geneid | 79670 |
---|---|
ensemblid | ENSG00000083223.18 |
hgncid | 25817 |
symbol | TUT7 |
name | terminal uridylyl transferase 7 |
refseq_nuc | NM_024617.4 |
refseq_prot | NP_078893.2 |
ensembl_nuc | ENST00000375963.8 |
ensembl_prot | ENSP00000365130.3 |
mane_status | MANE Select |
chr | chr9 |
start | 86287733 |
end | 86354410 |
strand | - |
ver | v1.2 |
region | chr9:86287733-86354410 |
region5000 | chr9:86282733-86359410 |
regionname0 | TUT7_chr9_86287733_86354410 |
regionname5000 | TUT7_chr9_86282733_86359410 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 1494 | 172 | 34 | 36 | 74 | 8 | 20 | 62 | TUT7_chr9_86282733_86359410 | TUT7 | copy fasta | chr9 | 86282733 | 86359410 |
a0002 | 1/1 | 1495 | 163 | 38 | 28 | 73 | 7 | 15 | 55 | TUT7_chr9_86282733_86359410 | TUT7 | copy fasta | chr9 | 86282733 | 86359410 |
a0003 | 0/0 | 1494 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | copy fasta | chr9 | 86282733 | 86359410 |
a0004 | 0/0 | 1494 | 5 | 4 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | copy fasta | chr9 | 86282733 | 86359410 |
a0005 | 0/0 | 1494 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | copy fasta | chr9 | 86282733 | 86359410 |
a0006 | 0/0 | 1495 | 2 | 0 | 1 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | copy fasta | chr9 | 86282733 | 86359410 |
a0007 | 0/0 | 1495 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | copy fasta | chr9 | 86282733 | 86359410 |
a0008 | 0/0 | 1495 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | copy fasta | chr9 | 86282733 | 86359410 |
a0009 | 0/0 | 1494 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | copy fasta | chr9 | 86282733 | 86359410 |
a0010 | 0/0 | 1494 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | copy fasta | chr9 | 86282733 | 86359410 |
a0011 | 0/0 | 1495 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | copy fasta | chr9 | 86282733 | 86359410 |
a0012 | 0/0 | 1495 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | copy fasta | chr9 | 86282733 | 86359410 |
a0013 | 0/0 | 1494 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | copy fasta | chr9 | 86282733 | 86359410 |
a0014 | 0/0 | 1494 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | copy fasta | chr9 | 86282733 | 86359410 |
a0015 | 0/0 | 1494 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | copy fasta | chr9 | 86282733 | 86359410 |
a0016 | 0/0 | 1494 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | copy fasta | chr9 | 86282733 | 86359410 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 4485 | 170 | 33 | 35 | 74 | 8 | 20 | TUT7_chr9_86282733_86359410 | TUT7 | copy fasta | chr9 | 86282733 | 86359410 |
c0002 | 1/1 | 4488 | 121 | 17 | 24 | 59 | 7 | 12 | TUT7_chr9_86282733_86359410 | TUT7 | copy fasta | chr9 | 86282733 | 86359410 |
c0003 | 0/0 | 4488 | 42 | 21 | 4 | 14 | 0 | 3 | TUT7_chr9_86282733_86359410 | TUT7 | copy fasta | chr9 | 86282733 | 86359410 |
c0004 | 0/0 | 4485 | 6 | 6 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | copy fasta | chr9 | 86282733 | 86359410 |
c0005 | 0/0 | 4485 | 5 | 4 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | copy fasta | chr9 | 86282733 | 86359410 |
c0006 | 0/0 | 4485 | 4 | 4 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | copy fasta | chr9 | 86282733 | 86359410 |
c0007 | 0/0 | 4488 | 2 | 0 | 1 | 0 | 1 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | copy fasta | chr9 | 86282733 | 86359410 |
c0008 | 0/0 | 4488 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | copy fasta | chr9 | 86282733 | 86359410 |
c0009 | 0/0 | 4485 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | copy fasta | chr9 | 86282733 | 86359410 |
c0010 | 0/0 | 4485 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | copy fasta | chr9 | 86282733 | 86359410 |
c0011 | 0/0 | 4488 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | copy fasta | chr9 | 86282733 | 86359410 |
c0012 | 0/0 | 4485 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | copy fasta | chr9 | 86282733 | 86359410 |
c0013 | 0/0 | 4485 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | copy fasta | chr9 | 86282733 | 86359410 |
c0014 | 0/0 | 4485 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | copy fasta | chr9 | 86282733 | 86359410 |
c0015 | 0/0 | 4485 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | copy fasta | chr9 | 86282733 | 86359410 |
c0016 | 0/0 | 4485 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | copy fasta | chr9 | 86282733 | 86359410 |
c0017 | 0/0 | 4485 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | copy fasta | chr9 | 86282733 | 86359410 |
c0018 | 0/0 | 4488 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | copy fasta | chr9 | 86282733 | 86359410 |
c0019 | 0/0 | 4488 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | copy fasta | chr9 | 86282733 | 86359410 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 1116 | 317 | 79 | 48 | 147 | 10 | 32 | TUT7_chr9_86282733_86359410 | TUT7 | copy fasta | chr9 | 86282733 | 86359410 |
t0002 | 1/0 | 1116 | 31 | 1 | 17 | 2 | 6 | 4 | TUT7_chr9_86282733_86359410 | TUT7 | copy fasta | chr9 | 86282733 | 86359410 |
t0003 | 0/0 | 1116 | 3 | 3 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | copy fasta | chr9 | 86282733 | 86359410 |
t0004 | 0/0 | 1116 | 3 | 3 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | copy fasta | chr9 | 86282733 | 86359410 |
t0005 | 0/0 | 1116 | 2 | 0 | 1 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | copy fasta | chr9 | 86282733 | 86359410 |
t0006 | 0/0 | 1116 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | copy fasta | chr9 | 86282733 | 86359410 |
t0007 | 0/0 | 1116 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | copy fasta | chr9 | 86282733 | 86359410 |
t0008 | 0/0 | 1116 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | copy fasta | chr9 | 86282733 | 86359410 |
t0009 | 0/0 | 1116 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | copy fasta | chr9 | 86282733 | 86359410 |
t0010 | 0/0 | 1116 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | copy fasta | chr9 | 86282733 | 86359410 |
t0011 | 0/0 | 1116 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | copy fasta | chr9 | 86282733 | 86359410 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 11 | 5 | 2 | 3 | 1 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0002 | 0/0 | 8 | 0 | 5 | 0 | 1 | 2 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0003 | 0/0 | 4 | 0 | 0 | 2 | 0 | 2 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0004 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0005 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0006 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0008 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0010 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0017 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0018 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0027 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0028 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0030 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0032 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0037 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0198 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0211 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 4485 | 170 | 33 | 35 | 74 | 8 | 20 | TUT7_chr9_86282733_86359410 | TUT7 | copy fasta | chr9 | 86282733 | 86359410 |
a0001c0009 | 0/0 | 4485 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | copy fasta | chr9 | 86282733 | 86359410 |
a0001c0014 | 0/0 | 4485 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | copy fasta | chr9 | 86282733 | 86359410 |
a0002c0002 | 1/1 | 4488 | 121 | 17 | 24 | 59 | 7 | 12 | TUT7_chr9_86282733_86359410 | TUT7 | copy fasta | chr9 | 86282733 | 86359410 |
a0002c0003 | 0/0 | 4488 | 42 | 21 | 4 | 14 | 0 | 3 | TUT7_chr9_86282733_86359410 | TUT7 | copy fasta | chr9 | 86282733 | 86359410 |
a0003c0004 | 0/0 | 4485 | 6 | 6 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | copy fasta | chr9 | 86282733 | 86359410 |
a0004c0005 | 0/0 | 4485 | 5 | 4 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | copy fasta | chr9 | 86282733 | 86359410 |
a0005c0006 | 0/0 | 4485 | 4 | 4 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | copy fasta | chr9 | 86282733 | 86359410 |
a0006c0007 | 0/0 | 4488 | 2 | 0 | 1 | 0 | 1 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | copy fasta | chr9 | 86282733 | 86359410 |
a0007c0008 | 0/0 | 4488 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | copy fasta | chr9 | 86282733 | 86359410 |
a0008c0019 | 0/0 | 4488 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | copy fasta | chr9 | 86282733 | 86359410 |
a0009c0017 | 0/0 | 4485 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | copy fasta | chr9 | 86282733 | 86359410 |
a0010c0016 | 0/0 | 4485 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | copy fasta | chr9 | 86282733 | 86359410 |
a0011c0011 | 0/0 | 4488 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | copy fasta | chr9 | 86282733 | 86359410 |
a0012c0018 | 0/0 | 4488 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | copy fasta | chr9 | 86282733 | 86359410 |
a0013c0012 | 0/0 | 4485 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | copy fasta | chr9 | 86282733 | 86359410 |
a0014c0013 | 0/0 | 4485 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | copy fasta | chr9 | 86282733 | 86359410 |
a0015c0015 | 0/0 | 4485 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | copy fasta | chr9 | 86282733 | 86359410 |
a0016c0010 | 0/0 | 4485 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | copy fasta | chr9 | 86282733 | 86359410 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 5600 | 136 | 26 | 20 | 72 | 2 | 16 | TUT7_chr9_86282733_86359410 | TUT7 | copy fasta | chr9 | 86282733 | 86359410 |
a0001c0001t0002 | 0/0 | 5600 | 28 | 1 | 15 | 2 | 6 | 4 | TUT7_chr9_86282733_86359410 | TUT7 | copy fasta | chr9 | 86282733 | 86359410 |
a0001c0001t0003 | 0/0 | 5600 | 3 | 3 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | copy fasta | chr9 | 86282733 | 86359410 |
a0001c0001t0004 | 0/0 | 5600 | 2 | 2 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | copy fasta | chr9 | 86282733 | 86359410 |
a0001c0001t0010 | 0/0 | 5600 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | copy fasta | chr9 | 86282733 | 86359410 |
a0001c0009t0001 | 0/0 | 5600 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | copy fasta | chr9 | 86282733 | 86359410 |
a0001c0014t0011 | 0/0 | 5600 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | copy fasta | chr9 | 86282733 | 86359410 |
a0002c0002t0001 | 0/1 | 5603 | 114 | 16 | 21 | 58 | 7 | 11 | TUT7_chr9_86282733_86359410 | TUT7 | copy fasta | chr9 | 86282733 | 86359410 |
a0002c0002t0002 | 1/0 | 5603 | 3 | 0 | 2 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | copy fasta | chr9 | 86282733 | 86359410 |
a0002c0002t0005 | 0/0 | 5603 | 2 | 0 | 1 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | copy fasta | chr9 | 86282733 | 86359410 |
a0002c0002t0006 | 0/0 | 5603 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | copy fasta | chr9 | 86282733 | 86359410 |
a0002c0002t0009 | 0/0 | 5603 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | copy fasta | chr9 | 86282733 | 86359410 |
a0002c0003t0001 | 0/0 | 5603 | 41 | 21 | 4 | 14 | 0 | 2 | TUT7_chr9_86282733_86359410 | TUT7 | copy fasta | chr9 | 86282733 | 86359410 |
a0002c0003t0007 | 0/0 | 5603 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | copy fasta | chr9 | 86282733 | 86359410 |
a0003c0004t0001 | 0/0 | 5600 | 6 | 6 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | copy fasta | chr9 | 86282733 | 86359410 |
a0004c0005t0001 | 0/0 | 5600 | 5 | 4 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | copy fasta | chr9 | 86282733 | 86359410 |
a0005c0006t0001 | 0/0 | 5600 | 4 | 4 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | copy fasta | chr9 | 86282733 | 86359410 |
a0006c0007t0001 | 0/0 | 5603 | 2 | 0 | 1 | 0 | 1 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | copy fasta | chr9 | 86282733 | 86359410 |
a0007c0008t0001 | 0/0 | 5603 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | copy fasta | chr9 | 86282733 | 86359410 |
a0008c0019t0001 | 0/0 | 5603 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | copy fasta | chr9 | 86282733 | 86359410 |
a0009c0017t0001 | 0/0 | 5600 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | copy fasta | chr9 | 86282733 | 86359410 |
a0010c0016t0001 | 0/0 | 5600 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | copy fasta | chr9 | 86282733 | 86359410 |
a0011c0011t0001 | 0/0 | 5603 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | copy fasta | chr9 | 86282733 | 86359410 |
a0012c0018t0001 | 0/0 | 5603 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | copy fasta | chr9 | 86282733 | 86359410 |
a0013c0012t0008 | 0/0 | 5600 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | copy fasta | chr9 | 86282733 | 86359410 |
a0014c0013t0001 | 0/0 | 5600 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | copy fasta | chr9 | 86282733 | 86359410 |
a0015c0015t0004 | 0/0 | 5600 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | copy fasta | chr9 | 86282733 | 86359410 |
a0016c0010t0001 | 0/0 | 5600 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | copy fasta | chr9 | 86282733 | 86359410 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 4 | 0 | 0 | 2 | 0 | 2 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0004 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0005 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0006 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0010 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0002g0002 | 0/0 | 8 | 0 | 5 | 0 | 1 | 2 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0002g0008 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0002g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0003g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0003g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0004g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0004g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0001t0010g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0009t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0001c0014t0011g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0001g0001 | 0/0 | 11 | 5 | 2 | 3 | 1 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0001g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0001g0027 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0001g0028 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0001g0030 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0001g0032 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0001g0211 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0002g0198 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0005g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0005g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0006g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0002t0009g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0003t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0003t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0003t0001g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0003t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0003t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0003t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0003t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0003t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0003t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0003t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0003t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0003t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0003t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0003t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0003t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0003t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0003t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0003t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0003t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0003t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0003t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0003t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0003t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0003t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0003t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0003t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0003t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0003t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0003t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0003t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0003t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0003t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0003t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0003t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0003t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0003t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0002c0003t0007g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0003c0004t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0003c0004t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0003c0004t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0003c0004t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0003c0004t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0003c0004t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0004c0005t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0004c0005t0001g0037 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0004c0005t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0005c0006t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0005c0006t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0005c0006t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0005c0006t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0006c0007t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0006c0007t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0007c0008t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0008c0019t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0009c0017t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0010c0016t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0011c0011t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0012c0018t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0013c0012t0008g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0014c0013t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0015c0015t0004g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
a0016c0010t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0006 | c0007 | t0001 | g0197 | EUR | GBR | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0048 | EUR | GBR | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG00140 | hp1 | a0002 | c0002 | t0001 | g0027 | EUR | GBR | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0078 | EUR | GBR | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0002 | EUR | FIN | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0018 | EUR | FIN | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG00323 | hp1 | a0002 | c0002 | t0001 | g0188 | EUR | FIN | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0046 | EUR | FIN | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | CHS | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG00438 | hp2 | a0002 | c0002 | t0001 | g0180 | EAS | CHS | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG00544 | hp1 | a0002 | c0002 | t0001 | g0184 | EAS | CHS | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG00544 | hp2 | a0002 | c0002 | t0001 | g0234 | EAS | CHS | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG00558 | hp1 | a0002 | c0002 | t0001 | g0029 | EAS | CHS | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | CHS | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | CHS | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG00597 | hp2 | a0002 | c0002 | t0001 | g0192 | EAS | CHS | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | CHS | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG00639 | hp1 | a0002 | c0002 | t0001 | g0257 | AMR | PUR | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0014 | AMR | PUR | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG00642 | hp2 | a0002 | c0002 | t0001 | g0221 | AMR | PUR | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG00733 | hp1 | a0002 | c0003 | t0001 | g0267 | AMR | PUR | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG00735 | hp1 | a0002 | c0003 | t0001 | g0266 | AMR | PUR | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG00735 | hp2 | a0002 | c0002 | t0001 | g0199 | AMR | PUR | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | PUR | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG00738 | hp2 | a0002 | c0002 | t0001 | g0175 | AMR | PUR | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG00741 | hp2 | a0002 | c0002 | t0001 | g0027 | AMR | PUR | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0051 | AMR | PUR | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG01070 | hp1 | a0002 | c0002 | t0001 | g0189 | AMR | PUR | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0054 | AMR | PUR | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG01099 | hp2 | a0002 | c0002 | t0001 | g0190 | AMR | PUR | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG01106 | hp1 | a0002 | c0002 | t0001 | g0191 | AMR | PUR | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG01109 | hp2 | a0002 | c0003 | t0001 | g0282 | AMR | PUR | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG01167 | hp2 | a0002 | c0002 | t0001 | g0258 | AMR | PUR | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG01168 | hp1 | a0002 | c0002 | t0001 | g0171 | AMR | PUR | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG01168 | hp2 | a0002 | c0002 | t0001 | g0225 | AMR | PUR | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG01169 | hp1 | a0002 | c0002 | t0001 | g0032 | AMR | PUR | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0050 | AMR | PUR | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG01243 | hp1 | a0004 | c0005 | t0001 | g0037 | AMR | PUR | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG01255 | hp1 | a0002 | c0002 | t0001 | g0208 | AMR | CLM | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG01255 | hp2 | a0002 | c0003 | t0001 | g0289 | AMR | CLM | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG01256 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG01256 | hp2 | a0002 | c0002 | t0002 | g0177 | AMR | CLM | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG01257 | hp2 | a0002 | c0002 | t0001 | g0228 | AMR | CLM | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0055 | AMR | CLM | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG01258 | hp2 | a0002 | c0002 | t0002 | g0176 | AMR | CLM | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG01261 | hp1 | a0002 | c0002 | t0005 | g0227 | AMR | CLM | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG01261 | hp2 | a0002 | c0002 | t0001 | g0186 | AMR | CLM | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG01361 | hp1 | a0002 | c0002 | t0001 | g0244 | AMR | CLM | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0052 | AMR | CLM | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG01433 | hp1 | a0006 | c0007 | t0001 | g0259 | AMR | CLM | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | CLM | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0043 | EUR | IBS | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG01515 | hp2 | a0002 | c0002 | t0001 | g0028 | EUR | IBS | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG01516 | hp1 | a0002 | c0002 | t0001 | g0028 | EUR | IBS | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0008 | EUR | IBS | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | ACB | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG01884 | hp2 | a0001 | c0014 | t0011 | g0294 | AFR | ACB | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0049 | AMR | PEL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG01943 | hp1 | a0002 | c0002 | t0001 | g0206 | AMR | PEL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PEL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG01978 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PEL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG02040 | hp1 | a0002 | c0002 | t0001 | g0238 | EAS | KHV | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG02040 | hp2 | a0002 | c0003 | t0001 | g0262 | EAS | KHV | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | ACB | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG02055 | hp2 | a0002 | c0003 | t0001 | g0290 | AFR | ACB | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG02071 | hp1 | a0002 | c0002 | t0001 | g0214 | EAS | KHV | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG02074 | hp1 | a0002 | c0002 | t0001 | g0182 | EAS | KHV | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG02074 | hp2 | a0002 | c0002 | t0001 | g0268 | EAS | KHV | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | KHV | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG02129 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG02132 | hp2 | a0002 | c0002 | t0001 | g0011 | EAS | KHV | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG02135 | hp1 | a0002 | c0002 | t0001 | g0249 | EAS | KHV | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG02145 | hp1 | a0001 | c0001 | t0002 | g0044 | AFR | ACB | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG02145 | hp2 | a0002 | c0002 | t0001 | g0001 | AFR | ACB | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG02148 | hp2 | a0001 | c0001 | t0002 | g0045 | AMR | PEL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG02165 | hp1 | a0002 | c0002 | t0001 | g0181 | EAS | CDX | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CDX | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG02257 | hp1 | a0002 | c0003 | t0001 | g0035 | AFR | ACB | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG02257 | hp2 | a0003 | c0004 | t0001 | g0273 | AFR | ACB | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG02258 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | ACB | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG02258 | hp2 | a0001 | c0001 | t0010 | g0160 | AFR | ACB | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG02280 | hp1 | a0002 | c0003 | t0001 | g0035 | AFR | ACB | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG02280 | hp2 | a0001 | c0001 | t0003 | g0020 | AFR | ACB | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PEL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG02293 | hp2 | a0002 | c0002 | t0001 | g0196 | AMR | PEL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG02300 | hp2 | a0002 | c0002 | t0001 | g0170 | AMR | PEL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG02451 | hp1 | a0002 | c0003 | t0001 | g0038 | AFR | ACB | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | ACB | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG02523 | hp2 | a0002 | c0002 | t0001 | g0183 | EAS | KHV | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG02602 | hp1 | a0010 | c0016 | t0001 | g0153 | SAS | PJL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG02602 | hp2 | a0002 | c0002 | t0001 | g0179 | SAS | PJL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG02615 | hp1 | a0009 | c0017 | t0001 | g0096 | AFR | GWD | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG02615 | hp2 | a0003 | c0004 | t0001 | g0274 | AFR | GWD | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG02622 | hp1 | a0005 | c0006 | t0001 | g0090 | AFR | GWD | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG02622 | hp2 | a0002 | c0002 | t0001 | g0147 | AFR | GWD | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG02630 | hp1 | a0002 | c0003 | t0001 | g0013 | AFR | GWD | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG02630 | hp2 | a0002 | c0003 | t0001 | g0246 | AFR | GWD | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG02683 | hp1 | a0002 | c0002 | t0001 | g0205 | SAS | PJL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG02698 | hp2 | a0002 | c0003 | t0001 | g0034 | SAS | PJL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG02717 | hp1 | a0002 | c0003 | t0001 | g0038 | AFR | GWD | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG02723 | hp2 | a0011 | c0011 | t0001 | g0286 | AFR | GWD | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG02738 | hp1 | a0002 | c0002 | t0001 | g0261 | SAS | PJL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG02809 | hp2 | a0002 | c0003 | t0001 | g0270 | AFR | GWD | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG02818 | hp2 | a0002 | c0003 | t0001 | g0288 | AFR | GWD | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG02886 | hp1 | a0003 | c0004 | t0001 | g0271 | AFR | GWD | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG02886 | hp2 | a0002 | c0002 | t0001 | g0209 | AFR | GWD | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | GWD | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG02895 | hp2 | a0005 | c0006 | t0001 | g0091 | AFR | GWD | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG02896 | hp1 | a0002 | c0003 | t0001 | g0284 | AFR | GWD | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG02896 | hp2 | a0002 | c0002 | t0001 | g0293 | AFR | GWD | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG02897 | hp1 | a0002 | c0003 | t0001 | g0285 | AFR | GWD | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG02897 | hp2 | a0005 | c0006 | t0001 | g0089 | AFR | GWD | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG02922 | hp2 | a0002 | c0002 | t0001 | g0216 | AFR | ESN | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG02965 | hp1 | a0004 | c0005 | t0001 | g0036 | AFR | ESN | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | ESN | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG02970 | hp1 | a0002 | c0002 | t0001 | g0230 | AFR | ESN | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG02970 | hp2 | a0002 | c0003 | t0001 | g0291 | AFR | ESN | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | ESN | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG02976 | hp2 | a0002 | c0002 | t0006 | g0173 | AFR | ESN | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG03017 | hp1 | a0012 | c0018 | t0001 | g0202 | SAS | PJL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG03041 | hp1 | a0001 | c0001 | t0004 | g0087 | AFR | GWD | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG03041 | hp2 | a0004 | c0005 | t0001 | g0036 | AFR | GWD | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | MSL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0281 | AFR | MSL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | ESN | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG03130 | hp2 | a0002 | c0003 | t0001 | g0287 | AFR | ESN | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG03139 | hp1 | a0002 | c0003 | t0001 | g0039 | AFR | ESN | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG03139 | hp2 | a0002 | c0003 | t0001 | g0269 | AFR | ESN | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG03195 | hp1 | a0004 | c0005 | t0001 | g0280 | AFR | ESN | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG03195 | hp2 | a0001 | c0001 | t0004 | g0085 | AFR | ESN | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG03209 | hp1 | a0015 | c0015 | t0004 | g0086 | AFR | MSL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG03209 | hp2 | a0002 | c0002 | t0001 | g0063 | AFR | MSL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG03225 | hp1 | a0013 | c0012 | t0008 | g0151 | AFR | MSL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG03225 | hp2 | a0002 | c0002 | t0001 | g0001 | AFR | MSL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG03239 | hp2 | a0002 | c0002 | t0001 | g0030 | SAS | PJL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG03453 | hp1 | a0002 | c0003 | t0001 | g0279 | AFR | MSL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | MSL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG03491 | hp2 | a0002 | c0002 | t0001 | g0245 | SAS | PJL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | ESN | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG03516 | hp2 | a0002 | c0003 | t0001 | g0169 | AFR | ESN | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG03540 | hp1 | a0002 | c0003 | t0001 | g0040 | AFR | GWD | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG03540 | hp2 | a0003 | c0004 | t0001 | g0272 | AFR | GWD | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG03654 | hp2 | a0002 | c0002 | t0001 | g0172 | SAS | PJL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG03669 | hp1 | a0002 | c0002 | t0001 | g0210 | SAS | PJL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | BEB | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG03834 | hp2 | a0002 | c0002 | t0001 | g0229 | SAS | BEB | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0080 | SAS | BEB | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0075 | SAS | BEB | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG03942 | hp1 | a0002 | c0002 | t0009 | g0167 | SAS | BEB | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG03942 | hp2 | a0002 | c0003 | t0001 | g0034 | SAS | BEB | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG04115 | hp1 | a0002 | c0002 | t0001 | g0201 | SAS | STU | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0060 | SAS | STU | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG04184 | hp1 | a0014 | c0013 | t0001 | g0072 | SAS | BEB | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG04184 | hp2 | a0002 | c0002 | t0001 | g0223 | SAS | BEB | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | STU | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0047 | SAS | STU | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG04228 | hp1 | a0002 | c0003 | t0007 | g0148 | SAS | STU | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG04228 | hp2 | a0002 | c0002 | t0001 | g0174 | SAS | STU | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA18522 | hp1 | a0002 | c0002 | t0001 | g0032 | AFR | YRI | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA18522 | hp2 | a0002 | c0002 | t0001 | g0222 | AFR | YRI | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA18612 | hp1 | a0002 | c0002 | t0001 | g0207 | EAS | CHB | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | CHB | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA18747 | hp1 | a0002 | c0003 | t0001 | g0247 | EAS | CHB | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA18747 | hp2 | a0002 | c0002 | t0001 | g0212 | EAS | CHB | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA18906 | hp1 | a0003 | c0004 | t0001 | g0276 | AFR | YRI | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | YRI | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA18942 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA18944 | hp2 | a0002 | c0002 | t0001 | g0242 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA18945 | hp2 | a0002 | c0002 | t0001 | g0215 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA18946 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA18947 | hp2 | a0002 | c0002 | t0001 | g0030 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA18948 | hp2 | a0002 | c0002 | t0005 | g0203 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA18950 | hp1 | a0002 | c0003 | t0001 | g0253 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA18951 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA18952 | hp2 | a0002 | c0002 | t0001 | g0235 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA18954 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA18956 | hp1 | a0002 | c0002 | t0001 | g0226 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA18957 | hp1 | a0002 | c0003 | t0001 | g0265 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA18957 | hp2 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA18959 | hp1 | a0002 | c0003 | t0001 | g0264 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA18960 | hp1 | a0002 | c0002 | t0001 | g0237 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA18963 | hp2 | a0002 | c0003 | t0001 | g0137 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA18966 | hp2 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA18967 | hp2 | a0007 | c0008 | t0001 | g0168 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA18968 | hp2 | a0002 | c0002 | t0001 | g0185 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA18969 | hp2 | a0002 | c0002 | t0001 | g0220 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA18971 | hp1 | a0002 | c0002 | t0001 | g0194 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA18973 | hp1 | a0002 | c0002 | t0001 | g0204 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA18974 | hp2 | a0002 | c0002 | t0001 | g0178 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA18975 | hp1 | a0002 | c0002 | t0001 | g0231 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA18977 | hp2 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA18978 | hp2 | a0002 | c0003 | t0001 | g0254 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA18980 | hp2 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA18981 | hp1 | a0002 | c0002 | t0001 | g0031 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA18983 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA18985 | hp1 | a0002 | c0002 | t0001 | g0029 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA18987 | hp1 | a0002 | c0002 | t0001 | g0260 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA18989 | hp2 | a0002 | c0002 | t0001 | g0164 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA18990 | hp1 | a0002 | c0002 | t0001 | g0240 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA18991 | hp1 | a0002 | c0002 | t0001 | g0233 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA18992 | hp1 | a0002 | c0002 | t0001 | g0200 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA18992 | hp2 | a0002 | c0003 | t0001 | g0252 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA18995 | hp1 | a0002 | c0002 | t0001 | g0239 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA18998 | hp1 | a0002 | c0003 | t0001 | g0263 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA18998 | hp2 | a0002 | c0002 | t0001 | g0232 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA18999 | hp1 | a0002 | c0003 | t0001 | g0255 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA18999 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA19002 | hp2 | a0002 | c0002 | t0001 | g0218 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA19005 | hp1 | a0002 | c0002 | t0001 | g0243 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA19005 | hp2 | a0002 | c0003 | t0001 | g0165 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA19007 | hp1 | a0016 | c0010 | t0001 | g0132 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA19009 | hp1 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA19012 | hp2 | a0002 | c0002 | t0001 | g0213 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA19030 | hp1 | a0002 | c0002 | t0001 | g0001 | AFR | LWK | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | LWK | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA19043 | hp1 | a0002 | c0002 | t0001 | g0193 | AFR | LWK | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | LWK | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA19056 | hp2 | a0002 | c0002 | t0001 | g0195 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA19060 | hp2 | a0002 | c0002 | t0001 | g0187 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA19062 | hp1 | a0008 | c0019 | t0001 | g0256 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA19068 | hp1 | a0002 | c0002 | t0001 | g0236 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA19070 | hp1 | a0002 | c0003 | t0001 | g0251 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA19070 | hp2 | a0002 | c0002 | t0001 | g0219 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA19074 | hp2 | a0002 | c0003 | t0001 | g0033 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA19079 | hp2 | a0002 | c0002 | t0001 | g0241 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA19080 | hp1 | a0002 | c0003 | t0001 | g0033 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA19081 | hp1 | a0002 | c0002 | t0001 | g0031 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA19085 | hp2 | a0002 | c0002 | t0001 | g0248 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | YRI | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA19240 | hp2 | a0001 | c0001 | t0003 | g0122 | AFR | YRI | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA20129 | hp1 | a0003 | c0004 | t0001 | g0275 | AFR | ASW | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA20129 | hp2 | a0002 | c0003 | t0001 | g0283 | AFR | ASW | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA20752 | hp1 | a0002 | c0002 | t0001 | g0001 | EUR | TSI | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0008 | EUR | TSI | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA20805 | hp1 | a0002 | c0002 | t0001 | g0224 | EUR | TSI | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA20805 | hp2 | a0002 | c0002 | t0001 | g0149 | EUR | TSI | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0053 | SAS | GIH | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | GIH | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG01123 | hp1 | a0001 | c0009 | t0001 | g0069 | AMR | CLM | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG02109 | hp2 | a0005 | c0006 | t0001 | g0088 | AFR | ACB | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG02486 | hp2 | a0001 | c0001 | t0003 | g0020 | AFR | ACB | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | MSL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG03471 | hp2 | a0002 | c0003 | t0001 | g0292 | AFR | MSL | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG06807 | hp1 | a0002 | c0003 | t0001 | g0013 | AFR | USA | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | USA | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA20300 | hp1 | a0004 | c0005 | t0001 | g0037 | AFR | USA | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA20300 | hp2 | a0002 | c0002 | t0001 | g0001 | AFR | USA | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA21309 | hp1 | a0002 | c0002 | t0001 | g0217 | AFR | LWK | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
NA21309 | hp2 | a0002 | c0002 | t0001 | g0166 | AFR | LWK | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0001 | g0211 | REF | REF | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
homoSapiens_grch38 | hp1 | a0002 | c0002 | t0002 | g0198 | REF | REF | TUT7_chr9_86282733_86359410 | TUT7 | chr9 | 86282733 | 86359410 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:86301359
|
T | C | 1 | a0005 | 4 | HG02109.hp2 HG02622.hp1 HG02895.hp2 others(1): Show |
missense_variant | MODERATE | c.4337A>G | p.Lys1446Arg | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/27 | 4508/5603 | 4337/4488 | 1446/1495 | chr9 | 86301359 | ||
chr9:86301593
|
C | T | 1 | a0012 | 1 | HG03017.hp1 | missense_variant | MODERATE | c.4103G>A | p.Arg1368Gln | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/27 | 4274/5603 | 4103/4488 | 1368/1495 | chr9 | 86301593 | ||
chr9:86309220
|
C | G | 1 | a0014 | 1 | HG04184.hp1 | missense_variant | MODERATE | c.3652G>C | p.Asp1218His | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 21/27 | 3823/5603 | 3652/4488 | 1218/1495 | chr9 | 86309220 | ||
chr9:86322456
|
C | A | 1 | a0011 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.2897G>T | p.Ser966Ile | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 14/27 | 3068/5603 | 2897/4488 | 966/1495 | chr9 | 86322456 | ||
chr9:86322456
|
C | T | 1 | a0013 | 1 | HG03225.hp1 | missense_variant | MODERATE | c.2897G>A | p.Ser966Asn | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 14/27 | 3068/5603 | 2897/4488 | 966/1495 | chr9 | 86322456 | ||
chr9:86322457
|
T | G | 1 | a0011 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.2896A>C | p.Ser966Arg | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 14/27 | 3067/5603 | 2896/4488 | 966/1495 | chr9 | 86322457 | ||
chr9:86322936
|
ATTT | A | 10 | a0001a0003a0004others(7): Show | 193 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(190): Show |
disruptive_inframe_deletion | MODERATE | c.2811_2813delAAA | p.Lys937del | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 13/27 | 2984/5603 | 2811/4488 | 937/1495 | chr9 | 86322936 | ||
chr9:86323133
|
T | C | 1 | a0015 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.2617A>G | p.Met873Val | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 13/27 | 2788/5603 | 2617/4488 | 873/1495 | chr9 | 86323133 | ||
chr9:86323171
|
G | A | 1 | a0010 | 1 | HG02602.hp1 | missense_variant | MODERATE | c.2579C>T | p.Pro860Leu | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 13/27 | 2750/5603 | 2579/4488 | 860/1495 | chr9 | 86323171 | ||
chr9:86323199
|
C | T | 1 | a0016 | 1 | NA19007.hp1 | missense_variant | MODERATE | c.2551G>A | p.Asp851Asn | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 13/27 | 2722/5603 | 2551/4488 | 851/1495 | chr9 | 86323199 | ||
chr9:86323541
|
T | C | 1 | a0009 | 1 | HG02615.hp1 | missense_variant | MODERATE | c.2209A>G | p.Lys737Glu | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 13/27 | 2380/5603 | 2209/4488 | 737/1495 | chr9 | 86323541 | ||
chr9:86323753
|
G | A | 1 | a0006 | 2 | HG00099.hp1 HG01433.hp1 |
