geneid | 79368 |
---|---|
ensemblid | ENSG00000132704.16 |
hgncid | 14875 |
symbol | FCRL2 |
name | Fc receptor like 2 |
refseq_nuc | NM_030764.4 |
refseq_prot | NP_110391.2 |
ensembl_nuc | ENST00000361516.8 |
ensembl_prot | ENSP00000355157.3 |
mane_status | MANE Select |
chr | chr1 |
start | 157745733 |
end | 157777132 |
strand | - |
ver | v1.2 |
region | chr1:157745733-157777132 |
region5000 | chr1:157740733-157782132 |
regionname0 | FCRL2_chr1_157745733_157777132 |
regionname5000 | FCRL2_chr1_157740733_157782132 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 508 | 374 | 87 | 71 | 168 | 14 | 32 | 126 | FCRL2_chr1_157740733_157782132 | FCRL2 | copy fasta | chr1 | 157740733 | 157782132 |
a0002 | 0/0 | 508 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | copy fasta | chr1 | 157740733 | 157782132 |
a0003 | 0/0 | 317 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | copy fasta | chr1 | 157740733 | 157782132 |
a0004 | 0/0 | 508 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | copy fasta | chr1 | 157740733 | 157782132 |
a0005 | 0/0 | 508 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | copy fasta | chr1 | 157740733 | 157782132 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1527 | 360 | 75 | 69 | 168 | 14 | 32 | FCRL2_chr1_157740733_157782132 | FCRL2 | copy fasta | chr1 | 157740733 | 157782132 |
c0002 | 0/0 | 1527 | 11 | 11 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | copy fasta | chr1 | 157740733 | 157782132 |
c0003 | 0/0 | 1527 | 3 | 3 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | copy fasta | chr1 | 157740733 | 157782132 |
c0004 | 0/0 | 1527 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | copy fasta | chr1 | 157740733 | 157782132 |
c0005 | 0/0 | 1527 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | copy fasta | chr1 | 157740733 | 157782132 |
c0006 | 0/0 | 1527 | 1 | 0 | 0 | 0 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | copy fasta | chr1 | 157740733 | 157782132 |
c0007 | 0/0 | 1527 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | copy fasta | chr1 | 157740733 | 157782132 |
c0008 | 0/0 | 1527 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | copy fasta | chr1 | 157740733 | 157782132 |
c0009 | 0/0 | 1527 | 1 | 0 | 0 | 0 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | copy fasta | chr1 | 157740733 | 157782132 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 1063 | 298 | 51 | 58 | 153 | 12 | 23 | FCRL2_chr1_157740733_157782132 | FCRL2 | copy fasta | chr1 | 157740733 | 157782132 |
t0002 | 0/0 | 1063 | 18 | 0 | 4 | 5 | 0 | 9 | FCRL2_chr1_157740733_157782132 | FCRL2 | copy fasta | chr1 | 157740733 | 157782132 |
t0003 | 0/0 | 1063 | 18 | 0 | 6 | 9 | 2 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | copy fasta | chr1 | 157740733 | 157782132 |
t0004 | 0/0 | 1063 | 16 | 16 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | copy fasta | chr1 | 157740733 | 157782132 |
t0005 | 0/0 | 1063 | 11 | 11 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | copy fasta | chr1 | 157740733 | 157782132 |
t0006 | 0/0 | 1063 | 8 | 7 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | copy fasta | chr1 | 157740733 | 157782132 |
t0007 | 0/1 | 1063 | 5 | 0 | 3 | 0 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | copy fasta | chr1 | 157740733 | 157782132 |
t0008 | 0/0 | 1063 | 3 | 3 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | copy fasta | chr1 | 157740733 | 157782132 |
t0009 | 0/0 | 1063 | 2 | 2 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | copy fasta | chr1 | 157740733 | 157782132 |
t0010 | 0/0 | 1063 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | copy fasta | chr1 | 157740733 | 157782132 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 11 | 0 | 4 | 7 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0002 | 0/0 | 8 | 0 | 2 | 6 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0003 | 0/0 | 7 | 0 | 1 | 6 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0004 | 0/0 | 7 | 0 | 0 | 6 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0007 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0008 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0010 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0011 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0012 | 0/0 | 4 | 0 | 2 | 1 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0013 | 0/0 | 4 | 1 | 1 | 0 | 0 | 2 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0014 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0015 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0017 | 0/0 | 3 | 1 | 0 | 1 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0018 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0020 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0030 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0032 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0036 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0037 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0137 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0163 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1527 | 360 | 75 | 69 | 168 | 14 | 32 | FCRL2_chr1_157740733_157782132 | FCRL2 | copy fasta | chr1 | 157740733 | 157782132 |
a0001c0002 | 0/0 | 1527 | 11 | 11 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | copy fasta | chr1 | 157740733 | 157782132 |
a0001c0004 | 0/0 | 1527 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | copy fasta | chr1 | 157740733 | 157782132 |
a0001c0007 | 0/0 | 1527 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | copy fasta | chr1 | 157740733 | 157782132 |
a0001c0008 | 0/0 | 1527 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | copy fasta | chr1 | 157740733 | 157782132 |
a0002c0003 | 0/0 | 1527 | 3 | 3 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | copy fasta | chr1 | 157740733 | 157782132 |
a0003c0005 | 0/0 | 1527 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | copy fasta | chr1 | 157740733 | 157782132 |
a0004c0006 | 0/0 | 1527 | 1 | 0 | 0 | 0 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | copy fasta | chr1 | 157740733 | 157782132 |
a0005c0009 | 0/0 | 1527 | 1 | 0 | 0 | 0 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | copy fasta | chr1 | 157740733 | 157782132 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 2589 | 290 | 47 | 56 | 153 | 12 | 21 | FCRL2_chr1_157740733_157782132 | FCRL2 | copy fasta | chr1 | 157740733 | 157782132 |
a0001c0001t0002 | 0/0 | 2589 | 17 | 0 | 3 | 5 | 0 | 9 | FCRL2_chr1_157740733_157782132 | FCRL2 | copy fasta | chr1 | 157740733 | 157782132 |
a0001c0001t0003 | 0/0 | 2589 | 18 | 0 | 6 | 9 | 2 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | copy fasta | chr1 | 157740733 | 157782132 |
a0001c0001t0004 | 0/0 | 2589 | 16 | 16 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | copy fasta | chr1 | 157740733 | 157782132 |
a0001c0001t0006 | 0/0 | 2589 | 8 | 7 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | copy fasta | chr1 | 157740733 | 157782132 |
a0001c0001t0007 | 0/1 | 2589 | 5 | 0 | 3 | 0 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | copy fasta | chr1 | 157740733 | 157782132 |
a0001c0001t0008 | 0/0 | 2589 | 3 | 3 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | copy fasta | chr1 | 157740733 | 157782132 |
a0001c0001t0009 | 0/0 | 2589 | 2 | 2 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | copy fasta | chr1 | 157740733 | 157782132 |
a0001c0001t0010 | 0/0 | 2589 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | copy fasta | chr1 | 157740733 | 157782132 |
a0001c0002t0001 | 0/0 | 2589 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | copy fasta | chr1 | 157740733 | 157782132 |
a0001c0002t0005 | 0/0 | 2589 | 10 | 10 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | copy fasta | chr1 | 157740733 | 157782132 |
a0001c0004t0005 | 0/0 | 2589 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | copy fasta | chr1 | 157740733 | 157782132 |
a0001c0007t0001 | 0/0 | 2589 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | copy fasta | chr1 | 157740733 | 157782132 |
a0001c0008t0002 | 0/0 | 2589 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | copy fasta | chr1 | 157740733 | 157782132 |
a0002c0003t0001 | 0/0 | 2589 | 3 | 3 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | copy fasta | chr1 | 157740733 | 157782132 |
a0003c0005t0001 | 0/0 | 2589 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | copy fasta | chr1 | 157740733 | 157782132 |
a0004c0006t0001 | 0/0 | 2589 | 1 | 0 | 0 | 0 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | copy fasta | chr1 | 157740733 | 157782132 |
a0005c0009t0001 | 0/0 | 2589 | 1 | 0 | 0 | 0 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | copy fasta | chr1 | 157740733 | 157782132 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 11 | 0 | 4 | 7 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0002 | 0/0 | 8 | 0 | 2 | 6 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0003 | 0/0 | 7 | 0 | 1 | 6 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0004 | 0/0 | 7 | 0 | 0 | 6 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0007 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0008 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0010 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0011 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0012 | 0/0 | 4 | 0 | 2 | 1 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0013 | 0/0 | 4 | 1 | 1 | 0 | 0 | 2 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0015 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0017 | 0/0 | 3 | 1 | 0 | 1 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0018 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0030 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0036 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0163 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0002g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0003g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0003g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0003g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0003g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0003g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0003g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0004g0014 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0004g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0004g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0004g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0004g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0004g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0004g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0004g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0004g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0004g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0004g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0004g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0006g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0006g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0006g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0006g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0006g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0006g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0006g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0007g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0007g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0007g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0007g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0007g0137 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0008g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0008g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0008g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0009g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0009g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0001t0010g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0002t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0002t0005g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0002t0005g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0002t0005g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0002t0005g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0002t0005g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0002t0005g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0002t0005g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0002t0005g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0002t0005g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0004t0005g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0007t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0001c0008t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0002c0003t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0002c0003t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0002c0003t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0003c0005t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0004c0006t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
a0005c0009t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0060 | EUR | GBR | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0030 | EUR | GBR | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG00140 | hp1 | a0001 | c0001 | t0003 | g0053 | EUR | GBR | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0071 | EUR | GBR | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0188 | EUR | FIN | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0136 | EUR | FIN | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | CHS | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG00408 | hp2 | a0001 | c0001 | t0003 | g0072 | EAS | CHS | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG00423 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | CHS | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | CHS | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | CHS | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | CHS | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | CHS | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | CHS | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | CHS | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0226 | EAS | CHS | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG00621 | hp1 | a0001 | c0001 | t0010 | g0171 | EAS | CHS | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | CHS | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0227 | AMR | PUR | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0225 | EAS | CHS | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG00735 | hp1 | a0001 | c0001 | t0003 | g0110 | AMR | PUR | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG01069 | hp1 | a0001 | c0001 | t0003 | g0054 | AMR | PUR | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG01070 | hp2 | a0001 | c0001 | t0003 | g0021 | AMR | PUR | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG01071 | hp2 | a0001 | c0001 | t0003 | g0021 | AMR | PUR | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG01106 | hp1 | a0001 | c0001 | t0007 | g0125 | AMR | PUR | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0271 | AMR | PUR | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG01109 | hp1 | a0001 | c0001 | t0006 | g0104 | AMR | PUR | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0230 | AMR | PUR | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG01192 | hp2 | a0001 | c0001 | t0003 | g0057 | AMR | PUR | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | CLM | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | CLM | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | CLM | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | CLM | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG01346 | hp2 | a0001 | c0001 | t0007 | g0119 | AMR | CLM | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | CLM | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | CLM | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | CLM | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | CLM | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0267 | AMR | CLM | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | CLM | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0037 | EUR | IBS | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0015 | EUR | IBS | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG01516 | hp1 | a0001 | c0001 | t0003 | g0063 | EUR | IBS | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0018 | EUR | IBS | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG01884 | hp2 | a0001 | c0001 | t0004 | g0242 | AFR | ACB | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG01891 | hp1 | a0001 | c0001 | t0008 | g0273 | AFR | ACB | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG01891 | hp2 | a0001 | c0001 | t0006 | g0105 | AFR | ACB | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG01934 | hp2 | a0001 | c0001 | t0003 | g0056 | AMR | PEL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PEL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | PEL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PEL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PEL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PEL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG01981 | hp1 | a0003 | c0005 | t0001 | g0211 | AMR | PEL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | PEL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PEL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG02004 | hp2 | a0001 | c0007 | t0001 | g0253 | AMR | PEL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | KHV | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | KHV | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | KHV | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG02055 | hp1 | a0001 | c0001 | t0004 | g0244 | AFR | ACB | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | ACB | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | KHV | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | KHV | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG02080 | hp1 | a0001 | c0001 | t0003 | g0061 | EAS | KHV | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | KHV | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG02145 | hp2 | a0001 | c0001 | t0008 | g0274 | AFR | ACB | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG02148 | hp2 | a0001 | c0008 | t0002 | g0254 | AMR | PEL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CDX | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | CDX | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | CDX | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | CDX | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG02257 | hp1 | a0002 | c0003 | t0001 | g0270 | AFR | ACB | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG02257 | hp2 | a0001 | c0002 | t0005 | g0283 | AFR | ACB | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG02258 | hp1 | a0001 | c0001 | t0008 | g0252 | AFR | ACB | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | ACB | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG02280 | hp1 | a0001 | c0001 | t0004 | g0246 | AFR | ACB | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG02300 | hp1 | a0001 | c0001 | t0007 | g0118 | AMR | PEL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | ACB | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG02572 | hp1 | a0001 | c0001 | t0006 | g0107 | AFR | GWD | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0217 | SAS | PJL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG02615 | hp1 | a0001 | c0001 | t0004 | g0039 | AFR | GWD | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG02622 | hp1 | a0001 | c0002 | t0005 | g0276 | AFR | GWD | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | GWD | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | GWD | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG02630 | hp2 | a0002 | c0003 | t0001 | g0268 | AFR | GWD | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0260 | SAS | PJL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG02683 | hp2 | a0005 | c0009 | t0001 | g0214 | SAS | PJL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG02717 | hp1 | a0001 | c0001 | t0004 | g0014 | AFR | GWD | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | GWD | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | GWD | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0224 | SAS | PJL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0223 | SAS | PJL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | GWD | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG02809 | hp2 | a0001 | c0001 | t0004 | g0014 | AFR | GWD | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG02818 | hp1 | a0001 | c0002 | t0005 | g0281 | AFR | GWD | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | GWD | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG02886 | hp1 | a0001 | c0002 | t0005 | g0043 | AFR | GWD | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG02886 | hp2 | a0001 | c0001 | t0006 | g0102 | AFR | GWD | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0240 | AFR | GWD | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG02895 | hp2 | a0001 | c0002 | t0005 | g0275 | AFR | GWD | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | ESN | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG02922 | hp2 | a0001 | c0002 | t0005 | g0282 | AFR | ESN | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG02965 | hp1 | a0001 | c0002 | t0005 | g0279 | AFR | ESN | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG02965 | hp2 | a0002 | c0003 | t0001 | g0269 | AFR | ESN | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | ESN | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG02970 | hp2 | a0001 | c0001 | t0006 | g0106 | AFR | ESN | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | ESN | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG02976 | hp2 | a0001 | c0001 | t0004 | g0247 | AFR | ESN | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0229 | SAS | PJL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG03041 | hp1 | a0001 | c0002 | t0005 | g0043 | AFR | GWD | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG03041 | hp2 | a0001 | c0001 | t0006 | g0103 | AFR | GWD | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0251 | AFR | ESN | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | ESN | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG03139 | hp1 | a0001 | c0002 | t0005 | g0277 | AFR | ESN | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | ESN | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ESN | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | ESN | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | MSL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG03209 | hp2 | a0001 | c0001 | t0004 | g0149 | AFR | MSL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG03225 | hp1 | a0001 | c0001 | t0006 | g0024 | AFR | MSL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | MSL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | PJL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0218 | SAS | PJL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG03453 | hp1 | a0001 | c0001 | t0004 | g0014 | AFR | MSL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG03453 | hp2 | a0001 | c0001 | t0009 | g0145 | AFR | MSL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG03486 | hp1 | a0001 | c0004 | t0005 | g0284 | AFR | MSL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG03486 | hp2 | a0001 | c0001 | t0009 | g0144 | AFR | MSL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG03490 | hp1 | a0001 | c0001 | t0007 | g0121 | SAS | PJL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0219 | SAS | PJL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG03516 | hp1 | a0001 | c0001 | t0004 | g0248 | AFR | ESN | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | ESN | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0258 | AFR | MSL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG03579 | hp2 | a0001 | c0001 | t0004 | g0249 | AFR | MSL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG03654 | hp1 | a0004 | c0006 | t0001 | g0212 | SAS | PJL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0228 | SAS | PJL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0070 | SAS | STU | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0220 | SAS | STU | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | BEB | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | BEB | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG04115 | hp1 | a0001 | c0001 | t0003 | g0055 | SAS | STU | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | STU | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0196 | SAS | BEB | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0259 | SAS | BEB | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | STU | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0189 | SAS | STU | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | STU | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0069 | SAS | STU | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | YRI | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA18522 | hp2 | a0001 | c0001 | t0004 | g0014 | AFR | YRI | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | CHB | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | CHB | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0272 | AFR | YRI | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA18906 | hp2 | a0001 | c0002 | t0005 | g0278 | AFR | YRI | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA18945 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA18951 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA18960 | hp2 | a0001 | c0001 | t0003 | g0074 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA18983 | hp1 | a0001 | c0001 | t0003 | g0115 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA18989 | hp1 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA19003 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA19009 | hp1 | a0001 | c0001 | t0003 | g0099 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA19030 | hp1 | a0001 | c0001 | t0004 | g0243 | AFR | LWK | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA19030 | hp2 | a0001 | c0002 | t0001 | g0280 | AFR | LWK | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | LWK | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | LWK | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA19059 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA19059 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | YRI | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA19240 | hp2 | a0001 | c0001 | t0004 | g0245 | AFR | YRI | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA20129 | hp1 | a0001 | c0001 | t0006 | g0024 | AFR | ASW | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ASW | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0075 | EUR | TSI | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0015 | EUR | TSI | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0066 | EUR | TSI | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0018 | EUR | TSI | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | CLM | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | CLM | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | ACB | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG02109 | hp2 | a0001 | c0001 | t0004 | g0039 | AFR | ACB | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG02486 | hp1 | a0001 | c0001 | t0004 | g0250 | AFR | ACB | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | ACB | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | ACB | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | MSL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | MSL | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | USA | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | USA | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | LWK | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | LWK | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0007 | g0137 | REF | REF | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0163 | REF | REF | FCRL2_chr1_157740733_157782132 | FCRL2 | chr1 | 157740733 | 157782132 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:157767441
|
C | A | 1 | a0003 | 1 | HG01981.hp1 | stop_gained | HIGH | c.952G>T | p.Glu318* | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 6/12 | 1011/2589 | 952/1527 | 318/508 | chr1 | 157767441 | ||
chr1:157767480
|
T | A | 1 | a0004 | 1 | HG03654.hp1 | missense_variant | MODERATE | c.913A>T | p.Arg305Trp | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 6/12 | 972/2589 | 913/1527 | 305/508 | chr1 | 157767480 | ||
chr1:157768692
|
A | T | 1 | a0002 | 3 | HG02257.hp1 HG02630.hp2 HG02965.hp2 |
missense_variant | MODERATE | c.605T>A | p.Ile202Asn | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 5/12 | 664/2589 | 605/1527 | 202/508 | chr1 | 157768692 | ||
chr1:157769983
|
G | A | 1 | a0005 | 1 | HG02683.hp2 | missense_variant | MODERATE | c.478C>T | p.Pro160Ser | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 4/12 | 537/2589 | 478/1527 | 160/508 | chr1 | 157769983 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:157766883
|
C | T | 2 | a0001c0002a0001c0004 | 12 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(9): Show |
synonymous_variant | LOW | c.1251G>A | p.Leu417Leu | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/12 | 1310/2589 | 1251/1527 | 417/508 | chr1 | 157766883 | ||
chr1:157767451
|
C | T | 1 | a0001c0004 | 1 | HG03486.hp1 | synonymous_variant | LOW | c.942G>A | p.Gly314Gly | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 6/12 | 1001/2589 | 942/1527 | 314/508 | chr1 | 157767451 | ||
chr1:157768484
|
G | A | 1 | a0001c0007 | 1 | HG02004.hp2 | synonymous_variant | LOW | c.813C>T | p.Gly271Gly | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 5/12 | 872/2589 | 813/1527 | 271/508 | chr1 | 157768484 | ||
chr1:157768694
|
G | A | 1 | a0001c0008 | 1 | HG02148.hp2 | synonymous_variant | LOW | c.603C>T | p.Pro201Pro | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 5/12 | 662/2589 | 603/1527 | 201/508 | chr1 | 157768694 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:157745937
|
T | C | 1 | a0001c0001t0006 | 8 | HG01109.hp1 HG01891.hp2 HG02572.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*799A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 12/12 | 799 | chr1 | 157745937 | |||||
chr1:157745993
|
C | T | 1 | a0001c0001t0004 | 16 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*743G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 12/12 | 743 | chr1 | 157745993 | |||||
chr1:157746016
|
A | C | 1 | a0001c0001t0007 | 5 | HG01106.hp1 HG01346.hp2 HG02300.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*720T>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 12/12 | 720 | chr1 | 157746016 | |||||
chr1:157746044
|
C | T | 3 | a0001c0001t0006a0001c0002t0005a0001c0004t0005 | 19 | HG01109.hp1 HG01891.hp2 HG02257.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*692G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 12/12 | 692 | chr1 | 157746044 | |||||
chr1:157746053
|
C | T | 4 | a0001c0001t0006a0001c0001t0008a0001c0002t0005others(1): Show | 22 | HG01109.hp1 HG01891.hp1 HG01891.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*683G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 12/12 | 683 | chr1 | 157746053 | |||||
chr1:157746108
|
C | G | 1 | a0001c0001t0003 | 18 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*628G>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 12/12 | 628 | chr1 | 157746108 | |||||
chr1:157746428
|
A | C | 2 | a0001c0001t0002a0001c0008t0002 | 18 | HG00609.hp2 HG00642.hp2 HG00673.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*308T>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 12/12 | 308 | chr1 | 157746428 | |||||
chr1:157746505
|
A | G | 1 | a0001c0001t0010 | 1 | HG00621.hp1 | 3_prime_UTR_variant | MODIFIER | c.*231T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 12/12 | 231 | chr1 | 157746505 | |||||
chr1:157746610
|
G | T | 3 | a0001c0001t0006a0001c0002t0005a0001c0004t0005 | 19 | HG01109.hp1 HG01891.hp2 HG02257.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*126C>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 12/12 | 126 | chr1 | 157746610 | |||||
chr1:157746625
|
C | T | 1 | a0001c0001t0009 | 2 | HG03453.hp2 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*111G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 12/12 | 111 | chr1 | 157746625 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:157746789
|
C | T | 17 | a0001c0001t0006g0024a0001c0001t0006g0102a0001c0001t0006g0103others(14): Show | 19 | HG01109.hp1 HG01891.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.1489-15G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 11/11 | chr1 | 157746789 | ||||||
chr1:157746802
|
T | C | 17 | a0001c0001t0006g0024a0001c0001t0006g0102a0001c0001t0006g0103others(14): Show | 19 | HG01109.hp1 HG01891.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.1489-28A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 11/11 | chr1 | 157746802 | ||||||
chr1:157746830
|
A | G | 17 | a0001c0001t0006g0024a0001c0001t0006g0102a0001c0001t0006g0103others(14): Show | 19 | HG01109.hp1 HG01891.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.1488+41T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 11/11 | chr1 | 157746830 | ||||||
chr1:157746934
|
C | G | 17 | a0001c0001t0006g0024a0001c0001t0006g0102a0001c0001t0006g0103others(14): Show | 19 | HG01109.hp1 HG01891.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.1460-35G>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 10/11 | chr1 | 157746934 | ||||||
chr1:157747007
|
C | T | 1 | a0001c0001t0008g0252 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1460-108G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 10/11 | chr1 | 157747007 | ||||||
chr1:157747046
|
T | G | 20 | a0001c0001t0001g0232a0001c0001t0001g0272a0001c0001t0002g0217others(17): Show | 20 | HG00609.hp2 HG00642.hp2 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.1460-147A>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 10/11 | chr1 | 157747046 | ||||||
chr1:157747073
|
A | G | 12 | a0001c0001t0004g0014a0001c0001t0004g0039a0001c0001t0004g0149others(9): Show | 16 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.1460-174T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 10/11 | chr1 | 157747073 | ||||||
chr1:157747113
|
C | T | 17 | a0001c0001t0006g0024a0001c0001t0006g0102a0001c0001t0006g0103others(14): Show | 19 | HG01109.hp1 HG01891.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.1460-214G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 10/11 | chr1 | 157747113 | ||||||
chr1:157747184
|
G | A | 17 | a0001c0001t0006g0024a0001c0001t0006g0102a0001c0001t0006g0103others(14): Show | 19 | HG01109.hp1 HG01891.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.1460-285C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 10/11 | chr1 | 157747184 | ||||||
chr1:157747238
|
A | G | 37 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0010others(34): Show | 59 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.1460-339T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 10/11 | chr1 | 157747238 | ||||||
chr1:157747277
|
