geneid | 3566 |
---|---|
ensemblid | ENSG00000077238.14 |
hgncid | 6015 |
symbol | IL4R |
name | interleukin 4 receptor |
refseq_nuc | NM_000418.4 |
refseq_prot | NP_000409.1 |
ensembl_nuc | ENST00000395762.7 |
ensembl_prot | ENSP00000379111.2 |
mane_status | MANE Select |
chr | chr16 |
start | 27313974 |
end | 27364778 |
strand | + |
ver | v1.2 |
region | chr16:27313974-27364778 |
region5000 | chr16:27308974-27369778 |
regionname0 | IL4R_chr16_27313974_27364778 |
regionname5000 | IL4R_chr16_27308974_27369778 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 825 | 100 | 13 | 11 | 60 | 6 | 10 | 44 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0002 | 1/1 | 825 | 85 | 9 | 25 | 31 | 6 | 12 | 22 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0003 | 0/0 | 825 | 28 | 9 | 5 | 13 | 0 | 1 | 10 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0004 | 0/0 | 825 | 18 | 0 | 3 | 9 | 0 | 6 | 6 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0005 | 0/0 | 825 | 14 | 2 | 9 | 3 | 0 | 0 | 3 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0006 | 0/0 | 825 | 11 | 11 | 0 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0007 | 0/0 | 825 | 8 | 0 | 0 | 8 | 0 | 0 | 8 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0008 | 0/0 | 825 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0009 | 0/0 | 825 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0010 | 0/0 | 825 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0011 | 0/0 | 825 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0012 | 0/0 | 825 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0013 | 0/0 | 825 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0014 | 0/0 | 825 | 4 | 1 | 0 | 0 | 0 | 3 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0015 | 0/0 | 825 | 3 | 0 | 1 | 0 | 2 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0016 | 0/0 | 825 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0017 | 0/0 | 825 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0018 | 0/0 | 825 | 3 | 1 | 0 | 1 | 0 | 1 | 1 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0019 | 0/0 | 825 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0020 | 0/0 | 825 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0021 | 0/0 | 825 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0022 | 0/0 | 825 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0023 | 0/0 | 825 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0024 | 0/0 | 825 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0025 | 0/0 | 825 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0026 | 0/0 | 825 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0027 | 0/0 | 825 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0028 | 0/0 | 825 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0029 | 0/0 | 825 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0030 | 0/0 | 825 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0031 | 0/0 | 825 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0032 | 0/0 | 825 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0033 | 0/0 | 825 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0034 | 0/0 | 825 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 2478 | 93 | 11 | 8 | 60 | 4 | 10 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
c0002 | 1/0 | 2478 | 81 | 8 | 23 | 31 | 6 | 12 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
c0003 | 0/0 | 2478 | 28 | 9 | 5 | 13 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
c0004 | 0/0 | 2478 | 18 | 0 | 3 | 9 | 0 | 6 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
c0005 | 0/0 | 2478 | 12 | 0 | 9 | 3 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
c0006 | 0/0 | 2478 | 10 | 10 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
c0007 | 0/0 | 2478 | 8 | 0 | 0 | 8 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
c0008 | 0/0 | 2478 | 7 | 2 | 3 | 0 | 2 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
c0009 | 0/0 | 2478 | 6 | 6 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
c0010 | 0/0 | 2478 | 5 | 5 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
c0011 | 0/0 | 2478 | 4 | 4 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
c0012 | 0/0 | 2478 | 4 | 4 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
c0013 | 0/1 | 2478 | 4 | 1 | 2 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
c0014 | 0/0 | 2478 | 3 | 0 | 1 | 0 | 2 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
c0015 | 0/0 | 2478 | 3 | 1 | 0 | 1 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
c0016 | 0/0 | 2478 | 3 | 2 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
c0017 | 0/0 | 2478 | 3 | 3 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
c0018 | 0/0 | 2478 | 3 | 2 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
c0019 | 0/0 | 2478 | 3 | 0 | 0 | 0 | 0 | 3 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
c0020 | 0/0 | 2478 | 2 | 2 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
c0021 | 0/0 | 2478 | 2 | 2 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
c0022 | 0/0 | 2478 | 2 | 2 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
c0023 | 0/0 | 2478 | 2 | 2 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
c0024 | 0/0 | 2478 | 2 | 2 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
c0025 | 0/0 | 2478 | 1 | 0 | 0 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
c0026 | 0/0 | 2478 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
c0027 | 0/0 | 2478 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
c0028 | 0/0 | 2478 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
c0029 | 0/0 | 2478 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
c0030 | 0/0 | 2478 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
c0031 | 0/0 | 2478 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
c0032 | 0/0 | 2478 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
c0033 | 0/0 | 2478 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
c0034 | 0/0 | 2478 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
c0035 | 0/0 | 2478 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
c0036 | 0/0 | 2478 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
c0037 | 0/0 | 2478 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
c0038 | 0/0 | 2478 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
c0039 | 0/0 | 2478 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
c0040 | 0/0 | 2478 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
c0041 | 0/0 | 2478 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
c0042 | 0/0 | 2478 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
c0043 | 0/0 | 2478 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
c0044 | 0/0 | 2478 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
c0045 | 0/0 | 2478 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
c0046 | 0/0 | 2478 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
c0047 | 0/0 | 2478 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
c0048 | 0/0 | 2478 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 1147 | 122 | 19 | 20 | 62 | 10 | 10 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
t0002 | 0/1 | 1147 | 116 | 16 | 32 | 46 | 4 | 17 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
t0003 | 0/0 | 1147 | 16 | 0 | 3 | 10 | 0 | 3 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
t0004 | 0/0 | 1147 | 12 | 12 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
t0005 | 0/0 | 1147 | 10 | 10 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
t0006 | 0/0 | 1147 | 9 | 8 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
t0007 | 0/0 | 1147 | 9 | 0 | 1 | 7 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
t0008 | 0/0 | 1147 | 7 | 7 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
t0009 | 0/0 | 1147 | 4 | 4 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
t0010 | 0/0 | 1147 | 4 | 4 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
t0011 | 0/0 | 1147 | 3 | 3 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
t0012 | 0/0 | 1147 | 3 | 0 | 0 | 0 | 0 | 3 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
t0013 | 0/0 | 1147 | 3 | 3 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
t0014 | 0/0 | 1147 | 2 | 2 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
t0015 | 0/0 | 1147 | 2 | 2 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
t0016 | 0/0 | 1147 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
t0017 | 0/0 | 1147 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
t0018 | 0/0 | 1147 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
t0019 | 0/0 | 1147 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
t0020 | 0/0 | 1147 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
t0021 | 0/0 | 1147 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
t0022 | 0/0 | 1147 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
t0023 | 0/0 | 1120 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
t0024 | 0/0 | 1147 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
t0025 | 0/0 | 1147 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
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 | 12 | 0 | 2 | 10 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0002 | 0/0 | 7 | 0 | 0 | 6 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0004 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0005 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0009 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0016 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0018 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0021 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0024 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0029 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0147 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0226 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 2478 | 93 | 11 | 8 | 60 | 4 | 10 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0001c0008 | 0/0 | 2478 | 7 | 2 | 3 | 0 | 2 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0002c0002 | 1/0 | 2478 | 81 | 8 | 23 | 31 | 6 | 12 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0002c0013 | 0/1 | 2478 | 4 | 1 | 2 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0003c0003 | 0/0 | 2478 | 28 | 9 | 5 | 13 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0004c0004 | 0/0 | 2478 | 18 | 0 | 3 | 9 | 0 | 6 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0005c0005 | 0/0 | 2478 | 12 | 0 | 9 | 3 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0005c0022 | 0/0 | 2478 | 2 | 2 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0006c0006 | 0/0 | 2478 | 10 | 10 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0006c0031 | 0/0 | 2478 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0007c0007 | 0/0 | 2478 | 8 | 0 | 0 | 8 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0008c0009 | 0/0 | 2478 | 6 | 6 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0008c0047 | 0/0 | 2478 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0009c0017 | 0/0 | 2478 | 3 | 3 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0009c0035 | 0/0 | 2478 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0009c0037 | 0/0 | 2478 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0009c0044 | 0/0 | 2478 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0009c0046 | 0/0 | 2478 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0010c0012 | 0/0 | 2478 | 4 | 4 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0010c0024 | 0/0 | 2478 | 2 | 2 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0010c0034 | 0/0 | 2478 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0011c0010 | 0/0 | 2478 | 5 | 5 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0012c0011 | 0/0 | 2478 | 4 | 4 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0013c0016 | 0/0 | 2478 | 3 | 2 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0013c0042 | 0/0 | 2478 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0014c0019 | 0/0 | 2478 | 3 | 0 | 0 | 0 | 0 | 3 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0014c0041 | 0/0 | 2478 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0015c0014 | 0/0 | 2478 | 3 | 0 | 1 | 0 | 2 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0016c0020 | 0/0 | 2478 | 2 | 2 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0016c0032 | 0/0 | 2478 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0017c0018 | 0/0 | 2478 | 3 | 2 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0018c0015 | 0/0 | 2478 | 3 | 1 | 0 | 1 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0019c0023 | 0/0 | 2478 | 2 | 2 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0020c0021 | 0/0 | 2478 | 2 | 2 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0021c0025 | 0/0 | 2478 | 1 | 0 | 0 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0022c0033 | 0/0 | 2478 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0023c0026 | 0/0 | 2478 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0024c0030 | 0/0 | 2478 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0025c0029 | 0/0 | 2478 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0026c0028 | 0/0 | 2478 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0027c0027 | 0/0 | 2478 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0028c0038 | 0/0 | 2478 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0029c0043 | 0/0 | 2478 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0030c0045 | 0/0 | 2478 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0031c0036 | 0/0 | 2478 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0032c0040 | 0/0 | 2478 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0033c0039 | 0/0 | 2478 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0034c0048 | 0/0 | 2478 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3624 | 74 | 11 | 5 | 47 | 2 | 9 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0001c0001t0002 | 0/0 | 3624 | 10 | 0 | 2 | 5 | 2 | 1 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0001c0001t0007 | 0/0 | 3624 | 8 | 0 | 1 | 7 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0001c0001t0021 | 0/0 | 3624 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0001c0008t0001 | 0/0 | 3624 | 1 | 0 | 0 | 0 | 1 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0001c0008t0002 | 0/0 | 3624 | 4 | 0 | 3 | 0 | 1 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0001c0008t0019 | 0/0 | 3624 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0001c0008t0025 | 0/0 | 3624 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0002c0002t0001 | 1/0 | 3624 | 25 | 3 | 5 | 10 | 5 | 1 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0002c0002t0002 | 0/0 | 3624 | 55 | 5 | 18 | 21 | 1 | 10 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0002c0002t0007 | 0/0 | 3624 | 1 | 0 | 0 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0002c0013t0002 | 0/1 | 3624 | 4 | 1 | 2 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0003c0003t0001 | 0/0 | 3624 | 6 | 3 | 3 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0003c0003t0002 | 0/0 | 3624 | 22 | 6 | 2 | 13 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0004c0004t0002 | 0/0 | 3624 | 5 | 0 | 1 | 0 | 0 | 4 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0004c0004t0003 | 0/0 | 3624 | 13 | 0 | 2 | 9 | 0 | 2 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0005c0005t0001 | 0/0 | 3624 | 5 | 0 | 5 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0005c0005t0002 | 0/0 | 3624 | 7 | 0 | 4 | 3 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0005c0022t0002 | 0/0 | 3624 | 2 | 2 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0006c0006t0006 | 0/0 | 3624 | 6 | 6 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0006c0006t0009 | 0/0 | 3624 | 4 | 4 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0006c0031t0005 | 0/0 | 3624 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0007c0007t0001 | 0/0 | 3624 | 2 | 0 | 0 | 2 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0007c0007t0002 | 0/0 | 3624 | 4 | 0 | 0 | 4 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0007c0007t0016 | 0/0 | 3624 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0007c0007t0022 | 0/0 | 3624 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0008c0009t0008 | 0/0 | 3624 | 5 | 5 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0008c0009t0017 | 0/0 | 3624 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0008c0047t0008 | 0/0 | 3624 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0009c0017t0013 | 0/0 | 3624 | 3 | 3 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0009c0035t0005 | 0/0 | 3624 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0009c0037t0002 | 0/0 | 3624 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0009c0044t0005 | 0/0 | 3624 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0009c0046t0005 | 0/0 | 3624 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0010c0012t0004 | 0/0 | 3624 | 4 | 4 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0010c0024t0004 | 0/0 | 3624 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0010c0024t0005 | 0/0 | 3624 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0010c0034t0005 | 0/0 | 3624 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0011c0010t0004 | 0/0 | 3624 | 5 | 5 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0012c0011t0010 | 0/0 | 3624 | 4 | 4 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0013c0016t0006 | 0/0 | 3624 | 3 | 2 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0013c0042t0008 | 0/0 | 3624 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0014c0019t0012 | 0/0 | 3624 | 3 | 0 | 0 | 0 | 0 | 3 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0014c0041t0005 | 0/0 | 3624 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0015c0014t0001 | 0/0 | 3624 | 3 | 0 | 1 | 0 | 2 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0016c0020t0011 | 0/0 | 3624 | 2 | 2 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0016c0032t0011 | 0/0 | 3624 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0017c0018t0005 | 0/0 | 3624 | 2 | 2 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0017c0018t0023 | 0/0 | 3597 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0018c0015t0002 | 0/0 | 3624 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0018c0015t0003 | 0/0 | 3624 | 2 | 0 | 0 | 1 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0019c0023t0014 | 0/0 | 3624 | 2 | 2 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0020c0021t0001 | 0/0 | 3624 | 2 | 2 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0021c0025t0002 | 0/0 | 3624 | 1 | 0 | 0 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0022c0033t0004 | 0/0 | 3624 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0023c0026t0001 | 0/0 | 3624 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0024c0030t0020 | 0/0 | 3624 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0025c0029t0015 | 0/0 | 3624 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0026c0028t0005 | 0/0 | 3624 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0027c0027t0003 | 0/0 | 3624 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0028c0038t0001 | 0/0 | 3624 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0029c0043t0018 | 0/0 | 3624 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0030c0045t0024 | 0/0 | 3624 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0031c0036t0015 | 0/0 | 3624 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0032c0040t0001 | 0/0 | 3624 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0033c0039t0004 | 0/0 | 3624 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
a0034c0048t0001 | 0/0 | 3624 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | copy fasta | chr16 | 27308974 | 27369778 |
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 | 7 | 0 | 0 | 6 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0001g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0002g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0002g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0007g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0007g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0007g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0007g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0007g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0007g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0001t0021g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0008t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0008t0002g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0008t0002g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0008t0002g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0008t0019g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0001c0008t0025g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0001g0016 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0001g0147 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0002g0001 | 0/0 | 10 | 0 | 2 | 8 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0002g0005 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0002g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0002g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0002g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0002g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0002g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0002g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0002g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0002g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0002g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0002g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0002g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0002t0007g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0013t0002g0024 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0013t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0002c0013t0002g0226 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0003c0003t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0003c0003t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0003c0003t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0003c0003t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0003c0003t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0003c0003t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0003c0003t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0003c0003t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0003c0003t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0003c0003t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0003c0003t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0003c0003t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0003c0003t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0003c0003t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0003c0003t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0003c0003t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0003c0003t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0003c0003t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0003c0003t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0003c0003t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0003c0003t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0003c0003t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0003c0003t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0003c0003t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0003c0003t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0003c0003t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0003c0003t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0003c0003t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0004c0004t0002g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0004c0004t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0004c0004t0002g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0004c0004t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0004c0004t0003g0018 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0004c0004t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0004c0004t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0004c0004t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0004c0004t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0004c0004t0003g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0004c0004t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0004c0004t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0004c0004t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0004c0004t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0004c0004t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0004c0004t0003g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0005c0005t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0005c0005t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0005c0005t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0005c0005t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0005c0005t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0005c0005t0002g0009 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0005c0005t0002g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0005c0005t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0005c0005t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0005c0005t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0005c0022t0002g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0006c0006t0006g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0006c0006t0006g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0006c0006t0006g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0006c0006t0006g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0006c0006t0006g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0006c0006t0009g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0006c0006t0009g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0006c0031t0005g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0007c0007t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0007c0007t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0007c0007t0002g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0007c0007t0002g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0007c0007t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0007c0007t0016g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0007c0007t0022g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0008c0009t0008g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0008c0009t0008g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0008c0009t0008g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0008c0009t0008g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0008c0009t0017g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0008c0047t0008g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0009c0017t0013g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0009c0017t0013g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0009c0017t0013g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0009c0035t0005g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0009c0037t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0009c0044t0005g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0009c0046t0005g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0010c0012t0004g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0010c0012t0004g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0010c0012t0004g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0010c0024t0004g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0010c0024t0005g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0010c0034t0005g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0011c0010t0004g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0011c0010t0004g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0011c0010t0004g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0011c0010t0004g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0011c0010t0004g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0012c0011t0010g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0012c0011t0010g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0012c0011t0010g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0013c0016t0006g0029 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0013c0016t0006g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0013c0042t0008g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0014c0019t0012g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0014c0019t0012g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0014c0019t0012g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0014c0041t0005g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0015c0014t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0015c0014t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0015c0014t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0016c0020t0011g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0016c0020t0011g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0016c0032t0011g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0017c0018t0005g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0017c0018t0005g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0017c0018t0023g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0018c0015t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0018c0015t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0018c0015t0003g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0019c0023t0014g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0019c0023t0014g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0020c0021t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0021c0025t0002g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0022c0033t0004g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0023c0026t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0024c0030t0020g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0025c0029t0015g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0026c0028t0005g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0027c0027t0003g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0028c0038t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0029c0043t0018g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0030c0045t0024g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0031c0036t0015g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0032c0040t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0033c0039t0004g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