missense_variant | MODERATE | c.1997C>T | p.Thr666Ile | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 13/27 | 2168/5603 | 1997/4488 | 666/1495 | chr9 | 86323753 | ||
chr9:86346438
|
G | A | 1 | a0003 | 6 | HG02257.hp2 HG02615.hp2 HG02886.hp1 others(3): Show |
missense_variant | MODERATE | c.563C>T | p.Thr188Ile | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 3/27 | 734/5603 | 563/4488 | 188/1495 | chr9 | 86346438 | ||
chr9:86346438
|
G | C | 1 | a0008 | 1 | NA19062.hp1 | missense_variant | MODERATE | c.563C>G | p.Thr188Ser | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 3/27 | 734/5603 | 563/4488 | 188/1495 | chr9 | 86346438 | ||
chr9:86346444
|
C | T | 1 | a0007 | 1 | NA18967.hp2 | missense_variant | MODERATE | c.557G>A | p.Arg186Gln | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 3/27 | 728/5603 | 557/4488 | 186/1495 | chr9 | 86346444 | ||
chr9:86353148
|
T | A | 1 | a0004 | 5 | HG01243.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
missense_variant | MODERATE | c.52A>T | p.Thr18Ser | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/27 | 223/5603 | 52/4488 | 18/1495 | chr9 | 86353148 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:86304865
|
G | T | 1 | a0001c0014 | 1 | HG01884.hp2 | synonymous_variant | LOW | c.3969C>A | p.Pro1323Pro | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 24/27 | 4140/5603 | 3969/4488 | 1323/1495 | chr9 | 86304865 | ||
chr9:86345023
|
C | T | 15 | a0001c0001a0001c0009a0001c0014others(12): Show | 237 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(234): Show |
synonymous_variant | LOW | c.951G>A | p.Leu317Leu | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 5/27 | 1122/5603 | 951/4488 | 317/1495 | chr9 | 86345023 | ||
chr9:86346419
|
C | T | 1 | a0001c0009 | 1 | HG01123.hp1 | synonymous_variant | LOW | c.582G>A | p.Glu194Glu | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 3/27 | 753/5603 | 582/4488 | 194/1495 | chr9 | 86346419 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:86287748
|
C | T | 26 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(23): Show | 331 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(328): Show |
3_prime_UTR_variant | MODIFIER | c.*929G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 27/27 | 929 | chr9 | 86287748 | |||||
chr9:86287976
|
T | C | 1 | a0002c0002t0009 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*701A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 27/27 | 701 | chr9 | 86287976 | |||||
chr9:86288160
|
C | T | 1 | a0001c0014t0011 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*517G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 27/27 | 517 | chr9 | 86288160 | |||||
chr9:86288232
|
T | C | 1 | a0002c0002t0005 | 2 | HG01261.hp1 NA18948.hp2 |
3_prime_UTR_variant | MODIFIER | c.*445A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 27/27 | 445 | chr9 | 86288232 | |||||
chr9:86288240
|
C | T | 1 | a0001c0001t0003 | 3 | HG02280.hp2 HG02486.hp2 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*437G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 27/27 | 437 | chr9 | 86288240 | |||||
chr9:86288305
|
C | T | 1 | a0013c0012t0008 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*372G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 27/27 | 372 | chr9 | 86288305 | |||||
chr9:86288452
|
T | A | 26 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(23): Show | 331 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(328): Show |
3_prime_UTR_variant | MODIFIER | c.*225A>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 27/27 | 225 | chr9 | 86288452 | |||||
chr9:86288500
|
C | G | 1 | a0002c0003t0007 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*177G>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 27/27 | 177 | chr9 | 86288500 | |||||
chr9:86288562
|
C | T | 3 | a0001c0001t0003a0001c0001t0004a0015c0015t0004 | 6 | HG02280.hp2 HG02486.hp2 HG03041.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*115G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 27/27 | 115 | chr9 | 86288562 | |||||
chr9:86288603
|
T | C | 1 | a0001c0001t0010 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*74A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 27/27 | 74 | chr9 | 86288603 | |||||
chr9:86288638
|
C | T | 1 | a0002c0002t0006 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*39G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 27/27 | 39 | chr9 | 86288638 | |||||
chr9:86354355
|
G | A | 1 | a0001c0014t0011 | 1 | HG01884.hp2 | 5_prime_UTR_variant | MODIFIER | c.-116C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 1/27 | 1156 | chr9 | 86354355 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:86288932
|
T | A | 1 | a0002c0003t0001g0246 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.4421-188A>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86288932 | ||||||
chr9:86289092
|
T | C | 3 | a0002c0002t0001g0063a0004c0005t0001g0037a0004c0005t0001g0280 | 4 | HG01243.hp1 HG03195.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.4421-348A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86289092 | ||||||
chr9:86289146
|
C | T | 4 | a0002c0003t0001g0033a0002c0003t0001g0253a0002c0003t0001g0255others(1): Show | 5 | NA18950.hp1 NA18999.hp1 NA19062.hp1 others(2): Show |
intron_variant | MODIFIER | c.4421-402G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86289146 | ||||||
chr9:86289235
|
A | C | 18 | a0001c0001t0001g0278a0002c0003t0001g0033a0002c0003t0001g0034others(15): Show | 20 | HG00733.hp1 HG00735.hp1 HG02040.hp2 others(17): Show |
intron_variant | MODIFIER | c.4421-491T>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86289235 | ||||||
chr9:86289404
|
A | C | 1 | a0004c0005t0001g0036 | 2 | HG02965.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.4421-660T>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86289404 | ||||||
chr9:86289553
|
G | A | 1 | a0002c0002t0001g0063 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.4421-809C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86289553 | ||||||
chr9:86289554
|
TAAGA | T | 134 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(131): Show | 164 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(161): Show |
intron_variant | MODIFIER | c.4421-814_4421-811d others(6): Show |
TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86289554 | ||||||
chr9:86289697
|
A | G | 18 | a0001c0001t0001g0278a0002c0003t0001g0033a0002c0003t0001g0034others(15): Show | 20 | HG00733.hp1 HG00735.hp1 HG02040.hp2 others(17): Show |
intron_variant | MODIFIER | c.4421-953T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86289697 | ||||||
chr9:86289742
|
CA | C | 5 | a0001c0001t0001g0093a0001c0001t0001g0110a0001c0001t0001g0111others(2): Show | 5 | HG03453.hp1 NA18948.hp1 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.4421-999delT | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86289742 | ||||||
chr9:86290033
|
A | G | 1 | a0002c0002t0001g0236 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.4421-1289T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86290033 | ||||||
chr9:86290073
|
G | A | 2 | a0004c0005t0001g0037a0004c0005t0001g0280 | 3 | HG01243.hp1 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.4421-1329C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86290073 | ||||||
chr9:86290092
|
C | G | 5 | a0002c0002t0001g0032a0002c0002t0001g0147a0002c0002t0001g0225others(2): Show | 6 | HG01168.hp2 HG01169.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.4421-1348G>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86290092 | ||||||
chr9:86290323
|
T | C | 1 | a0013c0012t0008g0151 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.4421-1579A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86290323 | ||||||
chr9:86290415
|
G | A | 100 | a0002c0002t0001g0001a0002c0002t0001g0007a0002c0002t0001g0011others(97): Show | 123 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.4421-1671C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86290415 | ||||||
chr9:86290686
|
C | CA | 45 | a0001c0001t0001g0059a0001c0001t0001g0071a0001c0001t0001g0075others(42): Show | 47 | HG00733.hp1 HG00735.hp1 HG00741.hp1 others(44): Show |
intron_variant | MODIFIER | c.4421-1943dupT | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86290686 | ||||||
chr9:86290686
|
CA | C | 7 | a0001c0001t0001g0058a0001c0001t0001g0061a0001c0001t0001g0106others(4): Show | 8 | HG00323.hp1 HG01070.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.4421-1943delT | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86290686 | ||||||
chr9:86290779
|
C | T | 1 | a0013c0012t0008g0151 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.4421-2035G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86290779 | ||||||
chr9:86290822
|
T | G | 48 | a0001c0001t0001g0005a0001c0001t0001g0021a0001c0001t0001g0024others(45): Show | 55 | HG00558.hp2 HG00597.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.4421-2078A>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86290822 | ||||||
chr9:86290909
|
C | A | 1 | a0001c0001t0001g0123 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.4421-2165G>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86290909 | ||||||
chr9:86290929
|
A | G | 3 | a0001c0001t0001g0092a0001c0001t0001g0139a0001c0001t0001g0145 | 3 | HG02723.hp1 HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.4421-2185T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86290929 | ||||||
chr9:86291165
|
T | C | 3 | a0001c0001t0001g0024a0001c0001t0001g0099a0001c0001t0001g0101 | 4 | HG01928.hp2 HG01934.hp1 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.4421-2421A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86291165 | ||||||
chr9:86291368
|
C | T | 1 | a0001c0001t0001g0084 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.4421-2624G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86291368 | ||||||
chr9:86291464
|
G | A | 2 | a0001c0001t0001g0154a0001c0001t0001g0155 | 2 | HG01192.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.4421-2720C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86291464 | ||||||
chr9:86291521
|
G | A | 2 | a0004c0005t0001g0037a0004c0005t0001g0280 | 3 | HG01243.hp1 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.4421-2777C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86291521 | ||||||
chr9:86291572
|
C | CA | 7 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0120others(4): Show | 7 | HG01255.hp1 HG02129.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.4421-2829dupT | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86291572 | ||||||
chr9:86291572
|
CA | C | 9 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0161others(6): Show | 9 | HG01070.hp1 HG01167.hp2 HG01257.hp2 others(6): Show |
intron_variant | MODIFIER | c.4421-2829delT | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86291572 | ||||||
chr9:86291736
|
C | T | 1 | a0001c0014t0011g0294 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.4421-2992G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86291736 | ||||||
chr9:86291780
|
C | G | 273 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(270): Show | 331 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(328): Show |
intron_variant | MODIFIER | c.4421-3036G>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86291780 | ||||||
chr9:86291795
|
T | C | 1 | a0002c0003t0007g0148 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.4421-3051A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86291795 | ||||||
chr9:86291905
|
T | C | 1 | a0002c0003t0001g0039 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.4421-3161A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86291905 | ||||||
chr9:86292049
|
A | T | 1 | a0002c0002t0001g0186 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.4421-3305T>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86292049 | ||||||
chr9:86292239
|
T | C | 2 | a0002c0003t0001g0252a0002c0003t0001g0254 | 2 | NA18978.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.4421-3495A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86292239 | ||||||
chr9:86292290
|
A | C | 1 | a0002c0002t0001g0178 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.4421-3546T>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86292290 | ||||||
chr9:86292417
|
A | G | 135 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(132): Show | 165 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(162): Show |
intron_variant | MODIFIER | c.4421-3673T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86292417 | ||||||
chr9:86292468
|
C | CA | 16 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0058others(13): Show | 18 | HG00621.hp1 HG02109.hp2 HG02622.hp1 others(15): Show |
intron_variant | MODIFIER | c.4421-3725dupT | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86292468 | ||||||
chr9:86292475
|
A | G | 1 | a0001c0001t0002g0048 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.4421-3731T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86292475 | ||||||
chr9:86292607
|
T | TA | 5 | a0001c0001t0001g0042a0001c0001t0001g0092a0001c0001t0001g0139others(2): Show | 7 | HG01109.hp1 HG01516.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.4421-3864dupT | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86292607 | ||||||
chr9:86292607
|
TA | T | 14 | a0001c0001t0001g0066a0001c0001t0001g0077a0001c0001t0001g0126others(11): Show | 14 | HG00323.hp2 HG00544.hp1 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.4421-3864delT | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86292607 | ||||||
chr9:86293340
|
T | A | 135 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(132): Show | 165 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(162): Show |
intron_variant | MODIFIER | c.4421-4596A>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86293340 | ||||||
chr9:86293533
|
C | A | 1 | a0004c0005t0001g0280 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.4421-4789G>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86293533 | ||||||
chr9:86293621
|
T | C | 1 | a0001c0001t0010g0160 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.4421-4877A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86293621 | ||||||
chr9:86293886
|
T | C | 102 | a0002c0002t0001g0001a0002c0002t0001g0007a0002c0002t0001g0011others(99): Show | 125 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.4421-5142A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86293886 | ||||||
chr9:86293888
|
G | A | 1 | a0013c0012t0008g0151 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.4421-5144C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86293888 | ||||||
chr9:86293965
|
G | A | 2 | a0002c0003t0001g0247a0002c0003t0001g0262 | 2 | HG02040.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.4421-5221C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86293965 | ||||||
chr9:86294026
|
G | A | 1 | a0002c0002t0001g0204 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.4421-5282C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86294026 | ||||||
chr9:86294026
|
G | T | 1 | a0001c0001t0001g0140 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.4421-5282C>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86294026 | ||||||
chr9:86294038
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.4421-5294C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86294038 | ||||||
chr9:86294052
|
A | C | 1 | a0002c0002t0001g0226 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.4421-5308T>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86294052 | ||||||
chr9:86294274
|
C | CA | 12 | a0001c0001t0001g0278a0001c0001t0002g0043a0001c0001t0002g0044others(9): Show | 12 | HG00099.hp2 HG00323.hp2 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.4421-5531dupT | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86294274 | ||||||
chr9:86294274
|
CA | C | 119 | a0001c0001t0001g0023a0001c0001t0001g0071a0001c0001t0001g0104others(116): Show | 145 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.4421-5531delT | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86294274 | ||||||
chr9:86294274
|
CAA | C | 119 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(116): Show | 148 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(145): Show |
intron_variant | MODIFIER | c.4421-5532_4421-553 others(6): Show |
TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86294274 | ||||||
chr9:86294328
|
G | T | 1 | a0010c0016t0001g0153 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.4421-5584C>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86294328 | ||||||
chr9:86294366
|
A | G | 1 | a0013c0012t0008g0151 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.4421-5622T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86294366 | ||||||
chr9:86294440
|
G | T | 141 | a0001c0001t0001g0123a0001c0001t0001g0278a0002c0002t0001g0001others(138): Show | 169 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.4421-5696C>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86294440 | ||||||
chr9:86294442
|
T | C | 1 | a0002c0002t0001g0222 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.4421-5698A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86294442 | ||||||
chr9:86294586
|
T | TA | 275 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(272): Show | 333 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(330): Show |
intron_variant | MODIFIER | c.4421-5843dupT | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86294586 | ||||||
chr9:86294715
|
A | T | 1 | a0001c0001t0001g0092 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.4421-5971T>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86294715 | ||||||
chr9:86294745
|
TTTA | T | 2 | a0002c0002t0001g0164a0002c0003t0001g0035 | 3 | HG02257.hp1 HG02280.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.4421-6004_4421-600 others(7): Show |
TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86294745 | ||||||
chr9:86294822
|
T | C | 1 | a0001c0001t0001g0061 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.4421-6078A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86294822 | ||||||
chr9:86294847
|
C | T | 1 | a0001c0001t0001g0103 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.4421-6103G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86294847 | ||||||
chr9:86294978
|
A | T | 140 | a0001c0001t0001g0278a0002c0002t0001g0001a0002c0002t0001g0007others(137): Show | 168 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.4421-6234T>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86294978 | ||||||
chr9:86295122
|
TCAAA | T | 7 | a0002c0003t0001g0013a0002c0003t0001g0035a0002c0003t0001g0040others(4): Show | 9 | HG02257.hp1 HG02280.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.4420+6150_4420+615 others(8): Show |
TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86295122 | ||||||
chr9:86295154
|
C | T | 2 | a0003c0004t0001g0271a0003c0004t0001g0272 | 2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.4420+6122G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86295154 | ||||||
chr9:86295246
|
T | C | 140 | a0001c0001t0001g0278a0002c0002t0001g0001a0002c0002t0001g0007others(137): Show | 168 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.4420+6030A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86295246 | ||||||
chr9:86295344
|
G | A | 116 | a0002c0002t0001g0001a0002c0002t0001g0007a0002c0002t0001g0011others(113): Show | 140 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.4420+5932C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86295344 | ||||||
chr9:86295413
|
G | A | 1 | a0002c0003t0001g0283 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.4420+5863C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86295413 | ||||||
chr9:86295643
|
T | C | 18 | a0001c0001t0001g0278a0002c0003t0001g0033a0002c0003t0001g0034others(15): Show | 20 | HG00733.hp1 HG00735.hp1 HG02040.hp2 others(17): Show |
intron_variant | MODIFIER | c.4420+5633A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86295643 | ||||||
chr9:86295823
|
GAATA | G | 140 | a0001c0001t0001g0278a0002c0002t0001g0001a0002c0002t0001g0007others(137): Show | 168 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.4420+5449_4420+545 others(8): Show |
TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86295823 | ||||||
chr9:86296150
|
T | C | 1 | a0002c0002t0001g0031 | 2 | NA18981.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.4420+5126A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86296150 | ||||||
chr9:86296154
|
G | A | 18 | a0001c0001t0001g0278a0002c0003t0001g0033a0002c0003t0001g0034others(15): Show | 20 | HG00733.hp1 HG00735.hp1 HG02040.hp2 others(17): Show |
intron_variant | MODIFIER | c.4420+5122C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86296154 | ||||||
chr9:86296493
|
C | G | 105 | a0001c0001t0001g0074a0001c0001t0001g0079a0001c0001t0001g0081others(102): Show | 128 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.4420+4783G>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86296493 | ||||||
chr9:86296636
|
G | A | 6 | a0002c0002t0001g0178a0002c0002t0001g0181a0002c0002t0001g0182others(3): Show | 6 | HG00544.hp1 HG02074.hp1 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.4420+4640C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86296636 | ||||||
chr9:86296870
|
G | A | 1 | a0001c0001t0001g0076 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.4420+4406C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86296870 | ||||||
chr9:86296954
|
G | A | 1 | a0002c0003t0001g0283 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.4420+4322C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86296954 | ||||||
chr9:86297079
|
A | G | 1 | a0001c0001t0001g0103 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.4420+4197T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86297079 | ||||||
chr9:86297086
|
T | C | 1 | a0002c0003t0001g0246 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.4420+4190A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86297086 | ||||||
chr9:86297154
|
G | A | 1 | a0002c0002t0001g0209 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.4420+4122C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86297154 | ||||||
chr9:86297256
|
C | G | 1 | a0001c0001t0010g0160 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.4420+4020G>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86297256 | ||||||
chr9:86297380
|
G | C | 1 | a0002c0002t0001g0217 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.4420+3896C>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86297380 | ||||||
chr9:86297447
|
C | T | 6 | a0003c0004t0001g0271a0003c0004t0001g0272a0003c0004t0001g0273others(3): Show | 6 | HG02257.hp2 HG02615.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.4420+3829G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86297447 | ||||||
chr9:86297623
|
T | C | 1 | a0001c0001t0010g0160 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.4420+3653A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86297623 | ||||||
