Item | Value |
---|---|
geneid | 23016 |
ensemblid | ENSG00000075914.13 |
hgncid | 28112 |
symbol | EXOSC7 |
name | exosome component 7 |
refseq_nuc | NM_015004.4 |
refseq_prot | NP_055819.2 |
ensembl_nuc | ENST00000265564.8 |
ensembl_prot | ENSP00000265564.7 |
mane_status | MANE Select |
chr | chr3 |
start | 44976244 |
end | 45011471 |
strand | + |
ver | v1.2 |
region | chr3:44976244-45011471 |
region5000 | chr3:44971244-45016471 |
regionname0 | EXOSC7_chr3_44976244_45011471 |
regionname5000 | EXOSC7_chr3_44971244_45016471 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0000 | 0/0 | 0 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | copy fasta | chr3 | 44971244 | 45016471 |
a0001 | 0/0 | 291 | 211 | 62 | 35 | 84 | 7 | 23 | 62 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | copy fasta | chr3 | 44971244 | 45016471 |
a0002 | 1/1 | 291 | 92 | 22 | 29 | 24 | 7 | 8 | 19 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | copy fasta | chr3 | 44971244 | 45016471 |
a0003 | 0/0 | 291 | 20 | 0 | 7 | 7 | 2 | 4 | 6 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | copy fasta | chr3 | 44971244 | 45016471 |
a0004 | 0/0 | 291 | 13 | 10 | 3 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | copy fasta | chr3 | 44971244 | 45016471 |
a0005 | 0/0 | 291 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | copy fasta | chr3 | 44971244 | 45016471 |
a0006 | 0/0 | 291 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | copy fasta | chr3 | 44971244 | 45016471 |
a0007 | 0/0 | 291 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | copy fasta | chr3 | 44971244 | 45016471 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 876 | 207 | 59 | 35 | 83 | 7 | 23 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | copy fasta | chr3 | 44971244 | 45016471 |
c0002 | 1/1 | 876 | 91 | 22 | 28 | 24 | 7 | 8 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | copy fasta | chr3 | 44971244 | 45016471 |
c0003 | 0/0 | 876 | 18 | 0 | 5 | 7 | 2 | 4 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | copy fasta | chr3 | 44971244 | 45016471 |
c0004 | 0/0 | 876 | 13 | 10 | 3 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | copy fasta | chr3 | 44971244 | 45016471 |
c0005 | 0/0 | 876 | 3 | 3 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | copy fasta | chr3 | 44971244 | 45016471 |
c0006 | 0/0 | 876 | 2 | 0 | 2 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | copy fasta | chr3 | 44971244 | 45016471 |
c0007 | 0/0 | 876 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | copy fasta | chr3 | 44971244 | 45016471 |
c0008 | 0/0 | 596 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | copy fasta | chr3 | 44971244 | 45016471 |
c0009 | 0/0 | 876 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | copy fasta | chr3 | 44971244 | 45016471 |
c0010 | 0/0 | 876 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | copy fasta | chr3 | 44971244 | 45016471 |
c0011 | 0/0 | 876 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | copy fasta | chr3 | 44971244 | 45016471 |
c0012 | 0/0 | 876 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | copy fasta | chr3 | 44971244 | 45016471 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 167 | 340 | 94 | 74 | 116 | 16 | 38 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | copy fasta | chr3 | 44971244 | 45016471 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 14 | 2 | 6 | 5 | 0 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0002 | 0/0 | 7 | 0 | 1 | 5 | 1 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0003 | 0/0 | 7 | 0 | 1 | 6 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0004 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0006 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0007 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0008 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0009 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0010 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0014 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0020 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0021 | 0/1 | 2 | 0 | 0 | 0 | 0 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0023 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0030 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0034 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0035 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0000c0008 | 0/0 | 596 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | copy fasta | chr3 | 44971244 | 45016471 |
a0001c0001 | 0/0 | 876 | 207 | 59 | 35 | 83 | 7 | 23 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | copy fasta | chr3 | 44971244 | 45016471 |
a0001c0005 | 0/0 | 876 | 3 | 3 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | copy fasta | chr3 | 44971244 | 45016471 |
a0001c0012 | 0/0 | 876 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | copy fasta | chr3 | 44971244 | 45016471 |
a0002c0002 | 1/1 | 876 | 91 | 22 | 28 | 24 | 7 | 8 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | copy fasta | chr3 | 44971244 | 45016471 |
a0002c0007 | 0/0 | 876 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | copy fasta | chr3 | 44971244 | 45016471 |
a0003c0003 | 0/0 | 876 | 18 | 0 | 5 | 7 | 2 | 4 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | copy fasta | chr3 | 44971244 | 45016471 |
a0003c0006 | 0/0 | 876 | 2 | 0 | 2 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | copy fasta | chr3 | 44971244 | 45016471 |
a0004c0004 | 0/0 | 876 | 13 | 10 | 3 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | copy fasta | chr3 | 44971244 | 45016471 |
a0005c0009 | 0/0 | 876 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | copy fasta | chr3 | 44971244 | 45016471 |
a0006c0011 | 0/0 | 876 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | copy fasta | chr3 | 44971244 | 45016471 |
a0007c0010 | 0/0 | 876 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | copy fasta | chr3 | 44971244 | 45016471 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0000c0008t0001 | 0/0 | 762 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | copy fasta | chr3 | 44971244 | 45016471 |
a0001c0001t0001 | 0/0 | 1042 | 207 | 59 | 35 | 83 | 7 | 23 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | copy fasta | chr3 | 44971244 | 45016471 |
a0001c0005t0001 | 0/0 | 1042 | 3 | 3 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | copy fasta | chr3 | 44971244 | 45016471 |
a0001c0012t0001 | 0/0 | 1042 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | copy fasta | chr3 | 44971244 | 45016471 |
a0002c0002t0001 | 1/1 | 1042 | 91 | 22 | 28 | 24 | 7 | 8 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | copy fasta | chr3 | 44971244 | 45016471 |
a0002c0007t0001 | 0/0 | 1042 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | copy fasta | chr3 | 44971244 | 45016471 |
a0003c0003t0001 | 0/0 | 1042 | 18 | 0 | 5 | 7 | 2 | 4 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | copy fasta | chr3 | 44971244 | 45016471 |
a0003c0006t0001 | 0/0 | 1042 | 2 | 0 | 2 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | copy fasta | chr3 | 44971244 | 45016471 |
a0004c0004t0001 | 0/0 | 1042 | 13 | 10 | 3 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | copy fasta | chr3 | 44971244 | 45016471 |
a0005c0009t0001 | 0/0 | 1042 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | copy fasta | chr3 | 44971244 | 45016471 |
a0006c0011t0001 | 0/0 | 1042 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | copy fasta | chr3 | 44971244 | 45016471 |
a0007c0010t0001 | 0/0 | 1042 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | copy fasta | chr3 | 44971244 | 45016471 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0000c0008t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0001 | 0/0 | 14 | 2 | 6 | 5 | 0 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0003 | 0/0 | 7 | 0 | 1 | 6 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0004 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0006 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0005t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0005t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0001c0012t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0002c0002t0001g0002 | 0/0 | 7 | 0 | 1 | 5 | 1 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0002c0002t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0002c0002t0001g0009 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0002c0002t0001g0010 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0002c0002t0001g0020 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0002c0002t0001g0021 | 0/1 | 2 | 0 | 0 | 0 | 0 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0002c0002t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0002c0002t0001g0023 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0002c0002t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0002c0002t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0002c0002t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0002c0002t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0002c0002t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0002c0002t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0002c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0002c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0002c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0002c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0002c0002t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0002c0002t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0002c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0002c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0002c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0002c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0002c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0002c0002t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0002c0002t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0002c0002t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0002c0002t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0002c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0002c0002t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0002c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0002c0002t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0002c0002t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0002c0002t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0002c0002t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0002c0002t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0002c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0002c0002t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0002c0002t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0002c0002t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0002c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0002c0002t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0002c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0002c0002t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0002c0002t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0002c0002t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0002c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0002c0002t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0002c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0002c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0002c0002t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0002c0002t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0002c0002t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0002c0002t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0002c0002t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0002c0002t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0002c0002t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0002c0002t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0002c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0002c0002t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0002c0002t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0002c0002t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0002c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0002c0002t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0002c0002t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0002c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0002c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0002c0002t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0002c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0002c0007t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0003c0003t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0003c0003t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0003c0003t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0003c0003t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0003c0003t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0003c0003t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0003c0003t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0003c0003t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0003c0003t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0003c0003t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0003c0003t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0003c0003t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0003c0003t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0003c0003t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0003c0003t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0003c0003t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0003c0006t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0004c0004t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0004c0004t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0004c0004t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0004c0004t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0004c0004t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0004c0004t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0004c0004t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0004c0004t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0004c0004t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0004c0004t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0004c0004t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0005c0009t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0006c0011t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
