.849+131T>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96886920 | ||||||
chr5:96886923
|
G | A | 178 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(175): Show | 202 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.849+134G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96886923 | ||||||
chr5:96887060
|
G | A | 1 | a0003c0003t0009g0034 | 2 | NA18973.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.849+271G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96887060 | ||||||
chr5:96887072
|
A | AGT | 16 | a0001c0004t0006g0128a0001c0004t0006g0132a0001c0004t0006g0147others(13): Show | 16 | HG01109.hp1 HG01496.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.849+284_849+285dup others(2): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr5 | 96887072 | |||||
chr5:96887073
|
G | GTA | 55 | a0001c0001t0001g0065a0002c0002t0002g0001a0002c0002t0002g0002others(52): Show | 72 | HG00423.hp1 HG00544.hp1 HG00609.hp2 others(69): Show |
intron_variant | MODIFIER | c.849+311_849+312dup others(2): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr5 | 96887073 | |||||
chr5:96887073
|
G | GTATA | 16 | a0001c0001t0001g0020a0002c0002t0002g0013a0002c0002t0002g0019others(13): Show | 19 | HG01192.hp1 HG02083.hp2 HG02135.hp1 others(16): Show |
intron_variant | MODIFIER | c.849+309_849+312dup others(4): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr5 | 96887073 | |||||
chr5:96887073
|
G | GTATATA | 7 | a0002c0002t0002g0017a0002c0002t0002g0046a0002c0002t0002g0087others(4): Show | 8 | HG00140.hp2 HG00323.hp2 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.849+307_849+312dup others(6): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr5 | 96887073 | |||||
chr5:96887073
|
G | GTATATAT others(1): Show |
3 | a0002c0002t0002g0105a0002c0002t0003g0104a0013c0019t0002g0072 | 3 | NA18972.hp1 NA18977.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.849+305_849+312dup others(8): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr5 | 96887073 | |||||
chr5:96887073
|
GTATA | G | 6 | a0001c0001t0001g0198a0001c0007t0001g0266a0005c0006t0005g0264others(3): Show | 6 | HG01361.hp1 HG02004.hp2 HG02040.hp1 others(3): Show |
intron_variant | MODIFIER | c.849+309_849+312del others(4): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr5 | 96887073 | |||||
chr5:96887075
|
A | G | 154 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(151): Show | 178 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.849+286A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96887075 | ||||||
chr5:96887077
|
A | G | 1 | a0001c0004t0006g0130 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.849+288A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96887077 | ||||||
chr5:96887079
|
A | G | 6 | a0001c0001t0001g0198a0001c0007t0001g0266a0005c0006t0005g0264others(3): Show | 6 | HG01361.hp1 HG02004.hp2 HG02040.hp1 others(3): Show |
intron_variant | MODIFIER | c.849+290A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96887079 | ||||||
chr5:96887094
|
T | C | 30 | a0001c0001t0001g0012a0001c0001t0001g0040a0001c0001t0001g0127others(27): Show | 32 | HG00597.hp2 HG01175.hp1 HG01192.hp2 others(29): Show |
intron_variant | MODIFIER | c.849+305T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96887094 | ||||||
chr5:96887094
|
TATATATA others(1): Show |
T | 9 | a0005c0006t0005g0038a0005c0006t0005g0212a0005c0006t0005g0327others(6): Show | 9 | HG00642.hp1 HG00735.hp1 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.849+307_849+314del others(8): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr5 | 96887094 | |||||
chr5:96887094
|
TATATATA others(3): Show |
T | 1 | a0005c0006t0013g0331 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.849+307_849+316del others(10): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr5 | 96887094 | |||||
chr5:96887096
|
T | C | 148 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(145): Show | 172 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.849+307T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96887096 | ||||||
chr5:96887096
|
TATATACA others(3): Show |
T | 1 | a0002c0002t0002g0325 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.849+309_849+318del others(10): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr5 | 96887096 | |||||
chr5:96887098
|
TATAC | T | 2 | a0002c0002t0009g0023a0002c0002t0009g0138 | 3 | HG01243.hp2 HG02647.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.849+311_849+314del others(4): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr5 | 96887098 | |||||
chr5:96887098
|
TATACAC | T | 3 | a0002c0002t0012g0241a0002c0002t0012g0242a0002c0002t0012g0243 | 3 | HG02559.hp2 HG02976.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.849+311_849+316del others(6): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr5 | 96887098 | |||||
chr5:96887098
|
TATACACA others(3): Show |
T | 1 | a0004c0005t0016g0304 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.849+311_849+320del others(10): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr5 | 96887098 | |||||
chr5:96887100
|
T | C | 1 | a0002c0002t0002g0113 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.849+311T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96887100 | ||||||
chr5:96887100
|
TAC | T | 8 | a0001c0004t0007g0114a0001c0004t0007g0115a0002c0002t0002g0086others(5): Show | 9 | HG00558.hp2 HG01257.hp1 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.849+337_849+338del others(2): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr5 | 96887100 | |||||
chr5:96887100
|
TACAC | T | 4 | a0004c0005t0002g0036a0004c0005t0003g0320a0011c0017t0001g0319others(1): Show | 5 | HG02055.hp1 HG02148.hp1 NA18948.hp1 others(2): Show |
intron_variant | MODIFIER | c.849+335_849+338del others(4): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr5 | 96887100 | |||||
chr5:96887100
|
TACACAC | T | 164 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(161): Show | 191 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.849+333_849+338del others(6): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr5 | 96887100 | |||||
chr5:96887100
|
TACACACA others(1): Show |
T | 3 | a0002c0002t0010g0039a0002c0002t0010g0336a0012c0020t0010g0334 | 4 | HG00738.hp2 HG01975.hp1 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.849+331_849+338del others(8): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr5 | 96887100 | |||||
chr5:96887102
|
C | T | 26 | a0001c0004t0007g0116a0001c0004t0022g0225a0001c0004t0030g0226others(23): Show | 27 | HG01943.hp2 HG02056.hp2 HG02738.hp1 others(24): Show |
intron_variant | MODIFIER | c.849+313C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96887102 | ||||||
chr5:96887104
|
C | T | 55 | a0001c0001t0001g0198a0001c0004t0006g0128a0001c0004t0006g0130others(52): Show | 57 | HG00558.hp2 HG01109.hp1 HG01243.hp1 others(54): Show |
intron_variant | MODIFIER | c.849+315C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96887104 | ||||||
chr5:96887106
|
C | T | 60 | a0001c0001t0001g0198a0001c0004t0006g0128a0001c0004t0006g0130others(57): Show | 63 | HG00558.hp2 HG01109.hp1 HG01243.hp1 others(60): Show |
intron_variant | MODIFIER | c.849+317C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96887106 | ||||||
chr5:96887108
|
C | T | 39 | a0002c0002t0002g0113a0002c0002t0010g0335a0003c0003t0004g0032others(36): Show | 44 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.849+319C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96887108 | ||||||
chr5:96887110
|
C | T | 178 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(175): Show | 202 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.849+321C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96887110 | ||||||
chr5:96887300
|
C | T | 1 | a0001c0001t0027g0333 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.849+511C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96887300 | ||||||
chr5:96887303
|
C | CT | 174 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(171): Show | 198 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.849+529dupT | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr5 | 96887303 | |||||
chr5:96887341
|
G | C | 178 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(175): Show | 202 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.849+552G>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96887341 | ||||||
chr5:96887370
|
G | A | 1 | a0013c0019t0002g0072 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.849+581G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96887370 | ||||||
chr5:96887396
|
A | G | 178 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(175): Show | 202 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.849+607A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96887396 | ||||||
chr5:96887468
|
T | G | 14 | a0004c0005t0002g0036a0004c0005t0003g0021a0004c0005t0003g0037others(11): Show | 17 | HG00597.hp1 HG02148.hp1 NA18747.hp2 others(14): Show |
intron_variant | MODIFIER | c.849+679T>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96887468 | ||||||
chr5:96887495
|
T | C | 2 | a0002c0002t0002g0015a0002c0002t0002g0090 | 3 | NA18960.hp2 NA18988.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.849+706T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96887495 | ||||||
chr5:96887588
|
C | G | 2 | a0002c0002t0009g0023a0002c0002t0009g0138 | 3 | HG01243.hp2 HG02647.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.849+799C>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96887588 | ||||||
chr5:96887596
|
G | A | 1 | a0002c0002t0002g0103 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.849+807G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96887596 | ||||||
chr5:96887598
|
C | T | 178 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(175): Show | 202 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.849+809C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96887598 | ||||||
chr5:96887607
|
A | G | 3 | a0001c0001t0001g0024a0001c0001t0001g0140a0001c0001t0008g0024 | 3 | HG00738.hp1 HG02818.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.849+818A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96887607 | ||||||
chr5:96887724
|
G | A | 4 | a0001c0004t0007g0114a0001c0004t0007g0115a0001c0004t0007g0116others(1): Show | 4 | HG02622.hp2 HG02809.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.849+935G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96887724 | ||||||
chr5:96887725
|
C | T | 1 | a0001c0004t0006g0131 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.849+936C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96887725 | ||||||
chr5:96887776
|
A | G | 178 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(175): Show | 202 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.849+987A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96887776 | ||||||
chr5:96887810
|
A | G | 2 | a0001c0001t0001g0262a0001c0001t0001g0263 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.849+1021A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96887810 | ||||||
chr5:96887848
|
G | A | 26 | a0001c0001t0001g0012a0001c0001t0001g0040a0001c0001t0001g0127others(23): Show | 28 | HG00597.hp2 HG01192.hp2 HG01358.hp1 others(25): Show |
intron_variant | MODIFIER | c.849+1059G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96887848 | ||||||
chr5:96888056
|
C | T | 178 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(175): Show | 202 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.850-1129C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96888056 | ||||||
chr5:96888129
|
G | GA | 180 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(177): Show | 204 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.850-1045dupA | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr5 | 96888129 | |||||
chr5:96888163
|
AAAAAG | A | 5 | a0002c0002t0012g0241a0002c0002t0012g0242a0002c0002t0012g0243others(2): Show | 5 | HG02559.hp2 HG02896.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.850-1017_850-1013d others(7): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr5 | 96888163 | |||||
chr5:96888164
|
A | AAG | 178 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(175): Show | 202 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.850-1020_850-1019i others(4): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr5 | 96888164 | |||||
chr5:96888165
|
A | G | 14 | a0002c0002t0010g0039a0002c0002t0010g0335a0002c0002t0010g0336others(11): Show | 15 | HG00642.hp1 HG00735.hp1 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.850-1020A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96888165 | ||||||
chr5:96888176
|
T | G | 203 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(200): Show | 229 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.850-1009T>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96888176 | ||||||
chr5:96888210
|
T | TA | 7 | a0002c0002t0009g0023a0002c0002t0009g0138a0002c0002t0012g0241others(4): Show | 8 | HG01243.hp2 HG02559.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.850-974dupA | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr5 | 96888210 | |||||
chr5:96888241
|
T | C | 1 | a0001c0001t0028g0189 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.850-944T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96888241 | ||||||
chr5:96888417
|
A | G | 178 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(175): Show | 202 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.850-768A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96888417 | ||||||
chr5:96888462
|
T | C | 1 | a0002c0002t0002g0103 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.850-723T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96888462 | ||||||
chr5:96888472
|
A | G | 185 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(182): Show | 210 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.850-713A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96888472 | ||||||
chr5:96888613
|
A | G | 1 | a0001c0004t0006g0131 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.850-572A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96888613 | ||||||
chr5:96888626
|
C | T | 12 | a0001c0001t0001g0047a0001c0001t0008g0045a0001c0007t0001g0031others(9): Show | 13 | HG00323.hp1 HG01167.hp1 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.850-559C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96888626 | ||||||
chr5:96888767
|
T | C | 7 | a0002c0002t0009g0023a0002c0002t0009g0138a0002c0002t0012g0241others(4): Show | 8 | HG01243.hp2 HG02559.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.850-418T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96888767 | ||||||
chr5:96888801
|
T | C | 1 | a0002c0002t0002g0325 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.850-384T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96888801 | ||||||
chr5:96888816
|
G | A | 1 | a0001c0001t0001g0301 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.850-369G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96888816 | ||||||
chr5:96888866
|
T | C | 7 | a0002c0002t0009g0023a0002c0002t0009g0138a0002c0002t0012g0241others(4): Show | 8 | HG01243.hp2 HG02559.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.850-319T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96888866 | ||||||
chr5:96888875
|
C | T | 178 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(175): Show | 202 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.850-310C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96888875 | ||||||
chr5:96888902
|
T | C | 1 | a0001c0001t0001g0173 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.850-283T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96888902 | ||||||
chr5:96888950
|
