geneid | 84640 |
---|---|
ensemblid | ENSG00000170185.11 |
hgncid | 20067 |
symbol | USP38 |
name | ubiquitin specific peptidase 38 |
refseq_nuc | NM_032557.6 |
refseq_prot | NP_115946.2 |
ensembl_nuc | ENST00000307017.9 |
ensembl_prot | ENSP00000303434.4 |
mane_status | MANE Select |
chr | chr4 |
start | 143184917 |
end | 143223874 |
strand | + |
ver | v1.2 |
region | chr4:143184917-143223874 |
region5000 | chr4:143179917-143228874 |
regionname0 | USP38_chr4_143184917_143223874 |
regionname5000 | USP38_chr4_143179917_143228874 |
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 | 1042 | 247 | 89 | 49 | 66 | 8 | 33 | 50 | USP38_chr4_143179917_143228874 | USP38 | copy fasta | chr4 | 143179917 | 143228874 |
a0002 | 0/0 | 1042 | 5 | 4 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | copy fasta | chr4 | 143179917 | 143228874 |
a0003 | 0/0 | 1042 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | USP38_chr4_143179917_143228874 | USP38 | copy fasta | chr4 | 143179917 | 143228874 |
a0004 | 0/0 | 1042 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | USP38_chr4_143179917_143228874 | USP38 | copy fasta | chr4 | 143179917 | 143228874 |
a0005 | 0/0 | 1042 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | USP38_chr4_143179917_143228874 | USP38 | copy fasta | chr4 | 143179917 | 143228874 |
a0006 | 0/0 | 1042 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | copy fasta | chr4 | 143179917 | 143228874 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 3129 | 140 | 57 | 30 | 33 | 3 | 16 | USP38_chr4_143179917_143228874 | USP38 | copy fasta | chr4 | 143179917 | 143228874 |
c0002 | 1/0 | 3129 | 76 | 14 | 15 | 30 | 2 | 14 | USP38_chr4_143179917_143228874 | USP38 | copy fasta | chr4 | 143179917 | 143228874 |
c0003 | 0/0 | 3129 | 26 | 18 | 3 | 1 | 3 | 1 | USP38_chr4_143179917_143228874 | USP38 | copy fasta | chr4 | 143179917 | 143228874 |
c0004 | 0/0 | 3129 | 5 | 4 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | copy fasta | chr4 | 143179917 | 143228874 |
c0005 | 0/0 | 3129 | 3 | 0 | 0 | 3 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | copy fasta | chr4 | 143179917 | 143228874 |
c0006 | 0/0 | 3129 | 2 | 0 | 0 | 0 | 0 | 2 | USP38_chr4_143179917_143228874 | USP38 | copy fasta | chr4 | 143179917 | 143228874 |
c0007 | 0/0 | 3129 | 1 | 0 | 0 | 0 | 0 | 1 | USP38_chr4_143179917_143228874 | USP38 | copy fasta | chr4 | 143179917 | 143228874 |
c0008 | 0/0 | 3129 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | copy fasta | chr4 | 143179917 | 143228874 |
c0009 | 0/0 | 3129 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | copy fasta | chr4 | 143179917 | 143228874 |
c0010 | 0/0 | 3129 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | copy fasta | chr4 | 143179917 | 143228874 |
c0011 | 0/0 | 3129 | 1 | 0 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | copy fasta | chr4 | 143179917 | 143228874 |
c0012 | 0/0 | 3129 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | copy fasta | chr4 | 143179917 | 143228874 |
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 | 3952 | 92 | 17 | 23 | 37 | 3 | 11 | USP38_chr4_143179917_143228874 | USP38 | copy fasta | chr4 | 143179917 | 143228874 |
t0002 | 1/0 | 3953 | 73 | 14 | 13 | 32 | 0 | 13 | USP38_chr4_143179917_143228874 | USP38 | copy fasta | chr4 | 143179917 | 143228874 |
t0003 | 0/0 | 3952 | 19 | 16 | 3 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | copy fasta | chr4 | 143179917 | 143228874 |
t0004 | 0/0 | 3952 | 13 | 13 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | copy fasta | chr4 | 143179917 | 143228874 |
t0005 | 0/0 | 3952 | 12 | 9 | 1 | 0 | 0 | 2 | USP38_chr4_143179917_143228874 | USP38 | copy fasta | chr4 | 143179917 | 143228874 |
t0006 | 0/0 | 3952 | 11 | 1 | 3 | 1 | 3 | 3 | USP38_chr4_143179917_143228874 | USP38 | copy fasta | chr4 | 143179917 | 143228874 |
t0007 | 0/0 | 3952 | 8 | 7 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | copy fasta | chr4 | 143179917 | 143228874 |
t0008 | 0/0 | 3954 | 5 | 5 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | copy fasta | chr4 | 143179917 | 143228874 |
t0009 | 0/0 | 3953 | 4 | 0 | 2 | 0 | 2 | 0 | USP38_chr4_143179917_143228874 | USP38 | copy fasta | chr4 | 143179917 | 143228874 |
t0010 | 0/0 | 3952 | 3 | 3 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | copy fasta | chr4 | 143179917 | 143228874 |
t0011 | 0/0 | 3952 | 2 | 2 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | copy fasta | chr4 | 143179917 | 143228874 |
t0012 | 0/0 | 3952 | 2 | 2 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | copy fasta | chr4 | 143179917 | 143228874 |
t0013 | 0/0 | 3952 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | copy fasta | chr4 | 143179917 | 143228874 |
t0014 | 0/0 | 3953 | 1 | 0 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | copy fasta | chr4 | 143179917 | 143228874 |
t0015 | 0/0 | 3953 | 1 | 0 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | copy fasta | chr4 | 143179917 | 143228874 |
t0016 | 0/0 | 3952 | 1 | 0 | 0 | 0 | 0 | 1 | USP38_chr4_143179917_143228874 | USP38 | copy fasta | chr4 | 143179917 | 143228874 |
t0017 | 0/0 | 3952 | 1 | 0 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | copy fasta | chr4 | 143179917 | 143228874 |
t0018 | 0/0 | 3952 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | copy fasta | chr4 | 143179917 | 143228874 |
t0019 | 0/0 | 3952 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | copy fasta | chr4 | 143179917 | 143228874 |
t0020 | 0/0 | 3952 | 1 | 0 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | copy fasta | chr4 | 143179917 | 143228874 |
t0021 | 0/0 | 3952 | 1 | 0 | 0 | 0 | 0 | 1 | USP38_chr4_143179917_143228874 | USP38 | copy fasta | chr4 | 143179917 | 143228874 |
t0022 | 0/0 | 3952 | 1 | 0 | 0 | 0 | 0 | 1 | USP38_chr4_143179917_143228874 | USP38 | copy fasta | chr4 | 143179917 | 143228874 |
t0023 | 0/0 | 3952 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | copy fasta | chr4 | 143179917 | 143228874 |
t0024 | 0/0 | 3952 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | copy fasta | chr4 | 143179917 | 143228874 |
t0025 | 0/0 | 3953 | 1 | 0 | 0 | 0 | 0 | 1 | USP38_chr4_143179917_143228874 | USP38 | copy fasta | chr4 | 143179917 | 143228874 |
t0026 | 0/0 | 3953 | 1 | 0 | 0 | 0 | 0 | 1 | USP38_chr4_143179917_143228874 | USP38 | copy fasta | chr4 | 143179917 | 143228874 |
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 | 40 | 1 | 13 | 19 | 2 | 5 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0002 | 0/0 | 17 | 3 | 5 | 4 | 0 | 5 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0003 | 0/0 | 16 | 0 | 2 | 11 | 1 | 2 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0004 | 0/0 | 8 | 8 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0005 | 0/0 | 7 | 6 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0006 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0007 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0008 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0009 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0010 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0011 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0015 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0017 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0018 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0020 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0021 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0025 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0028 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0117 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
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 | 0/1 | 3129 | 140 | 57 | 30 | 33 | 3 | 16 | USP38_chr4_143179917_143228874 | USP38 | copy fasta | chr4 | 143179917 | 143228874 |
a0001c0002 | 1/0 | 3129 | 76 | 14 | 15 | 30 | 2 | 14 | USP38_chr4_143179917_143228874 | USP38 | copy fasta | chr4 | 143179917 | 143228874 |
a0001c0003 | 0/0 | 3129 | 26 | 18 | 3 | 1 | 3 | 1 | USP38_chr4_143179917_143228874 | USP38 | copy fasta | chr4 | 143179917 | 143228874 |
a0001c0006 | 0/0 | 3129 | 2 | 0 | 0 | 0 | 0 | 2 | USP38_chr4_143179917_143228874 | USP38 | copy fasta | chr4 | 143179917 | 143228874 |
a0001c0008 | 0/0 | 3129 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | copy fasta | chr4 | 143179917 | 143228874 |
a0001c0009 | 0/0 | 3129 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | copy fasta | chr4 | 143179917 | 143228874 |
a0001c0011 | 0/0 | 3129 | 1 | 0 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | copy fasta | chr4 | 143179917 | 143228874 |
a0002c0004 | 0/0 | 3129 | 5 | 4 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | copy fasta | chr4 | 143179917 | 143228874 |
a0003c0005 | 0/0 | 3129 | 3 | 0 | 0 | 3 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | copy fasta | chr4 | 143179917 | 143228874 |
a0004c0012 | 0/0 | 3129 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | copy fasta | chr4 | 143179917 | 143228874 |
a0005c0007 | 0/0 | 3129 | 1 | 0 | 0 | 0 | 0 | 1 | USP38_chr4_143179917_143228874 | USP38 | copy fasta | chr4 | 143179917 | 143228874 |
a0006c0010 | 0/0 | 3129 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | copy fasta | chr4 | 143179917 | 143228874 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 7080 | 88 | 17 | 23 | 33 | 3 | 11 | USP38_chr4_143179917_143228874 | USP38 | copy fasta | chr4 | 143179917 | 143228874 |
a0001c0001t0003 | 0/0 | 7080 | 14 | 12 | 2 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | copy fasta | chr4 | 143179917 | 143228874 |
a0001c0001t0005 | 0/0 | 7080 | 12 | 9 | 1 | 0 | 0 | 2 | USP38_chr4_143179917_143228874 | USP38 | copy fasta | chr4 | 143179917 | 143228874 |
a0001c0001t0007 | 0/0 | 7080 | 8 | 7 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | copy fasta | chr4 | 143179917 | 143228874 |
a0001c0001t0008 | 0/0 | 7082 | 5 | 5 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | copy fasta | chr4 | 143179917 | 143228874 |
a0001c0001t0010 | 0/0 | 7080 | 3 | 3 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | copy fasta | chr4 | 143179917 | 143228874 |
a0001c0001t0014 | 0/0 | 7081 | 1 | 0 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | copy fasta | chr4 | 143179917 | 143228874 |
a0001c0001t0016 | 0/0 | 7080 | 1 | 0 | 0 | 0 | 0 | 1 | USP38_chr4_143179917_143228874 | USP38 | copy fasta | chr4 | 143179917 | 143228874 |
a0001c0001t0017 | 0/0 | 7080 | 1 | 0 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | copy fasta | chr4 | 143179917 | 143228874 |
a0001c0001t0018 | 0/0 | 7080 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | copy fasta | chr4 | 143179917 | 143228874 |
a0001c0001t0019 | 0/0 | 7080 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | copy fasta | chr4 | 143179917 | 143228874 |
a0001c0001t0020 | 0/0 | 7080 | 1 | 0 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | copy fasta | chr4 | 143179917 | 143228874 |
a0001c0001t0021 | 0/0 | 7080 | 1 | 0 | 0 | 0 | 0 | 1 | USP38_chr4_143179917_143228874 | USP38 | copy fasta | chr4 | 143179917 | 143228874 |
a0001c0001t0022 | 0/0 | 7080 | 1 | 0 | 0 | 0 | 0 | 1 | USP38_chr4_143179917_143228874 | USP38 | copy fasta | chr4 | 143179917 | 143228874 |
a0001c0001t0023 | 0/0 | 7080 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | copy fasta | chr4 | 143179917 | 143228874 |
a0001c0001t0024 | 0/0 | 7080 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | copy fasta | chr4 | 143179917 | 143228874 |
a0001c0002t0002 | 1/0 | 7081 | 69 | 14 | 12 | 30 | 0 | 12 | USP38_chr4_143179917_143228874 | USP38 | copy fasta | chr4 | 143179917 | 143228874 |
a0001c0002t0009 | 0/0 | 7081 | 4 | 0 | 2 | 0 | 2 | 0 | USP38_chr4_143179917_143228874 | USP38 | copy fasta | chr4 | 143179917 | 143228874 |
a0001c0002t0015 | 0/0 | 7081 | 1 | 0 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | copy fasta | chr4 | 143179917 | 143228874 |
a0001c0002t0025 | 0/0 | 7081 | 1 | 0 | 0 | 0 | 0 | 1 | USP38_chr4_143179917_143228874 | USP38 | copy fasta | chr4 | 143179917 | 143228874 |
a0001c0002t0026 | 0/0 | 7081 | 1 | 0 | 0 | 0 | 0 | 1 | USP38_chr4_143179917_143228874 | USP38 | copy fasta | chr4 | 143179917 | 143228874 |
a0001c0003t0004 | 0/0 | 7080 | 13 | 13 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | copy fasta | chr4 | 143179917 | 143228874 |
a0001c0003t0006 | 0/0 | 7080 | 9 | 1 | 3 | 1 | 3 | 1 | USP38_chr4_143179917_143228874 | USP38 | copy fasta | chr4 | 143179917 | 143228874 |
a0001c0003t0011 | 0/0 | 7080 | 2 | 2 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | copy fasta | chr4 | 143179917 | 143228874 |
a0001c0003t0012 | 0/0 | 7080 | 2 | 2 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | copy fasta | chr4 | 143179917 | 143228874 |
a0001c0006t0006 | 0/0 | 7080 | 2 | 0 | 0 | 0 | 0 | 2 | USP38_chr4_143179917_143228874 | USP38 | copy fasta | chr4 | 143179917 | 143228874 |
a0001c0008t0002 | 0/0 | 7081 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | copy fasta | chr4 | 143179917 | 143228874 |
a0001c0009t0002 | 0/0 | 7081 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | copy fasta | chr4 | 143179917 | 143228874 |
a0001c0011t0002 | 0/0 | 7081 | 1 | 0 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | copy fasta | chr4 | 143179917 | 143228874 |
a0002c0004t0003 | 0/0 | 7080 | 5 | 4 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | copy fasta | chr4 | 143179917 | 143228874 |
a0003c0005t0001 | 0/0 | 7080 | 3 | 0 | 0 | 3 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | copy fasta | chr4 | 143179917 | 143228874 |
a0004c0012t0001 | 0/0 | 7080 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | copy fasta | chr4 | 143179917 | 143228874 |
a0005c0007t0002 | 0/0 | 7081 | 1 | 0 | 0 | 0 | 0 | 1 | USP38_chr4_143179917_143228874 | USP38 | copy fasta | chr4 | 143179917 | 143228874 |
a0006c0010t0013 | 0/0 | 7080 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | copy fasta | chr4 | 143179917 | 143228874 |