a0007c0010t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0002 | t0001 | g0186 | EUR | GBR | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG00099 | hp2 | a0003 | c0003 | t0001 | g0041 | EUR | GBR | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG00140 | hp1 | a0002 | c0002 | t0001 | g0002 | EUR | GBR | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG00140 | hp2 | a0002 | c0002 | t0001 | g0073 | EUR | GBR | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG00280 | hp1 | a0002 | c0002 | t0001 | g0087 | EUR | FIN | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0224 | EUR | FIN | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG00408 | hp2 | a0002 | c0002 | t0001 | g0086 | EAS | CHS | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | CHS | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | CHS | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | CHS | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | CHS | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | CHS | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | CHS | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG00639 | hp2 | a0003 | c0006 | t0001 | g0007 | AMR | PUR | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | CHS | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0257 | AMR | PUR | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG00733 | hp2 | a0002 | c0002 | t0001 | g0090 | AMR | PUR | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG00735 | hp1 | a0002 | c0002 | t0001 | g0094 | AMR | PUR | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG00735 | hp2 | a0002 | c0002 | t0001 | g0129 | AMR | PUR | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG00741 | hp2 | a0002 | c0002 | t0001 | g0128 | AMR | PUR | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG01070 | hp2 | a0003 | c0003 | t0001 | g0048 | AMR | PUR | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG01071 | hp1 | a0002 | c0002 | t0001 | g0082 | AMR | PUR | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG01071 | hp2 | a0003 | c0003 | t0001 | g0016 | AMR | PUR | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG01074 | hp1 | a0003 | c0003 | t0001 | g0016 | AMR | PUR | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG01074 | hp2 | a0002 | c0002 | t0001 | g0009 | AMR | PUR | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0251 | AMR | PUR | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG01106 | hp1 | a0003 | c0006 | t0001 | g0007 | AMR | PUR | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG01106 | hp2 | a0002 | c0002 | t0001 | g0109 | AMR | PUR | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG01109 | hp1 | a0002 | c0002 | t0001 | g0099 | AMR | PUR | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0247 | AMR | PUR | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG01167 | hp2 | a0004 | c0004 | t0001 | g0017 | AMR | PUR | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG01168 | hp2 | a0002 | c0002 | t0001 | g0115 | AMR | PUR | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG01169 | hp2 | a0004 | c0004 | t0001 | g0017 | AMR | PUR | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG01175 | hp1 | a0002 | c0002 | t0001 | g0083 | AMR | PUR | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG01192 | hp2 | a0002 | c0002 | t0001 | g0020 | AMR | PUR | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG01243 | hp1 | a0002 | c0007 | t0001 | g0008 | AMR | PUR | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG01243 | hp2 | a0002 | c0002 | t0001 | g0118 | AMR | PUR | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG01256 | hp1 | a0003 | c0003 | t0001 | g0007 | AMR | CLM | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG01256 | hp2 | a0002 | c0002 | t0001 | g0122 | AMR | CLM | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG01258 | hp1 | a0002 | c0002 | t0001 | g0124 | AMR | CLM | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG01258 | hp2 | a0002 | c0002 | t0001 | g0092 | AMR | CLM | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | CLM | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG01261 | hp2 | a0002 | c0002 | t0001 | g0010 | AMR | CLM | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG01346 | hp1 | a0002 | c0002 | t0001 | g0106 | AMR | CLM | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG01346 | hp2 | a0002 | c0002 | t0001 | g0123 | AMR | CLM | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG01358 | hp1 | a0002 | c0002 | t0001 | g0075 | AMR | CLM | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG01361 | hp2 | a0002 | c0002 | t0001 | g0105 | AMR | CLM | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG01433 | hp1 | a0002 | c0002 | t0001 | g0074 | AMR | CLM | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG01496 | hp1 | a0002 | c0002 | t0001 | g0107 | AMR | CLM | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0232 | EUR | IBS | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG01515 | hp2 | a0002 | c0002 | t0001 | g0010 | EUR | IBS | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG01516 | hp1 | a0003 | c0003 | t0001 | g0047 | EUR | IBS | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0255 | EUR | IBS | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0256 | EUR | IBS | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0231 | EUR | IBS | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG01884 | hp1 | a0004 | c0004 | t0001 | g0018 | AFR | ACB | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | ACB | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | ACB | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0252 | AFR | ACB | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PEL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PEL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG01934 | hp2 | a0004 | c0004 | t0001 | g0057 | AMR | PEL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG01943 | hp1 | a0002 | c0002 | t0001 | g0091 | AMR | PEL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0250 | AMR | PEL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG01952 | hp2 | a0002 | c0002 | t0001 | g0101 | AMR | PEL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PEL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG01975 | hp2 | a0002 | c0002 | t0001 | g0120 | AMR | PEL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PEL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | PEL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG01981 | hp1 | a0002 | c0002 | t0001 | g0125 | AMR | PEL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PEL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | PEL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | ACB | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | KHV | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG02056 | hp2 | a0002 | c0002 | t0001 | g0130 | EAS | KHV | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG02071 | hp2 | a0002 | c0002 | t0001 | g0077 | EAS | KHV | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG02074 | hp1 | a0002 | c0002 | t0001 | g0079 | EAS | KHV | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG02129 | hp1 | a0002 | c0002 | t0001 | g0084 | EAS | KHV | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | KHV | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | KHV | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | KHV | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG02145 | hp1 | a0002 | c0002 | t0001 | g0121 | AFR | ACB | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | ACB | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PEL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG02148 | hp2 | a0003 | c0003 | t0001 | g0059 | AMR | PEL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | CDX | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | CDX | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG02257 | hp1 | a0002 | c0002 | t0001 | g0135 | AFR | ACB | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG02257 | hp2 | a0004 | c0004 | t0001 | g0064 | AFR | ACB | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | ACB | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG02258 | hp2 | a0001 | c0005 | t0001 | g0138 | AFR | ACB | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | ACB | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | ACB | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG02293 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG02300 | hp1 | a0002 | c0002 | t0001 | g0127 | AMR | PEL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | ACB | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG02523 | hp1 | a0003 | c0003 | t0001 | g0042 | EAS | KHV | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | KHV | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | GWD | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | GWD | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG02602 | hp1 | a0003 | c0003 | t0001 | g0050 | SAS | PJL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0195 | SAS | PJL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | GWD | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG02615 | hp2 | a0002 | c0002 | t0001 | g0119 | AFR | GWD | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG02630 | hp2 | a0002 | c0002 | t0001 | g0100 | AFR | GWD | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0243 | SAS | PJL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG02698 | hp2 | a0002 | c0002 | t0001 | g0126 | SAS | PJL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | GWD | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | GWD | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG02723 | hp2 | a0004 | c0004 | t0001 | g0062 | AFR | GWD | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | GWD | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | GWD | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG02818 | hp1 | a0001 | c0005 | t0001 | g0026 | AFR | GWD | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG02886 | hp1 | a0004 | c0004 | t0001 | g0063 | AFR | GWD | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | GWD | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG02896 | hp1 | a0002 | c0002 | t0001 | g0024 | AFR | GWD | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG02897 | hp1 | a0002 | c0002 | t0001 | g0024 | AFR | GWD | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | ESN | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | ESN | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | ESN | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG02965 | hp2 | a0002 | c0002 | t0001 | g0009 | AFR | ESN | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | ESN | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG02976 | hp2 | a0002 | c0002 | t0001 | g0025 | AFR | ESN | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG03017 | hp2 | a0007 | c0010 | t0001 | g0030 | SAS | PJL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG03041 | hp1 | a0002 | c0002 | t0001 | g0113 | AFR | GWD | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG03041 | hp2 | a0004 | c0004 | t0001 | g0060 | AFR | GWD | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG03098 | hp1 | a0002 | c0002 | t0001 | g0089 | AFR | MSL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | MSL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | ESN | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG03130 | hp2 | a0002 | c0002 | t0001 | g0008 | AFR | ESN | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG03139 | hp1 | a0004 | c0004 | t0001 | g0018 | AFR | ESN | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG03139 | hp2 | a0002 | c0002 | t0001 | g0025 | AFR | ESN | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG03195 | hp1 | a0002 | c0002 | t0001 | g0009 | AFR | ESN | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG03195 | hp2 | a0002 | c0002 | t0001 | g0008 | AFR | ESN | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG03209 | hp1 | a0002 | c0002 | t0001 | g0112 | AFR | MSL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | MSL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG03225 | hp1 | a0002 | c0002 | t0001 | g0102 | AFR | MSL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | MSL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG03239 | hp2 | a0002 | c0002 | t0001 | g0104 | SAS | PJL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG03453 | hp1 | a0002 | c0002 | t0001 | g0132 | AFR | MSL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG03453 | hp2 | a0002 | c0002 | t0001 | g0076 | AFR | MSL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG03486 | hp1 | a0004 | c0004 | t0001 | g0061 | AFR | MSL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | MSL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG03490 | hp1 | a0002 | c0002 | t0001 | g0110 | SAS | PJL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG03491 | hp1 | a0002 | c0002 | t0001 | g0021 | SAS | PJL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG03516 | hp1 | a0004 | c0004 | t0001 | g0052 | AFR | ESN | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | GWD | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG03540 | hp2 | a0001 | c0005 | t0001 | g0026 | AFR | GWD | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0227 | SAS | PJL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG03654 | hp2 | a0002 | c0002 | t0001 | g0108 | SAS | PJL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0175 | SAS | PJL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG03704 | hp1 | a0002 | c0002 | t0001 | g0010 | SAS | PJL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0222 | SAS | PJL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG03831 | hp1 | a0002 | c0002 | t0001 | g0117 | SAS | BEB | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0165 | SAS | BEB | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0148 | SAS | BEB | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG03834 | hp2 | a0003 | c0003 | t0001 | g0058 | SAS | BEB | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG03942 | hp1 | a0006 | c0011 | t0001 | g0034 | SAS | BEB | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0198 | SAS | BEB | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0167 | SAS | STU | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0240 | SAS | STU | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0154 | SAS | BEB | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0196 | SAS | BEB | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | STU | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0166 | SAS | STU | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG04204 | hp1 | a0002 | c0002 | t0001 | g0081 | SAS | STU | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG04204 | hp2 | a0005 | c0009 | t0001 | g0080 | SAS | STU | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | STU | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG04228 | hp2 | a0003 | c0003 | t0001 | g0043 | SAS | STU | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA18522 | hp1 | a0002 | c0002 | t0001 | g0131 | AFR | YRI | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | YRI | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHB | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | CHB | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA18906 | hp1 | a0002 | c0002 | t0001 | g0111 | AFR | YRI | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | YRI | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA18940 | hp1 | a0002 | c0002 | t0001 | g0088 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA18942 | hp1 | a0003 | c0003 | t0001 | g0015 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA18942 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA18947 | hp2 | a0002 | c0002 | t0001 | g0098 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA18948 | hp1 | a0002 | c0002 | t0001 | g0078 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA18952 | hp1 | a0002 | c0002 | t0001 | g0133 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA18953 | hp2 | a0002 | c0002 | t0001 | g0096 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA18956 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA18957 | hp2 | a0002 | c0002 | t0001 | g0022 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA18960 | hp2 | a0001 | c0012 | t0001 | g0171 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA18961 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA18964 | hp1 | a0003 | c0003 | t0001 | g0040 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA18967 | hp2 | a0002 | c0002 | t0001 | g0093 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA18970 | hp2 | a0002 | c0002 | t0001 | g0134 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA18973 | hp1 | a0002 | c0002 | t0001 | g0097 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA18977 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA18978 | hp2 | a0002 | c0002 | t0001 | g0095 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA18979 | hp1 | a0002 | c0002 | t0001 | g0114 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA18981 | hp2 | a0003 | c0003 | t0001 | g0044 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA18995 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA19002 | hp2 | a0002 | c0002 | t0001 | g0116 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | LWK | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA19030 | hp2 | a0002 | c0002 | t0001 | g0103 | AFR | LWK | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | LWK | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | LWK | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA19056 | hp2 | a0003 | c0003 | t0001 | g0049 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA19057 | hp1 | a0000 | c0008 | t0001 | g0258 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA19065 | hp2 | a0003 | c0003 | t0001 | g0015 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA19076 | hp1 | a0002 | c0002 | t0001 | g0022 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA19077 | hp1 | a0003 | c0003 | t0001 | g0046 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA19077 | hp2 | a0002 | c0002 | t0001 | g0085 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA19240 | hp1 | a0002 | c0002 | t0001 | g0072 | AFR | YRI | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | YRI | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | ASW | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | ASW | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA20752 | hp1 | a0002 | c0002 | t0001 | g0023 | EUR | TSI | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0035 | EUR | TSI | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA20805 | hp1 | a0002 | c0002 | t0001 | g0023 | EUR | TSI | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0070 | EUR | TSI | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA20905 | hp1 | a0003 | c0003 | t0001 | g0045 | SAS | GIH | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0245 | SAS | GIH | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | ACB | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | ACB | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | ACB | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | MSL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | MSL | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG06807 | hp1 | a0004 | c0004 | t0001 | g0053 | AFR | USA | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | USA | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA20300 | hp1 | a0004 | c0004 | t0001 | g0051 | AFR | USA | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | USA | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | LWK | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | LWK | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0001 | g0021 | REF | REF | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
homoSapiens_grch38 | hp1 | a0002 | c0002 | t0001 | g0020 | REF | REF | EXOSC7_chr3_44971244_45016471 | EXOSC7 | chr3 | 44971244 | 45016471 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:44976290
|
A | G | 1 | a0003 | 20 | HG00099.hp2 HG00639.hp2 HG01070.hp2 others(17): Show |
missense_variant | MODERATE | c.13A>G | p.Thr5Ala | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/8 | 47/1042 | 13/876 | 5/291 | chr3 | 44976290 | ||
chr3:45003609
|
TAGCTGGA others(6001): Show |
T | 1 | a0000 | 1 | NA19057.hp1 | exon_loss_variant | HIGH | c.492-1677_772-1614d others(2): Show |
EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr3 | 45003609 | |||||
chr3:45005305
|
G | A | 1 | a0004 | 13 | HG01167.hp2 HG01169.hp2 HG01884.hp1 others(10): Show |
missense_variant | MODERATE | c.506G>A | p.Arg169Gln | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/8 | 540/1042 | 506/876 | 169/291 | chr3 | 45005305 | ||
chr3:45007424
|
G | A | 1 | a0005 | 1 | HG04204.hp2 | missense_variant | MODERATE | c.620G>A | p.Gly207Asp | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 7/8 | 654/1042 | 620/876 | 207/291 | chr3 | 45007424 | ||
chr3:45007567
|
A | T | 1 | a0006 | 1 | HG03942.hp1 | missense_variant | MODERATE | c.763A>T | p.Met255Leu | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 7/8 | 797/1042 | 763/876 | 255/291 | chr3 | 45007567 | ||
chr3:45011245
|
G | A | 1 | a0007 | 1 | HG03017.hp2 | missense_variant | MODERATE | c.782G>A | p.Arg261His | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 8/8 | 816/1042 | 782/876 | 261/291 | chr3 | 45011245 | ||
chr3:45011283
|
G | C | 6 | a0000a0001a0003others(3): Show | 247 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(244): Show |
missense_variant | MODERATE | c.820G>C | p.Val274Leu | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 8/8 | 854/1042 | 820/876 | 274/291 | chr3 | 45011283 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:44976310
|
G | A | 1 | a0002c0007 | 1 | HG01243.hp1 | synonymous_variant | LOW | c.33G>A | p.Lys11Lys | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/8 | 67/1042 | 33/876 | 11/291 | chr3 | 44976310 | ||
chr3:44989160
|
C | T | 1 | a0001c0012 | 1 | NA18960.hp2 | synonymous_variant | LOW | c.78C>T | p.Gly26Gly | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 2/8 | 112/1042 | 78/876 | 26/291 | chr3 | 44989160 | ||
chr3:45001603
|
T | C | 1 | a0001c0005 | 3 | HG02258.hp2 HG02818.hp1 HG03540.hp2 |
synonymous_variant | LOW | c.486T>C | p.Asn162Asn | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 5/8 | 520/1042 | 486/876 | 162/291 | chr3 | 45001603 | ||
chr3:45005297
|
A | G | 1 | a0003c0006 | 2 | HG00639.hp2 HG01106.hp1 |
synonymous_variant | LOW | c.498A>G | p.Pro166Pro | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/8 | 532/1042 | 498/876 | 166/291 | chr3 | 45005297 |
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:44976366
|
C | G | 9 | a0000c0008t0001g0258a0001c0001t0001g0005a0001c0001t0001g0038others(6): Show | 14 | NA18984.hp1 NA18991.hp1 NA18998.hp1 others(11): Show |
intron_variant | MODIFIER | c.57+32C>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44976366 | ||||||
chr3:44976412
|
A | T | 139 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(136): Show | 182 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.57+78A>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44976412 | ||||||
chr3:44976413
|
G | T | 139 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(136): Show | 182 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.57+79G>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44976413 | ||||||
chr3:44976494
|
C | A | 9 | a0000c0008t0001g0258a0001c0001t0001g0005a0001c0001t0001g0038others(6): Show | 14 | NA18984.hp1 NA18991.hp1 NA18998.hp1 others(11): Show |
intron_variant | MODIFIER | c.57+160C>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44976494 | ||||||
chr3:44976556
|
C | T | 3 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0257 | 3 | HG00733.hp1 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.57+222C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44976556 | ||||||
chr3:44976688
|
G | T | 1 | a0001c0001t0001g0254 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.57+354G>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44976688 | ||||||
chr3:44976704
|
T | C | 32 | a0001c0001t0001g0039a0001c0001t0001g0054a0001c0001t0001g0055others(29): Show | 37 | HG00099.hp2 HG00639.hp2 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.57+370T>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44976704 | ||||||
chr3:44976782
|
A | G | 3 | a0001c0001t0001g0037a0001c0001t0001g0252a0001c0001t0001g0253 | 4 | HG01891.hp2 HG02280.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.57+448A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44976782 | ||||||
chr3:44976828
|
A | G | 4 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(1): Show | 4 | HG01081.hp2 HG01943.hp2 NA18948.hp2 others(1): Show |
intron_variant | MODIFIER | c.57+494A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44976828 | ||||||
chr3:44976979
|
T | C | 2 | a0001c0001t0001g0140a0001c0001t0001g0141 | 2 | HG02523.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.57+645T>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44976979 | ||||||
chr3:44977034
|
C | CA | 8 | a0001c0001t0001g0019a0001c0001t0001g0065a0001c0001t0001g0066others(5): Show | 9 | HG00738.hp2 HG02055.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.57+709dupA | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 44977034 | |||||
chr3:44977091
|
A | G | 193 | a0000c0008t0001g0258a0001c0001t0001g0001a0001c0001t0001g0003others(190): Show | 248 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.57+757A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44977091 | ||||||
chr3:44977213
|
A | T | 1 | a0002c0002t0001g0135 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.57+879A>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44977213 | ||||||
chr3:44977215
|
C | T | 1 | a0001c0001t0001g0247 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.57+881C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44977215 | ||||||
chr3:44977568
|
A | G | 193 | a0000c0008t0001g0258a0001c0001t0001g0001a0001c0001t0001g0003others(190): Show | 248 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.57+1234A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44977568 | ||||||
chr3:44977647
|
G | A | 1 | a0001c0001t0001g0136 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.57+1313G>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44977647 | ||||||
chr3:44977653
|
A | C | 1 | a0001c0001t0001g0036 | 2 | HG00673.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.57+1319A>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44977653 | ||||||
chr3:44977683
|
T | C | 1 | a0002c0002t0001g0072 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.57+1349T>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44977683 | ||||||
chr3:44978144
|
A | G | 1 | a0001c0001t0001g0246 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.57+1810A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44978144 | ||||||
chr3:44978323
|
AAG | A | 4 | a0001c0001t0001g0027a0001c0001t0001g0142a0001c0001t0001g0143others(1): Show | 5 | HG01978.hp2 HG01981.hp2 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.57+1991_57+1992del others(2): Show |
EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 44978323 | |||||
chr3:44978343
|
A | T | 6 | a0002c0002t0001g0025a0002c0002t0001g0130a0002c0002t0001g0131others(3): Show | 7 | HG02056.hp2 HG02976.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.57+2009A>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44978343 | ||||||
chr3:44978488
|
T | C | 1 | a0002c0002t0001g0073 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.57+2154T>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44978488 | ||||||
chr3:44978714
|
C | G | 7 | a0004c0004t0001g0017a0004c0004t0001g0018a0004c0004t0001g0060others(4): Show | 9 | HG01167.hp2 HG01169.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.57+2380C>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44978714 | ||||||
chr3:44979012
|
T | C | 1 | a0001c0001t0001g0039 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.57+2678T>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44979012 | ||||||
chr3:44979046
|
C | T | 1 | a0001c0001t0001g0039 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.57+2712C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44979046 | ||||||
chr3:44979174
|
A | G | 1 | a0003c0003t0001g0059 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.57+2840A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44979174 | ||||||
chr3:44979215
|
T | G | 1 | a0001c0001t0001g0140 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.57+2881T>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44979215 | ||||||
chr3:44979301
|
A | G | 1 | a0001c0001t0001g0245 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.57+2967A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44979301 | ||||||
chr3:44979504
|
A | C | 1 | a0001c0001t0001g0247 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.57+3170A>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44979504 | ||||||
chr3:44979518
|
C | A | 1 | a0002c0002t0001g0074 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.57+3184C>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44979518 | ||||||
chr3:44979521
|
C | T | 1 | a0001c0001t0001g0244 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.57+3187C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44979521 | ||||||
chr3:44979537
|
G | T | 1 | a0001c0001t0001g0244 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.57+3203G>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44979537 | ||||||
chr3:44979550
|
G | A | 1 | a0002c0002t0001g0075 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.57+3216G>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44979550 | ||||||
chr3:44979589
|
T | G | 1 | a0001c0001t0001g0039 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.57+3255T>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44979589 | ||||||
chr3:44979598
|
T | C | 3 | a0001c0001t0001g0136a0001c0001t0001g0255a0001c0001t0001g0256 | 3 | HG01516.hp2 HG01517.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.57+3264T>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44979598 | ||||||
chr3:44979598
|
T | TTC | 130 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(127): Show | 172 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.57+3264_57+3265ins others(2): Show |
EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44979598 | ||||||
chr3:44979924
|
G | A | 1 | a0001c0001t0001g0150 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.57+3590G>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44979924 | ||||||
chr3:44980047
|
T | G | 2 | a0001c0001t0001g0151a0001c0001t0001g0152 | 2 | HG01928.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.57+3713T>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44980047 | ||||||
chr3:44980048
|
A | G | 2 | a0001c0001t0001g0151a0001c0001t0001g0152 | 2 | HG01928.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.57+3714A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44980048 | ||||||
chr3:44980049
|
T | A | 2 | a0001c0001t0001g0151a0001c0001t0001g0152 | 2 | HG01928.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.57+3715T>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44980049 | ||||||
chr3:44980052
|
C | G | 2 | a0001c0001t0001g0151a0001c0001t0001g0152 | 2 | HG01928.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.57+3718C>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44980052 | ||||||
chr3:44980053
|
C | G | 2 | a0001c0001t0001g0151a0001c0001t0001g0152 | 2 | HG01928.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.57+3719C>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44980053 | ||||||
chr3:44980054
|
A | C | 2 | a0001c0001t0001g0151a0001c0001t0001g0152 | 2 | HG01928.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.57+3720A>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44980054 | ||||||
chr3:44980057
|
T | G | 2 | a0001c0001t0001g0151a0001c0001t0001g0152 | 2 | HG01928.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.57+3723T>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44980057 | ||||||
chr3:44980058
|
T | G | 2 | a0001c0001t0001g0151a0001c0001t0001g0152 | 2 | HG01928.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.57+3724T>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44980058 | ||||||
chr3:44980059
|
T | TGCAGTGG others(47): Show |
2 | a0001c0001t0001g0151a0001c0001t0001g0152 | 2 | HG01928.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.57+3725_57+3726ins others(54): Show |
EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44980059 | ||||||
chr3:44980482
|
C | T | 9 | a0000c0008t0001g0258a0001c0001t0001g0005a0001c0001t0001g0038others(6): Show | 14 | NA18984.hp1 NA18991.hp1 NA18998.hp1 others(11): Show |
intron_variant | MODIFIER | c.57+4148C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44980482 | ||||||
chr3:44980501
|
G | A | 4 | a0001c0001t0001g0137a0001c0001t0001g0139a0001c0005t0001g0026others(1): Show | 5 | HG02258.hp2 HG02818.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.57+4167G>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44980501 | ||||||
chr3:44980544
|
A | G | 1 | a0003c0003t0001g0058 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.57+4210A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44980544 | ||||||