A | T | 2 | a0001c0004t0022g0225a0001c0004t0030g0226 | 2 | HG02738.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.850-235A>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96888950 | ||||||
chr5:96889005
|
A | G | 10 | a0005c0006t0005g0038a0005c0006t0005g0212a0005c0006t0005g0327others(7): Show | 10 | HG00642.hp1 HG00735.hp1 HG01123.hp1 others(7): Show |
intron_variant | MODIFIER | c.850-180A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96889005 | ||||||
chr5:96889122
|
T | C | 1 | a0010c0015t0001g0144 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.850-63T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 4/18 | chr5 | 96889122 | ||||||
chr5:96889375
|
CTCTT | C | 2 | a0001c0001t0001g0029a0001c0001t0023g0216 | 3 | HG01884.hp1 HG02886.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.970+74_970+77delTT others(2): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr5 | 96889375 | |||||
chr5:96889398
|
G | C | 1 | a0003c0003t0004g0289 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.970+93G>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96889398 | ||||||
chr5:96889423
|
G | A | 1 | a0002c0002t0002g0002 | 4 | NA18970.hp2 NA18975.hp1 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.970+118G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96889423 | ||||||
chr5:96889548
|
G | A | 178 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(175): Show | 202 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.970+243G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96889548 | ||||||
chr5:96889613
|
G | A | 2 | a0002c0002t0002g0059a0002c0002t0002g0100 | 2 | HG01123.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.970+308G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96889613 | ||||||
chr5:96889818
|
A | T | 178 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(175): Show | 202 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.970+513A>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96889818 | ||||||
chr5:96889831
|
T | TAC | 8 | a0002c0002t0002g0015a0002c0002t0002g0055a0002c0002t0002g0060others(5): Show | 9 | HG01361.hp2 HG01934.hp2 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.970+557_970+558dup others(2): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr5 | 96889831 | |||||
chr5:96889831
|
T | TACAC | 5 | a0002c0002t0002g0119a0002c0002t0012g0241a0002c0002t0012g0242others(2): Show | 5 | HG01496.hp2 HG02559.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.970+555_970+558dup others(4): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr5 | 96889831 | |||||
chr5:96889831
|
TAC | T | 65 | a0001c0001t0001g0040a0001c0001t0001g0127a0001c0001t0001g0227others(62): Show | 73 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.970+557_970+558del others(2): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr5 | 96889831 | |||||
chr5:96889831
|
TACAC | T | 21 | a0001c0001t0001g0235a0001c0004t0007g0114a0001c0004t0007g0115others(18): Show | 22 | HG00423.hp1 HG00642.hp1 HG00735.hp1 others(19): Show |
intron_variant | MODIFIER | c.970+555_970+558del others(4): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr5 | 96889831 | |||||
chr5:96889831
|
TACACAC | T | 18 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(15): Show | 18 | HG00280.hp2 HG01070.hp2 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.970+553_970+558del others(6): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr5 | 96889831 | |||||
chr5:96889831
|
TACACACA others(1): Show |
T | 132 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(129): Show | 154 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.970+551_970+558del others(8): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr5 | 96889831 | |||||
chr5:96889835
|
C | T | 1 | a0002c0002t0002g0098 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.970+530C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96889835 | ||||||
chr5:96889862
|
A | G | 1 | a0002c0002t0002g0074 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.970+557A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96889862 | ||||||
chr5:96889893
|
T | C | 7 | a0002c0002t0009g0023a0002c0002t0009g0138a0002c0002t0012g0241others(4): Show | 8 | HG01243.hp2 HG02559.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.970+588T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96889893 | ||||||
chr5:96890070
|
T | C | 178 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(175): Show | 202 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.970+765T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96890070 | ||||||
chr5:96890152
|
C | A | 1 | a0001c0001t0001g0227 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.970+847C>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96890152 | ||||||
chr5:96890155
|
T | A | 2 | a0003c0003t0004g0280a0003c0003t0009g0279 | 2 | NA18964.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.970+850T>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96890155 | ||||||
chr5:96890423
|
C | T | 1 | a0001c0004t0006g0132 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.970+1118C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96890423 | ||||||
chr5:96890434
|
C | T | 64 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(61): Show | 82 | HG00140.hp1 HG00423.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.970+1129C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96890434 | ||||||
chr5:96890492
|
A | G | 244 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(241): Show | 276 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.970+1187A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96890492 | ||||||
chr5:96890508
|
G | A | 1 | a0001c0004t0006g0139 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.970+1203G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96890508 | ||||||
chr5:96890610
|
G | A | 1 | a0001c0001t0001g0228 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.970+1305G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96890610 | ||||||
chr5:96890664
|
T | C | 1 | a0001c0007t0001g0296 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.970+1359T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96890664 | ||||||
chr5:96890703
|
A | C | 7 | a0002c0002t0009g0023a0002c0002t0009g0138a0002c0002t0012g0241others(4): Show | 8 | HG01243.hp2 HG02559.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.970+1398A>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96890703 | ||||||
chr5:96890749
|
C | A | 1 | a0002c0002t0002g0113 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.970+1444C>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96890749 | ||||||
chr5:96890826
|
T | TTA | 14 | a0002c0002t0010g0039a0002c0002t0010g0335a0002c0002t0010g0336others(11): Show | 15 | HG00642.hp1 HG00735.hp1 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.971-1469_971-1468d others(4): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr5 | 96890826 | |||||
chr5:96890831
|
T | C | 185 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(182): Show | 210 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.971-1468T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96890831 | ||||||
chr5:96890991
|
G | T | 178 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(175): Show | 202 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.971-1308G>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96890991 | ||||||
chr5:96891000
|
C | T | 1 | a0002c0002t0026g0041 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.971-1299C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96891000 | ||||||
chr5:96891025
|
G | A | 178 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(175): Show | 202 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.971-1274G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96891025 | ||||||
chr5:96891026
|
A | G | 178 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(175): Show | 202 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.971-1273A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96891026 | ||||||
chr5:96891074
|
T | C | 1 | a0002c0002t0002g0016 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.971-1225T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96891074 | ||||||
chr5:96891159
|
A | G | 10 | a0005c0006t0005g0038a0005c0006t0005g0212a0005c0006t0005g0327others(7): Show | 10 | HG00642.hp1 HG00735.hp1 HG01123.hp1 others(7): Show |
intron_variant | MODIFIER | c.971-1140A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96891159 | ||||||
chr5:96891221
|
C | T | 1 | a0001c0004t0007g0303 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.971-1078C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96891221 | ||||||
chr5:96891322
|
C | T | 1 | a0001c0004t0007g0303 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.971-977C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96891322 | ||||||
chr5:96891367
|
ATG | A | 157 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(154): Show | 181 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.971-928_971-927del others(2): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr5 | 96891367 | |||||
chr5:96891369
|
G | GTA | 4 | a0002c0002t0012g0241a0002c0002t0012g0242a0002c0002t0012g0243others(1): Show | 4 | HG02559.hp2 HG02896.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.971-929_971-928ins others(2): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr5 | 96891369 | |||||
chr5:96891371
|
G | A | 28 | a0001c0004t0006g0128a0001c0004t0006g0130a0001c0004t0006g0131others(25): Show | 29 | HG01109.hp1 HG01243.hp1 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.971-928G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96891371 | ||||||
chr5:96891371
|
G | GTA | 39 | a0001c0004t0007g0114a0001c0004t0007g0115a0001c0004t0007g0116others(36): Show | 43 | HG00558.hp2 HG00609.hp1 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.971-914_971-913dup others(2): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr5 | 96891371 | |||||
chr5:96891371
|
GTA | G | 10 | a0005c0006t0005g0038a0005c0006t0005g0212a0005c0006t0005g0327others(7): Show | 10 | HG00642.hp1 HG00735.hp1 HG01123.hp1 others(7): Show |
intron_variant | MODIFIER | c.971-914_971-913del others(2): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr5 | 96891371 | |||||
chr5:96891385
|
A | G | 178 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(175): Show | 202 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.971-914A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96891385 | ||||||
chr5:96891447
|
A | G | 1 | a0001c0001t0001g0234 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.971-852A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96891447 | ||||||
chr5:96891450
|
TAC | T | 2 | a0002c0002t0029g0117a0004c0005t0003g0021 | 3 | NA18955.hp2 NA18982.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.971-837_971-836del others(2): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr5 | 96891450 | |||||
chr5:96891471
|
G | T | 2 | a0001c0004t0022g0225a0001c0004t0030g0226 | 2 | HG02738.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.971-828G>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96891471 | ||||||
chr5:96891471
|
GTA | G | 17 | a0001c0001t0001g0153a0001c0001t0001g0213a0001c0001t0001g0215others(14): Show | 18 | HG01069.hp2 HG01071.hp2 HG01975.hp2 others(15): Show |
intron_variant | MODIFIER | c.971-816_971-815del others(2): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr5 | 96891471 | |||||
chr5:96891471
|
GTATA | G | 4 | a0001c0001t0001g0218a0001c0001t0001g0220a0001c0001t0001g0221others(1): Show | 4 | HG04184.hp2 NA18949.hp1 NA19067.hp1 others(1): Show |
intron_variant | MODIFIER | c.971-818_971-815del others(4): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr5 | 96891471 | |||||
chr5:96891483
|
A | G | 164 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(161): Show | 188 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.971-816A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96891483 | ||||||
chr5:96891485
|
G | A | 4 | a0002c0002t0010g0039a0002c0002t0010g0335a0002c0002t0010g0336others(1): Show | 5 | HG00738.hp2 HG01167.hp2 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.971-814G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96891485 | ||||||
chr5:96891497
|
G | GTA | 27 | a0003c0003t0004g0032a0003c0003t0004g0033a0003c0003t0004g0250others(24): Show | 30 | HG00558.hp2 HG00609.hp1 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.971-801_971-800ins others(2): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr5 | 96891497 | |||||
chr5:96891499
|
G | A | 27 | a0003c0003t0004g0032a0003c0003t0004g0033a0003c0003t0004g0250others(24): Show | 30 | HG00558.hp2 HG00609.hp1 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.971-800G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96891499 | ||||||
chr5:96891499
|
GTA | G | 31 | a0001c0004t0007g0114a0001c0004t0007g0115a0001c0004t0007g0116others(28): Show | 35 | HG00597.hp1 HG00642.hp1 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.971-784_971-783del others(2): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr5 | 96891499 | |||||
chr5:96891501
|
A | G | 34 | a0001c0001t0001g0186a0001c0001t0001g0218a0001c0001t0001g0220others(31): Show | 35 | HG00738.hp2 HG01109.hp1 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.971-798A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96891501 | ||||||
chr5:96891503
|
A | G | 21 | a0002c0002t0009g0023a0002c0002t0009g0138a0002c0002t0010g0039others(18): Show | 23 | HG00642.hp1 HG00735.hp1 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.971-796A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96891503 | ||||||
chr5:96891504
|
TATATATA others(9): Show |
T | 153 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(150): Show | 177 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.971-789_971-774del others(16): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr5 | 96891504 | |||||
chr5:96891505
|
A | G | 4 | a0002c0002t0012g0241a0002c0002t0012g0242a0002c0002t0012g0243others(1): Show | 4 | HG02559.hp2 HG02896.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.971-794A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96891505 | ||||||
chr5:96891506
|
TATATATA others(7): Show |
T | 25 | a0001c0001t0001g0218a0001c0001t0001g0220a0001c0001t0001g0221others(22): Show | 25 | HG01109.hp1 HG01243.hp1 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.971-787_971-774del others(14): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr5 | 96891506 | |||||
chr5:96891525
|
A | G | 178 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(175): Show | 202 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.971-774A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96891525 | ||||||
chr5:96891528
|
G | GTA | 25 | a0003c0003t0004g0032a0003c0003t0004g0033a0003c0003t0004g0250others(22): Show | 28 | HG00558.hp2 HG00609.hp1 HG01257.hp1 others(25): Show |
intron_variant | MODIFIER | c.971-764_971-763dup others(2): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr5 | 96891528 | |||||
chr5:96891533
|
T | TAC | 12 | a0004c0005t0002g0036a0004c0005t0003g0021a0004c0005t0003g0037others(9): Show | 15 | HG00597.hp1 HG02148.hp1 NA18747.hp2 others(12): Show |
intron_variant | MODIFIER | c.971-765_971-764ins others(2): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr5 | 96891533 | |||||
chr5:96891535
|
T | C | 16 | a0002c0002t0002g0099a0002c0002t0002g0103a0004c0005t0002g0036others(13): Show | 19 | HG00597.hp1 HG02056.hp2 HG02148.hp1 others(16): Show |
intron_variant | MODIFIER | c.971-764T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96891535 | ||||||
chr5:96891535
|
TAC | T | 153 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(150): Show | 177 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(174): Show |
