geneid | 9818 |
---|---|
ensemblid | ENSG00000139496.18 |
hgncid | 20261 |
symbol | NUP58 |
name | nucleoporin 58 |
refseq_nuc | NM_014089.4 |
refseq_prot | NP_054808.1 |
ensembl_nuc | ENST00000381736.8 |
ensembl_prot | ENSP00000371155.3 |
mane_status | MANE Select |
chr | chr13 |
start | 25301625 |
end | 25342421 |
strand | + |
ver | v1.2 |
region | chr13:25301625-25342421 |
region5000 | chr13:25296625-25347421 |
regionname0 | NUP58_chr13_25301625_25342421 |
regionname5000 | NUP58_chr13_25296625_25347421 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 599 | 223 | 71 | 39 | 79 | 11 | 22 | 67 | NUP58_chr13_25296625_25347421 | NUP58 | copy fasta | chr13 | 25296625 | 25347421 |
a0002 | 0/0 | 599 | 115 | 11 | 17 | 70 | 5 | 12 | 58 | NUP58_chr13_25296625_25347421 | NUP58 | copy fasta | chr13 | 25296625 | 25347421 |
a0003 | 0/0 | 599 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | copy fasta | chr13 | 25296625 | 25347421 |
a0004 | 0/1 | 599 | 2 | 0 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | copy fasta | chr13 | 25296625 | 25347421 |
a0005 | 0/0 | 599 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | copy fasta | chr13 | 25296625 | 25347421 |
a0006 | 0/0 | 595 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | copy fasta | chr13 | 25296625 | 25347421 |
a0007 | 0/0 | 599 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | copy fasta | chr13 | 25296625 | 25347421 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 1800 | 198 | 66 | 32 | 66 | 11 | 22 | NUP58_chr13_25296625_25347421 | NUP58 | copy fasta | chr13 | 25296625 | 25347421 |
c0002 | 0/0 | 1800 | 115 | 11 | 17 | 70 | 5 | 12 | NUP58_chr13_25296625_25347421 | NUP58 | copy fasta | chr13 | 25296625 | 25347421 |
c0003 | 0/0 | 1800 | 14 | 0 | 1 | 13 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | copy fasta | chr13 | 25296625 | 25347421 |
c0004 | 0/0 | 1800 | 7 | 7 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | copy fasta | chr13 | 25296625 | 25347421 |
c0005 | 0/0 | 1800 | 4 | 4 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | copy fasta | chr13 | 25296625 | 25347421 |
c0006 | 0/0 | 1800 | 4 | 0 | 4 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | copy fasta | chr13 | 25296625 | 25347421 |
c0007 | 0/1 | 1800 | 2 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | copy fasta | chr13 | 25296625 | 25347421 |
c0008 | 0/0 | 1800 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | copy fasta | chr13 | 25296625 | 25347421 |
c0009 | 0/0 | 1800 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | copy fasta | chr13 | 25296625 | 25347421 |
c0010 | 0/0 | 1800 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | copy fasta | chr13 | 25296625 | 25347421 |
c0011 | 0/0 | 1788 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | copy fasta | chr13 | 25296625 | 25347421 |
c0012 | 0/0 | 1800 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | copy fasta | chr13 | 25296625 | 25347421 |
c0013 | 0/0 | 1800 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | copy fasta | chr13 | 25296625 | 25347421 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 2437 | 217 | 60 | 31 | 100 | 5 | 20 | NUP58_chr13_25296625_25347421 | NUP58 | copy fasta | chr13 | 25296625 | 25347421 |
t0002 | 0/0 | 2437 | 46 | 0 | 8 | 33 | 0 | 5 | NUP58_chr13_25296625_25347421 | NUP58 | copy fasta | chr13 | 25296625 | 25347421 |
t0003 | 0/1 | 2437 | 35 | 12 | 12 | 0 | 7 | 3 | NUP58_chr13_25296625_25347421 | NUP58 | copy fasta | chr13 | 25296625 | 25347421 |
t0004 | 0/0 | 2437 | 14 | 0 | 0 | 14 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | copy fasta | chr13 | 25296625 | 25347421 |
t0005 | 0/0 | 2437 | 7 | 0 | 3 | 0 | 3 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | copy fasta | chr13 | 25296625 | 25347421 |
t0006 | 0/0 | 2437 | 6 | 6 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | copy fasta | chr13 | 25296625 | 25347421 |
t0007 | 0/0 | 2433 | 4 | 3 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | copy fasta | chr13 | 25296625 | 25347421 |
t0008 | 0/0 | 2437 | 2 | 0 | 0 | 2 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | copy fasta | chr13 | 25296625 | 25347421 |
t0009 | 0/0 | 2437 | 2 | 0 | 1 | 0 | 1 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | copy fasta | chr13 | 25296625 | 25347421 |
t0010 | 0/0 | 2437 | 2 | 2 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | copy fasta | chr13 | 25296625 | 25347421 |
t0011 | 0/0 | 2437 | 2 | 0 | 0 | 0 | 0 | 2 | NUP58_chr13_25296625_25347421 | NUP58 | copy fasta | chr13 | 25296625 | 25347421 |
t0012 | 0/0 | 2437 | 2 | 2 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | copy fasta | chr13 | 25296625 | 25347421 |
t0013 | 0/0 | 2437 | 2 | 2 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | copy fasta | chr13 | 25296625 | 25347421 |
t0014 | 0/0 | 2437 | 2 | 2 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | copy fasta | chr13 | 25296625 | 25347421 |
t0015 | 0/0 | 2437 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | copy fasta | chr13 | 25296625 | 25347421 |
t0016 | 0/0 | 2437 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | copy fasta | chr13 | 25296625 | 25347421 |
t0017 | 0/0 | 2437 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | copy fasta | chr13 | 25296625 | 25347421 |
t0018 | 0/0 | 2437 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | copy fasta | chr13 | 25296625 | 25347421 |
t0019 | 0/0 | 2437 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | copy fasta | chr13 | 25296625 | 25347421 |
t0020 | 0/0 | 2437 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | copy fasta | chr13 | 25296625 | 25347421 |
t0021 | 0/0 | 2437 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | copy fasta | chr13 | 25296625 | 25347421 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 10 | 0 | 3 | 7 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0002 | 0/0 | 9 | 0 | 0 | 7 | 0 | 2 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0003 | 0/0 | 7 | 0 | 2 | 0 | 5 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0004 | 0/0 | 4 | 0 | 0 | 2 | 0 | 2 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0005 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0007 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0009 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0012 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0015 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0016 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0025 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0146 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 1800 | 198 | 66 | 32 | 66 | 11 | 22 | NUP58_chr13_25296625_25347421 | NUP58 | copy fasta | chr13 | 25296625 | 25347421 |
a0001c0003 | 0/0 | 1800 | 14 | 0 | 1 | 13 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | copy fasta | chr13 | 25296625 | 25347421 |
a0001c0005 | 0/0 | 1800 | 4 | 4 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | copy fasta | chr13 | 25296625 | 25347421 |
a0001c0006 | 0/0 | 1800 | 4 | 0 | 4 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | copy fasta | chr13 | 25296625 | 25347421 |
a0001c0008 | 0/0 | 1800 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | copy fasta | chr13 | 25296625 | 25347421 |
a0001c0010 | 0/0 | 1800 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | copy fasta | chr13 | 25296625 | 25347421 |
a0001c0012 | 0/0 | 1800 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | copy fasta | chr13 | 25296625 | 25347421 |
a0002c0002 | 0/0 | 1800 | 115 | 11 | 17 | 70 | 5 | 12 | NUP58_chr13_25296625_25347421 | NUP58 | copy fasta | chr13 | 25296625 | 25347421 |
a0003c0004 | 0/0 | 1800 | 7 | 7 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | copy fasta | chr13 | 25296625 | 25347421 |
a0004c0007 | 0/1 | 1800 | 2 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | copy fasta | chr13 | 25296625 | 25347421 |
a0005c0013 | 0/0 | 1800 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | copy fasta | chr13 | 25296625 | 25347421 |
a0006c0011 | 0/0 | 1788 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | copy fasta | chr13 | 25296625 | 25347421 |
a0007c0009 | 0/0 | 1800 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | copy fasta | chr13 | 25296625 | 25347421 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 4236 | 88 | 37 | 8 | 33 | 0 | 9 | NUP58_chr13_25296625_25347421 | NUP58 | copy fasta | chr13 | 25296625 | 25347421 |
a0001c0001t0002 | 0/0 | 4236 | 46 | 0 | 8 | 33 | 0 | 5 | NUP58_chr13_25296625_25347421 | NUP58 | copy fasta | chr13 | 25296625 | 25347421 |
a0001c0001t0003 | 0/0 | 4236 | 32 | 12 | 10 | 0 | 7 | 3 | NUP58_chr13_25296625_25347421 | NUP58 | copy fasta | chr13 | 25296625 | 25347421 |
a0001c0001t0005 | 0/0 | 4236 | 7 | 0 | 3 | 0 | 3 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | copy fasta | chr13 | 25296625 | 25347421 |
a0001c0001t0006 | 0/0 | 4236 | 6 | 6 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | copy fasta | chr13 | 25296625 | 25347421 |
a0001c0001t0007 | 0/0 | 4232 | 4 | 3 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | copy fasta | chr13 | 25296625 | 25347421 |
a0001c0001t0009 | 0/0 | 4236 | 2 | 0 | 1 | 0 | 1 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | copy fasta | chr13 | 25296625 | 25347421 |
a0001c0001t0010 | 0/0 | 4236 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | copy fasta | chr13 | 25296625 | 25347421 |
a0001c0001t0011 | 0/0 | 4236 | 2 | 0 | 0 | 0 | 0 | 2 | NUP58_chr13_25296625_25347421 | NUP58 | copy fasta | chr13 | 25296625 | 25347421 |
a0001c0001t0012 | 0/0 | 4236 | 2 | 2 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | copy fasta | chr13 | 25296625 | 25347421 |
a0001c0001t0013 | 0/0 | 4236 | 2 | 2 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | copy fasta | chr13 | 25296625 | 25347421 |
a0001c0001t0014 | 0/0 | 4236 | 2 | 2 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | copy fasta | chr13 | 25296625 | 25347421 |
a0001c0001t0015 | 0/0 | 4236 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | copy fasta | chr13 | 25296625 | 25347421 |
a0001c0001t0017 | 0/0 | 4236 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | copy fasta | chr13 | 25296625 | 25347421 |
a0001c0001t0018 | 0/0 | 4236 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | copy fasta | chr13 | 25296625 | 25347421 |
a0001c0001t0019 | 0/0 | 4236 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | copy fasta | chr13 | 25296625 | 25347421 |
a0001c0003t0004 | 0/0 | 4236 | 13 | 0 | 0 | 13 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | copy fasta | chr13 | 25296625 | 25347421 |
a0001c0003t0020 | 0/0 | 4236 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | copy fasta | chr13 | 25296625 | 25347421 |
a0001c0005t0001 | 0/0 | 4236 | 4 | 4 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | copy fasta | chr13 | 25296625 | 25347421 |
a0001c0006t0001 | 0/0 | 4236 | 4 | 0 | 4 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | copy fasta | chr13 | 25296625 | 25347421 |
a0001c0008t0001 | 0/0 | 4236 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | copy fasta | chr13 | 25296625 | 25347421 |
a0001c0010t0001 | 0/0 | 4236 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | copy fasta | chr13 | 25296625 | 25347421 |
a0001c0012t0001 | 0/0 | 4236 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | copy fasta | chr13 | 25296625 | 25347421 |
a0002c0002t0001 | 0/0 | 4236 | 110 | 11 | 16 | 67 | 5 | 11 | NUP58_chr13_25296625_25347421 | NUP58 | copy fasta | chr13 | 25296625 | 25347421 |
a0002c0002t0003 | 0/0 | 4236 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | copy fasta | chr13 | 25296625 | 25347421 |
a0002c0002t0008 | 0/0 | 4236 | 2 | 0 | 0 | 2 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | copy fasta | chr13 | 25296625 | 25347421 |
a0002c0002t0016 | 0/0 | 4236 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | copy fasta | chr13 | 25296625 | 25347421 |
a0002c0002t0021 | 0/0 | 4236 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | copy fasta | chr13 | 25296625 | 25347421 |
a0003c0004t0001 | 0/0 | 4236 | 7 | 7 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | copy fasta | chr13 | 25296625 | 25347421 |
a0004c0007t0003 | 0/1 | 4236 | 2 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | copy fasta | chr13 | 25296625 | 25347421 |
a0005c0013t0010 | 0/0 | 4236 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | copy fasta | chr13 | 25296625 | 25347421 |
a0006c0011t0004 | 0/0 | 4224 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | copy fasta | chr13 | 25296625 | 25347421 |
a0007c0009t0001 | 0/0 | 4236 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | copy fasta | chr13 | 25296625 | 25347421 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 9 | 0 | 0 | 7 | 0 | 2 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0001g0007 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0001g0025 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0002g0001 | 0/0 | 10 | 0 | 3 | 7 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0002g0005 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0002g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0003g0003 | 0/0 | 5 | 0 | 1 | 0 | 4 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0003g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0003g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0003g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0003g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0003g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0003g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0003g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0003g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0003g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0003g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0003g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0003g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0003g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0003g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0003g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0003g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0003g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0003g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0003g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0003g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0005g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0005g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0005g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0005g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0005g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0005g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0005g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0006g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0006g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0006g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0006g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0006g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0007g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0007g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0007g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0007g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0009g0003 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0010g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0011g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0011g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0012g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0012g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0013g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0013g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0014g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0015g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0017g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0018g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0001t0019g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0003t0004g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0003t0004g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0003t0004g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0003t0004g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0003t0004g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0003t0004g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0003t0004g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0003t0004g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0003t0004g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0003t0004g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0003t0004g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0003t0004g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0003t0004g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0003t0020g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0005t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0005t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0005t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0006t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0006t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0006t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0006t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0008t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0010t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0001c0012t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0004 | 0/0 | 4 | 0 | 0 | 2 | 0 | 2 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0009 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0012 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0015 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0016 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0003g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0008g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0008g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0016g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0002c0002t0021g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0003c0004t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0003c0004t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0003c0004t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0003c0004t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0003c0004t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0003c0004t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0003c0004t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0004c0007t0003g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0004c0007t0003g0146 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0005c0013t0010g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0006c0011t0004g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
