geneid | 23190 |
---|---|
ensemblid | ENSG00000144224.17 |
hgncid | 14860 |
symbol | UBXN4 |
name | UBX domain protein 4 |
refseq_nuc | NM_014607.4 |
refseq_prot | NP_055422.1 |
ensembl_nuc | ENST00000272638.14 |
ensembl_prot | ENSP00000272638.9 |
mane_status | MANE Select |
chr | chr2 |
start | 135741855 |
end | 135785056 |
strand | + |
ver | v1.2 |
region | chr2:135741855-135785056 |
region5000 | chr2:135736855-135790056 |
regionname0 | UBXN4_chr2_135741855_135785056 |
regionname5000 | UBXN4_chr2_135736855_135790056 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 508 | 367 | 86 | 64 | 173 | 6 | 36 | 138 | UBXN4_chr2_135736855_135790056 | UBXN4 | copy fasta | chr2 | 135736855 | 135790056 |
a0002 | 0/0 | 508 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | copy fasta | chr2 | 135736855 | 135790056 |
a0003 | 0/0 | 508 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | copy fasta | chr2 | 135736855 | 135790056 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1527 | 270 | 76 | 41 | 120 | 4 | 27 | UBXN4_chr2_135736855_135790056 | UBXN4 | copy fasta | chr2 | 135736855 | 135790056 |
c0002 | 0/0 | 1527 | 62 | 10 | 17 | 28 | 2 | 5 | UBXN4_chr2_135736855_135790056 | UBXN4 | copy fasta | chr2 | 135736855 | 135790056 |
c0003 | 0/0 | 1527 | 25 | 0 | 2 | 22 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | copy fasta | chr2 | 135736855 | 135790056 |
c0004 | 0/0 | 1527 | 8 | 0 | 3 | 3 | 0 | 2 | UBXN4_chr2_135736855_135790056 | UBXN4 | copy fasta | chr2 | 135736855 | 135790056 |
c0005 | 0/0 | 1527 | 2 | 0 | 0 | 2 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | copy fasta | chr2 | 135736855 | 135790056 |
c0006 | 0/0 | 1527 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | copy fasta | chr2 | 135736855 | 135790056 |
c0007 | 0/0 | 1527 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | copy fasta | chr2 | 135736855 | 135790056 |
c0008 | 0/0 | 1527 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | copy fasta | chr2 | 135736855 | 135790056 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 2245 | 160 | 26 | 25 | 91 | 3 | 14 | UBXN4_chr2_135736855_135790056 | UBXN4 | copy fasta | chr2 | 135736855 | 135790056 |
t0002 | 0/0 | 2246 | 80 | 12 | 23 | 33 | 3 | 9 | UBXN4_chr2_135736855_135790056 | UBXN4 | copy fasta | chr2 | 135736855 | 135790056 |
t0003 | 0/0 | 2243 | 73 | 22 | 9 | 35 | 0 | 7 | UBXN4_chr2_135736855_135790056 | UBXN4 | copy fasta | chr2 | 135736855 | 135790056 |
t0004 | 0/0 | 2245 | 25 | 15 | 4 | 4 | 0 | 2 | UBXN4_chr2_135736855_135790056 | UBXN4 | copy fasta | chr2 | 135736855 | 135790056 |
t0005 | 0/0 | 2246 | 11 | 2 | 0 | 6 | 0 | 3 | UBXN4_chr2_135736855_135790056 | UBXN4 | copy fasta | chr2 | 135736855 | 135790056 |
t0006 | 0/0 | 2246 | 4 | 4 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | copy fasta | chr2 | 135736855 | 135790056 |
t0007 | 0/0 | 2243 | 2 | 2 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | copy fasta | chr2 | 135736855 | 135790056 |
t0008 | 0/0 | 2245 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | copy fasta | chr2 | 135736855 | 135790056 |
t0009 | 0/0 | 2245 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | copy fasta | chr2 | 135736855 | 135790056 |
t0010 | 0/0 | 2245 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | copy fasta | chr2 | 135736855 | 135790056 |
t0011 | 0/0 | 2245 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | copy fasta | chr2 | 135736855 | 135790056 |
t0012 | 0/0 | 2245 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | copy fasta | chr2 | 135736855 | 135790056 |
t0013 | 0/0 | 2243 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | copy fasta | chr2 | 135736855 | 135790056 |
t0014 | 0/0 | 2243 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | copy fasta | chr2 | 135736855 | 135790056 |
t0015 | 0/0 | 2245 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | copy fasta | chr2 | 135736855 | 135790056 |
t0016 | 0/0 | 2245 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | copy fasta | chr2 | 135736855 | 135790056 |
t0017 | 0/0 | 2244 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | copy fasta | chr2 | 135736855 | 135790056 |
t0018 | 0/0 | 2246 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | copy fasta | chr2 | 135736855 | 135790056 |
t0019 | 0/0 | 2246 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | copy fasta | chr2 | 135736855 | 135790056 |
t0020 | 1/0 | 2245 | 1 | 0 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | copy fasta | chr2 | 135736855 | 135790056 |
t0021 | 0/0 | 2245 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | copy fasta | chr2 | 135736855 | 135790056 |
t0022 | 0/0 | 2243 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | copy fasta | chr2 | 135736855 | 135790056 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 17 | 1 | 10 | 1 | 1 | 4 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0002 | 0/0 | 12 | 0 | 1 | 10 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0003 | 0/0 | 7 | 6 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0004 | 0/0 | 6 | 1 | 4 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0005 | 0/0 | 5 | 0 | 3 | 1 | 1 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0006 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0009 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0010 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0011 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0014 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0016 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0018 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0021 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0022 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0023 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0285 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1527 | 270 | 76 | 41 | 120 | 4 | 27 | UBXN4_chr2_135736855_135790056 | UBXN4 | copy fasta | chr2 | 135736855 | 135790056 |
a0001c0002 | 0/0 | 1527 | 62 | 10 | 17 | 28 | 2 | 5 | UBXN4_chr2_135736855_135790056 | UBXN4 | copy fasta | chr2 | 135736855 | 135790056 |
a0001c0003 | 0/0 | 1527 | 25 | 0 | 2 | 22 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | copy fasta | chr2 | 135736855 | 135790056 |
a0001c0004 | 0/0 | 1527 | 8 | 0 | 3 | 3 | 0 | 2 | UBXN4_chr2_135736855_135790056 | UBXN4 | copy fasta | chr2 | 135736855 | 135790056 |
a0001c0007 | 0/0 | 1527 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | copy fasta | chr2 | 135736855 | 135790056 |
a0001c0008 | 0/0 | 1527 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | copy fasta | chr2 | 135736855 | 135790056 |
a0002c0005 | 0/0 | 1527 | 2 | 0 | 0 | 2 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | copy fasta | chr2 | 135736855 | 135790056 |
a0003c0006 | 0/0 | 1527 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | copy fasta | chr2 | 135736855 | 135790056 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 3771 | 134 | 26 | 23 | 68 | 3 | 13 | UBXN4_chr2_135736855_135790056 | UBXN4 | copy fasta | chr2 | 135736855 | 135790056 |
a0001c0001t0002 | 0/0 | 3772 | 16 | 2 | 7 | 3 | 1 | 3 | UBXN4_chr2_135736855_135790056 | UBXN4 | copy fasta | chr2 | 135736855 | 135790056 |
a0001c0001t0003 | 0/0 | 3769 | 65 | 22 | 6 | 32 | 0 | 5 | UBXN4_chr2_135736855_135790056 | UBXN4 | copy fasta | chr2 | 135736855 | 135790056 |
a0001c0001t0004 | 0/0 | 3771 | 25 | 15 | 4 | 4 | 0 | 2 | UBXN4_chr2_135736855_135790056 | UBXN4 | copy fasta | chr2 | 135736855 | 135790056 |
a0001c0001t0005 | 0/0 | 3772 | 11 | 2 | 0 | 6 | 0 | 3 | UBXN4_chr2_135736855_135790056 | UBXN4 | copy fasta | chr2 | 135736855 | 135790056 |
a0001c0001t0006 | 0/0 | 3772 | 4 | 4 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | copy fasta | chr2 | 135736855 | 135790056 |
a0001c0001t0007 | 0/0 | 3769 | 2 | 2 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | copy fasta | chr2 | 135736855 | 135790056 |
a0001c0001t0008 | 0/0 | 3771 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | copy fasta | chr2 | 135736855 | 135790056 |
a0001c0001t0009 | 0/0 | 3771 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | copy fasta | chr2 | 135736855 | 135790056 |
a0001c0001t0010 | 0/0 | 3771 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | copy fasta | chr2 | 135736855 | 135790056 |
a0001c0001t0011 | 0/0 | 3771 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | copy fasta | chr2 | 135736855 | 135790056 |
a0001c0001t0012 | 0/0 | 3771 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | copy fasta | chr2 | 135736855 | 135790056 |
a0001c0001t0013 | 0/0 | 3769 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | copy fasta | chr2 | 135736855 | 135790056 |
a0001c0001t0014 | 0/0 | 3769 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | copy fasta | chr2 | 135736855 | 135790056 |
a0001c0001t0015 | 0/0 | 3771 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | copy fasta | chr2 | 135736855 | 135790056 |
a0001c0001t0016 | 0/0 | 3771 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | copy fasta | chr2 | 135736855 | 135790056 |
a0001c0001t0017 | 0/0 | 3770 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | copy fasta | chr2 | 135736855 | 135790056 |
a0001c0001t0020 | 1/0 | 3771 | 1 | 0 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | copy fasta | chr2 | 135736855 | 135790056 |
a0001c0001t0021 | 0/0 | 3771 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | copy fasta | chr2 | 135736855 | 135790056 |
a0001c0001t0022 | 0/0 | 3769 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | copy fasta | chr2 | 135736855 | 135790056 |
a0001c0002t0002 | 0/0 | 3772 | 61 | 10 | 16 | 28 | 2 | 5 | UBXN4_chr2_135736855_135790056 | UBXN4 | copy fasta | chr2 | 135736855 | 135790056 |
a0001c0002t0018 | 0/0 | 3772 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | copy fasta | chr2 | 135736855 | 135790056 |
a0001c0003t0001 | 0/0 | 3771 | 25 | 0 | 2 | 22 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | copy fasta | chr2 | 135736855 | 135790056 |
a0001c0004t0003 | 0/0 | 3769 | 8 | 0 | 3 | 3 | 0 | 2 | UBXN4_chr2_135736855_135790056 | UBXN4 | copy fasta | chr2 | 135736855 | 135790056 |
a0001c0007t0019 | 0/0 | 3772 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | copy fasta | chr2 | 135736855 | 135790056 |
a0001c0008t0002 | 0/0 | 3772 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | copy fasta | chr2 | 135736855 | 135790056 |
a0002c0005t0002 | 0/0 | 3772 | 2 | 0 | 0 | 2 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | copy fasta | chr2 | 135736855 | 135790056 |
a0003c0006t0001 | 0/0 | 3771 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | copy fasta | chr2 | 135736855 | 135790056 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 17 | 1 | 10 | 1 | 1 | 4 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0002 | 0/0 | 11 | 0 | 1 | 10 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0022 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0002g0005 | 0/0 | 5 | 0 | 3 | 1 | 1 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0002g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0002g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0002g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0002g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0003g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0003g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0003g0014 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0003g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0003g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0003g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0003g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0003g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0003g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0003g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0003g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0003g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0003g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0003g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0003g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0003g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0003g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0003g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0003g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0003g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0003g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0003g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0003g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0004g0003 | 0/0 | 7 | 6 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0004g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0004g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0004g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0004g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0004g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0004g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0004g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0004g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0004g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0004g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0004g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0004g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0004g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0004g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0004g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0004g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0004g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0004g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0005g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0005g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0005g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0005g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0005g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0005g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0005g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0005g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0005g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0005g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0006g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0006g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0006g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0006g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0007g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0007g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0008g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0009g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0010g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0011g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0012g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0013g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0014g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0015g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0016g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0017g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0020g0285 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0021g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0001t0022g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0002t0002g0004 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0002t0002g0006 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0002t0002g0009 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0002t0002g0010 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0002t0002g0011 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0002t0002g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0002t0002g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0002t0002g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0002t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0002t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0002t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0002t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0002t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0002t0002g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0002t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0002t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0002t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0002t0002g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0002t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0002t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0002t0002g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0002t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0002t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0002t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0002t0002g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0002t0002g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0002t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0002t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0002t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0002t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0002t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0002t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0002t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0002t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0002t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0002t0002g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0002t0002g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0002t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0002t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0002t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0002t0002g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0002t0002g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0002t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0002t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0002t0018g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0003t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0003t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0003t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0003t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0003t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0003t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0003t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0003t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0003t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0003t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0003t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0003t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0003t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0003t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0003t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0003t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0003t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0003t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0003t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0003t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0003t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0003t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0003t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0003t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0004t0003g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0004t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0004t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0004t0003g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0004t0003g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0004t0003g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0004t0003g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0004t0003g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0007t0019g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0001c0008t0002g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0002c0005t0002g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0002c0005t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