G | C | 17 | a0001c0001t0006g0024a0001c0001t0006g0102a0001c0001t0006g0103others(14): Show | 19 | HG01109.hp1 HG01891.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.1460-378C>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 10/11 | chr1 | 157747277 | ||||||
chr1:157747280
|
T | C | 1 | a0001c0001t0001g0195 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1460-381A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 10/11 | chr1 | 157747280 | ||||||
chr1:157747305
|
ACT | A | 5 | a0001c0001t0001g0019a0001c0001t0001g0044a0001c0001t0001g0045others(2): Show | 6 | HG02145.hp1 HG02280.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.1460-408_1460-407d others(4): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 10/11 | chr1 | 157747305 | ||||||
chr1:157747386
|
G | C | 1 | a0001c0001t0001g0066 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1460-487C>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 10/11 | chr1 | 157747386 | ||||||
chr1:157747784
|
G | A | 17 | a0001c0001t0006g0024a0001c0001t0006g0102a0001c0001t0006g0103others(14): Show | 19 | HG01109.hp1 HG01891.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.1459+769C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 10/11 | chr1 | 157747784 | ||||||
chr1:157747877
|
T | C | 17 | a0001c0001t0006g0024a0001c0001t0006g0102a0001c0001t0006g0103others(14): Show | 19 | HG01109.hp1 HG01891.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.1459+676A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 10/11 | chr1 | 157747877 | ||||||
chr1:157747995
|
T | C | 17 | a0001c0001t0006g0024a0001c0001t0006g0102a0001c0001t0006g0103others(14): Show | 19 | HG01109.hp1 HG01891.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.1459+558A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 10/11 | chr1 | 157747995 | ||||||
chr1:157748020
|
A | G | 17 | a0001c0001t0006g0024a0001c0001t0006g0102a0001c0001t0006g0103others(14): Show | 19 | HG01109.hp1 HG01891.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.1459+533T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 10/11 | chr1 | 157748020 | ||||||
chr1:157748020
|
AT | A | 6 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0073others(3): Show | 8 | HG00140.hp1 HG03239.hp2 HG03688.hp2 others(5): Show |
intron_variant | MODIFIER | c.1459+532delA | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 10/11 | chr1 | 157748020 | ||||||
chr1:157748041
|
C | T | 17 | a0001c0001t0006g0024a0001c0001t0006g0102a0001c0001t0006g0103others(14): Show | 19 | HG01109.hp1 HG01891.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.1459+512G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 10/11 | chr1 | 157748041 | ||||||
chr1:157748104
|
A | G | 17 | a0001c0001t0006g0024a0001c0001t0006g0102a0001c0001t0006g0103others(14): Show | 19 | HG01109.hp1 HG01891.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.1459+449T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 10/11 | chr1 | 157748104 | ||||||
chr1:157748189
|
C | T | 2 | a0001c0001t0004g0247a0001c0001t0004g0248 | 2 | HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1459+364G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 10/11 | chr1 | 157748189 | ||||||
chr1:157748358
|
G | T | 1 | a0001c0001t0001g0258 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1459+195C>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 10/11 | chr1 | 157748358 | ||||||
chr1:157748412
|
G | C | 2 | a0001c0001t0006g0024a0001c0001t0006g0103 | 3 | HG03041.hp2 HG03225.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1459+141C>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 10/11 | chr1 | 157748412 | ||||||
chr1:157748441
|
C | CAAAT | 91 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0010others(88): Show | 123 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.1459+108_1459+111d others(6): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 10/11 | chr1 | 157748441 | ||||||
chr1:157748441
|
C | CAAATAAA others(1): Show |
4 | a0001c0001t0001g0124a0001c0001t0001g0158a0001c0001t0002g0231others(1): Show | 4 | HG01952.hp1 HG02451.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1459+104_1459+111d others(10): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 10/11 | chr1 | 157748441 | ||||||
chr1:157748441
|
CAAAT | C | 36 | a0001c0001t0001g0012a0001c0001t0001g0020a0001c0001t0001g0027others(33): Show | 41 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(38): Show |
intron_variant | MODIFIER | c.1459+108_1459+111d others(6): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 10/11 | chr1 | 157748441 | ||||||
chr1:157748441
|
CAAATAAA others(1): Show |
C | 7 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0146others(4): Show | 7 | HG00741.hp2 HG02074.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1459+104_1459+111d others(10): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 10/11 | chr1 | 157748441 | ||||||
chr1:157748441
|
CAAATAAA others(5): Show |
C | 2 | a0001c0001t0001g0048a0001c0001t0001g0049 | 2 | HG02486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1459+100_1459+111d others(14): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 10/11 | chr1 | 157748441 | ||||||
chr1:157748441
|
CAAATAAA others(9): Show |
C | 17 | a0001c0001t0006g0024a0001c0001t0006g0102a0001c0001t0006g0103others(14): Show | 19 | HG01109.hp1 HG01891.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.1459+96_1459+111de others(17): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 10/11 | chr1 | 157748441 | ||||||
chr1:157748491
|
C | A | 1 | a0001c0001t0001g0258 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1459+62G>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 10/11 | chr1 | 157748491 | ||||||
chr1:157748493
|
A | T | 272 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(269): Show | 363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.1459+60T>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 10/11 | chr1 | 157748493 | ||||||
chr1:157748535
|
T | G | 86 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(83): Show | 112 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.1459+18A>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 10/11 | chr1 | 157748535 | ||||||
chr1:157748640
|
T | G | 86 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(83): Show | 112 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.1394-22A>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 9/11 | chr1 | 157748640 | ||||||
chr1:157748855
|
T | C | 86 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(83): Show | 112 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.1393+20A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 9/11 | chr1 | 157748855 | ||||||
chr1:157748990
|
A | G | 86 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(83): Show | 112 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.1308-30T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 8/11 | chr1 | 157748990 | ||||||
chr1:157749045
|
G | A | 86 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(83): Show | 112 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.1308-85C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 8/11 | chr1 | 157749045 | ||||||
chr1:157749056
|
A | C | 7 | a0001c0002t0005g0043a0001c0002t0005g0275a0001c0002t0005g0276others(4): Show | 8 | HG02622.hp1 HG02818.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1308-96T>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 8/11 | chr1 | 157749056 | ||||||
chr1:157749103
|
A | G | 1 | a0001c0001t0001g0168 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1308-143T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 8/11 | chr1 | 157749103 | ||||||
chr1:157749138
|
T | C | 1 | a0001c0001t0001g0179 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1308-178A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 8/11 | chr1 | 157749138 | ||||||
chr1:157749189
|
C | CT | 85 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(82): Show | 111 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.1308-230dupA | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 8/11 | chr1 | 157749189 | ||||||
chr1:157749199
|
C | T | 1 | a0001c0001t0001g0073 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1308-239G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 8/11 | chr1 | 157749199 | ||||||
chr1:157749283
|
C | T | 76 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(73): Show | 101 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(98): Show |
intron_variant | MODIFIER | c.1308-323G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 8/11 | chr1 | 157749283 | ||||||
chr1:157749330
|
G | T | 3 | a0002c0003t0001g0268a0002c0003t0001g0269a0002c0003t0001g0270 | 3 | HG02257.hp1 HG02630.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1307+320C>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 8/11 | chr1 | 157749330 | ||||||
chr1:157749429
|
G | A | 1 | a0001c0001t0001g0204 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1307+221C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 8/11 | chr1 | 157749429 | ||||||
chr1:157749634
|
T | C | 10 | a0001c0002t0005g0043a0001c0002t0005g0275a0001c0002t0005g0276others(7): Show | 11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1307+16A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 8/11 | chr1 | 157749634 | ||||||
chr1:157749690
|
T | C | 1 | a0001c0001t0001g0165 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1280-13A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157749690 | ||||||
chr1:157749738
|
G | C | 1 | a0001c0001t0001g0215 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1280-61C>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157749738 | ||||||
chr1:157749753
|
C | T | 1 | a0001c0001t0001g0023 | 2 | NA18973.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.1280-76G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157749753 | ||||||
chr1:157749909
|
G | A | 1 | a0001c0001t0002g0222 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1280-232C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157749909 | ||||||
chr1:157749943
|
T | A | 1 | a0001c0001t0006g0106 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1280-266A>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157749943 | ||||||
chr1:157749951
|
A | T | 10 | a0001c0002t0005g0043a0001c0002t0005g0275a0001c0002t0005g0276others(7): Show | 11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-274T>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157749951 | ||||||
chr1:157750120
|
G | A | 1 | a0001c0007t0001g0253 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1280-443C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157750120 | ||||||
chr1:157750123
|
A | G | 10 | a0001c0002t0005g0043a0001c0002t0005g0275a0001c0002t0005g0276others(7): Show | 11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-446T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157750123 | ||||||
chr1:157750150
|
A | G | 1 | a0001c0001t0001g0051 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1280-473T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157750150 | ||||||
chr1:157750162
|
C | T | 1 | a0001c0001t0001g0194 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1280-485G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157750162 | ||||||
chr1:157750163
|
G | A | 10 | a0001c0002t0005g0043a0001c0002t0005g0275a0001c0002t0005g0276others(7): Show | 11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-486C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157750163 | ||||||
chr1:157750219
|
G | A | 69 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(66): Show | 93 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(90): Show |
intron_variant | MODIFIER | c.1280-542C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157750219 | ||||||
chr1:157750233
|
T | C | 1 | a0001c0001t0001g0129 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1280-556A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157750233 | ||||||
chr1:157750346
|
C | A | 10 | a0001c0002t0005g0043a0001c0002t0005g0275a0001c0002t0005g0276others(7): Show | 11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-669G>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157750346 | ||||||
chr1:157750410
|
T | C | 10 | a0001c0002t0005g0043a0001c0002t0005g0275a0001c0002t0005g0276others(7): Show | 11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-733A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157750410 | ||||||
chr1:157750431
|
T | C | 10 | a0001c0002t0005g0043a0001c0002t0005g0275a0001c0002t0005g0276others(7): Show | 11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-754A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157750431 | ||||||
chr1:157750804
|
C | A | 2 | a0001c0001t0008g0273a0001c0001t0008g0274 | 2 | HG01891.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.1280-1127G>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157750804 | ||||||
chr1:157750886
|
G | C | 13 | a0001c0001t0008g0252a0001c0001t0008g0273a0001c0001t0008g0274others(10): Show | 14 | HG01891.hp1 HG02145.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1280-1209C>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157750886 | ||||||
chr1:157750911
|
A | C | 1 | a0001c0001t0001g0190 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1280-1234T>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157750911 | ||||||
chr1:157750935
|
C | T | 1 | a0001c0001t0008g0252 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1280-1258G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157750935 | ||||||
chr1:157750940
|
T | C | 1 | a0001c0001t0008g0252 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1280-1263A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157750940 | ||||||
chr1:157751060
|
C | T | 2 | a0001c0001t0001g0170a0001c0001t0001g0183 | 2 | NA18957.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.1280-1383G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157751060 | ||||||
chr1:157751064
|
T | C | 4 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0134others(1): Show | 4 | HG01516.hp1 HG02451.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.1280-1387A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157751064 | ||||||
chr1:157751078
|
A | G | 1 | a0002c0003t0001g0269 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1280-1401T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157751078 | ||||||
chr1:157751098
|
T | A | 1 | a0001c0001t0003g0072 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1280-1421A>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157751098 | ||||||
chr1:157751111
|
A | G | 10 | a0001c0002t0005g0043a0001c0002t0005g0275a0001c0002t0005g0276others(7): Show | 11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-1434T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157751111 | ||||||
chr1:157751201
|
A | G | 1 | a0001c0001t0001g0062 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1280-1524T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157751201 | ||||||
chr1:157751208
|
T | A | 1 | a0001c0001t0001g0062 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1280-1531A>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157751208 | ||||||
chr1:157751209
|
C | A | 1 | a0001c0001t0001g0062 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1280-1532G>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157751209 | ||||||
chr1:157751212
|
A | G | 1 | a0001c0001t0001g0062 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1280-1535T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157751212 | ||||||
chr1:157751218
|
T | A | 1 | a0001c0001t0001g0062 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1280-1541A>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157751218 | ||||||
chr1:157751221
|
C | T | 1 | a0001c0001t0001g0062 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1280-1544G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157751221 | ||||||
chr1:157751222
|
C | T | 1 | a0001c0001t0001g0062 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1280-1545G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157751222 | ||||||
chr1:157751224
|
T | G | 1 | a0001c0001t0001g0062 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1280-1547A>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157751224 | ||||||
chr1:157751234
|
A | G | 1 | a0001c0001t0001g0234 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1280-1557T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157751234 | ||||||
chr1:157751332
|
G | A | 3 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0134 | 3 | HG02451.hp2 HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1280-1655C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157751332 | ||||||
chr1:157751464
|
G | A | 10 | a0001c0002t0005g0043a0001c0002t0005g0275a0001c0002t0005g0276others(7): Show | 11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-1787C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157751464 | ||||||
chr1:157751549
|
A | T | 10 | a0001c0002t0005g0043a0001c0002t0005g0275a0001c0002t0005g0276others(7): Show | 11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-1872T>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157751549 | ||||||
chr1:157751550
|
C | T | 20 | a0001c0001t0001g0232a0001c0001t0001g0272a0001c0001t0002g0217others(17): Show | 20 | HG00609.hp2 HG00642.hp2 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.1280-1873G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157751550 | ||||||
chr1:157751672
|
T | C | 1 | a0001c0001t0001g0083 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1280-1995A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157751672 | ||||||
chr1:157751894
|
C | T | 1 | a0001c0001t0003g0074 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1280-2217G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157751894 | ||||||
chr1:157751894
|
