geneid | 6047 |
---|---|
ensemblid | ENSG00000063978.17 |
hgncid | 10067 |
symbol | RNF4 |
name | ring finger protein 4 |
refseq_nuc | NM_002938.5 |
refseq_prot | NP_002929.1 |
ensembl_nuc | ENST00000314289.13 |
ensembl_prot | ENSP00000315212.8 |
mane_status | MANE Select |
chr | chr4 |
start | 2469106 |
end | 2515857 |
strand | + |
ver | v1.2 |
region | chr4:2469106-2515857 |
region5000 | chr4:2464106-2520857 |
regionname0 | RNF4_chr4_2469106_2515857 |
regionname5000 | RNF4_chr4_2464106_2520857 |
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 | 190 | 376 | 92 | 64 | 156 | 18 | 44 | 114 | RNF4_chr4_2464106_2520857 | RNF4 | copy fasta | chr4 | 2464106 | 2520857 |
a0002 | 0/0 | 190 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | copy fasta | chr4 | 2464106 | 2520857 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 573 | 366 | 87 | 60 | 156 | 18 | 43 | RNF4_chr4_2464106_2520857 | RNF4 | copy fasta | chr4 | 2464106 | 2520857 |
c0002 | 0/0 | 573 | 6 | 4 | 2 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | copy fasta | chr4 | 2464106 | 2520857 |
c0003 | 0/0 | 573 | 3 | 1 | 2 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | copy fasta | chr4 | 2464106 | 2520857 |
c0004 | 0/0 | 573 | 2 | 2 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | copy fasta | chr4 | 2464106 | 2520857 |
c0005 | 0/0 | 573 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | copy fasta | chr4 | 2464106 | 2520857 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 2348 | 169 | 29 | 37 | 72 | 8 | 23 | RNF4_chr4_2464106_2520857 | RNF4 | copy fasta | chr4 | 2464106 | 2520857 |
t0002 | 0/1 | 2348 | 54 | 3 | 15 | 23 | 6 | 6 | RNF4_chr4_2464106_2520857 | RNF4 | copy fasta | chr4 | 2464106 | 2520857 |
t0003 | 0/0 | 2349 | 41 | 13 | 4 | 21 | 1 | 2 | RNF4_chr4_2464106_2520857 | RNF4 | copy fasta | chr4 | 2464106 | 2520857 |
t0004 | 0/0 | 2349 | 22 | 3 | 0 | 18 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | copy fasta | chr4 | 2464106 | 2520857 |
t0005 | 0/0 | 2348 | 14 | 2 | 4 | 2 | 0 | 6 | RNF4_chr4_2464106_2520857 | RNF4 | copy fasta | chr4 | 2464106 | 2520857 |
t0006 | 0/0 | 2346 | 14 | 14 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | copy fasta | chr4 | 2464106 | 2520857 |
t0007 | 1/0 | 2349 | 13 | 7 | 0 | 2 | 0 | 3 | RNF4_chr4_2464106_2520857 | RNF4 | copy fasta | chr4 | 2464106 | 2520857 |
t0008 | 0/0 | 2348 | 10 | 0 | 0 | 10 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | copy fasta | chr4 | 2464106 | 2520857 |
t0009 | 0/0 | 2349 | 6 | 6 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | copy fasta | chr4 | 2464106 | 2520857 |
t0010 | 0/0 | 2348 | 5 | 3 | 0 | 1 | 1 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | copy fasta | chr4 | 2464106 | 2520857 |
t0011 | 0/0 | 2348 | 4 | 4 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | copy fasta | chr4 | 2464106 | 2520857 |
t0012 | 0/0 | 2349 | 3 | 0 | 0 | 0 | 1 | 2 | RNF4_chr4_2464106_2520857 | RNF4 | copy fasta | chr4 | 2464106 | 2520857 |
t0013 | 0/0 | 2348 | 2 | 2 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | copy fasta | chr4 | 2464106 | 2520857 |
t0014 | 0/0 | 2348 | 2 | 1 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | copy fasta | chr4 | 2464106 | 2520857 |
t0015 | 0/0 | 2348 | 2 | 2 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | copy fasta | chr4 | 2464106 | 2520857 |
t0016 | 0/0 | 2346 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | copy fasta | chr4 | 2464106 | 2520857 |
t0017 | 0/0 | 2348 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | copy fasta | chr4 | 2464106 | 2520857 |
t0018 | 0/0 | 2348 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | copy fasta | chr4 | 2464106 | 2520857 |
t0019 | 0/0 | 2348 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | copy fasta | chr4 | 2464106 | 2520857 |
t0020 | 0/0 | 2348 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | copy fasta | chr4 | 2464106 | 2520857 |
t0021 | 0/0 | 2348 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | copy fasta | chr4 | 2464106 | 2520857 |
t0022 | 0/0 | 2349 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | copy fasta | chr4 | 2464106 | 2520857 |
t0023 | 0/0 | 2348 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | copy fasta | chr4 | 2464106 | 2520857 |
t0024 | 0/0 | 2348 | 1 | 0 | 0 | 0 | 1 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | copy fasta | chr4 | 2464106 | 2520857 |
t0025 | 0/0 | 2348 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | copy fasta | chr4 | 2464106 | 2520857 |
t0026 | 0/0 | 2348 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | copy fasta | chr4 | 2464106 | 2520857 |
t0027 | 0/0 | 2348 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | copy fasta | chr4 | 2464106 | 2520857 |
t0028 | 0/0 | 2348 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | copy fasta | chr4 | 2464106 | 2520857 |
t0029 | 0/0 | 2348 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | copy fasta | chr4 | 2464106 | 2520857 |
t0030 | 0/0 | 2349 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | copy fasta | chr4 | 2464106 | 2520857 |
t0031 | 0/0 | 2349 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | copy fasta | chr4 | 2464106 | 2520857 |
t0032 | 0/0 | 2348 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | copy fasta | chr4 | 2464106 | 2520857 |
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 | 2 | 0 | 0 | 2 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0003 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0180 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0319 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0348 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0370 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 573 | 366 | 87 | 60 | 156 | 18 | 43 | RNF4_chr4_2464106_2520857 | RNF4 | copy fasta | chr4 | 2464106 | 2520857 |
a0001c0002 | 0/0 | 573 | 6 | 4 | 2 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | copy fasta | chr4 | 2464106 | 2520857 |
a0001c0003 | 0/0 | 573 | 3 | 1 | 2 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | copy fasta | chr4 | 2464106 | 2520857 |
a0001c0005 | 0/0 | 573 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | copy fasta | chr4 | 2464106 | 2520857 |
a0002c0004 | 0/0 | 573 | 2 | 2 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | copy fasta | chr4 | 2464106 | 2520857 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2920 | 166 | 27 | 37 | 72 | 8 | 22 | RNF4_chr4_2464106_2520857 | RNF4 | copy fasta | chr4 | 2464106 | 2520857 |
a0001c0001t0002 | 0/1 | 2920 | 54 | 3 | 15 | 23 | 6 | 6 | RNF4_chr4_2464106_2520857 | RNF4 | copy fasta | chr4 | 2464106 | 2520857 |
a0001c0001t0003 | 0/0 | 2921 | 35 | 9 | 2 | 21 | 1 | 2 | RNF4_chr4_2464106_2520857 | RNF4 | copy fasta | chr4 | 2464106 | 2520857 |
a0001c0001t0004 | 0/0 | 2921 | 22 | 3 | 0 | 18 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | copy fasta | chr4 | 2464106 | 2520857 |
a0001c0001t0005 | 0/0 | 2920 | 14 | 2 | 4 | 2 | 0 | 6 | RNF4_chr4_2464106_2520857 | RNF4 | copy fasta | chr4 | 2464106 | 2520857 |
a0001c0001t0006 | 0/0 | 2918 | 14 | 14 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | copy fasta | chr4 | 2464106 | 2520857 |
a0001c0001t0007 | 1/0 | 2921 | 13 | 7 | 0 | 2 | 0 | 3 | RNF4_chr4_2464106_2520857 | RNF4 | copy fasta | chr4 | 2464106 | 2520857 |
a0001c0001t0008 | 0/0 | 2920 | 10 | 0 | 0 | 10 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | copy fasta | chr4 | 2464106 | 2520857 |
a0001c0001t0009 | 0/0 | 2921 | 6 | 6 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | copy fasta | chr4 | 2464106 | 2520857 |
a0001c0001t0010 | 0/0 | 2920 | 5 | 3 | 0 | 1 | 1 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | copy fasta | chr4 | 2464106 | 2520857 |
a0001c0001t0011 | 0/0 | 2920 | 4 | 4 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | copy fasta | chr4 | 2464106 | 2520857 |
a0001c0001t0012 | 0/0 | 2921 | 3 | 0 | 0 | 0 | 1 | 2 | RNF4_chr4_2464106_2520857 | RNF4 | copy fasta | chr4 | 2464106 | 2520857 |
a0001c0001t0013 | 0/0 | 2920 | 2 | 2 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | copy fasta | chr4 | 2464106 | 2520857 |
a0001c0001t0015 | 0/0 | 2920 | 2 | 2 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | copy fasta | chr4 | 2464106 | 2520857 |
a0001c0001t0016 | 0/0 | 2918 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | copy fasta | chr4 | 2464106 | 2520857 |
a0001c0001t0017 | 0/0 | 2920 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | copy fasta | chr4 | 2464106 | 2520857 |
a0001c0001t0018 | 0/0 | 2920 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | copy fasta | chr4 | 2464106 | 2520857 |
a0001c0001t0019 | 0/0 | 2920 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | copy fasta | chr4 | 2464106 | 2520857 |
a0001c0001t0020 | 0/0 | 2920 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | copy fasta | chr4 | 2464106 | 2520857 |
a0001c0001t0022 | 0/0 | 2921 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | copy fasta | chr4 | 2464106 | 2520857 |
a0001c0001t0023 | 0/0 | 2920 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | copy fasta | chr4 | 2464106 | 2520857 |
a0001c0001t0024 | 0/0 | 2920 | 1 | 0 | 0 | 0 | 1 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | copy fasta | chr4 | 2464106 | 2520857 |
a0001c0001t0025 | 0/0 | 2920 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | copy fasta | chr4 | 2464106 | 2520857 |
a0001c0001t0026 | 0/0 | 2920 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | copy fasta | chr4 | 2464106 | 2520857 |
a0001c0001t0027 | 0/0 | 2920 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | copy fasta | chr4 | 2464106 | 2520857 |
a0001c0001t0028 | 0/0 | 2920 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | copy fasta | chr4 | 2464106 | 2520857 |
a0001c0001t0029 | 0/0 | 2920 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | copy fasta | chr4 | 2464106 | 2520857 |
a0001c0001t0030 | 0/0 | 2921 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | copy fasta | chr4 | 2464106 | 2520857 |
a0001c0001t0031 | 0/0 | 2921 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | copy fasta | chr4 | 2464106 | 2520857 |
a0001c0001t0032 | 0/0 | 2920 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | copy fasta | chr4 | 2464106 | 2520857 |
a0001c0002t0003 | 0/0 | 2921 | 6 | 4 | 2 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | copy fasta | chr4 | 2464106 | 2520857 |
a0001c0003t0014 | 0/0 | 2920 | 2 | 1 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | copy fasta | chr4 | 2464106 | 2520857 |
a0001c0003t0021 | 0/0 | 2920 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | copy fasta | chr4 | 2464106 | 2520857 |
a0001c0005t0001 | 0/0 | 2920 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | copy fasta | chr4 | 2464106 | 2520857 |
a0002c0004t0001 | 0/0 | 2920 | 2 | 2 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | copy fasta | chr4 | 2464106 | 2520857 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0001g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0002g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0002g0180 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0002g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0002g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0003g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0003g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0003g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0003g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0003g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0003g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0003g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0003g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0003g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0003g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0003g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0003g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0003g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0003g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0003g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0003g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0003g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0003g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0003g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0003g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0004g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0004g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0004g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0004g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0004g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0004g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0004g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0004g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0004g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0004g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0004g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0004g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0004g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0004g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0004g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0004g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0004g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0004g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0004g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0004g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0004g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0004g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0005g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0005g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0005g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0005g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0005g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0005g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0005g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0005g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0005g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0005g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0005g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0005g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0005g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0005g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0006g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0006g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0006g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0006g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0006g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0006g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0006g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0006g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0006g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0006g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0006g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0006g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0006g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0006g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0007g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0007g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0007g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0007g0319 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0007g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0007g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0007g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0007g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0007g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0007g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0007g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0007g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0008g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0008g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0008g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0008g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0008g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0008g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0008g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0008g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0008g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0008g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0009g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0009g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0009g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0009g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0009g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0009g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0010g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0010g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0010g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0010g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0010g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0011g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0011g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0011g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0011g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0012g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0012g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0012g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0013g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0013g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0015g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0015g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0016g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0017g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0018g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0019g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0020g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0022g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0023g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0024g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0025g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0026g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0027g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0028g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0029g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0030g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0031g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0001t0032g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0002t0003g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0002t0003g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0002t0003g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0002t0003g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0002t0003g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0002t0003g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0003t0014g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0003t0014g0370 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0003t0021g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0001c0005t0001g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0002c0004t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
a0002c0004t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | GBR | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0037 | EUR | GBR | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG00140 | hp1 | a0001 | c0001 | t0024 | g0215 | EUR | GBR | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0110 | EUR | GBR | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0140 | EUR | FIN | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0188 | EUR | FIN | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0263 | EUR | FIN | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0265 | EUR | FIN | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | CHS | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG00408 | hp2 | a0001 | c0001 | t0003 | g0252 | EAS | CHS | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0339 | EAS | CHS | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG00438 | hp2 | a0001 | c0001 | t0010 | g0216 | EAS | CHS | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG00544 | hp1 | a0001 | c0001 | t0004 | g0331 | EAS | CHS | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG00544 | hp2 | a0001 | c0001 | t0008 | g0282 | EAS | CHS | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | CHS | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG00558 | hp2 | a0001 | c0001 | t0004 | g0276 | EAS | CHS | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG00597 | hp1 | a0001 | c0001 | t0004 | g0295 | EAS | CHS | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0342 | EAS | CHS | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | CHS | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG00609 | hp2 | a0001 | c0001 | t0008 | g0327 | EAS | CHS | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0206 | AMR | PUR | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0347 | AMR | PUR | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0058 | AMR | PUR | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0200 | EAS | CHS | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG00673 | hp2 | a0001 | c0001 | t0003 | g0239 | EAS | CHS | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0194 | AMR | PUR | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0143 | AMR | PUR | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG00738 | hp1 | a0001 | c0001 | t0003 | g0237 | AMR | PUR | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0191 | AMR | PUR | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0176 | AMR | PUR | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG01074 | hp1 | a0001 | c0001 | t0005 | g0015 | AMR | PUR | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG01081 | hp1 | a0001 | c0001 | t0005 | g0014 | AMR | PUR | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0187 | AMR | PUR | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0195 | AMR | PUR | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0168 | AMR | PUR | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0184 | AMR | PUR | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG01167 | hp2 | a0001 | c0003 | t0021 | g0306 | AMR | PUR | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0177 | AMR | PUR | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0314 | AMR | PUR | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG01243 | hp1 | a0001 | c0002 | t0003 | g0217 | AMR | PUR | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG01243 | hp2 | a0001 | c0003 | t0014 | g0370 | AMR | PUR | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG01255 | hp1 | a0001 | c0002 | t0003 | g0254 | AMR | CLM | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG01255 | hp2 | a0001 | c0001 | t0019 | g0087 | AMR | CLM | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0346 | AMR | CLM | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | CLM | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | CLM | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG01257 | hp2 | a0001 | c0001 | t0003 | g0260 | AMR | CLM | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0309 | AMR | CLM | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | CLM | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | CLM | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0198 | AMR | CLM | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | CLM | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | CLM | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | CLM | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG01496 | hp1 | a0001 | c0001 | t0026 | g0081 | AMR | CLM | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0178 | AMR | CLM | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0107 | EUR | IBS | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG01515 | hp2 | a0001 | c0001 | t0010 | g0253 | EUR | IBS | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG01516 | hp1 | a0001 | c0001 | t0012 | g0247 | EUR | IBS | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0199 | EUR | IBS | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG01517 | hp1 | a0001 | c0001 | t0002 | g0189 | EUR | IBS | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0059 | EUR | IBS | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0262 | AFR | ACB | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG01884 | hp2 | a0001 | c0002 | t0003 | g0236 | AFR | ACB | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG01891 | hp1 | a0001 | c0001 | t0007 | g0006 | AFR | ACB | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG01891 | hp2 | a0001 | c0001 | t0009 | g0220 | AFR | ACB | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PEL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0210 | AMR | PEL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG01975 | hp2 | a0001 | c0001 | t0005 | g0019 | AMR | PEL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PEL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG01978 | hp2 | a0001 | c0001 | t0005 | g0013 | AMR | PEL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PEL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0317 | AMR | PEL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0293 | AMR | PEL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PEL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG02015 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | KHV | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG02027 | hp1 | a0001 | c0001 | t0003 | g0294 | EAS | KHV | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | KHV | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | KHV | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | KHV | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG02055 | hp1 | a0001 | c0001 | t0003 | g0250 | AFR | ACB | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG02055 | hp2 | a0001 | c0002 | t0003 | g0234 | AFR | ACB | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | KHV | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | KHV | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG02071 | hp2 | a0001 | c0001 | t0027 | g0123 | EAS | KHV | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG02083 | hp1 | a0001 | c0001 | t0004 | g0278 | EAS | KHV | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0186 | EAS | KHV | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | KHV | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG02129 | hp2 | a0001 | c0001 | t0022 | g0045 | EAS | KHV | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0371 | EAS | KHV | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG02132 | hp2 | a0001 | c0001 | t0017 | g0009 | EAS | KHV | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG02135 | hp1 | a0001 | c0001 | t0008 | g0326 | EAS | KHV | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0120 | EAS | KHV | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0298 | AFR | ACB | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG02145 | hp2 | a0001 | c0001 | t0003 | g0244 | AFR | ACB | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | CDX | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG02155 | hp2 | a0001 | c0001 | t0023 | g0023 | EAS | CDX | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG02165 | hp1 | a0001 | c0001 | t0004 | g0277 | EAS | CDX | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | CDX | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG02257 | hp1 | a0001 | c0001 | t0011 | g0364 | AFR | ACB | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0287 | AFR | ACB | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0359 | AFR | ACB | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG02258 | hp2 | a0001 | c0001 | t0006 | g0155 | AFR | ACB | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG02280 | hp1 | a0001 | c0001 | t0007 | g0308 | AFR | ACB | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0289 | AFR | ACB | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PEL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PEL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG02451 | hp1 | a0001 | c0001 | t0006 | g0153 | AFR | ACB | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG02451 | hp2 | a0001 | c0001 | t0010 | g0249 | AFR | ACB | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG02523 | hp1 | a0001 | c0001 | t0007 | g0303 | EAS | KHV | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0202 | EAS | KHV | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0290 | AFR | GWD | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0179 | SAS | PJL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0358 | AFR | GWD | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0362 | AFR | GWD | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0354 | AFR | GWD | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0311 | AFR | GWD | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0355 | AFR | GWD | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG02630 | hp2 | a0001 | c0001 | t0020 | g0269 | AFR | GWD | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG02647 | hp1 | a0001 | c0003 | t0014 | g0357 | AFR | GWD | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG02647 | hp2 | a0001 | c0001 | t0006 | g0161 | AFR | GWD | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0335 | SAS | PJL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG02698 | hp2 | a0001 | c0001 | t0018 | g0010 | SAS | PJL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG02717 | hp1 | a0001 | c0001 | t0005 | g0020 | AFR | GWD | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG02717 | hp2 | a0001 | c0001 | t0009 | g0227 | AFR | GWD | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG02723 | hp1 | a0001 | c0001 | t0009 | g0232 | AFR | GWD | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0353 | AFR | GWD | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG02735 | hp2 | a0001 | c0005 | t0001 | g0312 | SAS | PJL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0172 | SAS | PJL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG02738 | hp2 | a0001 | c0001 | t0005 | g0016 | SAS | PJL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG02809 | hp1 | a0001 | c0001 | t0003 | g0248 | AFR | GWD | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG02809 | hp2 | a0001 | c0001 | t0006 | g0163 | AFR | GWD | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG02818 | hp1 | a0001 | c0001 | t0013 | g0369 | AFR | GWD | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG02818 | hp2 | a0001 | c0001 | t0007 | g0330 | AFR | GWD | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG02886 | hp1 | a0001 | c0001 | t0006 | g0162 | AFR | GWD | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG02895 | hp1 | a0001 | c0001 | t0007 | g0329 | AFR | GWD | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG02895 | hp2 | a0001 | c0001 | t0006 | g0151 | AFR | GWD | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0304 | AFR | GWD | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG02896 | hp2 | a0001 | c0001 | t0003 | g0257 | AFR | GWD | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG02897 | hp1 | a0001 | c0001 | t0003 | g0171 | AFR | GWD | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG02897 | hp2 | a0001 | c0001 | t0006 | g0152 | AFR | GWD | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG02970 | hp1 | a0001 | c0001 | t0004 | g0356 | AFR | ESN | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0285 | AFR | ESN | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG02976 | hp1 | a0001 | c0001 | t0003 | g0224 | AFR | ESN | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0286 | AFR | ESN | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0318 | SAS | PJL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG03041 | hp1 | a0001 | c0001 | t0004 | g0352 | AFR | GWD | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG03041 | hp2 | a0001 | c0001 | t0016 | g0158 | AFR | GWD | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG03098 | hp1 | a0001 | c0001 | t0007 | g0006 | AFR | MSL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0209 | AFR | MSL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG03130 | hp1 | a0001 | c0001 | t0015 | g0350 | AFR | ESN | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG03130 | hp2 | a0001 | c0001 | t0006 | g0156 | AFR | ESN | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG03139 | hp1 | a0001 | c0001 | t0004 | g0292 | AFR | ESN | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG03139 | hp2 | a0001 | c0002 | t0003 | g0233 | AFR | ESN | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG03195 | hp1 | a0001 | c0001 | t0009 | g0223 | AFR | ESN | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG03195 | hp2 | a0001 | c0001 | t0015 | g0351 | AFR | ESN | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0288 | AFR | MSL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG03209 | hp2 | a0001 | c0001 | t0029 | g0363 | AFR | MSL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG03225 | hp2 | a0001 | c0001 | t0013 | g0368 | AFR | MSL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG03239 | hp2 | a0001 | c0001 | t0007 | g0334 | SAS | PJL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG03453 | hp1 | a0002 | c0004 | t0001 | g0057 | AFR | MSL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0361 | AFR | MSL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG03486 | hp1 | a0001 | c0001 | t0010 | g0222 | AFR | MSL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | MSL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG03490 | hp1 | a0001 | c0001 | t0005 | g0296 | SAS | PJL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0069 | SAS | PJL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG03492 | hp2 | a0001 | c0001 | t0005 | g0297 | SAS | PJL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0313 | AFR | ESN | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG03516 | hp2 | a0001 | c0001 | t0011 | g0366 | AFR | ESN | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG03540 | hp1 | a0001 | c0001 | t0006 | g0154 | AFR | GWD | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0207 | AFR | GWD | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | MSL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG03579 | hp2 | a0001 | c0001 | t0009 | g0226 | AFR | MSL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG03654 | hp1 | a0001 | c0001 | t0005 | g0021 | SAS | PJL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG03654 | hp2 | a0001 | c0001 | t0003 | g0240 | SAS | PJL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG03669 | hp1 | a0001 | c0001 | t0005 | g0017 | SAS | PJL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG03688 | hp1 | a0001 | c0001 | t0004 | g0046 | SAS | STU | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG03688 | hp2 | a0001 | c0001 | t0005 | g0018 | SAS | STU | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG03704 | hp1 | a0001 | c0001 | t0012 | g0221 | SAS | PJL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0173 | SAS | PJL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG03710 | hp1 | a0001 | c0001 | t0003 | g0266 | SAS | PJL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0316 | SAS | BEB | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG03831 | hp2 | a0001 | c0001 | t0012 | g0246 | SAS | BEB | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0310 | SAS | BEB | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0302 | SAS | BEB | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0190 | SAS | BEB | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG03942 | hp2 | a0001 | c0001 | t0007 | g0324 | SAS | BEB | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0174 | SAS | BEB | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | BEB | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | STU | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | STU | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG04228 | hp1 | a0001 | c0001 | t0007 | g0325 | SAS | STU | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | STU | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | YRI | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA18522 | hp2 | a0001 | c0001 | t0032 | g0360 | AFR | YRI | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | CHB | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | CHB | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | CHB | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | CHB | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA18906 | hp1 | a0001 | c0001 | t0009 | g0256 | AFR | YRI | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA18906 | hp2 | a0001 | c0001 | t0011 | g0365 | AFR | YRI | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0336 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA18940 | hp2 | a0001 | c0001 | t0003 | g0230 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA18942 | hp1 | a0001 | c0001 | t0004 | g0283 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA18943 | hp2 | a0001 | c0001 | t0008 | g0322 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0343 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA18950 | hp1 | a0001 | c0001 | t0003 | g0235 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA18950 | hp2 | a0001 | c0001 | t0004 | g0042 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA18951 | hp2 | a0001 | c0001 | t0008 | g0307 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA18952 | hp2 | a0001 | c0001 | t0008 | g0323 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA18953 | hp1 | a0001 | c0001 | t0005 | g0012 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA18960 | hp2 | a0001 | c0001 | t0003 | g0268 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA18962 | hp1 | a0001 | c0001 | t0004 | g0281 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA18964 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA18966 | hp1 | a0001 | c0001 | t0008 | g0321 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA18967 | hp2 | a0001 | c0001 | t0025 | g0126 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA18968 | hp1 | a0001 | c0001 | t0003 | g0170 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA18968 | hp2 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA18970 | hp1 | a0001 | c0001 | t0004 | g0270 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA18977 | hp2 | a0001 | c0001 | t0003 | g0238 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA18980 | hp1 | a0001 | c0001 | t0004 | g0033 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0340 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA18982 | hp1 | a0001 | c0001 | t0003 | g0272 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA18984 | hp2 | a0001 | c0001 | t0005 | g0011 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA18986 | hp1 | a0001 | c0001 | t0004 | g0063 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA18986 | hp2 | a0001 | c0001 | t0003 | g0279 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA18989 | hp2 | a0001 | c0001 | t0003 | g0273 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0341 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA18995 | hp1 | a0001 | c0001 | t0004 | g0274 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA18999 | hp1 | a0001 | c0001 | t0003 | g0218 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA18999 | hp2 | a0001 | c0001 | t0004 | g0041 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA19000 | hp1 | a0001 | c0001 | t0003 | g0291 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA19001 | hp1 | a0001 | c0001 | t0003 | g0258 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA19004 | hp1 | a0001 | c0001 | t0007 | g0333 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA19007 | hp2 | a0001 | c0001 | t0008 | g0066 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA19009 | hp1 | a0001 | c0001 | t0003 | g0251 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0344 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA19010 | hp2 | a0001 | c0001 | t0004 | g0275 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA19011 | hp1 | a0001 | c0001 | t0028 | g0332 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA19012 | hp1 | a0001 | c0001 | t0003 | g0271 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA19012 | hp2 | a0001 | c0001 | t0004 | g0040 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA19030 | hp1 | a0001 | c0001 | t0007 | g0320 | AFR | LWK | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA19030 | hp2 | a0001 | c0002 | t0003 | g0255 | AFR | LWK | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA19043 | hp1 | a0001 | c0001 | t0003 | g0267 | AFR | LWK | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA19043 | hp2 | a0001 | c0001 | t0003 | g0243 | AFR | LWK | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA19054 | hp1 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA19054 | hp2 | a0001 | c0001 | t0008 | g0345 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA19057 | hp1 | a0001 | c0001 | t0008 | g0305 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA19058 | hp1 | a0001 | c0001 | t0003 | g0261 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA19058 | hp2 | a0001 | c0001 | t0004 | g0084 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA19060 | hp2 | a0001 | c0001 | t0030 | g0231 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA19066 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA19067 | hp2 | a0001 | c0001 | t0004 | g0284 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA19074 | hp1 | a0001 | c0001 | t0003 | g0229 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0349 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA19077 | hp1 | a0001 | c0001 | t0003 | g0259 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA19079 | hp1 | a0001 | c0001 | t0004 | g0280 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA19079 | hp2 | a0001 | c0001 | t0003 | g0241 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA19082 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA19084 | hp1 | a0001 | c0001 | t0003 | g0219 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0337 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA20129 | hp1 | a0001 | c0001 | t0006 | g0160 | AFR | ASW | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0315 | AFR | ASW | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0205 | EUR | TSI | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0348 | EUR | TSI | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA20805 | hp1 | a0001 | c0001 | t0003 | g0225 | EUR | TSI | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0211 | EUR | TSI | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0175 | SAS | GIH | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | GIH | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG02109 | hp1 | a0001 | c0001 | t0005 | g0022 | AFR | ACB | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG02109 | hp2 | a0001 | c0001 | t0003 | g0242 | AFR | ACB | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG02486 | hp1 | a0001 | c0001 | t0006 | g0165 | AFR | ACB | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG02486 | hp2 | a0001 | c0001 | t0010 | g0245 | AFR | ACB | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG02559 | hp1 | a0001 | c0001 | t0006 | g0159 | AFR | ACB | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG02559 | hp2 | a0001 | c0001 | t0031 | g0228 | AFR | ACB | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG03471 | hp1 | a0001 | c0001 | t0011 | g0367 | AFR | MSL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG03471 | hp2 | a0001 | c0001 | t0006 | g0157 | AFR | MSL | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0208 | AFR | USA | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0299 | AFR | USA | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0338 | EAS | JPT | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA20300 | hp1 | a0001 | c0001 | t0007 | g0328 | AFR | USA | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA20300 | hp2 | a0002 | c0004 | t0001 | g0055 | AFR | USA | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | LWK | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
NA21309 | hp2 | a0001 | c0001 | t0006 | g0166 | AFR | LWK | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0180 | REF | REF | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0007 | g0319 | REF | REF | RNF4_chr4_2464106_2520857 | RNF4 | chr4 | 2464106 | 2520857 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:2469258
|
G | A | 1 | a0001 | 1 | HG01255.hp2 | splice_region_variant | LOW | c.-158G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/8 | chr4 | 2469258 | ||||||
chr4:2512575
|
G | A | 1 | a0002 | 2 | HG03453.hp1 NA20300.hp2 |
missense_variant | MODERATE | c.352G>A | p.Asp118Asn | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 6/8 | 662/2921 | 352/573 | 118/190 | chr4 | 2512575 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:2497042
|
A | G | 1 | a0001c0005 | 1 | HG02735.hp2 | synonymous_variant | LOW | c.45A>G | p.Gln15Gln | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/8 | 355/2921 | 45/573 | 15/190 | chr4 | 2497042 | ||
chr4:2513089
|
A | G | 1 | a0001c0003 | 3 | HG01167.hp2 HG01243.hp2 HG02647.hp1 |
synonymous_variant | LOW | c.381A>G | p.Ser127Ser | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 7/8 | 691/2921 | 381/573 | 127/190 | chr4 | 2513089 | ||
chr4:2513119
|
C | T | 1 | a0001c0002 | 6 | HG01243.hp1 HG01255.hp1 HG01884.hp2 others(3): Show |
synonymous_variant | LOW | c.411C>T | p.Asp137Asp | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 7/8 | 721/2921 | 411/573 | 137/190 | chr4 | 2513119 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:2469147
|
A | G | 1 | a0001c0001t0032 | 1 | NA18522.hp2 | 5_prime_UTR_variant | MODIFIER | c.-269A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/8 | 21347 | chr4 | 2469147 | |||||
chr4:2469165
|
C | G | 7 | a0001c0001t0003a0001c0001t0009a0001c0001t0010others(4): Show | 57 | HG00408.hp2 HG00438.hp2 HG00673.hp2 others(54): Show |
5_prime_UTR_variant | MODIFIER | c.-251C>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/8 | 21329 | chr4 | 2469165 | |||||
chr4:2469188
|
G | A | 1 | a0001c0001t0016 | 1 | HG03041.hp2 | 5_prime_UTR_variant | MODIFIER | c.-228G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/8 | 21306 | chr4 | 2469188 | |||||
chr4:2469229
|
G | A | 3 | a0001c0001t0005a0001c0001t0017a0001c0001t0018 | 16 | HG01074.hp1 HG01081.hp1 HG01975.hp2 others(13): Show |
5_prime_UTR_variant | MODIFIER | c.-187G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/8 | 21265 | chr4 | 2469229 | |||||
chr4:2490464
|
T | C | 4 | a0001c0001t0005a0001c0001t0013a0001c0001t0017others(1): Show | 18 | HG01074.hp1 HG01081.hp1 HG01975.hp2 others(15): Show |
5_prime_UTR_variant | MODIFIER | c.-30T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/8 | 30 | chr4 | 2490464 | |||||
chr4:2513830
|
G | A | 1 | a0001c0001t0020 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*11G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 8/8 | 11 | chr4 | 2513830 | |||||
chr4:2514064
|
A | G | 1 | a0001c0001t0029 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*245A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 8/8 | 245 | chr4 | 2514064 | |||||
chr4:2514166
|
G | C | 1 | a0001c0001t0012 | 3 | HG01516.hp1 HG03704.hp1 HG03831.hp2 |
3_prime_UTR_variant | MODIFIER | c.*347G>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 8/8 | 347 | chr4 | 2514166 | |||||
chr4:2514268
|
G | C | 2 | a0001c0003t0014a0001c0003t0021 | 3 | HG01167.hp2 HG01243.hp2 HG02647.hp1 |
3_prime_UTR_variant | MODIFIER | c.*449G>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 8/8 | 449 | chr4 | 2514268 | |||||
chr4:2514395
|
ACT | A | 2 | a0001c0001t0006a0001c0001t0016 | 15 | HG02258.hp2 HG02451.hp1 HG02486.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*579_*580delCT | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 8/8 | 579 | INFO_REALIGN_3_PRIME | chr4 | 2514395 | ||||
chr4:2514465
|
C | T | 1 | a0001c0001t0015 | 2 | HG03130.hp1 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*646C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 8/8 | 646 | chr4 | 2514465 | |||||
chr4:2514543
|
C | T | 3 | a0001c0001t0008a0001c0001t0027a0001c0001t0028 | 12 | HG00544.hp2 HG00609.hp2 HG02071.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*724C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 8/8 | 724 | chr4 | 2514543 | |||||
chr4:2514715
|
C | G | 1 | a0001c0001t0018 | 1 | HG02698.hp2 | 3_prime_UTR_variant | MODIFIER | c.*896C>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 8/8 | 896 | chr4 | 2514715 | |||||
chr4:2514720
|
G | C | 1 | a0001c0003t0021 | 1 | HG01167.hp2 | 3_prime_UTR_variant | MODIFIER | c.*901G>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 8/8 | 901 | chr4 | 2514720 | |||||
chr4:2514733
|
T | C | 1 | a0001c0001t0027 | 1 | HG02071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*914T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 8/8 | 914 | chr4 | 2514733 | |||||
chr4:2514890
|
C | T | 3 | a0001c0001t0008a0001c0001t0027a0001c0001t0028 | 12 | HG00544.hp2 HG00609.hp2 HG02071.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1071C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 8/8 | 1071 | chr4 | 2514890 | |||||
chr4:2514979
|
G | A | 2 | a0001c0003t0014a0001c0003t0021 | 3 | HG01167.hp2 HG01243.hp2 HG02647.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1160G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 8/8 | 1160 | chr4 | 2514979 | |||||
chr4:2515031
|
C | T | 1 | a0001c0001t0026 | 1 | HG01496.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1212C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 8/8 | 1212 | chr4 | 2515031 | |||||
chr4:2515057
|
TG | T | 26 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(23): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
3_prime_UTR_variant | MODIFIER | c.*1244delG | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 8/8 | 1244 | INFO_REALIGN_3_PRIME | chr4 | 2515057 | ||||
chr4:2515100
|
T | G | 1 | a0001c0001t0028 | 1 | NA19011.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1281T>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 8/8 | 1281 | chr4 | 2515100 | |||||
chr4:2515176
|
C | T | 1 | a0001c0001t0017 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1357C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 8/8 | 1357 | chr4 | 2515176 | |||||
chr4:2515270
|
C | T | 1 | a0001c0001t0025 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1451C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 8/8 | 1451 | chr4 | 2515270 | |||||
chr4:2515271
|
G | A | 1 | a0001c0001t0011 | 4 | HG02257.hp1 HG03471.hp1 HG03516.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1452G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 8/8 | 1452 | chr4 | 2515271 | |||||
chr4:2515329
|
G | A | 1 | a0001c0001t0022 | 1 | HG02129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1510G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 8/8 | 1510 | chr4 | 2515329 | |||||
chr4:2515340
|
