geneid | 9655 |
---|---|
ensemblid | ENSG00000171150.9 |
hgncid | 16852 |
symbol | SOCS5 |
name | suppressor of cytokine signaling 5 |
refseq_nuc | NM_144949.3 |
refseq_prot | NP_659198.1 |
ensembl_nuc | ENST00000394861.3 |
ensembl_prot | ENSP00000378330.2 |
mane_status | MANE Select |
chr | chr2 |
start | 46699295 |
end | 46763129 |
strand | + |
ver | v1.2 |
region | chr2:46699295-46763129 |
region5000 | chr2:46694295-46768129 |
regionname0 | SOCS5_chr2_46699295_46763129 |
regionname5000 | SOCS5_chr2_46694295_46768129 |
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 | 536 | 379 | 88 | 70 | 165 | 16 | 38 | 133 | SOCS5_chr2_46694295_46768129 | SOCS5 | copy fasta | chr2 | 46694295 | 46768129 |
a0002 | 0/0 | 536 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | copy fasta | chr2 | 46694295 | 46768129 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 1611 | 277 | 70 | 36 | 141 | 6 | 23 | SOCS5_chr2_46694295_46768129 | SOCS5 | copy fasta | chr2 | 46694295 | 46768129 |
c0002 | 0/1 | 1611 | 70 | 14 | 22 | 15 | 7 | 11 | SOCS5_chr2_46694295_46768129 | SOCS5 | copy fasta | chr2 | 46694295 | 46768129 |
c0003 | 0/0 | 1611 | 21 | 2 | 8 | 7 | 2 | 2 | SOCS5_chr2_46694295_46768129 | SOCS5 | copy fasta | chr2 | 46694295 | 46768129 |
c0004 | 0/0 | 1611 | 7 | 0 | 3 | 1 | 1 | 2 | SOCS5_chr2_46694295_46768129 | SOCS5 | copy fasta | chr2 | 46694295 | 46768129 |
c0005 | 0/0 | 1611 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | copy fasta | chr2 | 46694295 | 46768129 |
c0006 | 0/0 | 1611 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | copy fasta | chr2 | 46694295 | 46768129 |
c0007 | 0/0 | 1611 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | copy fasta | chr2 | 46694295 | 46768129 |
c0008 | 0/0 | 1611 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | copy fasta | chr2 | 46694295 | 46768129 |
c0009 | 0/0 | 1611 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | copy fasta | chr2 | 46694295 | 46768129 |
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 | 3156 | 103 | 12 | 12 | 71 | 1 | 7 | SOCS5_chr2_46694295_46768129 | SOCS5 | copy fasta | chr2 | 46694295 | 46768129 |
t0002 | 1/0 | 3156 | 94 | 8 | 8 | 61 | 4 | 12 | SOCS5_chr2_46694295_46768129 | SOCS5 | copy fasta | chr2 | 46694295 | 46768129 |
t0003 | 0/1 | 3156 | 63 | 12 | 21 | 14 | 5 | 10 | SOCS5_chr2_46694295_46768129 | SOCS5 | copy fasta | chr2 | 46694295 | 46768129 |
t0004 | 0/0 | 3156 | 26 | 23 | 2 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | copy fasta | chr2 | 46694295 | 46768129 |
t0005 | 0/0 | 3156 | 23 | 2 | 10 | 7 | 2 | 2 | SOCS5_chr2_46694295_46768129 | SOCS5 | copy fasta | chr2 | 46694295 | 46768129 |
t0006 | 0/0 | 3154 | 20 | 5 | 8 | 5 | 0 | 2 | SOCS5_chr2_46694295_46768129 | SOCS5 | copy fasta | chr2 | 46694295 | 46768129 |
t0007 | 0/0 | 3156 | 15 | 11 | 4 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | copy fasta | chr2 | 46694295 | 46768129 |
t0008 | 0/0 | 3144 | 6 | 5 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | copy fasta | chr2 | 46694295 | 46768129 |
t0009 | 0/0 | 3156 | 4 | 0 | 0 | 4 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | copy fasta | chr2 | 46694295 | 46768129 |
t0010 | 0/0 | 3156 | 4 | 0 | 1 | 0 | 2 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | copy fasta | chr2 | 46694295 | 46768129 |
t0011 | 0/0 | 3156 | 4 | 0 | 1 | 1 | 1 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | copy fasta | chr2 | 46694295 | 46768129 |
t0012 | 0/0 | 3156 | 3 | 1 | 0 | 1 | 1 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | copy fasta | chr2 | 46694295 | 46768129 |
t0013 | 0/0 | 3156 | 3 | 0 | 2 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | copy fasta | chr2 | 46694295 | 46768129 |
t0014 | 0/0 | 3156 | 2 | 2 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | copy fasta | chr2 | 46694295 | 46768129 |
t0015 | 0/0 | 3156 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | copy fasta | chr2 | 46694295 | 46768129 |
t0016 | 0/0 | 3156 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | copy fasta | chr2 | 46694295 | 46768129 |
t0017 | 0/0 | 3156 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | copy fasta | chr2 | 46694295 | 46768129 |
t0018 | 0/0 | 3156 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | copy fasta | chr2 | 46694295 | 46768129 |
t0019 | 0/0 | 3156 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | copy fasta | chr2 | 46694295 | 46768129 |
t0020 | 0/0 | 3156 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | copy fasta | chr2 | 46694295 | 46768129 |
t0021 | 0/0 | 3156 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | copy fasta | chr2 | 46694295 | 46768129 |
t0022 | 0/0 | 3156 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | copy fasta | chr2 | 46694295 | 46768129 |
t0023 | 0/0 | 3156 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | copy fasta | chr2 | 46694295 | 46768129 |
t0024 | 0/0 | 3156 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | copy fasta | chr2 | 46694295 | 46768129 |
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 | 5 | 0 | 2 | 1 | 1 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0002 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0004 | 0/0 | 4 | 0 | 1 | 2 | 1 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0009 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0010 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0012 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0013 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0017 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0018 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0026 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0035 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0111 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0326 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 1611 | 277 | 70 | 36 | 141 | 6 | 23 | SOCS5_chr2_46694295_46768129 | SOCS5 | copy fasta | chr2 | 46694295 | 46768129 |
a0001c0002 | 0/1 | 1611 | 70 | 14 | 22 | 15 | 7 | 11 | SOCS5_chr2_46694295_46768129 | SOCS5 | copy fasta | chr2 | 46694295 | 46768129 |
a0001c0003 | 0/0 | 1611 | 21 | 2 | 8 | 7 | 2 | 2 | SOCS5_chr2_46694295_46768129 | SOCS5 | copy fasta | chr2 | 46694295 | 46768129 |
a0001c0004 | 0/0 | 1611 | 7 | 0 | 3 | 1 | 1 | 2 | SOCS5_chr2_46694295_46768129 | SOCS5 | copy fasta | chr2 | 46694295 | 46768129 |
a0001c0005 | 0/0 | 1611 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | copy fasta | chr2 | 46694295 | 46768129 |
a0001c0006 | 0/0 | 1611 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | copy fasta | chr2 | 46694295 | 46768129 |
a0001c0008 | 0/0 | 1611 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | copy fasta | chr2 | 46694295 | 46768129 |
a0001c0009 | 0/0 | 1611 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | copy fasta | chr2 | 46694295 | 46768129 |
a0002c0007 | 0/0 | 1611 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | copy fasta | chr2 | 46694295 | 46768129 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4766 | 102 | 12 | 12 | 70 | 1 | 7 | SOCS5_chr2_46694295_46768129 | SOCS5 | copy fasta | chr2 | 46694295 | 46768129 |
a0001c0001t0002 | 1/0 | 4766 | 93 | 8 | 8 | 60 | 4 | 12 | SOCS5_chr2_46694295_46768129 | SOCS5 | copy fasta | chr2 | 46694295 | 46768129 |
a0001c0001t0004 | 0/0 | 4766 | 26 | 23 | 2 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | copy fasta | chr2 | 46694295 | 46768129 |
a0001c0001t0005 | 0/0 | 4766 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | copy fasta | chr2 | 46694295 | 46768129 |
a0001c0001t0006 | 0/0 | 4764 | 20 | 5 | 8 | 5 | 0 | 2 | SOCS5_chr2_46694295_46768129 | SOCS5 | copy fasta | chr2 | 46694295 | 46768129 |
a0001c0001t0007 | 0/0 | 4766 | 15 | 11 | 4 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | copy fasta | chr2 | 46694295 | 46768129 |
a0001c0001t0008 | 0/0 | 4754 | 5 | 4 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | copy fasta | chr2 | 46694295 | 46768129 |
a0001c0001t0009 | 0/0 | 4766 | 4 | 0 | 0 | 4 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | copy fasta | chr2 | 46694295 | 46768129 |
a0001c0001t0012 | 0/0 | 4766 | 1 | 0 | 0 | 0 | 1 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | copy fasta | chr2 | 46694295 | 46768129 |
a0001c0001t0014 | 0/0 | 4766 | 2 | 2 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | copy fasta | chr2 | 46694295 | 46768129 |
a0001c0001t0017 | 0/0 | 4766 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | copy fasta | chr2 | 46694295 | 46768129 |
a0001c0001t0018 | 0/0 | 4766 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | copy fasta | chr2 | 46694295 | 46768129 |
a0001c0001t0019 | 0/0 | 4766 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | copy fasta | chr2 | 46694295 | 46768129 |
a0001c0001t0020 | 0/0 | 4766 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | copy fasta | chr2 | 46694295 | 46768129 |
a0001c0001t0021 | 0/0 | 4766 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | copy fasta | chr2 | 46694295 | 46768129 |
a0001c0001t0022 | 0/0 | 4766 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | copy fasta | chr2 | 46694295 | 46768129 |
a0001c0001t0023 | 0/0 | 4766 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | copy fasta | chr2 | 46694295 | 46768129 |
a0001c0001t0024 | 0/0 | 4766 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | copy fasta | chr2 | 46694295 | 46768129 |
a0001c0002t0003 | 0/1 | 4766 | 63 | 12 | 21 | 14 | 5 | 10 | SOCS5_chr2_46694295_46768129 | SOCS5 | copy fasta | chr2 | 46694295 | 46768129 |
a0001c0002t0010 | 0/0 | 4766 | 4 | 0 | 1 | 0 | 2 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | copy fasta | chr2 | 46694295 | 46768129 |
a0001c0002t0012 | 0/0 | 4766 | 2 | 1 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | copy fasta | chr2 | 46694295 | 46768129 |
a0001c0002t0015 | 0/0 | 4766 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | copy fasta | chr2 | 46694295 | 46768129 |
a0001c0003t0005 | 0/0 | 4766 | 21 | 2 | 8 | 7 | 2 | 2 | SOCS5_chr2_46694295_46768129 | SOCS5 | copy fasta | chr2 | 46694295 | 46768129 |
a0001c0004t0011 | 0/0 | 4766 | 4 | 0 | 1 | 1 | 1 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | copy fasta | chr2 | 46694295 | 46768129 |
a0001c0004t0013 | 0/0 | 4766 | 3 | 0 | 2 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | copy fasta | chr2 | 46694295 | 46768129 |
a0001c0005t0008 | 0/0 | 4754 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | copy fasta | chr2 | 46694295 | 46768129 |
a0001c0006t0002 | 0/0 | 4766 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | copy fasta | chr2 | 46694295 | 46768129 |
a0001c0008t0016 | 0/0 | 4766 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | copy fasta | chr2 | 46694295 | 46768129 |
a0001c0009t0005 | 0/0 | 4766 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | copy fasta | chr2 | 46694295 | 46768129 |
a0002c0007t0001 | 0/0 | 4766 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | copy fasta | chr2 | 46694295 | 46768129 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0002g0004 | 0/0 | 4 | 0 | 1 | 2 | 1 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0002g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0002g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0002g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0002g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0002g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0002g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0002g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0002g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0002g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0002g0035 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0002g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0002g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0002g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0002g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0002g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0002g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0002g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0002g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0002g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0002g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0002g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0002g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0004g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0004g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0004g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0004g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0004g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0004g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0004g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0004g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0004g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0004g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0004g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0004g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0004g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0004g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0004g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0004g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0004g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0004g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0004g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0004g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0004g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0004g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0004g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0004g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0004g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0005g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0006g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0006g0009 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0006g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0006g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0006g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0006g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0006g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0006g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0006g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0006g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0006g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0006g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0006g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0006g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0006g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0006g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0006g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0006g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0007g0010 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0007g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0007g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0007g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0007g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0007g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0007g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0007g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0007g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0007g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0007g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0007g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0007g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0007g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0008g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0008g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0008g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0008g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0009g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0012g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0014g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0014g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0017g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0018g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0019g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0020g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0021g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0022g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0023g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0001t0024g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0002t0003g0001 | 0/0 | 5 | 0 | 2 | 1 | 1 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0002t0003g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0002t0003g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0002t0003g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0002t0003g0017 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0002t0003g0018 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0002t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0002t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0002t0003g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0002t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0002t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0002t0003g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0002t0003g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0002t0003g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0002t0003g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0002t0003g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0002t0003g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0002t0003g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0002t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0002t0003g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0002t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0002t0003g0111 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0002t0003g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0002t0003g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0002t0003g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0002t0003g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0002t0003g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0002t0003g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0002t0003g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0002t0003g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0002t0003g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0002t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0002t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0002t0003g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0002t0003g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0002t0003g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0002t0003g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0002t0003g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0002t0003g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0002t0003g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0002t0003g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0002t0003g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0002t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0002t0003g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0002t0003g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0002t0003g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0002t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0002t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0002t0003g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0002t0003g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0002t0003g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0002t0003g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0002t0003g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0002t0003g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0002t0010g0012 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0002t0010g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0002t0010g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0002t0012g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0002t0012g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0002t0015g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0003t0005g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0003t0005g0013 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0003t0005g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0003t0005g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0003t0005g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0003t0005g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0003t0005g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0003t0005g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0003t0005g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0003t0005g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0003t0005g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0003t0005g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0003t0005g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0003t0005g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0003t0005g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0003t0005g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0003t0005g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0003t0005g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0003t0005g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0004t0011g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0004t0011g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0004t0011g0326 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0004t0011g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0004t0013g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0004t0013g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0005t0008g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0006t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0008t0016g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0001c0009t0005g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
a0002c0007t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0002 | t0003 | g0140 | EUR | GBR | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0210 | EUR | GBR | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG00280 | hp1 | a0001 | c0002 | t0003 | g0118 | EUR | FIN | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG00280 | hp2 | a0001 | c0001 | t0012 | g0126 | EUR | FIN | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0269 | EUR | FIN | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG00323 | hp2 | a0001 | c0002 | t0003 | g0153 | EUR | FIN | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | CHS | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0317 | EAS | CHS | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | CHS | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG00438 | hp2 | a0001 | c0002 | t0003 | g0133 | EAS | CHS | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | CHS | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0314 | EAS | CHS | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0280 | EAS | CHS | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | CHS | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG00639 | hp1 | a0001 | c0002 | t0003 | g0099 | AMR | PUR | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0283 | AMR | PUR | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0285 | AMR | PUR | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG00733 | hp1 | a0001 | c0003 | t0005 | g0256 | AMR | PUR | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG00733 | hp2 | a0001 | c0001 | t0006 | g0008 | AMR | PUR | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG00738 | hp1 | a0001 | c0001 | t0004 | g0190 | AMR | PUR | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG00738 | hp2 | a0001 | c0002 | t0003 | g0134 | AMR | PUR | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG00741 | hp1 | a0001 | c0001 | t0007 | g0010 | AMR | PUR | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG00741 | hp2 | a0001 | c0002 | t0003 | g0124 | AMR | PUR | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0034 | AMR | PUR | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG01069 | hp2 | a0001 | c0003 | t0005 | g0042 | AMR | PUR | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG01070 | hp1 | a0001 | c0002 | t0003 | g0257 | AMR | PUR | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG01070 | hp2 | a0001 | c0004 | t0011 | g0324 | AMR | PUR | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0034 | AMR | PUR | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG01071 | hp2 | a0001 | c0002 | t0003 | g0258 | AMR | PUR | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG01074 | hp1 | a0001 | c0002 | t0003 | g0016 | AMR | PUR | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG01074 | hp2 | a0001 | c0003 | t0005 | g0084 | AMR | PUR | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG01081 | hp2 | a0001 | c0001 | t0007 | g0064 | AMR | PUR | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG01099 | hp2 | a0001 | c0002 | t0003 | g0016 | AMR | PUR | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG01106 | hp2 | a0001 | c0002 | t0003 | g0131 | AMR | PUR | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG01109 | hp1 | a0001 | c0001 | t0004 | g0331 | AMR | PUR | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG01109 | hp2 | a0001 | c0001 | t0008 | g0155 | AMR | PUR | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG01167 | hp1 | a0001 | c0002 | t0003 | g0152 | AMR | PUR | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG01167 | hp2 | a0001 | c0001 | t0006 | g0045 | AMR | PUR | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG01175 | hp1 | a0001 | c0001 | t0006 | g0044 | AMR | PUR | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG01175 | hp2 | a0001 | c0002 | t0003 | g0135 | AMR | PUR | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG01192 | hp1 | a0001 | c0002 | t0003 | g0137 | AMR | PUR | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG01243 | hp1 | a0001 | c0001 | t0007 | g0071 | AMR | PUR | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG01243 | hp2 | a0001 | c0001 | t0007 | g0072 | AMR | PUR | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0282 | AMR | CLM | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | CLM | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | CLM | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG01256 | hp2 | a0001 | c0002 | t0003 | g0101 | AMR | CLM | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG01257 | hp1 | a0001 | c0003 | t0005 | g0255 | AMR | CLM | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG01257 | hp2 | a0001 | c0004 | t0013 | g0021 | AMR | CLM | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | CLM | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG01258 | hp2 | a0001 | c0004 | t0013 | g0021 | AMR | CLM | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG01346 | hp1 | a0001 | c0001 | t0006 | g0049 | AMR | CLM | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG01346 | hp2 | a0001 | c0003 | t0005 | g0013 | AMR | CLM | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG01358 | hp1 | a0001 | c0002 | t0003 | g0114 | AMR | CLM | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG01358 | hp2 | a0001 | c0001 | t0006 | g0009 | AMR | CLM | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG01361 | hp1 | a0001 | c0001 | t0006 | g0046 | AMR | CLM | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG01361 | hp2 | a0001 | c0003 | t0005 | g0027 | AMR | CLM | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG01433 | hp1 | a0001 | c0009 | t0005 | g0027 | AMR | CLM | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG01433 | hp2 | a0001 | c0002 | t0010 | g0090 | AMR | CLM | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0304 | AMR | CLM | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG01496 | hp2 | a0001 | c0001 | t0005 | g0167 | AMR | CLM | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG01515 | hp1 | a0001 | c0004 | t0011 | g0326 | EUR | IBS | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG01515 | hp2 | a0001 | c0003 | t0005 | g0088 | EUR | IBS | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG01516 | hp1 | a0001 | c0002 | t0010 | g0012 | EUR | IBS | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0265 | EUR | IBS | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG01517 | hp1 | a0001 | c0003 | t0005 | g0013 | EUR | IBS | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG01517 | hp2 | a0001 | c0002 | t0010 | g0012 | EUR | IBS | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0035 | AMR | PEL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG01952 | hp2 | a0001 | c0002 | t0003 | g0018 | AMR | PEL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG01975 | hp1 | a0001 | c0002 | t0003 | g0113 | AMR | PEL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | PEL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG01978 | hp1 | a0001 | c0001 | t0006 | g0008 | AMR | PEL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG01978 | hp2 | a0001 | c0002 | t0003 | g0120 | AMR | PEL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG01981 | hp1 | a0001 | c0002 | t0003 | g0017 | AMR | PEL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG02004 | hp1 | a0001 | c0002 | t0003 | g0001 | AMR | PEL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | PEL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG02015 | hp2 | a0001 | c0002 | t0003 | g0110 | EAS | KHV | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0259 | EAS | KHV | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0309 | EAS | KHV | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG02055 | hp1 | a0001 | c0001 | t0007 | g0073 | AFR | ACB | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG02055 | hp2 | a0001 | c0001 | t0019 | g0263 | AFR | ACB | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG02056 | hp1 | a0001 | c0003 | t0005 | g0093 | EAS | KHV | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | KHV | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0300 | EAS | KHV | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | KHV | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG02080 | hp1 | a0001 | c0001 | t0006 | g0059 | EAS | KHV | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | KHV | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | KHV | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0266 | EAS | KHV | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG02132 | hp1 | a0001 | c0004 | t0011 | g0325 | EAS | KHV | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | KHV | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG02135 | hp2 | a0001 | c0001 | t0006 | g0052 | EAS | KHV | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG02145 | hp1 | a0001 | c0001 | t0004 | g0136 | AFR | ACB | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | ACB | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | CDX | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | CDX | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | CDX | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG02165 | hp2 | a0001 | c0002 | t0003 | g0139 | EAS | CDX | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG02257 | hp1 | a0001 | c0001 | t0007 | g0063 | AFR | ACB | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | ACB | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0319 | AFR | ACB | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG02258 | hp2 | a0001 | c0001 | t0004 | g0253 | AFR | ACB | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG02273 | hp1 | a0001 | c0002 | t0003 | g0129 | AMR | PEL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG02280 | hp1 | a0001 | c0001 | t0007 | g0069 | AFR | ACB | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG02280 | hp2 | a0001 | c0002 | t0003 | g0017 | AFR | ACB | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PEL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG02293 | hp2 | a0001 | c0002 | t0003 | g0001 | AMR | PEL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG02300 | hp1 | a0001 | c0003 | t0005 | g0085 | AMR | PEL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG02300 | hp2 | a0001 | c0003 | t0005 | g0254 | AMR | PEL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG02451 | hp1 | a0001 | c0005 | t0008 | g0081 | AFR | ACB | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | ACB | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG02572 | hp1 | a0001 | c0001 | t0004 | g0078 | AFR | GWD | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG02572 | hp2 | a0001 | c0001 | t0002 | g0281 | AFR | GWD | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG02615 | hp1 | a0001 | c0001 | t0004 | g0143 | AFR | GWD | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG02615 | hp2 | a0001 | c0001 | t0006 | g0057 | AFR | GWD | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG02622 | hp1 | a0001 | c0001 | t0007 | g0067 | AFR | GWD | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG02622 | hp2 | a0001 | c0001 | t0002 | g0032 | AFR | GWD | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG02630 | hp1 | a0001 | c0003 | t0005 | g0097 | AFR | GWD | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG02630 | hp2 | a0001 | c0002 | t0003 | g0127 | AFR | GWD | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG02647 | hp1 | a0001 | c0002 | t0012 | g0156 | AFR | GWD | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG02647 | hp2 | a0001 | c0003 | t0005 | g0149 | AFR | GWD | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0284 | SAS | PJL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG02683 | hp2 | a0001 | c0004 | t0013 | g0189 | SAS | PJL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG02698 | hp1 | a0001 | c0003 | t0005 | g0041 | SAS | PJL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG02698 | hp2 | a0001 | c0002 | t0003 | g0018 | SAS | PJL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG02717 | hp1 | a0001 | c0001 | t0006 | g0050 | AFR | GWD | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG02735 | hp1 | a0001 | c0002 | t0010 | g0086 | SAS | PJL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0172 | SAS | PJL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0237 | SAS | PJL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG02738 | hp2 | a0001 | c0002 | t0003 | g0123 | SAS | PJL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0264 | AFR | GWD | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG02818 | hp1 | a0001 | c0001 | t0004 | g0082 | AFR | GWD | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG02818 | hp2 | a0001 | c0001 | t0004 | g0076 | AFR | GWD | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG02886 | hp1 | a0001 | c0001 | t0004 | g0147 | AFR | GWD | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG02886 | hp2 | a0001 | c0002 | t0003 | g0015 | AFR | GWD | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG02895 | hp1 | a0001 | c0001 | t0004 | g0230 | AFR | GWD | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG02895 | hp2 | a0001 | c0002 | t0003 | g0105 | AFR | GWD | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | GWD | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG02896 | hp2 | a0001 | c0001 | t0004 | g0077 | AFR | GWD | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG02897 | hp1 | a0001 | c0001 | t0004 | g0075 | AFR | GWD | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG02897 | hp2 | a0001 | c0002 | t0003 | g0104 | AFR | GWD | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG02922 | hp1 | a0001 | c0002 | t0003 | g0117 | AFR | ESN | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG02922 | hp2 | a0001 | c0001 | t0007 | g0066 | AFR | ESN | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG02965 | hp1 | a0001 | c0001 | t0017 | g0180 | AFR | ESN | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG02965 | hp2 | a0001 | c0001 | t0007 | g0010 | AFR | ESN | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG02970 | hp1 | a0001 | c0001 | t0008 | g0154 | AFR | ESN | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG02970 | hp2 | a0001 | c0001 | t0004 | g0148 | AFR | ESN | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | ESN | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG02976 | hp2 | a0001 | c0001 | t0018 | g0141 | AFR | ESN | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG03041 | hp1 | a0001 | c0002 | t0003 | g0015 | AFR | GWD | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0032 | AFR | GWD | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG03098 | hp1 | a0001 | c0001 | t0004 | g0198 | AFR | MSL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG03098 | hp2 | a0001 | c0001 | t0014 | g0150 | AFR | MSL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG03130 | hp1 | a0001 | c0001 | t0008 | g0019 | AFR | ESN | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG03130 | hp2 | a0001 | c0001 | t0007 | g0070 | AFR | ESN | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0031 | AFR | ESN | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | ESN | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG03195 | hp1 | a0001 | c0001 | t0007 | g0065 | AFR | ESN | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG03195 | hp2 | a0001 | c0001 | t0004 | g0038 | AFR | ESN | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | MSL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG03209 | hp2 | a0001 | c0001 | t0020 | g0051 | AFR | MSL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | MSL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG03225 | hp2 | a0001 | c0001 | t0008 | g0080 | AFR | MSL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG03239 | hp1 | a0001 | c0002 | t0003 | g0109 | SAS | PJL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG03239 | hp2 | a0001 | c0001 | t0006 | g0047 | SAS | PJL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG03453 | hp1 | a0001 | c0001 | t0004 | g0028 | AFR | MSL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG03453 | hp2 | a0001 | c0001 | t0004 | g0142 | AFR | MSL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG03486 | hp1 | a0001 | c0001 | t0004 | g0083 | AFR | MSL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG03486 | hp2 | a0001 | c0008 | t0016 | g0145 | AFR | MSL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0321 | SAS | PJL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG03516 | hp1 | a0001 | c0001 | t0007 | g0074 | AFR | ESN | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG03516 | hp2 | a0001 | c0001 | t0008 | g0019 | AFR | ESN | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG03540 | hp1 | a0001 | c0002 | t0003 | g0125 | AFR | GWD | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG03540 | hp2 | a0001 | c0002 | t0003 | g0106 | AFR | GWD | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG03579 | hp1 | a0001 | c0001 | t0004 | g0144 | AFR | MSL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG03579 | hp2 | a0001 | c0001 | t0004 | g0192 | AFR | MSL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG03654 | hp1 | a0001 | c0001 | t0006 | g0009 | SAS | PJL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0279 | SAS | PJL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0267 | SAS | PJL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG03669 | hp2 | a0001 | c0001 | t0004 | g0222 | SAS | PJL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0322 | SAS | STU | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG03688 | hp2 | a0001 | c0002 | t0003 | g0130 | SAS | STU | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0252 | SAS | PJL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG03704 | hp2 | a0001 | c0002 | t0003 | g0119 | SAS | PJL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG03710 | hp1 | a0001 | c0002 | t0003 | g0115 | SAS | PJL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0261 | SAS | PJL | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG03831 | hp1 | a0001 | c0003 | t0005 | g0089 | SAS | BEB | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG03831 | hp2 | a0001 | c0004 | t0011 | g0327 | SAS | BEB | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0271 | SAS | BEB | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG03834 | hp2 | a0001 | c0002 | t0003 | g0001 | SAS | BEB | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG03942 | hp1 | a0001 | c0002 | t0003 | g0116 | SAS | BEB | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0260 | SAS | BEB | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0246 | SAS | STU | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0323 | SAS | STU | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0270 | SAS | BEB | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG04184 | hp2 | a0001 | c0002 | t0003 | g0157 | SAS | BEB | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG04199 | hp1 | a0001 | c0002 | t0003 | g0132 | SAS | STU | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0214 | SAS | STU | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0215 | SAS | STU | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG04204 | hp2 | a0001 | c0001 | t0024 | g0320 | SAS | STU | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA18522 | hp1 | a0001 | c0001 | t0004 | g0039 | AFR | YRI | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA18522 | hp2 | a0001 | c0001 | t0006 | g0055 | AFR | YRI | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0303 | EAS | CHB | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | CHB | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA18747 | hp1 | a0001 | c0003 | t0005 | g0087 | EAS | CHB | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | CHB | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA18906 | hp1 | a0001 | c0001 | t0006 | g0056 | AFR | YRI | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA18906 | hp2 | a0001 | c0001 | t0004 | g0037 | AFR | YRI | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA18939 | hp2 | a0001 | c0002 | t0012 | g0102 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA18943 | hp1 | a0001 | c0003 | t0005 | g0011 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA18944 | hp1 | a0001 | c0001 | t0006 | g0054 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA18945 | hp2 | a0001 | c0001 | t0022 | g0174 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA18946 | hp1 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA18946 | hp2 | a0001 | c0003 | t0005 | g0092 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA18952 | hp1 | a0001 | c0001 | t0006 | g0053 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA18952 | hp2 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA18953 | hp2 | a0001 | c0001 | t0009 | g0003 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA18956 | hp1 | a0001 | c0001 | t0002 | g0308 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA18956 | hp2 | a0001 | c0001 | t0009 | g0003 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA18957 | hp1 | a0001 | c0001 | t0002 | g0298 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA18959 | hp2 | a0001 | c0001 | t0002 | g0289 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0328 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA18961 | hp2 | a0001 | c0001 | t0002 | g0297 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0295 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA18965 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA18965 | hp2 | a0001 | c0001 | t0021 | g0241 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA18968 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0296 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0288 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA18971 | hp2 | a0001 | c0002 | t0003 | g0014 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA18972 | hp2 | a0001 | c0001 | t0002 | g0311 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0315 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0302 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA18977 | hp1 | a0001 | c0002 | t0003 | g0043 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA18978 | hp1 | a0001 | c0003 | t0005 | g0091 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA18980 | hp2 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA18985 | hp2 | a0001 | c0001 | t0002 | g0294 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA18987 | hp1 | a0001 | c0001 | t0002 | g0310 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA18990 | hp1 | a0001 | c0001 | t0002 | g0293 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA18992 | hp2 | a0001 | c0001 | t0002 | g0290 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA18993 | hp1 | a0002 | c0007 | t0001 | g0196 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA18993 | hp2 | a0001 | c0002 | t0003 | g0121 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA18994 | hp1 | a0001 | c0001 | t0006 | g0058 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA18998 | hp2 | a0001 | c0003 | t0005 | g0011 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0306 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0292 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA19002 | hp1 | a0001 | c0003 | t0005 | g0098 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0299 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA19003 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA19004 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA19006 | hp2 | a0001 | c0001 | t0009 | g0003 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0329 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA19011 | hp1 | a0001 | c0002 | t0003 | g0079 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA19030 | hp1 | a0001 | c0001 | t0007 | g0068 | AFR | LWK | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | LWK | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA19043 | hp1 | a0001 | c0002 | t0015 | g0103 | AFR | LWK | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA19043 | hp2 | a0001 | c0001 | t0004 | g0028 | AFR | LWK | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA19056 | hp1 | a0001 | c0002 | t0003 | g0108 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA19056 | hp2 | a0001 | c0001 | t0002 | g0318 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA19057 | hp1 | a0001 | c0002 | t0003 | g0095 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA19058 | hp2 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA19063 | hp1 | a0001 | c0001 | t0002 | g0332 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0305 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA19064 | hp1 | a0001 | c0002 | t0003 | g0122 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0307 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA19068 | hp1 | a0001 | c0001 | t0009 | g0003 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA19075 | hp2 | a0001 | c0001 | t0002 | g0316 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA19076 | hp1 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0313 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA19079 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA19082 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA19083 | hp2 | a0001 | c0002 | t0003 | g0138 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA19087 | hp1 | a0001 | c0006 | t0002 | g0291 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0312 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA19091 | hp2 | a0001 | c0002 | t0003 | g0014 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0031 | AFR | YRI | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA19240 | hp2 | a0001 | c0001 | t0014 | g0151 | AFR | YRI | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA20129 | hp1 | a0001 | c0001 | t0007 | g0040 | AFR | ASW | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA20129 | hp2 | a0001 | c0001 | t0006 | g0060 | AFR | ASW | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA20752 | hp1 | a0001 | c0002 | t0003 | g0100 | EUR | TSI | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0004 | EUR | TSI | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA20805 | hp1 | a0001 | c0002 | t0003 | g0001 | EUR | TSI | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0278 | EUR | TSI | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0274 | SAS | GIH | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0195 | SAS | GIH | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG01123 | hp1 | a0001 | c0002 | t0003 | g0094 | AMR | CLM | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG01123 | hp2 | a0001 | c0001 | t0006 | g0048 | AMR | CLM | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG02109 | hp1 | a0001 | c0002 | t0003 | g0128 | AFR | ACB | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG02109 | hp2 | a0001 | c0002 | t0003 | g0107 | AFR | ACB | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG02486 | hp1 | a0001 | c0001 | t0002 | g0286 | AFR | ACB | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG02486 | hp2 | a0001 | c0001 | t0023 | g0238 | AFR | ACB | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG02559 | hp1 | a0001 | c0001 | t0004 | g0202 | AFR | ACB | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
HG02559 | hp2 | a0001 | c0001 | t0004 | g0146 | AFR | ACB | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA18955 | hp2 | a0001 | c0002 | t0003 | g0096 | EAS | JPT | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA21309 | hp1 | a0001 | c0002 | t0003 | g0112 | AFR | LWK | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | LWK | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0003 | g0111 | REF | REF | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0035 | REF | REF | SOCS5_chr2_46694295_46768129 | SOCS5 | chr2 | 46694295 | 46768129 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:46759662
|
G | A | 1 | a0002 | 1 | NA18993.hp1 | missense_variant | MODERATE | c.1132G>A | p.Gly378Arg | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 2/2 | 1299/4766 | 1132/1611 | 378/536 | chr2 | 46759662 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:46758866
|
T | C | 1 | a0001c0005 | 1 | HG02451.hp1 | synonymous_variant | LOW | c.336T>C | p.Asp112Asp | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 2/2 | 503/4766 | 336/1611 | 112/536 | chr2 | 46758866 | ||
chr2:46759043
|
T | G | 1 | a0001c0006 | 1 | NA19087.hp1 | synonymous_variant | LOW | c.513T>G | p.Thr171Thr | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 2/2 | 680/4766 | 513/1611 | 171/536 | chr2 | 46759043 | ||
chr2:46759277
|
A | G | 1 | a0001c0002 | 70 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(67): Show |
synonymous_variant | LOW | c.747A>G | p.Thr249Thr | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 2/2 | 914/4766 | 747/1611 | 249/536 | chr2 | 46759277 | ||
chr2:46759577
|
C | G | 1 | a0001c0004 | 7 | HG01070.hp2 HG01257.hp2 HG01258.hp2 others(4): Show |
synonymous_variant | LOW | c.1047C>G | p.Thr349Thr | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 2/2 | 1214/4766 | 1047/1611 | 349/536 | chr2 | 46759577 | ||
chr2:46759670
|
C | A | 1 | a0001c0008 | 1 | HG03486.hp2 | synonymous_variant | LOW | c.1140C>A | p.Pro380Pro | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 2/2 | 1307/4766 | 1140/1611 | 380/536 | chr2 | 46759670 | ||
chr2:46760000
|
G | A | 2 | a0001c0003a0001c0009 | 22 | HG00733.hp1 HG01069.hp2 HG01074.hp2 others(19): Show |
synonymous_variant | LOW | c.1470G>A | p.Ala490Ala | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 2/2 | 1637/4766 | 1470/1611 | 490/536 | chr2 | 46760000 | ||
chr2:46760027
|
T | C | 1 | a0001c0009 | 1 | HG01433.hp1 | synonymous_variant | LOW | c.1497T>C | p.Asp499Asp | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 2/2 | 1664/4766 | 1497/1611 | 499/536 | chr2 | 46760027 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:46699392
|
G | A | 1 | a0001c0001t0009 | 4 | NA18953.hp2 NA18956.hp2 NA19006.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-70G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/2 | 59139 | chr2 | 46699392 | |||||
chr2:46760161
|
T | G | 25 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(22): Show | 277 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(274): Show |
3_prime_UTR_variant | MODIFIER | c.*20T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 2/2 | 20 | chr2 | 46760161 | |||||
chr2:46760199
|
C | T | 1 | a0001c0001t0006 | 20 | HG00733.hp2 HG01123.hp2 HG01167.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*58C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 2/2 | 58 | chr2 | 46760199 | |||||
chr2:46760202
|
C | T | 1 | a0001c0001t0006 | 20 | HG00733.hp2 HG01123.hp2 HG01167.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*61C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 2/2 | 61 | chr2 | 46760202 | |||||
chr2:46760316
|
G | A | 1 | a0001c0002t0015 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*175G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 2/2 | 175 | chr2 | 46760316 | |||||
chr2:46760405
|
G | A | 1 | a0001c0001t0006 | 20 | HG00733.hp2 HG01123.hp2 HG01167.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*264G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 2/2 | 264 | chr2 | 46760405 | |||||
chr2:46760628
|
A | G | 4 | a0001c0001t0005a0001c0002t0010a0001c0003t0005others(1): Show | 27 | HG00733.hp1 HG01069.hp2 HG01074.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*487A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 2/2 | 487 | chr2 | 46760628 | |||||
chr2:46760796
|
T | G | 18 | a0001c0001t0004a0001c0001t0005a0001c0001t0007others(15): Show | 148 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(145): Show |
3_prime_UTR_variant | MODIFIER | c.*655T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 2/2 | 655 | chr2 | 46760796 | |||||
chr2:46760840
|
C | T | 1 | a0001c0001t0024 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*699C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 2/2 | 699 | chr2 | 46760840 | |||||
chr2:46760933
|
G | T | 1 | a0001c0001t0023 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*792G>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 2/2 | 792 | chr2 | 46760933 | |||||
chr2:46760934
|
T | C | 3 | a0001c0001t0009a0001c0004t0011a0001c0004t0013 | 11 | HG01070.hp2 HG01257.hp2 HG01258.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*793T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 2/2 | 793 | chr2 | 46760934 | |||||
chr2:46760946
|
C | T | 1 | a0001c0001t0020 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*805C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 2/2 | 805 | chr2 | 46760946 | |||||
chr2:46761136
|
G | A | 2 | a0001c0002t0003a0001c0002t0015 | 64 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*995G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 2/2 | 995 | chr2 | 46761136 | |||||
chr2:46761370
|
G | A | 1 | a0001c0008t0016 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1229G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 2/2 | 1229 | chr2 | 46761370 | |||||
chr2:46761490
|
A | G | 1 | a0001c0001t0019 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1349A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 2/2 | 1349 | chr2 | 46761490 | |||||
chr2:46761651
|
G | T | 1 | a0001c0001t0022 | 1 | NA18945.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1510G>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 2/2 | 1510 | chr2 | 46761651 | |||||
chr2:46762123
|
A | T | 2 | a0001c0001t0009a0001c0004t0011 | 8 | HG01070.hp2 HG01515.hp1 HG02132.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1982A>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 2/2 | 1982 | chr2 | 46762123 | |||||
chr2:46762219
|
A | C | 1 | a0001c0001t0018 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2078A>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 2/2 | 2078 | chr2 | 46762219 | |||||
chr2:46762262
|
T | G | 1 | a0001c0001t0014 | 2 | HG03098.hp2 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2121T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 2/2 | 2121 | chr2 | 46762262 | |||||
chr2:46762291
|
T | C | 1 | a0001c0001t0009 | 4 | NA18953.hp2 NA18956.hp2 NA19006.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2150T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 2/2 | 2150 | chr2 | 46762291 | |||||
chr2:46762730
|
T | G | 5 | a0001c0001t0012a0001c0002t0003a0001c0002t0010others(2): Show | 71 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*2589T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 2/2 | 2589 | chr2 | 46762730 | |||||
chr2:46762731
|
GTTAACGG others(5): Show |
G | 2 | a0001c0001t0008a0001c0005t0008 | 6 | HG01109.hp2 HG02451.hp1 HG02970.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2595_*2606delCGGT others(8): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 2/2 | 2595 | INFO_REALIGN_3_PRIME | chr2 | 46762731 | ||||
chr2:46762873
|
TAC | T | 1 | a0001c0001t0006 | 20 | HG00733.hp2 HG01123.hp2 HG01167.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*2747_*2748delAC | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 2/2 | 2747 | INFO_REALIGN_3_PRIME | chr2 | 46762873 | ||||
chr2:46763052
|
G | T | 1 | a0001c0001t0017 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2911G>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 2/2 | 2911 | chr2 | 46763052 | |||||
chr2:46763071
|
A | G | 1 | a0001c0001t0007 | 15 | HG00741.hp1 HG01081.hp2 HG01243.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2930A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 2/2 | 2930 | chr2 | 46763071 | |||||
chr2:46763099
|
G | C | 1 | a0001c0001t0021 | 1 | NA18965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2958G>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 2/2 | 2958 | chr2 | 46763099 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:46699508
|
G | T | 1 | a0001c0001t0002g0332 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-13+59G>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46699508 | ||||||
chr2:46699512
|
G | A | 1 | a0001c0001t0001g0036 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-13+63G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46699512 | ||||||
chr2:46699545
|
C | T | 1 | a0001c0001t0004g0331 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-13+96C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46699545 | ||||||
chr2:46699574
|
C | A | 3 | a0001c0001t0004g0037a0001c0001t0004g0038a0001c0001t0004g0039 | 3 | HG03195.hp2 NA18522.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-13+125C>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46699574 | ||||||
chr2:46699580
|
G | C | 247 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0022others(244): Show | 273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.-13+131G>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46699580 | ||||||
chr2:46699608
|
G | A | 1 | a0001c0001t0009g0003 | 4 | NA18953.hp2 NA18956.hp2 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13+159G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46699608 | ||||||
chr2:46699823
|
G | A | 1 | a0001c0001t0007g0040 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-13+374G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46699823 | ||||||
chr2:46699887
|
G | A | 1 | a0001c0001t0002g0259 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-13+438G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46699887 | ||||||
chr2:46699919
|
G | T | 2 | a0001c0002t0003g0257a0001c0002t0003g0258 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-13+470G>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46699919 | ||||||
chr2:46700228
|
A | T | 5 | a0001c0003t0005g0027a0001c0003t0005g0254a0001c0003t0005g0255others(2): Show | 5 | HG00733.hp1 HG01257.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.-13+779A>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46700228 | ||||||
chr2:46700229
|
C | T | 5 | a0001c0003t0005g0027a0001c0003t0005g0254a0001c0003t0005g0255others(2): Show | 5 | HG00733.hp1 HG01257.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.-13+780C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46700229 | ||||||
chr2:46700253
|
T | C | 1 | a0001c0001t0002g0260 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-13+804T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46700253 | ||||||
chr2:46700463
|
T | C | 2 | a0001c0003t0005g0041a0001c0003t0005g0042 | 2 | HG01069.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.-13+1014T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46700463 | ||||||
chr2:46700539
|
A | C | 1 | a0001c0001t0004g0253 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-13+1090A>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46700539 | ||||||
chr2:46700724
|
A | G | 108 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0022others(105): Show | 118 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.-13+1275A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46700724 | ||||||
chr2:46700769
|
G | A | 1 | a0001c0001t0009g0003 | 4 | NA18953.hp2 NA18956.hp2 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13+1320G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46700769 | ||||||