chr3:44980604
|
C | T | 10 | a0002c0002t0001g0024a0002c0002t0001g0121a0002c0002t0001g0122others(7): Show | 11 | HG00735.hp2 HG00741.hp2 HG01256.hp2 others(8): Show |
intron_variant | MODIFIER | c.57+4270C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44980604 | ||||||
chr3:44980624
|
C | T | 6 | a0002c0002t0001g0025a0002c0002t0001g0130a0002c0002t0001g0131others(3): Show | 7 | HG02056.hp2 HG02976.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.57+4290C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44980624 | ||||||
chr3:44981656
|
A | T | 9 | a0000c0008t0001g0258a0001c0001t0001g0005a0001c0001t0001g0038others(6): Show | 14 | NA18984.hp1 NA18991.hp1 NA18998.hp1 others(11): Show |
intron_variant | MODIFIER | c.57+5322A>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44981656 | ||||||
chr3:44982098
|
G | C | 72 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0011others(69): Show | 98 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.57+5764G>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44982098 | ||||||
chr3:44982127
|
T | G | 1 | a0001c0001t0001g0153 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.57+5793T>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44982127 | ||||||
chr3:44982264
|
A | G | 10 | a0000c0008t0001g0258a0001c0001t0001g0005a0001c0001t0001g0038others(7): Show | 15 | NA18984.hp1 NA18991.hp1 NA18998.hp1 others(12): Show |
intron_variant | MODIFIER | c.57+5930A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44982264 | ||||||
chr3:44982278
|
C | G | 1 | a0001c0001t0001g0243 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.57+5944C>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44982278 | ||||||
chr3:44982278
|
C | T | 1 | a0001c0001t0001g0136 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.57+5944C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44982278 | ||||||
chr3:44982342
|
G | A | 1 | a0002c0002t0001g0072 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.57+6008G>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44982342 | ||||||
chr3:44982352
|
T | C | 17 | a0003c0003t0001g0007a0003c0003t0001g0015a0003c0003t0001g0016others(14): Show | 20 | HG00099.hp2 HG00639.hp2 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.57+6018T>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44982352 | ||||||
chr3:44982418
|
T | C | 193 | a0000c0008t0001g0258a0001c0001t0001g0001a0001c0001t0001g0003others(190): Show | 248 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.57+6084T>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44982418 | ||||||
chr3:44982509
|
A | G | 1 | a0004c0004t0001g0057 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.57+6175A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44982509 | ||||||
chr3:44982563
|
G | T | 1 | a0002c0002t0001g0120 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.57+6229G>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44982563 | ||||||
chr3:44982583
|
G | A | 6 | a0002c0002t0001g0025a0002c0002t0001g0130a0002c0002t0001g0131others(3): Show | 7 | HG02056.hp2 HG02976.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.57+6249G>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44982583 | ||||||
chr3:44982719
|
A | G | 263 | a0000c0008t0001g0258a0001c0001t0001g0001a0001c0001t0001g0003others(260): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.57+6385A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44982719 | ||||||
chr3:44982941
|
G | T | 1 | a0001c0001t0001g0242 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.58-6199G>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44982941 | ||||||
chr3:44983061
|
A | T | 1 | a0001c0001t0001g0251 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.58-6079A>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44983061 | ||||||
chr3:44983183
|
C | G | 2 | a0001c0001t0001g0153a0001c0001t0001g0200 | 2 | HG00423.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.58-5957C>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44983183 | ||||||
chr3:44983335
|
G | C | 1 | a0000c0008t0001g0258 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.58-5805G>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44983335 | ||||||
chr3:44983410
|
C | T | 36 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0034others(33): Show | 43 | HG00280.hp2 HG00609.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.58-5730C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44983410 | ||||||
chr3:44983448
|
A | G | 1 | a0001c0001t0001g0199 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.58-5692A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44983448 | ||||||
chr3:44983523
|
T | C | 1 | a0001c0001t0001g0143 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.58-5617T>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44983523 | ||||||
chr3:44983641
|
T | C | 143 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(140): Show | 187 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.58-5499T>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44983641 | ||||||
chr3:44983760
|
C | T | 1 | a0002c0002t0001g0129 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.58-5380C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44983760 | ||||||
chr3:44983785
|
CTG | C | 72 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0011others(69): Show | 98 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.58-5352_58-5351del others(2): Show |
EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 44983785 | |||||
chr3:44983848
|
A | G | 3 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056 | 3 | HG02486.hp2 HG02630.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.58-5292A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44983848 | ||||||
chr3:44983865
|
T | TA | 137 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(134): Show | 180 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.58-5265dupA | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 44983865 | |||||
chr3:44983913
|
T | A | 9 | a0000c0008t0001g0258a0001c0001t0001g0005a0001c0001t0001g0038others(6): Show | 14 | NA18984.hp1 NA18991.hp1 NA18998.hp1 others(11): Show |
intron_variant | MODIFIER | c.58-5227T>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44983913 | ||||||
chr3:44984200
|
G | A | 1 | a0001c0001t0001g0136 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.58-4940G>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44984200 | ||||||
chr3:44984319
|
A | C | 1 | a0001c0001t0001g0241 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.58-4821A>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44984319 | ||||||
chr3:44984450
|
G | C | 2 | a0001c0001t0001g0220a0001c0001t0001g0221 | 2 | HG02970.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.58-4690G>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44984450 | ||||||
chr3:44984521
|
A | G | 1 | a0002c0002t0001g0128 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.58-4619A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44984521 | ||||||
chr3:44984611
|
G | A | 3 | a0001c0001t0001g0012a0001c0001t0001g0201a0001c0001t0001g0202 | 5 | HG01884.hp2 HG01891.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.58-4529G>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44984611 | ||||||
chr3:44984635
|
A | G | 11 | a0004c0004t0001g0017a0004c0004t0001g0018a0004c0004t0001g0051others(8): Show | 13 | HG01167.hp2 HG01169.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.58-4505A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44984635 | ||||||
chr3:44984719
|
A | G | 32 | a0001c0001t0001g0039a0001c0001t0001g0054a0001c0001t0001g0055others(29): Show | 37 | HG00099.hp2 HG00639.hp2 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.58-4421A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44984719 | ||||||
chr3:44984942
|
A | T | 9 | a0000c0008t0001g0258a0001c0001t0001g0005a0001c0001t0001g0038others(6): Show | 14 | NA18984.hp1 NA18991.hp1 NA18998.hp1 others(11): Show |
intron_variant | MODIFIER | c.58-4198A>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44984942 | ||||||
chr3:44985011
|
A | G | 1 | a0001c0001t0001g0218 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.58-4129A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44985011 | ||||||
chr3:44985024
|
A | T | 3 | a0001c0001t0001g0012a0001c0001t0001g0201a0001c0001t0001g0202 | 5 | HG01884.hp2 HG01891.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.58-4116A>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44985024 | ||||||
chr3:44985297
|
A | G | 1 | a0002c0002t0001g0075 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.58-3843A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44985297 | ||||||
chr3:44985359
|
T | G | 1 | a0001c0001t0001g0154 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.58-3781T>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44985359 | ||||||
chr3:44985418
|
C | T | 1 | a0001c0001t0001g0242 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.58-3722C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44985418 | ||||||
chr3:44985450
|
C | T | 1 | a0004c0004t0001g0064 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.58-3690C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44985450 | ||||||
chr3:44985570
|
G | A | 1 | a0001c0001t0001g0136 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.58-3570G>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44985570 | ||||||
chr3:44985597
|
G | A | 8 | a0001c0001t0001g0019a0001c0001t0001g0065a0001c0001t0001g0066others(5): Show | 9 | HG00738.hp2 HG02055.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.58-3543G>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44985597 | ||||||
chr3:44985619
|
C | T | 8 | a0001c0001t0001g0019a0001c0001t0001g0065a0001c0001t0001g0066others(5): Show | 9 | HG00738.hp2 HG02055.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.58-3521C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44985619 | ||||||
chr3:44985652
|
A | T | 1 | a0002c0002t0001g0119 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.58-3488A>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44985652 | ||||||
chr3:44985721
|
G | A | 1 | a0001c0001t0001g0248 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.58-3419G>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44985721 | ||||||
chr3:44985732
|
G | A | 2 | a0001c0001t0001g0203a0001c0001t0001g0222 | 2 | HG03704.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.58-3408G>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44985732 | ||||||
chr3:44986017
|
C | A | 1 | a0001c0001t0001g0155 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.58-3123C>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44986017 | ||||||
chr3:44986205
|
A | G | 199 | a0000c0008t0001g0258a0001c0001t0001g0001a0001c0001t0001g0003others(196): Show | 255 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(252): Show |
intron_variant | MODIFIER | c.58-2935A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44986205 | ||||||
chr3:44986220
|
T | TG | 11 | a0001c0001t0001g0149a0001c0001t0001g0195a0001c0001t0001g0196others(8): Show | 11 | HG01192.hp1 HG02135.hp2 HG02602.hp1 others(8): Show |
intron_variant | MODIFIER | c.58-2917dupG | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 44986220 | |||||
chr3:44986224
|
A | G | 193 | a0000c0008t0001g0258a0001c0001t0001g0001a0001c0001t0001g0003others(190): Show | 248 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.58-2916A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44986224 | ||||||
chr3:44986243
|
A | G | 1 | a0004c0004t0001g0057 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.58-2897A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44986243 | ||||||
chr3:44986365
|
C | T | 1 | a0001c0001t0001g0150 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.58-2775C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44986365 | ||||||
chr3:44986401
|
C | T | 18 | a0001c0001t0001g0039a0003c0003t0001g0007a0003c0003t0001g0015others(15): Show | 21 | HG00099.hp2 HG00639.hp2 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.58-2739C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44986401 | ||||||
chr3:44986429
|
C | T | 3 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056 | 3 | HG02486.hp2 HG02630.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.58-2711C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44986429 | ||||||
chr3:44986437
|
C | T | 1 | a0001c0001t0001g0136 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.58-2703C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44986437 | ||||||
chr3:44986450
|
C | T | 1 | a0001c0001t0001g0136 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.58-2690C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44986450 | ||||||
chr3:44986594
|
G | A | 1 | a0001c0001t0001g0153 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.58-2546G>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44986594 | ||||||
chr3:44986619
|
C | T | 1 | a0001c0001t0001g0039 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.58-2521C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44986619 | ||||||
chr3:44986620
|
A | G | 193 | a0000c0008t0001g0258a0001c0001t0001g0001a0001c0001t0001g0003others(190): Show | 248 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.58-2520A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44986620 | ||||||
chr3:44986717
|
A | G | 1 | a0002c0002t0001g0118 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.58-2423A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44986717 | ||||||
chr3:44986719
|
C | G | 1 | a0002c0002t0001g0117 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.58-2421C>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44986719 | ||||||
chr3:44986759
|
C | T | 10 | a0000c0008t0001g0258a0001c0001t0001g0005a0001c0001t0001g0038others(7): Show | 15 | NA18984.hp1 NA18991.hp1 NA18998.hp1 others(12): Show |
intron_variant | MODIFIER | c.58-2381C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44986759 | ||||||
chr3:44986807
|
G | C | 1 | a0001c0001t0001g0156 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.58-2333G>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44986807 | ||||||
chr3:44987015
|
A | G | 8 | a0001c0001t0001g0019a0001c0001t0001g0065a0001c0001t0001g0066others(5): Show | 9 | HG00738.hp2 HG02055.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.58-2125A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44987015 | ||||||
chr3:44987085
|
TAA | T | 151 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(148): Show | 196 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.58-2054_58-2053del others(2): Show |
EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44987085 | ||||||
chr3:44987092
|
T | TA | 12 | a0001c0001t0001g0065a0001c0001t0001g0136a0002c0002t0001g0025others(9): Show | 13 | HG02055.hp2 HG02056.hp2 HG02071.hp2 others(10): Show |
intron_variant | MODIFIER | c.58-2032dupA | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 44987092 | |||||
chr3:44987092
|
TA | T | 18 | a0001c0001t0001g0037a0001c0001t0001g0146a0001c0001t0001g0192others(15): Show | 19 | HG01070.hp2 HG01168.hp2 HG01516.hp2 others(16): Show |
intron_variant | MODIFIER | c.58-2032delA | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 44987092 | |||||
chr3:44987098
|
AAAAAAAA others(36): Show |
A | 1 | a0001c0001t0001g0194 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.58-2039_58-1997del others(43): Show |
EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 44987098 | |||||
chr3:44987132
|
C | A | 3 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056 | 3 | HG02486.hp2 HG02630.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.58-2008C>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44987132 | ||||||
chr3:44987487
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.58-1653G>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44987487 | ||||||
chr3:44987494
|