T | C | 1 | a0001c0001t0030 | 1 | NA19060.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1521T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 8/8 | 1521 | chr4 | 2515340 | |||||
chr4:2515496
|
A | G | 3 | a0001c0001t0002a0001c0001t0020a0001c0001t0024 | 56 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*1677A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 8/8 | 1677 | chr4 | 2515496 | |||||
chr4:2515511
|
G | T | 4 | a0001c0001t0008a0001c0001t0015a0001c0001t0027others(1): Show | 14 | HG00544.hp2 HG00609.hp2 HG02071.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1692G>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 8/8 | 1692 | chr4 | 2515511 | |||||
chr4:2515564
|
C | T | 1 | a0001c0001t0009 | 6 | HG01891.hp2 HG02717.hp2 HG02723.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1745C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 8/8 | 1745 | chr4 | 2515564 | |||||
chr4:2515672
|
T | C | 1 | a0001c0001t0024 | 1 | HG00140.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1853T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 8/8 | 1853 | chr4 | 2515672 | |||||
chr4:2515720
|
G | A | 30 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(27): Show | 352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
3_prime_UTR_variant | MODIFIER | c.*1901G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 8/8 | 1901 | chr4 | 2515720 | |||||
chr4:2515751
|
T | A | 1 | a0001c0001t0023 | 1 | HG02155.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1932T>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 8/8 | 1932 | chr4 | 2515751 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:2469331
|
G | C | 1 | a0001c0001t0001g0008 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-158+73G>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2469331 | ||||||
chr4:2469387
|
A | C | 1 | a0001c0001t0001g0371 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-158+129A>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2469387 | ||||||
chr4:2469410
|
G | A | 296 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(293): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.-158+152G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2469410 | ||||||
chr4:2469463
|
A | G | 2 | a0001c0001t0005g0296a0001c0001t0005g0297 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-158+205A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2469463 | ||||||
chr4:2469476
|
G | C | 2 | a0001c0001t0001g0298a0001c0001t0001g0299 | 2 | HG02145.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-158+218G>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2469476 | ||||||
chr4:2469490
|
C | T | 1 | a0001c0001t0004g0295 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-158+232C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2469490 | ||||||
chr4:2469509
|
G | A | 16 | a0001c0001t0005g0011a0001c0001t0005g0012a0001c0001t0005g0013others(13): Show | 16 | HG01074.hp1 HG01081.hp1 HG01975.hp2 others(13): Show |
intron_variant | MODIFIER | c.-158+251G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2469509 | ||||||
chr4:2469742
|
G | T | 21 | a0001c0001t0001g0298a0001c0001t0001g0299a0001c0001t0001g0353others(18): Show | 21 | HG01243.hp2 HG02145.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.-158+484G>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2469742 | ||||||
chr4:2469772
|
G | C | 1 | a0001c0001t0001g0008 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-158+514G>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2469772 | ||||||
chr4:2469953
|
C | A | 1 | a0001c0001t0023g0023 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-158+695C>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2469953 | ||||||
chr4:2470075
|
A | G | 318 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(315): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.-158+817A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2470075 | ||||||
chr4:2470075
|
A | T | 1 | a0001c0001t0003g0294 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-158+817A>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2470075 | ||||||
chr4:2470082
|
A | G | 1 | a0001c0001t0002g0293 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-158+824A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2470082 | ||||||
chr4:2470087
|
C | T | 1 | a0001c0003t0014g0370 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-158+829C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2470087 | ||||||
chr4:2470181
|
A | G | 1 | a0001c0001t0004g0292 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-158+923A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2470181 | ||||||
chr4:2470247
|
T | C | 132 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(129): Show | 135 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.-158+989T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2470247 | ||||||
chr4:2470352
|
T | C | 1 | a0001c0001t0001g0302 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-158+1094T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2470352 | ||||||
chr4:2470403
|
C | T | 1 | a0001c0001t0003g0291 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-158+1145C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2470403 | ||||||
chr4:2470546
|
G | A | 33 | a0001c0001t0001g0150a0001c0001t0001g0164a0001c0001t0005g0011others(30): Show | 33 | HG01074.hp1 HG01081.hp1 HG01975.hp2 others(30): Show |
intron_variant | MODIFIER | c.-158+1288G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2470546 | ||||||
chr4:2470599
|
A | G | 1 | a0001c0001t0001g0290 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-158+1341A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2470599 | ||||||
chr4:2470633
|
A | T | 22 | a0001c0001t0001g0008a0001c0001t0001g0164a0001c0001t0001g0285others(19): Show | 22 | HG02257.hp2 HG02258.hp2 HG02280.hp2 others(19): Show |
intron_variant | MODIFIER | c.-158+1375A>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2470633 | ||||||
chr4:2470634
|
C | T | 17 | a0001c0001t0003g0271a0001c0001t0003g0272a0001c0001t0003g0273others(14): Show | 17 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(14): Show |
intron_variant | MODIFIER | c.-158+1376C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2470634 | ||||||
chr4:2470694
|
G | A | 2 | a0001c0001t0001g0024a0001c0001t0001g0025 | 2 | HG00738.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.-158+1436G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2470694 | ||||||
chr4:2470756
|
G | A | 1 | a0001c0001t0007g0303 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-158+1498G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2470756 | ||||||
chr4:2470827
|
CT | C | 190 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0026others(187): Show | 192 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.-158+1580delT | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2470827 | |||||
chr4:2470882
|
AAATGCCA others(30): Show |
A | 1 | a0001c0001t0001g0149 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-158+1625_-158+166 others(41): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2470882 | ||||||
chr4:2470943
|
T | C | 1 | a0001c0001t0017g0009 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-158+1685T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2470943 | ||||||
chr4:2470962
|
CT | C | 280 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(277): Show | 284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.-158+1725delT | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2470962 | |||||
chr4:2470962
|
CTT | C | 22 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(19): Show | 22 | HG01109.hp2 HG01243.hp2 HG02622.hp1 others(19): Show |
intron_variant | MODIFIER | c.-158+1724_-158+172 others(6): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2470962 | |||||
chr4:2471073
|
TCTC | T | 22 | a0001c0001t0001g0008a0001c0001t0001g0164a0001c0001t0001g0285others(19): Show | 22 | HG02257.hp2 HG02258.hp2 HG02280.hp2 others(19): Show |
intron_variant | MODIFIER | c.-158+1818_-158+182 others(7): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2471073 | |||||
chr4:2471191
|
G | A | 2 | a0001c0001t0001g0005a0001c0001t0001g0262 | 3 | HG01884.hp1 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-158+1933G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2471191 | ||||||
chr4:2471200
|
C | G | 1 | a0001c0001t0001g0141 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-158+1942C>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2471200 | ||||||
chr4:2471218
|
C | T | 263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(260): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.-158+1960C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2471218 | ||||||
chr4:2471365
|
A | T | 130 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(127): Show | 133 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.-158+2107A>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2471365 | ||||||
chr4:2471460
|
C | T | 1 | a0001c0001t0024g0215 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-158+2202C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2471460 | ||||||
chr4:2471460
|
CCAGTCAG others(28): Show |
C | 16 | a0001c0001t0005g0011a0001c0001t0005g0012a0001c0001t0005g0013others(13): Show | 16 | HG01074.hp1 HG01081.hp1 HG01975.hp2 others(13): Show |
intron_variant | MODIFIER | c.-158+2211_-158+224 others(39): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2471460 | |||||
chr4:2471525
|
G | C | 322 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(319): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.-158+2267G>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2471525 | ||||||
chr4:2471549
|
G | A | 1 | a0001c0001t0010g0216 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-158+2291G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2471549 | ||||||
chr4:2471560
|
G | A | 1 | a0001c0001t0005g0011 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.-158+2302G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2471560 | ||||||
chr4:2471589
|
A | G | 1 | a0001c0001t0001g0290 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-158+2331A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2471589 | ||||||
chr4:2471771
|
G | C | 2 | a0001c0001t0003g0271a0001c0001t0003g0272 | 2 | NA18982.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.-158+2513G>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2471771 | ||||||
chr4:2472008
|
A | G | 1 | a0001c0001t0001g0214 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-158+2750A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2472008 | ||||||
chr4:2472131
|
T | G | 2 | a0001c0001t0001g0358a0001c0001t0001g0359 | 2 | HG02258.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.-158+2873T>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2472131 | ||||||
chr4:2472138
|
A | C | 1 | a0001c0001t0001g0349 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-158+2880A>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2472138 | ||||||
chr4:2472180
|
C | G | 2 | a0001c0001t0002g0212a0001c0001t0002g0213 | 2 | NA18943.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.-158+2922C>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2472180 | ||||||
chr4:2472197
|
A | G | 3 | a0001c0001t0001g0290a0001c0001t0015g0350a0001c0001t0015g0351 | 3 | HG02572.hp1 HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-158+2939A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2472197 | ||||||
chr4:2472315
|
G | C | 2 | a0001c0001t0001g0300a0001c0001t0001g0301 | 2 | NA18964.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.-158+3057G>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2472315 | ||||||
chr4:2472480
|
A | G | 320 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(317): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.-158+3222A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2472480 | ||||||
chr4:2472554
|
C | A | 7 | a0001c0001t0001g0001a0001c0001t0001g0030a0001c0001t0001g0031others(4): Show | 8 | NA18612.hp1 NA18945.hp1 NA18967.hp1 others(5): Show |
intron_variant | MODIFIER | c.-158+3296C>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2472554 | ||||||
chr4:2472601
|
TA | T | 165 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(162): Show | 169 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.-158+3361delA | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2472601 | |||||
chr4:2472601
|
TAA | T | 14 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0133others(11): Show | 14 | HG00558.hp1 HG00738.hp2 HG02015.hp1 others(11): Show |
intron_variant | MODIFIER | c.-158+3360_-158+336 others(6): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2472601 | |||||
chr4:2472601
|
TAAAAA | T | 55 | a0001c0001t0001g0140a0001c0001t0001g0182a0001c0001t0001g0214others(52): Show | 56 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(53): Show |
intron_variant | MODIFIER | c.-158+3357_-158+336 others(9): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2472601 | |||||
chr4:2472709
|
A | T | 17 | a0001c0001t0001g0132a0001c0001t0005g0011a0001c0001t0005g0012others(14): Show | 17 | HG01074.hp1 HG01081.hp1 HG01358.hp2 others(14): Show |
intron_variant | MODIFIER | c.-158+3451A>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2472709 | ||||||
chr4:2472807
|
G | A | 1 | a0001c0001t0020g0269 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-158+3549G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2472807 | ||||||
chr4:2472890
|
A | C | 319 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(316): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.-158+3632A>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2472890 | ||||||
chr4:2472900
|
C | A | 1 | a0001c0001t0002g0173 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-158+3642C>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2472900 | ||||||
chr4:2472910
|
G | T | 2 | a0001c0001t0008g0305a0001c0001t0008g0345 | 2 | NA19054.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.-158+3652G>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2472910 | ||||||
chr4:2472912
|
C | T | 2 | a0001c0001t0002g0210a0001c0001t0002g0211 | 2 | HG01934.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.-158+3654C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2472912 | ||||||
chr4:2472989
|
A | G | 320 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(317): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.-158+3731A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2472989 | ||||||
chr4:2473045
|
A | G | 1 | a0001c0001t0001g0029 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-158+3787A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2473045 | ||||||
chr4:2473046
|
G | A | 1 | a0001c0001t0001g0029 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-158+3788G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2473046 | ||||||
chr4:2473054
|
A | G | 16 | a0001c0001t0005g0011a0001c0001t0005g0012a0001c0001t0005g0013others(13): Show | 16 | HG01074.hp1 HG01081.hp1 HG01975.hp2 others(13): Show |
intron_variant | MODIFIER | c.-158+3796A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2473054 | ||||||
chr4:2473119
|
C | T | 2 | a0001c0001t0001g0005a0001c0001t0001g0262 | 3 | HG01884.hp1 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-158+3861C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2473119 | ||||||
chr4:2473136
|
C | CT | 2 | a0001c0001t0001g0005a0001c0001t0001g0262 | 3 | HG01884.hp1 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-158+3881dupT | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2473136 | |||||
chr4:2473179
|
T | C | 320 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(317): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.-158+3921T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2473179 | ||||||
chr4:2473281
|
A | G | 320 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(317): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.-158+4023A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2473281 | ||||||
chr4:2473298
|
C | T | 52 | a0001c0001t0001g0182a0001c0001t0001g0214a0001c0001t0001g0371others(49): Show | 53 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(50): Show |
intron_variant | MODIFIER | c.-158+4040C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2473298 | ||||||
chr4:2473347
|
G | A | 1 | a0001c0001t0001g0262 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-158+4089G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2473347 | ||||||
chr4:2473381
|
T | TA | 18 | a0001c0001t0003g0171a0001c0001t0003g0257a0001c0001t0005g0012others(15): Show | 18 | HG02258.hp2 HG02451.hp1 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.-158+4134dupA | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2473381 | |||||
chr4:2473381
|
T | TC | 3 | a0001c0001t0001g0039a0001c0001t0001g0047a0001c0001t0001g0048 | 3 | HG01978.hp1 NA19001.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.-158+4123_-158+412 others(5): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2473381 | ||||||
chr4:2473382
|
A | C | 124 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(121): Show | 127 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.-158+4124A>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2473382 | ||||||
chr4:2473403
|
C | T | 2 | a0001c0002t0003g0254a0001c0002t0003g0255 | 2 | HG01255.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-158+4145C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2473403 | ||||||
chr4:2473468
|
A | G | 4 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(1): Show | 4 | HG01069.hp1 HG01071.hp2 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.-158+4210A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2473468 | ||||||
chr4:2473473
|
A | G | 1 | a0001c0001t0020g0269 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-158+4215A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2473473 | ||||||
chr4:2473629
|
GTGAAAC | G | 52 | a0001c0001t0001g0182a0001c0001t0001g0214a0001c0001t0001g0371others(49): Show | 53 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(50): Show |
intron_variant | MODIFIER | c.-158+4372_-158+437 others(10): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2473629 | ||||||
chr4:2473639
|
G | A | 1 | a0001c0001t0001g0302 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-158+4381G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2473639 | ||||||
chr4:2473660
|
A | C | 2 | a0001c0001t0001g0343a0001c0001t0001g0344 | 2 | NA18947.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.-158+4402A>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2473660 | ||||||
chr4:2473822
|
G | T | 4 | a0001c0001t0011g0364a0001c0001t0011g0365a0001c0001t0011g0366others(1): Show | 4 | HG02257.hp1 HG03471.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-158+4564G>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2473822 | ||||||
chr4:2473930
|
A | G | 320 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(317): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.-158+4672A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2473930 | ||||||
chr4:2474195
|
G | T | 2 | a0001c0001t0001g0127a0001c0001t0025g0126 | 2 | NA18967.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.-158+4937G>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2474195 | ||||||
chr4:2474220
|
AC | A | 320 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(317): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.-158+4963delC | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2474220 | ||||||
chr4:2474318
|
C | T | 11 | a0001c0001t0001g0300a0001c0001t0001g0301a0001c0001t0001g0337others(8): Show | 11 | HG00438.hp1 HG00597.hp2 NA18947.hp2 others(8): Show |
intron_variant | MODIFIER | c.-158+5060C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2474318 | ||||||
chr4:2474327
|
G | A | 3 | a0001c0001t0001g0290a0001c0001t0015g0350a0001c0001t0015g0351 | 3 | HG02572.hp1 HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-158+5069G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2474327 | ||||||
chr4:2474381
|
C | CA | 20 | a0001c0001t0001g0027a0001c0001t0001g0049a0001c0001t0001g0050others(17): Show | 21 | HG01074.hp1 HG01081.hp1 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.-158+5142dupA | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2474381 | |||||
chr4:2474381
|
CA | C | 165 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0035others(162): Show | 167 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.-158+5142delA | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2474381 | |||||
chr4:2474381
|
CAA | C | 6 | a0001c0001t0001g0298a0001c0001t0001g0299a0001c0001t0002g0169others(3): Show | 6 | HG02145.hp1 HG03130.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.-158+5141_-158+514 others(6): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2474381 | |||||
chr4:2474598
|
G | A | 317 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(314): Show | 322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.-158+5340G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2474598 | ||||||
chr4:2474752
|
C | T | 2 | a0001c0001t0015g0350a0001c0001t0015g0351 | 2 | HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-158+5494C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2474752 | ||||||
chr4:2474843
|
G | A | 20 | a0001c0001t0001g0298a0001c0001t0001g0299a0001c0001t0001g0353others(17): Show | 20 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.-158+5585G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2474843 | ||||||
chr4:2474859
|
G | A | 1 | a0001c0001t0001g0053 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-158+5601G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2474859 | ||||||
chr4:2474860
|
A | C | 52 | a0001c0001t0001g0182a0001c0001t0001g0214a0001c0001t0001g0371others(49): Show | 53 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(50): Show |
intron_variant | MODIFIER | c.-158+5602A>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2474860 | ||||||
chr4:2474919
|
C | T | 2 | a0001c0001t0015g0350a0001c0001t0015g0351 | 2 | HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-158+5661C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2474919 | ||||||
chr4:2474983
|
C | T | 121 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(118): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-158+5725C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2474983 | ||||||
chr4:2475052
|
A | G | 2 | a0001c0001t0015g0350a0001c0001t0015g0351 | 2 | HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-158+5794A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2475052 | ||||||
chr4:2475075
|
C | T | 1 | a0001c0001t0001g0290 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-158+5817C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2475075 | ||||||
chr4:2475102
|
C | T | 1 | a0001c0001t0001g0290 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-158+5844C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2475102 | ||||||
chr4:2475162
|
A | G | 317 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(314): Show | 322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.-158+5904A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2475162 | ||||||
chr4:2475168
|
A | G | 16 | a0001c0001t0005g0011a0001c0001t0005g0012a0001c0001t0005g0013others(13): Show | 16 | HG01074.hp1 HG01081.hp1 HG01975.hp2 others(13): Show |
intron_variant | MODIFIER | c.-158+5910A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2475168 | ||||||
chr4:2475195
|
T | A | 126 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(123): Show | 129 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.-158+5937T>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2475195 | ||||||
chr4:2475214
|
G | A | 1 | a0001c0001t0020g0269 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-158+5956G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2475214 | ||||||
chr4:2475310
|
C | T | 2 | a0001c0001t0005g0296a0001c0001t0005g0297 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-158+6052C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2475310 | ||||||
chr4:2475331
|
T | TTTTG | 51 | a0001c0001t0001g0182a0001c0001t0001g0214a0001c0001t0001g0371others(48): Show | 52 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.-158+6093_-158+609 others(8): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2475331 | |||||
chr4:2475443
|
A | G | 1 | a0001c0001t0001g0335 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-158+6185A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2475443 | ||||||
chr4:2475501
|
G | A | 2 | a0001c0001t0015g0350a0001c0001t0015g0351 | 2 | HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-158+6243G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2475501 | ||||||
chr4:2475554
|
G | A | 265 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(262): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.-158+6296G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2475554 | ||||||
chr4:2475618
|
G | A | 2 | a0001c0001t0003g0218a0001c0001t0003g0219 | 2 | NA18999.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.-158+6360G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2475618 | ||||||
chr4:2476008
|
T | C | 1 | a0001c0001t0006g0153 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-158+6750T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2476008 | ||||||
chr4:2476078
|
A | G | 320 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(317): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.-158+6820A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2476078 | ||||||
chr4:2476269
|
T | C | 2 | a0001c0001t0002g0058a0001c0001t0002g0143 | 2 | HG00642.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.-158+7011T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2476269 | ||||||
chr4:2476533
|