a0034c0048t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0002 | t0001 | g0141 | EUR | GBR | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0102 | EUR | GBR | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG00140 | hp1 | a0001 | c0001 | t0002 | g0100 | EUR | GBR | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0162 | EUR | GBR | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0119 | EUR | FIN | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG00280 | hp2 | a0002 | c0002 | t0002 | g0241 | EUR | FIN | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG00408 | hp1 | a0004 | c0004 | t0003 | g0121 | EAS | CHS | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | CHS | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG00438 | hp2 | a0002 | c0002 | t0002 | g0244 | EAS | CHS | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | CHS | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG00597 | hp2 | a0003 | c0003 | t0002 | g0146 | EAS | CHS | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG00609 | hp1 | a0002 | c0002 | t0001 | g0072 | EAS | CHS | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | CHS | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | CHS | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG00621 | hp2 | a0002 | c0002 | t0001 | g0077 | EAS | CHS | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG00639 | hp1 | a0002 | c0002 | t0001 | g0159 | AMR | PUR | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG00639 | hp2 | a0003 | c0003 | t0002 | g0129 | AMR | PUR | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG00642 | hp1 | a0002 | c0002 | t0002 | g0220 | AMR | PUR | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG00642 | hp2 | a0001 | c0008 | t0002 | g0272 | AMR | PUR | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG00673 | hp1 | a0001 | c0001 | t0007 | g0238 | EAS | CHS | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | CHS | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG00735 | hp1 | a0002 | c0002 | t0002 | g0021 | AMR | PUR | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG00735 | hp2 | a0030 | c0045 | t0024 | g0170 | AMR | PUR | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG00738 | hp1 | a0015 | c0014 | t0001 | g0017 | AMR | PUR | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG00741 | hp1 | a0002 | c0002 | t0002 | g0182 | AMR | PUR | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG00741 | hp2 | a0017 | c0018 | t0023 | g0174 | AMR | PUR | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01069 | hp1 | a0002 | c0002 | t0002 | g0219 | AMR | PUR | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01069 | hp2 | a0005 | c0005 | t0002 | g0010 | AMR | PUR | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01070 | hp1 | a0027 | c0027 | t0003 | g0205 | AMR | PUR | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01074 | hp1 | a0002 | c0002 | t0002 | g0214 | AMR | PUR | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01074 | hp2 | a0003 | c0003 | t0001 | g0060 | AMR | PUR | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01081 | hp1 | a0005 | c0005 | t0001 | g0259 | AMR | PUR | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01081 | hp2 | a0002 | c0002 | t0001 | g0150 | AMR | PUR | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01099 | hp1 | a0005 | c0005 | t0001 | g0260 | AMR | PUR | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01106 | hp1 | a0002 | c0002 | t0002 | g0213 | AMR | PUR | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01106 | hp2 | a0001 | c0008 | t0002 | g0028 | AMR | PUR | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01109 | hp1 | a0002 | c0002 | t0002 | g0243 | AMR | PUR | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01109 | hp2 | a0013 | c0016 | t0006 | g0029 | AMR | PUR | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01167 | hp1 | a0003 | c0003 | t0001 | g0059 | AMR | PUR | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01168 | hp1 | a0002 | c0013 | t0002 | g0024 | AMR | PUR | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01168 | hp2 | a0001 | c0008 | t0002 | g0028 | AMR | PUR | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01169 | hp1 | a0003 | c0003 | t0001 | g0058 | AMR | PUR | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01169 | hp2 | a0002 | c0013 | t0002 | g0190 | AMR | PUR | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01175 | hp1 | a0002 | c0002 | t0002 | g0023 | AMR | PUR | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0056 | AMR | PUR | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01243 | hp1 | a0005 | c0005 | t0001 | g0193 | AMR | PUR | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01243 | hp2 | a0029 | c0043 | t0018 | g0045 | AMR | PUR | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01258 | hp1 | a0005 | c0005 | t0002 | g0010 | AMR | CLM | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01258 | hp2 | a0002 | c0002 | t0002 | g0023 | AMR | CLM | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | CLM | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01346 | hp2 | a0002 | c0002 | t0001 | g0143 | AMR | CLM | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01358 | hp1 | a0003 | c0003 | t0002 | g0206 | AMR | CLM | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01358 | hp2 | a0002 | c0002 | t0002 | g0183 | AMR | CLM | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01361 | hp1 | a0002 | c0002 | t0002 | g0017 | AMR | CLM | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01361 | hp2 | a0005 | c0005 | t0002 | g0009 | AMR | CLM | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01433 | hp1 | a0005 | c0005 | t0001 | g0271 | AMR | CLM | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01433 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | CLM | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01496 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | CLM | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01496 | hp2 | a0004 | c0004 | t0002 | g0232 | AMR | CLM | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01515 | hp1 | a0002 | c0002 | t0001 | g0224 | EUR | IBS | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01515 | hp2 | a0015 | c0014 | t0001 | g0152 | EUR | IBS | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01516 | hp1 | a0002 | c0002 | t0001 | g0016 | EUR | IBS | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01516 | hp2 | a0001 | c0008 | t0002 | g0262 | EUR | IBS | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01517 | hp1 | a0002 | c0002 | t0001 | g0016 | EUR | IBS | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01517 | hp2 | a0002 | c0002 | t0001 | g0215 | EUR | IBS | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01884 | hp1 | a0003 | c0003 | t0001 | g0250 | AFR | ACB | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01884 | hp2 | a0002 | c0002 | t0001 | g0235 | AFR | ACB | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0258 | AFR | ACB | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01891 | hp2 | a0001 | c0008 | t0019 | g0261 | AFR | ACB | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01928 | hp1 | a0002 | c0002 | t0002 | g0188 | AMR | PEL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01928 | hp2 | a0002 | c0002 | t0001 | g0207 | AMR | PEL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01934 | hp1 | a0002 | c0002 | t0002 | g0005 | AMR | PEL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0265 | AMR | PEL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01943 | hp1 | a0002 | c0002 | t0001 | g0256 | AMR | PEL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01943 | hp2 | a0002 | c0002 | t0002 | g0225 | AMR | PEL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01952 | hp1 | a0004 | c0004 | t0003 | g0202 | AMR | PEL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG01952 | hp2 | a0028 | c0038 | t0001 | g0140 | AMR | PEL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02004 | hp1 | a0002 | c0002 | t0002 | g0005 | AMR | PEL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02004 | hp2 | a0005 | c0005 | t0002 | g0145 | AMR | PEL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02040 | hp1 | a0002 | c0002 | t0002 | g0254 | EAS | KHV | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | KHV | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02055 | hp1 | a0016 | c0020 | t0011 | g0240 | AFR | ACB | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02055 | hp2 | a0008 | c0009 | t0008 | g0084 | AFR | ACB | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02056 | hp1 | a0004 | c0004 | t0003 | g0201 | EAS | KHV | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02056 | hp2 | a0034 | c0048 | t0001 | g0126 | EAS | KHV | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02071 | hp1 | a0003 | c0003 | t0002 | g0154 | EAS | KHV | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | KHV | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02074 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | KHV | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | KHV | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02129 | hp1 | a0002 | c0002 | t0002 | g0198 | EAS | KHV | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02135 | hp1 | a0003 | c0003 | t0002 | g0137 | EAS | KHV | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02135 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | KHV | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02145 | hp1 | a0019 | c0023 | t0014 | g0030 | AFR | ACB | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02145 | hp2 | a0031 | c0036 | t0015 | g0051 | AFR | ACB | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02148 | hp1 | a0004 | c0004 | t0003 | g0018 | AMR | PEL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02148 | hp2 | a0002 | c0002 | t0002 | g0222 | AMR | PEL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02155 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | CDX | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | CDX | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02258 | hp1 | a0009 | c0046 | t0005 | g0037 | AFR | ACB | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | ACB | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02280 | hp1 | a0003 | c0003 | t0002 | g0163 | AFR | ACB | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02300 | hp1 | a0005 | c0005 | t0001 | g0264 | AMR | PEL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02300 | hp2 | a0001 | c0001 | t0007 | g0164 | AMR | PEL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02451 | hp1 | a0016 | c0032 | t0011 | g0043 | AFR | ACB | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02451 | hp2 | a0002 | c0002 | t0001 | g0128 | AFR | ACB | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02523 | hp1 | a0002 | c0002 | t0002 | g0231 | EAS | KHV | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | KHV | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02572 | hp1 | a0011 | c0010 | t0004 | g0180 | AFR | GWD | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02572 | hp2 | a0009 | c0017 | t0013 | g0177 | AFR | GWD | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02615 | hp1 | a0009 | c0017 | t0013 | g0276 | AFR | GWD | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02622 | hp1 | a0008 | c0047 | t0008 | g0039 | AFR | GWD | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02622 | hp2 | a0003 | c0003 | t0002 | g0252 | AFR | GWD | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02630 | hp1 | a0006 | c0006 | t0006 | g0233 | AFR | GWD | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02647 | hp1 | a0003 | c0003 | t0001 | g0127 | AFR | GWD | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02647 | hp2 | a0012 | c0011 | t0010 | g0019 | AFR | GWD | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02698 | hp2 | a0002 | c0002 | t0002 | g0239 | SAS | PJL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02717 | hp1 | a0020 | c0021 | t0001 | g0015 | AFR | GWD | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02717 | hp2 | a0013 | c0042 | t0008 | g0279 | AFR | GWD | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02723 | hp1 | a0010 | c0024 | t0005 | g0172 | AFR | GWD | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02723 | hp2 | a0003 | c0003 | t0002 | g0234 | AFR | GWD | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | PJL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02735 | hp2 | a0004 | c0004 | t0003 | g0018 | SAS | PJL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02738 | hp1 | a0014 | c0019 | t0012 | g0270 | SAS | PJL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0142 | SAS | PJL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02809 | hp1 | a0012 | c0011 | t0010 | g0019 | AFR | GWD | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02809 | hp2 | a0033 | c0039 | t0004 | g0275 | AFR | GWD | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02818 | hp1 | a0017 | c0018 | t0005 | g0175 | AFR | GWD | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02818 | hp2 | a0006 | c0006 | t0006 | g0236 | AFR | GWD | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02886 | hp1 | a0003 | c0003 | t0002 | g0044 | AFR | GWD | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02886 | hp2 | a0020 | c0021 | t0001 | g0015 | AFR | GWD | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02895 | hp1 | a0005 | c0022 | t0002 | g0020 | AFR | GWD | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02895 | hp2 | a0013 | c0016 | t0006 | g0282 | AFR | GWD | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02896 | hp1 | a0002 | c0002 | t0002 | g0208 | AFR | GWD | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02896 | hp2 | a0012 | c0011 | t0010 | g0179 | AFR | GWD | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02897 | hp1 | a0002 | c0002 | t0002 | g0228 | AFR | GWD | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02897 | hp2 | a0005 | c0022 | t0002 | g0020 | AFR | GWD | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02922 | hp1 | a0010 | c0024 | t0004 | g0281 | AFR | ESN | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02922 | hp2 | a0010 | c0012 | t0004 | g0011 | AFR | ESN | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02965 | hp1 | a0009 | c0017 | t0013 | g0176 | AFR | ESN | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02965 | hp2 | a0010 | c0012 | t0004 | g0011 | AFR | ESN | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02976 | hp1 | a0006 | c0006 | t0006 | g0210 | AFR | ESN | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0263 | SAS | PJL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG03017 | hp2 | a0002 | c0002 | t0002 | g0027 | SAS | PJL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG03041 | hp1 | a0010 | c0012 | t0004 | g0065 | AFR | GWD | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG03041 | hp2 | a0011 | c0010 | t0004 | g0047 | AFR | GWD | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG03098 | hp1 | a0009 | c0037 | t0002 | g0050 | AFR | MSL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG03098 | hp2 | a0024 | c0030 | t0020 | g0237 | AFR | MSL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG03130 | hp1 | a0017 | c0018 | t0005 | g0280 | AFR | ESN | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG03130 | hp2 | a0008 | c0009 | t0008 | g0007 | AFR | ESN | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG03139 | hp1 | a0006 | c0006 | t0009 | g0004 | AFR | ESN | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG03139 | hp2 | a0008 | c0009 | t0017 | g0251 | AFR | ESN | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | ESN | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG03195 | hp2 | a0019 | c0023 | t0014 | g0031 | AFR | ESN | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG03209 | hp1 | a0012 | c0011 | t0010 | g0048 | AFR | MSL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | MSL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG03225 | hp1 | a0006 | c0031 | t0005 | g0036 | AFR | MSL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG03225 | hp2 | a0006 | c0006 | t0006 | g0004 | AFR | MSL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG03239 | hp1 | a0014 | c0019 | t0012 | g0268 | SAS | PJL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG03453 | hp1 | a0009 | c0035 | t0005 | g0038 | AFR | MSL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG03453 | hp2 | a0002 | c0002 | t0001 | g0034 | AFR | MSL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG03486 | hp1 | a0010 | c0034 | t0005 | g0178 | AFR | MSL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG03486 | hp2 | a0003 | c0003 | t0002 | g0122 | AFR | MSL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG03490 | hp1 | a0002 | c0002 | t0002 | g0032 | SAS | PJL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG03490 | hp2 | a0004 | c0004 | t0002 | g0008 | SAS | PJL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG03491 | hp1 | a0002 | c0002 | t0002 | g0186 | SAS | PJL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG03491 | hp2 | a0002 | c0002 | t0002 | g0184 | SAS | PJL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG03492 | hp1 | a0004 | c0004 | t0002 | g0008 | SAS | PJL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG03492 | hp2 | a0002 | c0002 | t0002 | g0247 | SAS | PJL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG03540 | hp1 | a0011 | c0010 | t0004 | g0035 | AFR | GWD | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG03540 | hp2 | a0008 | c0009 | t0008 | g0041 | AFR | GWD | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG03579 | hp1 | a0011 | c0010 | t0004 | g0033 | AFR | MSL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG03579 | hp2 | a0002 | c0002 | t0002 | g0278 | AFR | MSL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG03669 | hp1 | a0004 | c0004 | t0002 | g0134 | SAS | PJL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG03669 | hp2 | a0021 | c0025 | t0002 | g0021 | SAS | PJL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG03704 | hp1 | a0002 | c0002 | t0002 | g0229 | SAS | PJL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG03710 | hp1 | a0004 | c0004 | t0003 | g0135 | SAS | PJL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG03710 | hp2 | a0014 | c0019 | t0012 | g0267 | SAS | PJL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG03834 | hp1 | a0004 | c0004 | t0002 | g0136 | SAS | BEB | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG03834 | hp2 | a0002 | c0002 | t0007 | g0211 | SAS | BEB | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG03942 | hp1 | a0003 | c0003 | t0002 | g0181 | SAS | BEB | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG03942 | hp2 | a0002 | c0002 | t0002 | g0027 | SAS | BEB | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0079 | SAS | BEB | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG04184 | hp2 | a0018 | c0015 | t0003 | g0253 | SAS | BEB | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG04199 | hp1 | a0002 | c0002 | t0002 | g0185 | SAS | STU | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG04199 | hp2 | a0002 | c0002 | t0002 | g0242 | SAS | STU | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0054 | SAS | STU | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0269 | SAS | STU | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG04228 | hp2 | a0002 | c0002 | t0001 | g0192 | SAS | STU | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18522 | hp1 | a0010 | c0012 | t0004 | g0049 | AFR | YRI | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18522 | hp2 | a0016 | c0020 | t0011 | g0042 | AFR | YRI | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | CHB | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18747 | hp2 | a0004 | c0004 | t0003 | g0195 | EAS | CHB | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18906 | hp1 | a0013 | c0016 | t0006 | g0029 | AFR | YRI | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0274 | AFR | YRI | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18940 | hp1 | a0002 | c0002 | t0002 | g0248 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18945 | hp1 | a0007 | c0007 | t0001 | g0091 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18950 | hp1 | a0001 | c0001 | t0007 | g0061 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18954 | hp1 | a0003 | c0003 | t0002 | g0156 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18954 | hp2 | a0007 | c0007 | t0001 | g0189 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18956 | hp2 | a0001 | c0001 | t0007 | g0006 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18957 | hp1 | a0002 | c0002 | t0001 | g0221 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18957 | hp2 | a0003 | c0003 | t0002 | g0161 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18960 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18964 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18966 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18967 | hp1 | a0003 | c0003 | t0002 | g0160 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18973 | hp2 | a0002 | c0002 | t0001 | g0148 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18974 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18974 | hp2 | a0003 | c0003 | t0002 | g0144 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18975 | hp1 | a0004 | c0004 | t0003 | g0070 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18975 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18977 | hp2 | a0002 | c0002 | t0002 | g0196 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18979 | hp1 | a0003 | c0003 | t0002 | g0153 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18983 | hp1 | a0005 | c0005 | t0002 | g0057 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18983 | hp2 | a0005 | c0005 | t0002 | g0105 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18986 | hp1 | a0007 | c0007 | t0002 | g0022 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18987 | hp1 | a0002 | c0002 | t0001 | g0273 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18988 | hp1 | a0002 | c0002 | t0002 | g0217 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18988 | hp2 | a0003 | c0003 | t0002 | g0157 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18990 | hp1 | a0003 | c0003 | t0002 | g0149 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18990 | hp2 | a0001 | c0001 | t0007 | g0006 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18994 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18998 | hp1 | a0001 | c0001 | t0021 | g0098 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA18998 | hp2 | a0007 | c0007 | t0022 | g0025 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19001 | hp2 | a0002 | c0002 | t0002 | g0025 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19002 | hp1 | a0002 | c0002 | t0002 | g0209 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19002 | hp2 | a0032 | c0040 | t0001 | g0014 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19003 | hp1 | a0001 | c0001 | t0007 | g0063 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19003 | hp2 | a0007 | c0007 | t0002 | g0001 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19005 | hp1 | a0002 | c0002 | t0001 | g0138 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19005 | hp2 | a0004 | c0004 | t0003 | g0197 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19009 | hp1 | a0003 | c0003 | t0002 | g0245 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19011 | hp1 | a0018 | c0015 | t0003 | g0115 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19011 | hp2 | a0003 | c0003 | t0002 | g0158 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19012 | hp1 | a0007 | c0007 | t0002 | g0022 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19012 | hp2 | a0004 | c0004 | t0003 | g0066 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19030 | hp1 | a0003 | c0003 | t0001 | g0249 | AFR | LWK | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19030 | hp2 | a0008 | c0009 | t0008 | g0040 | AFR | LWK | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19043 | hp1 | a0022 | c0033 | t0004 | g0118 | AFR | LWK | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19043 | hp2 | a0006 | c0006 | t0009 | g0004 | AFR | LWK | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19056 | hp2 | a0002 | c0002 | t0001 | g0204 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19057 | hp1 | a0003 | c0003 | t0002 | g0155 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19057 | hp2 | a0002 | c0002 | t0002 | g0216 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19060 | hp1 | a0002 | c0002 | t0002 | g0223 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19060 | hp2 | a0005 | c0005 | t0002 | g0009 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19062 | hp1 | a0002 | c0002 | t0002 | g0194 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19062 | hp2 | a0004 | c0004 | t0003 | g0069 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19066 | hp1 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19066 | hp2 | a0001 | c0001 | t0007 | g0006 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19068 | hp2 | a0004 | c0004 | t0003 | g0200 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19077 | hp1 | a0007 | c0007 | t0016 | g0227 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19081 | hp1 | a0023 | c0026 | t0001 | g0246 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19084 | hp1 | a0001 | c0001 | t0007 | g0073 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19084 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19085 | hp1 | a0002 | c0002 | t0001 | g0139 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19085 | hp2 | a0007 | c0007 | t0002 | g0218 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19086 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19086 | hp2 | a0004 | c0004 | t0003 | g0199 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19090 | hp2 | a0002 | c0002 | t0001 | g0171 | EAS | JPT | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19240 | hp1 | a0006 | c0006 | t0009 | g0026 | AFR | YRI | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA19240 | hp2 | a0018 | c0015 | t0002 | g0120 | AFR | YRI | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA20129 | hp1 | a0009 | c0044 | t0005 | g0257 | AFR | ASW | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA20129 | hp2 | a0002 | c0002 | t0002 | g0203 | AFR | ASW | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA20805 | hp1 | a0015 | c0014 | t0001 | g0151 | EUR | TSI | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA20805 | hp2 | a0001 | c0008 | t0001 | g0266 | EUR | TSI | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02109 | hp1 | a0025 | c0029 | t0015 | g0123 | AFR | ACB | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02109 | hp2 | a0002 | c0002 | t0002 | g0212 | AFR | ACB | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02486 | hp1 | a0026 | c0028 | t0005 | g0124 | AFR | ACB | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02486 | hp2 | a0003 | c0003 | t0002 | g0173 | AFR | ACB | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02559 | hp1 | a0006 | c0006 | t0006 | g0255 | AFR | ACB | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG02559 | hp2 | a0008 | c0009 | t0008 | g0007 | AFR | ACB | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG03471 | hp1 | a0006 | c0006 | t0009 | g0026 | AFR | MSL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | MSL | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG06807 | hp1 | a0001 | c0008 | t0025 | g0169 | AFR | USA | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
