geneid | 2208 |
---|---|
ensemblid | ENSG00000104921.15 |
hgncid | 3612 |
symbol | FCER2 |
name | Fc epsilon receptor II |
refseq_nuc | NM_001220500.2 |
refseq_prot | NP_001207429.1 |
ensembl_nuc | ENST00000597921.6 |
ensembl_prot | ENSP00000471974.1 |
mane_status | MANE Select |
chr | chr19 |
start | 7688776 |
end | 7702131 |
strand | - |
ver | v1.2 |
region | chr19:7688776-7702131 |
region5000 | chr19:7683776-7707131 |
regionname0 | FCER2_chr19_7688776_7702131 |
regionname5000 | FCER2_chr19_7683776_7707131 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 321 | 360 | 66 | 72 | 180 | 13 | 27 | 138 | FCER2_chr19_7683776_7707131 | FCER2 | copy fasta | chr19 | 7683776 | 7707131 |
a0002 | 0/0 | 321 | 79 | 28 | 9 | 16 | 4 | 22 | 9 | FCER2_chr19_7683776_7707131 | FCER2 | copy fasta | chr19 | 7683776 | 7707131 |
a0003 | 0/0 | 321 | 7 | 0 | 3 | 3 | 1 | 0 | 2 | FCER2_chr19_7683776_7707131 | FCER2 | copy fasta | chr19 | 7683776 | 7707131 |
a0004 | 0/0 | 321 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | copy fasta | chr19 | 7683776 | 7707131 |
a0005 | 0/0 | 321 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | copy fasta | chr19 | 7683776 | 7707131 |
a0006 | 0/0 | 321 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | copy fasta | chr19 | 7683776 | 7707131 |
a0007 | 0/0 | 321 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | copy fasta | chr19 | 7683776 | 7707131 |
a0008 | 0/0 | 321 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | copy fasta | chr19 | 7683776 | 7707131 |
a0009 | 0/0 | 321 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | copy fasta | chr19 | 7683776 | 7707131 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 966 | 227 | 34 | 47 | 115 | 11 | 18 | FCER2_chr19_7683776_7707131 | FCER2 | copy fasta | chr19 | 7683776 | 7707131 |
c0002 | 0/0 | 966 | 63 | 22 | 8 | 12 | 4 | 17 | FCER2_chr19_7683776_7707131 | FCER2 | copy fasta | chr19 | 7683776 | 7707131 |
c0003 | 0/0 | 966 | 60 | 21 | 6 | 26 | 2 | 5 | FCER2_chr19_7683776_7707131 | FCER2 | copy fasta | chr19 | 7683776 | 7707131 |
c0004 | 0/0 | 966 | 40 | 6 | 17 | 16 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | copy fasta | chr19 | 7683776 | 7707131 |
c0005 | 0/0 | 966 | 31 | 4 | 2 | 22 | 0 | 3 | FCER2_chr19_7683776_7707131 | FCER2 | copy fasta | chr19 | 7683776 | 7707131 |
c0006 | 0/0 | 966 | 11 | 2 | 1 | 4 | 0 | 4 | FCER2_chr19_7683776_7707131 | FCER2 | copy fasta | chr19 | 7683776 | 7707131 |
c0007 | 0/0 | 966 | 5 | 5 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | copy fasta | chr19 | 7683776 | 7707131 |
c0008 | 0/0 | 966 | 4 | 0 | 3 | 0 | 1 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | copy fasta | chr19 | 7683776 | 7707131 |
c0009 | 0/0 | 966 | 4 | 3 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | copy fasta | chr19 | 7683776 | 7707131 |
c0010 | 0/0 | 966 | 3 | 0 | 0 | 3 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | copy fasta | chr19 | 7683776 | 7707131 |
c0011 | 0/0 | 966 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | copy fasta | chr19 | 7683776 | 7707131 |
c0012 | 0/0 | 966 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | copy fasta | chr19 | 7683776 | 7707131 |
c0013 | 0/0 | 966 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | copy fasta | chr19 | 7683776 | 7707131 |
c0014 | 0/0 | 966 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | copy fasta | chr19 | 7683776 | 7707131 |
c0015 | 0/0 | 966 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | copy fasta | chr19 | 7683776 | 7707131 |
c0016 | 0/0 | 966 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | copy fasta | chr19 | 7683776 | 7707131 |
c0017 | 0/0 | 966 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | copy fasta | chr19 | 7683776 | 7707131 |
c0018 | 0/0 | 966 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | copy fasta | chr19 | 7683776 | 7707131 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 620 | 412 | 86 | 76 | 184 | 16 | 48 | FCER2_chr19_7683776_7707131 | FCER2 | copy fasta | chr19 | 7683776 | 7707131 |
t0002 | 0/0 | 556 | 26 | 4 | 8 | 10 | 2 | 2 | FCER2_chr19_7683776_7707131 | FCER2 | copy fasta | chr19 | 7683776 | 7707131 |
t0003 | 0/0 | 620 | 9 | 9 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | copy fasta | chr19 | 7683776 | 7707131 |
t0004 | 0/0 | 620 | 4 | 0 | 0 | 4 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | copy fasta | chr19 | 7683776 | 7707131 |
t0005 | 0/0 | 652 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | copy fasta | chr19 | 7683776 | 7707131 |
t0006 | 0/0 | 588 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | copy fasta | chr19 | 7683776 | 7707131 |
t0007 | 0/0 | 620 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | copy fasta | chr19 | 7683776 | 7707131 |
t0008 | 0/0 | 620 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | copy fasta | chr19 | 7683776 | 7707131 |
t0009 | 0/0 | 620 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | copy fasta | chr19 | 7683776 | 7707131 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 13 | 1 | 6 | 3 | 2 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0002 | 0/0 | 11 | 1 | 4 | 4 | 0 | 2 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0003 | 0/0 | 9 | 0 | 3 | 0 | 1 | 5 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0004 | 0/0 | 9 | 0 | 0 | 8 | 1 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0005 | 0/0 | 8 | 0 | 8 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0006 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0007 | 0/0 | 7 | 0 | 3 | 4 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0008 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0009 | 0/0 | 6 | 0 | 5 | 0 | 1 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0010 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0011 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0012 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0013 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0017 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0019 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0021 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0024 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0026 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0027 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0028 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0029 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0032 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0046 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0049 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0053 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0054 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0055 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0056 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0057 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0058 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0059 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0060 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0061 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0102 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0120 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 966 | 227 | 34 | 47 | 115 | 11 | 18 | FCER2_chr19_7683776_7707131 | FCER2 | copy fasta | chr19 | 7683776 | 7707131 |
a0001c0003 | 0/0 | 966 | 60 | 21 | 6 | 26 | 2 | 5 | FCER2_chr19_7683776_7707131 | FCER2 | copy fasta | chr19 | 7683776 | 7707131 |
a0001c0004 | 0/0 | 966 | 40 | 6 | 17 | 16 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | copy fasta | chr19 | 7683776 | 7707131 |
a0001c0005 | 0/0 | 966 | 31 | 4 | 2 | 22 | 0 | 3 | FCER2_chr19_7683776_7707131 | FCER2 | copy fasta | chr19 | 7683776 | 7707131 |
a0001c0012 | 0/0 | 966 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | copy fasta | chr19 | 7683776 | 7707131 |
a0001c0017 | 0/0 | 966 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | copy fasta | chr19 | 7683776 | 7707131 |
a0002c0002 | 0/0 | 966 | 63 | 22 | 8 | 12 | 4 | 17 | FCER2_chr19_7683776_7707131 | FCER2 | copy fasta | chr19 | 7683776 | 7707131 |
a0002c0006 | 0/0 | 966 | 11 | 2 | 1 | 4 | 0 | 4 | FCER2_chr19_7683776_7707131 | FCER2 | copy fasta | chr19 | 7683776 | 7707131 |
a0002c0009 | 0/0 | 966 | 4 | 3 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | copy fasta | chr19 | 7683776 | 7707131 |
a0002c0014 | 0/0 | 966 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | copy fasta | chr19 | 7683776 | 7707131 |
a0003c0008 | 0/0 | 966 | 4 | 0 | 3 | 0 | 1 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | copy fasta | chr19 | 7683776 | 7707131 |
a0003c0010 | 0/0 | 966 | 3 | 0 | 0 | 3 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | copy fasta | chr19 | 7683776 | 7707131 |
a0004c0007 | 0/0 | 966 | 5 | 5 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | copy fasta | chr19 | 7683776 | 7707131 |
a0005c0011 | 0/0 | 966 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | copy fasta | chr19 | 7683776 | 7707131 |
a0006c0015 | 0/0 | 966 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | copy fasta | chr19 | 7683776 | 7707131 |
a0007c0016 | 0/0 | 966 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | copy fasta | chr19 | 7683776 | 7707131 |
a0008c0013 | 0/0 | 966 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | copy fasta | chr19 | 7683776 | 7707131 |
a0009c0018 | 0/0 | 966 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | copy fasta | chr19 | 7683776 | 7707131 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 1585 | 224 | 34 | 46 | 113 | 11 | 18 | FCER2_chr19_7683776_7707131 | FCER2 | copy fasta | chr19 | 7683776 | 7707131 |
a0001c0001t0005 | 0/0 | 1617 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | copy fasta | chr19 | 7683776 | 7707131 |
a0001c0001t0007 | 0/0 | 1585 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | copy fasta | chr19 | 7683776 | 7707131 |
a0001c0001t0008 | 0/0 | 1585 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | copy fasta | chr19 | 7683776 | 7707131 |
a0001c0003t0001 | 0/0 | 1585 | 40 | 13 | 0 | 24 | 0 | 3 | FCER2_chr19_7683776_7707131 | FCER2 | copy fasta | chr19 | 7683776 | 7707131 |
a0001c0003t0002 | 0/0 | 1521 | 16 | 4 | 6 | 2 | 2 | 2 | FCER2_chr19_7683776_7707131 | FCER2 | copy fasta | chr19 | 7683776 | 7707131 |
a0001c0003t0003 | 0/0 | 1585 | 3 | 3 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | copy fasta | chr19 | 7683776 | 7707131 |
a0001c0003t0009 | 0/0 | 1585 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | copy fasta | chr19 | 7683776 | 7707131 |
a0001c0004t0001 | 0/0 | 1585 | 40 | 6 | 17 | 16 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | copy fasta | chr19 | 7683776 | 7707131 |
a0001c0005t0001 | 0/0 | 1585 | 21 | 4 | 0 | 14 | 0 | 3 | FCER2_chr19_7683776_7707131 | FCER2 | copy fasta | chr19 | 7683776 | 7707131 |
a0001c0005t0002 | 0/0 | 1521 | 10 | 0 | 2 | 8 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | copy fasta | chr19 | 7683776 | 7707131 |
a0001c0012t0001 | 0/0 | 1585 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | copy fasta | chr19 | 7683776 | 7707131 |
a0001c0017t0001 | 0/0 | 1585 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | copy fasta | chr19 | 7683776 | 7707131 |
a0002c0002t0001 | 0/0 | 1585 | 54 | 17 | 8 | 8 | 4 | 17 | FCER2_chr19_7683776_7707131 | FCER2 | copy fasta | chr19 | 7683776 | 7707131 |
a0002c0002t0003 | 0/0 | 1585 | 5 | 5 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | copy fasta | chr19 | 7683776 | 7707131 |
a0002c0002t0004 | 0/0 | 1585 | 4 | 0 | 0 | 4 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | copy fasta | chr19 | 7683776 | 7707131 |
a0002c0006t0001 | 0/0 | 1585 | 11 | 2 | 1 | 4 | 0 | 4 | FCER2_chr19_7683776_7707131 | FCER2 | copy fasta | chr19 | 7683776 | 7707131 |
a0002c0009t0001 | 0/0 | 1585 | 4 | 3 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | copy fasta | chr19 | 7683776 | 7707131 |
a0002c0014t0003 | 0/0 | 1585 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | copy fasta | chr19 | 7683776 | 7707131 |
a0003c0008t0001 | 0/0 | 1585 | 3 | 0 | 2 | 0 | 1 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | copy fasta | chr19 | 7683776 | 7707131 |
a0003c0008t0006 | 0/0 | 1553 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | copy fasta | chr19 | 7683776 | 7707131 |
a0003c0010t0001 | 0/0 | 1585 | 3 | 0 | 0 | 3 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | copy fasta | chr19 | 7683776 | 7707131 |
a0004c0007t0001 | 0/0 | 1585 | 5 | 5 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | copy fasta | chr19 | 7683776 | 7707131 |
a0005c0011t0001 | 0/0 | 1585 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | copy fasta | chr19 | 7683776 | 7707131 |
a0006c0015t0001 | 0/0 | 1585 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | copy fasta | chr19 | 7683776 | 7707131 |
a0007c0016t0001 | 0/0 | 1585 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | copy fasta | chr19 | 7683776 | 7707131 |
a0008c0013t0001 | 0/0 | 1585 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | copy fasta | chr19 | 7683776 | 7707131 |
a0009c0018t0001 | 0/0 | 1585 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | copy fasta | chr19 | 7683776 | 7707131 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 13 | 1 | 6 | 3 | 2 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0002 | 0/0 | 11 | 1 | 4 | 4 | 0 | 2 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0004 | 0/0 | 9 | 0 | 0 | 8 | 1 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0006 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0007 | 0/0 | 7 | 0 | 3 | 4 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0008 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0011 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0012 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0021 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0024 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0026 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0028 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0032 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0049 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0054 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0055 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0058 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0061 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0102 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0120 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0005g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0007g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0001t0008g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0003t0001g0013 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0003t0001g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0003t0001g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0003t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0003t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0003t0001g0053 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0003t0001g0057 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0003t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0003t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0003t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0003t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0003t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0003t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0003t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0003t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0003t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0003t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0003t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0003t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0003t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0003t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0003t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0003t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0003t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0003t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0003t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0003t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0003t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0003t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0003t0002g0009 | 0/0 | 6 | 0 | 5 | 0 | 1 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0003t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0003t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0003t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0003t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0003t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0003t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0003t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0003t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0003t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0003t0002g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0003t0003g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0003t0003g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0003t0003g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0003t0009g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0004t0001g0005 | 0/0 | 8 | 0 | 8 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0004t0001g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0004t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0004t0001g0046 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0004t0001g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0004t0001g0059 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0004t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0004t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0004t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0004t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0004t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0004t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0004t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0004t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0004t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0004t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0004t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0004t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0004t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0004t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0004t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0004t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0004t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0004t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0004t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0004t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0004t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0004t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0005t0001g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0005t0001g0027 