a0007c0009t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0003 | g0174 | EUR | GBR | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG00099 | hp2 | a0002 | c0002 | t0001 | g0160 | EUR | GBR | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG00140 | hp1 | a0002 | c0002 | t0001 | g0161 | EUR | GBR | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG00140 | hp2 | a0001 | c0001 | t0009 | g0003 | EUR | GBR | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG00280 | hp1 | a0001 | c0001 | t0003 | g0003 | EUR | FIN | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG00280 | hp2 | a0001 | c0001 | t0003 | g0024 | EUR | FIN | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG00323 | hp1 | a0002 | c0002 | t0001 | g0015 | EUR | FIN | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG00323 | hp2 | a0001 | c0001 | t0005 | g0159 | EUR | FIN | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | CHS | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG00423 | hp2 | a0002 | c0002 | t0001 | g0041 | EAS | CHS | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG00438 | hp1 | a0002 | c0002 | t0021 | g0013 | EAS | CHS | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0225 | EAS | CHS | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG00558 | hp1 | a0002 | c0002 | t0001 | g0064 | EAS | CHS | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | CHS | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | CHS | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG00609 | hp2 | a0002 | c0002 | t0001 | g0084 | EAS | CHS | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG00639 | hp2 | a0001 | c0001 | t0003 | g0134 | AMR | PUR | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG00642 | hp1 | a0002 | c0002 | t0001 | g0100 | AMR | PUR | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG00733 | hp1 | a0002 | c0002 | t0001 | g0101 | AMR | PUR | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG00733 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG00735 | hp1 | a0002 | c0002 | t0001 | g0115 | AMR | PUR | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG00738 | hp2 | a0001 | c0008 | t0001 | g0215 | AMR | PUR | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG00741 | hp1 | a0002 | c0002 | t0001 | g0082 | AMR | PUR | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG00741 | hp2 | a0002 | c0002 | t0001 | g0060 | AMR | PUR | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG01069 | hp1 | a0002 | c0002 | t0001 | g0180 | AMR | PUR | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0240 | AMR | PUR | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG01070 | hp1 | a0002 | c0002 | t0001 | g0077 | AMR | PUR | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG01070 | hp2 | a0001 | c0001 | t0003 | g0135 | AMR | PUR | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG01074 | hp1 | a0001 | c0006 | t0001 | g0261 | AMR | PUR | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG01074 | hp2 | a0001 | c0001 | t0015 | g0158 | AMR | PUR | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG01099 | hp1 | a0007 | c0009 | t0001 | g0114 | AMR | PUR | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG01099 | hp2 | a0001 | c0001 | t0005 | g0147 | AMR | PUR | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG01106 | hp1 | a0002 | c0002 | t0001 | g0061 | AMR | PUR | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG01109 | hp2 | a0002 | c0002 | t0001 | g0119 | AMR | PUR | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG01175 | hp1 | a0001 | c0001 | t0003 | g0039 | AMR | PUR | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0290 | AMR | PUR | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG01243 | hp2 | a0001 | c0012 | t0001 | g0073 | AMR | PUR | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG01255 | hp1 | a0002 | c0002 | t0001 | g0009 | AMR | CLM | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | CLM | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG01256 | hp1 | a0001 | c0001 | t0009 | g0003 | AMR | CLM | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0213 | AMR | CLM | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG01257 | hp1 | a0001 | c0001 | t0003 | g0089 | AMR | CLM | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG01261 | hp1 | a0001 | c0001 | t0003 | g0172 | AMR | CLM | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG01261 | hp2 | a0001 | c0001 | t0005 | g0132 | AMR | CLM | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG01346 | hp1 | a0004 | c0007 | t0003 | g0145 | AMR | CLM | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG01346 | hp2 | a0002 | c0002 | t0001 | g0016 | AMR | CLM | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG01358 | hp1 | a0002 | c0002 | t0001 | g0182 | AMR | CLM | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG01358 | hp2 | a0001 | c0001 | t0003 | g0178 | AMR | CLM | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG01361 | hp1 | a0001 | c0001 | t0003 | g0107 | AMR | CLM | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG01361 | hp2 | a0001 | c0001 | t0003 | g0029 | AMR | CLM | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG01496 | hp1 | a0001 | c0003 | t0020 | g0198 | AMR | CLM | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG01496 | hp2 | a0001 | c0001 | t0007 | g0042 | AMR | CLM | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG01515 | hp1 | a0001 | c0001 | t0003 | g0003 | EUR | IBS | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG01515 | hp2 | a0002 | c0002 | t0001 | g0079 | EUR | IBS | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG01516 | hp1 | a0001 | c0001 | t0005 | g0282 | EUR | IBS | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG01516 | hp2 | a0001 | c0001 | t0003 | g0003 | EUR | IBS | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG01517 | hp1 | a0001 | c0001 | t0005 | g0283 | EUR | IBS | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG01517 | hp2 | a0001 | c0001 | t0003 | g0003 | EUR | IBS | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | ACB | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | ACB | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | ACB | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG01891 | hp2 | a0001 | c0001 | t0006 | g0189 | AFR | ACB | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG01928 | hp1 | a0002 | c0002 | t0001 | g0012 | AMR | PEL | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG01928 | hp2 | a0001 | c0006 | t0001 | g0251 | AMR | PEL | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG01934 | hp1 | a0001 | c0006 | t0001 | g0247 | AMR | PEL | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0248 | AMR | PEL | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG01978 | hp1 | a0001 | c0001 | t0003 | g0108 | AMR | PEL | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0214 | AMR | PEL | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG01981 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | PEL | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG01981 | hp2 | a0002 | c0002 | t0003 | g0097 | AMR | PEL | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG02015 | hp1 | a0001 | c0003 | t0004 | g0203 | EAS | KHV | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG02015 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | KHV | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG02055 | hp1 | a0003 | c0004 | t0001 | g0296 | AFR | ACB | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | ACB | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0222 | EAS | KHV | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG02074 | hp2 | a0002 | c0002 | t0001 | g0019 | EAS | KHV | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG02129 | hp2 | a0002 | c0002 | t0001 | g0139 | EAS | KHV | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG02132 | hp1 | a0002 | c0002 | t0001 | g0016 | EAS | KHV | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG02132 | hp2 | a0001 | c0003 | t0004 | g0202 | EAS | KHV | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG02135 | hp1 | a0002 | c0002 | t0001 | g0070 | EAS | KHV | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | KHV | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | ACB | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | ACB | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG02148 | hp1 | a0002 | c0002 | t0001 | g0181 | AMR | PEL | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG02148 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG02155 | hp1 | a0002 | c0002 | t0001 | g0187 | EAS | CDX | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG02155 | hp2 | a0001 | c0003 | t0004 | g0284 | EAS | CDX | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0236 | EAS | CDX | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG02165 | hp2 | a0002 | c0002 | t0001 | g0019 | EAS | CDX | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG02257 | hp1 | a0001 | c0005 | t0001 | g0023 | AFR | ACB | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG02257 | hp2 | a0001 | c0001 | t0003 | g0276 | AFR | ACB | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG02258 | hp1 | a0001 | c0001 | t0007 | g0104 | AFR | ACB | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG02258 | hp2 | a0001 | c0001 | t0010 | g0131 | AFR | ACB | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG02280 | hp1 | a0001 | c0005 | t0001 | g0074 | AFR | ACB | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | ACB | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG02293 | hp1 | a0001 | c0006 | t0001 | g0254 | AMR | PEL | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG02293 | hp2 | a0002 | c0002 | t0001 | g0193 | AMR | PEL | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG02451 | hp2 | a0005 | c0013 | t0010 | g0127 | AFR | ACB | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG02572 | hp1 | a0002 | c0002 | t0001 | g0051 | AFR | GWD | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG02615 | hp1 | a0003 | c0004 | t0001 | g0293 | AFR | GWD | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG02615 | hp2 | a0001 | c0001 | t0003 | g0176 | AFR | GWD | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG02622 | hp1 | a0003 | c0004 | t0001 | g0295 | AFR | GWD | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG02622 | hp2 | a0002 | c0002 | t0001 | g0043 | AFR | GWD | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG02630 | hp1 | a0001 | c0001 | t0003 | g0030 | AFR | GWD | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG02630 | hp2 | a0002 | c0002 | t0001 | g0137 | AFR | GWD | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG02683 | hp1 | a0001 | c0001 | t0003 | g0173 | SAS | PJL | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG02683 | hp2 | a0002 | c0002 | t0001 | g0046 | SAS | PJL | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG02698 | hp1 | a0002 | c0002 | t0001 | g0167 | SAS | PJL | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0231 | SAS | PJL | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG02717 | hp2 | a0003 | c0004 | t0001 | g0294 | AFR | GWD | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | GWD | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0286 | SAS | PJL | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG02738 | hp1 | a0002 | c0002 | t0001 | g0071 | SAS | PJL | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0032 | SAS | PJL | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | GWD | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG02809 | hp2 | a0002 | c0002 | t0001 | g0093 | AFR | GWD | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG02818 | hp1 | a0001 | c0001 | t0003 | g0109 | AFR | GWD | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | GWD | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG02886 | hp1 | a0001 | c0010 | t0001 | g0106 | AFR | GWD | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG02886 | hp2 | a0003 | c0004 | t0001 | g0291 | AFR | GWD | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | GWD | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG02922 | hp1 | a0001 | c0001 | t0014 | g0011 | AFR | ESN | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG02922 | hp2 | a0001 | c0001 | t0013 | g0209 | AFR | ESN | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG02965 | hp1 | a0001 | c0001 | t0012 | g0152 | AFR | ESN | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG02965 | hp2 | a0001 | c0001 | t0006 | g0190 | AFR | ESN | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG02970 | hp1 | a0001 | c0005 | t0001 | g0023 | AFR | ESN | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG02970 | hp2 | a0001 | c0001 | t0006 | g0020 | AFR | ESN | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG02976 | hp1 | a0002 | c0002 | t0001 | g0010 | AFR | ESN | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | ESN | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG03098 | hp1 | a0001 | c0001 | t0006 | g0192 | AFR | MSL | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG03098 | hp2 | a0002 | c0002 | t0001 | g0050 | AFR | MSL | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG03130 | hp1 | a0001 | c0001 | t0006 | g0020 | AFR | ESN | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | ESN | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | ESN | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | ESN | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG03209 | hp1 | a0001 | c0001 | t0007 | g0171 | AFR | MSL | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG03209 | hp2 | a0001 | c0001 | t0003 | g0279 | AFR | MSL | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | MSL | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG03453 | hp2 | a0001 | c0001 | t0007 | g0072 | AFR | MSL | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | MSL | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | MSL | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0258 | SAS | PJL | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG03490 | hp2 | a0002 | c0002 | t0001 | g0059 | SAS | PJL | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG03491 | hp1 | a0001 | c0001 | t0018 | g0288 | SAS | PJL | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG03491 | hp2 | a0002 | c0002 | t0001 | g0004 | SAS | PJL | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG03492 | hp2 | a0002 | c0002 | t0001 | g0004 | SAS | PJL | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | ESN | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG03516 | hp2 | a0001 | c0001 | t0006 | g0191 | AFR | ESN | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG03540 | hp1 | a0001 | c0001 | t0003 | g0031 | AFR | GWD | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | MSL | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG03654 | hp1 | a0001 | c0001 | t0003 | g0177 | SAS | PJL | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG03654 | hp2 | a0001 | c0001 | t0019 | g0205 | SAS | PJL | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0285 | SAS | STU | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0256 | SAS | STU | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG03704 | hp1 | a0002 | c0002 | t0001 | g0138 | SAS | PJL | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG03704 | hp2 | a0001 | c0001 | t0011 | g0267 | SAS | PJL | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG03710 | hp1 | a0002 | c0002 | t0016 | g0062 | SAS | PJL | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0218 | SAS | PJL | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG03831 | hp1 | a0002 | c0002 | t0001 | g0117 | SAS | BEB | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG03831 | hp2 | a0001 | c0001 | t0011 | g0270 | SAS | BEB | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0233 | SAS | BEB | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG03942 | hp2 | a0001 | c0001 | t0003 | g0133 | SAS | BEB | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0232 | SAS | STU | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG04115 | hp2 | a0002 | c0002 | t0001 | g0053 | SAS | STU | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG04184 | hp1 | a0002 | c0002 | t0001 | g0112 | SAS | BEB | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0217 | SAS | BEB | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0252 | SAS | STU | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0275 | SAS | STU | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG04228 | hp1 | a0002 | c0002 | t0001 | g0066 | SAS | STU | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG04228 | hp2 | a0001 | c0001 | t0005 | g0148 | SAS | STU | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA18522 | hp1 | a0001 | c0001 | t0003 | g0058 | AFR | YRI | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA18522 | hp2 | a0002 | c0002 | t0001 | g0010 | AFR | YRI | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHB | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA18612 | hp2 | a0002 | c0002 | t0001 | g0068 | EAS | CHB | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | YRI | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA18906 | hp2 | a0001 | c0001 | t0003 | g0090 | AFR | YRI | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA18939 | hp1 | a0001 | c0003 | t0004 | g0197 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA18939 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA18940 | hp1 | a0002 | c0002 | t0001 | g0047 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA18940 | hp2 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA18942 | hp2 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA18944 | hp2 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA18945 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA18946 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA18946 | hp2 | a0002 | c0002 | t0001 | g0179 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA18950 | hp2 | a0002 | c0002 | t0001 | g0055 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA18952 | hp1 | a0002 | c0002 | t0001 | g0044 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA18952 | hp2 | a0001 | c0003 | t0004 | g0207 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA18953 | hp2 | a0002 | c0002 | t0001 | g0212 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA18956 | hp1 | a0002 | c0002 | t0001 | g0057 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA18962 | hp1 | a0002 | c0002 | t0001 | g0098 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA18963 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA18963 | hp2 | a0001 | c0003 | t0004 | g0194 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA18964 | hp1 | a0002 | c0002 | t0001 | g0125 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA18965 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA18966 | hp2 | a0002 | c0002 | t0001 | g0122 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA18968 | hp2 | a0002 | c0002 | t0001 | g0056 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA18970 | hp1 | a0002 | c0002 | t0001 | g0052 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA18970 | hp2 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA18971 | hp2 | a0002 | c0002 | t0001 | g0065 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA18973 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA18975 | hp1 | a0002 | c0002 | t0001 | g0184 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA18975 | hp2 | a0001 | c0003 | t0004 | g0208 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA18977 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA18977 | hp2 | a0002 | c0002 | t0001 | g0099 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA18978 | hp1 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA18978 | hp2 | a0002 | c0002 | t0001 | g0281 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA18979 | hp2 | a0001 | c0003 | t0004 | g0204 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA18980 | hp1 | a0002 | c0002 | t0001 | g0186 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA18980 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA18981 | hp1 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA18981 | hp2 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA18982 | hp1 | a0002 | c0002 | t0001 | g0287 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA18984 | hp1 | a0002 | c0002 | t0001 | g0094 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA18986 | hp2 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA18987 | hp1 | a0001 | c0003 | t0004 | g0206 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA18987 | hp2 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA18990 | hp1 | a0002 | c0002 | t0008 | g0170 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA18990 | hp2 | a0002 | c0002 | t0001 | g0280 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA18992 | hp1 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA18992 | hp2 | a0002 | c0002 | t0001 | g0081 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA18993 | hp1 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA18993 | hp2 | a0002 | c0002 | t0001 | g0113 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA18994 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA19001 | hp1 | a0002 | c0002 | t0001 | g0069 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA19003 | hp1 | a0002 | c0002 | t0001 | g0054 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA19004 | hp2 | a0002 | c0002 | t0001 | g0083 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA19006 | hp1 | a0002 | c0002 | t0001 | g0124 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA19011 | hp2 | a0002 | c0002 | t0001 | g0040 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA19012 | hp1 | a0002 | c0002 | t0001 | g0123 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA19012 | hp2 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA19043 | hp1 | a0001 | c0001 | t0003 | g0033 | AFR | LWK | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA19043 | hp2 | a0001 | c0001 | t0003 | g0144 | AFR | LWK | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA19054 | hp2 | a0002 | c0002 | t0001 | g0045 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA19055 | hp1 | a0002 | c0002 | t0001 | g0063 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA19055 | hp2 | a0001 | c0003 | t0004 | g0201 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA19057 | hp2 | a0001 | c0003 | t0004 | g0200 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA19058 | hp1 | a0002 | c0002 | t0001 | g0188 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA19058 | hp2 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA19063 | hp1 | a0002 | c0002 | t0001 | g0116 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA19063 | hp2 | a0001 | c0003 | t0004 | g0195 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA19065 | hp1 | a0002 | c0002 | t0001 | g0185 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA19067 | hp1 | a0002 | c0002 | t0001 | g0120 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA19068 | hp2 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA19070 | hp2 | a0002 | c0002 | t0001 | g0086 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA19072 | hp1 | a0006 | c0011 | t0004 | g0199 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA19072 | hp2 | a0002 | c0002 | t0001 | g0096 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA19075 | hp1 | a0002 | c0002 | t0001 | g0121 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA19076 | hp1 | a0002 | c0002 | t0001 | g0049 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA19077 | hp2 | a0002 | c0002 | t0001 | g0067 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA19078 | hp1 | a0002 | c0002 | t0001 | g0076 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA19079 | hp1 | a0002 | c0002 | t0008 | g0169 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA19082 | hp1 | a0002 | c0002 | t0001 | g0165 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA19083 | hp1 | a0002 | c0002 | t0001 | g0183 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA19084 | hp1 | a0001 | c0003 | t0004 | g0196 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA19084 | hp2 | a0002 | c0002 | t0001 | g0085 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA19086 | hp1 | a0002 | c0002 | t0001 | g0080 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA19090 | hp1 | a0002 | c0002 | t0001 | g0095 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA19091 | hp2 | a0002 | c0002 | t0001 | g0048 | EAS | JPT | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA19240 | hp1 | a0001 | c0001 | t0014 | g0011 | AFR | YRI | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0289 | AFR | YRI | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA20129 | hp1 | a0002 | c0002 | t0001 | g0015 | AFR | ASW | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA20129 | hp2 | a0001 | c0001 | t0003 | g0277 | AFR | ASW | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA20805 | hp1 | a0001 | c0001 | t0003 | g0175 | EUR | TSI | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA20805 | hp2 | a0002 | c0002 | t0001 | g0118 | EUR | TSI | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG01123 | hp1 | a0001 | c0001 | t0005 | g0149 | AMR | CLM | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG01123 | hp2 | a0002 | c0002 | t0001 | g0140 | AMR | CLM | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG02109 | hp1 | a0001 | c0005 | t0001 | g0075 | AFR | ACB | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG02109 | hp2 | a0001 | c0001 | t0003 | g0278 | AFR | ACB | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG02486 | hp1 | a0003 | c0004 | t0001 | g0297 | AFR | ACB | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | ACB | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG02559 | hp1 | a0001 | c0001 | t0013 | g0210 | AFR | ACB | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG02559 | hp2 | a0002 | c0002 | t0001 | g0010 | AFR | ACB | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | MSL | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | MSL | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG06807 | hp1 | a0002 | c0002 | t0001 | g0009 | AFR | USA | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