intron_variant | MODIFIER | c.971-736_971-735del others(2): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr5 | 96891535 | |||||
chr5:96891535
|
TACAC | T | 44 | a0001c0001t0001g0029a0001c0001t0001g0043a0001c0001t0001g0048others(41): Show | 46 | HG00280.hp1 HG00280.hp2 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.971-738_971-735del others(4): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr5 | 96891535 | |||||
chr5:96891537
|
C | T | 14 | a0001c0001t0001g0127a0001c0001t0001g0233a0001c0004t0007g0303others(11): Show | 15 | HG00738.hp2 HG01167.hp2 HG01168.hp2 others(12): Show |
intron_variant | MODIFIER | c.971-762C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96891537 | ||||||
chr5:96891539
|
C | T | 150 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(147): Show | 173 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(170): Show |
intron_variant | MODIFIER | c.971-760C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96891539 | ||||||
chr5:96891541
|
C | T | 63 | a0001c0001t0001g0029a0001c0001t0001g0043a0001c0001t0001g0048others(60): Show | 65 | HG00280.hp1 HG00280.hp2 HG01069.hp2 others(62): Show |
intron_variant | MODIFIER | c.971-758C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96891541 | ||||||
chr5:96891543
|
C | T | 2 | a0001c0001t0001g0157a0002c0002t0002g0113 | 2 | HG03130.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.971-756C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96891543 | ||||||
chr5:96891545
|
C | T | 1 | a0002c0002t0029g0117 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.971-754C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96891545 | ||||||
chr5:96891563
|
C | T | 160 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(157): Show | 184 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(181): Show |
intron_variant | MODIFIER | c.971-736C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96891563 | ||||||
chr5:96891565
|
T | C | 1 | a0002c0002t0002g0099 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.971-734T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96891565 | ||||||
chr5:96891571
|
G | GTA | 42 | a0001c0001t0001g0141a0001c0001t0001g0161a0001c0001t0001g0192others(39): Show | 46 | HG00558.hp2 HG00609.hp1 HG01243.hp2 others(43): Show |
intron_variant | MODIFIER | c.971-727_971-726dup others(2): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr5 | 96891571 | |||||
chr5:96891572
|
TAC | T | 23 | a0001c0001t0001g0065a0001c0001t0001g0312a0001c0004t0007g0114others(20): Show | 27 | HG00597.hp1 HG00597.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.971-706_971-705del others(2): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr5 | 96891572 | |||||
chr5:96891572
|
TACAC | T | 2 | a0004c0005t0003g0037a0018c0026t0003g0317 | 3 | NA18942.hp2 NA18978.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.971-708_971-705del others(4): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr5 | 96891572 | |||||
chr5:96891574
|
C | T | 182 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(179): Show | 207 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.971-725C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96891574 | ||||||
chr5:96891576
|
C | T | 6 | a0001c0001t0001g0312a0001c0004t0007g0114a0001c0004t0007g0115others(3): Show | 6 | HG00597.hp2 HG02622.hp2 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.971-723C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96891576 | ||||||
chr5:96891687
|
A | G | 2 | a0001c0004t0022g0225a0001c0004t0030g0226 | 2 | HG02738.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.971-612A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96891687 | ||||||
chr5:96891750
|
TAGA | T | 4 | a0002c0002t0012g0241a0002c0002t0012g0242a0002c0002t0012g0243others(1): Show | 4 | HG02559.hp2 HG02896.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.971-544_971-542del others(3): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr5 | 96891750 | |||||
chr5:96891882
|
A | G | 178 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(175): Show | 202 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.971-417A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96891882 | ||||||
chr5:96891916
|
A | T | 4 | a0002c0002t0012g0241a0002c0002t0012g0242a0002c0002t0012g0243others(1): Show | 4 | HG02559.hp2 HG02896.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.971-383A>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96891916 | ||||||
chr5:96891923
|
A | G | 1 | a0016c0013t0002g0067 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.971-376A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96891923 | ||||||
chr5:96892021
|
A | G | 1 | a0002c0002t0002g0073 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.971-278A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96892021 | ||||||
chr5:96892028
|
C | T | 1 | a0001c0001t0001g0252 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.971-271C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96892028 | ||||||
chr5:96892271
|
C | T | 17 | a0001c0004t0006g0128a0001c0004t0006g0130a0001c0004t0006g0131others(14): Show | 17 | HG01109.hp1 HG01243.hp1 HG01496.hp1 others(14): Show |
intron_variant | MODIFIER | c.971-28C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 5/18 | chr5 | 96892271 | ||||||
chr5:96892536
|
A | G | 21 | a0001c0004t0006g0128a0001c0004t0006g0130a0001c0004t0006g0131others(18): Show | 21 | HG01109.hp1 HG01243.hp1 HG01496.hp1 others(18): Show |
intron_variant | MODIFIER | c.1125+83A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 6/18 | chr5 | 96892536 | ||||||
chr5:96892724
|
G | A | 178 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(175): Show | 202 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.1125+271G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 6/18 | chr5 | 96892724 | ||||||
chr5:96892758
|
G | C | 1 | a0016c0013t0002g0067 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1125+305G>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 6/18 | chr5 | 96892758 | ||||||
chr5:96892763
|
C | T | 1 | a0002c0002t0002g0095 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1125+310C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 6/18 | chr5 | 96892763 | ||||||
chr5:96892933
|
T | A | 4 | a0002c0002t0010g0039a0002c0002t0010g0335a0002c0002t0010g0336others(1): Show | 5 | HG00738.hp2 HG01167.hp2 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.1125+480T>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 6/18 | chr5 | 96892933 | ||||||
chr5:96892996
|
A | AGCTGTTC | 3 | a0001c0001t0001g0030a0001c0001t0001g0219a0014c0023t0001g0217 | 4 | HG01106.hp2 HG01257.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.1125+544_1125+550d others(9): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 96892996 | |||||
chr5:96893031
|
G | A | 1 | a0001c0001t0001g0175 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1125+578G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 6/18 | chr5 | 96893031 | ||||||
chr5:96893073
|
T | C | 2 | a0002c0002t0009g0023a0002c0002t0009g0138 | 3 | HG01243.hp2 HG02647.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1125+620T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 6/18 | chr5 | 96893073 | ||||||
chr5:96893078
|
A | T | 178 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(175): Show | 202 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.1125+625A>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 6/18 | chr5 | 96893078 | ||||||
chr5:96893119
|
C | T | 1 | a0002c0002t0002g0054 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1125+666C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 6/18 | chr5 | 96893119 | ||||||
chr5:96893150
|
C | T | 4 | a0001c0004t0007g0114a0001c0004t0007g0115a0001c0004t0007g0116others(1): Show | 4 | HG02622.hp2 HG02809.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1125+697C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 6/18 | chr5 | 96893150 | ||||||
chr5:96893355
|
C | T | 1 | a0002c0002t0003g0058 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1125+902C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 6/18 | chr5 | 96893355 | ||||||
chr5:96893374
|
T | G | 1 | a0002c0002t0002g0325 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1125+921T>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 6/18 | chr5 | 96893374 | ||||||
chr5:96893488
|
C | A | 1 | a0001c0001t0001g0048 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1125+1035C>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 6/18 | chr5 | 96893488 | ||||||
chr5:96893521
|
G | T | 166 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(163): Show | 185 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.1125+1068G>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 6/18 | chr5 | 96893521 | ||||||
chr5:96893568
|
G | A | 147 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(144): Show | 169 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.1125+1115G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 6/18 | chr5 | 96893568 | ||||||
chr5:96893693
|
A | T | 1 | a0001c0004t0007g0299 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1125+1240A>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 6/18 | chr5 | 96893693 | ||||||
chr5:96893720
|
C | T | 1 | a0001c0001t0001g0185 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1125+1267C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 6/18 | chr5 | 96893720 | ||||||
chr5:96893723
|
T | C | 1 | a0002c0002t0002g0113 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1125+1270T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 6/18 | chr5 | 96893723 | ||||||
chr5:96893838
|
T | G | 133 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(130): Show | 159 | HG00140.hp1 HG00423.hp2 HG00558.hp1 others(156): Show |
intron_variant | MODIFIER | c.1125+1385T>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 6/18 | chr5 | 96893838 | ||||||
chr5:96893841
|
T | A | 3 | a0001c0001t0001g0024a0001c0001t0001g0140a0001c0001t0008g0024 | 3 | HG00738.hp1 HG02818.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1125+1388T>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 6/18 | chr5 | 96893841 | ||||||
chr5:96894046
|
G | T | 182 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(179): Show | 207 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.1126-1200G>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 6/18 | chr5 | 96894046 | ||||||
chr5:96894404
|
T | C | 47 | a0002c0002t0003g0068a0002c0002t0003g0104a0002c0002t0009g0023others(44): Show | 53 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.1126-842T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 6/18 | chr5 | 96894404 | ||||||
chr5:96894418
|
G | T | 155 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(152): Show | 180 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.1126-828G>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 6/18 | chr5 | 96894418 | ||||||
chr5:96894474
|
G | A | 181 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(178): Show | 206 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.1126-772G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 6/18 | chr5 | 96894474 | ||||||
chr5:96894513
|
CA | C | 181 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(178): Show | 206 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.1126-732delA | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 6/18 | chr5 | 96894513 | ||||||
chr5:96894535
|
A | G | 1 | a0001c0004t0011g0136 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1126-711A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 6/18 | chr5 | 96894535 | ||||||
chr5:96894679
|
A | G | 1 | a0001c0004t0007g0303 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1126-567A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 6/18 | chr5 | 96894679 | ||||||
chr5:96894699
|
G | A | 181 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(178): Show | 206 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.1126-547G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 6/18 | chr5 | 96894699 | ||||||
chr5:96894830
|
C | A | 1 | a0001c0001t0001g0175 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1126-416C>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 6/18 | chr5 | 96894830 | ||||||
chr5:96894921
|
A | G | 1 | a0002c0002t0002g0098 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1126-325A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 6/18 | chr5 | 96894921 | ||||||
chr5:96894990
|
T | C | 2 | a0002c0002t0002g0077a0002c0002t0002g0201 | 2 | HG00609.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.1126-256T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 6/18 | chr5 | 96894990 | ||||||
chr5:96895000
|
G | C | 1 | a0005c0006t0005g0268 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1126-246G>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 6/18 | chr5 | 96895000 | ||||||
chr5:96895140
|
G | A | 17 | a0002c0002t0010g0039a0002c0002t0010g0335a0002c0002t0010g0336others(14): Show | 18 | HG00642.hp1 HG00735.hp1 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.1126-106G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 6/18 | chr5 | 96895140 | ||||||
chr5:96895154
|
T | TA | 189 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(186): Show | 218 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.1126-83dupA | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 96895154 | |||||
chr5:96895179
|
A | ATT | 181 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(178): Show | 206 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.1126-62_1126-61dup others(2): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr5 | 96895179 | |||||
chr5:96895371
|
A | G | 1 | a0013c0019t0002g0072 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1239+12A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 7/18 | chr5 | 96895371 | ||||||
chr5:96895391
|
T | C | 1 | a0007c0012t0001g0152 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1239+32T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 7/18 | chr5 | 96895391 | ||||||
chr5:96895496
|
C | T | 13 | a0005c0006t0005g0038a0005c0006t0005g0212a0005c0006t0005g0264others(10): Show | 13 | HG00642.hp1 HG00735.hp1 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.1239+137C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 7/18 | chr5 | 96895496 | ||||||
chr5:96895649
|
T | C | 1 | a0001c0001t0001g0048 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1239+290T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 7/18 | chr5 | 96895649 | ||||||
chr5:96895668
|
T | C | 241 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(238): Show | 273 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(270): Show |
intron_variant | MODIFIER | c.1239+309T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 7/18 | chr5 | 96895668 | ||||||
chr5:96895732
|
G | A | 1 | a0002c0002t0002g0126 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1239+373G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 7/18 | chr5 | 96895732 | ||||||
chr5:96895800
|
C | T | 181 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(178): Show | 206 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.1239+441C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 7/18 | chr5 | 96895800 | ||||||
chr5:96895816
|
G | T | 181 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(178): Show | 206 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.1239+457G>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 7/18 | chr5 | 96895816 | ||||||
chr5:96895819
|
T | C | 47 | a0002c0002t0003g0068a0002c0002t0003g0104a0002c0002t0009g0023others(44): Show | 53 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.1239+460T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 7/18 | chr5 | 96895819 | ||||||