C | T | 1 | a0001c0001t0001g0044 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-158+7275C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2476533 | ||||||
chr4:2476550
|
G | A | 2 | a0001c0001t0001g0005a0001c0001t0001g0262 | 3 | HG01884.hp1 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-158+7292G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2476550 | ||||||
chr4:2476586
|
G | C | 126 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(123): Show | 129 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.-158+7328G>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2476586 | ||||||
chr4:2476604
|
G | T | 2 | a0001c0001t0001g0005a0001c0001t0001g0262 | 3 | HG01884.hp1 HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-158+7346G>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2476604 | ||||||
chr4:2476642
|
C | T | 1 | a0001c0001t0001g0038 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-158+7384C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2476642 | ||||||
chr4:2476683
|
G | A | 16 | a0001c0001t0005g0011a0001c0001t0005g0012a0001c0001t0005g0013others(13): Show | 16 | HG01074.hp1 HG01081.hp1 HG01975.hp2 others(13): Show |
intron_variant | MODIFIER | c.-158+7425G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2476683 | ||||||
chr4:2476690
|
C | G | 1 | a0001c0001t0010g0253 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-158+7432C>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2476690 | ||||||
chr4:2476704
|
C | CT | 89 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(86): Show | 89 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.-158+7462dupT | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2476704 | |||||
chr4:2476704
|
CT | C | 15 | a0001c0001t0001g0029a0001c0001t0001g0035a0001c0001t0001g0049others(12): Show | 15 | HG00609.hp1 HG01069.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.-158+7462delT | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2476704 | |||||
chr4:2476707
|
T | TC | 5 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0287others(2): Show | 5 | HG02257.hp2 HG02280.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.-158+7449_-158+745 others(5): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2476707 | ||||||
chr4:2476740
|
T | C | 1 | a0001c0001t0001g0150 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-158+7482T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2476740 | ||||||
chr4:2476754
|
G | A | 2 | a0001c0001t0002g0058a0001c0001t0002g0143 | 2 | HG00642.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.-158+7496G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2476754 | ||||||
chr4:2476794
|
G | A | 55 | a0001c0001t0001g0182a0001c0001t0001g0214a0001c0001t0001g0290others(52): Show | 56 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.-158+7536G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2476794 | ||||||
chr4:2476812
|
C | CT | 18 | a0001c0001t0003g0219a0001c0001t0005g0011a0001c0001t0005g0012others(15): Show | 18 | HG01074.hp1 HG01081.hp1 HG01975.hp2 others(15): Show |
intron_variant | MODIFIER | c.-158+7568dupT | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2476812 | |||||
chr4:2476812
|
CT | C | 20 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0064others(17): Show | 20 | HG01169.hp1 HG01496.hp2 HG01515.hp2 others(17): Show |
intron_variant | MODIFIER | c.-158+7568delT | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2476812 | |||||
chr4:2477366
|
C | A | 1 | a0001c0001t0002g0174 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-158+8108C>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2477366 | ||||||
chr4:2477374
|
T | C | 1 | a0001c0001t0008g0066 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-158+8116T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2477374 | ||||||
chr4:2477388
|
G | C | 2 | a0001c0001t0015g0350a0001c0001t0015g0351 | 2 | HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-158+8130G>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2477388 | ||||||
chr4:2477401
|
A | G | 17 | a0001c0001t0003g0252a0001c0001t0005g0011a0001c0001t0005g0012others(14): Show | 17 | HG00408.hp2 HG01074.hp1 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.-158+8143A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2477401 | ||||||
chr4:2477413
|
T | C | 89 | a0001c0001t0001g0047a0001c0001t0001g0050a0001c0001t0001g0053others(86): Show | 90 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.-158+8155T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2477413 | ||||||
chr4:2477529
|
G | A | 4 | a0001c0001t0005g0019a0001c0001t0006g0154a0001c0001t0013g0368others(1): Show | 4 | HG01975.hp2 HG02818.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-158+8271G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2477529 | ||||||
chr4:2477575
|
C | T | 1 | a0001c0001t0001g0142 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-158+8317C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2477575 | ||||||
chr4:2477793
|
G | A | 1 | a0001c0001t0001g0290 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-158+8535G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2477793 | ||||||
chr4:2477804
|
C | T | 1 | a0001c0001t0002g0209 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-158+8546C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2477804 | ||||||
chr4:2477836
|
A | G | 1 | a0001c0001t0007g0334 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-158+8578A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2477836 | ||||||
chr4:2477992
|
G | A | 1 | a0001c0001t0001g0077 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-158+8734G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2477992 | ||||||
chr4:2477993
|
A | T | 1 | a0001c0001t0023g0023 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-158+8735A>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2477993 | ||||||
chr4:2478033
|
A | G | 1 | a0001c0001t0003g0251 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-158+8775A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2478033 | ||||||
chr4:2478086
|
T | G | 123 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0024others(120): Show | 125 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.-158+8828T>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2478086 | ||||||
chr4:2478284
|
C | T | 1 | a0001c0001t0002g0209 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-158+9026C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2478284 | ||||||
chr4:2478372
|
C | T | 1 | a0001c0003t0021g0306 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-158+9114C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2478372 | ||||||
chr4:2478397
|
A | G | 2 | a0001c0001t0001g0121a0001c0001t0001g0147 | 2 | HG02056.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.-158+9139A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2478397 | ||||||
chr4:2478509
|
G | T | 2 | a0001c0003t0014g0357a0001c0003t0014g0370 | 2 | HG01243.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-158+9251G>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2478509 | ||||||
chr4:2478544
|
C | T | 28 | a0001c0001t0002g0122a0001c0001t0002g0200a0001c0001t0002g0201others(25): Show | 29 | HG00544.hp1 HG00609.hp2 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.-158+9286C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2478544 | ||||||
chr4:2478550
|
A | C | 2 | a0001c0003t0014g0357a0001c0003t0014g0370 | 2 | HG01243.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-158+9292A>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2478550 | ||||||
chr4:2478591
|
T | C | 334 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(331): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(336): Show |
intron_variant | MODIFIER | c.-158+9333T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2478591 | ||||||
chr4:2478651
|
G | A | 1 | a0001c0002t0003g0255 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-158+9393G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2478651 | ||||||
chr4:2478752
|
G | A | 2 | a0001c0001t0001g0078a0001c0001t0001g0079 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-158+9494G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2478752 | ||||||
chr4:2478834
|
G | A | 4 | a0001c0001t0001g0309a0001c0001t0001g0310a0001c0001t0001g0311others(1): Show | 4 | HG01256.hp1 HG01258.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.-158+9576G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2478834 | ||||||
chr4:2478994
|
G | A | 1 | a0001c0001t0001g0304 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-158+9736G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2478994 | ||||||
chr4:2479352
|
T | C | 1 | a0001c0001t0001g0054 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-158+10094T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2479352 | ||||||
chr4:2479361
|
A | T | 120 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0024others(117): Show | 122 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.-158+10103A>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2479361 | ||||||
chr4:2479405
|
G | C | 38 | a0001c0001t0001g0008a0001c0001t0001g0164a0001c0001t0001g0285others(35): Show | 38 | HG02145.hp1 HG02257.hp1 HG02257.hp2 others(35): Show |
intron_variant | MODIFIER | c.-158+10147G>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2479405 | ||||||
chr4:2479414
|
A | T | 3 | a0001c0001t0003g0248a0001c0001t0003g0250a0001c0001t0010g0249 | 3 | HG02055.hp1 HG02451.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.-158+10156A>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2479414 | ||||||
chr4:2479557
|
C | T | 7 | a0001c0001t0001g0008a0001c0001t0001g0285a0001c0001t0001g0286others(4): Show | 7 | HG02257.hp2 HG02280.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.-158+10299C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2479557 | ||||||
chr4:2479602
|
C | G | 1 | a0001c0001t0002g0209 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-158+10344C>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2479602 | ||||||
chr4:2479636
|
C | T | 2 | a0001c0003t0014g0357a0001c0003t0014g0370 | 2 | HG01243.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-158+10378C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2479636 | ||||||
chr4:2479700
|
G | A | 1 | a0001c0001t0001g0080 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-158+10442G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2479700 | ||||||
chr4:2479719
|
G | A | 1 | a0001c0001t0002g0205 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-158+10461G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2479719 | ||||||
chr4:2479746
|
C | T | 1 | a0001c0001t0001g0304 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-158+10488C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2479746 | ||||||
chr4:2479763
|
G | A | 72 | a0001c0001t0003g0170a0001c0001t0003g0171a0001c0001t0003g0218others(69): Show | 72 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.-158+10505G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2479763 | ||||||
chr4:2479765
|
C | G | 3 | a0001c0001t0012g0221a0001c0001t0012g0246a0001c0001t0012g0247 | 3 | HG01516.hp1 HG03704.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.-158+10507C>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2479765 | ||||||
chr4:2479916
|
GAGGAGCT others(5): Show |
G | 1 | a0001c0001t0001g0304 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-157-10419_-157-10 others(18): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2479916 | |||||
chr4:2479933
|
T | C | 1 | a0001c0001t0002g0180 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-157-10404T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2479933 | ||||||
chr4:2479942
|
G | GTCGGTGT others(3): Show |
1 | a0001c0001t0008g0282 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-157-10394_-157-10 others(16): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2479942 | |||||
chr4:2480077
|
C | T | 2 | a0001c0001t0001g0035a0001c0001t0001g0127 | 2 | NA19007.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.-157-10260C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2480077 | ||||||
chr4:2480272
|
C | CT | 16 | a0001c0001t0001g0027a0001c0001t0001g0121a0001c0001t0001g0130others(13): Show | 16 | HG01515.hp2 HG01516.hp1 HG01516.hp2 others(13): Show |
intron_variant | MODIFIER | c.-157-10047dupT | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2480272 | |||||
chr4:2480272
|
CT | C | 24 | a0001c0001t0001g0005a0001c0001t0001g0035a0001c0001t0001g0050others(21): Show | 25 | HG01070.hp1 HG01169.hp1 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.-157-10047delT | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2480272 | |||||
chr4:2480297
|
A | G | 1 | a0001c0001t0001g0304 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-157-10040A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2480297 | ||||||
chr4:2480333
|
C | T | 2 | a0001c0001t0001g0262a0001c0001t0029g0363 | 2 | HG01884.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-157-10004C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2480333 | ||||||
chr4:2480429
|
T | C | 2 | a0001c0003t0014g0357a0001c0003t0014g0370 | 2 | HG01243.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-157-9908T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2480429 | ||||||
chr4:2480458
|
A | T | 1 | a0001c0001t0001g0164 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-157-9879A>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2480458 | ||||||
chr4:2480524
|
T | C | 335 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(332): Show | 340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.-157-9813T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2480524 | ||||||
chr4:2480583
|
GA | G | 7 | a0001c0001t0001g0353a0001c0001t0001g0354a0001c0001t0001g0355others(4): Show | 7 | HG02615.hp2 HG02622.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.-157-9742delA | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2480583 | |||||
chr4:2480764
|
G | A | 1 | a0001c0001t0001g0005 | 2 | HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-157-9573G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2480764 | ||||||
chr4:2480784
|
G | A | 2 | a0001c0001t0015g0350a0001c0001t0015g0351 | 2 | HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-157-9553G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2480784 | ||||||
chr4:2480866
|
G | T | 1 | a0001c0001t0010g0245 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-157-9471G>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2480866 | ||||||
chr4:2480972
|
C | T | 2 | a0001c0001t0001g0005a0001c0001t0002g0174 | 3 | HG03225.hp1 HG04184.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-157-9365C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2480972 | ||||||
chr4:2481137
|
A | G | 1 | a0001c0001t0010g0253 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-157-9200A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2481137 | ||||||
chr4:2481310
|
A | G | 1 | a0001c0001t0002g0204 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-157-9027A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2481310 | ||||||
chr4:2481419
|
A | G | 1 | a0001c0001t0001g0043 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-157-8918A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2481419 | ||||||
chr4:2481479
|
T | G | 18 | a0001c0001t0005g0011a0001c0001t0005g0012a0001c0001t0005g0013others(15): Show | 18 | HG01074.hp1 HG01081.hp1 HG01975.hp2 others(15): Show |
intron_variant | MODIFIER | c.-157-8858T>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2481479 | ||||||
chr4:2481668
|
A | G | 6 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0287others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.-157-8669A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2481668 | ||||||
chr4:2481707
|
G | A | 2 | a0001c0001t0001g0068a0001c0001t0001g0069 | 2 | HG03490.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.-157-8630G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2481707 | ||||||
chr4:2481959
|
G | A | 1 | a0001c0001t0007g0320 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-157-8378G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2481959 | ||||||
chr4:2481983
|
C | T | 3 | a0001c0003t0014g0357a0001c0003t0014g0370a0001c0003t0021g0306 | 3 | HG01167.hp2 HG01243.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-157-8354C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2481983 | ||||||
chr4:2482127
|
C | G | 35 | a0001c0001t0003g0171a0001c0001t0003g0224a0001c0001t0003g0242others(32): Show | 35 | HG01074.hp1 HG01081.hp1 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.-157-8210C>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2482127 | ||||||
chr4:2482173
|
C | A | 1 | a0001c0001t0024g0215 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-157-8164C>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2482173 | ||||||
chr4:2482190
|
G | A | 2 | a0001c0001t0001g0262a0001c0001t0029g0363 | 2 | HG01884.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-157-8147G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2482190 | ||||||
chr4:2482443
|
C | G | 19 | a0001c0001t0001g0005a0001c0001t0005g0011a0001c0001t0005g0012others(16): Show | 20 | HG01074.hp1 HG01081.hp1 HG01975.hp2 others(17): Show |
intron_variant | MODIFIER | c.-157-7894C>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2482443 | ||||||
chr4:2482476
|
C | T | 38 | a0001c0001t0001g0008a0001c0001t0001g0164a0001c0001t0001g0285others(35): Show | 38 | HG02145.hp1 HG02257.hp1 HG02257.hp2 others(35): Show |
intron_variant | MODIFIER | c.-157-7861C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2482476 | ||||||
chr4:2482480
|
G | A | 1 | a0001c0003t0014g0357 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-157-7857G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2482480 | ||||||
chr4:2482481
|
G | T | 1 | a0001c0003t0014g0357 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-157-7856G>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2482481 | ||||||
chr4:2482668
|
T | C | 1 | a0001c0001t0001g0286 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-157-7669T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2482668 | ||||||
chr4:2482849
|
GCCTGT | G | 123 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0024others(120): Show | 125 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.-157-7486_-157-748 others(9): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2482849 | |||||
chr4:2482916
|
G | T | 18 | a0001c0001t0005g0011a0001c0001t0005g0012a0001c0001t0005g0013others(15): Show | 18 | HG01074.hp1 HG01081.hp1 HG01975.hp2 others(15): Show |
intron_variant | MODIFIER | c.-157-7421G>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2482916 | ||||||
chr4:2482931
|
C | T | 1 | a0001c0003t0021g0306 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-157-7406C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2482931 | ||||||
chr4:2482984
|
T | C | 1 | a0001c0001t0003g0294 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-157-7353T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2482984 | ||||||
chr4:2483130
|
T | C | 1 | a0001c0001t0002g0183 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-157-7207T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2483130 | ||||||
chr4:2483328
|
T | C | 2 | a0001c0003t0014g0357a0001c0003t0014g0370 | 2 | HG01243.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-157-7009T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2483328 | ||||||
chr4:2483364
|
A | C | 1 | a0001c0003t0021g0306 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-157-6973A>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2483364 | ||||||
chr4:2483370
|
G | C | 1 | a0001c0003t0021g0306 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-157-6967G>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2483370 | ||||||
chr4:2483371
|
T | A | 1 | a0001c0003t0021g0306 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-157-6966T>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2483371 | ||||||
chr4:2483404
|
C | A | 1 | a0001c0001t0002g0180 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-157-6933C>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2483404 | ||||||
chr4:2483568
|
T | C | 338 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(335): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.-157-6769T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2483568 | ||||||
chr4:2483578
|
C | G | 1 | a0001c0001t0002g0209 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-157-6759C>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2483578 | ||||||
chr4:2483660
|
C | T | 94 | a0001c0001t0003g0171a0001c0001t0003g0218a0001c0001t0003g0219others(91): Show | 95 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.-157-6677C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2483660 | ||||||
chr4:2483675
|
G | A | 1 | a0001c0001t0003g0225 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-157-6662G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2483675 | ||||||
chr4:2483850
|
T | C | 1 | a0001c0001t0001g0054 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-157-6487T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2483850 | ||||||
chr4:2483888
|
A | C | 51 | a0001c0001t0002g0004a0001c0001t0002g0122a0001c0001t0002g0167others(48): Show | 52 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.-157-6449A>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2483888 | ||||||
chr4:2483895
|
C | T | 1 | a0001c0001t0001g0005 | 2 | HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-157-6442C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2483895 | ||||||
chr4:2483901
|
C | T | 2 | a0001c0001t0001g0262a0001c0001t0029g0363 | 2 | HG01884.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-157-6436C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2483901 | ||||||
chr4:2483946
|
G | C | 4 | a0001c0001t0020g0269a0001c0003t0014g0357a0001c0003t0014g0370others(1): Show | 4 | HG01167.hp2 HG01243.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.-157-6391G>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2483946 | ||||||
chr4:2483949
|
C | T | 1 | a0001c0001t0003g0294 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-157-6388C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2483949 | ||||||
chr4:2483971
|
C | T | 38 | a0001c0001t0001g0008a0001c0001t0001g0164a0001c0001t0001g0285others(35): Show | 38 | HG02145.hp1 HG02257.hp1 HG02257.hp2 others(35): Show |
intron_variant | MODIFIER | c.-157-6366C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2483971 | ||||||
chr4:2483983
|
C | T | 1 | a0001c0003t0021g0306 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-157-6354C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2483983 | ||||||
chr4:2484042
|
G | A | 1 | a0001c0001t0003g0267 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-157-6295G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2484042 | ||||||
chr4:2484047
|
G | A | 1 | a0001c0001t0032g0360 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-157-6290G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2484047 | ||||||
chr4:2484067
|
T | TCCCCC | 15 | a0001c0001t0001g0318a0001c0001t0001g0358a0001c0001t0001g0359others(12): Show | 16 | HG00544.hp1 HG00544.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-157-6266_-157-626 others(9): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2484067 | |||||
chr4:2484067
|
T | TCCCCCC | 25 | a0001c0001t0001g0115a0001c0001t0001g0132a0001c0001t0001g0144others(22): Show | 25 | HG00408.hp2 HG01257.hp2 HG01358.hp1 others(22): Show |
intron_variant | MODIFIER | c.-157-6267_-157-626 others(10): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2484067 | |||||
chr4:2484067
|
T | TCCCCCCC others(1): Show |
17 | a0001c0001t0001g0039a0001c0001t0001g0083a0001c0001t0001g0125others(14): Show | 17 | HG00735.hp1 HG01106.hp2 HG02004.hp1 others(14): Show |
intron_variant | MODIFIER | c.-157-6269_-157-626 others(12): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2484067 | |||||
chr4:2484067
|
T | TCCCCCCC others(9): Show |
1 | a0001c0001t0003g0259 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-157-6262_-157-626 others(20): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2484067 | |||||
chr4:2484067
|
T | TCCCCCCC others(3): Show |
2 | a0001c0001t0001g0300a0001c0001t0006g0154 | 2 | HG03540.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.-157-6262_-157-626 others(14): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2484067 | |||||
chr4:2484067
|
T | TCCCCCCC others(4): Show |
11 | a0001c0001t0001g0007a0001c0001t0001g0034a0001c0001t0001g0114others(8): Show | 12 | HG00438.hp1 HG00639.hp2 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.-157-6262_-157-626 others(15): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2484067 | |||||
chr4:2484067
|
T | TCCCCCCC others(5): Show |
13 | a0001c0001t0001g0001a0001c0001t0001g0079a0001c0001t0001g0110others(10): Show | 14 | HG00140.hp2 HG00323.hp1 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.-157-6262_-157-626 others(16): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2484067 | |||||
chr4:2484067
|
T | TCCCCCCC others(6): Show |
16 | a0001c0001t0001g0047a0001c0001t0001g0069a0001c0001t0001g0073others(13): Show | 16 | HG00280.hp1 HG01257.hp1 HG01515.hp1 others(13): Show |
intron_variant | MODIFIER | c.-157-6262_-157-626 others(17): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2484067 | |||||
chr4:2484067
|
T | TCCCCCCC others(7): Show |
14 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0052others(11): Show | 15 | HG00099.hp1 HG00741.hp1 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.-157-6262_-157-626 others(18): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2484067 | |||||