HG06807 | hp2 | a0001 | c0001 | t0017 | g0155 | AFR | USA | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA20300 | hp1 | a0001 | c0001 | t0012 | g0151 | AFR | USA | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA20300 | hp2 | a0003 | c0004 | t0001 | g0292 | AFR | USA | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA21309 | hp1 | a0002 | c0002 | t0001 | g0136 | AFR | LWK | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | LWK | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
homoSapiens_chm13v2 | hp1 | a0004 | c0007 | t0003 | g0146 | REF | REF | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0025 | REF | REF | NUP58_chr13_25296625_25347421 | NUP58 | chr13 | 25296625 | 25347421 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:25301868
|
C | T | 1 | a0005 | 1 | HG02451.hp2 | missense_variant | MODERATE | c.95C>T | p.Thr32Met | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/16 | 244/4236 | 95/1800 | 32/599 | chr13 | 25301868 | ||
chr13:25301873
|
G | A | 2 | a0002a0007 | 116 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(113): Show |
missense_variant | MODERATE | c.100G>A | p.Ala34Thr | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/16 | 249/4236 | 100/1800 | 34/599 | chr13 | 25301873 | ||
chr13:25312934
|
A | G | 1 | a0003 | 7 | HG02055.hp1 HG02486.hp1 HG02615.hp1 others(4): Show |
missense_variant | MODERATE | c.338A>G | p.Asn113Ser | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 4/16 | 487/4236 | 338/1800 | 113/599 | chr13 | 25312934 | ||
chr13:25313673
|
T | C | 1 | a0007 | 1 | HG01099.hp1 | missense_variant | MODERATE | c.496T>C | p.Ser166Pro | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 5/16 | 645/4236 | 496/1800 | 166/599 | chr13 | 25313673 | ||
chr13:25315357
|
G | A | 1 | a0004 | 2 | HG01346.hp1 homoSapiens_chm13v2.hp1 |
missense_variant&splice_region_variant | MODERATE | c.575G>A | p.Gly192Glu | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/16 | 724/4236 | 575/1800 | 192/599 | chr13 | 25315357 | ||
chr13:25319334
|
ACGGGAAC others(5): Show |
A | 1 | a0006 | 1 | NA19072.hp1 | disruptive_inframe_deletion | MODERATE | c.696_707delGGGAACAA others(4): Show |
p.Gly233_Pro236del | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 7/16 | 845/4236 | 696/1800 | 232/599 | INFO_REALIGN_3_PRIME | chr13 | 25319334 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:25301869
|
G | C | 1 | a0001c0008 | 1 | HG00738.hp2 | synonymous_variant | LOW | c.96G>C | p.Thr32Thr | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/16 | 245/4236 | 96/1800 | 32/599 | chr13 | 25301869 | ||
chr13:25313640
|
T | C | 2 | a0001c0005a0001c0010 | 5 | HG02109.hp1 HG02257.hp1 HG02280.hp1 others(2): Show |
synonymous_variant | LOW | c.463T>C | p.Leu155Leu | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 5/16 | 612/4236 | 463/1800 | 155/599 | chr13 | 25313640 | ||
chr13:25313684
|
C | T | 1 | a0001c0010 | 1 | HG02886.hp1 | synonymous_variant | LOW | c.507C>T | p.Leu169Leu | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 5/16 | 656/4236 | 507/1800 | 169/599 | chr13 | 25313684 | ||
chr13:25326994
|
T | C | 1 | a0001c0012 | 1 | HG01243.hp2 | synonymous_variant | LOW | c.1110T>C | p.His370His | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 11/16 | 1259/4236 | 1110/1800 | 370/599 | chr13 | 25326994 | ||
chr13:25327027
|
C | G | 1 | a0001c0006 | 4 | HG01074.hp1 HG01928.hp2 HG01934.hp1 others(1): Show |
synonymous_variant | LOW | c.1143C>G | p.Thr381Thr | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 11/16 | 1292/4236 | 1143/1800 | 381/599 | chr13 | 25327027 | ||
chr13:25340083
|
A | G | 2 | a0001c0003a0006c0011 | 15 | HG01496.hp1 HG02015.hp1 HG02132.hp2 others(12): Show |
synonymous_variant | LOW | c.1749A>G | p.Gln583Gln | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 16/16 | 1898/4236 | 1749/1800 | 583/599 | chr13 | 25340083 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:25301639
|
C | G | 1 | a0001c0001t0014 | 2 | HG02922.hp1 NA19240.hp1 |
5_prime_UTR_variant | MODIFIER | c.-135C>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/16 | 135 | chr13 | 25301639 | |||||
chr13:25301706
|
G | T | 1 | a0002c0002t0021 | 1 | HG00438.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-68G>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/16 | chr13 | 25301706 | ||||||
chr13:25301741
|
C | T | 4 | a0001c0001t0019a0001c0003t0004a0001c0003t0020others(1): Show | 16 | HG01496.hp1 HG02015.hp1 HG02132.hp2 others(13): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-33C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/16 | chr13 | 25301741 | ||||||
chr13:25301772
|
A | C | 1 | a0001c0001t0007 | 4 | HG01496.hp2 HG02258.hp1 HG03209.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-2A>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/16 | 2 | chr13 | 25301772 | |||||
chr13:25340272
|
C | T | 1 | a0001c0001t0014 | 2 | HG02922.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*138C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 16/16 | 138 | chr13 | 25340272 | |||||
chr13:25340328
|
C | T | 6 | a0001c0001t0006a0001c0001t0014a0001c0001t0018others(3): Show | 24 | HG01496.hp1 HG01891.hp2 HG02015.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*194C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 16/16 | 194 | chr13 | 25340328 | |||||
chr13:25340687
|
C | T | 1 | a0001c0001t0017 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*553C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 16/16 | 553 | chr13 | 25340687 | |||||
chr13:25340713
|
G | A | 1 | a0001c0001t0002 | 46 | HG00438.hp2 HG00733.hp2 HG01069.hp2 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*579G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 16/16 | 579 | chr13 | 25340713 | |||||
chr13:25340767
|
A | G | 1 | a0001c0001t0013 | 2 | HG02559.hp1 HG02922.hp2 |
3_prime_UTR_variant | MODIFIER | c.*633A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 16/16 | 633 | chr13 | 25340767 | |||||
chr13:25340843
|
G | A | 1 | a0001c0003t0020 | 1 | HG01496.hp1 | 3_prime_UTR_variant | MODIFIER | c.*709G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 16/16 | 709 | chr13 | 25340843 | |||||
chr13:25340876
|
C | T | 3 | a0001c0003t0004a0001c0003t0020a0006c0011t0004 | 15 | HG01496.hp1 HG02015.hp1 HG02132.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*742C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 16/16 | 742 | chr13 | 25340876 | |||||
chr13:25341004
|
G | C | 1 | a0002c0002t0008 | 2 | NA18990.hp1 NA19079.hp1 |
3_prime_UTR_variant | MODIFIER | c.*870G>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 16/16 | 870 | chr13 | 25341004 | |||||
chr13:25341235
|
C | A | 1 | a0001c0001t0014 | 2 | HG02922.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1101C>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 16/16 | 1101 | chr13 | 25341235 | |||||
chr13:25341389
|
A | G | 1 | a0001c0001t0012 | 2 | HG02965.hp1 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1255A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 16/16 | 1255 | chr13 | 25341389 | |||||
chr13:25341654
|
A | C | 2 | a0001c0001t0006a0001c0001t0012 | 8 | HG01891.hp2 HG02965.hp1 HG02965.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1520A>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 16/16 | 1520 | chr13 | 25341654 | |||||
chr13:25341749
|
A | G | 1 | a0001c0001t0005 | 7 | HG00323.hp2 HG01099.hp2 HG01123.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1615A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 16/16 | 1615 | chr13 | 25341749 | |||||
chr13:25341810
|
A | G | 1 | a0002c0002t0016 | 1 | HG03710.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1676A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 16/16 | 1676 | chr13 | 25341810 | |||||
chr13:25341835
|
G | T | 2 | a0001c0001t0006a0001c0001t0012 | 8 | HG01891.hp2 HG02965.hp1 HG02965.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1701G>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 16/16 | 1701 | chr13 | 25341835 | |||||
chr13:25341885
|
A | G | 1 | a0001c0001t0011 | 2 | HG03704.hp2 HG03831.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1751A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 16/16 | 1751 | chr13 | 25341885 | |||||
chr13:25341921
|
T | C | 5 | a0001c0001t0003a0001c0001t0005a0001c0001t0009others(2): Show | 44 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*1787T>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 16/16 | 1787 | chr13 | 25341921 | |||||
chr13:25341985
|
A | G | 1 | a0001c0001t0009 | 2 | HG00140.hp2 HG01256.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1851A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 16/16 | 1851 | chr13 | 25341985 | |||||
chr13:25342055
|
ATTAT | A | 1 | a0001c0001t0007 | 4 | HG01496.hp2 HG02258.hp1 HG03209.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1926_*1929delTTAT | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 16/16 | 1926 | INFO_REALIGN_3_PRIME | chr13 | 25342055 | ||||
chr13:25342090
|
T | C | 2 | a0001c0001t0010a0005c0013t0010 | 2 | HG02258.hp2 HG02451.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1956T>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 16/16 | 1956 | chr13 | 25342090 | |||||
chr13:25342205
|
T | A | 1 | a0001c0001t0014 | 2 | HG02922.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2071T>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 16/16 | 2071 | chr13 | 25342205 | |||||
chr13:25342305
|
G | A | 1 | a0001c0001t0015 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2171G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 16/16 | 2171 | chr13 | 25342305 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:25301894
|
C | T | 7 | a0003c0004t0001g0291a0003c0004t0001g0292a0003c0004t0001g0293others(4): Show | 7 | HG02055.hp1 HG02486.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.107+14C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25301894 | ||||||
chr13:25301909
|
C | A | 1 | a0001c0001t0003g0024 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.107+29C>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25301909 | ||||||
chr13:25301983
|
C | T | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | HG01243.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.107+103C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25301983 | ||||||
chr13:25302135
|
A | G | 296 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0017others(293): Show | 347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.107+255A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25302135 | ||||||
chr13:25302232
|
A | G | 1 | a0001c0001t0018g0288 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.107+352A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25302232 | ||||||
chr13:25302317
|
C | T | 1 | a0002c0002t0001g0287 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.107+437C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25302317 | ||||||
chr13:25302537
|
T | G | 1 | a0001c0001t0001g0028 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.107+657T>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25302537 | ||||||
chr13:25302587
|
T | A | 3 | a0001c0001t0003g0029a0001c0001t0003g0030a0001c0001t0003g0031 | 3 | HG01361.hp2 HG02630.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.107+707T>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25302587 | ||||||
chr13:25302647
|
A | G | 2 | a0001c0001t0002g0285a0001c0001t0002g0286 | 2 | HG02735.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.107+767A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25302647 | ||||||
chr13:25302773
|
G | A | 1 | a0001c0001t0002g0032 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.107+893G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25302773 | ||||||
chr13:25302784
|
A | C | 1 | a0001c0001t0003g0031 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.107+904A>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25302784 | ||||||
chr13:25302942
|
T | C | 2 | a0001c0001t0014g0011a0001c0001t0018g0288 | 3 | HG02922.hp1 HG03491.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.107+1062T>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25302942 | ||||||
chr13:25303088
|
C | T | 1 | a0001c0003t0004g0284 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.107+1208C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25303088 | ||||||
chr13:25303117
|
A | G | 2 | a0001c0001t0005g0282a0001c0001t0005g0283 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.107+1237A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25303117 | ||||||
chr13:25303128
|
C | T | 1 | a0001c0001t0018g0288 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.107+1248C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25303128 | ||||||
chr13:25303202
|
C | T | 2 | a0002c0002t0001g0280a0002c0002t0001g0281 | 2 | NA18978.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.107+1322C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25303202 | ||||||
chr13:25303297
|
G | C | 1 | a0001c0001t0003g0033 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.107+1417G>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25303297 | ||||||
chr13:25303348
|
A | G | 6 | a0001c0001t0003g0033a0001c0001t0003g0276a0001c0001t0003g0277others(3): Show | 7 | HG02109.hp2 HG02257.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.107+1468A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25303348 | ||||||
chr13:25303377
|
TAACTG | T | 6 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0035others(3): Show | 8 | HG00738.hp1 HG01109.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.107+1500_107+1504d others(7): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25303377 | |||||
chr13:25303444
|
C | CT | 77 | a0001c0001t0001g0002a0001c0001t0001g0021a0001c0001t0001g0022others(74): Show | 103 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.107+1575dupT | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25303444 | |||||
chr13:25303502
|
G | T | 1 | a0001c0001t0014g0011 | 2 | HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.107+1622G>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25303502 | ||||||
chr13:25303755
|
T | C | 1 | a0001c0001t0001g0211 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.107+1875T>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25303755 | ||||||
chr13:25303911
|
C | T | 4 | a0003c0004t0001g0294a0003c0004t0001g0295a0003c0004t0001g0296others(1): Show | 4 | HG02055.hp1 HG02486.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.107+2031C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25303911 | ||||||
chr13:25303913
|
A | G | 1 | a0001c0001t0001g0275 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.107+2033A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25303913 | ||||||
chr13:25303957
|
C | T | 2 | a0001c0001t0013g0209a0001c0001t0013g0210 | 2 | HG02559.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.107+2077C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25303957 | ||||||
chr13:25303991
|
C | T | 1 | a0001c0001t0014g0011 | 2 | HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.107+2111C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25303991 | ||||||
chr13:25304282
|
A | G | 16 | a0001c0001t0019g0205a0001c0003t0004g0194a0001c0003t0004g0195others(13): Show | 16 | HG01496.hp1 HG02015.hp1 HG02132.hp2 others(13): Show |
intron_variant | MODIFIER | c.107+2402A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25304282 | ||||||
chr13:25304305
|
G | C | 2 | a0001c0001t0003g0029a0001c0001t0003g0039 | 2 | HG01175.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.107+2425G>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25304305 | ||||||
chr13:25304336
|
G | A | 1 | a0001c0001t0014g0011 | 2 | HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.107+2456G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25304336 | ||||||
chr13:25304463
|
G | T | 1 | a0002c0002t0001g0193 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.107+2583G>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25304463 | ||||||
chr13:25304473
|
C | G | 5 | a0001c0001t0006g0020a0001c0001t0006g0189a0001c0001t0006g0190others(2): Show | 6 | HG01891.hp2 HG02965.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.107+2593C>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25304473 | ||||||
chr13:25304478
|
T | TTA | 17 | a0001c0001t0001g0007a0001c0001t0001g0087a0001c0001t0001g0088others(14): Show | 22 | HG00438.hp1 HG00609.hp2 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.107+2636_107+2637d others(4): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25304478 | |||||
chr13:25304478
|
T | TTATA | 23 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(20): Show | 25 | HG00558.hp1 HG00738.hp1 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.107+2634_107+2637d others(6): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25304478 | |||||
chr13:25304478
|
T | TTATATA | 9 | a0001c0001t0001g0034a0002c0002t0001g0050a0002c0002t0001g0051others(6): Show | 9 | HG02572.hp1 HG03098.hp2 HG03579.hp1 others(6): Show |
intron_variant | MODIFIER | c.107+2632_107+2637d others(8): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25304478 | |||||
chr13:25304478
|
T | TTATATAT others(1): Show |
8 | a0002c0002t0001g0008a0002c0002t0001g0043a0002c0002t0001g0044others(5): Show | 10 | HG02015.hp2 HG02622.hp2 HG02683.hp2 others(7): Show |
intron_variant | MODIFIER | c.107+2630_107+2637d others(10): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25304478 | |||||
chr13:25304478
|
T | TTATATAT others(3): Show |
2 | a0001c0001t0007g0042a0002c0002t0001g0041 | 2 | HG00423.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.107+2628_107+2637d others(12): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25304478 | |||||
chr13:25304478
|
TTA | T | 34 | a0001c0001t0001g0027a0001c0001t0001g0110a0001c0001t0001g0111others(31): Show | 38 | HG00323.hp1 HG00735.hp1 HG01099.hp1 others(35): Show |
intron_variant | MODIFIER | c.107+2636_107+2637d others(4): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25304478 | |||||