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 | 34 | 1 | 12 | 15 | 2 | 4 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0001t0001g0005 | 0/0 | 7 | 6 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0001t0001g0010 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0001t0001g0117 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0001t0003g0004 | 0/0 | 8 | 8 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0001t0003g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0001t0003g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0001t0003g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0001t0003g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0001t0003g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0001t0005g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0001t0005g0025 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0001t0005g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0001t0005g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0001t0005g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0001t0005g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0001t0005g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0001t0007g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0001t0007g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0001t0007g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0001t0007g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0001t0007g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0001t0008g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0001t0008g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0001t0010g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0001t0010g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0001t0014g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0001t0016g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0001t0017g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0001t0018g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0001t0019g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0001t0020g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0001t0021g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0001t0022g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0001t0023g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0001t0024g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0002t0002g0002 | 0/0 | 15 | 3 | 4 | 4 | 0 | 4 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0002t0002g0003 | 0/0 | 14 | 0 | 1 | 11 | 0 | 2 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0002t0002g0007 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0002t0002g0008 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0002t0002g0009 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0002t0002g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0002t0002g0018 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0002t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0002t0002g0020 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0002t0002g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0002t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0002t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0002t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0002t0009g0003 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0002t0009g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0002t0009g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0002t0015g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0002t0025g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0002t0026g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0003t0004g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0003t0004g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0003t0004g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0003t0004g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0003t0004g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0003t0004g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0003t0004g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0003t0004g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0003t0004g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0003t0006g0011 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0003t0006g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0003t0006g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0003t0006g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0003t0006g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0003t0006g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0003t0006g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0003t0011g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0003t0012g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0006t0006g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0006t0006g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0008t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0009t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0001c0011t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0002c0004t0003g0015 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0002c0004t0003g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0002c0004t0003g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0003c0005t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0004c0012t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0005c0007t0002g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
a0006c0010t0013g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG00140 | hp2 | a0001 | c0003 | t0006 | g0011 | EUR | GBR | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG00280 | hp1 | a0001 | c0003 | t0006 | g0011 | EUR | FIN | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG00280 | hp2 | a0001 | c0002 | t0009 | g0003 | EUR | FIN | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG00408 | hp1 | a0001 | c0002 | t0002 | g0060 | EAS | CHS | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG00639 | hp1 | a0001 | c0002 | t0009 | g0003 | AMR | PUR | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG00642 | hp2 | a0001 | c0001 | t0017 | g0001 | AMR | PUR | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG00741 | hp1 | a0001 | c0002 | t0015 | g0002 | AMR | PUR | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG01069 | hp2 | a0001 | c0002 | t0002 | g0008 | AMR | PUR | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG01070 | hp1 | a0001 | c0001 | t0003 | g0031 | AMR | PUR | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG01071 | hp2 | a0001 | c0001 | t0003 | g0031 | AMR | PUR | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG01081 | hp1 | a0001 | c0002 | t0009 | g0053 | AMR | PUR | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG01081 | hp2 | a0001 | c0002 | t0002 | g0056 | AMR | PUR | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG01099 | hp2 | a0001 | c0011 | t0002 | g0050 | AMR | PUR | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG01109 | hp1 | a0001 | c0003 | t0006 | g0041 | AMR | PUR | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG01192 | hp1 | a0001 | c0001 | t0007 | g0126 | AMR | PUR | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG01243 | hp2 | a0002 | c0004 | t0003 | g0015 | AMR | PUR | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG01346 | hp2 | a0001 | c0002 | t0002 | g0009 | AMR | CLM | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG01358 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | CLM | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | CLM | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG01361 | hp2 | a0001 | c0002 | t0002 | g0020 | AMR | CLM | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG01433 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | CLM | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG01496 | hp2 | a0001 | c0001 | t0005 | g0025 | AMR | CLM | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG01516 | hp1 | a0001 | c0002 | t0009 | g0059 | EUR | IBS | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0028 | EUR | IBS | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG01884 | hp1 | a0001 | c0003 | t0004 | g0022 | AFR | ACB | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG01884 | hp2 | a0001 | c0002 | t0002 | g0002 | AFR | ACB | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG01891 | hp1 | a0001 | c0001 | t0003 | g0004 | AFR | ACB | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG01891 | hp2 | a0001 | c0003 | t0004 | g0037 | AFR | ACB | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG01934 | hp1 | a0001 | c0002 | t0002 | g0008 | AMR | PEL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG01978 | hp1 | a0001 | c0003 | t0006 | g0038 | AMR | PEL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG01981 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | PEL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PEL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG01993 | hp2 | a0001 | c0001 | t0020 | g0106 | AMR | PEL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG02027 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | KHV | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | KHV | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG02040 | hp2 | a0001 | c0002 | t0002 | g0051 | EAS | KHV | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG02055 | hp1 | a0001 | c0003 | t0004 | g0016 | AFR | ACB | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG02055 | hp2 | a0001 | c0001 | t0023 | g0074 | AFR | ACB | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | KHV | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | KHV | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG02129 | hp2 | a0001 | c0002 | t0002 | g0062 | EAS | KHV | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG02145 | hp1 | a0001 | c0002 | t0002 | g0009 | AFR | ACB | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG02145 | hp2 | a0001 | c0003 | t0011 | g0006 | AFR | ACB | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG02148 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | PEL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PEL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | CDX | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | CDX | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG02257 | hp1 | a0001 | c0001 | t0008 | g0023 | AFR | ACB | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG02258 | hp1 | a0001 | c0001 | t0018 | g0070 | AFR | ACB | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG02258 | hp2 | a0001 | c0003 | t0011 | g0006 | AFR | ACB | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG02273 | hp1 | a0001 | c0002 | t0002 | g0008 | AMR | PEL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PEL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG02280 | hp2 | a0001 | c0001 | t0007 | g0034 | AFR | ACB | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG02293 | hp1 | a0001 | c0002 | t0002 | g0008 | AMR | PEL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG02300 | hp1 | a0001 | c0001 | t0014 | g0111 | AMR | PEL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | ACB | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG02451 | hp2 | a0002 | c0004 | t0003 | g0121 | AFR | ACB | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG02523 | hp2 | a0001 | c0002 | t0002 | g0058 | EAS | KHV | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG02572 | hp1 | a0001 | c0001 | t0005 | g0014 | AFR | GWD | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG02615 | hp1 | a0001 | c0001 | t0003 | g0122 | AFR | GWD | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG02615 | hp2 | a0001 | c0003 | t0004 | g0065 | AFR | GWD | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG02622 | hp1 | a0001 | c0002 | t0002 | g0052 | AFR | GWD | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG02622 | hp2 | a0002 | c0004 | t0003 | g0015 | AFR | GWD | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG02630 | hp1 | a0001 | c0002 | t0002 | g0002 | AFR | GWD | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG02630 | hp2 | a0001 | c0001 | t0005 | g0097 | AFR | GWD | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG02647 | hp1 | a0001 | c0002 | t0002 | g0009 | AFR | GWD | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG02647 | hp2 | a0001 | c0003 | t0012 | g0033 | AFR | GWD | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG02698 | hp1 | a0001 | c0002 | t0002 | g0002 | SAS | PJL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG02717 | hp2 | a0001 | c0003 | t0004 | g0006 | AFR | GWD | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG02723 | hp1 | a0001 | c0001 | t0007 | g0128 | AFR | GWD | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG02723 | hp2 | a0001 | c0001 | t0005 | g0014 | AFR | GWD | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG02735 | hp1 | a0001 | c0001 | t0005 | g0029 | SAS | PJL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG02738 | hp2 | a0001 | c0002 | t0002 | g0002 | SAS | PJL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG02809 | hp1 | a0001 | c0001 | t0005 | g0014 | AFR | GWD | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG02809 | hp2 | a0001 | c0002 | t0002 | g0002 | AFR | GWD | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG02886 | hp2 | a0001 | c0001 | t0005 | g0027 | AFR | GWD | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG02895 | hp1 | a0001 | c0003 | t0004 | g0006 | AFR | GWD | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG02895 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | GWD | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG02896 | hp1 | a0001 | c0003 | t0004 | g0068 | AFR | GWD | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG02897 | hp1 | a0001 | c0001 | t0003 | g0123 | AFR | GWD | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | ESN | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG02922 | hp2 | a0001 | c0001 | t0008 | g0013 | AFR | ESN | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | ESN | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG02965 | hp2 | a0001 | c0003 | t0004 | g0046 | AFR | ESN | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG02970 | hp1 | a0001 | c0001 | t0007 | g0036 | AFR | ESN | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG02970 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | ESN | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG02976 | hp1 | a0006 | c0010 | t0013 | g0118 | AFR | ESN | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG02976 | hp2 | a0001 | c0001 | t0005 | g0025 | AFR | ESN | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG03017 | hp1 | a0001 | c0002 | t0002 | g0003 | SAS | PJL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG03041 | hp1 | a0001 | c0002 | t0002 | g0048 | AFR | GWD | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG03098 | hp1 | a0001 | c0001 | t0007 | g0035 | AFR | MSL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG03098 | hp2 | a0001 | c0001 | t0008 | g0013 | AFR | MSL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG03130 | hp1 | a0001 | c0001 | t0019 | g0127 | AFR | ESN | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG03130 | hp2 | a0001 | c0001 | t0010 | g0124 | AFR | ESN | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG03139 | hp1 | a0001 | c0001 | t0003 | g0004 | AFR | ESN | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG03195 | hp1 | a0001 | c0003 | t0004 | g0047 | AFR | ESN | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG03195 | hp2 | a0001 | c0001 | t0005 | g0079 | AFR | ESN | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG03209 | hp1 | a0001 | c0001 | t0007 | g0036 | AFR | MSL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG03209 | hp2 | a0001 | c0001 | t0010 | g0032 | AFR | MSL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG03225 | hp1 | a0001 | c0002 | t0002 | g0007 | AFR | MSL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG03225 | hp2 | a0001 | c0003 | t0004 | g0066 | AFR | MSL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG03453 | hp1 | a0001 | c0002 | t0002 | g0007 | AFR | MSL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG03486 | hp1 | a0001 | c0001 | t0007 | g0034 | AFR | MSL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG03486 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | MSL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG03490 | hp1 | a0001 | c0001 | t0022 | g0102 | SAS | PJL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG03490 | hp2 | a0001 | c0002 | t0002 | g0018 | SAS | PJL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG03491 | hp2 | a0001 | c0002 | t0002 | g0054 | SAS | PJL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG03492 | hp1 | a0001 | c0002 | t0002 | g0018 | SAS | PJL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG03540 | hp1 | a0001 | c0003 | t0004 | g0006 | AFR | GWD | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG03540 | hp2 | a0001 | c0003 | t0006 | g0067 | AFR | GWD | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG03579 | hp1 | a0001 | c0001 | t0024 | g0072 | AFR | MSL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | MSL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG03654 | hp1 | a0001 | c0003 | t0006 | g0042 | SAS | PJL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG03654 | hp2 | a0001 | c0002 | t0002 | g0055 | SAS | PJL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG03669 | hp1 | a0001 | c0002 | t0002 | g0002 | SAS | PJL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG03688 | hp1 | a0001 | c0001 | t0005 | g0029 | SAS | STU | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG03688 | hp2 | a0001 | c0002 | t0026 | g0021 | SAS | STU | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG03834 | hp1 | a0001 | c0001 | t0021 | g0001 | SAS | BEB | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG03834 | hp2 | a0001 | c0006 | t0006 | g0039 | SAS | BEB | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG03942 | hp1 | a0001 | c0006 | t0006 | g0017 | SAS | BEB | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG03942 | hp2 | a0001 | c0002 | t0002 | g0044 | SAS | BEB | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG04184 | hp1 | a0001 | c0002 | t0002 | g0003 | SAS | BEB | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG04184 | hp2 | a0001 | c0002 | t0025 | g0021 | SAS | BEB | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | STU | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG04199 | hp2 | a0001 | c0002 | t0002 | g0002 | SAS | STU | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | STU | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG04204 | hp2 | a0001 | c0002 | t0002 | g0057 | SAS | STU | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG04228 | hp1 | a0005 | c0007 | t0002 | g0002 | SAS | STU | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG04228 | hp2 | a0001 | c0001 | t0016 | g0108 | SAS | STU | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
NA18522 | hp1 | a0002 | c0004 | t0003 | g0015 | AFR | YRI | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
NA18522 | hp2 | a0001 | c0001 | t0008 | g0023 | AFR | YRI | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | CHB | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | CHB | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
NA18906 | hp1 | a0001 | c0002 | t0002 | g0024 | AFR | YRI | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
NA18906 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | YRI | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
NA18940 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
NA18945 | hp1 | a0001 | c0002 | t0002 | g0012 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
NA18947 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
NA18952 | hp1 | a0003 | c0005 | t0001 | g0001 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
NA18952 | hp2 | a0001 | c0003 | t0006 | g0040 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
NA18957 | hp1 | a0001 | c0002 | t0002 | g0012 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
NA18960 | hp1 | a0001 | c0002 | t0002 | g0012 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
NA18961 | hp1 | a0001 | c0002 | t0002 | g0043 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
NA18961 | hp2 | a0003 | c0005 | t0001 | g0001 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
NA18962 | hp2 | a0001 | c0002 | t0002 | g0049 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
NA18965 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
NA18967 | hp2 | a0001 | c0002 | t0002 | g0019 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
NA18971 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
NA18973 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
NA18981 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
NA18983 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
NA18990 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
NA18991 | hp2 | a0001 | c0009 | t0002 | g0064 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
NA18998 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
NA18999 | hp1 | a0003 | c0005 | t0001 | g0001 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
NA18999 | hp2 | a0001 | c0002 | t0002 | g0063 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
NA19000 | hp2 | a0001 | c0002 | t0002 | g0019 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
NA19005 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
NA19011 | hp1 | a0001 | c0008 | t0002 | g0071 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
NA19011 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
NA19030 | hp1 | a0001 | c0001 | t0005 | g0078 | AFR | LWK | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
NA19030 | hp2 | a0001 | c0002 | t0002 | g0007 | AFR | LWK | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
NA19043 | hp1 | a0001 | c0003 | t0004 | g0016 | AFR | LWK | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
NA19043 | hp2 | a0001 | c0002 | t0002 | g0024 | AFR | LWK | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
NA19062 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
NA19063 | hp1 | a0001 | c0002 | t0002 | g0061 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
NA19063 | hp2 | a0004 | c0012 | t0001 | g0001 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
NA19070 | hp2 | a0001 | c0002 | t0002 | g0045 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
NA19080 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
NA19085 | hp1 | a0001 | c0002 | t0002 | g0069 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
NA19091 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | YRI | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
NA19240 | hp2 | a0001 | c0001 | t0005 | g0027 | AFR | YRI | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | ASW | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
NA20129 | hp2 | a0002 | c0004 | t0003 | g0120 | AFR | ASW | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
NA20805 | hp1 | a0001 | c0003 | t0006 | g0017 | EUR | TSI | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG01123 | hp1 | a0001 | c0003 | t0006 | g0011 | AMR | CLM | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG01123 | hp2 | a0001 | c0002 | t0002 | g0003 | AMR | CLM | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG02109 | hp1 | a0001 | c0001 | t0008 | g0013 | AFR | ACB | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG02109 | hp2 | a0001 | c0001 | t0003 | g0125 | AFR | ACB | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG02486 | hp1 | a0001 | c0002 | t0002 | g0007 | AFR | ACB | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG02486 | hp2 | a0001 | c0001 | t0007 | g0035 | AFR | ACB | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG02559 | hp1 | a0001 | c0001 | t0003 | g0004 | AFR | ACB | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG02559 | hp2 | a0001 | c0002 | t0002 | g0009 | AFR | ACB | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG03471 | hp1 | a0001 | c0001 | t0010 | g0032 | AFR | MSL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG03471 | hp2 | a0001 | c0003 | t0012 | g0033 | AFR | MSL | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG06807 | hp1 | a0001 | c0001 | t0003 | g0004 | AFR | USA | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
HG06807 | hp2 | a0001 | c0001 | t0003 | g0119 | AFR | USA | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
NA21309 | hp1 | a0001 | c0003 | t0004 | g0022 | AFR | LWK | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | LWK | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0117 | REF | REF | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
homoSapiens_grch38 | hp1 | a0001 | c0002 | t0002 | g0020 | REF | REF | USP38_chr4_143179917_143228874 | USP38 | chr4 | 143179917 | 143228874 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:143185533
|
C | T | 1 | a0004 | 1 | NA19063.hp2 | missense_variant | MODERATE | c.83C>T | p.Ser28Leu | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 1/10 | 617/7081 | 83/3129 | 28/1042 | chr4 | 143185533 | ||
chr4:143186034
|
T | C | 1 | a0005 | 1 | HG04228.hp1 | missense_variant | MODERATE | c.584T>C | p.Val195Ala | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 1/10 | 1118/7081 | 584/3129 | 195/1042 | chr4 | 143186034 | ||
chr4:143213771
|
C | T | 1 | a0002 | 5 | HG01243.hp2 HG02451.hp2 HG02622.hp2 others(2): Show |
missense_variant | MODERATE | c.1795C>T | p.Arg599Cys | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 9/10 | 2329/7081 | 1795/3129 | 599/1042 | chr4 | 143213771 | ||
chr4:143214059
|
A | G | 1 | a0006 | 1 | HG02976.hp1 | missense_variant | MODERATE | c.2083A>G | p.Asn695Asp | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 9/10 | 2617/7081 | 2083/3129 | 695/1042 | chr4 | 143214059 | ||
chr4:143214828
|
G | A | 1 | a0003 | 3 | NA18952.hp1 NA18961.hp2 NA18999.hp1 |
missense_variant | MODERATE | c.2852G>A | p.Ser951Asn | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 9/10 | 3386/7081 | 2852/3129 | 951/1042 | chr4 | 143214828 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:143185618
|
C | T | 1 | a0001c0006 | 2 | HG03834.hp2 HG03942.hp1 |
synonymous_variant | LOW | c.168C>T | p.Phe56Phe | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 1/10 | 702/7081 | 168/3129 | 56/1042 | chr4 | 143185618 | ||
chr4:143186098
|
C | T | 1 | a0001c0011 | 1 | HG01099.hp2 | synonymous_variant | LOW | c.648C>T | p.Ser216Ser | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 1/10 | 1182/7081 | 648/3129 | 216/1042 | chr4 | 143186098 | ||
chr4:143209597
|
T | C | 2 | a0001c0003a0001c0006 | 28 | HG00140.hp2 HG00280.hp1 HG01109.hp1 others(25): Show |
synonymous_variant | LOW | c.1437T>C | p.Asn479Asn | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 7/10 | 1971/7081 | 1437/3129 | 479/1042 | chr4 | 143209597 | ||
chr4:143213827
|
G | C | 1 | a0001c0008 | 1 | NA19011.hp1 | synonymous_variant | LOW | c.1851G>C | p.Ser617Ser | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 9/10 | 2385/7081 | 1851/3129 | 617/1042 | chr4 | 143213827 | ||
chr4:143214565
|
G | A | 7 | a0001c0001a0001c0003a0001c0006others(4): Show | 178 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(175): Show |
synonymous_variant | LOW | c.2589G>A | p.Arg863Arg | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 9/10 | 3123/7081 | 2589/3129 | 863/1042 | chr4 | 143214565 | ||
chr4:143214880
|
A | G | 1 | a0001c0009 | 1 | NA18991.hp2 | synonymous_variant | LOW | c.2904A>G | p.Gly968Gly | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 9/10 | 3438/7081 | 2904/3129 | 968/1042 | chr4 | 143214880 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:143184961
