geneid | 56254 |
---|---|
ensemblid | ENSG00000155827.12 |
hgncid | 10062 |
symbol | RNF20 |
name | ring finger protein 20 |
refseq_nuc | NM_019592.7 |
refseq_prot | NP_062538.5 |
ensembl_nuc | ENST00000389120.8 |
ensembl_prot | ENSP00000373772.3 |
mane_status | MANE Select |
chr | chr9 |
start | 101533853 |
end | 101563344 |
strand | + |
ver | v1.2 |
region | chr9:101533853-101563344 |
region5000 | chr9:101528853-101568344 |
regionname0 | RNF20_chr9_101533853_101563344 |
regionname5000 | RNF20_chr9_101528853_101568344 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 975 | 398 | 84 | 80 | 176 | 16 | 40 | 139 | RNF20_chr9_101528853_101568344 | RNF20 | copy fasta | chr9 | 101528853 | 101568344 |
a0002 | 0/0 | 975 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | copy fasta | chr9 | 101528853 | 101568344 |
a0003 | 0/0 | 975 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RNF20_chr9_101528853_101568344 | RNF20 | copy fasta | chr9 | 101528853 | 101568344 |
a0004 | 0/0 | 975 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RNF20_chr9_101528853_101568344 | RNF20 | copy fasta | chr9 | 101528853 | 101568344 |
a0005 | 0/0 | 975 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | copy fasta | chr9 | 101528853 | 101568344 |
a0006 | 0/0 | 975 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RNF20_chr9_101528853_101568344 | RNF20 | copy fasta | chr9 | 101528853 | 101568344 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 2928 | 224 | 64 | 50 | 84 | 9 | 16 | RNF20_chr9_101528853_101568344 | RNF20 | copy fasta | chr9 | 101528853 | 101568344 |
c0002 | 0/0 | 2928 | 77 | 0 | 9 | 55 | 2 | 11 | RNF20_chr9_101528853_101568344 | RNF20 | copy fasta | chr9 | 101528853 | 101568344 |
c0003 | 0/0 | 2928 | 57 | 14 | 11 | 22 | 5 | 5 | RNF20_chr9_101528853_101568344 | RNF20 | copy fasta | chr9 | 101528853 | 101568344 |
c0004 | 0/1 | 2928 | 28 | 0 | 9 | 13 | 0 | 5 | RNF20_chr9_101528853_101568344 | RNF20 | copy fasta | chr9 | 101528853 | 101568344 |
c0005 | 0/0 | 2928 | 4 | 4 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | copy fasta | chr9 | 101528853 | 101568344 |
c0006 | 0/0 | 2928 | 4 | 4 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | copy fasta | chr9 | 101528853 | 101568344 |
c0007 | 0/0 | 2928 | 3 | 0 | 0 | 0 | 0 | 3 | RNF20_chr9_101528853_101568344 | RNF20 | copy fasta | chr9 | 101528853 | 101568344 |
c0008 | 0/0 | 2928 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | copy fasta | chr9 | 101528853 | 101568344 |
c0009 | 0/0 | 2928 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | copy fasta | chr9 | 101528853 | 101568344 |
c0010 | 0/0 | 2928 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | copy fasta | chr9 | 101528853 | 101568344 |
c0011 | 0/0 | 2928 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | copy fasta | chr9 | 101528853 | 101568344 |
c0012 | 0/0 | 2928 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | copy fasta | chr9 | 101528853 | 101568344 |
c0013 | 0/0 | 2928 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | copy fasta | chr9 | 101528853 | 101568344 |
c0014 | 0/0 | 2928 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | copy fasta | chr9 | 101528853 | 101568344 |
c0015 | 0/0 | 2928 | 1 | 0 | 1 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | copy fasta | chr9 | 101528853 | 101568344 |
c0016 | 0/0 | 2928 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | copy fasta | chr9 | 101528853 | 101568344 |
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 | 1/0 | 1011 | 366 | 82 | 69 | 164 | 15 | 35 | RNF20_chr9_101528853_101568344 | RNF20 | copy fasta | chr9 | 101528853 | 101568344 |
t0002 | 0/1 | 1011 | 19 | 0 | 1 | 13 | 0 | 4 | RNF20_chr9_101528853_101568344 | RNF20 | copy fasta | chr9 | 101528853 | 101568344 |
t0003 | 0/0 | 1011 | 9 | 0 | 8 | 0 | 0 | 1 | RNF20_chr9_101528853_101568344 | RNF20 | copy fasta | chr9 | 101528853 | 101568344 |
t0004 | 0/0 | 1011 | 3 | 0 | 0 | 3 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | copy fasta | chr9 | 101528853 | 101568344 |
t0005 | 0/0 | 1011 | 3 | 3 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | copy fasta | chr9 | 101528853 | 101568344 |
t0006 | 0/0 | 1011 | 2 | 0 | 1 | 0 | 1 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | copy fasta | chr9 | 101528853 | 101568344 |
t0007 | 0/0 | 1011 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | copy fasta | chr9 | 101528853 | 101568344 |
t0008 | 0/0 | 1011 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | copy fasta | chr9 | 101528853 | 101568344 |
t0009 | 0/0 | 1011 | 1 | 0 | 1 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | copy fasta | chr9 | 101528853 | 101568344 |
t0010 | 0/0 | 1011 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | copy fasta | chr9 | 101528853 | 101568344 |
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 | 50 | 0 | 6 | 36 | 1 | 7 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0002 | 1/0 | 41 | 7 | 10 | 18 | 3 | 2 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0003 | 0/0 | 26 | 4 | 5 | 16 | 1 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0004 | 0/0 | 22 | 2 | 5 | 14 | 0 | 1 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0005 | 0/0 | 20 | 0 | 4 | 14 | 1 | 1 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0006 | 0/1 | 13 | 0 | 1 | 7 | 0 | 4 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0007 | 0/0 | 9 | 0 | 4 | 0 | 4 | 1 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0008 | 0/0 | 7 | 6 | 1 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0009 | 0/0 | 7 | 6 | 1 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0010 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0011 | 0/0 | 6 | 0 | 6 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0012 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0013 | 0/0 | 5 | 0 | 1 | 0 | 1 | 3 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0014 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0015 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0017 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0019 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0020 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0022 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0028 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0032 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0040 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0042 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0043 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0044 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 2928 | 224 | 64 | 50 | 84 | 9 | 16 | RNF20_chr9_101528853_101568344 | RNF20 | copy fasta | chr9 | 101528853 | 101568344 |
a0001c0002 | 0/0 | 2928 | 77 | 0 | 9 | 55 | 2 | 11 | RNF20_chr9_101528853_101568344 | RNF20 | copy fasta | chr9 | 101528853 | 101568344 |
a0001c0003 | 0/0 | 2928 | 57 | 14 | 11 | 22 | 5 | 5 | RNF20_chr9_101528853_101568344 | RNF20 | copy fasta | chr9 | 101528853 | 101568344 |
a0001c0004 | 0/1 | 2928 | 28 | 0 | 9 | 13 | 0 | 5 | RNF20_chr9_101528853_101568344 | RNF20 | copy fasta | chr9 | 101528853 | 101568344 |
a0001c0006 | 0/0 | 2928 | 4 | 4 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | copy fasta | chr9 | 101528853 | 101568344 |
a0001c0007 | 0/0 | 2928 | 3 | 0 | 0 | 0 | 0 | 3 | RNF20_chr9_101528853_101568344 | RNF20 | copy fasta | chr9 | 101528853 | 101568344 |
a0001c0009 | 0/0 | 2928 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | copy fasta | chr9 | 101528853 | 101568344 |
a0001c0010 | 0/0 | 2928 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | copy fasta | chr9 | 101528853 | 101568344 |
a0001c0011 | 0/0 | 2928 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | copy fasta | chr9 | 101528853 | 101568344 |
a0001c0012 | 0/0 | 2928 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | copy fasta | chr9 | 101528853 | 101568344 |
a0001c0015 | 0/0 | 2928 | 1 | 0 | 1 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | copy fasta | chr9 | 101528853 | 101568344 |
a0002c0005 | 0/0 | 2928 | 4 | 4 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | copy fasta | chr9 | 101528853 | 101568344 |
a0003c0008 | 0/0 | 2928 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | copy fasta | chr9 | 101528853 | 101568344 |
a0004c0013 | 0/0 | 2928 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | copy fasta | chr9 | 101528853 | 101568344 |
a0005c0014 | 0/0 | 2928 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | copy fasta | chr9 | 101528853 | 101568344 |
a0006c0016 | 0/0 | 2928 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | copy fasta | chr9 | 101528853 | 101568344 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 3938 | 216 | 59 | 48 | 84 | 8 | 16 | RNF20_chr9_101528853_101568344 | RNF20 | copy fasta | chr9 | 101528853 | 101568344 |
a0001c0001t0005 | 0/0 | 3938 | 3 | 3 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | copy fasta | chr9 | 101528853 | 101568344 |
a0001c0001t0006 | 0/0 | 3938 | 2 | 0 | 1 | 0 | 1 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | copy fasta | chr9 | 101528853 | 101568344 |
a0001c0001t0008 | 0/0 | 3938 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | copy fasta | chr9 | 101528853 | 101568344 |
a0001c0001t0009 | 0/0 | 3938 | 1 | 0 | 1 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | copy fasta | chr9 | 101528853 | 101568344 |
a0001c0001t0010 | 0/0 | 3938 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | copy fasta | chr9 | 101528853 | 101568344 |
a0001c0002t0001 | 0/0 | 3938 | 74 | 0 | 9 | 52 | 2 | 11 | RNF20_chr9_101528853_101568344 | RNF20 | copy fasta | chr9 | 101528853 | 101568344 |
a0001c0002t0004 | 0/0 | 3938 | 3 | 0 | 0 | 3 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | copy fasta | chr9 | 101528853 | 101568344 |
a0001c0003t0001 | 0/0 | 3938 | 57 | 14 | 11 | 22 | 5 | 5 | RNF20_chr9_101528853_101568344 | RNF20 | copy fasta | chr9 | 101528853 | 101568344 |
a0001c0004t0002 | 0/1 | 3938 | 19 | 0 | 1 | 13 | 0 | 4 | RNF20_chr9_101528853_101568344 | RNF20 | copy fasta | chr9 | 101528853 | 101568344 |
a0001c0004t0003 | 0/0 | 3938 | 9 | 0 | 8 | 0 | 0 | 1 | RNF20_chr9_101528853_101568344 | RNF20 | copy fasta | chr9 | 101528853 | 101568344 |
a0001c0006t0001 | 0/0 | 3938 | 4 | 4 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | copy fasta | chr9 | 101528853 | 101568344 |
a0001c0007t0001 | 0/0 | 3938 | 3 | 0 | 0 | 0 | 0 | 3 | RNF20_chr9_101528853_101568344 | RNF20 | copy fasta | chr9 | 101528853 | 101568344 |
a0001c0009t0001 | 0/0 | 3938 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | copy fasta | chr9 | 101528853 | 101568344 |
a0001c0010t0001 | 0/0 | 3938 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | copy fasta | chr9 | 101528853 | 101568344 |
a0001c0011t0007 | 0/0 | 3938 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | copy fasta | chr9 | 101528853 | 101568344 |
a0001c0012t0001 | 0/0 | 3938 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | copy fasta | chr9 | 101528853 | 101568344 |
a0001c0015t0001 | 0/0 | 3938 | 1 | 0 | 1 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | copy fasta | chr9 | 101528853 | 101568344 |
a0002c0005t0001 | 0/0 | 3938 | 4 | 4 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | copy fasta | chr9 | 101528853 | 101568344 |
a0003c0008t0001 | 0/0 | 3938 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | copy fasta | chr9 | 101528853 | 101568344 |
a0004c0013t0001 | 0/0 | 3938 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | copy fasta | chr9 | 101528853 | 101568344 |
a0005c0014t0001 | 0/0 | 3938 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | copy fasta | chr9 | 101528853 | 101568344 |