a0003c0006t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00280 | hp1 | a0001 | c0001 | t0002 | g0005 | EUR | FIN | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG00408 | hp2 | a0001 | c0003 | t0001 | g0054 | EAS | CHS | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG00423 | hp2 | a0001 | c0003 | t0001 | g0045 | EAS | CHS | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG00544 | hp1 | a0001 | c0003 | t0001 | g0060 | EAS | CHS | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | CHS | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG00558 | hp1 | a0001 | c0003 | t0001 | g0063 | EAS | CHS | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG00558 | hp2 | a0001 | c0001 | t0009 | g0120 | EAS | CHS | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG00621 | hp1 | a0001 | c0001 | t0004 | g0131 | EAS | CHS | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG00639 | hp1 | a0001 | c0007 | t0019 | g0043 | AMR | PUR | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG00639 | hp2 | a0001 | c0001 | t0010 | g0132 | AMR | PUR | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG00642 | hp2 | a0001 | c0002 | t0002 | g0249 | AMR | PUR | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | CHS | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG00673 | hp2 | a0001 | c0002 | t0002 | g0237 | EAS | CHS | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG00733 | hp1 | a0001 | c0002 | t0002 | g0010 | AMR | PUR | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG00735 | hp1 | a0001 | c0001 | t0004 | g0003 | AMR | PUR | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG00735 | hp2 | a0001 | c0002 | t0002 | g0004 | AMR | PUR | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG00738 | hp1 | a0001 | c0002 | t0002 | g0006 | AMR | PUR | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0273 | AMR | PUR | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG01069 | hp1 | a0001 | c0002 | t0002 | g0009 | AMR | PUR | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG01071 | hp1 | a0001 | c0002 | t0002 | g0009 | AMR | PUR | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG01099 | hp2 | a0001 | c0002 | t0002 | g0009 | AMR | PUR | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG01167 | hp1 | a0001 | c0002 | t0002 | g0004 | AMR | PUR | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG01175 | hp1 | a0001 | c0001 | t0004 | g0133 | AMR | PUR | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG01175 | hp2 | a0001 | c0002 | t0002 | g0262 | AMR | PUR | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG01192 | hp2 | a0001 | c0002 | t0002 | g0243 | AMR | PUR | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG01243 | hp1 | a0001 | c0002 | t0002 | g0238 | AMR | PUR | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG01243 | hp2 | a0001 | c0001 | t0004 | g0119 | AMR | PUR | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG01255 | hp1 | a0001 | c0003 | t0001 | g0049 | AMR | CLM | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG01255 | hp2 | a0001 | c0002 | t0002 | g0235 | AMR | CLM | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0267 | AMR | CLM | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | CLM | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG01257 | hp2 | a0001 | c0002 | t0002 | g0241 | AMR | CLM | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | CLM | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG01261 | hp2 | a0001 | c0001 | t0003 | g0074 | AMR | CLM | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG01346 | hp1 | a0001 | c0001 | t0003 | g0072 | AMR | CLM | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG01358 | hp1 | a0001 | c0004 | t0003 | g0068 | AMR | CLM | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG01358 | hp2 | a0001 | c0002 | t0018 | g0004 | AMR | CLM | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | CLM | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | CLM | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG01496 | hp2 | a0001 | c0002 | t0002 | g0233 | AMR | CLM | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG01515 | hp1 | a0001 | c0002 | t0002 | g0260 | EUR | IBS | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0018 | EUR | IBS | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG01884 | hp2 | a0001 | c0001 | t0004 | g0032 | AFR | ACB | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0272 | AMR | PEL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG01943 | hp1 | a0001 | c0002 | t0002 | g0006 | AMR | PEL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG01943 | hp2 | a0001 | c0001 | t0002 | g0226 | AMR | PEL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG01952 | hp2 | a0001 | c0001 | t0003 | g0086 | AMR | PEL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG01978 | hp1 | a0001 | c0001 | t0003 | g0014 | AMR | PEL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG01978 | hp2 | a0001 | c0001 | t0004 | g0124 | AMR | PEL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG01981 | hp1 | a0001 | c0001 | t0003 | g0095 | AMR | PEL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG01993 | hp1 | a0001 | c0004 | t0003 | g0066 | AMR | PEL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | KHV | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG02015 | hp2 | a0001 | c0003 | t0001 | g0051 | EAS | KHV | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | KHV | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG02055 | hp1 | a0001 | c0002 | t0002 | g0240 | AFR | ACB | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG02055 | hp2 | a0001 | c0001 | t0003 | g0297 | AFR | ACB | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | KHV | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG02056 | hp2 | a0001 | c0001 | t0003 | g0101 | EAS | KHV | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG02071 | hp1 | a0001 | c0002 | t0002 | g0250 | EAS | KHV | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | KHV | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG02074 | hp1 | a0001 | c0003 | t0001 | g0012 | EAS | KHV | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG02074 | hp2 | a0002 | c0005 | t0002 | g0257 | EAS | KHV | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | KHV | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG02080 | hp2 | a0001 | c0002 | t0002 | g0011 | EAS | KHV | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG02083 | hp2 | a0001 | c0002 | t0002 | g0025 | EAS | KHV | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG02129 | hp1 | a0001 | c0003 | t0001 | g0059 | EAS | KHV | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | KHV | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG02132 | hp2 | a0001 | c0001 | t0013 | g0090 | EAS | KHV | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG02135 | hp2 | a0001 | c0002 | t0002 | g0236 | EAS | KHV | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG02145 | hp1 | a0001 | c0002 | t0002 | g0264 | AFR | ACB | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG02145 | hp2 | a0001 | c0001 | t0004 | g0134 | AFR | ACB | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PEL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG02148 | hp2 | a0001 | c0003 | t0001 | g0293 | AMR | PEL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | CDX | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG02165 | hp2 | a0001 | c0001 | t0003 | g0083 | EAS | CDX | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG02258 | hp1 | a0001 | c0001 | t0006 | g0282 | AFR | ACB | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | ACB | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG02280 | hp1 | a0001 | c0001 | t0014 | g0037 | AFR | ACB | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG02280 | hp2 | a0001 | c0001 | t0003 | g0112 | AFR | ACB | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG02293 | hp1 | a0001 | c0004 | t0003 | g0067 | AMR | PEL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG02300 | hp1 | a0001 | c0001 | t0003 | g0107 | AMR | PEL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PEL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG02451 | hp1 | a0001 | c0001 | t0003 | g0078 | AFR | ACB | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG02451 | hp2 | a0001 | c0001 | t0003 | g0091 | AFR | ACB | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG02615 | hp2 | a0001 | c0001 | t0003 | g0071 | AFR | GWD | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG02622 | hp1 | a0001 | c0001 | t0003 | g0038 | AFR | GWD | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG02622 | hp2 | a0001 | c0001 | t0004 | g0003 | AFR | GWD | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0279 | AFR | GWD | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG02630 | hp2 | a0001 | c0001 | t0004 | g0125 | AFR | GWD | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG02647 | hp1 | a0001 | c0001 | t0004 | g0003 | AFR | GWD | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG02647 | hp2 | a0001 | c0001 | t0003 | g0036 | AFR | GWD | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG02683 | hp1 | a0001 | c0002 | t0002 | g0258 | SAS | PJL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG02683 | hp2 | a0001 | c0003 | t0001 | g0050 | SAS | PJL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG02698 | hp1 | a0001 | c0001 | t0003 | g0117 | SAS | PJL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG02809 | hp1 | a0001 | c0001 | t0003 | g0070 | AFR | GWD | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG02809 | hp2 | a0001 | c0001 | t0003 | g0040 | AFR | GWD | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG02818 | hp1 | a0001 | c0001 | t0003 | g0104 | AFR | GWD | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG02886 | hp1 | a0001 | c0002 | t0002 | g0248 | AFR | GWD | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | GWD | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | GWD | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | GWD | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | ESN | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG02922 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | ESN | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG02965 | hp1 | a0001 | c0001 | t0004 | g0003 | AFR | ESN | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG02965 | hp2 | a0001 | c0001 | t0006 | g0283 | AFR | ESN | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG02970 | hp1 | a0001 | c0001 | t0004 | g0035 | AFR | ESN | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG02970 | hp2 | a0001 | c0001 | t0003 | g0147 | AFR | ESN | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | ESN | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG02976 | hp2 | a0001 | c0001 | t0003 | g0039 | AFR | ESN | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG03017 | hp1 | a0001 | c0004 | t0003 | g0294 | SAS | PJL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG03017 | hp2 | a0001 | c0001 | t0005 | g0284 | SAS | PJL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG03041 | hp1 | a0001 | c0001 | t0004 | g0034 | AFR | GWD | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG03041 | hp2 | a0001 | c0002 | t0002 | g0244 | AFR | GWD | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG03130 | hp1 | a0001 | c0001 | t0003 | g0073 | AFR | ESN | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG03130 | hp2 | a0001 | c0001 | t0005 | g0290 | AFR | ESN | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | ESN | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG03139 | hp2 | a0001 | c0001 | t0003 | g0080 | AFR | ESN | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG03195 | hp1 | a0001 | c0002 | t0002 | g0245 | AFR | ESN | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | ESN | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | MSL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG03209 | hp2 | a0001 | c0001 | t0004 | g0003 | AFR | MSL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | MSL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG03225 | hp2 | a0001 | c0001 | t0007 | g0041 | AFR | MSL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG03239 | hp2 | a0001 | c0001 | t0004 | g0136 | SAS | PJL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG03453 | hp1 | a0001 | c0001 | t0004 | g0003 | AFR | MSL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG03453 | hp2 | a0001 | c0002 | t0002 | g0004 | AFR | MSL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | MSL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG03486 | hp2 | a0001 | c0002 | t0002 | g0265 | AFR | MSL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0271 | SAS | PJL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0202 | SAS | PJL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG03516 | hp1 | a0001 | c0001 | t0006 | g0281 | AFR | ESN | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | ESN | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG03540 | hp1 | a0001 | c0001 | t0003 | g0042 | AFR | GWD | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG03579 | hp1 | a0001 | c0001 | t0015 | g0298 | AFR | MSL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | MSL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG03654 | hp2 | a0001 | c0001 | t0005 | g0286 | SAS | PJL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG03669 | hp1 | a0001 | c0001 | t0004 | g0129 | SAS | PJL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG03688 | hp1 | a0001 | c0001 | t0003 | g0118 | SAS | STU | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0166 | SAS | STU | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG03704 | hp1 | a0001 | c0001 | t0021 | g0002 | SAS | PJL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG03704 | hp2 | a0001 | c0001 | t0005 | g0291 | SAS | PJL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0231 | SAS | BEB | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG03831 | hp2 | a0001 | c0002 | t0002 | g0011 | SAS | BEB | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG03942 | hp1 | a0001 | c0002 | t0002 | g0239 | SAS | BEB | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG03942 | hp2 | a0001 | c0001 | t0003 | g0109 | SAS | BEB | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG04115 | hp1 | a0001 | c0008 | t0002 | g0259 | SAS | STU | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0270 | SAS | STU | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | BEB | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG04184 | hp2 | a0001 | c0004 | t0003 | g0299 | SAS | BEB | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG04199 | hp1 | a0001 | c0002 | t0002 | g0234 | SAS | STU | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0141 | SAS | STU | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | STU | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG04204 | hp2 | a0001 | c0002 | t0002 | g0242 | SAS | STU | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG04228 | hp1 | a0001 | c0001 | t0003 | g0069 | SAS | STU | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | STU | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA18522 | hp1 | a0001 | c0001 | t0003 | g0079 | AFR | YRI | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA18522 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | YRI | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA18747 | hp1 | a0001 | c0001 | t0004 | g0143 | EAS | CHB | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA18747 | hp2 | a0001 | c0001 | t0003 | g0077 | EAS | CHB | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA18906 | hp1 | a0001 | c0002 | t0002 | g0246 | AFR | YRI | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA18906 | hp2 | a0001 | c0001 | t0004 | g0130 | AFR | YRI | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA18939 | hp1 | a0001 | c0001 | t0003 | g0100 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA18940 | hp2 | a0001 | c0002 | t0002 | g0229 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA18941 | hp2 | a0001 | c0001 | t0003 | g0110 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA18943 | hp1 | a0001 | c0002 | t0002 | g0261 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA18944 | hp2 | a0001 | c0003 | t0001 | g0012 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA18945 | hp1 | a0001 | c0001 | t0003 | g0102 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA18947 | hp1 | a0001 | c0001 | t0005 | g0027 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA18947 | hp2 | a0001 | c0001 | t0003 | g0096 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA18950 | hp1 | a0001 | c0003 | t0001 | g0044 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA18952 | hp2 | a0001 | c0001 | t0005 | g0292 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA18954 | hp1 | a0001 | c0001 | t0003 | g0111 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA18956 | hp1 | a0001 | c0002 | t0002 | g0256 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA18957 | hp2 | a0001 | c0003 | t0001 | g0062 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA18959 | hp2 | a0001 | c0001 | t0017 | g0093 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA18960 | hp2 | a0001 | c0002 | t0002 | g0011 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA18967 | hp1 | a0001 | c0001 | t0012 | g0153 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA18967 | hp2 | a0001 | c0001 | t0003 | g0222 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA18968 | hp1 | a0001 | c0003 | t0001 | g0061 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA18968 | hp2 | a0001 | c0002 | t0002 | g0254 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA18969 | hp2 | a0001 | c0001 | t0003 | g0081 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA18970 | hp1 | a0001 | c0001 | t0003 | g0089 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA18971 | hp1 | a0001 | c0001 | t0005 | g0287 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA18971 | hp2 | a0001 | c0001 | t0016 | g0205 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA18972 | hp2 | a0001 | c0001 | t0003 | g0221 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA18973 | hp2 | a0001 | c0003 | t0001 | g0064 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA18974 | hp2 | a0001 | c0002 | t0002 | g0228 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA18979 | hp1 | a0001 | c0002 | t0002 | g0225 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA18979 | hp2 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA18981 | hp1 | a0001 | c0001 | t0004 | g0121 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA18981 | hp2 | a0001 | c0003 | t0001 | g0055 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA18982 | hp2 | a0001 | c0001 | t0003 | g0220 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA18983 | hp2 | a0001 | c0002 | t0002 | g0025 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA18986 | hp1 | a0001 | c0001 | t0003 | g0108 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA18986 | hp2 | a0002 | c0005 | t0002 | g0004 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA18988 | hp2 | a0001 | c0003 | t0001 | g0046 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA18990 | hp1 | a0001 | c0001 | t0005 | g0289 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA18992 | hp1 | a0001 | c0001 | t0003 | g0087 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA18993 | hp1 | a0001 | c0001 | t0022 | g0092 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA18994 | hp1 | a0001 | c0002 | t0002 | g0253 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA18998 | hp2 | a0001 | c0002 | t0002 | g0024 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA18999 | hp2 | a0001 | c0001 | t0003 | g0084 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA19000 | hp1 | a0001 | c0002 | t0002 | g0026 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA19001 | hp1 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA19001 | hp2 | a0001 | c0003 | t0001 | g0057 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA19002 | hp1 | a0001 | c0004 | t0003 | g0029 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA19002 | hp2 | a0001 | c0002 | t0002 | g0227 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA19003 | hp2 | a0001 | c0002 | t0002 | g0266 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA19004 | hp1 | a0001 | c0002 | t0002 | g0026 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA19004 | hp2 | a0001 | c0001 | t0005 | g0027 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA19006 | hp1 | a0001 | c0004 | t0003 | g0028 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA19006 | hp2 | a0001 | c0003 | t0001 | g0048 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA19007 | hp1 | a0001 | c0001 | t0003 | g0106 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA19007 | hp2 | a0001 | c0002 | t0002 | g0255 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA19009 | hp1 | a0001 | c0003 | t0001 | g0058 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA19009 | hp2 | a0001 | c0002 | t0002 | g0263 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA19010 | hp2 | a0001 | c0001 | t0003 | g0113 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA19030 | hp1 | a0001 | c0001 | t0011 | g0150 | AFR | LWK | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA19030 | hp2 | a0001 | c0001 | t0003 | g0148 | AFR | LWK | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA19043 | hp1 | a0001 | c0001 | t0003 | g0076 | AFR | LWK | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA19043 | hp2 | a0001 | c0001 | t0006 | g0280 | AFR | LWK | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA19054 | hp1 | a0001 | c0003 | t0001 | g0047 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA19056 | hp2 | a0001 | c0001 | t0003 | g0075 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA19057 | hp1 | a0001 | c0002 | t0002 | g0230 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA19058 | hp1 | a0001 | c0003 | t0001 | g0056 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA19058 | hp2 | a0001 | c0001 | t0003 | g0085 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA19060 | hp1 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA19062 | hp2 | a0001 | c0003 | t0001 | g0053 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA19063 | hp1 | a0003 | c0006 | t0001 | g0203 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA19063 | hp2 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA19064 | hp1 | a0001 | c0001 | t0003 | g0098 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA19065 | hp2 | a0001 | c0001 | t0003 | g0097 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA19067 | hp2 | a0001 | c0002 | t0002 | g0251 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0269 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA19074 | hp1 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA19074 | hp2 | a0001 | c0001 | t0003 | g0105 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA19075 | hp1 | a0001 | c0003 | t0001 | g0052 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA19077 | hp1 | a0001 | c0001 | t0003 | g0082 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA19077 | hp2 | a0001 | c0004 | t0003 | g0030 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA19078 | hp1 | a0001 | c0001 | t0003 | g0094 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA19079 | hp2 | a0001 | c0001 | t0003 | g0116 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA19082 | hp2 | a0001 | c0001 | t0003 | g0114 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA19083 | hp1 | a0001 | c0001 | t0005 | g0288 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA19084 | hp1 | a0001 | c0001 | t0004 | g0122 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA19085 | hp2 | a0001 | c0002 | t0002 | g0274 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA19086 | hp2 | a0001 | c0002 | t0002 | g0024 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA19087 | hp1 | a0001 | c0002 | t0002 | g0252 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA19088 | hp2 | a0001 | c0001 | t0003 | g0099 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA19089 | hp2 | a0001 | c0001 | t0008 | g0123 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA19091 | hp1 | a0001 | c0001 | t0003 | g0223 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA19240 | hp1 | a0001 | c0001 | t0004 | g0003 | AFR | YRI | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA19240 | hp2 | a0001 | c0001 | t0007 | g0007 | AFR | YRI | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA20129 | hp1 | a0001 | c0001 | t0005 | g0295 | AFR | ASW | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0232 | AFR | ASW | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0156 | EUR | TSI | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA20805 | hp2 | a0001 | c0002 | t0002 | g0010 | EUR | TSI | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA20905 | hp1 | a0001 | c0001 | t0003 | g0088 | SAS | GIH | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG01123 | hp1 | a0001 | c0002 | t0002 | g0004 | AMR | CLM | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG02109 | hp1 | a0001 | c0001 | t0004 | g0126 | AFR | ACB | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0275 | AFR | ACB | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG02486 | hp1 | a0001 | c0001 | t0004 | g0128 | AFR | ACB | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG02486 | hp2 | a0001 | c0001 | t0003 | g0115 | AFR | ACB | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | ACB | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG02559 | hp2 | a0001 | c0001 | t0004 | g0033 | AFR | ACB | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | MSL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | MSL | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA18955 | hp1 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA18955 | hp2 | a0001 | c0003 | t0001 | g0065 | EAS | JPT | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA20300 | hp1 | a0001 | c0002 | t0002 | g0247 | AFR | USA | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA20300 | hp2 | a0001 | c0001 | t0003 | g0103 | AFR | USA | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA21309 | hp1 | a0001 | c0002 | t0002 | g0010 | AFR | LWK | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
NA21309 | hp2 | a0001 | c0001 | t0002 | g0277 | AFR | LWK | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0022 | REF | REF | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0020 | g0285 | REF | REF | UBXN4_chr2_135736855_135790056 | UBXN4 | chr2 | 135736855 | 135790056 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:135769798
|
A | C | 1 | a0003 | 1 | NA19063.hp1 | missense_variant | MODERATE | c.632A>C | p.Glu211Ala | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 7/13 | 707/3771 | 632/1527 | 211/508 | chr2 | 135769798 | ||
chr2:135780371
|
C | G | 1 | a0002 | 2 | HG02074.hp2 NA18986.hp2 |
missense_variant | MODERATE | c.1374C>G | p.Ser458Arg | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 12/13 | 1449/3771 | 1374/1527 | 458/508 | chr2 | 135780371 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:135754247
|
A | G | 3 | a0001c0002a0001c0008a0002c0005 | 65 | HG00642.hp2 HG00673.hp2 HG00733.hp1 others(62): Show |
synonymous_variant | LOW | c.303A>G | p.Glu101Glu | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 4/13 | 378/3771 | 303/1527 | 101/508 | chr2 | 135754247 | ||
chr2:135754272
|
C | A | 1 | a0001c0003 | 25 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(22): Show |
synonymous_variant | LOW | c.328C>A | p.Arg110Arg | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 4/13 | 403/3771 | 328/1527 | 110/508 | chr2 | 135754272 | ||
chr2:135755609
|
C | T | 1 | a0001c0007 | 1 | HG00639.hp1 | synonymous_variant | LOW | c.426C>T | p.Asn142Asn | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/13 | 501/3771 | 426/1527 | 142/508 | chr2 | 135755609 | ||
chr2:135761846
|
C | G | 1 | a0001c0008 | 1 | HG04115.hp1 | synonymous_variant | LOW | c.537C>G | p.Ser179Ser | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/13 | 612/3771 | 537/1527 | 179/508 | chr2 | 135761846 | ||
chr2:135780341
|
G | A | 1 | a0001c0004 | 8 | HG01358.hp1 HG01993.hp1 HG02293.hp1 others(5): Show |
synonymous_variant | LOW | c.1344G>A | p.Ser448Ser | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 12/13 | 1419/3771 | 1344/1527 | 448/508 | chr2 | 135780341 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:135741872
|
C | T | 1 | a0001c0001t0022 | 1 | NA18993.hp1 | 5_prime_UTR_variant | MODIFIER | c.-58C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/13 | 58 | chr2 | 135741872 | |||||
chr2:135741879
|
C | T | 1 | a0001c0001t0021 | 1 | HG03704.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-51C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/13 | chr2 | 135741879 | ||||||
chr2:135741888
|
G | A | 4 | a0001c0001t0004a0001c0001t0008a0001c0001t0009others(1): Show | 28 | HG00558.hp2 HG00621.hp1 HG00639.hp2 others(25): Show |
5_prime_UTR_variant | MODIFIER | c.-42G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/13 | 42 | chr2 | 135741888 | |||||
chr2:135783082
|
C | G | 1 | a0001c0001t0010 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*195C>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 13/13 | 195 | chr2 | 135783082 | |||||
chr2:135783342
|
T | C | 1 | a0001c0001t0011 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*455T>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 13/13 | 455 | chr2 | 135783342 | |||||
chr2:135783439
|
T | C | 1 | a0001c0001t0006 | 4 | HG02258.hp1 HG02965.hp2 HG03516.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*552T>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 13/13 | 552 | chr2 | 135783439 | |||||
chr2:135783491
|
AT | A | 18 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(15): Show | 271 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(268): Show |
3_prime_UTR_variant | MODIFIER | c.*615delT | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 13/13 | 615 | INFO_REALIGN_3_PRIME | chr2 | 135783491 | ||||
chr2:135783543
|
C | T | 1 | a0001c0001t0009 | 1 | HG00558.hp2 | 3_prime_UTR_variant | MODIFIER | c.*656C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 13/13 | 656 | chr2 | 135783543 | |||||
chr2:135783546
|
G | C | 1 | a0001c0001t0012 | 1 | NA18967.hp1 | 3_prime_UTR_variant | MODIFIER | c.*659G>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 13/13 | 659 | chr2 | 135783546 | |||||
chr2:135783644
|
G | A | 1 | a0001c0001t0013 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*757G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 13/13 | 757 | chr2 | 135783644 | |||||
chr2:135783885
|
A | G | 1 | a0001c0001t0016 | 1 | NA18971.hp2 | 3_prime_UTR_variant | MODIFIER | c.*998A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 13/13 | 998 | chr2 | 135783885 | |||||
chr2:135784017
|
TTC | T | 7 | a0001c0001t0003a0001c0001t0007a0001c0001t0013others(4): Show | 79 | HG01261.hp2 HG01346.hp1 HG01358.hp1 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*1132_*1133delCT | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 13/13 | 1132 | INFO_REALIGN_3_PRIME | chr2 | 135784017 | ||||
chr2:135784284
|
T | C | 1 | a0001c0001t0015 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1397T>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 13/13 | 1397 | chr2 | 135784284 | |||||
chr2:135784374
|
A | G | 1 | a0001c0001t0007 | 2 | HG03225.hp2 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1487A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 13/13 | 1487 | chr2 | 135784374 | |||||
chr2:135784464
|
T | C | 1 | a0001c0001t0014 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1577T>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 13/13 | 1577 | chr2 | 135784464 | |||||
chr2:135784824
|
G | T | 1 | a0001c0001t0008 | 1 | NA19089.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1937G>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 13/13 | 1937 | chr2 | 135784824 | |||||
chr2:135784857
|
T | TA | 27 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(24): Show | 369 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(366): Show |
3_prime_UTR_variant | MODIFIER | c.*1974dupA | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 13/13 | 1975 | INFO_REALIGN_3_PRIME | chr2 | 135784857 | ||||
chr2:135784989
|
G | A | 6 | a0001c0001t0002a0001c0002t0002a0001c0002t0018others(3): Show | 82 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*2102G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 13/13 | 2102 | chr2 | 135784989 | |||||
chr2:135784990
|
A | G | 6 | a0001c0001t0002a0001c0002t0002a0001c0002t0018others(3): Show | 82 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*2103A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 13/13 | 2103 | chr2 | 135784990 | |||||
chr2:135785003
|
G | A | 1 | a0001c0002t0018 | 1 | HG01358.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2116G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 13/13 | 2116 | chr2 | 135785003 | |||||
chr2:135785019
|
G | A | 1 | a0001c0007t0019 | 1 | HG00639.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2132G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 13/13 | 2132 | chr2 | 135785019 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:135742031
|
G | C | 3 | a0001c0004t0003g0028a0001c0004t0003g0029a0001c0004t0003g0030 | 3 | NA19002.hp1 NA19006.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.82+20G>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135742031 | ||||||
chr2:135742090
|
G | T | 1 | a0001c0004t0003g0299 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.82+79G>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135742090 | ||||||
chr2:135742184
|
C | G | 1 | a0001c0001t0015g0298 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.82+173C>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135742184 | ||||||
chr2:135742228
|
G | T | 1 | a0001c0001t0003g0297 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.82+217G>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135742228 | ||||||
chr2:135742237
|
G | T | 1 | a0001c0001t0001g0296 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.82+226G>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135742237 | ||||||
chr2:135742300
|
C | T | 1 | a0001c0001t0005g0295 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.82+289C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135742300 | ||||||
chr2:135742326
|
C | T | 1 | a0001c0004t0003g0294 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.82+315C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135742326 | ||||||
chr2:135742653
|
G | C | 1 | a0001c0001t0001g0031 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.82+642G>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135742653 | ||||||
chr2:135742728
|
A | G | 1 | a0001c0003t0001g0293 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.82+717A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135742728 | ||||||
chr2:135742768
|
T | A | 288 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(285): Show | 354 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(351): Show |
intron_variant | MODIFIER | c.82+757T>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135742768 | ||||||
chr2:135742905
|
A | G | 66 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0278others(63): Show | 85 | HG00280.hp1 HG00642.hp2 HG00673.hp2 others(82): Show |
intron_variant | MODIFIER | c.82+894A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135742905 | ||||||
chr2:135742938
|
T | A | 1 | a0001c0001t0004g0032 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.82+927T>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135742938 | ||||||
chr2:135742939
|
C | G | 1 | a0001c0001t0001g0224 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.82+928C>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135742939 | ||||||
chr2:135743027
|
A | T | 288 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(285): Show | 354 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(351): Show |
intron_variant | MODIFIER | c.82+1016A>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135743027 | ||||||
chr2:135743107
|
G | A | 3 | a0001c0001t0004g0033a0001c0001t0004g0034a0001c0001t0004g0035 | 3 | HG02559.hp2 HG02970.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.82+1096G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135743107 | ||||||
chr2:135743339
|
C | T | 4 | a0001c0001t0003g0220a0001c0001t0003g0221a0001c0001t0003g0222others(1): Show | 4 | NA18967.hp2 NA18972.hp2 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.82+1328C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135743339 | ||||||
chr2:135743725
|
G | A | 1 | a0001c0002t0002g0225 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.82+1714G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135743725 | ||||||
chr2:135743863
|
G | GTA | 88 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(85): Show | 125 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.82+1863_82+1864dup others(2): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 135743863 | |||||
chr2:135743939
|
T | G | 61 | a0001c0001t0002g0005a0001c0001t0002g0226a0001c0001t0002g0231others(58): Show | 80 | HG00280.hp1 HG00642.hp2 HG00673.hp2 others(77): Show |
intron_variant | MODIFIER | c.82+1928T>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135743939 | ||||||
chr2:135744091
|
C | T | 4 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0146others(1): Show | 4 | HG02896.hp2 HG02897.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.82+2080C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135744091 | ||||||
chr2:135744117
|
C | G | 2 | a0001c0004t0003g0294a0001c0004t0003g0299 | 2 | HG03017.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.82+2106C>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135744117 | ||||||
chr2:135744270
|
A | G | 117 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(114): Show | 160 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(157): Show |
intron_variant | MODIFIER | c.82+2259A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135744270 | ||||||
chr2:135744362
|
A | G | 4 | a0001c0001t0001g0216a0001c0001t0001g0217a0001c0001t0001g0218others(1): Show | 4 | NA18945.hp2 NA18957.hp1 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.82+2351A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135744362 | ||||||
chr2:135744368
|
C | T | 1 | a0001c0001t0005g0292 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.82+2357C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135744368 | ||||||
chr2:135744374
|
A | G | 1 | a0001c0001t0001g0215 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.82+2363A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135744374 | ||||||
chr2:135744394
|
C | CAAATTAA others(1470): Show |
1 | a0001c0001t0001g0214 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.82+2400_82+2401ins others(1477): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 135744394 | |||||
chr2:135744394
|
C | CAAATTAA others(1471): Show |
1 | a0001c0001t0001g0213 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.82+2400_82+2401ins others(1478): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 135744394 | |||||
chr2:135744394
|
CAAATT | C | 66 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0003g0069others(63): Show | 68 | HG01261.hp2 HG01346.hp1 HG01358.hp1 others(65): Show |
intron_variant | MODIFIER | c.82+2386_82+2390del others(5): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 135744394 | |||||
chr2:135744460
|
A | G | 3 | a0001c0001t0001g0008a0001c0001t0001g0211a0001c0001t0001g0212 | 5 | HG00621.hp2 NA18983.hp1 NA19060.hp2 others(2): Show |
intron_variant | MODIFIER | c.82+2449A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135744460 | ||||||
chr2:135744610
|
T | C | 8 | a0001c0004t0003g0028a0001c0004t0003g0029a0001c0004t0003g0030others(5): Show | 8 | HG01358.hp1 HG01993.hp1 HG02293.hp1 others(5): Show |
intron_variant | MODIFIER | c.82+2599T>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135744610 | ||||||
chr2:135744625
|
A | ATT | 24 | a0001c0003t0001g0012a0001c0003t0001g0044a0001c0003t0001g0045others(21): Show | 25 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.82+2616_82+2617dup others(2): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 135744625 | |||||
chr2:135744629
|
A | T | 288 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(285): Show | 354 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(351): Show |
intron_variant | MODIFIER | c.82+2618A>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135744629 | ||||||
chr2:135744725
|
G | A | 1 | a0001c0001t0001g0149 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.82+2714G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135744725 | ||||||
chr2:135745050
|
G | C | 1 | a0001c0001t0004g0119 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.82+3039G>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135745050 | ||||||
chr2:135745058
|
C | G | 2 | a0001c0001t0003g0147a0001c0001t0003g0148 | 2 | HG02970.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.82+3047C>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135745058 | ||||||
chr2:135745103
|
G | A | 4 | a0001c0001t0006g0280a0001c0001t0006g0281a0001c0001t0006g0282others(1): Show | 4 | HG02258.hp1 HG02965.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.82+3092G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135745103 | ||||||
chr2:135745204
|
G | A | 1 | a0001c0001t0004g0033 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.83-3063G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135745204 | ||||||
chr2:135745222
|
C | G | 84 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(81): Show | 121 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.83-3045C>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135745222 | ||||||
chr2:135745549
|
A | G | 1 | a0001c0002t0002g0274 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.83-2718A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135745549 | ||||||
chr2:135745587
|
A | G | 84 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(81): Show | 121 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.83-2680A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135745587 | ||||||
chr2:135745748
|
G | T | 1 | a0001c0001t0004g0143 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.83-2519G>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135745748 | ||||||
chr2:135745818
|
CTAATGGA others(7): Show |
C | 3 | a0001c0001t0001g0023a0001c0001t0001g0209a0001c0001t0001g0210 | 4 | HG00673.hp1 HG01993.hp2 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.83-2436_83-2423del others(14): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 135745818 | |||||
chr2:135745875
|
C | CTT | 46 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0278others(43): Show | 59 | HG00639.hp1 HG00642.hp2 HG00673.hp2 others(56): Show |
intron_variant | MODIFIER | c.83-2372_83-2371dup others(2): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 135745875 | |||||
chr2:135745875
|
C | CTTT | 7 | a0001c0002t0002g0011a0001c0002t0002g0225a0001c0002t0002g0262others(4): Show | 9 | HG01175.hp2 HG02080.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.83-2373_83-2371dup others(3): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 135745875 | |||||
chr2:135745875
|
C | CTTTTTTT others(1): Show |
64 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0151others(61): Show | 70 | HG00280.hp1 HG01256.hp1 HG01433.hp1 others(67): Show |
intron_variant | MODIFIER | c.83-2378_83-2371dup others(8): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 135745875 | |||||
chr2:135745875
|
C | CTTTTTTT others(2): Show |