chr4:2484067
|
T | TCCCCCCC others(8): Show |
16 | a0001c0001t0001g0032a0001c0001t0001g0061a0001c0001t0001g0062others(13): Show | 16 | HG00438.hp2 HG00609.hp1 HG01069.hp1 others(13): Show |
intron_variant | MODIFIER | c.-157-6262_-157-626 others(19): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2484067 | |||||
chr4:2484067
|
T | TCCCCCCC others(9): Show |
33 | a0001c0001t0001g0029a0001c0001t0001g0031a0001c0001t0001g0035others(30): Show | 33 | HG00558.hp1 HG00738.hp1 HG01169.hp2 others(30): Show |
intron_variant | MODIFIER | c.-157-6262_-157-626 others(20): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2484067 | |||||
chr4:2484067
|
T | TCCCCCCC others(10): Show |
24 | a0001c0001t0001g0026a0001c0001t0001g0038a0001c0001t0001g0064others(21): Show | 24 | HG00323.hp2 HG00558.hp2 HG00597.hp1 others(21): Show |
intron_variant | MODIFIER | c.-157-6262_-157-626 others(21): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2484067 | |||||
chr4:2484067
|
T | TCCCCCCC others(11): Show |
23 | a0001c0001t0001g0027a0001c0001t0001g0037a0001c0001t0001g0093others(20): Show | 23 | HG00099.hp2 HG00408.hp1 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.-157-6262_-157-626 others(22): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2484067 | |||||
chr4:2484067
|
T | TCCCCCCC others(12): Show |
18 | a0001c0001t0001g0036a0001c0001t0001g0091a0001c0001t0001g0092others(15): Show | 18 | HG00609.hp2 HG01074.hp2 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.-157-6262_-157-626 others(23): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2484067 | |||||
chr4:2484067
|
T | TCCCCCCC others(13): Show |
19 | a0001c0001t0001g0051a0001c0001t0001g0089a0001c0001t0001g0090others(16): Show | 19 | HG00140.hp1 HG00280.hp2 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.-157-6262_-157-626 others(24): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2484067 | |||||
chr4:2484067
|
T | TCCCCCCC others(14): Show |
11 | a0001c0001t0001g0002a0001c0001t0001g0086a0001c0001t0001g0088others(8): Show | 12 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.-157-6262_-157-626 others(25): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2484067 | |||||
chr4:2484067
|
T | TCCCCCCC others(15): Show |
15 | a0001c0001t0001g0028a0001c0001t0001g0347a0001c0001t0002g0187others(12): Show | 16 | HG00642.hp1 HG01099.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.-157-6262_-157-626 others(26): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2484067 | |||||
chr4:2484067
|
T | TCCCCCCC others(16): Show |
9 | a0001c0001t0001g0060a0001c0001t0001g0085a0001c0001t0001g0353others(6): Show | 9 | HG02056.hp1 HG02083.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.-157-6262_-157-626 others(27): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2484067 | |||||
chr4:2484067
|
T | TCCCCCCC others(17): Show |
8 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0002g0175others(5): Show | 8 | HG00673.hp1 HG01169.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.-157-6262_-157-626 others(28): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2484067 | |||||
chr4:2484067
|
T | TCCCCCCC others(18): Show |
5 | a0001c0001t0002g0264a0001c0001t0003g0248a0001c0001t0004g0084others(2): Show | 5 | HG02809.hp1 HG03195.hp1 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.-157-6262_-157-626 others(29): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2484067 | |||||
chr4:2484067
|
T | TCCCCCCC others(19): Show |
2 | a0001c0001t0001g0348a0001c0001t0002g0185 | 2 | NA18968.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-157-6262_-157-626 others(30): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2484067 | |||||
chr4:2484067
|
T | TCCCCCCC others(20): Show |
2 | a0001c0001t0002g0184a0001c0001t0002g0208 | 2 | HG01167.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-157-6262_-157-626 others(31): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2484067 | |||||
chr4:2484067
|
T | TCCCCCCC others(21): Show |
1 | a0001c0005t0001g0312 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-157-6262_-157-626 others(32): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2484067 | |||||
chr4:2484067
|
T | TCCCCCCC others(23): Show |
1 | a0001c0001t0004g0278 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-157-6262_-157-626 others(34): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2484067 | |||||
chr4:2484067
|
T | TCCCCCCC others(28): Show |
1 | a0001c0001t0001g0304 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-157-6262_-157-626 others(39): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2484067 | |||||
chr4:2484067
|
T | TCCCCCGC others(8): Show |
1 | a0001c0001t0001g0150 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-157-6265_-157-626 others(19): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2484067 | |||||
chr4:2484067
|
T | TTCCCCCC others(4): Show |
1 | a0001c0001t0004g0292 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-157-6270_-157-626 others(15): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2484067 | ||||||
chr4:2484067
|
T | TTCCCCCC others(10): Show |
1 | a0001c0001t0001g0076 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-157-6270_-157-626 others(21): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2484067 | ||||||
chr4:2484068
|
C | T | 1 | a0001c0003t0021g0306 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-157-6269C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2484068 | ||||||
chr4:2484071
|
C | CCCCCCCC others(6): Show |
1 | a0001c0001t0001g0074 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-157-6262_-157-626 others(17): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2484071 | |||||
chr4:2484071
|
C | CCCCCCCC others(5): Show |
3 | a0001c0001t0001g0075a0001c0001t0002g0058a0001c0001t0002g0143 | 3 | HG00642.hp2 HG00735.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.-157-6262_-157-626 others(16): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2484071 | |||||
chr4:2484071
|
C | CCCCG | 19 | a0001c0001t0001g0005a0001c0001t0005g0011a0001c0001t0005g0012others(16): Show | 20 | HG01074.hp1 HG01081.hp1 HG01975.hp2 others(17): Show |
intron_variant | MODIFIER | c.-157-6263_-157-626 others(8): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2484071 | |||||
chr4:2484074
|
C | CCCCCCCC others(9): Show |
1 | a0001c0001t0001g0059 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-157-6262_-157-626 others(20): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2484074 | |||||
chr4:2484076
|
G | C | 1 | a0001c0003t0021g0306 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-157-6261G>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2484076 | ||||||
chr4:2484080
|
C | T | 1 | a0001c0001t0001g0150 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-157-6257C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2484080 | ||||||
chr4:2484094
|
G | T | 2 | a0001c0003t0014g0357a0001c0003t0014g0370 | 2 | HG01243.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-157-6243G>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2484094 | ||||||
chr4:2484205
|
T | C | 1 | a0001c0001t0010g0222 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-157-6132T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2484205 | ||||||
chr4:2484214
|
A | G | 370 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(367): Show | 377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.-157-6123A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2484214 | ||||||
chr4:2484513
|
A | G | 1 | a0001c0001t0001g0335 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-157-5824A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2484513 | ||||||
chr4:2484576
|
A | G | 1 | a0001c0001t0002g0168 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-157-5761A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2484576 | ||||||
chr4:2484589
|
A | G | 1 | a0001c0001t0002g0203 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-157-5748A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2484589 | ||||||
chr4:2484599
|
A | G | 2 | a0001c0003t0014g0357a0001c0003t0014g0370 | 2 | HG01243.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-157-5738A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2484599 | ||||||
chr4:2484759
|
C | T | 95 | a0001c0001t0003g0170a0001c0001t0003g0171a0001c0001t0003g0218others(92): Show | 96 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.-157-5578C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2484759 | ||||||
chr4:2484798
|
G | A | 1 | a0001c0003t0014g0357 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-157-5539G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2484798 | ||||||
chr4:2484877
|
C | G | 1 | a0001c0001t0001g0302 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-157-5460C>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2484877 | ||||||
chr4:2484894
|
A | G | 1 | a0001c0001t0002g0173 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-157-5443A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2484894 | ||||||
chr4:2484974
|
G | T | 2 | a0001c0001t0002g0188a0001c0001t0002g0265 | 2 | HG00280.hp2 HG00323.hp2 |
intron_variant | MODIFIER | c.-157-5363G>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2484974 | ||||||
chr4:2485174
|
C | T | 1 | a0001c0001t0008g0345 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-157-5163C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2485174 | ||||||
chr4:2485358
|
A | C | 1 | a0001c0003t0014g0357 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-157-4979A>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2485358 | ||||||
chr4:2485377
|
A | G | 1 | a0001c0001t0004g0033 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-157-4960A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2485377 | ||||||
chr4:2485424
|
C | G | 6 | a0001c0001t0001g0358a0001c0001t0001g0359a0001c0001t0011g0364others(3): Show | 6 | HG02257.hp1 HG02258.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.-157-4913C>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2485424 | ||||||
chr4:2485593
|
A | G | 1 | a0001c0001t0009g0232 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-157-4744A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2485593 | ||||||
chr4:2485639
|
C | T | 124 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0024others(121): Show | 126 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(123): Show |
intron_variant | MODIFIER | c.-157-4698C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2485639 | ||||||
chr4:2485698
|
C | A | 1 | a0001c0001t0003g0170 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-157-4639C>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2485698 | ||||||
chr4:2485780
|
G | A | 2 | a0001c0003t0014g0357a0001c0003t0014g0370 | 2 | HG01243.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-157-4557G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2485780 | ||||||
chr4:2485850
|
G | A | 14 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0044others(11): Show | 14 | HG02004.hp2 NA18612.hp2 NA18747.hp1 others(11): Show |
intron_variant | MODIFIER | c.-157-4487G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2485850 | ||||||
chr4:2485919
|
T | G | 1 | a0001c0001t0002g0176 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-157-4418T>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2485919 | ||||||
chr4:2485994
|
G | A | 1 | a0001c0001t0006g0161 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-157-4343G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2485994 | ||||||
chr4:2486703
|
A | C | 1 | a0001c0001t0002g0120 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-157-3634A>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2486703 | ||||||
chr4:2486704
|
G | C | 1 | a0001c0001t0002g0120 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-157-3633G>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2486704 | ||||||
chr4:2486761
|
C | T | 91 | a0001c0001t0003g0171a0001c0001t0003g0218a0001c0001t0003g0219others(88): Show | 92 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.-157-3576C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2486761 | ||||||
chr4:2486868
|
C | T | 1 | a0001c0001t0001g0071 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-157-3469C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2486868 | ||||||
chr4:2486982
|
G | A | 91 | a0001c0001t0003g0171a0001c0001t0003g0218a0001c0001t0003g0219others(88): Show | 92 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.-157-3355G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2486982 | ||||||
chr4:2487069
|
G | A | 1 | a0001c0001t0002g0198 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-157-3268G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2487069 | ||||||
chr4:2487113
|
C | A | 1 | a0001c0001t0017g0009 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-157-3224C>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2487113 | ||||||
chr4:2487216
|
C | G | 1 | a0001c0001t0002g0213 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-157-3121C>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2487216 | ||||||
chr4:2487280
|
A | C | 32 | a0001c0001t0001g0008a0001c0001t0001g0164a0001c0001t0001g0285others(29): Show | 32 | HG02145.hp1 HG02257.hp1 HG02257.hp2 others(29): Show |
intron_variant | MODIFIER | c.-157-3057A>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2487280 | ||||||
chr4:2487430
|
C | T | 2 | a0001c0001t0015g0350a0001c0001t0015g0351 | 2 | HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-157-2907C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2487430 | ||||||
chr4:2487651
|
G | A | 2 | a0001c0001t0009g0226a0001c0001t0009g0232 | 2 | HG02723.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-157-2686G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2487651 | ||||||
chr4:2487804
|
T | C | 1 | a0001c0001t0001g0358 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-157-2533T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2487804 | ||||||
chr4:2487866
|
A | G | 1 | a0001c0001t0001g0005 | 2 | HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-157-2471A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2487866 | ||||||
chr4:2487905
|
C | T | 1 | a0001c0001t0001g0150 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-157-2432C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2487905 | ||||||
chr4:2488022
|
C | T | 1 | a0001c0001t0029g0363 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-157-2315C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2488022 | ||||||
chr4:2488072
|
C | T | 3 | a0001c0001t0001g0262a0001c0001t0015g0350a0001c0001t0015g0351 | 3 | HG01884.hp1 HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-157-2265C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2488072 | ||||||
chr4:2488106
|
G | A | 2 | a0001c0001t0008g0066a0001c0001t0008g0327 | 2 | HG00609.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.-157-2231G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2488106 | ||||||
chr4:2488229
|
G | A | 1 | a0001c0001t0003g0260 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-157-2108G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2488229 | ||||||
chr4:2488371
|
G | C | 1 | a0001c0001t0001g0110 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-157-1966G>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2488371 | ||||||
chr4:2488375
|
A | C | 1 | a0001c0001t0001g0337 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-157-1962A>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2488375 | ||||||
chr4:2488473
|
C | A | 22 | a0001c0001t0001g0005a0001c0001t0001g0074a0001c0001t0001g0150others(19): Show | 23 | HG01261.hp1 HG02258.hp2 HG02451.hp1 others(20): Show |
intron_variant | MODIFIER | c.-157-1864C>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2488473 | ||||||
chr4:2488476
|
A | C | 4 | a0001c0001t0001g0071a0001c0003t0014g0357a0001c0003t0014g0370others(1): Show | 4 | HG01167.hp2 HG01243.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.-157-1861A>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2488476 | ||||||
chr4:2488518
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-157-1819C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2488518 | ||||||
chr4:2488548
|
G | A | 117 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0024others(114): Show | 119 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(116): Show |
intron_variant | MODIFIER | c.-157-1789G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2488548 | ||||||
chr4:2488757
|
C | T | 1 | a0001c0003t0021g0306 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-157-1580C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2488757 | ||||||
chr4:2488809
|
A | ATTAT | 60 | a0001c0001t0001g0053a0001c0001t0001g0077a0001c0001t0001g0097others(57): Show | 61 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.-157-1526_-157-152 others(8): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2488809 | |||||
chr4:2488812
|
T | A | 177 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0024others(174): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.-157-1525T>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2488812 | ||||||
chr4:2488824
|
A | T | 93 | a0001c0001t0001g0008a0001c0001t0003g0171a0001c0001t0003g0218others(90): Show | 94 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.-157-1513A>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2488824 | ||||||
chr4:2488855
|
G | A | 2 | a0001c0003t0014g0357a0001c0003t0014g0370 | 2 | HG01243.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-157-1482G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2488855 | ||||||
chr4:2488888
|
G | A | 1 | a0001c0003t0021g0306 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-157-1449G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2488888 | ||||||
chr4:2488971
|
A | C | 336 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(333): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.-157-1366A>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2488971 | ||||||
chr4:2488991
|
C | A | 1 | a0001c0001t0001g0150 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-157-1346C>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2488991 | ||||||
chr4:2489040
|
T | G | 21 | a0001c0001t0001g0164a0001c0001t0001g0285a0001c0001t0001g0286others(18): Show | 21 | HG02257.hp2 HG02258.hp2 HG02280.hp2 others(18): Show |
intron_variant | MODIFIER | c.-157-1297T>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2489040 | ||||||
chr4:2489053
|
T | TC | 24 | a0001c0001t0007g0006a0001c0001t0007g0303a0001c0001t0007g0308others(21): Show | 25 | HG00544.hp2 HG00609.hp2 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.-157-1282dupC | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 2489053 | |||||
chr4:2489113
|
G | A | 1 | a0001c0001t0032g0360 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-157-1224G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2489113 | ||||||
chr4:2489184
|
C | T | 1 | a0001c0002t0003g0255 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-157-1153C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2489184 | ||||||
chr4:2489233
|
T | G | 1 | a0001c0001t0003g0259 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-157-1104T>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2489233 | ||||||
chr4:2489247
|
C | G | 1 | a0001c0001t0029g0363 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-157-1090C>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2489247 | ||||||
chr4:2489280
|
A | T | 1 | a0001c0001t0002g0209 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-157-1057A>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2489280 | ||||||
chr4:2489417
|
T | A | 1 | a0001c0001t0020g0269 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-157-920T>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2489417 | ||||||
chr4:2489420
|
G | T | 1 | a0001c0001t0029g0363 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-157-917G>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2489420 | ||||||
chr4:2489422
|
C | G | 1 | a0001c0001t0029g0363 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-157-915C>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2489422 | ||||||
chr4:2489488
|
A | G | 94 | a0001c0001t0001g0008a0001c0001t0003g0170a0001c0001t0003g0171others(91): Show | 95 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.-157-849A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2489488 | ||||||
chr4:2489556
|
G | A | 2 | a0001c0001t0005g0013a0001c0001t0005g0014 | 2 | HG01081.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.-157-781G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2489556 | ||||||
chr4:2489701
|
A | G | 1 | a0001c0001t0006g0163 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-157-636A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2489701 | ||||||
chr4:2489762
|
A | G | 1 | a0001c0001t0001g0005 | 2 | HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-157-575A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2489762 | ||||||
chr4:2489794
|
C | A | 1 | a0001c0001t0001g0135 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-157-543C>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2489794 | ||||||
chr4:2489827
|
C | G | 1 | a0001c0001t0002g0209 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-157-510C>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2489827 | ||||||
chr4:2489832
|
C | T | 1 | a0001c0001t0029g0363 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-157-505C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2489832 | ||||||
chr4:2489948
|
A | G | 2 | a0001c0001t0002g0183a0001c0001t0002g0197 | 2 | NA18952.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.-157-389A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2489948 | ||||||
chr4:2489968
|
G | A | 36 | a0001c0001t0001g0028a0001c0001t0001g0039a0001c0001t0001g0049others(33): Show | 36 | HG00140.hp2 HG00609.hp1 HG01069.hp2 others(33): Show |
intron_variant | MODIFIER | c.-157-369G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2489968 | ||||||
chr4:2490221
|
C | T | 1 | a0001c0003t0021g0306 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-157-116C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2490221 | ||||||
chr4:2490230
|
G | A | 1 | a0001c0001t0007g0324 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-157-107G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 1/7 | chr4 | 2490230 | ||||||
chr4:2490669
|
C | T | 1 | a0001c0001t0002g0202 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.9+167C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2490669 | ||||||
chr4:2491077
|
T | TA | 3 | a0001c0003t0014g0357a0001c0003t0014g0370a0001c0003t0021g0306 | 3 | HG01167.hp2 HG01243.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.9+578dupA | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 2491077 | |||||
chr4:2491090
|
A | G | 1 | a0001c0003t0021g0306 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.9+588A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2491090 | ||||||
chr4:2491156
|
A | T | 18 | a0001c0001t0005g0011a0001c0001t0005g0012a0001c0001t0005g0013others(15): Show | 18 | HG01074.hp1 HG01081.hp1 HG01975.hp2 others(15): Show |
intron_variant | MODIFIER | c.9+654A>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2491156 | ||||||
chr4:2491528
|
C | T | 2 | a0001c0003t0014g0357a0001c0003t0014g0370 | 2 | HG01243.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.9+1026C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2491528 | ||||||
chr4:2491589
|
C | T | 1 | a0001c0001t0001g0002 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.9+1087C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2491589 | ||||||
chr4:2491622
|
A | G | 5 | a0001c0001t0001g0026a0001c0001t0001g0133a0001c0001t0001g0134others(2): Show | 5 | NA18951.hp1 NA18977.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.9+1120A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2491622 | ||||||
chr4:2491765
|
A | C | 54 | a0001c0001t0002g0004a0001c0001t0002g0122a0001c0001t0002g0167others(51): Show | 55 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(52): Show |
intron_variant | MODIFIER | c.9+1263A>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2491765 | ||||||
chr4:2491791
|
T | G | 1 | a0001c0001t0002g0193 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.9+1289T>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2491791 | ||||||
chr4:2492061
|
A | C | 94 | a0001c0001t0001g0008a0001c0001t0003g0170a0001c0001t0003g0171others(91): Show | 95 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.9+1559A>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2492061 | ||||||
chr4:2492237
|
G | A | 1 | a0001c0001t0006g0160 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.9+1735G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2492237 | ||||||
chr4:2492313
|
G | A | 1 | a0001c0001t0029g0363 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.9+1811G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2492313 | ||||||
chr4:2492458
|
G | A | 2 | a0001c0001t0015g0350a0001c0001t0015g0351 | 2 | HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.9+1956G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2492458 | ||||||
chr4:2492512
|
G | A | 54 | a0001c0001t0002g0004a0001c0001t0002g0122a0001c0001t0002g0167others(51): Show | 55 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(52): Show |
intron_variant | MODIFIER | c.9+2010G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2492512 | ||||||
chr4:2492975
|
A | T | 336 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(333): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.9+2473A>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2492975 | ||||||
chr4:2492981
|