chr9:86297665
|
A | C | 1 | a0002c0002t0001g0186 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.4420+3611T>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86297665 | ||||||
chr9:86297850
|
C | T | 82 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(79): Show | 104 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.4420+3426G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86297850 | ||||||
chr9:86297921
|
C | CTTTTTTT | 6 | a0001c0001t0001g0077a0001c0001t0001g0080a0001c0001t0001g0123others(3): Show | 8 | HG01069.hp1 HG01243.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.4420+3348_4420+335 others(11): Show |
TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86297921 | ||||||
chr9:86297921
|
C | CTTTTTTT others(1): Show |
112 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(109): Show | 140 | HG00140.hp2 HG00280.hp2 HG00558.hp2 others(137): Show |
intron_variant | MODIFIER | c.4420+3347_4420+335 others(12): Show |
TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86297921 | ||||||
chr9:86297921
|
C | CTTTTTTT others(2): Show |
14 | a0001c0001t0001g0073a0001c0001t0001g0094a0001c0001t0001g0097others(11): Show | 14 | HG00438.hp1 HG02109.hp2 HG02135.hp2 others(11): Show |
intron_variant | MODIFIER | c.4420+3346_4420+335 others(13): Show |
TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86297921 | ||||||
chr9:86297921
|
C | CTTTTTTT others(3): Show |
4 | a0001c0001t0010g0160a0002c0003t0001g0262a0002c0003t0007g0148others(1): Show | 4 | HG02040.hp2 HG02258.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.4420+3345_4420+335 others(14): Show |
TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86297921 | ||||||
chr9:86297921
|
C | CTTTTTTT others(4): Show |
20 | a0001c0001t0001g0278a0002c0002t0001g0225a0002c0003t0001g0033others(17): Show | 23 | HG00733.hp1 HG00735.hp1 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.4420+3344_4420+335 others(15): Show |
TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86297921 | ||||||
chr9:86297921
|
C | CTTTTTTT others(5): Show |
33 | a0002c0002t0001g0032a0002c0002t0001g0147a0002c0002t0001g0166others(30): Show | 36 | HG01109.hp2 HG01167.hp2 HG01169.hp1 others(33): Show |
intron_variant | MODIFIER | c.4420+3343_4420+335 others(16): Show |
TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86297921 | ||||||
chr9:86297921
|
C | CTTTTTTT others(6): Show |
64 | a0002c0002t0001g0001a0002c0002t0001g0027a0002c0002t0001g0028others(61): Show | 79 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.4420+3342_4420+335 others(17): Show |
TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86297921 | ||||||
chr9:86297921
|
C | CTTTTTTT others(7): Show |
17 | a0002c0002t0001g0007a0002c0002t0001g0011a0002c0002t0001g0012others(14): Show | 24 | HG00544.hp2 HG00738.hp2 HG01258.hp2 others(21): Show |
intron_variant | MODIFIER | c.4420+3341_4420+335 others(18): Show |
TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86297921 | ||||||
chr9:86297921
|
C | CTTTTTTT others(8): Show |
2 | a0002c0002t0001g0195a0002c0002t0001g0240 | 2 | NA18990.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.4420+3354_4420+335 others(19): Show |
TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86297921 | ||||||
chr9:86297954
|
C | T | 2 | a0001c0001t0001g0006a0001c0001t0001g0125 | 5 | HG01123.hp2 HG02109.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.4420+3322G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86297954 | ||||||
chr9:86298058
|
G | A | 2 | a0001c0001t0001g0074a0001c0001t0001g0081 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.4420+3218C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86298058 | ||||||
chr9:86298189
|
A | G | 1 | a0001c0001t0001g0159 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.4420+3087T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86298189 | ||||||
chr9:86298196
|
T | C | 275 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(272): Show | 333 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(330): Show |
intron_variant | MODIFIER | c.4420+3080A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86298196 | ||||||
chr9:86298591
|
G | C | 132 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(129): Show | 160 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(157): Show |
intron_variant | MODIFIER | c.4420+2685C>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86298591 | ||||||
chr9:86298747
|
T | G | 1 | a0001c0001t0001g0095 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.4420+2529A>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86298747 | ||||||
chr9:86298861
|
T | G | 1 | a0001c0001t0001g0277 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.4420+2415A>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86298861 | ||||||
chr9:86298944
|
T | C | 1 | a0001c0001t0001g0075 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.4420+2332A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86298944 | ||||||
chr9:86299088
|
G | A | 140 | a0001c0001t0001g0278a0002c0002t0001g0001a0002c0002t0001g0007others(137): Show | 168 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.4420+2188C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86299088 | ||||||
chr9:86299219
|
G | C | 2 | a0001c0001t0001g0009a0001c0001t0001g0083 | 4 | HG02165.hp2 NA19007.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.4420+2057C>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86299219 | ||||||
chr9:86299222
|
T | C | 2 | a0001c0001t0001g0162a0001c0001t0001g0163 | 2 | HG02572.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.4420+2054A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86299222 | ||||||
chr9:86299335
|
AACTTTCA others(7): Show |
A | 135 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(132): Show | 165 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(162): Show |
intron_variant | MODIFIER | c.4420+1927_4420+194 others(18): Show |
TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86299335 | ||||||
chr9:86299435
|
A | G | 13 | a0002c0003t0001g0038a0002c0003t0001g0039a0002c0003t0001g0282others(10): Show | 14 | HG01109.hp2 HG01255.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.4420+1841T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86299435 | ||||||
chr9:86299484
|
A | G | 1 | a0001c0001t0001g0067 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.4420+1792T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86299484 | ||||||
chr9:86299624
|
T | C | 1 | a0001c0001t0001g0281 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4420+1652A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86299624 | ||||||
chr9:86299639
|
G | T | 135 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(132): Show | 165 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(162): Show |
intron_variant | MODIFIER | c.4420+1637C>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86299639 | ||||||
chr9:86299779
|
G | A | 1 | a0002c0003t0001g0262 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.4420+1497C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86299779 | ||||||
chr9:86299899
|
T | C | 1 | a0002c0002t0001g0171 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.4420+1377A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86299899 | ||||||
chr9:86300651
|
A | T | 100 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(97): Show | 127 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.4420+625T>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86300651 | ||||||
chr9:86300927
|
G | A | 6 | a0003c0004t0001g0271a0003c0004t0001g0272a0003c0004t0001g0273others(3): Show | 6 | HG02257.hp2 HG02615.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.4420+349C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86300927 | ||||||
chr9:86300980
|
T | G | 1 | a0001c0001t0001g0078 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.4420+296A>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 26/26 | chr9 | 86300980 | ||||||
chr9:86301614
|
T | C | 1 | a0002c0002t0001g0183 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.4095-13A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 25/26 | chr9 | 86301614 | ||||||
chr9:86301660
|
G | A | 6 | a0002c0003t0001g0013a0002c0003t0001g0035a0002c0003t0001g0040others(3): Show | 8 | HG02257.hp1 HG02280.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.4095-59C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 25/26 | chr9 | 86301660 | ||||||
chr9:86301898
|
A | T | 1 | a0002c0002t0001g0194 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.4095-297T>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 25/26 | chr9 | 86301898 | ||||||
chr9:86301899
|
A | C | 1 | a0002c0002t0001g0194 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.4095-298T>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 25/26 | chr9 | 86301899 | ||||||
chr9:86301930
|
C | T | 1 | a0002c0002t0001g0193 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4095-329G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 25/26 | chr9 | 86301930 | ||||||
chr9:86302082
|
G | A | 13 | a0001c0001t0001g0015a0001c0001t0001g0058a0001c0001t0001g0059others(10): Show | 14 | HG02109.hp2 HG02622.hp1 HG02723.hp1 others(11): Show |
intron_variant | MODIFIER | c.4095-481C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 25/26 | chr9 | 86302082 | ||||||
chr9:86302257
|
G | A | 2 | a0001c0001t0001g0150a0001c0001t0001g0250 | 2 | HG00741.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.4095-656C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 25/26 | chr9 | 86302257 | ||||||
chr9:86302302
|
T | C | 2 | a0001c0001t0001g0154a0001c0001t0001g0155 | 2 | HG01192.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.4095-701A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 25/26 | chr9 | 86302302 | ||||||
chr9:86302309
|
A | C | 5 | a0001c0001t0003g0020a0001c0001t0003g0122a0001c0001t0004g0085others(2): Show | 6 | HG02280.hp2 HG02486.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.4095-708T>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 25/26 | chr9 | 86302309 | ||||||
chr9:86302331
|
TACAA | T | 139 | a0001c0001t0001g0278a0002c0002t0001g0001a0002c0002t0001g0007others(136): Show | 167 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.4095-734_4095-731d others(6): Show |
TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 25/26 | chr9 | 86302331 | ||||||
chr9:86302423
|
A | T | 18 | a0001c0001t0001g0278a0002c0003t0001g0033a0002c0003t0001g0034others(15): Show | 20 | HG00733.hp1 HG00735.hp1 HG02040.hp2 others(17): Show |
intron_variant | MODIFIER | c.4094+663T>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 25/26 | chr9 | 86302423 | ||||||
chr9:86302617
|
C | CT | 132 | a0001c0001t0001g0108a0001c0001t0001g0115a0001c0001t0001g0278others(129): Show | 160 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.4094+468dupA | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 25/26 | chr9 | 86302617 | ||||||
chr9:86302763
|
C | T | 1 | a0001c0001t0001g0065 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.4094+323G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 25/26 | chr9 | 86302763 | ||||||
chr9:86302832
|
C | A | 1 | a0002c0003t0001g0269 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.4094+254G>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 25/26 | chr9 | 86302832 | ||||||
chr9:86303228
|
C | G | 1 | a0002c0003t0001g0169 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.3979-27G>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 24/26 | chr9 | 86303228 | ||||||
chr9:86303518
|
A | G | 1 | a0002c0003t0001g0279 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3979-317T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 24/26 | chr9 | 86303518 | ||||||
chr9:86303623
|
T | G | 1 | a0002c0002t0001g0193 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3979-422A>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 24/26 | chr9 | 86303623 | ||||||
chr9:86303679
|
G | A | 2 | a0001c0001t0001g0026a0001c0001t0001g0144 | 3 | NA18943.hp1 NA18973.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.3979-478C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 24/26 | chr9 | 86303679 | ||||||
chr9:86304024
|
TAGAC | T | 13 | a0002c0003t0001g0038a0002c0003t0001g0039a0002c0003t0001g0282others(10): Show | 14 | HG01109.hp2 HG01255.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.3979-827_3979-824d others(6): Show |
TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 24/26 | chr9 | 86304024 | ||||||
chr9:86304146
|
GAT | G | 135 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(132): Show | 165 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(162): Show |
intron_variant | MODIFIER | c.3978+708_3978+709d others(4): Show |
TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 24/26 | chr9 | 86304146 | ||||||
chr9:86304186
|
T | C | 1 | a0001c0001t0001g0119 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.3978+670A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 24/26 | chr9 | 86304186 | ||||||
chr9:86304257
|
G | A | 2 | a0001c0001t0001g0154a0001c0001t0001g0155 | 2 | HG01192.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.3978+599C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 24/26 | chr9 | 86304257 | ||||||
chr9:86304415
|
T | G | 2 | a0001c0001t0002g0056a0001c0001t0002g0057 | 2 | NA18943.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.3978+441A>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 24/26 | chr9 | 86304415 | ||||||
chr9:86304521
|
G | T | 1 | a0002c0002t0001g0172 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.3978+335C>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 24/26 | chr9 | 86304521 | ||||||
chr9:86304538
|
C | T | 107 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(104): Show | 134 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.3978+318G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 24/26 | chr9 | 86304538 | ||||||
chr9:86304660
|
A | G | 1 | a0002c0002t0001g0235 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.3978+196T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 24/26 | chr9 | 86304660 | ||||||
chr9:86304689
|
G | A | 6 | a0002c0002t0001g0178a0002c0002t0001g0181a0002c0002t0001g0182others(3): Show | 6 | HG00544.hp1 HG02074.hp1 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.3978+167C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 24/26 | chr9 | 86304689 | ||||||
chr9:86304733
|
A | T | 292 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(289): Show | 360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.3978+123T>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 24/26 | chr9 | 86304733 | ||||||
chr9:86305033
|
C | T | 1 | a0001c0001t0001g0024 | 2 | HG01928.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.3887-86G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 23/26 | chr9 | 86305033 | ||||||
chr9:86305179
|
C | T | 18 | a0001c0001t0001g0278a0002c0003t0001g0033a0002c0003t0001g0034others(15): Show | 20 | HG00733.hp1 HG00735.hp1 HG02040.hp2 others(17): Show |
intron_variant | MODIFIER | c.3886+13G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 23/26 | chr9 | 86305179 | ||||||
chr9:86305313
|
C | T | 13 | a0001c0001t0001g0015a0001c0001t0001g0058a0001c0001t0001g0059others(10): Show | 14 | HG02109.hp2 HG02622.hp1 HG02723.hp1 others(11): Show |
intron_variant | MODIFIER | c.3839-74G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 22/26 | chr9 | 86305313 | ||||||
chr9:86305401
|
T | G | 1 | a0001c0001t0001g0076 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.3839-162A>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 22/26 | chr9 | 86305401 | ||||||
chr9:86305588
|
G | A | 1 | a0001c0001t0010g0160 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3839-349C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 22/26 | chr9 | 86305588 | ||||||
chr9:86306055
|
A | T | 13 | a0002c0003t0001g0038a0002c0003t0001g0039a0002c0003t0001g0282others(10): Show | 14 | HG01109.hp2 HG01255.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.3839-816T>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 22/26 | chr9 | 86306055 | ||||||
chr9:86306295
|
G | A | 1 | a0002c0002t0001g0187 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.3839-1056C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 22/26 | chr9 | 86306295 | ||||||
chr9:86306305
|
G | A | 2 | a0001c0001t0001g0161a0001c0001t0001g0281 | 2 | HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.3839-1066C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 22/26 | chr9 | 86306305 | ||||||
chr9:86306313
|
T | C | 140 | a0001c0001t0001g0278a0002c0002t0001g0001a0002c0002t0001g0007others(137): Show | 168 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.3839-1074A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 22/26 | chr9 | 86306313 | ||||||
chr9:86306375
|
G | A | 135 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(132): Show | 165 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(162): Show |
intron_variant | MODIFIER | c.3839-1136C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 22/26 | chr9 | 86306375 | ||||||
chr9:86306668
|
T | A | 135 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(132): Show | 165 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(162): Show |
intron_variant | MODIFIER | c.3839-1429A>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 22/26 | chr9 | 86306668 | ||||||
chr9:86306730
|
C | T | 1 | a0002c0003t0001g0264 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.3839-1491G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 22/26 | chr9 | 86306730 | ||||||
chr9:86306800
|
C | G | 60 | a0002c0002t0001g0001a0002c0002t0001g0007a0002c0002t0001g0011others(57): Show | 79 | HG00099.hp1 HG00544.hp2 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.3839-1561G>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 22/26 | chr9 | 86306800 | ||||||
chr9:86306806
|
A | G | 102 | a0002c0002t0001g0001a0002c0002t0001g0007a0002c0002t0001g0011others(99): Show | 125 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.3839-1567T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 22/26 | chr9 | 86306806 | ||||||
chr9:86306819
|
G | A | 1 | a0002c0002t0001g0224 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.3839-1580C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 22/26 | chr9 | 86306819 | ||||||
chr9:86306869
|
A | G | 1 | a0002c0002t0001g0211 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.3838+1560T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 22/26 | chr9 | 86306869 | ||||||
chr9:86306933
|
G | A | 275 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(272): Show | 333 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(330): Show |
intron_variant | MODIFIER | c.3838+1496C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 22/26 | chr9 | 86306933 | ||||||
chr9:86306980
|
C | T | 2 | a0001c0001t0001g0161a0001c0001t0001g0281 | 2 | HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.3838+1449G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 22/26 | chr9 | 86306980 | ||||||
chr9:86307039
|
G | C | 2 | a0001c0001t0001g0071a0001c0001t0001g0077 | 2 | HG01069.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.3838+1390C>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 22/26 | chr9 | 86307039 | ||||||
chr9:86307359
|
A | G | 3 | a0002c0002t0001g0201a0002c0002t0001g0223a0002c0002t0001g0245 | 3 | HG03491.hp2 HG04115.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.3838+1070T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 22/26 | chr9 | 86307359 | ||||||
chr9:86307542
|
T | C | 2 | a0001c0001t0001g0150a0001c0001t0001g0250 | 2 | HG00741.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.3838+887A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 22/26 | chr9 | 86307542 | ||||||
chr9:86307884
|
C | T | 13 | a0001c0001t0001g0015a0001c0001t0001g0058a0001c0001t0001g0059others(10): Show | 14 | HG02109.hp2 HG02622.hp1 HG02723.hp1 others(11): Show |
intron_variant | MODIFIER | c.3838+545G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 22/26 | chr9 | 86307884 | ||||||
chr9:86308059
|
A | G | 1 | a0006c0007t0001g0259 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.3838+370T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 22/26 | chr9 | 86308059 | ||||||
chr9:86308098
|
G | C | 1 | a0002c0003t0001g0279 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3838+331C>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 22/26 | chr9 | 86308098 | ||||||
chr9:86308136
|
C | A | 24 | a0001c0001t0001g0278a0002c0003t0001g0013a0002c0003t0001g0033others(21): Show | 28 | HG00733.hp1 HG00735.hp1 HG02040.hp2 others(25): Show |
intron_variant | MODIFIER | c.3838+293G>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 22/26 | chr9 | 86308136 | ||||||
chr9:86308358
|
G | A | 1 | a0001c0001t0002g0051 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.3838+71C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 22/26 | chr9 | 86308358 | ||||||
chr9:86308371
|
T | C | 9 | a0001c0001t0001g0278a0002c0003t0001g0033a0002c0003t0001g0165others(6): Show | 10 | NA18950.hp1 NA18978.hp2 NA18992.hp2 others(7): Show |
intron_variant | MODIFIER | c.3838+58A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 22/26 | chr9 | 86308371 | ||||||
chr9:86308383
|
T | G | 6 | a0002c0003t0001g0013a0002c0003t0001g0035a0002c0003t0001g0040others(3): Show | 8 | HG02257.hp1 HG02280.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.3838+46A>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 22/26 | chr9 | 86308383 | ||||||
chr9:86308965
|
G | C | 1 | a0002c0002t0001g0183 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.3660+247C>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 21/26 | chr9 | 86308965 | ||||||
chr9:86309142
|
A | C | 275 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(272): Show | 333 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(330): Show |
intron_variant | MODIFIER | c.3660+70T>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 21/26 | chr9 | 86309142 | ||||||
chr9:86309154
|
T | C | 7 | a0001c0001t0001g0026a0001c0001t0001g0068a0001c0001t0001g0105others(4): Show | 8 | HG01106.hp2 HG02129.hp1 NA18943.hp1 others(5): Show |
intron_variant | MODIFIER | c.3660+58A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 21/26 | chr9 | 86309154 | ||||||
chr9:86309424
|
A | G | 1 | a0002c0002t0001g0210 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.3582+39T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 20/26 | chr9 | 86309424 | ||||||
chr9:86310061
|
A | G | 4 | a0002c0002t0001g0231a0002c0002t0001g0232a0002c0002t0001g0233others(1): Show | 4 | NA18975.hp1 NA18991.hp1 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.3379-44T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 18/26 | chr9 | 86310061 | ||||||