HG06807 | hp2 | a0006 | c0006 | t0006 | g0004 | AFR | USA | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | USA | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA20300 | hp2 | a0011 | c0010 | t0004 | g0046 | AFR | USA | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA21309 | hp1 | a0002 | c0013 | t0002 | g0024 | AFR | LWK | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
NA21309 | hp2 | a0014 | c0041 | t0005 | g0230 | AFR | LWK | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
homoSapiens_chm13v2 | hp1 | a0002 | c0013 | t0002 | g0226 | REF | REF | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
homoSapiens_grch38 | hp1 | a0002 | c0002 | t0001 | g0147 | REF | REF | IL4R_chr16_27308974_27369778 | IL4R | chr16 | 27308974 | 27369778 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:27330196
|
C | A | 1 | a0007 | 1 | NA19077.hp1 | splice_region_variant | LOW | c.-21C>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/11 | chr16 | 27330196 | ||||||
chr16:27342126
|
A | G | 1 | a0034 | 1 | HG02056.hp2 | missense_variant | MODERATE | c.76A>G | p.Met26Val | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 4/11 | 274/3624 | 76/2478 | 26/825 | chr16 | 27342126 | ||
chr16:27344882
|
A | G | 17 | a0001a0005a0009others(14): Show | 153 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(150): Show |
missense_variant | MODERATE | c.223A>G | p.Ile75Val | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 5/11 | 421/3624 | 223/2478 | 75/825 | chr16 | 27344882 | ||
chr16:27344903
|
G | A | 1 | a0007 | 8 | NA18945.hp1 NA18954.hp2 NA18986.hp1 others(5): Show |
missense_variant | MODERATE | c.244G>A | p.Ala82Thr | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 5/11 | 442/3624 | 244/2478 | 82/825 | chr16 | 27344903 | ||
chr16:27346548
|
C | A | 1 | a0021 | 1 | HG03669.hp2 | missense_variant | MODERATE | c.443C>A | p.Pro148His | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/11 | 641/3624 | 443/2478 | 148/825 | chr16 | 27346548 | ||
chr16:27346578
|
C | T | 1 | a0022 | 1 | NA19043.hp1 | missense_variant | MODERATE | c.473C>T | p.Thr158Ile | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/11 | 671/3624 | 473/2478 | 158/825 | chr16 | 27346578 | ||
chr16:27352580
|
G | A | 1 | a0028 | 1 | HG01952.hp2 | missense_variant | MODERATE | c.554G>A | p.Arg185His | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 7/11 | 752/3624 | 554/2478 | 185/825 | chr16 | 27352580 | ||
chr16:27352625
|
G | A | 1 | a0023 | 1 | NA19081.hp1 | missense_variant | MODERATE | c.599G>A | p.Arg200Gln | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 7/11 | 797/3624 | 599/2478 | 200/825 | chr16 | 27352625 | ||
chr16:27362433
|
T | C | 1 | a0027 | 1 | HG01070.hp1 | missense_variant | MODERATE | c.1081T>C | p.Cys361Arg | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 11/11 | 1279/3624 | 1081/2478 | 361/825 | chr16 | 27362433 | ||
chr16:27362452
|
C | A | 1 | a0026 | 1 | HG02486.hp1 | missense_variant | MODERATE | c.1100C>A | p.Ala367Asp | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 11/11 | 1298/3624 | 1100/2478 | 367/825 | chr16 | 27362452 | ||
chr16:27362496
|
G | A | 1 | a0033 | 1 | HG02809.hp2 | missense_variant | MODERATE | c.1144G>A | p.Gly382Arg | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 11/11 | 1342/3624 | 1144/2478 | 382/825 | chr16 | 27362496 | ||
chr16:27362551
|
A | C | 13 | a0003a0005a0006others(10): Show | 85 | HG00597.hp2 HG00639.hp2 HG00741.hp2 others(82): Show |
missense_variant | MODERATE | c.1199A>C | p.Glu400Ala | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 11/11 | 1397/3624 | 1199/2478 | 400/825 | chr16 | 27362551 | ||
chr16:27362643
|
T | C | 2 | a0003a0005 | 42 | HG00597.hp2 HG00639.hp2 HG01069.hp2 others(39): Show |
missense_variant | MODERATE | c.1291T>C | p.Cys431Arg | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 11/11 | 1489/3624 | 1291/2478 | 431/825 | chr16 | 27362643 | ||
chr16:27362659
|
C | T | 2 | a0012a0014 | 8 | HG02647.hp2 HG02738.hp1 HG02809.hp1 others(5): Show |
missense_variant | MODERATE | c.1307C>T | p.Ser436Leu | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 11/11 | 1505/3624 | 1307/2478 | 436/825 | chr16 | 27362659 | ||
chr16:27362826
|
G | A | 1 | a0016 | 3 | HG02055.hp1 HG02451.hp1 NA18522.hp2 |
missense_variant | MODERATE | c.1474G>A | p.Ala492Thr | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 11/11 | 1672/3624 | 1474/2478 | 492/825 | chr16 | 27362826 | ||
chr16:27362827
|
C | T | 1 | a0026 | 1 | HG02486.hp1 | missense_variant | MODERATE | c.1475C>T | p.Ala492Val | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 11/11 | 1673/3624 | 1475/2478 | 492/825 | chr16 | 27362827 | ||
chr16:27362859
|
T | C | 11 | a0003a0005a0006others(8): Show | 77 | HG00597.hp2 HG00639.hp2 HG00735.hp2 others(74): Show |
missense_variant | MODERATE | c.1507T>C | p.Ser503Pro | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 11/11 | 1705/3624 | 1507/2478 | 503/825 | chr16 | 27362859 | ||
chr16:27363079
|
A | G | 25 | a0003a0004a0005others(22): Show | 131 | HG00408.hp1 HG00597.hp2 HG00639.hp2 others(128): Show |
missense_variant | MODERATE | c.1727A>G | p.Gln576Arg | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 11/11 | 1925/3624 | 1727/2478 | 576/825 | chr16 | 27363079 | ||
chr16:27363087
|
G | A | 4 | a0016a0017a0024others(1): Show | 8 | HG00741.hp2 HG02055.hp1 HG02109.hp1 others(5): Show |
missense_variant | MODERATE | c.1735G>A | p.Val579Ile | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 11/11 | 1933/3624 | 1735/2478 | 579/825 | chr16 | 27363087 | ||
chr16:27363126
|
G | T | 1 | a0025 | 1 | HG02109.hp1 | missense_variant | MODERATE | c.1774G>T | p.Val592Leu | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 11/11 | 1972/3624 | 1774/2478 | 592/825 | chr16 | 27363126 | ||
chr16:27363375
|
C | T | 1 | a0015 | 3 | HG00738.hp1 HG01515.hp2 NA20805.hp1 |
missense_variant | MODERATE | c.2023C>T | p.Pro675Ser | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 11/11 | 2221/3624 | 2023/2478 | 675/825 | chr16 | 27363375 | ||
chr16:27363601
|
A | G | 1 | a0032 | 1 | NA19002.hp2 | missense_variant | MODERATE | c.2249A>G | p.Asp750Gly | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 11/11 | 2447/3624 | 2249/2478 | 750/825 | chr16 | 27363601 | ||
chr16:27363606
|
T | G | 13 | a0008a0010a0011others(10): Show | 42 | HG00735.hp2 HG00741.hp2 HG01109.hp2 others(39): Show |
missense_variant | MODERATE | c.2254T>G | p.Ser752Ala | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 11/11 | 2452/3624 | 2254/2478 | 752/825 | chr16 | 27363606 | ||
chr16:27363708
|
T | C | 2 | a0019a0030 | 3 | HG00735.hp2 HG02145.hp1 HG03195.hp2 |
missense_variant | MODERATE | c.2356T>C | p.Ser786Pro | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 11/11 | 2554/3624 | 2356/2478 | 786/825 | chr16 | 27363708 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:27342158
|
C | T | 1 | a0002c0013 | 4 | HG01168.hp1 HG01169.hp2 NA21309.hp1 others(1): Show |
synonymous_variant | LOW | c.108C>T | p.Ser36Ser | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 4/11 | 306/3624 | 108/2478 | 36/825 | chr16 | 27342158 | ||
chr16:27342257
|
C | T | 1 | a0008c0047 | 1 | HG02622.hp1 | splice_region_variant&synonymous_variant | LOW | c.207C>T | p.Ser69Ser | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 4/11 | 405/3624 | 207/2478 | 69/825 | chr16 | 27342257 | ||
chr16:27344896
|
C | T | 1 | a0009c0046 | 1 | HG02258.hp1 | synonymous_variant | LOW | c.237C>T | p.Asn79Asn | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 5/11 | 435/3624 | 237/2478 | 79/825 | chr16 | 27344896 | ||
chr16:27344950
|
T | C | 5 | a0009c0035a0009c0037a0009c0046others(2): Show | 5 | HG02145.hp2 HG02258.hp1 HG03098.hp1 others(2): Show |
synonymous_variant | LOW | c.291T>C | p.Asp97Asp | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 5/11 | 489/3624 | 291/2478 | 97/825 | chr16 | 27344950 | ||
chr16:27346606
|
C | T | 5 | a0001c0008a0010c0024a0014c0019others(2): Show | 15 | HG00642.hp2 HG00735.hp2 HG01106.hp2 others(12): Show |
synonymous_variant | LOW | c.501C>T | p.Asn167Asn | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/11 | 699/3624 | 501/2478 | 167/825 | chr16 | 27346606 | ||
chr16:27352623
|
A | C | 2 | a0009c0037a0031c0036 | 2 | HG02145.hp2 HG03098.hp1 |
synonymous_variant | LOW | c.597A>C | p.Ala199Ala | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 7/11 | 795/3624 | 597/2478 | 199/825 | chr16 | 27352623 | ||
chr16:27355905
|
C | G | 3 | a0005c0022a0016c0032a0017c0018 | 6 | HG00741.hp2 HG02451.hp1 HG02818.hp1 others(3): Show |
splice_region_variant&synonymous_variant | LOW | c.768C>G | p.Thr256Thr | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/11 | 966/3624 | 768/2478 | 256/825 | chr16 | 27355905 | ||
chr16:27362594
|
G | T | 22 | a0003c0003a0005c0005a0005c0022others(19): Show | 85 | HG00597.hp2 HG00639.hp2 HG00741.hp2 others(82): Show |
synonymous_variant | LOW | c.1242G>T | p.Leu414Leu | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 11/11 | 1440/3624 | 1242/2478 | 414/825 | chr16 | 27362594 | ||
chr16:27362645
|
C | T | 11 | a0006c0031a0009c0035a0009c0044others(8): Show | 13 | HG00735.hp2 HG02055.hp1 HG02109.hp1 others(10): Show |
synonymous_variant | LOW | c.1293C>T | p.Cys431Cys | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 11/11 | 1491/3624 | 1293/2478 | 431/825 | chr16 | 27362645 | ||
chr16:27362651
|
T | C | 29 | a0003c0003a0005c0005a0005c0022others(26): Show | 94 | HG00597.hp2 HG00639.hp2 HG00735.hp2 others(91): Show |
synonymous_variant | LOW | c.1299T>C | p.Leu433Leu | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 11/11 | 1497/3624 | 1299/2478 | 433/825 | chr16 | 27362651 | ||
chr16:27363095
|
G | A | 1 | a0025c0029 | 1 | HG02109.hp1 | synonymous_variant | LOW | c.1743G>A | p.Ala581Ala | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 11/11 | 1941/3624 | 1743/2478 | 581/825 | chr16 | 27363095 | ||
chr16:27363704
|
C | T | 1 | a0013c0016 | 3 | HG01109.hp2 HG02895.hp2 NA18906.hp1 |
synonymous_variant | LOW | c.2352C>T | p.Gly784Gly | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 11/11 | 2550/3624 | 2352/2478 | 784/825 | chr16 | 27363704 | ||
chr16:27363749
|
T | C | 3 | a0006c0006a0025c0029a0031c0036 | 12 | HG02109.hp1 HG02145.hp2 HG02559.hp1 others(9): Show |
synonymous_variant | LOW | c.2397T>C | p.Pro799Pro | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 11/11 | 2595/3624 | 2397/2478 | 799/825 | chr16 | 27363749 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:27313979
|
C | T | 2 | a0001c0008t0025a0030c0045t0024 | 2 | HG00735.hp2 HG06807.hp1 |
5_prime_UTR_variant | MODIFIER | c.-193C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/11 | 26225 | chr16 | 27313979 | |||||
chr16:27363836
|
T | C | 12 | a0004c0004t0003a0008c0009t0008a0008c0009t0017others(9): Show | 36 | HG00408.hp1 HG01070.hp1 HG01952.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*6T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 11/11 | 6 | chr16 | 27363836 | |||||
chr16:27363838
|
T | C | 12 | a0006c0006t0006a0006c0006t0009a0008c0009t0008others(9): Show | 27 | HG00735.hp2 HG01109.hp2 HG01243.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*8T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 11/11 | 8 | chr16 | 27363838 | |||||
chr16:27363879
|
C | T | 1 | a0009c0017t0013 | 3 | HG02572.hp2 HG02615.hp1 HG02965.hp1 |
3_prime_UTR_variant | MODIFIER | c.*49C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 11/11 | 49 | chr16 | 27363879 | |||||
chr16:27363918
|
C | G | 2 | a0012c0011t0010a0014c0019t0012 | 7 | HG02647.hp2 HG02738.hp1 HG02809.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*88C>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 11/11 | 88 | chr16 | 27363918 | |||||
chr16:27363954
|
T | A | 1 | a0008c0009t0017 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*124T>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 11/11 | 124 | chr16 | 27363954 | |||||
chr16:27364102
|
G | A | 2 | a0016c0020t0011a0016c0032t0011 | 3 | HG02055.hp1 HG02451.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*272G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 11/11 | 272 | chr16 | 27364102 | |||||
chr16:27364112
|
C | A | 1 | a0006c0006t0009 | 4 | HG03139.hp1 HG03471.hp1 NA19043.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*282C>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 11/11 | 282 | chr16 | 27364112 | |||||
chr16:27364129
|
G | C | 2 | a0001c0008t0019a0029c0043t0018 | 2 | HG01243.hp2 HG01891.hp2 |
3_prime_UTR_variant | MODIFIER | c.*299G>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 11/11 | 299 | chr16 | 27364129 | |||||
chr16:27364199
|
TGCCCACC others(20): Show |
T | 1 | a0017c0018t0023 | 1 | HG00741.hp2 | 3_prime_UTR_variant | MODIFIER | c.*377_*403delAGATCA others(21): Show |
IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 11/11 | 377 | INFO_REALIGN_3_PRIME | chr16 | 27364199 | ||||
chr16:27364221
|
G | A | 19 | a0001c0001t0002a0001c0008t0002a0001c0008t0025others(16): Show | 137 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(134): Show |
3_prime_UTR_variant | MODIFIER | c.*391G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 11/11 | 391 | chr16 | 27364221 | |||||
chr16:27364235
|
G | A | 1 | a0024c0030t0020 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*405G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 11/11 | 405 | chr16 | 27364235 | |||||
chr16:27364280
|
G | A | 1 | a0019c0023t0014 | 2 | HG02145.hp1 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*450G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 11/11 | 450 | chr16 | 27364280 | |||||
chr16:27364466
|
A | G | 21 | a0001c0001t0002a0001c0001t0007a0001c0008t0002others(18): Show | 146 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(143): Show |
3_prime_UTR_variant | MODIFIER | c.*636A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 11/11 | 636 | chr16 | 27364466 | |||||
chr16:27364561
|
T | C | 1 | a0001c0001t0021 | 1 | NA18998.hp1 | 3_prime_UTR_variant | MODIFIER | c.*731T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 11/11 | 731 | chr16 | 27364561 | |||||
chr16:27364568
|
C | T | 20 | a0006c0006t0006a0006c0006t0009a0006c0031t0005others(17): Show | 40 | HG00741.hp2 HG01109.hp2 HG02258.hp1 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*738C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 11/11 | 738 | chr16 | 27364568 | |||||
chr16:27364745
|
A | G | 1 | a0007c0007t0022 | 1 | NA18998.hp2 | 3_prime_UTR_variant | MODIFIER | c.*915A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 11/11 | 915 | chr16 | 27364745 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:27314101
|
C | T | 3 | a0010c0024t0004g0281a0013c0016t0006g0029a0013c0016t0006g0282 | 4 | HG01109.hp2 HG02895.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-152+81C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27314101 | ||||||
chr16:27314105
|
C | T | 1 | a0017c0018t0005g0280 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-152+85C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27314105 | ||||||
chr16:27314194
|
C | T | 5 | a0001c0001t0001g0277a0002c0002t0002g0278a0009c0017t0013g0276others(2): Show | 5 | HG02615.hp1 HG02717.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-152+174C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27314194 | ||||||
chr16:27314200
|
C | T | 1 | a0001c0001t0001g0274 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-152+180C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27314200 | ||||||
chr16:27314313
|
G | A | 2 | a0019c0023t0014g0030a0019c0023t0014g0031 | 2 | HG02145.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-152+293G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27314313 | ||||||
chr16:27314339
|
G | GC | 5 | a0002c0002t0001g0034a0002c0002t0002g0032a0006c0031t0005g0036others(2): Show | 5 | HG03225.hp1 HG03453.hp2 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.-152+323dupC | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 27314339 | |||||
chr16:27314446
|
T | C | 8 | a0008c0009t0008g0007a0008c0009t0008g0040a0008c0009t0008g0041others(5): Show | 9 | HG02258.hp1 HG02451.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.-152+426T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27314446 | ||||||
chr16:27314452
|
A | G | 1 | a0002c0002t0001g0273 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-152+432A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27314452 | ||||||
chr16:27314534
|
G | C | 1 | a0004c0004t0002g0008 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-152+514G>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27314534 | ||||||
chr16:27314610
|
C | G | 1 | a0001c0008t0002g0272 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-152+590C>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27314610 | ||||||
chr16:27314662
|
G | C | 1 | a0003c0003t0002g0044 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-152+642G>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27314662 | ||||||
chr16:27314885
|
A | C | 15 | a0001c0001t0001g0263a0001c0001t0001g0269a0001c0001t0002g0265others(12): Show | 16 | HG01081.hp1 HG01099.hp1 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.-152+865A>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27314885 | ||||||
chr16:27314947
|
G | T | 141 | a0001c0001t0001g0191a0001c0001t0001g0258a0001c0001t0001g0263others(138): Show | 165 | HG00280.hp2 HG00438.hp2 HG00642.hp1 others(162): Show |
intron_variant | MODIFIER | c.-152+927G>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27314947 | ||||||
chr16:27314958
|
G | C | 2 | a0001c0008t0025g0169a0030c0045t0024g0170 | 2 | HG00735.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-152+938G>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27314958 | ||||||
chr16:27315448
|
G | A | 1 | a0002c0002t0001g0171 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-152+1428G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27315448 | ||||||
chr16:27315479
|
G | A | 1 | a0001c0008t0025g0169 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-152+1459G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27315479 | ||||||
chr16:27315521
|
T | G | 154 | a0001c0001t0001g0191a0001c0001t0001g0263a0001c0001t0001g0269others(151): Show | 179 | HG00280.hp2 HG00438.hp2 HG00642.hp1 others(176): Show |
intron_variant | MODIFIER | c.-152+1501T>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27315521 | ||||||
chr16:27315542
|
C | T | 4 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0167others(1): Show | 4 | NA18940.hp2 NA18964.hp1 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.-152+1522C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27315542 | ||||||
chr16:27315592
|
G | C | 2 | a0001c0001t0001g0052a0001c0001t0001g0053 | 2 | HG02258.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-152+1572G>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27315592 | ||||||
chr16:27315612
|
G | C | 1 | a0029c0043t0018g0045 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-152+1592G>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27315612 | ||||||
chr16:27315743
|
C | G | 1 | a0002c0002t0001g0256 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-152+1723C>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27315743 | ||||||
chr16:27315795
|
A | G | 99 | a0001c0001t0001g0191a0001c0001t0002g0187a0001c0001t0007g0006others(96): Show | 119 | HG00280.hp2 HG00438.hp2 HG00642.hp1 others(116): Show |
intron_variant | MODIFIER | c.-152+1775A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27315795 | ||||||
chr16:27315871
|
A | G | 8 | a0008c0009t0008g0007a0008c0009t0008g0040a0008c0009t0008g0041others(5): Show | 9 | HG02258.hp1 HG02451.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.-152+1851A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27315871 | ||||||
chr16:27315880
|
G | A | 2 | a0002c0002t0002g0182a0002c0002t0002g0183 | 2 | HG00741.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.-152+1860G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27315880 | ||||||
chr16:27315893
|
T | G | 152 | a0001c0001t0001g0191a0001c0001t0001g0263a0001c0001t0001g0269others(149): Show | 177 | HG00280.hp2 HG00438.hp2 HG00642.hp1 others(174): Show |
intron_variant | MODIFIER | c.-152+1873T>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27315893 | ||||||
chr16:27315914
|
G | C | 2 | a0002c0002t0002g0184a0002c0002t0002g0185 | 2 | HG03491.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.-152+1894G>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27315914 | ||||||
chr16:27315938
|
T | C | 2 | a0009c0035t0005g0038a0009c0046t0005g0037 | 2 | HG02258.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-152+1918T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27315938 | ||||||
chr16:27315994
|
G | A | 1 | a0001c0001t0001g0054 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-152+1974G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27315994 | ||||||
chr16:27316096
|
G | A | 2 | a0005c0005t0001g0259a0005c0005t0001g0260 | 2 | HG01081.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.-152+2076G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27316096 | ||||||
chr16:27316300
|
G | A | 1 | a0010c0024t0005g0172 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-152+2280G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27316300 | ||||||
chr16:27316424
|
A | G | 1 | a0006c0006t0006g0255 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-152+2404A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27316424 | ||||||
chr16:27316624
|
A | G | 1 | a0001c0001t0007g0164 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-152+2604A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27316624 | ||||||
chr16:27316633
|
C | A | 1 | a0003c0003t0002g0173 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-152+2613C>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27316633 | ||||||
chr16:27316683
|
C | T | 1 | a0002c0002t0002g0254 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-152+2663C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27316683 | ||||||
chr16:27316851
|
C | A | 4 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0055others(1): Show | 4 | HG02258.hp2 HG02615.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-152+2831C>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27316851 | ||||||
chr16:27316906
|
C | CTT | 143 | a0001c0001t0001g0191a0001c0001t0001g0263a0001c0001t0001g0269others(140): Show | 168 | HG00280.hp2 HG00438.hp2 HG00642.hp1 others(165): Show |
intron_variant | MODIFIER | c.-152+2899_-152+290 others(6): Show |
IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 27316906 | |||||
chr16:27316967
|
A | G | 1 | a0003c0003t0002g0163 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-152+2947A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27316967 | ||||||
chr16:27317045
|
AGGTGTGT others(9): Show |
A | 1 | a0001c0008t0019g0261 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-152+3027_-152+304 others(20): Show |
IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 27317045 | |||||
chr16:27317222
|
C | T | 39 | a0001c0001t0001g0263a0001c0001t0001g0269a0001c0001t0001g0277others(36): Show | 42 | HG00735.hp2 HG01081.hp1 HG01099.hp1 others(39): Show |
intron_variant | MODIFIER | c.-152+3202C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27317222 | ||||||
chr16:27317228
|
C | T | 8 | a0008c0009t0008g0007a0008c0009t0008g0040a0008c0009t0008g0041others(5): Show | 9 | HG02258.hp1 HG02451.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.-152+3208C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27317228 | ||||||
chr16:27317502
|
G | A | 4 | a0001c0001t0002g0056a0005c0005t0002g0009a0005c0005t0002g0010others(1): Show | 6 | HG01069.hp2 HG01175.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.-152+3482G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27317502 | ||||||
chr16:27317551
|
C | T | 3 | a0010c0024t0004g0281a0013c0016t0006g0029a0013c0016t0006g0282 | 4 | HG01109.hp2 HG02895.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-152+3531C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27317551 | ||||||
chr16:27317552
|
G | A | 1 | a0002c0002t0002g0032 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-152+3532G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27317552 | ||||||
chr16:27317604
|
C | T | 1 | a0001c0001t0001g0162 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-152+3584C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27317604 | ||||||
chr16:27317625
|
A | G | 1 | a0003c0003t0002g0044 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-152+3605A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27317625 | ||||||
chr16:27317642
|
G | A | 2 | a0017c0018t0005g0175a0017c0018t0023g0174 | 2 | HG00741.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.-152+3622G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27317642 | ||||||
chr16:27317682
|
G | C | 3 | a0003c0003t0001g0058a0003c0003t0001g0059a0003c0003t0001g0060 | 3 | HG01074.hp2 HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-152+3662G>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27317682 | ||||||
chr16:27317732
|
C | T | 1 | a0012c0011t0010g0179 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-152+3712C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27317732 | ||||||
chr16:27317757
|
T | C | 5 | a0010c0024t0004g0281a0013c0016t0006g0029a0013c0016t0006g0282others(2): Show | 6 | HG00741.hp2 HG01109.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.-152+3737T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27317757 | ||||||