C | T | 1 | a0001c0001t0001g0139 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.58-1646C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44987494 | ||||||
chr3:44987495
|
G | A | 2 | a0001c0001t0001g0029a0001c0001t0001g0195 | 3 | HG02602.hp2 HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.58-1645G>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44987495 | ||||||
chr3:44987565
|
A | G | 1 | a0003c0003t0001g0047 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.58-1575A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44987565 | ||||||
chr3:44987683
|
C | CT | 32 | a0001c0001t0001g0039a0001c0001t0001g0054a0001c0001t0001g0055others(29): Show | 37 | HG00099.hp2 HG00639.hp2 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.58-1456dupT | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 44987683 | |||||
chr3:44988056
|
C | G | 3 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0001g0218 | 3 | HG02717.hp2 HG02886.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.58-1084C>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44988056 | ||||||
chr3:44988175
|
G | T | 1 | a0001c0001t0001g0144 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.58-965G>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44988175 | ||||||
chr3:44988737
|
T | C | 36 | a0001c0001t0001g0039a0001c0001t0001g0054a0001c0001t0001g0055others(33): Show | 42 | HG00099.hp2 HG00639.hp2 HG01070.hp2 others(39): Show |
intron_variant | MODIFIER | c.58-403T>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44988737 | ||||||
chr3:44988790
|
A | G | 199 | a0000c0008t0001g0258a0001c0001t0001g0001a0001c0001t0001g0003others(196): Show | 255 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(252): Show |
intron_variant | MODIFIER | c.58-350A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44988790 | ||||||
chr3:44988971
|
A | G | 9 | a0001c0001t0001g0037a0001c0001t0001g0212a0001c0001t0001g0213others(6): Show | 10 | HG01891.hp2 HG02280.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.58-169A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44988971 | ||||||
chr3:44989072
|
T | C | 32 | a0001c0001t0001g0039a0001c0001t0001g0054a0001c0001t0001g0055others(29): Show | 37 | HG00099.hp2 HG00639.hp2 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.58-68T>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44989072 | ||||||
chr3:44989105
|
G | C | 5 | a0002c0002t0001g0081a0002c0002t0001g0082a0002c0002t0001g0083others(2): Show | 5 | HG01071.hp1 HG01168.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.58-35G>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44989105 | ||||||
chr3:44989106
|
G | T | 4 | a0002c0002t0001g0081a0002c0002t0001g0082a0002c0002t0001g0083others(1): Show | 4 | HG01071.hp1 HG01168.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.58-34G>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 1/7 | chr3 | 44989106 | ||||||
chr3:44989257
|
A | G | 32 | a0001c0001t0001g0039a0001c0001t0001g0054a0001c0001t0001g0055others(29): Show | 37 | HG00099.hp2 HG00639.hp2 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.159+16A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 2/7 | chr3 | 44989257 | ||||||
chr3:44989258
|
T | C | 1 | a0002c0002t0001g0084 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.159+17T>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 2/7 | chr3 | 44989258 | ||||||
chr3:44989310
|
C | T | 6 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(3): Show | 6 | HG00438.hp1 NA18957.hp1 NA18994.hp2 others(3): Show |
intron_variant | MODIFIER | c.159+69C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 2/7 | chr3 | 44989310 | ||||||
chr3:44989373
|
G | C | 2 | a0001c0001t0001g0151a0001c0001t0001g0152 | 2 | HG01928.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.159+132G>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 2/7 | chr3 | 44989373 | ||||||
chr3:44989375
|
A | AG | 17 | a0003c0003t0001g0007a0003c0003t0001g0015a0003c0003t0001g0016others(14): Show | 20 | HG00099.hp2 HG00639.hp2 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.159+141dupG | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 44989375 | |||||
chr3:44989377
|
G | T | 28 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0034others(25): Show | 35 | HG00609.hp1 HG00639.hp1 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.159+136G>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 2/7 | chr3 | 44989377 | ||||||
chr3:44989858
|
C | G | 10 | a0000c0008t0001g0258a0001c0001t0001g0005a0001c0001t0001g0038others(7): Show | 15 | NA18979.hp1 NA18984.hp1 NA18991.hp1 others(12): Show |
intron_variant | MODIFIER | c.254+214C>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44989858 | ||||||
chr3:44989873
|
C | T | 4 | a0004c0004t0001g0051a0004c0004t0001g0052a0004c0004t0001g0053others(1): Show | 4 | HG01934.hp2 HG03516.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.254+229C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44989873 | ||||||
chr3:44990241
|
T | C | 1 | a0001c0001t0001g0239 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.254+597T>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44990241 | ||||||
chr3:44990294
|
GA | G | 143 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(140): Show | 187 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.254+651delA | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44990294 | ||||||
chr3:44990379
|
T | C | 1 | a0001c0001t0001g0195 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.254+735T>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44990379 | ||||||
chr3:44990512
|
G | T | 1 | a0002c0002t0001g0113 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.254+868G>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44990512 | ||||||
chr3:44990653
|
A | ACTCCTCA others(35): Show |
1 | a0001c0001t0001g0194 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.254+1009_254+1010i others(44): Show |
EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44990653 | ||||||
chr3:44990730
|
C | T | 1 | a0001c0001t0001g0243 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.254+1086C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44990730 | ||||||
chr3:44990983
|
C | T | 8 | a0001c0001t0001g0019a0001c0001t0001g0065a0001c0001t0001g0066others(5): Show | 9 | HG00738.hp2 HG02055.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.254+1339C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44990983 | ||||||
chr3:44991016
|
CG | C | 32 | a0001c0001t0001g0039a0001c0001t0001g0054a0001c0001t0001g0055others(29): Show | 37 | HG00099.hp2 HG00639.hp2 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.254+1373delG | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44991016 | ||||||
chr3:44991362
|
A | G | 1 | a0002c0002t0001g0112 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.254+1718A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44991362 | ||||||
chr3:44991572
|
C | T | 9 | a0001c0001t0001g0037a0001c0001t0001g0212a0001c0001t0001g0213others(6): Show | 10 | HG01891.hp2 HG02280.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.254+1928C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44991572 | ||||||
chr3:44991704
|
T | C | 194 | a0000c0008t0001g0258a0001c0001t0001g0001a0001c0001t0001g0003others(191): Show | 249 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(246): Show |
intron_variant | MODIFIER | c.254+2060T>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44991704 | ||||||
chr3:44991729
|
C | G | 1 | a0002c0002t0001g0111 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.254+2085C>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44991729 | ||||||
chr3:44991861
|
A | G | 29 | a0001c0001t0001g0039a0003c0003t0001g0007a0003c0003t0001g0015others(26): Show | 34 | HG00099.hp2 HG00639.hp2 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.254+2217A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44991861 | ||||||
chr3:44992001
|
G | A | 72 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0011others(69): Show | 98 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.254+2357G>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44992001 | ||||||
chr3:44992069
|
A | G | 72 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0011others(69): Show | 98 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.254+2425A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44992069 | ||||||
chr3:44992525
|
T | C | 2 | a0001c0001t0001g0054a0001c0001t0001g0055 | 2 | HG02630.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.254+2881T>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44992525 | ||||||
chr3:44992527
|
G | T | 1 | a0001c0001t0001g0252 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.254+2883G>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44992527 | ||||||
chr3:44992718
|
C | G | 1 | a0002c0002t0001g0111 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.254+3074C>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44992718 | ||||||
chr3:44992847
|
TAGAG | T | 8 | a0001c0001t0001g0019a0001c0001t0001g0065a0001c0001t0001g0066others(5): Show | 9 | HG00738.hp2 HG02055.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.254+3206_254+3209d others(6): Show |
EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr3 | 44992847 | |||||
chr3:44992919
|
C | T | 193 | a0000c0008t0001g0258a0001c0001t0001g0001a0001c0001t0001g0003others(190): Show | 248 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.254+3275C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44992919 | ||||||
chr3:44993128
|
G | A | 8 | a0001c0001t0001g0019a0001c0001t0001g0065a0001c0001t0001g0066others(5): Show | 9 | HG00738.hp2 HG02055.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.254+3484G>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44993128 | ||||||
chr3:44993589
|
C | A | 1 | a0001c0001t0001g0226 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.255-3498C>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44993589 | ||||||
chr3:44994039
|
T | C | 9 | a0000c0008t0001g0258a0001c0001t0001g0005a0001c0001t0001g0038others(6): Show | 14 | NA18984.hp1 NA18991.hp1 NA18998.hp1 others(11): Show |
intron_variant | MODIFIER | c.255-3048T>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44994039 | ||||||
chr3:44994245
|
TA | T | 24 | a0001c0001t0001g0039a0001c0001t0001g0054a0001c0001t0001g0055others(21): Show | 27 | HG00099.hp2 HG00639.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.255-2825delA | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr3 | 44994245 | |||||
chr3:44994261
|
AAG | A | 68 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0011others(65): Show | 94 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.255-2824_255-2823d others(4): Show |
EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr3 | 44994261 | |||||
chr3:44994262
|
A | T | 10 | a0000c0008t0001g0258a0001c0001t0001g0005a0001c0001t0001g0038others(7): Show | 15 | NA18984.hp1 NA18991.hp1 NA18998.hp1 others(12): Show |
intron_variant | MODIFIER | c.255-2825A>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44994262 | ||||||
chr3:44994263
|
GA | G | 5 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0159others(2): Show | 5 | HG00423.hp1 HG00423.hp2 HG02071.hp1 others(2): Show |
intron_variant | MODIFIER | c.255-2823delA | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44994263 | ||||||
chr3:44994264
|
A | G | 194 | a0000c0008t0001g0258a0001c0001t0001g0001a0001c0001t0001g0003others(191): Show | 250 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(247): Show |
intron_variant | MODIFIER | c.255-2823A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44994264 | ||||||
chr3:44994274
|
CCTT | C | 2 | a0001c0001t0001g0019a0001c0001t0001g0066 | 3 | HG02809.hp2 HG02895.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.255-2809_255-2807d others(5): Show |
EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr3 | 44994274 | |||||
chr3:44994279
|
T | G | 1 | a0001c0001t0001g0155 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.255-2808T>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44994279 | ||||||
chr3:44994369
|
A | AT | 9 | a0001c0001t0001g0037a0001c0001t0001g0212a0001c0001t0001g0213others(6): Show | 10 | HG01891.hp2 HG02280.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.255-2704dupT | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr3 | 44994369 | |||||
chr3:44994605
|
A | G | 1 | a0002c0002t0001g0110 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.255-2482A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44994605 | ||||||
chr3:44994683
|
G | A | 193 | a0000c0008t0001g0258a0001c0001t0001g0001a0001c0001t0001g0003others(190): Show | 248 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.255-2404G>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44994683 | ||||||
chr3:44994856
|
G | GGT | 7 | a0002c0002t0001g0072a0002c0002t0001g0078a0002c0002t0001g0085others(4): Show | 7 | HG01975.hp2 HG01981.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.255-2182_255-2181d others(4): Show |
EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr3 | 44994856 | |||||
chr3:44994856
|
G | GGTGT | 10 | a0002c0002t0001g0025a0002c0002t0001g0077a0002c0002t0001g0087others(7): Show | 11 | HG00280.hp1 HG01256.hp2 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.255-2184_255-2181d others(6): Show |
EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr3 | 44994856 | |||||
chr3:44994856
|
G | GGTGTGT | 5 | a0002c0002t0001g0081a0002c0002t0001g0121a0002c0002t0001g0131others(2): Show | 5 | HG02145.hp1 HG03041.hp2 HG04204.hp1 others(2): Show |
intron_variant | MODIFIER | c.255-2186_255-2181d others(8): Show |
EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr3 | 44994856 | |||||
chr3:44994856
|
G | GGTGTGTG others(1): Show |
3 | a0002c0002t0001g0130a0004c0004t0001g0017a0004c0004t0001g0064 | 4 | HG01167.hp2 HG01169.hp2 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.255-2188_255-2181d others(10): Show |
EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr3 | 44994856 | |||||
chr3:44994856
|
G | GGTGTGTG others(3): Show |
1 | a0002c0002t0001g0086 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.255-2190_255-2181d others(12): Show |
EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr3 | 44994856 | |||||
chr3:44994856
|
G | GGTGTGTG others(5): Show |
1 | a0002c0002t0001g0128 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.255-2192_255-2181d others(14): Show |
EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr3 | 44994856 | |||||
chr3:44994856
|
GGT | G | 29 | a0001c0001t0001g0019a0001c0001t0001g0065a0001c0001t0001g0066others(26): Show | 35 | HG00140.hp2 HG00735.hp2 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.255-2182_255-2181d others(4): Show |
EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr3 | 44994856 | |||||
chr3:44994856
|
GGTGT | G | 25 | a0001c0001t0001g0014a0001c0001t0001g0034a0001c0001t0001g0071others(22): Show | 28 | HG00609.hp1 HG00639.hp1 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.255-2184_255-2181d others(6): Show |
EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr3 | 44994856 | |||||
chr3:44994856
|
GGTGTGT | G | 17 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0035others(14): Show | 25 | HG00639.hp2 HG01081.hp2 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.255-2186_255-2181d others(8): Show |
EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr3 | 44994856 | |||||
chr3:44994856
|
GGTGTGTG others(1): Show |
G | 39 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0039others(36): Show | 44 | HG00280.hp2 HG00609.hp2 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.255-2188_255-2181d others(10): Show |
EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr3 | 44994856 | |||||
chr3:44994856
|
GGTGTGTG others(3): Show |
G | 89 | a0000c0008t0001g0258a0001c0001t0001g0001a0001c0001t0001g0003others(86): Show | 125 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.255-2190_255-2181d others(12): Show |
EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr3 | 44994856 | |||||
chr3:44994856
|
GGTGTGTG others(5): Show |