chr9:86310070
|
C | CT | 266 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(263): Show | 323 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(320): Show |
intron_variant | MODIFIER | c.3379-54dupA | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 18/26 | chr9 | 86310070 | ||||||
chr9:86310391
|
T | C | 2 | a0001c0001t0001g0021a0001c0001t0001g0104 | 3 | NA18953.hp1 NA18978.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.3378+315A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 18/26 | chr9 | 86310391 | ||||||
chr9:86310605
|
C | A | 1 | a0013c0012t0008g0151 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3378+101G>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 18/26 | chr9 | 86310605 | ||||||
chr9:86310619
|
ATG | A | 275 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(272): Show | 333 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(330): Show |
intron_variant | MODIFIER | c.3378+85_3378+86del others(2): Show |
TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 18/26 | chr9 | 86310619 | ||||||
chr9:86310859
|
A | G | 31 | a0002c0002t0001g0027a0002c0002t0001g0028a0002c0002t0001g0029others(28): Show | 34 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(31): Show |
intron_variant | MODIFIER | c.3275-50T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86310859 | ||||||
chr9:86311194
|
T | C | 135 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(132): Show | 165 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(162): Show |
intron_variant | MODIFIER | c.3275-385A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86311194 | ||||||
chr9:86311462
|
G | A | 102 | a0002c0002t0001g0001a0002c0002t0001g0007a0002c0002t0001g0011others(99): Show | 125 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.3275-653C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86311462 | ||||||
chr9:86311560
|
T | C | 2 | a0004c0005t0001g0037a0004c0005t0001g0280 | 3 | HG01243.hp1 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.3275-751A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86311560 | ||||||
chr9:86311589
|
T | TCCCTCTC | 139 | a0001c0001t0001g0278a0002c0002t0001g0001a0002c0002t0001g0007others(136): Show | 167 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.3275-787_3275-781d others(9): Show |
TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86311589 | ||||||
chr9:86311632
|
A | ACGGTCTC others(10): Show |
130 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(127): Show | 157 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(154): Show |
intron_variant | MODIFIER | c.3275-840_3275-824d others(19): Show |
TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86311632 | ||||||
chr9:86311632
|
ACGGTCTC others(10): Show |
A | 1 | a0002c0002t0001g0193 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3275-840_3275-824d others(19): Show |
TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86311632 | ||||||
chr9:86311651
|
G | GGTCTCCC others(10): Show |
1 | a0003c0004t0001g0272 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.3275-843_3275-842i others(19): Show |
TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86311651 | ||||||
chr9:86311668
|
G | A | 2 | a0002c0003t0001g0269a0002c0003t0001g0270 | 2 | HG02809.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.3275-859C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86311668 | ||||||
chr9:86311672
|
C | G | 2 | a0001c0001t0001g0154a0001c0001t0001g0155 | 2 | HG01192.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.3275-863G>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86311672 | ||||||
chr9:86311721
|
C | A | 2 | a0001c0001t0002g0046a0001c0001t0002g0052 | 2 | HG00323.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.3275-912G>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86311721 | ||||||
chr9:86311744
|
C | T | 2 | a0001c0001t0010g0160a0002c0002t0006g0173 | 2 | HG02258.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.3275-935G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86311744 | ||||||
chr9:86311745
|
G | A | 3 | a0001c0001t0003g0020a0001c0001t0003g0122a0001c0001t0004g0087 | 4 | HG02280.hp2 HG02486.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.3275-936C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86311745 | ||||||
chr9:86311766
|
C | T | 135 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(132): Show | 165 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(162): Show |
intron_variant | MODIFIER | c.3275-957G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86311766 | ||||||
chr9:86311812
|
G | C | 140 | a0001c0001t0001g0278a0002c0002t0001g0001a0002c0002t0001g0007others(137): Show | 168 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.3275-1003C>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86311812 | ||||||
chr9:86311826
|
T | G | 1 | a0002c0003t0001g0137 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.3275-1017A>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86311826 | ||||||
chr9:86311837
|
G | C | 135 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(132): Show | 165 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(162): Show |
intron_variant | MODIFIER | c.3275-1028C>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86311837 | ||||||
chr9:86311855
|
C | T | 9 | a0001c0001t0001g0023a0001c0001t0001g0062a0001c0001t0001g0084others(6): Show | 10 | HG02572.hp1 HG02615.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.3275-1046G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86311855 | ||||||
chr9:86311885
|
G | T | 1 | a0001c0001t0001g0019 | 2 | HG02071.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.3275-1076C>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86311885 | ||||||
chr9:86311926
|
A | G | 140 | a0001c0001t0001g0278a0002c0002t0001g0001a0002c0002t0001g0007others(137): Show | 168 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.3275-1117T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86311926 | ||||||
chr9:86311943
|
G | C | 18 | a0001c0001t0001g0278a0002c0003t0001g0033a0002c0003t0001g0034others(15): Show | 20 | HG00733.hp1 HG00735.hp1 HG02040.hp2 others(17): Show |
intron_variant | MODIFIER | c.3275-1134C>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86311943 | ||||||
chr9:86311953
|
G | A | 3 | a0004c0005t0001g0036a0004c0005t0001g0037a0004c0005t0001g0280 | 5 | HG01243.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.3275-1144C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86311953 | ||||||
chr9:86312032
|
C | T | 2 | a0002c0002t0001g0209a0002c0002t0001g0258 | 2 | HG01167.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.3275-1223G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86312032 | ||||||
chr9:86312045
|
G | A | 2 | a0001c0001t0001g0080a0010c0016t0001g0153 | 2 | HG02602.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.3275-1236C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86312045 | ||||||
chr9:86312179
|
G | A | 1 | a0001c0001t0010g0160 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3275-1370C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86312179 | ||||||
chr9:86312185
|
T | C | 1 | a0001c0001t0010g0160 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3275-1376A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86312185 | ||||||
chr9:86312246
|
G | A | 1 | a0002c0002t0001g0184 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.3275-1437C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86312246 | ||||||
chr9:86312276
|
C | T | 1 | a0002c0003t0001g0289 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.3275-1467G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86312276 | ||||||
chr9:86312433
|
C | T | 3 | a0001c0001t0001g0015a0001c0001t0001g0058a0001c0001t0001g0059 | 4 | NA18953.hp2 NA18955.hp2 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.3275-1624G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86312433 | ||||||
chr9:86312451
|
C | T | 3 | a0002c0002t0001g0174a0002c0002t0001g0175a0002c0002t0009g0167 | 3 | HG00738.hp2 HG03942.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3275-1642G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86312451 | ||||||
chr9:86312456
|
C | A | 1 | a0002c0002t0005g0227 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.3275-1647G>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86312456 | ||||||
chr9:86312473
|
C | T | 140 | a0001c0001t0001g0278a0002c0002t0001g0001a0002c0002t0001g0007others(137): Show | 168 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.3275-1664G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86312473 | ||||||
chr9:86312474
|
A | G | 275 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(272): Show | 333 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(330): Show |
intron_variant | MODIFIER | c.3275-1665T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86312474 | ||||||
chr9:86312478
|
G | A | 1 | a0002c0003t0001g0279 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3275-1669C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86312478 | ||||||
chr9:86312501
|
C | T | 140 | a0001c0001t0001g0278a0002c0002t0001g0001a0002c0002t0001g0007others(137): Show | 168 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.3275-1692G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86312501 | ||||||
chr9:86312510
|
G | A | 3 | a0003c0004t0001g0271a0003c0004t0001g0272a0003c0004t0001g0273 | 3 | HG02257.hp2 HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.3275-1701C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86312510 | ||||||
chr9:86312522
|
C | T | 1 | a0013c0012t0008g0151 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3275-1713G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86312522 | ||||||
chr9:86312633
|
C | T | 2 | a0002c0002t0001g0229a0002c0002t0001g0261 | 2 | HG02738.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.3275-1824G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86312633 | ||||||
chr9:86312634
|
A | G | 275 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(272): Show | 333 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(330): Show |
intron_variant | MODIFIER | c.3275-1825T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86312634 | ||||||
chr9:86312653
|
G | A | 1 | a0001c0001t0001g0281 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3275-1844C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86312653 | ||||||
chr9:86312665
|
T | C | 135 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(132): Show | 165 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(162): Show |
intron_variant | MODIFIER | c.3275-1856A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86312665 | ||||||
chr9:86312910
|
C | T | 1 | a0004c0005t0001g0036 | 2 | HG02965.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.3275-2101G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86312910 | ||||||
chr9:86313005
|
C | G | 1 | a0002c0003t0001g0169 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.3275-2196G>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86313005 | ||||||
chr9:86313126
|
T | TAATA | 109 | a0001c0001t0001g0026a0001c0001t0001g0070a0001c0001t0001g0078others(106): Show | 134 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.3275-2321_3275-231 others(8): Show |
TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86313126 | ||||||
chr9:86313126
|
T | TAATAAAT others(1): Show |
4 | a0002c0002t0001g0012a0002c0002t0001g0172a0002c0002t0001g0222others(1): Show | 6 | HG03491.hp2 HG03654.hp2 NA18522.hp2 others(3): Show |
intron_variant | MODIFIER | c.3275-2325_3275-231 others(12): Show |
TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86313126 | ||||||
chr9:86313126
|
T | TAATAAAT others(5): Show |
1 | a0006c0007t0001g0259 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.3275-2329_3275-231 others(16): Show |
TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86313126 | ||||||
chr9:86313126
|
TAATA | T | 70 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0022others(67): Show | 89 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.3275-2321_3275-231 others(8): Show |
TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86313126 | ||||||
chr9:86313126
|
TAATAAAT others(1): Show |
T | 3 | a0001c0001t0001g0105a0001c0001t0010g0160a0013c0012t0008g0151 | 3 | HG02258.hp2 HG03225.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.3275-2325_3275-231 others(12): Show |
TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86313126 | ||||||
chr9:86313126
|
TAATAAAT others(5): Show |
T | 1 | a0002c0003t0001g0034 | 2 | HG02698.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.3275-2329_3275-231 others(16): Show |
TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86313126 | ||||||
chr9:86313150
|
A | T | 2 | a0001c0001t0001g0021a0001c0001t0001g0104 | 3 | NA18953.hp1 NA18978.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.3275-2341T>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86313150 | ||||||
chr9:86313183
|
G | A | 135 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(132): Show | 165 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(162): Show |
intron_variant | MODIFIER | c.3275-2374C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86313183 | ||||||
chr9:86313200
|
A | G | 1 | a0002c0003t0001g0251 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.3275-2391T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86313200 | ||||||
chr9:86313283
|
G | T | 1 | a0002c0003t0001g0169 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.3275-2474C>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86313283 | ||||||
chr9:86313417
|
G | A | 2 | a0001c0001t0001g0278a0002c0003t0001g0251 | 2 | NA18997.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.3275-2608C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86313417 | ||||||
chr9:86313485
|
G | C | 1 | a0002c0003t0001g0292 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3275-2676C>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86313485 | ||||||
chr9:86313576
|
T | C | 4 | a0001c0001t0001g0010a0001c0001t0001g0018a0001c0001t0001g0070others(1): Show | 7 | HG00280.hp2 HG01123.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.3275-2767A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86313576 | ||||||
chr9:86313646
|
G | C | 140 | a0001c0001t0001g0278a0002c0002t0001g0001a0002c0002t0001g0007others(137): Show | 168 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.3275-2837C>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86313646 | ||||||
chr9:86313760
|
C | A | 1 | a0002c0002t0001g0221 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.3275-2951G>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86313760 | ||||||
chr9:86313763
|
A | T | 1 | a0002c0002t0001g0239 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.3275-2954T>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86313763 | ||||||
chr9:86314016
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.3274+3203C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86314016 | ||||||
chr9:86314017
|
C | T | 1 | a0009c0017t0001g0096 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3274+3202G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86314017 | ||||||
chr9:86314075
|
A | G | 2 | a0001c0001t0001g0026a0001c0001t0001g0144 | 3 | NA18943.hp1 NA18973.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.3274+3144T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86314075 | ||||||
chr9:86314390
|
C | CA | 138 | a0002c0002t0001g0001a0002c0002t0001g0007a0002c0002t0001g0011others(135): Show | 166 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.3274+2828dupT | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86314390 | ||||||
chr9:86314593
|
T | G | 1 | a0002c0002t0001g0205 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.3274+2626A>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86314593 | ||||||
chr9:86314595
|
G | A | 2 | a0001c0001t0001g0154a0001c0001t0001g0155 | 2 | HG01192.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.3274+2624C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86314595 | ||||||
chr9:86314679
|
C | G | 3 | a0002c0002t0001g0174a0002c0002t0001g0175a0002c0002t0009g0167 | 3 | HG00738.hp2 HG03942.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.3274+2540G>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86314679 | ||||||
chr9:86314809
|
G | A | 1 | a0001c0001t0001g0117 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.3274+2410C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86314809 | ||||||
chr9:86314829
|
T | C | 2 | a0001c0001t0001g0162a0001c0001t0001g0163 | 2 | HG02572.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.3274+2390A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86314829 | ||||||
chr9:86314847
|
C | T | 1 | a0002c0002t0001g0217 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3274+2372G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86314847 | ||||||
chr9:86314894
|
A | G | 2 | a0001c0001t0001g0006a0001c0001t0001g0125 | 5 | HG01123.hp2 HG02109.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.3274+2325T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86314894 | ||||||
chr9:86315009
|
C | T | 1 | a0002c0003t0001g0279 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3274+2210G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86315009 | ||||||
chr9:86315107
|
AC | A | 6 | a0001c0001t0001g0154a0001c0001t0001g0155a0002c0002t0001g0223others(3): Show | 6 | HG01192.hp1 HG01884.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.3274+2111delG | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86315107 | ||||||
chr9:86315243
|
G | A | 109 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(106): Show | 136 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(133): Show |
intron_variant | MODIFIER | c.3274+1976C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86315243 | ||||||
chr9:86315299
|
C | G | 1 | a0001c0001t0001g0099 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.3274+1920G>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86315299 | ||||||
chr9:86315310
|
C | T | 1 | a0001c0001t0001g0099 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.3274+1909G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86315310 | ||||||
chr9:86315763
|
T | A | 1 | a0002c0002t0001g0185 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.3274+1456A>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86315763 | ||||||
chr9:86315763
|
T | TA | 136 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(133): Show | 166 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(163): Show |
intron_variant | MODIFIER | c.3274+1455dupT | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86315763 | ||||||
chr9:86315806
|
A | G | 3 | a0002c0003t0001g0263a0002c0003t0001g0264a0002c0003t0001g0265 | 3 | NA18957.hp1 NA18959.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.3274+1413T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86315806 | ||||||
chr9:86315929
|
G | A | 1 | a0001c0001t0001g0139 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3274+1290C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86315929 | ||||||
chr9:86315994
|
C | T | 1 | a0002c0003t0001g0288 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3274+1225G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86315994 | ||||||
chr9:86316028
|
G | A | 1 | a0004c0005t0001g0036 | 2 | HG02965.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.3274+1191C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86316028 | ||||||
chr9:86316073
|
C | T | 1 | a0002c0002t0001g0200 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.3274+1146G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86316073 | ||||||
chr9:86316141
|
C | T | 1 | a0001c0001t0001g0143 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.3274+1078G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86316141 | ||||||
chr9:86316194
|
C | T | 1 | a0002c0002t0001g0221 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.3274+1025G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86316194 | ||||||
chr9:86316586
|
C | T | 1 | a0002c0002t0001g0175 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.3274+633G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86316586 | ||||||
chr9:86316713
|
C | G | 1 | a0001c0001t0010g0160 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3274+506G>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86316713 | ||||||
chr9:86316789
|
A | G | 154 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(151): Show | 194 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.3274+430T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86316789 | ||||||
chr9:86316882
|
CAACT | C | 4 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(1): Show | 4 | HG00558.hp2 HG00597.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.3274+333_3274+336d others(6): Show |
TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86316882 | ||||||
chr9:86316898
|
AACGAT | A | 6 | a0002c0003t0001g0013a0002c0003t0001g0035a0002c0003t0001g0040others(3): Show | 8 | HG02257.hp1 HG02280.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.3274+316_3274+320d others(7): Show |
TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86316898 | ||||||
chr9:86316909
|
A | G | 1 | a0016c0010t0001g0132 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.3274+310T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86316909 | ||||||
chr9:86316946
|
T | G | 1 | a0001c0014t0011g0294 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3274+273A>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86316946 | ||||||
chr9:86317077
|
A | AT | 101 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(98): Show | 128 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.3274+141dupA | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 17/26 | chr9 | 86317077 | ||||||
chr9:86317287
|
G | A | 2 | a0001c0001t0001g0154a0001c0001t0001g0155 | 2 | HG01192.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.3217-11C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 16/26 | chr9 | 86317287 | ||||||
chr9:86317298
|
G | T | 1 | a0002c0002t0001g0258 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.3217-22C>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 16/26 | chr9 | 86317298 | ||||||
chr9:86317311
|
A | G | 17 | a0002c0002t0001g0030a0002c0002t0001g0164a0002c0002t0001g0200others(14): Show | 18 | HG01261.hp1 HG02040.hp1 HG02683.hp1 others(15): Show |
intron_variant | MODIFIER | c.3217-35T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 16/26 | chr9 | 86317311 | ||||||
chr9:86317348
|
T | C | 1 | a0006c0007t0001g0197 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.3217-72A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 16/26 | chr9 | 86317348 | ||||||
chr9:86317442
|