chr13:25304478
|
TTATA | T | 14 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0002g0213others(11): Show | 16 | HG01123.hp2 HG01256.hp2 HG01346.hp2 others(13): Show |
intron_variant | MODIFIER | c.107+2634_107+2637d others(6): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25304478 | |||||
chr13:25304478
|
TTATATA | T | 16 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0156others(13): Show | 19 | HG00639.hp1 HG00642.hp2 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.107+2632_107+2637d others(8): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25304478 | |||||
chr13:25304478
|
TTATATAT others(1): Show |
T | 38 | a0001c0001t0001g0021a0001c0001t0001g0163a0001c0001t0001g0223others(35): Show | 52 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.107+2630_107+2637d others(10): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25304478 | |||||
chr13:25304478
|
TTATATAT others(3): Show |
T | 32 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0022others(29): Show | 42 | HG00558.hp2 HG00609.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.107+2628_107+2637d others(12): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25304478 | |||||
chr13:25304478
|
TTATATAT others(7): Show |
T | 1 | a0002c0002t0001g0167 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.107+2624_107+2637d others(16): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25304478 | |||||
chr13:25304478
|
TTATATAT others(9): Show |
T | 4 | a0001c0001t0001g0274a0001c0001t0007g0171a0002c0002t0008g0169others(1): Show | 4 | HG03209.hp1 NA18982.hp2 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.107+2622_107+2637d others(18): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25304478 | |||||
chr13:25304478
|
TTATATAT others(11): Show |
T | 1 | a0002c0002t0001g0018 | 2 | NA18942.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.107+2620_107+2637d others(20): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25304478 | |||||
chr13:25304478
|
TTATATAT others(15): Show |
T | 1 | a0001c0001t0018g0288 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.107+2616_107+2637d others(24): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25304478 | |||||
chr13:25304478
|
TTATATAT others(17): Show |
T | 11 | a0002c0002t0001g0019a0002c0002t0001g0180a0002c0002t0001g0181others(8): Show | 12 | HG01069.hp1 HG01358.hp1 HG02074.hp2 others(9): Show |
intron_variant | MODIFIER | c.107+2614_107+2637d others(26): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25304478 | |||||
chr13:25304494
|
A | G | 1 | a0002c0002t0001g0179 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.107+2614A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25304494 | ||||||
chr13:25304496
|
ATATATAT others(18): Show |
A | 1 | a0002c0002t0001g0179 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.107+2618_107+2642d others(27): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25304496 | |||||
chr13:25304500
|
A | G | 10 | a0001c0001t0003g0003a0001c0001t0003g0024a0001c0001t0003g0172others(7): Show | 15 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(12): Show |
intron_variant | MODIFIER | c.107+2620A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25304500 | ||||||
chr13:25304502
|
A | G | 1 | a0001c0001t0001g0168 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.107+2622A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25304502 | ||||||
chr13:25304502
|
ATATATAT others(12): Show |
A | 10 | a0001c0001t0003g0003a0001c0001t0003g0024a0001c0001t0003g0172others(7): Show | 15 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(12): Show |
intron_variant | MODIFIER | c.107+2624_107+2642d others(21): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25304502 | |||||
chr13:25304504
|
A | G | 1 | a0001c0003t0004g0208 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.107+2624A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25304504 | ||||||
chr13:25304504
|
ATATATAT others(10): Show |
A | 1 | a0001c0001t0001g0168 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.107+2626_107+2642d others(19): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25304504 | |||||
chr13:25304506
|
A | G | 1 | a0001c0001t0014g0011 | 2 | HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.107+2626A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25304506 | ||||||
chr13:25304506
|
ATATATAT others(8): Show |
A | 1 | a0001c0003t0004g0208 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.107+2628_107+2642d others(17): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25304506 | |||||
chr13:25304508
|
A | G | 2 | a0001c0003t0004g0207a0003c0004t0001g0293 | 2 | HG02615.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.107+2628A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25304508 | ||||||
chr13:25304508
|
ATATATAT others(7): Show |
A | 1 | a0001c0001t0014g0011 | 2 | HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.107+2630_107+2643d others(16): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25304508 | |||||
chr13:25304510
|
A | G | 5 | a0001c0001t0001g0164a0001c0001t0002g0248a0001c0001t0002g0249others(2): Show | 5 | HG00323.hp2 HG01934.hp1 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.107+2630A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25304510 | ||||||
chr13:25304510
|
ATATATAT others(4): Show |
A | 2 | a0001c0003t0004g0207a0003c0004t0001g0293 | 2 | HG02615.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.107+2632_107+2642d others(13): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25304510 | |||||
chr13:25304512
|
A | G | 12 | a0001c0001t0001g0150a0001c0001t0001g0164a0001c0001t0003g0144others(9): Show | 12 | HG01099.hp2 HG01123.hp1 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.107+2632A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25304512 | ||||||
chr13:25304513
|
TATATGTA | T | 3 | a0001c0001t0002g0248a0001c0001t0002g0249a0001c0006t0001g0247 | 3 | HG01934.hp1 HG01934.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.107+2634_107+2640d others(9): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25304513 | ||||||
chr13:25304514
|
A | G | 8 | a0001c0001t0001g0290a0001c0001t0003g0029a0001c0001t0003g0039others(5): Show | 8 | HG00639.hp2 HG01070.hp2 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.107+2634A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25304514 | ||||||
chr13:25304514
|
ATATGTAT | A | 12 | a0001c0001t0001g0150a0001c0001t0001g0164a0001c0001t0003g0144others(9): Show | 12 | HG01099.hp2 HG01123.hp1 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.107+2636_107+2642d others(9): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25304514 | |||||
chr13:25304516
|
A | G | 1 | a0001c0001t0001g0143 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.107+2636A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25304516 | ||||||
chr13:25304516
|
ATGTAT | A | 8 | a0001c0001t0001g0290a0001c0001t0003g0029a0001c0001t0003g0039others(5): Show | 8 | HG00639.hp2 HG01070.hp2 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.107+2638_107+2642d others(7): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25304516 | |||||
chr13:25304518
|
G | A | 25 | a0001c0001t0001g0078a0001c0001t0001g0289a0001c0001t0003g0058others(22): Show | 25 | HG01070.hp1 HG01496.hp1 HG02015.hp1 others(22): Show |
intron_variant | MODIFIER | c.107+2638G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25304518 | ||||||
chr13:25304520
|
A | ATATATAT others(6): Show |
1 | a0002c0002t0001g0040 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.107+2641_107+2642i others(15): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25304520 | |||||
chr13:25304520
|
A | G | 7 | a0001c0001t0001g0078a0001c0001t0001g0289a0001c0005t0001g0074others(4): Show | 7 | HG01070.hp1 HG02109.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.107+2640A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25304520 | ||||||
chr13:25304520
|
AT | A | 15 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0110others(12): Show | 15 | HG01257.hp1 HG01361.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.107+2655delT | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25304520 | |||||
chr13:25304521
|
T | TA | 4 | a0001c0001t0001g0078a0001c0001t0001g0289a0002c0002t0001g0076others(1): Show | 4 | HG01070.hp1 HG03139.hp1 NA19078.hp1 others(1): Show |
intron_variant | MODIFIER | c.107+2641_107+2642i others(3): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25304521 | ||||||
chr13:25304521
|
T | TATATGTA | 9 | a0001c0001t0013g0209a0001c0003t0004g0194a0001c0003t0004g0195others(6): Show | 9 | HG01496.hp1 HG02155.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.107+2641_107+2642i others(9): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25304521 | ||||||
chr13:25304521
|
T | TATGTA | 4 | a0001c0003t0004g0200a0001c0003t0004g0201a0001c0003t0004g0202others(1): Show | 4 | HG02132.hp2 HG02717.hp2 NA19055.hp2 others(1): Show |
intron_variant | MODIFIER | c.107+2641_107+2642i others(7): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25304521 | ||||||
chr13:25304521
|
T | TGTA | 6 | a0001c0001t0003g0058a0001c0001t0019g0205a0001c0003t0004g0203others(3): Show | 6 | HG02015.hp1 HG03490.hp2 HG03654.hp2 others(3): Show |
intron_variant | MODIFIER | c.107+2641_107+2642i others(5): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25304521 | ||||||
chr13:25304578
|
G | A | 1 | a0002c0002t0001g0060 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.107+2698G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25304578 | ||||||
chr13:25304790
|
A | C | 1 | a0002c0002t0001g0188 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.107+2910A>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25304790 | ||||||
chr13:25304871
|
A | G | 1 | a0001c0001t0015g0158 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.108-2935A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25304871 | ||||||
chr13:25305025
|
G | A | 1 | a0001c0001t0001g0153 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.108-2781G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25305025 | ||||||
chr13:25305047
|
G | A | 1 | a0001c0003t0004g0200 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.108-2759G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25305047 | ||||||
chr13:25305057
|
T | C | 1 | a0001c0008t0001g0215 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.108-2749T>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25305057 | ||||||
chr13:25305130
|
G | GT | 11 | a0001c0001t0001g0026a0001c0001t0001g0088a0001c0001t0001g0105others(8): Show | 11 | HG01175.hp2 HG01243.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.108-2645dupT | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25305130 | |||||
chr13:25305130
|
G | GTT | 9 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(6): Show | 9 | HG02055.hp2 HG02145.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.108-2646_108-2645d others(4): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25305130 | |||||
chr13:25305130
|
G | GTTT | 10 | a0001c0001t0006g0190a0001c0001t0006g0191a0001c0001t0019g0205others(7): Show | 10 | HG01496.hp1 HG02132.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.108-2647_108-2645d others(5): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25305130 | |||||
chr13:25305130
|
G | GTTTTTTT others(4): Show |
1 | a0001c0010t0001g0106 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.108-2655_108-2645d others(13): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25305130 | |||||
chr13:25305130
|
G | GTTTTTTT others(10): Show |
1 | a0001c0005t0001g0074 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.108-2661_108-2645d others(19): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25305130 | |||||
chr13:25305130
|
G | GTTTTTTT others(12): Show |
1 | a0001c0005t0001g0075 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.108-2663_108-2645d others(21): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25305130 | |||||
chr13:25305130
|
GTTTTTTT others(3): Show |
G | 1 | a0001c0001t0006g0192 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.108-2654_108-2645d others(12): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25305130 | |||||
chr13:25305130
|
GTTTTTTT others(4): Show |
G | 4 | a0003c0004t0001g0291a0003c0004t0001g0292a0003c0004t0001g0293others(1): Show | 4 | HG02055.hp1 HG02615.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.108-2655_108-2645d others(13): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25305130 | |||||
chr13:25305130
|
GTTTTTTT others(5): Show |
G | 4 | a0001c0003t0004g0194a0003c0004t0001g0294a0003c0004t0001g0295others(1): Show | 4 | HG02486.hp1 HG02622.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.108-2656_108-2645d others(14): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25305130 | |||||
chr13:25305130
|
GTTTTTTT others(6): Show |
G | 6 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0035others(3): Show | 8 | HG00738.hp1 HG01109.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.108-2657_108-2645d others(15): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25305130 | |||||
chr13:25305139
|
T | G | 1 | a0001c0001t0003g0144 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.108-2667T>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25305139 | ||||||
chr13:25305139
|
T | TTTGTTTG | 134 | a0001c0001t0001g0028a0001c0001t0001g0164a0001c0001t0003g0003others(131): Show | 155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.108-2665_108-2664i others(9): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25305139 | |||||
chr13:25305139
|
T | TTTTGTTT others(1): Show |
8 | a0001c0001t0001g0166a0001c0001t0001g0250a0001c0001t0001g0252others(5): Show | 8 | HG00735.hp2 HG01928.hp2 HG02074.hp1 others(5): Show |
intron_variant | MODIFIER | c.108-2664_108-2663i others(10): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25305139 | |||||
chr13:25305142
|
T | G | 5 | a0002c0002t0001g0049a0002c0002t0001g0057a0002c0002t0001g0125others(2): Show | 5 | HG01123.hp2 NA18956.hp1 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.108-2664T>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25305142 | ||||||
chr13:25305143
|
T | G | 143 | a0001c0001t0001g0028a0001c0001t0001g0164a0001c0001t0001g0166others(140): Show | 164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.108-2663T>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25305143 | ||||||
chr13:25305143
|
T | TTTTGTTT others(1): Show |
64 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0021others(61): Show | 90 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.108-2660_108-2659i others(10): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25305143 | |||||
chr13:25305144
|
T | G | 1 | a0001c0001t0014g0011 | 2 | HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.108-2662T>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25305144 | ||||||
chr13:25305146
|
T | G | 8 | a0001c0001t0001g0078a0001c0001t0001g0091a0001c0001t0001g0092others(5): Show | 8 | HG01123.hp2 HG01884.hp1 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.108-2660T>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25305146 | ||||||
chr13:25305146
|
T | TTGTTTGT others(3): Show |
1 | a0001c0001t0002g0214 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.108-2659_108-2658i others(12): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25305146 | |||||
chr13:25305147
|
T | G | 217 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0021others(214): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.108-2659T>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25305147 | ||||||
chr13:25305147
|
T | TGTTTGTT others(2): Show |
4 | a0001c0001t0001g0245a0001c0001t0001g0246a0001c0001t0001g0272others(1): Show | 4 | NA18979.hp1 NA18984.hp2 NA19001.hp2 others(1): Show |
intron_variant | MODIFIER | c.108-2659_108-2658i others(11): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25305147 | ||||||
chr13:25305148
|
T | G | 1 | a0001c0001t0014g0011 | 2 | HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.108-2658T>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25305148 | ||||||
chr13:25305151
|
T | G | 2 | a0002c0002t0001g0079a0002c0002t0001g0093 | 2 | HG01515.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.108-2655T>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25305151 | ||||||
chr13:25305152
|
T | G | 1 | a0001c0001t0014g0011 | 2 | HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.108-2654T>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25305152 | ||||||
chr13:25305253
|
T | A | 4 | a0002c0002t0001g0010a0002c0002t0001g0043a0002c0002t0001g0050others(1): Show | 6 | HG02559.hp2 HG02572.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.108-2553T>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25305253 | ||||||
chr13:25305279
|
G | C | 1 | a0001c0001t0002g0216 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.108-2527G>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25305279 | ||||||
chr13:25305352
|
G | A | 1 | a0001c0001t0018g0288 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.108-2454G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25305352 | ||||||
chr13:25305460
|
C | T | 1 | a0001c0001t0001g0252 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.108-2346C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25305460 | ||||||
chr13:25305504
|
C | T | 1 | a0001c0001t0014g0011 | 2 | HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.108-2302C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25305504 | ||||||
chr13:25305872
|
C | T | 1 | a0001c0001t0018g0288 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.108-1934C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25305872 | ||||||
chr13:25305918
|
T | C | 1 | a0001c0001t0001g0253 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.108-1888T>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25305918 | ||||||
chr13:25305995
|
C | A | 1 | a0001c0012t0001g0073 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.108-1811C>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25305995 | ||||||
chr13:25306133
|
C | T | 4 | a0001c0001t0007g0042a0001c0001t0007g0072a0001c0001t0007g0104others(1): Show | 4 | HG01496.hp2 HG02258.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.108-1673C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25306133 | ||||||
chr13:25306150
|
A | C | 3 | a0002c0002t0001g0185a0002c0002t0001g0186a0002c0002t0001g0187 | 3 | HG02155.hp1 NA18980.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.108-1656A>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25306150 | ||||||
chr13:25306154
|
C | T | 1 | a0001c0001t0001g0028 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.108-1652C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25306154 | ||||||
chr13:25306368
|
T | C | 1 | a0001c0001t0014g0011 | 2 | HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.108-1438T>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25306368 | ||||||
chr13:25306388
|
C | T | 1 | a0001c0001t0018g0288 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.108-1418C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25306388 | ||||||
chr13:25306393
|
C | CA | 63 | a0001c0001t0001g0028a0001c0001t0001g0078a0001c0001t0001g0091others(60): Show | 63 | HG00438.hp2 HG01106.hp1 HG01261.hp1 others(60): Show |
intron_variant | MODIFIER | c.108-1391dupA | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25306393 | |||||
chr13:25306393
|
C | CAA | 8 | a0001c0001t0001g0153a0001c0001t0007g0042a0001c0001t0007g0072others(5): Show | 8 | HG01496.hp2 HG02145.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.108-1392_108-1391d others(4): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25306393 | |||||
chr13:25306486
|
G | A | 2 | a0001c0001t0012g0151a0001c0001t0012g0152 | 2 | HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.108-1320G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25306486 | ||||||
chr13:25306544
|
G | A | 1 | a0002c0002t0001g0082 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.108-1262G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25306544 | ||||||
chr13:25306595
|
A | T | 1 | a0001c0001t0001g0275 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.108-1211A>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25306595 | ||||||
chr13:25306601
|
T | C | 1 | a0001c0001t0018g0288 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.108-1205T>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25306601 | ||||||
chr13:25306695
|
A | G | 1 | a0001c0001t0006g0191 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.108-1111A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25306695 | ||||||
chr13:25306749
|
C | A | 1 | a0001c0001t0002g0218 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.108-1057C>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25306749 | ||||||
chr13:25306807
|
G | A | 1 | a0001c0001t0001g0141 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.108-999G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25306807 | ||||||