chr2:46700974
|
C | T | 3 | a0001c0001t0008g0019a0001c0001t0008g0154a0001c0001t0008g0155 | 4 | HG01109.hp2 HG02970.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-13+1525C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46700974 | ||||||
chr2:46701027
|
C | G | 106 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0022others(103): Show | 116 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.-13+1578C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46701027 | ||||||
chr2:46701149
|
C | T | 1 | a0001c0002t0003g0153 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-13+1700C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46701149 | ||||||
chr2:46701187
|
C | A | 1 | a0001c0002t0003g0043 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-13+1738C>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46701187 | ||||||
chr2:46701339
|
T | A | 1 | a0001c0001t0001g0158 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-13+1890T>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46701339 | ||||||
chr2:46701443
|
A | G | 1 | a0001c0002t0003g0152 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-13+1994A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46701443 | ||||||
chr2:46701811
|
T | TTTTTTTT others(289): Show |
13 | a0001c0001t0007g0010a0001c0001t0007g0063a0001c0001t0007g0064others(10): Show | 14 | HG00741.hp1 HG01081.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.-13+2365_-13+2366i others(298): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46701811 | |||||
chr2:46701811
|
T | TTTTTTTT others(289): Show |
4 | a0001c0001t0004g0075a0001c0001t0004g0076a0001c0001t0004g0077others(1): Show | 4 | HG02572.hp1 HG02818.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13+2365_-13+2366i others(298): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46701811 | |||||
chr2:46701811
|
T | TTTTTTTT others(280): Show |
1 | a0001c0002t0003g0079 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-13+2365_-13+2366i others(289): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46701811 | |||||
chr2:46701811
|
T | TTTTTTTT others(294): Show |
2 | a0001c0001t0008g0019a0001c0001t0008g0154 | 3 | HG02970.hp1 HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-13+2365_-13+2366i others(303): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46701811 | |||||
chr2:46701811
|
T | TTTTTTTT others(295): Show |
5 | a0001c0001t0001g0020a0001c0001t0004g0082a0001c0001t0008g0080others(2): Show | 6 | HG01109.hp2 HG02451.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.-13+2365_-13+2366i others(304): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46701811 | |||||
chr2:46701811
|
T | TTTTTTTT others(296): Show |
2 | a0001c0001t0001g0159a0001c0001t0004g0083 | 2 | HG03486.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.-13+2365_-13+2366i others(305): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46701811 | |||||
chr2:46701811
|
T | TTTTTTTT others(297): Show |
6 | a0001c0003t0005g0041a0001c0003t0005g0084a0001c0003t0005g0085others(3): Show | 6 | HG00733.hp1 HG01074.hp2 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.-13+2365_-13+2366i others(306): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46701811 | |||||
chr2:46701811
|
T | TTTTTTTT others(298): Show |
12 | a0001c0002t0010g0012a0001c0002t0010g0086a0001c0002t0010g0090others(9): Show | 15 | HG01069.hp2 HG01346.hp2 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.-13+2365_-13+2366i others(307): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46701811 | |||||
chr2:46701811
|
T | TTTTTTTT others(286): Show |
1 | a0001c0002t0003g0094 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-13+2365_-13+2366i others(295): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46701811 | |||||
chr2:46701811
|
T | TTTTTTTT others(299): Show |
2 | a0001c0003t0005g0092a0001c0003t0005g0093 | 2 | HG02056.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.-13+2365_-13+2366i others(308): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46701811 | |||||
chr2:46701811
|
T | TTTTTTTT others(285): Show |
2 | a0001c0002t0003g0095a0001c0002t0003g0096 | 2 | NA18955.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.-13+2365_-13+2366i others(294): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46701811 | |||||
chr2:46701811
|
T | TTTTTTTT others(287): Show |
34 | a0001c0001t0012g0126a0001c0002t0003g0001a0001c0002t0003g0014others(31): Show | 41 | HG00280.hp1 HG00280.hp2 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.-13+2365_-13+2366i others(296): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46701811 | |||||
chr2:46701811
|
T | TTTTTTTT others(300): Show |
2 | a0001c0003t0005g0097a0001c0003t0005g0098 | 2 | HG02630.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.-13+2365_-13+2366i others(309): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46701811 | |||||
chr2:46701811
|
T | TTTTTTTT others(288): Show |
14 | a0001c0002t0003g0017a0001c0002t0003g0018a0001c0002t0003g0127others(11): Show | 16 | HG00323.hp2 HG00438.hp2 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.-13+2365_-13+2366i others(297): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46701811 | |||||
chr2:46701811
|
T | TTTTTTTT others(289): Show |
3 | a0001c0002t0003g0137a0001c0002t0003g0138a0001c0002t0003g0139 | 3 | HG01192.hp1 HG02165.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.-13+2365_-13+2366i others(298): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46701811 | |||||
chr2:46701811
|
T | TTTTTTTT others(302): Show |
2 | a0001c0001t0001g0160a0001c0001t0004g0136 | 2 | HG02145.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.-13+2365_-13+2366i others(311): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46701811 | |||||
chr2:46701811
|
T | TTTTTTTT others(290): Show |
1 | a0001c0002t0003g0140 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-13+2365_-13+2366i others(299): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46701811 | |||||
chr2:46701811
|
T | TTTTTTTT others(303): Show |
7 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0163others(4): Show | 7 | HG02451.hp2 HG02647.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.-13+2365_-13+2366i others(312): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46701811 | |||||
chr2:46701811
|
T | TTTTTTTT others(304): Show |
49 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0036others(46): Show | 54 | HG00408.hp1 HG00558.hp1 HG00738.hp1 others(51): Show |
intron_variant | MODIFIER | c.-13+2365_-13+2366i others(313): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46701811 | |||||
chr2:46701811
|
T | TTTTTTTT others(304): Show |
1 | a0001c0001t0001g0208 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-13+2365_-13+2366i others(313): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46701811 | |||||
chr2:46701811
|
T | TTTTTTTT others(305): Show |
28 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0209others(25): Show | 30 | HG00140.hp2 HG00438.hp1 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.-13+2365_-13+2366i others(314): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46701811 | |||||
chr2:46701811
|
T | TTTTTTTT others(305): Show |
3 | a0001c0001t0001g0025a0001c0001t0001g0235a0001c0001t0001g0236 | 4 | NA18948.hp1 NA18998.hp1 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13+2365_-13+2366i others(314): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46701811 | |||||
chr2:46701811
|
T | TTTTTTTT others(306): Show |
11 | a0001c0001t0001g0026a0001c0001t0001g0237a0001c0001t0001g0239others(8): Show | 12 | HG02293.hp1 HG02486.hp2 HG02738.hp1 others(9): Show |
intron_variant | MODIFIER | c.-13+2365_-13+2366i others(315): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46701811 | |||||
chr2:46701811
|
T | TTTTTTTT others(306): Show |
1 | a0001c0001t0001g0247 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-13+2365_-13+2366i others(315): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46701811 | |||||
chr2:46701811
|
T | TTTTTTTT others(294): Show |
1 | a0001c0002t0003g0157 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-13+2365_-13+2366i others(303): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46701811 | |||||
chr2:46701811
|
T | TTTTTTTT others(307): Show |
5 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(2): Show | 5 | HG02976.hp2 NA18906.hp2 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.-13+2365_-13+2366i others(316): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46701811 | |||||
chr2:46701811
|
T | TTTTTTTT others(307): Show |
1 | a0001c0001t0001g0251 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.-13+2365_-13+2366i others(316): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46701811 | |||||
chr2:46701811
|
T | TTTTTTTT others(308): Show |
3 | a0001c0001t0004g0038a0001c0001t0004g0039a0001c0001t0004g0142 | 3 | HG03195.hp2 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-13+2365_-13+2366i others(317): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46701811 | |||||
chr2:46701811
|
T | TTTTTTTT others(309): Show |
3 | a0001c0001t0004g0143a0001c0001t0004g0144a0001c0008t0016g0145 | 3 | HG02615.hp1 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-13+2365_-13+2366i others(318): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46701811 | |||||
chr2:46701811
|
T | TTTTTTTT others(310): Show |
4 | a0001c0001t0001g0252a0001c0001t0004g0146a0001c0001t0004g0147others(1): Show | 4 | HG01109.hp1 HG02559.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-13+2365_-13+2366i others(319): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46701811 | |||||
chr2:46701811
|
T | TTTTTTTT others(312): Show |
1 | a0001c0001t0004g0148 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-13+2365_-13+2366i others(321): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46701811 | |||||
chr2:46701811
|
T | TTTTTTTT others(314): Show |
1 | a0001c0003t0005g0149 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-13+2365_-13+2366i others(323): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46701811 | |||||
chr2:46701811
|
T | TTTTTTTT others(316): Show |
1 | a0001c0001t0014g0150 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-13+2365_-13+2366i others(325): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46701811 | |||||
chr2:46701811
|
T | TTTTTTTT others(321): Show |
1 | a0001c0001t0014g0151 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-13+2365_-13+2366i others(330): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46701811 | |||||
chr2:46701863
|
A | G | 248 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0022others(245): Show | 274 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.-13+2414A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46701863 | ||||||
chr2:46702068
|
A | G | 2 | a0001c0001t0002g0328a0001c0001t0002g0329 | 2 | NA18960.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.-13+2619A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46702068 | ||||||
chr2:46702096
|
G | A | 1 | a0001c0001t0002g0261 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-13+2647G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46702096 | ||||||
chr2:46702427
|
A | G | 22 | a0001c0002t0010g0012a0001c0002t0010g0086a0001c0002t0010g0090others(19): Show | 25 | HG00733.hp1 HG01069.hp2 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.-13+2978A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46702427 | ||||||
chr2:46702504
|
G | C | 1 | a0001c0003t0005g0011 | 2 | NA18943.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.-13+3055G>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46702504 | ||||||
chr2:46702569
|
T | C | 10 | a0001c0001t0004g0037a0001c0001t0004g0038a0001c0001t0004g0039others(7): Show | 10 | HG02572.hp1 HG02818.hp2 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.-13+3120T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46702569 | ||||||
chr2:46702678
|
T | G | 7 | a0001c0001t0004g0075a0001c0001t0004g0076a0001c0001t0004g0077others(4): Show | 7 | HG02572.hp1 HG02818.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.-13+3229T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46702678 | ||||||
chr2:46702722
|
CAT | C | 10 | a0001c0001t0004g0037a0001c0001t0004g0038a0001c0001t0004g0039others(7): Show | 10 | HG02572.hp1 HG02818.hp2 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.-13+3276_-13+3277d others(4): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46702722 | |||||
chr2:46702734
|
T | C | 55 | a0001c0002t0003g0001a0001c0002t0003g0014a0001c0002t0003g0015others(52): Show | 64 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.-13+3285T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46702734 | ||||||
chr2:46702812
|
G | C | 130 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0022others(127): Show | 142 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.-13+3363G>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46702812 | ||||||
chr2:46702831
|
T | G | 1 | a0001c0001t0006g0044 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-13+3382T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46702831 | ||||||
chr2:46702963
|
A | G | 130 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0022others(127): Show | 142 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.-13+3514A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46702963 | ||||||
chr2:46703030
|
A | G | 4 | a0001c0004t0011g0324a0001c0004t0011g0325a0001c0004t0011g0326others(1): Show | 4 | HG01070.hp2 HG01515.hp1 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.-13+3581A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46703030 | ||||||
chr2:46703206
|
A | G | 3 | a0001c0001t0002g0321a0001c0001t0002g0322a0001c0001t0002g0323 | 3 | HG03491.hp1 HG03688.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.-13+3757A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46703206 | ||||||
chr2:46703276
|
T | A | 7 | a0001c0001t0007g0010a0001c0001t0007g0063a0001c0001t0007g0064others(4): Show | 8 | HG00741.hp1 HG01081.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.-13+3827T>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46703276 | ||||||
chr2:46703354
|
G | GTT | 129 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0022others(126): Show | 141 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.-13+3916_-13+3917d others(4): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46703354 | |||||
chr2:46703374
|
G | A | 256 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0022others(253): Show | 286 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.-13+3925G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46703374 | ||||||
chr2:46703637
|
T | C | 110 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0022others(107): Show | 120 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.-13+4188T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46703637 | ||||||
chr2:46703774
|
A | G | 1 | a0001c0002t0003g0079 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-13+4325A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46703774 | ||||||
chr2:46703829
|
A | G | 1 | a0001c0001t0001g0207 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-13+4380A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46703829 | ||||||
chr2:46703886
|
T | G | 1 | a0001c0001t0001g0166 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-13+4437T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46703886 | ||||||
chr2:46704004
|
A | G | 1 | a0001c0001t0004g0083 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-13+4555A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46704004 | ||||||
chr2:46704032
|
A | G | 2 | a0001c0001t0001g0061a0001c0001t0001g0062 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-13+4583A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46704032 | ||||||
chr2:46704102
|
C | G | 11 | a0001c0001t0004g0037a0001c0001t0004g0038a0001c0001t0004g0039others(8): Show | 11 | HG02572.hp1 HG02818.hp2 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.-13+4653C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46704102 | ||||||
chr2:46704255
|
C | T | 1 | a0001c0001t0024g0320 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-13+4806C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46704255 | ||||||
chr2:46704293
|
C | T | 1 | a0001c0001t0007g0040 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-13+4844C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46704293 | ||||||
chr2:46704357
|
A | G | 1 | a0001c0001t0004g0037 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-13+4908A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46704357 | ||||||
chr2:46704534
|
T | A | 9 | a0001c0001t0004g0136a0001c0001t0004g0142a0001c0001t0004g0143others(6): Show | 9 | HG01109.hp1 HG02145.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.-13+5085T>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46704534 | ||||||
chr2:46704588
|
T | A | 2 | a0001c0001t0001g0061a0001c0001t0001g0062 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-13+5139T>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46704588 | ||||||
chr2:46704713
|
A | G | 2 | a0001c0001t0004g0038a0001c0001t0004g0039 | 2 | HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-13+5264A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46704713 | ||||||
chr2:46704829
|
A | C | 2 | a0001c0001t0001g0159a0001c0001t0001g0250 | 2 | NA19076.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.-13+5380A>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46704829 | ||||||
chr2:46705062
|
G | C | 9 | a0001c0001t0004g0136a0001c0001t0004g0142a0001c0001t0004g0143others(6): Show | 9 | HG01109.hp1 HG02145.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.-13+5613G>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46705062 | ||||||
chr2:46705321
|
A | C | 1 | a0001c0001t0007g0010 | 2 | HG00741.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-13+5872A>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46705321 | ||||||
chr2:46705378
|
T | A | 1 | a0001c0002t0010g0012 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-13+5929T>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46705378 | ||||||
chr2:46705384
|
G | A | 251 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0022others(248): Show | 278 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.-13+5935G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46705384 | ||||||
chr2:46705405
|
T | G | 58 | a0001c0001t0012g0126a0001c0002t0003g0001a0001c0002t0003g0014others(55): Show | 67 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.-13+5956T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46705405 | ||||||
chr2:46705409
|
A | T | 1 | a0001c0002t0010g0012 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-13+5960A>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46705409 | ||||||
chr2:46705416
|
G | A | 330 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0022others(327): Show | 375 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(372): Show |
intron_variant | MODIFIER | c.-13+5967G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46705416 | ||||||
chr2:46705526
|
GATTACCA | G | 7 | a0001c0001t0004g0082a0001c0001t0004g0083a0001c0001t0008g0019others(4): Show | 8 | HG01109.hp2 HG02451.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.-13+6078_-13+6084d others(9): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46705526 | ||||||
chr2:46705527
|
A | G | 117 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0004g0028others(114): Show | 131 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.-13+6078A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46705527 | ||||||
chr2:46705658
|
T | A | 251 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0022others(248): Show | 278 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.-13+6209T>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46705658 | ||||||
chr2:46705773
|
A | G | 7 | a0001c0001t0004g0082a0001c0001t0004g0083a0001c0001t0008g0019others(4): Show | 8 | HG01109.hp2 HG02451.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.-13+6324A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46705773 | ||||||
chr2:46705810
|
C | A | 8 | a0001c0001t0006g0008a0001c0001t0006g0009a0001c0001t0006g0044others(5): Show | 10 | HG00733.hp2 HG01123.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.-13+6361C>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46705810 | ||||||
chr2:46705882
|
A | G | 1 | a0001c0001t0004g0083 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-13+6433A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46705882 | ||||||
chr2:46705926
|
A | T | 21 | a0001c0002t0010g0012a0001c0002t0010g0086a0001c0002t0010g0090others(18): Show | 24 | HG00733.hp1 HG01069.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.-13+6477A>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46705926 | ||||||
chr2:46705990
|
A | G | 1 | a0001c0001t0001g0206 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-13+6541A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46705990 | ||||||
chr2:46705994
|
G | C | 1 | a0001c0002t0003g0099 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-13+6545G>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46705994 | ||||||
chr2:46706076
|
G | A | 11 | a0001c0001t0004g0037a0001c0001t0004g0038a0001c0001t0004g0039others(8): Show | 11 | HG02572.hp1 HG02818.hp2 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.-13+6627G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46706076 | ||||||
chr2:46706116
|
T | C | 1 | a0001c0001t0006g0050 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-13+6667T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46706116 | ||||||
chr2:46706314
|
G | A | 1 | a0001c0001t0009g0003 | 4 | NA18953.hp2 NA18956.hp2 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13+6865G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46706314 | ||||||
chr2:46706405
|
T | C | 1 | a0001c0002t0003g0099 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-13+6956T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46706405 | ||||||
chr2:46706468
|
C | G | 2 | a0001c0001t0002g0317a0001c0001t0002g0318 | 2 | HG00408.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.-13+7019C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46706468 | ||||||
chr2:46706684
|
A | T | 1 | a0001c0001t0002g0316 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-13+7235A>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46706684 | ||||||
chr2:46706823
|
G | T | 13 | a0001c0001t0007g0010a0001c0001t0007g0063a0001c0001t0007g0064others(10): Show | 14 | HG00741.hp1 HG01081.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.-13+7374G>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46706823 | ||||||
chr2:46706859
|
C | G | 1 | a0001c0001t0004g0082 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-13+7410C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46706859 | ||||||
chr2:46706873
|
A | G | 1 | a0001c0003t0005g0149 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-13+7424A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46706873 | ||||||
chr2:46706918
|
C | T | 3 | a0001c0001t0004g0037a0001c0001t0004g0038a0001c0001t0004g0039 | 3 | HG03195.hp2 NA18522.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-13+7469C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46706918 | ||||||
chr2:46707005
|
TGCTG | T | 4 | a0001c0003t0005g0091a0001c0003t0005g0092a0001c0003t0005g0093others(1): Show | 4 | HG02056.hp1 NA18946.hp2 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.-13+7557_-13+7560d others(6): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46707005 | ||||||
chr2:46707011
|
A | T | 4 | a0001c0003t0005g0091a0001c0003t0005g0092a0001c0003t0005g0093others(1): Show | 4 | HG02056.hp1 NA18946.hp2 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.-13+7562A>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46707011 | ||||||
chr2:46707012
|
C | T | 4 | a0001c0003t0005g0091a0001c0003t0005g0092a0001c0003t0005g0093others(1): Show | 4 | HG02056.hp1 NA18946.hp2 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.-13+7563C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46707012 | ||||||
chr2:46707176
|
G | T | 1 | a0001c0001t0002g0315 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-13+7727G>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46707176 | ||||||
chr2:46707209
|
T | C | 2 | a0001c0001t0001g0061a0001c0001t0001g0062 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-13+7760T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46707209 | ||||||
chr2:46707311
|
C | A | 1 | a0001c0003t0005g0149 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-13+7862C>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46707311 | ||||||
chr2:46707366
|
T | C | 57 | a0001c0001t0012g0126a0001c0002t0003g0001a0001c0002t0003g0014others(54): Show | 66 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.-13+7917T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46707366 | ||||||
chr2:46707436
|
T | C | 1 | a0001c0001t0002g0317 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-13+7987T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46707436 | ||||||
chr2:46707481
|
A | G | 2 | a0001c0001t0002g0313a0001c0001t0002g0314 | 2 | HG00558.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.-13+8032A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46707481 | ||||||
chr2:46707570
|
G | A | 1 | a0001c0008t0016g0145 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-13+8121G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46707570 | ||||||
chr2:46707693
|
G | A | 11 | a0001c0001t0006g0050a0001c0001t0006g0052a0001c0001t0006g0053others(8): Show | 11 | HG02080.hp1 HG02135.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.-13+8244G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46707693 | ||||||
chr2:46707769
|
C | T | 128 | a0001c0001t0004g0028a0001c0001t0004g0037a0001c0001t0004g0038others(125): Show | 145 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.-13+8320C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46707769 | ||||||
chr2:46707797
|
G | T | 110 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0022others(107): Show | 120 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.-13+8348G>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46707797 | ||||||
chr2:46707934
|
T | G | 2 | a0001c0001t0001g0061a0001c0001t0001g0062 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-13+8485T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46707934 | ||||||
chr2:46708001
|
C | A | 11 | a0001c0001t0006g0050a0001c0001t0006g0052a0001c0001t0006g0053others(8): Show | 11 | HG02080.hp1 HG02135.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.-13+8552C>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46708001 | ||||||
chr2:46708054
|
CTGTT | C | 1 | a0001c0001t0009g0003 | 4 | NA18953.hp2 NA18956.hp2 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13+8609_-13+8612d others(6): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46708054 | |||||
chr2:46708115
|
T | C | 8 | a0001c0001t0004g0075a0001c0001t0004g0076a0001c0001t0004g0077others(5): Show | 8 | HG02572.hp1 HG02818.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.-13+8666T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46708115 | ||||||
chr2:46708176
|
A | G | 1 | a0001c0001t0007g0074 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-13+8727A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46708176 | ||||||
chr2:46708343
|
G | C | 1 | a0001c0001t0019g0263 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-13+8894G>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46708343 | ||||||
chr2:46708433
|
C | T | 11 | a0001c0001t0006g0050a0001c0001t0006g0052a0001c0001t0006g0053others(8): Show | 11 | HG02080.hp1 HG02135.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.-13+8984C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46708433 | ||||||
chr2:46708434
|
G | A | 1 | a0001c0001t0007g0010 | 2 | HG00741.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-13+8985G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46708434 | ||||||
chr2:46708569
|
G | A | 11 | a0001c0001t0006g0050a0001c0001t0006g0052a0001c0001t0006g0053others(8): Show | 11 | HG02080.hp1 HG02135.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.-13+9120G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46708569 | ||||||
chr2:46708652
|
G | C | 68 | a0001c0001t0004g0037a0001c0001t0004g0038a0001c0001t0004g0039others(65): Show | 77 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(74): Show |
intron_variant | MODIFIER | c.-13+9203G>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46708652 | ||||||
chr2:46708782
|
G | C | 4 | a0001c0001t0001g0168a0001c0001t0001g0209a0001c0001t0001g0210others(1): Show | 4 | HG00140.hp2 HG01099.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13+9333G>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46708782 | ||||||
chr2:46708880
|
C | CT | 25 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0033others(22): Show | 30 | HG01496.hp1 HG02027.hp1 HG02027.hp2 others(27): Show |
intron_variant | MODIFIER | c.-13+9456dupT | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46708880 | |||||
chr2:46708880
|
CT | C | 26 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0233others(23): Show | 27 | HG01175.hp2 HG01346.hp1 HG01516.hp1 others(24): Show |
intron_variant | MODIFIER | c.-13+9456delT | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46708880 | |||||
chr2:46708880
|
CTT | C | 212 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0022others(209): Show | 240 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.-13+9455_-13+9456d others(4): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46708880 | |||||
chr2:46708880
|
CTTT | C | 17 | a0001c0001t0001g0161a0001c0001t0001g0169a0001c0001t0001g0170others(14): Show | 18 | HG00741.hp1 HG01070.hp1 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.-13+9454_-13+9456d others(5): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46708880 | |||||
chr2:46709037
|
C | T | 3 | a0001c0001t0004g0037a0001c0001t0004g0038a0001c0001t0004g0039 | 3 | HG03195.hp2 NA18522.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-13+9588C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46709037 | ||||||
chr2:46709044
|
G | A | 1 | a0001c0001t0005g0167 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-13+9595G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46709044 | ||||||
chr2:46709126
|
C | T | 13 | a0001c0001t0007g0010a0001c0001t0007g0063a0001c0001t0007g0064others(10): Show | 14 | HG00741.hp1 HG01081.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.-13+9677C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46709126 | ||||||