|
C | T | 2 | a0001c0002t0025a0001c0002t0026 | 2 | HG03688.hp2 HG04184.hp2 |
5_prime_UTR_variant | MODIFIER | c.-490C>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 1/10 | 490 | chr4 | 143184961 | |||||
chr4:143185278
|
G | A | 1 | a0006c0010t0013 | 1 | HG02976.hp1 | 5_prime_UTR_variant | MODIFIER | c.-173G>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 1/10 | 173 | chr4 | 143185278 | |||||
chr4:143185308
|
G | A | 1 | a0001c0001t0010 | 3 | HG03130.hp2 HG03209.hp2 HG03471.hp1 |
5_prime_UTR_variant | MODIFIER | c.-143G>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 1/10 | 143 | chr4 | 143185308 | |||||
chr4:143220522
|
C | G | 1 | a0001c0001t0024 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*66C>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 10/10 | 66 | chr4 | 143220522 | |||||
chr4:143220632
|
GA | G | 24 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(21): Show | 177 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(174): Show |
3_prime_UTR_variant | MODIFIER | c.*185delA | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 10/10 | 185 | INFO_REALIGN_3_PRIME | chr4 | 143220632 | ||||
chr4:143220684
|
T | C | 1 | a0001c0001t0016 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*228T>C | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 10/10 | 228 | chr4 | 143220684 | |||||
chr4:143220715
|
C | A | 1 | a0001c0002t0025 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*259C>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 10/10 | 259 | chr4 | 143220715 | |||||
chr4:143220798
|
T | A | 1 | a0001c0001t0005 | 12 | HG01496.hp2 HG02572.hp1 HG02630.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*342T>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 10/10 | 342 | chr4 | 143220798 | |||||
chr4:143220843
|
A | T | 1 | a0001c0001t0023 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*387A>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 10/10 | 387 | chr4 | 143220843 | |||||
chr4:143220880
|
A | T | 1 | a0001c0003t0012 | 2 | HG02647.hp2 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*424A>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 10/10 | 424 | chr4 | 143220880 | |||||
chr4:143220888
|
C | T | 1 | a0001c0002t0015 | 1 | HG00741.hp1 | 3_prime_UTR_variant | MODIFIER | c.*432C>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 10/10 | 432 | chr4 | 143220888 | |||||
chr4:143221398
|
G | C | 1 | a0001c0001t0017 | 1 | HG00642.hp2 | 3_prime_UTR_variant | MODIFIER | c.*942G>C | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 10/10 | 942 | chr4 | 143221398 | |||||
chr4:143221448
|
T | C | 1 | a0001c0002t0009 | 4 | HG00280.hp2 HG00639.hp1 HG01081.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*992T>C | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 10/10 | 992 | chr4 | 143221448 | |||||
chr4:143221728
|
A | C | 1 | a0001c0001t0022 | 1 | HG03490.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1272A>C | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 10/10 | 1272 | chr4 | 143221728 | |||||
chr4:143221806
|
C | G | 1 | a0001c0001t0021 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1350C>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 10/10 | 1350 | chr4 | 143221806 | |||||
chr4:143221829
|
G | A | 2 | a0001c0001t0008a0001c0001t0018 | 6 | HG02109.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1373G>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 10/10 | 1373 | chr4 | 143221829 | |||||
chr4:143221867
|
C | T | 5 | a0001c0003t0004a0001c0003t0006a0001c0003t0011others(2): Show | 28 | HG00140.hp2 HG00280.hp1 HG01109.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*1411C>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 10/10 | 1411 | chr4 | 143221867 | |||||
chr4:143221967
|
T | TTA | 1 | a0001c0001t0008 | 5 | HG02109.hp1 HG02257.hp1 HG02922.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1514_*1515dupTA | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 10/10 | 1516 | INFO_REALIGN_3_PRIME | chr4 | 143221967 | ||||
chr4:143222187
|
T | G | 25 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(22): Show | 178 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(175): Show |
3_prime_UTR_variant | MODIFIER | c.*1731T>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 10/10 | 1731 | chr4 | 143222187 | |||||
chr4:143222243
|
A | T | 1 | a0001c0001t0008 | 5 | HG02109.hp1 HG02257.hp1 HG02922.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1787A>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 10/10 | 1787 | chr4 | 143222243 | |||||
chr4:143222256
|
A | C | 1 | a0001c0001t0024 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1800A>C | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 10/10 | 1800 | chr4 | 143222256 | |||||
chr4:143222425
|
C | T | 11 | a0001c0001t0001a0001c0001t0005a0001c0001t0014others(8): Show | 111 | HG00140.hp1 HG00408.hp2 HG00639.hp2 others(108): Show |
3_prime_UTR_variant | MODIFIER | c.*1969C>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 10/10 | 1969 | chr4 | 143222425 | |||||
chr4:143222521
|
T | C | 1 | a0001c0001t0019 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2065T>C | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 10/10 | 2065 | chr4 | 143222521 | |||||
chr4:143223093
|
A | G | 1 | a0001c0001t0020 | 1 | HG01993.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2637A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 10/10 | 2637 | chr4 | 143223093 | |||||
chr4:143223121
|
T | C | 1 | a0001c0003t0011 | 2 | HG02145.hp2 HG02258.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2665T>C | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 10/10 | 2665 | chr4 | 143223121 | |||||
chr4:143223209
|
T | G | 2 | a0001c0001t0007a0001c0001t0019 | 9 | HG01192.hp1 HG02280.hp2 HG02486.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2753T>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 10/10 | 2753 | chr4 | 143223209 | |||||
chr4:143223514
|
C | A | 25 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(22): Show | 178 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(175): Show |
3_prime_UTR_variant | MODIFIER | c.*3058C>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 10/10 | 3058 | chr4 | 143223514 | |||||
chr4:143223570
|
T | C | 2 | a0001c0001t0007a0001c0001t0019 | 9 | HG01192.hp1 HG02280.hp2 HG02486.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3114T>C | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 10/10 | 3114 | chr4 | 143223570 | |||||
chr4:143223808
|
T | G | 2 | a0001c0003t0006a0001c0006t0006 | 11 | HG00140.hp2 HG00280.hp1 HG01109.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3352T>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 10/10 | 3352 | chr4 | 143223808 | |||||
chr4:143223839
|
C | T | 1 | a0001c0001t0024 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3383C>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 10/10 | 3383 | chr4 | 143223839 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:143186184
|
T | C | 4 | a0001c0003t0004g0006a0001c0003t0004g0016a0001c0003t0004g0037others(1): Show | 8 | HG01891.hp2 HG02055.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.682+52T>C | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 1/9 | chr4 | 143186184 | ||||||
chr4:143186191
|
C | T | 6 | a0001c0001t0007g0034a0001c0001t0007g0035a0001c0001t0007g0036others(3): Show | 9 | HG01192.hp1 HG02280.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.682+59C>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 1/9 | chr4 | 143186191 | ||||||
chr4:143186453
|
T | C | 8 | a0001c0003t0006g0011a0001c0003t0006g0017a0001c0003t0006g0038others(5): Show | 10 | HG00140.hp2 HG00280.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.682+321T>C | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 1/9 | chr4 | 143186453 | ||||||
chr4:143186652
|
C | G | 1 | a0001c0003t0012g0033 | 2 | HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.682+520C>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 1/9 | chr4 | 143186652 | ||||||
chr4:143186669
|
A | G | 78 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(75): Show | 144 | HG00140.hp1 HG00408.hp2 HG00639.hp2 others(141): Show |
intron_variant | MODIFIER | c.682+537A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 1/9 | chr4 | 143186669 | ||||||
chr4:143186871
|
C | T | 18 | a0001c0001t0003g0004a0001c0001t0003g0031a0001c0001t0003g0119others(15): Show | 32 | HG01070.hp1 HG01071.hp2 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.682+739C>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 1/9 | chr4 | 143186871 | ||||||
chr4:143186981
|
A | G | 1 | a0001c0001t0001g0117 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.683-845A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 1/9 | chr4 | 143186981 | ||||||
chr4:143187008
|
A | T | 59 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(56): Show | 111 | HG00140.hp1 HG00408.hp2 HG00639.hp2 others(108): Show |
intron_variant | MODIFIER | c.683-818A>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 1/9 | chr4 | 143187008 | ||||||
chr4:143187011
|
C | T | 1 | a0001c0001t0001g0116 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.683-815C>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 1/9 | chr4 | 143187011 | ||||||
chr4:143187036
|
A | G | 2 | a0001c0002t0002g0024a0001c0008t0002g0071 | 3 | NA18906.hp1 NA19011.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.683-790A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 1/9 | chr4 | 143187036 | ||||||
chr4:143187089
|
T | A | 1 | a0001c0001t0001g0073 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.683-737T>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 1/9 | chr4 | 143187089 | ||||||
chr4:143187091
|
T | G | 1 | a0001c0003t0004g0037 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.683-735T>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 1/9 | chr4 | 143187091 | ||||||
chr4:143187132
|
A | G | 3 | a0001c0001t0008g0013a0001c0001t0008g0023a0001c0001t0018g0070 | 6 | HG02109.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.683-694A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 1/9 | chr4 | 143187132 | ||||||
chr4:143187360
|
A | G | 1 | a0001c0001t0018g0070 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.683-466A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 1/9 | chr4 | 143187360 | ||||||
chr4:143187372
|
T | C | 1 | a0001c0002t0002g0043 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.683-454T>C | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 1/9 | chr4 | 143187372 | ||||||
chr4:143187417
|
A | G | 1 | a0001c0001t0001g0115 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.683-409A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 1/9 | chr4 | 143187417 | ||||||
chr4:143187456
|
G | C | 2 | a0001c0002t0002g0018a0001c0002t0002g0044 | 3 | HG03490.hp2 HG03492.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.683-370G>C | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 1/9 | chr4 | 143187456 | ||||||
chr4:143187488
|
A | G | 59 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(56): Show | 111 | HG00140.hp1 HG00408.hp2 HG00639.hp2 others(108): Show |
intron_variant | MODIFIER | c.683-338A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 1/9 | chr4 | 143187488 | ||||||
chr4:143187622
|
A | G | 1 | a0001c0002t0002g0069 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.683-204A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 1/9 | chr4 | 143187622 | ||||||
chr4:143188382
|
T | C | 59 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(56): Show | 111 | HG00140.hp1 HG00408.hp2 HG00639.hp2 others(108): Show |
intron_variant | MODIFIER | c.818+421T>C | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143188382 | ||||||
chr4:143188482
|
C | T | 2 | a0001c0001t0008g0013a0001c0001t0008g0023 | 5 | HG02109.hp1 HG02257.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.818+521C>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143188482 | ||||||
chr4:143188527
|
G | A | 3 | a0001c0001t0008g0013a0001c0001t0008g0023a0001c0001t0018g0070 | 6 | HG02109.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.818+566G>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143188527 | ||||||
chr4:143188789
|
A | G | 1 | a0001c0001t0001g0114 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.818+828A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143188789 | ||||||
chr4:143189099
|
AT | A | 2 | a0001c0003t0006g0011a0001c0003t0006g0038 | 4 | HG00140.hp2 HG00280.hp1 HG01123.hp1 others(1): Show |
intron_variant | MODIFIER | c.818+1142delT | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 143189099 | |||||
chr4:143189179
|
G | C | 1 | a0001c0002t0002g0045 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.818+1218G>C | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143189179 | ||||||
chr4:143189344
|
C | T | 1 | a0001c0001t0001g0113 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.818+1383C>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143189344 | ||||||
chr4:143189737
|
A | T | 1 | a0001c0001t0001g0112 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.818+1776A>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143189737 | ||||||
chr4:143189823
|
T | C | 1 | a0001c0003t0004g0016 | 2 | HG02055.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.818+1862T>C | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143189823 | ||||||
chr4:143189874
|
T | C | 1 | a0006c0010t0013g0118 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.818+1913T>C | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143189874 | ||||||
chr4:143190054
|
C | T | 1 | a0001c0003t0004g0068 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.818+2093C>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143190054 | ||||||
chr4:143190114
|