G | 5 | a0001c0001t0001g0210a0001c0001t0001g0218a0001c0001t0001g0247others(2): Show | 5 | HG01109.hp2 HG02717.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.255-2192_255-2181d others(14): Show |
EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr3 | 44994856 | |||||
chr3:44994856
|
GGTGTGTG others(7): Show |
G | 2 | a0001c0001t0001g0244a0003c0003t0001g0045 | 2 | NA19030.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.255-2194_255-2181d others(16): Show |
EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr3 | 44994856 | |||||
chr3:44994856
|
GGTGTGTG others(11): Show |
G | 2 | a0001c0001t0001g0236a0001c0001t0001g0239 | 2 | HG02132.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.255-2198_255-2181d others(20): Show |
EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr3 | 44994856 | |||||
chr3:44994870
|
T | G | 1 | a0001c0001t0001g0161 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.255-2217T>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44994870 | ||||||
chr3:44994944
|
A | C | 5 | a0001c0001t0001g0203a0001c0001t0001g0209a0001c0001t0001g0210others(2): Show | 5 | HG02451.hp1 HG02717.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.255-2143A>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44994944 | ||||||
chr3:44994947
|
C | T | 9 | a0000c0008t0001g0258a0001c0001t0001g0005a0001c0001t0001g0038others(6): Show | 14 | NA18984.hp1 NA18991.hp1 NA18998.hp1 others(11): Show |
intron_variant | MODIFIER | c.255-2140C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44994947 | ||||||
chr3:44994954
|
C | CA | 7 | a0001c0001t0001g0033a0001c0001t0001g0137a0001c0001t0001g0139others(4): Show | 9 | HG02258.hp2 HG02818.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.255-2124dupA | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr3 | 44994954 | |||||
chr3:44995047
|
C | T | 13 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0028others(10): Show | 20 | HG00642.hp1 HG01109.hp2 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.255-2040C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44995047 | ||||||
chr3:44995230
|
G | A | 3 | a0002c0002t0001g0021a0002c0002t0001g0023a0002c0002t0001g0090 | 5 | HG00733.hp2 HG03491.hp1 NA20752.hp1 others(2): Show |
intron_variant | MODIFIER | c.255-1857G>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44995230 | ||||||
chr3:44995308
|
G | A | 39 | a0002c0002t0001g0002a0002c0002t0001g0009a0002c0002t0001g0021others(36): Show | 50 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(47): Show |
intron_variant | MODIFIER | c.255-1779G>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44995308 | ||||||
chr3:44996018
|
A | G | 29 | a0001c0001t0001g0039a0003c0003t0001g0007a0003c0003t0001g0015others(26): Show | 34 | HG00099.hp2 HG00639.hp2 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.255-1069A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44996018 | ||||||
chr3:44996158
|
G | C | 192 | a0000c0008t0001g0258a0001c0001t0001g0001a0001c0001t0001g0003others(189): Show | 247 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(244): Show |
intron_variant | MODIFIER | c.255-929G>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44996158 | ||||||
chr3:44996178
|
T | G | 140 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(137): Show | 183 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.255-909T>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44996178 | ||||||
chr3:44996277
|
T | G | 8 | a0001c0001t0001g0019a0001c0001t0001g0065a0001c0001t0001g0066others(5): Show | 9 | HG00738.hp2 HG02055.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.255-810T>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44996277 | ||||||
chr3:44996299
|
CA | C | 159 | a0000c0008t0001g0258a0001c0001t0001g0001a0001c0001t0001g0003others(156): Show | 209 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(206): Show |
intron_variant | MODIFIER | c.255-783delA | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr3 | 44996299 | |||||
chr3:44996412
|
G | A | 9 | a0000c0008t0001g0258a0001c0001t0001g0005a0001c0001t0001g0038others(6): Show | 14 | NA18984.hp1 NA18991.hp1 NA18998.hp1 others(11): Show |
intron_variant | MODIFIER | c.255-675G>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44996412 | ||||||
chr3:44996556
|
A | G | 7 | a0004c0004t0001g0017a0004c0004t0001g0018a0004c0004t0001g0060others(4): Show | 9 | HG01167.hp2 HG01169.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.255-531A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44996556 | ||||||
chr3:44996753
|
A | G | 1 | a0001c0001t0001g0217 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.255-334A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44996753 | ||||||
chr3:44996847
|
A | G | 4 | a0001c0001t0001g0137a0001c0001t0001g0139a0001c0005t0001g0026others(1): Show | 5 | HG02258.hp2 HG02818.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.255-240A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44996847 | ||||||
chr3:44996852
|
A | G | 6 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(3): Show | 6 | HG00438.hp1 NA18957.hp1 NA18994.hp2 others(3): Show |
intron_variant | MODIFIER | c.255-235A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44996852 | ||||||
chr3:44996963
|
A | G | 1 | a0001c0001t0001g0070 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.255-124A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44996963 | ||||||
chr3:44997002
|
A | G | 6 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(3): Show | 6 | HG00438.hp1 NA18957.hp1 NA18994.hp2 others(3): Show |
intron_variant | MODIFIER | c.255-85A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44997002 | ||||||
chr3:44997050
|
A | G | 1 | a0001c0001t0001g0139 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.255-37A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 3/7 | chr3 | 44997050 | ||||||
chr3:44997852
|
A | G | 1 | a0001c0001t0001g0151 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.420+600A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 4/7 | chr3 | 44997852 | ||||||
chr3:44997886
|
C | T | 4 | a0001c0001t0001g0137a0001c0001t0001g0139a0001c0005t0001g0026others(1): Show | 5 | HG02258.hp2 HG02818.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.420+634C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 4/7 | chr3 | 44997886 | ||||||
chr3:44997991
|
G | A | 1 | a0002c0002t0001g0105 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.420+739G>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 4/7 | chr3 | 44997991 | ||||||
chr3:44998031
|
G | GT | 22 | a0003c0003t0001g0007a0003c0003t0001g0015a0003c0003t0001g0016others(19): Show | 27 | HG00639.hp2 HG01070.hp2 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.420+786dupT | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr3 | 44998031 | |||||
chr3:44998031
|
G | GTT | 5 | a0001c0001t0001g0039a0003c0003t0001g0040a0003c0003t0001g0043others(2): Show | 5 | HG01934.hp2 HG02818.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.420+785_420+786dup others(2): Show |
EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr3 | 44998031 | |||||
chr3:44998039
|
G | GT | 6 | a0001c0001t0001g0146a0001c0001t0001g0184a0001c0001t0001g0185others(3): Show | 6 | HG01261.hp1 HG03209.hp1 HG03654.hp2 others(3): Show |
intron_variant | MODIFIER | c.420+801dupT | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr3 | 44998039 | |||||
chr3:44998039
|
G | T | 32 | a0001c0001t0001g0039a0001c0001t0001g0054a0001c0001t0001g0055others(29): Show | 37 | HG00639.hp2 HG01070.hp2 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.420+787G>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 4/7 | chr3 | 44998039 | ||||||
chr3:44998060
|
G | A | 1 | a0003c0003t0001g0042 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.420+808G>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 4/7 | chr3 | 44998060 | ||||||
chr3:44998093
|
T | C | 1 | a0001c0001t0001g0056 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.420+841T>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 4/7 | chr3 | 44998093 | ||||||
chr3:44998396
|
C | T | 1 | a0001c0001t0001g0199 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.420+1144C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 4/7 | chr3 | 44998396 | ||||||
chr3:44998596
|
T | C | 3 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0056 | 3 | HG02486.hp2 HG02630.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.420+1344T>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 4/7 | chr3 | 44998596 | ||||||
chr3:44998828
|
A | G | 3 | a0001c0001t0001g0032a0001c0001t0001g0168a0001c0001t0001g0183 | 4 | HG01928.hp1 HG01975.hp1 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.420+1576A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 4/7 | chr3 | 44998828 | ||||||
chr3:44998969
|
G | A | 4 | a0001c0001t0001g0028a0001c0001t0001g0147a0001c0001t0001g0148others(1): Show | 5 | HG00642.hp1 HG01192.hp1 HG03669.hp2 others(2): Show |
intron_variant | MODIFIER | c.420+1717G>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 4/7 | chr3 | 44998969 | ||||||
chr3:44999015
|
G | A | 142 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(139): Show | 186 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.420+1763G>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 4/7 | chr3 | 44999015 | ||||||
chr3:44999148
|
GC | G | 17 | a0003c0003t0001g0007a0003c0003t0001g0015a0003c0003t0001g0016others(14): Show | 20 | HG00099.hp2 HG00639.hp2 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.420+1898delC | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr3 | 44999148 | |||||
chr3:44999181
|
G | C | 1 | a0001c0001t0001g0246 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.420+1929G>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 4/7 | chr3 | 44999181 | ||||||
chr3:44999190
|
T | C | 150 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(147): Show | 195 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(192): Show |
intron_variant | MODIFIER | c.420+1938T>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 4/7 | chr3 | 44999190 | ||||||
chr3:44999236
|
G | T | 1 | a0001c0001t0001g0137 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.420+1984G>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 4/7 | chr3 | 44999236 | ||||||
chr3:44999243
|
A | T | 1 | a0005c0009t0001g0080 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.420+1991A>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 4/7 | chr3 | 44999243 | ||||||
chr3:44999277
|
T | C | 1 | a0002c0002t0001g0125 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.420+2025T>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 4/7 | chr3 | 44999277 | ||||||
chr3:44999295
|
T | G | 1 | a0001c0001t0001g0136 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.420+2043T>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 4/7 | chr3 | 44999295 | ||||||
chr3:44999354
|
G | C | 1 | a0001c0001t0001g0212 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.420+2102G>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 4/7 | chr3 | 44999354 | ||||||
chr3:44999397
|
G | T | 14 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0028others(11): Show | 21 | HG00642.hp1 HG01109.hp2 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.421-2141G>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 4/7 | chr3 | 44999397 | ||||||
chr3:44999513
|
A | C | 3 | a0002c0002t0001g0130a0002c0002t0001g0133a0002c0002t0001g0134 | 3 | HG02056.hp2 NA18952.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.421-2025A>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 4/7 | chr3 | 44999513 | ||||||
chr3:44999689
|
TA | T | 5 | a0001c0001t0001g0033a0001c0001t0001g0162a0002c0002t0001g0022others(2): Show | 7 | HG02129.hp1 HG02922.hp1 NA18947.hp2 others(4): Show |
intron_variant | MODIFIER | c.421-1836delA | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr3 | 44999689 | |||||
chr3:45000001
|
T | TA | 32 | a0001c0001t0001g0039a0001c0001t0001g0054a0001c0001t0001g0055others(29): Show | 37 | HG00099.hp2 HG00639.hp2 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.421-1536dupA | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr3 | 45000001 | |||||
chr3:45000459
|
C | T | 1 | a0002c0002t0001g0113 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.421-1079C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 4/7 | chr3 | 45000459 | ||||||
chr3:45000555
|
G | C | 3 | a0002c0002t0001g0082a0002c0002t0001g0083a0002c0002t0001g0115 | 3 | HG01071.hp1 HG01168.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.421-983G>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 4/7 | chr3 | 45000555 | ||||||
chr3:45000560
|
G | A | 1 | a0001c0001t0001g0136 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.421-978G>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 4/7 | chr3 | 45000560 | ||||||
chr3:45000571
|
T | C | 18 | a0002c0002t0001g0117a0003c0003t0001g0007a0003c0003t0001g0015others(15): Show | 21 | HG00099.hp2 HG00639.hp2 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.421-967T>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 4/7 | chr3 | 45000571 | ||||||
chr3:45000629
|
A | G | 1 | a0001c0001t0001g0136 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.421-909A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 4/7 | chr3 | 45000629 | ||||||
chr3:45000805
|
C | G | 2 | a0002c0002t0001g0104a0002c0002t0001g0110 | 2 | HG03239.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.421-733C>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 4/7 | chr3 | 45000805 | ||||||
chr3:45001145
|
G | A | 53 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0014others(50): Show | 63 | HG00280.hp2 HG00609.hp1 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.421-393G>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 4/7 | chr3 | 45001145 | ||||||
chr3:45001228
|
G | A | 2 | a0001c0001t0001g0229a0001c0001t0001g0230 | 2 | HG01070.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.421-310G>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 4/7 | chr3 | 45001228 | ||||||
chr3:45001229
|
G | T | 1 | a0001c0001t0001g0155 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.421-309G>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 4/7 | chr3 | 45001229 | ||||||
chr3:45001239
|
G | A | 1 | a0001c0001t0001g0036 | 2 | HG00673.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.421-299G>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 4/7 | chr3 | 45001239 | ||||||
chr3:45001314
|
A | T | 9 | a0000c0008t0001g0258a0001c0001t0001g0005a0001c0001t0001g0038others(6): Show | 14 | NA18984.hp1 NA18991.hp1 NA18998.hp1 others(11): Show |
intron_variant | MODIFIER | c.421-224A>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 4/7 | chr3 | 45001314 | ||||||
chr3:45001335
|
C | T | 1 | a0002c0002t0001g0119 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.421-203C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 4/7 | chr3 | 45001335 | ||||||
chr3:45002187
|
CTGAT | C | 8 | a0001c0001t0001g0019a0001c0001t0001g0065a0001c0001t0001g0066others(5): Show | 9 | HG00738.hp2 HG02055.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.491+583_491+586del others(4): Show |
EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 45002187 | |||||
chr3:45002278
|
A | G | 1 | a0001c0001t0001g0216 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.491+670A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 5/7 | chr3 | 45002278 | ||||||
chr3:45002338
|
C | A | 1 | a0002c0002t0001g0130 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.491+730C>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 5/7 | chr3 | 45002338 | ||||||
chr3:45002363
|
T | C | 1 | a0002c0002t0001g0077 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.491+755T>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 5/7 | chr3 | 45002363 | ||||||
chr3:45002370
|
A | C | 2 | a0001c0001t0001g0153a0001c0001t0001g0200 | 2 | HG00423.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.491+762A>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 5/7 | chr3 | 45002370 | ||||||