chr2:46709151
|
T | G | 1 | a0001c0002t0003g0157 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-13+9702T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46709151 | ||||||
chr2:46709178
|
C | G | 251 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0022others(248): Show | 278 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.-13+9729C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46709178 | ||||||
chr2:46709311
|
C | G | 1 | a0001c0003t0005g0097 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-13+9862C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46709311 | ||||||
chr2:46709610
|
G | A | 1 | a0001c0002t0012g0102 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-13+10161G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46709610 | ||||||
chr2:46709645
|
T | G | 1 | a0001c0002t0015g0103 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-13+10196T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46709645 | ||||||
chr2:46709698
|
A | T | 21 | a0001c0002t0010g0012a0001c0002t0010g0086a0001c0002t0010g0090others(18): Show | 24 | HG00733.hp1 HG01069.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.-13+10249A>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46709698 | ||||||
chr2:46709755
|
A | G | 18 | a0001c0001t0004g0136a0001c0001t0004g0142a0001c0001t0004g0143others(15): Show | 20 | HG00280.hp2 HG00733.hp2 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.-13+10306A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46709755 | ||||||
chr2:46709836
|
C | T | 1 | a0001c0001t0002g0295 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-13+10387C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46709836 | ||||||
chr2:46709948
|
G | T | 1 | a0001c0008t0016g0145 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-13+10499G>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46709948 | ||||||
chr2:46709989
|
C | G | 1 | a0001c0002t0003g0124 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-13+10540C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46709989 | ||||||
chr2:46710131
|
T | G | 1 | a0001c0001t0001g0171 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-13+10682T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46710131 | ||||||
chr2:46710202
|
A | G | 259 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0022others(256): Show | 292 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.-13+10753A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46710202 | ||||||
chr2:46710277
|
A | G | 11 | a0001c0001t0006g0050a0001c0001t0006g0052a0001c0001t0006g0053others(8): Show | 11 | HG02080.hp1 HG02135.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.-13+10828A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46710277 | ||||||
chr2:46710348
|
C | T | 1 | a0001c0002t0012g0102 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-13+10899C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46710348 | ||||||
chr2:46710349
|
G | A | 1 | a0001c0001t0020g0051 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-13+10900G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46710349 | ||||||
chr2:46710425
|
G | T | 11 | a0001c0001t0006g0050a0001c0001t0006g0052a0001c0001t0006g0053others(8): Show | 11 | HG02080.hp1 HG02135.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.-13+10976G>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46710425 | ||||||
chr2:46710431
|
C | T | 1 | a0001c0001t0006g0058 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-13+10982C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46710431 | ||||||
chr2:46710547
|
T | G | 2 | a0001c0001t0001g0061a0001c0001t0001g0062 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-13+11098T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46710547 | ||||||
chr2:46710600
|
A | G | 22 | a0001c0002t0010g0012a0001c0002t0010g0086a0001c0002t0010g0090others(19): Show | 25 | HG00733.hp1 HG01069.hp2 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.-13+11151A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46710600 | ||||||
chr2:46710638
|
A | T | 1 | a0001c0001t0002g0265 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-13+11189A>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46710638 | ||||||
chr2:46710726
|
A | G | 1 | a0001c0002t0003g0139 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-13+11277A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46710726 | ||||||
chr2:46710879
|
C | A | 11 | a0001c0001t0006g0050a0001c0001t0006g0052a0001c0001t0006g0053others(8): Show | 11 | HG02080.hp1 HG02135.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.-13+11430C>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46710879 | ||||||
chr2:46711120
|
T | G | 4 | a0001c0004t0011g0324a0001c0004t0011g0325a0001c0004t0011g0326others(1): Show | 4 | HG01070.hp2 HG01515.hp1 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.-13+11671T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46711120 | ||||||
chr2:46711165
|
A | T | 2 | a0001c0001t0001g0061a0001c0001t0001g0062 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-13+11716A>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46711165 | ||||||
chr2:46711246
|
A | G | 53 | a0001c0001t0012g0126a0001c0002t0003g0001a0001c0002t0003g0014others(50): Show | 62 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.-13+11797A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46711246 | ||||||
chr2:46711254
|
A | C | 53 | a0001c0001t0012g0126a0001c0002t0003g0001a0001c0002t0003g0014others(50): Show | 62 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.-13+11805A>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46711254 | ||||||
chr2:46711365
|
C | A | 3 | a0001c0001t0004g0037a0001c0001t0004g0038a0001c0001t0004g0039 | 3 | HG03195.hp2 NA18522.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-13+11916C>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46711365 | ||||||
chr2:46711597
|
C | T | 55 | a0001c0002t0003g0001a0001c0002t0003g0014a0001c0002t0003g0015others(52): Show | 64 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.-13+12148C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46711597 | ||||||
chr2:46711643
|
C | A | 1 | a0001c0001t0023g0238 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-13+12194C>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46711643 | ||||||
chr2:46711650
|
T | C | 56 | a0001c0001t0012g0126a0001c0002t0003g0001a0001c0002t0003g0014others(53): Show | 65 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.-13+12201T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46711650 | ||||||
chr2:46711853
|
G | A | 1 | a0001c0003t0005g0011 | 2 | NA18943.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.-13+12404G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46711853 | ||||||
chr2:46711898
|
A | G | 2 | a0001c0001t0004g0028a0001c0001t0019g0263 | 3 | HG02055.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-13+12449A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46711898 | ||||||
chr2:46711953
|
A | G | 1 | a0001c0001t0004g0083 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-13+12504A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46711953 | ||||||
chr2:46712003
|
G | T | 1 | a0001c0001t0006g0057 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-13+12554G>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46712003 | ||||||
chr2:46712010
|
T | C | 11 | a0001c0001t0004g0037a0001c0001t0004g0038a0001c0001t0004g0039others(8): Show | 11 | HG02572.hp1 HG02818.hp2 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.-13+12561T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46712010 | ||||||
chr2:46712139
|
T | C | 1 | a0001c0001t0009g0003 | 4 | NA18953.hp2 NA18956.hp2 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13+12690T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46712139 | ||||||
chr2:46712306
|
C | CT | 175 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0022others(172): Show | 191 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(188): Show |
intron_variant | MODIFIER | c.-13+12867dupT | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46712306 | |||||
chr2:46712316
|
T | TC | 20 | a0001c0001t0006g0008a0001c0001t0006g0009a0001c0001t0006g0044others(17): Show | 22 | HG00280.hp2 HG00733.hp2 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.-13+12870dupC | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46712316 | |||||
chr2:46712336
|
C | CT | 52 | a0001c0001t0002g0259a0001c0001t0002g0292a0001c0001t0002g0293others(49): Show | 60 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.-13+12912dupT | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46712336 | |||||
chr2:46712336
|
C | CTT | 6 | a0001c0002t0003g0018a0001c0002t0003g0096a0001c0002t0003g0123others(3): Show | 7 | HG00438.hp2 HG00738.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.-13+12911_-13+1291 others(6): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46712336 | |||||
chr2:46712336
|
CT | C | 49 | a0001c0001t0002g0296a0001c0001t0004g0083a0001c0001t0004g0142others(46): Show | 57 | HG00280.hp2 HG00733.hp1 HG00733.hp2 others(54): Show |
intron_variant | MODIFIER | c.-13+12912delT | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46712336 | |||||
chr2:46712336
|
CTT | C | 50 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0200others(47): Show | 53 | HG00741.hp1 HG01081.hp2 HG01109.hp2 others(50): Show |
intron_variant | MODIFIER | c.-13+12911_-13+1291 others(6): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46712336 | |||||
chr2:46712336
|
CTTT | C | 97 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0022others(94): Show | 107 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(104): Show |
intron_variant | MODIFIER | c.-13+12910_-13+1291 others(7): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46712336 | |||||
chr2:46712449
|
T | G | 5 | a0001c0001t0001g0168a0001c0001t0001g0172a0001c0001t0001g0209others(2): Show | 5 | HG00140.hp2 HG01099.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.-13+13000T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46712449 | ||||||
chr2:46712490
|
C | T | 2 | a0001c0001t0007g0072a0001c0001t0007g0073 | 2 | HG01243.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.-13+13041C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46712490 | ||||||
chr2:46712491
|
G | A | 1 | a0001c0001t0002g0321 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-13+13042G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46712491 | ||||||
chr2:46712492
|
T | A | 20 | a0001c0001t0006g0008a0001c0001t0006g0009a0001c0001t0006g0044others(17): Show | 22 | HG00280.hp2 HG00733.hp2 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.-13+13043T>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46712492 | ||||||
chr2:46712500
|
C | T | 1 | a0001c0001t0004g0082 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-13+13051C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46712500 | ||||||
chr2:46712518
|
A | G | 2 | a0001c0002t0003g0121a0001c0002t0003g0122 | 2 | NA18993.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.-13+13069A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46712518 | ||||||
chr2:46712544
|
A | G | 11 | a0001c0001t0006g0050a0001c0001t0006g0052a0001c0001t0006g0053others(8): Show | 11 | HG02080.hp1 HG02135.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.-13+13095A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46712544 | ||||||
chr2:46712585
|
G | A | 1 | a0001c0001t0001g0172 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-13+13136G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46712585 | ||||||
chr2:46712621
|
C | T | 1 | a0001c0002t0003g0132 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-13+13172C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46712621 | ||||||
chr2:46712633
|
T | C | 251 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0022others(248): Show | 278 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.-13+13184T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46712633 | ||||||
chr2:46712756
|
C | T | 1 | a0001c0001t0007g0040 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-13+13307C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46712756 | ||||||
chr2:46712794
|
C | T | 1 | a0001c0001t0001g0199 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-13+13345C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46712794 | ||||||
chr2:46712971
|
G | A | 4 | a0001c0004t0011g0324a0001c0004t0011g0325a0001c0004t0011g0326others(1): Show | 4 | HG01070.hp2 HG01515.hp1 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.-13+13522G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46712971 | ||||||
chr2:46713138
|
T | C | 2 | a0001c0001t0001g0061a0001c0001t0001g0062 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-13+13689T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46713138 | ||||||
chr2:46713224
|
C | T | 2 | a0001c0001t0001g0061a0001c0001t0001g0062 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-13+13775C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46713224 | ||||||
chr2:46713225
|
G | A | 1 | a0001c0003t0005g0087 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-13+13776G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46713225 | ||||||
chr2:46713366
|
G | T | 20 | a0001c0001t0006g0008a0001c0001t0006g0009a0001c0001t0006g0044others(17): Show | 22 | HG00280.hp2 HG00733.hp2 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.-13+13917G>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46713366 | ||||||
chr2:46713427
|
G | T | 1 | a0001c0001t0001g0262 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-13+13978G>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46713427 | ||||||
chr2:46713521
|
C | T | 1 | a0001c0001t0023g0238 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-13+14072C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46713521 | ||||||
chr2:46713547
|
T | C | 13 | a0001c0001t0007g0010a0001c0001t0007g0063a0001c0001t0007g0064others(10): Show | 14 | HG00741.hp1 HG01081.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.-13+14098T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46713547 | ||||||
chr2:46713564
|
T | C | 13 | a0001c0001t0007g0010a0001c0001t0007g0063a0001c0001t0007g0064others(10): Show | 14 | HG00741.hp1 HG01081.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.-13+14115T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46713564 | ||||||
chr2:46713581
|
A | G | 20 | a0001c0001t0006g0008a0001c0001t0006g0009a0001c0001t0006g0044others(17): Show | 22 | HG00280.hp2 HG00733.hp2 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.-13+14132A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46713581 | ||||||
chr2:46713612
|
C | T | 1 | a0001c0001t0004g0198 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-13+14163C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46713612 | ||||||
chr2:46713659
|
G | T | 4 | a0001c0001t0001g0020a0001c0001t0001g0197a0001c0001t0001g0199others(1): Show | 5 | NA18977.hp2 NA18980.hp1 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.-13+14210G>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46713659 | ||||||
chr2:46713730
|
G | A | 1 | a0001c0001t0002g0266 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-13+14281G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46713730 | ||||||
chr2:46713733
|
A | C | 1 | a0001c0001t0023g0238 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-13+14284A>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46713733 | ||||||
chr2:46713747
|
T | C | 13 | a0001c0001t0007g0010a0001c0001t0007g0063a0001c0001t0007g0064others(10): Show | 14 | HG00741.hp1 HG01081.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.-13+14298T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46713747 | ||||||
chr2:46713992
|
C | T | 1 | a0001c0008t0016g0145 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-13+14543C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46713992 | ||||||
chr2:46714088
|
G | A | 10 | a0001c0001t0004g0037a0001c0001t0004g0038a0001c0001t0004g0039others(7): Show | 10 | HG02572.hp1 HG02818.hp2 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.-13+14639G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46714088 | ||||||
chr2:46714108
|
G | T | 2 | a0001c0001t0001g0170a0001c0001t0001g0330 | 2 | NA18951.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.-13+14659G>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46714108 | ||||||
chr2:46714162
|
A | G | 9 | a0001c0001t0002g0289a0001c0001t0002g0290a0001c0001t0002g0293others(6): Show | 9 | HG00408.hp2 HG00558.hp2 NA18956.hp1 others(6): Show |
intron_variant | MODIFIER | c.-13+14713A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46714162 | ||||||
chr2:46714218
|
A | G | 3 | a0001c0001t0001g0036a0001c0001t0004g0028a0001c0001t0019g0263 | 4 | HG02055.hp2 HG02809.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-13+14769A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46714218 | ||||||
chr2:46714419
|
G | A | 2 | a0001c0001t0001g0211a0001c0002t0003g0135 | 2 | HG01175.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.-13+14970G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46714419 | ||||||
chr2:46714496
|
C | G | 2 | a0001c0001t0002g0287a0001c0001t0002g0288 | 2 | NA18946.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.-13+15047C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46714496 | ||||||
chr2:46714526
|
A | G | 7 | a0001c0001t0004g0082a0001c0001t0004g0083a0001c0001t0008g0019others(4): Show | 8 | HG01109.hp2 HG02451.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.-13+15077A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46714526 | ||||||
chr2:46714650
|
C | T | 1 | a0001c0002t0015g0103 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-13+15201C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46714650 | ||||||
chr2:46714693
|
A | G | 20 | a0001c0001t0006g0008a0001c0001t0006g0009a0001c0001t0006g0044others(17): Show | 22 | HG00280.hp2 HG00733.hp2 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.-13+15244A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46714693 | ||||||
chr2:46714798
|
T | G | 5 | a0001c0001t0002g0267a0001c0004t0011g0324a0001c0004t0011g0325others(2): Show | 5 | HG01070.hp2 HG01515.hp1 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.-13+15349T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46714798 | ||||||
chr2:46715149
|
G | C | 1 | a0001c0001t0002g0289 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-13+15700G>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46715149 | ||||||
chr2:46715150
|
C | A | 1 | a0001c0002t0012g0156 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-13+15701C>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46715150 | ||||||
chr2:46715371
|
C | CA | 25 | a0001c0001t0001g0161a0001c0001t0001g0203a0001c0001t0001g0212others(22): Show | 27 | HG00280.hp2 HG00733.hp2 HG01123.hp2 others(24): Show |
intron_variant | MODIFIER | c.-13+15936dupA | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46715371 | |||||
chr2:46715371
|
CA | C | 59 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0002g0329others(56): Show | 68 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.-13+15936delA | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46715371 | |||||
chr2:46715409
|
T | C | 1 | a0001c0002t0003g0124 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-13+15960T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46715409 | ||||||
chr2:46715494
|
T | G | 1 | a0001c0001t0018g0141 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-13+16045T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46715494 | ||||||
chr2:46715652
|
T | A | 6 | a0001c0001t0002g0005a0001c0001t0002g0268a0001c0001t0002g0294others(3): Show | 9 | NA18948.hp2 NA18950.hp1 NA18960.hp2 others(6): Show |
intron_variant | MODIFIER | c.-13+16203T>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46715652 | ||||||
chr2:46715830
|
T | A | 4 | a0001c0004t0011g0324a0001c0004t0011g0325a0001c0004t0011g0326others(1): Show | 4 | HG01070.hp2 HG01515.hp1 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.-13+16381T>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46715830 | ||||||
chr2:46715915
|
A | G | 1 | a0001c0002t0003g0079 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-13+16466A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46715915 | ||||||
chr2:46715984
|
C | T | 4 | a0001c0004t0011g0324a0001c0004t0011g0325a0001c0004t0011g0326others(1): Show | 4 | HG01070.hp2 HG01515.hp1 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.-13+16535C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46715984 | ||||||
chr2:46716052
|
T | C | 229 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0022others(226): Show | 254 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.-13+16603T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46716052 | ||||||
chr2:46716110
|
C | G | 13 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0259others(10): Show | 17 | HG01496.hp1 HG02027.hp1 HG02080.hp2 others(14): Show |
intron_variant | MODIFIER | c.-13+16661C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46716110 | ||||||
chr2:46716111
|
CT | C | 228 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0022others(225): Show | 253 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.-13+16676delT | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46716111 | |||||
chr2:46716147
|
C | T | 249 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0022others(246): Show | 276 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.-13+16698C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46716147 | ||||||
chr2:46716194
|
T | C | 1 | a0001c0001t0002g0261 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-13+16745T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46716194 | ||||||
chr2:46716303
|
G | T | 2 | a0001c0001t0001g0194a0001c0001t0001g0195 | 2 | HG03491.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.-13+16854G>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46716303 | ||||||
chr2:46716367
|
A | AT | 11 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0004g0147others(8): Show | 11 | HG00733.hp1 HG01109.hp1 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.-13+16947dupT | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46716367 | |||||
chr2:46716367
|
AT | A | 130 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0187others(127): Show | 155 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.-13+16947delT | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46716367 | |||||
chr2:46716367
|
ATT | A | 118 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0022others(115): Show | 129 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.-13+16946_-13+1694 others(6): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46716367 | |||||
chr2:46716367
|
ATTTTTTT others(7): Show |
A | 3 | a0001c0001t0001g0036a0001c0001t0004g0028a0001c0001t0019g0263 | 4 | HG02055.hp2 HG02809.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-13+16934_-13+1694 others(18): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46716367 | |||||
chr2:46716388
|
T | C | 11 | a0001c0001t0006g0050a0001c0001t0006g0052a0001c0001t0006g0053others(8): Show | 11 | HG02080.hp1 HG02135.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.-13+16939T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46716388 | ||||||
chr2:46716457
|
C | G | 1 | a0001c0002t0003g0094 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-13+17008C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46716457 | ||||||
chr2:46716549
|
C | T | 7 | a0001c0001t0004g0075a0001c0001t0004g0076a0001c0001t0004g0077others(4): Show | 7 | HG02572.hp1 HG02818.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.-13+17100C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46716549 | ||||||
chr2:46716637
|
C | G | 2 | a0001c0001t0001g0061a0001c0001t0001g0062 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-13+17188C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46716637 | ||||||
chr2:46716662
|
G | A | 3 | a0001c0003t0005g0013a0001c0003t0005g0085a0001c0003t0005g0088 | 4 | HG01346.hp2 HG01515.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.-13+17213G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46716662 | ||||||
chr2:46716673
|
C | T | 19 | a0001c0001t0006g0008a0001c0001t0006g0009a0001c0001t0006g0044others(16): Show | 21 | HG00733.hp2 HG01123.hp2 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.-13+17224C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46716673 | ||||||
chr2:46716733
|
C | G | 2 | a0001c0001t0001g0185a0001c0001t0001g0186 | 2 | NA19010.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.-13+17284C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46716733 | ||||||
chr2:46716815
|
A | G | 7 | a0001c0001t0001g0026a0001c0001t0001g0166a0001c0001t0001g0184others(4): Show | 8 | HG00438.hp1 HG00642.hp2 HG01975.hp2 others(5): Show |
intron_variant | MODIFIER | c.-13+17366A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46716815 | ||||||
chr2:46716928
|
A | G | 19 | a0001c0001t0006g0008a0001c0001t0006g0009a0001c0001t0006g0044others(16): Show | 21 | HG00733.hp2 HG01123.hp2 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.-13+17479A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46716928 | ||||||
chr2:46717003
|
G | A | 1 | a0001c0001t0006g0057 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-13+17554G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46717003 | ||||||
chr2:46717041
|
T | G | 233 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0022others(230): Show | 258 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.-13+17592T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46717041 | ||||||
chr2:46717126
|
A | G | 252 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0022others(249): Show | 279 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.-13+17677A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46717126 | ||||||
chr2:46717252
|
A | C | 2 | a0001c0001t0001g0205a0001c0001t0001g0243 | 2 | NA18964.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.-13+17803A>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46717252 | ||||||
chr2:46717368
|
G | A | 1 | a0001c0001t0005g0167 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-13+17919G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46717368 | ||||||
chr2:46717414
|
G | C | 230 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0022others(227): Show | 255 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.-13+17965G>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46717414 | ||||||
chr2:46717525
|
G | A | 1 | a0001c0001t0002g0267 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-13+18076G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46717525 | ||||||
chr2:46717558
|
A | G | 1 | a0001c0001t0001g0232 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-13+18109A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46717558 | ||||||
chr2:46717692
|
T | C | 1 | a0001c0004t0011g0326 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-13+18243T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46717692 | ||||||
chr2:46717760
|
G | A | 1 | a0001c0003t0005g0087 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-13+18311G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46717760 | ||||||
chr2:46717778
|
A | G | 1 | a0001c0003t0005g0042 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-13+18329A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46717778 | ||||||
chr2:46717797
|
G | C | 4 | a0001c0001t0001g0171a0001c0001t0001g0201a0001c0001t0001g0204others(1): Show | 4 | NA18944.hp2 NA18949.hp2 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.-13+18348G>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46717797 | ||||||
chr2:46717888
|
A | T | 1 | a0001c0004t0011g0324 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-13+18439A>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46717888 | ||||||
chr2:46717903
|
A | C | 1 | a0001c0001t0001g0183 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-13+18454A>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46717903 | ||||||
chr2:46717970
|
T | C | 3 | a0001c0001t0004g0037a0001c0001t0004g0038a0001c0001t0004g0039 | 3 | HG03195.hp2 NA18522.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-13+18521T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46717970 | ||||||
chr2:46718022
|
G | C | 11 | a0001c0001t0006g0050a0001c0001t0006g0052a0001c0001t0006g0053others(8): Show | 11 | HG02080.hp1 HG02135.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.-13+18573G>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46718022 | ||||||
chr2:46718095
|
TTG | T | 328 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0022others(325): Show | 370 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(367): Show |
intron_variant | MODIFIER | c.-13+18668_-13+1866 others(6): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46718095 | |||||
chr2:46718214
|
A | G | 1 | a0001c0006t0002g0291 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-13+18765A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46718214 | ||||||
chr2:46718256
|
G | A | 2 | a0001c0001t0002g0317a0001c0001t0002g0318 | 2 | HG00408.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.-13+18807G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46718256 | ||||||
chr2:46718349
|
T | C | 1 | a0001c0001t0001g0194 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-13+18900T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46718349 | ||||||
chr2:46718460
|
T | A | 1 | a0001c0004t0011g0325 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-13+19011T>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46718460 | ||||||
chr2:46718511
|
A | G | 1 | a0001c0001t0009g0003 | 4 | NA18953.hp2 NA18956.hp2 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13+19062A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46718511 | ||||||
chr2:46718754
|
G | A | 4 | a0001c0004t0011g0324a0001c0004t0011g0325a0001c0004t0011g0326others(1): Show | 4 | HG01070.hp2 HG01515.hp1 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.-13+19305G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46718754 | ||||||
chr2:46718815
|
G | T | 4 | a0001c0004t0011g0324a0001c0004t0011g0325a0001c0004t0011g0326others(1): Show | 4 | HG01070.hp2 HG01515.hp1 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.-13+19366G>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46718815 | ||||||
chr2:46718884
|
G | A | 6 | a0001c0001t0002g0005a0001c0001t0002g0268a0001c0001t0002g0294others(3): Show | 9 | NA18948.hp2 NA18950.hp1 NA18960.hp2 others(6): Show |