CG | C | 3 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0134 | 3 | HG02451.hp2 HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1280-2218delC | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157751894 | ||||||
chr1:157751903
|
C | CGAGCAAA others(19): Show |
3 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0134 | 3 | HG02451.hp2 HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1280-2227_1280-222 others(30): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157751903 | ||||||
chr1:157751904
|
T | A | 3 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0134 | 3 | HG02451.hp2 HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1280-2227A>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157751904 | ||||||
chr1:157751908
|
G | C | 10 | a0001c0002t0005g0043a0001c0002t0005g0275a0001c0002t0005g0276others(7): Show | 11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-2231C>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157751908 | ||||||
chr1:157751922
|
A | G | 10 | a0001c0002t0005g0043a0001c0002t0005g0275a0001c0002t0005g0276others(7): Show | 11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-2245T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157751922 | ||||||
chr1:157751945
|
G | A | 10 | a0001c0002t0005g0043a0001c0002t0005g0275a0001c0002t0005g0276others(7): Show | 11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-2268C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157751945 | ||||||
chr1:157751949
|
T | C | 1 | a0001c0001t0001g0135 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1280-2272A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157751949 | ||||||
chr1:157752008
|
T | C | 2 | a0001c0001t0001g0232a0001c0001t0001g0272 | 2 | HG03195.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1280-2331A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157752008 | ||||||
chr1:157752010
|
C | T | 3 | a0001c0001t0008g0252a0001c0001t0008g0273a0001c0001t0008g0274 | 3 | HG01891.hp1 HG02145.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.1280-2333G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157752010 | ||||||
chr1:157752013
|
T | A | 1 | a0001c0001t0001g0132 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1280-2336A>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157752013 | ||||||
chr1:157752266
|
G | A | 10 | a0001c0002t0005g0043a0001c0002t0005g0275a0001c0002t0005g0276others(7): Show | 11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-2589C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157752266 | ||||||
chr1:157752267
|
T | C | 10 | a0001c0002t0005g0043a0001c0002t0005g0275a0001c0002t0005g0276others(7): Show | 11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-2590A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157752267 | ||||||
chr1:157752318
|
A | G | 2 | a0001c0001t0001g0232a0001c0001t0001g0272 | 2 | HG03195.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1280-2641T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157752318 | ||||||
chr1:157752548
|
G | A | 3 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0134 | 3 | HG02451.hp2 HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1280-2871C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157752548 | ||||||
chr1:157752763
|
T | C | 1 | a0001c0001t0001g0062 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1280-3086A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157752763 | ||||||
chr1:157752860
|
G | A | 10 | a0001c0002t0005g0043a0001c0002t0005g0275a0001c0002t0005g0276others(7): Show | 11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-3183C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157752860 | ||||||
chr1:157752920
|
G | A | 10 | a0001c0002t0005g0043a0001c0002t0005g0275a0001c0002t0005g0276others(7): Show | 11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-3243C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157752920 | ||||||
chr1:157753105
|
A | T | 7 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068others(4): Show | 7 | HG00140.hp2 HG00733.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.1280-3428T>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157753105 | ||||||
chr1:157753365
|
C | A | 3 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0134 | 3 | HG02451.hp2 HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1280-3688G>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157753365 | ||||||
chr1:157753398
|
C | A | 10 | a0001c0002t0005g0043a0001c0002t0005g0275a0001c0002t0005g0276others(7): Show | 11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-3721G>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157753398 | ||||||
chr1:157753664
|
T | C | 1 | a0001c0001t0001g0174 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1280-3987A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157753664 | ||||||
chr1:157753725
|
A | G | 10 | a0001c0002t0005g0043a0001c0002t0005g0275a0001c0002t0005g0276others(7): Show | 11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-4048T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157753725 | ||||||
chr1:157754045
|
C | G | 69 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(66): Show | 93 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(90): Show |
intron_variant | MODIFIER | c.1280-4368G>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157754045 | ||||||
chr1:157754047
|
G | A | 69 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(66): Show | 93 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(90): Show |
intron_variant | MODIFIER | c.1280-4370C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157754047 | ||||||
chr1:157754049
|
A | AATATTTC others(5): Show |
69 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(66): Show | 93 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(90): Show |
intron_variant | MODIFIER | c.1280-4373_1280-437 others(16): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157754049 | ||||||
chr1:157754050
|
C | T | 69 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(66): Show | 93 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(90): Show |
intron_variant | MODIFIER | c.1280-4373G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157754050 | ||||||
chr1:157754150
|
C | T | 1 | a0001c0001t0001g0260 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1280-4473G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157754150 | ||||||
chr1:157754402
|
G | T | 10 | a0001c0002t0005g0043a0001c0002t0005g0275a0001c0002t0005g0276others(7): Show | 11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-4725C>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157754402 | ||||||
chr1:157754449
|
A | C | 10 | a0001c0002t0005g0043a0001c0002t0005g0275a0001c0002t0005g0276others(7): Show | 11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-4772T>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157754449 | ||||||
chr1:157754471
|
G | C | 2 | a0001c0001t0001g0175a0001c0001t0001g0209 | 2 | HG01192.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1280-4794C>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157754471 | ||||||
chr1:157754499
|
C | A | 1 | a0001c0001t0001g0178 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1280-4822G>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157754499 | ||||||
chr1:157754773
|
C | T | 10 | a0001c0002t0005g0043a0001c0002t0005g0275a0001c0002t0005g0276others(7): Show | 11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-5096G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157754773 | ||||||
chr1:157754774
|
C | T | 10 | a0001c0002t0005g0043a0001c0002t0005g0275a0001c0002t0005g0276others(7): Show | 11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-5097G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157754774 | ||||||
chr1:157754777
|
G | A | 10 | a0001c0002t0005g0043a0001c0002t0005g0275a0001c0002t0005g0276others(7): Show | 11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-5100C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157754777 | ||||||
chr1:157754832
|
G | A | 4 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0134others(1): Show | 4 | HG02451.hp2 HG02647.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1280-5155C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157754832 | ||||||
chr1:157754870
|
G | A | 1 | a0001c0002t0005g0282 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1280-5193C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157754870 | ||||||
chr1:157754914
|
C | T | 10 | a0001c0002t0005g0043a0001c0002t0005g0275a0001c0002t0005g0276others(7): Show | 11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-5237G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157754914 | ||||||
chr1:157754953
|
G | A | 2 | a0001c0001t0001g0068a0001c0001t0001g0070 | 2 | HG01175.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.1280-5276C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157754953 | ||||||
chr1:157754965
|
C | CA | 19 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0023others(16): Show | 30 | HG00597.hp2 HG00621.hp2 HG01256.hp2 others(27): Show |
intron_variant | MODIFIER | c.1280-5289dupT | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157754965 | ||||||
chr1:157754967
|
A | G | 2 | a0001c0001t0001g0140a0001c0001t0001g0141 | 2 | HG03139.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1280-5290T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157754967 | ||||||
chr1:157755006
|
C | A | 3 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0007t0001g0253 | 3 | HG02004.hp2 HG02055.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1280-5329G>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157755006 | ||||||
chr1:157755073
|
A | G | 1 | a0001c0001t0001g0155 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1280-5396T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157755073 | ||||||
chr1:157755123
|
A | G | 1 | a0001c0001t0001g0157 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1280-5446T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157755123 | ||||||
chr1:157755195
|
C | T | 10 | a0001c0002t0005g0043a0001c0002t0005g0275a0001c0002t0005g0276others(7): Show | 11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-5518G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157755195 | ||||||
chr1:157755257
|
C | T | 11 | a0001c0001t0007g0118a0001c0002t0005g0043a0001c0002t0005g0275others(8): Show | 12 | HG02257.hp2 HG02300.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1280-5580G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157755257 | ||||||
chr1:157755325
|
G | A | 10 | a0001c0002t0005g0043a0001c0002t0005g0275a0001c0002t0005g0276others(7): Show | 11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-5648C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157755325 | ||||||
chr1:157755331
|
C | A | 10 | a0001c0002t0005g0043a0001c0002t0005g0275a0001c0002t0005g0276others(7): Show | 11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-5654G>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157755331 | ||||||
chr1:157755420
|
G | A | 2 | a0001c0001t0001g0034a0001c0001t0001g0189 | 3 | HG03017.hp1 HG03831.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1280-5743C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157755420 | ||||||
chr1:157755474
|
T | G | 186 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(183): Show | 240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.1280-5797A>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157755474 | ||||||
chr1:157755586
|
C | G | 5 | a0001c0001t0001g0019a0001c0001t0001g0044a0001c0001t0001g0045others(2): Show | 6 | HG02145.hp1 HG02280.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.1280-5909G>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157755586 | ||||||
chr1:157755655
|
C | T | 2 | a0001c0001t0001g0031a0001c0001t0001g0169 | 3 | NA18978.hp1 NA18999.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.1280-5978G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157755655 | ||||||
chr1:157755800
|
T | C | 12 | a0001c0001t0004g0014a0001c0001t0004g0039a0001c0001t0004g0149others(9): Show | 16 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.1280-6123A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157755800 | ||||||
chr1:157755944
|
T | C | 10 | a0001c0002t0005g0043a0001c0002t0005g0275a0001c0002t0005g0276others(7): Show | 11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-6267A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157755944 | ||||||
chr1:157756044
|
G | A | 1 | a0001c0001t0006g0102 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1280-6367C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157756044 | ||||||
chr1:157756071
|
T | A | 5 | a0001c0001t0001g0019a0001c0001t0001g0044a0001c0001t0001g0045others(2): Show | 6 | HG02145.hp1 HG02280.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.1280-6394A>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157756071 | ||||||
chr1:157756100
|
G | T | 10 | a0001c0002t0005g0043a0001c0002t0005g0275a0001c0002t0005g0276others(7): Show | 11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-6423C>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157756100 | ||||||
chr1:157756212
|
A | G | 1 | a0001c0001t0001g0169 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1280-6535T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157756212 | ||||||
chr1:157756230
|
G | A | 1 | a0001c0001t0001g0234 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1280-6553C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157756230 | ||||||
chr1:157756333
|
T | C | 18 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0002g0219others(15): Show | 18 | HG00609.hp2 HG00642.hp2 HG00673.hp1 others(15): Show |
intron_variant | MODIFIER | c.1280-6656A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157756333 | ||||||
chr1:157756389
|
T | G | 1 | a0001c0001t0001g0200 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1280-6712A>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157756389 | ||||||
chr1:157756453
|
T | C | 10 | a0001c0002t0005g0043a0001c0002t0005g0275a0001c0002t0005g0276others(7): Show | 11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-6776A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157756453 | ||||||
chr1:157756462
|
C | T | 1 | a0001c0001t0001g0265 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1280-6785G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157756462 | ||||||
chr1:157756468
|
A | G | 3 | a0001c0001t0001g0238a0001c0001t0001g0239a0001c0001t0001g0240 | 3 | HG02630.hp1 HG02895.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1280-6791T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157756468 | ||||||
chr1:157756543
|
G | A | 37 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0010others(34): Show | 59 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.1280-6866C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157756543 | ||||||
chr1:157756587
|
G | A | 10 | a0001c0002t0005g0043a0001c0002t0005g0275a0001c0002t0005g0276others(7): Show | 11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-6910C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157756587 | ||||||
chr1:157756617
|
C | T | 41 | a0001c0001t0001g0019a0001c0001t0001g0044a0001c0001t0001g0045others(38): Show | 42 | HG00609.hp2 HG00642.hp2 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.1280-6940G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157756617 | ||||||
chr1:157756631
|
T | A | 10 | a0001c0002t0005g0043a0001c0002t0005g0275a0001c0002t0005g0276others(7): Show | 11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-6954A>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157756631 | ||||||
chr1:157756649
|
G | T | 1 | a0001c0002t0005g0278 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1280-6972C>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157756649 | ||||||
chr1:157756662
|
C | G | 10 | a0001c0002t0005g0043a0001c0002t0005g0275a0001c0002t0005g0276others(7): Show | 11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-6985G>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157756662 | ||||||
chr1:157756670
|
C | T | 56 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0010others(53): Show | 83 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.1280-6993G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157756670 | ||||||
chr1:157756679
|
G | GA | 165 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(162): Show | 214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.1280-7003dupT | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157756679 | ||||||
chr1:157756679
|
GAA | G | 10 | a0001c0002t0005g0043a0001c0002t0005g0275a0001c0002t0005g0276others(7): Show | 11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-7004_1280-700 others(6): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157756679 | ||||||
chr1:157756696
|
G | A | 1 | a0001c0001t0001g0258 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1280-7019C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157756696 | ||||||
chr1:157756696
|
G | C | 10 | a0001c0002t0005g0043a0001c0002t0005g0275a0001c0002t0005g0276others(7): Show | 11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-7019C>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157756696 | ||||||
chr1:157756886
|
C | T | 10 | a0001c0002t0005g0043a0001c0002t0005g0275a0001c0002t0005g0276others(7): Show | 11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-7209G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157756886 | ||||||
chr1:157757031
|
G | C | 3 | a0001c0001t0008g0252a0001c0001t0008g0273a0001c0001t0008g0274 | 3 | HG01891.hp1 HG02145.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.1280-7354C>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157757031 | ||||||
chr1:157757100
|