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0005t0001g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0005t0001g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0005t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0005t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0005t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0005t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0005t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0005t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0005t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0005t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0005t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0005t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0005t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0005t0002g0010 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0005t0002g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0005t0002g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0005t0002g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0012t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0001c0017t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0002c0002t0001g0003 | 0/0 | 9 | 0 | 3 | 0 | 1 | 5 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0002c0002t0001g0019 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0002c0002t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0002c0002t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0002c0002t0001g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0002c0002t0001g0056 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0002c0002t0001g0060 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0002c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0002c0002t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0002c0002t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0002c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0002c0002t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0002c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0002c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0002c0002t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0002c0002t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0002c0002t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0002c0002t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0002c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0002c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0002c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0002c0002t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0002c0002t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0002c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0002c0002t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0002c0002t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0002c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0002c0002t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0002c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0002c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0002c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0002c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0002c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0002c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0002c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0002c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0002c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0002c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0002c0002t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0002c0002t0003g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0002c0002t0003g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0002c0002t0003g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0002c0002t0004g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0002c0002t0004g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0002c0006t0001g0017 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0002c0006t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0002c0006t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0002c0006t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0002c0006t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0002c0006t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0002c0006t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0002c0006t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0002c0006t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0002c0009t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0002c0009t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0002c0009t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0002c0014t0003g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0003c0008t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0003c0008t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0003c0008t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0003c0008t0006g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0003c0010t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0003c0010t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0003c0010t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0004c0007t0001g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0004c0007t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0004c0007t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0004c0007t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0005c0011t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0006c0015t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0007c0016t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0008c0013t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
a0009c0018t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0024 | EUR | GBR | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0082 | EUR | GBR | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0091 | EUR | GBR | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG00140 | hp2 | a0002 | c0002 | t0001 | g0273 | EUR | GBR | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0096 | EUR | FIN | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG00280 | hp2 | a0001 | c0003 | t0002 | g0009 | EUR | FIN | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | FIN | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG00323 | hp2 | a0002 | c0002 | t0001 | g0003 | EUR | FIN | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG00423 | hp1 | a0002 | c0002 | t0004 | g0134 | EAS | CHS | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | CHS | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG00438 | hp1 | a0001 | c0003 | t0001 | g0013 | EAS | CHS | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG00438 | hp2 | a0002 | c0002 | t0001 | g0064 | EAS | CHS | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | CHS | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | CHS | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | CHS | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG00597 | hp1 | a0001 | c0003 | t0001 | g0037 | EAS | CHS | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | CHS | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG00609 | hp1 | a0001 | c0005 | t0002 | g0010 | EAS | CHS | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG00609 | hp2 | a0002 | c0002 | t0001 | g0255 | EAS | CHS | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | CHS | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG00621 | hp2 | a0002 | c0006 | t0001 | g0017 | EAS | CHS | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG00642 | hp1 | a0001 | c0005 | t0002 | g0282 | AMR | PUR | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | CHS | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG00673 | hp2 | a0002 | c0006 | t0001 | g0127 | EAS | CHS | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG00733 | hp1 | a0003 | c0008 | t0006 | g0183 | AMR | PUR | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0271 | AMR | PUR | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG00735 | hp2 | a0001 | c0004 | t0001 | g0005 | AMR | PUR | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0254 | AMR | PUR | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG00741 | hp2 | a0001 | c0003 | t0002 | g0009 | AMR | PUR | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG01069 | hp1 | a0001 | c0003 | t0002 | g0009 | AMR | PUR | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG01069 | hp2 | a0001 | c0004 | t0001 | g0005 | AMR | PUR | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG01070 | hp2 | a0002 | c0002 | t0001 | g0003 | AMR | PUR | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG01071 | hp1 | a0002 | c0002 | t0001 | g0003 | AMR | PUR | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG01071 | hp2 | a0001 | c0003 | t0002 | g0009 | AMR | PUR | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG01074 | hp2 | a0002 | c0002 | t0001 | g0135 | AMR | PUR | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG01099 | hp1 | a0001 | c0004 | t0001 | g0005 | AMR | PUR | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG01106 | hp2 | a0007 | c0016 | t0001 | g0189 | AMR | PUR | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG01109 | hp2 | a0002 | c0002 | t0001 | g0232 | AMR | PUR | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG01167 | hp1 | a0001 | c0004 | t0001 | g0046 | AMR | PUR | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG01167 | hp2 | a0002 | c0002 | t0001 | g0019 | AMR | PUR | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG01169 | hp1 | a0001 | c0004 | t0001 | g0046 | AMR | PUR | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0290 | AMR | PUR | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG01192 | hp1 | a0001 | c0003 | t0002 | g0009 | AMR | PUR | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG01192 | hp2 | a0002 | c0002 | t0001 | g0136 | AMR | PUR | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG01243 | hp2 | a0001 | c0005 | t0002 | g0283 | AMR | PUR | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG01255 | hp1 | a0001 | c0003 | t0002 | g0009 | AMR | CLM | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG01255 | hp2 | a0003 | c0008 | t0001 | g0292 | AMR | CLM | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | CLM | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | CLM | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG01261 | hp1 | a0002 | c0006 | t0001 | g0067 | AMR | CLM | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0299 | AMR | CLM | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG01346 | hp2 | a0001 | c0003 | t0002 | g0112 | AMR | CLM | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG01358 | hp1 | a0001 | c0004 | t0001 | g0030 | AMR | CLM | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG01361 | hp2 | a0001 | c0004 | t0001 | g0005 | AMR | CLM | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | CLM | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | CLM | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG01496 | hp2 | a0001 | c0004 | t0001 | g0274 | AMR | CLM | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0270 | EUR | IBS | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0054 | EUR | IBS | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG01516 | hp1 | a0002 | c0002 | t0001 | g0272 | EUR | IBS | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0269 | EUR | IBS | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | ACB | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG01884 | hp2 | a0002 | c0002 | t0003 | g0020 | AFR | ACB | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG01891 | hp1 | a0002 | c0014 | t0003 | g0087 | AFR | ACB | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG01891 | hp2 | a0001 | c0004 | t0001 | g0170 | AFR | ACB | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG01928 | hp1 | a0005 | c0011 | t0001 | g0196 | AMR | PEL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG01928 | hp2 | a0001 | c0004 | t0001 | g0177 | AMR | PEL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PEL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG01943 | hp1 | a0001 | c0004 | t0001 | g0030 | AMR | PEL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0300 | AMR | PEL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG01952 | hp1 | a0001 | c0004 | t0001 | g0005 | AMR | PEL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG01952 | hp2 | a0002 | c0002 | t0001 | g0110 | AMR | PEL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG01975 | hp1 | a0001 | c0004 | t0001 | g0279 | AMR | PEL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PEL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG01978 | hp1 | a0001 | c0001 | t0008 | g0184 | AMR | PEL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG01993 | hp2 | a0001 | c0004 | t0001 | g0005 | AMR | PEL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | PEL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02004 | hp2 | a0003 | c0008 | t0001 | g0116 | AMR | PEL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | KHV | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | KHV | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02027 | hp2 | a0001 | c0003 | t0002 | g0219 | EAS | KHV | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02040 | hp2 | a0001 | c0003 | t0001 | g0297 | EAS | KHV | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02055 | hp1 | a0002 | c0002 | t0001 | g0125 | AFR | ACB | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | KHV | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | KHV | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02074 | hp1 | a0001 | c0003 | t0001 | g0057 | EAS | KHV | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02074 | hp2 | a0001 | c0004 | t0001 | g0191 | EAS | KHV | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02080 | hp1 | a0001 | c0004 | t0001 | g0280 | EAS | KHV | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | KHV | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02083 | hp1 | a0001 | c0003 | t0001 | g0294 | EAS | KHV | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02083 | hp2 | a0001 | c0003 | t0001 | g0057 | EAS | KHV | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | KHV | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | KHV | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02132 | hp1 | a0003 | c0010 | t0001 | g0284 | EAS | KHV | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02132 | hp2 | a0001 | c0003 | t0001 | g0108 | EAS | KHV | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | KHV | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | KHV | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02145 | hp1 | a0002 | c0002 | t0001 | g0090 | AFR | ACB | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02145 | hp2 | a0002 | c0009 | t0001 | g0041 | AFR | ACB | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PEL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02155 | hp1 | a0001 | c0004 | t0001 | g0047 | EAS | CDX | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02155 | hp2 | a0001 | c0001 | t0007 | g0132 | EAS | CDX | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CDX | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | CDX | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02257 | hp1 | a0002 | c0009 | t0001 | g0041 | AFR | ACB | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | ACB | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02258 | hp1 | a0001 | c0003 | t0001 | g0074 | AFR | ACB | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02273 | hp1 | a0001 | c0004 | t0001 | g0059 | AMR | PEL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02273 | hp2 | a0001 | c0004 | t0001 | g0005 | AMR | PEL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02280 | hp1 | a0002 | c0002 | t0003 | g0086 | AFR | ACB | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02280 | hp2 | a0001 | c0005 | t0001 | g0042 | AFR | ACB | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PEL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02300 | hp1 | a0001 | c0004 | t0001 | g0197 | AMR | PEL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PEL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | ACB | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02451 | hp2 | a0002 | c0002 | t0001 | g0033 | AFR | ACB | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | KHV | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02572 | hp1 | a0001 | c0003 | t0001 | g0018 | AFR | GWD | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02572 | hp2 | a0002 | c0002 | t0003 | g0020 | AFR | GWD | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02602 | hp1 | a0002 | c0002 | t0001 | g0176 | SAS | PJL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02602 | hp2 | a0001 | c0003 | t0001 | g0094 | SAS | PJL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02615 | hp1 | a0004 | c0007 | t0001 | g0088 | AFR | GWD | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0307 | AFR | GWD | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02622 | hp1 | a0002 | c0002 | t0001 | g0040 | AFR | GWD | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0298 | AFR | GWD | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02630 | hp1 | a0002 | c0002 | t0001 | g0051 | AFR | GWD | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02630 | hp2 | a0001 | c0004 | t0001 | g0167 | AFR | GWD | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | GWD | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02647 | hp2 | a0001 | c0003 | t0009 | g0306 | AFR | GWD | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02683 | hp1 | a0001 | c0003 | t0002 | g0291 | SAS | PJL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02683 | hp2 | a0001 | c0003 | t0001 | g0118 | SAS | PJL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02698 | hp1 | a0002 | c0002 | t0001 | g0079 | SAS | PJL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | GWD | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02723 | hp1 | a0002 | c0006 | t0001 | g0305 | AFR | GWD | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02723 | hp2 | a0004 | c0007 | t0001 | g0043 | AFR | GWD | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02735 | hp1 | a0002 | c0002 | t0001 | g0003 | SAS | PJL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0237 | SAS | PJL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02738 | hp2 | a0002 | c0002 | t0001 | g0003 | SAS | PJL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02809 | hp1 | a0001 | c0003 | t0001 | g0018 | AFR | GWD | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02809 | hp2 | a0002 | c0002 | t0001 | g0223 | AFR | GWD | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02818 | hp2 | a0001 | c0003 | t0002 | g0225 | AFR | GWD | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02886 | hp1 | a0001 | c0003 | t0002 | g0159 | AFR | GWD | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02886 | hp2 | a0001 | c0017 | t0001 | g0303 | AFR | GWD | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02895 | hp2 | a0002 | c0002 | t0001 | g0056 | AFR | GWD | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02896 | hp1 | a0001 | c0005 | t0001 | g0224 | AFR | GWD | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02896 | hp2 | a0004 | c0007 | t0001 | g0164 | AFR | GWD | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02897 | hp1 | a0004 | c0007 | t0001 | g0043 | AFR | GWD | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02897 | hp2 | a0002 | c0002 | t0001 | g0056 | AFR | GWD | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02922 | hp1 | a0001 | c0004 | t0001 | g0163 | AFR | ESN | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02922 | hp2 | a0001 | c0003 | t0001 | g0018 | AFR | ESN | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02965 | hp1 | a0001 | c0005 | t0001 | g0042 | AFR | ESN | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02965 | hp2 | a0001 | c0003 | t0001 | g0153 | AFR | ESN | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02970 | hp1 | a0002 | c0002 | t0001 | g0166 | AFR | ESN | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02970 | hp2 | a0002 | c0002 | t0003 | g0122 | AFR | ESN | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | ESN | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02976 | hp2 | a0002 | c0002 | t0001 | g0040 | AFR | ESN | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG03017 | hp1 | a0002 | c0006 | t0001 | g0017 | SAS | PJL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG03017 | hp2 | a0002 | c0006 | t0001 | g0085 | SAS | PJL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG03041 | hp1 | a0001 | c0003 | t0003 | g0152 | AFR | GWD | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | GWD | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG03098 | hp1 | a0001 | c0003 | t0001 | g0034 | AFR | MSL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG03098 | hp2 | a0004 | c0007 | t0001 | g0066 | AFR | MSL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG03130 | hp1 | a0001 | c0003 | t0001 | g0023 | AFR | ESN | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG03130 | hp2 | a0001 | c0004 | t0001 | g0165 | AFR | ESN | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG03139 | hp1 | a0002 | c0002 | t0003 | g0020 | AFR | ESN | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG03139 | hp2 | a0002 | c0002 | t0001 | g0075 | AFR | ESN | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG03195 | hp1 | a0001 | c0004 | t0001 | g0228 | AFR | ESN | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG03195 | hp2 | a0001 | c0003 | t0001 | g0023 | AFR | ESN | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG03209 | hp1 | a0001 | c0004 | t0001 | g0301 | AFR | MSL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | MSL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG03225 | hp1 | a0002 | c0006 | t0001 | g0171 | AFR | MSL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG03225 | hp2 | a0002 | c0002 | t0001 | g0169 | AFR | MSL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG03239 | hp1 | a0002 | c0002 | t0001 | g0003 | SAS | PJL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG03453 | hp1 | a0001 | c0003 | t0001 | g0053 | AFR | MSL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG03453 | hp2 | a0008 | c0013 | t0001 | g0080 | AFR | MSL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG03486 | hp1 | a0002 | c0002 | t0001 | g0211 | AFR | MSL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG03486 | hp2 | a0001 | c0003 | t0001 | g0023 | AFR | MSL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG03490 | hp1 | a0002 | c0002 | t0001 | g0019 | SAS | PJL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0058 | SAS | PJL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG03491 | hp1 | a0002 | c0002 | t0001 | g0060 | SAS | PJL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG03491 | hp2 | a0002 | c0002 | t0001 | g0139 | SAS | PJL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | PJL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG03492 | hp2 | a0002 | c0002 | t0001 | g0060 | SAS | PJL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | ESN | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG03516 | hp2 | a0002 | c0002 | t0001 | g0078 | AFR | ESN | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG03579 | hp1 | a0001 | c0003 | t0001 | g0053 | AFR | MSL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG03579 | hp2 | a0002 | c0002 | t0001 | g0051 | AFR | MSL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG03654 | hp1 | a0002 | c0006 | t0001 | g0103 | SAS | PJL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG03654 | hp2 | a0001 | c0003 | t0001 | g0013 | SAS | PJL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0264 | SAS | PJL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG03688 | hp1 | a0002 | c0002 | t0001 | g0092 | SAS | STU | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG03688 | hp2 | a0002 | c0002 | t0001 | g0137 | SAS | STU | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG03704 | hp1 | a0001 | c0005 | t0001 | g0084 | SAS | PJL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG03710 | hp1 | a0002 | c0006 | t0001 | g0117 | SAS | PJL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG03831 | hp1 | a0002 | c0002 | t0001 | g0003 | SAS | BEB | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0244 | SAS | BEB | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG03834 | hp1 | a0001 | c0005 | t0001 | g0027 | SAS | BEB | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG03834 | hp2 | a0002 | c0002 | t0001 | g0261 | SAS | BEB | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0252 | SAS | BEB | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG03927 | hp2 | a0002 | c0002 | t0001 | g0019 | SAS | BEB | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG03942 | hp1 | a0001 | c0003 | t0002 | g0107 | SAS | BEB | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0250 | SAS | BEB | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG04115 | hp1 | a0002 | c0002 | t0001 | g0233 | SAS | STU | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0069 | SAS | STU | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0248 | SAS | BEB | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | BEB | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG04199 | hp1 | a0002 | c0002 | t0001 | g0253 | SAS | STU | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG04199 | hp2 | a0002 | c0009 | t0001 | g0210 | SAS | STU | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG04204 | hp1 | a0002 | c0002 | t0001 | g0003 | SAS | STU | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG04228 | hp1 | a0001 | c0004 | t0001 | g0155 | SAS | STU | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | YRI | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | YRI | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | CHB | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA18612 | hp2 | a0002 | c0006 | t0001 | g0128 | EAS | CHB | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA18747 | hp1 | a0002 | c0002 | t0001 | g0231 | EAS | CHB | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | YRI | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | YRI | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA18940 | hp2 | a0002 | c0002 | t0004 | g0022 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA18942 | hp1 | a0001 | c0004 | t0001 | g0195 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA18942 | hp2 | a0001 | c0005 | t0001 | g0251 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA18943 | hp1 | a0001 | c0003 | t0002 | g0222 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA18944 | hp1 | a0001 | c0004 | t0001 | g0059 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA18945 | hp2 | a0001 | c0005 | t0001 | g0027 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA18946 | hp1 | a0001 | c0003 | t0001 | g0063 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA18946 | hp2 | a0001 | c0005 | t0002 | g0010 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA18950 | hp1 | a0001 | c0004 | t0001 | g0293 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA18950 | hp2 | a0001 | c0003 | t0001 | g0239 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA18952 | hp2 | a0001 | c0012 | t0001 | g0205 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA18953 | hp2 | a0001 | c0005 | t0002 | g0035 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA18954 | hp2 | a0002 | c0002 | t0001 | g0267 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA18957 | hp1 | a0001 | c0005 | t0001 | g0203 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA18960 | hp1 | a0001 | c0003 | t0001 | g0241 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA18961 | hp2 | a0001 | c0003 | t0001 | g0207 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA18962 | hp1 | a0001 | c0003 | t0001 | g0095 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA18967 | hp1 | a0001 | c0003 | t0001 | g0037 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA18969 | hp2 | a0001 | c0003 | t0001 | g0093 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA18970 | hp2 | a0001 | c0001 | t0005 | g0289 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA18971 | hp2 | a0001 | c0005 | t0001 | g0048 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA18972 | hp1 | a0001 | c0005 | t0002 | g0010 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA18973 | hp2 | a0001 | c0004 | t0001 | g0126 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA18975 | hp1 | a0001 | c0003 | t0001 | g0097 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA18975 | hp2 | a0006 | c0015 | t0001 | g0098 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA18977 | hp1 | a0001 | c0005 | t0001 | g0048 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA18977 | hp2 | a0002 | c0002 | t0004 | g0022 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA18979 | hp2 | a0001 | c0003 | t0001 | g0013 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA18980 | hp2 | a0001 | c0003 | t0001 | g0101 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA18982 | hp1 | a0001 | c0003 | t0001 | g0013 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA18985 | hp2 | a0002 | c0002 | t0001 | g0247 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA18986 | hp1 | a0001 | c0004 | t0001 | g0045 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA18988 | hp1 | a0001 | c0004 | t0001 | g0158 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA18988 | hp2 | a0001 | c0005 | t0001 | g0025 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA18989 | hp1 | a0001 | c0003 | t0001 | g0068 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA18991 | hp1 | a0001 | c0005 | t0001 | g0025 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA18993 | hp2 | a0001 | c0005 | t0001 | g0027 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA18994 | hp1 | a0002 | c0002 | t0001 | g0268 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA18994 | hp2 | a0001 | c0005 | t0001 | g0227 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA18998 | hp2 | a0001 | c0004 | t0001 | g0045 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA19000 | hp2 | a0001 | c0004 | t0001 | g0198 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA19001 | hp1 | a0001 | c0004 | t0001 | g0192 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA19003 | hp1 | a0001 | c0005 | t0001 | g0204 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA19004 | hp1 | a0002 | c0002 | t0001 | g0100 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA19005 | hp1 | a0001 | c0003 | t0001 | g0256 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA19007 | hp2 | a0001 | c0005 | t0002 | g0010 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA19030 | hp1 | a0001 | c0003 | t0001 | g0034 | AFR | LWK | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA19030 | hp2 | a0001 | c0003 | t0001 | g0142 | AFR | LWK | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA19043 | hp1 | a0001 | c0003 | t0003 | g0154 | AFR | LWK | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | LWK | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA19055 | hp2 | a0001 | c0005 | t0001 | g0200 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA19056 | hp2 | a0001 | c0005 | t0001 | g0025 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA19059 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA19059 | hp2 | a0001 | c0004 | t0001 | g0047 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA19062 | hp1 | a0001 | c0003 | t0001 | g0286 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA19062 | hp2 | a0001 | c0003 | t0001 | g0123 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA19064 | hp1 | a0003 | c0010 | t0001 | g0214 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA19064 | hp2 | a0001 | c0005 | t0001 | g0201 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA19066 | hp1 | a0001 | c0004 | t0001 | g0281 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA19066 | hp2 | a0001 | c0005 | t0002 | g0010 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA19067 | hp2 | a0002 | c0006 | t0001 | g0017 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA19079 | hp1 | a0001 | c0003 | t0001 | g0221 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA19080 | hp1 | a0001 | c0004 | t0001 | g0193 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA19080 | hp2 | a0003 | c0010 | t0001 | g0218 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA19081 | hp1 | a0002 | c0002 | t0001 | g0266 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA19082 | hp1 | a0001 | c0004 | t0001 | g0278 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA19082 | hp2 | a0001 | c0005 | t0002 | g0010 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA19084 | hp1 | a0001 | c0005 | t0002 | g0035 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA19084 | hp2 | a0002 | c0002 | t0004 | g0022 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA19087 | hp1 | a0001 | c0003 | t0001 | g0129 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA19091 | hp1 | a0001 | c0005 | t0001 | g0144 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA19240 | hp1 | a0001 | c0003 | t0002 | g0208 | AFR | YRI | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA19240 | hp2 | a0002 | c0002 | t0001 | g0308 | AFR | YRI | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA20129 | hp1 | a0002 | c0009 | t0001 | g0077 | AFR | ASW | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | ASW | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA20752 | hp1 | a0002 | c0002 | t0001 | g0138 | EUR | TSI | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA20752 | hp2 | a0001 | c0003 | t0002 | g0133 | EUR | TSI | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA20805 | hp1 | a0003 | c0008 | t0001 | g0182 | EUR | TSI | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0024 | EUR | TSI | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA20905 | hp1 | a0009 | c0018 | t0001 | g0162 | SAS | GIH | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA20905 | hp2 | a0001 | c0005 | t0001 | g0157 | SAS | GIH | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG01123 | hp1 | a0002 | c0002 | t0001 | g0003 | AMR | CLM | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG01123 | hp2 | a0001 | c0004 | t0001 | g0005 | AMR | CLM | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02109 | hp1 | a0001 | c0005 | t0001 | g0257 | AFR | ACB | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02109 | hp2 | a0002 | c0002 | t0001 | g0033 | AFR | ACB | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02486 | hp1 | a0001 | c0003 | t0003 | g0304 | AFR | ACB | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | ACB | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | ACB | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG02559 | hp2 | a0001 | c0003 | t0002 | g0147 | AFR | ACB | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | MSL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | MSL | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | USA | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | USA | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | USA | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | USA | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | LWK | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | LWK | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0120 | REF | REF | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0102 | REF | REF | FCER2_chr19_7683776_7707131 | FCER2 | chr19 | 7683776 | 7707131 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:7689213
|
A | G | 1 | a0008 | 1 | HG03453.hp2 | missense_variant | MODERATE | c.946T>C | p.Ser316Pro | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 11/11 | 1148/1585 | 946/966 | 316/321 | chr19 | 7689213 | ||