intron_variant | MODIFIER | c.-13+19435G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46718884 | ||||||
chr2:46718887
|
A | G | 1 | a0001c0001t0004g0083 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-13+19438A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46718887 | ||||||
chr2:46718992
|
A | G | 4 | a0001c0001t0004g0078a0001c0001t0004g0148a0001c0001t0014g0150others(1): Show | 4 | HG02572.hp1 HG02970.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13+19543A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46718992 | ||||||
chr2:46719050
|
A | G | 1 | a0001c0002t0012g0156 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-13+19601A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46719050 | ||||||
chr2:46719140
|
A | G | 2 | a0001c0002t0003g0099a0001c0002t0003g0131 | 2 | HG00639.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.-13+19691A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46719140 | ||||||
chr2:46719204
|
A | G | 1 | a0001c0001t0001g0223 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.-13+19755A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46719204 | ||||||
chr2:46719246
|
T | C | 1 | a0001c0001t0001g0183 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-13+19797T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46719246 | ||||||
chr2:46719385
|
A | G | 1 | a0001c0001t0001g0237 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-13+19936A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46719385 | ||||||
chr2:46719416
|
G | A | 4 | a0001c0004t0011g0324a0001c0004t0011g0325a0001c0004t0011g0326others(1): Show | 4 | HG01070.hp2 HG01515.hp1 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.-13+19967G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46719416 | ||||||
chr2:46719535
|
T | G | 1 | a0001c0001t0002g0271 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-13+20086T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46719535 | ||||||
chr2:46719652
|
C | G | 2 | a0001c0001t0008g0019a0001c0001t0008g0155 | 3 | HG01109.hp2 HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-13+20203C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46719652 | ||||||
chr2:46719694
|
G | A | 2 | a0001c0001t0008g0080a0001c0005t0008g0081 | 2 | HG02451.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-13+20245G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46719694 | ||||||
chr2:46719802
|
T | A | 5 | a0001c0001t0008g0019a0001c0001t0008g0080a0001c0001t0008g0154others(2): Show | 6 | HG01109.hp2 HG02451.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.-13+20353T>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46719802 | ||||||
chr2:46719870
|
C | T | 2 | a0001c0001t0007g0072a0001c0001t0007g0073 | 2 | HG01243.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.-13+20421C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46719870 | ||||||
chr2:46719980
|
A | G | 1 | a0001c0001t0004g0147 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-13+20531A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46719980 | ||||||
chr2:46720065
|
T | G | 5 | a0001c0002t0003g0104a0001c0002t0003g0105a0001c0002t0003g0106others(2): Show | 5 | HG02109.hp2 HG02630.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-13+20616T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46720065 | ||||||
chr2:46720277
|
G | T | 7 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0002t0003g0104others(4): Show | 7 | HG01256.hp1 HG01258.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.-13+20828G>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46720277 | ||||||
chr2:46720291
|
G | A | 1 | a0001c0003t0005g0084 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-13+20842G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46720291 | ||||||
chr2:46720301
|
G | A | 19 | a0001c0003t0005g0011a0001c0003t0005g0013a0001c0003t0005g0027others(16): Show | 21 | HG00733.hp1 HG01069.hp2 HG01074.hp2 others(18): Show |
intron_variant | MODIFIER | c.-13+20852G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46720301 | ||||||
chr2:46720537
|
T | C | 20 | a0001c0001t0006g0008a0001c0001t0006g0009a0001c0001t0006g0044others(17): Show | 22 | HG00280.hp2 HG00733.hp2 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.-13+21088T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46720537 | ||||||
chr2:46720607
|
A | C | 1 | a0001c0008t0016g0145 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-13+21158A>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46720607 | ||||||
chr2:46720662
|
T | C | 1 | a0001c0001t0009g0003 | 4 | NA18953.hp2 NA18956.hp2 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13+21213T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46720662 | ||||||
chr2:46720896
|
C | T | 13 | a0001c0001t0007g0010a0001c0001t0007g0063a0001c0001t0007g0064others(10): Show | 14 | HG00741.hp1 HG01081.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.-13+21447C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46720896 | ||||||
chr2:46720936
|
C | T | 19 | a0001c0001t0006g0008a0001c0001t0006g0009a0001c0001t0006g0044others(16): Show | 21 | HG00733.hp2 HG01123.hp2 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.-13+21487C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46720936 | ||||||
chr2:46721011
|
C | G | 59 | a0001c0002t0003g0001a0001c0002t0003g0014a0001c0002t0003g0015others(56): Show | 69 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.-13+21562C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46721011 | ||||||
chr2:46721036
|
T | C | 195 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0022others(192): Show | 218 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.-13+21587T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46721036 | ||||||
chr2:46721067
|
C | T | 1 | a0001c0001t0004g0142 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-13+21618C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46721067 | ||||||
chr2:46721175
|
A | G | 3 | a0001c0001t0002g0282a0001c0001t0002g0283a0001c0001t0002g0285 | 3 | HG00639.hp2 HG00642.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.-13+21726A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46721175 | ||||||
chr2:46721306
|
C | CT | 1 | a0001c0001t0009g0003 | 4 | NA18953.hp2 NA18956.hp2 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13+21858dupT | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46721306 | |||||
chr2:46721461
|
A | C | 1 | a0001c0001t0002g0304 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-13+22012A>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46721461 | ||||||
chr2:46721520
|
A | G | 1 | a0001c0003t0005g0149 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-13+22071A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46721520 | ||||||
chr2:46721563
|
C | G | 9 | a0001c0001t0006g0008a0001c0001t0006g0009a0001c0001t0006g0044others(6): Show | 11 | HG00280.hp2 HG00733.hp2 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.-13+22114C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46721563 | ||||||
chr2:46721595
|
C | A | 1 | a0001c0001t0006g0046 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-13+22146C>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46721595 | ||||||
chr2:46721627
|
G | C | 1 | a0001c0001t0006g0046 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-13+22178G>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46721627 | ||||||
chr2:46721698
|
T | C | 2 | a0001c0001t0001g0061a0001c0001t0001g0062 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-13+22249T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46721698 | ||||||
chr2:46721714
|
G | C | 1 | a0001c0003t0005g0011 | 2 | NA18943.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.-13+22265G>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46721714 | ||||||
chr2:46721722
|
G | C | 1 | a0001c0003t0005g0041 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-13+22273G>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46721722 | ||||||
chr2:46721877
|
A | G | 1 | a0001c0002t0003g0140 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-13+22428A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46721877 | ||||||
chr2:46721882
|
G | A | 1 | a0001c0003t0005g0149 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-13+22433G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46721882 | ||||||
chr2:46721883
|
C | T | 1 | a0001c0001t0001g0242 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-13+22434C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46721883 | ||||||
chr2:46722198
|
A | G | 252 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0022others(249): Show | 282 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.-13+22749A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46722198 | ||||||
chr2:46722263
|
C | A | 1 | a0001c0008t0016g0145 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-13+22814C>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46722263 | ||||||
chr2:46722301
|
A | C | 2 | a0001c0001t0001g0061a0001c0001t0001g0062 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-13+22852A>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46722301 | ||||||
chr2:46722310
|
G | C | 1 | a0001c0001t0001g0213 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-13+22861G>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46722310 | ||||||
chr2:46722333
|
GA | G | 225 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0022others(222): Show | 249 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.-13+22891delA | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46722333 | |||||
chr2:46722545
|
A | G | 110 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0022others(107): Show | 120 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.-13+23096A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46722545 | ||||||
chr2:46722605
|
A | C | 1 | a0001c0002t0003g0130 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-13+23156A>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46722605 | ||||||
chr2:46722877
|
T | C | 1 | a0001c0001t0001g0224 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-13+23428T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46722877 | ||||||
chr2:46722980
|
T | G | 1 | a0001c0003t0005g0093 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-13+23531T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46722980 | ||||||
chr2:46723087
|
T | A | 1 | a0001c0008t0016g0145 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-13+23638T>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46723087 | ||||||
chr2:46723282
|
G | T | 256 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0022others(253): Show | 286 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.-13+23833G>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46723282 | ||||||
chr2:46723444
|
T | C | 21 | a0001c0002t0010g0012a0001c0002t0010g0086a0001c0002t0010g0090others(18): Show | 24 | HG00733.hp1 HG01069.hp2 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.-13+23995T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46723444 | ||||||
chr2:46723530
|
T | A | 2 | a0001c0001t0001g0061a0001c0001t0001g0062 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-13+24081T>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46723530 | ||||||
chr2:46723573
|
T | C | 7 | a0001c0001t0004g0082a0001c0001t0004g0083a0001c0001t0008g0019others(4): Show | 8 | HG01109.hp2 HG02451.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.-13+24124T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46723573 | ||||||
chr2:46723630
|
C | T | 227 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0022others(224): Show | 252 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.-13+24181C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46723630 | ||||||
chr2:46723819
|
G | T | 1 | a0001c0001t0001g0158 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-13+24370G>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46723819 | ||||||
chr2:46723973
|
T | C | 5 | a0001c0002t0003g0104a0001c0002t0003g0105a0001c0002t0003g0106others(2): Show | 5 | HG02109.hp2 HG02630.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-13+24524T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46723973 | ||||||
chr2:46724050
|
A | C | 1 | a0001c0001t0009g0003 | 4 | NA18953.hp2 NA18956.hp2 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13+24601A>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46724050 | ||||||
chr2:46724105
|
C | T | 1 | a0001c0001t0001g0191 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-13+24656C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46724105 | ||||||
chr2:46724335
|
C | G | 1 | a0001c0001t0009g0003 | 4 | NA18953.hp2 NA18956.hp2 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13+24886C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46724335 | ||||||
chr2:46724388
|
C | T | 2 | a0001c0001t0001g0061a0001c0001t0001g0062 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-13+24939C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46724388 | ||||||
chr2:46724451
|
T | G | 1 | a0001c0002t0003g0111 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-13+25002T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46724451 | ||||||
chr2:46724467
|
T | G | 1 | a0001c0001t0007g0074 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-13+25018T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46724467 | ||||||
chr2:46724627
|
C | T | 7 | a0001c0001t0004g0136a0001c0001t0004g0142a0001c0001t0004g0143others(4): Show | 7 | HG01109.hp1 HG02145.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.-13+25178C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46724627 | ||||||
chr2:46724664
|
G | A | 16 | a0001c0001t0006g0050a0001c0001t0006g0052a0001c0001t0006g0053others(13): Show | 19 | HG01070.hp2 HG01515.hp1 HG02080.hp1 others(16): Show |
intron_variant | MODIFIER | c.-13+25215G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46724664 | ||||||
chr2:46724724
|
A | G | 1 | a0001c0008t0016g0145 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-13+25275A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46724724 | ||||||
chr2:46724774
|
G | A | 1 | a0001c0001t0002g0272 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-13+25325G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46724774 | ||||||
chr2:46724960
|
T | C | 2 | a0001c0001t0004g0028a0001c0001t0019g0263 | 3 | HG02055.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-13+25511T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46724960 | ||||||
chr2:46724977
|
G | A | 18 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0006g0050others(15): Show | 21 | HG01070.hp2 HG01256.hp1 HG01258.hp1 others(18): Show |
intron_variant | MODIFIER | c.-13+25528G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46724977 | ||||||
chr2:46724999
|
C | G | 2 | a0001c0001t0001g0061a0001c0001t0001g0062 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-13+25550C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46724999 | ||||||
chr2:46725039
|
A | T | 7 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0009g0003others(4): Show | 10 | HG01070.hp2 HG01256.hp1 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.-13+25590A>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46725039 | ||||||
chr2:46725295
|
C | G | 1 | a0001c0001t0007g0040 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-13+25846C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46725295 | ||||||
chr2:46725307
|
A | G | 20 | a0001c0001t0006g0008a0001c0001t0006g0009a0001c0001t0006g0044others(17): Show | 22 | HG00280.hp2 HG00733.hp2 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.-13+25858A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46725307 | ||||||
chr2:46725330
|
T | C | 1 | a0001c0001t0009g0003 | 4 | NA18953.hp2 NA18956.hp2 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13+25881T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46725330 | ||||||
chr2:46725619
|
T | C | 16 | a0001c0001t0001g0162a0001c0001t0001g0173a0001c0001t0007g0010others(13): Show | 17 | HG00741.hp1 HG01081.hp2 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.-13+26170T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46725619 | ||||||
chr2:46725648
|
C | A | 1 | a0001c0001t0008g0155 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-13+26199C>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46725648 | ||||||
chr2:46725715
|
T | G | 1 | a0001c0001t0001g0161 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-13+26266T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46725715 | ||||||
chr2:46726095
|
T | G | 1 | a0001c0001t0001g0215 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-13+26646T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46726095 | ||||||
chr2:46726128
|
G | A | 1 | a0001c0003t0005g0097 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-13+26679G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46726128 | ||||||
chr2:46726266
|
T | G | 1 | a0001c0001t0002g0313 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-13+26817T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46726266 | ||||||
chr2:46726313
|
A | C | 20 | a0001c0001t0006g0008a0001c0001t0006g0009a0001c0001t0006g0044others(17): Show | 22 | HG00280.hp2 HG00733.hp2 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.-13+26864A>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46726313 | ||||||
chr2:46726326
|
A | G | 248 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0022others(245): Show | 278 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.-13+26877A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46726326 | ||||||
chr2:46726343
|
G | C | 26 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0006g0008others(23): Show | 31 | HG00733.hp2 HG01070.hp2 HG01123.hp2 others(28): Show |
intron_variant | MODIFIER | c.-13+26894G>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46726343 | ||||||
chr2:46726366
|
A | G | 30 | a0001c0001t0001g0036a0001c0001t0001g0061a0001c0001t0001g0062others(27): Show | 36 | HG00280.hp2 HG00733.hp2 HG01070.hp2 others(33): Show |
intron_variant | MODIFIER | c.-13+26917A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46726366 | ||||||
chr2:46726452
|
G | C | 1 | a0001c0001t0004g0076 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-13+27003G>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46726452 | ||||||
chr2:46726502
|
T | C | 2 | a0001c0001t0001g0061a0001c0001t0001g0062 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-13+27053T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46726502 | ||||||
chr2:46726544
|
G | A | 3 | a0001c0002t0003g0121a0001c0002t0003g0122a0001c0002t0012g0102 | 3 | NA18939.hp2 NA18993.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.-13+27095G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46726544 | ||||||
chr2:46726551
|
G | A | 4 | a0001c0004t0011g0324a0001c0004t0011g0325a0001c0004t0011g0326others(1): Show | 4 | HG01070.hp2 HG01515.hp1 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.-13+27102G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46726551 | ||||||
chr2:46726574
|
C | G | 2 | a0001c0001t0004g0028a0001c0001t0019g0263 | 3 | HG02055.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-13+27125C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46726574 | ||||||
chr2:46726624
|
C | T | 55 | a0001c0002t0003g0001a0001c0002t0003g0014a0001c0002t0003g0015others(52): Show | 64 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.-13+27175C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46726624 | ||||||
chr2:46726628
|
A | T | 9 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0004g0028others(6): Show | 13 | HG01070.hp2 HG01256.hp1 HG01258.hp1 others(10): Show |
intron_variant | MODIFIER | c.-13+27179A>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46726628 | ||||||
chr2:46726645
|
A | G | 2 | a0001c0001t0006g0050a0001c0001t0006g0060 | 2 | HG02717.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-13+27196A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46726645 | ||||||
chr2:46726720
|
CAGTATTT others(15): Show |
C | 1 | a0001c0002t0003g0139 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-13+27272_-13+2729 others(26): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46726720 | ||||||
chr2:46726734
|
T | G | 21 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0023others(18): Show | 26 | HG00621.hp2 HG02015.hp1 HG02273.hp2 others(23): Show |
intron_variant | MODIFIER | c.-13+27285T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46726734 | ||||||
chr2:46726738
|
A | AATT | 5 | a0001c0001t0002g0264a0001c0001t0002g0265a0001c0001t0002g0266others(2): Show | 5 | HG01516.hp2 HG02129.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-13+27320_-13+2732 others(7): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46726738 | |||||
chr2:46726738
|
A | AATTATTA others(5): Show |
1 | a0001c0001t0014g0151 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-13+27311_-13+2732 others(16): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46726738 | |||||
chr2:46726738
|
A | AATTATTA others(8): Show |
3 | a0001c0001t0004g0075a0001c0001t0004g0077a0001c0001t0004g0078 | 3 | HG02572.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-13+27308_-13+2732 others(19): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46726738 | |||||
chr2:46726738
|
AATT | A | 207 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0022others(204): Show | 231 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.-13+27320_-13+2732 others(7): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46726738 | |||||
chr2:46726738
|
AATTATT | A | 23 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0006g0008others(20): Show | 28 | HG00280.hp2 HG00733.hp2 HG01123.hp2 others(25): Show |
intron_variant | MODIFIER | c.-13+27317_-13+2732 others(10): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46726738 | |||||
chr2:46726811
|
C | A | 1 | a0001c0001t0001g0211 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-13+27362C>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46726811 | ||||||
chr2:46726917
|
C | T | 5 | a0001c0001t0001g0213a0001c0001t0004g0190a0001c0001t0004g0198others(2): Show | 5 | HG00738.hp1 HG02071.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-13+27468C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46726917 | ||||||
chr2:46726948
|
G | T | 3 | a0001c0003t0005g0013a0001c0003t0005g0085a0001c0003t0005g0088 | 4 | HG01346.hp2 HG01515.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.-13+27499G>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46726948 | ||||||
chr2:46727144
|
C | CT | 9 | a0001c0001t0001g0062a0001c0001t0001g0199a0001c0001t0004g0146others(6): Show | 9 | HG00738.hp1 HG01258.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.-13+27717dupT | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46727144 | |||||
chr2:46727144
|
C | CTTTT | 8 | a0001c0001t0006g0009a0001c0001t0006g0044a0001c0001t0006g0045others(5): Show | 9 | HG00280.hp2 HG01123.hp2 HG01167.hp2 others(6): Show |
intron_variant | MODIFIER | c.-13+27714_-13+2771 others(8): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46727144 | |||||
chr2:46727144
|
C | CTTTTTT | 9 | a0001c0001t0006g0053a0001c0001t0006g0054a0001c0001t0006g0055others(6): Show | 9 | HG02080.hp1 HG02615.hp2 HG03209.hp2 others(6): Show |
intron_variant | MODIFIER | c.-13+27712_-13+2771 others(10): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46727144 | |||||
chr2:46727144
|
CT | C | 162 | a0001c0001t0001g0172a0001c0001t0001g0203a0001c0001t0001g0235others(159): Show | 190 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(187): Show |
intron_variant | MODIFIER | c.-13+27717delT | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46727144 | |||||
chr2:46727144
|
CTT | C | 23 | a0001c0001t0002g0265a0001c0001t0002g0273a0001c0001t0002g0274others(20): Show | 24 | HG00323.hp2 HG01109.hp2 HG01516.hp2 others(21): Show |
intron_variant | MODIFIER | c.-13+27716_-13+2771 others(6): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46727144 | |||||
chr2:46727218
|
A | G | 27 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0006g0008others(24): Show | 32 | HG00280.hp2 HG00733.hp2 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.-13+27769A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46727218 | ||||||
chr2:46727235
|
G | A | 1 | a0001c0001t0009g0003 | 4 | NA18953.hp2 NA18956.hp2 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13+27786G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46727235 | ||||||
chr2:46727250
|
G | A | 1 | a0001c0001t0001g0218 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-13+27801G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46727250 | ||||||
chr2:46727263
|
C | T | 1 | a0001c0003t0005g0089 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-13+27814C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46727263 | ||||||
chr2:46727270
|
T | A | 5 | a0001c0002t0003g0104a0001c0002t0003g0105a0001c0002t0003g0106others(2): Show | 5 | HG02109.hp2 HG02630.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-13+27821T>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46727270 | ||||||
chr2:46727273
|
C | T | 2 | a0001c0001t0002g0292a0001c0001t0002g0301 | 2 | NA18980.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.-13+27824C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46727273 | ||||||
chr2:46727690
|
C | G | 1 | a0001c0004t0013g0189 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-13+28241C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46727690 | ||||||
chr2:46727743
|
G | A | 6 | a0001c0001t0002g0029a0001c0001t0002g0273a0001c0001t0002g0275others(3): Show | 7 | HG02027.hp2 HG02155.hp2 NA18955.hp1 others(4): Show |
intron_variant | MODIFIER | c.-13+28294G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46727743 | ||||||
chr2:46727823
|
C | G | 1 | a0001c0001t0009g0003 | 4 | NA18953.hp2 NA18956.hp2 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13+28374C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46727823 | ||||||
chr2:46727894
|
G | A | 1 | a0001c0001t0005g0167 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-13+28445G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46727894 | ||||||
chr2:46727924
|
T | C | 1 | a0001c0002t0003g0112 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-13+28475T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46727924 | ||||||
chr2:46727949
|
TTGA | T | 107 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0022others(104): Show | 117 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.-13+28503_-13+2850 others(7): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46727949 | |||||
chr2:46728035
|
C | T | 2 | a0001c0001t0001g0177a0001c0001t0001g0187 | 2 | NA18962.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.-13+28586C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46728035 | ||||||
chr2:46728041
|
G | T | 11 | a0001c0001t0006g0050a0001c0001t0006g0052a0001c0001t0006g0053others(8): Show | 11 | HG02080.hp1 HG02135.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.-13+28592G>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46728041 | ||||||
chr2:46728046
|
T | C | 255 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0022others(252): Show | 285 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.-13+28597T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46728046 | ||||||
chr2:46728218
|
A | T | 5 | a0001c0001t0001g0168a0001c0001t0001g0172a0001c0001t0001g0209others(2): Show | 5 | HG00140.hp2 HG01099.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.-13+28769A>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46728218 | ||||||
chr2:46728240
|
C | T | 102 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0022others(99): Show | 112 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.-13+28791C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46728240 | ||||||
chr2:46728311
|
G | A | 1 | a0001c0002t0003g0157 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-13+28862G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46728311 | ||||||
chr2:46728404
|
C | T | 1 | a0001c0001t0009g0003 | 4 | NA18953.hp2 NA18956.hp2 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13+28955C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46728404 | ||||||
chr2:46728460
|
G | T | 19 | a0001c0003t0005g0011a0001c0003t0005g0013a0001c0003t0005g0027others(16): Show | 21 | HG00733.hp1 HG01069.hp2 HG01074.hp2 others(18): Show |
intron_variant | MODIFIER | c.-13+29011G>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46728460 | ||||||
chr2:46728495
|
T | G | 1 | a0001c0001t0020g0051 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-13+29046T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46728495 | ||||||
chr2:46728634
|
C | T | 1 | a0001c0002t0003g0111 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-13+29185C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46728634 | ||||||
chr2:46728716
|
C | T | 8 | a0001c0001t0004g0136a0001c0001t0004g0142a0001c0001t0004g0143others(5): Show | 8 | HG01109.hp1 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.-13+29267C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46728716 | ||||||
chr2:46728752
|
C | T | 3 | a0001c0001t0004g0136a0001c0001t0004g0144a0001c0001t0004g0147 | 3 | HG02145.hp1 HG02886.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-13+29303C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46728752 | ||||||
chr2:46728800
|
G | A | 109 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0022others(106): Show | 120 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.-13+29351G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46728800 | ||||||
chr2:46728808
|
T | C | 247 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0022others(244): Show | 277 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.-13+29359T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46728808 | ||||||
chr2:46728818
|
A | C | 4 | a0001c0004t0011g0324a0001c0004t0011g0325a0001c0004t0011g0326others(1): Show | 4 | HG01070.hp2 HG01515.hp1 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.-13+29369A>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46728818 | ||||||
chr2:46728896
|
C | G | 1 | a0001c0001t0002g0313 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-13+29447C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46728896 | ||||||
chr2:46728901
|
A | T | 27 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0006g0008others(24): Show | 32 | HG00280.hp2 HG00733.hp2 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.-13+29452A>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46728901 | ||||||