chr16:27317797
|
G | A | 256 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(253): Show | 296 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(293): Show |
intron_variant | MODIFIER | c.-152+3777G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27317797 | ||||||
chr16:27317812
|
A | G | 3 | a0004c0004t0002g0134a0004c0004t0002g0136a0004c0004t0003g0135 | 3 | HG03669.hp1 HG03710.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.-152+3792A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27317812 | ||||||
chr16:27318247
|
C | T | 1 | a0001c0001t0001g0133 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-152+4227C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27318247 | ||||||
chr16:27318307
|
ATGTC | A | 3 | a0002c0002t0001g0034a0011c0010t0004g0033a0011c0010t0004g0035 | 3 | HG03453.hp2 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-152+4290_-152+429 others(8): Show |
IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 27318307 | |||||
chr16:27318447
|
G | GAA | 103 | a0001c0001t0001g0191a0001c0001t0007g0006a0001c0001t0007g0238others(100): Show | 124 | HG00280.hp2 HG00438.hp2 HG00642.hp1 others(121): Show |
intron_variant | MODIFIER | c.-152+4428_-152+442 others(6): Show |
IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 27318447 | |||||
chr16:27318555
|
C | T | 4 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0055others(1): Show | 4 | HG02258.hp2 HG02615.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-152+4535C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27318555 | ||||||
chr16:27318638
|
C | T | 1 | a0001c0008t0019g0261 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-152+4618C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27318638 | ||||||
chr16:27318725
|
C | T | 1 | a0029c0043t0018g0045 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-152+4705C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27318725 | ||||||
chr16:27318863
|
G | A | 1 | a0003c0003t0002g0137 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-152+4843G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27318863 | ||||||
chr16:27319488
|
G | C | 3 | a0003c0003t0002g0173a0003c0003t0002g0181a0011c0010t0004g0180 | 3 | HG02486.hp2 HG02572.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-152+5468G>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27319488 | ||||||
chr16:27319573
|
C | T | 3 | a0010c0024t0004g0281a0013c0016t0006g0029a0013c0016t0006g0282 | 4 | HG01109.hp2 HG02895.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-152+5553C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27319573 | ||||||
chr16:27319613
|
A | T | 4 | a0001c0001t0001g0277a0002c0002t0002g0278a0009c0017t0013g0276others(1): Show | 4 | HG02615.hp1 HG02717.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-152+5593A>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27319613 | ||||||
chr16:27319616
|
A | G | 5 | a0010c0024t0004g0281a0013c0016t0006g0029a0013c0016t0006g0282others(2): Show | 6 | HG00741.hp2 HG01109.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.-152+5596A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27319616 | ||||||
chr16:27319709
|
G | A | 88 | a0001c0001t0001g0191a0001c0001t0007g0006a0001c0001t0007g0238others(85): Show | 108 | HG00280.hp2 HG00438.hp2 HG00642.hp1 others(105): Show |
intron_variant | MODIFIER | c.-152+5689G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27319709 | ||||||
chr16:27319846
|
C | T | 3 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132 | 3 | HG02040.hp2 NA19081.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.-152+5826C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27319846 | ||||||
chr16:27319926
|
A | G | 2 | a0002c0002t0002g0278a0013c0042t0008g0279 | 2 | HG02717.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-152+5906A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27319926 | ||||||
chr16:27320175
|
G | A | 2 | a0002c0002t0002g0184a0002c0002t0002g0185 | 2 | HG03491.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.-152+6155G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27320175 | ||||||
chr16:27320393
|
C | T | 2 | a0009c0037t0002g0050a0031c0036t0015g0051 | 2 | HG02145.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-152+6373C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27320393 | ||||||
chr16:27320476
|
C | G | 1 | a0002c0002t0002g0248 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-152+6456C>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27320476 | ||||||
chr16:27320573
|
A | G | 154 | a0001c0001t0001g0191a0001c0001t0001g0263a0001c0001t0001g0269others(151): Show | 179 | HG00280.hp2 HG00438.hp2 HG00639.hp2 others(176): Show |
intron_variant | MODIFIER | c.-152+6553A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27320573 | ||||||
chr16:27320593
|
T | G | 2 | a0012c0011t0010g0019a0012c0011t0010g0179 | 3 | HG02647.hp2 HG02809.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.-152+6573T>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27320593 | ||||||
chr16:27320653
|
C | G | 154 | a0001c0001t0001g0191a0001c0001t0001g0263a0001c0001t0001g0269others(151): Show | 179 | HG00280.hp2 HG00438.hp2 HG00639.hp2 others(176): Show |
intron_variant | MODIFIER | c.-152+6633C>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27320653 | ||||||
chr16:27320676
|
C | T | 1 | a0006c0006t0006g0255 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-152+6656C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27320676 | ||||||
chr16:27320852
|
T | C | 1 | a0002c0002t0002g0188 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-152+6832T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27320852 | ||||||
chr16:27320948
|
C | CT | 117 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(114): Show | 139 | HG00280.hp2 HG00438.hp2 HG00639.hp2 others(136): Show |
intron_variant | MODIFIER | c.-152+6941dupT | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 27320948 | |||||
chr16:27321005
|
G | A | 1 | a0009c0037t0002g0050 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-152+6985G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27321005 | ||||||
chr16:27321013
|
A | G | 154 | a0001c0001t0001g0191a0001c0001t0001g0263a0001c0001t0001g0269others(151): Show | 179 | HG00280.hp2 HG00438.hp2 HG00639.hp2 others(176): Show |
intron_variant | MODIFIER | c.-152+6993A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27321013 | ||||||
chr16:27321175
|
C | A | 1 | a0010c0024t0004g0281 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-152+7155C>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27321175 | ||||||
chr16:27321186
|
C | T | 3 | a0002c0002t0002g0027a0002c0002t0002g0186a0002c0002t0002g0247 | 4 | HG03017.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.-152+7166C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27321186 | ||||||
chr16:27321190
|
C | T | 2 | a0002c0002t0001g0128a0003c0003t0001g0127 | 2 | HG02451.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-152+7170C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27321190 | ||||||
chr16:27321290
|
T | G | 2 | a0019c0023t0014g0030a0019c0023t0014g0031 | 2 | HG02145.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-152+7270T>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27321290 | ||||||
chr16:27321337
|
T | C | 3 | a0001c0001t0002g0062a0001c0001t0007g0061a0001c0001t0007g0063 | 3 | NA18950.hp1 NA19003.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.-152+7317T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27321337 | ||||||
chr16:27321820
|
A | C | 1 | a0034c0048t0001g0126 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-152+7800A>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27321820 | ||||||
chr16:27322060
|
A | C | 24 | a0001c0001t0001g0263a0001c0001t0001g0269a0001c0001t0001g0277others(21): Show | 26 | HG01081.hp1 HG01099.hp1 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.-151-8006A>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27322060 | ||||||
chr16:27322086
|
T | C | 6 | a0001c0001t0001g0277a0002c0002t0002g0278a0009c0017t0013g0276others(3): Show | 6 | HG02615.hp1 HG02717.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-151-7980T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27322086 | ||||||
chr16:27322103
|
G | GT | 129 | a0001c0001t0001g0162a0001c0001t0001g0263a0001c0001t0001g0269others(126): Show | 152 | HG00140.hp2 HG00280.hp2 HG00639.hp2 others(149): Show |
intron_variant | MODIFIER | c.-151-7950dupT | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 27322103 | |||||
chr16:27322103
|
G | GTT | 19 | a0001c0001t0001g0277a0002c0002t0002g0244a0002c0002t0002g0278others(16): Show | 20 | HG00438.hp2 HG00741.hp2 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.-151-7951_-151-795 others(6): Show |
IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 27322103 | |||||
chr16:27322212
|
T | G | 2 | a0008c0009t0008g0040a0008c0047t0008g0039 | 2 | HG02622.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-151-7854T>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27322212 | ||||||
chr16:27322333
|
C | T | 3 | a0002c0002t0002g0241a0002c0002t0002g0242a0002c0002t0002g0243 | 3 | HG00280.hp2 HG01109.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.-151-7733C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27322333 | ||||||
chr16:27322334
|
G | A | 2 | a0019c0023t0014g0030a0019c0023t0014g0031 | 2 | HG02145.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-151-7732G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27322334 | ||||||
chr16:27322343
|
A | C | 1 | a0016c0020t0011g0240 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-151-7723A>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27322343 | ||||||
chr16:27322618
|
G | A | 1 | a0001c0001t0001g0064 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-151-7448G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27322618 | ||||||
chr16:27322702
|
A | G | 1 | a0017c0018t0005g0175 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-151-7364A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27322702 | ||||||
chr16:27322750
|
A | C | 3 | a0010c0012t0004g0049a0012c0011t0010g0048a0029c0043t0018g0045 | 3 | HG01243.hp2 HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-151-7316A>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27322750 | ||||||
chr16:27322852
|
A | C | 4 | a0009c0017t0013g0176a0009c0017t0013g0177a0011c0010t0004g0046others(1): Show | 4 | HG02572.hp2 HG02965.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-151-7214A>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27322852 | ||||||
chr16:27322927
|
C | T | 1 | a0020c0021t0001g0015 | 2 | HG02717.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-151-7139C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27322927 | ||||||
chr16:27322968
|
A | C | 2 | a0010c0012t0004g0049a0012c0011t0010g0048 | 2 | HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-151-7098A>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27322968 | ||||||
chr16:27323084
|
C | T | 3 | a0003c0003t0002g0173a0003c0003t0002g0181a0011c0010t0004g0180 | 3 | HG02486.hp2 HG02572.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-151-6982C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27323084 | ||||||
chr16:27323209
|
C | T | 1 | a0002c0002t0002g0239 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-151-6857C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27323209 | ||||||
chr16:27323249
|
A | G | 2 | a0001c0001t0007g0006a0001c0001t0007g0238 | 4 | HG00673.hp1 NA18956.hp2 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.-151-6817A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27323249 | ||||||
chr16:27323309
|
C | A | 1 | a0029c0043t0018g0045 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-151-6757C>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27323309 | ||||||
chr16:27323386
|
C | T | 1 | a0024c0030t0020g0237 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-151-6680C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27323386 | ||||||
chr16:27323414
|
AAG | A | 8 | a0008c0009t0008g0007a0008c0009t0008g0040a0008c0009t0008g0041others(5): Show | 9 | HG02258.hp1 HG02451.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.-151-6649_-151-664 others(6): Show |
IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 27323414 | |||||
chr16:27323457
|
C | T | 2 | a0003c0003t0002g0160a0003c0003t0002g0161 | 2 | NA18957.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.-151-6609C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27323457 | ||||||
chr16:27323642
|
G | C | 2 | a0002c0002t0002g0021a0021c0025t0002g0021 | 2 | HG00735.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.-151-6424G>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27323642 | ||||||
chr16:27323681
|
G | C | 20 | a0001c0001t0001g0263a0001c0001t0001g0269a0001c0001t0002g0265others(17): Show | 22 | HG01081.hp1 HG01099.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.-151-6385G>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27323681 | ||||||
chr16:27323690
|
C | T | 11 | a0002c0002t0001g0235a0003c0003t0002g0234a0004c0004t0002g0232others(8): Show | 14 | HG01496.hp2 HG01884.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.-151-6376C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27323690 | ||||||
chr16:27323801
|
A | G | 1 | a0008c0009t0008g0040 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-151-6265A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27323801 | ||||||
chr16:27323847
|
C | T | 1 | a0002c0002t0002g0231 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-151-6219C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27323847 | ||||||
chr16:27323951
|
G | A | 2 | a0010c0012t0004g0011a0010c0012t0004g0065 | 3 | HG02922.hp2 HG02965.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-151-6115G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27323951 | ||||||
chr16:27324277
|
T | TG | 111 | a0001c0001t0001g0191a0001c0001t0007g0006a0001c0001t0007g0238others(108): Show | 133 | HG00280.hp2 HG00438.hp2 HG00639.hp2 others(130): Show |
intron_variant | MODIFIER | c.-151-5787dupG | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 27324277 | |||||
chr16:27324316
|
C | T | 1 | a0002c0002t0001g0192 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-151-5750C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27324316 | ||||||
chr16:27324357
|
G | A | 1 | a0010c0024t0004g0281 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-151-5709G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27324357 | ||||||
chr16:27324801
|
G | A | 4 | a0009c0017t0013g0176a0009c0017t0013g0177a0009c0037t0002g0050others(1): Show | 4 | HG02145.hp2 HG02572.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-151-5265G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27324801 | ||||||
chr16:27324841
|
G | A | 3 | a0010c0024t0004g0281a0013c0016t0006g0029a0013c0016t0006g0282 | 4 | HG01109.hp2 HG02895.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-151-5225G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27324841 | ||||||
chr16:27325106
|
G | A | 118 | a0001c0001t0001g0191a0001c0001t0001g0277a0001c0001t0007g0006others(115): Show | 139 | HG00280.hp2 HG00438.hp2 HG00639.hp2 others(136): Show |
intron_variant | MODIFIER | c.-151-4960G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27325106 | ||||||
chr16:27325116
|
C | T | 135 | a0001c0001t0001g0191a0001c0001t0001g0277a0001c0001t0007g0006others(132): Show | 158 | HG00280.hp2 HG00438.hp2 HG00639.hp2 others(155): Show |
intron_variant | MODIFIER | c.-151-4950C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27325116 | ||||||
chr16:27325232
|
G | A | 1 | a0029c0043t0018g0045 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-151-4834G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27325232 | ||||||
chr16:27325241
|
T | C | 5 | a0001c0001t0001g0067a0001c0001t0001g0068a0004c0004t0003g0066others(2): Show | 5 | NA18949.hp1 NA18975.hp1 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.-151-4825T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27325241 | ||||||
chr16:27325284
|
A | G | 2 | a0010c0012t0004g0049a0012c0011t0010g0048 | 2 | HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-151-4782A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27325284 | ||||||
chr16:27325312
|
C | T | 1 | a0001c0001t0001g0133 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-151-4754C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27325312 | ||||||
chr16:27325328
|
T | C | 1 | a0014c0041t0005g0230 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-151-4738T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27325328 | ||||||
chr16:27325407
|
G | A | 3 | a0010c0012t0004g0049a0012c0011t0010g0048a0029c0043t0018g0045 | 3 | HG01243.hp2 HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-151-4659G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27325407 | ||||||
chr16:27325417
|
C | CA | 7 | a0010c0012t0004g0049a0010c0024t0004g0281a0012c0011t0010g0048others(4): Show | 8 | HG01109.hp2 HG01243.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.-151-4642dupA | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 27325417 | |||||
chr16:27325573
|
CA | C | 14 | a0002c0002t0002g0228a0002c0002t0002g0229a0003c0003t0002g0044others(11): Show | 15 | HG00639.hp2 HG00741.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.-151-4480delA | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 27325573 | |||||
chr16:27325715
|
A | G | 1 | a0003c0003t0002g0129 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-151-4351A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27325715 | ||||||
chr16:27326274
|
T | C | 2 | a0017c0018t0005g0175a0017c0018t0023g0174 | 2 | HG00741.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.-151-3792T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27326274 | ||||||
chr16:27326329
|
A | G | 2 | a0010c0012t0004g0049a0012c0011t0010g0048 | 2 | HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-151-3737A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27326329 | ||||||
chr16:27326401
|
G | A | 20 | a0001c0001t0001g0071a0002c0002t0001g0204a0002c0002t0001g0207others(17): Show | 22 | HG00438.hp2 HG01070.hp1 HG01358.hp1 others(19): Show |
intron_variant | MODIFIER | c.-151-3665G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27326401 | ||||||
chr16:27326527
|
A | G | 1 | a0014c0041t0005g0230 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-151-3539A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27326527 | ||||||
chr16:27326594
|
A | G | 1 | a0003c0003t0002g0044 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-151-3472A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27326594 | ||||||
chr16:27326615
|
G | A | 18 | a0001c0001t0001g0277a0002c0002t0002g0278a0003c0003t0002g0044others(15): Show | 19 | HG00741.hp2 HG01109.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.-151-3451G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27326615 | ||||||
chr16:27326647
|
G | T | 2 | a0011c0010t0004g0046a0011c0010t0004g0047 | 2 | HG03041.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-151-3419G>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27326647 | ||||||
chr16:27326648
|
A | C | 1 | a0001c0001t0001g0054 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-151-3418A>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27326648 | ||||||
chr16:27326648
|
A | T | 2 | a0011c0010t0004g0046a0011c0010t0004g0047 | 2 | HG03041.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-151-3418A>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27326648 | ||||||
chr16:27326649
|
G | A | 2 | a0011c0010t0004g0046a0011c0010t0004g0047 | 2 | HG03041.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-151-3417G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27326649 | ||||||
chr16:27326650
|
A | G | 2 | a0011c0010t0004g0046a0011c0010t0004g0047 | 2 | HG03041.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-151-3416A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27326650 | ||||||
chr16:27326728
|
C | A | 8 | a0002c0002t0001g0128a0003c0003t0001g0127a0008c0009t0008g0007others(5): Show | 9 | HG02451.hp1 HG02451.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.-151-3338C>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27326728 | ||||||
chr16:27326759
|
G | A | 2 | a0017c0018t0005g0175a0017c0018t0023g0174 | 2 | HG00741.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.-151-3307G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27326759 | ||||||
chr16:27326811
|
T | C | 2 | a0017c0018t0005g0175a0017c0018t0023g0174 | 2 | HG00741.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.-151-3255T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27326811 | ||||||
chr16:27327106
|
G | A | 2 | a0019c0023t0014g0030a0019c0023t0014g0031 | 2 | HG02145.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-151-2960G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27327106 | ||||||
chr16:27327125
|
C | T | 3 | a0003c0003t0002g0044a0017c0018t0005g0175a0017c0018t0023g0174 | 3 | HG00741.hp2 HG02818.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-151-2941C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27327125 | ||||||
chr16:27327309
|
C | T | 8 | a0002c0002t0001g0128a0003c0003t0001g0127a0008c0009t0008g0007others(5): Show | 9 | HG02451.hp1 HG02451.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.-151-2757C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27327309 | ||||||
chr16:27327316
|
T | C | 1 | a0029c0043t0018g0045 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-151-2750T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27327316 | ||||||
chr16:27327343
|
G | A | 2 | a0002c0002t0002g0208a0002c0002t0002g0228 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-151-2723G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27327343 | ||||||
chr16:27327429
|
A | T | 1 | a0001c0001t0001g0125 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-151-2637A>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27327429 | ||||||
chr16:27327444
|
A | C | 6 | a0008c0009t0008g0007a0008c0009t0008g0040a0008c0009t0008g0041others(3): Show | 7 | HG02451.hp1 HG02559.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-151-2622A>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27327444 | ||||||
chr16:27327508
|
G | A | 1 | a0002c0002t0001g0072 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-151-2558G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27327508 | ||||||
chr16:27327636
|
T | G | 2 | a0002c0002t0001g0138a0002c0002t0001g0139 | 2 | NA19005.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.-151-2430T>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27327636 | ||||||
chr16:27327703
|
T | C | 98 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(95): Show | 114 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.-151-2363T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27327703 | ||||||
chr16:27327706
|
T | C | 100 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(97): Show | 116 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(113): Show |
intron_variant | MODIFIER | c.-151-2360T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27327706 | ||||||
chr16:27327794
|
G | A | 3 | a0002c0002t0001g0034a0011c0010t0004g0033a0011c0010t0004g0035 | 3 | HG03453.hp2 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-151-2272G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27327794 | ||||||
chr16:27327799
|
G | A | 2 | a0017c0018t0005g0175a0017c0018t0023g0174 | 2 | HG00741.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.-151-2267G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27327799 | ||||||
chr16:27327824
|
T | C | 93 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(90): Show | 108 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(105): Show |
intron_variant | MODIFIER | c.-151-2242T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27327824 | ||||||
chr16:27327936
|
G | A | 2 | a0001c0001t0002g0012a0001c0001t0007g0073 | 3 | HG00621.hp1 HG00673.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.-151-2130G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27327936 | ||||||
chr16:27327968
|
A | G | 1 | a0018c0015t0002g0120 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-151-2098A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27327968 | ||||||
chr16:27327986
|
C | G | 2 | a0017c0018t0005g0175a0017c0018t0023g0174 | 2 | HG00741.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.-151-2080C>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27327986 | ||||||
chr16:27328136
|
C | T | 4 | a0003c0003t0002g0044a0011c0010t0004g0035a0017c0018t0005g0175others(1): Show | 4 | HG00741.hp2 HG02818.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-151-1930C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27328136 | ||||||
chr16:27328137
|
G | A | 1 | a0001c0001t0001g0074 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-151-1929G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27328137 | ||||||
chr16:27328190
|
A | G | 8 | a0002c0002t0001g0128a0003c0003t0001g0127a0008c0009t0008g0007others(5): Show | 9 | HG02451.hp1 HG02451.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.-151-1876A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27328190 | ||||||
chr16:27328194
|
A | G | 1 | a0010c0024t0005g0172 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-151-1872A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27328194 | ||||||
chr16:27328205
|
C | CAAAAAAA others(2): Show |
17 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0052others(14): Show | 21 | HG00408.hp2 HG00558.hp2 HG02040.hp2 others(18): Show |
intron_variant | MODIFIER | c.-151-1851_-151-184 others(13): Show |
IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 27328205 | |||||
chr16:27328205
|
C | CAAAAAAA others(3): Show |
59 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0054others(56): Show | 68 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(65): Show |
intron_variant | MODIFIER | c.-151-1852_-151-184 others(14): Show |
IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 27328205 | |||||
chr16:27328205
|
C | CAAAAAAA others(4): Show |
14 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(11): Show | 16 | HG00621.hp1 HG00621.hp2 HG00673.hp2 others(13): Show |
intron_variant | MODIFIER | c.-151-1853_-151-184 others(15): Show |
IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 27328205 | |||||
chr16:27328205
|
C | CAAAAAAA others(5): Show |
2 | a0001c0001t0001g0075a0001c0001t0007g0073 | 2 | HG01346.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.-151-1854_-151-184 others(16): Show |
IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 27328205 | |||||
chr16:27328205
|
C | CAAAAAAA others(6): Show |
2 | a0017c0018t0005g0175a0017c0018t0023g0174 | 2 | HG00741.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.-151-1855_-151-184 others(17): Show |
IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 27328205 | |||||
chr16:27328205
|
C | CAAAAAAA others(8): Show |
3 | a0003c0003t0002g0044a0009c0037t0002g0050a0031c0036t0015g0051 | 3 | HG02145.hp2 HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-151-1857_-151-184 others(19): Show |
IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 27328205 | |||||
chr16:27328205
|
CAA | C | 9 | a0001c0001t0001g0277a0002c0002t0002g0278a0009c0017t0013g0176others(6): Show | 9 | HG02572.hp2 HG02615.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.-151-1844_-151-184 others(6): Show |
IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 27328205 | |||||
chr16:27328224
|
G | A | 20 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0052others(17): Show | 24 | HG00408.hp2 HG00558.hp2 HG02040.hp2 others(21): Show |
intron_variant | MODIFIER | c.-151-1842G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27328224 | ||||||
chr16:27328253
|