T | G | 1 | a0002c0003t0001g0246 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3217-166A>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 16/26 | chr9 | 86317442 | ||||||
chr9:86317451
|
T | C | 1 | a0002c0002t0001g0216 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3217-175A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 16/26 | chr9 | 86317451 | ||||||
chr9:86317841
|
G | A | 1 | a0004c0005t0001g0036 | 2 | HG02965.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.3217-565C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 16/26 | chr9 | 86317841 | ||||||
chr9:86318066
|
T | C | 1 | a0002c0002t0001g0170 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.3217-790A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 16/26 | chr9 | 86318066 | ||||||
chr9:86318193
|
C | T | 1 | a0002c0002t0001g0166 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3216+765G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 16/26 | chr9 | 86318193 | ||||||
chr9:86318330
|
A | G | 3 | a0002c0003t0001g0013a0002c0003t0001g0040a0002c0003t0001g0279 | 4 | HG02630.hp1 HG03453.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.3216+628T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 16/26 | chr9 | 86318330 | ||||||
chr9:86318411
|
C | G | 1 | a0001c0001t0001g0127 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3216+547G>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 16/26 | chr9 | 86318411 | ||||||
chr9:86318420
|
A | G | 13 | a0001c0001t0001g0015a0001c0001t0001g0058a0001c0001t0001g0059others(10): Show | 14 | HG02109.hp2 HG02622.hp1 HG02723.hp1 others(11): Show |
intron_variant | MODIFIER | c.3216+538T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 16/26 | chr9 | 86318420 | ||||||
chr9:86318475
|
G | A | 2 | a0001c0001t0001g0060a0001c0001t0001g0061 | 2 | HG03017.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.3216+483C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 16/26 | chr9 | 86318475 | ||||||
chr9:86318542
|
T | C | 3 | a0001c0001t0001g0117a0001c0001t0001g0156a0001c0001t0001g0157 | 3 | NA18956.hp2 NA18974.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.3216+416A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 16/26 | chr9 | 86318542 | ||||||
chr9:86318688
|
A | G | 1 | a0001c0001t0001g0071 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.3216+270T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 16/26 | chr9 | 86318688 | ||||||
chr9:86318757
|
A | G | 209 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(206): Show | 256 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.3216+201T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 16/26 | chr9 | 86318757 | ||||||
chr9:86318758
|
G | A | 13 | a0002c0003t0001g0038a0002c0003t0001g0039a0002c0003t0001g0282others(10): Show | 14 | HG01109.hp2 HG01255.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.3216+200C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 16/26 | chr9 | 86318758 | ||||||
chr9:86318759
|
T | G | 13 | a0002c0003t0001g0038a0002c0003t0001g0039a0002c0003t0001g0282others(10): Show | 14 | HG01109.hp2 HG01255.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.3216+199A>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 16/26 | chr9 | 86318759 | ||||||
chr9:86318764
|
G | T | 13 | a0002c0003t0001g0038a0002c0003t0001g0039a0002c0003t0001g0282others(10): Show | 14 | HG01109.hp2 HG01255.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.3216+194C>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 16/26 | chr9 | 86318764 | ||||||
chr9:86319331
|
A | G | 1 | a0013c0012t0008g0151 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3115+253T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 15/26 | chr9 | 86319331 | ||||||
chr9:86319419
|
C | T | 1 | a0001c0001t0001g0161 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3115+165G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 15/26 | chr9 | 86319419 | ||||||
chr9:86319484
|
G | A | 1 | a0002c0002t0001g0237 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.3115+100C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 15/26 | chr9 | 86319484 | ||||||
chr9:86319709
|
G | T | 191 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(188): Show | 236 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.3029-39C>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 14/26 | chr9 | 86319709 | ||||||
chr9:86319723
|
G | C | 1 | a0002c0002t0001g0063 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3029-53C>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 14/26 | chr9 | 86319723 | ||||||
chr9:86319923
|
C | A | 13 | a0001c0001t0001g0015a0001c0001t0001g0058a0001c0001t0001g0059others(10): Show | 14 | HG02109.hp2 HG02622.hp1 HG02723.hp1 others(11): Show |
intron_variant | MODIFIER | c.3029-253G>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 14/26 | chr9 | 86319923 | ||||||
chr9:86319932
|
A | C | 18 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0014others(15): Show | 28 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.3029-262T>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 14/26 | chr9 | 86319932 | ||||||
chr9:86320009
|
C | T | 18 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0014others(15): Show | 28 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.3029-339G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 14/26 | chr9 | 86320009 | ||||||
chr9:86320067
|
G | A | 18 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0014others(15): Show | 28 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.3029-397C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 14/26 | chr9 | 86320067 | ||||||
chr9:86320257
|
C | CA | 8 | a0001c0001t0001g0118a0002c0002t0001g0215a0002c0003t0001g0246others(5): Show | 8 | HG02257.hp2 HG02615.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.3029-588dupT | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 14/26 | chr9 | 86320257 | ||||||
chr9:86320257
|
C | CAA | 19 | a0001c0001t0001g0121a0001c0001t0002g0002a0001c0001t0002g0008others(16): Show | 29 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(26): Show |
intron_variant | MODIFIER | c.3029-589_3029-588d others(4): Show |
TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 14/26 | chr9 | 86320257 | ||||||
chr9:86320257
|
CA | C | 16 | a0001c0001t0001g0015a0001c0001t0001g0058a0001c0001t0001g0059others(13): Show | 17 | HG00323.hp1 HG02109.hp2 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.3029-588delT | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 14/26 | chr9 | 86320257 | ||||||
chr9:86320258
|
A | C | 2 | a0002c0002t0001g0230a0002c0002t0001g0293 | 2 | HG02896.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.3029-588T>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 14/26 | chr9 | 86320258 | ||||||
chr9:86320259
|
A | C | 5 | a0001c0001t0001g0015a0001c0001t0001g0058a0001c0001t0001g0059others(2): Show | 6 | HG03017.hp2 HG04115.hp2 NA18953.hp2 others(3): Show |
intron_variant | MODIFIER | c.3029-589T>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 14/26 | chr9 | 86320259 | ||||||
chr9:86320304
|
C | T | 1 | a0001c0001t0001g0070 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3029-634G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 14/26 | chr9 | 86320304 | ||||||
chr9:86320308
|
T | G | 1 | a0002c0002t0001g0216 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3029-638A>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 14/26 | chr9 | 86320308 | ||||||
chr9:86320343
|
C | T | 1 | a0002c0002t0001g0164 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.3029-673G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 14/26 | chr9 | 86320343 | ||||||
chr9:86320470
|
C | T | 1 | a0001c0001t0001g0103 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.3029-800G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 14/26 | chr9 | 86320470 | ||||||
chr9:86320473
|
T | C | 18 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0014others(15): Show | 28 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.3029-803A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 14/26 | chr9 | 86320473 | ||||||
chr9:86320500
|
T | C | 1 | a0002c0002t0001g0166 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3029-830A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 14/26 | chr9 | 86320500 | ||||||
chr9:86320522
|
T | C | 17 | a0002c0002t0001g0029a0002c0002t0001g0149a0002c0002t0001g0174others(14): Show | 18 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(15): Show |
intron_variant | MODIFIER | c.3029-852A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 14/26 | chr9 | 86320522 | ||||||
chr9:86320764
|
T | C | 1 | a0002c0002t0001g0217 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3029-1094A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 14/26 | chr9 | 86320764 | ||||||
chr9:86320848
|
A | G | 2 | a0002c0003t0001g0269a0002c0003t0001g0270 | 2 | HG02809.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.3029-1178T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 14/26 | chr9 | 86320848 | ||||||
chr9:86320857
|
G | C | 292 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(289): Show | 360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.3029-1187C>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 14/26 | chr9 | 86320857 | ||||||
chr9:86320895
|
T | G | 5 | a0001c0001t0001g0015a0001c0001t0001g0058a0001c0001t0001g0059others(2): Show | 6 | HG03017.hp2 HG04115.hp2 NA18953.hp2 others(3): Show |
intron_variant | MODIFIER | c.3029-1225A>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 14/26 | chr9 | 86320895 | ||||||
chr9:86321075
|
G | A | 13 | a0001c0001t0001g0015a0001c0001t0001g0058a0001c0001t0001g0059others(10): Show | 14 | HG02109.hp2 HG02622.hp1 HG02723.hp1 others(11): Show |
intron_variant | MODIFIER | c.3028+1250C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 14/26 | chr9 | 86321075 | ||||||
chr9:86321127
|
C | T | 3 | a0001c0001t0001g0150a0001c0001t0001g0250a0001c0014t0011g0294 | 3 | HG00741.hp1 HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.3028+1198G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 14/26 | chr9 | 86321127 | ||||||
chr9:86321190
|
T | TA | 16 | a0001c0001t0002g0053a0002c0003t0001g0033a0002c0003t0001g0034others(13): Show | 18 | HG00733.hp1 HG00735.hp1 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.3028+1134dupT | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 14/26 | chr9 | 86321190 | ||||||
chr9:86321190
|
TA | T | 6 | a0001c0001t0001g0082a0001c0001t0001g0102a0001c0001t0001g0123others(3): Show | 6 | HG00323.hp2 HG00639.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.3028+1134delT | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 14/26 | chr9 | 86321190 | ||||||
chr9:86321235
|
T | C | 5 | a0002c0003t0001g0282a0002c0003t0001g0283a0002c0003t0001g0284others(2): Show | 5 | HG01109.hp2 HG02723.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.3028+1090A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 14/26 | chr9 | 86321235 | ||||||
chr9:86321312
|
G | A | 18 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0014others(15): Show | 28 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.3028+1013C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 14/26 | chr9 | 86321312 | ||||||
chr9:86321445
|
C | T | 2 | a0002c0002t0002g0176a0002c0002t0002g0177 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.3028+880G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 14/26 | chr9 | 86321445 | ||||||
chr9:86321580
|
T | C | 1 | a0002c0002t0001g0224 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.3028+745A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 14/26 | chr9 | 86321580 | ||||||
chr9:86321628
|
T | C | 1 | a0001c0001t0001g0093 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.3028+697A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 14/26 | chr9 | 86321628 | ||||||
chr9:86321729
|
A | T | 154 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(151): Show | 194 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.3028+596T>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 14/26 | chr9 | 86321729 | ||||||
chr9:86322037
|
C | T | 3 | a0005c0006t0001g0088a0005c0006t0001g0089a0005c0006t0001g0091 | 3 | HG02109.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.3028+288G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 14/26 | chr9 | 86322037 | ||||||
chr9:86322092
|
T | A | 2 | a0001c0001t0001g0006a0001c0001t0001g0125 | 5 | HG01123.hp2 HG02109.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.3028+233A>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 14/26 | chr9 | 86322092 | ||||||
chr9:86322174
|
C | A | 109 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(106): Show | 136 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(133): Show |
intron_variant | MODIFIER | c.3028+151G>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 14/26 | chr9 | 86322174 | ||||||
chr9:86322512
|
C | T | 1 | a0002c0002t0001g0175 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2878-37G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 13/26 | chr9 | 86322512 | ||||||
chr9:86322702
|
T | A | 18 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0014others(15): Show | 28 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.2877+171A>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 13/26 | chr9 | 86322702 | ||||||
chr9:86322781
|
T | C | 135 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(132): Show | 165 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(162): Show |
intron_variant | MODIFIER | c.2877+92A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 13/26 | chr9 | 86322781 | ||||||
chr9:86324061
|
A | G | 4 | a0001c0001t0001g0024a0001c0001t0001g0099a0001c0001t0001g0100others(1): Show | 5 | HG01928.hp2 HG01934.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.1790-101T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 12/26 | chr9 | 86324061 | ||||||
chr9:86324253
|
T | C | 1 | a0002c0002t0001g0218 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1790-293A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 12/26 | chr9 | 86324253 | ||||||
chr9:86324254
|
C | T | 9 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(6): Show | 9 | HG00558.hp2 HG00597.hp1 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.1790-294G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 12/26 | chr9 | 86324254 | ||||||
chr9:86324609
|
T | C | 3 | a0001c0001t0001g0068a0001c0001t0001g0119a0001c0001t0001g0131 | 3 | HG01106.hp2 NA19081.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1790-649A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 12/26 | chr9 | 86324609 | ||||||
chr9:86324617
|
GA | G | 153 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(150): Show | 193 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.1790-658delT | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 12/26 | chr9 | 86324617 | ||||||
chr9:86324821
|
T | C | 2 | a0002c0002t0001g0219a0002c0002t0001g0220 | 2 | NA18969.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1789+513A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 12/26 | chr9 | 86324821 | ||||||
chr9:86325086
|
C | T | 2 | a0004c0005t0001g0037a0004c0005t0001g0280 | 3 | HG01243.hp1 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1789+248G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 12/26 | chr9 | 86325086 | ||||||
chr9:86325148
|
G | A | 1 | a0001c0001t0001g0098 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1789+186C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 12/26 | chr9 | 86325148 | ||||||
chr9:86325277
|
A | G | 1 | a0002c0002t0001g0221 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1789+57T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 12/26 | chr9 | 86325277 | ||||||
chr9:86325312
|
T | C | 1 | a0001c0001t0001g0277 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1789+22A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 12/26 | chr9 | 86325312 | ||||||
chr9:86325654
|
T | C | 2 | a0002c0002t0001g0032a0002c0002t0001g0225 | 3 | HG01168.hp2 HG01169.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1609-140A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 11/26 | chr9 | 86325654 | ||||||
chr9:86325708
|
T | C | 18 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0014others(15): Show | 28 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1609-194A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 11/26 | chr9 | 86325708 | ||||||
chr9:86325875
|
G | A | 1 | a0002c0003t0001g0246 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1609-361C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 11/26 | chr9 | 86325875 | ||||||
chr9:86326082
|
C | A | 1 | a0002c0002t0001g0221 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1609-568G>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 11/26 | chr9 | 86326082 | ||||||
chr9:86326086
|
G | A | 1 | a0002c0003t0001g0279 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1609-572C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 11/26 | chr9 | 86326086 | ||||||
chr9:86326149
|
T | C | 1 | a0002c0002t0001g0063 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1609-635A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 11/26 | chr9 | 86326149 | ||||||
chr9:86326152
|
T | C | 135 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(132): Show | 165 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(162): Show |
intron_variant | MODIFIER | c.1609-638A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 11/26 | chr9 | 86326152 | ||||||
chr9:86326245
|
T | C | 1 | a0001c0001t0001g0095 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1609-731A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 11/26 | chr9 | 86326245 | ||||||
chr9:86326634
|
C | A | 153 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(150): Show | 193 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.1609-1120G>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 11/26 | chr9 | 86326634 | ||||||
chr9:86326798
|
AC | A | 3 | a0002c0003t0001g0013a0002c0003t0001g0040a0002c0003t0001g0279 | 4 | HG02630.hp1 HG03453.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1609-1285delG | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 11/26 | chr9 | 86326798 | ||||||
chr9:86326829
|
A | C | 1 | a0001c0001t0002g0056 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1609-1315T>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 11/26 | chr9 | 86326829 | ||||||
chr9:86326856
|
T | C | 1 | a0001c0001t0001g0158 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1609-1342A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 11/26 | chr9 | 86326856 | ||||||
chr9:86327156
|
T | G | 7 | a0001c0001t0001g0023a0001c0001t0001g0062a0001c0001t0001g0126others(4): Show | 8 | HG02572.hp1 HG02615.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1608+1184A>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 11/26 | chr9 | 86327156 | ||||||
chr9:86327442
|
T | C | 1 | a0011c0011t0001g0286 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1608+898A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 11/26 | chr9 | 86327442 | ||||||
chr9:86327523
|
A | G | 2 | a0001c0001t0003g0020a0001c0001t0003g0122 | 3 | HG02280.hp2 HG02486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1608+817T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 11/26 | chr9 | 86327523 | ||||||
chr9:86327639
|
C | T | 1 | a0006c0007t0001g0197 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1608+701G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 11/26 | chr9 | 86327639 | ||||||
chr9:86327642
|
C | T | 1 | a0001c0001t0010g0160 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1608+698G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 11/26 | chr9 | 86327642 | ||||||
chr9:86327759
|
A | G | 154 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(151): Show | 194 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.1608+581T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 11/26 | chr9 | 86327759 | ||||||
chr9:86327776
|
C | T | 1 | a0002c0002t0001g0170 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1608+564G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 11/26 | chr9 | 86327776 | ||||||
chr9:86327840
|
C | T | 1 | a0003c0004t0001g0273 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1608+500G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 11/26 | chr9 | 86327840 | ||||||
chr9:86328085
|
T | C | 2 | a0001c0001t0001g0150a0001c0001t0001g0250 | 2 | HG00741.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.1608+255A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 11/26 | chr9 | 86328085 | ||||||
chr9:86328090
|
T | C | 13 | a0001c0001t0001g0015a0001c0001t0001g0058a0001c0001t0001g0059others(10): Show | 14 | HG02109.hp2 HG02622.hp1 HG02723.hp1 others(11): Show |
intron_variant | MODIFIER | c.1608+250A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 11/26 | chr9 | 86328090 | ||||||
chr9:86328256
|
T | C | 18 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0014others(15): Show | 28 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1608+84A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 11/26 | chr9 | 86328256 | ||||||
chr9:86328534
|
T | A | 1 | a0001c0001t0001g0120 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1456-42A>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86328534 | ||||||
chr9:86328619
|
A | C | 2 | a0004c0005t0001g0037a0004c0005t0001g0280 | 3 | HG01243.hp1 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1456-127T>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86328619 | ||||||
chr9:86328817
|
G | C | 1 | a0001c0001t0001g0067 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1456-325C>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86328817 | ||||||
chr9:86328842
|
T | C | 1 | a0001c0001t0001g0017 | 2 | HG03491.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1456-350A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86328842 | ||||||
chr9:86329032
|
T | A | 103 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(100): Show | 130 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.1456-540A>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86329032 | ||||||
chr9:86329070
|
A | G | 13 | a0002c0003t0001g0038a0002c0003t0001g0039a0002c0003t0001g0282others(10): Show | 14 | HG01109.hp2 HG01255.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.1456-578T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86329070 | ||||||
chr9:86329248
|
G | A | 2 | a0001c0001t0001g0150a0001c0001t0001g0250 | 2 | HG00741.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.1456-756C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86329248 | ||||||
chr9:86329280
|
T | C | 1 | a0002c0002t0001g0268 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1456-788A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86329280 | ||||||
chr9:86329299
|