chr2:46728962
|
G | C | 1 | a0001c0001t0004g0082 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-13+29513G>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46728962 | ||||||
chr2:46729154
|
G | A | 7 | a0001c0001t0004g0075a0001c0001t0004g0077a0001c0001t0004g0078others(4): Show | 7 | HG02572.hp1 HG02896.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.-12-29365G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46729154 | ||||||
chr2:46729230
|
T | C | 9 | a0001c0001t0004g0136a0001c0001t0004g0142a0001c0001t0004g0143others(6): Show | 9 | HG01109.hp1 HG02145.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.-12-29289T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46729230 | ||||||
chr2:46729301
|
T | G | 1 | a0001c0002t0003g0133 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-12-29218T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46729301 | ||||||
chr2:46729340
|
A | AT | 27 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0006g0008others(24): Show | 32 | HG00280.hp2 HG00733.hp2 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.-12-29179_-12-2917 others(5): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46729340 | ||||||
chr2:46729370
|
A | C | 1 | a0001c0008t0016g0145 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-12-29149A>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46729370 | ||||||
chr2:46729438
|
A | G | 1 | a0001c0001t0007g0065 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-12-29081A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46729438 | ||||||
chr2:46729479
|
C | T | 2 | a0001c0001t0004g0028a0001c0001t0019g0263 | 3 | HG02055.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-12-29040C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46729479 | ||||||
chr2:46729480
|
G | A | 1 | a0001c0001t0001g0216 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-12-29039G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46729480 | ||||||
chr2:46729621
|
C | T | 1 | a0001c0001t0007g0071 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-12-28898C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46729621 | ||||||
chr2:46729650
|
C | T | 8 | a0001c0001t0004g0136a0001c0001t0004g0142a0001c0001t0004g0143others(5): Show | 8 | HG01109.hp1 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.-12-28869C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46729650 | ||||||
chr2:46729655
|
A | G | 2 | a0001c0001t0002g0032a0001c0001t0002g0281 | 3 | HG02572.hp2 HG02622.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-12-28864A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46729655 | ||||||
chr2:46729671
|
G | C | 246 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0022others(243): Show | 276 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.-12-28848G>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46729671 | ||||||
chr2:46729874
|
A | T | 1 | a0001c0008t0016g0145 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-12-28645A>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46729874 | ||||||
chr2:46729881
|
C | G | 1 | a0001c0008t0016g0145 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-12-28638C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46729881 | ||||||
chr2:46730070
|
C | G | 8 | a0001c0001t0006g0008a0001c0001t0006g0009a0001c0001t0006g0044others(5): Show | 10 | HG00733.hp2 HG01123.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.-12-28449C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46730070 | ||||||
chr2:46730077
|
A | G | 1 | a0001c0001t0009g0003 | 4 | NA18953.hp2 NA18956.hp2 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.-12-28442A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46730077 | ||||||
chr2:46730116
|
T | C | 1 | a0001c0001t0009g0003 | 4 | NA18953.hp2 NA18956.hp2 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.-12-28403T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46730116 | ||||||
chr2:46730339
|
G | A | 2 | a0001c0001t0001g0061a0001c0001t0001g0062 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-12-28180G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46730339 | ||||||
chr2:46730376
|
G | A | 19 | a0001c0003t0005g0011a0001c0003t0005g0013a0001c0003t0005g0027others(16): Show | 21 | HG00733.hp1 HG01069.hp2 HG01074.hp2 others(18): Show |
intron_variant | MODIFIER | c.-12-28143G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46730376 | ||||||
chr2:46730509
|
C | T | 1 | a0001c0003t0005g0097 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-12-28010C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46730509 | ||||||
chr2:46730512
|
A | G | 2 | a0001c0001t0004g0143a0001c0001t0018g0141 | 2 | HG02615.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-12-28007A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46730512 | ||||||
chr2:46730567
|
T | C | 1 | a0001c0001t0002g0276 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-12-27952T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46730567 | ||||||
chr2:46730580
|
A | G | 13 | a0001c0001t0007g0010a0001c0001t0007g0063a0001c0001t0007g0064others(10): Show | 14 | HG00741.hp1 HG01081.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.-12-27939A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46730580 | ||||||
chr2:46730609
|
G | A | 18 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0006g0050others(15): Show | 21 | HG01070.hp2 HG01256.hp1 HG01258.hp1 others(18): Show |
intron_variant | MODIFIER | c.-12-27910G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46730609 | ||||||
chr2:46730642
|
C | G | 1 | a0001c0003t0005g0042 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-12-27877C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46730642 | ||||||
chr2:46730648
|
A | G | 4 | a0001c0004t0011g0324a0001c0004t0011g0325a0001c0004t0011g0326others(1): Show | 4 | HG01070.hp2 HG01515.hp1 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.-12-27871A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46730648 | ||||||
chr2:46730706
|
A | G | 56 | a0001c0001t0012g0126a0001c0002t0003g0001a0001c0002t0003g0014others(53): Show | 66 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.-12-27813A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46730706 | ||||||
chr2:46730762
|
A | G | 1 | a0001c0001t0001g0213 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-12-27757A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46730762 | ||||||
chr2:46730915
|
A | G | 1 | a0001c0001t0001g0212 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-12-27604A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46730915 | ||||||
chr2:46730960
|
C | T | 1 | a0001c0001t0004g0083 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-12-27559C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46730960 | ||||||
chr2:46730974
|
C | G | 1 | a0001c0001t0009g0003 | 4 | NA18953.hp2 NA18956.hp2 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.-12-27545C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46730974 | ||||||
chr2:46731019
|
A | G | 1 | a0001c0001t0002g0299 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-12-27500A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46731019 | ||||||
chr2:46731046
|
G | T | 2 | a0001c0001t0001g0061a0001c0001t0001g0062 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-12-27473G>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46731046 | ||||||
chr2:46731055
|
T | G | 2 | a0001c0001t0001g0061a0001c0001t0001g0062 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-12-27464T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46731055 | ||||||
chr2:46731143
|
T | G | 1 | a0001c0001t0001g0036 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-12-27376T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46731143 | ||||||
chr2:46731212
|
G | T | 3 | a0001c0002t0003g0111a0001c0002t0003g0119a0001c0002t0003g0125 | 3 | HG03540.hp1 HG03704.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-12-27307G>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46731212 | ||||||
chr2:46731229
|
G | T | 5 | a0001c0001t0001g0022a0001c0001t0001g0207a0001c0001t0001g0218others(2): Show | 6 | NA18939.hp1 NA18953.hp1 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12-27290G>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46731229 | ||||||
chr2:46731253
|
C | T | 1 | a0001c0008t0016g0145 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-12-27266C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46731253 | ||||||
chr2:46731271
|
T | A | 1 | a0001c0001t0007g0069 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-12-27248T>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46731271 | ||||||
chr2:46731356
|
A | G | 1 | a0001c0002t0003g0129 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-12-27163A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46731356 | ||||||
chr2:46731523
|
A | G | 1 | a0001c0001t0019g0263 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-12-26996A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46731523 | ||||||
chr2:46731776
|
T | TA | 1 | a0001c0001t0009g0003 | 4 | NA18953.hp2 NA18956.hp2 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.-12-26741dupA | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46731776 | |||||
chr2:46732070
|
G | A | 2 | a0001c0001t0001g0061a0001c0001t0001g0062 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-12-26449G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46732070 | ||||||
chr2:46732114
|
T | G | 1 | a0001c0001t0002g0277 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-12-26405T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46732114 | ||||||
chr2:46732151
|
G | T | 7 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0009g0003others(4): Show | 10 | HG01070.hp2 HG01256.hp1 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.-12-26368G>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46732151 | ||||||
chr2:46732201
|
T | C | 1 | a0001c0001t0002g0310 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-12-26318T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46732201 | ||||||
chr2:46732212
|
A | G | 1 | a0001c0001t0004g0083 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-12-26307A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46732212 | ||||||
chr2:46732221
|
A | G | 1 | a0001c0001t0002g0281 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-12-26298A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46732221 | ||||||
chr2:46732268
|
C | T | 1 | a0001c0001t0002g0283 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-12-26251C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46732268 | ||||||
chr2:46732274
|
A | T | 1 | a0001c0001t0001g0182 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-12-26245A>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46732274 | ||||||
chr2:46732492
|
G | A | 19 | a0001c0001t0006g0008a0001c0001t0006g0009a0001c0001t0006g0044others(16): Show | 21 | HG00733.hp2 HG01123.hp2 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.-12-26027G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46732492 | ||||||
chr2:46732531
|
G | A | 1 | a0001c0001t0018g0141 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-12-25988G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46732531 | ||||||
chr2:46732588
|
C | G | 5 | a0001c0001t0008g0019a0001c0001t0008g0080a0001c0001t0008g0154others(2): Show | 6 | HG01109.hp2 HG02451.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12-25931C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46732588 | ||||||
chr2:46732623
|
C | G | 2 | a0001c0001t0002g0328a0001c0001t0002g0329 | 2 | NA18960.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.-12-25896C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46732623 | ||||||
chr2:46732865
|
G | A | 56 | a0001c0002t0003g0001a0001c0002t0003g0014a0001c0002t0003g0015others(53): Show | 65 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.-12-25654G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46732865 | ||||||
chr2:46732920
|
C | T | 7 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0009g0003others(4): Show | 10 | HG01070.hp2 HG01256.hp1 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.-12-25599C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46732920 | ||||||
chr2:46732940
|
A | C | 1 | a0001c0001t0009g0003 | 4 | NA18953.hp2 NA18956.hp2 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.-12-25579A>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46732940 | ||||||
chr2:46732962
|
T | A | 17 | a0001c0002t0010g0012a0001c0002t0010g0086a0001c0002t0010g0090others(14): Show | 20 | HG01069.hp2 HG01074.hp2 HG01346.hp2 others(17): Show |
intron_variant | MODIFIER | c.-12-25557T>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46732962 | ||||||
chr2:46732973
|
C | G | 1 | a0001c0001t0001g0237 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-12-25546C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46732973 | ||||||
chr2:46732978
|
G | T | 1 | a0001c0001t0006g0056 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-12-25541G>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46732978 | ||||||
chr2:46733037
|
C | T | 1 | a0001c0001t0007g0068 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-12-25482C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46733037 | ||||||
chr2:46733158
|
G | A | 18 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0006g0050others(15): Show | 21 | HG01070.hp2 HG01256.hp1 HG01258.hp1 others(18): Show |
intron_variant | MODIFIER | c.-12-25361G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46733158 | ||||||
chr2:46733180
|
C | T | 1 | a0001c0001t0009g0003 | 4 | NA18953.hp2 NA18956.hp2 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.-12-25339C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46733180 | ||||||
chr2:46733190
|
G | T | 70 | a0001c0001t0007g0010a0001c0001t0007g0063a0001c0001t0007g0064others(67): Show | 80 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.-12-25329G>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46733190 | ||||||
chr2:46733199
|
A | T | 11 | a0001c0001t0006g0050a0001c0001t0006g0052a0001c0001t0006g0053others(8): Show | 11 | HG02080.hp1 HG02135.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.-12-25320A>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46733199 | ||||||
chr2:46733276
|
G | A | 1 | a0001c0001t0002g0034 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.-12-25243G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46733276 | ||||||
chr2:46733419
|
G | T | 1 | a0001c0008t0016g0145 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-12-25100G>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46733419 | ||||||
chr2:46733483
|
G | A | 1 | a0001c0001t0006g0056 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-12-25036G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46733483 | ||||||
chr2:46733568
|
C | CA | 16 | a0001c0001t0004g0076a0001c0002t0010g0012a0001c0002t0010g0090others(13): Show | 19 | HG01069.hp2 HG01074.hp2 HG01346.hp2 others(16): Show |
intron_variant | MODIFIER | c.-12-24939dupA | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46733568 | |||||
chr2:46733568
|
CA | C | 16 | a0001c0001t0004g0136a0001c0001t0004g0142a0001c0001t0004g0143others(13): Show | 18 | HG00733.hp2 HG01109.hp1 HG01123.hp2 others(15): Show |
intron_variant | MODIFIER | c.-12-24939delA | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46733568 | |||||
chr2:46733577
|
AAAAG | A | 10 | a0001c0001t0006g0052a0001c0001t0006g0053a0001c0001t0006g0054others(7): Show | 13 | HG02080.hp1 HG02135.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.-12-24938_-12-2493 others(8): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46733577 | |||||
chr2:46733581
|
G | A | 5 | a0001c0002t0010g0086a0001c0003t0005g0041a0001c0004t0011g0325others(2): Show | 5 | HG01515.hp1 HG02132.hp1 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.-12-24938G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46733581 | ||||||
chr2:46733581
|
G | GA | 6 | a0001c0001t0001g0237a0001c0001t0002g0272a0001c0002t0003g0113others(3): Show | 6 | HG01975.hp1 HG02738.hp1 NA18993.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12-24923dupA | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46733581 | |||||
chr2:46733581
|
GA | G | 12 | a0001c0001t0002g0313a0001c0001t0004g0075a0001c0001t0004g0077others(9): Show | 13 | HG01074.hp1 HG01099.hp2 HG01256.hp2 others(10): Show |
intron_variant | MODIFIER | c.-12-24923delA | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46733581 | |||||
chr2:46733582
|
A | G | 2 | a0001c0002t0010g0086a0001c0003t0005g0041 | 2 | HG02698.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.-12-24937A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46733582 | ||||||
chr2:46733647
|
G | A | 1 | a0001c0001t0008g0080 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-12-24872G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46733647 | ||||||
chr2:46733650
|
A | T | 1 | a0001c0002t0003g0118 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-12-24869A>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46733650 | ||||||
chr2:46733688
|
A | T | 18 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0006g0050others(15): Show | 21 | HG01070.hp2 HG01256.hp1 HG01258.hp1 others(18): Show |
intron_variant | MODIFIER | c.-12-24831A>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46733688 | ||||||
chr2:46733857
|
G | A | 18 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0006g0050others(15): Show | 21 | HG01070.hp2 HG01256.hp1 HG01258.hp1 others(18): Show |
intron_variant | MODIFIER | c.-12-24662G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46733857 | ||||||
chr2:46733887
|
AAC | A | 3 | a0001c0001t0004g0037a0001c0001t0004g0038a0001c0001t0004g0039 | 3 | HG03195.hp2 NA18522.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-12-24630_-12-2462 others(6): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46733887 | |||||
chr2:46733891
|
T | G | 1 | a0001c0002t0015g0103 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-12-24628T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46733891 | ||||||
chr2:46733898
|
C | T | 8 | a0001c0001t0004g0136a0001c0001t0004g0142a0001c0001t0004g0143others(5): Show | 8 | HG01109.hp1 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.-12-24621C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46733898 | ||||||
chr2:46733921
|
A | C | 19 | a0001c0001t0006g0008a0001c0001t0006g0009a0001c0001t0006g0044others(16): Show | 21 | HG00733.hp2 HG01123.hp2 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.-12-24598A>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46733921 | ||||||
chr2:46733958
|
A | G | 1 | a0001c0002t0015g0103 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-12-24561A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46733958 | ||||||
chr2:46734176
|
A | G | 4 | a0001c0001t0006g0050a0001c0001t0006g0055a0001c0001t0006g0056others(1): Show | 4 | HG02717.hp1 NA18522.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.-12-24343A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46734176 | ||||||
chr2:46734217
|
T | A | 1 | a0001c0001t0009g0003 | 4 | NA18953.hp2 NA18956.hp2 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.-12-24302T>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46734217 | ||||||
chr2:46734228
|
T | A | 26 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0006g0008others(23): Show | 31 | HG00733.hp2 HG01070.hp2 HG01123.hp2 others(28): Show |
intron_variant | MODIFIER | c.-12-24291T>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46734228 | ||||||
chr2:46734243
|
A | G | 1 | a0001c0001t0002g0307 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-12-24276A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46734243 | ||||||
chr2:46734501
|
T | G | 3 | a0001c0001t0002g0286a0001c0001t0002g0297a0001c0001t0002g0304 | 3 | HG01496.hp1 HG02486.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.-12-24018T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46734501 | ||||||
chr2:46734559
|
A | G | 2 | a0001c0001t0007g0064a0001c0001t0007g0065 | 2 | HG01081.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-12-23960A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46734559 | ||||||
chr2:46734649
|
G | C | 6 | a0001c0001t0004g0075a0001c0001t0004g0077a0001c0001t0004g0078others(3): Show | 6 | HG02572.hp1 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12-23870G>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46734649 | ||||||
chr2:46734652
|
C | G | 1 | a0001c0001t0001g0171 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-12-23867C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46734652 | ||||||
chr2:46734653
|
C | G | 1 | a0001c0001t0004g0076 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-12-23866C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46734653 | ||||||
chr2:46734869
|
T | C | 1 | a0001c0002t0003g0139 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-12-23650T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46734869 | ||||||
chr2:46734871
|
T | C | 2 | a0001c0001t0001g0061a0001c0001t0001g0062 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-12-23648T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46734871 | ||||||
chr2:46734998
|
A | T | 2 | a0001c0001t0001g0061a0001c0001t0001g0062 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-12-23521A>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46734998 | ||||||
chr2:46735024
|
A | G | 1 | a0001c0003t0005g0041 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-12-23495A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46735024 | ||||||
chr2:46735184
|
G | C | 1 | a0001c0001t0001g0237 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-12-23335G>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46735184 | ||||||
chr2:46735240
|
G | A | 1 | a0001c0001t0001g0237 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-12-23279G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46735240 | ||||||
chr2:46735600
|
A | T | 246 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0022others(243): Show | 276 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.-12-22919A>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46735600 | ||||||
chr2:46735727
|
A | G | 3 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0181 | 3 | HG02257.hp2 HG02451.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-12-22792A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46735727 | ||||||
chr2:46735738
|
G | T | 1 | a0001c0001t0004g0222 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-12-22781G>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46735738 | ||||||
chr2:46735817
|
C | T | 1 | a0001c0001t0002g0261 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-12-22702C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46735817 | ||||||
chr2:46735867
|
A | G | 13 | a0001c0001t0007g0010a0001c0001t0007g0063a0001c0001t0007g0064others(10): Show | 14 | HG00741.hp1 HG01081.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.-12-22652A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46735867 | ||||||
chr2:46736018
|
C | G | 2 | a0001c0003t0005g0092a0001c0003t0005g0098 | 2 | NA18946.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.-12-22501C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46736018 | ||||||
chr2:46736096
|
G | A | 11 | a0001c0001t0006g0050a0001c0001t0006g0052a0001c0001t0006g0053others(8): Show | 11 | HG02080.hp1 HG02135.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.-12-22423G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46736096 | ||||||
chr2:46736131
|
T | G | 22 | a0001c0002t0010g0012a0001c0002t0010g0086a0001c0002t0010g0090others(19): Show | 25 | HG00733.hp1 HG01069.hp2 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.-12-22388T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46736131 | ||||||
chr2:46736243
|
A | G | 6 | a0001c0002t0003g0016a0001c0002t0003g0101a0001c0002t0003g0109others(3): Show | 7 | HG01074.hp1 HG01099.hp2 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.-12-22276A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46736243 | ||||||
chr2:46736395
|
T | A | 1 | a0001c0001t0002g0278 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-12-22124T>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46736395 | ||||||
chr2:46736396
|
C | G | 8 | a0001c0001t0004g0075a0001c0001t0004g0076a0001c0001t0004g0077others(5): Show | 8 | HG02572.hp1 HG02818.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.-12-22123C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46736396 | ||||||
chr2:46736471
|
A | G | 22 | a0001c0002t0010g0012a0001c0002t0010g0086a0001c0002t0010g0090others(19): Show | 25 | HG00733.hp1 HG01069.hp2 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.-12-22048A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46736471 | ||||||
chr2:46736688
|
C | T | 1 | a0001c0002t0003g0139 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-12-21831C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46736688 | ||||||
chr2:46736714
|
T | C | 1 | a0001c0001t0004g0148 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-12-21805T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46736714 | ||||||
chr2:46736842
|
A | AT | 26 | a0001c0001t0004g0075a0001c0001t0004g0076a0001c0001t0004g0077others(23): Show | 28 | HG00280.hp2 HG00733.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.-12-21664dupT | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46736842 | |||||
chr2:46736842
|
AT | A | 112 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0022others(109): Show | 125 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.-12-21664delT | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46736842 | |||||
chr2:46736921
|
A | G | 1 | a0001c0001t0001g0249 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-12-21598A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46736921 | ||||||
chr2:46737114
|
C | G | 13 | a0001c0001t0007g0010a0001c0001t0007g0063a0001c0001t0007g0064others(10): Show | 14 | HG00741.hp1 HG01081.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.-12-21405C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46737114 | ||||||
chr2:46737149
|
A | T | 131 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0022others(128): Show | 144 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.-12-21370A>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46737149 | ||||||
chr2:46737240
|
T | G | 1 | a0001c0001t0001g0203 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-12-21279T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46737240 | ||||||
chr2:46737643
|
G | A | 11 | a0001c0001t0006g0050a0001c0001t0006g0052a0001c0001t0006g0053others(8): Show | 11 | HG02080.hp1 HG02135.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.-12-20876G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46737643 | ||||||
chr2:46737661
|
A | G | 1 | a0001c0001t0009g0003 | 4 | NA18953.hp2 NA18956.hp2 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.-12-20858A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46737661 | ||||||
chr2:46737856
|
T | TA | 14 | a0001c0001t0001g0036a0001c0001t0004g0028a0001c0001t0006g0050others(11): Show | 15 | HG02055.hp2 HG02080.hp1 HG02135.hp2 others(12): Show |
intron_variant | MODIFIER | c.-12-20649dupA | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46737856 | |||||
chr2:46737871
|
T | C | 49 | a0001c0001t0012g0126a0001c0002t0003g0001a0001c0002t0003g0014others(46): Show | 57 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(54): Show |
intron_variant | MODIFIER | c.-12-20648T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46737871 | ||||||
chr2:46737975
|
A | G | 20 | a0001c0001t0006g0008a0001c0001t0006g0009a0001c0001t0006g0044others(17): Show | 22 | HG00280.hp2 HG00733.hp2 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.-12-20544A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46737975 | ||||||
chr2:46738223
|
A | T | 11 | a0001c0001t0006g0050a0001c0001t0006g0052a0001c0001t0006g0053others(8): Show | 11 | HG02080.hp1 HG02135.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.-12-20296A>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46738223 | ||||||
chr2:46738252
|
C | T | 2 | a0001c0001t0001g0061a0001c0001t0001g0062 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-12-20267C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46738252 | ||||||
chr2:46738363
|
C | G | 1 | a0001c0001t0004g0222 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-12-20156C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46738363 | ||||||
chr2:46738488
|
C | G | 19 | a0001c0001t0006g0008a0001c0001t0006g0009a0001c0001t0006g0044others(16): Show | 21 | HG00733.hp2 HG01123.hp2 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.-12-20031C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46738488 | ||||||
chr2:46738504
|
T | G | 13 | a0001c0001t0007g0010a0001c0001t0007g0063a0001c0001t0007g0064others(10): Show | 14 | HG00741.hp1 HG01081.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.-12-20015T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46738504 | ||||||
chr2:46738566
|
C | G | 1 | a0001c0001t0002g0275 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-12-19953C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46738566 | ||||||
chr2:46738867
|
G | A | 11 | a0001c0001t0006g0050a0001c0001t0006g0052a0001c0001t0006g0053others(8): Show | 11 | HG02080.hp1 HG02135.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.-12-19652G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46738867 | ||||||
chr2:46738869
|
G | A | 18 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0006g0050others(15): Show | 21 | HG01070.hp2 HG01256.hp1 HG01258.hp1 others(18): Show |
intron_variant | MODIFIER | c.-12-19650G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46738869 | ||||||
chr2:46738926
|
G | A | 6 | a0001c0002t0003g0104a0001c0002t0003g0105a0001c0002t0003g0106others(3): Show | 6 | HG02109.hp2 HG02451.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.-12-19593G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46738926 | ||||||
chr2:46739030
|
C | T | 2 | a0001c0001t0004g0028a0001c0001t0019g0263 | 3 | HG02055.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-12-19489C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46739030 | ||||||
chr2:46739228
|
A | G | 1 | a0001c0001t0017g0180 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-12-19291A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46739228 | ||||||
chr2:46739301
|
A | G | 3 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0181 | 3 | HG02257.hp2 HG02451.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-12-19218A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46739301 | ||||||