chr3:45002403
|
C | T | 1 | a0002c0002t0001g0097 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.491+795C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 5/7 | chr3 | 45002403 | ||||||
chr3:45002435
|
A | G | 1 | a0001c0001t0001g0242 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.491+827A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 5/7 | chr3 | 45002435 | ||||||
chr3:45002501
|
A | G | 138 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(135): Show | 181 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(178): Show |
intron_variant | MODIFIER | c.491+893A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 5/7 | chr3 | 45002501 | ||||||
chr3:45002707
|
A | G | 1 | a0001c0001t0001g0243 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.491+1099A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 5/7 | chr3 | 45002707 | ||||||
chr3:45002908
|
G | A | 1 | a0002c0002t0001g0108 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.491+1300G>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 5/7 | chr3 | 45002908 | ||||||
chr3:45002992
|
A | G | 2 | a0001c0001t0001g0167a0001c0001t0001g0196 | 2 | HG04115.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.491+1384A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 5/7 | chr3 | 45002992 | ||||||
chr3:45003326
|
TGTGC | T | 73 | a0001c0001t0001g0247a0002c0002t0001g0002a0002c0002t0001g0008others(70): Show | 89 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(86): Show |
intron_variant | MODIFIER | c.491+1742_491+1745d others(6): Show |
EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 45003326 | |||||
chr3:45003326
|
TGTGCGTG others(1): Show |
T | 61 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0012others(58): Show | 77 | HG00639.hp1 HG00738.hp2 HG01070.hp1 others(74): Show |
intron_variant | MODIFIER | c.491+1738_491+1745d others(10): Show |
EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 45003326 | |||||
chr3:45003326
|
TGTGCGTG others(5): Show |
T | 65 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0011others(62): Show | 90 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.491+1734_491+1745d others(14): Show |
EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 45003326 | |||||
chr3:45003334
|
CGTGCGTG others(11): Show |
C | 1 | a0001c0001t0001g0139 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.491+1730_491+1747d others(20): Show |
EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 45003334 | |||||
chr3:45003335
|
G | A | 1 | a0001c0001t0001g0137 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.491+1727G>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 5/7 | chr3 | 45003335 | ||||||
chr3:45003340
|
TGCGTGCG others(3): Show |
T | 14 | a0000c0008t0001g0258a0001c0001t0001g0005a0001c0001t0001g0031others(11): Show | 20 | HG00642.hp2 HG02602.hp1 NA18953.hp1 others(17): Show |
intron_variant | MODIFIER | c.491+1734_491+1743d others(12): Show |
EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 45003340 | |||||
chr3:45003342
|
CGTGCGTG others(3): Show |
C | 1 | a0001c0001t0001g0242 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.491+1738_491+1747d others(12): Show |
EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 45003342 | |||||
chr3:45003342
|
CGTGCGTG others(5): Show |
C | 6 | a0001c0001t0001g0013a0001c0001t0001g0137a0001c0001t0001g0206others(3): Show | 9 | HG02145.hp2 HG02258.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.491+1738_491+1749d others(14): Show |
EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 45003342 | |||||
chr3:45003344
|
TGCGTGC | T | 45 | a0001c0001t0001g0039a0001c0001t0001g0054a0001c0001t0001g0055others(42): Show | 50 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.491+1738_491+1743d others(8): Show |
EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 45003344 | |||||
chr3:45003350
|
C | T | 1 | a0001c0001t0001g0247 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.491+1742C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 5/7 | chr3 | 45003350 | ||||||
chr3:45003351
|
G | A | 1 | a0001c0001t0001g0203 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.491+1743G>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 5/7 | chr3 | 45003351 | ||||||
chr3:45003363
|
A | G | 160 | a0000c0008t0001g0258a0001c0001t0001g0001a0001c0001t0001g0003others(157): Show | 210 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(207): Show |
intron_variant | MODIFIER | c.491+1755A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 5/7 | chr3 | 45003363 | ||||||
chr3:45003381
|
T | C | 9 | a0001c0001t0001g0037a0001c0001t0001g0212a0001c0001t0001g0213others(6): Show | 10 | HG01891.hp2 HG02280.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.491+1773T>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 5/7 | chr3 | 45003381 | ||||||
chr3:45003386
|
A | G | 198 | a0000c0008t0001g0258a0001c0001t0001g0001a0001c0001t0001g0003others(195): Show | 254 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(251): Show |
intron_variant | MODIFIER | c.491+1778A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 5/7 | chr3 | 45003386 | ||||||
chr3:45003775
|
G | A | 1 | a0003c0003t0001g0058 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.492-1516G>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 5/7 | chr3 | 45003775 | ||||||
chr3:45004227
|
A | G | 1 | a0002c0002t0001g0074 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.492-1064A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 5/7 | chr3 | 45004227 | ||||||
chr3:45004324
|
C | T | 1 | a0001c0001t0001g0069 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.492-967C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 5/7 | chr3 | 45004324 | ||||||
chr3:45004325
|
A | G | 3 | a0001c0001t0001g0037a0001c0001t0001g0252a0001c0001t0001g0253 | 4 | HG01891.hp2 HG02280.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.492-966A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 5/7 | chr3 | 45004325 | ||||||
chr3:45004475
|
C | T | 8 | a0001c0001t0001g0019a0001c0001t0001g0065a0001c0001t0001g0066others(5): Show | 9 | HG00738.hp2 HG02055.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.492-816C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 5/7 | chr3 | 45004475 | ||||||
chr3:45004502
|
C | T | 6 | a0002c0002t0001g0025a0002c0002t0001g0130a0002c0002t0001g0131others(3): Show | 7 | HG02056.hp2 HG02976.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.492-789C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 5/7 | chr3 | 45004502 | ||||||
chr3:45004555
|
G | GT | 57 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0035others(54): Show | 64 | HG00735.hp1 HG00735.hp2 HG01070.hp1 others(61): Show |
intron_variant | MODIFIER | c.492-723dupT | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 45004555 | |||||
chr3:45004555
|
G | GTT | 10 | a0001c0001t0001g0034a0001c0001t0001g0151a0001c0001t0001g0152others(7): Show | 10 | HG00609.hp1 HG00639.hp1 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.492-724_492-723dup others(2): Show |
EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 45004555 | |||||
chr3:45004555
|
GT | G | 28 | a0001c0001t0001g0039a0003c0003t0001g0007a0003c0003t0001g0015others(25): Show | 33 | HG00099.hp2 HG00639.hp2 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.492-723delT | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 45004555 | |||||
chr3:45004557
|
T | G | 1 | a0001c0001t0001g0158 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.492-734T>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 5/7 | chr3 | 45004557 | ||||||
chr3:45004569
|
G | T | 78 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0034others(75): Show | 96 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.492-722G>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 5/7 | chr3 | 45004569 | ||||||
chr3:45004573
|
T | G | 3 | a0001c0001t0001g0012a0001c0001t0001g0201a0001c0001t0001g0202 | 5 | HG01884.hp2 HG01891.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.492-718T>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 5/7 | chr3 | 45004573 | ||||||
chr3:45004575
|
T | G | 32 | a0001c0001t0001g0039a0001c0001t0001g0054a0001c0001t0001g0055others(29): Show | 37 | HG00099.hp2 HG00639.hp2 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.492-716T>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 5/7 | chr3 | 45004575 | ||||||
chr3:45004680
|
TCAGA | T | 11 | a0004c0004t0001g0017a0004c0004t0001g0018a0004c0004t0001g0051others(8): Show | 13 | HG01167.hp2 HG01169.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.492-607_492-604del others(4): Show |
EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 45004680 | |||||
chr3:45005123
|
G | A | 8 | a0001c0001t0001g0005a0001c0001t0001g0038a0001c0001t0001g0259others(5): Show | 13 | NA18984.hp1 NA18991.hp1 NA18998.hp1 others(10): Show |
intron_variant | MODIFIER | c.492-168G>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 5/7 | chr3 | 45005123 | ||||||
chr3:45005138
|
TTGACAGG others(2): Show |
T | 8 | a0001c0001t0001g0005a0001c0001t0001g0038a0001c0001t0001g0259others(5): Show | 13 | NA18984.hp1 NA18991.hp1 NA18998.hp1 others(10): Show |
intron_variant | MODIFIER | c.492-140_492-132del others(9): Show |
EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 45005138 | |||||
chr3:45005620
|
T | C | 255 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(252): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.615+206T>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | chr3 | 45005620 | ||||||
chr3:45005949
|
C | T | 1 | a0003c0003t0001g0045 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.615+535C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | chr3 | 45005949 | ||||||
chr3:45006068
|
C | CT | 71 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0014others(68): Show | 94 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.615+683dupT | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr3 | 45006068 | |||||
chr3:45006068
|
C | CTT | 53 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(50): Show | 69 | HG00423.hp1 HG00438.hp2 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.615+682_615+683dup others(2): Show |
EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr3 | 45006068 | |||||
chr3:45006068
|
CT | C | 46 | a0001c0001t0001g0013a0001c0001t0001g0028a0001c0001t0001g0147others(43): Show | 63 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(60): Show |
intron_variant | MODIFIER | c.615+683delT | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr3 | 45006068 | |||||
chr3:45006068
|
CTT | C | 12 | a0001c0001t0001g0005a0001c0001t0001g0038a0001c0001t0001g0136others(9): Show | 17 | HG02056.hp2 NA18952.hp1 NA18970.hp2 others(14): Show |
intron_variant | MODIFIER | c.615+682_615+683del others(2): Show |
EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr3 | 45006068 | |||||
chr3:45006068
|
CTTTTTTT others(1): Show |
C | 15 | a0001c0012t0001g0171a0003c0003t0001g0007a0003c0003t0001g0015others(12): Show | 18 | HG00099.hp2 HG00639.hp2 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.615+676_615+683del others(8): Show |
EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr3 | 45006068 | |||||
chr3:45006068
|
CTTTTTTT others(5): Show |
C | 8 | a0001c0001t0001g0019a0001c0001t0001g0065a0001c0001t0001g0066others(5): Show | 9 | HG00738.hp2 HG02055.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.615+672_615+683del others(12): Show |
EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr3 | 45006068 | |||||
chr3:45006068
|
CTTTTTTT others(11): Show |
C | 2 | a0001c0001t0001g0223a0001c0001t0001g0224 | 2 | HG00280.hp2 HG01167.hp1 |
intron_variant | MODIFIER | c.615+666_615+683del others(18): Show |
EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr3 | 45006068 | |||||
chr3:45006116
|
C | T | 142 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(139): Show | 186 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.615+702C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | chr3 | 45006116 | ||||||
chr3:45006120
|
C | G | 1 | a0001c0001t0001g0176 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.615+706C>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | chr3 | 45006120 | ||||||
chr3:45006126
|
G | A | 1 | a0002c0002t0001g0126 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.615+712G>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | chr3 | 45006126 | ||||||
chr3:45006139
|
G | A | 142 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(139): Show | 186 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.615+725G>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | chr3 | 45006139 | ||||||
chr3:45006229
|
C | T | 1 | a0001c0001t0001g0065 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.615+815C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | chr3 | 45006229 | ||||||
chr3:45006266
|
C | T | 1 | a0002c0002t0001g0130 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.615+852C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | chr3 | 45006266 | ||||||
chr3:45006267
|
G | A | 69 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0011others(66): Show | 95 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.615+853G>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | chr3 | 45006267 | ||||||
chr3:45006345
|
C | T | 1 | a0001c0001t0001g0260 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.615+931C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | chr3 | 45006345 | ||||||
chr3:45006404
|
G | GT | 9 | a0001c0001t0001g0136a0001c0001t0001g0207a0002c0002t0001g0087others(6): Show | 9 | HG00280.hp1 HG01106.hp2 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.616-993dupT | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr3 | 45006404 | |||||
chr3:45006404
|
GT | G | 128 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0011others(125): Show | 170 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.616-993delT | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr3 | 45006404 | |||||
chr3:45006404
|
GTT | G | 66 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(63): Show | 86 | HG00609.hp1 HG00639.hp1 HG00642.hp1 others(83): Show |
intron_variant | MODIFIER | c.616-994_616-993del others(2): Show |
EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr3 | 45006404 | |||||
chr3:45006404
|
GTTT | G | 9 | a0001c0001t0001g0214a0001c0001t0001g0217a0001c0001t0001g0249others(6): Show | 10 | HG02056.hp2 HG02559.hp2 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.616-995_616-993del others(3): Show |
EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr3 | 45006404 | |||||
chr3:45006411
|
T | G | 1 | a0004c0004t0001g0063 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.615+997T>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | chr3 | 45006411 | ||||||
chr3:45006412
|
T | G | 11 | a0001c0001t0001g0065a0004c0004t0001g0017a0004c0004t0001g0018others(8): Show | 13 | HG01167.hp2 HG01169.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.615+998T>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | chr3 | 45006412 | ||||||
chr3:45006440
|
C | T | 1 | a0001c0001t0001g0039 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.616-980C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | chr3 | 45006440 | ||||||
chr3:45006449
|
G | A | 1 | a0003c0003t0001g0050 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.616-971G>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | chr3 | 45006449 | ||||||
chr3:45006458
|
G | A | 2 | a0002c0002t0001g0104a0002c0002t0001g0110 | 2 | HG03239.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.616-962G>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | chr3 | 45006458 | ||||||
chr3:45006477
|
T | C | 191 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(188): Show | 246 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(243): Show |
intron_variant | MODIFIER | c.616-943T>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | chr3 | 45006477 | ||||||
chr3:45006478
|