chr5:96895830
|
G | A | 2 | a0001c0001t0001g0065a0001c0001t0001g0236 | 2 | HG00741.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.1239+471G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 7/18 | chr5 | 96895830 | ||||||
chr5:96895859
|
G | T | 24 | a0001c0004t0006g0128a0001c0004t0006g0130a0001c0004t0006g0131others(21): Show | 24 | HG01109.hp1 HG01243.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.1239+500G>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 7/18 | chr5 | 96895859 | ||||||
chr5:96895874
|
A | C | 17 | a0002c0002t0010g0039a0002c0002t0010g0335a0002c0002t0010g0336others(14): Show | 18 | HG00642.hp1 HG00735.hp1 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.1240-499A>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 7/18 | chr5 | 96895874 | ||||||
chr5:96895938
|
CTCT | C | 3 | a0001c0004t0007g0297a0001c0004t0007g0298a0001c0004t0007g0299 | 3 | HG02451.hp1 NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1240-430_1240-428d others(5): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr5 | 96895938 | |||||
chr5:96896040
|
TTGACAGG others(8): Show |
T | 1 | a0002c0002t0017g0070 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1240-329_1240-315d others(17): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr5 | 96896040 | |||||
chr5:96896308
|
A | G | 1 | a0001c0004t0015g0129 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1240-65A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 7/18 | chr5 | 96896308 | ||||||
chr5:96896518
|
G | C | 181 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(178): Show | 206 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.1371+14G>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 8/18 | chr5 | 96896518 | ||||||
chr5:96896519
|
G | A | 4 | a0003c0003t0004g0250a0003c0003t0004g0281a0003c0003t0004g0282others(1): Show | 4 | NA18962.hp1 NA18991.hp1 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.1371+15G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 8/18 | chr5 | 96896519 | ||||||
chr5:96896546
|
G | GAAA | 181 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(178): Show | 206 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.1371+42_1371+43ins others(3): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 8/18 | chr5 | 96896546 | ||||||
chr5:96896582
|
C | T | 181 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(178): Show | 206 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.1371+78C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 8/18 | chr5 | 96896582 | ||||||
chr5:96896641
|
CAT | C | 155 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(152): Show | 180 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.1372-90_1372-89del others(2): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 8/18 | chr5 | 96896641 | ||||||
chr5:96896698
|
T | A | 179 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(176): Show | 204 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.1372-34T>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 8/18 | chr5 | 96896698 | ||||||
chr5:96896864
|
G | GTAAGTCA others(93): Show |
154 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(151): Show | 178 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.1503+3_1503+102dup others(100): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr5 | 96896864 | |||||
chr5:96896892
|
T | C | 13 | a0002c0002t0003g0068a0002c0002t0003g0104a0004c0005t0003g0021others(10): Show | 15 | HG00597.hp1 HG02083.hp2 NA18942.hp2 others(12): Show |
intron_variant | MODIFIER | c.1503+29T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | chr5 | 96896892 | ||||||
chr5:96896995
|
A | G | 181 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(178): Show | 206 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.1503+132A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | chr5 | 96896995 | ||||||
chr5:96896996
|
T | C | 17 | a0002c0002t0010g0039a0002c0002t0010g0335a0002c0002t0010g0336others(14): Show | 18 | HG00642.hp1 HG00735.hp1 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.1503+133T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | chr5 | 96896996 | ||||||
chr5:96896996
|
T | G | 4 | a0002c0002t0012g0241a0002c0002t0012g0242a0002c0002t0012g0243others(1): Show | 4 | HG02559.hp2 HG02896.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1503+133T>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | chr5 | 96896996 | ||||||
chr5:96897045
|
G | T | 2 | a0001c0001t0001g0156a0001c0001t0001g0158 | 2 | NA19009.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1503+182G>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | chr5 | 96897045 | ||||||
chr5:96897085
|
C | G | 1 | a0001c0004t0007g0303 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1503+222C>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | chr5 | 96897085 | ||||||
chr5:96897102
|
C | T | 155 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(152): Show | 180 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.1503+239C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | chr5 | 96897102 | ||||||
chr5:96897544
|
C | CT | 181 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(178): Show | 206 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.1503+688dupT | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr5 | 96897544 | |||||
chr5:96897652
|
A | G | 1 | a0003c0003t0004g0282 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1503+789A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | chr5 | 96897652 | ||||||
chr5:96897746
|
T | A | 181 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(178): Show | 206 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.1503+883T>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | chr5 | 96897746 | ||||||
chr5:96897759
|
C | G | 111 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(108): Show | 132 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.1503+896C>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | chr5 | 96897759 | ||||||
chr5:96897904
|
G | A | 181 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(178): Show | 206 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.1503+1041G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | chr5 | 96897904 | ||||||
chr5:96897919
|
G | A | 4 | a0002c0002t0012g0241a0002c0002t0012g0242a0002c0002t0012g0243others(1): Show | 4 | HG02559.hp2 HG02896.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1503+1056G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | chr5 | 96897919 | ||||||
chr5:96897921
|
G | A | 4 | a0001c0001t0001g0174a0001c0001t0001g0187a0001c0001t0001g0190others(1): Show | 4 | NA18947.hp1 NA18972.hp2 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.1503+1058G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | chr5 | 96897921 | ||||||
chr5:96898392
|
T | TA | 26 | a0003c0003t0004g0033a0003c0003t0004g0250a0003c0003t0004g0272others(23): Show | 28 | HG00558.hp2 HG00609.hp1 HG02602.hp1 others(25): Show |
intron_variant | MODIFIER | c.1503+1530dupA | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr5 | 96898392 | |||||
chr5:96898488
|
T | C | 4 | a0002c0002t0002g0004a0002c0002t0002g0056a0002c0002t0002g0120others(1): Show | 7 | HG00741.hp2 HG02965.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.1503+1625T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | chr5 | 96898488 | ||||||
chr5:96898508
|
G | A | 155 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(152): Show | 180 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.1504-1613G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | chr5 | 96898508 | ||||||
chr5:96898510
|
G | A | 181 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(178): Show | 206 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.1504-1611G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | chr5 | 96898510 | ||||||
chr5:96898532
|
A | T | 47 | a0002c0002t0003g0068a0002c0002t0003g0104a0002c0002t0009g0023others(44): Show | 53 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.1504-1589A>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | chr5 | 96898532 | ||||||
chr5:96898565
|
T | C | 2 | a0007c0012t0001g0152a0007c0012t0001g0154 | 2 | HG01074.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1504-1556T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | chr5 | 96898565 | ||||||
chr5:96898572
|
C | CA | 22 | a0002c0002t0002g0052a0002c0002t0002g0120a0002c0002t0003g0066others(19): Show | 23 | HG00642.hp1 HG00735.hp1 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.1504-1529dupA | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr5 | 96898572 | |||||
chr5:96898572
|
C | CAA | 42 | a0001c0001t0001g0161a0001c0001t0001g0209a0001c0011t0001g0184others(39): Show | 48 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.1504-1530_1504-152 others(6): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr5 | 96898572 | |||||
chr5:96898572
|
C | CAAA | 143 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(140): Show | 166 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.1504-1531_1504-152 others(7): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr5 | 96898572 | |||||
chr5:96898572
|
C | CAAAA | 16 | a0001c0001t0001g0025a0001c0001t0001g0030a0001c0001t0001g0088others(13): Show | 18 | HG00423.hp2 HG01074.hp1 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.1504-1532_1504-152 others(8): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr5 | 96898572 | |||||
chr5:96898572
|
C | CAAAAA | 16 | a0001c0004t0006g0128a0001c0004t0006g0130a0001c0004t0006g0131others(13): Show | 16 | HG01109.hp1 HG01243.hp1 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.1504-1533_1504-152 others(9): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr5 | 96898572 | |||||
chr5:96898572
|
C | CAAAAAA | 8 | a0001c0004t0006g0224a0001c0004t0007g0114a0001c0004t0007g0297others(5): Show | 8 | HG02055.hp2 HG02738.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1504-1534_1504-152 others(10): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr5 | 96898572 | |||||
chr5:96898602
|
T | C | 181 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(178): Show | 206 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.1504-1519T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | chr5 | 96898602 | ||||||
chr5:96898611
|
T | G | 246 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(243): Show | 278 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(275): Show |
intron_variant | MODIFIER | c.1504-1510T>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | chr5 | 96898611 | ||||||
chr5:96898648
|
G | A | 181 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(178): Show | 206 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.1504-1473G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | chr5 | 96898648 | ||||||
chr5:96898671
|
C | T | 181 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(178): Show | 206 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.1504-1450C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | chr5 | 96898671 | ||||||
chr5:96898829
|
A | T | 245 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(242): Show | 277 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(274): Show |
intron_variant | MODIFIER | c.1504-1292A>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | chr5 | 96898829 | ||||||
chr5:96898874
|
G | A | 155 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(152): Show | 180 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.1504-1247G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | chr5 | 96898874 | ||||||
chr5:96898917
|
C | T | 181 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(178): Show | 206 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.1504-1204C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | chr5 | 96898917 | ||||||
chr5:96898979
|
A | C | 13 | a0005c0006t0005g0038a0005c0006t0005g0212a0005c0006t0005g0264others(10): Show | 13 | HG00642.hp1 HG00735.hp1 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.1504-1142A>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | chr5 | 96898979 | ||||||
chr5:96899022
|
T | TAAAAAGA others(331): Show |
2 | a0003c0003t0004g0293a0003c0003t0004g0294 | 2 | NA18985.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.1504-1084_1504-108 others(342): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr5 | 96899022 | |||||
chr5:96899168
|
T | C | 181 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(178): Show | 206 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.1504-953T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | chr5 | 96899168 | ||||||
chr5:96899232
|
T | TTCTGAC | 245 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(242): Show | 277 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(274): Show |
intron_variant | MODIFIER | c.1504-886_1504-885i others(8): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr5 | 96899232 | |||||
chr5:96899289
|
T | TCCCACCC others(6): Show |
1 | a0002c0002t0017g0070 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1504-829_1504-828i others(15): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr5 | 96899289 | |||||
chr5:96899334
|
T | C | 228 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(225): Show | 259 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(256): Show |
intron_variant | MODIFIER | c.1504-787T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | chr5 | 96899334 | ||||||
chr5:96899400
|
T | A | 1 | a0004c0016t0002g0318 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1504-721T>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | chr5 | 96899400 | ||||||
chr5:96899415
|
C | T | 1 | a0002c0002t0002g0080 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1504-706C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | chr5 | 96899415 | ||||||
chr5:96899520
|
T | C | 1 | a0004c0016t0002g0318 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1504-601T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | chr5 | 96899520 | ||||||
chr5:96899568
|
A | G | 1 | a0001c0001t0001g0167 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1504-553A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | chr5 | 96899568 | ||||||
chr5:96899659
|
G | A | 1 | a0002c0002t0002g0121 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1504-462G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | chr5 | 96899659 | ||||||
chr5:96899759
|
T | C | 1 | a0002c0002t0002g0091 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1504-362T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | chr5 | 96899759 | ||||||
chr5:96899789
|
A | G | 1 | a0009c0014t0001g0302 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1504-332A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | chr5 | 96899789 | ||||||
chr5:96899889
|
T | G | 17 | a0002c0002t0010g0039a0002c0002t0010g0335a0002c0002t0010g0336others(14): Show | 18 | HG00642.hp1 HG00735.hp1 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.1504-232T>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | chr5 | 96899889 | ||||||
chr5:96900013
|
A | G | 13 | a0005c0006t0005g0038a0005c0006t0005g0212a0005c0006t0005g0264others(10): Show | 13 | HG00642.hp1 HG00735.hp1 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.1504-108A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 9/18 | chr5 | 96900013 | ||||||
chr5:96900192
|
A | G | 181 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(178): Show | 206 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(203): Show |
splice_region_variant&intron_variant | LOW | c.1572+3A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 10/18 | chr5 | 96900192 | ||||||