G | T | 1 | a0001c0001t0001g0109 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.9+2479G>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2492981 | ||||||
chr4:2493180
|
C | A | 1 | a0001c0001t0004g0274 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.9+2678C>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2493180 | ||||||
chr4:2493221
|
G | T | 1 | a0001c0001t0001g0214 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.9+2719G>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2493221 | ||||||
chr4:2493300
|
G | C | 1 | a0001c0001t0001g0060 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.9+2798G>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2493300 | ||||||
chr4:2493433
|
A | C | 1 | a0001c0001t0001g0060 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.9+2931A>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2493433 | ||||||
chr4:2493503
|
A | G | 2 | a0001c0001t0011g0365a0001c0001t0011g0366 | 2 | HG03516.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.9+3001A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2493503 | ||||||
chr4:2493743
|
T | TA | 12 | a0001c0001t0001g0026a0001c0001t0001g0048a0001c0001t0001g0075others(9): Show | 12 | HG00408.hp1 HG00438.hp1 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.10-3242dupA | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 2493743 | |||||
chr4:2493743
|
T | TAA | 51 | a0001c0001t0001g0290a0001c0001t0002g0004a0001c0001t0002g0168others(48): Show | 52 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.10-3243_10-3242dup others(2): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 2493743 | |||||
chr4:2493743
|
TA | T | 109 | a0001c0001t0001g0008a0001c0001t0001g0083a0001c0001t0001g0088others(106): Show | 109 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.10-3242delA | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 2493743 | |||||
chr4:2493743
|
TAAAAAAA others(3): Show |
T | 1 | a0001c0001t0001g0142 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.10-3251_10-3242del others(10): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 2493743 | |||||
chr4:2493794
|
C | T | 1 | a0001c0001t0001g0150 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.10-3213C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2493794 | ||||||
chr4:2493998
|
A | G | 337 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(334): Show | 342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.10-3009A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2493998 | ||||||
chr4:2494000
|
G | A | 54 | a0001c0001t0002g0004a0001c0001t0002g0122a0001c0001t0002g0167others(51): Show | 55 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(52): Show |
intron_variant | MODIFIER | c.10-3007G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2494000 | ||||||
chr4:2494032
|
G | A | 1 | a0001c0002t0003g0255 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.10-2975G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2494032 | ||||||
chr4:2494094
|
G | A | 2 | a0001c0001t0002g0169a0001c0001t0002g0192 | 2 | NA18966.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.10-2913G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2494094 | ||||||
chr4:2494110
|
T | A | 1 | a0001c0001t0001g0005 | 2 | HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.10-2897T>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2494110 | ||||||
chr4:2494146
|
A | G | 1 | a0001c0001t0001g0262 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.10-2861A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2494146 | ||||||
chr4:2494165
|
G | A | 2 | a0002c0004t0001g0055a0002c0004t0001g0057 | 2 | HG03453.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.10-2842G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2494165 | ||||||
chr4:2494172
|
C | T | 339 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(336): Show | 344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.10-2835C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2494172 | ||||||
chr4:2494194
|
A | T | 3 | a0001c0003t0014g0357a0001c0003t0014g0370a0001c0003t0021g0306 | 3 | HG01167.hp2 HG01243.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.10-2813A>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2494194 | ||||||
chr4:2494227
|
A | G | 1 | a0001c0001t0007g0303 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.10-2780A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2494227 | ||||||
chr4:2494304
|
A | G | 336 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(333): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.10-2703A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2494304 | ||||||
chr4:2494351
|
C | G | 1 | a0001c0001t0003g0279 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.10-2656C>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2494351 | ||||||
chr4:2494373
|
C | CT | 62 | a0001c0001t0001g0034a0001c0001t0001g0289a0001c0001t0001g0290others(59): Show | 63 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.10-2614dupT | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 2494373 | |||||
chr4:2494373
|
C | CTT | 8 | a0001c0001t0001g0304a0001c0001t0002g0167a0001c0001t0002g0172others(5): Show | 8 | HG00140.hp1 HG00741.hp2 HG01167.hp2 others(5): Show |
intron_variant | MODIFIER | c.10-2615_10-2614dup others(2): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 2494373 | |||||
chr4:2494373
|
CT | C | 122 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0024others(119): Show | 124 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.10-2614delT | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 2494373 | |||||
chr4:2494373
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0003g0294 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.10-2624_10-2614del others(11): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 2494373 | |||||
chr4:2494394
|
G | T | 3 | a0001c0003t0014g0357a0001c0003t0014g0370a0001c0003t0021g0306 | 3 | HG01167.hp2 HG01243.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.10-2613G>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2494394 | ||||||
chr4:2494416
|
G | A | 1 | a0001c0001t0010g0216 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.10-2591G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2494416 | ||||||
chr4:2494570
|
T | C | 1 | a0001c0001t0002g0169 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.10-2437T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2494570 | ||||||
chr4:2494571
|
G | A | 1 | a0001c0001t0002g0169 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.10-2436G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2494571 | ||||||
chr4:2494571
|
G | C | 1 | a0001c0001t0017g0009 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.10-2436G>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2494571 | ||||||
chr4:2494579
|
T | A | 1 | a0001c0001t0002g0169 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.10-2428T>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2494579 | ||||||
chr4:2494580
|
A | C | 1 | a0001c0001t0002g0169 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.10-2427A>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2494580 | ||||||
chr4:2494582
|
G | A | 1 | a0001c0001t0002g0169 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.10-2425G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2494582 | ||||||
chr4:2494607
|
T | C | 1 | a0001c0001t0002g0169 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.10-2400T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2494607 | ||||||
chr4:2494622
|
C | T | 2 | a0001c0001t0001g0059a0001c0001t0001g0107 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.10-2385C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2494622 | ||||||
chr4:2494623
|
G | A | 1 | a0001c0001t0002g0169 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.10-2384G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2494623 | ||||||
chr4:2494628
|
C | T | 1 | a0001c0001t0002g0169 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.10-2379C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2494628 | ||||||
chr4:2494634
|
C | A | 1 | a0001c0001t0002g0169 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.10-2373C>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2494634 | ||||||
chr4:2494660
|
A | G | 1 | a0001c0001t0002g0169 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.10-2347A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2494660 | ||||||
chr4:2494662
|
G | C | 1 | a0001c0001t0002g0169 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.10-2345G>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2494662 | ||||||
chr4:2494663
|
C | A | 1 | a0001c0001t0002g0169 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.10-2344C>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2494663 | ||||||
chr4:2494817
|
T | C | 1 | a0001c0001t0001g0262 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.10-2190T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2494817 | ||||||
chr4:2494825
|
C | G | 1 | a0001c0001t0001g0054 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.10-2182C>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2494825 | ||||||
chr4:2495046
|
A | G | 1 | a0001c0001t0002g0207 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.10-1961A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2495046 | ||||||
chr4:2495086
|
G | A | 127 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0024others(124): Show | 129 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.10-1921G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2495086 | ||||||
chr4:2495087
|
T | G | 127 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0024others(124): Show | 129 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.10-1920T>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2495087 | ||||||
chr4:2495088
|
GTCAGCTC others(4): Show |
G | 127 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0024others(124): Show | 129 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.10-1918_10-1908del others(11): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2495088 | ||||||
chr4:2495168
|
C | T | 6 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0287others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.10-1839C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2495168 | ||||||
chr4:2495180
|
T | A | 1 | a0001c0001t0004g0046 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.10-1827T>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2495180 | ||||||
chr4:2495181
|
C | T | 1 | a0001c0001t0004g0046 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.10-1826C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2495181 | ||||||
chr4:2495331
|
A | G | 2 | a0001c0001t0001g0102a0001c0001t0001g0106 | 2 | HG01981.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.10-1676A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2495331 | ||||||
chr4:2495386
|
C | G | 1 | a0001c0001t0001g0262 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.10-1621C>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2495386 | ||||||
chr4:2495426
|
G | A | 1 | a0001c0001t0002g0192 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.10-1581G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2495426 | ||||||
chr4:2495476
|
C | T | 1 | a0001c0001t0007g0303 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.10-1531C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2495476 | ||||||
chr4:2495599
|
A | AT | 3 | a0001c0003t0014g0357a0001c0003t0014g0370a0001c0003t0021g0306 | 3 | HG01167.hp2 HG01243.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.10-1407dupT | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 2495599 | |||||
chr4:2495638
|
T | TGG | 4 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0002g0173others(1): Show | 4 | HG03471.hp2 HG03704.hp2 NA18951.hp1 others(1): Show |
intron_variant | MODIFIER | c.10-1369_10-1368ins others(2): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2495638 | ||||||
chr4:2495639
|
T | G | 9 | a0001c0001t0001g0124a0001c0001t0001g0133a0001c0001t0001g0134others(6): Show | 10 | HG01243.hp2 HG01891.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.10-1368T>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2495639 | ||||||
chr4:2495639
|
T | TG | 71 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0287others(68): Show | 72 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.10-1359dupG | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 2495639 | |||||
chr4:2495639
|
T | TGG | 124 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0024others(121): Show | 126 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(123): Show |
intron_variant | MODIFIER | c.10-1360_10-1359dup others(2): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 2495639 | |||||
chr4:2495640
|
G | T | 3 | a0001c0001t0015g0350a0001c0001t0015g0351a0001c0003t0021g0306 | 3 | HG01167.hp2 HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.10-1367G>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2495640 | ||||||
chr4:2495641
|
G | T | 1 | a0001c0003t0021g0306 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.10-1366G>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2495641 | ||||||
chr4:2495642
|
G | A | 2 | a0001c0001t0015g0350a0001c0001t0015g0351 | 2 | HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.10-1365G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2495642 | ||||||
chr4:2495646
|
G | C | 19 | a0001c0001t0005g0011a0001c0001t0005g0012a0001c0001t0005g0013others(16): Show | 19 | HG01074.hp1 HG01081.hp1 HG01975.hp2 others(16): Show |
intron_variant | MODIFIER | c.10-1361G>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2495646 | ||||||
chr4:2495646
|
G | T | 8 | a0001c0001t0003g0171a0001c0001t0003g0243a0001c0001t0003g0248others(5): Show | 8 | HG01255.hp1 HG02055.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.10-1361G>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2495646 | ||||||
chr4:2495647
|
G | C | 1 | a0001c0001t0007g0328 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.10-1360G>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2495647 | ||||||
chr4:2495647
|
G | T | 1 | a0001c0001t0001g0150 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.10-1360G>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2495647 | ||||||
chr4:2496096
|
G | A | 1 | a0001c0003t0021g0306 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.10-911G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2496096 | ||||||
chr4:2496371
|
T | G | 3 | a0001c0003t0014g0357a0001c0003t0014g0370a0001c0003t0021g0306 | 3 | HG01167.hp2 HG01243.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.10-636T>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2496371 | ||||||
chr4:2496717
|
C | T | 1 | a0001c0001t0001g0112 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.10-290C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 2/7 | chr4 | 2496717 | ||||||
chr4:2497201
|
T | C | 1 | a0001c0001t0004g0046 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.124+80T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2497201 | ||||||
chr4:2497239
|
C | T | 3 | a0001c0001t0007g0006a0001c0001t0007g0308a0001c0001t0007g0328 | 4 | HG01891.hp1 HG02280.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.124+118C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2497239 | ||||||
chr4:2497245
|
A | G | 1 | a0001c0001t0001g0052 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.124+124A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2497245 | ||||||
chr4:2497356
|
G | A | 1 | a0001c0001t0001g0150 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.124+235G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2497356 | ||||||
chr4:2497381
|
A | G | 1 | a0001c0001t0001g0150 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.124+260A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2497381 | ||||||
chr4:2497390
|
T | G | 127 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0024others(124): Show | 129 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.124+269T>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2497390 | ||||||
chr4:2497431
|
C | T | 2 | a0001c0003t0014g0357a0001c0003t0014g0370 | 2 | HG01243.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.124+310C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2497431 | ||||||
chr4:2497624
|
T | C | 2 | a0001c0001t0003g0271a0001c0001t0003g0272 | 2 | NA18982.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.124+503T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2497624 | ||||||
chr4:2497659
|
G | C | 3 | a0001c0003t0014g0357a0001c0003t0014g0370a0001c0003t0021g0306 | 3 | HG01167.hp2 HG01243.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.124+538G>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2497659 | ||||||
chr4:2497673
|
C | T | 1 | a0001c0001t0002g0208 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.124+552C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2497673 | ||||||
chr4:2497881
|
G | A | 1 | a0001c0001t0002g0207 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.124+760G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2497881 | ||||||
chr4:2497941
|
C | G | 2 | a0001c0003t0014g0357a0001c0003t0014g0370 | 2 | HG01243.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.124+820C>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2497941 | ||||||
chr4:2498069
|
C | G | 1 | a0001c0001t0001g0290 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.124+948C>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2498069 | ||||||
chr4:2498111
|
C | T | 1 | a0001c0001t0001g0262 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.124+990C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2498111 | ||||||
chr4:2498141
|
C | T | 1 | a0001c0001t0007g0303 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.124+1020C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2498141 | ||||||
chr4:2498205
|
G | A | 339 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(336): Show | 344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.124+1084G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2498205 | ||||||
chr4:2498319
|
G | A | 1 | a0001c0001t0004g0046 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.124+1198G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2498319 | ||||||
chr4:2498427
|
A | G | 2 | a0001c0001t0002g0188a0001c0001t0002g0265 | 2 | HG00280.hp2 HG00323.hp2 |
intron_variant | MODIFIER | c.124+1306A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2498427 | ||||||
chr4:2498479
|
G | T | 2 | a0001c0001t0001g0287a0001c0001t0001g0289 | 2 | HG02257.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.124+1358G>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2498479 | ||||||
chr4:2498603
|
G | A | 1 | a0001c0001t0001g0302 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.124+1482G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2498603 | ||||||
chr4:2498742
|
A | C | 1 | a0001c0001t0001g0005 | 2 | HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.124+1621A>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2498742 | ||||||
chr4:2498849
|
C | T | 1 | a0001c0001t0029g0363 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.124+1728C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2498849 | ||||||
chr4:2498922
|
C | T | 6 | a0001c0001t0001g0358a0001c0001t0001g0359a0001c0001t0011g0364others(3): Show | 6 | HG02257.hp1 HG02258.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.125-1737C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2498922 | ||||||
chr4:2498962
|
C | T | 8 | a0001c0001t0001g0029a0001c0001t0001g0092a0001c0001t0001g0094others(5): Show | 8 | HG00408.hp1 HG00558.hp1 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.125-1697C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2498962 | ||||||
chr4:2498968
|
G | A | 1 | a0001c0001t0007g0330 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.125-1691G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2498968 | ||||||
chr4:2499070
|
G | A | 43 | a0001c0001t0002g0004a0001c0001t0002g0122a0001c0001t0002g0167others(40): Show | 44 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.125-1589G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2499070 | ||||||
chr4:2499173
|
G | A | 2 | a0001c0001t0007g0324a0001c0001t0007g0334 | 2 | HG03239.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.125-1486G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2499173 | ||||||
chr4:2499175
|
C | T | 1 | a0001c0001t0006g0161 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.125-1484C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2499175 | ||||||
chr4:2499183
|
C | T | 1 | a0001c0003t0021g0306 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.125-1476C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2499183 | ||||||
chr4:2499308
|
T | C | 2 | a0001c0003t0014g0357a0001c0003t0014g0370 | 2 | HG01243.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.125-1351T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2499308 | ||||||
chr4:2499369
|
G | A | 1 | a0001c0001t0001g0371 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.125-1290G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2499369 | ||||||
chr4:2499451
|
T | G | 1 | a0001c0001t0002g0200 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.125-1208T>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2499451 | ||||||
chr4:2499495
|
C | T | 2 | a0001c0003t0014g0357a0001c0003t0014g0370 | 2 | HG01243.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.125-1164C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2499495 | ||||||
chr4:2499506
|
C | T | 1 | a0001c0001t0001g0150 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.125-1153C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2499506 | ||||||
chr4:2499518
|
C | A | 1 | a0001c0001t0001g0335 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.125-1141C>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2499518 | ||||||
chr4:2499588
|
TTTAATA | T | 124 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0024others(121): Show | 126 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(123): Show |
intron_variant | MODIFIER | c.125-1058_125-1053d others(8): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 2499588 | |||||
chr4:2499632
|
C | T | 1 | a0001c0001t0007g0330 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.125-1027C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2499632 | ||||||
chr4:2499667
|
G | A | 1 | a0001c0003t0021g0306 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.125-992G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2499667 | ||||||
chr4:2499843
|
G | T | 1 | a0001c0003t0021g0306 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.125-816G>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2499843 | ||||||
chr4:2500031
|
G | A | 1 | a0001c0001t0010g0216 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.125-628G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2500031 | ||||||
chr4:2500156
|
C | CA | 12 | a0001c0001t0001g0005a0001c0001t0001g0035a0001c0001t0001g0043others(9): Show | 13 | HG00280.hp2 HG00323.hp2 HG02129.hp1 others(10): Show |
intron_variant | MODIFIER | c.125-482dupA | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 2500156 | |||||
chr4:2500156
|
CA | C | 126 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0049others(123): Show | 127 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(124): Show |
intron_variant | MODIFIER | c.125-482delA | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 2500156 | |||||
chr4:2500156
|
CAA | C | 6 | a0001c0001t0001g0039a0001c0001t0015g0350a0001c0001t0015g0351others(3): Show | 6 | HG01167.hp2 HG01243.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.125-483_125-482del others(2): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 2500156 | |||||
chr4:2500197
|
C | T | 2 | a0001c0001t0002g0183a0001c0001t0002g0197 | 2 | NA18952.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.125-462C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2500197 | ||||||
chr4:2500207
|
A | C | 2 | a0001c0001t0015g0350a0001c0001t0015g0351 | 2 | HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.125-452A>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2500207 | ||||||
chr4:2500274
|
G | A | 1 | a0001c0001t0002g0178 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.125-385G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2500274 | ||||||
chr4:2500301
|
A | T | 1 | a0001c0001t0001g0290 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.125-358A>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2500301 | ||||||
chr4:2500421
|
C | A | 1 | a0001c0001t0005g0012 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.125-238C>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2500421 | ||||||
chr4:2500457
|
C | T | 1 | a0001c0001t0009g0256 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.125-202C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2500457 | ||||||
chr4:2500469
|
T | A | 1 | a0001c0001t0005g0011 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.125-190T>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2500469 | ||||||
chr4:2500497
|
T | A | 1 | a0001c0001t0005g0012 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.125-162T>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2500497 | ||||||
chr4:2500514
|
G | A | 1 | a0001c0001t0001g0130 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.125-145G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2500514 | ||||||
chr4:2500572
|
A | ATT | 337 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(334): Show | 342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.125-87_125-86insTT | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 3/7 | chr4 | 2500572 | ||||||
chr4:2500777
|
