geneid | 3344 |
---|---|
ensemblid | ENSG00000170802.17 |
hgncid | 5281 |
symbol | FOXN2 |
name | forkhead box N2 |
refseq_nuc | NM_002158.4 |
refseq_prot | NP_002149.2 |
ensembl_nuc | ENST00000340553.8 |
ensembl_prot | ENSP00000343633.3 |
mane_status | MANE Select |
chr | chr2 |
start | 48314682 |
end | 48379295 |
strand | + |
ver | v1.2 |
region | chr2:48314682-48379295 |
region5000 | chr2:48309682-48384295 |
regionname0 | FOXN2_chr2_48314682_48379295 |
regionname5000 | FOXN2_chr2_48309682_48384295 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 431 | 341 | 80 | 60 | 141 | 14 | 44 | 109 | FOXN2_chr2_48309682_48384295 | FOXN2 | copy fasta | chr2 | 48309682 | 48384295 |
a0002 | 0/0 | 431 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | copy fasta | chr2 | 48309682 | 48384295 |
a0003 | 0/0 | 431 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | copy fasta | chr2 | 48309682 | 48384295 |
a0004 | 0/0 | 431 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | copy fasta | chr2 | 48309682 | 48384295 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1296 | 215 | 57 | 39 | 74 | 8 | 35 | FOXN2_chr2_48309682_48384295 | FOXN2 | copy fasta | chr2 | 48309682 | 48384295 |
c0002 | 0/0 | 1296 | 106 | 11 | 17 | 67 | 5 | 6 | FOXN2_chr2_48309682_48384295 | FOXN2 | copy fasta | chr2 | 48309682 | 48384295 |
c0003 | 0/0 | 1296 | 12 | 11 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | copy fasta | chr2 | 48309682 | 48384295 |
c0004 | 0/0 | 1296 | 8 | 1 | 3 | 0 | 1 | 3 | FOXN2_chr2_48309682_48384295 | FOXN2 | copy fasta | chr2 | 48309682 | 48384295 |
c0005 | 0/0 | 1296 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | copy fasta | chr2 | 48309682 | 48384295 |
c0006 | 0/0 | 1296 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | copy fasta | chr2 | 48309682 | 48384295 |
c0007 | 0/0 | 1296 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | copy fasta | chr2 | 48309682 | 48384295 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 4142 | 170 | 42 | 35 | 56 | 8 | 27 | FOXN2_chr2_48309682_48384295 | FOXN2 | copy fasta | chr2 | 48309682 | 48384295 |
t0002 | 0/0 | 4142 | 95 | 8 | 12 | 63 | 2 | 10 | FOXN2_chr2_48309682_48384295 | FOXN2 | copy fasta | chr2 | 48309682 | 48384295 |
t0003 | 0/0 | 4141 | 17 | 10 | 4 | 0 | 1 | 2 | FOXN2_chr2_48309682_48384295 | FOXN2 | copy fasta | chr2 | 48309682 | 48384295 |
t0004 | 0/0 | 4142 | 17 | 0 | 0 | 17 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | copy fasta | chr2 | 48309682 | 48384295 |
t0005 | 0/0 | 4142 | 14 | 11 | 1 | 0 | 0 | 2 | FOXN2_chr2_48309682_48384295 | FOXN2 | copy fasta | chr2 | 48309682 | 48384295 |
t0006 | 0/0 | 4142 | 7 | 0 | 3 | 0 | 3 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | copy fasta | chr2 | 48309682 | 48384295 |
t0007 | 0/0 | 4142 | 2 | 2 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | copy fasta | chr2 | 48309682 | 48384295 |
t0008 | 0/0 | 4142 | 2 | 2 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | copy fasta | chr2 | 48309682 | 48384295 |
t0009 | 0/0 | 4142 | 2 | 0 | 0 | 2 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | copy fasta | chr2 | 48309682 | 48384295 |
t0010 | 0/0 | 4141 | 2 | 1 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | copy fasta | chr2 | 48309682 | 48384295 |
t0011 | 0/0 | 4142 | 2 | 0 | 0 | 1 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | copy fasta | chr2 | 48309682 | 48384295 |
t0012 | 0/0 | 4142 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | copy fasta | chr2 | 48309682 | 48384295 |
t0013 | 0/0 | 4142 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | copy fasta | chr2 | 48309682 | 48384295 |
t0014 | 0/0 | 4142 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | copy fasta | chr2 | 48309682 | 48384295 |
t0015 | 0/0 | 4142 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | copy fasta | chr2 | 48309682 | 48384295 |
t0016 | 0/0 | 4142 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | copy fasta | chr2 | 48309682 | 48384295 |
t0017 | 0/0 | 4142 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | copy fasta | chr2 | 48309682 | 48384295 |
t0018 | 0/0 | 4142 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | copy fasta | chr2 | 48309682 | 48384295 |
t0019 | 0/0 | 4142 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | copy fasta | chr2 | 48309682 | 48384295 |
t0020 | 0/0 | 4142 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | copy fasta | chr2 | 48309682 | 48384295 |
t0021 | 0/0 | 4142 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | copy fasta | chr2 | 48309682 | 48384295 |
t0022 | 0/0 | 4141 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | copy fasta | chr2 | 48309682 | 48384295 |
t0023 | 0/0 | 4142 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | copy fasta | chr2 | 48309682 | 48384295 |
t0024 | 0/0 | 4142 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | copy fasta | chr2 | 48309682 | 48384295 |
t0025 | 0/0 | 4142 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | copy fasta | chr2 | 48309682 | 48384295 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0003 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0008 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0009 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0078 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1296 | 215 | 57 | 39 | 74 | 8 | 35 | FOXN2_chr2_48309682_48384295 | FOXN2 | copy fasta | chr2 | 48309682 | 48384295 |
a0001c0002 | 0/0 | 1296 | 106 | 11 | 17 | 67 | 5 | 6 | FOXN2_chr2_48309682_48384295 | FOXN2 | copy fasta | chr2 | 48309682 | 48384295 |
a0001c0003 | 0/0 | 1296 | 12 | 11 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | copy fasta | chr2 | 48309682 | 48384295 |
a0001c0004 | 0/0 | 1296 | 8 | 1 | 3 | 0 | 1 | 3 | FOXN2_chr2_48309682_48384295 | FOXN2 | copy fasta | chr2 | 48309682 | 48384295 |