chr13:25306939
|
A | G | 79 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0021others(76): Show | 105 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.108-867A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25306939 | ||||||
chr13:25306968
|
T | A | 2 | a0001c0001t0005g0282a0001c0001t0005g0283 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.108-838T>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25306968 | ||||||
chr13:25307050
|
G | C | 1 | a0007c0009t0001g0114 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.108-756G>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25307050 | ||||||
chr13:25307196
|
G | A | 6 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0035others(3): Show | 8 | HG00738.hp1 HG01109.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.108-610G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25307196 | ||||||
chr13:25307211
|
A | AT | 24 | a0001c0001t0001g0028a0001c0001t0001g0105a0001c0001t0001g0111others(21): Show | 26 | HG01243.hp2 HG01496.hp2 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.108-574dupT | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25307211 | |||||
chr13:25307211
|
A | ATT | 26 | a0001c0001t0001g0078a0001c0001t0001g0091a0001c0001t0001g0110others(23): Show | 26 | HG00735.hp1 HG01243.hp1 HG01257.hp1 others(23): Show |
intron_variant | MODIFIER | c.108-575_108-574dup others(2): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25307211 | |||||
chr13:25307211
|
A | ATTT | 158 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0021others(155): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.108-576_108-574dup others(3): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25307211 | |||||
chr13:25307211
|
A | ATTTT | 39 | a0001c0001t0001g0143a0001c0001t0001g0164a0001c0001t0001g0245others(36): Show | 51 | HG00733.hp2 HG01069.hp2 HG01123.hp1 others(48): Show |
intron_variant | MODIFIER | c.108-577_108-574dup others(4): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25307211 | |||||
chr13:25307211
|
A | ATTTTT | 8 | a0001c0001t0001g0227a0001c0001t0002g0006a0001c0001t0002g0032others(5): Show | 11 | HG00438.hp2 HG02738.hp2 NA18940.hp2 others(8): Show |
intron_variant | MODIFIER | c.108-578_108-574dup others(5): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25307211 | |||||
chr13:25307211
|
AT | A | 15 | a0001c0001t0019g0205a0001c0003t0004g0194a0001c0003t0004g0195others(12): Show | 15 | HG01496.hp1 HG02015.hp1 HG02132.hp2 others(12): Show |
intron_variant | MODIFIER | c.108-574delT | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr13 | 25307211 | |||||
chr13:25307348
|
A | G | 5 | a0001c0003t0004g0200a0001c0003t0004g0201a0001c0003t0004g0203others(2): Show | 5 | HG02015.hp1 NA18979.hp2 NA18987.hp1 others(2): Show |
intron_variant | MODIFIER | c.108-458A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25307348 | ||||||
chr13:25307465
|
C | T | 1 | a0001c0006t0001g0251 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.108-341C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25307465 | ||||||
chr13:25307555
|
G | A | 4 | a0001c0001t0001g0087a0001c0001t0001g0102a0001c0001t0001g0103others(1): Show | 4 | HG02280.hp2 HG02818.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.108-251G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 1/15 | chr13 | 25307555 | ||||||
chr13:25308151
|
C | T | 80 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0021others(77): Show | 106 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.250+203C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 2/15 | chr13 | 25308151 | ||||||
chr13:25308241
|
A | G | 1 | a0001c0001t0018g0288 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.250+293A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 2/15 | chr13 | 25308241 | ||||||
chr13:25308355
|
C | T | 2 | a0001c0005t0001g0074a0001c0005t0001g0075 | 2 | HG02109.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.250+407C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 2/15 | chr13 | 25308355 | ||||||
chr13:25308465
|
G | A | 1 | a0001c0008t0001g0215 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.250+517G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 2/15 | chr13 | 25308465 | ||||||
chr13:25308469
|
A | AT | 8 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0256others(5): Show | 8 | HG02486.hp2 HG02723.hp2 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.250+540dupT | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr13 | 25308469 | |||||
chr13:25308469
|
AT | A | 165 | a0001c0001t0001g0017a0001c0001t0001g0028a0001c0001t0001g0143others(162): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.250+540delT | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr13 | 25308469 | |||||
chr13:25308492
|
T | G | 24 | a0002c0002t0001g0008a0002c0002t0001g0018a0002c0002t0001g0040others(21): Show | 27 | HG00423.hp2 HG00558.hp1 HG00609.hp2 others(24): Show |
intron_variant | MODIFIER | c.250+544T>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 2/15 | chr13 | 25308492 | ||||||
chr13:25308586
|
T | C | 1 | a0001c0001t0014g0011 | 2 | HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.250+638T>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 2/15 | chr13 | 25308586 | ||||||
chr13:25308653
|
T | C | 4 | a0002c0002t0001g0010a0002c0002t0001g0043a0002c0002t0001g0050others(1): Show | 6 | HG02559.hp2 HG02572.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.251-594T>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 2/15 | chr13 | 25308653 | ||||||
chr13:25308864
|
A | G | 3 | a0001c0001t0007g0042a0001c0001t0007g0072a0001c0001t0007g0104 | 3 | HG01496.hp2 HG02258.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.251-383A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 2/15 | chr13 | 25308864 | ||||||
chr13:25309082
|
A | G | 2 | a0001c0001t0013g0209a0001c0001t0013g0210 | 2 | HG02559.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.251-165A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 2/15 | chr13 | 25309082 | ||||||
chr13:25309174
|
C | T | 4 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0134others(1): Show | 4 | HG00639.hp2 HG01070.hp2 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.251-73C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 2/15 | chr13 | 25309174 | ||||||
chr13:25309425
|
C | T | 2 | a0001c0001t0001g0143a0001c0001t0001g0164 | 2 | HG02145.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.286+143C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | chr13 | 25309425 | ||||||
chr13:25309583
|
C | A | 1 | a0001c0001t0014g0011 | 2 | HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.286+301C>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | chr13 | 25309583 | ||||||
chr13:25309619
|
T | A | 1 | a0001c0001t0002g0236 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.286+337T>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | chr13 | 25309619 | ||||||
chr13:25309666
|
T | C | 3 | a0002c0002t0001g0012a0002c0002t0001g0048a0002c0002t0001g0081 | 4 | HG01928.hp1 NA18992.hp2 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.286+384T>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | chr13 | 25309666 | ||||||
chr13:25309726
|
C | T | 4 | a0001c0001t0007g0042a0001c0001t0007g0072a0001c0001t0007g0104others(1): Show | 4 | HG01496.hp2 HG02258.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.286+444C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | chr13 | 25309726 | ||||||
chr13:25309792
|
GAAAGGAA others(52): Show |
G | 1 | a0001c0001t0015g0158 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.286+560_286+618del others(59): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr13 | 25309792 | |||||
chr13:25309842
|
A | G | 4 | a0001c0001t0007g0042a0001c0001t0007g0072a0001c0001t0007g0104others(1): Show | 4 | HG01496.hp2 HG02258.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.286+560A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | chr13 | 25309842 | ||||||
chr13:25309860
|
GGAAAA | G | 31 | a0001c0001t0001g0227a0001c0001t0002g0001a0001c0001t0002g0005others(28): Show | 46 | HG00438.hp2 HG00733.hp2 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.286+580_286+584del others(5): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr13 | 25309860 | |||||
chr13:25309963
|
A | G | 20 | a0001c0001t0001g0078a0001c0001t0001g0091a0001c0001t0001g0092others(17): Show | 21 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.286+681A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | chr13 | 25309963 | ||||||
chr13:25310009
|
A | G | 4 | a0001c0001t0007g0042a0001c0001t0007g0072a0001c0001t0007g0104others(1): Show | 4 | HG01496.hp2 HG02258.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.286+727A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | chr13 | 25310009 | ||||||
chr13:25310029
|
C | A | 1 | a0001c0001t0018g0288 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.286+747C>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | chr13 | 25310029 | ||||||
chr13:25310102
|
G | A | 2 | a0002c0002t0001g0112a0002c0002t0001g0117 | 2 | HG03831.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.286+820G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | chr13 | 25310102 | ||||||
chr13:25310142
|
A | G | 4 | a0002c0002t0001g0116a0002c0002t0001g0122a0002c0002t0001g0123others(1): Show | 4 | NA18966.hp2 NA19006.hp1 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.286+860A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | chr13 | 25310142 | ||||||
chr13:25310206
|
A | AT | 24 | a0001c0001t0001g0026a0001c0001t0001g0088a0001c0001t0001g0126others(21): Show | 24 | HG01175.hp2 HG01496.hp1 HG02015.hp1 others(21): Show |
intron_variant | MODIFIER | c.286+954dupT | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr13 | 25310206 | |||||
chr13:25310206
|
AT | A | 66 | a0001c0001t0001g0143a0001c0001t0001g0166a0001c0001t0001g0229others(63): Show | 81 | HG00558.hp1 HG00609.hp2 HG00642.hp1 others(78): Show |
intron_variant | MODIFIER | c.286+954delT | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr13 | 25310206 | |||||
chr13:25310206
|
ATT | A | 100 | a0001c0001t0001g0017a0001c0001t0001g0028a0001c0001t0001g0154others(97): Show | 119 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(116): Show |
intron_variant | MODIFIER | c.286+953_286+954del others(2): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr13 | 25310206 | |||||
chr13:25310206
|
ATTTT | A | 6 | a0001c0001t0006g0020a0001c0001t0006g0190a0001c0001t0006g0191others(3): Show | 8 | HG02486.hp1 HG02922.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.286+951_286+954del others(4): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr13 | 25310206 | |||||
chr13:25310206
|
ATTTTT | A | 13 | a0001c0001t0001g0078a0001c0001t0001g0091a0001c0001t0001g0092others(10): Show | 13 | HG01884.hp1 HG02055.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.286+950_286+954del others(5): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr13 | 25310206 | |||||
chr13:25310206
|
ATTTTTTT others(3): Show |
A | 3 | a0001c0001t0007g0042a0001c0001t0007g0072a0001c0001t0007g0104 | 3 | HG01496.hp2 HG02258.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.286+945_286+954del others(10): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr13 | 25310206 | |||||
chr13:25310206
|
ATTTTTTT others(5): Show |
A | 1 | a0001c0001t0001g0259 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.286+943_286+954del others(12): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr13 | 25310206 | |||||
chr13:25310206
|
ATTTTTTT others(6): Show |
A | 1 | a0001c0012t0001g0073 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.286+942_286+954del others(13): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr13 | 25310206 | |||||
chr13:25310206
|
ATTTTTTT others(7): Show |
A | 2 | a0001c0001t0002g0224a0001c0001t0002g0237 | 2 | NA18978.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.286+941_286+954del others(14): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr13 | 25310206 | |||||
chr13:25310236
|
T | A | 2 | a0001c0001t0014g0011a0001c0001t0018g0288 | 3 | HG02922.hp1 HG03491.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.286+954T>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | chr13 | 25310236 | ||||||
chr13:25310278
|
T | C | 1 | a0001c0001t0001g0262 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.286+996T>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | chr13 | 25310278 | ||||||
chr13:25310283
|
C | T | 20 | a0001c0001t0001g0078a0001c0001t0001g0091a0001c0001t0001g0092others(17): Show | 21 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.286+1001C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | chr13 | 25310283 | ||||||
chr13:25310307
|
G | A | 2 | a0001c0001t0001g0154a0001c0001t0001g0163 | 2 | HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.286+1025G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | chr13 | 25310307 | ||||||
chr13:25310374
|
C | T | 2 | a0001c0001t0005g0147a0001c0001t0005g0148 | 2 | HG01099.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.286+1092C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | chr13 | 25310374 | ||||||
chr13:25310440
|
G | A | 7 | a0003c0004t0001g0291a0003c0004t0001g0292a0003c0004t0001g0293others(4): Show | 7 | HG02055.hp1 HG02486.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.286+1158G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | chr13 | 25310440 | ||||||
chr13:25310479
|
C | T | 1 | a0001c0005t0001g0074 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.286+1197C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | chr13 | 25310479 | ||||||
chr13:25310480
|
G | A | 1 | a0002c0002t0001g0061 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.286+1198G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | chr13 | 25310480 | ||||||
chr13:25310519
|
C | CT | 179 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0022others(176): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.286+1260dupT | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr13 | 25310519 | |||||
chr13:25310519
|
C | CTT | 58 | a0001c0001t0001g0021a0001c0001t0001g0211a0001c0001t0001g0220others(55): Show | 74 | HG00423.hp1 HG00438.hp2 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.286+1259_286+1260d others(4): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr13 | 25310519 | |||||
chr13:25310519
|
C | CTTT | 11 | a0001c0001t0001g0255a0001c0001t0002g0032a0001c0001t0002g0221others(8): Show | 11 | HG01069.hp2 HG01361.hp1 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.286+1258_286+1260d others(5): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr13 | 25310519 | |||||
chr13:25310519
|
CT | C | 20 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0102others(17): Show | 21 | HG01891.hp1 HG01891.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.286+1260delT | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr13 | 25310519 | |||||
chr13:25310712
|
C | T | 2 | a0001c0001t0003g0030a0001c0001t0003g0031 | 2 | HG02630.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.286+1430C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | chr13 | 25310712 | ||||||
chr13:25310801
|
C | T | 1 | a0001c0001t0002g0240 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.286+1519C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | chr13 | 25310801 | ||||||
chr13:25310955
|
T | A | 1 | a0002c0002t0001g0167 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.286+1673T>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | chr13 | 25310955 | ||||||
chr13:25311028
|
G | C | 1 | a0001c0012t0001g0073 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.286+1746G>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | chr13 | 25311028 | ||||||
chr13:25311109
|
C | T | 2 | a0001c0001t0014g0011a0001c0001t0018g0288 | 3 | HG02922.hp1 HG03491.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.287-1774C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | chr13 | 25311109 | ||||||
chr13:25311138
|
G | A | 1 | a0001c0001t0001g0027 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.287-1745G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | chr13 | 25311138 | ||||||
chr13:25311174
|
T | C | 1 | a0001c0001t0001g0263 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.287-1709T>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | chr13 | 25311174 | ||||||
chr13:25311191
|
A | G | 3 | a0003c0004t0001g0291a0003c0004t0001g0292a0003c0004t0001g0293 | 3 | HG02615.hp1 HG02886.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.287-1692A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | chr13 | 25311191 | ||||||
chr13:25311454
|
C | T | 1 | a0001c0001t0001g0150 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.287-1429C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | chr13 | 25311454 | ||||||
chr13:25311501
|
G | A | 1 | a0002c0002t0001g0187 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.287-1382G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | chr13 | 25311501 | ||||||
chr13:25311664
|
G | T | 1 | a0001c0001t0018g0288 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.287-1219G>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | chr13 | 25311664 | ||||||
chr13:25311673
|
CT | C | 123 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0028others(120): Show | 156 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.287-1189delT | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr13 | 25311673 | |||||
chr13:25311673
|
CTT | C | 21 | a0001c0001t0001g0078a0001c0001t0001g0091a0001c0001t0001g0092others(18): Show | 21 | HG00099.hp1 HG01884.hp1 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.287-1190_287-1189d others(4): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr13 | 25311673 | |||||
chr13:25311673
|
CTTT | C | 14 | a0001c0001t0012g0152a0001c0001t0019g0205a0001c0003t0004g0194others(11): Show | 14 | HG01496.hp1 HG02015.hp1 HG02132.hp2 others(11): Show |
intron_variant | MODIFIER | c.287-1191_287-1189d others(5): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr13 | 25311673 | |||||
chr13:25311693
|
T | G | 1 | a0002c0002t0001g0093 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.287-1190T>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | chr13 | 25311693 | ||||||
chr13:25311812
|
G | A | 1 | a0001c0001t0014g0011 | 2 | HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.287-1071G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | chr13 | 25311812 | ||||||
chr13:25312046
|
C | A | 1 | a0001c0001t0014g0011 | 2 | HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.287-837C>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | chr13 | 25312046 | ||||||
chr13:25312224
|
A | G | 1 | a0001c0001t0014g0011 | 2 | HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.287-659A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | chr13 | 25312224 | ||||||
chr13:25312524
|
C | T | 1 | a0001c0012t0001g0073 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.287-359C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | chr13 | 25312524 | ||||||
chr13:25312568
|
G | A | 2 | a0001c0001t0014g0011a0001c0001t0018g0288 | 3 | HG02922.hp1 HG03491.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.287-315G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | chr13 | 25312568 | ||||||
chr13:25312607
|
A | G | 1 | a0001c0001t0014g0011 | 2 | HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.287-276A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | chr13 | 25312607 | ||||||
chr13:25312648
|
G | T | 1 | a0001c0001t0001g0250 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.287-235G>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | chr13 | 25312648 | ||||||
chr13:25312723
|
C | T | 5 | a0001c0001t0001g0150a0001c0001t0001g0154a0001c0001t0001g0163others(2): Show | 5 | HG01243.hp1 HG01884.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.287-160C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | chr13 | 25312723 | ||||||
chr13:25312769
|
C | T | 1 | a0003c0004t0001g0296 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.287-114C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | chr13 | 25312769 | ||||||
chr13:25312794
|
A | G | 277 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0017others(274): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.287-89A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 3/15 | chr13 | 25312794 | ||||||
chr13:25313087
|
G | A | 1 | a0001c0001t0018g0288 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.436+55G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 4/15 | chr13 | 25313087 | ||||||
chr13:25313451
|
T | C | 1 | a0001c0001t0002g0237 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.437-163T>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 4/15 | chr13 | 25313451 | ||||||
chr13:25313544
|
G | A | 1 | a0002c0002t0001g0118 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.437-70G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 4/15 | chr13 | 25313544 | ||||||
chr13:25313600
|