G | A | 2 | a0001c0003t0004g0046a0001c0003t0004g0047 | 2 | HG02965.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.818+2153G>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143190114 | ||||||
chr4:143190262
|
ATAG | A | 76 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(73): Show | 142 | HG00140.hp1 HG00408.hp2 HG00639.hp2 others(139): Show |
intron_variant | MODIFIER | c.818+2305_818+2307d others(5): Show |
USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 143190262 | |||||
chr4:143190290
|
A | C | 1 | a0001c0001t0024g0072 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.818+2329A>C | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143190290 | ||||||
chr4:143190493
|
C | CT | 10 | a0001c0001t0001g0101a0001c0001t0001g0103a0001c0001t0001g0104others(7): Show | 10 | HG01099.hp1 HG01361.hp1 HG01993.hp2 others(7): Show |
intron_variant | MODIFIER | c.818+2534dupT | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 143190493 | |||||
chr4:143190579
|
A | G | 77 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(74): Show | 143 | HG00140.hp1 HG00408.hp2 HG00639.hp2 others(140): Show |
intron_variant | MODIFIER | c.818+2618A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143190579 | ||||||
chr4:143190679
|
T | G | 3 | a0001c0001t0008g0013a0001c0001t0008g0023a0001c0001t0018g0070 | 6 | HG02109.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.818+2718T>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143190679 | ||||||
chr4:143190744
|
G | A | 3 | a0001c0001t0008g0013a0001c0001t0008g0023a0001c0001t0018g0070 | 6 | HG02109.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.818+2783G>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143190744 | ||||||
chr4:143190802
|
C | T | 100 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(97): Show | 177 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.818+2841C>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143190802 | ||||||
chr4:143190896
|
A | G | 1 | a0001c0001t0024g0072 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.818+2935A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143190896 | ||||||
chr4:143191048
|
G | GTGATCCT others(6): Show |
1 | a0001c0001t0024g0072 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.818+3099_818+3100i others(15): Show |
USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 143191048 | |||||
chr4:143191276
|
A | C | 1 | a0001c0001t0001g0110 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.818+3315A>C | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143191276 | ||||||
chr4:143191844
|
G | A | 1 | a0001c0002t0002g0043 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.819-3872G>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143191844 | ||||||
chr4:143192145
|
T | A | 5 | a0001c0001t0003g0119a0001c0001t0003g0122a0002c0004t0003g0015others(2): Show | 7 | HG01243.hp2 HG02451.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.819-3571T>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143192145 | ||||||
chr4:143192345
|
G | T | 1 | a0001c0003t0012g0033 | 2 | HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.819-3371G>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143192345 | ||||||
chr4:143192459
|
C | T | 8 | a0001c0003t0006g0011a0001c0003t0006g0017a0001c0003t0006g0038others(5): Show | 10 | HG00140.hp2 HG00280.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.819-3257C>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143192459 | ||||||
chr4:143192479
|
A | C | 1 | a0001c0001t0001g0100 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.819-3237A>C | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143192479 | ||||||
chr4:143192550
|
C | CT | 12 | a0001c0001t0001g0026a0001c0001t0001g0073a0001c0001t0001g0075others(9): Show | 13 | HG01099.hp1 HG02027.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.819-3145dupT | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 143192550 | |||||
chr4:143192550
|
C | CTT | 52 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(49): Show | 108 | HG00140.hp1 HG00408.hp2 HG00639.hp2 others(105): Show |
intron_variant | MODIFIER | c.819-3146_819-3145d others(4): Show |
USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 143192550 | |||||
chr4:143192550
|
C | CTTT | 15 | a0001c0001t0001g0030a0001c0001t0001g0098a0001c0001t0001g0099others(12): Show | 23 | HG01243.hp2 HG01993.hp1 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.819-3147_819-3145d others(5): Show |
USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 143192550 | |||||
chr4:143192550
|
CT | C | 10 | a0001c0001t0018g0070a0001c0002t0002g0048a0001c0002t0002g0049others(7): Show | 15 | HG01099.hp2 HG01891.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.819-3145delT | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 143192550 | |||||
chr4:143192550
|
CTT | C | 2 | a0001c0001t0008g0013a0001c0001t0008g0023 | 5 | HG02109.hp1 HG02257.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.819-3146_819-3145d others(4): Show |
USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 143192550 | |||||
chr4:143192574
|
T | G | 1 | a0001c0001t0001g0077 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.819-3142T>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143192574 | ||||||
chr4:143192647
|
T | A | 78 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(75): Show | 144 | HG00140.hp1 HG00408.hp2 HG00639.hp2 others(141): Show |
intron_variant | MODIFIER | c.819-3069T>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143192647 | ||||||
chr4:143192769
|
G | A | 18 | a0001c0001t0003g0004a0001c0001t0003g0031a0001c0001t0003g0119others(15): Show | 32 | HG01070.hp1 HG01071.hp2 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.819-2947G>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143192769 | ||||||
chr4:143192827
|
T | A | 1 | a0001c0002t0002g0019 | 2 | NA18967.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.819-2889T>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143192827 | ||||||
chr4:143192828
|
A | G | 1 | a0001c0002t0002g0019 | 2 | NA18967.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.819-2888A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143192828 | ||||||
chr4:143192888
|
G | T | 1 | a0001c0001t0001g0096 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.819-2828G>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143192888 | ||||||
chr4:143193042
|
C | T | 49 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(46): Show | 96 | HG00140.hp1 HG00408.hp2 HG00639.hp2 others(93): Show |
intron_variant | MODIFIER | c.819-2674C>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143193042 | ||||||
chr4:143193126
|
T | C | 1 | a0001c0001t0024g0072 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.819-2590T>C | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143193126 | ||||||
chr4:143193260
|
A | G | 18 | a0001c0003t0004g0006a0001c0003t0004g0016a0001c0003t0004g0022others(15): Show | 25 | HG00140.hp2 HG00280.hp1 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.819-2456A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143193260 | ||||||
chr4:143193274
|
A | G | 3 | a0002c0004t0003g0015a0002c0004t0003g0120a0002c0004t0003g0121 | 5 | HG01243.hp2 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.819-2442A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143193274 | ||||||
chr4:143193521
|
G | A | 3 | a0001c0001t0008g0013a0001c0001t0008g0023a0001c0001t0018g0070 | 6 | HG02109.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.819-2195G>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143193521 | ||||||
chr4:143193778
|
C | A | 4 | a0001c0003t0004g0006a0001c0003t0004g0016a0001c0003t0004g0037others(1): Show | 8 | HG01891.hp2 HG02055.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.819-1938C>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143193778 | ||||||
chr4:143193878
|
G | A | 1 | a0001c0001t0001g0098 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.819-1838G>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143193878 | ||||||
chr4:143194149
|
T | C | 1 | a0001c0002t0002g0051 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.819-1567T>C | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143194149 | ||||||
chr4:143194513
|
C | CT | 12 | a0001c0001t0001g0095a0001c0001t0003g0004a0001c0001t0003g0031others(9): Show | 23 | HG01070.hp1 HG01071.hp2 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.819-1192dupT | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 143194513 | |||||
chr4:143194536
|
C | G | 1 | a0001c0001t0007g0036 | 2 | HG02970.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.819-1180C>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143194536 | ||||||
chr4:143194577
|
G | A | 2 | a0001c0001t0010g0032a0001c0001t0010g0124 | 3 | HG03130.hp2 HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.819-1139G>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143194577 | ||||||
chr4:143194610
|
C | T | 1 | a0001c0001t0024g0072 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.819-1106C>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143194610 | ||||||
chr4:143194630
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.819-1086C>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143194630 | ||||||
chr4:143194870
|
G | T | 1 | a0001c0001t0023g0074 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.819-846G>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143194870 | ||||||
chr4:143194892
|
T | A | 1 | a0001c0001t0003g0122 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.819-824T>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143194892 | ||||||
chr4:143194893
|
A | C | 1 | a0001c0001t0003g0122 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.819-823A>C | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143194893 | ||||||
chr4:143194894
|
C | CT | 32 | a0001c0001t0003g0031a0001c0001t0003g0119a0001c0001t0007g0034others(29): Show | 57 | HG00280.hp2 HG00408.hp1 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.819-807dupT | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 143194894 | |||||
chr4:143194894
|
C | T | 1 | a0001c0001t0003g0122 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.819-822C>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143194894 | ||||||
chr4:143194894
|
CT | C | 17 | a0001c0001t0001g0081a0001c0001t0003g0125a0001c0001t0005g0027others(14): Show | 24 | HG00140.hp2 HG00280.hp1 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.819-807delT | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 143194894 | |||||
chr4:143195024
|
TTTG | T | 3 | a0002c0004t0003g0015a0002c0004t0003g0120a0002c0004t0003g0121 | 5 | HG01243.hp2 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.819-689_819-687del others(3): Show |
USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 143195024 | |||||
chr4:143195457
|
C | T | 2 | a0001c0001t0001g0005a0001c0001t0001g0099 | 8 | HG01243.hp1 HG02280.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.819-259C>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143195457 | ||||||
chr4:143195458
|
G | A | 1 | a0001c0003t0004g0068 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.819-258G>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143195458 | ||||||
chr4:143195486
|
C | A | 1 | a0001c0001t0001g0080 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.819-230C>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143195486 | ||||||
chr4:143195539
|
A | G | 1 | a0001c0003t0012g0033 | 2 | HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.819-177A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 2/9 | chr4 | 143195539 | ||||||
chr4:143195944
|
GTTA | G | 6 | a0001c0001t0007g0034a0001c0001t0007g0035a0001c0001t0007g0036others(3): Show | 9 | HG01192.hp1 HG02280.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.948+102_948+104del others(3): Show |
USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | 143195944 | |||||
chr4:143195950
|
GTTGTT | G | 20 | a0001c0003t0004g0006a0001c0003t0004g0016a0001c0003t0004g0022others(17): Show | 28 | HG00140.hp2 HG00280.hp1 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.948+114_948+118del others(5): Show |
USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | 143195950 | |||||
chr4:143196135
|
G | A | 1 | a0001c0002t0002g0044 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.948+290G>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 3/9 | chr4 | 143196135 | ||||||
chr4:143196237
|
C | T | 1 | a0001c0002t0002g0058 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.948+392C>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 3/9 | chr4 | 143196237 | ||||||
chr4:143196278
|
C | T | 58 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(55): Show | 110 | HG00140.hp1 HG00408.hp2 HG00639.hp2 others(107): Show |
intron_variant | MODIFIER | c.948+433C>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 3/9 | chr4 | 143196278 | ||||||
chr4:143196332
|
A | T | 1 | a0001c0003t0006g0067 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.948+487A>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 3/9 | chr4 | 143196332 | ||||||
chr4:143196499
|
G | A | 101 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(98): Show | 178 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.948+654G>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 3/9 | chr4 | 143196499 | ||||||
chr4:143196515
|
A | G | 7 | a0001c0001t0005g0014a0001c0001t0005g0025a0001c0001t0005g0027others(4): Show | 12 | HG01496.hp2 HG02572.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.948+670A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 3/9 | chr4 | 143196515 | ||||||
chr4:143196740
|
T | G | 3 | a0001c0001t0008g0013a0001c0001t0008g0023a0001c0001t0018g0070 | 6 | HG02109.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.948+895T>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 3/9 | chr4 | 143196740 | ||||||