89 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(86): Show | 130 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.83-2379_83-2371dup others(9): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 135745875 | |||||
chr2:135745875
|
C | CTTTTTTT others(3): Show |
26 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0135others(23): Show | 28 | HG00621.hp1 HG00639.hp2 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.83-2380_83-2371dup others(10): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 135745875 | |||||
chr2:135745875
|
C | CTTTTTTT others(4): Show |
23 | a0001c0001t0001g0204a0001c0001t0001g0206a0001c0001t0001g0207others(20): Show | 24 | HG00408.hp2 HG00544.hp1 HG01192.hp1 others(21): Show |
intron_variant | MODIFIER | c.83-2381_83-2371dup others(11): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 135745875 | |||||
chr2:135745875
|
C | CTTTTTTT others(5): Show |
4 | a0001c0001t0004g0119a0001c0003t0001g0063a0001c0003t0001g0064others(1): Show | 4 | HG00558.hp1 HG01243.hp2 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.83-2382_83-2371dup others(12): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 135745875 | |||||
chr2:135745875
|
C | CTTTTTTT others(7): Show |
1 | a0001c0001t0001g0139 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.83-2384_83-2371dup others(14): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 135745875 | |||||
chr2:135745875
|
C | CTTTTTTT others(10): Show |
1 | a0001c0001t0001g0140 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.83-2387_83-2371dup others(17): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 135745875 | |||||
chr2:135745875
|
C | CTTTTTTT others(11): Show |
2 | a0001c0001t0001g0141a0001c0001t0001g0142 | 2 | HG03654.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.83-2388_83-2371dup others(18): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 135745875 | |||||
chr2:135745875
|
CTTT | C | 13 | a0001c0001t0001g0154a0001c0001t0003g0007a0001c0001t0003g0036others(10): Show | 14 | HG00738.hp2 HG02055.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.83-2373_83-2371del others(3): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 135745875 | |||||
chr2:135745998
|
C | T | 2 | a0001c0001t0001g0151a0001c0001t0001g0152 | 2 | HG02615.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.83-2269C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135745998 | ||||||
chr2:135746034
|
C | T | 1 | a0001c0001t0004g0033 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.83-2233C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135746034 | ||||||
chr2:135746161
|
G | A | 1 | a0001c0003t0001g0063 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.83-2106G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135746161 | ||||||
chr2:135746531
|
A | C | 60 | a0001c0001t0002g0005a0001c0001t0002g0226a0001c0001t0002g0231others(57): Show | 79 | HG00280.hp1 HG00642.hp2 HG00673.hp2 others(76): Show |
intron_variant | MODIFIER | c.83-1736A>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135746531 | ||||||
chr2:135746579
|
C | T | 1 | a0001c0001t0001g0145 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.83-1688C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135746579 | ||||||
chr2:135746668
|
G | A | 1 | a0001c0003t0001g0048 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.83-1599G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135746668 | ||||||
chr2:135746882
|
C | CT | 66 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0278others(63): Show | 85 | HG00280.hp1 HG00642.hp2 HG00673.hp2 others(82): Show |
intron_variant | MODIFIER | c.83-1374dupT | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 135746882 | |||||
chr2:135746882
|
CT | C | 8 | a0001c0004t0003g0028a0001c0004t0003g0029a0001c0004t0003g0030others(5): Show | 8 | HG01358.hp1 HG01993.hp1 HG02293.hp1 others(5): Show |
intron_variant | MODIFIER | c.83-1374delT | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 135746882 | |||||
chr2:135746993
|
TTAG | T | 3 | a0001c0001t0001g0022a0001c0001t0001g0202a0001c0001t0001g0208 | 4 | HG00733.hp2 HG01192.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.83-1269_83-1267del others(3): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 135746993 | |||||
chr2:135747158
|
C | T | 4 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0146others(1): Show | 4 | HG02896.hp2 HG02897.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.83-1109C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135747158 | ||||||
chr2:135747191
|
CA | C | 220 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(217): Show | 267 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(264): Show |
intron_variant | MODIFIER | c.83-1069delA | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 135747191 | |||||
chr2:135747284
|
A | G | 1 | a0001c0001t0004g0119 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.83-983A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135747284 | ||||||
chr2:135747290
|
A | G | 1 | a0001c0003t0001g0293 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.83-977A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135747290 | ||||||
chr2:135747348
|
CA | C | 87 | a0001c0001t0001g0276a0001c0001t0001g0278a0001c0001t0001g0279others(84): Show | 107 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.83-895delA | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 135747348 | |||||
chr2:135747348
|
CAA | C | 19 | a0001c0001t0001g0015a0001c0001t0001g0159a0001c0001t0001g0160others(16): Show | 21 | HG00423.hp1 HG00558.hp2 HG01515.hp1 others(18): Show |
intron_variant | MODIFIER | c.83-896_83-895delAA | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 135747348 | |||||
chr2:135747348
|
CAAA | C | 30 | a0001c0001t0001g0016a0001c0001t0001g0021a0001c0001t0001g0127others(27): Show | 38 | HG00621.hp1 HG00639.hp2 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.83-897_83-895delAA others(1): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 135747348 | |||||
chr2:135747348
|
CAAAA | C | 83 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(80): Show | 117 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(114): Show |
intron_variant | MODIFIER | c.83-898_83-895delAA others(2): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 135747348 | |||||
chr2:135747348
|
CAAAAA | C | 65 | a0001c0001t0001g0193a0001c0001t0003g0013a0001c0001t0003g0014others(62): Show | 67 | HG01261.hp2 HG01346.hp1 HG01358.hp1 others(64): Show |
intron_variant | MODIFIER | c.83-899_83-895delAA others(3): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 135747348 | |||||
chr2:135747348
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0002t0002g0261 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.83-906_83-895delAA others(10): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 135747348 | |||||
chr2:135747398
|
G | A | 2 | a0001c0003t0001g0049a0001c0003t0001g0293 | 2 | HG01255.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.83-869G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135747398 | ||||||
chr2:135747693
|
G | A | 2 | a0001c0001t0001g0213a0001c0001t0001g0214 | 2 | HG02559.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.83-574G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135747693 | ||||||
chr2:135747701
|
C | G | 1 | a0001c0001t0001g0275 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.83-566C>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135747701 | ||||||
chr2:135747754
|
C | A | 2 | a0001c0001t0001g0151a0001c0001t0001g0152 | 2 | HG02615.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.83-513C>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135747754 | ||||||
chr2:135747833
|
C | T | 24 | a0001c0003t0001g0012a0001c0003t0001g0044a0001c0003t0001g0045others(21): Show | 25 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.83-434C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135747833 | ||||||
chr2:135747868
|
G | A | 10 | a0001c0001t0003g0007a0001c0001t0003g0036a0001c0001t0003g0038others(7): Show | 11 | HG02055.hp2 HG02280.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.83-399G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135747868 | ||||||
chr2:135747894
|
T | A | 1 | a0001c0002t0002g0262 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.83-373T>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135747894 | ||||||
chr2:135747972
|
G | A | 2 | a0001c0001t0001g0151a0001c0001t0001g0152 | 2 | HG02615.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.83-295G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135747972 | ||||||
chr2:135747976
|
C | T | 140 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(137): Show | 184 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(181): Show |
intron_variant | MODIFIER | c.83-291C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135747976 | ||||||
chr2:135748233
|
A | G | 3 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0192 | 3 | NA18939.hp2 NA18941.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.83-34A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 1/12 | chr2 | 135748233 | ||||||
chr2:135748510
|
G | A | 1 | a0001c0001t0001g0276 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.185+141G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135748510 | ||||||
chr2:135748566
|
T | G | 1 | a0001c0001t0003g0077 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.185+197T>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135748566 | ||||||
chr2:135748724
|
CA | C | 135 | a0001c0001t0001g0127a0001c0001t0001g0135a0001c0001t0001g0137others(132): Show | 145 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(142): Show |
intron_variant | MODIFIER | c.185+371delA | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 135748724 | |||||
chr2:135748724
|
CAA | C | 85 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(82): Show | 122 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.185+370_185+371del others(2): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 135748724 | |||||
chr2:135748805
|
G | A | 220 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(217): Show | 267 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(264): Show |
intron_variant | MODIFIER | c.185+436G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135748805 | ||||||
chr2:135749044
|
A | G | 1 | a0001c0001t0001g0189 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.185+675A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135749044 | ||||||
chr2:135749067
|
T | C | 2 | a0001c0001t0001g0144a0001c0001t0001g0146 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.185+698T>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135749067 | ||||||
chr2:135749357
|
A | C | 220 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(217): Show | 267 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(264): Show |
intron_variant | MODIFIER | c.185+988A>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135749357 | ||||||
chr2:135749425
|
G | A | 288 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(285): Show | 354 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(351): Show |
intron_variant | MODIFIER | c.185+1056G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135749425 | ||||||
chr2:135749469
|
A | G | 84 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(81): Show | 121 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.185+1100A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135749469 | ||||||
chr2:135749578
|
TCAC | T | 4 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0146others(1): Show | 4 | HG02896.hp2 HG02897.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.185+1210_185+1212d others(5): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135749578 | ||||||
chr2:135749633
|
A | AGTATTGT others(348): Show |
1 | a0001c0001t0011g0150 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.185+1280_185+1281i others(357): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 135749633 | |||||
chr2:135749796
|
G | A | 1 | a0001c0001t0005g0292 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.185+1427G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135749796 | ||||||
chr2:135749811
|
G | A | 1 | a0001c0001t0003g0036 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.185+1442G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135749811 | ||||||
chr2:135749864
|
A | T | 2 | a0001c0001t0003g0069a0001c0001t0003g0109 | 2 | HG03942.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.185+1495A>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135749864 | ||||||
chr2:135749946
|
A | G | 1 | a0001c0001t0002g0232 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.185+1577A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135749946 | ||||||
chr2:135749960
|
A | G | 1 | a0001c0001t0001g0145 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.185+1591A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135749960 | ||||||
chr2:135750195
|
A | C | 1 | a0001c0001t0001g0207 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.185+1826A>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135750195 | ||||||
chr2:135750234
|
A | G | 288 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(285): Show | 354 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(351): Show |
intron_variant | MODIFIER | c.185+1865A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135750234 | ||||||
chr2:135750249
|
C | T | 1 | a0001c0004t0003g0029 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.185+1880C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135750249 | ||||||
chr2:135750308
|
G | T | 4 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0146others(1): Show | 4 | HG02896.hp2 HG02897.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.185+1939G>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135750308 | ||||||
chr2:135750344
|
G | A | 1 | a0001c0001t0001g0163 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.185+1975G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135750344 | ||||||
chr2:135750429
|
C | T | 1 | a0001c0001t0011g0150 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.185+2060C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135750429 | ||||||
chr2:135750437
|
C | G | 1 | a0001c0001t0003g0069 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.185+2068C>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135750437 | ||||||
chr2:135750553
|
A | G | 2 | a0001c0001t0001g0188a0001c0001t0001g0206 | 2 | HG02886.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.185+2184A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135750553 | ||||||
chr2:135750693
|
CT | C | 19 | a0001c0001t0004g0003a0001c0001t0004g0032a0001c0001t0004g0119others(16): Show | 25 | HG00558.hp2 HG00621.hp1 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.185+2335delT | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 135750693 | |||||
chr2:135750802
|
T | A | 10 | a0001c0001t0003g0007a0001c0001t0003g0036a0001c0001t0003g0038others(7): Show | 11 | HG02055.hp2 HG02280.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.185+2433T>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135750802 | ||||||
chr2:135750835
|
C | CTT | 7 | a0001c0001t0003g0039a0001c0001t0003g0040a0001c0001t0003g0042others(4): Show | 7 | HG02055.hp2 HG02809.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.185+2503_185+2504d others(4): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 135750835 | |||||
chr2:135750835
|
C | CTTTT | 7 | a0001c0001t0006g0282a0001c0003t0001g0044a0001c0003t0001g0046others(4): Show | 7 | HG00408.hp2 HG02258.hp1 NA18950.hp1 others(4): Show |
intron_variant | MODIFIER | c.185+2501_185+2504d others(6): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 135750835 | |||||
chr2:135750835
|
C | CTTTTT | 6 | a0001c0003t0001g0047a0001c0003t0001g0049a0001c0003t0001g0055others(3): Show | 6 | HG01255.hp1 HG02148.hp2 NA18981.hp2 others(3): Show |
intron_variant | MODIFIER | c.185+2500_185+2504d others(7): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 135750835 | |||||
chr2:135750835
|
C | CTTTTTT | 5 | a0001c0003t0001g0012a0001c0003t0001g0048a0001c0003t0001g0058others(2): Show | 6 | HG02074.hp1 HG02129.hp1 NA18944.hp2 others(3): Show |
intron_variant | MODIFIER | c.185+2499_185+2504d others(8): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 135750835 | |||||
chr2:135750835
|
C | CTTTTTTT others(3): Show |
2 | a0001c0003t0001g0045a0001c0003t0001g0065 | 2 | HG00423.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.185+2495_185+2504d others(12): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 135750835 | |||||
chr2:135750835
|
C | CTTTTTTT others(4): Show |
1 | a0001c0003t0001g0063 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.185+2494_185+2504d others(13): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 135750835 | |||||
chr2:135750835
|
C | CTTTTTTT others(5): Show |
1 | a0001c0003t0001g0060 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.185+2493_185+2504d others(14): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 135750835 | |||||
chr2:135750835
|
C | CTTTTTTT others(14): Show |
1 | a0001c0003t0001g0061 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.185+2484_185+2504d others(23): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 135750835 | |||||
chr2:135750835
|
CT | C | 12 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0157others(9): Show | 12 | HG01261.hp2 HG02300.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.185+2504delT | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 135750835 | |||||
chr2:135750835
|
CTT | C | 10 | a0001c0001t0003g0072a0001c0001t0003g0073a0001c0001t0003g0100others(7): Show | 10 | HG01346.hp1 HG02056.hp2 HG02698.hp1 others(7): Show |
intron_variant | MODIFIER | c.185+2503_185+2504d others(4): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 135750835 | |||||
chr2:135750835
|
CTTT | C | 19 | a0001c0001t0001g0139a0001c0001t0003g0013a0001c0001t0003g0014others(16): Show | 21 | HG01433.hp2 HG01978.hp1 HG01981.hp1 others(18): Show |
intron_variant | MODIFIER | c.185+2502_185+2504d others(5): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 135750835 | |||||
chr2:135750835
|
CTTTT | C | 18 | a0001c0001t0001g0135a0001c0001t0001g0141a0001c0001t0001g0142others(15): Show | 18 | HG01952.hp2 HG02132.hp2 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.185+2501_185+2504d others(6): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 135750835 | |||||
chr2:135750835
|
CTTTTT | C | 16 | a0001c0001t0001g0127a0001c0001t0001g0137a0001c0001t0001g0138others(13): Show | 16 | HG01358.hp1 HG02165.hp2 HG02293.hp1 others(13): Show |
intron_variant | MODIFIER | c.185+2500_185+2504d others(7): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 135750835 | |||||
chr2:135750835
|
CTTTTTT | C | 7 | a0001c0001t0003g0078a0001c0001t0003g0079a0001c0001t0011g0150others(4): Show | 7 | HG01993.hp1 HG02451.hp1 HG03017.hp1 others(4): Show |
intron_variant | MODIFIER | c.185+2499_185+2504d others(8): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 135750835 | |||||
chr2:135750835
|
CTTTTTTT others(6): Show |
C | 14 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0154others(11): Show | 16 | HG00673.hp1 HG00738.hp2 HG01928.hp1 others(13): Show |
intron_variant | MODIFIER | c.185+2492_185+2504d others(15): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 135750835 | |||||
chr2:135750835
|
CTTTTTTT others(7): Show |
C | 62 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(59): Show | 97 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.185+2491_185+2504d others(16): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 135750835 | |||||
chr2:135750835
|
CTTTTTTT others(8): Show |
C | 2 | a0001c0001t0001g0190a0001c0001t0001g0217 | 2 | NA18957.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.185+2490_185+2504d others(17): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 135750835 | |||||
chr2:135750835
|
CTTTTTTT others(9): Show |
C | 3 | a0001c0001t0001g0155a0001c0001t0004g0126a0001c0001t0004g0134 | 3 | HG02109.hp1 HG02145.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.185+2489_185+2504d others(18): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 135750835 | |||||
chr2:135750835
|
CTTTTTTT others(10): Show |
C | 17 | a0001c0001t0004g0003a0001c0001t0004g0032a0001c0001t0004g0119others(14): Show | 23 | HG00558.hp2 HG00621.hp1 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.185+2488_185+2504d others(19): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 135750835 | |||||
chr2:135750835
|
CTTTTTTT others(13): Show |
C | 6 | a0001c0001t0002g0231a0001c0001t0002g0272a0001c0002t0002g0235others(3): Show | 6 | HG01255.hp2 HG01928.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.185+2485_185+2504d others(22): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 135750835 | |||||
chr2:135750835
|
CTTTTTTT others(14): Show |
C | 60 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0278others(57): Show | 79 | HG00280.hp1 HG00642.hp2 HG00673.hp2 others(76): Show |
intron_variant | MODIFIER | c.185+2484_185+2504d others(23): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 135750835 | |||||
chr2:135750925
|
G | A | 4 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(1): Show | 4 | HG01433.hp2 HG03491.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.185+2556G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135750925 | ||||||
chr2:135750925
|