C | T | 1 | a0007c0009t0001g0114 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.437-14C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 4/15 | chr13 | 25313600 | ||||||
chr13:25313890
|
G | C | 1 | a0002c0002t0001g0064 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.574+139G>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 5/15 | chr13 | 25313890 | ||||||
chr13:25313956
|
T | C | 4 | a0001c0001t0001g0088a0001c0001t0001g0129a0001c0001t0001g0130others(1): Show | 4 | HG02055.hp2 HG02897.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.574+205T>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 5/15 | chr13 | 25313956 | ||||||
chr13:25314099
|
T | A | 139 | a0001c0001t0003g0003a0001c0001t0003g0024a0001c0001t0003g0029others(136): Show | 159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): Show |
intron_variant | MODIFIER | c.574+348T>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 5/15 | chr13 | 25314099 | ||||||
chr13:25314170
|
T | A | 1 | a0002c0002t0001g0113 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.574+419T>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 5/15 | chr13 | 25314170 | ||||||
chr13:25314176
|
G | A | 4 | a0001c0001t0007g0042a0001c0001t0007g0072a0001c0001t0007g0104others(1): Show | 4 | HG01496.hp2 HG02258.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.574+425G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 5/15 | chr13 | 25314176 | ||||||
chr13:25314296
|
C | G | 240 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0021others(237): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.574+545C>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 5/15 | chr13 | 25314296 | ||||||
chr13:25314310
|
T | TTTAAGGA others(10): Show |
2 | a0001c0001t0012g0151a0001c0001t0012g0152 | 2 | HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.574+561_574+577dup others(17): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr13 | 25314310 | |||||
chr13:25314314
|
A | C | 1 | a0001c0001t0018g0288 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.574+563A>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 5/15 | chr13 | 25314314 | ||||||
chr13:25314380
|
T | G | 2 | a0001c0001t0014g0011a0001c0001t0018g0288 | 3 | HG02922.hp1 HG03491.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.574+629T>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 5/15 | chr13 | 25314380 | ||||||
chr13:25314417
|
T | C | 1 | a0001c0001t0018g0288 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.574+666T>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 5/15 | chr13 | 25314417 | ||||||
chr13:25314423
|
C | T | 101 | a0002c0002t0001g0004a0002c0002t0001g0008a0002c0002t0001g0009others(98): Show | 116 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.574+672C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 5/15 | chr13 | 25314423 | ||||||
chr13:25314607
|
A | G | 1 | a0001c0001t0001g0111 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.575-750A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 5/15 | chr13 | 25314607 | ||||||
chr13:25314610
|
A | G | 1 | a0001c0001t0001g0036 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.575-747A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 5/15 | chr13 | 25314610 | ||||||
chr13:25314665
|
A | C | 2 | a0001c0001t0001g0266a0001c0001t0001g0273 | 2 | NA19004.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.575-692A>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 5/15 | chr13 | 25314665 | ||||||
chr13:25314682
|
C | T | 5 | a0001c0001t0003g0033a0001c0001t0003g0276a0001c0001t0003g0277others(2): Show | 5 | HG02109.hp2 HG02257.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.575-675C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 5/15 | chr13 | 25314682 | ||||||
chr13:25314746
|
G | T | 1 | a0001c0001t0014g0011 | 2 | HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.575-611G>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 5/15 | chr13 | 25314746 | ||||||
chr13:25314850
|
G | A | 270 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0021others(267): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.575-507G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 5/15 | chr13 | 25314850 | ||||||
chr13:25315062
|
G | C | 101 | a0002c0002t0001g0004a0002c0002t0001g0008a0002c0002t0001g0009others(98): Show | 116 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.575-295G>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 5/15 | chr13 | 25315062 | ||||||
chr13:25315141
|
GA | G | 4 | a0001c0005t0001g0023a0001c0005t0001g0074a0001c0005t0001g0075others(1): Show | 5 | HG02109.hp1 HG02257.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.575-211delA | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr13 | 25315141 | |||||
chr13:25315232
|
G | A | 2 | a0001c0001t0014g0011a0001c0001t0018g0288 | 3 | HG02922.hp1 HG03491.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.575-125G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 5/15 | chr13 | 25315232 | ||||||
chr13:25315531
|
A | G | 2 | a0001c0001t0014g0011a0001c0001t0018g0288 | 3 | HG02922.hp1 HG03491.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.685+64A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | chr13 | 25315531 | ||||||
chr13:25315567
|
TTAG | T | 5 | a0001c0001t0003g0033a0001c0001t0003g0276a0001c0001t0003g0277others(2): Show | 5 | HG02109.hp2 HG02257.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.685+106_685+108del others(3): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr13 | 25315567 | |||||
chr13:25315682
|
TTGTC | T | 221 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0021others(218): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.685+220_685+223del others(4): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr13 | 25315682 | |||||
chr13:25315699
|
T | C | 3 | a0003c0004t0001g0291a0003c0004t0001g0292a0003c0004t0001g0293 | 3 | HG02615.hp1 HG02886.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.685+232T>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | chr13 | 25315699 | ||||||
chr13:25315794
|
T | A | 1 | a0001c0001t0001g0252 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.685+327T>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | chr13 | 25315794 | ||||||
chr13:25315948
|
G | A | 1 | a0001c0001t0003g0175 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.685+481G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | chr13 | 25315948 | ||||||
chr13:25315952
|
T | C | 1 | a0001c0001t0001g0028 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.685+485T>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | chr13 | 25315952 | ||||||
chr13:25316125
|
A | C | 16 | a0001c0001t0019g0205a0001c0003t0004g0194a0001c0003t0004g0195others(13): Show | 16 | HG01496.hp1 HG02015.hp1 HG02132.hp2 others(13): Show |
intron_variant | MODIFIER | c.685+658A>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | chr13 | 25316125 | ||||||
chr13:25316413
|
G | A | 1 | a0001c0001t0003g0089 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.685+946G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | chr13 | 25316413 | ||||||
chr13:25316447
|
CT | C | 253 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0021others(250): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.685+989delT | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr13 | 25316447 | |||||
chr13:25316457
|
A | T | 2 | a0001c0001t0013g0209a0001c0001t0013g0210 | 2 | HG02559.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.685+990A>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | chr13 | 25316457 | ||||||
chr13:25316560
|
C | G | 3 | a0003c0004t0001g0291a0003c0004t0001g0292a0003c0004t0001g0293 | 3 | HG02615.hp1 HG02886.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.685+1093C>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | chr13 | 25316560 | ||||||
chr13:25316568
|
G | A | 270 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0021others(267): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.685+1101G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | chr13 | 25316568 | ||||||
chr13:25316580
|
A | T | 7 | a0003c0004t0001g0291a0003c0004t0001g0292a0003c0004t0001g0293others(4): Show | 7 | HG02055.hp1 HG02486.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.685+1113A>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | chr13 | 25316580 | ||||||
chr13:25316690
|
A | G | 1 | a0002c0002t0001g0060 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.685+1223A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | chr13 | 25316690 | ||||||
chr13:25316694
|
C | T | 279 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0017others(276): Show | 330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.685+1227C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | chr13 | 25316694 | ||||||
chr13:25317032
|
C | CT | 7 | a0001c0001t0002g0285a0001c0001t0003g0033a0001c0001t0003g0276others(4): Show | 8 | HG02109.hp2 HG02257.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.685+1574dupT | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr13 | 25317032 | |||||
chr13:25317066
|
A | G | 4 | a0003c0004t0001g0294a0003c0004t0001g0295a0003c0004t0001g0296others(1): Show | 4 | HG02055.hp1 HG02486.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.685+1599A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | chr13 | 25317066 | ||||||
chr13:25317073
|
G | A | 4 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0245others(1): Show | 6 | HG00423.hp1 HG00558.hp2 HG00609.hp1 others(3): Show |
intron_variant | MODIFIER | c.685+1606G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | chr13 | 25317073 | ||||||
chr13:25317125
|
G | A | 31 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0006others(28): Show | 46 | HG00438.hp2 HG00733.hp2 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.685+1658G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | chr13 | 25317125 | ||||||
chr13:25317137
|
A | G | 89 | a0002c0002t0001g0004a0002c0002t0001g0008a0002c0002t0001g0009others(86): Show | 102 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.685+1670A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | chr13 | 25317137 | ||||||
chr13:25317267
|
TCCTTATT others(2): Show |
T | 7 | a0001c0001t0006g0020a0001c0001t0006g0189a0001c0001t0006g0190others(4): Show | 8 | HG01891.hp2 HG02965.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.685+1803_685+1811d others(11): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr13 | 25317267 | |||||
chr13:25317401
|
A | G | 1 | a0001c0001t0003g0135 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.686-1925A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | chr13 | 25317401 | ||||||
chr13:25317557
|
TGTAA | T | 4 | a0003c0004t0001g0294a0003c0004t0001g0295a0003c0004t0001g0296others(1): Show | 4 | HG02055.hp1 HG02486.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.686-1765_686-1762d others(6): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr13 | 25317557 | |||||
chr13:25317586
|
T | C | 3 | a0003c0004t0001g0291a0003c0004t0001g0292a0003c0004t0001g0293 | 3 | HG02615.hp1 HG02886.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.686-1740T>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | chr13 | 25317586 | ||||||
chr13:25317694
|
G | A | 296 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0017others(293): Show | 347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.686-1632G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | chr13 | 25317694 | ||||||
chr13:25317739
|
GA | G | 4 | a0001c0001t0001g0150a0001c0001t0001g0289a0001c0001t0001g0290others(1): Show | 5 | HG01243.hp1 HG01884.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.686-1580delA | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr13 | 25317739 | |||||
chr13:25317814
|
C | G | 14 | a0001c0001t0006g0020a0001c0001t0006g0189a0001c0001t0006g0190others(11): Show | 15 | HG01891.hp2 HG02055.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.686-1512C>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | chr13 | 25317814 | ||||||
chr13:25317858
|
A | AT | 187 | a0001c0001t0001g0002a0001c0001t0001g0021a0001c0001t0001g0022others(184): Show | 228 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.686-1447dupT | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr13 | 25317858 | |||||
chr13:25317858
|
A | ATT | 22 | a0001c0001t0001g0017a0001c0001t0001g0078a0001c0001t0001g0091others(19): Show | 23 | HG00735.hp2 HG01074.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.686-1448_686-1447d others(4): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr13 | 25317858 | |||||
chr13:25317882
|
GA | G | 3 | a0001c0005t0001g0074a0001c0005t0001g0075a0001c0010t0001g0106 | 3 | HG02109.hp1 HG02280.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.686-1443delA | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | chr13 | 25317882 | ||||||
chr13:25317893
|
T | G | 238 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0021others(235): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.686-1433T>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | chr13 | 25317893 | ||||||
chr13:25317915
|
A | C | 1 | a0001c0001t0001g0264 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.686-1411A>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | chr13 | 25317915 | ||||||
chr13:25317940
|
T | C | 1 | a0001c0001t0005g0147 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.686-1386T>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | chr13 | 25317940 | ||||||
chr13:25317942
|
C | T | 6 | a0001c0001t0003g0033a0001c0001t0003g0276a0001c0001t0003g0277others(3): Show | 7 | HG02109.hp2 HG02257.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.686-1384C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | chr13 | 25317942 | ||||||
chr13:25317977
|
C | T | 1 | a0002c0002t0001g0059 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.686-1349C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | chr13 | 25317977 | ||||||
chr13:25318010
|
C | T | 1 | a0001c0001t0001g0229 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.686-1316C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | chr13 | 25318010 | ||||||
chr13:25318032
|
T | C | 1 | a0001c0001t0001g0028 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.686-1294T>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | chr13 | 25318032 | ||||||
chr13:25318067
|
C | T | 4 | a0003c0004t0001g0294a0003c0004t0001g0295a0003c0004t0001g0296others(1): Show | 4 | HG02055.hp1 HG02486.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.686-1259C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | chr13 | 25318067 | ||||||
chr13:25318074
|
A | T | 1 | a0001c0001t0014g0011 | 2 | HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.686-1252A>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | chr13 | 25318074 | ||||||
chr13:25318195
|
G | T | 3 | a0003c0004t0001g0291a0003c0004t0001g0292a0003c0004t0001g0293 | 3 | HG02615.hp1 HG02886.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.686-1131G>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | chr13 | 25318195 | ||||||
chr13:25318322
|
C | T | 7 | a0003c0004t0001g0291a0003c0004t0001g0292a0003c0004t0001g0293others(4): Show | 7 | HG02055.hp1 HG02486.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.686-1004C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | chr13 | 25318322 | ||||||
chr13:25318365
|
C | T | 1 | a0001c0001t0001g0038 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.686-961C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | chr13 | 25318365 | ||||||
chr13:25318699
|
G | A | 1 | a0001c0001t0003g0174 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.686-627G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | chr13 | 25318699 | ||||||
chr13:25318801
|
T | C | 2 | a0001c0001t0012g0151a0001c0001t0012g0152 | 2 | HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.686-525T>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | chr13 | 25318801 | ||||||
chr13:25318866
|
G | C | 1 | a0001c0001t0011g0267 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.686-460G>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | chr13 | 25318866 | ||||||
chr13:25318885
|
G | A | 1 | a0003c0004t0001g0294 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.686-441G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | chr13 | 25318885 | ||||||
chr13:25318924
|
A | C | 1 | a0002c0002t0001g0070 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.686-402A>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | chr13 | 25318924 | ||||||
chr13:25319083
|
T | A | 134 | a0001c0001t0003g0003a0001c0001t0003g0024a0001c0001t0003g0029others(131): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.686-243T>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | chr13 | 25319083 | ||||||
chr13:25319165
|
G | A | 3 | a0003c0004t0001g0291a0003c0004t0001g0292a0003c0004t0001g0293 | 3 | HG02615.hp1 HG02886.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.686-161G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | chr13 | 25319165 | ||||||
chr13:25319189
|
A | G | 3 | a0001c0005t0001g0074a0001c0005t0001g0075a0001c0010t0001g0106 | 3 | HG02109.hp1 HG02280.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.686-137A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | chr13 | 25319189 | ||||||
chr13:25319225
|
GTTTATA | G | 216 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0021others(213): Show | 262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.686-94_686-89delTT others(4): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr13 | 25319225 | |||||
chr13:25319402
|
T | C | 17 | a0001c0001t0014g0011a0001c0001t0019g0205a0001c0003t0004g0194others(14): Show | 18 | HG01496.hp1 HG02015.hp1 HG02132.hp2 others(15): Show |
intron_variant | MODIFIER | c.710+52T>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 7/15 | chr13 | 25319402 | ||||||
chr13:25319466
|
T | C | 16 | a0001c0001t0019g0205a0001c0003t0004g0194a0001c0003t0004g0195others(13): Show | 16 | HG01496.hp1 HG02015.hp1 HG02132.hp2 others(13): Show |
intron_variant | MODIFIER | c.710+116T>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 7/15 | chr13 | 25319466 | ||||||
chr13:25319468
|
T | C | 3 | a0001c0001t0001g0021a0001c0001t0001g0245a0001c0001t0001g0246 | 4 | HG00423.hp1 NA19001.hp2 NA19075.hp2 others(1): Show |
intron_variant | MODIFIER | c.710+118T>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 7/15 | chr13 | 25319468 | ||||||
chr13:25319595
|
CTAATA | C | 7 | a0003c0004t0001g0291a0003c0004t0001g0292a0003c0004t0001g0293others(4): Show | 7 | HG02055.hp1 HG02486.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.710+249_710+253del others(5): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr13 | 25319595 | |||||
chr13:25319631
|
T | C | 1 | a0002c0002t0001g0101 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.710+281T>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 7/15 | chr13 | 25319631 | ||||||
chr13:25319707
|
A | T | 1 | a0003c0004t0001g0292 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.710+357A>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 7/15 | chr13 | 25319707 | ||||||
chr13:25319766
|
A | G | 16 | a0001c0001t0019g0205a0001c0003t0004g0194a0001c0003t0004g0195others(13): Show | 16 | HG01496.hp1 HG02015.hp1 HG02132.hp2 others(13): Show |
intron_variant | MODIFIER | c.710+416A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 7/15 | chr13 | 25319766 | ||||||
chr13:25319796
|
A | G | 7 | a0003c0004t0001g0291a0003c0004t0001g0292a0003c0004t0001g0293others(4): Show | 7 | HG02055.hp1 HG02486.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.710+446A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 7/15 | chr13 | 25319796 | ||||||
chr13:25319802
|
T | A | 16 | a0001c0001t0019g0205a0001c0003t0004g0194a0001c0003t0004g0195others(13): Show | 16 | HG01496.hp1 HG02015.hp1 HG02132.hp2 others(13): Show |
intron_variant | MODIFIER | c.710+452T>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 7/15 | chr13 | 25319802 | ||||||
chr13:25319886
|
A | G | 1 | a0001c0001t0001g0163 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.710+536A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 7/15 | chr13 | 25319886 | ||||||
chr13:25319923
|
A | G | 5 | a0001c0001t0006g0020a0001c0001t0006g0189a0001c0001t0006g0190others(2): Show | 6 | HG01891.hp2 HG02965.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.710+573A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 7/15 | chr13 | 25319923 | ||||||
chr13:25319959
|
C | G | 1 | a0001c0001t0018g0288 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.711-571C>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 7/15 | chr13 | 25319959 | ||||||
chr13:25319976
|
A | T | 16 | a0001c0001t0019g0205a0001c0003t0004g0194a0001c0003t0004g0195others(13): Show | 16 | HG01496.hp1 HG02015.hp1 HG02132.hp2 others(13): Show |
intron_variant | MODIFIER | c.711-554A>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 7/15 | chr13 | 25319976 | ||||||
chr13:25320091
|