chr4:143196905
|
T | A | 1 | a0001c0002t0002g0018 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.949-918T>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 3/9 | chr4 | 143196905 | ||||||
chr4:143197019
|
C | T | 6 | a0001c0001t0007g0034a0001c0001t0007g0035a0001c0001t0007g0036others(3): Show | 9 | HG01192.hp1 HG02280.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.949-804C>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 3/9 | chr4 | 143197019 | ||||||
chr4:143197097
|
T | G | 1 | a0001c0001t0001g0082 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.949-726T>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 3/9 | chr4 | 143197097 | ||||||
chr4:143198020
|
A | G | 1 | a0001c0001t0007g0035 | 2 | HG02486.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1050+96A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 4/9 | chr4 | 143198020 | ||||||
chr4:143198169
|
G | A | 1 | a0001c0001t0003g0031 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1050+245G>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 4/9 | chr4 | 143198169 | ||||||
chr4:143198171
|
A | C | 1 | a0001c0001t0024g0072 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1050+247A>C | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 4/9 | chr4 | 143198171 | ||||||
chr4:143198290
|
A | G | 1 | a0001c0002t0002g0057 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1050+366A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 4/9 | chr4 | 143198290 | ||||||
chr4:143198529
|
T | A | 20 | a0001c0003t0004g0006a0001c0003t0004g0016a0001c0003t0004g0022others(17): Show | 28 | HG00140.hp2 HG00280.hp1 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.1050+605T>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 4/9 | chr4 | 143198529 | ||||||
chr4:143198780
|
G | A | 77 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(74): Show | 143 | HG00140.hp1 HG00408.hp2 HG00639.hp2 others(140): Show |
intron_variant | MODIFIER | c.1050+856G>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 4/9 | chr4 | 143198780 | ||||||
chr4:143198961
|
T | G | 20 | a0001c0003t0004g0006a0001c0003t0004g0016a0001c0003t0004g0022others(17): Show | 28 | HG00140.hp2 HG00280.hp1 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.1050+1037T>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 4/9 | chr4 | 143198961 | ||||||
chr4:143199051
|
A | G | 101 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(98): Show | 178 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.1050+1127A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 4/9 | chr4 | 143199051 | ||||||
chr4:143199053
|
G | A | 1 | a0006c0010t0013g0118 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1050+1129G>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 4/9 | chr4 | 143199053 | ||||||
chr4:143199146
|
G | T | 12 | a0001c0001t0003g0004a0001c0001t0003g0031a0001c0001t0003g0119others(9): Show | 23 | HG01070.hp1 HG01071.hp2 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.1050+1222G>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 4/9 | chr4 | 143199146 | ||||||
chr4:143199212
|
C | T | 1 | a0001c0001t0003g0125 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1050+1288C>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 4/9 | chr4 | 143199212 | ||||||
chr4:143199213
|
G | A | 6 | a0001c0001t0007g0034a0001c0001t0007g0035a0001c0001t0007g0036others(3): Show | 9 | HG01192.hp1 HG02280.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1050+1289G>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 4/9 | chr4 | 143199213 | ||||||
chr4:143199377
|
A | G | 1 | a0001c0003t0004g0066 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1050+1453A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 4/9 | chr4 | 143199377 | ||||||
chr4:143199527
|
C | T | 77 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(74): Show | 143 | HG00140.hp1 HG00408.hp2 HG00639.hp2 others(140): Show |
intron_variant | MODIFIER | c.1050+1603C>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 4/9 | chr4 | 143199527 | ||||||
chr4:143199776
|
GTCT | G | 6 | a0001c0001t0007g0034a0001c0001t0007g0035a0001c0001t0007g0036others(3): Show | 9 | HG01192.hp1 HG02280.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1050+1857_1050+185 others(7): Show |
USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr4 | 143199776 | |||||
chr4:143200011
|
A | T | 100 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(97): Show | 177 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.1050+2087A>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 4/9 | chr4 | 143200011 | ||||||
chr4:143200158
|
G | A | 1 | a0001c0003t0006g0011 | 3 | HG00140.hp2 HG00280.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.1050+2234G>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 4/9 | chr4 | 143200158 | ||||||
chr4:143200231
|
G | A | 1 | a0001c0001t0024g0072 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1050+2307G>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 4/9 | chr4 | 143200231 | ||||||
chr4:143200659
|
G | T | 9 | a0001c0003t0004g0006a0001c0003t0004g0016a0001c0003t0004g0022others(6): Show | 14 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.1050+2735G>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 4/9 | chr4 | 143200659 | ||||||
chr4:143200714
|
G | A | 3 | a0001c0001t0008g0013a0001c0001t0008g0023a0001c0001t0018g0070 | 6 | HG02109.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1051-2694G>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 4/9 | chr4 | 143200714 | ||||||
chr4:143200890
|
T | C | 1 | a0001c0001t0005g0078 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1051-2518T>C | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 4/9 | chr4 | 143200890 | ||||||
chr4:143201024
|
C | T | 1 | a0001c0003t0004g0066 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1051-2384C>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 4/9 | chr4 | 143201024 | ||||||
chr4:143201074
|
A | G | 39 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(36): Show | 86 | HG00140.hp1 HG00408.hp2 HG00639.hp2 others(83): Show |
intron_variant | MODIFIER | c.1051-2334A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 4/9 | chr4 | 143201074 | ||||||
chr4:143201220
|
C | T | 2 | a0001c0001t0001g0110a0001c0001t0020g0106 | 2 | HG01993.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.1051-2188C>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 4/9 | chr4 | 143201220 | ||||||
chr4:143201277
|
G | A | 3 | a0001c0001t0008g0013a0001c0001t0008g0023a0001c0001t0018g0070 | 6 | HG02109.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1051-2131G>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 4/9 | chr4 | 143201277 | ||||||
chr4:143201294
|
C | T | 1 | a0001c0001t0024g0072 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1051-2114C>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 4/9 | chr4 | 143201294 | ||||||
chr4:143201359
|
C | T | 1 | a0001c0003t0004g0066 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1051-2049C>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 4/9 | chr4 | 143201359 | ||||||
chr4:143201401
|
A | G | 1 | a0001c0001t0005g0079 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1051-2007A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 4/9 | chr4 | 143201401 | ||||||
chr4:143201523
|
T | C | 20 | a0001c0003t0004g0006a0001c0003t0004g0016a0001c0003t0004g0022others(17): Show | 28 | HG00140.hp2 HG00280.hp1 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.1051-1885T>C | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 4/9 | chr4 | 143201523 | ||||||
chr4:143201646
|
G | T | 2 | a0001c0001t0008g0013a0001c0001t0008g0023 | 5 | HG02109.hp1 HG02257.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1051-1762G>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 4/9 | chr4 | 143201646 | ||||||
chr4:143201989
|
C | A | 2 | a0001c0001t0001g0084a0001c0001t0001g0100 | 2 | HG00642.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.1051-1419C>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 4/9 | chr4 | 143201989 | ||||||
chr4:143202029
|
ATTAC | A | 1 | a0001c0003t0004g0016 | 2 | HG02055.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1051-1376_1051-137 others(8): Show |
USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr4 | 143202029 | |||||
chr4:143202101
|
CTT | C | 9 | a0001c0003t0004g0006a0001c0003t0004g0016a0001c0003t0004g0022others(6): Show | 14 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.1051-1304_1051-130 others(6): Show |
USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr4 | 143202101 | |||||
chr4:143202219
|
A | G | 1 | a0001c0001t0024g0072 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1051-1189A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 4/9 | chr4 | 143202219 | ||||||
chr4:143202257
|
A | G | 1 | a0001c0001t0001g0105 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1051-1151A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 4/9 | chr4 | 143202257 | ||||||
chr4:143202337
|
A | G | 1 | a0001c0003t0004g0066 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1051-1071A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 4/9 | chr4 | 143202337 | ||||||
chr4:143202339
|
G | A | 1 | a0001c0001t0003g0031 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1051-1069G>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 4/9 | chr4 | 143202339 | ||||||
chr4:143202414
|
C | T | 101 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(98): Show | 178 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.1051-994C>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 4/9 | chr4 | 143202414 | ||||||
chr4:143202473
|
T | G | 1 | a0006c0010t0013g0118 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1051-935T>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 4/9 | chr4 | 143202473 | ||||||
chr4:143202492
|
T | G | 6 | a0001c0001t0007g0034a0001c0001t0007g0035a0001c0001t0007g0036others(3): Show | 9 | HG01192.hp1 HG02280.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1051-916T>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 4/9 | chr4 | 143202492 | ||||||
chr4:143203065
|
G | A | 2 | a0001c0002t0002g0048a0001c0002t0002g0052 | 2 | HG02622.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1051-343G>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 4/9 | chr4 | 143203065 | ||||||
chr4:143203119
|
G | T | 8 | a0001c0003t0006g0011a0001c0003t0006g0017a0001c0003t0006g0038others(5): Show | 10 | HG00140.hp2 HG00280.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1051-289G>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 4/9 | chr4 | 143203119 | ||||||
chr4:143203125
|
T | C | 101 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(98): Show | 178 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.1051-283T>C | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 4/9 | chr4 | 143203125 | ||||||
chr4:143203339
|
G | A | 77 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(74): Show | 143 | HG00140.hp1 HG00408.hp2 HG00639.hp2 others(140): Show |
intron_variant | MODIFIER | c.1051-69G>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 4/9 | chr4 | 143203339 | ||||||
chr4:143203694
|
A | G | 1 | a0001c0001t0001g0093 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1209+128A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 5/9 | chr4 | 143203694 | ||||||
chr4:143203894
|
G | T | 3 | a0001c0001t0003g0004a0001c0001t0003g0123a0001c0001t0003g0125 | 10 | HG01891.hp1 HG02109.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1209+328G>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 5/9 | chr4 | 143203894 | ||||||
chr4:143203932
|
A | C | 59 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(56): Show | 111 | HG00140.hp1 HG00408.hp2 HG00639.hp2 others(108): Show |
intron_variant | MODIFIER | c.1209+366A>C | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 5/9 | chr4 | 143203932 | ||||||
chr4:143204008
|
G | A | 1 | a0001c0001t0001g0028 | 2 | HG01192.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.1209+442G>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 5/9 | chr4 | 143204008 | ||||||
chr4:143204095
|
C | A | 1 | a0001c0001t0001g0075 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1209+529C>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 5/9 | chr4 | 143204095 | ||||||
chr4:143204142
|
C | T | 1 | a0001c0009t0002g0064 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1209+576C>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 5/9 | chr4 | 143204142 | ||||||
chr4:143204303
|
G | A | 1 | a0001c0002t0002g0012 | 3 | NA18945.hp1 NA18957.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.1209+737G>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 5/9 | chr4 | 143204303 | ||||||
chr4:143204351
|
G | T | 6 | a0001c0001t0007g0034a0001c0001t0007g0035a0001c0001t0007g0036others(3): Show | 9 | HG01192.hp1 HG02280.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1209+785G>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 5/9 | chr4 | 143204351 | ||||||
chr4:143204453
|
G | A | 2 | a0001c0001t0001g0084a0001c0001t0001g0100 | 2 | HG00642.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.1209+887G>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 5/9 | chr4 | 143204453 | ||||||
chr4:143204458
|
C | T | 1 | a0001c0001t0001g0092 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1209+892C>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 5/9 | chr4 | 143204458 | ||||||
chr4:143204516
|
A | G | 1 | a0001c0003t0004g0066 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1209+950A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 5/9 | chr4 | 143204516 | ||||||
chr4:143204577
|
CG | C | 3 | a0001c0003t0004g0006a0001c0003t0004g0037a0001c0003t0011g0006 | 6 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1209+1015delG | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr4 | 143204577 | |||||