a0006c0016t0001 | 0/0 | 3938 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | copy fasta | chr9 | 101528853 | 101568344 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 1/0 | 40 | 6 | 10 | 18 | 3 | 2 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0001t0001g0003 | 0/0 | 22 | 1 | 4 | 16 | 1 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0001t0001g0004 | 0/0 | 22 | 2 | 5 | 14 | 0 | 1 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0001t0001g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0001t0001g0008 | 0/0 | 7 | 6 | 1 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0001t0001g0009 | 0/0 | 7 | 6 | 1 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0001t0001g0013 | 0/0 | 5 | 0 | 1 | 0 | 1 | 3 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0001t0001g0014 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0001t0001g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0001t0001g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0001t0001g0019 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0001t0001g0020 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0001t0001g0022 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0001t0001g0040 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0001t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0001t0001g0043 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0001t0005g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0001t0006g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0001t0006g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0001t0008g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0001t0009g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0001t0010g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0002t0001g0001 | 0/0 | 46 | 0 | 5 | 33 | 1 | 7 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0002t0001g0015 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0002t0001g0017 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0002t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0002t0001g0032 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0002t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0002t0001g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0002t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0002t0004g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0003t0001g0005 | 0/0 | 16 | 0 | 4 | 10 | 1 | 1 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0003t0001g0007 | 0/0 | 9 | 0 | 4 | 0 | 4 | 1 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0003t0001g0010 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0003t0001g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0003t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0003t0001g0042 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0003t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0003t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0003t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0003t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0003t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0003t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0003t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0003t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0003t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0003t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0003t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0003t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0003t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0003t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0003t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0003t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0004t0002g0006 | 0/1 | 13 | 0 | 1 | 7 | 0 | 4 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0004t0002g0012 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0004t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0004t0003g0011 | 0/0 | 6 | 0 | 6 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0004t0003g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0004t0003g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0004t0003g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0006t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0006t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0006t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0007t0001g0044 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0007t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0009t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0010t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0011t0007g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0012t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0001c0015t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0002c0005t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0002c0005t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0002c0005t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0003c0008t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0004c0013t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0005c0014t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
a0006c0016t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0040 | EUR | GBR | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG00099 | hp2 | a0001 | c0003 | t0001 | g0007 | EUR | GBR | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG00140 | hp1 | a0001 | c0003 | t0001 | g0005 | EUR | GBR | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0013 | EUR | GBR | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG00280 | hp2 | a0001 | c0001 | t0006 | g0120 | EUR | FIN | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG00408 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | CHS | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | CHS | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG00438 | hp1 | a0001 | c0003 | t0001 | g0135 | EAS | CHS | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG00544 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG00642 | hp2 | a0001 | c0002 | t0001 | g0032 | AMR | PUR | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG00733 | hp2 | a0001 | c0004 | t0003 | g0011 | AMR | PUR | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG00741 | hp1 | a0001 | c0003 | t0001 | g0007 | AMR | PUR | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG01069 | hp1 | a0001 | c0002 | t0001 | g0031 | AMR | PUR | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG01070 | hp1 | a0001 | c0004 | t0003 | g0055 | AMR | PUR | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG01071 | hp2 | a0001 | c0002 | t0001 | g0031 | AMR | PUR | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG01081 | hp1 | a0001 | c0001 | t0006 | g0122 | AMR | PUR | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG01099 | hp1 | a0001 | c0004 | t0003 | g0011 | AMR | PUR | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG01106 | hp1 | a0001 | c0002 | t0001 | g0111 | AMR | PUR | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG01168 | hp1 | a0001 | c0003 | t0001 | g0007 | AMR | PUR | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG01192 | hp1 | a0001 | c0004 | t0003 | g0011 | AMR | PUR | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG01192 | hp2 | a0001 | c0003 | t0001 | g0136 | AMR | PUR | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG01243 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG01255 | hp1 | a0001 | c0001 | t0009 | g0003 | AMR | CLM | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG01256 | hp1 | a0001 | c0004 | t0003 | g0011 | AMR | CLM | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG01256 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG01257 | hp1 | a0001 | c0003 | t0001 | g0007 | AMR | CLM | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG01258 | hp1 | a0001 | c0003 | t0001 | g0007 | AMR | CLM | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG01258 | hp2 | a0001 | c0004 | t0003 | g0011 | AMR | CLM | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG01261 | hp2 | a0001 | c0003 | t0001 | g0144 | AMR | CLM | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG01346 | hp1 | a0001 | c0003 | t0001 | g0145 | AMR | CLM | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG01346 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG01361 | hp1 | a0001 | c0003 | t0001 | g0005 | AMR | CLM | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | CLM | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | CLM | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG01496 | hp2 | a0001 | c0004 | t0002 | g0006 | AMR | CLM | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0054 | EUR | IBS | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG01515 | hp2 | a0001 | c0002 | t0001 | g0001 | EUR | IBS | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG01516 | hp1 | a0001 | c0003 | t0001 | g0007 | EUR | IBS | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG01516 | hp2 | a0001 | c0002 | t0001 | g0102 | EUR | IBS | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG01517 | hp1 | a0001 | c0003 | t0001 | g0007 | EUR | IBS | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG01884 | hp1 | a0001 | c0003 | t0001 | g0152 | AFR | ACB | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | ACB | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PEL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PEL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG01978 | hp1 | a0001 | c0003 | t0001 | g0005 | AMR | PEL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PEL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG01981 | hp1 | a0001 | c0004 | t0003 | g0011 | AMR | PEL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG01981 | hp2 | a0001 | c0003 | t0001 | g0005 | AMR | PEL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG01993 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG01993 | hp2 | a0001 | c0003 | t0001 | g0005 | AMR | PEL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG02015 | hp1 | a0001 | c0002 | t0001 | g0098 | EAS | KHV | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG02040 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | ACB | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG02056 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | KHV | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG02071 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG02071 | hp2 | a0001 | c0002 | t0001 | g0099 | EAS | KHV | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG02074 | hp1 | a0001 | c0002 | t0001 | g0015 | EAS | KHV | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG02080 | hp1 | a0001 | c0004 | t0002 | g0012 | EAS | KHV | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG02080 | hp2 | a0001 | c0002 | t0001 | g0030 | EAS | KHV | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG02129 | hp2 | a0001 | c0004 | t0002 | g0012 | EAS | KHV | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG02135 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | ACB | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG02148 | hp1 | a0001 | c0015 | t0001 | g0001 | AMR | PEL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG02155 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CDX | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG02165 | hp1 | a0001 | c0004 | t0002 | g0006 | EAS | CDX | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG02165 | hp2 | a0001 | c0004 | t0002 | g0012 | EAS | CDX | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | ACB | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | ACB | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG02273 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG02280 | hp2 | a0001 | c0011 | t0007 | g0064 | AFR | ACB | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG02293 | hp2 | a0001 | c0004 | t0003 | g0052 | AMR | PEL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | PEL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG02451 | hp1 | a0001 | c0003 | t0001 | g0010 | AFR | ACB | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG02523 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG02523 | hp2 | a0005 | c0014 | t0001 | g0030 | EAS | KHV | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG02572 | hp1 | a0001 | c0003 | t0001 | g0010 | AFR | GWD | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG02602 | hp2 | a0001 | c0003 | t0001 | g0007 | SAS | PJL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | GWD | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG02622 | hp2 | a0001 | c0010 | t0001 | g0105 | AFR | GWD | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG02630 | hp2 | a0001 | c0003 | t0001 | g0150 | AFR | GWD | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG02647 | hp1 | a0001 | c0003 | t0001 | g0147 | AFR | GWD | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG02647 | hp2 | a0001 | c0006 | t0001 | g0037 | AFR | GWD | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG02698 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG02698 | hp2 | a0001 | c0004 | t0002 | g0006 | SAS | PJL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG02735 | hp2 | a0001 | c0004 | t0002 | g0006 | SAS | PJL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG02738 | hp2 | a0001 | c0002 | t0001 | g0034 | SAS | PJL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG02886 | hp1 | a0001 | c0001 | t0008 | g0121 | AFR | GWD | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG02886 | hp2 | a0001 | c0006 | t0001 | g0113 | AFR | GWD | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG02895 | hp2 | a0001 | c0003 | t0001 | g0149 | AFR | GWD | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | GWD | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG02922 | hp2 | a0001 | c0003 | t0001 | g0010 | AFR | ESN | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG02965 | hp1 | a0001 | c0003 | t0001 | g0010 | AFR | ESN | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | ESN | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG02970 | hp1 | a0001 | c0003 | t0001 | g0151 | AFR | ESN | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG02976 | hp2 | a0001 | c0001 | t0005 | g0003 | AFR | ESN | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG03017 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG03017 | hp2 | a0001 | c0003 | t0001 | g0005 | SAS | PJL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG03098 | hp1 | a0001 | c0001 | t0005 | g0003 | AFR | MSL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG03098 | hp2 | a0001 | c0003 | t0001 | g0148 | AFR | MSL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG03130 | hp2 | a0002 | c0005 | t0001 | g0023 | AFR | ESN | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG03195 | hp1 | a0001 | c0001 | t0010 | g0060 | AFR | ESN | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | ESN | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG03209 | hp2 | a0001 | c0003 | t0001 | g0010 | AFR | MSL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG03239 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | MSL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | MSL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | MSL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG03490 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG03491 | hp2 | a0001 | c0007 | t0001 | g0044 | SAS | PJL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | ESN | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG03516 | hp2 | a0001 | c0003 | t0001 | g0010 | AFR | ESN | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | MSL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG03704 | hp1 | a0001 | c0002 | t0001 | g0104 | SAS | PJL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG03710 | hp1 | a0001 | c0004 | t0002 | g0006 | SAS | PJL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG03710 | hp2 | a0001 | c0007 | t0001 | g0044 | SAS | PJL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG03834 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | BEB | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG03834 | hp2 | a0001 | c0004 | t0002 | g0006 | SAS | BEB | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG03927 | hp1 | a0001 | c0003 | t0001 | g0042 | SAS | BEB | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG03927 | hp2 | a0001 | c0002 | t0001 | g0017 | SAS | BEB | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG03942 | hp2 | a0001 | c0007 | t0001 | g0137 | SAS | BEB | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | STU | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG04115 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | STU | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | STU | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG04199 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | STU | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG04204 | hp1 | a0001 | c0003 | t0001 | g0042 | SAS | STU | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0119 | SAS | STU | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG04228 | hp1 | a0001 | c0004 | t0003 | g0050 | SAS | STU | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG04228 | hp2 | a0001 | c0002 | t0001 | g0034 | SAS | STU | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA18522 | hp1 | a0002 | c0005 | t0001 | g0023 | AFR | YRI | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | YRI | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHB | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA18612 | hp2 | a0001 | c0004 | t0002 | g0006 | EAS | CHB | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHB | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA18747 | hp2 | a0001 | c0009 | t0001 | g0062 | EAS | CHB | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | YRI | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA18906 | hp2 | a0002 | c0005 | t0001 | g0047 | AFR | YRI | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA18939 | hp2 | a0001 | c0002 | t0001 | g0015 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA18943 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA18945 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA18946 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA18947 | hp1 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA18948 | hp1 | a0003 | c0008 | t0001 | g0134 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA18950 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA18950 | hp2 | a0001 | c0003 | t0001 | g0005 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA18951 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA18953 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA18953 | hp2 | a0001 | c0003 | t0001 | g0005 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA18954 | hp1 | a0001 | c0002 | t0001 | g0101 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA18959 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA18960 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA18960 | hp2 | a0001 | c0003 | t0001 | g0005 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA18961 | hp2 | a0001 | c0003 | t0001 | g0005 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA18962 | hp2 | a0001 | c0002 | t0004 | g0001 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA18964 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA18965 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA18965 | hp2 | a0001 | c0003 | t0001 | g0141 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA18967 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA18968 | hp2 | a0001 | c0003 | t0001 | g0005 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA18970 | hp2 | a0001 | c0004 | t0002 | g0012 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA18971 | hp1 | a0001 | c0004 | t0002 | g0006 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA18971 | hp2 | a0001 | c0002 | t0004 | g0001 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA18973 | hp2 | a0001 | c0003 | t0001 | g0021 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA18974 | hp1 | a0001 | c0003 | t0001 | g0046 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA18974 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA18975 | hp2 | a0001 | c0003 | t0001 | g0005 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA18977 | hp1 | a0001 | c0002 | t0001 | g0033 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA18979 | hp1 | a0001 | c0002 | t0001 | g0033 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA18979 | hp2 | a0001 | c0002 | t0001 | g0015 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA18981 | hp1 | a0001 | c0002 | t0001 | g0072 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA18984 | hp2 | a0001 | c0004 | t0002 | g0006 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA18985 | hp1 | a0001 | c0012 | t0001 | g0017 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA18986 | hp2 | a0001 | c0002 | t0001 | g0015 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA18988 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA18990 | hp2 | a0001 | c0002 | t0001 | g0100 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA18991 | hp1 | a0001 | c0002 | t0001 | g0103 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA18993 | hp1 | a0001 | c0003 | t0001 | g0045 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA18993 | hp2 | a0001 | c0002 | t0004 | g0001 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA18997 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA18999 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA19000 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA19000 | hp2 | a0001 | c0003 | t0001 | g0005 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA19001 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA19002 | hp2 | a0001 | c0004 | t0002 | g0051 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA19005 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA19010 | hp1 | a0001 | c0004 | t0002 | g0006 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | LWK | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | LWK | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA19043 | hp1 | a0001 | c0006 | t0001 | g0112 | AFR | LWK | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | LWK | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA19054 | hp1 | a0001 | c0002 | t0001 | g0032 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA19054 | hp2 | a0001 | c0004 | t0002 | g0006 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA19055 | hp1 | a0006 | c0016 | t0001 | g0068 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA19055 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA19056 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA19056 | hp2 | a0001 | c0003 | t0001 | g0039 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA19057 | hp1 | a0004 | c0013 | t0001 | g0059 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA19060 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA19060 | hp2 | a0001 | c0004 | t0002 | g0006 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA19062 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA19064 | hp2 | a0001 | c0002 | t0001 | g0063 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA19065 | hp1 | a0001 | c0003 | t0001 | g0142 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA19068 | hp2 | a0001 | c0004 | t0002 | g0012 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA19070 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA19076 | hp1 | a0001 | c0002 | t0001 | g0058 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA19077 | hp2 | a0001 | c0002 | t0001 | g0015 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA19078 | hp2 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA19079 | hp1 | a0001 | c0003 | t0001 | g0039 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA19080 | hp1 | a0001 | c0003 | t0001 | g0005 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA19080 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA19081 | hp2 | a0001 | c0003 | t0001 | g0045 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA19082 | hp2 | a0001 | c0003 | t0001 | g0005 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA19084 | hp1 | a0001 | c0003 | t0001 | g0021 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA19087 | hp1 | a0001 | c0003 | t0001 | g0021 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA19088 | hp2 | a0001 | c0003 | t0001 | g0005 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA19090 | hp2 | a0001 | c0003 | t0001 | g0046 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA19240 | hp1 | a0001 | c0003 | t0001 | g0010 | AFR | YRI | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA19240 | hp2 | a0001 | c0006 | t0001 | g0037 | AFR | YRI | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | ASW | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA20129 | hp2 | a0001 | c0001 | t0005 | g0003 | AFR | ASW | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA20752 | hp2 | a0001 | c0003 | t0001 | g0007 | EUR | TSI | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0019 | EUR | TSI | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA20905 | hp1 | a0001 | c0003 | t0001 | g0143 | SAS | GIH | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | GIH | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | CLM | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG02559 | hp1 | a0001 | c0003 | t0001 | g0146 | AFR | ACB | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | MSL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | MSL | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG06807 | hp1 | a0002 | c0005 | t0001 | g0002 | AFR | USA | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | USA | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA18955 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | USA | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | USA | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