chr5:96900378
|
C | T | 1 | a0001c0004t0011g0136 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1572+189C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 10/18 | chr5 | 96900378 | ||||||
chr5:96900440
|
G | A | 3 | a0002c0002t0002g0017a0002c0002t0002g0046a0002c0002t0002g0101 | 4 | HG00140.hp2 HG00323.hp2 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.1572+251G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 10/18 | chr5 | 96900440 | ||||||
chr5:96900614
|
G | A | 181 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(178): Show | 206 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.1572+425G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 10/18 | chr5 | 96900614 | ||||||
chr5:96900708
|
A | G | 245 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(242): Show | 277 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(274): Show |
intron_variant | MODIFIER | c.1572+519A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 10/18 | chr5 | 96900708 | ||||||
chr5:96900757
|
A | C | 3 | a0008c0009t0002g0022a0008c0009t0025g0022a0016c0013t0002g0067 | 3 | HG02055.hp1 HG02572.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1572+568A>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 10/18 | chr5 | 96900757 | ||||||
chr5:96900837
|
C | T | 24 | a0001c0004t0006g0128a0001c0004t0006g0130a0001c0004t0006g0131others(21): Show | 24 | HG01109.hp1 HG01243.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.1572+648C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 10/18 | chr5 | 96900837 | ||||||
chr5:96900916
|
T | C | 245 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(242): Show | 277 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(274): Show |
intron_variant | MODIFIER | c.1573-590T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 10/18 | chr5 | 96900916 | ||||||
chr5:96901139
|
C | T | 155 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(152): Show | 180 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.1573-367C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 10/18 | chr5 | 96901139 | ||||||
chr5:96901152
|
T | C | 27 | a0003c0003t0004g0032a0003c0003t0004g0033a0003c0003t0004g0250others(24): Show | 30 | HG00558.hp2 HG00609.hp1 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.1573-354T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 10/18 | chr5 | 96901152 | ||||||
chr5:96901188
|
G | GTTTT | 168 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(165): Show | 193 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.1573-318_1573-317i others(6): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 10/18 | chr5 | 96901188 | ||||||
chr5:96901189
|
A | T | 13 | a0001c0001t0001g0043a0001c0001t0001g0048a0001c0001t0001g0110others(10): Show | 13 | HG00280.hp1 HG01070.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.1573-317A>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 10/18 | chr5 | 96901189 | ||||||
chr5:96901193
|
T | A | 13 | a0001c0001t0001g0043a0001c0001t0001g0048a0001c0001t0001g0110others(10): Show | 13 | HG00280.hp1 HG01070.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.1573-313T>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 10/18 | chr5 | 96901193 | ||||||
chr5:96901194
|
G | T | 13 | a0001c0001t0001g0043a0001c0001t0001g0048a0001c0001t0001g0110others(10): Show | 13 | HG00280.hp1 HG01070.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.1573-312G>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 10/18 | chr5 | 96901194 | ||||||
chr5:96901410
|
C | G | 181 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(178): Show | 206 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.1573-96C>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 10/18 | chr5 | 96901410 | ||||||
chr5:96901451
|
C | A | 1 | a0004c0016t0002g0318 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1573-55C>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 10/18 | chr5 | 96901451 | ||||||
chr5:96901709
|
C | T | 181 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(178): Show | 206 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.1748+28C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 11/18 | chr5 | 96901709 | ||||||
chr5:96901845
|
C | T | 2 | a0008c0009t0002g0022a0008c0009t0025g0022 | 2 | HG02572.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1748+164C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 11/18 | chr5 | 96901845 | ||||||
chr5:96901892
|
T | C | 4 | a0001c0001t0001g0024a0001c0001t0001g0140a0001c0001t0008g0024others(1): Show | 4 | HG00738.hp1 HG02818.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1748+211T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 11/18 | chr5 | 96901892 | ||||||
chr5:96901920
|
T | C | 24 | a0001c0004t0006g0128a0001c0004t0006g0130a0001c0004t0006g0131others(21): Show | 24 | HG01109.hp1 HG01243.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.1748+239T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 11/18 | chr5 | 96901920 | ||||||
chr5:96902007
|
T | C | 17 | a0002c0002t0010g0039a0002c0002t0010g0335a0002c0002t0010g0336others(14): Show | 18 | HG00642.hp1 HG00735.hp1 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.1749-267T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 11/18 | chr5 | 96902007 | ||||||
chr5:96902034
|
A | G | 2 | a0007c0012t0001g0152a0007c0012t0001g0154 | 2 | HG01074.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1749-240A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 11/18 | chr5 | 96902034 | ||||||
chr5:96902039
|
T | C | 1 | a0001c0004t0006g0139 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1749-235T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 11/18 | chr5 | 96902039 | ||||||
chr5:96902052
|
C | T | 1 | a0003c0003t0004g0288 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1749-222C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 11/18 | chr5 | 96902052 | ||||||
chr5:96902066
|
T | G | 1 | a0002c0002t0003g0104 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1749-208T>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 11/18 | chr5 | 96902066 | ||||||
chr5:96902175
|
G | A | 1 | a0001c0001t0001g0157 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1749-99G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 11/18 | chr5 | 96902175 | ||||||
chr5:96902398
|
A | G | 2 | a0002c0002t0009g0023a0002c0002t0009g0138 | 3 | HG01243.hp2 HG02647.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1828+45A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 12/18 | chr5 | 96902398 | ||||||
chr5:96902403
|
G | T | 1 | a0001c0001t0001g0247 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1828+50G>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 12/18 | chr5 | 96902403 | ||||||
chr5:96902413
|
A | G | 3 | a0001c0004t0007g0114a0001c0004t0007g0115a0001c0004t0007g0116 | 3 | HG02622.hp2 HG02809.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1828+60A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 12/18 | chr5 | 96902413 | ||||||
chr5:96902552
|
C | T | 1 | a0002c0002t0002g0064 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1828+199C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 12/18 | chr5 | 96902552 | ||||||
chr5:96902565
|
TAG | T | 47 | a0002c0002t0003g0068a0002c0002t0003g0104a0002c0002t0009g0023others(44): Show | 53 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.1828+216_1828+217d others(4): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr5 | 96902565 | |||||
chr5:96902607
|
T | A | 1 | a0002c0002t0002g0325 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1828+254T>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 12/18 | chr5 | 96902607 | ||||||
chr5:96902697
|
A | G | 181 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(178): Show | 206 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.1828+344A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 12/18 | chr5 | 96902697 | ||||||
chr5:96902847
|
T | G | 13 | a0005c0006t0005g0038a0005c0006t0005g0212a0005c0006t0005g0264others(10): Show | 13 | HG00642.hp1 HG00735.hp1 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.1828+494T>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 12/18 | chr5 | 96902847 | ||||||
chr5:96902874
|
C | T | 250 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(247): Show | 282 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.1829-503C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 12/18 | chr5 | 96902874 | ||||||
chr5:96902910
|
A | G | 13 | a0005c0006t0005g0038a0005c0006t0005g0212a0005c0006t0005g0264others(10): Show | 13 | HG00642.hp1 HG00735.hp1 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.1829-467A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 12/18 | chr5 | 96902910 | ||||||
chr5:96902990
|
A | G | 3 | a0001c0001t0001g0030a0001c0001t0001g0219a0014c0023t0001g0217 | 4 | HG01106.hp2 HG01257.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.1829-387A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 12/18 | chr5 | 96902990 | ||||||
chr5:96903109
|
C | A | 13 | a0005c0006t0005g0038a0005c0006t0005g0212a0005c0006t0005g0264others(10): Show | 13 | HG00642.hp1 HG00735.hp1 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.1829-268C>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 12/18 | chr5 | 96903109 | ||||||
chr5:96903235
|
C | T | 47 | a0002c0002t0003g0068a0002c0002t0003g0104a0002c0002t0009g0023others(44): Show | 53 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.1829-142C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 12/18 | chr5 | 96903235 | ||||||
chr5:96903256
|
C | T | 1 | a0002c0002t0002g0201 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1829-121C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 12/18 | chr5 | 96903256 | ||||||
chr5:96903590
|
A | G | 181 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(178): Show | 206 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.2012+30A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96903590 | ||||||
chr5:96903647
|
G | A | 1 | a0002c0002t0002g0057 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2012+87G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96903647 | ||||||
chr5:96903726
|
G | GACCCAC | 27 | a0003c0003t0004g0032a0003c0003t0004g0033a0003c0003t0004g0250others(24): Show | 30 | HG00558.hp2 HG00609.hp1 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.2012+169_2012+174d others(8): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr5 | 96903726 | |||||
chr5:96903941
|
G | C | 181 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(178): Show | 206 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.2012+381G>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96903941 | ||||||
chr5:96904009
|
G | C | 181 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(178): Show | 206 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.2012+449G>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96904009 | ||||||
chr5:96904010
|
T | A | 181 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(178): Show | 206 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.2012+450T>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96904010 | ||||||
chr5:96904043
|
T | A | 1 | a0001c0001t0001g0176 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.2012+483T>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96904043 | ||||||
chr5:96904133
|
G | A | 155 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(152): Show | 180 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.2012+573G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96904133 | ||||||
chr5:96904223
|
T | C | 245 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(242): Show | 277 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(274): Show |
intron_variant | MODIFIER | c.2012+663T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96904223 | ||||||
chr5:96904318
|
T | G | 2 | a0001c0004t0022g0225a0001c0004t0030g0226 | 2 | HG02738.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.2012+758T>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96904318 | ||||||
chr5:96904370
|
T | C | 1 | a0002c0002t0002g0119 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2012+810T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96904370 | ||||||
chr5:96904439
|
A | G | 3 | a0001c0001t0001g0027a0001c0001t0001g0198a0001c0001t0008g0197 | 4 | NA18980.hp1 NA18987.hp2 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.2012+879A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96904439 | ||||||
chr5:96904510
|
C | A | 47 | a0002c0002t0003g0068a0002c0002t0003g0104a0002c0002t0009g0023others(44): Show | 53 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.2012+950C>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96904510 | ||||||
chr5:96904516
|
T | C | 155 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(152): Show | 180 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.2012+956T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96904516 | ||||||
chr5:96904520
|
G | A | 47 | a0002c0002t0003g0068a0002c0002t0003g0104a0002c0002t0009g0023others(44): Show | 53 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.2012+960G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96904520 | ||||||
chr5:96904584
|
C | G | 1 | a0002c0002t0002g0073 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2012+1024C>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96904584 | ||||||
chr5:96904682
|
A | G | 181 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(178): Show | 206 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.2012+1122A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96904682 | ||||||
chr5:96904934
|
C | T | 1 | a0002c0002t0029g0117 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2012+1374C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96904934 | ||||||
chr5:96904984
|
TTTTTTAA others(2): Show |
T | 13 | a0005c0006t0005g0038a0005c0006t0005g0212a0005c0006t0005g0264others(10): Show | 13 | HG00642.hp1 HG00735.hp1 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.2012+1432_2012+144 others(13): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr5 | 96904984 | |||||
chr5:96905245
|
G | C | 3 | a0008c0009t0002g0022a0008c0009t0025g0022a0016c0013t0002g0067 | 3 | HG02055.hp1 HG02572.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2012+1685G>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96905245 | ||||||
chr5:96905307
|
A | G | 1 | a0001c0001t0001g0235 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2012+1747A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96905307 | ||||||
chr5:96905358
|
G | C | 1 | a0005c0006t0013g0326 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2012+1798G>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96905358 | ||||||
chr5:96905412
|
A | C | 24 | a0001c0004t0006g0128a0001c0004t0006g0130a0001c0004t0006g0131others(21): Show | 24 | HG01109.hp1 HG01243.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.2012+1852A>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96905412 | ||||||
chr5:96905490
|
T | C | 4 | a0002c0002t0002g0084a0002c0002t0002g0105a0002c0002t0017g0069others(1): Show | 4 | HG02300.hp1 NA18949.hp2 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.2012+1930T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96905490 | ||||||
chr5:96905944
|
A | AT | 177 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(174): Show | 202 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.2012+2399dupT | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr5 | 96905944 | |||||
chr5:96905944
|
AT | A | 47 | a0002c0002t0003g0068a0002c0002t0003g0104a0002c0002t0009g0023others(44): Show | 53 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.2012+2399delT | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr5 | 96905944 | |||||