chr4:143204814
|
T | C | 3 | a0001c0001t0005g0027a0001c0001t0005g0078a0001c0001t0005g0097 | 4 | HG02630.hp2 HG02886.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1210-1219T>C | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 5/9 | chr4 | 143204814 | ||||||
chr4:143204824
|
A | G | 1 | a0001c0003t0012g0033 | 2 | HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1210-1209A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 5/9 | chr4 | 143204824 | ||||||
chr4:143204948
|
T | A | 1 | a0001c0001t0001g0109 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1210-1085T>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 5/9 | chr4 | 143204948 | ||||||
chr4:143205139
|
T | G | 1 | a0001c0003t0006g0040 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1210-894T>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 5/9 | chr4 | 143205139 | ||||||
chr4:143205190
|
C | T | 5 | a0001c0001t0003g0119a0001c0001t0003g0122a0002c0004t0003g0015others(2): Show | 7 | HG01243.hp2 HG02451.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1210-843C>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 5/9 | chr4 | 143205190 | ||||||
chr4:143205219
|
C | T | 1 | a0001c0003t0004g0066 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1210-814C>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 5/9 | chr4 | 143205219 | ||||||
chr4:143205324
|
G | A | 3 | a0001c0001t0008g0013a0001c0001t0008g0023a0001c0001t0018g0070 | 6 | HG02109.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1210-709G>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 5/9 | chr4 | 143205324 | ||||||
chr4:143205349
|
T | C | 8 | a0001c0003t0006g0011a0001c0003t0006g0017a0001c0003t0006g0038others(5): Show | 10 | HG00140.hp2 HG00280.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1210-684T>C | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 5/9 | chr4 | 143205349 | ||||||
chr4:143205697
|
A | G | 1 | a0001c0003t0004g0066 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1210-336A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 5/9 | chr4 | 143205697 | ||||||
chr4:143205833
|
A | G | 20 | a0001c0003t0004g0006a0001c0003t0004g0016a0001c0003t0004g0022others(17): Show | 28 | HG00140.hp2 HG00280.hp1 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.1210-200A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 5/9 | chr4 | 143205833 | ||||||
chr4:143205943
|
T | TAAGAATC others(348): Show |
1 | a0001c0001t0001g0095 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1210-71_1210-70ins others(355): Show |
USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr4 | 143205943 | |||||
chr4:143206029
|
A | G | 1 | a0001c0006t0006g0039 | 1 | HG03834.hp2 | splice_region_variant&intron_variant | LOW | c.1210-4A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 5/9 | chr4 | 143206029 | ||||||
chr4:143206246
|
T | G | 3 | a0001c0001t0008g0013a0001c0001t0008g0023a0001c0001t0018g0070 | 6 | HG02109.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1403+20T>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 6/9 | chr4 | 143206246 | ||||||
chr4:143206330
|
A | G | 1 | a0001c0003t0012g0033 | 2 | HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1403+104A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 6/9 | chr4 | 143206330 | ||||||
chr4:143206333
|
A | G | 1 | a0006c0010t0013g0118 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1403+107A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 6/9 | chr4 | 143206333 | ||||||
chr4:143206372
|
T | C | 20 | a0001c0003t0004g0006a0001c0003t0004g0016a0001c0003t0004g0022others(17): Show | 28 | HG00140.hp2 HG00280.hp1 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.1403+146T>C | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 6/9 | chr4 | 143206372 | ||||||
chr4:143206428
|
G | A | 1 | a0001c0001t0024g0072 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1403+202G>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 6/9 | chr4 | 143206428 | ||||||
chr4:143206582
|
C | T | 5 | a0001c0001t0003g0119a0001c0001t0003g0122a0002c0004t0003g0015others(2): Show | 7 | HG01243.hp2 HG02451.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1403+356C>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 6/9 | chr4 | 143206582 | ||||||
chr4:143206600
|
G | T | 1 | a0001c0003t0004g0016 | 2 | HG02055.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1403+374G>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 6/9 | chr4 | 143206600 | ||||||
chr4:143206625
|
G | A | 16 | a0001c0002t0002g0003a0001c0002t0002g0009a0001c0002t0002g0045others(13): Show | 33 | HG00280.hp2 HG00408.hp1 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.1403+399G>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 6/9 | chr4 | 143206625 | ||||||
chr4:143207252
|
G | A | 1 | a0001c0001t0001g0096 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1403+1026G>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 6/9 | chr4 | 143207252 | ||||||
chr4:143207288
|
C | G | 1 | a0001c0001t0018g0070 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1403+1062C>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 6/9 | chr4 | 143207288 | ||||||
chr4:143207325
|
G | A | 2 | a0001c0001t0010g0032a0001c0001t0010g0124 | 3 | HG03130.hp2 HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1403+1099G>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 6/9 | chr4 | 143207325 | ||||||
chr4:143207326
|
T | G | 1 | a0001c0001t0007g0036 | 2 | HG02970.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1403+1100T>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 6/9 | chr4 | 143207326 | ||||||
chr4:143207327
|
C | T | 18 | a0001c0001t0003g0004a0001c0001t0003g0031a0001c0001t0003g0119others(15): Show | 32 | HG01070.hp1 HG01071.hp2 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.1403+1101C>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 6/9 | chr4 | 143207327 | ||||||
chr4:143207337
|
A | G | 1 | a0006c0010t0013g0118 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1403+1111A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 6/9 | chr4 | 143207337 | ||||||
chr4:143207380
|
A | T | 8 | a0001c0003t0006g0011a0001c0003t0006g0017a0001c0003t0006g0038others(5): Show | 10 | HG00140.hp2 HG00280.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1403+1154A>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 6/9 | chr4 | 143207380 | ||||||
chr4:143207408
|
T | C | 100 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(97): Show | 177 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.1403+1182T>C | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 6/9 | chr4 | 143207408 | ||||||
chr4:143207427
|
A | G | 1 | a0006c0010t0013g0118 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1403+1201A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 6/9 | chr4 | 143207427 | ||||||
chr4:143207648
|
GGTTT | G | 3 | a0001c0001t0001g0109a0001c0001t0016g0108a0001c0001t0022g0102 | 3 | HG03490.hp1 HG04199.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1403+1429_1403+143 others(8): Show |
USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | 143207648 | |||||
chr4:143207666
|
AT | A | 100 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(97): Show | 177 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.1403+1454delT | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | 143207666 | |||||
chr4:143207821
|
G | A | 5 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0076others(2): Show | 14 | HG01243.hp1 HG02280.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1403+1595G>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 6/9 | chr4 | 143207821 | ||||||
chr4:143207884
|
G | A | 3 | a0001c0001t0008g0013a0001c0001t0008g0023a0001c0001t0018g0070 | 6 | HG02109.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1403+1658G>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 6/9 | chr4 | 143207884 | ||||||
chr4:143207923
|
C | A | 77 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(74): Show | 143 | HG00140.hp1 HG00408.hp2 HG00639.hp2 others(140): Show |
intron_variant | MODIFIER | c.1404-1641C>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 6/9 | chr4 | 143207923 | ||||||
chr4:143208409
|
A | C | 1 | a0001c0002t0002g0061 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1404-1155A>C | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 6/9 | chr4 | 143208409 | ||||||
chr4:143208518
|
T | A | 1 | a0001c0001t0001g0117 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1404-1046T>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 6/9 | chr4 | 143208518 | ||||||
chr4:143208526
|
A | G | 1 | a0001c0002t0002g0024 | 2 | NA18906.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1404-1038A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 6/9 | chr4 | 143208526 | ||||||
chr4:143208698
|
A | G | 137 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(134): Show | 256 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.1404-866A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 6/9 | chr4 | 143208698 | ||||||
chr4:143208716
|
G | A | 6 | a0001c0001t0007g0034a0001c0001t0007g0035a0001c0001t0007g0036others(3): Show | 9 | HG01192.hp1 HG02280.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1404-848G>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 6/9 | chr4 | 143208716 | ||||||
chr4:143208808
|
A | G | 101 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(98): Show | 178 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.1404-756A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 6/9 | chr4 | 143208808 | ||||||
chr4:143208851
|
T | A | 1 | a0001c0003t0012g0033 | 2 | HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1404-713T>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 6/9 | chr4 | 143208851 | ||||||
chr4:143208950
|
C | T | 1 | a0001c0002t0002g0009 | 4 | HG01346.hp2 HG02145.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1404-614C>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 6/9 | chr4 | 143208950 | ||||||
chr4:143208965
|
C | T | 78 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(75): Show | 144 | HG00140.hp1 HG00408.hp2 HG00639.hp2 others(141): Show |
intron_variant | MODIFIER | c.1404-599C>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 6/9 | chr4 | 143208965 | ||||||
chr4:143209013
|
C | T | 2 | a0001c0001t0010g0032a0001c0001t0010g0124 | 3 | HG03130.hp2 HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1404-551C>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 6/9 | chr4 | 143209013 | ||||||
chr4:143209035
|
T | C | 1 | a0001c0001t0024g0072 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1404-529T>C | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 6/9 | chr4 | 143209035 | ||||||
chr4:143209065
|
A | AT | 8 | a0001c0003t0006g0011a0001c0003t0006g0017a0001c0003t0006g0038others(5): Show | 10 | HG00140.hp2 HG00280.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1404-492dupT | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | 143209065 | |||||
chr4:143209104
|
ACTTAT | A | 77 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(74): Show | 143 | HG00140.hp1 HG00408.hp2 HG00639.hp2 others(140): Show |
intron_variant | MODIFIER | c.1404-454_1404-450d others(7): Show |
USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | 143209104 | |||||
chr4:143209129
|
A | T | 1 | a0001c0001t0001g0094 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1404-435A>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 6/9 | chr4 | 143209129 | ||||||
chr4:143209371
|
G | A | 1 | a0001c0001t0001g0112 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1404-193G>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 6/9 | chr4 | 143209371 | ||||||
chr4:143209444
|
T | C | 20 | a0001c0003t0004g0006a0001c0003t0004g0016a0001c0003t0004g0022others(17): Show | 28 | HG00140.hp2 HG00280.hp1 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.1404-120T>C | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 6/9 | chr4 | 143209444 | ||||||
chr4:143209509
|
A | G | 18 | a0001c0001t0003g0004a0001c0001t0003g0031a0001c0001t0003g0119others(15): Show | 32 | HG01070.hp1 HG01071.hp2 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.1404-55A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 6/9 | chr4 | 143209509 | ||||||
chr4:143209812
|
C | T | 6 | a0001c0001t0007g0034a0001c0001t0007g0035a0001c0001t0007g0036others(3): Show | 9 | HG01192.hp1 HG02280.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1497+155C>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 7/9 | chr4 | 143209812 | ||||||
chr4:143209826
|
A | AT | 77 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(74): Show | 143 | HG00140.hp1 HG00408.hp2 HG00639.hp2 others(140): Show |
intron_variant | MODIFIER | c.1497+177dupT | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr4 | 143209826 | |||||
chr4:143210153
|
T | A | 1 | a0001c0001t0024g0072 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1497+496T>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 7/9 | chr4 | 143210153 | ||||||
chr4:143210188
|
G | A | 1 | a0001c0001t0008g0023 | 2 | HG02257.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1497+531G>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 7/9 | chr4 | 143210188 | ||||||
chr4:143210204
|
G | A | 101 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(98): Show | 178 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.1497+547G>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 7/9 | chr4 | 143210204 | ||||||
chr4:143210216
|
A | G | 1 | a0001c0002t0002g0008 | 4 | HG01069.hp2 HG01934.hp1 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.1497+559A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 7/9 | chr4 | 143210216 | ||||||
chr4:143210217
|
A | G | 1 | a0001c0002t0002g0056 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1497+560A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 7/9 | chr4 | 143210217 | ||||||