T | A | 10 | a0001c0002t0005g0043a0001c0002t0005g0275a0001c0002t0005g0276others(7): Show | 11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-7423A>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157757100 | ||||||
chr1:157757123
|
T | G | 10 | a0001c0002t0005g0043a0001c0002t0005g0275a0001c0002t0005g0276others(7): Show | 11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-7446A>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157757123 | ||||||
chr1:157757448
|
G | A | 1 | a0005c0009t0001g0214 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1280-7771C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157757448 | ||||||
chr1:157757468
|
C | T | 1 | a0001c0001t0008g0252 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1280-7791G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157757468 | ||||||
chr1:157757508
|
C | T | 1 | a0001c0001t0001g0066 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1280-7831G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157757508 | ||||||
chr1:157757551
|
C | T | 10 | a0001c0002t0005g0043a0001c0002t0005g0275a0001c0002t0005g0276others(7): Show | 11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-7874G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157757551 | ||||||
chr1:157757552
|
G | A | 1 | a0001c0001t0001g0185 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1280-7875C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157757552 | ||||||
chr1:157757684
|
T | C | 10 | a0001c0002t0005g0043a0001c0002t0005g0275a0001c0002t0005g0276others(7): Show | 11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-8007A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157757684 | ||||||
chr1:157757701
|
A | T | 10 | a0001c0002t0005g0043a0001c0002t0005g0275a0001c0002t0005g0276others(7): Show | 11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-8024T>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157757701 | ||||||
chr1:157757731
|
T | G | 10 | a0001c0002t0005g0043a0001c0002t0005g0275a0001c0002t0005g0276others(7): Show | 11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-8054A>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157757731 | ||||||
chr1:157757786
|
C | A | 10 | a0001c0002t0005g0043a0001c0002t0005g0275a0001c0002t0005g0276others(7): Show | 11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-8109G>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157757786 | ||||||
chr1:157757831
|
G | A | 2 | a0001c0001t0001g0177a0001c0001t0001g0186 | 2 | NA18945.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.1280-8154C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157757831 | ||||||
chr1:157757835
|
G | A | 1 | a0001c0001t0006g0104 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1280-8158C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157757835 | ||||||
chr1:157757839
|
G | C | 10 | a0001c0002t0005g0043a0001c0002t0005g0275a0001c0002t0005g0276others(7): Show | 11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-8162C>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157757839 | ||||||
chr1:157757841
|
A | T | 10 | a0001c0002t0005g0043a0001c0002t0005g0275a0001c0002t0005g0276others(7): Show | 11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-8164T>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157757841 | ||||||
chr1:157757842
|
G | T | 10 | a0001c0002t0005g0043a0001c0002t0005g0275a0001c0002t0005g0276others(7): Show | 11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-8165C>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157757842 | ||||||
chr1:157757858
|
A | G | 1 | a0001c0001t0008g0252 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1280-8181T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157757858 | ||||||
chr1:157757894
|
A | G | 10 | a0001c0002t0005g0043a0001c0002t0005g0275a0001c0002t0005g0276others(7): Show | 11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-8217T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157757894 | ||||||
chr1:157757897
|
G | T | 10 | a0001c0002t0005g0043a0001c0002t0005g0275a0001c0002t0005g0276others(7): Show | 11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-8220C>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157757897 | ||||||
chr1:157757927
|
G | A | 1 | a0001c0001t0001g0187 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1280-8250C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157757927 | ||||||
chr1:157757956
|
C | G | 1 | a0001c0001t0009g0144 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1280-8279G>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157757956 | ||||||
chr1:157758064
|
C | T | 10 | a0001c0002t0005g0043a0001c0002t0005g0275a0001c0002t0005g0276others(7): Show | 11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-8387G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157758064 | ||||||
chr1:157758094
|
T | A | 10 | a0001c0002t0005g0043a0001c0002t0005g0275a0001c0002t0005g0276others(7): Show | 11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-8417A>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157758094 | ||||||
chr1:157758161
|
A | G | 10 | a0001c0002t0005g0043a0001c0002t0005g0275a0001c0002t0005g0276others(7): Show | 11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1280-8484T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157758161 | ||||||
chr1:157758293
|
G | C | 10 | a0001c0002t0005g0043a0001c0002t0005g0275a0001c0002t0005g0276others(7): Show | 11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1279+8562C>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157758293 | ||||||
chr1:157758310
|
G | A | 10 | a0001c0002t0005g0043a0001c0002t0005g0275a0001c0002t0005g0276others(7): Show | 11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1279+8545C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157758310 | ||||||
chr1:157758358
|
T | C | 3 | a0001c0002t0005g0277a0001c0002t0005g0278a0001c0002t0005g0283 | 3 | HG02257.hp2 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1279+8497A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157758358 | ||||||
chr1:157758409
|
C | T | 10 | a0001c0002t0005g0043a0001c0002t0005g0275a0001c0002t0005g0276others(7): Show | 11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1279+8446G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157758409 | ||||||
chr1:157758442
|
A | C | 1 | a0001c0001t0001g0126 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1279+8413T>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157758442 | ||||||
chr1:157758511
|
T | C | 3 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0134 | 3 | HG02451.hp2 HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1279+8344A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157758511 | ||||||
chr1:157758525
|
C | G | 10 | a0001c0002t0005g0043a0001c0002t0005g0275a0001c0002t0005g0276others(7): Show | 11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1279+8330G>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157758525 | ||||||
chr1:157758538
|
G | A | 10 | a0001c0002t0005g0043a0001c0002t0005g0275a0001c0002t0005g0276others(7): Show | 11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1279+8317C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157758538 | ||||||
chr1:157758547
|
C | T | 1 | a0001c0001t0003g0057 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1279+8308G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157758547 | ||||||
chr1:157758567
|
A | G | 1 | a0001c0004t0005g0284 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1279+8288T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157758567 | ||||||
chr1:157758661
|
T | C | 1 | a0001c0001t0001g0065 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1279+8194A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157758661 | ||||||
chr1:157758664
|
C | T | 3 | a0001c0001t0008g0252a0001c0001t0008g0273a0001c0001t0008g0274 | 3 | HG01891.hp1 HG02145.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.1279+8191G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157758664 | ||||||
chr1:157758665
|
C | T | 1 | a0001c0001t0001g0065 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1279+8190G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157758665 | ||||||
chr1:157758667
|
A | G | 1 | a0001c0001t0001g0065 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1279+8188T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157758667 | ||||||
chr1:157758669
|
G | T | 1 | a0001c0001t0001g0065 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1279+8186C>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157758669 | ||||||
chr1:157758671
|
A | C | 1 | a0001c0001t0001g0065 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1279+8184T>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157758671 | ||||||
chr1:157758674
|
C | G | 1 | a0001c0001t0001g0065 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1279+8181G>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157758674 | ||||||
chr1:157758675
|
C | T | 1 | a0001c0001t0001g0065 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1279+8180G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157758675 | ||||||
chr1:157758676
|
C | T | 1 | a0001c0001t0001g0065 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1279+8179G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157758676 | ||||||
chr1:157758679
|
G | T | 2 | a0001c0001t0001g0048a0001c0001t0001g0049 | 2 | HG02486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1279+8176C>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157758679 | ||||||
chr1:157758680
|
C | CA | 53 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0035others(50): Show | 59 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.1279+8174dupT | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157758680 | ||||||
chr1:157758680
|
C | CAA | 7 | a0001c0001t0001g0148a0001c0001t0001g0168a0001c0001t0001g0180others(4): Show | 7 | HG01123.hp1 HG02145.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1279+8173_1279+817 others(6): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157758680 | ||||||
chr1:157758680
|
CA | C | 25 | a0001c0001t0001g0034a0001c0001t0001g0048a0001c0001t0001g0049others(22): Show | 31 | HG01109.hp1 HG01884.hp2 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.1279+8174delT | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157758680 | ||||||
chr1:157758773
|
A | G | 1 | a0001c0001t0001g0182 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.1279+8082T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157758773 | ||||||
chr1:157758943
|
T | C | 1 | a0001c0001t0001g0178 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1279+7912A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157758943 | ||||||
chr1:157758957
|
A | G | 3 | a0001c0001t0001g0238a0001c0001t0001g0239a0001c0001t0001g0240 | 3 | HG02630.hp1 HG02895.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1279+7898T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157758957 | ||||||
chr1:157759106
|
G | A | 10 | a0001c0002t0005g0043a0001c0002t0005g0275a0001c0002t0005g0276others(7): Show | 11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1279+7749C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157759106 | ||||||
chr1:157759110
|
T | C | 1 | a0001c0001t0001g0241 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1279+7745A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157759110 | ||||||
chr1:157759302
|
A | G | 10 | a0001c0002t0005g0043a0001c0002t0005g0275a0001c0002t0005g0276others(7): Show | 11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1279+7553T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157759302 | ||||||
chr1:157759345
|
C | A | 3 | a0001c0001t0001g0238a0001c0001t0001g0239a0001c0001t0001g0240 | 3 | HG02630.hp1 HG02895.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1279+7510G>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157759345 | ||||||
chr1:157759470
|
C | A | 10 | a0001c0002t0005g0043a0001c0002t0005g0275a0001c0002t0005g0276others(7): Show | 11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1279+7385G>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157759470 | ||||||
chr1:157759514
|
T | A | 11 | a0001c0001t0001g0109a0001c0001t0001g0140a0001c0001t0001g0141others(8): Show | 11 | HG02004.hp2 HG02055.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1279+7341A>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157759514 | ||||||
chr1:157759565
|
C | G | 1 | a0001c0002t0005g0283 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1279+7290G>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157759565 | ||||||
chr1:157759580
|
A | T | 3 | a0001c0001t0001g0238a0001c0001t0001g0239a0001c0001t0001g0240 | 3 | HG02630.hp1 HG02895.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1279+7275T>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157759580 | ||||||
chr1:157759765
|
C | A | 4 | a0001c0001t0001g0040a0001c0001t0001g0148a0001c0001t0001g0241others(1): Show | 5 | HG02723.hp1 HG02922.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1279+7090G>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157759765 | ||||||
chr1:157759821
|
G | A | 10 | a0001c0002t0005g0043a0001c0002t0005g0275a0001c0002t0005g0276others(7): Show | 11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1279+7034C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157759821 | ||||||
chr1:157759967
|
G | A | 1 | a0001c0001t0001g0093 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1279+6888C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157759967 | ||||||
chr1:157760090
|
C | T | 1 | a0001c0001t0001g0082 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1279+6765G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760090 | ||||||
chr1:157760131
|
T | C | 10 | a0001c0002t0005g0043a0001c0002t0005g0275a0001c0002t0005g0276others(7): Show | 11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1279+6724A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760131 | ||||||
chr1:157760238
|
T | C | 37 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0010others(34): Show | 59 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.1279+6617A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760238 | ||||||
chr1:157760359
|
A | G | 2 | a0001c0001t0008g0273a0001c0001t0008g0274 | 2 | HG01891.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.1279+6496T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760359 | ||||||
chr1:157760460
|
T | TA | 10 | a0001c0002t0005g0043a0001c0002t0005g0275a0001c0002t0005g0276others(7): Show | 11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1279+6394dupT | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760460 | ||||||
chr1:157760489
|
G | A | 5 | a0001c0001t0001g0019a0001c0001t0001g0044a0001c0001t0001g0045others(2): Show | 6 | HG02145.hp1 HG02280.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.1279+6366C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760489 | ||||||
chr1:157760588
|
T | C | 10 | a0001c0002t0005g0043a0001c0002t0005g0275a0001c0002t0005g0276others(7): Show | 11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1279+6267A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760588 | ||||||
chr1:157760591
|
C | T | 1 | a0001c0001t0001g0181 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1279+6264G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760591 | ||||||
chr1:157760654
|
A | AGAAG | 22 | a0001c0001t0001g0019a0001c0001t0001g0044a0001c0001t0001g0045others(19): Show | 27 | HG00140.hp1 HG00423.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.1279+6197_1279+620 others(8): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760654 | ||||||
chr1:157760654
|
A | G | 1 | a0001c0001t0001g0193 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1279+6201T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760654 | ||||||
chr1:157760654
|
AGAAG | A | 11 | a0001c0001t0001g0109a0001c0001t0001g0135a0001c0001t0001g0140others(8): Show | 11 | HG02004.hp2 HG02055.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1279+6197_1279+620 others(8): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760654 | ||||||
chr1:157760654
|
AGAAGGAA others(5): Show |
A | 1 | a0001c0001t0001g0006 | 5 | HG02056.hp1 NA18939.hp1 NA18952.hp2 others(2): Show |
intron_variant | MODIFIER | c.1279+6189_1279+620 others(16): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760654 | ||||||
chr1:157760658
|
G | A | 10 | a0001c0002t0005g0043a0001c0002t0005g0275a0001c0002t0005g0276others(7): Show | 11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1279+6197C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760658 | ||||||
chr1:157760662
|
G | A | 7 | a0001c0002t0005g0043a0001c0002t0005g0275a0001c0002t0005g0276others(4): Show | 8 | HG02622.hp1 HG02818.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1279+6193C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760662 | ||||||
chr1:157760678
|
G | A | 3 | a0001c0001t0001g0152a0001c0001t0001g0193a0001c0001t0001g0258 | 3 | HG01981.hp2 HG02723.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1279+6177C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760678 | ||||||
chr1:157760680
|
A | AAAGAAAG others(127): Show |
1 | a0001c0001t0002g0229 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1279+6174_1279+617 others(138): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760680 | ||||||
chr1:157760680
|
A | AAAGAAAG others(123): Show |
6 | a0001c0001t0002g0225a0001c0001t0002g0226a0001c0001t0002g0227others(3): Show | 6 | HG00609.hp2 HG00642.hp2 HG00673.hp1 others(3): Show |
intron_variant | MODIFIER | c.1279+6174_1279+617 others(134): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760680 | ||||||
chr1:157760682
|
A | G | 18 | a0001c0001t0001g0071a0001c0001t0001g0132a0001c0001t0003g0061others(15): Show | 19 | HG00140.hp2 HG00408.hp2 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.1279+6173T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760682 | ||||||