C | G | 3 | a0001c0001t0001g0219a0001c0001t0001g0220a0001c0001t0003g0144 | 3 | HG00639.hp1 HG00642.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.711-439C>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 7/15 | chr13 | 25320091 | ||||||
chr13:25320151
|
T | C | 3 | a0001c0001t0001g0150a0001c0001t0001g0289a0001c0001t0001g0290 | 3 | HG01243.hp1 HG01884.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.711-379T>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 7/15 | chr13 | 25320151 | ||||||
chr13:25320247
|
T | C | 1 | a0002c0002t0001g0055 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.711-283T>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 7/15 | chr13 | 25320247 | ||||||
chr13:25320332
|
A | G | 4 | a0002c0002t0001g0010a0002c0002t0001g0043a0002c0002t0001g0050others(1): Show | 6 | HG02559.hp2 HG02572.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.711-198A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 7/15 | chr13 | 25320332 | ||||||
chr13:25320409
|
A | C | 3 | a0003c0004t0001g0294a0003c0004t0001g0295a0003c0004t0001g0297 | 3 | HG02486.hp1 HG02622.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.711-121A>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 7/15 | chr13 | 25320409 | ||||||
chr13:25320525
|
C | A | 2 | a0001c0005t0001g0074a0001c0005t0001g0075 | 2 | HG02109.hp1 HG02280.hp1 |
splice_region_variant&intron_variant | LOW | c.711-5C>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 7/15 | chr13 | 25320525 | ||||||
chr13:25320689
|
A | T | 1 | a0002c0002t0001g0065 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.776+94A>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 8/15 | chr13 | 25320689 | ||||||
chr13:25321238
|
T | C | 1 | a0001c0001t0003g0174 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.951+145T>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 9/15 | chr13 | 25321238 | ||||||
chr13:25321368
|
A | G | 1 | a0001c0001t0018g0288 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.951+275A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 9/15 | chr13 | 25321368 | ||||||
chr13:25321447
|
C | T | 4 | a0001c0005t0001g0023a0001c0005t0001g0074a0001c0005t0001g0075others(1): Show | 5 | HG02109.hp1 HG02257.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.951+354C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 9/15 | chr13 | 25321447 | ||||||
chr13:25321565
|
A | G | 79 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0021others(76): Show | 105 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.951+472A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 9/15 | chr13 | 25321565 | ||||||
chr13:25321745
|
C | T | 3 | a0001c0001t0005g0282a0001c0001t0005g0283a0001c0012t0001g0073 | 3 | HG01243.hp2 HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.951+652C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 9/15 | chr13 | 25321745 | ||||||
chr13:25321746
|
G | A | 1 | a0001c0001t0001g0102 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.951+653G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 9/15 | chr13 | 25321746 | ||||||
chr13:25321854
|
T | G | 1 | a0006c0011t0004g0199 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.951+761T>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 9/15 | chr13 | 25321854 | ||||||
chr13:25322029
|
G | A | 1 | a0001c0001t0014g0011 | 2 | HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.951+936G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 9/15 | chr13 | 25322029 | ||||||
chr13:25322228
|
G | A | 5 | a0001c0001t0006g0020a0001c0001t0006g0189a0001c0001t0006g0190others(2): Show | 6 | HG01891.hp2 HG02965.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.951+1135G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 9/15 | chr13 | 25322228 | ||||||
chr13:25322232
|
T | G | 1 | a0006c0011t0004g0199 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.951+1139T>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 9/15 | chr13 | 25322232 | ||||||
chr13:25322355
|
C | T | 1 | a0005c0013t0010g0127 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.951+1262C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 9/15 | chr13 | 25322355 | ||||||
chr13:25322459
|
C | G | 1 | a0001c0001t0018g0288 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.951+1366C>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 9/15 | chr13 | 25322459 | ||||||
chr13:25322936
|
T | A | 16 | a0001c0001t0019g0205a0001c0003t0004g0194a0001c0003t0004g0195others(13): Show | 16 | HG01496.hp1 HG02015.hp1 HG02132.hp2 others(13): Show |
intron_variant | MODIFIER | c.951+1843T>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 9/15 | chr13 | 25322936 | ||||||
chr13:25323023
|
C | T | 8 | a0001c0001t0001g0078a0001c0001t0001g0091a0001c0001t0001g0092others(5): Show | 8 | HG01884.hp1 HG02723.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.951+1930C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 9/15 | chr13 | 25323023 | ||||||
chr13:25323140
|
T | A | 1 | a0001c0001t0002g0286 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.952-1849T>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 9/15 | chr13 | 25323140 | ||||||
chr13:25323368
|
T | C | 1 | a0002c0002t0001g0193 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.952-1621T>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 9/15 | chr13 | 25323368 | ||||||
chr13:25323377
|
AT | A | 133 | a0001c0001t0003g0003a0001c0001t0003g0024a0001c0001t0003g0029others(130): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.952-1610delT | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr13 | 25323377 | |||||
chr13:25323379
|
T | TA | 16 | a0001c0001t0019g0205a0001c0003t0004g0194a0001c0003t0004g0195others(13): Show | 16 | HG01496.hp1 HG02015.hp1 HG02132.hp2 others(13): Show |
intron_variant | MODIFIER | c.952-1599dupA | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr13 | 25323379 | |||||
chr13:25323379
|
TA | T | 106 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0021others(103): Show | 133 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(130): Show |
intron_variant | MODIFIER | c.952-1599delA | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr13 | 25323379 | |||||
chr13:25323462
|
A | G | 1 | a0001c0001t0013g0209 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.952-1527A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 9/15 | chr13 | 25323462 | ||||||
chr13:25323502
|
A | C | 1 | a0001c0001t0018g0288 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.952-1487A>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 9/15 | chr13 | 25323502 | ||||||
chr13:25323592
|
C | T | 214 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0021others(211): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.952-1397C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 9/15 | chr13 | 25323592 | ||||||
chr13:25323714
|
GTTTAAA | G | 214 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0021others(211): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.952-1272_952-1267d others(8): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr13 | 25323714 | |||||
chr13:25323733
|
G | A | 1 | a0003c0004t0001g0292 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.952-1256G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 9/15 | chr13 | 25323733 | ||||||
chr13:25323962
|
A | G | 214 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0021others(211): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.952-1027A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 9/15 | chr13 | 25323962 | ||||||
chr13:25324024
|
C | T | 1 | a0001c0001t0018g0288 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.952-965C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 9/15 | chr13 | 25324024 | ||||||
chr13:25324282
|
T | C | 6 | a0001c0001t0003g0024a0001c0001t0003g0172a0001c0001t0003g0173others(3): Show | 6 | HG00280.hp2 HG01261.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.952-707T>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 9/15 | chr13 | 25324282 | ||||||
chr13:25324386
|
G | T | 6 | a0001c0001t0006g0020a0001c0001t0006g0189a0001c0001t0006g0190others(3): Show | 7 | HG01891.hp2 HG02486.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.952-603G>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 9/15 | chr13 | 25324386 | ||||||
chr13:25324397
|
A | T | 2 | a0001c0005t0001g0074a0001c0005t0001g0075 | 2 | HG02109.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.952-592A>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 9/15 | chr13 | 25324397 | ||||||
chr13:25324420
|
T | G | 1 | a0001c0001t0014g0011 | 2 | HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.952-569T>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 9/15 | chr13 | 25324420 | ||||||
chr13:25324907
|
T | C | 1 | a0001c0001t0003g0172 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.952-82T>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 9/15 | chr13 | 25324907 | ||||||
chr13:25324936
|
A | G | 1 | a0001c0001t0002g0248 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.952-53A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 9/15 | chr13 | 25324936 | ||||||
chr13:25324953
|
C | CT | 94 | a0001c0001t0001g0028a0002c0002t0001g0004a0002c0002t0001g0008others(91): Show | 107 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.952-20dupT | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr13 | 25324953 | |||||
chr13:25325079
|
G | A | 1 | a0001c0001t0018g0288 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1031+11G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 10/15 | chr13 | 25325079 | ||||||
chr13:25325086
|
TA | T | 2 | a0001c0001t0001g0017a0001c0001t0001g0166 | 3 | HG00735.hp2 HG03195.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1031+23delA | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr13 | 25325086 | |||||
chr13:25325195
|
G | T | 5 | a0001c0001t0006g0020a0001c0001t0006g0189a0001c0001t0006g0190others(2): Show | 6 | HG01891.hp2 HG02965.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1031+127G>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 10/15 | chr13 | 25325195 | ||||||
chr13:25325340
|
A | G | 4 | a0001c0001t0003g0107a0001c0001t0003g0108a0001c0001t0003g0134others(1): Show | 4 | HG00639.hp2 HG01070.hp2 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.1031+272A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 10/15 | chr13 | 25325340 | ||||||
chr13:25325392
|
G | A | 2 | a0001c0001t0012g0151a0001c0001t0012g0152 | 2 | HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1031+324G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 10/15 | chr13 | 25325392 | ||||||
chr13:25325489
|
C | T | 1 | a0003c0004t0001g0293 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1031+421C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 10/15 | chr13 | 25325489 | ||||||
chr13:25325546
|
A | G | 10 | a0001c0001t0003g0033a0001c0001t0003g0276a0001c0001t0003g0277others(7): Show | 11 | HG01496.hp2 HG02109.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1031+478A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 10/15 | chr13 | 25325546 | ||||||
chr13:25325698
|
G | A | 1 | a0001c0001t0003g0144 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1031+630G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 10/15 | chr13 | 25325698 | ||||||
chr13:25325804
|
C | T | 1 | a0001c0012t0001g0073 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1031+736C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 10/15 | chr13 | 25325804 | ||||||
chr13:25325856
|
G | C | 1 | a0001c0001t0015g0158 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1031+788G>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 10/15 | chr13 | 25325856 | ||||||
chr13:25325886
|
T | C | 1 | a0002c0002t0001g0212 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1031+818T>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 10/15 | chr13 | 25325886 | ||||||
chr13:25326077
|
C | T | 1 | a0001c0001t0001g0102 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1032-839C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 10/15 | chr13 | 25326077 | ||||||
chr13:25326161
|
C | T | 1 | a0002c0002t0001g0121 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1032-755C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 10/15 | chr13 | 25326161 | ||||||
chr13:25326174
|
T | C | 5 | a0001c0001t0006g0020a0001c0001t0006g0189a0001c0001t0006g0190others(2): Show | 6 | HG01891.hp2 HG02965.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1032-742T>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 10/15 | chr13 | 25326174 | ||||||
chr13:25326294
|
G | GA | 5 | a0001c0001t0006g0020a0001c0001t0006g0189a0001c0001t0006g0190others(2): Show | 6 | HG01891.hp2 HG02965.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1032-619dupA | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr13 | 25326294 | |||||
chr13:25326302
|
T | C | 10 | a0001c0001t0003g0033a0001c0001t0003g0276a0001c0001t0003g0277others(7): Show | 11 | HG01496.hp2 HG02109.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1032-614T>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 10/15 | chr13 | 25326302 | ||||||
chr13:25326336
|
C | CT | 30 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0142others(27): Show | 33 | HG01243.hp2 HG01361.hp2 HG01496.hp2 others(30): Show |
intron_variant | MODIFIER | c.1032-567dupT | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr13 | 25326336 | |||||
chr13:25326337
|
T | C | 1 | a0001c0001t0018g0288 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1032-579T>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 10/15 | chr13 | 25326337 | ||||||
chr13:25326700
|
C | T | 134 | a0001c0001t0003g0003a0001c0001t0003g0024a0001c0001t0003g0029others(131): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.1032-216C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 10/15 | chr13 | 25326700 | ||||||
chr13:25327115
|
A | C | 1 | a0002c0002t0001g0118 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1150+81A>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 11/15 | chr13 | 25327115 | ||||||
chr13:25327135
|
A | C | 1 | a0001c0001t0002g0239 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1150+101A>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 11/15 | chr13 | 25327135 | ||||||
chr13:25327250
|
A | C | 1 | a0002c0002t0001g0060 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1151-180A>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 11/15 | chr13 | 25327250 | ||||||
chr13:25327276
|
G | A | 5 | a0001c0001t0006g0020a0001c0001t0006g0189a0001c0001t0006g0190others(2): Show | 6 | HG01891.hp2 HG02965.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1151-154G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 11/15 | chr13 | 25327276 | ||||||
chr13:25327317
|
T | C | 1 | a0001c0001t0014g0011 | 2 | HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1151-113T>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 11/15 | chr13 | 25327317 | ||||||
chr13:25327346
|
A | G | 2 | a0001c0001t0013g0209a0001c0001t0013g0210 | 2 | HG02559.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1151-84A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 11/15 | chr13 | 25327346 | ||||||
chr13:25327389
|
A | G | 1 | a0001c0001t0018g0288 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1151-41A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 11/15 | chr13 | 25327389 | ||||||
chr13:25327643
|
A | C | 271 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0021others(268): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.1233+131A>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 12/15 | chr13 | 25327643 | ||||||
chr13:25327671
|
A | G | 1 | a0001c0001t0006g0189 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1233+159A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 12/15 | chr13 | 25327671 | ||||||
chr13:25327708
|
C | T | 1 | a0002c0002t0001g0070 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1233+196C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 12/15 | chr13 | 25327708 | ||||||
chr13:25327709
|
G | A | 2 | a0001c0001t0012g0151a0001c0001t0012g0152 | 2 | HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1233+197G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 12/15 | chr13 | 25327709 | ||||||
chr13:25327729
|
CT | C | 4 | a0002c0002t0001g0054a0002c0002t0001g0055a0002c0002t0001g0057others(1): Show | 4 | NA18950.hp2 NA18956.hp1 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.1233+225delT | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr13 | 25327729 | |||||
chr13:25327833
|
A | G | 2 | a0001c0001t0012g0151a0001c0001t0012g0152 | 2 | HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1233+321A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 12/15 | chr13 | 25327833 | ||||||
chr13:25327918
|
TAGTC | T | 6 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0035others(3): Show | 8 | HG00738.hp1 HG01109.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1233+409_1233+412d others(6): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr13 | 25327918 | |||||
chr13:25327966
|
C | T | 1 | a0002c0002t0001g0137 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1233+454C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 12/15 | chr13 | 25327966 | ||||||
chr13:25327981
|
A | G | 1 | a0001c0001t0014g0011 | 2 | HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1233+469A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 12/15 | chr13 | 25327981 | ||||||
chr13:25328026
|
C | G | 3 | a0001c0001t0001g0150a0001c0001t0001g0289a0001c0001t0001g0290 | 3 | HG01243.hp1 HG01884.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1233+514C>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 12/15 | chr13 | 25328026 | ||||||
chr13:25328032
|
C | G | 5 | a0001c0001t0006g0020a0001c0001t0006g0189a0001c0001t0006g0190others(2): Show | 6 | HG01891.hp2 HG02965.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1233+520C>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 12/15 | chr13 | 25328032 | ||||||
chr13:25328055
|
C | T | 3 | a0001c0001t0001g0150a0001c0001t0001g0289a0001c0001t0001g0290 | 3 | HG01243.hp1 HG01884.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1233+543C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 12/15 | chr13 | 25328055 | ||||||
chr13:25328114
|
G | A | 4 | a0002c0002t0001g0116a0002c0002t0001g0122a0002c0002t0001g0123others(1): Show | 4 | NA18966.hp2 NA19006.hp1 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.1233+602G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 12/15 | chr13 | 25328114 | ||||||
chr13:25328140
|
A | G | 10 | a0001c0001t0003g0033a0001c0001t0003g0276a0001c0001t0003g0277others(7): Show | 11 | HG01496.hp2 HG02109.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1233+628A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 12/15 | chr13 | 25328140 | ||||||
chr13:25328200
|
A | G | 7 | a0003c0004t0001g0291a0003c0004t0001g0292a0003c0004t0001g0293others(4): Show | 7 | HG02055.hp1 HG02486.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1233+688A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 12/15 | chr13 | 25328200 | ||||||
chr13:25328246
|
C | T | 1 | a0002c0002t0001g0181 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1233+734C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 12/15 | chr13 | 25328246 | ||||||
chr13:25328340
|
T | G | 1 | a0001c0001t0018g0288 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1233+828T>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 12/15 | chr13 | 25328340 | ||||||
chr13:25328395
|
CT | C | 235 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0017others(232): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.1233+901delT | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr13 | 25328395 | |||||
chr13:25328420
|
G | A | 1 | a0001c0001t0018g0288 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1233+908G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 12/15 | chr13 | 25328420 | ||||||
chr13:25328438
|
C | T | 1 | a0001c0001t0001g0028 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1233+926C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 12/15 | chr13 | 25328438 | ||||||
chr13:25328512
|
C | T | 15 | a0001c0003t0004g0194a0001c0003t0004g0195a0001c0003t0004g0196others(12): Show | 15 | HG01496.hp1 HG02015.hp1 HG02132.hp2 others(12): Show |
intron_variant | MODIFIER | c.1233+1000C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 12/15 | chr13 | 25328512 | ||||||
chr13:25328523
|
A | C | 215 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0021others(212): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.1233+1011A>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 12/15 | chr13 | 25328523 | ||||||
chr13:25328646
|
C | G | 1 | a0001c0001t0005g0159 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1233+1134C>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 12/15 | chr13 | 25328646 | ||||||
chr13:25328694
|
A | G | 10 | a0001c0001t0003g0033a0001c0001t0003g0276a0001c0001t0003g0277others(7): Show | 11 | HG01496.hp2 HG02109.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1233+1182A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 12/15 | chr13 | 25328694 | ||||||