chr19:7689215
|
G | A | 1 | a0004 | 5 | HG02615.hp1 HG02723.hp2 HG02896.hp2 others(2): Show |
missense_variant | MODERATE | c.944C>T | p.Pro315Leu | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 11/11 | 1146/1585 | 944/966 | 315/321 | chr19 | 7689215 | ||
chr19:7689308
|
C | T | 1 | a0007 | 1 | HG01106.hp2 | missense_variant | MODERATE | c.851G>A | p.Arg284Gln | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 11/11 | 1053/1585 | 851/966 | 284/321 | chr19 | 7689308 | ||
chr19:7689422
|
G | T | 1 | a0009 | 1 | NA20905.hp1 | missense_variant | MODERATE | c.737C>A | p.Ala246Asp | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 11/11 | 939/1585 | 737/966 | 246/321 | chr19 | 7689422 | ||
chr19:7690464
|
C | T | 1 | a0006 | 1 | NA18975.hp2 | missense_variant | MODERATE | c.563G>A | p.Arg188Gln | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 9/11 | 765/1585 | 563/966 | 188/321 | chr19 | 7690464 | ||
chr19:7696869
|
C | T | 1 | a0005 | 1 | HG01928.hp1 | missense_variant | MODERATE | c.425G>A | p.Arg142Gln | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/11 | 627/1585 | 425/966 | 142/321 | chr19 | 7696869 | ||
chr19:7697554
|
C | T | 1 | a0003 | 7 | HG00733.hp1 HG01255.hp2 HG02004.hp2 others(4): Show |
missense_variant | MODERATE | c.226G>A | p.Gly76Ser | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 5/11 | 428/1585 | 226/966 | 76/321 | chr19 | 7697554 | ||
chr19:7698362
|
G | A | 2 | a0002a0009 | 80 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(77): Show |
missense_variant | MODERATE | c.184C>T | p.Arg62Trp | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 4/11 | 386/1585 | 184/966 | 62/321 | chr19 | 7698362 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:7689235
|
A | G | 1 | a0001c0012 | 1 | NA18952.hp2 | synonymous_variant | LOW | c.924T>C | p.Pro308Pro | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 11/11 | 1126/1585 | 924/966 | 308/321 | chr19 | 7689235 | ||
chr19:7689325
|
G | A | 1 | a0001c0017 | 1 | HG02886.hp2 | synonymous_variant | LOW | c.834C>T | p.Gly278Gly | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 11/11 | 1036/1585 | 834/966 | 278/321 | chr19 | 7689325 | ||
chr19:7689340
|
G | A | 1 | a0002c0014 | 1 | HG01891.hp1 | synonymous_variant | LOW | c.819C>T | p.Cys273Cys | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 11/11 | 1021/1585 | 819/966 | 273/321 | chr19 | 7689340 | ||
chr19:7690170
|
G | A | 10 | a0001c0003a0001c0005a0001c0012others(7): Show | 178 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(175): Show |
synonymous_variant | LOW | c.717C>T | p.His239His | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 10/11 | 919/1585 | 717/966 | 239/321 | chr19 | 7690170 | ||
chr19:7698817
|
A | G | 7 | a0001c0004a0001c0005a0001c0012others(4): Show | 86 | HG00609.hp1 HG00621.hp2 HG00642.hp1 others(83): Show |
synonymous_variant | LOW | c.60T>C | p.Arg20Arg | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 3/11 | 262/1585 | 60/966 | 20/321 | chr19 | 7698817 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:7688835
|
G | A | 1 | a0002c0002t0004 | 4 | HG00423.hp1 NA18940.hp2 NA18977.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*358C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 11/11 | 358 | chr19 | 7688835 | |||||
chr19:7688879
|
G | GCATCTGG others(25): Show |
1 | a0001c0001t0005 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*282_*313dupAGAGTA others(26): Show |
FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 11/11 | 313 | chr19 | 7688879 | |||||
chr19:7688879
|
GCATCTGG others(25): Show |
G | 1 | a0003c0008t0006 | 1 | HG00733.hp1 | 3_prime_UTR_variant | MODIFIER | c.*282_*313delAGAGTA others(26): Show |
FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 11/11 | 282 | chr19 | 7688879 | |||||
chr19:7688879
|
GCATCTGG others(57): Show |
G | 2 | a0001c0003t0002a0001c0005t0002 | 26 | HG00280.hp2 HG00609.hp1 HG00642.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*250_*313delAGAGTA others(58): Show |
FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 11/11 | 250 | chr19 | 7688879 | |||||
chr19:7688920
|
G | A | 1 | a0001c0001t0007 | 1 | HG02155.hp2 | 3_prime_UTR_variant | MODIFIER | c.*273C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 11/11 | 273 | chr19 | 7688920 | |||||
chr19:7688929
|
G | C | 3 | a0001c0003t0003a0002c0002t0003a0002c0014t0003 | 9 | HG01884.hp2 HG01891.hp1 HG02280.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*264C>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 11/11 | 264 | chr19 | 7688929 | |||||
chr19:7689169
|
C | A | 1 | a0001c0001t0008 | 1 | HG01978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*24G>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 11/11 | 24 | chr19 | 7689169 | |||||
chr19:7689184
|
T | C | 1 | a0001c0003t0009 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9A>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 11/11 | 9 | chr19 | 7689184 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:7689448
|
G | A | 1 | a0008c0013t0001g0080 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.729-18C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 10/10 | chr19 | 7689448 | ||||||
chr19:7689474
|
G | T | 1 | a0002c0006t0001g0305 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.729-44C>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 10/10 | chr19 | 7689474 | ||||||
chr19:7689558
|
G | C | 1 | a0002c0002t0001g0079 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.729-128C>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 10/10 | chr19 | 7689558 | ||||||
chr19:7689659
|
C | T | 88 | a0001c0001t0001g0104a0001c0003t0001g0023a0001c0003t0001g0034others(85): Show | 125 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.729-229G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 10/10 | chr19 | 7689659 | ||||||
chr19:7689682
|
C | G | 1 | a0001c0001t0001g0015 | 4 | NA18983.hp1 NA19001.hp2 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.729-252G>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 10/10 | chr19 | 7689682 | ||||||
chr19:7689705
|
C | A | 5 | a0001c0001t0001g0199a0001c0001t0001g0209a0001c0001t0001g0275others(2): Show | 5 | NA18960.hp2 NA18973.hp2 NA19003.hp2 others(2): Show |
intron_variant | MODIFIER | c.729-275G>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 10/10 | chr19 | 7689705 | ||||||
chr19:7689705
|
C | T | 137 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0061others(134): Show | 190 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.729-275G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 10/10 | chr19 | 7689705 | ||||||
chr19:7689743
|
T | C | 136 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0061others(133): Show | 189 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(186): Show |
intron_variant | MODIFIER | c.729-313A>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 10/10 | chr19 | 7689743 | ||||||
chr19:7689790
|
C | T | 124 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0061others(121): Show | 171 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(168): Show |
intron_variant | MODIFIER | c.729-360G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 10/10 | chr19 | 7689790 | ||||||
chr19:7689810
|
G | C | 137 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0061others(134): Show | 190 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.728+349C>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 10/10 | chr19 | 7689810 | ||||||
chr19:7689816
|
G | T | 137 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0061others(134): Show | 190 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.728+343C>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 10/10 | chr19 | 7689816 | ||||||
chr19:7689819
|
A | G | 137 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0061others(134): Show | 190 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.728+340T>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 10/10 | chr19 | 7689819 | ||||||
chr19:7689880
|
C | T | 137 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0061others(134): Show | 190 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.728+279G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 10/10 | chr19 | 7689880 | ||||||
chr19:7689897
|
C | T | 5 | a0002c0014t0003g0087a0004c0007t0001g0043a0004c0007t0001g0066others(2): Show | 6 | HG01891.hp1 HG02615.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.728+262G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 10/10 | chr19 | 7689897 | ||||||
chr19:7689912
|
G | A | 137 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0061others(134): Show | 190 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.728+247C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 10/10 | chr19 | 7689912 | ||||||
chr19:7689966
|
C | A | 1 | a0001c0001t0001g0141 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.728+193G>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 10/10 | chr19 | 7689966 | ||||||
chr19:7690026
|
G | A | 140 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0036others(137): Show | 193 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.728+133C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 10/10 | chr19 | 7690026 | ||||||
chr19:7690031
|
T | C | 140 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0036others(137): Show | 193 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.728+128A>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 10/10 | chr19 | 7690031 | ||||||
chr19:7690053
|
C | T | 4 | a0001c0001t0001g0036a0001c0001t0001g0160a0001c0001t0001g0206others(1): Show | 5 | HG01891.hp2 HG02818.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.728+106G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 10/10 | chr19 | 7690053 | ||||||
chr19:7690056
|
A | C | 134 | a0001c0001t0001g0036a0001c0001t0001g0160a0001c0001t0001g0206others(131): Show | 185 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.728+103T>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 10/10 | chr19 | 7690056 | ||||||
chr19:7690078
|
T | C | 134 | a0001c0001t0001g0036a0001c0001t0001g0160a0001c0001t0001g0206others(131): Show | 185 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.728+81A>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 10/10 | chr19 | 7690078 | ||||||
chr19:7690082
|
A | G | 134 | a0001c0001t0001g0036a0001c0001t0001g0160a0001c0001t0001g0206others(131): Show | 185 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.728+77T>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 10/10 | chr19 | 7690082 | ||||||
chr19:7690085
|
C | T | 134 | a0001c0001t0001g0036a0001c0001t0001g0160a0001c0001t0001g0206others(131): Show | 185 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.728+74G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 10/10 | chr19 | 7690085 | ||||||
chr19:7690132
|
C | G | 1 | a0002c0002t0001g0176 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.728+27G>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 10/10 | chr19 | 7690132 | ||||||
chr19:7690145
|
G | A | 6 | a0001c0001t0001g0036a0001c0001t0001g0160a0001c0001t0001g0206others(3): Show | 7 | HG01891.hp2 HG02615.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.728+14C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 10/10 | chr19 | 7690145 | ||||||
chr19:7690273
|
A | G | 128 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(125): Show | 178 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(175): Show |
splice_region_variant&intron_variant | LOW | c.622-8T>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 9/10 | chr19 | 7690273 | ||||||
chr19:7690327
|
C | T | 128 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(125): Show | 178 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.622-62G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 9/10 | chr19 | 7690327 | ||||||
chr19:7690348
|
G | A | 1 | a0001c0001t0001g0186 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.621+58C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 9/10 | chr19 | 7690348 | ||||||
chr19:7690355
|
T | TC | 66 | a0001c0003t0001g0023a0001c0003t0001g0034a0001c0003t0001g0053others(63): Show | 91 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.621+50dupG | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 9/10 | chr19 | 7690355 | ||||||
chr19:7690372
|
T | C | 2 | a0001c0001t0001g0174a0001c0004t0001g0228 | 2 | HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.621+34A>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 9/10 | chr19 | 7690372 | ||||||
chr19:7690399
|
A | G | 127 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(124): Show | 177 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(174): Show |
splice_region_variant&intron_variant | LOW | c.621+7T>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 9/10 | chr19 | 7690399 | ||||||
chr19:7690583
|
T | C | 125 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(122): Show | 175 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.470-26A>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7690583 | ||||||
chr19:7690586
|
G | T | 125 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(122): Show | 175 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.470-29C>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7690586 | ||||||
chr19:7690592
|
T | C | 125 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(122): Show | 175 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.470-35A>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7690592 | ||||||
chr19:7690593
|
G | A | 125 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(122): Show | 175 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.470-36C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7690593 | ||||||
chr19:7690596
|
A | G | 125 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(122): Show | 175 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.470-39T>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7690596 | ||||||
chr19:7690599
|
G | A | 125 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(122): Show | 175 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.470-42C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7690599 | ||||||
chr19:7690600
|
C | T | 58 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0037others(55): Show | 83 | HG00280.hp2 HG00438.hp1 HG00597.hp1 others(80): Show |
intron_variant | MODIFIER | c.470-43G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7690600 | ||||||
chr19:7690632
|
A | G | 125 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(122): Show | 175 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.470-75T>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7690632 | ||||||
chr19:7690685
|
G | A | 125 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(122): Show | 175 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.470-128C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7690685 | ||||||
chr19:7690695
|
C | T | 1 | a0002c0002t0001g0135 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.470-138G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7690695 | ||||||
chr19:7690696
|
A | G | 123 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(120): Show | 173 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.470-139T>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7690696 | ||||||
chr19:7690807
|
C | T | 6 | a0001c0001t0001g0036a0001c0001t0001g0160a0001c0001t0001g0206others(3): Show | 7 | HG01891.hp2 HG02615.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.470-250G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7690807 | ||||||
chr19:7690830
|
A | G | 125 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(122): Show | 175 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.470-273T>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7690830 | ||||||
chr19:7690859
|
A | G | 125 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(122): Show | 175 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.470-302T>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7690859 | ||||||
chr19:7690909
|
G | C | 47 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0037others(44): Show | 60 | HG00438.hp1 HG00597.hp1 HG00733.hp1 others(57): Show |
intron_variant | MODIFIER | c.470-352C>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7690909 | ||||||
chr19:7691026
|
C | T | 18 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0044others(15): Show | 26 | HG02015.hp1 HG02015.hp2 HG02071.hp1 others(23): Show |
intron_variant | MODIFIER | c.470-469G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7691026 | ||||||
chr19:7691043
|
A | G | 1 | a0001c0003t0002g0159 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.470-486T>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7691043 | ||||||
chr19:7691051
|
T | TATCACCA others(177): Show |
1 | a0001c0001t0001g0174 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.470-495_470-494ins others(184): Show |
FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7691051 | ||||||
chr19:7691051
|
T | TATCATCA others(85): Show |
1 | a0003c0008t0006g0183 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.470-495_470-494ins others(92): Show |
FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7691051 | ||||||
chr19:7691056
|
C | T | 124 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(121): Show | 174 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.470-499G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7691056 | ||||||
chr19:7691078
|
G | A | 1 | a0003c0008t0006g0183 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.470-521C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7691078 | ||||||
chr19:7691078
|
G | GGCCCCTC others(85): Show |
41 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0037others(38): Show | 54 | HG00438.hp1 HG00597.hp1 HG01255.hp2 others(51): Show |
intron_variant | MODIFIER | c.470-522_470-521ins others(92): Show |
FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7691078 | ||||||
chr19:7691078
|
G | GGCCCCTC others(85): Show |
67 | a0001c0003t0001g0023a0001c0003t0001g0034a0001c0003t0001g0053others(64): Show | 92 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.470-522_470-521ins others(92): Show |
FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7691078 | ||||||
chr19:7691078