T | C | 2 | a0017c0018t0005g0175a0017c0018t0023g0174 | 2 | HG00741.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.-151-1813T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27328253 | ||||||
chr16:27328347
|
G | A | 1 | a0002c0002t0002g0188 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-151-1719G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27328347 | ||||||
chr16:27328348
|
A | G | 1 | a0001c0001t0001g0093 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-151-1718A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27328348 | ||||||
chr16:27328412
|
C | T | 1 | a0003c0003t0002g0161 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-151-1654C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27328412 | ||||||
chr16:27328441
|
T | G | 152 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(149): Show | 172 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.-151-1625T>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27328441 | ||||||
chr16:27328652
|
G | C | 2 | a0007c0007t0001g0189a0007c0007t0002g0022 | 3 | NA18954.hp2 NA18986.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.-151-1414G>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27328652 | ||||||
chr16:27328943
|
A | G | 2 | a0001c0001t0001g0013a0001c0001t0001g0092 | 3 | HG02280.hp2 HG02976.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-151-1123A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27328943 | ||||||
chr16:27328982
|
C | T | 1 | a0002c0002t0002g0243 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-151-1084C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27328982 | ||||||
chr16:27329043
|
G | A | 2 | a0002c0002t0001g0072a0002c0002t0001g0077 | 2 | HG00609.hp1 HG00621.hp2 |
intron_variant | MODIFIER | c.-151-1023G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27329043 | ||||||
chr16:27329054
|
C | T | 3 | a0010c0012t0004g0011a0010c0012t0004g0049a0010c0012t0004g0065 | 4 | HG02922.hp2 HG02965.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-151-1012C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27329054 | ||||||
chr16:27329349
|
T | G | 2 | a0009c0037t0002g0050a0031c0036t0015g0051 | 2 | HG02145.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-151-717T>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27329349 | ||||||
chr16:27329414
|
T | C | 106 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(103): Show | 123 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(120): Show |
intron_variant | MODIFIER | c.-151-652T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27329414 | ||||||
chr16:27329633
|
C | G | 1 | a0010c0034t0005g0178 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-151-433C>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27329633 | ||||||
chr16:27329676
|
C | CA | 91 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0014others(88): Show | 106 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(103): Show |
intron_variant | MODIFIER | c.-151-373dupA | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 27329676 | |||||
chr16:27329676
|
C | CAA | 9 | a0001c0001t0001g0013a0001c0001t0001g0052a0001c0001t0001g0053others(6): Show | 10 | HG02258.hp2 HG02280.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.-151-374_-151-373d others(4): Show |
IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 27329676 | |||||
chr16:27329676
|
CA | C | 32 | a0001c0001t0001g0263a0001c0001t0001g0269a0001c0001t0001g0277others(29): Show | 35 | HG00639.hp1 HG01081.hp1 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.-151-373delA | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 27329676 | |||||
chr16:27329738
|
A | G | 97 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(94): Show | 112 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.-151-328A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27329738 | ||||||
chr16:27329833
|
C | A | 1 | a0003c0003t0002g0173 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-151-233C>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27329833 | ||||||
chr16:27329836
|
T | C | 1 | a0010c0034t0005g0178 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-151-230T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27329836 | ||||||
chr16:27329869
|
TG | T | 3 | a0001c0001t0001g0064a0001c0001t0001g0095a0028c0038t0001g0140 | 3 | HG01952.hp2 HG02698.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.-151-196delG | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27329869 | ||||||
chr16:27329899
|
T | A | 1 | a0006c0006t0006g0210 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-151-167T>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27329899 | ||||||
chr16:27330021
|
T | C | 6 | a0001c0001t0001g0277a0009c0017t0013g0176a0009c0017t0013g0177others(3): Show | 6 | HG02572.hp2 HG02615.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-151-45T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27330021 | ||||||
chr16:27330027
|
C | A | 1 | a0006c0006t0006g0255 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-151-39C>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 1/10 | chr16 | 27330027 | ||||||
chr16:27330214
|
C | T | 3 | a0017c0018t0005g0175a0017c0018t0023g0174a0020c0021t0001g0015 | 4 | HG00741.hp2 HG02717.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+16C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27330214 | ||||||
chr16:27330232
|
T | C | 112 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(109): Show | 129 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.-19+34T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27330232 | ||||||
chr16:27330280
|
G | C | 1 | a0003c0003t0002g0044 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-19+82G>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27330280 | ||||||
chr16:27330386
|
C | CA | 130 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(127): Show | 148 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.-19+202dupA | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 27330386 | |||||
chr16:27330449
|
G | A | 1 | a0010c0034t0005g0178 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-19+251G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27330449 | ||||||
chr16:27330457
|
C | T | 2 | a0002c0002t0002g0184a0002c0002t0002g0185 | 2 | HG03491.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.-19+259C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27330457 | ||||||
chr16:27330497
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-19+299C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27330497 | ||||||
chr16:27330657
|
T | C | 3 | a0010c0024t0004g0281a0013c0016t0006g0029a0013c0016t0006g0282 | 4 | HG01109.hp2 HG02895.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+459T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27330657 | ||||||
chr16:27331055
|
CA | C | 19 | a0001c0001t0001g0263a0001c0001t0001g0269a0001c0001t0002g0265others(16): Show | 21 | HG01081.hp1 HG01099.hp1 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.-19+858delA | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27331055 | ||||||
chr16:27331058
|
A | G | 19 | a0001c0001t0001g0263a0001c0001t0001g0269a0001c0001t0002g0265others(16): Show | 21 | HG01081.hp1 HG01099.hp1 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.-19+860A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27331058 | ||||||
chr16:27331060
|
T | C | 19 | a0001c0001t0001g0263a0001c0001t0001g0269a0001c0001t0002g0265others(16): Show | 21 | HG01081.hp1 HG01099.hp1 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.-19+862T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27331060 | ||||||
chr16:27331087
|
C | T | 1 | a0010c0024t0005g0172 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-19+889C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27331087 | ||||||
chr16:27331227
|
G | T | 1 | a0001c0001t0002g0083 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-19+1029G>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27331227 | ||||||
chr16:27331275
|
T | A | 111 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(108): Show | 128 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.-19+1077T>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27331275 | ||||||
chr16:27331294
|
T | C | 1 | a0002c0002t0002g0278 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-19+1096T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27331294 | ||||||
chr16:27331371
|
A | G | 6 | a0001c0001t0001g0277a0009c0017t0013g0176a0009c0017t0013g0177others(3): Show | 6 | HG02572.hp2 HG02615.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-19+1173A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27331371 | ||||||
chr16:27331411
|
G | A | 3 | a0010c0024t0004g0281a0013c0016t0006g0029a0013c0016t0006g0282 | 4 | HG01109.hp2 HG02895.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+1213G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27331411 | ||||||
chr16:27331422
|
AAAT | A | 12 | a0001c0001t0001g0014a0001c0001t0001g0082a0001c0001t0001g0113others(9): Show | 12 | HG02155.hp2 NA18747.hp1 NA18940.hp2 others(9): Show |
intron_variant | MODIFIER | c.-19+1229_-19+1231d others(5): Show |
IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 27331422 | |||||
chr16:27331441
|
A | G | 1 | a0002c0002t0002g0209 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-19+1243A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27331441 | ||||||
chr16:27331558
|
C | T | 32 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0052others(29): Show | 38 | HG00408.hp2 HG00558.hp2 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.-19+1360C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27331558 | ||||||
chr16:27331692
|
A | G | 1 | a0030c0045t0024g0170 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-19+1494A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27331692 | ||||||
chr16:27331717
|
C | G | 1 | a0001c0008t0019g0261 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-19+1519C>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27331717 | ||||||
chr16:27332097
|
C | T | 1 | a0002c0002t0001g0072 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-19+1899C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27332097 | ||||||
chr16:27332158
|
A | G | 78 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0054others(75): Show | 89 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(86): Show |
intron_variant | MODIFIER | c.-19+1960A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27332158 | ||||||
chr16:27332194
|
T | C | 108 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(105): Show | 125 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.-19+1996T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27332194 | ||||||
chr16:27332214
|
A | G | 2 | a0001c0001t0001g0067a0001c0001t0001g0068 | 2 | NA18949.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.-19+2016A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27332214 | ||||||
chr16:27332256
|
A | G | 1 | a0009c0037t0002g0050 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-19+2058A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27332256 | ||||||
chr16:27332304
|
C | A | 1 | a0009c0017t0013g0276 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-19+2106C>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27332304 | ||||||
chr16:27332393
|
A | G | 12 | a0001c0001t0001g0014a0001c0001t0001g0082a0001c0001t0001g0113others(9): Show | 12 | HG02155.hp2 NA18747.hp1 NA18940.hp2 others(9): Show |
intron_variant | MODIFIER | c.-19+2195A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27332393 | ||||||
chr16:27332427
|
G | A | 1 | a0010c0034t0005g0178 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-19+2229G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27332427 | ||||||
chr16:27332577
|
G | A | 1 | a0002c0002t0001g0256 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-19+2379G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27332577 | ||||||
chr16:27332642
|
T | C | 76 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0054others(73): Show | 87 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(84): Show |
intron_variant | MODIFIER | c.-19+2444T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27332642 | ||||||
chr16:27332680
|
A | G | 1 | a0004c0004t0002g0136 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-19+2482A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27332680 | ||||||
chr16:27332685
|
C | T | 8 | a0003c0003t0002g0153a0003c0003t0002g0154a0003c0003t0002g0155others(5): Show | 8 | HG02071.hp1 NA18954.hp1 NA18957.hp2 others(5): Show |
intron_variant | MODIFIER | c.-19+2487C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27332685 | ||||||
chr16:27332780
|
T | C | 2 | a0009c0037t0002g0050a0031c0036t0015g0051 | 2 | HG02145.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-19+2582T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27332780 | ||||||
chr16:27332794
|
T | C | 32 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0052others(29): Show | 38 | HG00408.hp2 HG00558.hp2 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.-19+2596T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27332794 | ||||||
chr16:27332838
|
C | T | 1 | a0001c0001t0001g0112 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-19+2640C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27332838 | ||||||
chr16:27332878
|
T | G | 58 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0052others(55): Show | 67 | HG00408.hp2 HG00558.hp2 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.-19+2680T>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27332878 | ||||||
chr16:27332956
|
C | G | 1 | a0010c0024t0004g0281 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-19+2758C>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27332956 | ||||||
chr16:27332956
|
C | T | 2 | a0002c0002t0001g0128a0003c0003t0001g0127 | 2 | HG02451.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-19+2758C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27332956 | ||||||
chr16:27333100
|
T | A | 3 | a0010c0024t0005g0172a0019c0023t0014g0030a0019c0023t0014g0031 | 3 | HG02145.hp1 HG02723.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-19+2902T>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27333100 | ||||||
chr16:27333190
|
C | T | 1 | a0002c0013t0002g0226 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-19+2992C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27333190 | ||||||
chr16:27333199
|
C | CTT | 28 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0052others(25): Show | 33 | HG00408.hp2 HG00558.hp2 HG02040.hp2 others(30): Show |
intron_variant | MODIFIER | c.-19+3013_-19+3014d others(4): Show |
IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 27333199 | |||||
chr16:27333311
|
G | A | 2 | a0009c0037t0002g0050a0031c0036t0015g0051 | 2 | HG02145.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-19+3113G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27333311 | ||||||
chr16:27333373
|
C | T | 2 | a0001c0008t0025g0169a0030c0045t0024g0170 | 2 | HG00735.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-19+3175C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27333373 | ||||||
chr16:27333793
|
A | G | 146 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(143): Show | 166 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.-19+3595A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27333793 | ||||||
chr16:27333800
|
T | C | 21 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0052others(18): Show | 25 | HG00408.hp2 HG00558.hp2 HG02040.hp2 others(22): Show |
intron_variant | MODIFIER | c.-19+3602T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27333800 | ||||||
chr16:27333888
|
CT | C | 108 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(105): Show | 124 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.-19+3702delT | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 27333888 | |||||
chr16:27333896
|
T | C | 3 | a0010c0024t0004g0281a0013c0016t0006g0029a0013c0016t0006g0282 | 4 | HG01109.hp2 HG02895.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+3698T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27333896 | ||||||
chr16:27333909
|
G | C | 11 | a0001c0001t0001g0277a0003c0003t0002g0044a0009c0017t0013g0176others(8): Show | 12 | HG01243.hp2 HG02572.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.-19+3711G>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27333909 | ||||||
chr16:27334031
|
C | T | 65 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0054others(62): Show | 75 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(72): Show |
intron_variant | MODIFIER | c.-19+3833C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27334031 | ||||||
chr16:27334034
|
C | T | 1 | a0017c0018t0005g0175 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-19+3836C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27334034 | ||||||
chr16:27334150
|
G | C | 2 | a0009c0035t0005g0038a0009c0046t0005g0037 | 2 | HG02258.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-19+3952G>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27334150 | ||||||
chr16:27334161
|
C | T | 1 | a0006c0006t0006g0236 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-19+3963C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27334161 | ||||||
chr16:27334378
|
A | G | 1 | a0001c0008t0019g0261 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-19+4180A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27334378 | ||||||
chr16:27334390
|
C | T | 2 | a0002c0002t0001g0138a0002c0002t0001g0139 | 2 | NA19005.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.-19+4192C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27334390 | ||||||
chr16:27334418
|
G | A | 3 | a0010c0012t0004g0011a0010c0012t0004g0049a0010c0012t0004g0065 | 4 | HG02922.hp2 HG02965.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+4220G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27334418 | ||||||
chr16:27335033
|
T | C | 161 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(158): Show | 184 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.-19+4835T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27335033 | ||||||
chr16:27335054
|
G | A | 1 | a0001c0001t0001g0096 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-19+4856G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27335054 | ||||||
chr16:27335266
|
G | A | 1 | a0001c0001t0001g0263 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-18-4920G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27335266 | ||||||
chr16:27335271
|
T | C | 2 | a0001c0008t0025g0169a0030c0045t0024g0170 | 2 | HG00735.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-18-4915T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27335271 | ||||||
chr16:27335477
|
C | G | 1 | a0018c0015t0002g0120 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-18-4709C>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27335477 | ||||||
chr16:27335918
|
G | A | 1 | a0005c0022t0002g0020 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-18-4268G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27335918 | ||||||
chr16:27336011
|
A | G | 2 | a0012c0011t0010g0019a0012c0011t0010g0179 | 3 | HG02647.hp2 HG02809.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.-18-4175A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27336011 | ||||||
chr16:27336079
|
G | A | 1 | a0004c0004t0002g0008 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-18-4107G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27336079 | ||||||
chr16:27336152
|
A | G | 1 | a0002c0002t0002g0225 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-18-4034A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27336152 | ||||||
chr16:27336194
|
G | A | 1 | a0003c0003t0002g0153 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.-18-3992G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27336194 | ||||||
chr16:27336207
|
C | T | 3 | a0010c0024t0004g0281a0013c0016t0006g0029a0013c0016t0006g0282 | 4 | HG01109.hp2 HG02895.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18-3979C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27336207 | ||||||
chr16:27336298
|
G | A | 5 | a0004c0004t0002g0232a0012c0011t0010g0019a0012c0011t0010g0048others(2): Show | 6 | HG01243.hp2 HG01496.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.-18-3888G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27336298 | ||||||
chr16:27336324
|
A | G | 4 | a0011c0010t0004g0046a0011c0010t0004g0047a0014c0041t0005g0230others(1): Show | 4 | HG03041.hp2 NA19043.hp1 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18-3862A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27336324 | ||||||
chr16:27336659
|
CAG | C | 3 | a0002c0002t0001g0207a0002c0002t0001g0256a0003c0003t0002g0206 | 3 | HG01358.hp1 HG01928.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.-18-3524_-18-3523d others(4): Show |
IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 27336659 | |||||
chr16:27336676
|
C | CA | 6 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0097others(3): Show | 6 | HG03239.hp2 HG04228.hp2 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.-18-3490dupA | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 27336676 | |||||
chr16:27336676
|
CA | C | 41 | a0001c0001t0001g0068a0001c0001t0001g0071a0001c0001t0001g0107others(38): Show | 44 | HG00642.hp2 HG01070.hp1 HG01081.hp1 others(41): Show |
intron_variant | MODIFIER | c.-18-3490delA | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 27336676 | |||||
chr16:27336676
|
CAA | C | 15 | a0001c0001t0001g0277a0005c0005t0001g0260a0009c0017t0013g0176others(12): Show | 17 | HG00741.hp2 HG01099.hp1 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.-18-3491_-18-3490d others(4): Show |
IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 27336676 | |||||
chr16:27336694
|
A | AAAGGAAA others(37): Show |
1 | a0009c0037t0002g0050 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-18-3490_-18-3447d others(46): Show |
IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 27336694 | |||||
chr16:27336694
|
A | AAGGAAAG others(36): Show |
1 | a0031c0036t0015g0051 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-18-3491_-18-3490i others(45): Show |
IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 27336694 | |||||
chr16:27336712
|
G | T | 1 | a0006c0031t0005g0036 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-18-3474G>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27336712 | ||||||
chr16:27336719
|
C | T | 4 | a0011c0010t0004g0046a0011c0010t0004g0047a0014c0041t0005g0230others(1): Show | 4 | HG03041.hp2 NA19043.hp1 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18-3467C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27336719 | ||||||
chr16:27336843
|
C | T | 1 | a0002c0002t0002g0242 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-18-3343C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27336843 | ||||||
chr16:27336844
|
T | C | 44 | a0001c0001t0001g0263a0001c0001t0001g0269a0001c0001t0001g0277others(41): Show | 49 | HG00642.hp2 HG00741.hp2 HG01081.hp1 others(46): Show |
intron_variant | MODIFIER | c.-18-3342T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27336844 | ||||||
chr16:27336914
|
A | G | 2 | a0009c0037t0002g0050a0031c0036t0015g0051 | 2 | HG02145.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-18-3272A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27336914 | ||||||
chr16:27336954
|
G | A | 4 | a0011c0010t0004g0046a0011c0010t0004g0047a0014c0041t0005g0230others(1): Show | 4 | HG03041.hp2 NA19043.hp1 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18-3232G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27336954 | ||||||
chr16:27337001
|
T | C | 44 | a0001c0001t0001g0263a0001c0001t0001g0269a0001c0001t0001g0277others(41): Show | 49 | HG00642.hp2 HG00741.hp2 HG01081.hp1 others(46): Show |
intron_variant | MODIFIER | c.-18-3185T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27337001 | ||||||
chr16:27337009
|
G | A | 3 | a0010c0024t0004g0281a0013c0016t0006g0029a0013c0016t0006g0282 | 4 | HG01109.hp2 HG02895.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18-3177G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27337009 | ||||||
chr16:27337057
|
A | G | 1 | a0014c0041t0005g0230 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-18-3129A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27337057 | ||||||
chr16:27337111
|
G | A | 2 | a0009c0037t0002g0050a0031c0036t0015g0051 | 2 | HG02145.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-18-3075G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27337111 | ||||||
chr16:27337124
|
A | AAAG | 44 | a0001c0001t0001g0263a0001c0001t0001g0269a0001c0001t0001g0277others(41): Show | 49 | HG00642.hp2 HG00741.hp2 HG01081.hp1 others(46): Show |
intron_variant | MODIFIER | c.-18-3055_-18-3053d others(5): Show |
IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 27337124 | |||||
chr16:27337163
|
G | C | 2 | a0001c0008t0025g0169a0030c0045t0024g0170 | 2 | HG00735.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-18-3023G>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27337163 | ||||||
chr16:27337199
|
G | T | 1 | a0001c0001t0001g0112 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-18-2987G>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27337199 | ||||||
chr16:27337271
|
C | T | 3 | a0010c0024t0004g0281a0013c0016t0006g0029a0013c0016t0006g0282 | 4 | HG01109.hp2 HG02895.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18-2915C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27337271 | ||||||
chr16:27337309
|
G | A | 91 | a0001c0001t0001g0191a0002c0002t0001g0001a0002c0002t0001g0072others(88): Show | 109 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.-18-2877G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27337309 | ||||||
chr16:27337328
|
C | T | 1 | a0002c0002t0001g0128 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-18-2858C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27337328 | ||||||
chr16:27337404
|
A | G | 3 | a0003c0003t0002g0173a0003c0003t0002g0181a0011c0010t0004g0180 | 3 | HG02486.hp2 HG02572.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-18-2782A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27337404 | ||||||
chr16:27337410
|
A | G | 1 | a0005c0022t0002g0020 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-18-2776A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27337410 | ||||||
chr16:27337489
|
G | C | 1 | a0001c0001t0001g0112 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-18-2697G>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27337489 | ||||||
chr16:27337561
|
C | CT | 4 | a0011c0010t0004g0046a0011c0010t0004g0047a0014c0041t0005g0230others(1): Show | 4 | HG03041.hp2 NA19043.hp1 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18-2618dupT | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 27337561 | |||||
chr16:27337619
|
G | A | 2 | a0003c0003t0001g0249a0003c0003t0001g0250 | 2 | HG01884.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-18-2567G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27337619 | ||||||
chr16:27337648
|
C | T | 1 | a0001c0001t0001g0117 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-18-2538C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27337648 | ||||||
chr16:27337766
|
G | C | 1 | a0001c0001t0001g0074 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-18-2420G>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27337766 | ||||||
chr16:27337847
|
C | T | 65 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0054others(62): Show | 75 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(72): Show |
intron_variant | MODIFIER | c.-18-2339C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27337847 | ||||||
chr16:27337853
|
C | G | 1 | a0006c0031t0005g0036 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-18-2333C>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27337853 | ||||||
chr16:27337922
|