homoSapiens_chm13v2 | hp1 | a0001 | c0004 | t0002 | g0006 | REF | REF | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0002 | REF | REF | RNF20_chr9_101528853_101568344 | RNF20 | chr9 | 101528853 | 101568344 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:101540967
|
A | G | 1 | a0006 | 1 | NA19055.hp1 | missense_variant | MODERATE | c.620A>G | p.Asn207Ser | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 5/20 | 708/3938 | 620/2928 | 207/975 | chr9 | 101540967 | ||
chr9:101551685
|
G | A | 1 | a0003 | 1 | NA18948.hp1 | missense_variant&splice_region_variant | MODERATE | c.1274G>A | p.Arg425Gln | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 11/20 | 1362/3938 | 1274/2928 | 425/975 | chr9 | 101551685 | ||
chr9:101552453
|
C | T | 1 | a0005 | 1 | HG02523.hp2 | missense_variant | MODERATE | c.1601C>T | p.Ala534Val | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 13/20 | 1689/3938 | 1601/2928 | 534/975 | chr9 | 101552453 | ||
chr9:101552664
|
A | C | 1 | a0004 | 1 | NA19057.hp1 | missense_variant | MODERATE | c.1812A>C | p.Arg604Ser | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 13/20 | 1900/3938 | 1812/2928 | 604/975 | chr9 | 101552664 | ||
chr9:101561177
|
G | A | 1 | a0002 | 4 | HG03130.hp2 HG06807.hp1 NA18522.hp1 others(1): Show |
missense_variant | MODERATE | c.2596G>A | p.Val866Met | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 18/20 | 2684/3938 | 2596/2928 | 866/975 | chr9 | 101561177 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:101540343
|
A | G | 1 | a0001c0004 | 28 | HG00733.hp2 HG01070.hp1 HG01099.hp1 others(25): Show |
synonymous_variant | LOW | c.270A>G | p.Leu90Leu | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 3/20 | 358/3938 | 270/2928 | 90/975 | chr9 | 101540343 | ||
chr9:101544780
|
G | T | 1 | a0001c0007 | 3 | HG03491.hp2 HG03710.hp2 HG03942.hp2 |
synonymous_variant | LOW | c.642G>T | p.Val214Val | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 6/20 | 730/3938 | 642/2928 | 214/975 | chr9 | 101544780 | ||
chr9:101547163
|
T | C | 2 | a0001c0003a0003c0008 | 58 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(55): Show |
synonymous_variant | LOW | c.921T>C | p.Tyr307Tyr | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 8/20 | 1009/3938 | 921/2928 | 307/975 | chr9 | 101547163 | ||
chr9:101547172
|
G | C | 1 | a0001c0009 | 1 | NA18747.hp2 | synonymous_variant | LOW | c.930G>C | p.Gly310Gly | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 8/20 | 1018/3938 | 930/2928 | 310/975 | chr9 | 101547172 | ||
chr9:101547416
|
A | G | 1 | a0001c0015 | 1 | HG02148.hp1 | synonymous_variant | LOW | c.990A>G | p.Ala330Ala | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 9/20 | 1078/3938 | 990/2928 | 330/975 | chr9 | 101547416 | ||
chr9:101550656
|
T | C | 1 | a0001c0010 | 1 | HG02622.hp2 | synonymous_variant | LOW | c.1143T>C | p.Tyr381Tyr | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 10/20 | 1231/3938 | 1143/2928 | 381/975 | chr9 | 101550656 | ||
chr9:101552733
|
A | G | 1 | a0001c0006 | 4 | HG02647.hp2 HG02886.hp2 NA19043.hp1 others(1): Show |
synonymous_variant | LOW | c.1881A>G | p.Lys627Lys | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 13/20 | 1969/3938 | 1881/2928 | 627/975 | chr9 | 101552733 | ||
chr9:101554063
|
C | T | 1 | a0001c0012 | 1 | NA18985.hp1 | synonymous_variant | LOW | c.1977C>T | p.Asp659Asp | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 14/20 | 2065/3938 | 1977/2928 | 659/975 | chr9 | 101554063 | ||
chr9:101554087
|
G | A | 1 | a0001c0011 | 1 | HG02280.hp2 | synonymous_variant | LOW | c.2001G>A | p.Glu667Glu | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 14/20 | 2089/3938 | 2001/2928 | 667/975 | chr9 | 101554087 | ||
chr9:101562263
|
G | A | 5 | a0001c0002a0001c0009a0001c0012others(2): Show | 81 | HG00408.hp2 HG00544.hp2 HG00642.hp2 others(78): Show |
synonymous_variant | LOW | c.2769G>A | p.Pro923Pro | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 20/20 | 2857/3938 | 2769/2928 | 923/975 | chr9 | 101562263 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:101533882
|
G | C | 1 | a0001c0002t0004 | 3 | NA18962.hp2 NA18971.hp2 NA18993.hp2 |
5_prime_UTR_variant | MODIFIER | c.-59G>C | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 1/20 | 1542 | chr9 | 101533882 | |||||
chr9:101533899
|
C | A | 1 | a0001c0011t0007 | 1 | HG02280.hp2 | 5_prime_UTR_variant | MODIFIER | c.-42C>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 1/20 | 1525 | chr9 | 101533899 | |||||
chr9:101535411
|
T | A | 2 | a0001c0004t0002a0001c0004t0003 | 28 | HG00733.hp2 HG01070.hp1 HG01099.hp1 others(25): Show |
5_prime_UTR_variant | MODIFIER | c.-13T>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/20 | 13 | chr9 | 101535411 | |||||
chr9:101562581
|
G | A | 1 | a0001c0001t0008 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*159G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 20/20 | 159 | chr9 | 101562581 | |||||
chr9:101562652
|
T | C | 1 | a0001c0001t0009 | 1 | HG01255.hp1 | 3_prime_UTR_variant | MODIFIER | c.*230T>C | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 20/20 | 230 | chr9 | 101562652 | |||||
chr9:101562920
|
C | T | 2 | a0001c0001t0006a0001c0004t0002 | 21 | HG00280.hp2 HG01081.hp1 HG01496.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*498C>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 20/20 | 498 | chr9 | 101562920 | |||||
chr9:101563068
|
T | A | 1 | a0001c0001t0010 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*646T>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 20/20 | 646 | chr9 | 101563068 | |||||
chr9:101563205
|
A | G | 1 | a0001c0001t0005 | 3 | HG02976.hp2 HG03098.hp1 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*783A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 20/20 | 783 | chr9 | 101563205 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:101533991
|
A | G | 54 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0022others(51): Show | 120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.-27+77A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 1/19 | chr9 | 101533991 | ||||||
chr9:101534036
|
G | T | 1 | a0001c0001t0001g0153 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-27+122G>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 1/19 | chr9 | 101534036 | ||||||
chr9:101534061
|
A | G | 1 | a0001c0003t0001g0152 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-27+147A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 1/19 | chr9 | 101534061 | ||||||
chr9:101534462
|
G | C | 2 | a0002c0005t0001g0023a0002c0005t0001g0047 | 3 | HG03130.hp2 NA18522.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-27+548G>C | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 1/19 | chr9 | 101534462 | ||||||
chr9:101534549
|
ATTCT | A | 3 | a0001c0001t0001g0024a0001c0001t0001g0048a0001c0001t0001g0049 | 4 | HG00639.hp1 HG00735.hp1 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.-27+640_-27+643del others(4): Show |
RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr9 | 101534549 | |||||
chr9:101534669
|
A | G | 12 | a0001c0003t0001g0007a0001c0003t0001g0010a0001c0003t0001g0143others(9): Show | 26 | HG00099.hp2 HG00741.hp1 HG01168.hp1 others(23): Show |
intron_variant | MODIFIER | c.-26-729A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 1/19 | chr9 | 101534669 | ||||||
chr9:101534909
|
CT | C | 8 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0004t0002g0006others(5): Show | 29 | HG00733.hp2 HG01099.hp1 HG01192.hp1 others(26): Show |
intron_variant | MODIFIER | c.-26-473delT | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr9 | 101534909 | |||||
chr9:101534930
|
C | G | 1 | a0001c0001t0001g0115 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-26-468C>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 1/19 | chr9 | 101534930 | ||||||
chr9:101535024
|
T | C | 7 | a0001c0004t0002g0006a0001c0004t0002g0012a0001c0004t0002g0051others(4): Show | 28 | HG00733.hp2 HG01070.hp1 HG01099.hp1 others(25): Show |
intron_variant | MODIFIER | c.-26-374T>C | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 1/19 | chr9 | 101535024 | ||||||
chr9:101535049
|
C | A | 7 | a0001c0004t0002g0006a0001c0004t0002g0012a0001c0004t0002g0051others(4): Show | 28 | HG00733.hp2 HG01070.hp1 HG01099.hp1 others(25): Show |
intron_variant | MODIFIER | c.-26-349C>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 1/19 | chr9 | 101535049 | ||||||
chr9:101535049
|
C | G | 1 | a0001c0001t0001g0114 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-26-349C>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 1/19 | chr9 | 101535049 | ||||||
chr9:101535109
|
G | A | 1 | a0002c0005t0001g0047 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-26-289G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 1/19 | chr9 | 101535109 | ||||||
chr9:101535202
|
C | G | 3 | a0001c0006t0001g0037a0001c0006t0001g0112a0001c0006t0001g0113 | 4 | HG02647.hp2 HG02886.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.-26-196C>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 1/19 | chr9 | 101535202 | ||||||
chr9:101535233
|
AT | A | 5 | a0001c0001t0001g0018a0001c0001t0001g0056a0001c0001t0001g0057others(2): Show | 7 | HG02280.hp1 HG02622.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.-26-151delT | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr9 | 101535233 | |||||
chr9:101535561
|
A | G | 1 | a0001c0006t0001g0113 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.129+9A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/19 | chr9 | 101535561 | ||||||
chr9:101535753
|
T | C | 1 | a0004c0013t0001g0059 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.129+201T>C | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/19 | chr9 | 101535753 | ||||||
chr9:101535874
|
C | T | 1 | a0001c0002t0001g0111 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.129+322C>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/19 | chr9 | 101535874 | ||||||
chr9:101536019
|
A | G | 2 | a0001c0001t0001g0036a0001c0001t0001g0110 | 3 | HG02055.hp1 HG03486.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.129+467A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/19 | chr9 | 101536019 | ||||||
chr9:101536102
|
A | G | 1 | a0001c0001t0001g0109 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.129+550A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/19 | chr9 | 101536102 | ||||||
chr9:101536152
|
A | C | 3 | a0001c0003t0001g0046a0001c0003t0001g0141a0001c0003t0001g0142 | 4 | NA18965.hp2 NA18974.hp1 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.129+600A>C | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/19 | chr9 | 101536152 | ||||||
chr9:101536243
|
T | C | 2 | a0001c0001t0001g0061a0001c0001t0010g0060 | 2 | HG03195.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.129+691T>C | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/19 | chr9 | 101536243 | ||||||