G | T | 24 | a0001c0003t0001g0012a0001c0003t0001g0044a0001c0003t0001g0045others(21): Show | 25 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.185+2556G>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135750925 | ||||||
chr2:135751022
|
A | AT | 108 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(105): Show | 145 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.186-2501dupT | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 135751022 | |||||
chr2:135751074
|
C | T | 1 | a0001c0001t0003g0117 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.186-2465C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135751074 | ||||||
chr2:135751099
|
C | T | 1 | a0001c0001t0011g0150 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.186-2440C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135751099 | ||||||
chr2:135751249
|
T | G | 24 | a0001c0003t0001g0012a0001c0003t0001g0044a0001c0003t0001g0045others(21): Show | 25 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.186-2290T>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135751249 | ||||||
chr2:135751331
|
C | T | 24 | a0001c0003t0001g0012a0001c0003t0001g0044a0001c0003t0001g0045others(21): Show | 25 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.186-2208C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135751331 | ||||||
chr2:135751436
|
C | T | 1 | a0001c0001t0003g0042 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.186-2103C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135751436 | ||||||
chr2:135751477
|
C | T | 8 | a0001c0001t0005g0027a0001c0001t0005g0284a0001c0001t0005g0286others(5): Show | 9 | HG03017.hp2 HG03654.hp2 HG03704.hp2 others(6): Show |
intron_variant | MODIFIER | c.186-2062C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135751477 | ||||||
chr2:135751561
|
A | G | 3 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142 | 3 | HG03491.hp2 HG03654.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.186-1978A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135751561 | ||||||
chr2:135751616
|
C | T | 300 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(297): Show | 367 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(364): Show |
intron_variant | MODIFIER | c.186-1923C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135751616 | ||||||
chr2:135751652
|
T | A | 288 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(285): Show | 354 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(351): Show |
intron_variant | MODIFIER | c.186-1887T>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135751652 | ||||||
chr2:135751685
|
G | A | 24 | a0001c0003t0001g0012a0001c0003t0001g0044a0001c0003t0001g0045others(21): Show | 25 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.186-1854G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135751685 | ||||||
chr2:135751791
|
A | C | 8 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0146others(5): Show | 8 | HG02109.hp2 HG02630.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.186-1748A>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135751791 | ||||||
chr2:135751890
|
G | C | 26 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(23): Show | 32 | HG00558.hp2 HG00621.hp1 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.186-1649G>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135751890 | ||||||
chr2:135751900
|
C | T | 4 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(1): Show | 4 | HG01433.hp2 HG03491.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.186-1639C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135751900 | ||||||
chr2:135751997
|
A | G | 1 | a0001c0001t0003g0117 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.186-1542A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135751997 | ||||||
chr2:135752003
|
T | C | 86 | a0001c0001t0002g0005a0001c0001t0002g0226a0001c0001t0002g0231others(83): Show | 93 | HG00280.hp1 HG00741.hp1 HG01256.hp1 others(90): Show |
intron_variant | MODIFIER | c.186-1536T>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135752003 | ||||||
chr2:135752009
|
A | C | 1 | a0001c0001t0001g0182 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.186-1530A>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135752009 | ||||||
chr2:135752057
|
C | CT | 288 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(285): Show | 354 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(351): Show |
intron_variant | MODIFIER | c.186-1474dupT | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 135752057 | |||||
chr2:135752158
|
C | G | 1 | a0001c0007t0019g0043 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.186-1381C>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135752158 | ||||||
chr2:135752268
|
C | T | 3 | a0001c0001t0004g0033a0001c0001t0004g0034a0001c0001t0004g0035 | 3 | HG02559.hp2 HG02970.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.186-1271C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135752268 | ||||||
chr2:135752298
|
C | T | 62 | a0001c0001t0002g0005a0001c0001t0002g0226a0001c0001t0002g0231others(59): Show | 81 | HG00280.hp1 HG00642.hp2 HG00673.hp2 others(78): Show |
intron_variant | MODIFIER | c.186-1241C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135752298 | ||||||
chr2:135752385
|
T | C | 8 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0146others(5): Show | 8 | HG02109.hp2 HG02630.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.186-1154T>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135752385 | ||||||
chr2:135752442
|
T | G | 224 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(221): Show | 271 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(268): Show |
intron_variant | MODIFIER | c.186-1097T>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135752442 | ||||||
chr2:135752489
|
G | A | 8 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0146others(5): Show | 8 | HG02109.hp2 HG02630.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.186-1050G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135752489 | ||||||
chr2:135752521
|
T | G | 288 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(285): Show | 354 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(351): Show |
intron_variant | MODIFIER | c.186-1018T>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135752521 | ||||||
chr2:135752588
|
G | C | 8 | a0001c0001t0001g0127a0001c0001t0001g0135a0001c0001t0001g0137others(5): Show | 8 | HG01433.hp2 HG02818.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.186-951G>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135752588 | ||||||
chr2:135752643
|
T | C | 1 | a0001c0007t0019g0043 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.186-896T>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135752643 | ||||||
chr2:135752732
|
C | A | 40 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0003g0069others(37): Show | 42 | HG01346.hp1 HG01952.hp2 HG01978.hp1 others(39): Show |
intron_variant | MODIFIER | c.186-807C>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135752732 | ||||||
chr2:135752966
|
C | T | 1 | a0001c0001t0001g0160 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.186-573C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135752966 | ||||||
chr2:135753013
|
C | T | 1 | a0001c0001t0005g0295 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.186-526C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135753013 | ||||||
chr2:135753017
|
CT | C | 86 | a0001c0001t0001g0144a0001c0001t0001g0146a0001c0001t0001g0186others(83): Show | 89 | HG00639.hp1 HG01261.hp2 HG01346.hp1 others(86): Show |
intron_variant | MODIFIER | c.186-499delT | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 135753017 | |||||
chr2:135753017
|
CTT | C | 109 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(106): Show | 151 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.186-500_186-499del others(2): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 135753017 | |||||
chr2:135753017
|
CTTT | C | 23 | a0001c0001t0001g0018a0001c0001t0001g0156a0001c0001t0001g0191others(20): Show | 25 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.186-501_186-499del others(3): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 135753017 | |||||
chr2:135753243
|
C | T | 1 | a0001c0001t0002g0226 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.186-296C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135753243 | ||||||
chr2:135753300
|
A | G | 1 | a0001c0001t0001g0185 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.186-239A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 2/12 | chr2 | 135753300 | ||||||
chr2:135753721
|
AT | A | 65 | a0001c0001t0002g0005a0001c0001t0002g0226a0001c0001t0002g0231others(62): Show | 71 | HG00280.hp1 HG00741.hp1 HG01256.hp1 others(68): Show |
intron_variant | MODIFIER | c.214+155delT | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 3/12 | chr2 | 135753721 | ||||||
chr2:135753852
|
T | C | 1 | a0003c0006t0001g0203 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.214+285T>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 3/12 | chr2 | 135753852 | ||||||
chr2:135753852
|
TA | T | 7 | a0001c0001t0003g0075a0001c0001t0003g0089a0001c0001t0003g0096others(4): Show | 7 | NA18941.hp2 NA18945.hp1 NA18947.hp2 others(4): Show |
intron_variant | MODIFIER | c.214+286delA | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 3/12 | chr2 | 135753852 | ||||||
chr2:135753855
|
A | T | 7 | a0001c0001t0003g0075a0001c0001t0003g0089a0001c0001t0003g0096others(4): Show | 7 | NA18941.hp2 NA18945.hp1 NA18947.hp2 others(4): Show |
intron_variant | MODIFIER | c.214+288A>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 3/12 | chr2 | 135753855 | ||||||
chr2:135753925
|
A | T | 1 | a0001c0007t0019g0043 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.215-234A>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 3/12 | chr2 | 135753925 | ||||||
chr2:135753930
|
T | C | 1 | a0001c0001t0001g0145 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.215-229T>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 3/12 | chr2 | 135753930 | ||||||
chr2:135754005
|
A | G | 84 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(81): Show | 121 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.215-154A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 3/12 | chr2 | 135754005 | ||||||
chr2:135754047
|
G | T | 24 | a0001c0003t0001g0012a0001c0003t0001g0044a0001c0003t0001g0045others(21): Show | 25 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.215-112G>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 3/12 | chr2 | 135754047 | ||||||
chr2:135754304
|
C | T | 76 | a0001c0001t0003g0007a0001c0001t0003g0013a0001c0001t0003g0014others(73): Show | 79 | HG01261.hp2 HG01346.hp1 HG01358.hp1 others(76): Show |
intron_variant | MODIFIER | c.333+27C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 4/12 | chr2 | 135754304 | ||||||
chr2:135754316
|
G | A | 24 | a0001c0003t0001g0012a0001c0003t0001g0044a0001c0003t0001g0045others(21): Show | 25 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.333+39G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 4/12 | chr2 | 135754316 | ||||||
chr2:135754328
|
A | AT | 76 | a0001c0001t0002g0005a0001c0001t0002g0226a0001c0001t0002g0231others(73): Show | 82 | HG00280.hp1 HG00741.hp1 HG01256.hp1 others(79): Show |
intron_variant | MODIFIER | c.333+62dupT | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr2 | 135754328 | |||||
chr2:135754381
|
G | C | 86 | a0001c0001t0002g0005a0001c0001t0002g0226a0001c0001t0002g0231others(83): Show | 93 | HG00280.hp1 HG00741.hp1 HG01256.hp1 others(90): Show |
intron_variant | MODIFIER | c.333+104G>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 4/12 | chr2 | 135754381 | ||||||
chr2:135754453
|
G | A | 1 | a0001c0001t0006g0282 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.333+176G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 4/12 | chr2 | 135754453 | ||||||
chr2:135754565
|
T | G | 2 | a0001c0001t0011g0150a0001c0007t0019g0043 | 2 | HG00639.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.333+288T>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 4/12 | chr2 | 135754565 | ||||||
chr2:135754569
|
C | T | 1 | a0001c0001t0001g0195 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.333+292C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 4/12 | chr2 | 135754569 | ||||||
chr2:135754575
|
G | A | 5 | a0001c0001t0003g0103a0001c0001t0003g0112a0001c0001t0003g0115others(2): Show | 6 | HG02280.hp2 HG02486.hp2 NA18998.hp2 others(3): Show |
intron_variant | MODIFIER | c.333+298G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 4/12 | chr2 | 135754575 | ||||||
chr2:135754748
|
G | A | 3 | a0001c0001t0004g0033a0001c0001t0004g0034a0001c0001t0004g0035 | 3 | HG02559.hp2 HG02970.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.333+471G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 4/12 | chr2 | 135754748 | ||||||
chr2:135754765
|
C | T | 3 | a0001c0001t0003g0078a0001c0001t0003g0147a0001c0001t0003g0148 | 3 | HG02451.hp1 HG02970.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.333+488C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 4/12 | chr2 | 135754765 | ||||||
chr2:135754929
|
G | A | 1 | a0001c0007t0019g0043 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.334-588G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 4/12 | chr2 | 135754929 | ||||||
chr2:135754972
|
C | T | 1 | a0001c0001t0004g0133 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.334-545C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 4/12 | chr2 | 135754972 | ||||||
chr2:135754975
|
A | G | 288 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(285): Show | 354 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(351): Show |
intron_variant | MODIFIER | c.334-542A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 4/12 | chr2 | 135754975 | ||||||
chr2:135755013
|
A | G | 4 | a0001c0001t0006g0280a0001c0001t0006g0281a0001c0001t0006g0282others(1): Show | 4 | HG02258.hp1 HG02965.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.334-504A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 4/12 | chr2 | 135755013 | ||||||
chr2:135755031
|
G | A | 3 | a0001c0001t0003g0013a0001c0001t0003g0084a0001c0001t0003g0113 | 4 | NA18955.hp1 NA18999.hp2 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.334-486G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 4/12 | chr2 | 135755031 | ||||||
chr2:135755211
|
T | TAATCATT others(17): Show |
1 | a0001c0001t0001g0187 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.334-302_334-279dup others(24): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr2 | 135755211 | |||||
chr2:135755296
|
G | T | 1 | a0001c0001t0003g0077 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.334-221G>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 4/12 | chr2 | 135755296 | ||||||
chr2:135755363
|
A | T | 1 | a0001c0001t0002g0232 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.334-154A>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 4/12 | chr2 | 135755363 | ||||||
chr2:135755703
|
T | C | 1 | a0001c0001t0002g0232 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.508+12T>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135755703 | ||||||
chr2:135755721
|
A | G | 3 | a0001c0001t0006g0280a0001c0001t0006g0281a0001c0001t0006g0283 | 3 | HG02965.hp2 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.508+30A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135755721 | ||||||
chr2:135755739
|
C | T | 1 | a0001c0001t0002g0271 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.508+48C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135755739 | ||||||
chr2:135755920
|
T | C | 2 | a0001c0001t0001g0165a0001c0001t0001g0196 | 2 | HG02148.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.508+229T>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135755920 | ||||||
chr2:135755992
|
A | G | 1 | a0001c0001t0011g0150 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.508+301A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135755992 | ||||||
chr2:135756100
|
T | A | 50 | a0001c0002t0002g0004a0001c0002t0002g0006a0001c0002t0002g0009others(47): Show | 65 | HG00642.hp2 HG00673.hp2 HG00733.hp1 others(62): Show |
intron_variant | MODIFIER | c.508+409T>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135756100 | ||||||
chr2:135756131
|
A | AAAT | 8 | a0001c0001t0001g0127a0001c0001t0001g0135a0001c0001t0001g0137others(5): Show | 8 | HG01433.hp2 HG02818.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.508+442_508+444dup others(3): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 135756131 | |||||
chr2:135756504
|
A | T | 24 | a0001c0003t0001g0012a0001c0003t0001g0044a0001c0003t0001g0045others(21): Show | 25 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.508+813A>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135756504 | ||||||
chr2:135756594
|
G | A | 10 | a0001c0001t0003g0007a0001c0001t0003g0036a0001c0001t0003g0038others(7): Show | 11 | HG02055.hp2 HG02280.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.508+903G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135756594 | ||||||
chr2:135756881
|
C | T | 1 | a0001c0001t0015g0298 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.508+1190C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135756881 | ||||||
chr2:135757139
|
G | T | 66 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0003g0069others(63): Show | 68 | HG01261.hp2 HG01346.hp1 HG01358.hp1 others(65): Show |
intron_variant | MODIFIER | c.508+1448G>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135757139 | ||||||
chr2:135757276
|
C | T | 10 | a0001c0001t0003g0007a0001c0001t0003g0036a0001c0001t0003g0038others(7): Show | 11 | HG02055.hp2 HG02280.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.508+1585C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135757276 | ||||||
chr2:135757431
|
G | A | 1 | a0001c0001t0005g0290 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.508+1740G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135757431 | ||||||
chr2:135757496
|
T | C | 3 | a0001c0001t0005g0284a0001c0001t0005g0286a0001c0001t0005g0291 | 3 | HG03017.hp2 HG03654.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.508+1805T>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135757496 | ||||||
chr2:135757700
|
A | T | 2 | a0001c0001t0001g0151a0001c0001t0001g0152 | 2 | HG02615.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.508+2009A>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135757700 | ||||||
chr2:135757785
|
A | AT | 6 | a0001c0001t0001g0181a0001c0001t0001g0219a0001c0001t0003g0074others(3): Show | 6 | HG01261.hp2 HG02055.hp2 HG02074.hp2 others(3): Show |
intron_variant | MODIFIER | c.508+2109dupT | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 135757785 | |||||
chr2:135757785
|
A | T | 10 | a0001c0001t0003g0088a0001c0002t0002g0006a0001c0002t0002g0026others(7): Show | 14 | HG00738.hp1 HG01496.hp2 HG01943.hp1 others(11): Show |
intron_variant | MODIFIER | c.508+2094A>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135757785 | ||||||
chr2:135757888
|
G | A | 52 | a0001c0001t0002g0232a0001c0001t0002g0277a0001c0002t0002g0004others(49): Show | 67 | HG00642.hp2 HG00673.hp2 HG00733.hp1 others(64): Show |
intron_variant | MODIFIER | c.508+2197G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135757888 | ||||||
chr2:135757972
|
A | G | 1 | a0001c0001t0001g0142 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.508+2281A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135757972 | ||||||
chr2:135758014
|
A | G | 6 | a0001c0001t0001g0155a0001c0001t0001g0157a0001c0001t0001g0158others(3): Show | 6 | HG02895.hp1 HG02897.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.508+2323A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135758014 | ||||||
chr2:135758075
|
A | AT | 88 | a0001c0001t0001g0137a0001c0001t0001g0144a0001c0001t0001g0145others(85): Show | 95 | HG00280.hp1 HG00741.hp1 HG01256.hp1 others(92): Show |
intron_variant | MODIFIER | c.508+2400dupT | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 135758075 | |||||
chr2:135758075
|
A | ATT | 149 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(146): Show | 193 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(190): Show |
intron_variant | MODIFIER | c.508+2399_508+2400d others(4): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 135758075 | |||||
chr2:135758151
|
C | T | 30 | a0001c0001t0001g0127a0001c0001t0001g0135a0001c0001t0001g0137others(27): Show | 36 | HG00558.hp2 HG00621.hp1 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.508+2460C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135758151 | ||||||
chr2:135758231
|
T | C | 30 | a0001c0001t0001g0127a0001c0001t0001g0135a0001c0001t0001g0137others(27): Show | 36 | HG00558.hp2 HG00621.hp1 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.508+2540T>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135758231 | ||||||
chr2:135758289
|
G | A | 76 | a0001c0001t0002g0005a0001c0001t0002g0226a0001c0001t0002g0231others(73): Show | 82 | HG00280.hp1 HG00741.hp1 HG01256.hp1 others(79): Show |
intron_variant | MODIFIER | c.508+2598G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135758289 | ||||||
chr2:135758354
|
A | G | 76 | a0001c0001t0002g0005a0001c0001t0002g0226a0001c0001t0002g0231others(73): Show | 82 | HG00280.hp1 HG00741.hp1 HG01256.hp1 others(79): Show |