chr13:25328852
|
A | G | 2 | a0001c0001t0014g0011a0001c0001t0018g0288 | 3 | HG02922.hp1 HG03491.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1233+1340A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 12/15 | chr13 | 25328852 | ||||||
chr13:25328855
|
G | A | 3 | a0001c0005t0001g0074a0001c0005t0001g0075a0001c0010t0001g0106 | 3 | HG02109.hp1 HG02280.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1233+1343G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 12/15 | chr13 | 25328855 | ||||||
chr13:25328953
|
G | A | 32 | a0001c0001t0003g0033a0001c0001t0003g0276a0001c0001t0003g0277others(29): Show | 35 | HG01496.hp1 HG01496.hp2 HG01891.hp2 others(32): Show |
intron_variant | MODIFIER | c.1233+1441G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 12/15 | chr13 | 25328953 | ||||||
chr13:25329230
|
C | T | 1 | a0002c0002t0001g0082 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1233+1718C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 12/15 | chr13 | 25329230 | ||||||
chr13:25329303
|
A | G | 1 | a0002c0002t0001g0085 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1233+1791A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 12/15 | chr13 | 25329303 | ||||||
chr13:25329320
|
CT | C | 3 | a0002c0002t0001g0012a0002c0002t0001g0048a0002c0002t0001g0081 | 4 | HG01928.hp1 NA18992.hp2 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.1233+1815delT | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr13 | 25329320 | |||||
chr13:25329329
|
C | G | 4 | a0001c0005t0001g0023a0001c0005t0001g0074a0001c0005t0001g0075others(1): Show | 5 | HG02109.hp1 HG02257.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.1233+1817C>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 12/15 | chr13 | 25329329 | ||||||
chr13:25329537
|
G | A | 2 | a0002c0002t0001g0180a0002c0002t0001g0181 | 2 | HG01069.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.1234-1820G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 12/15 | chr13 | 25329537 | ||||||
chr13:25329614
|
T | C | 15 | a0001c0003t0004g0194a0001c0003t0004g0195a0001c0003t0004g0196others(12): Show | 15 | HG01496.hp1 HG02015.hp1 HG02132.hp2 others(12): Show |
intron_variant | MODIFIER | c.1234-1743T>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 12/15 | chr13 | 25329614 | ||||||
chr13:25329705
|
G | A | 1 | a0002c0002t0001g0188 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1234-1652G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 12/15 | chr13 | 25329705 | ||||||
chr13:25329768
|
A | C | 1 | a0001c0001t0003g0109 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1234-1589A>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 12/15 | chr13 | 25329768 | ||||||
chr13:25329935
|
G | A | 1 | a0002c0002t0001g0139 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1234-1422G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 12/15 | chr13 | 25329935 | ||||||
chr13:25330261
|
C | T | 1 | a0003c0004t0001g0296 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1234-1096C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 12/15 | chr13 | 25330261 | ||||||
chr13:25330659
|
T | C | 97 | a0002c0002t0001g0004a0002c0002t0001g0008a0002c0002t0001g0009others(94): Show | 110 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.1234-698T>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 12/15 | chr13 | 25330659 | ||||||
chr13:25330766
|
A | G | 140 | a0001c0001t0003g0003a0001c0001t0003g0024a0001c0001t0003g0029others(137): Show | 161 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(158): Show |
intron_variant | MODIFIER | c.1234-591A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 12/15 | chr13 | 25330766 | ||||||
chr13:25330849
|
C | T | 1 | a0001c0001t0018g0288 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1234-508C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 12/15 | chr13 | 25330849 | ||||||
chr13:25331169
|
A | G | 7 | a0003c0004t0001g0291a0003c0004t0001g0292a0003c0004t0001g0293others(4): Show | 7 | HG02055.hp1 HG02486.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1234-188A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 12/15 | chr13 | 25331169 | ||||||
chr13:25331253
|
A | G | 5 | a0001c0001t0006g0020a0001c0001t0006g0189a0001c0001t0006g0190others(2): Show | 6 | HG01891.hp2 HG02965.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1234-104A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 12/15 | chr13 | 25331253 | ||||||
chr13:25331278
|
T | C | 283 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0017others(280): Show | 334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.1234-79T>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 12/15 | chr13 | 25331278 | ||||||
chr13:25331344
|
A | ATTTT | 40 | a0001c0001t0003g0033a0001c0001t0003g0276a0001c0001t0003g0277others(37): Show | 43 | HG01496.hp1 HG01496.hp2 HG01891.hp2 others(40): Show |
intron_variant | MODIFIER | c.1234-11_1234-10ins others(4): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr13 | 25331344 | |||||
chr13:25331566
|
C | T | 1 | a0002c0002t0001g0071 | 1 | HG02738.hp1 | splice_region_variant&intron_variant | LOW | c.1435+8C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 13/15 | chr13 | 25331566 | ||||||
chr13:25331804
|
A | T | 7 | a0001c0001t0006g0020a0001c0001t0006g0189a0001c0001t0006g0190others(4): Show | 9 | HG01891.hp2 HG02922.hp1 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.1435+246A>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 13/15 | chr13 | 25331804 | ||||||
chr13:25331819
|
T | G | 2 | a0001c0001t0014g0011a0001c0001t0018g0288 | 3 | HG02922.hp1 HG03491.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1435+261T>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 13/15 | chr13 | 25331819 | ||||||
chr13:25331868
|
AT | A | 7 | a0001c0001t0001g0087a0001c0001t0001g0102a0001c0001t0001g0103others(4): Show | 7 | HG01891.hp1 HG02258.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1435+312delT | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr13 | 25331868 | |||||
chr13:25331883
|
C | T | 7 | a0001c0001t0006g0020a0001c0001t0006g0189a0001c0001t0006g0190others(4): Show | 9 | HG01891.hp2 HG02922.hp1 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.1435+325C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 13/15 | chr13 | 25331883 | ||||||
chr13:25331946
|
A | T | 7 | a0001c0001t0001g0078a0001c0001t0001g0091a0001c0001t0001g0092others(4): Show | 7 | HG01884.hp1 HG02896.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.1435+388A>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 13/15 | chr13 | 25331946 | ||||||
chr13:25332052
|
A | G | 2 | a0001c0001t0001g0037a0001c0001t0018g0288 | 2 | HG02723.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.1435+494A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 13/15 | chr13 | 25332052 | ||||||
chr13:25332153
|
C | G | 1 | a0001c0001t0018g0288 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1435+595C>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 13/15 | chr13 | 25332153 | ||||||
chr13:25332231
|
A | G | 2 | a0001c0001t0003g0090a0001c0001t0003g0109 | 2 | HG02818.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1435+673A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 13/15 | chr13 | 25332231 | ||||||
chr13:25332537
|
C | A | 1 | a0001c0012t0001g0073 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1435+979C>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 13/15 | chr13 | 25332537 | ||||||
chr13:25332537
|
CAAAA | C | 133 | a0001c0001t0003g0003a0001c0001t0003g0024a0001c0001t0003g0029others(130): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.1435+983_1435+986d others(6): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr13 | 25332537 | |||||
chr13:25332565
|
A | G | 1 | a0002c0002t0001g0100 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1435+1007A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 13/15 | chr13 | 25332565 | ||||||
chr13:25332582
|
T | C | 1 | a0001c0001t0002g0224 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1435+1024T>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 13/15 | chr13 | 25332582 | ||||||
chr13:25332583
|
A | T | 1 | a0001c0001t0002g0224 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1435+1025A>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 13/15 | chr13 | 25332583 | ||||||
chr13:25332607
|
T | C | 1 | a0002c0002t0001g0099 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1435+1049T>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 13/15 | chr13 | 25332607 | ||||||
chr13:25332709
|
C | T | 1 | a0002c0002t0001g0125 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1435+1151C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 13/15 | chr13 | 25332709 | ||||||
chr13:25332713
|
G | A | 2 | a0003c0004t0001g0295a0003c0004t0001g0297 | 2 | HG02486.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1435+1155G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 13/15 | chr13 | 25332713 | ||||||
chr13:25332787
|
A | G | 215 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0021others(212): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.1435+1229A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 13/15 | chr13 | 25332787 | ||||||
chr13:25332854
|
A | G | 2 | a0001c0001t0012g0151a0001c0001t0012g0152 | 2 | HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1435+1296A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 13/15 | chr13 | 25332854 | ||||||
chr13:25332906
|
A | G | 8 | a0001c0001t0003g0033a0001c0001t0003g0276a0001c0001t0003g0277others(5): Show | 10 | HG02109.hp2 HG02257.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1435+1348A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 13/15 | chr13 | 25332906 | ||||||
chr13:25333061
|
G | T | 1 | a0001c0001t0002g0242 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1435+1503G>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 13/15 | chr13 | 25333061 | ||||||
chr13:25333162
|
T | C | 2 | a0001c0001t0014g0011a0001c0001t0018g0288 | 3 | HG02922.hp1 HG03491.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1435+1604T>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 13/15 | chr13 | 25333162 | ||||||
chr13:25333196
|
T | C | 3 | a0001c0001t0003g0108a0001c0001t0003g0134a0001c0001t0003g0135 | 3 | HG00639.hp2 HG01070.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.1435+1638T>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 13/15 | chr13 | 25333196 | ||||||
chr13:25333209
|
T | C | 22 | a0001c0001t0006g0020a0001c0001t0006g0189a0001c0001t0006g0190others(19): Show | 24 | HG01496.hp1 HG01891.hp2 HG02015.hp1 others(21): Show |
intron_variant | MODIFIER | c.1435+1651T>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 13/15 | chr13 | 25333209 | ||||||
chr13:25333643
|
G | A | 4 | a0001c0001t0007g0042a0001c0001t0007g0072a0001c0001t0007g0104others(1): Show | 4 | HG01496.hp2 HG02258.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1435+2085G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 13/15 | chr13 | 25333643 | ||||||
chr13:25333700
|
A | G | 2 | a0001c0001t0012g0151a0001c0001t0012g0152 | 2 | HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1435+2142A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 13/15 | chr13 | 25333700 | ||||||
chr13:25333816
|
A | T | 1 | a0001c0001t0014g0011 | 2 | HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1435+2258A>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 13/15 | chr13 | 25333816 | ||||||
chr13:25333840
|
TTGTTTTT others(9): Show |
T | 1 | a0003c0004t0001g0296 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1435+2287_1435+230 others(20): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr13 | 25333840 | |||||
chr13:25333910
|
A | G | 1 | a0001c0001t0003g0178 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1435+2352A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 13/15 | chr13 | 25333910 | ||||||
chr13:25334142
|
G | T | 1 | a0001c0001t0001g0274 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1435+2584G>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 13/15 | chr13 | 25334142 | ||||||
chr13:25334214
|
A | T | 2 | a0001c0001t0005g0282a0001c0001t0005g0283 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1435+2656A>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 13/15 | chr13 | 25334214 | ||||||
chr13:25334400
|
G | A | 5 | a0001c0001t0001g0227a0001c0001t0001g0253a0001c0001t0001g0255others(2): Show | 5 | NA18945.hp2 NA18950.hp1 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.1436-2536G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 13/15 | chr13 | 25334400 | ||||||
chr13:25334609
|
T | G | 2 | a0001c0001t0012g0151a0001c0001t0012g0152 | 2 | HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1436-2327T>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 13/15 | chr13 | 25334609 | ||||||
chr13:25334650
|
A | G | 2 | a0001c0001t0007g0042a0001c0001t0007g0104 | 2 | HG01496.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.1436-2286A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 13/15 | chr13 | 25334650 | ||||||
chr13:25334850
|
A | G | 1 | a0002c0002t0001g0212 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1436-2086A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 13/15 | chr13 | 25334850 | ||||||
chr13:25335021
|
A | T | 3 | a0001c0005t0001g0074a0001c0005t0001g0075a0001c0010t0001g0106 | 3 | HG02109.hp1 HG02280.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1436-1915A>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 13/15 | chr13 | 25335021 | ||||||
chr13:25335064
|
A | G | 2 | a0001c0001t0002g0285a0001c0001t0002g0286 | 2 | HG02735.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.1436-1872A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 13/15 | chr13 | 25335064 | ||||||
chr13:25335203
|
T | C | 1 | a0001c0001t0001g0230 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1436-1733T>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 13/15 | chr13 | 25335203 | ||||||
chr13:25335394
|
C | G | 1 | a0001c0001t0003g0279 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1436-1542C>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 13/15 | chr13 | 25335394 | ||||||
chr13:25335506
|
A | G | 2 | a0001c0001t0002g0221a0001c0001t0002g0239 | 2 | NA18981.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.1436-1430A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 13/15 | chr13 | 25335506 | ||||||
chr13:25335816
|
G | A | 80 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0021others(77): Show | 106 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.1436-1120G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 13/15 | chr13 | 25335816 | ||||||
chr13:25335975
|
T | A | 5 | a0001c0001t0003g0090a0001c0001t0003g0109a0001c0001t0006g0192others(2): Show | 5 | HG02818.hp1 HG03098.hp1 HG03710.hp1 others(2): Show |
intron_variant | MODIFIER | c.1436-961T>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 13/15 | chr13 | 25335975 | ||||||
chr13:25335976
|
A | T | 1 | a0002c0002t0001g0161 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1436-960A>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 13/15 | chr13 | 25335976 | ||||||
chr13:25336501
|
A | G | 7 | a0001c0001t0001g0078a0001c0001t0001g0091a0001c0001t0001g0092others(4): Show | 7 | HG01884.hp1 HG02896.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.1436-435A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 13/15 | chr13 | 25336501 | ||||||
chr13:25336609
|
G | A | 1 | a0001c0001t0014g0011 | 2 | HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1436-327G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 13/15 | chr13 | 25336609 | ||||||
chr13:25336912
|
A | AT | 12 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0168others(9): Show | 12 | HG02055.hp1 HG02486.hp1 HG02615.hp1 others(9): Show |
splice_region_variant&intron_variant | LOW | c.1436-8dupT | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr13 | 25336912 | |||||
chr13:25336912
|
AT | A | 6 | a0001c0001t0006g0020a0001c0001t0006g0189a0001c0001t0006g0190others(3): Show | 7 | HG01358.hp1 HG01891.hp2 HG02965.hp2 others(4): Show |
splice_region_variant&intron_variant | LOW | c.1436-8delT | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr13 | 25336912 | |||||
chr13:25337169
|
A | G | 1 | a0001c0010t0001g0106 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1534+135A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 14/15 | chr13 | 25337169 | ||||||
chr13:25337736
|
C | T | 1 | a0001c0001t0002g0238 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1534+702C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 14/15 | chr13 | 25337736 | ||||||
chr13:25337750
|
A | G | 1 | a0002c0002t0001g0061 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1534+716A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 14/15 | chr13 | 25337750 | ||||||
chr13:25337897
|
A | G | 168 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0017others(165): Show | 201 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(198): Show |
intron_variant | MODIFIER | c.1535-739A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 14/15 | chr13 | 25337897 | ||||||
chr13:25337944
|
G | A | 1 | a0001c0010t0001g0106 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1535-692G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 14/15 | chr13 | 25337944 | ||||||
chr13:25337991
|
T | A | 1 | a0001c0001t0018g0288 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1535-645T>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 14/15 | chr13 | 25337991 | ||||||
chr13:25338235
|
T | C | 2 | a0001c0001t0001g0017a0001c0001t0001g0166 | 3 | HG00735.hp2 HG03195.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1535-401T>C | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 14/15 | chr13 | 25338235 | ||||||
chr13:25338530
|
A | G | 1 | a0001c0001t0002g0236 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1535-106A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 14/15 | chr13 | 25338530 | ||||||
chr13:25338562
|
C | T | 1 | a0001c0001t0017g0155 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1535-74C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 14/15 | chr13 | 25338562 | ||||||
chr13:25338988
|
C | G | 1 | a0001c0001t0007g0042 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1630+257C>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 15/15 | chr13 | 25338988 | ||||||
chr13:25339038
|
TAC | T | 19 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0087others(16): Show | 19 | HG01175.hp2 HG01891.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.1630+309_1630+310d others(4): Show |
NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr13 | 25339038 | |||||
chr13:25339055
|
C | G | 1 | a0001c0001t0001g0230 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1630+324C>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 15/15 | chr13 | 25339055 | ||||||
chr13:25339068
|
T | A | 1 | a0001c0001t0001g0230 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1630+337T>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 15/15 | chr13 | 25339068 | ||||||
chr13:25339136
|
C | T | 1 | a0001c0008t0001g0215 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1630+405C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 15/15 | chr13 | 25339136 | ||||||
chr13:25339246
|
A | G | 4 | a0001c0001t0002g0006a0001c0001t0002g0226a0001c0001t0002g0243others(1): Show | 7 | NA18963.hp1 NA18964.hp2 NA18971.hp1 others(4): Show |
intron_variant | MODIFIER | c.1630+515A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 15/15 | chr13 | 25339246 | ||||||
chr13:25339380
|
C | T | 1 | a0001c0001t0001g0250 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1631-585C>T | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 15/15 | chr13 | 25339380 | ||||||
chr13:25339527
|
G | A | 15 | a0001c0003t0004g0194a0001c0003t0004g0195a0001c0003t0004g0196others(12): Show | 15 | HG01496.hp1 HG02015.hp1 HG02132.hp2 others(12): Show |
intron_variant | MODIFIER | c.1631-438G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 15/15 | chr13 | 25339527 | ||||||
chr13:25339533
|
T | G | 1 | a0001c0001t0014g0011 | 2 | HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1631-432T>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 15/15 | chr13 | 25339533 | ||||||
chr13:25339593
|
G | A | 1 | a0002c0002t0001g0161 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1631-372G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 15/15 | chr13 | 25339593 | ||||||
chr13:25339620
|
A | G | 2 | a0001c0001t0014g0011a0001c0001t0018g0288 | 3 | HG02922.hp1 HG03491.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1631-345A>G | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 15/15 | chr13 | 25339620 | ||||||
chr13:25339660
|
G | A | 134 | a0001c0001t0003g0003a0001c0001t0003g0024a0001c0001t0003g0029others(131): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.1631-305G>A | NUP58 | ENSG00000139496.18 | transcript | ENST00000381736.8 | protein_coding | 15/15 | chr13 | 25339660 |