chr9:101536424
|
G | C | 5 | a0001c0003t0001g0007a0001c0003t0001g0143a0001c0003t0001g0144others(2): Show | 13 | HG00099.hp2 HG00741.hp1 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.129+872G>C | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/19 | chr9 | 101536424 | ||||||
chr9:101536464
|
A | G | 2 | a0001c0001t0001g0107a0001c0001t0001g0108 | 2 | NA18986.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.129+912A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/19 | chr9 | 101536464 | ||||||
chr9:101536776
|
A | T | 1 | a0001c0001t0001g0153 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.129+1224A>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/19 | chr9 | 101536776 | ||||||
chr9:101536803
|
G | A | 1 | a0001c0009t0001g0062 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.129+1251G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/19 | chr9 | 101536803 | ||||||
chr9:101536917
|
T | C | 7 | a0001c0004t0002g0006a0001c0004t0002g0012a0001c0004t0002g0051others(4): Show | 28 | HG00733.hp2 HG01070.hp1 HG01099.hp1 others(25): Show |
intron_variant | MODIFIER | c.129+1365T>C | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/19 | chr9 | 101536917 | ||||||
chr9:101536933
|
C | T | 1 | a0001c0001t0001g0024 | 2 | HG00639.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.129+1381C>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/19 | chr9 | 101536933 | ||||||
chr9:101537011
|
C | T | 38 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0022others(35): Show | 89 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.129+1459C>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/19 | chr9 | 101537011 | ||||||
chr9:101537021
|
C | T | 1 | a0001c0001t0001g0106 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.129+1469C>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/19 | chr9 | 101537021 | ||||||
chr9:101537050
|
G | A | 1 | a0001c0001t0001g0118 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.129+1498G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/19 | chr9 | 101537050 | ||||||
chr9:101537197
|
A | T | 1 | a0001c0001t0001g0035 | 2 | NA18939.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.129+1645A>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/19 | chr9 | 101537197 | ||||||
chr9:101537203
|
G | C | 1 | a0001c0001t0001g0013 | 5 | HG00140.hp2 HG01257.hp2 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.129+1651G>C | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/19 | chr9 | 101537203 | ||||||
chr9:101537221
|
A | G | 1 | a0001c0001t0001g0140 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.129+1669A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/19 | chr9 | 101537221 | ||||||
chr9:101537277
|
G | A | 1 | a0001c0002t0001g0063 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.129+1725G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/19 | chr9 | 101537277 | ||||||
chr9:101537283
|
T | C | 38 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0022others(35): Show | 89 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.129+1731T>C | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/19 | chr9 | 101537283 | ||||||
chr9:101537523
|
TG | T | 7 | a0001c0004t0002g0006a0001c0004t0002g0012a0001c0004t0002g0051others(4): Show | 28 | HG00733.hp2 HG01070.hp1 HG01099.hp1 others(25): Show |
intron_variant | MODIFIER | c.129+1974delG | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | 101537523 | |||||
chr9:101537539
|
G | A | 1 | a0001c0011t0007g0064 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.129+1987G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/19 | chr9 | 101537539 | ||||||
chr9:101537591
|
A | G | 38 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0022others(35): Show | 89 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.129+2039A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/19 | chr9 | 101537591 | ||||||
chr9:101537798
|
A | G | 94 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0022others(91): Show | 240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.129+2246A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/19 | chr9 | 101537798 | ||||||
chr9:101537842
|
A | G | 3 | a0001c0001t0001g0097a0001c0001t0001g0107a0001c0001t0001g0108 | 3 | NA18986.hp1 NA19007.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.129+2290A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/19 | chr9 | 101537842 | ||||||
chr9:101537942
|
A | T | 1 | a0001c0001t0001g0029 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.130-2261A>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/19 | chr9 | 101537942 | ||||||
chr9:101537994
|
G | A | 2 | a0001c0001t0001g0036a0001c0001t0001g0110 | 3 | HG02055.hp1 HG03486.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.130-2209G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/19 | chr9 | 101537994 | ||||||
chr9:101537995
|
A | C | 1 | a0001c0001t0001g0115 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.130-2208A>C | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/19 | chr9 | 101537995 | ||||||
chr9:101538169
|
A | G | 1 | a0001c0001t0001g0153 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.130-2034A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/19 | chr9 | 101538169 | ||||||
chr9:101538300
|
G | A | 1 | a0001c0004t0003g0050 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.130-1903G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/19 | chr9 | 101538300 | ||||||
chr9:101538390
|
C | T | 3 | a0001c0001t0001g0061a0001c0001t0010g0060a0001c0010t0001g0105 | 3 | HG02622.hp2 HG03195.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.130-1813C>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/19 | chr9 | 101538390 | ||||||
chr9:101538550
|
G | C | 3 | a0001c0004t0002g0006a0001c0004t0002g0012a0001c0004t0002g0051 | 19 | HG01496.hp2 HG02080.hp1 HG02129.hp2 others(16): Show |
intron_variant | MODIFIER | c.130-1653G>C | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/19 | chr9 | 101538550 | ||||||
chr9:101538778
|
G | A | 1 | a0001c0001t0001g0116 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.130-1425G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/19 | chr9 | 101538778 | ||||||
chr9:101538818
|
T | C | 2 | a0001c0001t0001g0061a0001c0001t0010g0060 | 2 | HG03195.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.130-1385T>C | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/19 | chr9 | 101538818 | ||||||
chr9:101538857
|
G | T | 1 | a0001c0011t0007g0064 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.130-1346G>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/19 | chr9 | 101538857 | ||||||
chr9:101538990
|
C | T | 3 | a0001c0006t0001g0037a0001c0006t0001g0112a0001c0006t0001g0113 | 4 | HG02647.hp2 HG02886.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.130-1213C>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/19 | chr9 | 101538990 | ||||||
chr9:101539224
|
A | G | 92 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0022others(89): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.130-979A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/19 | chr9 | 101539224 | ||||||
chr9:101539226
|
A | G | 3 | a0001c0004t0002g0006a0001c0004t0002g0012a0001c0004t0002g0051 | 19 | HG01496.hp2 HG02080.hp1 HG02129.hp2 others(16): Show |
intron_variant | MODIFIER | c.130-977A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/19 | chr9 | 101539226 | ||||||
chr9:101539253
|
G | T | 1 | a0001c0001t0001g0057 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.130-950G>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/19 | chr9 | 101539253 | ||||||
chr9:101539274
|
C | T | 1 | a0001c0003t0001g0151 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.130-929C>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/19 | chr9 | 101539274 | ||||||
chr9:101539280
|
C | T | 1 | a0001c0001t0001g0153 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.130-923C>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/19 | chr9 | 101539280 | ||||||
chr9:101539602
|
C | T | 1 | a0001c0001t0001g0096 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.130-601C>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/19 | chr9 | 101539602 | ||||||
chr9:101539661
|
A | G | 23 | a0001c0002t0001g0001a0001c0002t0001g0015a0001c0002t0001g0017others(20): Show | 80 | HG00408.hp2 HG00544.hp2 HG00642.hp2 others(77): Show |
intron_variant | MODIFIER | c.130-542A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/19 | chr9 | 101539661 | ||||||
chr9:101539883
|
A | T | 92 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0022others(89): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.130-320A>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/19 | chr9 | 101539883 | ||||||
chr9:101539973
|
G | A | 1 | a0001c0002t0001g0098 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.130-230G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/19 | chr9 | 101539973 | ||||||
chr9:101540185
|
G | A | 2 | a0001c0001t0001g0153a0001c0010t0001g0105 | 2 | HG02145.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.130-18G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 2/19 | chr9 | 101540185 | ||||||
chr9:101540453
|
C | T | 1 | a0001c0003t0001g0045 | 2 | NA18993.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.298-37C>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 3/19 | chr9 | 101540453 | ||||||
chr9:101540454
|
C | G | 1 | a0001c0003t0001g0146 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.298-36C>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 3/19 | chr9 | 101540454 | ||||||
chr9:101540676
|
T | C | 2 | a0001c0001t0001g0036a0001c0001t0001g0110 | 3 | HG02055.hp1 HG03486.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.445+39T>C | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 4/19 | chr9 | 101540676 | ||||||
chr9:101541018
|
A | G | 1 | a0001c0001t0001g0095 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.628+43A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 5/19 | chr9 | 101541018 | ||||||
chr9:101541295
|
T | C | 24 | a0001c0002t0001g0001a0001c0002t0001g0015a0001c0002t0001g0017others(21): Show | 81 | HG00408.hp2 HG00544.hp2 HG00642.hp2 others(78): Show |
intron_variant | MODIFIER | c.628+320T>C | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 5/19 | chr9 | 101541295 | ||||||
chr9:101541371
|
A | G | 94 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0022others(91): Show | 240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.628+396A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 5/19 | chr9 | 101541371 | ||||||
chr9:101541399
|
A | G | 1 | a0001c0002t0001g0104 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.628+424A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 5/19 | chr9 | 101541399 | ||||||
chr9:101541607
|
G | A | 8 | a0001c0004t0002g0006a0001c0004t0002g0012a0001c0004t0002g0051others(5): Show | 29 | HG00733.hp2 HG01070.hp1 HG01099.hp1 others(26): Show |
intron_variant | MODIFIER | c.628+632G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 5/19 | chr9 | 101541607 | ||||||
chr9:101541946
|
A | C | 1 | a0001c0001t0001g0153 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.628+971A>C | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 5/19 | chr9 | 101541946 | ||||||
chr9:101542116
|
A | G | 1 | a0001c0010t0001g0105 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.628+1141A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 5/19 | chr9 | 101542116 | ||||||
chr9:101542206
|
A | G | 1 | a0001c0004t0003g0052 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.628+1231A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 5/19 | chr9 | 101542206 | ||||||
chr9:101542337
|
A | C | 1 | a0001c0001t0001g0115 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.628+1362A>C | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 5/19 | chr9 | 101542337 | ||||||
chr9:101542644
|
A | G | 1 | a0001c0003t0001g0142 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.628+1669A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 5/19 | chr9 | 101542644 | ||||||
chr9:101542816
|