T | C | 1 | a0014c0041t0005g0230 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-18-2264T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27337922 | ||||||
chr16:27337925
|
G | A | 2 | a0001c0001t0001g0067a0001c0001t0001g0068 | 2 | NA18949.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.-18-2261G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27337925 | ||||||
chr16:27337945
|
A | AT | 66 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0054others(63): Show | 76 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(73): Show |
intron_variant | MODIFIER | c.-18-2234dupT | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 27337945 | |||||
chr16:27337959
|
C | CT | 7 | a0001c0001t0001g0168a0002c0002t0002g0223a0003c0003t0002g0158others(4): Show | 7 | HG01433.hp1 HG02723.hp1 HG03710.hp1 others(4): Show |
intron_variant | MODIFIER | c.-18-2212dupT | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 27337959 | |||||
chr16:27337959
|
CT | C | 36 | a0001c0001t0001g0263a0001c0001t0001g0269a0001c0001t0001g0277others(33): Show | 41 | HG00642.hp2 HG00741.hp2 HG01081.hp1 others(38): Show |
intron_variant | MODIFIER | c.-18-2212delT | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 27337959 | |||||
chr16:27338031
|
G | A | 4 | a0001c0001t0002g0265a0005c0005t0001g0259a0005c0005t0001g0260others(1): Show | 4 | HG01081.hp1 HG01099.hp1 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18-2155G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27338031 | ||||||
chr16:27338073
|
C | T | 2 | a0009c0037t0002g0050a0031c0036t0015g0051 | 2 | HG02145.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-18-2113C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27338073 | ||||||
chr16:27338075
|
G | C | 2 | a0019c0023t0014g0030a0019c0023t0014g0031 | 2 | HG02145.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-18-2111G>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27338075 | ||||||
chr16:27338082
|
G | A | 4 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0258others(1): Show | 4 | HG01891.hp1 HG02630.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18-2104G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27338082 | ||||||
chr16:27338117
|
T | C | 130 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(127): Show | 151 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.-18-2069T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27338117 | ||||||
chr16:27338172
|
G | T | 38 | a0001c0001t0001g0263a0001c0001t0001g0269a0001c0001t0001g0277others(35): Show | 43 | HG00642.hp2 HG00741.hp2 HG01081.hp1 others(40): Show |
intron_variant | MODIFIER | c.-18-2014G>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27338172 | ||||||
chr16:27338197
|
C | T | 1 | a0030c0045t0024g0170 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-18-1989C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27338197 | ||||||
chr16:27338236
|
T | G | 1 | a0007c0007t0016g0227 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-18-1950T>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27338236 | ||||||
chr16:27338335
|
A | T | 4 | a0012c0011t0010g0019a0012c0011t0010g0048a0012c0011t0010g0179others(1): Show | 5 | HG01243.hp2 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-18-1851A>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27338335 | ||||||
chr16:27338526
|
AT | A | 140 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(137): Show | 162 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.-18-1653delT | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr16 | 27338526 | |||||
chr16:27338597
|
C | T | 3 | a0002c0002t0002g0203a0004c0004t0003g0202a0027c0027t0003g0205 | 3 | HG01070.hp1 HG01952.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-18-1589C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27338597 | ||||||
chr16:27338650
|
A | G | 1 | a0005c0022t0002g0020 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-18-1536A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27338650 | ||||||
chr16:27338691
|
C | T | 146 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(143): Show | 168 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.-18-1495C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27338691 | ||||||
chr16:27338719
|
C | A | 2 | a0002c0002t0001g0128a0003c0003t0001g0127 | 2 | HG02451.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-18-1467C>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27338719 | ||||||
chr16:27338801
|
G | T | 1 | a0005c0005t0002g0057 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-18-1385G>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27338801 | ||||||
chr16:27338893
|
G | A | 1 | a0011c0010t0004g0180 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-18-1293G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27338893 | ||||||
chr16:27339043
|
C | T | 1 | a0003c0003t0002g0044 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-18-1143C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27339043 | ||||||
chr16:27339293
|
T | C | 1 | a0034c0048t0001g0126 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-18-893T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27339293 | ||||||
chr16:27339366
|
A | G | 131 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(128): Show | 152 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.-18-820A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27339366 | ||||||
chr16:27339422
|
G | A | 1 | a0003c0003t0002g0173 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-18-764G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27339422 | ||||||
chr16:27339672
|
C | A | 1 | a0002c0002t0002g0196 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-18-514C>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27339672 | ||||||
chr16:27339707
|
A | T | 2 | a0008c0009t0008g0040a0008c0047t0008g0039 | 2 | HG02622.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-18-479A>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27339707 | ||||||
chr16:27339771
|
A | G | 1 | a0014c0041t0005g0230 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-18-415A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27339771 | ||||||
chr16:27339785
|
G | A | 1 | a0001c0001t0001g0071 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-18-401G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27339785 | ||||||
chr16:27339972
|
G | A | 7 | a0008c0009t0008g0007a0008c0009t0008g0040a0008c0009t0008g0041others(4): Show | 8 | HG02055.hp1 HG02451.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.-18-214G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27339972 | ||||||
chr16:27340017
|
A | G | 127 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(124): Show | 148 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.-18-169A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 2/10 | chr16 | 27340017 | ||||||
chr16:27340354
|
G | A | 2 | a0002c0002t0001g0143a0002c0002t0001g0159 | 2 | HG00639.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.70+81G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 3/10 | chr16 | 27340354 | ||||||
chr16:27340392
|
A | G | 1 | a0014c0041t0005g0230 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.70+119A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 3/10 | chr16 | 27340392 | ||||||
chr16:27340477
|
C | G | 2 | a0013c0016t0006g0029a0013c0016t0006g0282 | 3 | HG01109.hp2 HG02895.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.70+204C>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 3/10 | chr16 | 27340477 | ||||||
chr16:27340581
|
G | A | 4 | a0003c0003t0002g0044a0011c0010t0004g0046a0011c0010t0004g0047others(1): Show | 4 | HG02886.hp1 HG03041.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.70+308G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 3/10 | chr16 | 27340581 | ||||||
chr16:27340647
|
A | G | 3 | a0010c0024t0005g0172a0019c0023t0014g0030a0019c0023t0014g0031 | 3 | HG02145.hp1 HG02723.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.70+374A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 3/10 | chr16 | 27340647 | ||||||
chr16:27340677
|
G | A | 1 | a0014c0041t0005g0230 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.70+404G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 3/10 | chr16 | 27340677 | ||||||
chr16:27340678
|
C | T | 1 | a0002c0002t0001g0192 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.70+405C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 3/10 | chr16 | 27340678 | ||||||
chr16:27340792
|
G | C | 1 | a0001c0001t0001g0107 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.70+519G>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 3/10 | chr16 | 27340792 | ||||||
chr16:27340800
|
T | C | 22 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0052others(19): Show | 28 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.70+527T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 3/10 | chr16 | 27340800 | ||||||
chr16:27340857
|
G | A | 1 | a0002c0013t0002g0226 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.70+584G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 3/10 | chr16 | 27340857 | ||||||
chr16:27340918
|
G | A | 1 | a0002c0002t0002g0244 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.70+645G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 3/10 | chr16 | 27340918 | ||||||
chr16:27340920
|
C | T | 2 | a0001c0001t0001g0082a0001c0001t0001g0116 | 2 | HG02155.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.70+647C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 3/10 | chr16 | 27340920 | ||||||
chr16:27340927
|
G | T | 2 | a0013c0016t0006g0029a0013c0016t0006g0282 | 3 | HG01109.hp2 HG02895.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.70+654G>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 3/10 | chr16 | 27340927 | ||||||
chr16:27341271
|
G | A | 2 | a0013c0016t0006g0029a0013c0016t0006g0282 | 3 | HG01109.hp2 HG02895.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.71-850G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 3/10 | chr16 | 27341271 | ||||||
chr16:27341389
|
A | G | 1 | a0018c0015t0002g0120 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.71-732A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 3/10 | chr16 | 27341389 | ||||||
chr16:27341392
|
C | T | 27 | a0001c0001t0001g0263a0001c0001t0001g0269a0001c0001t0002g0142others(24): Show | 30 | HG00642.hp2 HG00741.hp2 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.71-729C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 3/10 | chr16 | 27341392 | ||||||
chr16:27341498
|
G | A | 27 | a0001c0001t0001g0263a0001c0001t0001g0269a0001c0001t0002g0142others(24): Show | 30 | HG00642.hp2 HG00741.hp2 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.71-623G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 3/10 | chr16 | 27341498 | ||||||
chr16:27341565
|
C | T | 5 | a0003c0003t0002g0044a0011c0010t0004g0046a0011c0010t0004g0047others(2): Show | 5 | HG02886.hp1 HG03041.hp2 NA19043.hp1 others(2): Show |
intron_variant | MODIFIER | c.71-556C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 3/10 | chr16 | 27341565 | ||||||
chr16:27341587
|
A | T | 2 | a0002c0002t0002g0186a0002c0002t0002g0247 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.71-534A>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 3/10 | chr16 | 27341587 | ||||||
chr16:27341604
|
T | G | 1 | a0003c0003t0002g0144 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.71-517T>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 3/10 | chr16 | 27341604 | ||||||
chr16:27341614
|
C | G | 9 | a0002c0002t0001g0128a0003c0003t0001g0127a0008c0009t0008g0007others(6): Show | 10 | HG02055.hp1 HG02451.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.71-507C>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 3/10 | chr16 | 27341614 | ||||||
chr16:27341617
|
T | A | 9 | a0002c0002t0001g0128a0003c0003t0001g0127a0008c0009t0008g0007others(6): Show | 10 | HG02055.hp1 HG02451.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.71-504T>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 3/10 | chr16 | 27341617 | ||||||
chr16:27341644
|
T | C | 5 | a0003c0003t0002g0044a0011c0010t0004g0046a0011c0010t0004g0047others(2): Show | 5 | HG02886.hp1 HG03041.hp2 NA19043.hp1 others(2): Show |
intron_variant | MODIFIER | c.71-477T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 3/10 | chr16 | 27341644 | ||||||
chr16:27341700
|
G | A | 2 | a0002c0013t0002g0024a0002c0013t0002g0190 | 3 | HG01168.hp1 HG01169.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.71-421G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 3/10 | chr16 | 27341700 | ||||||
chr16:27341797
|
G | A | 4 | a0012c0011t0010g0019a0012c0011t0010g0048a0012c0011t0010g0179others(1): Show | 5 | HG01243.hp2 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.71-324G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 3/10 | chr16 | 27341797 | ||||||
chr16:27341867
|
G | A | 4 | a0011c0010t0004g0046a0011c0010t0004g0047a0014c0041t0005g0230others(1): Show | 4 | HG03041.hp2 NA19043.hp1 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.71-254G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 3/10 | chr16 | 27341867 | ||||||
chr16:27341909
|
G | A | 31 | a0001c0001t0001g0263a0001c0001t0001g0269a0001c0001t0002g0142others(28): Show | 34 | HG00642.hp2 HG00741.hp2 HG01081.hp1 others(31): Show |
intron_variant | MODIFIER | c.71-212G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 3/10 | chr16 | 27341909 | ||||||
chr16:27342036
|
C | T | 27 | a0001c0001t0001g0263a0001c0001t0001g0269a0001c0001t0002g0142others(24): Show | 30 | HG00642.hp2 HG00741.hp2 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.71-85C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 3/10 | chr16 | 27342036 | ||||||
chr16:27342076
|
G | A | 2 | a0012c0011t0010g0019a0012c0011t0010g0179 | 3 | HG02647.hp2 HG02809.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.71-45G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 3/10 | chr16 | 27342076 | ||||||
chr16:27342268
|
G | C | 2 | a0013c0016t0006g0029a0013c0016t0006g0282 | 3 | HG01109.hp2 HG02895.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.209+9G>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 4/10 | chr16 | 27342268 | ||||||
chr16:27342304
|
A | G | 4 | a0012c0011t0010g0019a0012c0011t0010g0048a0012c0011t0010g0179others(1): Show | 5 | HG01243.hp2 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.209+45A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 4/10 | chr16 | 27342304 | ||||||
chr16:27342464
|
G | A | 5 | a0001c0001t0001g0277a0009c0017t0013g0176a0009c0017t0013g0177others(2): Show | 5 | HG02572.hp2 HG02615.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.209+205G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 4/10 | chr16 | 27342464 | ||||||
chr16:27342480
|
G | A | 4 | a0012c0011t0010g0019a0012c0011t0010g0048a0012c0011t0010g0179others(1): Show | 5 | HG01243.hp2 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.209+221G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 4/10 | chr16 | 27342480 | ||||||
chr16:27342554
|
T | G | 1 | a0001c0001t0001g0263 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.209+295T>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 4/10 | chr16 | 27342554 | ||||||
chr16:27342640
|
T | A | 1 | a0010c0024t0005g0172 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.209+381T>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 4/10 | chr16 | 27342640 | ||||||
chr16:27342694
|
G | C | 1 | a0004c0004t0003g0069 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.209+435G>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 4/10 | chr16 | 27342694 | ||||||
chr16:27342746
|
C | A | 27 | a0001c0001t0001g0263a0001c0001t0001g0269a0001c0001t0002g0142others(24): Show | 30 | HG00642.hp2 HG00741.hp2 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.209+487C>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 4/10 | chr16 | 27342746 | ||||||
chr16:27342834
|
G | A | 3 | a0016c0020t0011g0042a0016c0020t0011g0240a0016c0032t0011g0043 | 3 | HG02055.hp1 HG02451.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.209+575G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 4/10 | chr16 | 27342834 | ||||||
chr16:27342855
|
C | T | 1 | a0011c0010t0004g0046 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.209+596C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 4/10 | chr16 | 27342855 | ||||||
chr16:27342968
|
T | A | 13 | a0002c0002t0001g0128a0003c0003t0001g0127a0003c0003t0002g0044others(10): Show | 14 | HG02055.hp1 HG02451.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.209+709T>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 4/10 | chr16 | 27342968 | ||||||
chr16:27342969
|
G | A | 13 | a0002c0002t0001g0128a0003c0003t0001g0127a0003c0003t0002g0044others(10): Show | 14 | HG02055.hp1 HG02451.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.209+710G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 4/10 | chr16 | 27342969 | ||||||
chr16:27343005
|
C | A | 10 | a0002c0002t0002g0203a0004c0004t0003g0066a0004c0004t0003g0069others(7): Show | 10 | HG00408.hp1 HG01070.hp1 HG01952.hp1 others(7): Show |
intron_variant | MODIFIER | c.209+746C>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 4/10 | chr16 | 27343005 | ||||||
chr16:27343040
|
C | T | 40 | a0001c0001t0001g0263a0001c0001t0001g0269a0001c0001t0002g0142others(37): Show | 44 | HG00642.hp2 HG00741.hp2 HG01081.hp1 others(41): Show |
intron_variant | MODIFIER | c.209+781C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 4/10 | chr16 | 27343040 | ||||||
chr16:27343170
|
T | G | 3 | a0011c0010t0004g0046a0011c0010t0004g0047a0022c0033t0004g0118 | 3 | HG03041.hp2 NA19043.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.209+911T>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 4/10 | chr16 | 27343170 | ||||||
chr16:27343179
|
G | C | 2 | a0019c0023t0014g0030a0019c0023t0014g0031 | 2 | HG02145.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.209+920G>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 4/10 | chr16 | 27343179 | ||||||
chr16:27343210
|
C | G | 146 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(143): Show | 168 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.209+951C>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 4/10 | chr16 | 27343210 | ||||||
chr16:27343408
|
G | GTTTT | 26 | a0001c0001t0001g0263a0001c0001t0001g0269a0001c0001t0002g0142others(23): Show | 29 | HG00642.hp2 HG00741.hp2 HG01081.hp1 others(26): Show |
intron_variant | MODIFIER | c.209+1152_209+1155d others(6): Show |
IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 27343408 | |||||
chr16:27343411
|
T | TTTTG | 57 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0064others(54): Show | 66 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.209+1176_209+1179d others(6): Show |
IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 27343411 | |||||
chr16:27343413
|
TTG | T | 12 | a0002c0002t0001g0128a0003c0003t0001g0127a0008c0009t0008g0007others(9): Show | 13 | HG02055.hp1 HG02451.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.209+1156_209+1157d others(4): Show |
IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 27343413 | |||||
chr16:27343415
|
G | T | 2 | a0009c0037t0002g0050a0033c0039t0004g0275 | 2 | HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.209+1156G>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 4/10 | chr16 | 27343415 | ||||||
chr16:27343450
|
G | C | 1 | a0004c0004t0003g0202 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.209+1191G>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 4/10 | chr16 | 27343450 | ||||||
chr16:27343518
|
C | G | 13 | a0002c0002t0001g0128a0003c0003t0001g0127a0003c0003t0002g0044others(10): Show | 14 | HG02055.hp1 HG02451.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.209+1259C>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 4/10 | chr16 | 27343518 | ||||||
chr16:27343626
|
T | C | 40 | a0001c0001t0001g0263a0001c0001t0001g0269a0001c0001t0002g0142others(37): Show | 44 | HG00642.hp2 HG00741.hp2 HG01081.hp1 others(41): Show |
intron_variant | MODIFIER | c.210-1243T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 4/10 | chr16 | 27343626 | ||||||
chr16:27343680
|
A | G | 13 | a0002c0002t0001g0128a0003c0003t0001g0127a0003c0003t0002g0044others(10): Show | 14 | HG02055.hp1 HG02451.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.210-1189A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 4/10 | chr16 | 27343680 | ||||||
chr16:27343683
|
G | C | 140 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(137): Show | 162 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.210-1186G>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 4/10 | chr16 | 27343683 | ||||||
chr16:27343729
|
C | T | 9 | a0002c0002t0001g0128a0003c0003t0001g0127a0008c0009t0008g0007others(6): Show | 10 | HG02055.hp1 HG02451.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.210-1140C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 4/10 | chr16 | 27343729 | ||||||
chr16:27343867
|
G | GA | 3 | a0011c0010t0004g0046a0011c0010t0004g0047a0022c0033t0004g0118 | 3 | HG03041.hp2 NA19043.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.210-1001dupA | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 27343867 | |||||
chr16:27343964
|
G | T | 27 | a0001c0001t0001g0263a0001c0001t0001g0269a0001c0001t0002g0142others(24): Show | 30 | HG00642.hp2 HG00741.hp2 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.210-905G>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 4/10 | chr16 | 27343964 | ||||||
chr16:27344028
|
A | G | 40 | a0001c0001t0001g0263a0001c0001t0001g0269a0001c0001t0002g0142others(37): Show | 44 | HG00642.hp2 HG00741.hp2 HG01081.hp1 others(41): Show |
intron_variant | MODIFIER | c.210-841A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 4/10 | chr16 | 27344028 | ||||||
chr16:27344041
|
G | A | 89 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(86): Show | 105 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(102): Show |
intron_variant | MODIFIER | c.210-828G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 4/10 | chr16 | 27344041 | ||||||
chr16:27344109
|
G | A | 13 | a0002c0002t0001g0128a0003c0003t0001g0127a0003c0003t0002g0044others(10): Show | 14 | HG02055.hp1 HG02451.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.210-760G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 4/10 | chr16 | 27344109 | ||||||
chr16:27344174
|
G | A | 1 | a0029c0043t0018g0045 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.210-695G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 4/10 | chr16 | 27344174 | ||||||
chr16:27344288
|
G | A | 1 | a0002c0002t0001g0273 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.210-581G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 4/10 | chr16 | 27344288 | ||||||
chr16:27344303
|
A | AG | 5 | a0008c0009t0008g0040a0008c0047t0008g0039a0016c0020t0011g0042others(2): Show | 5 | HG02055.hp1 HG02451.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.210-564dupG | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 27344303 | |||||
chr16:27344337
|
C | T | 4 | a0009c0035t0005g0038a0009c0037t0002g0050a0009c0046t0005g0037others(1): Show | 4 | HG02145.hp2 HG02258.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.210-532C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 4/10 | chr16 | 27344337 | ||||||
chr16:27344364
|
C | CA | 16 | a0001c0001t0002g0142a0002c0002t0001g0128a0002c0002t0001g0192others(13): Show | 18 | HG01109.hp2 HG02451.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.210-487dupA | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 27344364 | |||||
chr16:27344364
|
CA | C | 16 | a0001c0001t0001g0125a0001c0001t0001g0277a0001c0001t0021g0098others(13): Show | 17 | HG00099.hp1 HG01884.hp2 HG02148.hp2 others(14): Show |
intron_variant | MODIFIER | c.210-487delA | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 27344364 | |||||
chr16:27344364
|
CAA | C | 85 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(82): Show | 101 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(98): Show |
intron_variant | MODIFIER | c.210-488_210-487del others(2): Show |
IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 27344364 | |||||
chr16:27344364
|
CAAA | C | 11 | a0001c0001t0001g0110a0001c0001t0001g0133a0001c0001t0001g0167others(8): Show | 11 | HG00735.hp2 HG02145.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.210-489_210-487del others(3): Show |
IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr16 | 27344364 | |||||
chr16:27344528
|
G | A | 2 | a0001c0008t0025g0169a0030c0045t0024g0170 | 2 | HG00735.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.210-341G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 4/10 | chr16 | 27344528 | ||||||
chr16:27344567
|
C | T | 5 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0167others(2): Show | 5 | HG03486.hp1 NA18940.hp2 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.210-302C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 4/10 | chr16 | 27344567 | ||||||
chr16:27345038
|
C | T | 76 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0054others(73): Show | 86 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(83): Show |
intron_variant | MODIFIER | c.361+18C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 5/10 | chr16 | 27345038 | ||||||
chr16:27345077
|
C | T | 106 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(103): Show | 123 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(120): Show |
intron_variant | MODIFIER | c.361+57C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 5/10 | chr16 | 27345077 | ||||||
chr16:27345091
|
G | A | 24 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0052others(21): Show | 30 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(27): Show |
intron_variant | MODIFIER | c.361+71G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 5/10 | chr16 | 27345091 | ||||||
chr16:27345133
|
C | T | 2 | a0002c0002t0002g0184a0002c0002t0002g0185 | 2 | HG03491.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.361+113C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 5/10 | chr16 | 27345133 | ||||||
chr16:27345286
|
A | G | 7 | a0009c0035t0005g0038a0009c0037t0002g0050a0009c0046t0005g0037others(4): Show | 8 | HG02145.hp2 HG02258.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.361+266A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 5/10 | chr16 | 27345286 | ||||||
chr16:27345334
|
G | T | 2 | a0001c0008t0025g0169a0030c0045t0024g0170 | 2 | HG00735.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.361+314G>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 5/10 | chr16 | 27345334 | ||||||
chr16:27345346
|
T | G | 121 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(118): Show | 141 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.361+326T>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 5/10 | chr16 | 27345346 | ||||||
chr16:27345359
|
G | A | 7 | a0009c0035t0005g0038a0009c0037t0002g0050a0009c0046t0005g0037others(4): Show | 8 | HG02145.hp2 HG02258.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.361+339G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 5/10 | chr16 | 27345359 | ||||||
chr16:27345368
|
G | C | 7 | a0009c0035t0005g0038a0009c0037t0002g0050a0009c0046t0005g0037others(4): Show | 8 | HG02145.hp2 HG02258.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.361+348G>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 5/10 | chr16 | 27345368 | ||||||
chr16:27345403
|
G | A | 3 | a0013c0016t0006g0029a0013c0016t0006g0282a0020c0021t0001g0015 | 5 | HG01109.hp2 HG02717.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.361+383G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 5/10 | chr16 | 27345403 | ||||||
chr16:27345420
|
C | T | 4 | a0010c0012t0004g0049a0011c0010t0004g0046a0011c0010t0004g0047others(1): Show | 4 | HG03041.hp2 NA18522.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.361+400C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 5/10 | chr16 | 27345420 | ||||||