chr2:46739365
|
C | G | 11 | a0001c0001t0006g0050a0001c0001t0006g0052a0001c0001t0006g0053others(8): Show | 11 | HG02080.hp1 HG02135.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.-12-19154C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46739365 | ||||||
chr2:46739392
|
G | A | 128 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0022others(125): Show | 141 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.-12-19127G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46739392 | ||||||
chr2:46739393
|
A | T | 17 | a0001c0002t0010g0012a0001c0002t0010g0086a0001c0002t0010g0090others(14): Show | 20 | HG01069.hp2 HG01074.hp2 HG01346.hp2 others(17): Show |
intron_variant | MODIFIER | c.-12-19126A>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46739393 | ||||||
chr2:46739414
|
A | G | 1 | a0001c0003t0005g0084 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-12-19105A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46739414 | ||||||
chr2:46739665
|
G | A | 1 | a0001c0008t0016g0145 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-12-18854G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46739665 | ||||||
chr2:46739691
|
G | A | 150 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0168others(147): Show | 173 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.-12-18828G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46739691 | ||||||
chr2:46739897
|
A | G | 3 | a0001c0001t0002g0031a0001c0001t0002g0032a0001c0001t0002g0281 | 5 | HG02572.hp2 HG02622.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-12-18622A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46739897 | ||||||
chr2:46739958
|
C | G | 1 | a0001c0001t0001g0248 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-12-18561C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46739958 | ||||||
chr2:46739979
|
C | T | 2 | a0001c0001t0001g0061a0001c0001t0001g0062 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-12-18540C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46739979 | ||||||
chr2:46740267
|
G | A | 1 | a0001c0003t0005g0254 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-12-18252G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46740267 | ||||||
chr2:46740335
|
T | A | 1 | a0001c0003t0005g0091 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-12-18184T>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46740335 | ||||||
chr2:46740555
|
A | G | 3 | a0001c0003t0005g0041a0001c0003t0005g0042a0001c0003t0005g0084 | 3 | HG01069.hp2 HG01074.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.-12-17964A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46740555 | ||||||
chr2:46740672
|
CTGATACC others(11126): Show |
C | 1 | a0001c0001t0008g0019 | 2 | HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-12-17846_-12-6714 others(3): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46740672 | ||||||
chr2:46740734
|
C | A | 7 | a0001c0001t0004g0075a0001c0001t0004g0077a0001c0001t0004g0078others(4): Show | 7 | HG02572.hp1 HG02896.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.-12-17785C>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46740734 | ||||||
chr2:46740912
|
C | T | 241 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0022others(238): Show | 270 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.-12-17607C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46740912 | ||||||
chr2:46740982
|
T | C | 1 | a0001c0003t0005g0149 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-12-17537T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46740982 | ||||||
chr2:46741042
|
T | C | 1 | a0001c0002t0010g0012 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-12-17477T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46741042 | ||||||
chr2:46741058
|
C | T | 1 | a0001c0001t0021g0241 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-12-17461C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46741058 | ||||||
chr2:46741111
|
C | T | 3 | a0001c0002t0003g0115a0001c0002t0003g0116a0001c0002t0003g0132 | 3 | HG03710.hp1 HG03942.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-12-17408C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46741111 | ||||||
chr2:46741122
|
C | G | 1 | a0001c0001t0001g0205 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-12-17397C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46741122 | ||||||
chr2:46741122
|
C | T | 8 | a0001c0001t0006g0008a0001c0001t0006g0009a0001c0001t0006g0044others(5): Show | 10 | HG00733.hp2 HG01123.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.-12-17397C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46741122 | ||||||
chr2:46741147
|
T | A | 13 | a0001c0001t0007g0010a0001c0001t0007g0063a0001c0001t0007g0064others(10): Show | 14 | HG00741.hp1 HG01081.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.-12-17372T>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46741147 | ||||||
chr2:46741154
|
T | A | 1 | a0001c0001t0007g0040 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-12-17365T>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46741154 | ||||||
chr2:46741274
|
C | G | 4 | a0001c0004t0011g0324a0001c0004t0011g0325a0001c0004t0011g0326others(1): Show | 4 | HG01070.hp2 HG01515.hp1 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.-12-17245C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46741274 | ||||||
chr2:46741314
|
G | A | 1 | a0001c0002t0003g0014 | 2 | NA18971.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.-12-17205G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46741314 | ||||||
chr2:46741322
|
C | T | 1 | a0001c0001t0001g0229 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-12-17197C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46741322 | ||||||
chr2:46741326
|
A | G | 259 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0022others(256): Show | 291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.-12-17193A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46741326 | ||||||
chr2:46741384
|
G | A | 19 | a0001c0001t0006g0008a0001c0001t0006g0009a0001c0001t0006g0044others(16): Show | 21 | HG00733.hp2 HG01123.hp2 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.-12-17135G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46741384 | ||||||
chr2:46741388
|
G | A | 1 | a0001c0001t0001g0225 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-12-17131G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46741388 | ||||||
chr2:46741422
|
A | C | 4 | a0001c0004t0011g0324a0001c0004t0011g0325a0001c0004t0011g0326others(1): Show | 4 | HG01070.hp2 HG01515.hp1 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.-12-17097A>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46741422 | ||||||
chr2:46741555
|
C | T | 19 | a0001c0001t0006g0008a0001c0001t0006g0009a0001c0001t0006g0044others(16): Show | 21 | HG00733.hp2 HG01123.hp2 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.-12-16964C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46741555 | ||||||
chr2:46741577
|
A | G | 294 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0022others(291): Show | 334 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(331): Show |
intron_variant | MODIFIER | c.-12-16942A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46741577 | ||||||
chr2:46741611
|
T | G | 4 | a0001c0004t0011g0324a0001c0004t0011g0325a0001c0004t0011g0326others(1): Show | 4 | HG01070.hp2 HG01515.hp1 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.-12-16908T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46741611 | ||||||
chr2:46741643
|
G | A | 1 | a0001c0002t0003g0131 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-12-16876G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46741643 | ||||||
chr2:46741841
|
A | G | 4 | a0001c0004t0011g0324a0001c0004t0011g0325a0001c0004t0011g0326others(1): Show | 4 | HG01070.hp2 HG01515.hp1 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.-12-16678A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46741841 | ||||||
chr2:46742058
|
A | G | 5 | a0001c0001t0009g0003a0001c0004t0011g0324a0001c0004t0011g0325others(2): Show | 8 | HG01070.hp2 HG01515.hp1 HG02132.hp1 others(5): Show |
intron_variant | MODIFIER | c.-12-16461A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46742058 | ||||||
chr2:46742215
|
T | C | 3 | a0001c0001t0001g0036a0001c0001t0004g0028a0001c0001t0019g0263 | 4 | HG02055.hp2 HG02809.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-12-16304T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46742215 | ||||||
chr2:46742252
|
C | G | 25 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0006g0008others(22): Show | 30 | HG00733.hp2 HG01070.hp2 HG01123.hp2 others(27): Show |
intron_variant | MODIFIER | c.-12-16267C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46742252 | ||||||
chr2:46742281
|
G | A | 1 | a0001c0001t0001g0229 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-12-16238G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46742281 | ||||||
chr2:46742304
|
T | G | 1 | a0001c0001t0002g0278 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-12-16215T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46742304 | ||||||
chr2:46742379
|
G | A | 8 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0173others(5): Show | 8 | HG01255.hp2 HG02145.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-12-16140G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46742379 | ||||||
chr2:46742402
|
T | A | 12 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0259others(9): Show | 16 | HG00558.hp2 HG02027.hp1 HG02080.hp2 others(13): Show |
intron_variant | MODIFIER | c.-12-16117T>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46742402 | ||||||
chr2:46742468
|
G | A | 5 | a0001c0001t0009g0003a0001c0004t0011g0324a0001c0004t0011g0325others(2): Show | 8 | HG01070.hp2 HG01515.hp1 HG02132.hp1 others(5): Show |
intron_variant | MODIFIER | c.-12-16051G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46742468 | ||||||
chr2:46742496
|
T | C | 3 | a0001c0001t0001g0169a0001c0001t0001g0177a0001c0001t0001g0187 | 3 | NA18957.hp2 NA18962.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.-12-16023T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46742496 | ||||||
chr2:46742727
|
G | A | 3 | a0001c0001t0004g0037a0001c0001t0004g0038a0001c0001t0004g0039 | 3 | HG03195.hp2 NA18522.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-12-15792G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46742727 | ||||||
chr2:46742783
|
A | G | 1 | a0001c0001t0001g0158 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-12-15736A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46742783 | ||||||
chr2:46742820
|
T | C | 4 | a0001c0004t0011g0324a0001c0004t0011g0325a0001c0004t0011g0326others(1): Show | 4 | HG01070.hp2 HG01515.hp1 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.-12-15699T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46742820 | ||||||
chr2:46743113
|
T | A | 1 | a0001c0008t0016g0145 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-12-15406T>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46743113 | ||||||
chr2:46743261
|
G | A | 2 | a0001c0001t0004g0192a0001c0001t0004g0253 | 2 | HG02258.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-12-15258G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46743261 | ||||||
chr2:46743327
|
G | A | 241 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0022others(238): Show | 270 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.-12-15192G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46743327 | ||||||
chr2:46743409
|
C | T | 7 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0009g0003others(4): Show | 10 | HG01070.hp2 HG01256.hp1 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.-12-15110C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46743409 | ||||||
chr2:46743448
|
A | G | 192 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0022others(189): Show | 214 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.-12-15071A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46743448 | ||||||
chr2:46743601
|
A | G | 4 | a0001c0001t0008g0080a0001c0001t0008g0154a0001c0001t0008g0155others(1): Show | 4 | HG01109.hp2 HG02451.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.-12-14918A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46743601 | ||||||
chr2:46743687
|
T | G | 27 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0006g0008others(24): Show | 32 | HG00280.hp2 HG00733.hp2 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.-12-14832T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46743687 | ||||||
chr2:46743748
|
A | G | 105 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0022others(102): Show | 115 | HG00408.hp1 HG00438.hp1 HG00558.hp1 others(112): Show |
intron_variant | MODIFIER | c.-12-14771A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46743748 | ||||||
chr2:46743769
|
T | C | 1 | a0001c0001t0006g0044 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-12-14750T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46743769 | ||||||
chr2:46743778
|
T | C | 2 | a0001c0001t0001g0061a0001c0001t0001g0062 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-12-14741T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46743778 | ||||||
chr2:46743878
|
T | C | 1 | a0001c0001t0001g0183 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-12-14641T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46743878 | ||||||
chr2:46743951
|
G | A | 1 | a0001c0001t0006g0046 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-12-14568G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46743951 | ||||||
chr2:46743987
|
A | G | 1 | a0001c0001t0002g0316 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-12-14532A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46743987 | ||||||
chr2:46743987
|
A | T | 26 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0006g0008others(23): Show | 31 | HG00733.hp2 HG01070.hp2 HG01123.hp2 others(28): Show |
intron_variant | MODIFIER | c.-12-14532A>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46743987 | ||||||
chr2:46743996
|
CT | C | 257 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0022others(254): Show | 289 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.-12-14512delT | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46743996 | |||||
chr2:46744050
|
C | T | 15 | a0001c0001t0002g0005a0001c0001t0002g0268a0001c0001t0002g0294others(12): Show | 18 | HG01109.hp1 HG02145.hp1 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.-12-14469C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46744050 | ||||||
chr2:46744056
|
C | T | 13 | a0001c0001t0007g0010a0001c0001t0007g0063a0001c0001t0007g0064others(10): Show | 14 | HG00741.hp1 HG01081.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.-12-14463C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46744056 | ||||||
chr2:46744080
|
C | T | 19 | a0001c0001t0006g0008a0001c0001t0006g0009a0001c0001t0006g0044others(16): Show | 21 | HG00733.hp2 HG01123.hp2 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.-12-14439C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46744080 | ||||||
chr2:46744084
|
G | A | 1 | a0001c0002t0003g0079 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-12-14435G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46744084 | ||||||
chr2:46744208
|
G | T | 5 | a0001c0001t0009g0003a0001c0004t0011g0324a0001c0004t0011g0325others(2): Show | 8 | HG01070.hp2 HG01515.hp1 HG02132.hp1 others(5): Show |
intron_variant | MODIFIER | c.-12-14311G>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46744208 | ||||||
chr2:46744242
|
GGCCTCCC others(531): Show |
G | 1 | a0001c0005t0008g0081 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-12-14264_-12-1372 others(4): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46744242 | |||||
chr2:46744249
|
C | T | 8 | a0001c0001t0006g0008a0001c0001t0006g0009a0001c0001t0006g0044others(5): Show | 10 | HG00733.hp2 HG01123.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.-12-14270C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46744249 | ||||||
chr2:46744276
|
C | T | 1 | a0001c0003t0005g0089 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-12-14243C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46744276 | ||||||
chr2:46744283
|
C | G | 1 | a0001c0001t0008g0080 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-12-14236C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46744283 | ||||||
chr2:46744299
|
C | A | 15 | a0001c0001t0004g0028a0001c0001t0007g0010a0001c0001t0007g0063others(12): Show | 17 | HG00741.hp1 HG01081.hp2 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.-12-14220C>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46744299 | ||||||
chr2:46744327
|
G | A | 11 | a0001c0001t0006g0050a0001c0001t0006g0052a0001c0001t0006g0053others(8): Show | 11 | HG02080.hp1 HG02135.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.-12-14192G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46744327 | ||||||
chr2:46744516
|
A | C | 2 | a0001c0002t0003g0095a0001c0002t0003g0096 | 2 | NA18955.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.-12-14003A>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46744516 | ||||||
chr2:46744528
|
C | CT | 6 | a0001c0001t0004g0190a0001c0001t0004g0192a0001c0001t0004g0198others(3): Show | 6 | HG00738.hp1 HG02258.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12-13978dupT | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46744528 | |||||
chr2:46744661
|
G | T | 8 | a0001c0001t0004g0136a0001c0001t0004g0142a0001c0001t0004g0143others(5): Show | 8 | HG01109.hp1 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.-12-13858G>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46744661 | ||||||
chr2:46744688
|
C | T | 13 | a0001c0001t0007g0010a0001c0001t0007g0063a0001c0001t0007g0064others(10): Show | 14 | HG00741.hp1 HG01081.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.-12-13831C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46744688 | ||||||
chr2:46744771
|
G | A | 1 | a0001c0001t0006g0046 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-12-13748G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46744771 | ||||||
chr2:46744792
|
T | A | 4 | a0001c0001t0008g0080a0001c0001t0008g0154a0001c0001t0008g0155others(1): Show | 4 | HG01109.hp2 HG02451.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.-12-13727T>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46744792 | ||||||
chr2:46744817
|
C | T | 1 | a0001c0002t0003g0135 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-12-13702C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46744817 | ||||||
chr2:46744827
|
T | C | 255 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0022others(252): Show | 287 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(284): Show |
intron_variant | MODIFIER | c.-12-13692T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46744827 | ||||||
chr2:46744883
|
G | A | 1 | a0001c0002t0003g0152 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-12-13636G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46744883 | ||||||
chr2:46745001
|
C | G | 13 | a0001c0001t0007g0010a0001c0001t0007g0063a0001c0001t0007g0064others(10): Show | 14 | HG00741.hp1 HG01081.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.-12-13518C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46745001 | ||||||
chr2:46745045
|
G | A | 13 | a0001c0001t0007g0010a0001c0001t0007g0063a0001c0001t0007g0064others(10): Show | 14 | HG00741.hp1 HG01081.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.-12-13474G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46745045 | ||||||
chr2:46745060
|
A | G | 1 | a0001c0001t0009g0003 | 4 | NA18953.hp2 NA18956.hp2 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.-12-13459A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46745060 | ||||||
chr2:46745070
|
C | T | 1 | a0001c0002t0003g0130 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-12-13449C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46745070 | ||||||
chr2:46745122
|
G | C | 1 | a0001c0008t0016g0145 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-12-13397G>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46745122 | ||||||
chr2:46745291
|
T | C | 1 | a0001c0001t0017g0180 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-12-13228T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46745291 | ||||||
chr2:46745524
|
T | G | 7 | a0001c0001t0009g0003a0001c0004t0011g0324a0001c0004t0011g0325others(4): Show | 11 | HG01070.hp2 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.-12-12995T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46745524 | ||||||
chr2:46745571
|
A | C | 8 | a0001c0001t0004g0075a0001c0001t0004g0076a0001c0001t0004g0077others(5): Show | 8 | HG02572.hp1 HG02818.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.-12-12948A>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46745571 | ||||||
chr2:46745585
|
T | C | 1 | a0001c0001t0001g0246 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-12-12934T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46745585 | ||||||
chr2:46745629
|
A | C | 65 | a0001c0001t0004g0075a0001c0001t0004g0076a0001c0001t0004g0077others(62): Show | 74 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.-12-12890A>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46745629 | ||||||
chr2:46745702
|
AG | A | 3 | a0001c0001t0001g0158a0001c0001t0001g0179a0001c0001t0001g0221 | 3 | HG00558.hp1 HG01081.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.-12-12814delG | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46745702 | |||||
chr2:46745738
|
A | G | 3 | a0001c0001t0004g0136a0001c0001t0004g0144a0001c0001t0004g0147 | 3 | HG02145.hp1 HG02886.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-12-12781A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46745738 | ||||||
chr2:46745767
|
T | G | 23 | a0001c0002t0010g0012a0001c0002t0010g0086a0001c0002t0010g0090others(20): Show | 26 | HG00733.hp1 HG01069.hp2 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.-12-12752T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46745767 | ||||||
chr2:46746050
|
GT | G | 9 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0009g0003others(6): Show | 13 | HG01070.hp2 HG01256.hp1 HG01257.hp2 others(10): Show |
intron_variant | MODIFIER | c.-12-12457delT | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46746050 | |||||
chr2:46746165
|
A | C | 1 | a0001c0001t0006g0047 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-12-12354A>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46746165 | ||||||
chr2:46746256
|
C | G | 1 | a0001c0001t0004g0028 | 2 | HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-12-12263C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46746256 | ||||||
chr2:46746261
|
T | A | 83 | a0001c0001t0004g0028a0001c0001t0004g0037a0001c0001t0004g0038others(80): Show | 95 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.-12-12258T>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46746261 | ||||||
chr2:46746316
|
C | T | 1 | a0001c0001t0002g0266 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-12-12203C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46746316 | ||||||
chr2:46746438
|
T | G | 1 | a0001c0001t0009g0003 | 4 | NA18953.hp2 NA18956.hp2 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.-12-12081T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46746438 | ||||||
chr2:46746543
|
C | T | 2 | a0001c0001t0001g0061a0001c0001t0001g0062 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-12-11976C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46746543 | ||||||
chr2:46746563
|
A | G | 1 | a0001c0002t0003g0130 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-12-11956A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46746563 | ||||||
chr2:46746630
|
G | C | 1 | a0001c0001t0001g0247 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-12-11889G>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46746630 | ||||||
chr2:46746646
|
C | CA | 21 | a0001c0001t0006g0008a0001c0001t0006g0009a0001c0001t0006g0044others(18): Show | 23 | HG00280.hp2 HG00733.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.-12-11860dupA | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46746646 | |||||
chr2:46746691
|
A | G | 2 | a0001c0001t0001g0061a0001c0001t0001g0062 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-12-11828A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46746691 | ||||||
chr2:46746767
|
C | T | 7 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0009g0003others(4): Show | 10 | HG01070.hp2 HG01256.hp1 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.-12-11752C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46746767 | ||||||
chr2:46746779
|
A | G | 19 | a0001c0001t0006g0008a0001c0001t0006g0009a0001c0001t0006g0044others(16): Show | 21 | HG00733.hp2 HG01123.hp2 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.-12-11740A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46746779 | ||||||
chr2:46746781
|
C | G | 19 | a0001c0001t0006g0008a0001c0001t0006g0009a0001c0001t0006g0044others(16): Show | 21 | HG00733.hp2 HG01123.hp2 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.-12-11738C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46746781 | ||||||
chr2:46746813
|
G | T | 20 | a0001c0001t0006g0008a0001c0001t0006g0009a0001c0001t0006g0044others(17): Show | 22 | HG00280.hp2 HG00733.hp2 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.-12-11706G>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46746813 | ||||||
chr2:46746922
|
C | CT | 75 | a0001c0001t0001g0165a0001c0001t0001g0183a0001c0001t0001g0187others(72): Show | 86 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.-12-11576dupT | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46746922 | |||||
chr2:46746922
|
CT | C | 10 | a0001c0001t0002g0292a0001c0001t0002g0301a0001c0001t0004g0082others(7): Show | 10 | HG01109.hp1 HG01515.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.-12-11576delT | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46746922 | |||||
chr2:46746922
|
CTTT | C | 19 | a0001c0001t0006g0008a0001c0001t0006g0009a0001c0001t0006g0044others(16): Show | 21 | HG00733.hp2 HG01123.hp2 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.-12-11578_-12-1157 others(7): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46746922 | |||||
chr2:46746922
|
CTTTTTTT | C | 13 | a0001c0001t0007g0010a0001c0001t0007g0063a0001c0001t0007g0064others(10): Show | 14 | HG00741.hp1 HG01081.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.-12-11582_-12-1157 others(11): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46746922 | |||||
chr2:46746926
|
T | C | 5 | a0001c0003t0005g0011a0001c0003t0005g0091a0001c0003t0005g0092others(2): Show | 6 | HG02056.hp1 NA18943.hp1 NA18946.hp2 others(3): Show |
intron_variant | MODIFIER | c.-12-11593T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46746926 | ||||||
chr2:46747011
|
G | A | 1 | a0001c0002t0003g0132 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-12-11508G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46747011 | ||||||
chr2:46747296
|
C | T | 1 | a0001c0002t0010g0012 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-12-11223C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46747296 | ||||||
chr2:46747399
|
A | T | 9 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0009g0003others(6): Show | 13 | HG01070.hp2 HG01256.hp1 HG01257.hp2 others(10): Show |
intron_variant | MODIFIER | c.-12-11120A>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46747399 | ||||||
chr2:46747470
|
C | T | 20 | a0001c0001t0006g0008a0001c0001t0006g0009a0001c0001t0006g0044others(17): Show | 22 | HG00280.hp2 HG00733.hp2 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.-12-11049C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46747470 | ||||||
chr2:46747482
|
C | T | 8 | a0001c0001t0004g0136a0001c0001t0004g0142a0001c0001t0004g0143others(5): Show | 8 | HG01109.hp1 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.-12-11037C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46747482 | ||||||
chr2:46747510
|
C | T | 1 | a0001c0001t0001g0203 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-12-11009C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46747510 | ||||||
chr2:46747527
|
A | T | 20 | a0001c0001t0006g0008a0001c0001t0006g0009a0001c0001t0006g0044others(17): Show | 22 | HG00280.hp2 HG00733.hp2 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.-12-10992A>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46747527 | ||||||
chr2:46747529
|
T | A | 9 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0009g0003others(6): Show | 13 | HG01070.hp2 HG01256.hp1 HG01257.hp2 others(10): Show |
intron_variant | MODIFIER | c.-12-10990T>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46747529 | ||||||
chr2:46747913
|
G | T | 6 | a0001c0003t0005g0013a0001c0003t0005g0041a0001c0003t0005g0042others(3): Show | 7 | HG01069.hp2 HG01074.hp2 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.-12-10606G>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46747913 | ||||||
chr2:46748122
|
C | T | 3 | a0001c0003t0005g0041a0001c0003t0005g0042a0001c0003t0005g0084 | 3 | HG01069.hp2 HG01074.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.-12-10397C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46748122 | ||||||
chr2:46748189
|
C | CT | 62 | a0001c0001t0001g0205a0001c0001t0002g0292a0001c0001t0002g0302others(59): Show | 74 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.-12-10314dupT | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46748189 | |||||
chr2:46748189
|
CT | C | 22 | a0001c0001t0001g0183a0001c0001t0006g0008a0001c0001t0006g0009others(19): Show | 24 | HG00280.hp2 HG00733.hp2 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.-12-10314delT | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46748189 | |||||
chr2:46748197
|
T | C | 15 | a0001c0003t0005g0011a0001c0003t0005g0013a0001c0003t0005g0041others(12): Show | 17 | HG01069.hp2 HG01074.hp2 HG01346.hp2 others(14): Show |
intron_variant | MODIFIER | c.-12-10322T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46748197 | ||||||
chr2:46748205
|
T | G | 1 | a0001c0001t0002g0267 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-12-10314T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46748205 | ||||||
chr2:46748230
|
G | A | 1 | a0001c0001t0004g0222 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-12-10289G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46748230 | ||||||
chr2:46748249
|
G | A | 1 | a0001c0001t0009g0003 | 4 | NA18953.hp2 NA18956.hp2 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.-12-10270G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46748249 | ||||||