C | T | 23 | a0001c0002t0001g0001a0001c0002t0001g0015a0001c0002t0001g0017others(20): Show | 80 | HG00408.hp2 HG00544.hp2 HG00642.hp2 others(77): Show |
intron_variant | MODIFIER | c.628+1841C>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 5/19 | chr9 | 101542816 | ||||||
chr9:101542893
|
A | T | 1 | a0001c0001t0001g0038 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.629-1874A>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 5/19 | chr9 | 101542893 | ||||||
chr9:101542954
|
T | G | 2 | a0001c0001t0001g0025a0001c0001t0001g0065 | 3 | HG01934.hp2 HG01943.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.629-1813T>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 5/19 | chr9 | 101542954 | ||||||
chr9:101543266
|
A | C | 1 | a0001c0011t0007g0064 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.629-1501A>C | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 5/19 | chr9 | 101543266 | ||||||
chr9:101543295
|
G | GCCAGGGC others(17): Show |
9 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0004t0002g0006others(6): Show | 30 | HG00733.hp2 HG01070.hp1 HG01099.hp1 others(27): Show |
intron_variant | MODIFIER | c.629-1424_629-1401d others(26): Show |
RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr9 | 101543295 | |||||
chr9:101543295
|
GCCAGGGC others(41): Show |
G | 1 | a0001c0001t0001g0038 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.629-1448_629-1401d others(50): Show |
RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr9 | 101543295 | |||||
chr9:101543372
|
G | A | 1 | a0001c0003t0001g0021 | 3 | NA18973.hp2 NA19084.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.629-1395G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 5/19 | chr9 | 101543372 | ||||||
chr9:101543372
|
GGCGGCAC others(16): Show |
G | 3 | a0001c0003t0001g0145a0001c0007t0001g0044a0001c0007t0001g0137 | 4 | HG01346.hp1 HG03491.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.629-1356_629-1334d others(25): Show |
RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr9 | 101543372 | |||||
chr9:101543375
|
G | GGCACTGT others(17): Show |
1 | a0001c0001t0001g0053 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.629-1379_629-1378i others(26): Show |
RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr9 | 101543375 | |||||
chr9:101543445
|
G | A | 4 | a0001c0001t0001g0008a0001c0001t0001g0066a0001c0001t0001g0067others(1): Show | 10 | HG01109.hp1 HG01884.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.629-1322G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 5/19 | chr9 | 101543445 | ||||||
chr9:101543468
|
A | AGCACTGT others(17): Show |
1 | a0001c0011t0007g0064 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.629-1279_629-1256d others(26): Show |
RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr9 | 101543468 | |||||
chr9:101543468
|
A | AGCACTGT others(16): Show |
2 | a0001c0001t0001g0028a0001c0001t0001g0092 | 3 | HG01167.hp2 HG03704.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.629-1286_629-1285i others(25): Show |
RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr9 | 101543468 | |||||
chr9:101543481
|
C | T | 2 | a0001c0001t0001g0093a0001c0001t0001g0094 | 2 | NA18973.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.629-1286C>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 5/19 | chr9 | 101543481 | ||||||
chr9:101543490
|
G | A | 1 | a0001c0003t0001g0039 | 2 | NA19056.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.629-1277G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 5/19 | chr9 | 101543490 | ||||||
chr9:101543499
|
TCTAACCC others(3): Show |
T | 15 | a0001c0003t0001g0007a0001c0003t0001g0010a0001c0003t0001g0143others(12): Show | 30 | HG00099.hp2 HG00741.hp1 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.629-1266_629-1257d others(12): Show |
RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr9 | 101543499 | |||||
chr9:101543539
|
C | T | 7 | a0001c0004t0002g0006a0001c0004t0002g0012a0001c0004t0002g0051others(4): Show | 28 | HG00733.hp2 HG01070.hp1 HG01099.hp1 others(25): Show |
intron_variant | MODIFIER | c.629-1228C>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 5/19 | chr9 | 101543539 | ||||||
chr9:101543583
|
AGCGGCAC others(17): Show |
A | 1 | a0001c0001t0001g0043 | 2 | HG01433.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.629-1167_629-1144d others(26): Show |
RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr9 | 101543583 | |||||
chr9:101543592
|
G | A | 1 | a0001c0004t0003g0052 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.629-1175G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 5/19 | chr9 | 101543592 | ||||||
chr9:101543679
|
T | C | 3 | a0001c0001t0001g0061a0001c0001t0010g0060a0001c0010t0001g0105 | 3 | HG02622.hp2 HG03195.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.629-1088T>C | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 5/19 | chr9 | 101543679 | ||||||
chr9:101543737
|
C | T | 12 | a0001c0001t0001g0005a0001c0001t0001g0133a0001c0003t0001g0005others(9): Show | 34 | HG00140.hp1 HG00438.hp1 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.629-1030C>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 5/19 | chr9 | 101543737 | ||||||
chr9:101543784
|
T | C | 1 | a0001c0010t0001g0105 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.629-983T>C | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 5/19 | chr9 | 101543784 | ||||||
chr9:101543879
|
A | G | 2 | a0001c0001t0001g0131a0001c0001t0001g0132 | 2 | HG02615.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.629-888A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 5/19 | chr9 | 101543879 | ||||||
chr9:101544044
|
ACT | A | 39 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0022others(36): Show | 90 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.629-718_629-717del others(2): Show |
RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr9 | 101544044 | |||||
chr9:101544146
|
A | G | 1 | a0001c0001t0001g0153 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.629-621A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 5/19 | chr9 | 101544146 | ||||||
chr9:101544151
|
G | A | 1 | a0001c0001t0001g0119 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.629-616G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 5/19 | chr9 | 101544151 | ||||||
chr9:101544348
|
T | C | 24 | a0001c0002t0001g0001a0001c0002t0001g0015a0001c0002t0001g0017others(21): Show | 81 | HG00408.hp2 HG00544.hp2 HG00642.hp2 others(78): Show |
intron_variant | MODIFIER | c.629-419T>C | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 5/19 | chr9 | 101544348 | ||||||
chr9:101544564
|
G | T | 3 | a0001c0006t0001g0037a0001c0006t0001g0112a0001c0006t0001g0113 | 4 | HG02647.hp2 HG02886.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.629-203G>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 5/19 | chr9 | 101544564 | ||||||
chr9:101544645
|
T | G | 3 | a0001c0002t0001g0015a0001c0002t0001g0098a0001c0002t0001g0099 | 7 | HG02015.hp1 HG02071.hp2 HG02074.hp1 others(4): Show |
intron_variant | MODIFIER | c.629-122T>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 5/19 | chr9 | 101544645 | ||||||
chr9:101544664
|
G | A | 2 | a0001c0003t0001g0147a0001c0003t0001g0152 | 2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.629-103G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 5/19 | chr9 | 101544664 | ||||||
chr9:101544706
|
T | TA | 13 | a0001c0001t0001g0065a0001c0001t0001g0069a0001c0001t0001g0070others(10): Show | 21 | HG00099.hp2 HG00741.hp1 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.629-45dupA | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr9 | 101544706 | |||||
chr9:101544706
|
TA | T | 15 | a0001c0001t0001g0091a0001c0001t0001g0115a0001c0001t0001g0117others(12): Show | 36 | HG00733.hp2 HG01070.hp1 HG01099.hp1 others(33): Show |
intron_variant | MODIFIER | c.629-45delA | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr9 | 101544706 | |||||
chr9:101544763
|
C | G | 2 | a0001c0001t0001g0071a0001c0001t0001g0090 | 2 | HG03540.hp2 NA19030.hp1 |
splice_region_variant&intron_variant | LOW | c.629-4C>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 5/19 | chr9 | 101544763 | ||||||
chr9:101545050
|
C | A | 1 | a0001c0002t0001g0100 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.747+165C>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 6/19 | chr9 | 101545050 | ||||||
chr9:101545252
|
G | C | 23 | a0001c0002t0001g0001a0001c0002t0001g0015a0001c0002t0001g0017others(20): Show | 80 | HG00408.hp2 HG00544.hp2 HG00642.hp2 others(77): Show |
intron_variant | MODIFIER | c.747+367G>C | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 6/19 | chr9 | 101545252 | ||||||
chr9:101545351
|
T | C | 27 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0025others(24): Show | 55 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.747+466T>C | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 6/19 | chr9 | 101545351 | ||||||
chr9:101545418
|
A | G | 1 | a0001c0001t0001g0049 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.747+533A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 6/19 | chr9 | 101545418 | ||||||
chr9:101545510
|
G | A | 4 | a0001c0001t0001g0008a0001c0001t0001g0066a0001c0001t0001g0067others(1): Show | 10 | HG01109.hp1 HG01884.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.747+625G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 6/19 | chr9 | 101545510 | ||||||
chr9:101545554
|
T | C | 1 | a0001c0011t0007g0064 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.747+669T>C | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 6/19 | chr9 | 101545554 | ||||||
chr9:101545593
|
T | A | 38 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0022others(35): Show | 89 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.747+708T>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 6/19 | chr9 | 101545593 | ||||||
chr9:101545629
|
G | A | 2 | a0001c0001t0001g0036a0001c0001t0001g0110 | 3 | HG02055.hp1 HG03486.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.747+744G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 6/19 | chr9 | 101545629 | ||||||
chr9:101545902
|
A | T | 1 | a0001c0010t0001g0105 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.748-918A>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 6/19 | chr9 | 101545902 | ||||||
chr9:101545931
|
A | C | 1 | a0001c0010t0001g0105 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.748-889A>C | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 6/19 | chr9 | 101545931 | ||||||
chr9:101546083
|
A | G | 41 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0022others(38): Show | 93 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.748-737A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 6/19 | chr9 | 101546083 | ||||||
chr9:101546094
|
G | T | 3 | a0001c0006t0001g0037a0001c0006t0001g0112a0001c0006t0001g0113 | 4 | HG02647.hp2 HG02886.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.748-726G>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 6/19 | chr9 | 101546094 | ||||||
chr9:101546160
|
C | G | 1 | a0001c0001t0001g0080 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.748-660C>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 6/19 | chr9 | 101546160 | ||||||
chr9:101546235
|
A | G | 1 | a0001c0001t0001g0026 | 2 | NA18945.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.748-585A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 6/19 | chr9 | 101546235 | ||||||
chr9:101546265
|
G | A | 1 | a0001c0011t0007g0064 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.748-555G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 6/19 | chr9 | 101546265 | ||||||
chr9:101546595
|
T | G | 1 | a0001c0001t0006g0120 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.748-225T>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 6/19 | chr9 | 101546595 | ||||||
chr9:101546646
|
GAC | G | 3 | a0001c0006t0001g0037a0001c0006t0001g0112a0001c0006t0001g0113 | 4 | HG02647.hp2 HG02886.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.748-170_748-169del others(2): Show |
RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr9 | 101546646 | |||||
chr9:101546666
|