intron_variant | MODIFIER | c.508+2663A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135758354 | ||||||
chr2:135758366
|
G | A | 1 | a0001c0001t0003g0039 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.508+2675G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135758366 | ||||||
chr2:135758441
|
T | A | 19 | a0001c0001t0004g0003a0001c0001t0004g0032a0001c0001t0004g0119others(16): Show | 25 | HG00558.hp2 HG00621.hp1 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.508+2750T>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135758441 | ||||||
chr2:135758558
|
C | T | 296 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(293): Show | 363 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(360): Show |
intron_variant | MODIFIER | c.508+2867C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135758558 | ||||||
chr2:135758738
|
A | T | 66 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0003g0069others(63): Show | 68 | HG01261.hp2 HG01346.hp1 HG01358.hp1 others(65): Show |
intron_variant | MODIFIER | c.508+3047A>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135758738 | ||||||
chr2:135758764
|
A | ATTTTTTT others(29): Show |
1 | a0001c0001t0002g0231 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.509-3042_509-3041i others(38): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 135758764 | |||||
chr2:135758782
|
A | G | 1 | a0001c0001t0002g0231 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.509-3036A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135758782 | ||||||
chr2:135758806
|
T | C | 1 | a0001c0001t0003g0118 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.509-3012T>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135758806 | ||||||
chr2:135758808
|
C | T | 2 | a0001c0001t0001g0180a0001c0001t0001g0224 | 2 | HG02129.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.509-3010C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135758808 | ||||||
chr2:135758846
|
C | T | 7 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0146others(4): Show | 7 | HG02109.hp2 HG02630.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.509-2972C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135758846 | ||||||
chr2:135758903
|
C | T | 21 | a0001c0001t0004g0003a0001c0001t0004g0032a0001c0001t0004g0119others(18): Show | 27 | HG00558.hp2 HG00621.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.509-2915C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135758903 | ||||||
chr2:135758938
|
T | C | 1 | a0001c0001t0001g0183 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.509-2880T>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135758938 | ||||||
chr2:135758978
|
C | T | 1 | a0001c0001t0011g0150 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.509-2840C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135758978 | ||||||
chr2:135759178
|
A | T | 116 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(113): Show | 159 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.509-2640A>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135759178 | ||||||
chr2:135759190
|
A | G | 1 | a0001c0001t0001g0179 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.509-2628A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135759190 | ||||||
chr2:135759324
|
T | TA | 10 | a0001c0001t0003g0007a0001c0001t0003g0036a0001c0001t0003g0038others(7): Show | 11 | HG02055.hp2 HG02280.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.509-2492dupA | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 135759324 | |||||
chr2:135759400
|
G | A | 53 | a0001c0001t0002g0232a0001c0001t0002g0277a0001c0001t0004g0129others(50): Show | 68 | HG00642.hp2 HG00673.hp2 HG00733.hp1 others(65): Show |
intron_variant | MODIFIER | c.509-2418G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135759400 | ||||||
chr2:135759451
|
C | T | 1 | a0001c0001t0001g0184 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.509-2367C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135759451 | ||||||
chr2:135759577
|
G | C | 1 | a0001c0001t0001g0008 | 3 | HG00621.hp2 NA19060.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.509-2241G>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135759577 | ||||||
chr2:135759607
|
A | G | 10 | a0001c0001t0003g0007a0001c0001t0003g0036a0001c0001t0003g0038others(7): Show | 11 | HG02055.hp2 HG02280.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.509-2211A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135759607 | ||||||
chr2:135759621
|
G | A | 1 | a0001c0001t0001g0166 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.509-2197G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135759621 | ||||||
chr2:135759766
|
A | AT | 26 | a0001c0001t0001g0127a0001c0001t0001g0135a0001c0001t0001g0137others(23): Show | 26 | HG00639.hp1 HG00673.hp2 HG01256.hp1 others(23): Show |
intron_variant | MODIFIER | c.509-2030dupT | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 135759766 | |||||
chr2:135759766
|
A | ATT | 160 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0015others(157): Show | 204 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(201): Show |
intron_variant | MODIFIER | c.509-2031_509-2030d others(4): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 135759766 | |||||
chr2:135759766
|
A | ATTT | 30 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0020others(27): Show | 50 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.509-2032_509-2030d others(5): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 135759766 | |||||
chr2:135759766
|
ATT | A | 60 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0003g0069others(57): Show | 62 | HG01261.hp2 HG01346.hp1 HG01358.hp1 others(59): Show |
intron_variant | MODIFIER | c.509-2031_509-2030d others(4): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 135759766 | |||||
chr2:135759799
|
C | T | 23 | a0001c0003t0001g0012a0001c0003t0001g0044a0001c0003t0001g0045others(20): Show | 24 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(21): Show |
intron_variant | MODIFIER | c.509-2019C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135759799 | ||||||
chr2:135759901
|
C | T | 287 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(284): Show | 353 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(350): Show |
intron_variant | MODIFIER | c.509-1917C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135759901 | ||||||
chr2:135760062
|
C | A | 1 | a0001c0007t0019g0043 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.509-1756C>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135760062 | ||||||
chr2:135760122
|
C | T | 1 | a0001c0001t0001g0142 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.509-1696C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135760122 | ||||||
chr2:135760201
|
G | T | 1 | a0001c0003t0001g0059 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.509-1617G>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135760201 | ||||||
chr2:135760533
|
T | A | 86 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(83): Show | 123 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.509-1285T>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135760533 | ||||||
chr2:135760603
|
C | CA | 3 | a0001c0001t0001g0161a0001c0001t0001g0170a0001c0001t0001g0194 | 3 | NA18952.hp1 NA19070.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.509-1215_509-1214i others(3): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135760603 | ||||||
chr2:135760691
|
A | G | 3 | a0001c0001t0001g0127a0001c0001t0001g0137a0001c0001t0001g0138 | 3 | HG02896.hp1 HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.509-1127A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135760691 | ||||||
chr2:135761411
|
C | T | 1 | a0001c0001t0001g0177 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.509-407C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135761411 | ||||||
chr2:135761430
|
TG | T | 158 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(155): Show | 203 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(200): Show |
intron_variant | MODIFIER | c.509-386delG | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 135761430 | |||||
chr2:135761547
|
C | T | 1 | a0001c0001t0003g0088 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.509-271C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 5/12 | chr2 | 135761547 | ||||||
chr2:135761936
|
C | A | 5 | a0001c0001t0001g0171a0001c0001t0001g0172a0001c0001t0001g0190others(2): Show | 5 | NA18939.hp2 NA18941.hp1 NA18956.hp2 others(2): Show |
intron_variant | MODIFIER | c.602+25C>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135761936 | ||||||
chr2:135761937
|
A | G | 1 | a0001c0007t0019g0043 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.602+26A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135761937 | ||||||
chr2:135762143
|
C | A | 1 | a0001c0001t0003g0118 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.602+232C>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135762143 | ||||||
chr2:135762292
|
C | T | 54 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0003g0069others(51): Show | 56 | HG01261.hp2 HG01346.hp1 HG01952.hp2 others(53): Show |
intron_variant | MODIFIER | c.602+381C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135762292 | ||||||
chr2:135762473
|
C | T | 63 | a0001c0001t0001g0210a0001c0001t0002g0005a0001c0001t0002g0226others(60): Show | 82 | HG00280.hp1 HG00642.hp2 HG00673.hp1 others(79): Show |
intron_variant | MODIFIER | c.602+562C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135762473 | ||||||
chr2:135762487
|
A | G | 2 | a0001c0002t0002g0244a0001c0002t0002g0265 | 2 | HG03041.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.602+576A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135762487 | ||||||
chr2:135762530
|
T | A | 66 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0003g0069others(63): Show | 68 | HG01261.hp2 HG01346.hp1 HG01358.hp1 others(65): Show |
intron_variant | MODIFIER | c.602+619T>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135762530 | ||||||
chr2:135762531
|
A | T | 1 | a0001c0001t0012g0153 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.602+620A>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135762531 | ||||||
chr2:135762578
|
T | A | 3 | a0001c0001t0003g0078a0001c0001t0003g0147a0001c0001t0003g0148 | 3 | HG02451.hp1 HG02970.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.602+667T>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135762578 | ||||||
chr2:135762616
|
T | G | 76 | a0001c0001t0002g0005a0001c0001t0002g0226a0001c0001t0002g0231others(73): Show | 82 | HG00280.hp1 HG00741.hp1 HG01256.hp1 others(79): Show |
intron_variant | MODIFIER | c.602+705T>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135762616 | ||||||
chr2:135762625
|
G | A | 3 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142 | 3 | HG03491.hp2 HG03654.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.602+714G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135762625 | ||||||
chr2:135762648
|
TC | T | 8 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0146others(5): Show | 8 | HG02109.hp2 HG02630.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.602+738delC | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135762648 | ||||||
chr2:135762665
|
A | C | 2 | a0001c0003t0001g0046a0001c0003t0001g0056 | 2 | NA18988.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.602+754A>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135762665 | ||||||
chr2:135762735
|
G | A | 10 | a0001c0001t0003g0007a0001c0001t0003g0036a0001c0001t0003g0038others(7): Show | 11 | HG02055.hp2 HG02280.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.602+824G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135762735 | ||||||
chr2:135763134
|
C | T | 1 | a0001c0001t0003g0091 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.602+1223C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135763134 | ||||||
chr2:135763341
|
TACTA | T | 10 | a0001c0001t0003g0007a0001c0001t0003g0036a0001c0001t0003g0038others(7): Show | 11 | HG02055.hp2 HG02280.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.602+1431_602+1434d others(6): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135763341 | ||||||
chr2:135763669
|
T | A | 1 | a0001c0002t0002g0235 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.602+1758T>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135763669 | ||||||
chr2:135763671
|
C | A | 1 | a0001c0002t0002g0235 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.602+1760C>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135763671 | ||||||
chr2:135763673
|
A | G | 10 | a0001c0001t0003g0007a0001c0001t0003g0036a0001c0001t0003g0038others(7): Show | 11 | HG02055.hp2 HG02280.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.602+1762A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135763673 | ||||||
chr2:135763862
|
C | T | 1 | a0001c0001t0003g0076 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.602+1951C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135763862 | ||||||
chr2:135763925
|
G | A | 1 | a0001c0001t0003g0118 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.602+2014G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135763925 | ||||||
chr2:135763944
|
G | A | 75 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(72): Show | 112 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.602+2033G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135763944 | ||||||
chr2:135764025
|
G | A | 66 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0003g0069others(63): Show | 68 | HG01261.hp2 HG01346.hp1 HG01358.hp1 others(65): Show |
intron_variant | MODIFIER | c.602+2114G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135764025 | ||||||
chr2:135764128
|
TAAATA | T | 129 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(126): Show | 168 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(165): Show |
intron_variant | MODIFIER | c.602+2236_602+2240d others(7): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 135764128 | |||||
chr2:135764134
|
A | C | 5 | a0001c0001t0003g0075a0001c0001t0003g0089a0001c0001t0003g0096others(2): Show | 5 | NA18947.hp2 NA18970.hp1 NA19056.hp2 others(2): Show |
intron_variant | MODIFIER | c.602+2223A>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135764134 | ||||||
chr2:135764160
|
A | G | 2 | a0001c0003t0001g0051a0001c0003t0001g0063 | 2 | HG00558.hp1 HG02015.hp2 |
intron_variant | MODIFIER | c.602+2249A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135764160 | ||||||
chr2:135764218
|
G | C | 1 | a0001c0001t0004g0033 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.602+2307G>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135764218 | ||||||
chr2:135764293
|
C | G | 1 | a0001c0003t0001g0050 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.602+2382C>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135764293 | ||||||
chr2:135764431
|
A | T | 10 | a0001c0001t0003g0007a0001c0001t0003g0036a0001c0001t0003g0038others(7): Show | 11 | HG02055.hp2 HG02280.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.602+2520A>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135764431 | ||||||
chr2:135764465
|
A | G | 24 | a0001c0003t0001g0012a0001c0003t0001g0044a0001c0003t0001g0045others(21): Show | 25 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.602+2554A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135764465 | ||||||
chr2:135764564
|
A | G | 2 | a0001c0001t0001g0144a0001c0001t0001g0146 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.602+2653A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135764564 | ||||||
chr2:135764620
|
A | G | 1 | a0001c0001t0011g0150 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.602+2709A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135764620 | ||||||
chr2:135764726
|
G | A | 2 | a0001c0001t0003g0111a0001c0001t0022g0092 | 2 | NA18954.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.602+2815G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135764726 | ||||||
chr2:135764806
|
T | C | 2 | a0001c0001t0001g0151a0001c0001t0001g0152 | 2 | HG02615.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.602+2895T>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135764806 | ||||||
chr2:135764807
|
G | A | 288 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(285): Show | 354 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(351): Show |
intron_variant | MODIFIER | c.602+2896G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135764807 | ||||||
chr2:135764824
|
G | T | 8 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0146others(5): Show | 8 | HG02109.hp2 HG02630.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.602+2913G>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135764824 | ||||||
chr2:135765033
|
C | T | 1 | a0001c0003t0001g0050 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.602+3122C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135765033 | ||||||
chr2:135765067
|
GCTT | G | 4 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(1): Show | 4 | HG01433.hp2 HG03491.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.602+3161_602+3163d others(5): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 135765067 | |||||
chr2:135765087
|
T | G | 24 | a0001c0003t0001g0012a0001c0003t0001g0044a0001c0003t0001g0045others(21): Show | 25 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.602+3176T>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135765087 | ||||||
chr2:135765105
|
C | T | 85 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(82): Show | 122 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.602+3194C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135765105 | ||||||
chr2:135765140
|
A | G | 116 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(113): Show | 159 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.602+3229A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135765140 | ||||||
chr2:135765187
|
T | G | 1 | a0001c0001t0001g0166 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.602+3276T>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135765187 | ||||||
chr2:135765208
|
G | GT | 8 | a0001c0001t0001g0169a0001c0001t0004g0121a0001c0001t0004g0125others(5): Show | 8 | HG00408.hp2 HG00639.hp1 HG00673.hp2 others(5): Show |
intron_variant | MODIFIER | c.602+3311dupT | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 135765208 | |||||
chr2:135765213
|
T | G | 93 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0146others(90): Show | 100 | HG00280.hp1 HG00741.hp1 HG01256.hp1 others(97): Show |
intron_variant | MODIFIER | c.602+3302T>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135765213 | ||||||
chr2:135765222
|
T | C | 1 | a0001c0001t0002g0232 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.602+3311T>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135765222 | ||||||
chr2:135765254
|
A | G | 41 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0003g0069others(38): Show | 43 | HG01346.hp1 HG01952.hp2 HG01978.hp1 others(40): Show |
intron_variant | MODIFIER | c.602+3343A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135765254 | ||||||
chr2:135765370
|
C | T | 1 | a0001c0001t0003g0087 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.602+3459C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135765370 | ||||||
chr2:135765371
|
G | A | 79 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(76): Show | 116 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.602+3460G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135765371 | ||||||
chr2:135765433
|
A | G | 1 | a0001c0004t0003g0068 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.602+3522A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135765433 | ||||||
chr2:135765475
|
T | C | 66 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0003g0069others(63): Show | 68 | HG01261.hp2 HG01346.hp1 HG01358.hp1 others(65): Show |
intron_variant | MODIFIER | c.602+3564T>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135765475 | ||||||
chr2:135765487
|
G | A | 4 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(1): Show | 4 | HG01433.hp2 HG03491.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.602+3576G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135765487 | ||||||
chr2:135765648
|
CT | C | 10 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0146others(7): Show | 10 | HG02109.hp2 HG02630.hp1 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.602+3748delT | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 135765648 | |||||
chr2:135765711
|
C | A | 10 | a0001c0001t0003g0007a0001c0001t0003g0036a0001c0001t0003g0038others(7): Show | 11 | HG02055.hp2 HG02280.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.602+3800C>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135765711 | ||||||
chr2:135765780
|
G | A | 2 | a0001c0003t0001g0044a0001c0003t0001g0045 | 2 | HG00423.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.602+3869G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135765780 | ||||||
chr2:135765824
|
C | G | 1 | a0001c0001t0001g0199 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.602+3913C>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135765824 | ||||||
chr2:135766104
|
G | A | 1 | a0001c0002t0002g0227 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.603-3665G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135766104 | ||||||