chr1:157760686
|
A | G | 7 | a0001c0002t0005g0043a0001c0002t0005g0275a0001c0002t0005g0276others(4): Show | 8 | HG02622.hp1 HG02818.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1279+6169T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760686 | ||||||
chr1:157760686
|
AGAAAGAA others(5): Show |
A | 4 | a0001c0001t0004g0014a0001c0001t0004g0247a0001c0001t0004g0248others(1): Show | 7 | HG02486.hp1 HG02717.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1279+6157_1279+616 others(16): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760686 | ||||||
chr1:157760690
|
AGAAAGAA others(1): Show |
A | 5 | a0001c0001t0004g0243a0001c0001t0004g0244a0001c0001t0004g0249others(2): Show | 6 | HG02055.hp1 HG02886.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1279+6157_1279+616 others(12): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760690 | ||||||
chr1:157760694
|
A | G | 3 | a0001c0001t0001g0188a0001c0001t0001g0193a0001c0001t0004g0039 | 4 | HG00280.hp1 HG01981.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.1279+6161T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760694 | ||||||
chr1:157760694
|
AGAAG | A | 4 | a0001c0001t0003g0110a0001c0001t0008g0252a0001c0002t0005g0276others(1): Show | 4 | HG00735.hp1 HG02257.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.1279+6157_1279+616 others(8): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760694 | ||||||
chr1:157760698
|
G | A | 19 | a0001c0001t0001g0071a0001c0001t0001g0132a0001c0001t0001g0152others(16): Show | 20 | HG00140.hp2 HG00408.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.1279+6157C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760698 | ||||||
chr1:157760698
|
G | GAAGAAAG others(7): Show |
1 | a0001c0001t0001g0201 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1279+6156_1279+615 others(18): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760698 | ||||||
chr1:157760698
|
G | GGAAA | 28 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(25): Show | 42 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(39): Show |
intron_variant | MODIFIER | c.1279+6153_1279+615 others(8): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760698 | ||||||
chr1:157760698
|
G | GGAAAGAA others(1): Show |
19 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0036others(16): Show | 30 | HG00408.hp1 HG00735.hp2 HG01123.hp1 others(27): Show |
intron_variant | MODIFIER | c.1279+6149_1279+615 others(12): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760698 | ||||||
chr1:157760698
|
G | GGAAAGAA others(5): Show |
4 | a0001c0001t0001g0154a0001c0001t0001g0157a0001c0001t0001g0199others(1): Show | 4 | HG01175.hp1 HG02559.hp2 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.1279+6145_1279+615 others(16): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760698 | ||||||
chr1:157760698
|
G | GGAAAGAA others(9): Show |
2 | a0001c0001t0001g0077a0001c0001t0001g0202 | 2 | NA18984.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.1279+6141_1279+615 others(20): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760698 | ||||||
chr1:157760698
|
G | GGAAAGAA others(9): Show |
7 | a0001c0001t0001g0010a0001c0001t0001g0127a0001c0001t0009g0144others(4): Show | 10 | HG00544.hp1 HG01167.hp1 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.1279+6156_1279+615 others(20): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760698 | ||||||
chr1:157760698
|
G | GGAAAGAA others(13): Show |
2 | a0001c0001t0001g0128a0001c0001t0006g0102 | 2 | HG01109.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1279+6156_1279+615 others(24): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760698 | ||||||
chr1:157760698
|
G | GGAAAGAA others(20): Show |
1 | a0002c0003t0001g0270 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1279+6156_1279+615 others(31): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760698 | ||||||
chr1:157760698
|
GGAAA | G | 22 | a0001c0001t0001g0008a0001c0001t0001g0031a0001c0001t0001g0032others(19): Show | 28 | HG00558.hp2 HG00597.hp1 HG00621.hp1 others(25): Show |
intron_variant | MODIFIER | c.1279+6153_1279+615 others(8): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760698 | ||||||
chr1:157760698
|
GGAAAGAA others(1): Show |
G | 19 | a0001c0001t0001g0020a0001c0001t0001g0058a0001c0001t0001g0060others(16): Show | 20 | HG00099.hp1 HG00733.hp1 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.1279+6149_1279+615 others(12): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760698 | ||||||
chr1:157760698
|
GGAAAGAA others(5): Show |
G | 12 | a0001c0001t0001g0051a0001c0001t0001g0059a0001c0001t0001g0085others(9): Show | 12 | HG01361.hp2 HG02559.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.1279+6145_1279+615 others(16): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760698 | ||||||
chr1:157760698
|
GGAAAGAA others(9): Show |
G | 2 | a0001c0001t0001g0235a0001c0001t0001g0236 | 2 | HG02055.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1279+6141_1279+615 others(20): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760698 | ||||||
chr1:157760699
|
G | GAAAGAAA others(5): Show |
9 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0081others(6): Show | 16 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(13): Show |
intron_variant | MODIFIER | c.1279+6155_1279+615 others(16): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760699 | ||||||
chr1:157760699
|
G | T | 2 | a0001c0001t0001g0258a0001c0001t0004g0246 | 2 | HG02280.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1279+6156C>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760699 | ||||||
chr1:157760702
|
A | AGAAAGAA others(127): Show |
1 | a0001c0001t0002g0224 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1279+6152_1279+615 others(138): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760702 | ||||||
chr1:157760702
|
A | AGAAAGAA others(123): Show |
1 | a0001c0001t0002g0222 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1279+6152_1279+615 others(134): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760702 | ||||||
chr1:157760702
|
A | AGAAAGAA others(119): Show |
1 | a0001c0001t0002g0221 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1279+6152_1279+615 others(130): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760702 | ||||||
chr1:157760702
|
A | AGAAAGAA others(115): Show |
1 | a0001c0001t0002g0271 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1279+6152_1279+615 others(126): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760702 | ||||||
chr1:157760702
|
A | G | 8 | a0001c0001t0001g0071a0001c0001t0001g0132a0001c0001t0003g0061others(5): Show | 8 | HG00140.hp2 HG00408.hp2 HG01516.hp1 others(5): Show |
intron_variant | MODIFIER | c.1279+6153T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760702 | ||||||
chr1:157760703
|
G | GAAAGAAA others(1): Show |
14 | a0001c0001t0001g0007a0001c0001t0001g0029a0001c0001t0001g0046others(11): Show | 19 | HG01106.hp1 HG01255.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.1279+6151_1279+615 others(12): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760703 | ||||||
chr1:157760703
|
G | GAAGGAAA others(1): Show |
2 | a0001c0001t0001g0040a0001c0001t0001g0148 | 3 | HG02922.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1279+6151_1279+615 others(12): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760703 | ||||||
chr1:157760703
|
G | T | 2 | a0001c0001t0001g0241a0001c0001t0004g0149 | 2 | HG02723.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1279+6152C>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760703 | ||||||
chr1:157760706
|
A | AGAAATAA others(123): Show |
1 | a0001c0001t0002g0220 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1279+6148_1279+614 others(134): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760706 | ||||||
chr1:157760706
|
A | AGAAATAA others(119): Show |
1 | a0001c0001t0002g0219 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1279+6148_1279+614 others(130): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760706 | ||||||
chr1:157760706
|
A | AGAAATAA others(115): Show |
1 | a0001c0001t0002g0217 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1279+6148_1279+614 others(126): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760706 | ||||||
chr1:157760706
|
A | AGAAATAA others(111): Show |
1 | a0001c0001t0001g0232 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1279+6148_1279+614 others(122): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760706 | ||||||
chr1:157760706
|
A | G | 6 | a0001c0001t0003g0110a0001c0001t0004g0014a0001c0001t0004g0247others(3): Show | 9 | HG00735.hp1 HG02258.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1279+6149T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760706 | ||||||
chr1:157760707
|
G | GAAAT | 27 | a0001c0001t0001g0016a0001c0001t0001g0025a0001c0001t0001g0028others(24): Show | 32 | HG00099.hp2 HG01123.hp2 HG01192.hp2 others(29): Show |
intron_variant | MODIFIER | c.1279+6147_1279+614 others(8): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760707 | ||||||
chr1:157760707
|
G | GAAATAAA others(139): Show |
1 | a0001c0001t0002g0259 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1279+6147_1279+614 others(150): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760707 | ||||||
chr1:157760707
|
G | GAAATAAA others(131): Show |
1 | a0001c0001t0002g0228 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1279+6147_1279+614 others(142): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760707 | ||||||
chr1:157760707
|
G | GAAATAAA others(119): Show |
1 | a0001c0001t0001g0272 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1279+6147_1279+614 others(130): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760707 | ||||||
chr1:157760707
|
G | T | 2 | a0001c0001t0001g0251a0001c0001t0004g0039 | 3 | HG02109.hp2 HG02615.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1279+6148C>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760707 | ||||||
chr1:157760711
|
G | T | 46 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(43): Show | 73 | HG00140.hp1 HG00423.hp2 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.1279+6144C>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760711 | ||||||
chr1:157760715
|
G | GAAAGAAA others(119): Show |
1 | a0001c0001t0002g0223 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1279+6139_1279+614 others(130): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760715 | ||||||
chr1:157760715
|
G | T | 18 | a0001c0001t0001g0071a0001c0001t0001g0073a0001c0001t0001g0080others(15): Show | 18 | HG00140.hp2 HG00408.hp2 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.1279+6140C>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760715 | ||||||
chr1:157760719
|
G | GAAAGAAA others(115): Show |
1 | a0001c0001t0002g0218 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1279+6135_1279+613 others(126): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760719 | ||||||
chr1:157760719
|
G | T | 24 | a0001c0001t0001g0020a0001c0001t0001g0058a0001c0001t0001g0060others(21): Show | 28 | HG00099.hp1 HG00733.hp1 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.1279+6136C>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760719 | ||||||
chr1:157760723
|
G | T | 7 | a0001c0001t0001g0059a0001c0001t0001g0085a0001c0001t0001g0091others(4): Show | 7 | HG01361.hp2 HG02559.hp1 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.1279+6132C>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760723 | ||||||
chr1:157760728
|
AAAGAAAG others(20): Show |
A | 1 | a0001c0001t0001g0086 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1279+6100_1279+612 others(31): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760728 | ||||||
chr1:157760731
|
GAAAGAAA others(3): Show |
G | 1 | a0001c0001t0001g0098 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1279+6114_1279+612 others(14): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760731 | ||||||
chr1:157760735
|
GAAAGAA | G | 20 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(17): Show | 39 | HG00597.hp2 HG00621.hp2 HG01256.hp2 others(36): Show |
intron_variant | MODIFIER | c.1279+6114_1279+611 others(10): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760735 | ||||||
chr1:157760743
|
GA | G | 3 | a0001c0002t0005g0275a0001c0002t0005g0281a0001c0002t0005g0282 | 3 | HG02818.hp1 HG02895.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1279+6111delT | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760743 | ||||||
chr1:157760746
|
AGAAAGAA others(39): Show |
A | 1 | a0001c0002t0005g0277 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1279+6063_1279+610 others(50): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760746 | ||||||
chr1:157760750
|
AGAAAGAA others(35): Show |
A | 1 | a0001c0002t0005g0278 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1279+6063_1279+610 others(46): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760750 | ||||||
chr1:157760754
|
AGAAGAAA others(31): Show |
A | 1 | a0001c0004t0005g0284 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1279+6063_1279+610 others(42): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760754 | ||||||
chr1:157760756
|
AAGAAAGA others(27): Show |
A | 3 | a0001c0002t0005g0275a0001c0002t0005g0281a0001c0002t0005g0282 | 3 | HG02818.hp1 HG02895.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1279+6065_1279+609 others(38): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760756 | ||||||
chr1:157760765
|
T | A | 4 | a0001c0002t0005g0043a0001c0002t0005g0276a0001c0002t0005g0279others(1): Show | 5 | HG02257.hp2 HG02622.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1279+6090A>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760765 | ||||||
chr1:157760769
|
AAAAGAAA others(16): Show |
A | 4 | a0001c0002t0005g0043a0001c0002t0005g0276a0001c0002t0005g0279others(1): Show | 5 | HG02257.hp2 HG02622.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1279+6063_1279+608 others(27): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760769 | ||||||
chr1:157760792
|
G | A | 3 | a0001c0002t0005g0275a0001c0002t0005g0281a0001c0002t0005g0282 | 3 | HG02818.hp1 HG02895.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1279+6063C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760792 | ||||||
chr1:157760812
|
G | GGGAA | 3 | a0001c0001t0008g0252a0001c0001t0008g0273a0001c0001t0008g0274 | 3 | HG01891.hp1 HG02145.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.1279+6039_1279+604 others(8): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157760812 | ||||||
chr1:157761066
|
G | A | 1 | a0001c0001t0001g0075 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1279+5789C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157761066 | ||||||
chr1:157761104
|
T | C | 1 | a0001c0001t0001g0241 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1279+5751A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157761104 | ||||||
chr1:157761174
|
T | C | 1 | a0001c0001t0001g0258 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1279+5681A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157761174 | ||||||
chr1:157761195
|
C | T | 10 | a0001c0002t0005g0043a0001c0002t0005g0275a0001c0002t0005g0276others(7): Show | 11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1279+5660G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157761195 | ||||||
chr1:157761199
|
T | C | 10 | a0001c0002t0005g0043a0001c0002t0005g0275a0001c0002t0005g0276others(7): Show | 11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1279+5656A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157761199 | ||||||
chr1:157761245
|
G | C | 1 | a0001c0001t0001g0204 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1279+5610C>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157761245 | ||||||
chr1:157761286
|
A | C | 10 | a0001c0002t0005g0043a0001c0002t0005g0275a0001c0002t0005g0276others(7): Show | 11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1279+5569T>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157761286 | ||||||
chr1:157761396
|
G | A | 68 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(65): Show | 92 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(89): Show |
intron_variant | MODIFIER | c.1279+5459C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157761396 | ||||||
chr1:157761481
|
G | A | 1 | a0001c0001t0008g0252 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1279+5374C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157761481 | ||||||
chr1:157761585
|
G | A | 10 | a0001c0002t0005g0043a0001c0002t0005g0275a0001c0002t0005g0276others(7): Show | 11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1279+5270C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157761585 | ||||||
chr1:157761612
|
C | A | 10 | a0001c0002t0005g0043a0001c0002t0005g0275a0001c0002t0005g0276others(7): Show | 11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1279+5243G>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157761612 | ||||||
chr1:157761623
|
CTT | C | 10 | a0001c0002t0005g0043a0001c0002t0005g0275a0001c0002t0005g0276others(7): Show | 11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1279+5230_1279+523 others(6): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157761623 | ||||||
chr1:157761670
|
C | T | 1 | a0001c0001t0008g0252 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1279+5185G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157761670 | ||||||
chr1:157761680
|
A | T | 10 | a0001c0002t0005g0043a0001c0002t0005g0275a0001c0002t0005g0276others(7): Show | 11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1279+5175T>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157761680 | ||||||
chr1:157761751
|
T | C | 1 | a0001c0001t0003g0063 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1279+5104A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157761751 | ||||||