|
G | GGCCCCTC others(85): Show |
1 | a0004c0007t0001g0088 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.470-522_470-521ins others(92): Show |
FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7691078 | ||||||
chr19:7691092
|
C | T | 39 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0031others(36): Show | 51 | HG01109.hp1 HG01891.hp2 HG01934.hp2 others(48): Show |
intron_variant | MODIFIER | c.470-535G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7691092 | ||||||
chr19:7691121
|
C | CTGA | 15 | a0001c0003t0002g0009a0001c0003t0002g0107a0001c0003t0002g0112others(12): Show | 27 | HG00280.hp2 HG00609.hp1 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.470-565_470-564ins others(3): Show |
FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7691121 | ||||||
chr19:7691123
|
A | G | 110 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(107): Show | 148 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(145): Show |
intron_variant | MODIFIER | c.470-566T>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7691123 | ||||||
chr19:7691124
|
A | ATAGCTCA others(82): Show |
15 | a0001c0003t0002g0009a0001c0003t0002g0107a0001c0003t0002g0112others(12): Show | 27 | HG00280.hp2 HG00609.hp1 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.470-568_470-567ins others(89): Show |
FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7691124 | ||||||
chr19:7691124
|
A | G | 110 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(107): Show | 148 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(145): Show |
intron_variant | MODIFIER | c.470-567T>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7691124 | ||||||
chr19:7691154
|
A | T | 2 | a0001c0001t0001g0269a0001c0001t0001g0270 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.470-597T>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7691154 | ||||||
chr19:7691182
|
G | A | 125 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(122): Show | 175 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.470-625C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7691182 | ||||||
chr19:7691202
|
T | C | 125 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(122): Show | 175 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.470-645A>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7691202 | ||||||
chr19:7691237
|
T | C | 125 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(122): Show | 175 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.470-680A>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7691237 | ||||||
chr19:7691305
|
C | T | 125 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(122): Show | 175 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.470-748G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7691305 | ||||||
chr19:7691385
|
A | T | 124 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(121): Show | 174 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.470-828T>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7691385 | ||||||
chr19:7691425
|
C | T | 124 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(121): Show | 174 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.470-868G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7691425 | ||||||
chr19:7691440
|
C | T | 60 | a0001c0003t0001g0023a0001c0003t0001g0034a0001c0003t0001g0074others(57): Show | 84 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.470-883G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7691440 | ||||||
chr19:7691442
|
A | C | 124 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(121): Show | 174 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.470-885T>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7691442 | ||||||
chr19:7691445
|
G | T | 124 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(121): Show | 174 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.470-888C>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7691445 | ||||||
chr19:7691449
|
A | ATAGT | 124 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(121): Show | 174 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.470-893_470-892ins others(4): Show |
FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7691449 | ||||||
chr19:7691465
|
A | T | 124 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(121): Show | 174 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.470-908T>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7691465 | ||||||
chr19:7691498
|
T | C | 1 | a0001c0001t0001g0058 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.470-941A>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7691498 | ||||||
chr19:7691545
|
C | T | 1 | a0001c0005t0002g0282 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.470-988G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7691545 | ||||||
chr19:7691577
|
A | G | 124 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(121): Show | 174 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.470-1020T>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7691577 | ||||||
chr19:7691591
|
C | G | 124 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(121): Show | 174 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.470-1034G>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7691591 | ||||||
chr19:7691596
|
C | T | 39 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0037others(36): Show | 51 | HG00438.hp1 HG00597.hp1 HG00733.hp1 others(48): Show |
intron_variant | MODIFIER | c.470-1039G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7691596 | ||||||
chr19:7691709
|
G | A | 118 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(115): Show | 168 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.470-1152C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7691709 | ||||||
chr19:7691748
|
A | C | 122 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(119): Show | 172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1191T>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7691748 | ||||||
chr19:7691771
|
T | C | 121 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(118): Show | 171 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(168): Show |
intron_variant | MODIFIER | c.470-1214A>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7691771 | ||||||
chr19:7691820
|
T | C | 122 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(119): Show | 172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1263A>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7691820 | ||||||
chr19:7691900
|
A | G | 1 | a0002c0006t0001g0127 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.470-1343T>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7691900 | ||||||
chr19:7691962
|
T | C | 122 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(119): Show | 172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1405A>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7691962 | ||||||
chr19:7691963
|
G | A | 122 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(119): Show | 172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1406C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7691963 | ||||||
chr19:7691964
|
T | C | 122 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(119): Show | 172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1407A>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7691964 | ||||||
chr19:7691969
|
C | A | 122 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(119): Show | 172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1412G>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7691969 | ||||||
chr19:7691970
|
ATT | A | 122 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(119): Show | 172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1415_470-1414d others(4): Show |
FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7691970 | ||||||
chr19:7691972
|
T | TCACACTC others(137): Show |
1 | a0001c0001t0001g0194 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.470-1416_470-1415i others(146): Show |
FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7691972 | ||||||
chr19:7691972
|
T | TCACATTC others(137): Show |
182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(179): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.470-1416_470-1415i others(146): Show |
FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7691972 | ||||||
chr19:7691972
|
T | TCACATTC others(281): Show |
1 | a0001c0001t0001g0115 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.470-1416_470-1415i others(290): Show |
FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7691972 | ||||||
chr19:7691972
|
T | TCACATTC others(137): Show |
1 | a0001c0001t0001g0015 | 4 | NA18983.hp1 NA19001.hp2 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.470-1416_470-1415i others(146): Show |
FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7691972 | ||||||
chr19:7692000
|
C | T | 122 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(119): Show | 172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1443G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692000 | ||||||
chr19:7692012
|
C | T | 122 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(119): Show | 172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1455G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692012 | ||||||
chr19:7692013
|
A | G | 122 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(119): Show | 172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1456T>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692013 | ||||||
chr19:7692014
|
G | T | 122 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(119): Show | 172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1457C>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692014 | ||||||
chr19:7692018
|
G | A | 122 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(119): Show | 172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1461C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692018 | ||||||
chr19:7692021
|
T | C | 122 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(119): Show | 172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1464A>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692021 | ||||||
chr19:7692024
|
A | ATTCACG | 122 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(119): Show | 172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1473_470-1468d others(8): Show |
FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692024 | ||||||
chr19:7692035
|
A | T | 122 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(119): Show | 172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1478T>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692035 | ||||||
chr19:7692048
|
T | C | 122 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(119): Show | 172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1491A>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692048 | ||||||
chr19:7692065
|
C | T | 122 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(119): Show | 172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1508G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692065 | ||||||
chr19:7692067
|
A | G | 122 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(119): Show | 172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1510T>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692067 | ||||||
chr19:7692068
|
G | A | 142 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0044others(139): Show | 200 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.470-1511C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692068 | ||||||
chr19:7692083
|
A | T | 122 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(119): Show | 172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1526T>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692083 | ||||||
chr19:7692089
|
C | A | 185 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(182): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.470-1532G>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692089 | ||||||
chr19:7692096
|
T | C | 122 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(119): Show | 172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1539A>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692096 | ||||||
chr19:7692107
|
T | C | 141 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(138): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.470-1550A>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692107 | ||||||
chr19:7692108
|
T | C | 122 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(119): Show | 172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1551A>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692108 | ||||||
chr19:7692109
|
G | A | 122 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(119): Show | 172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1552C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692109 | ||||||
chr19:7692110
|
T | C | 122 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(119): Show | 172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1553A>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692110 | ||||||
chr19:7692113
|
T | C | 123 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(120): Show | 173 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.470-1556A>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692113 | ||||||
chr19:7692115
|
A | G | 122 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(119): Show | 172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1558T>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692115 | ||||||
chr19:7692125
|
C | T | 122 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(119): Show | 172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1568G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692125 | ||||||
chr19:7692157
|
A | G | 122 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(119): Show | 172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1600T>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692157 | ||||||
chr19:7692161
|
C | T | 122 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(119): Show | 172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1604G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692161 | ||||||
chr19:7692164
|
A | G | 122 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(119): Show | 172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1607T>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692164 | ||||||
chr19:7692174
|
G | A | 137 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0036others(134): Show | 191 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.470-1617C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692174 | ||||||
chr19:7692190
|
A | T | 1 | a0001c0004t0001g0197 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.470-1633T>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692190 | ||||||
chr19:7692203
|
T | G | 122 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(119): Show | 172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1646A>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692203 | ||||||
chr19:7692204
|
C | T | 122 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(119): Show | 172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1647G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692204 | ||||||
chr19:7692205
|
A | G | 122 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(119): Show | 172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1648T>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692205 | ||||||
chr19:7692210
|
G | A | 122 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(119): Show | 172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1653C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692210 | ||||||
chr19:7692212
|
G | A | 122 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(119): Show | 172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1655C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692212 | ||||||
chr19:7692227
|
A | G | 122 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(119): Show | 172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1670T>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692227 | ||||||
chr19:7692233
|
A | C | 122 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(119): Show | 172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1676T>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692233 | ||||||
chr19:7692249
|
C | A | 122 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(119): Show | 172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1692G>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692249 | ||||||
chr19:7692251
|
C | T | 122 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(119): Show | 172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1694G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692251 | ||||||
chr19:7692252
|
T | C | 122 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(119): Show | 172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1695A>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692252 | ||||||
chr19:7692253
|
G | A | 122 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(119): Show | 172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1696C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692253 | ||||||
chr19:7692254
|
T | C | 122 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(119): Show | 172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1697A>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692254 | ||||||
chr19:7692269
|
C | T | 123 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(120): Show | 173 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.470-1712G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692269 | ||||||
chr19:7692275
|
T | G | 122 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(119): Show | 172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1718A>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692275 | ||||||
chr19:7692288
|
C | T | 122 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(119): Show | 172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1731G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692288 | ||||||