chr2:135766126
|
G | C | 288 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(285): Show | 354 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(351): Show |
intron_variant | MODIFIER | c.603-3643G>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135766126 | ||||||
chr2:135766304
|
G | A | 288 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(285): Show | 354 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(351): Show |
intron_variant | MODIFIER | c.603-3465G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135766304 | ||||||
chr2:135766306
|
T | G | 1 | a0001c0007t0019g0043 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.603-3463T>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135766306 | ||||||
chr2:135766341
|
T | C | 8 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0146others(5): Show | 8 | HG02109.hp2 HG02630.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.603-3428T>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135766341 | ||||||
chr2:135766352
|
T | C | 1 | a0001c0001t0001g0135 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.603-3417T>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135766352 | ||||||
chr2:135766409
|
C | T | 7 | a0001c0002t0002g0010a0001c0002t0002g0235a0001c0002t0002g0242others(4): Show | 9 | HG00642.hp2 HG00733.hp1 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.603-3360C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135766409 | ||||||
chr2:135766653
|
G | A | 2 | a0001c0001t0001g0213a0001c0001t0001g0214 | 2 | HG02559.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.603-3116G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135766653 | ||||||
chr2:135766796
|
A | G | 2 | a0001c0002t0002g0247a0001c0002t0002g0248 | 2 | HG02886.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.603-2973A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135766796 | ||||||
chr2:135767177
|
A | G | 29 | a0001c0001t0001g0127a0001c0001t0001g0135a0001c0001t0001g0137others(26): Show | 35 | HG00558.hp2 HG00621.hp1 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.603-2592A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135767177 | ||||||
chr2:135767196
|
A | G | 76 | a0001c0001t0002g0005a0001c0001t0002g0226a0001c0001t0002g0231others(73): Show | 82 | HG00280.hp1 HG00741.hp1 HG01256.hp1 others(79): Show |
intron_variant | MODIFIER | c.603-2573A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135767196 | ||||||
chr2:135767520
|
T | C | 1 | a0001c0001t0001g0163 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.603-2249T>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135767520 | ||||||
chr2:135767739
|
G | T | 52 | a0001c0001t0002g0232a0001c0001t0002g0277a0001c0002t0002g0004others(49): Show | 67 | HG00642.hp2 HG00673.hp2 HG00733.hp1 others(64): Show |
intron_variant | MODIFIER | c.603-2030G>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135767739 | ||||||
chr2:135767893
|
A | G | 29 | a0001c0001t0001g0127a0001c0001t0001g0135a0001c0001t0001g0137others(26): Show | 35 | HG00558.hp2 HG00621.hp1 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.603-1876A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135767893 | ||||||
chr2:135768176
|
T | C | 2 | a0001c0001t0001g0151a0001c0001t0001g0152 | 2 | HG02615.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.603-1593T>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135768176 | ||||||
chr2:135768286
|
C | A | 2 | a0001c0002t0002g0009a0001c0002t0002g0260 | 4 | HG01069.hp1 HG01071.hp1 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.603-1483C>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135768286 | ||||||
chr2:135768290
|
C | T | 1 | a0001c0001t0011g0150 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.603-1479C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135768290 | ||||||
chr2:135768357
|
C | T | 1 | a0001c0001t0001g0215 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.603-1412C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135768357 | ||||||
chr2:135768511
|
T | G | 3 | a0001c0001t0003g0078a0001c0001t0003g0147a0001c0001t0003g0148 | 3 | HG02451.hp1 HG02970.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.603-1258T>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135768511 | ||||||
chr2:135768603
|
G | A | 24 | a0001c0003t0001g0012a0001c0003t0001g0044a0001c0003t0001g0045others(21): Show | 25 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.603-1166G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135768603 | ||||||
chr2:135768617
|
A | T | 2 | a0001c0001t0001g0151a0001c0001t0001g0152 | 2 | HG02615.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.603-1152A>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135768617 | ||||||
chr2:135768732
|
T | C | 8 | a0001c0001t0005g0027a0001c0001t0005g0284a0001c0001t0005g0286others(5): Show | 9 | HG03017.hp2 HG03654.hp2 HG03704.hp2 others(6): Show |
intron_variant | MODIFIER | c.603-1037T>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135768732 | ||||||
chr2:135768754
|
C | G | 288 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(285): Show | 354 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(351): Show |
intron_variant | MODIFIER | c.603-1015C>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135768754 | ||||||
chr2:135768861
|
C | A | 1 | a0001c0002t0002g0238 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.603-908C>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135768861 | ||||||
chr2:135768910
|
C | G | 1 | a0001c0001t0001g0159 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.603-859C>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135768910 | ||||||
chr2:135769041
|
C | T | 24 | a0001c0003t0001g0012a0001c0003t0001g0044a0001c0003t0001g0045others(21): Show | 25 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.603-728C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135769041 | ||||||
chr2:135769202
|
A | G | 8 | a0001c0001t0001g0127a0001c0001t0001g0135a0001c0001t0001g0137others(5): Show | 8 | HG01433.hp2 HG02818.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.603-567A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135769202 | ||||||
chr2:135769397
|
G | GT | 64 | a0001c0001t0002g0005a0001c0001t0002g0226a0001c0001t0002g0231others(61): Show | 83 | HG00280.hp1 HG00642.hp2 HG00673.hp2 others(80): Show |
intron_variant | MODIFIER | c.603-358dupT | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 135769397 | |||||
chr2:135769397
|
GT | G | 12 | a0001c0001t0001g0178a0001c0001t0003g0007a0001c0001t0003g0036others(9): Show | 13 | HG01257.hp1 HG02258.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.603-358delT | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 135769397 | |||||
chr2:135769411
|
T | A | 87 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(84): Show | 124 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.603-358T>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135769411 | ||||||
chr2:135769550
|
G | C | 62 | a0001c0001t0002g0005a0001c0001t0002g0226a0001c0001t0002g0231others(59): Show | 81 | HG00280.hp1 HG00642.hp2 HG00673.hp2 others(78): Show |
intron_variant | MODIFIER | c.603-219G>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135769550 | ||||||
chr2:135769748
|
G | T | 1 | a0001c0001t0005g0288 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.603-21G>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | chr2 | 135769748 | ||||||
chr2:135769748
|
GT | G | 25 | a0001c0001t0003g0075a0001c0003t0001g0012a0001c0003t0001g0044others(22): Show | 26 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(23): Show |
splice_region_variant&intron_variant | LOW | c.603-8delT | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 135769748 | |||||
chr2:135769873
|
G | GTGAT | 85 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(82): Show | 122 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.657+56_657+59dupGA others(2): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 135769873 | |||||
chr2:135770201
|
T | C | 3 | a0001c0004t0003g0028a0001c0004t0003g0029a0001c0004t0003g0030 | 3 | NA19002.hp1 NA19006.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.658-370T>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 7/12 | chr2 | 135770201 | ||||||
chr2:135770231
|
A | G | 8 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0146others(5): Show | 8 | HG02109.hp2 HG02630.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.658-340A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 7/12 | chr2 | 135770231 | ||||||
chr2:135770416
|
T | C | 2 | a0001c0003t0001g0012a0001c0003t0001g0059 | 3 | HG02074.hp1 HG02129.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.658-155T>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 7/12 | chr2 | 135770416 | ||||||
chr2:135770434
|
C | G | 140 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(137): Show | 184 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(181): Show |
intron_variant | MODIFIER | c.658-137C>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 7/12 | chr2 | 135770434 | ||||||
chr2:135770436
|
A | G | 288 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(285): Show | 354 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(351): Show |
intron_variant | MODIFIER | c.658-135A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 7/12 | chr2 | 135770436 | ||||||
chr2:135770464
|
C | A | 51 | a0001c0001t0002g0232a0001c0002t0002g0004a0001c0002t0002g0006others(48): Show | 66 | HG00642.hp2 HG00673.hp2 HG00733.hp1 others(63): Show |
intron_variant | MODIFIER | c.658-107C>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 7/12 | chr2 | 135770464 | ||||||
chr2:135770476
|
T | C | 1 | a0001c0001t0001g0204 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.658-95T>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 7/12 | chr2 | 135770476 | ||||||
chr2:135770489
|
A | G | 1 | a0001c0001t0001g0149 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.658-82A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 7/12 | chr2 | 135770489 | ||||||
chr2:135770787
|
G | A | 1 | a0001c0001t0001g0031 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.822+52G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 8/12 | chr2 | 135770787 | ||||||
chr2:135771021
|
T | TACTACTA others(23): Show |
13 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0142others(10): Show | 14 | HG02055.hp2 HG02280.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.822+308_822+337dup others(30): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 135771021 | |||||
chr2:135771199
|
G | A | 2 | a0001c0001t0003g0111a0001c0001t0022g0092 | 2 | NA18954.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.822+464G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 8/12 | chr2 | 135771199 | ||||||
chr2:135771386
|
G | T | 1 | a0001c0002t0002g0241 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.822+651G>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 8/12 | chr2 | 135771386 | ||||||
chr2:135771414
|
T | G | 24 | a0001c0003t0001g0012a0001c0003t0001g0044a0001c0003t0001g0045others(21): Show | 25 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.822+679T>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 8/12 | chr2 | 135771414 | ||||||
chr2:135771430
|
G | C | 288 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(285): Show | 354 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(351): Show |
intron_variant | MODIFIER | c.822+695G>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 8/12 | chr2 | 135771430 | ||||||
chr2:135771533
|
G | T | 1 | a0001c0001t0001g0160 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.822+798G>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 8/12 | chr2 | 135771533 | ||||||
chr2:135772116
|
A | G | 1 | a0001c0001t0005g0284 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.823-304A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 8/12 | chr2 | 135772116 | ||||||
chr2:135772183
|
A | G | 1 | a0001c0001t0001g0209 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.823-237A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 8/12 | chr2 | 135772183 | ||||||
chr2:135772283
|
A | G | 2 | a0001c0003t0001g0044a0001c0003t0001g0045 | 2 | HG00423.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.823-137A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 8/12 | chr2 | 135772283 | ||||||
chr2:135772323
|
T | G | 1 | a0001c0001t0014g0037 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.823-97T>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 8/12 | chr2 | 135772323 | ||||||
chr2:135772327
|
T | TA | 27 | a0001c0001t0001g0182a0001c0002t0002g0244a0001c0003t0001g0012others(24): Show | 28 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(25): Show |
intron_variant | MODIFIER | c.823-81dupA | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 135772327 | |||||
chr2:135772587
|
G | A | 24 | a0001c0003t0001g0012a0001c0003t0001g0044a0001c0003t0001g0045others(21): Show | 25 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.950+40G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | chr2 | 135772587 | ||||||
chr2:135772678
|
G | A | 76 | a0001c0001t0003g0007a0001c0001t0003g0013a0001c0001t0003g0014others(73): Show | 79 | HG01261.hp2 HG01346.hp1 HG01358.hp1 others(76): Show |
intron_variant | MODIFIER | c.950+131G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | chr2 | 135772678 | ||||||
chr2:135772694
|
C | G | 8 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0146others(5): Show | 8 | HG02109.hp2 HG02630.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.950+147C>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | chr2 | 135772694 | ||||||
chr2:135772717
|
A | G | 1 | a0001c0001t0001g0135 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.950+170A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | chr2 | 135772717 | ||||||
chr2:135772809
|
C | T | 64 | a0001c0001t0002g0005a0001c0001t0002g0226a0001c0001t0002g0231others(61): Show | 83 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(80): Show |
intron_variant | MODIFIER | c.950+262C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | chr2 | 135772809 | ||||||
chr2:135772821
|
G | A | 58 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0003g0069others(55): Show | 60 | HG01261.hp2 HG01346.hp1 HG01952.hp2 others(57): Show |
intron_variant | MODIFIER | c.950+274G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | chr2 | 135772821 | ||||||
chr2:135772873
|
C | T | 62 | a0001c0001t0002g0005a0001c0001t0002g0226a0001c0001t0002g0231others(59): Show | 81 | HG00280.hp1 HG00642.hp2 HG00673.hp2 others(78): Show |
intron_variant | MODIFIER | c.950+326C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | chr2 | 135772873 | ||||||
chr2:135772906
|
G | A | 8 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0146others(5): Show | 8 | HG02109.hp2 HG02630.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.950+359G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | chr2 | 135772906 | ||||||
chr2:135772910
|
G | A | 4 | a0001c0001t0001g0204a0001c0001t0001g0207a0001c0001t0016g0205others(1): Show | 4 | HG02040.hp1 NA18954.hp2 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.950+363G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | chr2 | 135772910 | ||||||
chr2:135772968
|
C | T | 1 | a0001c0001t0002g0232 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.950+421C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | chr2 | 135772968 | ||||||
chr2:135772986
|
G | A | 76 | a0001c0001t0003g0007a0001c0001t0003g0013a0001c0001t0003g0014others(73): Show | 79 | HG01261.hp2 HG01346.hp1 HG01358.hp1 others(76): Show |
intron_variant | MODIFIER | c.950+439G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | chr2 | 135772986 | ||||||
chr2:135773037
|
C | CA | 27 | a0001c0001t0001g0171a0001c0001t0001g0173a0001c0001t0001g0174others(24): Show | 28 | HG00544.hp2 HG01175.hp1 HG01978.hp2 others(25): Show |
intron_variant | MODIFIER | c.950+511dupA | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 135773037 | |||||
chr2:135773037
|
C | CAAA | 51 | a0001c0001t0002g0005a0001c0001t0002g0226a0001c0001t0002g0231others(48): Show | 68 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.950+509_950+511dup others(3): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 135773037 | |||||
chr2:135773037
|
C | CAAAA | 11 | a0001c0001t0002g0270a0001c0001t0011g0150a0001c0002t0002g0009others(8): Show | 13 | HG01069.hp1 HG01071.hp1 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.950+508_950+511dup others(4): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 135773037 | |||||
chr2:135773037
|
CA | C | 11 | a0001c0001t0001g0140a0001c0001t0001g0144a0001c0001t0001g0145others(8): Show | 11 | HG02109.hp2 HG02630.hp1 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.950+511delA | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 135773037 | |||||
chr2:135773038
|
A | C | 1 | a0001c0001t0003g0095 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.950+491A>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | chr2 | 135773038 | ||||||
chr2:135773045
|
A | G | 2 | a0001c0001t0001g0213a0001c0001t0001g0214 | 2 | HG02559.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.950+498A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | chr2 | 135773045 | ||||||
chr2:135773070
|
A | G | 1 | a0001c0001t0001g0193 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.950+523A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | chr2 | 135773070 | ||||||
chr2:135773169
|
C | T | 4 | a0001c0001t0006g0280a0001c0001t0006g0281a0001c0001t0006g0282others(1): Show | 4 | HG02258.hp1 HG02965.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.950+622C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | chr2 | 135773169 | ||||||
chr2:135773645
|
T | A | 1 | a0001c0001t0009g0120 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.950+1098T>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | chr2 | 135773645 | ||||||
chr2:135773649
|
G | A | 1 | a0001c0002t0002g0255 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.950+1102G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | chr2 | 135773649 | ||||||
chr2:135773657
|
A | C | 1 | a0001c0001t0001g0198 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.950+1110A>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | chr2 | 135773657 | ||||||
chr2:135773682
|
C | A | 76 | a0001c0001t0003g0007a0001c0001t0003g0013a0001c0001t0003g0014others(73): Show | 79 | HG01261.hp2 HG01346.hp1 HG01358.hp1 others(76): Show |
intron_variant | MODIFIER | c.950+1135C>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | chr2 | 135773682 | ||||||
chr2:135774233
|
G | C | 1 | a0001c0001t0001g0201 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.950+1686G>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | chr2 | 135774233 | ||||||
chr2:135774477
|
G | A | 1 | a0001c0001t0004g0033 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.951-1772G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | chr2 | 135774477 | ||||||
chr2:135774480
|
A | G | 2 | a0001c0001t0001g0151a0001c0001t0001g0152 | 2 | HG02615.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.951-1769A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | chr2 | 135774480 | ||||||
chr2:135774501
|
A | G | 2 | a0001c0002t0002g0253a0001c0002t0002g0254 | 2 | NA18968.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.951-1748A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | chr2 | 135774501 | ||||||
chr2:135774632
|
G | T | 1 | a0001c0002t0002g0025 | 2 | HG02083.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.951-1617G>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | chr2 | 135774632 | ||||||
chr2:135774655
|
G | A | 53 | a0001c0001t0002g0232a0001c0001t0002g0277a0001c0002t0002g0004others(50): Show | 68 | HG00639.hp1 HG00642.hp2 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.951-1594G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | chr2 | 135774655 | ||||||
chr2:135774674
|
G | A | 1 | a0001c0002t0002g0251 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.951-1575G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | chr2 | 135774674 | ||||||
chr2:135774801
|
C | T | 1 | a0001c0001t0001g0198 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.951-1448C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | chr2 | 135774801 | ||||||
chr2:135774824
|
G | A | 8 | a0001c0004t0003g0028a0001c0004t0003g0029a0001c0004t0003g0030others(5): Show | 8 | HG01358.hp1 HG01993.hp1 HG02293.hp1 others(5): Show |
intron_variant | MODIFIER | c.951-1425G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | chr2 | 135774824 | ||||||
chr2:135774844
|
C | CA | 25 | a0001c0001t0001g0127a0001c0001t0001g0135a0001c0001t0001g0137others(22): Show | 26 | HG01433.hp2 HG01978.hp2 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.951-1390dupA | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 135774844 | |||||
chr2:135774948
|
T | G | 30 | a0001c0001t0001g0127a0001c0001t0001g0135a0001c0001t0001g0137others(27): Show | 36 | HG00558.hp2 HG00621.hp1 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.951-1301T>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | chr2 | 135774948 | ||||||
chr2:135774958
|
A | G | 8 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0146others(5): Show | 8 | HG02109.hp2 HG02630.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.951-1291A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | chr2 | 135774958 | ||||||