chr2:46748303
|
A | G | 1 | a0001c0001t0004g0222 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-12-10216A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46748303 | ||||||
chr2:46748377
|
C | T | 1 | a0001c0001t0002g0300 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-12-10142C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46748377 | ||||||
chr2:46748450
|
G | A | 6 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0173others(3): Show | 6 | HG01255.hp2 HG02145.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-12-10069G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46748450 | ||||||
chr2:46748468
|
T | A | 1 | a0001c0001t0017g0180 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-12-10051T>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46748468 | ||||||
chr2:46748500
|
T | C | 1 | a0001c0003t0005g0149 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-12-10019T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46748500 | ||||||
chr2:46748689
|
A | G | 100 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0022others(97): Show | 110 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.-12-9830A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46748689 | ||||||
chr2:46748710
|
A | G | 1 | a0001c0001t0006g0060 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-12-9809A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46748710 | ||||||
chr2:46748808
|
G | A | 20 | a0001c0001t0006g0008a0001c0001t0006g0009a0001c0001t0006g0044others(17): Show | 22 | HG00280.hp2 HG00733.hp2 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.-12-9711G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46748808 | ||||||
chr2:46748814
|
A | T | 3 | a0001c0002t0003g0111a0001c0002t0003g0119a0001c0002t0003g0125 | 3 | HG03540.hp1 HG03704.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-12-9705A>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46748814 | ||||||
chr2:46748829
|
G | A | 2 | a0001c0001t0001g0061a0001c0001t0001g0062 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-12-9690G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46748829 | ||||||
chr2:46749078
|
G | C | 59 | a0001c0002t0003g0001a0001c0002t0003g0014a0001c0002t0003g0015others(56): Show | 69 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.-12-9441G>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46749078 | ||||||
chr2:46749173
|
G | A | 20 | a0001c0001t0006g0008a0001c0001t0006g0009a0001c0001t0006g0044others(17): Show | 22 | HG00280.hp2 HG00733.hp2 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.-12-9346G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46749173 | ||||||
chr2:46749229
|
C | T | 1 | a0001c0001t0004g0142 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-12-9290C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46749229 | ||||||
chr2:46749233
|
C | G | 1 | a0001c0002t0010g0012 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-12-9286C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46749233 | ||||||
chr2:46749237
|
T | A | 20 | a0001c0001t0006g0008a0001c0001t0006g0009a0001c0001t0006g0044others(17): Show | 22 | HG00280.hp2 HG00733.hp2 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.-12-9282T>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46749237 | ||||||
chr2:46749402
|
G | A | 4 | a0001c0004t0011g0324a0001c0004t0011g0325a0001c0004t0011g0326others(1): Show | 4 | HG01070.hp2 HG01515.hp1 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.-12-9117G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46749402 | ||||||
chr2:46749516
|
C | G | 248 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0022others(245): Show | 277 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.-12-9003C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46749516 | ||||||
chr2:46749589
|
G | A | 6 | a0001c0001t0004g0075a0001c0001t0004g0077a0001c0001t0004g0078others(3): Show | 6 | HG02572.hp1 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12-8930G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46749589 | ||||||
chr2:46749604
|
A | G | 20 | a0001c0001t0006g0008a0001c0001t0006g0009a0001c0001t0006g0044others(17): Show | 22 | HG00280.hp2 HG00733.hp2 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.-12-8915A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46749604 | ||||||
chr2:46749670
|
T | C | 1 | a0001c0001t0002g0269 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-12-8849T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46749670 | ||||||
chr2:46749695
|
C | T | 27 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0006g0008others(24): Show | 32 | HG00280.hp2 HG00733.hp2 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.-12-8824C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46749695 | ||||||
chr2:46749728
|
C | G | 107 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0022others(104): Show | 117 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.-12-8791C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46749728 | ||||||
chr2:46749958
|
T | C | 4 | a0001c0004t0011g0324a0001c0004t0011g0325a0001c0004t0011g0326others(1): Show | 4 | HG01070.hp2 HG01515.hp1 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.-12-8561T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46749958 | ||||||
chr2:46750050
|
G | A | 9 | a0001c0001t0004g0037a0001c0001t0004g0038a0001c0001t0004g0039others(6): Show | 9 | HG01109.hp2 HG02451.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.-12-8469G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46750050 | ||||||
chr2:46750112
|
G | C | 248 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0022others(245): Show | 277 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.-12-8407G>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46750112 | ||||||
chr2:46750124
|
G | C | 7 | a0001c0001t0004g0075a0001c0001t0004g0076a0001c0001t0004g0077others(4): Show | 7 | HG02572.hp1 HG02818.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.-12-8395G>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46750124 | ||||||
chr2:46750173
|
G | A | 19 | a0001c0001t0006g0008a0001c0001t0006g0009a0001c0001t0006g0044others(16): Show | 21 | HG00733.hp2 HG01123.hp2 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.-12-8346G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46750173 | ||||||
chr2:46750273
|
C | T | 4 | a0001c0001t0001g0024a0001c0001t0001g0188a0001c0001t0001g0191others(1): Show | 5 | HG00408.hp1 NA18968.hp1 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.-12-8246C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46750273 | ||||||
chr2:46750280
|
C | G | 1 | a0001c0001t0021g0241 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-12-8239C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46750280 | ||||||
chr2:46750326
|
G | C | 1 | a0001c0008t0016g0145 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-12-8193G>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46750326 | ||||||
chr2:46750470
|
C | G | 1 | a0001c0001t0024g0320 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-12-8049C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46750470 | ||||||
chr2:46750523
|
T | C | 1 | a0001c0001t0017g0180 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-12-7996T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46750523 | ||||||
chr2:46750530
|
C | T | 19 | a0001c0001t0006g0008a0001c0001t0006g0009a0001c0001t0006g0044others(16): Show | 21 | HG00733.hp2 HG01123.hp2 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.-12-7989C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46750530 | ||||||
chr2:46750610
|
G | A | 4 | a0001c0001t0002g0007a0001c0001t0002g0259a0001c0001t0002g0305others(1): Show | 6 | HG02027.hp1 HG02080.hp2 NA18949.hp1 others(3): Show |
intron_variant | MODIFIER | c.-12-7909G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46750610 | ||||||
chr2:46750612
|
A | G | 4 | a0001c0004t0011g0324a0001c0004t0011g0325a0001c0004t0011g0326others(1): Show | 4 | HG01070.hp2 HG01515.hp1 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.-12-7907A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46750612 | ||||||
chr2:46750625
|
A | G | 1 | a0001c0001t0001g0176 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-12-7894A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46750625 | ||||||
chr2:46750627
|
A | G | 4 | a0001c0004t0011g0324a0001c0004t0011g0325a0001c0004t0011g0326others(1): Show | 4 | HG01070.hp2 HG01515.hp1 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.-12-7892A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46750627 | ||||||
chr2:46750631
|
C | T | 2 | a0001c0002t0003g0015a0001c0002t0003g0135 | 3 | HG01175.hp2 HG02886.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-12-7888C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46750631 | ||||||
chr2:46750730
|
G | A | 5 | a0001c0001t0004g0075a0001c0001t0004g0077a0001c0001t0004g0078others(2): Show | 5 | HG02572.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-12-7789G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46750730 | ||||||
chr2:46750754
|
A | G | 61 | a0001c0001t0004g0222a0001c0002t0003g0001a0001c0002t0003g0014others(58): Show | 71 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.-12-7765A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46750754 | ||||||
chr2:46750917
|
T | C | 243 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0022others(240): Show | 269 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.-12-7602T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46750917 | ||||||
chr2:46750951
|
C | T | 243 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0022others(240): Show | 269 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.-12-7568C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46750951 | ||||||
chr2:46750974
|
A | G | 16 | a0001c0001t0005g0167a0001c0003t0005g0011a0001c0003t0005g0013others(13): Show | 18 | HG01069.hp2 HG01074.hp2 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.-12-7545A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46750974 | ||||||
chr2:46751039
|
T | C | 1 | a0001c0003t0005g0256 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-12-7480T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46751039 | ||||||
chr2:46751065
|
A | C | 2 | a0001c0001t0001g0262a0001c0001t0004g0076 | 2 | HG02818.hp2 NA18939.hp1 |
intron_variant | MODIFIER | c.-12-7454A>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46751065 | ||||||
chr2:46751094
|
T | C | 1 | a0001c0001t0001g0248 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-12-7425T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46751094 | ||||||
chr2:46751150
|
G | A | 8 | a0001c0001t0001g0171a0001c0001t0001g0201a0001c0001t0001g0204others(5): Show | 8 | HG03195.hp2 NA18522.hp1 NA18906.hp2 others(5): Show |
intron_variant | MODIFIER | c.-12-7369G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46751150 | ||||||
chr2:46751150
|
G | T | 8 | a0001c0001t0004g0136a0001c0001t0004g0142a0001c0001t0004g0143others(5): Show | 8 | HG01109.hp1 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.-12-7369G>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46751150 | ||||||
chr2:46751210
|
A | G | 62 | a0001c0001t0004g0222a0001c0001t0012g0126a0001c0002t0003g0001others(59): Show | 72 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.-12-7309A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46751210 | ||||||
chr2:46751219
|
A | G | 1 | a0001c0002t0003g0128 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-12-7300A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46751219 | ||||||
chr2:46751498
|
A | G | 2 | a0001c0001t0007g0070a0001c0001t0007g0071 | 2 | HG01243.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-12-7021A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46751498 | ||||||
chr2:46751504
|
A | G | 329 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0022others(326): Show | 373 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(370): Show |
intron_variant | MODIFIER | c.-12-7015A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46751504 | ||||||
chr2:46751585
|
T | A | 8 | a0001c0001t0004g0136a0001c0001t0004g0142a0001c0001t0004g0143others(5): Show | 8 | HG01109.hp1 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.-12-6934T>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46751585 | ||||||
chr2:46751690
|
G | T | 19 | a0001c0001t0006g0008a0001c0001t0006g0009a0001c0001t0006g0044others(16): Show | 21 | HG00733.hp2 HG01123.hp2 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.-12-6829G>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46751690 | ||||||
chr2:46751691
|
C | T | 19 | a0001c0001t0006g0008a0001c0001t0006g0009a0001c0001t0006g0044others(16): Show | 21 | HG00733.hp2 HG01123.hp2 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.-12-6828C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46751691 | ||||||
chr2:46751806
|
A | G | 1 | a0001c0001t0008g0019 | 2 | HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-12-6713A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46751806 | ||||||
chr2:46751811
|
G | A | 8 | a0001c0001t0006g0008a0001c0001t0006g0009a0001c0001t0006g0044others(5): Show | 10 | HG00733.hp2 HG01123.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.-12-6708G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46751811 | ||||||
chr2:46751841
|
G | T | 19 | a0001c0001t0006g0008a0001c0001t0006g0009a0001c0001t0006g0044others(16): Show | 21 | HG00733.hp2 HG01123.hp2 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.-12-6678G>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46751841 | ||||||
chr2:46751914
|
T | C | 1 | a0001c0001t0006g0053 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-12-6605T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46751914 | ||||||
chr2:46752090
|
A | T | 6 | a0001c0004t0011g0324a0001c0004t0011g0325a0001c0004t0011g0326others(3): Show | 7 | HG01070.hp2 HG01257.hp2 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.-12-6429A>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46752090 | ||||||
chr2:46752091
|
C | T | 6 | a0001c0004t0011g0324a0001c0004t0011g0325a0001c0004t0011g0326others(3): Show | 7 | HG01070.hp2 HG01257.hp2 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.-12-6428C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46752091 | ||||||
chr2:46752105
|
G | A | 19 | a0001c0001t0006g0008a0001c0001t0006g0009a0001c0001t0006g0044others(16): Show | 21 | HG00733.hp2 HG01123.hp2 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.-12-6414G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46752105 | ||||||
chr2:46752108
|
G | A | 1 | a0001c0001t0009g0003 | 4 | NA18953.hp2 NA18956.hp2 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.-12-6411G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46752108 | ||||||
chr2:46752134
|
C | T | 2 | a0001c0001t0007g0066a0001c0001t0007g0067 | 2 | HG02622.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-12-6385C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46752134 | ||||||
chr2:46752168
|
CT | C | 24 | a0001c0001t0004g0075a0001c0001t0004g0077a0001c0001t0004g0078others(21): Show | 26 | HG00733.hp2 HG01123.hp2 HG01167.hp2 others(23): Show |
intron_variant | MODIFIER | c.-12-6337delT | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46752168 | |||||
chr2:46752269
|
C | T | 2 | a0001c0001t0002g0295a0001c0001t0004g0148 | 2 | HG02970.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.-12-6250C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46752269 | ||||||
chr2:46752358
|
C | G | 13 | a0001c0001t0007g0010a0001c0001t0007g0063a0001c0001t0007g0064others(10): Show | 14 | HG00741.hp1 HG01081.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.-12-6161C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46752358 | ||||||
chr2:46752517
|
T | C | 97 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0022others(94): Show | 107 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.-12-6002T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46752517 | ||||||
chr2:46752534
|
TG | T | 4 | a0001c0004t0011g0324a0001c0004t0011g0325a0001c0004t0011g0326others(1): Show | 4 | HG01070.hp2 HG01515.hp1 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.-12-5980delG | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46752534 | |||||
chr2:46752547
|
G | T | 7 | a0001c0001t0004g0082a0001c0001t0004g0083a0001c0001t0008g0019others(4): Show | 8 | HG01109.hp2 HG02451.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.-12-5972G>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46752547 | ||||||
chr2:46752574
|
G | C | 1 | a0001c0001t0001g0187 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-12-5945G>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46752574 | ||||||
chr2:46752691
|
A | G | 1 | a0001c0002t0003g0116 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-12-5828A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46752691 | ||||||
chr2:46752711
|
T | G | 1 | a0001c0001t0002g0279 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-12-5808T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46752711 | ||||||
chr2:46752758
|
A | T | 1 | a0001c0002t0003g0100 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-12-5761A>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46752758 | ||||||
chr2:46752809
|
T | C | 1 | a0001c0002t0003g0133 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-12-5710T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46752809 | ||||||
chr2:46752966
|
C | A | 19 | a0001c0001t0006g0008a0001c0001t0006g0009a0001c0001t0006g0044others(16): Show | 21 | HG00733.hp2 HG01123.hp2 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.-12-5553C>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46752966 | ||||||
chr2:46752997
|
G | C | 1 | a0001c0001t0008g0154 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-12-5522G>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46752997 | ||||||
chr2:46753200
|
C | T | 2 | a0001c0001t0001g0061a0001c0001t0001g0062 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-12-5319C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46753200 | ||||||
chr2:46753349
|
A | G | 1 | a0001c0003t0005g0041 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-12-5170A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46753349 | ||||||
chr2:46753402
|
G | T | 1 | a0001c0001t0001g0186 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.-12-5117G>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46753402 | ||||||
chr2:46753562
|
T | C | 7 | a0001c0001t0004g0082a0001c0001t0004g0083a0001c0001t0008g0019others(4): Show | 8 | HG01109.hp2 HG02451.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.-12-4957T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46753562 | ||||||
chr2:46753752
|
C | T | 1 | a0001c0001t0002g0311 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.-12-4767C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46753752 | ||||||
chr2:46753900
|
T | C | 24 | a0001c0001t0005g0167a0001c0002t0010g0012a0001c0002t0010g0086others(21): Show | 27 | HG00733.hp1 HG01069.hp2 HG01074.hp2 others(24): Show |
intron_variant | MODIFIER | c.-12-4619T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46753900 | ||||||
chr2:46753981
|
A | G | 2 | a0001c0001t0001g0061a0001c0001t0001g0062 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-12-4538A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46753981 | ||||||
chr2:46754068
|
G | A | 2 | a0001c0001t0001g0061a0001c0001t0001g0062 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-12-4451G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46754068 | ||||||
chr2:46754482
|
A | G | 107 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0022others(104): Show | 117 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.-12-4037A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46754482 | ||||||
chr2:46754559
|
G | A | 1 | a0001c0001t0001g0161 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-12-3960G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46754559 | ||||||
chr2:46754768
|
A | G | 3 | a0001c0001t0004g0037a0001c0001t0004g0038a0001c0001t0004g0039 | 3 | HG03195.hp2 NA18522.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-12-3751A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46754768 | ||||||
chr2:46754789
|
C | T | 1 | a0001c0001t0002g0289 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-12-3730C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46754789 | ||||||
chr2:46754920
|
C | A | 1 | a0001c0001t0004g0202 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-12-3599C>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46754920 | ||||||
chr2:46755138
|
G | A | 1 | a0001c0008t0016g0145 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-12-3381G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46755138 | ||||||
chr2:46755418
|
T | G | 2 | a0001c0001t0006g0048a0001c0001t0006g0049 | 2 | HG01123.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.-12-3101T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46755418 | ||||||
chr2:46755454
|
T | G | 1 | a0001c0001t0001g0240 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-12-3065T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46755454 | ||||||
chr2:46755472
|
G | A | 1 | a0001c0002t0015g0103 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-12-3047G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46755472 | ||||||
chr2:46755500
|
T | G | 13 | a0001c0001t0007g0010a0001c0001t0007g0063a0001c0001t0007g0064others(10): Show | 14 | HG00741.hp1 HG01081.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.-12-3019T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46755500 | ||||||
chr2:46755530
|
T | A | 1 | a0001c0002t0003g0117 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-12-2989T>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46755530 | ||||||
chr2:46755550
|
A | C | 20 | a0001c0001t0006g0008a0001c0001t0006g0009a0001c0001t0006g0044others(17): Show | 22 | HG00280.hp2 HG00733.hp2 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.-12-2969A>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46755550 | ||||||
chr2:46755756
|
C | G | 2 | a0001c0001t0008g0080a0001c0005t0008g0081 | 2 | HG02451.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-12-2763C>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46755756 | ||||||
chr2:46755806
|
G | A | 2 | a0001c0001t0004g0028a0001c0001t0019g0263 | 3 | HG02055.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-12-2713G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46755806 | ||||||
chr2:46755857
|
T | C | 7 | a0001c0001t0004g0075a0001c0001t0004g0076a0001c0001t0004g0077others(4): Show | 7 | HG02572.hp1 HG02818.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.-12-2662T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46755857 | ||||||
chr2:46755883
|
C | T | 2 | a0001c0002t0003g0095a0001c0002t0003g0096 | 2 | NA18955.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.-12-2636C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46755883 | ||||||
chr2:46755959
|
A | G | 108 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0022others(105): Show | 118 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.-12-2560A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46755959 | ||||||
chr2:46756046
|
G | A | 7 | a0001c0001t0004g0075a0001c0001t0004g0076a0001c0001t0004g0077others(4): Show | 7 | HG02572.hp1 HG02818.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.-12-2473G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46756046 | ||||||
chr2:46756139
|
G | A | 8 | a0001c0001t0004g0136a0001c0001t0004g0142a0001c0001t0004g0143others(5): Show | 8 | HG01109.hp1 HG02145.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.-12-2380G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46756139 | ||||||
chr2:46756147
|
G | A | 1 | a0001c0001t0017g0180 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-12-2372G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46756147 | ||||||
chr2:46756437
|
A | T | 1 | a0001c0001t0004g0083 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-12-2082A>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46756437 | ||||||
chr2:46756482
|
AGATTTGG others(12): Show |
A | 1 | a0001c0002t0003g0128 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-12-2035_-12-2017d others(21): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46756482 | |||||
chr2:46756547
|
T | G | 2 | a0001c0001t0001g0061a0001c0001t0001g0062 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-12-1972T>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46756547 | ||||||
chr2:46756583
|
G | A | 1 | a0001c0001t0002g0305 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-12-1936G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46756583 | ||||||
chr2:46756591
|
A | G | 2 | a0001c0001t0001g0061a0001c0001t0001g0062 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-12-1928A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46756591 | ||||||
chr2:46756611
|
T | A | 1 | a0001c0001t0001g0184 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-12-1908T>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46756611 | ||||||
chr2:46756637
|
G | C | 1 | a0001c0002t0003g0114 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-12-1882G>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46756637 | ||||||
chr2:46756707
|
A | G | 5 | a0001c0001t0001g0022a0001c0001t0001g0207a0001c0001t0001g0216others(2): Show | 6 | NA18953.hp1 NA18959.hp1 NA18970.hp2 others(3): Show |
intron_variant | MODIFIER | c.-12-1812A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46756707 | ||||||
chr2:46756772
|
C | T | 1 | a0001c0002t0003g0139 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-12-1747C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46756772 | ||||||
chr2:46756773
|
G | A | 18 | a0001c0001t0006g0008a0001c0001t0006g0009a0001c0001t0006g0044others(15): Show | 20 | HG00733.hp2 HG01123.hp2 HG01167.hp2 others(17): Show |
intron_variant | MODIFIER | c.-12-1746G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46756773 | ||||||
chr2:46756927
|
C | T | 4 | a0001c0001t0004g0037a0001c0001t0004g0038a0001c0001t0004g0039others(1): Show | 4 | HG03195.hp2 HG03209.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.-12-1592C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46756927 | ||||||
chr2:46757053
|
A | G | 2 | a0001c0002t0003g0121a0001c0002t0003g0122 | 2 | NA18993.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.-12-1466A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46757053 | ||||||
chr2:46757121
|
C | T | 1 | a0001c0002t0012g0102 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-12-1398C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46757121 | ||||||
chr2:46757142
|
G | A | 1 | a0001c0001t0001g0036 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-12-1377G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46757142 | ||||||
chr2:46757343
|
T | C | 222 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0022others(219): Show | 246 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.-12-1176T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46757343 | ||||||
chr2:46757459
|
A | T | 6 | a0001c0004t0011g0324a0001c0004t0011g0325a0001c0004t0011g0326others(3): Show | 7 | HG01070.hp2 HG01257.hp2 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.-12-1060A>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46757459 | ||||||
chr2:46757488
|
C | T | 240 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0022others(237): Show | 266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.-12-1031C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46757488 | ||||||
chr2:46757547
|
A | C | 2 | a0001c0001t0001g0175a0001c0001t0001g0227 | 2 | NA19009.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.-12-972A>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46757547 | ||||||
chr2:46757577
|
C | T | 1 | a0001c0002t0003g0112 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-12-942C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46757577 | ||||||
chr2:46757595
|
G | GGT | 6 | a0001c0004t0011g0324a0001c0004t0011g0325a0001c0004t0011g0326others(3): Show | 7 | HG01070.hp2 HG01257.hp2 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.-12-922_-12-921dup others(2): Show |
SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr2 | 46757595 | |||||
chr2:46757633
|
G | A | 1 | a0001c0001t0021g0241 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-12-886G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46757633 | ||||||
chr2:46757691
|
A | G | 106 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0022others(103): Show | 115 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.-12-828A>G | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46757691 | ||||||
chr2:46757700
|
C | T | 1 | a0001c0001t0012g0126 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-12-819C>T | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46757700 | ||||||
chr2:46757764
|
G | A | 1 | a0001c0002t0003g0043 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-12-755G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46757764 | ||||||
chr2:46757993
|
T | C | 2 | a0001c0001t0004g0028a0001c0001t0019g0263 | 3 | HG02055.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-12-526T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46757993 | ||||||
chr2:46758018
|
A | C | 1 | a0001c0001t0009g0003 | 4 | NA18953.hp2 NA18956.hp2 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.-12-501A>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46758018 | ||||||
chr2:46758044
|
C | A | 1 | a0001c0001t0002g0315 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-12-475C>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46758044 | ||||||
chr2:46758098
|
T | C | 1 | a0001c0001t0009g0003 | 4 | NA18953.hp2 NA18956.hp2 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.-12-421T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46758098 | ||||||
chr2:46758106
|
T | A | 1 | a0001c0003t0005g0149 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-12-413T>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46758106 | ||||||
chr2:46758353
|
T | C | 2 | a0001c0001t0004g0192a0001c0001t0004g0253 | 2 | HG02258.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-12-166T>C | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46758353 | ||||||
chr2:46758405
|
G | A | 13 | a0001c0001t0007g0010a0001c0001t0007g0063a0001c0001t0007g0064others(10): Show | 14 | HG00741.hp1 HG01081.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.-12-114G>A | SOCS5 | ENSG00000171150.9 | transcript | ENST00000394861.3 | protein_coding | 1/1 | chr2 | 46758405 |