a0002c0006 | 0/0 | 1296 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | copy fasta | chr2 | 48309682 | 48384295 |
a0003c0007 | 0/0 | 1296 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | copy fasta | chr2 | 48309682 | 48384295 |
a0004c0005 | 0/0 | 1296 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | copy fasta | chr2 | 48309682 | 48384295 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 5437 | 159 | 33 | 34 | 55 | 8 | 27 | FOXN2_chr2_48309682_48384295 | FOXN2 | copy fasta | chr2 | 48309682 | 48384295 |
a0001c0001t0002 | 0/0 | 5437 | 12 | 7 | 1 | 0 | 0 | 4 | FOXN2_chr2_48309682_48384295 | FOXN2 | copy fasta | chr2 | 48309682 | 48384295 |
a0001c0001t0004 | 0/0 | 5437 | 17 | 0 | 0 | 17 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | copy fasta | chr2 | 48309682 | 48384295 |
a0001c0001t0005 | 0/0 | 5437 | 14 | 11 | 1 | 0 | 0 | 2 | FOXN2_chr2_48309682_48384295 | FOXN2 | copy fasta | chr2 | 48309682 | 48384295 |
a0001c0001t0008 | 0/0 | 5437 | 2 | 2 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | copy fasta | chr2 | 48309682 | 48384295 |
a0001c0001t0011 | 0/0 | 5437 | 2 | 0 | 0 | 1 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | copy fasta | chr2 | 48309682 | 48384295 |
a0001c0001t0012 | 0/0 | 5437 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | copy fasta | chr2 | 48309682 | 48384295 |
a0001c0001t0014 | 0/0 | 5437 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | copy fasta | chr2 | 48309682 | 48384295 |
a0001c0001t0015 | 0/0 | 5437 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | copy fasta | chr2 | 48309682 | 48384295 |
a0001c0001t0017 | 0/0 | 5437 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | copy fasta | chr2 | 48309682 | 48384295 |
a0001c0001t0018 | 0/0 | 5437 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | copy fasta | chr2 | 48309682 | 48384295 |
a0001c0001t0019 | 0/0 | 5437 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | copy fasta | chr2 | 48309682 | 48384295 |
a0001c0001t0020 | 0/0 | 5437 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | copy fasta | chr2 | 48309682 | 48384295 |
a0001c0001t0021 | 0/0 | 5437 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | copy fasta | chr2 | 48309682 | 48384295 |
a0001c0001t0024 | 0/0 | 5437 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | copy fasta | chr2 | 48309682 | 48384295 |
a0001c0002t0002 | 0/0 | 5437 | 82 | 1 | 11 | 63 | 2 | 5 | FOXN2_chr2_48309682_48384295 | FOXN2 | copy fasta | chr2 | 48309682 | 48384295 |
a0001c0002t0003 | 0/0 | 5436 | 10 | 9 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | copy fasta | chr2 | 48309682 | 48384295 |
a0001c0002t0006 | 0/0 | 5437 | 7 | 0 | 3 | 0 | 3 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | copy fasta | chr2 | 48309682 | 48384295 |
a0001c0002t0009 | 0/0 | 5437 | 2 | 0 | 0 | 2 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | copy fasta | chr2 | 48309682 | 48384295 |
a0001c0002t0010 | 0/0 | 5436 | 2 | 1 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | copy fasta | chr2 | 48309682 | 48384295 |
a0001c0002t0022 | 0/0 | 5436 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | copy fasta | chr2 | 48309682 | 48384295 |
a0001c0002t0023 | 0/0 | 5437 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | copy fasta | chr2 | 48309682 | 48384295 |
a0001c0002t0025 | 0/0 | 5437 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | copy fasta | chr2 | 48309682 | 48384295 |
a0001c0003t0001 | 0/0 | 5437 | 9 | 8 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | copy fasta | chr2 | 48309682 | 48384295 |
a0001c0003t0007 | 0/0 | 5437 | 2 | 2 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | copy fasta | chr2 | 48309682 | 48384295 |
a0001c0003t0016 | 0/0 | 5437 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | copy fasta | chr2 | 48309682 | 48384295 |
a0001c0004t0002 | 0/0 | 5437 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | copy fasta | chr2 | 48309682 | 48384295 |
a0001c0004t0003 | 0/0 | 5436 | 7 | 1 | 3 | 0 | 1 | 2 | FOXN2_chr2_48309682_48384295 | FOXN2 | copy fasta | chr2 | 48309682 | 48384295 |
a0002c0006t0001 | 0/0 | 5437 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | copy fasta | chr2 | 48309682 | 48384295 |
a0003c0007t0013 | 0/0 | 5437 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | copy fasta | chr2 | 48309682 | 48384295 |
a0004c0005t0001 | 0/0 | 5437 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | copy fasta | chr2 | 48309682 | 48384295 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0008 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0078 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0004g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0004g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0004g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0004g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0004g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0004g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0004g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0004g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0004g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0004g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0004g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0004g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0004g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0004g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0005g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0005g0003 