chr2:135775018
|
T | C | 1 | a0001c0001t0002g0270 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.951-1231T>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | chr2 | 135775018 | ||||||
chr2:135775185
|
G | T | 1 | a0001c0001t0011g0150 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.951-1064G>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | chr2 | 135775185 | ||||||
chr2:135775243
|
C | T | 18 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0146others(15): Show | 19 | HG02055.hp2 HG02109.hp2 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.951-1006C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | chr2 | 135775243 | ||||||
chr2:135775347
|
C | G | 24 | a0001c0003t0001g0012a0001c0003t0001g0044a0001c0003t0001g0045others(21): Show | 25 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.951-902C>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | chr2 | 135775347 | ||||||
chr2:135775540
|
G | A | 1 | a0001c0002t0002g0244 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.951-709G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | chr2 | 135775540 | ||||||
chr2:135775591
|
G | A | 288 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(285): Show | 354 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(351): Show |
intron_variant | MODIFIER | c.951-658G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | chr2 | 135775591 | ||||||
chr2:135775625
|
G | A | 76 | a0001c0001t0003g0007a0001c0001t0003g0013a0001c0001t0003g0014others(73): Show | 79 | HG01261.hp2 HG01346.hp1 HG01358.hp1 others(76): Show |
intron_variant | MODIFIER | c.951-624G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | chr2 | 135775625 | ||||||
chr2:135775761
|
A | G | 1 | a0001c0001t0015g0298 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.951-488A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | chr2 | 135775761 | ||||||
chr2:135775798
|
G | A | 8 | a0001c0001t0001g0127a0001c0001t0001g0135a0001c0001t0001g0137others(5): Show | 8 | HG01433.hp2 HG02818.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.951-451G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | chr2 | 135775798 | ||||||
chr2:135775858
|
C | A | 2 | a0001c0001t0003g0085a0001c0001t0003g0116 | 2 | NA19058.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.951-391C>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | chr2 | 135775858 | ||||||
chr2:135775859
|
C | T | 1 | a0001c0001t0004g0035 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.951-390C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | chr2 | 135775859 | ||||||
chr2:135775917
|
A | G | 1 | a0001c0001t0003g0042 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.951-332A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | chr2 | 135775917 | ||||||
chr2:135776015
|
C | G | 10 | a0001c0001t0003g0007a0001c0001t0003g0036a0001c0001t0003g0038others(7): Show | 11 | HG02055.hp2 HG02280.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.951-234C>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | chr2 | 135776015 | ||||||
chr2:135776217
|
A | G | 1 | a0001c0001t0015g0298 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.951-32A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 9/12 | chr2 | 135776217 | ||||||
chr2:135776423
|
A | G | 24 | a0001c0003t0001g0012a0001c0003t0001g0044a0001c0003t0001g0045others(21): Show | 25 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.1053+72A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 10/12 | chr2 | 135776423 | ||||||
chr2:135776431
|
G | T | 1 | a0001c0001t0005g0287 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1053+80G>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 10/12 | chr2 | 135776431 | ||||||
chr2:135776598
|
T | C | 10 | a0001c0001t0003g0007a0001c0001t0003g0036a0001c0001t0003g0038others(7): Show | 11 | HG02055.hp2 HG02280.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.1053+247T>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 10/12 | chr2 | 135776598 | ||||||
chr2:135776696
|
C | T | 1 | a0001c0001t0001g0145 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1053+345C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 10/12 | chr2 | 135776696 | ||||||
chr2:135776733
|
T | TA | 8 | a0001c0001t0001g0127a0001c0001t0001g0135a0001c0001t0001g0137others(5): Show | 8 | HG01433.hp2 HG02818.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.1053+383dupA | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 135776733 | |||||
chr2:135777064
|
A | G | 24 | a0001c0003t0001g0012a0001c0003t0001g0044a0001c0003t0001g0045others(21): Show | 25 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.1053+713A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 10/12 | chr2 | 135777064 | ||||||
chr2:135777183
|
G | A | 1 | a0001c0001t0003g0099 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1053+832G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 10/12 | chr2 | 135777183 | ||||||
chr2:135777205
|
T | C | 1 | a0001c0001t0003g0040 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1053+854T>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 10/12 | chr2 | 135777205 | ||||||
chr2:135777349
|
C | T | 1 | a0001c0007t0019g0043 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1053+998C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 10/12 | chr2 | 135777349 | ||||||
chr2:135777379
|
T | G | 24 | a0001c0003t0001g0012a0001c0003t0001g0044a0001c0003t0001g0045others(21): Show | 25 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.1053+1028T>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 10/12 | chr2 | 135777379 | ||||||
chr2:135777665
|
T | A | 54 | a0001c0001t0002g0232a0001c0001t0002g0277a0001c0001t0011g0150others(51): Show | 69 | HG00639.hp1 HG00642.hp2 HG00673.hp2 others(66): Show |
intron_variant | MODIFIER | c.1054-1283T>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 10/12 | chr2 | 135777665 | ||||||
chr2:135777712
|
A | G | 4 | a0001c0001t0003g0070a0001c0001t0003g0071a0001c0001t0003g0073others(1): Show | 4 | HG01261.hp2 HG02615.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1054-1236A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 10/12 | chr2 | 135777712 | ||||||
chr2:135777719
|
C | G | 1 | a0001c0001t0011g0150 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1054-1229C>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 10/12 | chr2 | 135777719 | ||||||
chr2:135777775
|
C | T | 1 | a0001c0001t0011g0150 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1054-1173C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 10/12 | chr2 | 135777775 | ||||||
chr2:135777794
|
A | C | 76 | a0001c0001t0002g0005a0001c0001t0002g0226a0001c0001t0002g0231others(73): Show | 82 | HG00280.hp1 HG00741.hp1 HG01256.hp1 others(79): Show |
intron_variant | MODIFIER | c.1054-1154A>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 10/12 | chr2 | 135777794 | ||||||
chr2:135777840
|
G | T | 86 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(83): Show | 123 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.1054-1108G>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 10/12 | chr2 | 135777840 | ||||||
chr2:135777888
|
A | G | 1 | a0001c0001t0001g0138 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1054-1060A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 10/12 | chr2 | 135777888 | ||||||
chr2:135778137
|
A | C | 2 | a0001c0001t0011g0150a0001c0007t0019g0043 | 2 | HG00639.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1054-811A>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 10/12 | chr2 | 135778137 | ||||||
chr2:135778156
|
G | A | 4 | a0001c0001t0006g0280a0001c0001t0006g0281a0001c0001t0006g0282others(1): Show | 4 | HG02258.hp1 HG02965.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1054-792G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 10/12 | chr2 | 135778156 | ||||||
chr2:135778174
|
C | CA | 49 | a0001c0001t0001g0135a0001c0001t0001g0144a0001c0001t0001g0145others(46): Show | 51 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.1054-760dupA | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 135778174 | |||||
chr2:135778180
|
A | C | 5 | a0001c0001t0005g0027a0001c0001t0005g0287a0001c0001t0005g0288others(2): Show | 6 | NA18947.hp1 NA18952.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.1054-768A>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 10/12 | chr2 | 135778180 | ||||||
chr2:135778188
|
AC | A | 39 | a0001c0001t0002g0277a0001c0002t0002g0004a0001c0002t0002g0006others(36): Show | 53 | HG00642.hp2 HG00673.hp2 HG00733.hp1 others(50): Show |
intron_variant | MODIFIER | c.1054-759delC | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 10/12 | chr2 | 135778188 | ||||||
chr2:135778189
|
C | A | 11 | a0001c0001t0008g0123a0001c0002t0002g0026a0001c0002t0002g0239others(8): Show | 12 | HG01175.hp2 HG01192.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.1054-759C>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 10/12 | chr2 | 135778189 | ||||||
chr2:135778202
|
A | C | 1 | a0001c0001t0001g0176 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1054-746A>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 10/12 | chr2 | 135778202 | ||||||
chr2:135778306
|
G | A | 234 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(231): Show | 285 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(282): Show |
intron_variant | MODIFIER | c.1054-642G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 10/12 | chr2 | 135778306 | ||||||
chr2:135778321
|
C | T | 1 | a0001c0002t0002g0230 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1054-627C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 10/12 | chr2 | 135778321 | ||||||
chr2:135778525
|
G | A | 52 | a0001c0001t0002g0232a0001c0001t0002g0277a0001c0002t0002g0004others(49): Show | 67 | HG00642.hp2 HG00673.hp2 HG00733.hp1 others(64): Show |
intron_variant | MODIFIER | c.1054-423G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 10/12 | chr2 | 135778525 | ||||||
chr2:135778543
|
C | G | 76 | a0001c0001t0002g0005a0001c0001t0002g0226a0001c0001t0002g0231others(73): Show | 82 | HG00280.hp1 HG00741.hp1 HG01256.hp1 others(79): Show |
intron_variant | MODIFIER | c.1054-405C>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 10/12 | chr2 | 135778543 | ||||||
chr2:135778861
|
A | G | 1 | a0001c0001t0011g0150 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1054-87A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 10/12 | chr2 | 135778861 | ||||||
chr2:135779322
|
CA | C | 288 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(285): Show | 354 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(351): Show |
intron_variant | MODIFIER | c.1185+251delA | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr2 | 135779322 | |||||
chr2:135779375
|
A | T | 1 | a0001c0001t0003g0082 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1185+296A>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 11/12 | chr2 | 135779375 | ||||||
chr2:135779487
|
G | A | 86 | a0001c0001t0002g0005a0001c0001t0002g0226a0001c0001t0002g0231others(83): Show | 93 | HG00280.hp1 HG00741.hp1 HG01256.hp1 others(90): Show |
intron_variant | MODIFIER | c.1185+408G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 11/12 | chr2 | 135779487 | ||||||
chr2:135779536
|
A | G | 1 | a0001c0001t0001g0276 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1185+457A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 11/12 | chr2 | 135779536 | ||||||
chr2:135779595
|
G | A | 2 | a0001c0001t0001g0173a0001c0001t0001g0182 | 2 | HG00544.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1185+516G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 11/12 | chr2 | 135779595 | ||||||
chr2:135779633
|
A | G | 1 | a0001c0001t0002g0271 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1186-550A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 11/12 | chr2 | 135779633 | ||||||
chr2:135779689
|
A | G | 1 | a0001c0002t0002g0265 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1186-494A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 11/12 | chr2 | 135779689 | ||||||
chr2:135779819
|
CAAT | C | 24 | a0001c0003t0001g0012a0001c0003t0001g0044a0001c0003t0001g0045others(21): Show | 25 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.1186-362_1186-360d others(5): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr2 | 135779819 | |||||
chr2:135779843
|
TATTATAT others(6): Show |
T | 1 | a0001c0003t0001g0065 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1186-323_1186-311d others(15): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr2 | 135779843 | |||||
chr2:135779872
|
TTTATAA | T | 8 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0146others(5): Show | 8 | HG02109.hp2 HG02630.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.1186-303_1186-298d others(8): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr2 | 135779872 | |||||
chr2:135779880
|
TATA | T | 78 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(75): Show | 115 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.1186-299_1186-297d others(5): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr2 | 135779880 | |||||
chr2:135779902
|
AATAT | A | 86 | a0001c0001t0002g0005a0001c0001t0002g0226a0001c0001t0002g0231others(83): Show | 93 | HG00280.hp1 HG00741.hp1 HG01256.hp1 others(90): Show |
intron_variant | MODIFIER | c.1186-275_1186-272d others(6): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr2 | 135779902 | |||||
chr2:135779947
|
GTTA | G | 10 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0146others(7): Show | 10 | HG02109.hp2 HG02615.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1186-231_1186-229d others(5): Show |
UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr2 | 135779947 | |||||
chr2:135780051
|
T | C | 1 | a0001c0001t0003g0222 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1186-132T>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 11/12 | chr2 | 135780051 | ||||||
chr2:135780089
|
C | T | 3 | a0001c0001t0003g0085a0001c0001t0003g0094a0001c0001t0003g0116 | 3 | NA19058.hp2 NA19078.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.1186-94C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 11/12 | chr2 | 135780089 | ||||||
chr2:135780427
|
A | T | 1 | a0001c0001t0003g0094 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1388+42A>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 12/12 | chr2 | 135780427 | ||||||
chr2:135780479
|
T | C | 1 | a0001c0001t0001g0162 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1388+94T>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 12/12 | chr2 | 135780479 | ||||||
chr2:135780547
|
A | T | 8 | a0001c0001t0001g0144a0001c0001t0001g0145a0001c0001t0001g0146others(5): Show | 8 | HG02109.hp2 HG02630.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.1388+162A>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 12/12 | chr2 | 135780547 | ||||||
chr2:135781092
|
G | A | 1 | a0001c0001t0002g0277 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1388+707G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 12/12 | chr2 | 135781092 | ||||||
chr2:135781170
|
G | A | 4 | a0001c0001t0001g0127a0001c0001t0001g0135a0001c0001t0001g0137others(1): Show | 4 | HG02818.hp2 HG02896.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1388+785G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 12/12 | chr2 | 135781170 | ||||||
chr2:135781206
|
A | G | 296 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(293): Show | 363 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(360): Show |
intron_variant | MODIFIER | c.1388+821A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 12/12 | chr2 | 135781206 | ||||||
chr2:135781303
|
C | A | 1 | a0001c0002t0002g0228 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1388+918C>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 12/12 | chr2 | 135781303 | ||||||
chr2:135781317
|
G | T | 1 | a0001c0001t0004g0035 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1388+932G>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 12/12 | chr2 | 135781317 | ||||||
chr2:135781323
|
A | G | 3 | a0001c0001t0003g0100a0001c0001t0003g0114a0001c0001t0017g0093 | 3 | NA18939.hp1 NA18959.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.1388+938A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 12/12 | chr2 | 135781323 | ||||||
chr2:135781369
|
T | A | 225 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(222): Show | 272 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(269): Show |
intron_variant | MODIFIER | c.1388+984T>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 12/12 | chr2 | 135781369 | ||||||
chr2:135781374
|
G | A | 1 | a0001c0002t0002g0228 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1388+989G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 12/12 | chr2 | 135781374 | ||||||
chr2:135781375
|
C | G | 1 | a0001c0002t0002g0228 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1388+990C>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 12/12 | chr2 | 135781375 | ||||||
chr2:135781406
|
T | C | 1 | a0001c0001t0003g0111 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1388+1021T>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 12/12 | chr2 | 135781406 | ||||||
chr2:135781472
|
A | T | 1 | a0001c0001t0003g0081 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1388+1087A>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 12/12 | chr2 | 135781472 | ||||||
chr2:135781552
|
G | T | 87 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(84): Show | 124 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.1388+1167G>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 12/12 | chr2 | 135781552 | ||||||
chr2:135781583
|
G | A | 24 | a0001c0003t0001g0012a0001c0003t0001g0044a0001c0003t0001g0045others(21): Show | 25 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.1389-1166G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 12/12 | chr2 | 135781583 | ||||||
chr2:135781760
|
C | T | 62 | a0001c0001t0002g0005a0001c0001t0002g0226a0001c0001t0002g0231others(59): Show | 81 | HG00280.hp1 HG00642.hp2 HG00673.hp2 others(78): Show |
intron_variant | MODIFIER | c.1389-989C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 12/12 | chr2 | 135781760 | ||||||
chr2:135781763
|
G | A | 2 | a0001c0001t0001g0162a0001c0007t0019g0043 | 2 | HG00639.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.1389-986G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 12/12 | chr2 | 135781763 | ||||||
chr2:135781843
|
T | C | 288 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(285): Show | 354 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(351): Show |
intron_variant | MODIFIER | c.1389-906T>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 12/12 | chr2 | 135781843 | ||||||
chr2:135781922
|
T | C | 1 | a0001c0001t0002g0268 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1389-827T>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 12/12 | chr2 | 135781922 | ||||||
chr2:135781924
|
G | A | 1 | a0001c0001t0004g0131 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1389-825G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 12/12 | chr2 | 135781924 | ||||||
chr2:135781943
|
G | A | 141 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(138): Show | 185 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(182): Show |
intron_variant | MODIFIER | c.1389-806G>A | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 12/12 | chr2 | 135781943 | ||||||
chr2:135781972
|
G | C | 2 | a0001c0003t0001g0051a0001c0003t0001g0063 | 2 | HG00558.hp1 HG02015.hp2 |
intron_variant | MODIFIER | c.1389-777G>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 12/12 | chr2 | 135781972 | ||||||
chr2:135782006
|
T | C | 24 | a0001c0003t0001g0012a0001c0003t0001g0044a0001c0003t0001g0045others(21): Show | 25 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.1389-743T>C | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 12/12 | chr2 | 135782006 | ||||||
chr2:135782100
|
T | G | 62 | a0001c0001t0002g0005a0001c0001t0002g0226a0001c0001t0002g0231others(59): Show | 81 | HG00280.hp1 HG00642.hp2 HG00673.hp2 others(78): Show |
intron_variant | MODIFIER | c.1389-649T>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 12/12 | chr2 | 135782100 | ||||||
chr2:135782144
|
TA | T | 4 | a0001c0001t0001g0127a0001c0001t0001g0135a0001c0001t0001g0137others(1): Show | 4 | HG02818.hp2 HG02896.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1389-601delA | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 135782144 | |||||
chr2:135782245
|
A | G | 1 | a0001c0001t0011g0150 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1389-504A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 12/12 | chr2 | 135782245 | ||||||
chr2:135782327
|
C | T | 24 | a0001c0003t0001g0012a0001c0003t0001g0044a0001c0003t0001g0045others(21): Show | 25 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.1389-422C>T | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 12/12 | chr2 | 135782327 | ||||||
chr2:135782513
|
A | G | 62 | a0001c0001t0002g0005a0001c0001t0002g0226a0001c0001t0002g0231others(59): Show | 81 | HG00280.hp1 HG00642.hp2 HG00673.hp2 others(78): Show |
intron_variant | MODIFIER | c.1389-236A>G | UBXN4 | ENSG00000144224.17 | transcript | ENST00000272638.14 | protein_coding | 12/12 | chr2 | 135782513 |