chr19:7692300
|
C | T | 122 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(119): Show | 172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1743G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692300 | ||||||
chr19:7692301
|
A | G | 122 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(119): Show | 172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1744T>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692301 | ||||||
chr19:7692306
|
G | A | 122 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(119): Show | 172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1749C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692306 | ||||||
chr19:7692312
|
A | C | 122 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(119): Show | 172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1755T>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692312 | ||||||
chr19:7692318
|
G | A | 122 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(119): Show | 172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1761C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692318 | ||||||
chr19:7692322
|
A | G | 5 | a0001c0003t0003g0154a0004c0007t0001g0043a0004c0007t0001g0066others(2): Show | 6 | HG02615.hp1 HG02723.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.470-1765T>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692322 | ||||||
chr19:7692323
|
A | T | 122 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(119): Show | 172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1766T>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692323 | ||||||
chr19:7692329
|
C | T | 122 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(119): Show | 172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1772G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692329 | ||||||
chr19:7692349
|
A | G | 122 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(119): Show | 172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1792T>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692349 | ||||||
chr19:7692356
|
G | A | 122 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(119): Show | 172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1799C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692356 | ||||||
chr19:7692369
|
CAACAACA others(41): Show |
C | 122 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(119): Show | 172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1860_470-1813d others(50): Show |
FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692369 | ||||||
chr19:7692440
|
C | A | 6 | a0001c0001t0001g0036a0001c0001t0001g0160a0001c0001t0001g0206others(3): Show | 7 | HG01891.hp2 HG02615.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.470-1883G>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692440 | ||||||
chr19:7692445
|
G | A | 122 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(119): Show | 172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1888C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692445 | ||||||
chr19:7692450
|
G | GAACACAT others(6): Show |
1 | a0001c0005t0001g0204 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.470-1906_470-1894d others(15): Show |
FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692450 | ||||||
chr19:7692462
|
G | A | 5 | a0001c0003t0003g0154a0004c0007t0001g0043a0004c0007t0001g0066others(2): Show | 6 | HG02615.hp1 HG02723.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.470-1905C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692462 | ||||||
chr19:7692485
|
A | G | 122 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(119): Show | 172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1928T>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692485 | ||||||
chr19:7692492
|
C | T | 4 | a0004c0007t0001g0043a0004c0007t0001g0066a0004c0007t0001g0088others(1): Show | 5 | HG02615.hp1 HG02723.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.470-1935G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692492 | ||||||
chr19:7692493
|
A | G | 122 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(119): Show | 172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1936T>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692493 | ||||||
chr19:7692497
|
C | T | 2 | a0001c0001t0001g0174a0001c0004t0001g0228 | 2 | HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.470-1940G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692497 | ||||||
chr19:7692500
|
G | A | 84 | a0001c0003t0001g0018a0001c0003t0001g0023a0001c0003t0001g0034others(81): Show | 124 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.470-1943C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692500 | ||||||
chr19:7692501
|
C | T | 122 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(119): Show | 172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1944G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692501 | ||||||
chr19:7692541
|
A | G | 122 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(119): Show | 172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1984T>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692541 | ||||||
chr19:7692545
|
T | C | 122 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(119): Show | 172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-1988A>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692545 | ||||||
chr19:7692570
|
G | A | 122 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(119): Show | 172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-2013C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692570 | ||||||
chr19:7692586
|
G | A | 1 | a0002c0002t0001g0079 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.470-2029C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692586 | ||||||
chr19:7692599
|
CCTTACAG others(137): Show |
C | 3 | a0001c0005t0001g0224a0002c0002t0001g0033a0002c0002t0001g0078 | 4 | HG02109.hp2 HG02451.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.470-2186_470-2043d others(2): Show |
FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692599 | ||||||
chr19:7692629
|
C | T | 119 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(116): Show | 168 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.470-2072G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692629 | ||||||
chr19:7692630
|
ACCATCG | A | 119 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(116): Show | 168 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.470-2079_470-2074d others(8): Show |
FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692630 | ||||||
chr19:7692639
|
A | G | 6 | a0001c0001t0001g0036a0001c0001t0001g0160a0001c0001t0001g0206others(3): Show | 7 | HG01891.hp2 HG02615.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.470-2082T>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692639 | ||||||
chr19:7692643
|
G | A | 119 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(116): Show | 168 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.470-2086C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692643 | ||||||
chr19:7692649
|
C | T | 21 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0044others(18): Show | 29 | HG02015.hp1 HG02015.hp2 HG02071.hp1 others(26): Show |
intron_variant | MODIFIER | c.470-2092G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692649 | ||||||
chr19:7692650
|
G | A | 1 | a0002c0002t0003g0122 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.470-2093C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692650 | ||||||
chr19:7692678
|
A | G | 121 | a0001c0001t0001g0174a0001c0003t0001g0013a0001c0003t0001g0018others(118): Show | 170 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.470-2121T>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692678 | ||||||
chr19:7692727
|
G | A | 119 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(116): Show | 168 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.470-2170C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692727 | ||||||
chr19:7692729
|
T | C | 119 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(116): Show | 168 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.470-2172A>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692729 | ||||||
chr19:7692742
|
T | C | 119 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(116): Show | 168 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.470-2185A>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692742 | ||||||
chr19:7692781
|
A | G | 122 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(119): Show | 172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-2224T>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692781 | ||||||
chr19:7692842
|
C | T | 122 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(119): Show | 172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-2285G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692842 | ||||||
chr19:7692867
|
C | A | 122 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(119): Show | 172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-2310G>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692867 | ||||||
chr19:7692883
|
A | G | 122 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(119): Show | 172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-2326T>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692883 | ||||||
chr19:7692999
|
A | G | 1 | a0001c0004t0001g0192 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.470-2442T>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7692999 | ||||||
chr19:7693022
|
C | T | 21 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0044others(18): Show | 29 | HG02015.hp1 HG02015.hp2 HG02071.hp1 others(26): Show |
intron_variant | MODIFIER | c.470-2465G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7693022 | ||||||
chr19:7693028
|
C | A | 9 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0061others(6): Show | 12 | HG01934.hp2 HG02055.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.470-2471G>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7693028 | ||||||
chr19:7693041
|
A | G | 1 | a0001c0004t0001g0293 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.470-2484T>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7693041 | ||||||
chr19:7693113
|
C | T | 1 | a0001c0004t0001g0197 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.470-2556G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7693113 | ||||||
chr19:7693114
|
G | A | 122 | a0001c0003t0001g0013a0001c0003t0001g0018a0001c0003t0001g0023others(119): Show | 172 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.470-2557C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7693114 | ||||||
chr19:7693133
|
C | T | 1 | a0008c0013t0001g0080 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.470-2576G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7693133 | ||||||
chr19:7693151
|
T | G | 3 | a0001c0005t0001g0224a0002c0002t0001g0033a0002c0002t0001g0078 | 4 | HG02109.hp2 HG02451.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.470-2594A>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7693151 | ||||||
chr19:7693155
|
G | A | 2 | a0001c0003t0001g0053a0002c0002t0001g0075 | 3 | HG03139.hp2 HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.470-2598C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7693155 | ||||||
chr19:7693209
|
G | C | 1 | a0002c0002t0004g0134 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.470-2652C>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7693209 | ||||||
chr19:7693231
|
G | C | 122 | a0001c0001t0001g0039a0001c0001t0001g0243a0001c0003t0001g0013others(119): Show | 173 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.470-2674C>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7693231 | ||||||
chr19:7693268
|
T | A | 157 | a0001c0001t0001g0007a0001c0001t0001g0026a0001c0001t0001g0065others(154): Show | 223 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.470-2711A>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7693268 | ||||||
chr19:7693272
|
G | C | 157 | a0001c0001t0001g0007a0001c0001t0001g0026a0001c0001t0001g0065others(154): Show | 223 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.470-2715C>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7693272 | ||||||
chr19:7693308
|
C | T | 82 | a0001c0003t0001g0023a0001c0003t0001g0034a0001c0003t0001g0053others(79): Show | 120 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.470-2751G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7693308 | ||||||
chr19:7693374
|
G | C | 157 | a0001c0001t0001g0007a0001c0001t0001g0026a0001c0001t0001g0065others(154): Show | 223 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.470-2817C>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7693374 | ||||||
chr19:7693377
|
G | A | 157 | a0001c0001t0001g0007a0001c0001t0001g0026a0001c0001t0001g0065others(154): Show | 223 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.470-2820C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7693377 | ||||||
chr19:7693417
|
A | G | 157 | a0001c0001t0001g0007a0001c0001t0001g0026a0001c0001t0001g0065others(154): Show | 223 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.470-2860T>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7693417 | ||||||
chr19:7693430
|
C | G | 158 | a0001c0001t0001g0007a0001c0001t0001g0026a0001c0001t0001g0065others(155): Show | 224 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(221): Show |
intron_variant | MODIFIER | c.470-2873G>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7693430 | ||||||
chr19:7693443
|
A | T | 5 | a0001c0003t0003g0154a0004c0007t0001g0043a0004c0007t0001g0066others(2): Show | 6 | HG02615.hp1 HG02723.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.470-2886T>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7693443 | ||||||
chr19:7693453
|
T | C | 72 | a0001c0001t0001g0007a0001c0001t0001g0026a0001c0001t0001g0065others(69): Show | 98 | HG00280.hp1 HG00438.hp1 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.470-2896A>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7693453 | ||||||
chr19:7693503
|
T | C | 1 | a0001c0001t0001g0071 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.470-2946A>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7693503 | ||||||
chr19:7693551
|
A | T | 1 | a0002c0002t0003g0122 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.470-2994T>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7693551 | ||||||
chr19:7693584
|
T | A | 179 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0016others(176): Show | 253 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(250): Show |
intron_variant | MODIFIER | c.470-3027A>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7693584 | ||||||
chr19:7693591
|
G | A | 179 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0016others(176): Show | 253 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(250): Show |
intron_variant | MODIFIER | c.470-3034C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7693591 | ||||||
chr19:7693624
|
C | CT | 1 | a0001c0003t0001g0018 | 3 | HG02572.hp1 HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.470-3068dupA | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7693624 | ||||||
chr19:7693642
|
T | TTTTTG | 2 | a0002c0002t0001g0033a0002c0002t0001g0078 | 3 | HG02109.hp2 HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.470-3090_470-3086d others(7): Show |
FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7693642 | ||||||
chr19:7693732
|
T | C | 83 | a0001c0001t0001g0307a0001c0003t0001g0023a0001c0003t0001g0034others(80): Show | 121 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.469+3093A>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7693732 | ||||||
chr19:7693733
|
G | A | 1 | a0002c0002t0001g0137 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.469+3092C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7693733 | ||||||
chr19:7693839
|
G | A | 44 | a0001c0001t0001g0307a0001c0003t0001g0023a0001c0003t0001g0034others(41): Show | 63 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.469+2986C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7693839 | ||||||
chr19:7693907
|
C | A | 180 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0016others(177): Show | 253 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(250): Show |
intron_variant | MODIFIER | c.469+2918G>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7693907 | ||||||
chr19:7693953
|
A | AT | 32 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0036others(29): Show | 37 | HG00544.hp1 HG00621.hp1 HG01257.hp1 others(34): Show |
intron_variant | MODIFIER | c.469+2871dupA | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7693953 | ||||||
chr19:7693953
|
AT | A | 28 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0044others(25): Show | 38 | HG00741.hp1 HG01169.hp2 HG02015.hp1 others(35): Show |
intron_variant | MODIFIER | c.469+2871delA | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7693953 | ||||||
chr19:7693953
|
ATTTTTTT others(5): Show |
A | 83 | a0001c0001t0001g0307a0001c0003t0001g0023a0001c0003t0001g0034others(80): Show | 121 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.469+2860_469+2871d others(14): Show |
FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7693953 | ||||||
chr19:7693988
|
C | T | 2 | a0002c0002t0001g0136a0002c0002t0001g0272 | 2 | HG01192.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.469+2837G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7693988 | ||||||
chr19:7693994
|
C | G | 83 | a0001c0001t0001g0307a0001c0003t0001g0023a0001c0003t0001g0034others(80): Show | 121 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.469+2831G>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7693994 | ||||||
chr19:7694011
|
C | T | 83 | a0001c0001t0001g0307a0001c0003t0001g0023a0001c0003t0001g0034others(80): Show | 121 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.469+2814G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7694011 | ||||||
chr19:7694044
|
G | A | 83 | a0001c0001t0001g0307a0001c0003t0001g0023a0001c0003t0001g0034others(80): Show | 121 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.469+2781C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7694044 | ||||||
chr19:7694064
|
T | C | 1 | a0001c0001t0001g0072 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.469+2761A>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7694064 | ||||||