G | A | 1 | a0001c0001t0001g0018 | 2 | HG00280.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.1456-807C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86329299 | ||||||
chr9:86329391
|
C | T | 1 | a0001c0014t0011g0294 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1456-899G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86329391 | ||||||
chr9:86329511
|
G | A | 1 | a0002c0002t0006g0173 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1456-1019C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86329511 | ||||||
chr9:86329523
|
C | CA | 4 | a0002c0003t0001g0246a0004c0005t0001g0036a0004c0005t0001g0037others(1): Show | 6 | HG01243.hp1 HG02630.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1456-1032dupT | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86329523 | ||||||
chr9:86329523
|
CA | C | 150 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(147): Show | 188 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.1456-1032delT | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86329523 | ||||||
chr9:86329683
|
A | G | 2 | a0001c0001t0001g0161a0001c0001t0001g0281 | 2 | HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1456-1191T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86329683 | ||||||
chr9:86330015
|
T | C | 1 | a0001c0001t0001g0146 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1456-1523A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86330015 | ||||||
chr9:86330091
|
C | T | 154 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(151): Show | 194 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.1456-1599G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86330091 | ||||||
chr9:86330134
|
T | G | 5 | a0001c0001t0001g0015a0001c0001t0001g0058a0001c0001t0001g0059others(2): Show | 6 | HG03017.hp2 HG04115.hp2 NA18953.hp2 others(3): Show |
intron_variant | MODIFIER | c.1456-1642A>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86330134 | ||||||
chr9:86330223
|
A | C | 18 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0014others(15): Show | 28 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1456-1731T>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86330223 | ||||||
chr9:86330299
|
A | G | 1 | a0001c0001t0001g0159 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1456-1807T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86330299 | ||||||
chr9:86330331
|
A | G | 133 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(130): Show | 161 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.1456-1839T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86330331 | ||||||
chr9:86330351
|
T | G | 18 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0014others(15): Show | 28 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1456-1859A>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86330351 | ||||||
chr9:86330745
|
T | C | 133 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(130): Show | 161 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.1456-2253A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86330745 | ||||||
chr9:86330880
|
CT | C | 6 | a0002c0003t0001g0013a0002c0003t0001g0035a0002c0003t0001g0040others(3): Show | 8 | HG02257.hp1 HG02280.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1456-2389delA | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86330880 | ||||||
chr9:86331083
|
T | A | 3 | a0004c0005t0001g0036a0004c0005t0001g0037a0004c0005t0001g0280 | 5 | HG01243.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1456-2591A>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86331083 | ||||||
chr9:86331192
|
C | T | 13 | a0001c0001t0001g0015a0001c0001t0001g0058a0001c0001t0001g0059others(10): Show | 14 | HG02109.hp2 HG02622.hp1 HG02723.hp1 others(11): Show |
intron_variant | MODIFIER | c.1456-2700G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86331192 | ||||||
chr9:86331227
|
A | AT | 133 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(130): Show | 161 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.1456-2736dupA | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86331227 | ||||||
chr9:86331236
|
C | T | 1 | a0002c0002t0001g0166 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1456-2744G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86331236 | ||||||
chr9:86331323
|
T | C | 2 | a0001c0001t0001g0026a0001c0001t0001g0144 | 3 | NA18943.hp1 NA18973.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.1456-2831A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86331323 | ||||||
chr9:86331450
|
G | A | 1 | a0001c0001t0002g0054 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1456-2958C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86331450 | ||||||
chr9:86331806
|
A | C | 3 | a0002c0003t0001g0247a0002c0003t0001g0262a0002c0003t0007g0148 | 3 | HG02040.hp2 HG04228.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.1456-3314T>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86331806 | ||||||
chr9:86331808
|
A | C | 1 | a0001c0001t0001g0098 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1456-3316T>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86331808 | ||||||
chr9:86332332
|
T | G | 1 | a0002c0002t0001g0149 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1456-3840A>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86332332 | ||||||
chr9:86332339
|
C | T | 18 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0014others(15): Show | 28 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1456-3847G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86332339 | ||||||
chr9:86332359
|
TA | T | 102 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(99): Show | 129 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.1456-3868delT | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86332359 | ||||||
chr9:86332623
|
A | G | 1 | a0002c0002t0001g0231 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1456-4131T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86332623 | ||||||
chr9:86332755
|
T | A | 102 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(99): Show | 129 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.1456-4263A>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86332755 | ||||||
chr9:86333021
|
T | C | 1 | a0002c0002t0001g0166 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1455+4398A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86333021 | ||||||
chr9:86333182
|
A | G | 1 | a0004c0005t0001g0036 | 2 | HG02965.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1455+4237T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86333182 | ||||||
chr9:86333486
|
G | C | 18 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0014others(15): Show | 28 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1455+3933C>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86333486 | ||||||
chr9:86333522
|
G | A | 1 | a0001c0001t0001g0139 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1455+3897C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86333522 | ||||||
chr9:86333556
|
A | T | 1 | a0001c0001t0002g0045 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1455+3863T>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86333556 | ||||||
chr9:86333630
|
T | A | 17 | a0001c0001t0001g0006a0001c0001t0001g0023a0001c0001t0001g0062others(14): Show | 22 | HG01123.hp2 HG02109.hp1 HG02280.hp2 others(19): Show |
intron_variant | MODIFIER | c.1455+3789A>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86333630 | ||||||
chr9:86333773
|
T | C | 18 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0014others(15): Show | 28 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1455+3646A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86333773 | ||||||
chr9:86333809
|
T | C | 18 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0014others(15): Show | 28 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1455+3610A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86333809 | ||||||
chr9:86333833
|
TTA | T | 18 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0014others(15): Show | 28 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1455+3584_1455+358 others(6): Show |
TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86333833 | ||||||
chr9:86333848
|
T | C | 3 | a0004c0005t0001g0036a0004c0005t0001g0037a0004c0005t0001g0280 | 5 | HG01243.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1455+3571A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86333848 | ||||||
chr9:86333881
|
G | C | 1 | a0013c0012t0008g0151 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1455+3538C>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86333881 | ||||||
chr9:86334073
|
T | C | 18 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0014others(15): Show | 28 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1455+3346A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86334073 | ||||||
chr9:86334207
|
C | T | 1 | a0001c0001t0001g0097 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1455+3212G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86334207 | ||||||
chr9:86334236
|
T | C | 1 | a0002c0002t0001g0222 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1455+3183A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86334236 | ||||||
chr9:86334331
|
G | A | 1 | a0002c0002t0001g0223 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1455+3088C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86334331 | ||||||
chr9:86334364
|
G | A | 6 | a0002c0003t0001g0013a0002c0003t0001g0035a0002c0003t0001g0040others(3): Show | 8 | HG02257.hp1 HG02280.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1455+3055C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86334364 | ||||||
chr9:86334614
|
G | A | 6 | a0001c0001t0001g0015a0001c0001t0001g0058a0001c0001t0001g0059others(3): Show | 7 | HG03017.hp2 HG03540.hp1 HG04115.hp2 others(4): Show |
intron_variant | MODIFIER | c.1455+2805C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86334614 | ||||||
chr9:86334617
|
T | C | 6 | a0003c0004t0001g0271a0003c0004t0001g0272a0003c0004t0001g0273others(3): Show | 6 | HG02257.hp2 HG02615.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1455+2802A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86334617 | ||||||
chr9:86334708
|
T | G | 3 | a0004c0005t0001g0036a0004c0005t0001g0037a0004c0005t0001g0280 | 5 | HG01243.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1455+2711A>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86334708 | ||||||
chr9:86334949
|
T | C | 1 | a0002c0003t0001g0246 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1455+2470A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86334949 | ||||||
chr9:86335162
|
G | A | 1 | a0001c0001t0001g0024 | 2 | HG01928.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.1455+2257C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86335162 | ||||||
chr9:86335283
|
T | C | 6 | a0003c0004t0001g0271a0003c0004t0001g0272a0003c0004t0001g0273others(3): Show | 6 | HG02257.hp2 HG02615.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1455+2136A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86335283 | ||||||
chr9:86335474
|
A | C | 1 | a0002c0002t0001g0234 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1455+1945T>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86335474 | ||||||
chr9:86335542
|
A | G | 2 | a0001c0001t0001g0162a0001c0001t0001g0163 | 2 | HG02572.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1455+1877T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86335542 | ||||||
chr9:86335795
|
A | G | 1 | a0013c0012t0008g0151 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1455+1624T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86335795 | ||||||
chr9:86335988
|
T | C | 1 | a0001c0001t0010g0160 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1455+1431A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86335988 | ||||||
chr9:86336094
|
C | A | 1 | a0002c0002t0001g0249 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1455+1325G>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86336094 | ||||||
chr9:86336498
|
C | T | 6 | a0002c0003t0001g0013a0002c0003t0001g0035a0002c0003t0001g0040others(3): Show | 8 | HG02257.hp1 HG02280.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1455+921G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86336498 | ||||||
chr9:86336558
|
T | C | 1 | a0002c0002t0001g0224 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1455+861A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86336558 | ||||||
chr9:86336613
|
G | C | 1 | a0001c0001t0001g0130 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1455+806C>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86336613 | ||||||
chr9:86336721
|
T | G | 1 | a0007c0008t0001g0168 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1455+698A>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86336721 | ||||||
chr9:86336923
|
C | T | 190 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(187): Show | 235 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.1455+496G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86336923 | ||||||
chr9:86336972
|
T | G | 1 | a0001c0001t0001g0159 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1455+447A>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86336972 | ||||||
chr9:86337103
|
C | T | 1 | a0001c0014t0011g0294 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1455+316G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86337103 | ||||||
chr9:86337149
|
T | C | 6 | a0003c0004t0001g0271a0003c0004t0001g0272a0003c0004t0001g0273others(3): Show | 6 | HG02257.hp2 HG02615.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1455+270A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86337149 | ||||||
chr9:86337257
|
A | G | 3 | a0002c0002t0001g0007a0002c0002t0001g0194a0002c0002t0001g0195 | 6 | NA18942.hp2 NA18946.hp1 NA18951.hp1 others(3): Show |
intron_variant | MODIFIER | c.1455+162T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86337257 | ||||||
chr9:86337331
|
G | A | 2 | a0002c0002t0001g0032a0002c0002t0001g0225 | 3 | HG01168.hp2 HG01169.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1455+88C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86337331 | ||||||
chr9:86337366
|
T | A | 1 | a0001c0001t0001g0131 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1455+53A>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86337366 | ||||||
chr9:86337398
|
A | C | 3 | a0001c0001t0002g0014a0001c0001t0002g0043a0001c0001t0002g0044 | 4 | HG00639.hp2 HG00738.hp1 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.1455+21T>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 10/26 | chr9 | 86337398 | ||||||
chr9:86337648
|
T | C | 1 | a0002c0002t0001g0226 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1336-110A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 9/26 | chr9 | 86337648 | ||||||
chr9:86337705
|
G | A | 3 | a0004c0005t0001g0036a0004c0005t0001g0037a0004c0005t0001g0280 | 5 | HG01243.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1336-167C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 9/26 | chr9 | 86337705 | ||||||
chr9:86337719
|
T | A | 1 | a0001c0001t0001g0080 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1336-181A>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 9/26 | chr9 | 86337719 | ||||||
chr9:86337860
|
G | C | 5 | a0001c0001t0001g0015a0001c0001t0001g0058a0001c0001t0001g0059others(2): Show | 6 | HG03017.hp2 HG04115.hp2 NA18953.hp2 others(3): Show |
intron_variant | MODIFIER | c.1336-322C>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 9/26 | chr9 | 86337860 | ||||||
chr9:86337870
|
C | T | 3 | a0004c0005t0001g0036a0004c0005t0001g0037a0004c0005t0001g0280 | 5 | HG01243.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1336-332G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 9/26 | chr9 | 86337870 | ||||||
chr9:86337958
|
T | C | 3 | a0001c0001t0001g0092a0001c0001t0001g0139a0001c0001t0001g0145 | 3 | HG02723.hp1 HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1336-420A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 9/26 | chr9 | 86337958 | ||||||
chr9:86337962
|
C | T | 3 | a0004c0005t0001g0036a0004c0005t0001g0037a0004c0005t0001g0280 | 5 | HG01243.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1336-424G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 9/26 | chr9 | 86337962 | ||||||
chr9:86338158
|
A | G | 5 | a0002c0003t0001g0282a0002c0003t0001g0283a0002c0003t0001g0284others(2): Show | 5 | HG01109.hp2 HG02723.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1336-620T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 9/26 | chr9 | 86338158 | ||||||
chr9:86338210
|
CT | C | 13 | a0001c0001t0001g0081a0001c0001t0001g0092a0001c0001t0001g0145others(10): Show | 13 | HG01167.hp1 HG01257.hp2 HG01261.hp1 others(10): Show |
intron_variant | MODIFIER | c.1335+612delA | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 9/26 | chr9 | 86338210 | ||||||
chr9:86338210
|
CTTTTTTT others(4): Show |
C | 2 | a0002c0002t0001g0229a0002c0002t0001g0261 | 2 | HG02738.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1335+602_1335+612d others(13): Show |
TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 9/26 | chr9 | 86338210 | ||||||
chr9:86338275
|
G | A | 2 | a0001c0001t0001g0026a0001c0001t0001g0144 | 3 | NA18943.hp1 NA18973.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.1335+548C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 9/26 | chr9 | 86338275 | ||||||
chr9:86338322
|
T | C | 1 | a0001c0001t0002g0055 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1335+501A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 9/26 | chr9 | 86338322 | ||||||
chr9:86338514
|
G | T | 1 | a0009c0017t0001g0096 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1335+309C>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 9/26 | chr9 | 86338514 | ||||||
chr9:86338607
|
C | T | 110 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(107): Show | 137 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.1335+216G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 9/26 | chr9 | 86338607 | ||||||
chr9:86338639
|
C | T | 22 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0014others(19): Show | 34 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.1335+184G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 9/26 | chr9 | 86338639 | ||||||
chr9:86338720
|
T | C | 3 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0136 | 3 | HG02135.hp2 NA18946.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.1335+103A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 9/26 | chr9 | 86338720 | ||||||
chr9:86338772
|
A | G | 1 | a0013c0012t0008g0151 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1335+51T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 9/26 | chr9 | 86338772 | ||||||
chr9:86339042
|
C | A | 2 | a0001c0001t0001g0019a0001c0001t0001g0082 | 3 | HG02071.hp2 NA18969.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.1209-93G>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 8/26 | chr9 | 86339042 | ||||||
chr9:86339079
|
A | C | 1 | a0001c0001t0001g0095 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1209-130T>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 8/26 | chr9 | 86339079 | ||||||
chr9:86339138
|
C | T | 1 | a0001c0014t0011g0294 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1209-189G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 8/26 | chr9 | 86339138 | ||||||
chr9:86339254
|
T | C | 5 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(2): Show | 5 | HG02135.hp2 NA18946.hp2 NA18954.hp2 others(2): Show |
intron_variant | MODIFIER | c.1209-305A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 8/26 | chr9 | 86339254 | ||||||
chr9:86339449
|
C | T | 1 | a0001c0001t0001g0144 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1209-500G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 8/26 | chr9 | 86339449 | ||||||
chr9:86339789
|
C | T | 103 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(100): Show | 130 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.1208+247G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 8/26 | chr9 | 86339789 | ||||||
chr9:86339964
|
T | C | 3 | a0002c0002t0001g0147a0002c0002t0001g0230a0002c0002t0001g0293 | 3 | HG02622.hp2 HG02896.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1208+72A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 8/26 | chr9 | 86339964 | ||||||
chr9:86340014
|
A | T | 3 | a0004c0005t0001g0036a0004c0005t0001g0037a0004c0005t0001g0280 | 5 | HG01243.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1208+22T>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 8/26 | chr9 | 86340014 | ||||||
chr9:86340188
|
T | C | 1 | a0001c0001t0001g0139 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1139-83A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 7/26 | chr9 | 86340188 | ||||||
chr9:86340462
|
C | T | 21 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0014others(18): Show | 33 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.1139-357G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 7/26 | chr9 | 86340462 | ||||||
chr9:86340628
|
T | C | 1 | a0001c0001t0001g0136 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1138+374A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 7/26 | chr9 | 86340628 | ||||||
chr9:86340874
|
T | C | 18 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0014others(15): Show | 28 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1138+128A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 7/26 | chr9 | 86340874 | ||||||
chr9:86341102
|
C | T | 11 | a0002c0002t0001g0027a0002c0002t0001g0028a0002c0002t0001g0170others(8): Show | 13 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(10): Show |
intron_variant | MODIFIER | c.1087-49G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 6/26 | chr9 | 86341102 | ||||||
chr9:86341252
|
G | C | 1 | a0001c0001t0001g0142 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1087-199C>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 6/26 | chr9 | 86341252 | ||||||
chr9:86341363
|
A | G | 1 | a0001c0001t0001g0094 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1087-310T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 6/26 | chr9 | 86341363 | ||||||
chr9:86341416
|
A | G | 13 | a0001c0001t0001g0015a0001c0001t0001g0058a0001c0001t0001g0059others(10): Show | 14 | HG02109.hp2 HG02622.hp1 HG02723.hp1 others(11): Show |
intron_variant | MODIFIER | c.1087-363T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 6/26 | chr9 | 86341416 | ||||||
chr9:86341433
|
T | C | 6 | a0003c0004t0001g0271a0003c0004t0001g0272a0003c0004t0001g0273others(3): Show | 6 | HG02257.hp2 HG02615.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1087-380A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 6/26 | chr9 | 86341433 | ||||||
chr9:86341448
|