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0005g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0005g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0005g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0005g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0005g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0005g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0005g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0005g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0005g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0005g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0008g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0008g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0011g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0011g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0012g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0014g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0015g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0017g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0018g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0019g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0020g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0021g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0001t0024g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0002g0009 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0002g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0002g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0002g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0002g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0002g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0002g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0002g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0002g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0002g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0002g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0002g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0002g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0002g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0002g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0002g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0002g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0002g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0002g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0002g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0002g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0002g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0003g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0003g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0003g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0003g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0003g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0003g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0003g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0003g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0003g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0003g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0006g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0006g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0006g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0006g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0006g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0006g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0006g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0009g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0009g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0010g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0010g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0022g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0023g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0002t0025g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0003t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0003t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0003t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0003t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0003t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0003t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0003t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0003t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0003t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0003t0007g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0003t0007g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0003t0016g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0004t0002g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0004t0003g0001 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0004t0003g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0004t0003g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0004t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0001c0004t0003g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0002c0006t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0003c0007t0013g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
a0004c0005t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0232 | EUR | GBR | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0104 | EUR | GBR | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG00280 | hp1 | a0001 | c0002 | t0006 | g0242 | EUR | FIN | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG00280 | hp2 | a0001 | c0002 | t0002 | g0260 | EUR | FIN | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG00408 | hp1 | a0001 | c0002 | t0002 | g0321 | EAS | CHS | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | CHS | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | CHS | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | CHS | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG00438 | hp1 | a0001 | c0001 | t0004 | g0083 | EAS | CHS | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | CHS | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | CHS | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG00558 | hp2 | a0001 | c0002 | t0002 | g0302 | EAS | CHS | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG00609 | hp1 | a0001 | c0002 | t0002 | g0280 | EAS | CHS | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | CHS | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | CHS | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG00621 | hp2 | a0001 | c0002 | t0002 | g0314 | EAS | CHS | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG00738 | hp2 | a0001 | c0002 | t0003 | g0245 | AMR | PUR | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG01069 | hp1 | a0001 | c0001 | t0021 | g0034 | AMR | PUR | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | PUR | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG01070 | hp2 | a0001 | c0002 | t0022 | g0237 | AMR | PUR | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG01074 | hp1 | a0001 | c0003 | t0001 | g0141 | AMR | PUR | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG01074 | hp2 | a0001 | c0002 | t0002 | g0009 | AMR | PUR | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | PUR | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG01081 | hp2 | a0001 | c0002 | t0006 | g0241 | AMR | PUR | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG01106 | hp2 | a0001 | c0002 | t0002 | g0332 | AMR | PUR | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG01109 | hp1 | a0001 | c0002 | t0002 | g0265 | AMR | PUR | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG01109 | hp2 | a0001 | c0002 | t0010 | g0246 | AMR | PUR | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG01167 | hp2 | a0001 | c0002 | t0002 | g0284 | AMR | PUR | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG01169 | hp2 | a0001 | c0002 | t0002 | g0311 | AMR | PUR | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG01192 | hp2 | a0001 | c0004 | t0003 | g0001 | AMR | PUR | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0046 | AMR | PUR | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG01243 | hp2 | a0001 | c0001 | t0024 | g0201 | AMR | PUR | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG01255 | hp2 | a0001 | c0002 | t0006 | g0240 | AMR | CLM | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG01257 | hp1 | a0001 | c0002 | t0006 | g0238 | AMR | CLM | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | CLM | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | CLM | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | CLM | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | CLM | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG01346 | hp2 | a0001 | c0004 | t0003 | g0045 | AMR | CLM | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | CLM | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | CLM | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG01433 | hp1 | a0001 | c0002 | t0002 | g0333 | AMR | CLM | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG01433 | hp2 | a0001 | c0001 | t0005 | g0003 | AMR | CLM | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | CLM | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | CLM | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG01515 | hp1 | a0001 | c0004 | t0003 | g0001 | EUR | IBS | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0211 | EUR | IBS | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0216 | EUR | IBS | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG01516 | hp2 | a0001 | c0002 | t0006 | g0239 | EUR | IBS | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0210 | EUR | IBS | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG01517 | hp2 | a0001 | c0002 | t0006 | g0243 | EUR | IBS | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG01884 | hp1 | a0001 | c0001 | t0012 | g0044 | AFR | ACB | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG01884 | hp2 | a0001 | c0003 | t0001 | g0143 | AFR | ACB | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG01891 | hp1 | a0001 | c0001 | t0005 | g0030 | AFR | ACB | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0031 | AFR | ACB | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PEL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG01928 | hp2 | a0001 | c0002 | t0002 | g0258 | AMR | PEL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PEL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG01952 | hp2 | a0001 | c0002 | t0002 | g0317 | AMR | PEL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG01975 | hp1 | a0001 | c0002 | t0002 | g0282 | AMR | PEL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG01975 | hp2 | a0001 | c0001 | t0020 | g0117 | AMR | PEL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG01978 | hp1 | a0001 | c0002 | t0002 | g0320 | AMR | PEL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | PEL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PEL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PEL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | KHV | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | KHV | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG02040 | hp1 | a0001 | c0002 | t0002 | g0285 | EAS | KHV | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG02040 | hp2 | a0001 | c0001 | t0011 | g0074 | EAS | KHV | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG02055 | hp1 | a0001 | c0003 | t0007 | g0012 | AFR | ACB | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | ACB | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG02056 | hp1 | a0001 | c0002 | t0002 | g0329 | EAS | KHV | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | KHV | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG02071 | hp1 | a0001 | c0002 | t0002 | g0308 | EAS | KHV | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | KHV | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | KHV | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG02080 | hp2 | a0001 | c0002 | t0002 | g0318 | EAS | KHV | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG02132 | hp1 | a0001 | c0001 | t0004 | g0062 | EAS | KHV | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG02132 | hp2 | a0001 | c0002 | t0002 | g0272 | EAS | KHV | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0322 | EAS | KHV | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG02135 | hp2 | a0001 | c0002 | t0009 | g0325 | EAS | KHV | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | ACB | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG02145 | hp2 | a0001 | c0001 | t0002 | g0043 | AFR | ACB | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PEL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG02148 | hp2 | a0001 | c0002 | t0002 | g0313 | AMR | PEL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG02155 | hp1 | a0001 | c0002 | t0002 | g0273 | EAS | CDX | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG02155 | hp2 | a0001 | c0001 | t0004 | g0066 | EAS | CDX | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG02258 | hp1 | a0001 | c0004 | t0003 | g0021 | AFR | ACB | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG02258 | hp2 | a0001 | c0001 | t0005 | g0003 | AFR | ACB | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | ACB | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | ACB | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG02451 | hp1 | a0001 | c0001 | t0002 | g0035 | AFR | ACB | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG02451 | hp2 | a0001 | c0003 | t0001 | g0207 | AFR | ACB | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0191 | SAS | PJL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0213 | SAS | PJL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG02630 | hp1 | a0001 | c0003 | t0001 | g0138 | AFR | GWD | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | GWD | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | GWD | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0218 | SAS | PJL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | PJL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | GWD | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG02717 | hp2 | a0001 | c0002 | t0003 | g0016 | AFR | GWD | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG02723 | hp1 | a0004 | c0005 | t0001 | g0095 | AFR | GWD | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG02723 | hp2 | a0001 | c0001 | t0002 | g0018 | AFR | GWD | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG02735 | hp2 | a0001 | c0002 | t0006 | g0236 | SAS | PJL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0190 | SAS | PJL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0231 | SAS | PJL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG02809 | hp1 | a0001 | c0001 | t0008 | g0112 | AFR | GWD | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG02818 | hp1 | a0001 | c0001 | t0005 | g0047 | AFR | GWD | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG02895 | hp1 | a0001 | c0003 | t0001 | g0135 | AFR | GWD | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | GWD | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG02896 | hp2 | a0001 | c0001 | t0005 | g0002 | AFR | GWD | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG02897 | hp1 | a0001 | c0001 | t0005 | g0002 | AFR | GWD | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG02897 | hp2 | a0001 | c0003 | t0001 | g0134 | AFR | GWD | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | ESN | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG02965 | hp2 | a0001 | c0001 | t0005 | g0026 | AFR | ESN | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG02970 | hp1 | a0001 | c0003 | t0001 | g0149 | AFR | ESN | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | ESN | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | ESN | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG02976 | hp2 | a0001 | c0002 | t0003 | g0247 | AFR | ESN | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0233 | SAS | PJL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG03017 | hp2 | a0001 | c0001 | t0005 | g0123 | SAS | PJL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG03041 | hp1 | a0001 | c0001 | t0005 | g0024 | AFR | GWD | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | GWD | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG03098 | hp1 | a0001 | c0002 | t0003 | g0092 | AFR | MSL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG03098 | hp2 | a0001 | c0003 | t0007 | g0011 | AFR | MSL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG03130 | hp1 | a0001 | c0001 | t0005 | g0025 | AFR | ESN | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG03130 | hp2 | a0001 | c0003 | t0016 | g0136 | AFR | ESN | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG03139 | hp1 | a0001 | c0001 | t0008 | g0101 | AFR | ESN | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG03139 | hp2 | a0001 | c0001 | t0002 | g0023 | AFR | ESN | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | ESN | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG03195 | hp2 | a0001 | c0002 | t0003 | g0248 | AFR | ESN | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | MSL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG03209 | hp2 | a0001 | c0002 | t0003 | g0255 | AFR | MSL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | MSL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG03225 | hp2 | a0001 | c0002 | t0003 | g0249 | AFR | MSL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0033 | SAS | PJL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0235 | SAS | PJL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG03453 | hp1 | a0001 | c0002 | t0003 | g0250 | AFR | MSL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG03453 | hp2 | a0001 | c0001 | t0017 | g0331 | AFR | MSL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | MSL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | MSL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0227 | SAS | PJL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG03490 | hp2 | a0001 | c0004 | t0003 | g0019 | SAS | PJL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0230 | SAS | PJL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG03492 | hp2 | a0001 | c0004 | t0003 | g0001 | SAS | PJL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | ESN | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG03516 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | ESN | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG03540 | hp1 | a0001 | c0001 | t0005 | g0027 | AFR | GWD | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG03540 | hp2 | a0001 | c0003 | t0001 | g0182 | AFR | GWD | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG03579 | hp1 | a0001 | c0002 | t0003 | g0256 | AFR | MSL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG03579 | hp2 | a0003 | c0007 | t0013 | g0146 | AFR | MSL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0214 | SAS | PJL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0193 | SAS | STU | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0040 | SAS | STU | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG03704 | hp2 | a0001 | c0001 | t0005 | g0164 | SAS | PJL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0042 | SAS | PJL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG03710 | hp2 | a0001 | c0002 | t0002 | g0304 | SAS | PJL | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG03831 | hp1 | a0001 | c0001 | t0011 | g0088 | SAS | BEB | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0225 | SAS | BEB | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG03834 | hp1 | a0001 | c0002 | t0002 | g0278 | SAS | BEB | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG03834 | hp2 | a0001 | c0002 | t0002 | g0293 | SAS | BEB | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0226 | SAS | BEB | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0039 | SAS | BEB | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG03942 | hp1 | a0001 | c0002 | t0002 | g0294 | SAS | BEB | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG03942 | hp2 | a0001 | c0001 | t0019 | g0169 | SAS | BEB | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG04115 | hp1 | a0001 | c0004 | t0002 | g0022 | SAS | STU | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0053 | SAS | STU | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG04199 | hp1 | a0001 | c0002 | t0002 | g0287 | SAS | STU | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0054 | SAS | STU | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | STU | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0252 | SAS | STU | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | YRI | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA18522 | hp2 | a0001 | c0001 | t0002 | g0036 | AFR | YRI | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | CHB | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA18612 | hp2 | a0001 | c0002 | t0002 | g0267 | EAS | CHB | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA18747 | hp1 | a0001 | c0002 | t0002 | g0261 | EAS | CHB | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA18747 | hp2 | a0001 | c0001 | t0018 | g0106 | EAS | CHB | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA18906 | hp1 | a0001 | c0002 | t0002 | g0259 | AFR | YRI | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA18906 | hp2 | a0001 | c0002 | t0003 | g0251 | AFR | YRI | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA18941 | hp2 | a0001 | c0002 | t0002 | g0275 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA18942 | hp1 | a0001 | c0002 | t0002 | g0279 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA18944 | hp2 | a0001 | c0002 | t0002 | g0049 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA18945 | hp1 | a0001 | c0001 | t0004 | g0084 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA18945 | hp2 | a0001 | c0002 | t0002 | g0323 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA18946 | hp2 | a0001 | c0002 | t0002 | g0281 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA18949 | hp2 | a0001 | c0002 | t0002 | g0310 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA18950 | hp2 | a0001 | c0002 | t0002 | g0010 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA18954 | hp1 | a0001 | c0002 | t0002 | g0264 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA18954 | hp2 | a0001 | c0001 | t0004 | g0056 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA18956 | hp2 | a0001 | c0002 | t0002 | g0301 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA18960 | hp2 | a0001 | c0002 | t0002 | g0316 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA18963 | hp1 | a0001 | c0002 | t0002 | g0032 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA18969 | hp1 | a0001 | c0001 | t0004 | g0091 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA18969 | hp2 | a0001 | c0002 | t0002 | g0292 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA18970 | hp1 | a0001 | c0002 | t0002 | g0037 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA18972 | hp2 | a0001 | c0002 | t0002 | g0257 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA18975 | hp2 | a0001 | c0002 | t0002 | g0326 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA18978 | hp1 | a0001 | c0002 | t0002 | g0327 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA18980 | hp1 | a0001 | c0002 | t0023 | g0330 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA18980 | hp2 | a0001 | c0002 | t0002 | g0041 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA18982 | hp1 | a0001 | c0002 | t0009 | g0283 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA18982 | hp2 | a0001 | c0001 | t0004 | g0089 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA18988 | hp2 | a0001 | c0002 | t0002 | g0277 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA18989 | hp1 | a0001 | c0002 | t0002 | g0303 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA18990 | hp1 | a0001 | c0002 | t0002 | g0300 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA18991 | hp1 | a0001 | c0002 | t0002 | g0312 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA18992 | hp1 | a0001 | c0002 | t0002 | g0010 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA18992 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA18994 | hp2 | a0001 | c0002 | t0002 | g0324 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA18995 | hp1 | a0001 | c0002 | t0002 | g0048 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA18998 | hp1 | a0001 | c0002 | t0002 | g0289 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA18998 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA19000 | hp2 | a0001 | c0002 | t0002 | g0319 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA19002 | hp2 | a0001 | c0002 | t0002 | g0288 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA19004 | hp1 | a0001 | c0002 | t0002 | g0298 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA19004 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA19005 | hp2 | a0001 | c0002 | t0002 | g0315 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA19007 | hp2 | a0001 | c0002 | t0002 | g0229 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA19011 | hp1 | a0001 | c0001 | t0004 | g0067 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA19011 | hp2 | a0001 | c0002 | t0002 | g0307 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA19030 | hp1 | a0001 | c0001 | t0014 | g0161 | AFR | LWK | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA19030 | hp2 | a0001 | c0001 | t0015 | g0184 | AFR | LWK | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA19056 | hp1 | a0001 | c0002 | t0002 | g0270 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA19056 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA19057 | hp1 | a0002 | c0006 | t0001 | g0064 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA19057 | hp2 | a0001 | c0002 | t0002 | g0263 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA19058 | hp2 | a0001 | c0002 | t0002 | g0262 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA19060 | hp1 | a0001 | c0002 | t0002 | g0299 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA19060 | hp2 | a0001 | c0002 | t0002 | g0038 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA19063 | hp1 | a0001 | c0002 | t0002 | g0286 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA19064 | hp1 | a0001 | c0001 | t0004 | g0081 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA19064 | hp2 | a0001 | c0002 | t0002 | g0271 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA19068 | hp2 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA19072 | hp1 | a0001 | c0002 | t0002 | g0290 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA19072 | hp2 | a0001 | c0001 | t0004 | g0082 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA19074 | hp1 | a0001 | c0002 | t0002 | g0306 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA19075 | hp2 | a0001 | c0002 | t0002 | g0295 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA19077 | hp2 | a0001 | c0002 | t0002 | g0296 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA19078 | hp1 | a0001 | c0002 | t0002 | g0291 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA19079 | hp2 | a0001 | c0002 | t0002 | g0305 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA19083 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA19083 | hp2 | a0001 | c0002 | t0002 | g0266 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA19084 | hp1 | a0001 | c0002 | t0025 | g0060 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA19087 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA19087 | hp2 | a0001 | c0002 | t0002 | g0269 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA19088 | hp1 | a0001 | c0002 | t0002 | g0309 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA19089 | hp1 | a0001 | c0002 | t0002 | g0268 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA19090 | hp1 | a0001 | c0002 | t0002 | g0297 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA19090 | hp2 | a0001 | c0001 | t0004 | g0087 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA19240 | hp1 | a0001 | c0001 | t0005 | g0028 | AFR | YRI | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | YRI | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA20752 | hp1 | a0001 | c0002 | t0002 | g0274 | EUR | TSI | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0179 | EUR | TSI | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0050 | EUR | TSI | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0103 | EUR | TSI | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0071 | SAS | GIH | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0208 | SAS | GIH | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG01123 | hp1 | a0001 | c0004 | t0003 | g0020 | AMR | CLM | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0253 | AMR | CLM | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG02109 | hp1 | a0001 | c0003 | t0001 | g0137 | AFR | ACB | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG02559 | hp1 | a0001 | c0001 | t0005 | g0029 | AFR | ACB | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG02559 | hp2 | a0001 | c0002 | t0010 | g0244 | AFR | ACB | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | USA | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | USA | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA18955 | hp1 | a0001 | c0002 | t0002 | g0276 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | LWK | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | LWK | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0008 | REF | REF | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0078 | REF | REF | FOXN2_chr2_48309682_48384295 | FOXN2 | chr2 | 48309682 | 48384295 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:48346477