chr16:27345569
|
A | G | 1 | a0003c0003t0001g0127 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.361+549A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 5/10 | chr16 | 27345569 | ||||||
chr16:27345571
|
G | A | 9 | a0001c0001t0001g0277a0005c0022t0002g0020a0009c0017t0013g0176others(6): Show | 10 | HG00741.hp2 HG02572.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.361+551G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 5/10 | chr16 | 27345571 | ||||||
chr16:27345603
|
T | A | 1 | a0003c0003t0002g0044 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.361+583T>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 5/10 | chr16 | 27345603 | ||||||
chr16:27345641
|
G | A | 2 | a0001c0001t0001g0113a0001c0001t0001g0114 | 2 | NA18945.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.361+621G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 5/10 | chr16 | 27345641 | ||||||
chr16:27345692
|
C | T | 7 | a0003c0003t0001g0127a0008c0009t0008g0007a0008c0009t0008g0040others(4): Show | 8 | HG02055.hp1 HG02451.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.361+672C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 5/10 | chr16 | 27345692 | ||||||
chr16:27345693
|
G | A | 3 | a0013c0016t0006g0029a0013c0016t0006g0282a0020c0021t0001g0015 | 5 | HG01109.hp2 HG02717.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.361+673G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 5/10 | chr16 | 27345693 | ||||||
chr16:27345743
|
A | G | 7 | a0009c0035t0005g0038a0009c0037t0002g0050a0009c0046t0005g0037others(4): Show | 8 | HG02145.hp2 HG02258.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.361+723A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 5/10 | chr16 | 27345743 | ||||||
chr16:27345787
|
A | G | 7 | a0009c0035t0005g0038a0009c0037t0002g0050a0009c0046t0005g0037others(4): Show | 8 | HG02145.hp2 HG02258.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.362-680A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 5/10 | chr16 | 27345787 | ||||||
chr16:27345951
|
G | A | 1 | a0002c0002t0001g0128 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.362-516G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 5/10 | chr16 | 27345951 | ||||||
chr16:27345958
|
T | C | 7 | a0009c0035t0005g0038a0009c0037t0002g0050a0009c0046t0005g0037others(4): Show | 8 | HG02145.hp2 HG02258.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.362-509T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 5/10 | chr16 | 27345958 | ||||||
chr16:27346085
|
G | A | 1 | a0001c0001t0001g0125 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.362-382G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 5/10 | chr16 | 27346085 | ||||||
chr16:27346087
|
G | A | 2 | a0002c0002t0002g0186a0002c0002t0002g0247 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.362-380G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 5/10 | chr16 | 27346087 | ||||||
chr16:27346210
|
G | A | 5 | a0008c0009t0008g0084a0010c0012t0004g0049a0011c0010t0004g0046others(2): Show | 5 | HG02055.hp2 HG03041.hp2 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.362-257G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 5/10 | chr16 | 27346210 | ||||||
chr16:27346463
|
G | A | 9 | a0001c0008t0001g0266a0001c0008t0002g0028a0001c0008t0002g0262others(6): Show | 10 | HG00642.hp2 HG01106.hp2 HG01168.hp2 others(7): Show |
splice_region_variant&intron_variant | LOW | c.362-4G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 5/10 | chr16 | 27346463 | ||||||
chr16:27346639
|
G | A | 1 | a0001c0008t0001g0266 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.513+21G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27346639 | ||||||
chr16:27346719
|
C | T | 5 | a0008c0009t0008g0084a0010c0012t0004g0049a0011c0010t0004g0046others(2): Show | 5 | HG02055.hp2 HG03041.hp2 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.513+101C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27346719 | ||||||
chr16:27346724
|
G | A | 3 | a0002c0002t0001g0215a0002c0002t0001g0224a0002c0002t0002g0239 | 3 | HG01515.hp1 HG01517.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.513+106G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27346724 | ||||||
chr16:27346737
|
A | T | 6 | a0002c0002t0001g0034a0003c0003t0002g0173a0003c0003t0002g0181others(3): Show | 6 | HG02486.hp2 HG02572.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.513+119A>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27346737 | ||||||
chr16:27346777
|
A | C | 267 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(264): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.513+159A>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27346777 | ||||||
chr16:27346809
|
A | G | 1 | a0003c0003t0002g0044 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.513+191A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27346809 | ||||||
chr16:27346811
|
C | T | 94 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0054others(91): Show | 106 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(103): Show |
intron_variant | MODIFIER | c.513+193C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27346811 | ||||||
chr16:27346849
|
C | T | 1 | a0003c0003t0002g0234 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.513+231C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27346849 | ||||||
chr16:27346869
|
G | A | 16 | a0001c0008t0001g0266a0001c0008t0002g0028a0001c0008t0002g0262others(13): Show | 17 | HG00642.hp2 HG00735.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.513+251G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27346869 | ||||||
chr16:27346882
|
A | G | 155 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(152): Show | 178 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.513+264A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27346882 | ||||||
chr16:27347030
|
G | A | 9 | a0001c0008t0001g0266a0001c0008t0002g0028a0001c0008t0002g0262others(6): Show | 10 | HG00642.hp2 HG01106.hp2 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.513+412G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27347030 | ||||||
chr16:27347111
|
A | G | 1 | a0004c0004t0003g0121 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.513+493A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27347111 | ||||||
chr16:27347251
|
C | T | 1 | a0003c0003t0002g0149 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.513+633C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27347251 | ||||||
chr16:27347276
|
C | T | 1 | a0001c0001t0001g0071 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.513+658C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27347276 | ||||||
chr16:27347323
|
C | T | 3 | a0002c0002t0001g0128a0009c0035t0005g0038a0009c0046t0005g0037 | 3 | HG02258.hp1 HG02451.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.513+705C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27347323 | ||||||
chr16:27347442
|
T | C | 144 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0054others(141): Show | 162 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.513+824T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27347442 | ||||||
chr16:27347537
|
C | A | 2 | a0014c0041t0005g0230a0026c0028t0005g0124 | 2 | HG02486.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.513+919C>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27347537 | ||||||
chr16:27347554
|
A | T | 1 | a0014c0041t0005g0230 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.513+936A>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27347554 | ||||||
chr16:27347563
|
G | A | 1 | a0014c0041t0005g0230 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.513+945G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27347563 | ||||||
chr16:27347567
|
G | A | 61 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0052others(58): Show | 71 | HG00408.hp2 HG00558.hp2 HG00639.hp1 others(68): Show |
intron_variant | MODIFIER | c.513+949G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27347567 | ||||||
chr16:27347627
|
A | G | 181 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(178): Show | 206 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.513+1009A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27347627 | ||||||
chr16:27347700
|
A | C | 123 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0054others(120): Show | 138 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.513+1082A>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27347700 | ||||||
chr16:27347740
|
A | T | 115 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0054others(112): Show | 129 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.513+1122A>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27347740 | ||||||
chr16:27347745
|
A | G | 3 | a0013c0016t0006g0029a0013c0016t0006g0282a0020c0021t0001g0015 | 5 | HG01109.hp2 HG02717.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.513+1127A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27347745 | ||||||
chr16:27347873
|
G | T | 9 | a0001c0001t0001g0277a0005c0022t0002g0020a0009c0017t0013g0176others(6): Show | 10 | HG00741.hp2 HG02572.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.513+1255G>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27347873 | ||||||
chr16:27347902
|
G | A | 1 | a0033c0039t0004g0275 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.513+1284G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27347902 | ||||||
chr16:27347975
|
G | A | 22 | a0001c0008t0001g0266a0001c0008t0002g0028a0001c0008t0002g0262others(19): Show | 24 | HG00642.hp2 HG01106.hp2 HG01168.hp2 others(21): Show |
intron_variant | MODIFIER | c.513+1357G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27347975 | ||||||
chr16:27348194
|
C | A | 2 | a0001c0008t0025g0169a0030c0045t0024g0170 | 2 | HG00735.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.513+1576C>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27348194 | ||||||
chr16:27348254
|
G | A | 5 | a0008c0009t0008g0084a0010c0012t0004g0049a0011c0010t0004g0046others(2): Show | 5 | HG02055.hp2 HG03041.hp2 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.513+1636G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27348254 | ||||||
chr16:27348267
|
G | C | 4 | a0003c0003t0002g0044a0012c0011t0010g0019a0012c0011t0010g0048others(1): Show | 5 | HG02647.hp2 HG02809.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.513+1649G>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27348267 | ||||||
chr16:27348311
|
G | T | 1 | a0001c0001t0001g0090 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.513+1693G>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27348311 | ||||||
chr16:27348503
|
C | G | 1 | a0029c0043t0018g0045 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.513+1885C>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27348503 | ||||||
chr16:27348523
|
G | A | 149 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(146): Show | 171 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.513+1905G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27348523 | ||||||
chr16:27348671
|
G | A | 1 | a0001c0001t0001g0087 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.513+2053G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27348671 | ||||||
chr16:27348720
|
G | A | 2 | a0001c0001t0001g0099a0001c0001t0001g0162 | 2 | HG00140.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.513+2102G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27348720 | ||||||
chr16:27348764
|
T | C | 2 | a0010c0012t0004g0049a0022c0033t0004g0118 | 2 | NA18522.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.513+2146T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27348764 | ||||||
chr16:27348772
|
G | C | 1 | a0014c0041t0005g0230 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.513+2154G>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27348772 | ||||||
chr16:27348773
|
G | T | 1 | a0014c0041t0005g0230 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.513+2155G>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27348773 | ||||||
chr16:27348901
|
G | A | 3 | a0013c0016t0006g0029a0013c0016t0006g0282a0020c0021t0001g0015 | 5 | HG01109.hp2 HG02717.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.513+2283G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27348901 | ||||||
chr16:27348910
|
GA | G | 19 | a0001c0008t0001g0266a0001c0008t0002g0028a0001c0008t0002g0262others(16): Show | 22 | HG00642.hp2 HG00735.hp2 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.513+2293delA | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27348910 | ||||||
chr16:27348952
|
T | C | 1 | a0003c0003t0002g0044 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.513+2334T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27348952 | ||||||
chr16:27349136
|
G | A | 1 | a0002c0002t0002g0184 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.513+2518G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27349136 | ||||||
chr16:27349257
|
C | T | 1 | a0001c0001t0001g0114 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.513+2639C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27349257 | ||||||
chr16:27349279
|
G | A | 1 | a0002c0002t0001g0128 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.513+2661G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27349279 | ||||||
chr16:27349306
|
A | G | 164 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(161): Show | 187 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.513+2688A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27349306 | ||||||
chr16:27349307
|
T | C | 164 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(161): Show | 187 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.513+2689T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27349307 | ||||||
chr16:27349535
|
A | T | 4 | a0005c0022t0002g0020a0017c0018t0005g0175a0017c0018t0023g0174others(1): Show | 5 | HG00741.hp2 HG02809.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.513+2917A>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27349535 | ||||||
chr16:27349611
|
T | A | 4 | a0005c0022t0002g0020a0017c0018t0005g0175a0017c0018t0023g0174others(1): Show | 5 | HG00741.hp2 HG02809.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.514-2929T>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27349611 | ||||||
chr16:27349731
|
A | G | 16 | a0001c0008t0001g0266a0001c0008t0002g0028a0001c0008t0002g0262others(13): Show | 17 | HG00642.hp2 HG00735.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.514-2809A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27349731 | ||||||
chr16:27349747
|
T | TTTG | 3 | a0002c0002t0002g0196a0010c0012t0004g0011a0010c0012t0004g0065 | 4 | HG02922.hp2 HG02965.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.514-2774_514-2772d others(5): Show |
IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr16 | 27349747 | |||||
chr16:27349846
|
A | C | 111 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0054others(108): Show | 126 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.514-2694A>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27349846 | ||||||
chr16:27349906
|
C | T | 3 | a0003c0003t0001g0250a0009c0037t0002g0050a0031c0036t0015g0051 | 3 | HG01884.hp1 HG02145.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.514-2634C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27349906 | ||||||
chr16:27349992
|
C | A | 19 | a0001c0008t0001g0266a0001c0008t0002g0028a0001c0008t0002g0262others(16): Show | 22 | HG00642.hp2 HG00735.hp2 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.514-2548C>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27349992 | ||||||
chr16:27350016
|
G | A | 2 | a0009c0035t0005g0038a0009c0046t0005g0037 | 2 | HG02258.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.514-2524G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27350016 | ||||||
chr16:27350041
|
G | A | 37 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0052others(34): Show | 44 | HG00408.hp2 HG00558.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.514-2499G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27350041 | ||||||
chr16:27350256
|
A | G | 3 | a0002c0002t0001g0128a0009c0035t0005g0038a0009c0046t0005g0037 | 3 | HG02258.hp1 HG02451.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.514-2284A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27350256 | ||||||
chr16:27350395
|
A | G | 1 | a0001c0001t0001g0054 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.514-2145A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27350395 | ||||||
chr16:27350472
|
C | T | 45 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0052others(42): Show | 52 | HG00408.hp2 HG00558.hp2 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.514-2068C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27350472 | ||||||
chr16:27350674
|
G | A | 1 | a0001c0001t0001g0078 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.514-1866G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27350674 | ||||||
chr16:27350838
|
C | T | 1 | a0001c0001t0001g0089 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.514-1702C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27350838 | ||||||
chr16:27351128
|
A | G | 5 | a0001c0001t0001g0277a0009c0017t0013g0176a0009c0017t0013g0177others(2): Show | 5 | HG02572.hp2 HG02615.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.514-1412A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27351128 | ||||||
chr16:27351212
|
G | C | 16 | a0001c0008t0001g0266a0001c0008t0002g0028a0001c0008t0002g0262others(13): Show | 17 | HG00642.hp2 HG00735.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.514-1328G>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27351212 | ||||||
chr16:27351496
|
A | ATC | 41 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0052others(38): Show | 48 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.514-1030_514-1029d others(4): Show |
IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr16 | 27351496 | |||||
chr16:27351510
|
CT | C | 101 | a0001c0001t0001g0277a0001c0001t0002g0100a0001c0001t0002g0265others(98): Show | 119 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.514-1011delT | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr16 | 27351510 | |||||
chr16:27351510
|
CTT | C | 27 | a0002c0002t0001g0128a0002c0002t0002g0216a0002c0002t0002g0217others(24): Show | 30 | HG00741.hp2 HG01496.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.514-1012_514-1011d others(4): Show |
IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr16 | 27351510 | |||||
chr16:27351512
|
T | C | 41 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0052others(38): Show | 48 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.514-1028T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27351512 | ||||||
chr16:27351527
|
TTTC | T | 20 | a0001c0001t0001g0101a0001c0008t0001g0266a0001c0008t0002g0028others(17): Show | 23 | HG00642.hp2 HG00735.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.514-1012_514-1010d others(5): Show |
IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27351527 | ||||||
chr16:27351528
|
TTC | T | 89 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0054others(86): Show | 101 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.514-1011_514-1010d others(4): Show |
IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27351528 | ||||||
chr16:27351530
|
C | T | 1 | a0019c0023t0014g0031 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.514-1010C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27351530 | ||||||
chr16:27351714
|
C | T | 3 | a0013c0016t0006g0029a0013c0016t0006g0282a0020c0021t0001g0015 | 5 | HG01109.hp2 HG02717.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.514-826C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27351714 | ||||||
chr16:27351720
|
G | A | 19 | a0001c0008t0001g0266a0001c0008t0002g0028a0001c0008t0002g0262others(16): Show | 22 | HG00642.hp2 HG00735.hp2 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.514-820G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27351720 | ||||||
chr16:27351726
|
G | A | 14 | a0001c0008t0001g0266a0001c0008t0002g0028a0001c0008t0002g0262others(11): Show | 15 | HG00642.hp2 HG01106.hp2 HG01168.hp2 others(12): Show |
intron_variant | MODIFIER | c.514-814G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27351726 | ||||||
chr16:27351783
|
G | A | 1 | a0007c0007t0002g0218 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.514-757G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27351783 | ||||||
chr16:27351788
|
T | G | 2 | a0009c0037t0002g0050a0031c0036t0015g0051 | 2 | HG02145.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.514-752T>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27351788 | ||||||
chr16:27351909
|
T | C | 19 | a0001c0008t0001g0266a0001c0008t0002g0028a0001c0008t0002g0262others(16): Show | 22 | HG00642.hp2 HG00735.hp2 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.514-631T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27351909 | ||||||
chr16:27351944
|
T | C | 7 | a0008c0009t0008g0007a0008c0009t0008g0040a0008c0009t0008g0041others(4): Show | 8 | HG02055.hp1 HG02451.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.514-596T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27351944 | ||||||
chr16:27352032
|
C | T | 1 | a0001c0001t0001g0107 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.514-508C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27352032 | ||||||
chr16:27352182
|
G | C | 4 | a0003c0003t0002g0044a0012c0011t0010g0019a0012c0011t0010g0048others(1): Show | 5 | HG02647.hp2 HG02809.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.514-358G>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27352182 | ||||||
chr16:27352290
|
G | A | 19 | a0001c0008t0001g0266a0001c0008t0002g0028a0001c0008t0002g0262others(16): Show | 22 | HG00642.hp2 HG00735.hp2 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.514-250G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27352290 | ||||||
chr16:27352365
|
G | C | 248 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(245): Show | 288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.514-175G>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27352365 | ||||||
chr16:27352413
|
C | T | 3 | a0002c0002t0001g0128a0009c0035t0005g0038a0009c0046t0005g0037 | 3 | HG02258.hp1 HG02451.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.514-127C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 6/10 | chr16 | 27352413 | ||||||
chr16:27352837
|
C | T | 106 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0052others(103): Show | 128 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.670+141C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 7/10 | chr16 | 27352837 | ||||||
chr16:27352879
|
A | C | 213 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(210): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.670+183A>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 7/10 | chr16 | 27352879 | ||||||
chr16:27352912
|
G | A | 232 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(229): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.670+216G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 7/10 | chr16 | 27352912 | ||||||
chr16:27352932
|
C | T | 104 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0052others(101): Show | 126 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.670+236C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 7/10 | chr16 | 27352932 | ||||||
chr16:27353024
|
G | A | 232 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(229): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.670+328G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 7/10 | chr16 | 27353024 | ||||||
chr16:27353034
|
A | C | 1 | a0017c0018t0005g0280 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.670+338A>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 7/10 | chr16 | 27353034 | ||||||
chr16:27353124
|
C | T | 2 | a0002c0002t0002g0208a0002c0002t0002g0228 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.670+428C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 7/10 | chr16 | 27353124 | ||||||
chr16:27353151
|
T | A | 5 | a0001c0001t0001g0277a0009c0017t0013g0176a0009c0017t0013g0177others(2): Show | 5 | HG02572.hp2 HG02615.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.670+455T>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 7/10 | chr16 | 27353151 | ||||||
chr16:27353189
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.670+493G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 7/10 | chr16 | 27353189 | ||||||
chr16:27353251
|
A | G | 13 | a0008c0009t0008g0007a0008c0009t0008g0040a0008c0009t0008g0041others(10): Show | 14 | HG01243.hp2 HG02055.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.670+555A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 7/10 | chr16 | 27353251 | ||||||
chr16:27353343
|
G | GAAATA | 19 | a0001c0008t0001g0266a0001c0008t0002g0028a0001c0008t0002g0262others(16): Show | 22 | HG00642.hp2 HG00735.hp2 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.670+660_670+664dup others(5): Show |
IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 27353343 | |||||
chr16:27353485
|
G | A | 94 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0054others(91): Show | 106 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.670+789G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 7/10 | chr16 | 27353485 | ||||||
chr16:27353597
|
G | C | 248 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(245): Show | 288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.670+901G>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 7/10 | chr16 | 27353597 | ||||||
chr16:27353756
|
C | T | 2 | a0002c0002t0001g0141a0002c0002t0002g0032 | 2 | HG00099.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.670+1060C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 7/10 | chr16 | 27353756 | ||||||
chr16:27353797
|
C | T | 19 | a0001c0008t0001g0266a0001c0008t0002g0028a0001c0008t0002g0262others(16): Show | 22 | HG00642.hp2 HG00735.hp2 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.670+1101C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 7/10 | chr16 | 27353797 | ||||||
chr16:27353957
|
A | G | 5 | a0001c0008t0025g0169a0013c0016t0006g0029a0013c0016t0006g0282others(2): Show | 7 | HG00735.hp2 HG01109.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.670+1261A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 7/10 | chr16 | 27353957 | ||||||
chr16:27353989
|
G | A | 5 | a0001c0008t0025g0169a0013c0016t0006g0029a0013c0016t0006g0282others(2): Show | 7 | HG00735.hp2 HG01109.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.670+1293G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 7/10 | chr16 | 27353989 | ||||||
chr16:27353990
|
T | A | 1 | a0010c0034t0005g0178 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.670+1294T>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 7/10 | chr16 | 27353990 | ||||||
chr16:27354013
|
T | G | 1 | a0029c0043t0018g0045 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.670+1317T>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 7/10 | chr16 | 27354013 | ||||||
chr16:27354132
|
C | G | 93 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0054others(90): Show | 105 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.670+1436C>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 7/10 | chr16 | 27354132 | ||||||
chr16:27354147
|
A | G | 14 | a0001c0008t0001g0266a0001c0008t0002g0028a0001c0008t0002g0262others(11): Show | 15 | HG00642.hp2 HG01106.hp2 HG01168.hp2 others(12): Show |
intron_variant | MODIFIER | c.670+1451A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 7/10 | chr16 | 27354147 | ||||||
chr16:27354293
|
A | G | 104 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0052others(101): Show | 126 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.671-1515A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 7/10 | chr16 | 27354293 | ||||||