chr1:157761794
|
A | G | 10 | a0001c0002t0005g0043a0001c0002t0005g0275a0001c0002t0005g0276others(7): Show | 11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1279+5061T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157761794 | ||||||
chr1:157761874
|
T | C | 13 | a0001c0001t0008g0252a0001c0001t0008g0273a0001c0001t0008g0274others(10): Show | 14 | HG01891.hp1 HG02145.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1279+4981A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157761874 | ||||||
chr1:157762301
|
A | C | 68 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(65): Show | 92 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(89): Show |
intron_variant | MODIFIER | c.1279+4554T>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157762301 | ||||||
chr1:157762400
|
C | T | 2 | a0001c0001t0001g0116a0001c0001t0001g0117 | 2 | HG00738.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.1279+4455G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157762400 | ||||||
chr1:157762470
|
G | A | 10 | a0001c0002t0005g0043a0001c0002t0005g0275a0001c0002t0005g0276others(7): Show | 11 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1279+4385C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157762470 | ||||||
chr1:157762571
|
G | C | 1 | a0001c0001t0001g0258 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1279+4284C>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157762571 | ||||||
chr1:157762729
|
A | AACAAG | 37 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0010others(34): Show | 59 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.1279+4125_1279+412 others(9): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157762729 | ||||||
chr1:157762750
|
C | T | 1 | a0001c0001t0001g0215 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1279+4105G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157762750 | ||||||
chr1:157762773
|
G | A | 1 | a0001c0001t0002g0230 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1279+4082C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157762773 | ||||||
chr1:157762795
|
A | G | 1 | a0001c0001t0001g0095 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1279+4060T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157762795 | ||||||
chr1:157762899
|
C | A | 280 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(277): Show | 376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.1279+3956G>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157762899 | ||||||
chr1:157762925
|
G | A | 2 | a0001c0001t0001g0088a0001c0001t0001g0100 | 2 | HG01361.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.1279+3930C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157762925 | ||||||
chr1:157762990
|
G | T | 1 | a0001c0001t0001g0030 | 2 | HG00099.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.1279+3865C>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157762990 | ||||||
chr1:157763205
|
A | G | 1 | a0001c0001t0001g0267 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1279+3650T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157763205 | ||||||
chr1:157763235
|
T | C | 1 | a0001c0001t0001g0049 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1279+3620A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157763235 | ||||||
chr1:157763269
|
T | C | 1 | a0001c0001t0008g0252 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1279+3586A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157763269 | ||||||
chr1:157763300
|
G | C | 3 | a0001c0002t0005g0277a0001c0002t0005g0278a0001c0002t0005g0283 | 3 | HG02257.hp2 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1279+3555C>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157763300 | ||||||
chr1:157763321
|
G | A | 47 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0010others(44): Show | 70 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.1279+3534C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157763321 | ||||||
chr1:157763442
|
T | A | 47 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0010others(44): Show | 70 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.1279+3413A>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157763442 | ||||||
chr1:157763499
|
T | A | 3 | a0001c0002t0005g0277a0001c0002t0005g0278a0001c0002t0005g0283 | 3 | HG02257.hp2 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1279+3356A>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157763499 | ||||||
chr1:157763567
|
G | T | 2 | a0001c0001t0001g0048a0001c0001t0001g0049 | 2 | HG02486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1279+3288C>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157763567 | ||||||
chr1:157763589
|
T | G | 47 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0010others(44): Show | 70 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.1279+3266A>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157763589 | ||||||
chr1:157763708
|
T | C | 1 | a0001c0001t0001g0210 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1279+3147A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157763708 | ||||||
chr1:157763754
|
G | A | 9 | a0001c0002t0005g0043a0001c0002t0005g0275a0001c0002t0005g0276others(6): Show | 10 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.1279+3101C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157763754 | ||||||
chr1:157763789
|
G | A | 5 | a0001c0001t0001g0019a0001c0001t0001g0044a0001c0001t0001g0045others(2): Show | 6 | HG02145.hp1 HG02280.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.1279+3066C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157763789 | ||||||
chr1:157763978
|
C | T | 1 | a0001c0001t0001g0108 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1279+2877G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157763978 | ||||||
chr1:157764016
|
C | T | 1 | a0001c0001t0001g0022 | 2 | NA18984.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.1279+2839G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157764016 | ||||||
chr1:157764025
|
A | G | 190 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(187): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.1279+2830T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157764025 | ||||||
chr1:157764029
|
C | CA | 46 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0010others(43): Show | 70 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.1279+2825dupT | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157764029 | ||||||
chr1:157764029
|
C | CAAAA | 14 | a0001c0001t0006g0024a0001c0001t0006g0102a0001c0001t0006g0104others(11): Show | 16 | HG01109.hp1 HG01891.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.1279+2822_1279+282 others(8): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157764029 | ||||||
chr1:157764029
|
CA | C | 93 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(90): Show | 115 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(112): Show |
intron_variant | MODIFIER | c.1279+2825delT | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157764029 | ||||||
chr1:157764076
|
C | T | 2 | a0001c0001t0008g0273a0001c0001t0008g0274 | 2 | HG01891.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.1279+2779G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157764076 | ||||||
chr1:157764155
|
G | A | 1 | a0001c0001t0001g0146 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1279+2700C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157764155 | ||||||
chr1:157764166
|
C | T | 4 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0134others(1): Show | 4 | HG02451.hp2 HG02615.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.1279+2689G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157764166 | ||||||
chr1:157764171
|
T | G | 2 | a0001c0001t0008g0273a0001c0001t0008g0274 | 2 | HG01891.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.1279+2684A>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157764171 | ||||||
chr1:157764229
|
T | C | 18 | a0001c0001t0006g0024a0001c0001t0006g0102a0001c0001t0006g0103others(15): Show | 20 | HG01109.hp1 HG01891.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.1279+2626A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157764229 | ||||||
chr1:157764233
|
G | GA | 20 | a0001c0001t0006g0024a0001c0001t0006g0102a0001c0001t0006g0103others(17): Show | 22 | HG01109.hp1 HG01891.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.1279+2621dupT | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157764233 | ||||||
chr1:157764312
|
C | G | 1 | a0001c0001t0001g0025 | 2 | NA18952.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.1279+2543G>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157764312 | ||||||
chr1:157764404
|
T | C | 3 | a0001c0001t0001g0040a0001c0001t0001g0148a0001c0001t0001g0251 | 4 | HG02922.hp1 HG02970.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1279+2451A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157764404 | ||||||
chr1:157764480
|
A | G | 2 | a0001c0001t0001g0048a0001c0001t0001g0049 | 2 | HG02486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1279+2375T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157764480 | ||||||
chr1:157764792
|
A | G | 4 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0134others(1): Show | 4 | HG02451.hp2 HG02615.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.1279+2063T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157764792 | ||||||
chr1:157764991
|
T | C | 2 | a0001c0001t0008g0273a0001c0001t0008g0274 | 2 | HG01891.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.1279+1864A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157764991 | ||||||
chr1:157765117
|
C | T | 186 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(183): Show | 238 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.1279+1738G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157765117 | ||||||
chr1:157765326
|
G | A | 36 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0010others(33): Show | 59 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.1279+1529C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157765326 | ||||||
chr1:157765450
|
G | A | 18 | a0001c0001t0002g0217a0001c0001t0002g0218a0001c0001t0002g0219others(15): Show | 18 | HG00609.hp2 HG00642.hp2 HG00673.hp1 others(15): Show |
intron_variant | MODIFIER | c.1279+1405C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157765450 | ||||||
chr1:157765560
|
G | A | 11 | a0001c0002t0001g0280a0001c0002t0005g0043a0001c0002t0005g0275others(8): Show | 12 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.1279+1295C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157765560 | ||||||
chr1:157765575
|
C | T | 1 | a0001c0001t0001g0064 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1279+1280G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157765575 | ||||||
chr1:157765655
|
T | C | 1 | a0001c0001t0001g0095 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1279+1200A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157765655 | ||||||
chr1:157765737
|
G | A | 1 | a0001c0001t0001g0129 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1279+1118C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157765737 | ||||||
chr1:157765820
|
T | C | 1 | a0001c0001t0001g0092 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1279+1035A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157765820 | ||||||
chr1:157765836
|
A | C | 13 | a0001c0001t0008g0273a0001c0001t0008g0274a0001c0002t0001g0280others(10): Show | 14 | HG01891.hp1 HG02145.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1279+1019T>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157765836 | ||||||
chr1:157765917
|
A | G | 11 | a0001c0002t0001g0280a0001c0002t0005g0043a0001c0002t0005g0275others(8): Show | 12 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.1279+938T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157765917 | ||||||
chr1:157765966
|
G | C | 2 | a0001c0001t0001g0079a0001c0001t0001g0080 | 2 | HG01243.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.1279+889C>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157765966 | ||||||
chr1:157766287
|
T | C | 11 | a0001c0002t0001g0280a0001c0002t0005g0043a0001c0002t0005g0275others(8): Show | 12 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.1279+568A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157766287 | ||||||
chr1:157766308
|
A | G | 70 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(67): Show | 92 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(89): Show |
intron_variant | MODIFIER | c.1279+547T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157766308 | ||||||
chr1:157766332
|
G | T | 1 | a0001c0001t0003g0063 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1279+523C>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157766332 | ||||||
chr1:157766340
|
G | A | 1 | a0001c0001t0001g0150 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1279+515C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157766340 | ||||||
chr1:157766419
|
T | C | 11 | a0001c0002t0001g0280a0001c0002t0005g0043a0001c0002t0005g0275others(8): Show | 12 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.1279+436A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157766419 | ||||||
chr1:157766483
|
AT | A | 21 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(18): Show | 38 | HG00597.hp2 HG00621.hp2 HG01256.hp2 others(35): Show |
intron_variant | MODIFIER | c.1279+371delA | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157766483 | ||||||
chr1:157766484
|
T | A | 7 | a0001c0001t0001g0235a0001c0001t0001g0236a0001c0001t0001g0237others(4): Show | 7 | HG02004.hp2 HG02055.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1279+371A>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157766484 | ||||||
chr1:157766486
|
T | A | 21 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(18): Show | 38 | HG00597.hp2 HG00621.hp2 HG01256.hp2 others(35): Show |
intron_variant | MODIFIER | c.1279+369A>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157766486 | ||||||
chr1:157766531
|
G | A | 2 | a0001c0001t0001g0232a0001c0001t0001g0272 | 2 | HG03195.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1279+324C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157766531 | ||||||
chr1:157766641
|
C | A | 90 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(87): Show | 114 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.1279+214G>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157766641 | ||||||
chr1:157766647
|
CTA | C | 8 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0233others(5): Show | 8 | HG02004.hp2 HG02055.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.1279+206_1279+207d others(4): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157766647 | ||||||
chr1:157766772
|
C | T | 1 | a0001c0001t0001g0160 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1279+83G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 7/11 | chr1 | 157766772 | ||||||
chr1:157767122
|
C | A | 11 | a0001c0002t0001g0280a0001c0002t0005g0043a0001c0002t0005g0275others(8): Show | 12 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.1162+109G>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 6/11 | chr1 | 157767122 | ||||||
chr1:157767135
|
G | A | 5 | a0001c0001t0004g0014a0001c0001t0004g0247a0001c0001t0004g0248others(2): Show | 8 | HG02486.hp1 HG02717.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.1162+96C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 6/11 | chr1 | 157767135 | ||||||
chr1:157767141
|
C | T | 20 | a0001c0001t0001g0232a0001c0001t0001g0272a0001c0001t0002g0217others(17): Show | 20 | HG00609.hp2 HG00642.hp2 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.1162+90G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 6/11 | chr1 | 157767141 | ||||||
chr1:157767514
|
C | T | 5 | a0001c0001t0001g0019a0001c0001t0001g0044a0001c0001t0001g0045others(2): Show | 6 | HG02145.hp1 HG02280.hp2 HG03195.hp1 others(3): Show |
splice_region_variant&intron_variant | LOW | c.884-5G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 5/11 | chr1 | 157767514 | ||||||
chr1:157767714
|
G | A | 187 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(184): Show | 240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.884-205C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 5/11 | chr1 | 157767714 | ||||||
chr1:157768073
|
G | A | 1 | a0001c0001t0001g0251 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.883+341C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 5/11 | chr1 | 157768073 | ||||||
chr1:157768093
|
G | A | 1 | a0001c0001t0001g0213 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.883+321C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 5/11 | chr1 | 157768093 | ||||||
chr1:157768181
|
C | T | 1 | a0001c0001t0001g0062 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.883+233G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 5/11 | chr1 | 157768181 | ||||||
chr1:157768293
|
A | C | 1 | a0001c0001t0003g0061 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.883+121T>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 5/11 | chr1 | 157768293 | ||||||
chr1:157768304
|
G | A | 1 | a0001c0001t0008g0252 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.883+110C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 5/11 | chr1 | 157768304 | ||||||
chr1:157768403
|
G | C | 1 | a0001c0001t0006g0102 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.883+11C>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 5/11 | chr1 | 157768403 | ||||||
chr1:157768718
|
C | G | 1 | a0001c0001t0001g0159 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.596-17G>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 4/11 | chr1 | 157768718 | ||||||
chr1:157768942
|