chr5:96906185
|
CTTTT | C | 181 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(178): Show | 206 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.2012+2632_2012+263 others(8): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr5 | 96906185 | |||||
chr5:96906236
|
T | C | 1 | a0002c0002t0002g0113 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2012+2676T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96906236 | ||||||
chr5:96906240
|
T | C | 8 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0206others(5): Show | 13 | HG02258.hp1 HG02280.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.2012+2680T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96906240 | ||||||
chr5:96906370
|
G | A | 181 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(178): Show | 206 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.2013-2591G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96906370 | ||||||
chr5:96906417
|
C | T | 1 | a0002c0002t0003g0044 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.2013-2544C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96906417 | ||||||
chr5:96906566
|
A | C | 181 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(178): Show | 206 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.2013-2395A>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96906566 | ||||||
chr5:96906573
|
A | T | 1 | a0002c0002t0002g0109 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2013-2388A>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96906573 | ||||||
chr5:96906696
|
T | C | 17 | a0002c0002t0010g0039a0002c0002t0010g0335a0002c0002t0010g0336others(14): Show | 18 | HG00642.hp1 HG00735.hp1 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.2013-2265T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96906696 | ||||||
chr5:96906708
|
T | C | 181 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(178): Show | 206 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.2013-2253T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96906708 | ||||||
chr5:96906731
|
C | T | 2 | a0002c0002t0009g0023a0002c0002t0009g0138 | 3 | HG01243.hp2 HG02647.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2013-2230C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96906731 | ||||||
chr5:96906738
|
G | A | 181 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(178): Show | 206 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.2013-2223G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96906738 | ||||||
chr5:96906758
|
G | A | 181 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(178): Show | 206 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.2013-2203G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96906758 | ||||||
chr5:96906790
|
G | C | 2 | a0001c0001t0001g0110a0001c0001t0001g0111 | 2 | HG00280.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.2013-2171G>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96906790 | ||||||
chr5:96907099
|
A | G | 1 | a0001c0001t0001g0315 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2013-1862A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96907099 | ||||||
chr5:96907153
|
T | C | 112 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(109): Show | 133 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.2013-1808T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96907153 | ||||||
chr5:96907162
|
G | A | 181 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(178): Show | 206 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.2013-1799G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96907162 | ||||||
chr5:96907163
|
G | A | 1 | a0002c0002t0002g0057 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2013-1798G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96907163 | ||||||
chr5:96907277
|
C | T | 181 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(178): Show | 206 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.2013-1684C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96907277 | ||||||
chr5:96907573
|
A | AT | 70 | a0001c0001t0001g0030a0001c0001t0001g0219a0002c0002t0002g0063others(67): Show | 78 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.2013-1375dupT | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr5 | 96907573 | |||||
chr5:96907573
|
A | ATT | 176 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(173): Show | 200 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.2013-1376_2013-137 others(6): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr5 | 96907573 | |||||
chr5:96907604
|
G | A | 1 | a0003c0003t0004g0032 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.2013-1357G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96907604 | ||||||
chr5:96907652
|
C | T | 13 | a0005c0006t0005g0038a0005c0006t0005g0212a0005c0006t0005g0264others(10): Show | 13 | HG00642.hp1 HG00735.hp1 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.2013-1309C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96907652 | ||||||
chr5:96907653
|
G | A | 13 | a0002c0002t0003g0068a0002c0002t0003g0104a0004c0005t0003g0021others(10): Show | 15 | HG00597.hp1 HG02083.hp2 NA18942.hp2 others(12): Show |
intron_variant | MODIFIER | c.2013-1308G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96907653 | ||||||
chr5:96907839
|
T | C | 2 | a0005c0006t0005g0327a0005c0006t0013g0326 | 2 | HG00735.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.2013-1122T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96907839 | ||||||
chr5:96907883
|
CA | C | 58 | a0002c0002t0002g0028a0002c0002t0002g0113a0002c0002t0002g0125others(55): Show | 65 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.2013-1066delA | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr5 | 96907883 | |||||
chr5:96907883
|
CAAA | C | 181 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(178): Show | 206 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.2013-1068_2013-106 others(7): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr5 | 96907883 | |||||
chr5:96907892
|
A | T | 2 | a0002c0002t0009g0023a0002c0002t0009g0138 | 3 | HG01243.hp2 HG02647.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2013-1069A>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96907892 | ||||||
chr5:96907894
|
A | AT | 4 | a0002c0002t0003g0014a0002c0002t0003g0079a0002c0002t0003g0083others(1): Show | 5 | HG02027.hp2 HG03834.hp2 NA19010.hp1 others(2): Show |
intron_variant | MODIFIER | c.2013-1067_2013-106 others(5): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96907894 | ||||||
chr5:96907894
|
A | T | 174 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(171): Show | 200 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.2013-1067A>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96907894 | ||||||
chr5:96908305
|
C | T | 1 | a0009c0014t0001g0302 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2013-656C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96908305 | ||||||
chr5:96908377
|
G | C | 13 | a0005c0006t0005g0038a0005c0006t0005g0212a0005c0006t0005g0264others(10): Show | 13 | HG00642.hp1 HG00735.hp1 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.2013-584G>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96908377 | ||||||
chr5:96908385
|
C | T | 1 | a0002c0002t0003g0058 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2013-576C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96908385 | ||||||
chr5:96908845
|
C | T | 245 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(242): Show | 277 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(274): Show |
intron_variant | MODIFIER | c.2013-116C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96908845 | ||||||
chr5:96908881
|
A | C | 183 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(180): Show | 209 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.2013-80A>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96908881 | ||||||
chr5:96908934
|
A | G | 181 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(178): Show | 206 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.2013-27A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 13/18 | chr5 | 96908934 | ||||||
chr5:96909814
|
A | G | 181 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(178): Show | 206 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.2354+50A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | chr5 | 96909814 | ||||||
chr5:96909913
|
T | C | 181 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(178): Show | 206 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.2354+149T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | chr5 | 96909913 | ||||||
chr5:96909914
|
G | A | 1 | a0001c0001t0001g0153 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.2354+150G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | chr5 | 96909914 | ||||||
chr5:96910080
|
C | A | 2 | a0001c0004t0022g0225a0001c0004t0030g0226 | 2 | HG02738.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.2354+316C>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | chr5 | 96910080 | ||||||
chr5:96910187
|
C | T | 14 | a0001c0001t0001g0047a0001c0001t0001g0088a0001c0001t0001g0089others(11): Show | 15 | HG00323.hp1 HG01167.hp1 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.2354+423C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | chr5 | 96910187 | ||||||
chr5:96910188
|
C | T | 181 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(178): Show | 206 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.2354+424C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | chr5 | 96910188 | ||||||
chr5:96910199
|
A | C | 181 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(178): Show | 206 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.2354+435A>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | chr5 | 96910199 | ||||||
chr5:96910206
|
C | A | 181 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(178): Show | 206 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.2354+442C>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | chr5 | 96910206 | ||||||
chr5:96910264
|
C | CA | 212 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(209): Show | 247 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.2354+516dupA | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr5 | 96910264 | |||||
chr5:96910264
|
C | CAA | 28 | a0001c0001t0001g0200a0001c0001t0001g0222a0001c0004t0006g0128others(25): Show | 28 | HG01109.hp1 HG01243.hp1 HG01496.hp1 others(25): Show |
intron_variant | MODIFIER | c.2354+515_2354+516d others(4): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr5 | 96910264 | |||||
chr5:96910396
|
T | G | 5 | a0002c0002t0002g0018a0002c0002t0003g0044a0002c0002t0003g0082others(2): Show | 5 | HG00544.hp1 NA18948.hp2 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.2354+632T>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | chr5 | 96910396 | ||||||
chr5:96910453
|
G | GA | 64 | a0002c0002t0003g0068a0002c0002t0003g0104a0002c0002t0009g0023others(61): Show | 71 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.2354+700dupA | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr5 | 96910453 | |||||
chr5:96910634
|
T | C | 181 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(178): Show | 206 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.2354+870T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | chr5 | 96910634 | ||||||
chr5:96910705
|
G | T | 1 | a0001c0001t0001g0153 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.2354+941G>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | chr5 | 96910705 | ||||||
chr5:96910897
|
A | T | 181 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(178): Show | 206 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.2354+1133A>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | chr5 | 96910897 | ||||||
chr5:96911026
|
T | C | 2 | a0002c0002t0002g0015a0002c0002t0002g0090 | 3 | NA18960.hp2 NA18988.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.2354+1262T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | chr5 | 96911026 | ||||||
chr5:96911236
|
G | T | 181 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(178): Show | 206 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.2355-1401G>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | chr5 | 96911236 | ||||||
chr5:96911248
|
A | G | 2 | a0002c0002t0002g0051a0002c0002t0003g0076 | 2 | NA18990.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.2355-1389A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | chr5 | 96911248 | ||||||
chr5:96911552
|
G | A | 2 | a0001c0001t0001g0255a0001c0001t0001g0256 | 2 | HG02572.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2355-1085G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | chr5 | 96911552 | ||||||
chr5:96911569
|
A | T | 2 | a0007c0012t0001g0152a0007c0012t0001g0154 | 2 | HG01074.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2355-1068A>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | chr5 | 96911569 | ||||||
chr5:96911586
|
A | G | 47 | a0002c0002t0003g0068a0002c0002t0003g0104a0002c0002t0009g0023others(44): Show | 53 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.2355-1051A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | chr5 | 96911586 | ||||||
chr5:96911615
|
G | C | 1 | a0001c0004t0011g0133 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2355-1022G>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | chr5 | 96911615 | ||||||
chr5:96911723
|
A | G | 1 | a0001c0001t0001g0308 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2355-914A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | chr5 | 96911723 | ||||||
chr5:96911730
|
G | A | 245 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(242): Show | 277 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(274): Show |
intron_variant | MODIFIER | c.2355-907G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | chr5 | 96911730 | ||||||
chr5:96911740
|
C | T | 47 | a0002c0002t0003g0068a0002c0002t0003g0104a0002c0002t0009g0023others(44): Show | 53 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.2355-897C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | chr5 | 96911740 | ||||||
chr5:96911765
|
C | G | 1 | a0000c0010t0014g0026 | 2 | NA18983.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.2355-872C>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | chr5 | 96911765 | ||||||
chr5:96911818
|
G | T | 1 | a0001c0001t0001g0162 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2355-819G>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | chr5 | 96911818 | ||||||
chr5:96911858
|
C | A | 1 | a0002c0002t0002g0201 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2355-779C>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | chr5 | 96911858 | ||||||
chr5:96911866
|
C | CA | 10 | a0002c0002t0002g0061a0002c0002t0002g0062a0002c0002t0002g0063others(7): Show | 10 | HG00544.hp2 HG00609.hp2 HG02129.hp2 others(7): Show |
intron_variant | MODIFIER | c.2355-756dupA | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr5 | 96911866 | |||||
chr5:96911866
|
C | CAAAAAAA | 15 | a0001c0004t0006g0128a0001c0004t0006g0130a0001c0004t0006g0132others(12): Show | 15 | HG01109.hp1 HG01243.hp1 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.2355-762_2355-756d others(9): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr5 | 96911866 | |||||
chr5:96911866
|
C | CAAAAAAA others(1): Show |
7 | a0001c0004t0007g0114a0001c0004t0007g0115a0001c0004t0007g0116others(4): Show | 7 | HG02451.hp1 HG02622.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.2355-763_2355-756d others(10): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr5 | 96911866 | |||||
chr5:96911866
|
C | CAAAAAAA others(2): Show |