A | G | 1 | a0001c0001t0001g0089 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.748-154A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 6/19 | chr9 | 101546666 | ||||||
chr9:101546726
|
C | T | 1 | a0001c0001t0001g0079 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.748-94C>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 6/19 | chr9 | 101546726 | ||||||
chr9:101547597
|
C | T | 1 | a0001c0001t0001g0129 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1092+79C>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 9/19 | chr9 | 101547597 | ||||||
chr9:101547779
|
G | T | 1 | a0001c0001t0001g0020 | 3 | HG01167.hp1 HG01361.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.1092+261G>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 9/19 | chr9 | 101547779 | ||||||
chr9:101547989
|
A | G | 1 | a0001c0001t0001g0078 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1092+471A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 9/19 | chr9 | 101547989 | ||||||
chr9:101548102
|
G | A | 4 | a0001c0001t0001g0008a0001c0001t0001g0066a0001c0001t0001g0067others(1): Show | 10 | HG01109.hp1 HG01884.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.1092+584G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 9/19 | chr9 | 101548102 | ||||||
chr9:101548829
|
A | G | 1 | a0001c0004t0002g0051 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1092+1311A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 9/19 | chr9 | 101548829 | ||||||
chr9:101548864
|
C | T | 1 | a0001c0001t0001g0128 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1092+1346C>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 9/19 | chr9 | 101548864 | ||||||
chr9:101548993
|
C | T | 1 | a0001c0001t0001g0088 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1092+1475C>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 9/19 | chr9 | 101548993 | ||||||
chr9:101549069
|
T | G | 1 | a0001c0001t0001g0081 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1093-1537T>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 9/19 | chr9 | 101549069 | ||||||
chr9:101549081
|
C | T | 1 | a0001c0003t0001g0042 | 2 | HG03927.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1093-1525C>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 9/19 | chr9 | 101549081 | ||||||
chr9:101549112
|
A | G | 4 | a0001c0001t0001g0008a0001c0001t0001g0066a0001c0001t0001g0067others(1): Show | 10 | HG01109.hp1 HG01884.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.1093-1494A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 9/19 | chr9 | 101549112 | ||||||
chr9:101549165
|
G | A | 1 | a0001c0001t0008g0121 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1093-1441G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 9/19 | chr9 | 101549165 | ||||||
chr9:101549196
|
G | A | 1 | a0001c0002t0001g0072 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1093-1410G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 9/19 | chr9 | 101549196 | ||||||
chr9:101549330
|
A | T | 1 | a0001c0002t0001g0034 | 2 | HG02738.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1093-1276A>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 9/19 | chr9 | 101549330 | ||||||
chr9:101549429
|
G | A | 1 | a0001c0001t0001g0022 | 3 | HG01358.hp1 HG02145.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1093-1177G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 9/19 | chr9 | 101549429 | ||||||
chr9:101549471
|
G | A | 9 | a0001c0001t0006g0120a0001c0001t0006g0122a0001c0004t0002g0006others(6): Show | 30 | HG00280.hp2 HG00733.hp2 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.1093-1135G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 9/19 | chr9 | 101549471 | ||||||
chr9:101549499
|
A | G | 1 | a0001c0001t0001g0127 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1093-1107A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 9/19 | chr9 | 101549499 | ||||||
chr9:101549603
|
T | C | 1 | a0001c0011t0007g0064 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1093-1003T>C | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 9/19 | chr9 | 101549603 | ||||||
chr9:101549636
|
C | T | 2 | a0001c0001t0001g0038a0001c0001t0008g0121 | 3 | HG01070.hp2 HG01071.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1093-970C>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 9/19 | chr9 | 101549636 | ||||||
chr9:101549668
|
G | A | 1 | a0001c0002t0001g0111 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1093-938G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 9/19 | chr9 | 101549668 | ||||||
chr9:101549696
|
G | A | 9 | a0001c0001t0006g0120a0001c0001t0006g0122a0001c0004t0002g0006others(6): Show | 30 | HG00280.hp2 HG00733.hp2 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.1093-910G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 9/19 | chr9 | 101549696 | ||||||
chr9:101549809
|
G | T | 1 | a0001c0001t0001g0087 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1093-797G>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 9/19 | chr9 | 101549809 | ||||||
chr9:101549880
|
G | A | 3 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0091 | 7 | HG00639.hp2 HG01167.hp1 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.1093-726G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 9/19 | chr9 | 101549880 | ||||||
chr9:101549920
|
A | G | 5 | a0001c0001t0001g0041a0001c0001t0001g0126a0001c0001t0001g0131others(2): Show | 6 | HG02258.hp2 HG02615.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1093-686A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 9/19 | chr9 | 101549920 | ||||||
chr9:101550010
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1093-596C>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 9/19 | chr9 | 101550010 | ||||||
chr9:101550065
|
C | T | 25 | a0001c0002t0001g0001a0001c0002t0001g0015a0001c0002t0001g0017others(22): Show | 82 | HG00408.hp2 HG00544.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.1093-541C>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 9/19 | chr9 | 101550065 | ||||||
chr9:101550165
|
A | C | 24 | a0001c0002t0001g0001a0001c0002t0001g0015a0001c0002t0001g0017others(21): Show | 81 | HG00408.hp2 HG00544.hp2 HG00642.hp2 others(78): Show |
intron_variant | MODIFIER | c.1093-441A>C | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 9/19 | chr9 | 101550165 | ||||||
chr9:101550500
|
T | G | 1 | a0001c0001t0008g0121 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1093-106T>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 9/19 | chr9 | 101550500 | ||||||
chr9:101551147
|
A | G | 1 | a0001c0001t0001g0038 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1272+362A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 10/19 | chr9 | 101551147 | ||||||
chr9:101551171
|
C | G | 47 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0022others(44): Show | 112 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(109): Show |
intron_variant | MODIFIER | c.1272+386C>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 10/19 | chr9 | 101551171 | ||||||
chr9:101551200
|
A | G | 1 | a0001c0001t0001g0067 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1272+415A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 10/19 | chr9 | 101551200 | ||||||
chr9:101551215
|
G | C | 1 | a0001c0001t0001g0082 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1272+430G>C | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 10/19 | chr9 | 101551215 | ||||||
chr9:101551223
|
T | C | 1 | a0001c0001t0001g0109 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1272+438T>C | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 10/19 | chr9 | 101551223 | ||||||
chr9:101551550
|
A | C | 1 | a0001c0003t0001g0152 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1273-134A>C | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 10/19 | chr9 | 101551550 | ||||||
chr9:101551560
|
T | C | 2 | a0001c0003t0001g0147a0001c0003t0001g0152 | 2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1273-124T>C | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 10/19 | chr9 | 101551560 | ||||||
chr9:101551583
|
G | A | 1 | a0001c0001t0001g0153 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1273-101G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 10/19 | chr9 | 101551583 | ||||||
chr9:101551586
|
T | G | 2 | a0001c0006t0001g0037a0001c0006t0001g0113 | 3 | HG02647.hp2 HG02886.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1273-98T>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 10/19 | chr9 | 101551586 | ||||||
chr9:101551616
|
C | CATTATTG others(54): Show |
44 | a0001c0001t0001g0036a0001c0001t0001g0061a0001c0001t0001g0086others(41): Show | 117 | HG00099.hp2 HG00408.hp2 HG00544.hp2 others(114): Show |
intron_variant | MODIFIER | c.1273-66_1273-65ins others(61): Show |
RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr9 | 101551616 | |||||
chr9:101551885
|
A | G | 1 | a0001c0001t0001g0090 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1408+66A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 11/19 | chr9 | 101551885 | ||||||
chr9:101551946
|
T | A | 1 | a0001c0001t0001g0116 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1408+127T>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 11/19 | chr9 | 101551946 | ||||||
chr9:101552132
|
G | A | 1 | a0001c0001t0008g0121 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1409-9G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 11/19 | chr9 | 101552132 | ||||||
chr9:101552349
|
G | A | 2 | a0001c0007t0001g0044a0001c0007t0001g0137 | 3 | HG03491.hp2 HG03710.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1531-34G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 12/19 | chr9 | 101552349 | ||||||
chr9:101552896
|
C | G | 1 | a0001c0010t0001g0105 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1901+143C>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 13/19 | chr9 | 101552896 | ||||||
chr9:101552973
|
G | A | 24 | a0001c0002t0001g0001a0001c0002t0001g0015a0001c0002t0001g0017others(21): Show | 81 | HG00408.hp2 HG00544.hp2 HG00642.hp2 others(78): Show |
intron_variant | MODIFIER | c.1901+220G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 13/19 | chr9 | 101552973 | ||||||
chr9:101553166
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1901+413C>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 13/19 | chr9 | 101553166 | ||||||
chr9:101553301
|
G | A | 3 | a0001c0006t0001g0037a0001c0006t0001g0112a0001c0006t0001g0113 | 4 | HG02647.hp2 HG02886.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.1901+548G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 13/19 | chr9 | 101553301 | ||||||
chr9:101553413
|
A | G | 1 | a0001c0001t0001g0076 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1902-575A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 13/19 | chr9 | 101553413 | ||||||
chr9:101553649
|
T | G | 37 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0022others(34): Show | 88 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.1902-339T>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 13/19 | chr9 | 101553649 | ||||||
chr9:101553725
|
A | C | 1 | a0001c0001t0001g0066 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1902-263A>C | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 13/19 | chr9 | 101553725 | ||||||
chr9:101553896
|
T | C | 1 | a0001c0002t0001g0101 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1902-92T>C | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 13/19 | chr9 | 101553896 | ||||||
chr9:101554248
|
A | T | 1 | a0001c0001t0001g0038 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.2019+143A>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 14/19 | chr9 | 101554248 | ||||||
chr9:101554311
|
A | G | 1 | a0001c0001t0001g0085 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2019+206A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 14/19 | chr9 | 101554311 | ||||||
chr9:101554424
|
A | T | 1 | a0001c0001t0001g0126 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2020-270A>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 14/19 | chr9 | 101554424 | ||||||
chr9:101554557
|
G | A | 2 | a0001c0002t0001g0031a0001c0002t0001g0102 | 3 | HG01069.hp1 HG01071.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.2020-137G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 14/19 | chr9 | 101554557 | ||||||