G | A | 1 | a0003c0004t0001g0273 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1087-395C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 6/26 | chr9 | 86341448 | ||||||
chr9:86341517
|
T | G | 1 | a0002c0002t0001g0187 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1087-464A>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 6/26 | chr9 | 86341517 | ||||||
chr9:86341733
|
C | T | 13 | a0002c0003t0001g0038a0002c0003t0001g0039a0002c0003t0001g0282others(10): Show | 14 | HG01109.hp2 HG01255.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.1087-680G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 6/26 | chr9 | 86341733 | ||||||
chr9:86341931
|
G | A | 1 | a0002c0002t0001g0242 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1087-878C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 6/26 | chr9 | 86341931 | ||||||
chr9:86342019
|
G | A | 4 | a0002c0002t0001g0231a0002c0002t0001g0232a0002c0002t0001g0233others(1): Show | 4 | NA18975.hp1 NA18991.hp1 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.1087-966C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 6/26 | chr9 | 86342019 | ||||||
chr9:86342067
|
G | C | 6 | a0002c0003t0001g0013a0002c0003t0001g0035a0002c0003t0001g0040others(3): Show | 8 | HG02257.hp1 HG02280.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1086+1008C>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 6/26 | chr9 | 86342067 | ||||||
chr9:86342092
|
C | T | 18 | a0001c0001t0001g0278a0002c0003t0001g0033a0002c0003t0001g0034others(15): Show | 20 | HG00733.hp1 HG00735.hp1 HG02040.hp2 others(17): Show |
intron_variant | MODIFIER | c.1086+983G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 6/26 | chr9 | 86342092 | ||||||
chr9:86342172
|
A | AT | 3 | a0004c0005t0001g0036a0004c0005t0001g0037a0004c0005t0001g0280 | 5 | HG01243.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1086+902dupA | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 6/26 | chr9 | 86342172 | ||||||
chr9:86342393
|
T | G | 4 | a0002c0002t0001g0234a0002c0002t0001g0235a0002c0002t0001g0236others(1): Show | 4 | HG00544.hp2 NA18952.hp2 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.1086+682A>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 6/26 | chr9 | 86342393 | ||||||
chr9:86342691
|
A | G | 1 | a0002c0002t0001g0196 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1086+384T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 6/26 | chr9 | 86342691 | ||||||
chr9:86342757
|
C | T | 18 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0014others(15): Show | 28 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1086+318G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 6/26 | chr9 | 86342757 | ||||||
chr9:86342770
|
C | T | 3 | a0002c0002t0001g0007a0002c0002t0001g0194a0002c0002t0001g0195 | 6 | NA18942.hp2 NA18946.hp1 NA18951.hp1 others(3): Show |
intron_variant | MODIFIER | c.1086+305G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 6/26 | chr9 | 86342770 | ||||||
chr9:86342934
|
T | G | 4 | a0002c0002t0001g0188a0002c0002t0001g0189a0002c0002t0001g0190others(1): Show | 4 | HG00323.hp1 HG01070.hp1 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.1086+141A>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 6/26 | chr9 | 86342934 | ||||||
chr9:86342942
|
T | C | 2 | a0001c0001t0002g0056a0001c0001t0002g0057 | 2 | NA18943.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.1086+133A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 6/26 | chr9 | 86342942 | ||||||
chr9:86342951
|
G | C | 1 | a0002c0002t0001g0238 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1086+124C>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 6/26 | chr9 | 86342951 | ||||||
chr9:86343317
|
T | C | 18 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0014others(15): Show | 28 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.998-154A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 5/26 | chr9 | 86343317 | ||||||
chr9:86343488
|
T | C | 11 | a0002c0002t0001g0012a0002c0002t0001g0239a0002c0002t0001g0240others(8): Show | 13 | HG02257.hp2 HG02615.hp2 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.998-325A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 5/26 | chr9 | 86343488 | ||||||
chr9:86343831
|
C | T | 2 | a0004c0005t0001g0037a0004c0005t0001g0280 | 3 | HG01243.hp1 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.998-668G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 5/26 | chr9 | 86343831 | ||||||
chr9:86343865
|
T | C | 2 | a0004c0005t0001g0037a0004c0005t0001g0280 | 3 | HG01243.hp1 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.998-702A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 5/26 | chr9 | 86343865 | ||||||
chr9:86343916
|
A | G | 1 | a0001c0001t0001g0093 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.998-753T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 5/26 | chr9 | 86343916 | ||||||
chr9:86344020
|
T | G | 1 | a0002c0003t0001g0137 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.998-857A>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 5/26 | chr9 | 86344020 | ||||||
chr9:86344071
|
A | G | 1 | a0002c0002t0001g0193 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.997+906T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 5/26 | chr9 | 86344071 | ||||||
chr9:86344075
|
T | C | 111 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(108): Show | 138 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.997+902A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 5/26 | chr9 | 86344075 | ||||||
chr9:86344504
|
C | T | 18 | a0001c0001t0001g0278a0002c0003t0001g0033a0002c0003t0001g0034others(15): Show | 20 | HG00733.hp1 HG00735.hp1 HG02040.hp2 others(17): Show |
intron_variant | MODIFIER | c.997+473G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 5/26 | chr9 | 86344504 | ||||||
chr9:86344588
|
C | CT | 129 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(126): Show | 157 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(154): Show |
intron_variant | MODIFIER | c.997+388dupA | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 5/26 | chr9 | 86344588 | ||||||
chr9:86344663
|
G | A | 1 | a0001c0001t0001g0025 | 2 | NA18947.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.997+314C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 5/26 | chr9 | 86344663 | ||||||
chr9:86344723
|
A | G | 1 | a0002c0003t0001g0269 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.997+254T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 5/26 | chr9 | 86344723 | ||||||
chr9:86344734
|
C | T | 3 | a0004c0005t0001g0036a0004c0005t0001g0037a0004c0005t0001g0280 | 5 | HG01243.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.997+243G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 5/26 | chr9 | 86344734 | ||||||
chr9:86344846
|
C | CA | 18 | a0001c0001t0001g0278a0002c0003t0001g0033a0002c0003t0001g0034others(15): Show | 20 | HG00733.hp1 HG00735.hp1 HG02040.hp2 others(17): Show |
intron_variant | MODIFIER | c.997+130dupT | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 5/26 | chr9 | 86344846 | ||||||
chr9:86344881
|
G | A | 1 | a0001c0001t0001g0150 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.997+96C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 5/26 | chr9 | 86344881 | ||||||
chr9:86344888
|
A | C | 1 | a0002c0002t0009g0167 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.997+89T>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 5/26 | chr9 | 86344888 | ||||||
chr9:86345348
|
T | C | 1 | a0001c0001t0001g0139 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.820-194A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 4/26 | chr9 | 86345348 | ||||||
chr9:86345446
|
C | T | 1 | a0002c0003t0001g0246 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.819+223G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 4/26 | chr9 | 86345446 | ||||||
chr9:86345466
|
A | C | 13 | a0002c0003t0001g0038a0002c0003t0001g0039a0002c0003t0001g0282others(10): Show | 14 | HG01109.hp2 HG01255.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.819+203T>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 4/26 | chr9 | 86345466 | ||||||
chr9:86345517
|
T | G | 3 | a0004c0005t0001g0036a0004c0005t0001g0037a0004c0005t0001g0280 | 5 | HG01243.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.819+152A>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 4/26 | chr9 | 86345517 | ||||||
chr9:86346195
|
C | A | 3 | a0004c0005t0001g0036a0004c0005t0001g0037a0004c0005t0001g0280 | 5 | HG01243.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.702+104G>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 3/26 | chr9 | 86346195 | ||||||
chr9:86346281
|
T | C | 2 | a0002c0003t0001g0013a0002c0003t0001g0040 | 3 | HG02630.hp1 HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.702+18A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 3/26 | chr9 | 86346281 | ||||||
chr9:86346800
|
G | A | 4 | a0001c0001t0001g0025a0001c0001t0001g0140a0001c0001t0001g0141others(1): Show | 5 | HG00621.hp2 NA18612.hp2 NA18947.hp1 others(2): Show |
intron_variant | MODIFIER | c.521-320C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86346800 | ||||||
chr9:86346845
|
T | C | 1 | a0002c0002t0001g0243 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.521-365A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86346845 | ||||||
chr9:86346913
|
C | T | 5 | a0001c0001t0001g0084a0001c0001t0003g0020a0001c0001t0004g0085others(2): Show | 6 | HG02280.hp2 HG02486.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.521-433G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86346913 | ||||||
chr9:86347023
|
T | C | 4 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(1): Show | 4 | HG00558.hp2 HG00597.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.521-543A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86347023 | ||||||
chr9:86347063
|
G | A | 1 | a0001c0001t0001g0083 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.521-583C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86347063 | ||||||
chr9:86347252
|
C | A | 1 | a0002c0002t0001g0244 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.521-772G>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86347252 | ||||||
chr9:86347552
|
C | T | 25 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(22): Show | 36 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(33): Show |
intron_variant | MODIFIER | c.521-1072G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86347552 | ||||||
chr9:86347560
|
T | G | 1 | a0002c0002t0001g0245 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.521-1080A>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86347560 | ||||||
chr9:86347578
|
G | C | 1 | a0003c0004t0001g0276 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.521-1098C>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86347578 | ||||||
chr9:86347588
|
G | T | 6 | a0002c0003t0001g0013a0002c0003t0001g0035a0002c0003t0001g0040others(3): Show | 8 | HG02257.hp1 HG02280.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.521-1108C>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86347588 | ||||||
chr9:86347680
|
A | T | 1 | a0002c0002t0009g0167 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.521-1200T>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86347680 | ||||||
chr9:86347880
|
AT | A | 9 | a0002c0003t0001g0013a0002c0003t0001g0035a0002c0003t0001g0040others(6): Show | 13 | HG01243.hp1 HG02257.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.521-1401delA | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86347880 | ||||||
chr9:86348093
|
C | T | 30 | a0002c0002t0001g0027a0002c0002t0001g0028a0002c0002t0001g0029others(27): Show | 33 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(30): Show |
intron_variant | MODIFIER | c.521-1613G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86348093 | ||||||
chr9:86348451
|
T | C | 1 | a0001c0001t0001g0143 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.521-1971A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86348451 | ||||||
chr9:86348515
|
G | C | 2 | a0001c0001t0001g0026a0001c0001t0001g0144 | 3 | NA18943.hp1 NA18973.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.521-2035C>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86348515 | ||||||
chr9:86348658
|
C | T | 1 | a0001c0001t0001g0068 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.521-2178G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86348658 | ||||||
chr9:86348662
|
A | G | 1 | a0002c0003t0001g0251 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.521-2182T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86348662 | ||||||
chr9:86348708
|
C | T | 4 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(1): Show | 4 | HG00558.hp2 HG00597.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.521-2228G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86348708 | ||||||
chr9:86348803
|
T | A | 1 | a0001c0001t0001g0145 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.521-2323A>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86348803 | ||||||
chr9:86348852
|
T | C | 1 | a0002c0003t0001g0246 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.521-2372A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86348852 | ||||||
chr9:86349033
|
T | C | 177 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(174): Show | 221 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.521-2553A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86349033 | ||||||
chr9:86349065
|
G | A | 1 | a0002c0002t0001g0248 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.521-2585C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86349065 | ||||||
chr9:86349077
|
G | A | 1 | a0001c0001t0001g0146 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.521-2597C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86349077 | ||||||
chr9:86349392
|
C | T | 2 | a0002c0003t0001g0013a0002c0003t0001g0040 | 3 | HG02630.hp1 HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.521-2912G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86349392 | ||||||
chr9:86349573
|
GA | G | 3 | a0004c0005t0001g0036a0004c0005t0001g0037a0004c0005t0001g0280 | 5 | HG01243.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.521-3094delT | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86349573 | ||||||
chr9:86349603
|
A | G | 3 | a0004c0005t0001g0036a0004c0005t0001g0037a0004c0005t0001g0280 | 5 | HG01243.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.520+3077T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86349603 | ||||||
chr9:86349712
|
T | C | 1 | a0002c0002t0001g0249 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.520+2968A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86349712 | ||||||
chr9:86349792
|
C | G | 1 | a0002c0002t0001g0166 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.520+2888G>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86349792 | ||||||
chr9:86349823
|
G | T | 9 | a0001c0001t0001g0278a0002c0003t0001g0033a0002c0003t0001g0165others(6): Show | 10 | NA18950.hp1 NA18978.hp2 NA18992.hp2 others(7): Show |
intron_variant | MODIFIER | c.520+2857C>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86349823 | ||||||
chr9:86349892
|
C | T | 1 | a0002c0002t0001g0164 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.520+2788G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86349892 | ||||||
chr9:86350006
|
T | C | 6 | a0003c0004t0001g0271a0003c0004t0001g0272a0003c0004t0001g0273others(3): Show | 6 | HG02257.hp2 HG02615.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.520+2674A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86350006 | ||||||
chr9:86350202
|
G | A | 2 | a0001c0001t0001g0162a0001c0001t0001g0163 | 2 | HG02572.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.520+2478C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86350202 | ||||||
chr9:86350511
|
C | T | 2 | a0001c0001t0001g0150a0001c0001t0001g0250 | 2 | HG00741.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.520+2169G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86350511 | ||||||
chr9:86350518
|
G | A | 3 | a0004c0005t0001g0036a0004c0005t0001g0037a0004c0005t0001g0280 | 5 | HG01243.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.520+2162C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86350518 | ||||||
chr9:86350684
|
A | T | 133 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(130): Show | 161 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.520+1996T>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86350684 | ||||||
chr9:86350701
|
A | G | 1 | a0001c0001t0001g0064 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.520+1979T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86350701 | ||||||
chr9:86350753
|
T | C | 2 | a0004c0005t0001g0037a0004c0005t0001g0280 | 3 | HG01243.hp1 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.520+1927A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86350753 | ||||||
chr9:86350771
|
C | T | 1 | a0002c0002t0001g0149 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.520+1909G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86350771 | ||||||
chr9:86351000
|
G | T | 1 | a0002c0002t0001g0063 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.520+1680C>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86351000 | ||||||
chr9:86351074
|
C | T | 1 | a0001c0001t0001g0062 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.520+1606G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86351074 | ||||||
chr9:86351132
|
C | CA | 30 | a0001c0001t0001g0250a0001c0001t0001g0278a0001c0014t0011g0294others(27): Show | 33 | HG00639.hp1 HG00733.hp1 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.520+1547dupT | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86351132 | ||||||
chr9:86351132
|
CA | C | 133 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(130): Show | 173 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.520+1547delT | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86351132 | ||||||
chr9:86351177
|
T | C | 18 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0014others(15): Show | 28 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.520+1503A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86351177 | ||||||
chr9:86351217
|
C | A | 1 | a0002c0002t0001g0268 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.520+1463G>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86351217 | ||||||
chr9:86351392
|
C | T | 5 | a0001c0001t0001g0015a0001c0001t0001g0058a0001c0001t0001g0059others(2): Show | 6 | HG03017.hp2 HG04115.hp2 NA18953.hp2 others(3): Show |
intron_variant | MODIFIER | c.520+1288G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86351392 | ||||||
chr9:86351422
|
C | A | 6 | a0002c0003t0001g0013a0002c0003t0001g0035a0002c0003t0001g0040others(3): Show | 8 | HG02257.hp1 HG02280.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.520+1258G>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86351422 | ||||||
chr9:86351431
|
G | A | 6 | a0003c0004t0001g0271a0003c0004t0001g0272a0003c0004t0001g0273others(3): Show | 6 | HG02257.hp2 HG02615.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.520+1249C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86351431 | ||||||
chr9:86351455
|
A | G | 3 | a0004c0005t0001g0036a0004c0005t0001g0037a0004c0005t0001g0280 | 5 | HG01243.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.520+1225T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86351455 | ||||||
chr9:86351477
|
G | A | 3 | a0004c0005t0001g0036a0004c0005t0001g0037a0004c0005t0001g0280 | 5 | HG01243.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.520+1203C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86351477 | ||||||
chr9:86351519
|
C | T | 18 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0014others(15): Show | 28 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.520+1161G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86351519 | ||||||
chr9:86351620
|
T | C | 1 | a0001c0001t0001g0277 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.520+1060A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86351620 | ||||||
chr9:86351639
|
C | T | 1 | a0001c0014t0011g0294 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.520+1041G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86351639 | ||||||
chr9:86351859
|
T | C | 2 | a0004c0005t0001g0037a0004c0005t0001g0280 | 3 | HG01243.hp1 HG03195.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.520+821A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86351859 | ||||||
chr9:86351892
|
T | C | 1 | a0001c0001t0001g0278 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.520+788A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86351892 | ||||||
chr9:86352385
|
A | G | 21 | a0001c0001t0002g0002a0001c0001t0002g0008a0001c0001t0002g0014others(18): Show | 33 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.520+295T>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86352385 | ||||||
chr9:86352440
|
C | A | 3 | a0004c0005t0001g0036a0004c0005t0001g0037a0004c0005t0001g0280 | 5 | HG01243.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.520+240G>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 2/26 | chr9 | 86352440 | ||||||
chr9:86353494
|
G | A | 4 | a0002c0003t0001g0013a0002c0003t0001g0035a0002c0003t0001g0040others(1): Show | 6 | HG02257.hp1 HG02280.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-31-264C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 1/26 | chr9 | 86353494 | ||||||
chr9:86353536
|
T | C | 3 | a0004c0005t0001g0036a0004c0005t0001g0037a0004c0005t0001g0280 | 5 | HG01243.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-31-306A>G | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 1/26 | chr9 | 86353536 | ||||||
chr9:86353618
|
G | T | 2 | a0001c0001t0001g0041a0001c0001t0001g0042 | 2 | NA18966.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.-31-388C>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 1/26 | chr9 | 86353618 | ||||||
chr9:86353763
|
G | A | 1 | a0001c0001t0001g0281 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-32+508C>T | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 1/26 | chr9 | 86353763 | ||||||
chr9:86353929
|
C | G | 2 | a0002c0003t0001g0013a0002c0003t0001g0040 | 3 | HG02630.hp1 HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-32+342G>C | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 1/26 | chr9 | 86353929 | ||||||
chr9:86353955
|
CG | C | 14 | a0002c0002t0001g0293a0002c0003t0001g0038a0002c0003t0001g0039others(11): Show | 15 | HG01109.hp2 HG01255.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.-32+315delC | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 1/26 | chr9 | 86353955 | ||||||
chr9:86354093
|
C | T | 1 | a0002c0003t0001g0039 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-32+178G>A | TUT7 | ENSG00000083223.18 | transcript | ENST00000375963.8 | protein_coding | 1/26 | chr9 | 86354093 |