chr19:7694144
|
A | G | 75 | a0001c0001t0001g0007a0001c0001t0001g0026a0001c0001t0001g0065others(72): Show | 103 | HG00280.hp1 HG00438.hp1 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.469+2681T>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7694144 | ||||||
chr19:7694147
|
G | A | 75 | a0001c0001t0001g0007a0001c0001t0001g0026a0001c0001t0001g0065others(72): Show | 103 | HG00280.hp1 HG00438.hp1 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.469+2678C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7694147 | ||||||
chr19:7694150
|
C | G | 75 | a0001c0001t0001g0007a0001c0001t0001g0026a0001c0001t0001g0065others(72): Show | 103 | HG00280.hp1 HG00438.hp1 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.469+2675G>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7694150 | ||||||
chr19:7694168
|
G | T | 75 | a0001c0001t0001g0007a0001c0001t0001g0026a0001c0001t0001g0065others(72): Show | 103 | HG00280.hp1 HG00438.hp1 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.469+2657C>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7694168 | ||||||
chr19:7694169
|
T | G | 75 | a0001c0001t0001g0007a0001c0001t0001g0026a0001c0001t0001g0065others(72): Show | 103 | HG00280.hp1 HG00438.hp1 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.469+2656A>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7694169 | ||||||
chr19:7694189
|
G | C | 1 | a0002c0002t0001g0176 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.469+2636C>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7694189 | ||||||
chr19:7694215
|
G | C | 22 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0044others(19): Show | 32 | HG02015.hp1 HG02015.hp2 HG02071.hp1 others(29): Show |
intron_variant | MODIFIER | c.469+2610C>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7694215 | ||||||
chr19:7694267
|
A | G | 4 | a0003c0008t0001g0116a0003c0008t0001g0182a0003c0008t0001g0292others(1): Show | 4 | HG00733.hp1 HG01255.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.469+2558T>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7694267 | ||||||
chr19:7694286
|
C | T | 1 | a0001c0004t0001g0193 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.469+2539G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7694286 | ||||||
chr19:7694304
|
G | A | 2 | a0001c0003t0002g0208a0001c0003t0002g0225 | 2 | HG02818.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.469+2521C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7694304 | ||||||
chr19:7694319
|
T | C | 1 | a0001c0003t0001g0018 | 3 | HG02572.hp1 HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.469+2506A>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7694319 | ||||||
chr19:7694324
|
C | T | 5 | a0001c0001t0001g0111a0001c0001t0001g0172a0001c0001t0001g0174others(2): Show | 5 | HG01109.hp1 HG02976.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.469+2501G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7694324 | ||||||
chr19:7694367
|
A | C | 78 | a0001c0001t0001g0307a0001c0003t0001g0023a0001c0003t0001g0034others(75): Show | 115 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.469+2458T>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7694367 | ||||||
chr19:7694382
|
A | G | 3 | a0003c0010t0001g0214a0003c0010t0001g0218a0003c0010t0001g0284 | 3 | HG02132.hp1 NA19064.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.469+2443T>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7694382 | ||||||
chr19:7694394
|
C | T | 78 | a0001c0001t0001g0307a0001c0003t0001g0023a0001c0003t0001g0034others(75): Show | 115 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.469+2431G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7694394 | ||||||
chr19:7694583
|
G | T | 1 | a0002c0002t0001g0135 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.469+2242C>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7694583 | ||||||
chr19:7694683
|
T | C | 172 | a0001c0001t0001g0007a0001c0001t0001g0026a0001c0001t0001g0031others(169): Show | 240 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(237): Show |
intron_variant | MODIFIER | c.469+2142A>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7694683 | ||||||
chr19:7694734
|
G | C | 1 | a0001c0001t0001g0021 | 3 | HG01106.hp1 HG01358.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.469+2091C>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7694734 | ||||||
chr19:7694790
|
C | T | 201 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0016others(198): Show | 279 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(276): Show |
intron_variant | MODIFIER | c.469+2035G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7694790 | ||||||
chr19:7694827
|
C | T | 4 | a0001c0001t0001g0024a0001c0001t0001g0120a0001c0001t0001g0237others(1): Show | 6 | HG00099.hp1 HG01175.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.469+1998G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7694827 | ||||||
chr19:7694828
|
C | T | 1 | a0001c0004t0001g0126 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.469+1997G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7694828 | ||||||
chr19:7694829
|
G | C | 201 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0016others(198): Show | 279 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(276): Show |
intron_variant | MODIFIER | c.469+1996C>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7694829 | ||||||
chr19:7694837
|
AT | A | 85 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0036others(82): Show | 115 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.469+1987delA | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7694837 | ||||||
chr19:7695134
|
T | A | 66 | a0001c0001t0001g0307a0001c0003t0001g0023a0001c0003t0001g0034others(63): Show | 92 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.469+1691A>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7695134 | ||||||
chr19:7695284
|
C | T | 2 | a0001c0001t0001g0187a0001c0001t0001g0242 | 2 | NA18956.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.469+1541G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7695284 | ||||||
chr19:7695440
|
A | C | 4 | a0001c0003t0001g0018a0003c0010t0001g0214a0003c0010t0001g0218others(1): Show | 6 | HG02132.hp1 HG02572.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.469+1385T>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7695440 | ||||||
chr19:7695541
|
C | T | 1 | a0001c0003t0001g0018 | 3 | HG02572.hp1 HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.469+1284G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7695541 | ||||||
chr19:7695560
|
G | A | 62 | a0001c0001t0001g0307a0001c0003t0001g0034a0001c0003t0001g0053others(59): Show | 86 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.469+1265C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7695560 | ||||||
chr19:7695596
|
C | T | 62 | a0001c0001t0001g0307a0001c0003t0001g0034a0001c0003t0001g0053others(59): Show | 86 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.469+1229G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7695596 | ||||||
chr19:7695619
|
T | TA | 62 | a0001c0001t0001g0307a0001c0003t0001g0034a0001c0003t0001g0053others(59): Show | 86 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.469+1205dupT | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7695619 | ||||||
chr19:7695723
|
C | T | 62 | a0001c0001t0001g0307a0001c0003t0001g0034a0001c0003t0001g0053others(59): Show | 86 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.469+1102G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7695723 | ||||||
chr19:7695738
|
G | A | 7 | a0001c0003t0002g0009a0001c0003t0002g0107a0001c0003t0002g0133others(4): Show | 12 | HG00280.hp2 HG00642.hp1 HG00741.hp2 others(9): Show |
intron_variant | MODIFIER | c.469+1087C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7695738 | ||||||
chr19:7695783
|
G | A | 62 | a0001c0001t0001g0307a0001c0003t0001g0034a0001c0003t0001g0053others(59): Show | 86 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.469+1042C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7695783 | ||||||
chr19:7695793
|
C | T | 4 | a0004c0007t0001g0043a0004c0007t0001g0066a0004c0007t0001g0088others(1): Show | 5 | HG02615.hp1 HG02723.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.469+1032G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7695793 | ||||||
chr19:7695912
|
ATC | A | 3 | a0001c0003t0001g0074a0002c0002t0001g0255a0002c0002t0004g0134 | 3 | HG00423.hp1 HG00609.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.469+911_469+912del others(2): Show |
FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7695912 | ||||||
chr19:7695918
|
CTCT | C | 56 | a0001c0001t0001g0307a0001c0003t0001g0034a0001c0003t0001g0053others(53): Show | 80 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.469+904_469+906del others(3): Show |
FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7695918 | ||||||
chr19:7695920
|
C | CT | 24 | a0001c0001t0001g0012a0001c0001t0001g0028a0001c0001t0001g0081others(21): Show | 35 | HG00544.hp2 HG00609.hp1 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.469+904dupA | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7695920 | ||||||
chr19:7695920
|
CT | C | 91 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0016others(88): Show | 125 | HG00280.hp1 HG00438.hp1 HG00639.hp1 others(122): Show |
intron_variant | MODIFIER | c.469+904delA | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7695920 | ||||||
chr19:7695922
|
T | C | 17 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0036others(14): Show | 21 | HG01891.hp2 HG01934.hp2 HG01975.hp2 others(18): Show |
intron_variant | MODIFIER | c.469+903A>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7695922 | ||||||
chr19:7695949
|
C | T | 62 | a0001c0001t0001g0307a0001c0003t0001g0034a0001c0003t0001g0053others(59): Show | 86 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.469+876G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7695949 | ||||||
chr19:7695957
|
C | T | 62 | a0001c0001t0001g0307a0001c0003t0001g0034a0001c0003t0001g0053others(59): Show | 86 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.469+868G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7695957 | ||||||
chr19:7695975
|
T | G | 2 | a0001c0001t0001g0269a0001c0001t0001g0270 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.469+850A>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7695975 | ||||||
chr19:7696003
|
G | A | 62 | a0001c0001t0001g0307a0001c0003t0001g0034a0001c0003t0001g0053others(59): Show | 86 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.469+822C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7696003 | ||||||
chr19:7696093
|
C | G | 1 | a0001c0003t0003g0154 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.469+732G>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7696093 | ||||||
chr19:7696095
|
G | A | 1 | a0001c0001t0001g0277 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.469+730C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7696095 | ||||||
chr19:7696107
|
A | T | 1 | a0001c0004t0001g0280 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.469+718T>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7696107 | ||||||
chr19:7696140
|
G | A | 116 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0016others(113): Show | 155 | HG00280.hp1 HG00438.hp1 HG00597.hp1 others(152): Show |
intron_variant | MODIFIER | c.469+685C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7696140 | ||||||
chr19:7696161
|
G | A | 1 | a0002c0002t0003g0122 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.469+664C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7696161 | ||||||
chr19:7696192
|
C | T | 8 | a0001c0003t0002g0009a0001c0003t0002g0107a0001c0003t0002g0133others(5): Show | 13 | HG00280.hp2 HG00642.hp1 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.469+633G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7696192 | ||||||
chr19:7696193
|
G | A | 1 | a0008c0013t0001g0080 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.469+632C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7696193 | ||||||
chr19:7696247
|
G | T | 1 | a0001c0003t0001g0018 | 3 | HG02572.hp1 HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.469+578C>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7696247 | ||||||
chr19:7696333
|
T | C | 62 | a0001c0001t0001g0307a0001c0003t0001g0034a0001c0003t0001g0053others(59): Show | 86 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.469+492A>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7696333 | ||||||
chr19:7696336
|
C | A | 62 | a0001c0001t0001g0307a0001c0003t0001g0034a0001c0003t0001g0053others(59): Show | 86 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.469+489G>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7696336 | ||||||
chr19:7696381
|
G | A | 2 | a0001c0001t0001g0089a0001c0001t0001g0213 | 2 | HG03041.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.469+444C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7696381 | ||||||
chr19:7696393
|
G | A | 5 | a0001c0003t0001g0034a0002c0002t0001g0051a0002c0002t0001g0125others(2): Show | 7 | HG02055.hp1 HG02630.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.469+432C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7696393 | ||||||
chr19:7696527
|
C | T | 1 | a0002c0002t0003g0122 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.469+298G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7696527 | ||||||
chr19:7696528
|
G | A | 69 | a0001c0001t0001g0307a0001c0003t0001g0034a0001c0003t0001g0053others(66): Show | 98 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.469+297C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7696528 | ||||||
chr19:7696560
|
A | G | 3 | a0001c0001t0001g0111a0001c0001t0001g0172a0001c0004t0001g0301 | 3 | HG01109.hp1 HG03209.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.469+265T>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7696560 | ||||||
chr19:7696570
|
G | A | 61 | a0001c0001t0001g0007a0001c0001t0001g0026a0001c0001t0001g0065others(58): Show | 86 | HG00280.hp1 HG00438.hp1 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.469+255C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7696570 | ||||||
chr19:7696586
|
G | A | 69 | a0001c0001t0001g0307a0001c0003t0001g0034a0001c0003t0001g0053others(66): Show | 98 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.469+239C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7696586 | ||||||
chr19:7696608
|
CTT | C | 69 | a0001c0001t0001g0307a0001c0003t0001g0034a0001c0003t0001g0053others(66): Show | 98 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.469+215_469+216del others(2): Show |
FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7696608 | ||||||
chr19:7696623
|
G | A | 1 | a0002c0002t0001g0211 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.469+202C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7696623 | ||||||
chr19:7696631
|
G | A | 8 | a0001c0001t0001g0111a0001c0001t0001g0172a0001c0001t0001g0174others(5): Show | 8 | HG01109.hp1 HG02818.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.469+194C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7696631 | ||||||
chr19:7696781
|
A | G | 70 | a0001c0001t0001g0307a0001c0003t0001g0034a0001c0003t0001g0053others(67): Show | 99 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.469+44T>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7696781 | ||||||
chr19:7696795
|
G | A | 1 | a0001c0001t0001g0202 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.469+30C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7696795 | ||||||
chr19:7696799
|
T | C | 1 | a0001c0001t0001g0073 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.469+26A>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 8/10 | chr19 | 7696799 | ||||||
chr19:7696916
|
T | C | 1 | a0001c0001t0001g0187 | 1 | NA18962.hp2 | splice_acceptor_variant&intron_variant | HIGH | c.380-2A>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 7/10 | chr19 | 7696916 | ||||||
chr19:7696926
|
A | G | 195 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0016others(192): Show | 266 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(263): Show |
intron_variant | MODIFIER | c.380-12T>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 7/10 | chr19 | 7696926 | ||||||
chr19:7696962
|
C | T | 1 | a0001c0001t0001g0071 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.380-48G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 7/10 | chr19 | 7696962 | ||||||
chr19:7696984
|
C | A | 1 | a0001c0001t0001g0099 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.379+29G>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 7/10 | chr19 | 7696984 | ||||||
chr19:7697404
|
C | T | 1 | a0001c0004t0001g0274 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.254-106G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 5/10 | chr19 | 7697404 | ||||||
chr19:7697494
|
TCCCCTGC others(2): Show |
T | 82 | a0001c0001t0001g0307a0001c0003t0001g0018a0001c0003t0001g0034others(79): Show | 114 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.253+24_253+32delTT others(7): Show |
FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 5/10 | chr19 | 7697494 | ||||||
chr19:7697767
|
CTA | C | 96 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0031others(93): Show | 135 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.191-180_191-179del others(2): Show |
FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 4/10 | chr19 | 7697767 | ||||||
chr19:7697842
|
A | C | 1 | a0001c0003t0001g0018 | 3 | HG02572.hp1 HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.191-253T>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 4/10 | chr19 | 7697842 | ||||||
chr19:7697916
|
A | C | 1 | a0001c0001t0001g0236 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.191-327T>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 4/10 | chr19 | 7697916 | ||||||
chr19:7697939
|
C | T | 2 | a0002c0002t0001g0019a0002c0002t0001g0092 | 4 | HG01167.hp2 HG03490.hp1 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.191-350G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 4/10 | chr19 | 7697939 | ||||||
chr19:7698025
|
G | A | 100 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0031others(97): Show | 139 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.190+331C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 4/10 | chr19 | 7698025 | ||||||