chr16:27354351
|
G | A | 4 | a0003c0003t0002g0044a0012c0011t0010g0019a0012c0011t0010g0048others(1): Show | 5 | HG02647.hp2 HG02809.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.671-1457G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 7/10 | chr16 | 27354351 | ||||||
chr16:27354359
|
C | T | 4 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0055others(1): Show | 4 | HG02258.hp2 HG02615.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.671-1449C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 7/10 | chr16 | 27354359 | ||||||
chr16:27354361
|
G | A | 4 | a0003c0003t0002g0044a0012c0011t0010g0019a0012c0011t0010g0048others(1): Show | 5 | HG02647.hp2 HG02809.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.671-1447G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 7/10 | chr16 | 27354361 | ||||||
chr16:27354398
|
C | T | 1 | a0033c0039t0004g0275 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.671-1410C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 7/10 | chr16 | 27354398 | ||||||
chr16:27354615
|
G | A | 1 | a0003c0003t0002g0234 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.671-1193G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 7/10 | chr16 | 27354615 | ||||||
chr16:27354706
|
C | A | 1 | a0002c0002t0001g0235 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.671-1102C>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 7/10 | chr16 | 27354706 | ||||||
chr16:27354709
|
A | G | 249 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(246): Show | 289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.671-1099A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 7/10 | chr16 | 27354709 | ||||||
chr16:27354719
|
T | C | 1 | a0003c0003t0002g0158 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.671-1089T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 7/10 | chr16 | 27354719 | ||||||
chr16:27354782
|
G | A | 1 | a0010c0034t0005g0178 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.671-1026G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 7/10 | chr16 | 27354782 | ||||||
chr16:27354805
|
A | G | 20 | a0001c0008t0001g0266a0001c0008t0002g0028a0001c0008t0002g0262others(17): Show | 23 | HG00642.hp2 HG00735.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.671-1003A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 7/10 | chr16 | 27354805 | ||||||
chr16:27354975
|
T | C | 18 | a0001c0008t0001g0266a0001c0008t0002g0028a0001c0008t0002g0262others(15): Show | 19 | HG00642.hp2 HG01106.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.671-833T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 7/10 | chr16 | 27354975 | ||||||
chr16:27355067
|
C | T | 1 | a0001c0001t0001g0068 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.671-741C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 7/10 | chr16 | 27355067 | ||||||
chr16:27355178
|
A | G | 15 | a0001c0008t0001g0266a0001c0008t0002g0028a0001c0008t0002g0262others(12): Show | 17 | HG00642.hp2 HG01106.hp2 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.671-630A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 7/10 | chr16 | 27355178 | ||||||
chr16:27355241
|
A | G | 70 | a0001c0001t0001g0277a0001c0008t0001g0266a0001c0008t0002g0028others(67): Show | 75 | HG00639.hp2 HG00642.hp2 HG00735.hp2 others(72): Show |
intron_variant | MODIFIER | c.671-567A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 7/10 | chr16 | 27355241 | ||||||
chr16:27355413
|
G | T | 1 | a0002c0002t0002g0214 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.671-395G>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 7/10 | chr16 | 27355413 | ||||||
chr16:27355548
|
C | T | 10 | a0001c0001t0001g0277a0005c0022t0002g0020a0009c0017t0013g0176others(7): Show | 11 | HG00741.hp2 HG02572.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.671-260C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 7/10 | chr16 | 27355548 | ||||||
chr16:27355654
|
A | G | 1 | a0014c0041t0005g0230 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.671-154A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 7/10 | chr16 | 27355654 | ||||||
chr16:27355661
|
T | C | 9 | a0001c0008t0001g0266a0001c0008t0002g0028a0001c0008t0002g0262others(6): Show | 10 | HG00642.hp2 HG01106.hp2 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.671-147T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 7/10 | chr16 | 27355661 | ||||||
chr16:27355749
|
G | A | 1 | a0005c0005t0001g0193 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.671-59G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 7/10 | chr16 | 27355749 | ||||||
chr16:27355939
|
C | T | 4 | a0004c0004t0003g0195a0004c0004t0003g0200a0004c0004t0003g0202others(1): Show | 4 | HG01070.hp1 HG01952.hp1 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.770+32C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | chr16 | 27355939 | ||||||
chr16:27355958
|
G | A | 1 | a0010c0012t0004g0011 | 2 | HG02922.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.770+51G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | chr16 | 27355958 | ||||||
chr16:27356013
|
C | T | 229 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(226): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.770+106C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | chr16 | 27356013 | ||||||
chr16:27356037
|
C | G | 1 | a0001c0001t0007g0061 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.770+130C>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | chr16 | 27356037 | ||||||
chr16:27356084
|
C | CT | 7 | a0002c0002t0001g0034a0003c0003t0002g0157a0003c0003t0002g0160others(4): Show | 7 | HG02055.hp1 HG02258.hp1 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.770+202dupT | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 27356084 | |||||
chr16:27356084
|
CT | C | 199 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(196): Show | 233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.770+202delT | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 27356084 | |||||
chr16:27356084
|
CTT | C | 10 | a0001c0001t0001g0080a0001c0001t0001g0085a0001c0001t0001g0102others(7): Show | 12 | HG00099.hp2 HG01069.hp1 HG01070.hp2 others(9): Show |
intron_variant | MODIFIER | c.770+201_770+202del others(2): Show |
IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 27356084 | |||||
chr16:27356084
|
CTTTTTTT others(11): Show |
C | 5 | a0008c0009t0008g0084a0010c0012t0004g0049a0011c0010t0004g0046others(2): Show | 5 | HG02055.hp2 HG03041.hp2 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.770+185_770+202del others(18): Show |
IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 27356084 | |||||
chr16:27356088
|
T | C | 2 | a0008c0009t0008g0040a0008c0047t0008g0039 | 2 | HG02622.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.770+181T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | chr16 | 27356088 | ||||||
chr16:27356090
|
T | TC | 8 | a0001c0001t0001g0277a0005c0022t0002g0020a0009c0017t0013g0176others(5): Show | 9 | HG00741.hp2 HG02572.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.770+183_770+184ins others(1): Show |
IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | chr16 | 27356090 | ||||||
chr16:27356092
|
T | C | 2 | a0001c0001t0001g0106a0001c0001t0001g0116 | 2 | HG02155.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.770+185T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | chr16 | 27356092 | ||||||
chr16:27356093
|
T | C | 184 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(181): Show | 217 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.770+186T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | chr16 | 27356093 | ||||||
chr16:27356094
|
T | C | 8 | a0001c0001t0001g0080a0001c0001t0001g0085a0001c0001t0001g0102others(5): Show | 8 | HG00099.hp2 HG01069.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.770+187T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | chr16 | 27356094 | ||||||
chr16:27356184
|
C | T | 3 | a0010c0024t0005g0172a0029c0043t0018g0045a0033c0039t0004g0275 | 3 | HG01243.hp2 HG02723.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.770+277C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | chr16 | 27356184 | ||||||
chr16:27356206
|
C | T | 2 | a0009c0035t0005g0038a0009c0046t0005g0037 | 2 | HG02258.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.770+299C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | chr16 | 27356206 | ||||||
chr16:27356412
|
C | T | 1 | a0001c0001t0002g0142 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.770+505C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | chr16 | 27356412 | ||||||
chr16:27356412
|
CG | C | 7 | a0005c0022t0002g0020a0016c0020t0011g0042a0016c0020t0011g0240others(4): Show | 8 | HG00741.hp2 HG02055.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.770+507delG | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 27356412 | |||||
chr16:27356416
|
A | C | 7 | a0005c0022t0002g0020a0016c0020t0011g0042a0016c0020t0011g0240others(4): Show | 8 | HG00741.hp2 HG02055.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.770+509A>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | chr16 | 27356416 | ||||||
chr16:27356505
|
C | G | 218 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(215): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.770+598C>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | chr16 | 27356505 | ||||||
chr16:27356517
|
C | G | 1 | a0001c0008t0002g0272 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.770+610C>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | chr16 | 27356517 | ||||||
chr16:27356542
|
G | C | 9 | a0008c0009t0008g0007a0008c0009t0008g0040a0008c0009t0008g0041others(6): Show | 10 | HG02055.hp2 HG02559.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.770+635G>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | chr16 | 27356542 | ||||||
chr16:27356586
|
C | T | 5 | a0008c0009t0008g0084a0010c0012t0004g0049a0011c0010t0004g0046others(2): Show | 5 | HG02055.hp2 HG03041.hp2 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.770+679C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | chr16 | 27356586 | ||||||
chr16:27356651
|
G | A | 218 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(215): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.770+744G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | chr16 | 27356651 | ||||||
chr16:27356678
|
C | T | 244 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(241): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.770+771C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | chr16 | 27356678 | ||||||
chr16:27356777
|
C | T | 2 | a0009c0035t0005g0038a0009c0046t0005g0037 | 2 | HG02258.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.770+870C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | chr16 | 27356777 | ||||||
chr16:27357108
|
G | A | 1 | a0002c0002t0002g0242 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.770+1201G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | chr16 | 27357108 | ||||||
chr16:27357175
|
C | G | 3 | a0013c0016t0006g0029a0013c0016t0006g0282a0020c0021t0001g0015 | 5 | HG01109.hp2 HG02717.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.770+1268C>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | chr16 | 27357175 | ||||||
chr16:27357176
|
G | A | 2 | a0001c0001t0001g0108a0002c0002t0002g0231 | 2 | HG02523.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.770+1269G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | chr16 | 27357176 | ||||||
chr16:27357342
|
C | T | 3 | a0012c0011t0010g0019a0012c0011t0010g0048a0012c0011t0010g0179 | 4 | HG02647.hp2 HG02809.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.770+1435C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | chr16 | 27357342 | ||||||
chr16:27357355
|
C | T | 1 | a0008c0009t0017g0251 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.770+1448C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | chr16 | 27357355 | ||||||
chr16:27357424
|
C | T | 2 | a0009c0035t0005g0038a0009c0046t0005g0037 | 2 | HG02258.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.771-1492C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | chr16 | 27357424 | ||||||
chr16:27357469
|
A | T | 209 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(206): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.771-1447A>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | chr16 | 27357469 | ||||||
chr16:27357488
|
G | A | 1 | a0001c0001t0001g0104 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.771-1428G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | chr16 | 27357488 | ||||||
chr16:27357491
|
T | C | 1 | a0010c0034t0005g0178 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.771-1425T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | chr16 | 27357491 | ||||||
chr16:27357512
|
G | A | 194 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(191): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.771-1404G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | chr16 | 27357512 | ||||||
chr16:27357527
|
G | T | 1 | a0002c0002t0002g0213 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.771-1389G>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | chr16 | 27357527 | ||||||
chr16:27357779
|
TAG | T | 12 | a0001c0001t0001g0277a0005c0022t0002g0020a0009c0017t0013g0176others(9): Show | 13 | HG00741.hp2 HG02055.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.771-1133_771-1132d others(4): Show |
IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 27357779 | |||||
chr16:27357892
|
G | GT | 16 | a0001c0001t0001g0125a0001c0001t0001g0166a0001c0008t0025g0169others(13): Show | 16 | HG00735.hp2 HG01928.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.771-1009dupT | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 27357892 | |||||
chr16:27357898
|
T | G | 1 | a0003c0003t0002g0181 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.771-1018T>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | chr16 | 27357898 | ||||||
chr16:27357907
|
T | C | 2 | a0002c0002t0001g0016a0002c0002t0001g0150 | 3 | HG01081.hp2 HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.771-1009T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | chr16 | 27357907 | ||||||
chr16:27357916
|
T | G | 5 | a0009c0037t0002g0050a0012c0011t0010g0019a0012c0011t0010g0048others(2): Show | 6 | HG02145.hp2 HG02647.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.771-1000T>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | chr16 | 27357916 | ||||||
chr16:27357928
|
T | C | 1 | a0026c0028t0005g0124 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.771-988T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | chr16 | 27357928 | ||||||
chr16:27358174
|
G | A | 5 | a0008c0009t0008g0007a0008c0009t0008g0040a0008c0009t0008g0041others(2): Show | 6 | HG02559.hp2 HG02622.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.771-742G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | chr16 | 27358174 | ||||||
chr16:27358181
|
A | G | 213 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(210): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.771-735A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | chr16 | 27358181 | ||||||
chr16:27358240
|
G | A | 2 | a0012c0011t0010g0019a0012c0011t0010g0179 | 3 | HG02647.hp2 HG02809.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.771-676G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | chr16 | 27358240 | ||||||
chr16:27358275
|
C | T | 5 | a0001c0001t0001g0109a0001c0001t0007g0061a0001c0001t0007g0063others(2): Show | 5 | HG01167.hp2 HG02300.hp2 NA18950.hp1 others(2): Show |
intron_variant | MODIFIER | c.771-641C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | chr16 | 27358275 | ||||||
chr16:27358288
|
G | A | 20 | a0001c0001t0002g0100a0002c0002t0002g0021a0002c0002t0002g0023others(17): Show | 22 | HG00140.hp1 HG00280.hp2 HG00642.hp1 others(19): Show |
intron_variant | MODIFIER | c.771-628G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | chr16 | 27358288 | ||||||
chr16:27358462
|
G | A | 1 | a0033c0039t0004g0275 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.771-454G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | chr16 | 27358462 | ||||||
chr16:27358616
|
T | C | 1 | a0008c0009t0008g0007 | 2 | HG02559.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.771-300T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | chr16 | 27358616 | ||||||
chr16:27358701
|
C | T | 1 | a0003c0003t0002g0153 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.771-215C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | chr16 | 27358701 | ||||||
chr16:27358738
|
G | T | 1 | a0010c0034t0005g0178 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.771-178G>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 8/10 | chr16 | 27358738 | ||||||
chr16:27359007
|
G | A | 1 | a0003c0003t0002g0252 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.849+13G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 9/10 | chr16 | 27359007 | ||||||
chr16:27359133
|
A | G | 236 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(233): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.849+139A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 9/10 | chr16 | 27359133 | ||||||
chr16:27359196
|
A | T | 4 | a0013c0016t0006g0029a0013c0016t0006g0282a0020c0021t0001g0015others(1): Show | 6 | HG01109.hp2 HG02717.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.849+202A>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 9/10 | chr16 | 27359196 | ||||||
chr16:27359225
|
T | G | 4 | a0013c0016t0006g0029a0013c0016t0006g0282a0020c0021t0001g0015others(1): Show | 6 | HG01109.hp2 HG02717.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.849+231T>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 9/10 | chr16 | 27359225 | ||||||
chr16:27359484
|
T | G | 1 | a0009c0046t0005g0037 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.849+490T>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 9/10 | chr16 | 27359484 | ||||||
chr16:27359611
|
AGTG | A | 199 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(196): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.849+621_849+623del others(3): Show |
IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr16 | 27359611 | |||||
chr16:27359626
|
G | C | 2 | a0019c0023t0014g0030a0019c0023t0014g0031 | 2 | HG02145.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.849+632G>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 9/10 | chr16 | 27359626 | ||||||
chr16:27359665
|
G | A | 2 | a0019c0023t0014g0030a0019c0023t0014g0031 | 2 | HG02145.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.849+671G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 9/10 | chr16 | 27359665 | ||||||
chr16:27359837
|
C | T | 198 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(195): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.849+843C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 9/10 | chr16 | 27359837 | ||||||
chr16:27359927
|
C | T | 5 | a0009c0017t0013g0176a0009c0017t0013g0177a0009c0017t0013g0276others(2): Show | 5 | HG02109.hp1 HG02572.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.850-839C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 9/10 | chr16 | 27359927 | ||||||
chr16:27359984
|
G | A | 1 | a0002c0002t0002g0214 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.850-782G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 9/10 | chr16 | 27359984 | ||||||
chr16:27360041
|
G | A | 1 | a0018c0015t0002g0120 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.850-725G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 9/10 | chr16 | 27360041 | ||||||
chr16:27360075
|
C | T | 1 | a0011c0010t0004g0033 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.850-691C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 9/10 | chr16 | 27360075 | ||||||
chr16:27360076
|
G | A | 107 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0052others(104): Show | 131 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.850-690G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 9/10 | chr16 | 27360076 | ||||||
chr16:27360099
|
C | G | 1 | a0017c0018t0005g0280 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.850-667C>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 9/10 | chr16 | 27360099 | ||||||
chr16:27360103
|
T | C | 227 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(224): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.850-663T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 9/10 | chr16 | 27360103 | ||||||
chr16:27360206
|
G | T | 1 | a0002c0002t0001g0273 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.850-560G>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 9/10 | chr16 | 27360206 | ||||||
chr16:27360218
|
C | T | 212 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(209): Show | 247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.850-548C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 9/10 | chr16 | 27360218 | ||||||
chr16:27360250
|
G | A | 198 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(195): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.850-516G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 9/10 | chr16 | 27360250 | ||||||
chr16:27360263
|
T | C | 215 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(212): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.850-503T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 9/10 | chr16 | 27360263 | ||||||
chr16:27360331
|
C | T | 2 | a0001c0001t0001g0130a0001c0001t0001g0132 | 2 | NA19081.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.850-435C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 9/10 | chr16 | 27360331 | ||||||
chr16:27360348
|
G | A | 5 | a0001c0008t0025g0169a0012c0011t0010g0019a0012c0011t0010g0048others(2): Show | 6 | HG00735.hp2 HG02647.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.850-418G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 9/10 | chr16 | 27360348 | ||||||
chr16:27360383
|
G | A | 1 | a0010c0034t0005g0178 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.850-383G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 9/10 | chr16 | 27360383 | ||||||
chr16:27360628
|
A | G | 221 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(218): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.850-138A>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 9/10 | chr16 | 27360628 | ||||||
chr16:27360677
|
G | A | 1 | a0003c0003t0002g0044 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.850-89G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 9/10 | chr16 | 27360677 | ||||||
chr16:27360995
|
C | A | 7 | a0010c0012t0004g0049a0010c0024t0004g0281a0010c0024t0005g0172others(4): Show | 7 | HG02723.hp1 HG02809.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.899+180C>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 10/10 | chr16 | 27360995 | ||||||
chr16:27361074
|
G | T | 9 | a0010c0012t0004g0049a0010c0024t0004g0281a0011c0010t0004g0046others(6): Show | 9 | HG00741.hp2 HG02818.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.899+259G>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 10/10 | chr16 | 27361074 | ||||||
chr16:27361173
|
CTG | C | 46 | a0003c0003t0001g0127a0003c0003t0001g0249a0003c0003t0001g0250others(43): Show | 50 | HG00639.hp2 HG00735.hp2 HG00741.hp2 others(47): Show |
intron_variant | MODIFIER | c.899+361_899+362del others(2): Show |
IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 27361173 | |||||
chr16:27361202
|
G | A | 7 | a0012c0011t0010g0019a0012c0011t0010g0048a0012c0011t0010g0179others(4): Show | 8 | HG02647.hp2 HG02738.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.899+387G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 10/10 | chr16 | 27361202 | ||||||
chr16:27361329
|
T | G | 29 | a0004c0004t0002g0008a0004c0004t0002g0134a0004c0004t0002g0136others(26): Show | 32 | HG00408.hp1 HG01070.hp1 HG01081.hp1 others(29): Show |
intron_variant | MODIFIER | c.899+514T>G | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 10/10 | chr16 | 27361329 | ||||||
chr16:27361371
|
C | T | 5 | a0013c0016t0006g0029a0013c0016t0006g0282a0016c0020t0011g0042others(2): Show | 6 | HG01109.hp2 HG02055.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.899+556C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 10/10 | chr16 | 27361371 | ||||||
chr16:27361426
|
G | A | 2 | a0002c0002t0001g0215a0002c0002t0001g0224 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.899+611G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 10/10 | chr16 | 27361426 | ||||||
chr16:27361610
|
CT | C | 65 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0054others(62): Show | 71 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.900-620delT | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 27361610 | |||||
chr16:27361610
|
CTT | C | 53 | a0001c0001t0007g0073a0002c0002t0001g0256a0003c0003t0001g0058others(50): Show | 58 | HG00597.hp2 HG00639.hp2 HG00741.hp2 others(55): Show |
intron_variant | MODIFIER | c.900-621_900-620del others(2): Show |
IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 27361610 | |||||
chr16:27361610
|
CTTT | C | 46 | a0003c0003t0001g0059a0004c0004t0002g0008a0004c0004t0002g0134others(43): Show | 53 | HG00408.hp1 HG01070.hp1 HG01109.hp2 others(50): Show |
intron_variant | MODIFIER | c.900-622_900-620del others(3): Show |
IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 27361610 | |||||
chr16:27361610
|
CTTTT | C | 11 | a0006c0006t0006g0236a0009c0017t0013g0177a0009c0017t0013g0276others(8): Show | 11 | HG00735.hp2 HG02055.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.900-623_900-620del others(4): Show |
IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 27361610 | |||||
chr16:27361636
|
C | T | 3 | a0016c0020t0011g0042a0016c0020t0011g0240a0016c0032t0011g0043 | 3 | HG02055.hp1 HG02451.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.900-616C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 10/10 | chr16 | 27361636 | ||||||
chr16:27361642
|
G | T | 1 | a0001c0001t0002g0062 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.900-610G>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 10/10 | chr16 | 27361642 | ||||||
chr16:27361771
|
AT | A | 7 | a0012c0011t0010g0019a0012c0011t0010g0048a0012c0011t0010g0179others(4): Show | 8 | HG02647.hp2 HG02738.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.900-477delT | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 27361771 | |||||
chr16:27361810
|
G | A | 41 | a0006c0006t0006g0004a0006c0006t0006g0210a0006c0006t0006g0233others(38): Show | 47 | HG00741.hp2 HG01109.hp2 HG01243.hp2 others(44): Show |
intron_variant | MODIFIER | c.900-442G>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 10/10 | chr16 | 27361810 | ||||||
chr16:27362009
|
T | C | 1 | a0017c0018t0005g0175 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.900-243T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 10/10 | chr16 | 27362009 | ||||||
chr16:27362146
|
A | C | 23 | a0010c0012t0004g0011a0010c0012t0004g0049a0010c0012t0004g0065others(20): Show | 24 | HG00735.hp2 HG00741.hp2 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.900-106A>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 10/10 | chr16 | 27362146 | ||||||
chr16:27362149
|
T | C | 1 | a0020c0021t0001g0015 | 2 | HG02717.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.900-103T>C | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 10/10 | chr16 | 27362149 | ||||||
chr16:27362156
|
C | T | 1 | a0002c0002t0001g0150 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.900-96C>T | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 10/10 | chr16 | 27362156 | ||||||
chr16:27362237
|
C | A | 91 | a0003c0003t0001g0058a0003c0003t0001g0059a0003c0003t0001g0060others(88): Show | 100 | HG00597.hp2 HG00639.hp2 HG00735.hp2 others(97): Show |
intron_variant | MODIFIER | c.900-15C>A | IL4R | ENSG00000077238.14 | transcript | ENST00000395762.7 | protein_coding | 10/10 | chr16 | 27362237 |