7 | a0001c0001t0001g0047a0001c0001t0001g0169a0001c0001t0001g0186others(4): Show | 7 | HG00323.hp1 HG01167.hp1 HG02040.hp2 others(4): Show |
intron_variant | MODIFIER | c.2355-764_2355-756d others(11): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr5 | 96911866 | |||||
chr5:96911866
|
C | CAAAAAAA others(3): Show |
106 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(103): Show | 127 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.2355-765_2355-756d others(12): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr5 | 96911866 | |||||
chr5:96911866
|
C | CAAAAAAA others(4): Show |
39 | a0001c0001t0001g0012a0001c0001t0001g0020a0001c0001t0001g0040others(36): Show | 42 | HG00280.hp2 HG00597.hp2 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.2355-766_2355-756d others(13): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr5 | 96911866 | |||||
chr5:96911866
|
C | CAAAAAAA others(5): Show |
2 | a0001c0001t0001g0254a0001c0001t0020g0151 | 2 | HG01106.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.2355-767_2355-756d others(14): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr5 | 96911866 | |||||
chr5:96911866
|
C | CAAAAAAA others(6): Show |
1 | a0001c0001t0001g0252 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2355-768_2355-756d others(15): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr5 | 96911866 | |||||
chr5:96911866
|
CA | C | 26 | a0002c0002t0002g0053a0002c0002t0002g0113a0002c0002t0002g0325others(23): Show | 30 | HG00597.hp1 HG00738.hp2 HG01167.hp2 others(27): Show |
intron_variant | MODIFIER | c.2355-756delA | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr5 | 96911866 | |||||
chr5:96911882
|
G | A | 181 | a0000c0010t0014g0026a0001c0001t0001g0005a0001c0001t0001g0006others(178): Show | 206 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.2355-755G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | chr5 | 96911882 | ||||||
chr5:96911883
|
AAAGAAAG others(298): Show |
A | 1 | a0000c0010t0014g0026 | 2 | NA18983.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.2355-751_2355-447d others(2): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr5 | 96911883 | |||||
chr5:96911915
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2355-722C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | chr5 | 96911915 | ||||||
chr5:96911941
|
G | A | 1 | a0002c0002t0002g0102 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2355-696G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | chr5 | 96911941 | ||||||
chr5:96911954
|
C | G | 1 | a0001c0001t0028g0189 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2355-683C>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | chr5 | 96911954 | ||||||
chr5:96911965
|
G | A | 1 | a0004c0005t0003g0316 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2355-672G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | chr5 | 96911965 | ||||||
chr5:96911986
|
G | A | 6 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0206others(3): Show | 11 | HG02258.hp1 HG02280.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.2355-651G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | chr5 | 96911986 | ||||||
chr5:96912046
|
C | T | 180 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(177): Show | 204 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.2355-591C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | chr5 | 96912046 | ||||||
chr5:96912089
|
C | A | 1 | a0001c0001t0001g0164 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2355-548C>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | chr5 | 96912089 | ||||||
chr5:96912106
|
T | C | 244 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(241): Show | 275 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.2355-531T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | chr5 | 96912106 | ||||||
chr5:96912123
|
G | A | 180 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(177): Show | 204 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.2355-514G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | chr5 | 96912123 | ||||||
chr5:96912145
|
C | T | 1 | a0004c0005t0003g0021 | 2 | NA18955.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.2355-492C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | chr5 | 96912145 | ||||||
chr5:96912148
|
G | A | 2 | a0001c0007t0001g0259a0001c0007t0001g0266 | 2 | HG02004.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.2355-489G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | chr5 | 96912148 | ||||||
chr5:96912188
|
C | CA | 25 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0158others(22): Show | 25 | HG00280.hp1 HG00597.hp2 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.2355-433dupA | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr5 | 96912188 | |||||
chr5:96912194
|
AAAAAAAA others(4): Show |
A | 1 | a0001c0007t0001g0269 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2355-438_2355-428d others(13): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr5 | 96912194 | |||||
chr5:96912201
|
A | G | 1 | a0000c0010t0014g0026 | 2 | NA18983.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.2355-436A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | chr5 | 96912201 | ||||||
chr5:96912204
|
AG | A | 5 | a0001c0001t0001g0050a0001c0001t0001g0164a0001c0001t0001g0182others(2): Show | 5 | HG00558.hp1 HG02451.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.2355-432delG | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | chr5 | 96912204 | ||||||
chr5:96912205
|
G | A | 174 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(171): Show | 198 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.2355-432G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | chr5 | 96912205 | ||||||
chr5:96912265
|
T | TA | 55 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(52): Show | 67 | HG00140.hp1 HG00423.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.2355-362dupA | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr5 | 96912265 | |||||
chr5:96912289
|
A | G | 154 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(151): Show | 178 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.2355-348A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | chr5 | 96912289 | ||||||
chr5:96912294
|
G | A | 17 | a0001c0004t0006g0128a0001c0004t0006g0130a0001c0004t0006g0131others(14): Show | 17 | HG01109.hp1 HG01243.hp1 HG01496.hp1 others(14): Show |
intron_variant | MODIFIER | c.2355-343G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | chr5 | 96912294 | ||||||
chr5:96912513
|
G | T | 4 | a0006c0008t0008g0171a0006c0008t0008g0172a0006c0008t0008g0238others(1): Show | 4 | HG02040.hp1 HG02698.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.2355-124G>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | chr5 | 96912513 | ||||||
chr5:96912550
|
T | G | 17 | a0002c0002t0010g0039a0002c0002t0010g0335a0002c0002t0010g0336others(14): Show | 18 | HG00642.hp1 HG00735.hp1 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.2355-87T>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 15/18 | chr5 | 96912550 | ||||||
chr5:96912981
|
T | TGTTTCAT others(17): Show |
1 | a0002c0002t0003g0104 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.2516+183_2516+184i others(26): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 16/18 | chr5 | 96912981 | ||||||
chr5:96912983
|
G | C | 1 | a0002c0002t0003g0104 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.2516+185G>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 16/18 | chr5 | 96912983 | ||||||
chr5:96912985
|
T | A | 1 | a0002c0002t0003g0104 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.2516+187T>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 16/18 | chr5 | 96912985 | ||||||
chr5:96913003
|
G | T | 180 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(177): Show | 204 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.2516+205G>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 16/18 | chr5 | 96913003 | ||||||
chr5:96913091
|
T | C | 253 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(250): Show | 285 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(282): Show |
intron_variant | MODIFIER | c.2517-226T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 16/18 | chr5 | 96913091 | ||||||
chr5:96913158
|
T | C | 1 | a0002c0002t0002g0062 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.2517-159T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 16/18 | chr5 | 96913158 | ||||||
chr5:96913182
|
A | G | 180 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(177): Show | 204 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.2517-135A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 16/18 | chr5 | 96913182 | ||||||
chr5:96913201
|
A | G | 1 | a0002c0002t0029g0117 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2517-116A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 16/18 | chr5 | 96913201 | ||||||
chr5:96913619
|
G | A | 180 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(177): Show | 204 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.2657+162G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | chr5 | 96913619 | ||||||
chr5:96913647
|
T | A | 180 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(177): Show | 204 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.2657+190T>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | chr5 | 96913647 | ||||||
chr5:96913674
|
A | C | 180 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(177): Show | 204 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.2657+217A>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | chr5 | 96913674 | ||||||
chr5:96913930
|
A | C | 178 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(175): Show | 202 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.2657+473A>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | chr5 | 96913930 | ||||||
chr5:96913930
|
A | T | 2 | a0001c0004t0022g0225a0001c0004t0030g0226 | 2 | HG02738.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.2657+473A>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | chr5 | 96913930 | ||||||
chr5:96913944
|
T | C | 245 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(242): Show | 276 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.2657+487T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | chr5 | 96913944 | ||||||
chr5:96914041
|
A | G | 47 | a0002c0002t0003g0068a0002c0002t0003g0104a0002c0002t0009g0023others(44): Show | 53 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.2657+584A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | chr5 | 96914041 | ||||||
chr5:96914054
|
T | A | 1 | a0001c0001t0001g0227 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2657+597T>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | chr5 | 96914054 | ||||||
chr5:96914129
|
G | GTCTC | 20 | a0001c0001t0001g0257a0001c0004t0006g0128a0001c0004t0006g0130others(17): Show | 20 | HG01109.hp1 HG01243.hp1 HG01496.hp1 others(17): Show |
intron_variant | MODIFIER | c.2657+689_2657+692d others(6): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 96914129 | |||||
chr5:96914146
|
T | TCACACAC others(9): Show |
4 | a0002c0002t0012g0241a0002c0002t0012g0242a0002c0002t0012g0243others(1): Show | 4 | HG02559.hp2 HG02896.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.2657+690_2657+691i others(18): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 96914146 | |||||
chr5:96914148
|
T | A | 5 | a0001c0001t0001g0141a0002c0002t0012g0241a0002c0002t0012g0242others(2): Show | 5 | HG02280.hp2 HG02559.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.2657+691T>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | chr5 | 96914148 | ||||||
chr5:96914148
|
T | TCACA | 3 | a0001c0001t0001g0112a0001c0001t0001g0127a0001c0001t0001g0233 | 3 | HG02258.hp2 HG03453.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2657+708_2657+711d others(6): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 96914148 | |||||
chr5:96914148
|
T | TCACACAC others(5): Show |
1 | a0004c0005t0003g0320 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.2657+700_2657+711d others(14): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 96914148 | |||||
chr5:96914148
|
T | TCACACAC others(7): Show |
2 | a0002c0002t0002g0202a0002c0002t0002g0325 | 2 | HG01109.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2657+698_2657+711d others(16): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 96914148 | |||||
chr5:96914148
|
T | TCACACAC others(9): Show |
14 | a0002c0002t0002g0028a0002c0002t0002g0113a0002c0002t0003g0068others(11): Show | 15 | HG00597.hp1 HG02055.hp1 HG02083.hp2 others(12): Show |
intron_variant | MODIFIER | c.2657+696_2657+711d others(18): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 96914148 | |||||
chr5:96914148
|
T | TCACACAC others(11): Show |
5 | a0002c0002t0002g0204a0002c0002t0009g0023a0002c0002t0009g0138others(2): Show | 7 | HG01243.hp2 HG01255.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.2657+694_2657+711d others(20): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 96914148 | |||||
chr5:96914148
|
T | TCACACAC others(13): Show |
1 | a0003c0003t0004g0032 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.2657+692_2657+711d others(22): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 96914148 | |||||
chr5:96914148
|
T | TCACACAC others(17): Show |
3 | a0003c0003t0004g0033a0003c0003t0004g0277a0003c0003t0009g0287 | 4 | NA18950.hp1 NA18968.hp1 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.2657+711_2657+712i others(26): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 96914148 | |||||
chr5:96914148
|
T | TCTCA | 150 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(147): Show | 174 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.2657+692_2657+693i others(6): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 96914148 | |||||
chr5:96914148
|
T | TCTCACA | 5 | a0001c0001t0001g0155a0001c0001t0001g0181a0001c0001t0001g0191others(2): Show | 5 | HG02027.hp1 NA18612.hp1 NA18959.hp2 others(2): Show |
intron_variant | MODIFIER | c.2657+692_2657+693i others(8): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 96914148 | |||||
chr5:96914148
|
T | TCTCACAC others(3): Show |
4 | a0002c0002t0010g0039a0002c0002t0010g0335a0002c0002t0010g0336others(1): Show | 5 | HG00738.hp2 HG01167.hp2 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.2657+692_2657+693i others(12): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 96914148 | |||||
chr5:96914148
|
T | TCTCACAC others(9): Show |
11 | a0005c0006t0005g0038a0005c0006t0005g0212a0005c0006t0005g0264others(8): Show | 11 | HG00642.hp1 HG00735.hp1 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.2657+692_2657+693i others(18): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 96914148 | |||||
chr5:96914148
|
T | TCTCACAC others(11): Show |
4 | a0003c0003t0004g0289a0003c0003t0004g0291a0004c0005t0003g0037others(1): Show | 5 | NA18942.hp2 NA18978.hp2 NA19002.hp1 others(2): Show |
intron_variant | MODIFIER | c.2657+692_2657+693i others(20): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 96914148 | |||||
chr5:96914148
|
T | TCTCACAC others(13): Show |
1 | a0003c0003t0004g0274 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2657+692_2657+693i others(22): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 96914148 | |||||
chr5:96914148
|
T | TCTCACAC others(15): Show |
16 | a0003c0003t0004g0250a0003c0003t0004g0276a0003c0003t0004g0278others(13): Show | 16 | HG00558.hp2 HG00609.hp1 HG03688.hp2 others(13): Show |
intron_variant | MODIFIER | c.2657+692_2657+693i others(24): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 96914148 | |||||
chr5:96914148
|
T | TCTCACAC others(17): Show |