chr19:7698066
|
G | A | 1 | a0002c0002t0001g0138 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.190+290C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 4/10 | chr19 | 7698066 | ||||||
chr19:7698092
|
C | T | 92 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0031others(89): Show | 131 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.190+264G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 4/10 | chr19 | 7698092 | ||||||
chr19:7698159
|
C | A | 99 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0044others(96): Show | 137 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.190+197G>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 4/10 | chr19 | 7698159 | ||||||
chr19:7698217
|
C | T | 1 | a0001c0003t0002g0112 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.190+139G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 4/10 | chr19 | 7698217 | ||||||
chr19:7698247
|
T | C | 1 | a0002c0002t0001g0139 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.190+109A>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 4/10 | chr19 | 7698247 | ||||||
chr19:7698295
|
G | A | 1 | a0001c0001t0001g0212 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.190+61C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 4/10 | chr19 | 7698295 | ||||||
chr19:7698329
|
A | C | 1 | a0001c0005t0001g0200 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.190+27T>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 4/10 | chr19 | 7698329 | ||||||
chr19:7698330
|
C | A | 1 | a0001c0005t0001g0200 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.190+26G>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 4/10 | chr19 | 7698330 | ||||||
chr19:7698332
|
C | T | 1 | a0001c0001t0001g0111 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.190+24G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 4/10 | chr19 | 7698332 | ||||||
chr19:7698913
|
C | T | 1 | a0001c0003t0001g0093 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.23-59G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 2/10 | chr19 | 7698913 | ||||||
chr19:7698929
|
C | T | 1 | a0001c0001t0001g0071 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.23-75G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 2/10 | chr19 | 7698929 | ||||||
chr19:7698992
|
C | T | 115 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(112): Show | 183 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.23-138G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 2/10 | chr19 | 7698992 | ||||||
chr19:7699031
|
G | A | 151 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0011others(148): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.23-177C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 2/10 | chr19 | 7699031 | ||||||
chr19:7699044
|
A | T | 278 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(275): Show | 411 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(408): Show |
intron_variant | MODIFIER | c.23-190T>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 2/10 | chr19 | 7699044 | ||||||
chr19:7699091
|
A | C | 201 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0014others(198): Show | 286 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(283): Show |
intron_variant | MODIFIER | c.23-237T>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 2/10 | chr19 | 7699091 | ||||||
chr19:7699097
|
C | A | 38 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0016others(35): Show | 56 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.23-243G>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 2/10 | chr19 | 7699097 | ||||||
chr19:7699271
|
A | G | 158 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0014others(155): Show | 224 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(221): Show |
intron_variant | MODIFIER | c.23-417T>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 2/10 | chr19 | 7699271 | ||||||
chr19:7699477
|
G | GT | 6 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0003t0001g0068others(3): Show | 6 | HG01261.hp1 HG02809.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.22+261dupA | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 2/10 | chr19 | 7699477 | ||||||
chr19:7699477
|
GT | G | 5 | a0001c0001t0001g0021a0001c0001t0001g0104a0001c0001t0001g0105others(2): Show | 9 | HG01106.hp1 HG01358.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.22+261delA | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 2/10 | chr19 | 7699477 | ||||||
chr19:7699477
|
GTTT | G | 7 | a0001c0001t0001g0061a0001c0001t0001g0124a0001c0003t0001g0123others(4): Show | 8 | HG02451.hp1 HG02486.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.22+259_22+261delAA others(1): Show |
FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 2/10 | chr19 | 7699477 | ||||||
chr19:7699477
|
GTTTT | G | 76 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0036others(73): Show | 114 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.22+258_22+261delAA others(2): Show |
FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 2/10 | chr19 | 7699477 | ||||||
chr19:7699477
|
GTTTTT | G | 155 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(152): Show | 238 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(235): Show |
intron_variant | MODIFIER | c.22+257_22+261delAA others(3): Show |
FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 2/10 | chr19 | 7699477 | ||||||
chr19:7699487
|
T | C | 1 | a0001c0003t0001g0108 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.22+252A>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 2/10 | chr19 | 7699487 | ||||||
chr19:7699488
|
T | C | 1 | a0001c0001t0001g0109 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.22+251A>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 2/10 | chr19 | 7699488 | ||||||
chr19:7699512
|
G | A | 1 | a0001c0003t0009g0306 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.22+227C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 2/10 | chr19 | 7699512 | ||||||
chr19:7699550
|
G | T | 234 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(231): Show | 356 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(353): Show |
intron_variant | MODIFIER | c.22+189C>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 2/10 | chr19 | 7699550 | ||||||
chr19:7699587
|
C | A | 16 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0180others(13): Show | 21 | HG00280.hp2 HG00733.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.22+152G>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 2/10 | chr19 | 7699587 | ||||||
chr19:7699588
|
G | A | 8 | a0001c0001t0001g0044a0001c0001t0001g0172a0001c0001t0001g0173others(5): Show | 9 | HG01109.hp1 HG02886.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.22+151C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 2/10 | chr19 | 7699588 | ||||||
chr19:7699659
|
G | GC | 224 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(221): Show | 340 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(337): Show |
intron_variant | MODIFIER | c.22+79dupG | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 2/10 | chr19 | 7699659 | ||||||
chr19:7699855
|
G | A | 158 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(155): Show | 262 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(259): Show |
intron_variant | MODIFIER | c.-85-10C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 1/10 | chr19 | 7699855 | ||||||
chr19:7699878
|
C | G | 6 | a0001c0001t0001g0044a0001c0001t0001g0172a0001c0001t0001g0173others(3): Show | 7 | HG01109.hp1 HG02895.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.-85-33G>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 1/10 | chr19 | 7699878 | ||||||
chr19:7699886
|
T | C | 164 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(161): Show | 269 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(266): Show |
intron_variant | MODIFIER | c.-85-41A>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 1/10 | chr19 | 7699886 | ||||||
chr19:7699899
|
C | T | 1 | a0001c0004t0001g0301 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-85-54G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 1/10 | chr19 | 7699899 | ||||||
chr19:7699900
|
A | G | 6 | a0001c0001t0001g0044a0001c0001t0001g0172a0001c0001t0001g0173others(3): Show | 7 | HG01109.hp1 HG02895.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.-85-55T>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 1/10 | chr19 | 7699900 | ||||||
chr19:7699924
|
G | A | 13 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0181others(10): Show | 18 | HG00280.hp2 HG00733.hp1 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.-85-79C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 1/10 | chr19 | 7699924 | ||||||
chr19:7699926
|
C | G | 6 | a0001c0001t0001g0044a0001c0001t0001g0172a0001c0001t0001g0173others(3): Show | 7 | HG01109.hp1 HG02895.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.-85-81G>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 1/10 | chr19 | 7699926 | ||||||
chr19:7699933
|
G | C | 6 | a0001c0001t0001g0044a0001c0001t0001g0172a0001c0001t0001g0173others(3): Show | 7 | HG01109.hp1 HG02895.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.-85-88C>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 1/10 | chr19 | 7699933 | ||||||
chr19:7699940
|
T | C | 6 | a0001c0001t0001g0044a0001c0001t0001g0172a0001c0001t0001g0173others(3): Show | 7 | HG01109.hp1 HG02895.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.-85-95A>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 1/10 | chr19 | 7699940 | ||||||
chr19:7699979
|
G | A | 16 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0180others(13): Show | 21 | HG00280.hp2 HG00733.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.-85-134C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 1/10 | chr19 | 7699979 | ||||||
chr19:7699988
|
A | G | 6 | a0001c0001t0001g0044a0001c0001t0001g0172a0001c0001t0001g0173others(3): Show | 7 | HG01109.hp1 HG02895.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.-85-143T>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 1/10 | chr19 | 7699988 | ||||||
chr19:7699991
|
G | C | 5 | a0001c0001t0001g0044a0001c0001t0001g0172a0001c0001t0001g0173others(2): Show | 6 | HG01109.hp1 HG02895.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.-85-146C>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 1/10 | chr19 | 7699991 | ||||||
chr19:7700119
|
C | T | 1 | a0001c0003t0001g0239 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-85-274G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 1/10 | chr19 | 7700119 | ||||||
chr19:7700263
|
T | C | 1 | a0001c0001t0001g0160 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-85-418A>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 1/10 | chr19 | 7700263 | ||||||
chr19:7700289
|
A | G | 3 | a0001c0001t0001g0061a0001c0003t0003g0304a0001c0017t0001g0303 | 4 | HG02451.hp1 HG02486.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-85-444T>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 1/10 | chr19 | 7700289 | ||||||
chr19:7700328
|
G | A | 1 | a0001c0001t0001g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-85-483C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 1/10 | chr19 | 7700328 | ||||||
chr19:7700380
|
G | A | 228 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(225): Show | 350 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(347): Show |
intron_variant | MODIFIER | c.-85-535C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 1/10 | chr19 | 7700380 | ||||||
chr19:7700463
|
TCTC | T | 5 | a0001c0001t0001g0024a0001c0001t0001g0054a0001c0001t0001g0236others(2): Show | 8 | HG00099.hp1 HG00639.hp2 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.-85-621_-85-619del others(3): Show |
FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 1/10 | chr19 | 7700463 | ||||||
chr19:7700506
|
CTTTA | C | 228 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(225): Show | 350 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(347): Show |
intron_variant | MODIFIER | c.-85-665_-85-662del others(4): Show |
FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 1/10 | chr19 | 7700506 | ||||||
chr19:7700565
|
A | G | 1 | a0001c0001t0001g0062 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-85-720T>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 1/10 | chr19 | 7700565 | ||||||
chr19:7700633
|
G | A | 45 | a0001c0001t0001g0011a0001c0001t0001g0049a0001c0001t0001g0050others(42): Show | 56 | HG00423.hp2 HG00558.hp1 HG01167.hp1 others(53): Show |
intron_variant | MODIFIER | c.-85-788C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 1/10 | chr19 | 7700633 | ||||||
chr19:7700640
|
G | A | 1 | a0009c0018t0001g0162 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-85-795C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 1/10 | chr19 | 7700640 | ||||||
chr19:7700658
|
G | T | 147 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(144): Show | 249 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(246): Show |
intron_variant | MODIFIER | c.-85-813C>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 1/10 | chr19 | 7700658 | ||||||
chr19:7700704
|
G | A | 16 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0180others(13): Show | 21 | HG00280.hp2 HG00733.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.-85-859C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 1/10 | chr19 | 7700704 | ||||||
chr19:7700760
|
G | A | 1 | a0001c0001t0001g0299 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-85-915C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 1/10 | chr19 | 7700760 | ||||||
chr19:7700807
|
A | G | 12 | a0001c0001t0001g0194a0001c0001t0001g0199a0001c0004t0001g0045others(9): Show | 15 | HG00423.hp2 HG01167.hp1 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.-85-962T>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 1/10 | chr19 | 7700807 | ||||||
chr19:7700812
|
C | T | 1 | a0002c0006t0001g0305 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-85-967G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 1/10 | chr19 | 7700812 | ||||||
chr19:7700820
|
T | A | 1 | a0001c0001t0001g0300 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-85-975A>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 1/10 | chr19 | 7700820 | ||||||
chr19:7700842
|
G | A | 63 | a0001c0001t0001g0011a0001c0001t0001g0049a0001c0001t0001g0050others(60): Show | 80 | HG00280.hp2 HG00423.hp2 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.-85-997C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 1/10 | chr19 | 7700842 | ||||||
chr19:7700957
|
C | T | 2 | a0001c0001t0001g0234a0001c0001t0001g0235 | 2 | NA18947.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.-86+1058G>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 1/10 | chr19 | 7700957 | ||||||
chr19:7700964
|
C | A | 47 | a0001c0001t0001g0011a0001c0001t0001g0049a0001c0001t0001g0050others(44): Show | 59 | HG00423.hp2 HG00558.hp1 HG01167.hp1 others(56): Show |
intron_variant | MODIFIER | c.-86+1051G>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 1/10 | chr19 | 7700964 | ||||||
chr19:7701179
|
G | A | 1 | a0001c0005t0001g0227 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-86+836C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 1/10 | chr19 | 7701179 | ||||||
chr19:7701200
|
G | A | 1 | a0001c0001t0001g0015 | 4 | NA18983.hp1 NA19001.hp2 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.-86+815C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 1/10 | chr19 | 7701200 | ||||||
chr19:7701388
|
T | C | 228 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(225): Show | 350 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(347): Show |
intron_variant | MODIFIER | c.-86+627A>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 1/10 | chr19 | 7701388 | ||||||
chr19:7701401
|
G | A | 1 | a0001c0004t0001g0301 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-86+614C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 1/10 | chr19 | 7701401 | ||||||
chr19:7701667
|
T | C | 1 | a0001c0004t0001g0301 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-86+348A>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 1/10 | chr19 | 7701667 | ||||||
chr19:7701673
|
G | A | 1 | a0001c0004t0001g0228 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-86+342C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 1/10 | chr19 | 7701673 | ||||||
chr19:7701703
|
A | C | 2 | a0001c0003t0001g0063a0002c0002t0001g0064 | 2 | HG00438.hp2 NA18946.hp1 |
intron_variant | MODIFIER | c.-86+312T>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 1/10 | chr19 | 7701703 | ||||||
chr19:7701718
|
C | A | 5 | a0001c0001t0001g0016a0001c0001t0001g0052a0001c0001t0001g0229others(2): Show | 9 | HG00597.hp2 HG02071.hp1 HG02129.hp1 others(6): Show |
intron_variant | MODIFIER | c.-86+297G>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 1/10 | chr19 | 7701718 | ||||||
chr19:7701763
|
G | A | 1 | a0001c0003t0001g0053 | 2 | HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-86+252C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 1/10 | chr19 | 7701763 | ||||||
chr19:7701873
|
G | T | 1 | a0001c0001t0001g0062 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-86+142C>A | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 1/10 | chr19 | 7701873 | ||||||
chr19:7701961
|
G | A | 1 | a0002c0002t0001g0231 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-86+54C>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 1/10 | chr19 | 7701961 | ||||||
chr19:7701980
|
T | G | 88 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(85): Show | 143 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.-86+35A>C | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 1/10 | chr19 | 7701980 | ||||||
chr19:7701985
|
T | C | 3 | a0001c0001t0001g0061a0001c0003t0003g0304a0001c0017t0001g0303 | 4 | HG02451.hp1 HG02486.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-86+30A>G | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 1/10 | chr19 | 7701985 | ||||||
chr19:7702003
|
C | A | 4 | a0001c0001t0001g0307a0001c0003t0009g0306a0002c0002t0001g0308others(1): Show | 4 | HG02615.hp2 HG02647.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.-86+12G>T | FCER2 | ENSG00000104921.15 | transcript | ENST00000597921.6 | protein_coding | 1/10 | chr19 | 7702003 |