A | G | 11 | a0001c0002t0001g0280a0001c0002t0005g0043a0001c0002t0005g0275others(8): Show | 12 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.596-241T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 4/11 | chr1 | 157768942 | ||||||
chr1:157768970
|
A | G | 1 | a0001c0001t0001g0158 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.596-269T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 4/11 | chr1 | 157768970 | ||||||
chr1:157769195
|
G | C | 1 | a0001c0001t0001g0135 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.596-494C>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 4/11 | chr1 | 157769195 | ||||||
chr1:157769244
|
T | G | 11 | a0001c0002t0001g0280a0001c0002t0005g0043a0001c0002t0005g0275others(8): Show | 12 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.596-543A>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 4/11 | chr1 | 157769244 | ||||||
chr1:157769264
|
C | T | 1 | a0001c0001t0001g0108 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.596-563G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 4/11 | chr1 | 157769264 | ||||||
chr1:157769489
|
G | A | 11 | a0001c0002t0001g0280a0001c0002t0005g0043a0001c0002t0005g0275others(8): Show | 12 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.595+377C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 4/11 | chr1 | 157769489 | ||||||
chr1:157769497
|
G | A | 7 | a0001c0001t0006g0024a0001c0001t0006g0102a0001c0001t0006g0103others(4): Show | 8 | HG01109.hp1 HG01891.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.595+369C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 4/11 | chr1 | 157769497 | ||||||
chr1:157769716
|
C | T | 1 | a0001c0001t0001g0157 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.595+150G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 4/11 | chr1 | 157769716 | ||||||
chr1:157769841
|
C | T | 2 | a0001c0001t0001g0155a0001c0001t0001g0156 | 2 | HG00639.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.595+25G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 4/11 | chr1 | 157769841 | ||||||
chr1:157770396
|
GTC | G | 169 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(166): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.310+11_310+12delGA | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 3/11 | chr1 | 157770396 | ||||||
chr1:157770399
|
A | G | 169 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(166): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.310+10T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 3/11 | chr1 | 157770399 | ||||||
chr1:157770704
|
G | A | 7 | a0001c0001t0006g0024a0001c0001t0006g0102a0001c0001t0006g0103others(4): Show | 8 | HG01109.hp1 HG01891.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.53-38C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157770704 | ||||||
chr1:157770999
|
G | C | 69 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(66): Show | 91 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(88): Show |
intron_variant | MODIFIER | c.53-333C>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157770999 | ||||||
chr1:157771007
|
G | A | 1 | a0001c0001t0001g0131 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.53-341C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157771007 | ||||||
chr1:157771099
|
T | C | 1 | a0001c0001t0001g0215 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.53-433A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157771099 | ||||||
chr1:157771309
|
G | A | 3 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0095 | 3 | NA18986.hp1 NA19012.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.53-643C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157771309 | ||||||
chr1:157771361
|
T | C | 1 | a0001c0001t0001g0216 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.53-695A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157771361 | ||||||
chr1:157771447
|
T | A | 185 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(182): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.53-781A>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157771447 | ||||||
chr1:157771528
|
A | C | 67 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(64): Show | 89 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(86): Show |
intron_variant | MODIFIER | c.53-862T>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157771528 | ||||||
chr1:157771890
|
A | G | 7 | a0001c0001t0006g0024a0001c0001t0006g0102a0001c0001t0006g0103others(4): Show | 8 | HG01109.hp1 HG01891.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.53-1224T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157771890 | ||||||
chr1:157771938
|
G | A | 1 | a0001c0001t0001g0258 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.53-1272C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157771938 | ||||||
chr1:157772011
|
A | G | 40 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0010others(37): Show | 63 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.53-1345T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157772011 | ||||||
chr1:157772028
|
T | TTA | 13 | a0001c0001t0001g0136a0001c0001t0001g0256a0001c0001t0007g0137others(10): Show | 14 | HG00280.hp2 HG02071.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.53-1364_53-1363dup others(2): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157772028 | ||||||
chr1:157772028
|
T | TTATA | 55 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(52): Show | 76 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.53-1366_53-1363dup others(4): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157772028 | ||||||
chr1:157772028
|
T | TTATATA | 8 | a0001c0001t0001g0023a0001c0001t0001g0096a0001c0001t0001g0097others(5): Show | 9 | HG01192.hp2 HG01361.hp2 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.53-1368_53-1363dup others(6): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157772028 | ||||||
chr1:157772028
|
T | TTATATAT others(1): Show |
6 | a0001c0001t0001g0019a0001c0001t0001g0044a0001c0001t0001g0045others(3): Show | 7 | HG02145.hp1 HG02280.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.53-1370_53-1363dup others(8): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157772028 | ||||||
chr1:157772028
|
T | TTATATAT others(5): Show |
5 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0146others(2): Show | 5 | HG00741.hp2 HG02647.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.53-1374_53-1363dup others(12): Show |
FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157772028 | ||||||
chr1:157772227
|
C | A | 11 | a0001c0002t0001g0280a0001c0002t0005g0043a0001c0002t0005g0275others(8): Show | 12 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.53-1561G>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157772227 | ||||||
chr1:157772427
|
G | A | 1 | a0001c0001t0001g0147 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.53-1761C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157772427 | ||||||
chr1:157772447
|
A | C | 1 | a0001c0001t0001g0059 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.53-1781T>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157772447 | ||||||
chr1:157772514
|
T | C | 5 | a0001c0001t0001g0019a0001c0001t0001g0044a0001c0001t0001g0045others(2): Show | 6 | HG02145.hp1 HG02280.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.53-1848A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157772514 | ||||||
chr1:157772563
|
C | T | 2 | a0001c0001t0001g0153a0001c0001t0001g0154 | 2 | HG00642.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.53-1897G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157772563 | ||||||
chr1:157772564
|
G | A | 1 | a0001c0001t0002g0259 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.53-1898C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157772564 | ||||||
chr1:157772738
|
A | G | 2 | a0001c0001t0001g0151a0001c0001t0001g0152 | 2 | HG02723.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.53-2072T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157772738 | ||||||
chr1:157772748
|
G | A | 1 | a0001c0001t0001g0150 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.53-2082C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157772748 | ||||||
chr1:157772749
|
A | G | 1 | a0001c0001t0001g0150 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.53-2083T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157772749 | ||||||
chr1:157772826
|
T | C | 7 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0262others(4): Show | 9 | HG00438.hp1 NA18951.hp1 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.53-2160A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157772826 | ||||||
chr1:157772858
|
C | A | 3 | a0001c0002t0001g0280a0001c0002t0005g0281a0001c0002t0005g0282 | 3 | HG02818.hp1 HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.53-2192G>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157772858 | ||||||
chr1:157773037
|
C | T | 1 | a0001c0001t0004g0149 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.53-2371G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157773037 | ||||||
chr1:157773360
|
T | A | 1 | a0001c0001t0001g0100 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.52+2415A>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157773360 | ||||||
chr1:157773553
|
T | C | 11 | a0001c0002t0001g0280a0001c0002t0005g0043a0001c0002t0005g0275others(8): Show | 12 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.52+2222A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157773553 | ||||||
chr1:157773998
|
A | G | 1 | a0001c0001t0001g0148 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.52+1777T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157773998 | ||||||
chr1:157774075
|
A | G | 5 | a0001c0001t0001g0019a0001c0001t0001g0044a0001c0001t0001g0045others(2): Show | 6 | HG02145.hp1 HG02280.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.52+1700T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157774075 | ||||||
chr1:157774197
|
C | T | 1 | a0001c0001t0001g0058 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.52+1578G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157774197 | ||||||
chr1:157774214
|
A | G | 67 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(64): Show | 89 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(86): Show |
intron_variant | MODIFIER | c.52+1561T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157774214 | ||||||
chr1:157774352
|
A | T | 44 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0010others(41): Show | 67 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.52+1423T>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157774352 | ||||||
chr1:157774361
|
G | A | 1 | a0001c0001t0001g0260 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.52+1414C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157774361 | ||||||
chr1:157774366
|
T | C | 11 | a0001c0002t0001g0280a0001c0002t0005g0043a0001c0002t0005g0275others(8): Show | 12 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.52+1409A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157774366 | ||||||
chr1:157774431
|
T | C | 6 | a0001c0001t0006g0024a0001c0001t0006g0103a0001c0001t0006g0104others(3): Show | 7 | HG01109.hp1 HG01891.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.52+1344A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157774431 | ||||||
chr1:157774471
|
G | C | 8 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0261others(5): Show | 10 | HG00438.hp1 HG00544.hp2 NA18951.hp1 others(7): Show |
intron_variant | MODIFIER | c.52+1304C>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157774471 | ||||||
chr1:157774553
|
C | T | 5 | a0001c0001t0003g0053a0001c0001t0003g0054a0001c0001t0003g0055others(2): Show | 5 | HG00140.hp1 HG01069.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.52+1222G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157774553 | ||||||
chr1:157774710
|
T | G | 11 | a0001c0002t0001g0280a0001c0002t0005g0043a0001c0002t0005g0275others(8): Show | 12 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.52+1065A>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157774710 | ||||||
chr1:157774736
|
G | A | 1 | a0001c0001t0001g0267 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.52+1039C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157774736 | ||||||
chr1:157774942
|
T | A | 1 | a0001c0001t0001g0101 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.52+833A>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157774942 | ||||||
chr1:157774968
|
A | G | 7 | a0001c0001t0006g0024a0001c0001t0006g0102a0001c0001t0006g0103others(4): Show | 8 | HG01109.hp1 HG01891.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.52+807T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157774968 | ||||||
chr1:157774977
|
A | G | 1 | a0001c0001t0001g0050 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.52+798T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157774977 | ||||||
chr1:157774990
|
A | T | 2 | a0001c0001t0008g0273a0001c0001t0008g0274 | 2 | HG01891.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.52+785T>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157774990 | ||||||
chr1:157775058
|
C | T | 57 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(54): Show | 79 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(76): Show |
intron_variant | MODIFIER | c.52+717G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157775058 | ||||||
chr1:157775200
|
A | G | 1 | a0001c0001t0001g0052 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.52+575T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157775200 | ||||||
chr1:157775335
|
G | C | 2 | a0001c0001t0008g0273a0001c0001t0008g0274 | 2 | HG01891.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.52+440C>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157775335 | ||||||
chr1:157775373
|
T | C | 3 | a0002c0003t0001g0268a0002c0003t0001g0269a0002c0003t0001g0270 | 3 | HG02257.hp1 HG02630.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.52+402A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157775373 | ||||||
chr1:157775439
|
C | A | 1 | a0001c0001t0002g0271 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.52+336G>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157775439 | ||||||
chr1:157775525
|
C | T | 2 | a0001c0001t0008g0273a0001c0001t0008g0274 | 2 | HG01891.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.52+250G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157775525 | ||||||
chr1:157775601
|
A | G | 2 | a0001c0001t0001g0050a0001c0001t0001g0051 | 2 | NA18975.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.52+174T>C | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 2/11 | chr1 | 157775601 | ||||||
chr1:157775952
|
G | A | 2 | a0001c0001t0001g0048a0001c0001t0001g0049 | 2 | HG02486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.32-157C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 1/11 | chr1 | 157775952 | ||||||
chr1:157775967
|
T | A | 1 | a0001c0002t0005g0282 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.32-172A>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 1/11 | chr1 | 157775967 | ||||||
chr1:157775994
|
T | C | 2 | a0001c0001t0008g0273a0001c0001t0008g0274 | 2 | HG01891.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.32-199A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 1/11 | chr1 | 157775994 | ||||||
chr1:157776000
|
A | T | 2 | a0001c0001t0008g0273a0001c0001t0008g0274 | 2 | HG01891.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.32-205T>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 1/11 | chr1 | 157776000 | ||||||
chr1:157776018
|
G | A | 11 | a0001c0002t0001g0280a0001c0002t0005g0043a0001c0002t0005g0275others(8): Show | 12 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.32-223C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 1/11 | chr1 | 157776018 | ||||||
chr1:157776098
|
T | C | 1 | a0001c0002t0005g0283 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.32-303A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 1/11 | chr1 | 157776098 | ||||||
chr1:157776311
|
C | T | 2 | a0001c0001t0001g0048a0001c0001t0001g0049 | 2 | HG02486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.32-516G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 1/11 | chr1 | 157776311 | ||||||
chr1:157776321
|
G | A | 1 | a0001c0001t0001g0272 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.32-526C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 1/11 | chr1 | 157776321 | ||||||
chr1:157776471
|
T | C | 18 | a0001c0001t0001g0019a0001c0001t0001g0044a0001c0001t0001g0045others(15): Show | 20 | HG01891.hp1 HG02145.hp1 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.31+572A>G | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 1/11 | chr1 | 157776471 | ||||||
chr1:157776637
|
C | T | 5 | a0001c0001t0001g0019a0001c0001t0001g0044a0001c0001t0001g0045others(2): Show | 6 | HG02145.hp1 HG02280.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.31+406G>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 1/11 | chr1 | 157776637 | ||||||
chr1:157776789
|
A | T | 11 | a0001c0002t0001g0280a0001c0002t0005g0043a0001c0002t0005g0275others(8): Show | 12 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.31+254T>A | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 1/11 | chr1 | 157776789 | ||||||
chr1:157776996
|
C | A | 1 | a0001c0004t0005g0284 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.31+47G>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 1/11 | chr1 | 157776996 | ||||||
chr1:157777024
|
G | A | 11 | a0001c0002t0001g0280a0001c0002t0005g0043a0001c0002t0005g0275others(8): Show | 12 | HG02257.hp2 HG02622.hp1 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.31+19C>T | FCRL2 | ENSG00000132704.16 | transcript | ENST00000361516.8 | protein_coding | 1/11 | chr1 | 157777024 |