G | A | 1 | a0001c0012t0001g0171 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.616-942G>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | chr3 | 45006478 | ||||||
chr3:45006495
|
T | C | 197 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(194): Show | 253 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(250): Show |
intron_variant | MODIFIER | c.616-925T>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | chr3 | 45006495 | ||||||
chr3:45006502
|
C | T | 18 | a0001c0001t0001g0039a0003c0003t0001g0007a0003c0003t0001g0015others(15): Show | 21 | HG00099.hp2 HG00639.hp2 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.616-918C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | chr3 | 45006502 | ||||||
chr3:45006568
|
C | T | 8 | a0001c0001t0001g0005a0001c0001t0001g0038a0001c0001t0001g0259others(5): Show | 13 | NA18984.hp1 NA18991.hp1 NA18998.hp1 others(10): Show |
intron_variant | MODIFIER | c.616-852C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | chr3 | 45006568 | ||||||
chr3:45006597
|
T | C | 2 | a0001c0001t0001g0150a0001c0001t0001g0161 | 2 | HG00609.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.616-823T>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | chr3 | 45006597 | ||||||
chr3:45006648
|
C | A | 1 | a0001c0001t0001g0136 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.616-772C>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | chr3 | 45006648 | ||||||
chr3:45006648
|
C | T | 1 | a0002c0002t0001g0087 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.616-772C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | chr3 | 45006648 | ||||||
chr3:45006658
|
T | C | 197 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(194): Show | 253 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(250): Show |
intron_variant | MODIFIER | c.616-762T>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | chr3 | 45006658 | ||||||
chr3:45006659
|
G | A | 197 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(194): Show | 253 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(250): Show |
intron_variant | MODIFIER | c.616-761G>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | chr3 | 45006659 | ||||||
chr3:45006690
|
A | G | 1 | a0001c0001t0001g0136 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.616-730A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | chr3 | 45006690 | ||||||
chr3:45006703
|
A | G | 1 | a0001c0001t0001g0136 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.616-717A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | chr3 | 45006703 | ||||||
chr3:45006711
|
C | T | 4 | a0001c0001t0001g0137a0001c0001t0001g0139a0001c0005t0001g0026others(1): Show | 5 | HG02258.hp2 HG02818.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.616-709C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | chr3 | 45006711 | ||||||
chr3:45006795
|
A | G | 32 | a0001c0001t0001g0039a0001c0001t0001g0054a0001c0001t0001g0055others(29): Show | 37 | HG00099.hp2 HG00639.hp2 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.616-625A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | chr3 | 45006795 | ||||||
chr3:45006796
|
C | T | 1 | a0001c0001t0001g0175 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.616-624C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | chr3 | 45006796 | ||||||
chr3:45006802
|
C | A | 1 | a0001c0001t0001g0151 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.616-618C>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | chr3 | 45006802 | ||||||
chr3:45006811
|
C | T | 29 | a0001c0001t0001g0039a0003c0003t0001g0007a0003c0003t0001g0015others(26): Show | 34 | HG00099.hp2 HG00639.hp2 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.616-609C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | chr3 | 45006811 | ||||||
chr3:45006912
|
A | C | 32 | a0001c0001t0001g0039a0001c0001t0001g0054a0001c0001t0001g0055others(29): Show | 37 | HG00099.hp2 HG00639.hp2 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.616-508A>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | chr3 | 45006912 | ||||||
chr3:45006960
|
A | C | 1 | a0001c0001t0001g0174 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.616-460A>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | chr3 | 45006960 | ||||||
chr3:45006980
|
T | C | 190 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(187): Show | 245 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(242): Show |
intron_variant | MODIFIER | c.616-440T>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | chr3 | 45006980 | ||||||
chr3:45007119
|
T | A | 1 | a0001c0001t0001g0201 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.616-301T>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | chr3 | 45007119 | ||||||
chr3:45007129
|
T | C | 2 | a0001c0001t0001g0229a0001c0001t0001g0230 | 2 | HG01070.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.616-291T>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | chr3 | 45007129 | ||||||
chr3:45007315
|
T | C | 14 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0028others(11): Show | 21 | HG00642.hp1 HG01109.hp2 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.616-105T>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | chr3 | 45007315 | ||||||
chr3:45007400
|
C | T | 8 | a0001c0001t0001g0005a0001c0001t0001g0038a0001c0001t0001g0259others(5): Show | 13 | NA18984.hp1 NA18991.hp1 NA18998.hp1 others(10): Show |
intron_variant | MODIFIER | c.616-20C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | chr3 | 45007400 | ||||||
chr3:45007408
|
C | T | 6 | a0002c0002t0001g0025a0002c0002t0001g0130a0002c0002t0001g0131others(3): Show | 7 | HG02056.hp2 HG02976.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.616-12C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 6/7 | chr3 | 45007408 | ||||||
chr3:45007581
|
G | A | 1 | a0001c0001t0001g0219 | 1 | HG02451.hp1 | splice_region_variant&intron_variant | LOW | c.771+6G>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 7/7 | chr3 | 45007581 | ||||||
chr3:45007694
|
A | G | 197 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(194): Show | 253 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(250): Show |
intron_variant | MODIFIER | c.771+119A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 7/7 | chr3 | 45007694 | ||||||
chr3:45007799
|
A | C | 1 | a0002c0002t0001g0134 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.771+224A>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 7/7 | chr3 | 45007799 | ||||||
chr3:45007822
|
C | G | 142 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(139): Show | 186 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.771+247C>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 7/7 | chr3 | 45007822 | ||||||
chr3:45007879
|
C | G | 8 | a0001c0001t0001g0005a0001c0001t0001g0038a0001c0001t0001g0259others(5): Show | 13 | NA18984.hp1 NA18991.hp1 NA18998.hp1 others(10): Show |
intron_variant | MODIFIER | c.771+304C>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 7/7 | chr3 | 45007879 | ||||||
chr3:45007882
|
G | A | 1 | a0001c0001t0001g0246 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.771+307G>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 7/7 | chr3 | 45007882 | ||||||
chr3:45008098
|
C | G | 2 | a0003c0003t0001g0016a0003c0003t0001g0048 | 3 | HG01070.hp2 HG01071.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.771+523C>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 7/7 | chr3 | 45008098 | ||||||
chr3:45008109
|
A | G | 4 | a0001c0001t0001g0137a0001c0001t0001g0139a0001c0005t0001g0026others(1): Show | 5 | HG02258.hp2 HG02818.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.771+534A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 7/7 | chr3 | 45008109 | ||||||
chr3:45008161
|
T | C | 2 | a0001c0001t0001g0140a0001c0001t0001g0141 | 2 | HG02523.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.771+586T>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 7/7 | chr3 | 45008161 | ||||||
chr3:45008217
|
G | C | 1 | a0003c0003t0001g0044 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.771+642G>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 7/7 | chr3 | 45008217 | ||||||
chr3:45008473
|
T | C | 1 | a0001c0001t0001g0180 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.771+898T>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 7/7 | chr3 | 45008473 | ||||||
chr3:45008802
|
A | C | 1 | a0001c0001t0001g0208 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.771+1227A>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 7/7 | chr3 | 45008802 | ||||||
chr3:45008900
|
A | G | 1 | a0003c0003t0001g0050 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.771+1325A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 7/7 | chr3 | 45008900 | ||||||
chr3:45008971
|
T | C | 1 | a0001c0001t0001g0197 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.771+1396T>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 7/7 | chr3 | 45008971 | ||||||
chr3:45008991
|
G | C | 1 | a0001c0001t0001g0241 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.771+1416G>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 7/7 | chr3 | 45008991 | ||||||
chr3:45009080
|
T | C | 1 | a0002c0002t0001g0119 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.771+1505T>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 7/7 | chr3 | 45009080 | ||||||
chr3:45009218
|
G | A | 191 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(188): Show | 246 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(243): Show |
intron_variant | MODIFIER | c.771+1643G>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 7/7 | chr3 | 45009218 | ||||||
chr3:45009267
|
T | G | 2 | a0001c0001t0001g0151a0001c0001t0001g0152 | 2 | HG01928.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.771+1692T>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 7/7 | chr3 | 45009267 | ||||||
chr3:45009360
|
G | A | 3 | a0001c0001t0001g0031a0001c0001t0001g0180a0001c0001t0001g0181 | 4 | NA18953.hp1 NA18961.hp1 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.771+1785G>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 7/7 | chr3 | 45009360 | ||||||
chr3:45009472
|
A | G | 1 | a0001c0001t0001g0175 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.772-1763A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 7/7 | chr3 | 45009472 | ||||||
chr3:45009509
|
C | CT | 19 | a0002c0002t0001g0010a0002c0002t0001g0024a0002c0002t0001g0073others(16): Show | 22 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(19): Show |
intron_variant | MODIFIER | c.772-1718dupT | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr3 | 45009509 | |||||
chr3:45009510
|
T | A | 6 | a0002c0002t0001g0025a0002c0002t0001g0130a0002c0002t0001g0131others(3): Show | 7 | HG02056.hp2 HG02976.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.772-1725T>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 7/7 | chr3 | 45009510 | ||||||
chr3:45009556
|
T | C | 1 | a0001c0001t0001g0139 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.772-1679T>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 7/7 | chr3 | 45009556 | ||||||
chr3:45009587
|
C | T | 8 | a0001c0001t0001g0019a0001c0001t0001g0065a0001c0001t0001g0066others(5): Show | 9 | HG00738.hp2 HG02055.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.772-1648C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 7/7 | chr3 | 45009587 | ||||||
chr3:45009634
|
C | T | 8 | a0001c0001t0001g0019a0001c0001t0001g0065a0001c0001t0001g0066others(5): Show | 9 | HG00738.hp2 HG02055.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.772-1601C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 7/7 | chr3 | 45009634 | ||||||
chr3:45009642
|
T | TGGTTCAA others(37): Show |
1 | a0002c0002t0001g0124 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.772-1592_772-1549d others(46): Show |
EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr3 | 45009642 | |||||
chr3:45009653
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A | G | 32 | a0001c0001t0001g0039a0001c0001t0001g0054a0001c0001t0001g0055others(29): Show | 37 | HG00099.hp2 HG00639.hp2 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.772-1582A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 7/7 | chr3 | 45009653 | ||||||
chr3:45009683
|
T | C | 1 | a0001c0001t0001g0246 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.772-1552T>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 7/7 | chr3 | 45009683 | ||||||
chr3:45009848
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C | T | 1 | a0001c0001t0001g0223 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.772-1387C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 7/7 | chr3 | 45009848 | ||||||
chr3:45010291
|
A | G | 1 | a0001c0001t0001g0214 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.772-944A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 7/7 | chr3 | 45010291 | ||||||
chr3:45010330
|
C | T | 9 | a0000c0008t0001g0258a0001c0001t0001g0005a0001c0001t0001g0038others(6): Show | 14 | NA18984.hp1 NA18991.hp1 NA18998.hp1 others(11): Show |
intron_variant | MODIFIER | c.772-905C>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 7/7 | chr3 | 45010330 | ||||||
chr3:45010335
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A | C | 192 | a0000c0008t0001g0258a0001c0001t0001g0001a0001c0001t0001g0003others(189): Show | 247 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(244): Show |
intron_variant | MODIFIER | c.772-900A>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 7/7 | chr3 | 45010335 | ||||||
chr3:45010387
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A | G | 1 | a0003c0003t0001g0059 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.772-848A>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 7/7 | chr3 | 45010387 | ||||||
chr3:45010862
|
AG | A | 3 | a0002c0002t0001g0121a0002c0002t0001g0123a0002c0002t0001g0128 | 3 | HG00741.hp2 HG01346.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.772-372delG | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 7/7 | chr3 | 45010862 | ||||||
chr3:45011018
|
T | A | 1 | a0002c0002t0001g0124 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.772-217T>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 7/7 | chr3 | 45011018 | ||||||
chr3:45011029
|
T | A | 1 | a0002c0002t0001g0124 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.772-206T>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 7/7 | chr3 | 45011029 | ||||||
chr3:45011034
|
A | T | 1 | a0002c0002t0001g0124 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.772-201A>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 7/7 | chr3 | 45011034 | ||||||
chr3:45011047
|
C | A | 1 | a0002c0002t0001g0124 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.772-188C>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 7/7 | chr3 | 45011047 | ||||||
chr3:45011057
|
T | G | 1 | a0002c0002t0001g0124 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.772-178T>G | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 7/7 | chr3 | 45011057 | ||||||
chr3:45011066
|
G | T | 1 | a0002c0002t0001g0124 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.772-169G>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 7/7 | chr3 | 45011066 | ||||||
chr3:45011072
|
T | A | 1 | a0002c0002t0001g0124 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.772-163T>A | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 7/7 | chr3 | 45011072 | ||||||
chr3:45011076
|
G | T | 1 | a0002c0002t0001g0124 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.772-159G>T | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 7/7 | chr3 | 45011076 | ||||||
chr3:45011078
|
TTTTGTTT others(54): Show |
T | 1 | a0002c0002t0001g0124 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.772-155_772-95delT others(60): Show |
EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr3 | 45011078 | |||||
chr3:45011131
|
T | C | 1 | a0001c0001t0001g0039 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.772-104T>C | EXOSC7 | ENSG00000075914.13 | transcript | ENST00000265564.8 | protein_coding | 7/7 | chr3 | 45011131 |