1 | a0003c0003t0009g0034 | 2 | NA18973.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.2657+692_2657+693i others(26): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 96914148 | |||||
chr5:96914148
|
T | TCTCACAC others(19): Show |
2 | a0003c0003t0004g0272a0003c0003t0004g0273 | 2 | NA19010.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.2657+692_2657+693i others(28): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 96914148 | |||||
chr5:96914148
|
T | TCTCTCAC others(5): Show |
1 | a0003c0003t0004g0283 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2657+692_2657+693i others(14): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 96914148 | |||||
chr5:96914148
|
T | TCTCTCAC others(9): Show |
2 | a0005c0006t0005g0328a0005c0006t0005g0329 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.2657+692_2657+693i others(18): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 96914148 | |||||
chr5:96914148
|
T | TCTCTCAC others(15): Show |
1 | a0002c0002t0029g0117 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2657+692_2657+693i others(24): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 96914148 | |||||
chr5:96914324
|
T | A | 1 | a0002c0002t0002g0016 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.2657+867T>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | chr5 | 96914324 | ||||||
chr5:96914343
|
G | C | 13 | a0001c0004t0006g0131a0001c0004t0006g0132a0001c0004t0006g0147others(10): Show | 13 | HG01109.hp1 HG01496.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.2657+886G>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | chr5 | 96914343 | ||||||
chr5:96914560
|
C | A | 180 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(177): Show | 204 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.2657+1103C>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | chr5 | 96914560 | ||||||
chr5:96914631
|
A | ACCAT | 1 | a0002c0002t0002g0002 | 4 | NA18970.hp2 NA18975.hp1 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.2658-1056_2658-105 others(8): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 96914631 | |||||
chr5:96914753
|
G | A | 154 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(151): Show | 178 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.2658-935G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | chr5 | 96914753 | ||||||
chr5:96914875
|
A | G | 1 | a0001c0004t0007g0303 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2658-813A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | chr5 | 96914875 | ||||||
chr5:96914881
|
A | G | 17 | a0002c0002t0010g0039a0002c0002t0010g0335a0002c0002t0010g0336others(14): Show | 18 | HG00642.hp1 HG00735.hp1 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.2658-807A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | chr5 | 96914881 | ||||||
chr5:96914945
|
ATTAT | A | 178 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(175): Show | 202 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.2658-736_2658-733d others(6): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 96914945 | |||||
chr5:96915013
|
T | A | 17 | a0002c0002t0010g0039a0002c0002t0010g0335a0002c0002t0010g0336others(14): Show | 18 | HG00642.hp1 HG00735.hp1 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.2658-675T>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | chr5 | 96915013 | ||||||
chr5:96915076
|
T | C | 4 | a0002c0002t0010g0039a0002c0002t0010g0335a0002c0002t0010g0336others(1): Show | 5 | HG00738.hp2 HG01167.hp2 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.2658-612T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | chr5 | 96915076 | ||||||
chr5:96915100
|
C | T | 27 | a0003c0003t0004g0032a0003c0003t0004g0033a0003c0003t0004g0250others(24): Show | 30 | HG00558.hp2 HG00609.hp1 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.2658-588C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | chr5 | 96915100 | ||||||
chr5:96915224
|
G | A | 180 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(177): Show | 204 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.2658-464G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | chr5 | 96915224 | ||||||
chr5:96915235
|
C | G | 2 | a0001c0004t0022g0225a0001c0004t0030g0226 | 2 | HG02738.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.2658-453C>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | chr5 | 96915235 | ||||||
chr5:96915298
|
C | T | 4 | a0002c0002t0002g0004a0002c0002t0002g0056a0002c0002t0002g0120others(1): Show | 7 | HG00741.hp2 HG02965.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.2658-390C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | chr5 | 96915298 | ||||||
chr5:96915299
|
G | A | 180 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(177): Show | 204 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.2658-389G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | chr5 | 96915299 | ||||||
chr5:96915484
|
ATT | A | 180 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(177): Show | 204 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.2658-201_2658-200d others(4): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | 96915484 | |||||
chr5:96915539
|
T | A | 3 | a0001c0004t0007g0114a0001c0004t0007g0115a0001c0004t0007g0116 | 3 | HG02622.hp2 HG02809.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.2658-149T>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | chr5 | 96915539 | ||||||
chr5:96915557
|
T | C | 3 | a0001c0001t0001g0232a0001c0001t0001g0237a0001c0001t0020g0151 | 3 | HG01175.hp1 HG01993.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.2658-131T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | chr5 | 96915557 | ||||||
chr5:96915572
|
G | A | 1 | a0002c0002t0002g0046 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2658-116G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 17/18 | chr5 | 96915572 | ||||||
chr5:96915971
|
C | A | 96 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0003others(93): Show | 120 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.2739+202C>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 18/18 | chr5 | 96915971 | ||||||
chr5:96915975
|
C | T | 1 | a0004c0016t0002g0318 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2739+206C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 18/18 | chr5 | 96915975 | ||||||
chr5:96915997
|
T | C | 160 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0003others(157): Show | 191 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(188): Show |
intron_variant | MODIFIER | c.2739+228T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 18/18 | chr5 | 96915997 | ||||||
chr5:96916009
|
T | C | 47 | a0002c0002t0003g0068a0002c0002t0003g0104a0002c0002t0009g0023others(44): Show | 53 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.2739+240T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 18/18 | chr5 | 96916009 | ||||||
chr5:96916153
|
G | A | 1 | a0001c0001t0001g0155 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2739+384G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 18/18 | chr5 | 96916153 | ||||||
chr5:96916246
|
AC | A | 158 | a0001c0004t0022g0225a0001c0004t0030g0226a0002c0002t0002g0001others(155): Show | 188 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(185): Show |
intron_variant | MODIFIER | c.2739+478delC | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 18/18 | chr5 | 96916246 | ||||||
chr5:96916247
|
C | A | 24 | a0001c0004t0006g0128a0001c0004t0006g0130a0001c0004t0006g0131others(21): Show | 24 | HG01109.hp1 HG01243.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.2739+478C>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 18/18 | chr5 | 96916247 | ||||||
chr5:96916247
|
CA | C | 4 | a0002c0002t0010g0039a0002c0002t0010g0335a0002c0002t0010g0336others(1): Show | 5 | HG00738.hp2 HG01167.hp2 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.2739+484delA | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr5 | 96916247 | |||||
chr5:96916261
|
A | C | 2 | a0001c0004t0022g0225a0001c0004t0030g0226 | 2 | HG02738.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.2739+492A>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 18/18 | chr5 | 96916261 | ||||||
chr5:96916374
|
C | T | 25 | a0001c0001t0001g0173a0001c0004t0006g0128a0001c0004t0006g0130others(22): Show | 25 | HG01109.hp1 HG01243.hp1 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.2739+605C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 18/18 | chr5 | 96916374 | ||||||
chr5:96916375
|
G | A | 96 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0003others(93): Show | 120 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.2739+606G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 18/18 | chr5 | 96916375 | ||||||
chr5:96916456
|
C | CT | 29 | a0001c0001t0001g0141a0001c0001t0001g0155a0001c0001t0001g0158others(26): Show | 29 | HG00621.hp2 HG01192.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.2739+710dupT | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr5 | 96916456 | |||||
chr5:96916456
|
CT | C | 9 | a0001c0001t0001g0005a0001c0001t0001g0140a0001c0001t0001g0168others(6): Show | 12 | HG00140.hp1 HG00735.hp2 HG00738.hp1 others(9): Show |
intron_variant | MODIFIER | c.2739+710delT | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr5 | 96916456 | |||||
chr5:96916456
|
CTT | C | 6 | a0001c0004t0022g0225a0002c0002t0003g0104a0002c0002t0029g0117others(3): Show | 6 | HG02602.hp1 HG03831.hp1 NA18977.hp2 others(3): Show |
intron_variant | MODIFIER | c.2739+709_2739+710d others(4): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr5 | 96916456 | |||||
chr5:96916456
|
CTTT | C | 47 | a0002c0002t0002g0042a0002c0002t0002g0052a0002c0002t0002g0078others(44): Show | 52 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.2739+708_2739+710d others(5): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr5 | 96916456 | |||||
chr5:96916456
|
CTTTT | C | 83 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0003others(80): Show | 106 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.2739+707_2739+710d others(6): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr5 | 96916456 | |||||
chr5:96916456
|
CTTTTT | C | 24 | a0002c0002t0002g0028a0002c0002t0002g0202a0002c0002t0002g0204others(21): Show | 27 | HG00642.hp1 HG00735.hp1 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.2739+706_2739+710d others(7): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr5 | 96916456 | |||||
chr5:96916519
|
T | G | 1 | a0001c0001t0001g0110 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2739+750T>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 18/18 | chr5 | 96916519 | ||||||
chr5:96916550
|
G | A | 1 | a0001c0001t0001g0167 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2739+781G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 18/18 | chr5 | 96916550 | ||||||
chr5:96916588
|
C | T | 9 | a0002c0002t0002g0042a0002c0002t0002g0061a0002c0002t0002g0063others(6): Show | 9 | HG00423.hp1 HG00609.hp2 HG02129.hp2 others(6): Show |
intron_variant | MODIFIER | c.2739+819C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 18/18 | chr5 | 96916588 | ||||||
chr5:96916614
|
C | T | 1 | a0001c0001t0001g0251 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2739+845C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 18/18 | chr5 | 96916614 | ||||||
chr5:96916690
|
G | A | 1 | a0001c0004t0011g0133 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2740-772G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 18/18 | chr5 | 96916690 | ||||||
chr5:96916702
|
T | C | 13 | a0005c0006t0005g0038a0005c0006t0005g0212a0005c0006t0005g0264others(10): Show | 13 | HG00642.hp1 HG00735.hp1 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.2740-760T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 18/18 | chr5 | 96916702 | ||||||
chr5:96916725
|
C | T | 4 | a0002c0002t0012g0241a0002c0002t0012g0242a0002c0002t0012g0243others(1): Show | 4 | HG02559.hp2 HG02896.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.2740-737C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 18/18 | chr5 | 96916725 | ||||||
chr5:96916727
|
C | T | 24 | a0001c0004t0006g0128a0001c0004t0006g0130a0001c0004t0006g0131others(21): Show | 24 | HG01109.hp1 HG01243.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.2740-735C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 18/18 | chr5 | 96916727 | ||||||
chr5:96916728
|
G | A | 143 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0003others(140): Show | 173 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(170): Show |
intron_variant | MODIFIER | c.2740-734G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 18/18 | chr5 | 96916728 | ||||||
chr5:96916760
|
C | T | 1 | a0001c0001t0001g0312 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2740-702C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 18/18 | chr5 | 96916760 | ||||||
chr5:96916765
|
C | CT | 165 | a0001c0001t0001g0047a0001c0001t0001g0088a0001c0001t0001g0089others(162): Show | 194 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.2740-683dupT | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr5 | 96916765 | |||||
chr5:96916765
|
C | CTT | 7 | a0002c0002t0002g0015a0002c0002t0002g0090a0002c0002t0010g0039others(4): Show | 9 | HG00738.hp2 HG01167.hp2 HG01975.hp1 others(6): Show |
intron_variant | MODIFIER | c.2740-684_2740-683d others(4): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr5 | 96916765 | |||||
chr5:96916765
|
C | CTTT | 13 | a0005c0006t0005g0038a0005c0006t0005g0212a0005c0006t0005g0264others(10): Show | 13 | HG00642.hp1 HG00735.hp1 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.2740-685_2740-683d others(5): Show |
ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr5 | 96916765 | |||||
chr5:96916765
|
CT | C | 49 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(46): Show | 58 | HG00423.hp2 HG00558.hp1 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.2740-683delT | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr5 | 96916765 | |||||
chr5:96916779
|
T | C | 1 | a0001c0001t0001g0213 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.2740-683T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 18/18 | chr5 | 96916779 | ||||||
chr5:96916885
|
T | C | 143 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0003others(140): Show | 173 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(170): Show |
intron_variant | MODIFIER | c.2740-577T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 18/18 | chr5 | 96916885 | ||||||
chr5:96917098
|
C | T | 1 | a0002c0002t0002g0325 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2740-364C>T | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 18/18 | chr5 | 96917098 | ||||||
chr5:96917099
|
G | A | 95 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0003others(92): Show | 119 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.2740-363G>A | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 18/18 | chr5 | 96917099 | ||||||
chr5:96917239
|
TG | T | 96 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0003others(93): Show | 120 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.2740-220delG | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr5 | 96917239 | |||||
chr5:96917294
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A | G | 96 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0003others(93): Show | 120 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.2740-168A>G | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 18/18 | chr5 | 96917294 | ||||||
chr5:96917400
|
T | C | 96 | a0002c0002t0002g0001a0002c0002t0002g0002a0002c0002t0002g0003others(93): Show | 120 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.2740-62T>C | ERAP2 | ENSG00000164308.17 | transcript | ENST00000437043.8 | protein_coding | 18/18 | chr5 | 96917400 |