A | G | 2 | a0001c0003t0014g0357a0001c0003t0014g0370 | 2 | HG01243.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.204+39A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2500777 | ||||||
chr4:2500791
|
A | G | 1 | a0001c0001t0001g0263 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.204+53A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2500791 | ||||||
chr4:2500910
|
T | C | 97 | a0001c0001t0001g0008a0001c0001t0003g0170a0001c0001t0003g0171others(94): Show | 98 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.204+172T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2500910 | ||||||
chr4:2501078
|
G | C | 1 | a0001c0001t0002g0212 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.204+340G>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2501078 | ||||||
chr4:2501108
|
C | T | 2 | a0001c0001t0001g0315a0001c0001t0001g0316 | 2 | HG03831.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.204+370C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2501108 | ||||||
chr4:2501206
|
C | T | 1 | a0002c0004t0001g0057 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.204+468C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2501206 | ||||||
chr4:2501415
|
G | GGGAGGCT others(8): Show |
7 | a0001c0001t0001g0008a0001c0001t0001g0285a0001c0001t0001g0286others(4): Show | 7 | HG02257.hp2 HG02280.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.204+686_204+700dup others(15): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 2501415 | |||||
chr4:2501562
|
C | T | 1 | a0001c0003t0021g0306 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.204+824C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2501562 | ||||||
chr4:2501577
|
T | C | 1 | a0001c0003t0021g0306 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.204+839T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2501577 | ||||||
chr4:2501615
|
T | G | 1 | a0001c0003t0021g0306 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.204+877T>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2501615 | ||||||
chr4:2501667
|
C | G | 1 | a0001c0001t0002g0209 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.204+929C>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2501667 | ||||||
chr4:2501735
|
G | A | 1 | a0001c0001t0001g0262 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.204+997G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2501735 | ||||||
chr4:2501766
|
C | T | 1 | a0001c0001t0001g0005 | 2 | HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.204+1028C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2501766 | ||||||
chr4:2501860
|
T | C | 8 | a0001c0001t0002g0205a0001c0001t0002g0206a0001c0001t0002g0208others(5): Show | 8 | HG00639.hp1 HG02004.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.204+1122T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2501860 | ||||||
chr4:2501877
|
G | A | 1 | a0001c0001t0003g0235 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.204+1139G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2501877 | ||||||
chr4:2501909
|
C | A | 2 | a0001c0001t0015g0350a0001c0001t0015g0351 | 2 | HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.204+1171C>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2501909 | ||||||
chr4:2502108
|
C | A | 1 | a0001c0001t0001g0316 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.204+1370C>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2502108 | ||||||
chr4:2502195
|
A | G | 3 | a0001c0001t0001g0135a0001c0001t0001g0138a0001c0001t0001g0139 | 3 | HG02015.hp1 HG02040.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.204+1457A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2502195 | ||||||
chr4:2502240
|
T | C | 1 | a0001c0001t0001g0100 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.204+1502T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2502240 | ||||||
chr4:2502468
|
A | G | 117 | a0001c0001t0003g0170a0001c0001t0003g0171a0001c0001t0003g0218others(114): Show | 118 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(115): Show |
intron_variant | MODIFIER | c.204+1730A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2502468 | ||||||
chr4:2502562
|
T | C | 3 | a0001c0003t0014g0357a0001c0003t0014g0370a0001c0003t0021g0306 | 3 | HG01167.hp2 HG01243.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.204+1824T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2502562 | ||||||
chr4:2502630
|
T | C | 338 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(335): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.204+1892T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2502630 | ||||||
chr4:2502671
|
C | CA | 15 | a0001c0001t0001g0047a0001c0001t0001g0124a0001c0001t0001g0353others(12): Show | 15 | HG02135.hp2 HG02257.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.204+1948dupA | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 2502671 | |||||
chr4:2502843
|
C | CA | 6 | a0001c0001t0001g0290a0001c0001t0003g0258a0001c0001t0003g0291others(3): Show | 6 | HG02572.hp1 HG02723.hp1 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.204+2120dupA | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 2502843 | |||||
chr4:2502843
|
CA | C | 256 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(253): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.204+2120delA | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 2502843 | |||||
chr4:2502984
|
G | A | 2 | a0001c0001t0003g0258a0001c0001t0003g0291 | 2 | NA19000.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.204+2246G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2502984 | ||||||
chr4:2503092
|
T | A | 2 | a0001c0001t0001g0133a0001c0001t0001g0134 | 2 | NA18951.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.204+2354T>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2503092 | ||||||
chr4:2503168
|
C | G | 1 | a0001c0001t0002g0209 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.204+2430C>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2503168 | ||||||
chr4:2503183
|
T | C | 44 | a0001c0001t0002g0004a0001c0001t0002g0122a0001c0001t0002g0167others(41): Show | 45 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(42): Show |
intron_variant | MODIFIER | c.204+2445T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2503183 | ||||||
chr4:2503311
|
T | G | 14 | a0001c0001t0001g0298a0001c0001t0001g0299a0001c0001t0001g0353others(11): Show | 14 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.204+2573T>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2503311 | ||||||
chr4:2503320
|
A | G | 1 | a0001c0003t0021g0306 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.204+2582A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2503320 | ||||||
chr4:2503364
|
G | T | 98 | a0001c0001t0003g0171a0001c0001t0003g0218a0001c0001t0003g0219others(95): Show | 99 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.204+2626G>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2503364 | ||||||
chr4:2503517
|
C | T | 80 | a0001c0001t0003g0171a0001c0001t0003g0218a0001c0001t0003g0219others(77): Show | 81 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.204+2779C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2503517 | ||||||
chr4:2503580
|
A | G | 1 | a0001c0001t0001g0005 | 2 | HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.204+2842A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2503580 | ||||||
chr4:2503658
|
C | T | 1 | a0001c0001t0019g0087 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.204+2920C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2503658 | ||||||
chr4:2503736
|
C | G | 1 | a0001c0001t0005g0016 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.204+2998C>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2503736 | ||||||
chr4:2503800
|
C | T | 1 | a0001c0001t0001g0302 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.204+3062C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2503800 | ||||||
chr4:2503802
|
G | C | 18 | a0001c0001t0005g0011a0001c0001t0005g0012a0001c0001t0005g0013others(15): Show | 18 | HG01074.hp1 HG01081.hp1 HG01975.hp2 others(15): Show |
intron_variant | MODIFIER | c.204+3064G>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2503802 | ||||||
chr4:2503824
|
C | T | 1 | a0001c0003t0021g0306 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.204+3086C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2503824 | ||||||
chr4:2503879
|
C | T | 98 | a0001c0001t0003g0171a0001c0001t0003g0218a0001c0001t0003g0219others(95): Show | 99 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.204+3141C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2503879 | ||||||
chr4:2503996
|
C | A | 1 | a0001c0001t0001g0050 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.204+3258C>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2503996 | ||||||
chr4:2504000
|
T | G | 14 | a0001c0001t0008g0066a0001c0001t0008g0282a0001c0001t0008g0305others(11): Show | 14 | HG00544.hp2 HG00609.hp2 HG02071.hp2 others(11): Show |
intron_variant | MODIFIER | c.204+3262T>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2504000 | ||||||
chr4:2504260
|
G | A | 23 | a0001c0001t0001g0008a0001c0001t0001g0285a0001c0001t0001g0286others(20): Show | 23 | HG02257.hp2 HG02258.hp2 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.204+3522G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2504260 | ||||||
chr4:2504267
|
G | A | 5 | a0001c0001t0001g0054a0001c0001t0001g0056a0001c0001t0001g0142others(2): Show | 5 | HG01106.hp1 HG02886.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.204+3529G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2504267 | ||||||
chr4:2504276
|
G | A | 1 | a0001c0001t0023g0023 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.204+3538G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2504276 | ||||||
chr4:2504392
|
C | G | 1 | a0001c0001t0003g0229 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.204+3654C>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2504392 | ||||||
chr4:2504441
|
T | G | 3 | a0001c0003t0014g0357a0001c0003t0014g0370a0001c0003t0021g0306 | 3 | HG01167.hp2 HG01243.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.204+3703T>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2504441 | ||||||
chr4:2504482
|
T | A | 14 | a0001c0001t0001g0298a0001c0001t0001g0299a0001c0001t0001g0353others(11): Show | 14 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.204+3744T>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2504482 | ||||||
chr4:2504523
|
C | CATTT | 4 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0288others(1): Show | 4 | HG02970.hp2 HG02976.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.204+3785_204+3786i others(6): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2504523 | ||||||
chr4:2504524
|
T | A | 8 | a0001c0001t0001g0008a0001c0001t0001g0027a0001c0001t0001g0285others(5): Show | 8 | HG02257.hp2 HG02280.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.204+3786T>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2504524 | ||||||
chr4:2504524
|
T | TTTTA | 92 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0025others(89): Show | 93 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(90): Show |
intron_variant | MODIFIER | c.204+3826_204+3829d others(6): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 2504524 | |||||
chr4:2504524
|
T | TTTTATTT others(1): Show |
44 | a0001c0001t0001g0026a0001c0001t0001g0044a0001c0001t0001g0060others(41): Show | 45 | HG00140.hp1 HG00673.hp1 HG01167.hp1 others(42): Show |
intron_variant | MODIFIER | c.204+3822_204+3829d others(10): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 2504524 | |||||
chr4:2504524
|
T | TTTTATTT others(5): Show |
3 | a0001c0001t0001g0355a0001c0001t0006g0162a0001c0001t0006g0163 | 3 | HG02630.hp1 HG02809.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.204+3818_204+3829d others(14): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 2504524 | |||||
chr4:2504524
|
TTTTA | T | 108 | a0001c0001t0001g0005a0001c0001t0001g0054a0001c0001t0001g0056others(105): Show | 109 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.204+3826_204+3829d others(6): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 2504524 | |||||
chr4:2504524
|
TTTTATTT others(5): Show |
T | 17 | a0001c0001t0001g0028a0001c0001t0001g0039a0001c0001t0001g0049others(14): Show | 17 | HG00609.hp1 HG01975.hp1 HG02015.hp1 others(14): Show |
intron_variant | MODIFIER | c.204+3818_204+3829d others(14): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 2504524 | |||||
chr4:2504524
|
TTTTATTT others(9): Show |
T | 1 | a0001c0001t0001g0007 | 2 | HG00639.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.204+3814_204+3829d others(18): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 2504524 | |||||
chr4:2504613
|
T | C | 17 | a0001c0001t0008g0066a0001c0001t0008g0282a0001c0001t0008g0305others(14): Show | 17 | HG00544.hp2 HG00609.hp2 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.204+3875T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2504613 | ||||||
chr4:2504726
|
A | AT | 106 | a0001c0001t0001g0008a0001c0001t0001g0053a0001c0001t0001g0076others(103): Show | 108 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.204+4009dupT | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 2504726 | |||||
chr4:2504726
|
A | ATT | 11 | a0001c0001t0001g0150a0001c0001t0002g0172a0001c0001t0002g0180others(8): Show | 11 | HG00741.hp2 HG01099.hp1 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.204+4008_204+4009d others(4): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 2504726 | |||||
chr4:2504726
|
A | ATTT | 6 | a0001c0001t0001g0358a0001c0001t0001g0359a0001c0001t0011g0364others(3): Show | 6 | HG02257.hp1 HG02258.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.204+4007_204+4009d others(5): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 2504726 | |||||
chr4:2504726
|
A | ATTTTTTT others(1): Show |
7 | a0001c0001t0008g0066a0001c0001t0008g0282a0001c0001t0008g0305others(4): Show | 7 | HG00544.hp2 HG00609.hp2 HG02071.hp2 others(4): Show |
intron_variant | MODIFIER | c.204+4002_204+4009d others(10): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 2504726 | |||||
chr4:2504726
|
A | ATTTTTTT others(10): Show |
1 | a0001c0001t0015g0350 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.204+3993_204+4009d others(19): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 2504726 | |||||
chr4:2504726
|
A | ATTTTTTT others(11): Show |
1 | a0001c0001t0015g0351 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.204+3992_204+4009d others(20): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 2504726 | |||||
chr4:2504726
|
AT | A | 7 | a0001c0001t0001g0073a0001c0001t0001g0100a0001c0001t0001g0107others(4): Show | 7 | HG01515.hp1 HG01515.hp2 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.204+4009delT | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 2504726 | |||||
chr4:2504986
|
G | C | 1 | a0001c0001t0002g0205 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.204+4248G>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2504986 | ||||||
chr4:2505051
|
T | A | 7 | a0001c0001t0002g0004a0001c0001t0002g0167a0001c0001t0002g0181others(4): Show | 8 | NA18939.hp1 NA18952.hp1 NA18959.hp1 others(5): Show |
intron_variant | MODIFIER | c.204+4313T>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505051 | ||||||
chr4:2505091
|
G | A | 4 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(1): Show | 4 | HG01069.hp1 HG01071.hp2 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.204+4353G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505091 | ||||||
chr4:2505177
|
C | G | 6 | a0001c0001t0001g0309a0001c0001t0001g0310a0001c0001t0001g0311others(3): Show | 6 | HG01256.hp1 HG01258.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.204+4439C>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505177 | ||||||
chr4:2505233
|
G | C | 21 | a0001c0001t0005g0011a0001c0001t0005g0012a0001c0001t0005g0013others(18): Show | 21 | HG01074.hp1 HG01081.hp1 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.204+4495G>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505233 | ||||||
chr4:2505328
|
C | CT | 64 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(61): Show | 65 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.204+4605dupT | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 2505328 | |||||
chr4:2505328
|
CT | C | 7 | a0001c0001t0001g0064a0001c0001t0001g0069a0001c0001t0001g0286others(4): Show | 7 | HG02895.hp2 HG02976.hp2 HG03491.hp2 others(4): Show |
intron_variant | MODIFIER | c.204+4605delT | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 2505328 | |||||
chr4:2505353
|
T | G | 1 | a0001c0001t0005g0016 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.204+4615T>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505353 | ||||||
chr4:2505356
|
C | T | 17 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(14): Show | 17 | HG00099.hp2 HG00323.hp1 HG00544.hp2 others(14): Show |
intron_variant | MODIFIER | c.204+4618C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505356 | ||||||
chr4:2505364
|
T | C | 4 | a0001c0001t0001g0071a0001c0001t0005g0016a0001c0003t0014g0357others(1): Show | 4 | HG01167.hp2 HG02647.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.204+4626T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505364 | ||||||
chr4:2505365
|
G | T | 1 | a0001c0001t0001g0071 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.204+4627G>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505365 | ||||||
chr4:2505370
|
A | G | 102 | a0001c0001t0001g0035a0001c0001t0001g0047a0001c0001t0001g0064others(99): Show | 103 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.204+4632A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505370 | ||||||
chr4:2505379
|
A | G | 12 | a0001c0001t0004g0356a0001c0001t0007g0006a0001c0001t0007g0303others(9): Show | 13 | HG01891.hp1 HG02280.hp1 HG02523.hp1 others(10): Show |
intron_variant | MODIFIER | c.204+4641A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505379 | ||||||
chr4:2505388
|
C | T | 1 | a0001c0001t0001g0121 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.204+4650C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505388 | ||||||
chr4:2505394
|
T | G | 1 | a0001c0003t0021g0306 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.204+4656T>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505394 | ||||||
chr4:2505405
|
C | G | 1 | a0001c0001t0001g0121 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.204+4667C>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505405 | ||||||
chr4:2505418
|
T | C | 3 | a0001c0001t0002g0188a0001c0001t0002g0265a0001c0001t0003g0267 | 3 | HG00280.hp2 HG00323.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.204+4680T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505418 | ||||||
chr4:2505425
|
A | C | 1 | a0001c0001t0001g0304 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.204+4687A>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505425 | ||||||
chr4:2505427
|
A | G | 16 | a0001c0001t0001g0304a0001c0001t0003g0273a0001c0001t0004g0270others(13): Show | 16 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(13): Show |
intron_variant | MODIFIER | c.204+4689A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505427 | ||||||
chr4:2505437
|
T | G | 1 | a0001c0001t0001g0302 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.204+4699T>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505437 | ||||||
chr4:2505444
|
G | C | 1 | a0001c0001t0002g0193 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.204+4706G>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505444 | ||||||
chr4:2505450
|
A | C | 13 | a0001c0001t0001g0262a0001c0001t0001g0298a0001c0001t0001g0299others(10): Show | 13 | HG01243.hp2 HG01884.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.204+4712A>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505450 | ||||||
chr4:2505450
|
A | T | 5 | a0001c0001t0001g0353a0001c0001t0001g0354a0001c0001t0001g0355others(2): Show | 5 | HG02615.hp2 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.204+4712A>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505450 | ||||||
chr4:2505455
|
A | T | 2 | a0001c0003t0014g0357a0001c0003t0014g0370 | 2 | HG01243.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.204+4717A>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505455 | ||||||
chr4:2505464
|
T | G | 1 | a0001c0001t0001g0005 | 2 | HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.204+4726T>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505464 | ||||||
chr4:2505470
|
T | C | 7 | a0001c0001t0001g0005a0001c0001t0001g0039a0001c0001t0001g0091others(4): Show | 8 | HG01934.hp2 HG02647.hp1 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.204+4732T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505470 | ||||||
chr4:2505473
|
C | T | 1 | a0001c0001t0001g0005 | 2 | HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.204+4735C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505473 | ||||||
chr4:2505474
|
C | T | 1 | a0001c0003t0014g0370 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.204+4736C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505474 | ||||||
chr4:2505475
|
G | A | 2 | a0001c0001t0001g0044a0001c0003t0021g0306 | 2 | HG01167.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.204+4737G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505475 | ||||||
chr4:2505477
|
C | T | 1 | a0001c0001t0005g0013 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.204+4739C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505477 | ||||||
chr4:2505482
|
C | T | 1 | a0001c0001t0001g0148 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.204+4744C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505482 | ||||||
chr4:2505483
|
A | G | 3 | a0001c0001t0001g0148a0001c0001t0001g0150a0001c0001t0004g0356 | 3 | HG02970.hp1 HG03579.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.204+4745A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505483 | ||||||
chr4:2505486
|
C | T | 1 | a0001c0001t0001g0150 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.204+4748C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505486 | ||||||
chr4:2505505
|
T | G | 3 | a0001c0001t0002g0209a0001c0001t0015g0350a0001c0001t0015g0351 | 3 | HG03098.hp2 HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.204+4767T>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505505 | ||||||
chr4:2505526
|
C | T | 1 | a0001c0001t0032g0360 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.204+4788C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505526 | ||||||
chr4:2505527
|
A | G | 148 | a0001c0001t0001g0005a0001c0001t0001g0028a0001c0001t0001g0039others(145): Show | 151 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.204+4789A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505527 | ||||||
chr4:2505531
|
T | G | 6 | a0001c0001t0001g0029a0001c0001t0001g0092a0001c0001t0001g0094others(3): Show | 6 | HG00408.hp1 HG00558.hp1 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.204+4793T>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505531 | ||||||
chr4:2505532
|
A | T | 4 | a0001c0001t0001g0353a0001c0001t0001g0354a0001c0001t0001g0355others(1): Show | 4 | HG02615.hp2 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.204+4794A>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505532 | ||||||
chr4:2505533
|
G | C | 52 | a0001c0001t0001g0051a0001c0001t0001g0078a0001c0001t0001g0079others(49): Show | 53 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.204+4795G>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505533 | ||||||
chr4:2505535
|
C | T | 2 | a0001c0001t0002g0168a0001c0001t0009g0256 | 2 | HG01109.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.204+4797C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505535 | ||||||
chr4:2505536
|
A | G | 1 | a0001c0001t0003g0267 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.204+4798A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505536 | ||||||
chr4:2505546
|
C | A | 7 | a0001c0001t0001g0298a0001c0001t0001g0299a0001c0001t0001g0353others(4): Show | 7 | HG02145.hp1 HG02615.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.204+4808C>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505546 | ||||||
chr4:2505546
|
C | T | 148 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(145): Show | 150 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.204+4808C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505546 | ||||||
chr4:2505547
|
G | A | 125 | a0001c0001t0001g0024a0001c0001t0001g0029a0001c0001t0001g0078others(122): Show | 126 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.204+4809G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505547 | ||||||
chr4:2505547
|
G | C | 1 | a0001c0001t0015g0351 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.204+4809G>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505547 | ||||||
chr4:2505560
|
C | T | 225 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0024others(222): Show | 228 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(225): Show |
intron_variant | MODIFIER | c.204+4822C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505560 | ||||||
chr4:2505568
|
G | A | 33 | a0001c0001t0001g0008a0001c0001t0001g0150a0001c0001t0001g0285others(30): Show | 33 | HG01243.hp1 HG01884.hp2 HG02055.hp2 others(30): Show |
intron_variant | MODIFIER | c.204+4830G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505568 | ||||||
chr4:2505572
|
G | A | 313 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(310): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.204+4834G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505572 | ||||||
chr4:2505575
|
T | C | 1 | a0001c0001t0012g0221 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.204+4837T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505575 | ||||||
chr4:2505576
|