chr9:101554570
|
C | T | 3 | a0001c0006t0001g0037a0001c0006t0001g0112a0001c0006t0001g0113 | 4 | HG02647.hp2 HG02886.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.2020-124C>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 14/19 | chr9 | 101554570 | ||||||
chr9:101554617
|
A | G | 1 | a0001c0003t0001g0039 | 2 | NA19056.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.2020-77A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 14/19 | chr9 | 101554617 | ||||||
chr9:101554670
|
T | A | 5 | a0001c0001t0006g0120a0001c0001t0006g0122a0001c0004t0002g0006others(2): Show | 21 | HG00280.hp2 HG01081.hp1 HG01496.hp2 others(18): Show |
intron_variant | MODIFIER | c.2020-24T>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 14/19 | chr9 | 101554670 | ||||||
chr9:101554893
|
A | T | 1 | a0001c0002t0001g0103 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.2169+50A>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 15/19 | chr9 | 101554893 | ||||||
chr9:101555024
|
T | G | 1 | a0001c0001t0001g0083 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2169+181T>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 15/19 | chr9 | 101555024 | ||||||
chr9:101555348
|
T | A | 1 | a0001c0004t0002g0012 | 5 | HG02080.hp1 HG02129.hp2 HG02165.hp2 others(2): Show |
intron_variant | MODIFIER | c.2169+505T>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 15/19 | chr9 | 101555348 | ||||||
chr9:101555384
|
A | T | 1 | a0001c0003t0001g0150 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2169+541A>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 15/19 | chr9 | 101555384 | ||||||
chr9:101555454
|
A | G | 12 | a0001c0003t0001g0007a0001c0003t0001g0010a0001c0003t0001g0143others(9): Show | 26 | HG00099.hp2 HG00741.hp1 HG01168.hp1 others(23): Show |
intron_variant | MODIFIER | c.2169+611A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 15/19 | chr9 | 101555454 | ||||||
chr9:101555476
|
A | G | 1 | a0001c0001t0001g0115 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2169+633A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 15/19 | chr9 | 101555476 | ||||||
chr9:101555757
|
G | C | 1 | a0001c0001t0001g0027 | 2 | HG04115.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.2169+914G>C | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 15/19 | chr9 | 101555757 | ||||||
chr9:101555761
|
G | A | 1 | a0001c0003t0001g0143 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2169+918G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 15/19 | chr9 | 101555761 | ||||||
chr9:101555789
|
T | TA | 8 | a0001c0001t0001g0073a0001c0001t0001g0115a0001c0001t0001g0116others(5): Show | 10 | HG01261.hp2 HG03098.hp2 HG03195.hp2 others(7): Show |
intron_variant | MODIFIER | c.2169+961dupA | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr9 | 101555789 | |||||
chr9:101555827
|
C | T | 1 | a0001c0011t0007g0064 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2169+984C>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 15/19 | chr9 | 101555827 | ||||||
chr9:101555898
|
C | T | 3 | a0001c0006t0001g0037a0001c0006t0001g0112a0001c0006t0001g0113 | 4 | HG02647.hp2 HG02886.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.2169+1055C>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 15/19 | chr9 | 101555898 | ||||||
chr9:101555997
|
T | C | 1 | a0001c0004t0003g0050 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2169+1154T>C | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 15/19 | chr9 | 101555997 | ||||||
chr9:101556005
|
G | A | 3 | a0001c0001t0001g0036a0001c0001t0001g0110a0001c0001t0010g0060 | 4 | HG02055.hp1 HG03195.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2169+1162G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 15/19 | chr9 | 101556005 | ||||||
chr9:101556009
|
C | CT | 26 | a0001c0001t0001g0086a0001c0002t0001g0001a0001c0002t0001g0015others(23): Show | 83 | HG00408.hp2 HG00544.hp2 HG00642.hp2 others(80): Show |
intron_variant | MODIFIER | c.2169+1176dupT | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr9 | 101556009 | |||||
chr9:101556276
|
A | G | 1 | a0001c0001t0001g0140 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2170-1108A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 15/19 | chr9 | 101556276 | ||||||
chr9:101556528
|
A | T | 12 | a0001c0003t0001g0007a0001c0003t0001g0010a0001c0003t0001g0143others(9): Show | 26 | HG00099.hp2 HG00741.hp1 HG01168.hp1 others(23): Show |
intron_variant | MODIFIER | c.2170-856A>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 15/19 | chr9 | 101556528 | ||||||
chr9:101556552
|
A | G | 3 | a0001c0006t0001g0037a0001c0006t0001g0112a0001c0006t0001g0113 | 4 | HG02647.hp2 HG02886.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.2170-832A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 15/19 | chr9 | 101556552 | ||||||
chr9:101556610
|
A | G | 1 | a0001c0003t0001g0136 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2170-774A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 15/19 | chr9 | 101556610 | ||||||
chr9:101556620
|
G | A | 1 | a0001c0001t0001g0133 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2170-764G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 15/19 | chr9 | 101556620 | ||||||
chr9:101556691
|
A | C | 1 | a0001c0001t0001g0086 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2170-693A>C | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 15/19 | chr9 | 101556691 | ||||||
chr9:101556777
|
T | C | 81 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0022others(78): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.2170-607T>C | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 15/19 | chr9 | 101556777 | ||||||
chr9:101556832
|
A | T | 2 | a0001c0001t0001g0131a0001c0001t0001g0132 | 2 | HG02615.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2170-552A>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 15/19 | chr9 | 101556832 | ||||||
chr9:101557042
|
T | C | 1 | a0001c0001t0001g0040 | 2 | HG00099.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.2170-342T>C | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 15/19 | chr9 | 101557042 | ||||||
chr9:101557116
|
C | T | 1 | a0001c0010t0001g0105 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2170-268C>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 15/19 | chr9 | 101557116 | ||||||
chr9:101557117
|
G | A | 1 | a0001c0001t0001g0057 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.2170-267G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 15/19 | chr9 | 101557117 | ||||||
chr9:101557648
|
C | T | 1 | a0001c0001t0001g0139 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2382+52C>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 16/19 | chr9 | 101557648 | ||||||
chr9:101557845
|
C | T | 2 | a0001c0001t0001g0069a0001c0001t0001g0075 | 2 | HG02027.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.2382+249C>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 16/19 | chr9 | 101557845 | ||||||
chr9:101557867
|
G | A | 1 | a0001c0001t0001g0014 | 5 | HG01081.hp2 HG02451.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.2382+271G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 16/19 | chr9 | 101557867 | ||||||
chr9:101557958
|
G | T | 5 | a0001c0001t0006g0120a0001c0001t0006g0122a0001c0004t0002g0006others(2): Show | 21 | HG00280.hp2 HG01081.hp1 HG01496.hp2 others(18): Show |
intron_variant | MODIFIER | c.2382+362G>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 16/19 | chr9 | 101557958 | ||||||
chr9:101558006
|
CT | C | 23 | a0001c0001t0001g0016a0001c0001t0001g0056a0001c0001t0001g0074others(20): Show | 48 | HG00280.hp2 HG00642.hp2 HG00733.hp1 others(45): Show |
intron_variant | MODIFIER | c.2382+428delT | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr9 | 101558006 | |||||
chr9:101558032
|
C | T | 1 | a0001c0002t0001g0033 | 2 | NA18977.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.2382+436C>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 16/19 | chr9 | 101558032 | ||||||
chr9:101558149
|
A | G | 9 | a0001c0001t0006g0120a0001c0001t0006g0122a0001c0004t0002g0006others(6): Show | 30 | HG00280.hp2 HG00733.hp2 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.2382+553A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 16/19 | chr9 | 101558149 | ||||||
chr9:101558150
|
T | A | 1 | a0001c0001t0001g0109 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.2382+554T>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 16/19 | chr9 | 101558150 | ||||||
chr9:101558152
|
G | A | 1 | a0001c0001t0001g0124 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2382+556G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 16/19 | chr9 | 101558152 | ||||||
chr9:101558211
|
G | A | 6 | a0001c0001t0001g0041a0001c0001t0001g0123a0001c0001t0001g0126others(3): Show | 7 | HG02258.hp2 HG02615.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.2382+615G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 16/19 | chr9 | 101558211 | ||||||
chr9:101558381
|
G | A | 7 | a0001c0003t0001g0007a0001c0003t0001g0143a0001c0003t0001g0144others(4): Show | 15 | HG00099.hp2 HG00741.hp1 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.2382+785G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 16/19 | chr9 | 101558381 | ||||||
chr9:101558394
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2382+798G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 16/19 | chr9 | 101558394 | ||||||
chr9:101558414
|
A | G | 1 | a0001c0001t0001g0092 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2382+818A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 16/19 | chr9 | 101558414 | ||||||
chr9:101558565
|
C | A | 1 | a0001c0001t0001g0084 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2382+969C>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 16/19 | chr9 | 101558565 | ||||||
chr9:101558726
|
T | C | 1 | a0001c0011t0007g0064 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2382+1130T>C | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 16/19 | chr9 | 101558726 | ||||||
chr9:101558936
|
G | A | 24 | a0001c0002t0001g0001a0001c0002t0001g0015a0001c0002t0001g0017others(21): Show | 81 | HG00408.hp2 HG00544.hp2 HG00642.hp2 others(78): Show |
intron_variant | MODIFIER | c.2382+1340G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 16/19 | chr9 | 101558936 | ||||||
chr9:101558950
|
G | A | 5 | a0001c0003t0001g0010a0001c0003t0001g0148a0001c0003t0001g0149others(2): Show | 11 | HG02451.hp1 HG02572.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.2382+1354G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 16/19 | chr9 | 101558950 | ||||||
chr9:101559141
|
A | G | 2 | a0001c0001t0001g0009a0001c0001t0001g0085 | 8 | HG01952.hp2 HG02572.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.2382+1545A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 16/19 | chr9 | 101559141 | ||||||
chr9:101559154
|
G | T | 1 | a0001c0001t0001g0038 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.2382+1558G>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 16/19 | chr9 | 101559154 | ||||||
chr9:101559324
|
G | A | 1 | a0001c0007t0001g0137 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2383-1477G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 16/19 | chr9 | 101559324 | ||||||
chr9:101560524
|
T | A | 1 | a0001c0002t0001g0099 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2383-277T>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 16/19 | chr9 | 101560524 | ||||||
chr9:101560672
|
A | T | 1 | a0001c0003t0001g0135 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2383-129A>T | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 16/19 | chr9 | 101560672 | ||||||
chr9:101561360
|
A | G | 1 | a0001c0004t0002g0051 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.2649+130A>G | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 18/19 | chr9 | 101561360 | ||||||
chr9:101562214
|
G | A | 1 | a0001c0010t0001g0105 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2752-32G>A | RNF20 | ENSG00000155827.12 | transcript | ENST00000389120.8 | protein_coding | 19/19 | chr9 | 101562214 |