chr4:143210586
|
C | CA | 5 | a0001c0001t0008g0013a0001c0001t0008g0023a0001c0001t0018g0070others(2): Show | 8 | HG02109.hp1 HG02257.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1497+941dupA | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr4 | 143210586 | |||||
chr4:143210609
|
G | T | 1 | a0001c0003t0006g0041 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1497+952G>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 7/9 | chr4 | 143210609 | ||||||
chr4:143210910
|
TATACTCA others(1): Show |
T | 5 | a0001c0002t0002g0045a0001c0002t0002g0051a0001c0002t0002g0060others(2): Show | 5 | HG00408.hp1 HG02040.hp2 NA18999.hp2 others(2): Show |
intron_variant | MODIFIER | c.1497+1257_1497+126 others(12): Show |
USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr4 | 143210910 | |||||
chr4:143210946
|
A | G | 1 | a0001c0001t0019g0127 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1497+1289A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 7/9 | chr4 | 143210946 | ||||||
chr4:143211191
|
T | A | 101 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(98): Show | 178 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.1498-1127T>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 7/9 | chr4 | 143211191 | ||||||
chr4:143211339
|
T | A | 1 | a0001c0001t0024g0072 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1498-979T>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 7/9 | chr4 | 143211339 | ||||||
chr4:143211384
|
A | G | 1 | a0001c0001t0005g0029 | 2 | HG02735.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.1498-934A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 7/9 | chr4 | 143211384 | ||||||
chr4:143211395
|
C | T | 1 | a0001c0001t0001g0091 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1498-923C>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 7/9 | chr4 | 143211395 | ||||||
chr4:143211469
|
A | G | 100 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(97): Show | 177 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.1498-849A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 7/9 | chr4 | 143211469 | ||||||
chr4:143211519
|
T | C | 78 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(75): Show | 144 | HG00140.hp1 HG00408.hp2 HG00639.hp2 others(141): Show |
intron_variant | MODIFIER | c.1498-799T>C | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 7/9 | chr4 | 143211519 | ||||||
chr4:143211767
|
A | C | 1 | a0001c0001t0003g0125 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1498-551A>C | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 7/9 | chr4 | 143211767 | ||||||
chr4:143211813
|
A | G | 1 | a0001c0001t0001g0090 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1498-505A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 7/9 | chr4 | 143211813 | ||||||
chr4:143211939
|
T | C | 1 | a0001c0001t0003g0119 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1498-379T>C | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 7/9 | chr4 | 143211939 | ||||||
chr4:143212021
|
T | G | 2 | a0001c0002t0025g0021a0001c0002t0026g0021 | 2 | HG03688.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.1498-297T>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 7/9 | chr4 | 143212021 | ||||||
chr4:143212045
|
C | T | 8 | a0001c0003t0006g0011a0001c0003t0006g0017a0001c0003t0006g0038others(5): Show | 10 | HG00140.hp2 HG00280.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1498-273C>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 7/9 | chr4 | 143212045 | ||||||
chr4:143212099
|
T | A | 1 | a0001c0001t0003g0122 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1498-219T>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 7/9 | chr4 | 143212099 | ||||||
chr4:143212104
|
A | G | 1 | a0001c0003t0004g0037 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1498-214A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 7/9 | chr4 | 143212104 | ||||||
chr4:143212264
|
T | G | 1 | a0001c0001t0001g0085 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1498-54T>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 7/9 | chr4 | 143212264 | ||||||
chr4:143212305
|
T | C | 1 | a0001c0001t0001g0086 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1498-13T>C | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 7/9 | chr4 | 143212305 | ||||||
chr4:143212592
|
C | CT | 78 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(75): Show | 144 | HG00140.hp1 HG00408.hp2 HG00639.hp2 others(141): Show |
intron_variant | MODIFIER | c.1604+173dupT | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr4 | 143212592 | |||||
chr4:143212704
|
G | A | 78 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(75): Show | 144 | HG00140.hp1 HG00408.hp2 HG00639.hp2 others(141): Show |
intron_variant | MODIFIER | c.1604+280G>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 8/9 | chr4 | 143212704 | ||||||
chr4:143212890
|
A | T | 77 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(74): Show | 143 | HG00140.hp1 HG00408.hp2 HG00639.hp2 others(140): Show |
intron_variant | MODIFIER | c.1604+466A>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 8/9 | chr4 | 143212890 | ||||||
chr4:143213115
|
G | A | 3 | a0002c0004t0003g0015a0002c0004t0003g0120a0002c0004t0003g0121 | 5 | HG01243.hp2 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1605-466G>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 8/9 | chr4 | 143213115 | ||||||
chr4:143213124
|
C | T | 59 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(56): Show | 111 | HG00140.hp1 HG00408.hp2 HG00639.hp2 others(108): Show |
intron_variant | MODIFIER | c.1605-457C>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 8/9 | chr4 | 143213124 | ||||||
chr4:143213179
|
G | A | 1 | a0001c0001t0008g0023 | 2 | HG02257.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1605-402G>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 8/9 | chr4 | 143213179 | ||||||
chr4:143213420
|
T | G | 1 | a0001c0001t0016g0108 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1605-161T>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 8/9 | chr4 | 143213420 | ||||||
chr4:143213567
|
A | G | 1 | a0001c0001t0024g0072 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1605-14A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 8/9 | chr4 | 143213567 | ||||||
chr4:143215040
|
T | G | 101 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(98): Show | 178 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.2967+97T>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 9/9 | chr4 | 143215040 | ||||||
chr4:143215053
|
A | G | 20 | a0001c0003t0004g0006a0001c0003t0004g0016a0001c0003t0004g0022others(17): Show | 28 | HG00140.hp2 HG00280.hp1 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.2967+110A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 9/9 | chr4 | 143215053 | ||||||
chr4:143215068
|
C | T | 1 | a0001c0001t0024g0072 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2967+125C>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 9/9 | chr4 | 143215068 | ||||||
chr4:143215252
|
T | C | 78 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(75): Show | 144 | HG00140.hp1 HG00408.hp2 HG00639.hp2 others(141): Show |
intron_variant | MODIFIER | c.2967+309T>C | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 9/9 | chr4 | 143215252 | ||||||
chr4:143215689
|
A | T | 2 | a0001c0001t0005g0027a0001c0001t0005g0078 | 3 | HG02886.hp2 NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2967+746A>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 9/9 | chr4 | 143215689 | ||||||
chr4:143215833
|
C | T | 101 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(98): Show | 178 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.2967+890C>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 9/9 | chr4 | 143215833 | ||||||
chr4:143216069
|
C | T | 4 | a0001c0002t0002g0007a0001c0002t0002g0024a0001c0002t0002g0048others(1): Show | 8 | HG02486.hp1 HG02622.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.2967+1126C>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 9/9 | chr4 | 143216069 | ||||||
chr4:143216182
|
T | G | 1 | a0001c0001t0001g0087 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.2967+1239T>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 9/9 | chr4 | 143216182 | ||||||
chr4:143216206
|
A | G | 78 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(75): Show | 144 | HG00140.hp1 HG00408.hp2 HG00639.hp2 others(141): Show |
intron_variant | MODIFIER | c.2967+1263A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 9/9 | chr4 | 143216206 | ||||||
chr4:143216478
|
AT | A | 23 | a0001c0001t0008g0013a0001c0001t0008g0023a0001c0001t0024g0072others(20): Show | 34 | HG00140.hp2 HG00280.hp1 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.2967+1549delT | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr4 | 143216478 | |||||
chr4:143216655
|
T | A | 1 | a0001c0001t0001g0088 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2967+1712T>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 9/9 | chr4 | 143216655 | ||||||
chr4:143216673
|
G | A | 11 | a0001c0001t0003g0004a0001c0001t0003g0031a0001c0001t0003g0119others(8): Show | 22 | HG01070.hp1 HG01071.hp2 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.2967+1730G>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 9/9 | chr4 | 143216673 | ||||||
chr4:143216728
|
G | A | 1 | a0001c0001t0003g0119 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2967+1785G>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 9/9 | chr4 | 143216728 | ||||||
chr4:143216809
|
C | CATTT | 2 | a0001c0001t0008g0013a0001c0001t0008g0023 | 5 | HG02109.hp1 HG02257.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2967+1882_2967+188 others(8): Show |
USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr4 | 143216809 | |||||
chr4:143217083
|
A | G | 1 | a0001c0003t0006g0041 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2967+2140A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 9/9 | chr4 | 143217083 | ||||||
chr4:143217377
|
C | A | 1 | a0001c0001t0001g0103 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2967+2434C>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 9/9 | chr4 | 143217377 | ||||||
chr4:143217906
|
A | C | 1 | a0001c0003t0006g0067 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2968-2389A>C | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 9/9 | chr4 | 143217906 | ||||||
chr4:143218244
|
G | A | 1 | a0001c0001t0001g0087 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.2968-2051G>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 9/9 | chr4 | 143218244 | ||||||
chr4:143218320
|
C | A | 3 | a0001c0001t0008g0013a0001c0001t0008g0023a0001c0001t0018g0070 | 6 | HG02109.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.2968-1975C>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 9/9 | chr4 | 143218320 | ||||||
chr4:143218471
|
A | G | 1 | a0001c0003t0012g0033 | 2 | HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2968-1824A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 9/9 | chr4 | 143218471 | ||||||
chr4:143218559
|
T | A | 78 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(75): Show | 144 | HG00140.hp1 HG00408.hp2 HG00639.hp2 others(141): Show |
intron_variant | MODIFIER | c.2968-1736T>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 9/9 | chr4 | 143218559 | ||||||
chr4:143218815
|
T | C | 3 | a0001c0001t0008g0013a0001c0001t0008g0023a0001c0001t0018g0070 | 6 | HG02109.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.2968-1480T>C | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 9/9 | chr4 | 143218815 | ||||||
chr4:143218920
|
T | A | 1 | a0001c0002t0002g0055 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2968-1375T>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 9/9 | chr4 | 143218920 | ||||||
chr4:143218925
|
C | T | 1 | a0001c0001t0024g0072 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2968-1370C>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 9/9 | chr4 | 143218925 | ||||||
chr4:143219223
|
G | A | 77 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(74): Show | 143 | HG00140.hp1 HG00408.hp2 HG00639.hp2 others(140): Show |
intron_variant | MODIFIER | c.2968-1072G>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 9/9 | chr4 | 143219223 | ||||||
chr4:143219255
|
A | G | 9 | a0001c0003t0006g0011a0001c0003t0006g0017a0001c0003t0006g0038others(6): Show | 11 | HG00140.hp2 HG00280.hp1 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.2968-1040A>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 9/9 | chr4 | 143219255 | ||||||
chr4:143219439
|
G | A | 77 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(74): Show | 143 | HG00140.hp1 HG00408.hp2 HG00639.hp2 others(140): Show |
intron_variant | MODIFIER | c.2968-856G>A | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 9/9 | chr4 | 143219439 | ||||||
chr4:143219482
|
T | C | 1 | a0001c0001t0001g0089 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.2968-813T>C | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 9/9 | chr4 | 143219482 | ||||||
chr4:143219512
|
C | T | 77 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0010others(74): Show | 143 | HG00140.hp1 HG00408.hp2 HG00639.hp2 others(140): Show |
intron_variant | MODIFIER | c.2968-783C>T | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 9/9 | chr4 | 143219512 | ||||||
chr4:143219560
|
C | G | 9 | a0001c0003t0004g0006a0001c0003t0004g0016a0001c0003t0004g0022others(6): Show | 14 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.2968-735C>G | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 9/9 | chr4 | 143219560 | ||||||
chr4:143220179
|
T | C | 1 | a0001c0001t0007g0128 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2968-116T>C | USP38 | ENSG00000170185.11 | transcript | ENST00000307017.9 | protein_coding | 9/9 | chr4 | 143220179 |