C | T | 298 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(295): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.204+4838C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505576 | ||||||
chr4:2505584
|
C | T | 264 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(261): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.204+4846C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505584 | ||||||
chr4:2505600
|
T | C | 81 | a0001c0001t0001g0076a0001c0001t0001g0078a0001c0001t0001g0079others(78): Show | 82 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.204+4862T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505600 | ||||||
chr4:2505604
|
T | C | 67 | a0001c0001t0001g0076a0001c0001t0001g0078a0001c0001t0001g0079others(64): Show | 68 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.204+4866T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505604 | ||||||
chr4:2505614
|
C | G | 2 | a0001c0001t0015g0350a0001c0001t0015g0351 | 2 | HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.204+4876C>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505614 | ||||||
chr4:2505614
|
C | T | 238 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(235): Show | 241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.204+4876C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505614 | ||||||
chr4:2505616
|
C | G | 1 | a0001c0003t0021g0306 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.204+4878C>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505616 | ||||||
chr4:2505617
|
G | A | 1 | a0001c0003t0014g0370 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.204+4879G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505617 | ||||||
chr4:2505618
|
C | T | 1 | a0001c0001t0001g0005 | 2 | HG03225.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.204+4880C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505618 | ||||||
chr4:2505620
|
C | T | 1 | a0001c0001t0012g0246 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.204+4882C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505620 | ||||||
chr4:2505621
|
G | A | 2 | a0001c0001t0011g0364a0001c0001t0011g0367 | 2 | HG02257.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.204+4883G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505621 | ||||||
chr4:2505629
|
G | A | 2 | a0001c0001t0015g0350a0001c0001t0015g0351 | 2 | HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.204+4891G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505629 | ||||||
chr4:2505717
|
G | A | 22 | a0001c0001t0001g0008a0001c0001t0001g0285a0001c0001t0001g0286others(19): Show | 22 | HG02257.hp2 HG02258.hp2 HG02280.hp2 others(19): Show |
intron_variant | MODIFIER | c.204+4979G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505717 | ||||||
chr4:2505723
|
C | CTT | 6 | a0001c0001t0001g0309a0001c0001t0008g0305a0001c0001t0008g0321others(3): Show | 6 | HG01258.hp1 HG02071.hp2 NA18952.hp2 others(3): Show |
intron_variant | MODIFIER | c.204+5014_204+5015d others(4): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 2505723 | |||||
chr4:2505723
|
C | CTTTTTTT others(18): Show |
1 | a0001c0001t0015g0350 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.204+4991_204+5015d others(27): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 2505723 | |||||
chr4:2505723
|
C | CTTTTTTT others(19): Show |
1 | a0001c0001t0015g0351 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.204+4990_204+5015d others(28): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 2505723 | |||||
chr4:2505723
|
CT | C | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 159 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.204+5015delT | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 2505723 | |||||
chr4:2505723
|
CTT | C | 87 | a0001c0001t0001g0008a0001c0001t0001g0065a0001c0001t0001g0083others(84): Show | 87 | HG00408.hp2 HG00544.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.204+5014_204+5015d others(4): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 2505723 | |||||
chr4:2505723
|
CTTT | C | 15 | a0001c0001t0001g0005a0001c0001t0001g0262a0001c0001t0001g0298others(12): Show | 16 | HG01109.hp2 HG01243.hp2 HG01516.hp2 others(13): Show |
intron_variant | MODIFIER | c.204+5013_204+5015d others(5): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 2505723 | |||||
chr4:2505723
|
CTTTT | C | 44 | a0001c0001t0002g0004a0001c0001t0002g0122a0001c0001t0002g0167others(41): Show | 45 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(42): Show |
intron_variant | MODIFIER | c.204+5012_204+5015d others(6): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 2505723 | |||||
chr4:2505723
|
CTTTTTTT others(4): Show |
C | 2 | a0001c0001t0008g0066a0001c0001t0008g0327 | 2 | HG00609.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.204+5005_204+5015d others(13): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 2505723 | |||||
chr4:2505741
|
T | C | 2 | a0002c0004t0001g0055a0002c0004t0001g0057 | 2 | HG03453.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.204+5003T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505741 | ||||||
chr4:2505759
|
G | T | 1 | a0001c0001t0032g0360 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.204+5021G>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505759 | ||||||
chr4:2505790
|
G | A | 1 | a0001c0003t0014g0370 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.204+5052G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505790 | ||||||
chr4:2505907
|
G | A | 1 | a0001c0001t0004g0352 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.204+5169G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505907 | ||||||
chr4:2505910
|
C | T | 1 | a0001c0003t0014g0370 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.204+5172C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2505910 | ||||||
chr4:2506081
|
A | G | 2 | a0001c0001t0001g0113a0001c0001t0001g0115 | 2 | HG01175.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.204+5343A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2506081 | ||||||
chr4:2506180
|
T | C | 39 | a0001c0001t0001g0008a0001c0001t0001g0285a0001c0001t0001g0286others(36): Show | 39 | HG01167.hp2 HG01243.hp2 HG02145.hp1 others(36): Show |
intron_variant | MODIFIER | c.204+5442T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2506180 | ||||||
chr4:2506189
|
CT | C | 127 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0024others(124): Show | 129 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.204+5456delT | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 2506189 | |||||
chr4:2506200
|
CT | C | 6 | a0001c0001t0003g0171a0001c0001t0003g0243a0001c0001t0003g0248others(3): Show | 6 | HG02055.hp1 HG02451.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.204+5463delT | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2506200 | ||||||
chr4:2506215
|
G | A | 53 | a0001c0001t0002g0004a0001c0001t0002g0122a0001c0001t0002g0167others(50): Show | 54 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.204+5477G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2506215 | ||||||
chr4:2506219
|
T | C | 4 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0002g0058others(1): Show | 4 | HG00642.hp2 HG00735.hp2 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.204+5481T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2506219 | ||||||
chr4:2506223
|
G | A | 1 | a0001c0001t0002g0168 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.204+5485G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2506223 | ||||||
chr4:2506313
|
A | G | 2 | a0001c0001t0001g0097a0001c0001t0001g0104 | 2 | NA18971.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.204+5575A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2506313 | ||||||
chr4:2506356
|
G | A | 1 | a0001c0001t0001g0095 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.205-5600G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2506356 | ||||||
chr4:2506382
|
A | G | 12 | a0001c0001t0008g0066a0001c0001t0008g0282a0001c0001t0008g0305others(9): Show | 12 | HG00544.hp2 HG00609.hp2 HG02071.hp2 others(9): Show |
intron_variant | MODIFIER | c.205-5574A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2506382 | ||||||
chr4:2506462
|
G | A | 2 | a0001c0001t0015g0350a0001c0001t0015g0351 | 2 | HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.205-5494G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2506462 | ||||||
chr4:2506478
|
G | A | 2 | a0001c0001t0003g0258a0001c0001t0003g0291 | 2 | NA19000.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.205-5478G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2506478 | ||||||
chr4:2506571
|
C | CT | 12 | a0001c0001t0008g0066a0001c0001t0008g0282a0001c0001t0008g0305others(9): Show | 12 | HG00544.hp2 HG00609.hp2 HG02071.hp2 others(9): Show |
intron_variant | MODIFIER | c.205-5376dupT | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 2506571 | |||||
chr4:2506574
|
T | C | 2 | a0001c0001t0015g0350a0001c0001t0015g0351 | 2 | HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.205-5382T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2506574 | ||||||
chr4:2506635
|
A | C | 1 | a0001c0001t0006g0166 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.205-5321A>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2506635 | ||||||
chr4:2506636
|
C | T | 1 | a0001c0001t0006g0166 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.205-5320C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2506636 | ||||||
chr4:2506727
|
C | G | 22 | a0001c0001t0003g0258a0001c0001t0003g0271a0001c0001t0003g0272others(19): Show | 22 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(19): Show |
intron_variant | MODIFIER | c.205-5229C>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2506727 | ||||||
chr4:2506781
|
G | A | 1 | a0001c0001t0001g0118 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.205-5175G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2506781 | ||||||
chr4:2507381
|
A | G | 1 | a0001c0001t0001g0371 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.205-4575A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2507381 | ||||||
chr4:2507505
|
C | T | 1 | a0001c0001t0022g0045 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.205-4451C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2507505 | ||||||
chr4:2507602
|
C | A | 2 | a0001c0001t0015g0350a0001c0001t0015g0351 | 2 | HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.205-4354C>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2507602 | ||||||
chr4:2507678
|
G | A | 2 | a0001c0001t0005g0296a0001c0001t0005g0297 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.205-4278G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2507678 | ||||||
chr4:2507759
|
C | T | 2 | a0001c0003t0014g0357a0001c0003t0014g0370 | 2 | HG01243.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.205-4197C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2507759 | ||||||
chr4:2508104
|
C | T | 6 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0287others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.205-3852C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2508104 | ||||||
chr4:2508147
|
G | A | 2 | a0001c0001t0001g0298a0001c0001t0001g0299 | 2 | HG02145.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.205-3809G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2508147 | ||||||
chr4:2508186
|
A | C | 2 | a0001c0001t0002g0212a0001c0001t0002g0213 | 2 | NA18943.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.205-3770A>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2508186 | ||||||
chr4:2508248
|
T | G | 1 | a0001c0001t0002g0208 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.205-3708T>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2508248 | ||||||
chr4:2508357
|
T | C | 2 | a0001c0003t0014g0357a0001c0003t0014g0370 | 2 | HG01243.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.205-3599T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2508357 | ||||||
chr4:2508361
|
C | T | 2 | a0001c0001t0015g0350a0001c0001t0015g0351 | 2 | HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.205-3595C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2508361 | ||||||
chr4:2508400
|
C | G | 1 | a0001c0001t0001g0339 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.205-3556C>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2508400 | ||||||
chr4:2508592
|
T | G | 1 | a0001c0001t0002g0192 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.205-3364T>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2508592 | ||||||
chr4:2508662
|
G | A | 2 | a0001c0003t0014g0357a0001c0003t0014g0370 | 2 | HG01243.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.205-3294G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2508662 | ||||||
chr4:2508754
|
A | G | 245 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0024others(242): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.205-3202A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2508754 | ||||||
chr4:2508758
|
G | A | 1 | a0001c0001t0001g0262 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.205-3198G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2508758 | ||||||
chr4:2508911
|
C | CT | 98 | a0001c0001t0001g0008a0001c0001t0001g0034a0001c0001t0001g0150others(95): Show | 98 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.205-3020dupT | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 2508911 | |||||
chr4:2508911
|
C | CTT | 37 | a0001c0001t0001g0108a0001c0001t0001g0149a0001c0001t0001g0316others(34): Show | 38 | HG01074.hp1 HG01081.hp1 HG01257.hp1 others(35): Show |
intron_variant | MODIFIER | c.205-3021_205-3020d others(4): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 2508911 | |||||
chr4:2508911
|
C | CTTT | 107 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(104): Show | 110 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.205-3022_205-3020d others(5): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 2508911 | |||||
chr4:2508911
|
C | CTTTT | 19 | a0001c0001t0001g0026a0001c0001t0001g0036a0001c0001t0001g0037others(16): Show | 19 | HG00099.hp2 HG01099.hp2 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.205-3023_205-3020d others(6): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 2508911 | |||||
chr4:2509007
|
C | T | 1 | a0001c0001t0009g0220 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.205-2949C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2509007 | ||||||
chr4:2509009
|
C | G | 2 | a0001c0003t0014g0357a0001c0003t0014g0370 | 2 | HG01243.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.205-2947C>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2509009 | ||||||
chr4:2509012
|
G | A | 1 | a0001c0001t0001g0262 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.205-2944G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2509012 | ||||||
chr4:2509036
|
A | C | 2 | a0001c0001t0015g0350a0001c0001t0015g0351 | 2 | HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.205-2920A>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2509036 | ||||||
chr4:2509072
|
C | G | 1 | a0001c0001t0003g0268 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.205-2884C>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2509072 | ||||||
chr4:2509162
|
G | A | 12 | a0001c0001t0008g0066a0001c0001t0008g0282a0001c0001t0008g0305others(9): Show | 12 | HG00544.hp2 HG00609.hp2 HG02071.hp2 others(9): Show |
intron_variant | MODIFIER | c.205-2794G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2509162 | ||||||
chr4:2509228
|
T | C | 2 | a0001c0001t0002g0177a0001c0001t0002g0184 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.205-2728T>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2509228 | ||||||
chr4:2509308
|
C | T | 128 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0024others(125): Show | 130 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.205-2648C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2509308 | ||||||
chr4:2509344
|
A | T | 1 | a0001c0001t0003g0238 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.205-2612A>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2509344 | ||||||
chr4:2509451
|
C | T | 1 | a0001c0001t0002g0178 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.205-2505C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2509451 | ||||||
chr4:2509469
|
C | T | 1 | a0001c0001t0007g0329 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.205-2487C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2509469 | ||||||
chr4:2509508
|
G | A | 2 | a0001c0001t0001g0298a0001c0001t0001g0299 | 2 | HG02145.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.205-2448G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2509508 | ||||||
chr4:2509525
|
T | G | 18 | a0001c0001t0005g0011a0001c0001t0005g0012a0001c0001t0005g0013others(15): Show | 18 | HG01074.hp1 HG01081.hp1 HG01975.hp2 others(15): Show |
intron_variant | MODIFIER | c.205-2431T>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2509525 | ||||||
chr4:2509650
|
G | A | 1 | a0001c0001t0001g0113 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.205-2306G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2509650 | ||||||
chr4:2509768
|
G | A | 1 | a0001c0001t0001g0102 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.205-2188G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2509768 | ||||||
chr4:2509890
|
C | T | 1 | a0001c0001t0004g0280 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.205-2066C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2509890 | ||||||
chr4:2509976
|
A | G | 1 | a0001c0003t0021g0306 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.205-1980A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2509976 | ||||||
chr4:2510089
|
G | A | 1 | a0001c0003t0021g0306 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.205-1867G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2510089 | ||||||
chr4:2510289
|
G | C | 123 | a0001c0001t0001g0262a0001c0001t0003g0170a0001c0001t0003g0171others(120): Show | 124 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(121): Show |
intron_variant | MODIFIER | c.205-1667G>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2510289 | ||||||
chr4:2510324
|
C | T | 2 | a0001c0001t0001g0262a0001c0001t0029g0363 | 2 | HG01884.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.205-1632C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2510324 | ||||||
chr4:2510327
|
A | G | 124 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0024others(121): Show | 126 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(123): Show |
intron_variant | MODIFIER | c.205-1629A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2510327 | ||||||
chr4:2510480
|
C | T | 2 | a0001c0001t0001g0068a0001c0001t0001g0069 | 2 | HG03490.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.205-1476C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2510480 | ||||||
chr4:2510514
|
C | T | 1 | a0001c0003t0021g0306 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.205-1442C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2510514 | ||||||
chr4:2510517
|
C | T | 1 | a0001c0001t0003g0294 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.205-1439C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2510517 | ||||||
chr4:2510736
|
C | A | 12 | a0001c0001t0007g0006a0001c0001t0007g0303a0001c0001t0007g0308others(9): Show | 13 | HG01891.hp1 HG02280.hp1 HG02523.hp1 others(10): Show |
intron_variant | MODIFIER | c.205-1220C>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2510736 | ||||||
chr4:2510791
|
C | G | 1 | a0001c0001t0005g0012 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.205-1165C>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2510791 | ||||||
chr4:2511216
|
T | TAAGGTCC others(54): Show |
1 | a0001c0001t0020g0269 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.205-330_205-270dup others(61): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 2511216 | |||||
chr4:2511216
|
TAAGGTCC others(54): Show |
T | 154 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0008others(151): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.205-330_205-270del others(61): Show |
RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 2511216 | |||||
chr4:2511216
|
TAAGGTCC others(115): Show |
T | 19 | a0001c0001t0001g0101a0001c0001t0001g0164a0001c0001t0001g0298others(16): Show | 19 | HG00544.hp2 HG00609.hp2 HG01975.hp2 others(16): Show |
intron_variant | MODIFIER | c.205-391_205-270del | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 2511216 | |||||
chr4:2511216
|
TAAGGTCC others(176): Show |
T | 108 | a0001c0001t0001g0002a0001c0001t0001g0048a0001c0001t0001g0052others(105): Show | 110 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(107): Show |
intron_variant | MODIFIER | c.205-452_205-270del | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 2511216 | |||||
chr4:2511216
|
TAAGGTCC others(237): Show |
T | 3 | a0001c0001t0001g0262a0001c0003t0014g0357a0001c0003t0014g0370 | 3 | HG01243.hp2 HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.205-513_205-270del | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 2511216 | |||||
chr4:2511216
|
TAAGGTCC others(359): Show |
T | 1 | a0001c0003t0021g0306 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.205-635_205-270del | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 2511216 | |||||
chr4:2511347
|
C | T | 1 | a0001c0001t0002g0202 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.205-609C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2511347 | ||||||
chr4:2511446
|
C | T | 1 | a0001c0001t0001g0141 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.205-510C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2511446 | ||||||
chr4:2511467
|
C | T | 7 | a0001c0001t0001g0059a0001c0001t0001g0061a0001c0001t0001g0107others(4): Show | 7 | HG00140.hp2 HG01069.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.205-489C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2511467 | ||||||
chr4:2511532
|
G | C | 2 | a0001c0001t0003g0258a0001c0001t0003g0291 | 2 | NA19000.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.205-424G>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2511532 | ||||||
chr4:2511574
|
A | G | 1 | a0001c0001t0001g0141 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.205-382A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2511574 | ||||||
chr4:2511888
|
G | C | 117 | a0001c0001t0003g0170a0001c0001t0003g0171a0001c0001t0003g0218others(114): Show | 118 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(115): Show |
intron_variant | MODIFIER | c.205-68G>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2511888 | ||||||
chr4:2511893
|
G | A | 339 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(336): Show | 344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.205-63G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2511893 | ||||||
chr4:2511897
|
A | G | 128 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0024others(125): Show | 130 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.205-59A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 4/7 | chr4 | 2511897 | ||||||
chr4:2512027
|
G | A | 1 | a0001c0001t0003g0230 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.214+62G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 5/7 | chr4 | 2512027 | ||||||
chr4:2512086
|
A | T | 1 | a0001c0001t0003g0224 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.214+121A>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 5/7 | chr4 | 2512086 | ||||||
chr4:2512094
|
G | A | 2 | a0001c0003t0014g0357a0001c0003t0014g0370 | 2 | HG01243.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.214+129G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 5/7 | chr4 | 2512094 | ||||||
chr4:2512115
|
A | G | 337 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(334): Show | 342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.214+150A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 5/7 | chr4 | 2512115 | ||||||
chr4:2512241
|
G | A | 11 | a0001c0001t0003g0171a0001c0001t0003g0224a0001c0001t0003g0242others(8): Show | 11 | HG01255.hp1 HG02055.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.215-197G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 5/7 | chr4 | 2512241 | ||||||
chr4:2512606
|
G | A | 1 | a0001c0001t0001g0093 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.374+9G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 6/7 | chr4 | 2512606 | ||||||
chr4:2512651
|
C | T | 22 | a0001c0001t0001g0008a0001c0001t0001g0285a0001c0001t0001g0286others(19): Show | 22 | HG02257.hp2 HG02258.hp2 HG02280.hp2 others(19): Show |
intron_variant | MODIFIER | c.374+54C>T | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 6/7 | chr4 | 2512651 | ||||||
chr4:2512960
|
G | A | 1 | a0001c0001t0001g0262 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.375-123G>A | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 6/7 | chr4 | 2512960 | ||||||
chr4:2513335
|
A | G | 1 | a0001c0001t0001g0290 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.423+204A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 7/7 | chr4 | 2513335 | ||||||
chr4:2513341
|
C | G | 1 | a0001c0001t0001g0317 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.423+210C>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 7/7 | chr4 | 2513341 | ||||||
chr4:2513424
|
A | G | 3 | a0001c0001t0001g0035a0001c0001t0001g0127a0001c0001t0025g0126 | 3 | NA18967.hp2 NA19007.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.424-246A>G | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 7/7 | chr4 | 2513424 | ||||||
chr4:2513550
|
G | C | 18 | a0001c0001t0005g0011a0001c0001t0005g0012a0001c0001t0005g0013others(15): Show | 18 | HG01074.hp1 HG01081.hp1 HG01975.hp2 others(15): Show |
intron_variant | MODIFIER | c.424-120G>C | RNF4 | ENSG00000063978.17 | transcript | ENST00000314289.13 | protein_coding | 7/7 | chr4 | 2513550 |