|
T | C | 1 | a0004 | 1 | HG02723.hp1 | missense_variant | MODERATE | c.263T>C | p.Ile88Thr | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/7 | 552/5437 | 263/1296 | 88/431 | chr2 | 48346477 | ||
chr2:48359093
|
C | G | 1 | a0003 | 1 | HG03579.hp2 | missense_variant | MODERATE | c.584C>G | p.Pro195Arg | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 4/7 | 873/5437 | 584/1296 | 195/431 | chr2 | 48359093 | ||
chr2:48375195
|
G | C | 1 | a0002 | 1 | NA19057.hp1 | missense_variant | MODERATE | c.1048G>C | p.Glu350Gln | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 7/7 | 1337/5437 | 1048/1296 | 350/431 | chr2 | 48375195 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:48375047
|
A | G | 1 | a0001c0004 | 8 | HG01123.hp1 HG01192.hp2 HG01346.hp2 others(5): Show |
synonymous_variant | LOW | c.900A>G | p.Glu300Glu | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 7/7 | 1189/5437 | 900/1296 | 300/431 | chr2 | 48375047 | ||
chr2:48375092
|
A | T | 1 | a0001c0003 | 12 | HG01074.hp1 HG01884.hp2 HG02055.hp1 others(9): Show |
synonymous_variant | LOW | c.945A>T | p.Ala315Ala | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 7/7 | 1234/5437 | 945/1296 | 315/431 | chr2 | 48375092 | ||
chr2:48375113
|
C | T | 2 | a0001c0002a0001c0004 | 114 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(111): Show |
synonymous_variant | LOW | c.966C>T | p.Ser322Ser | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 7/7 | 1255/5437 | 966/1296 | 322/431 | chr2 | 48375113 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:48314754
|
G | A | 1 | a0001c0003t0007 | 2 | HG02055.hp1 HG03098.hp2 |
5_prime_UTR_variant | MODIFIER | c.-217G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/7 | 31461 | chr2 | 48314754 | |||||
chr2:48328588
|
C | G | 2 | a0001c0001t0004a0001c0002t0025 | 18 | HG00438.hp1 HG02132.hp1 HG02155.hp2 others(15): Show |
5_prime_UTR_variant | MODIFIER | c.-129C>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/7 | 17627 | chr2 | 48328588 | |||||
chr2:48328681
|
A | C | 1 | a0001c0001t0011 | 2 | HG02040.hp2 HG03831.hp1 |
5_prime_UTR_variant | MODIFIER | c.-36A>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/7 | 17534 | chr2 | 48328681 | |||||
chr2:48375456
|
T | C | 1 | a0001c0001t0012 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*13T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 7/7 | 13 | chr2 | 48375456 | |||||
chr2:48375712
|
C | T | 1 | a0001c0002t0010 | 2 | HG01109.hp2 HG02559.hp2 |
3_prime_UTR_variant | MODIFIER | c.*269C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 7/7 | 269 | chr2 | 48375712 | |||||
chr2:48375859
|
A | G | 1 | a0001c0001t0024 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*416A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 7/7 | 416 | chr2 | 48375859 | |||||
chr2:48375886
|
G | A | 1 | a0003c0007t0013 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*443G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 7/7 | 443 | chr2 | 48375886 | |||||
chr2:48376344
|
A | C | 14 | a0001c0001t0002a0001c0001t0005a0001c0001t0012others(11): Show | 142 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(139): Show |
3_prime_UTR_variant | MODIFIER | c.*901A>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 7/7 | 901 | chr2 | 48376344 | |||||
chr2:48376598
|
A | G | 1 | a0001c0001t0020 | 1 | HG01975.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1155A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 7/7 | 1155 | chr2 | 48376598 | |||||
chr2:48376905
|
C | T | 1 | a0001c0001t0019 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1462C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 7/7 | 1462 | chr2 | 48376905 | |||||
chr2:48377090
|
T | A | 1 | a0001c0001t0021 | 1 | HG01069.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1647T>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 7/7 | 1647 | chr2 | 48377090 | |||||
chr2:48377418
|
A | T | 1 | a0001c0001t0018 | 1 | NA18747.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1975A>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 7/7 | 1975 | chr2 | 48377418 | |||||
chr2:48377578
|
G | C | 2 | a0001c0002t0006a0001c0002t0022 | 8 | HG00280.hp1 HG01070.hp2 HG01081.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2135G>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 7/7 | 2135 | chr2 | 48377578 | |||||
chr2:48377629
|
C | T | 1 | a0001c0002t0023 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2186C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 7/7 | 2186 | chr2 | 48377629 | |||||
chr2:48377775
|
T | C | 1 | a0001c0001t0014 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2332T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 7/7 | 2332 | chr2 | 48377775 | |||||
chr2:48377788
|
A | G | 1 | a0001c0001t0017 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2345A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 7/7 | 2345 | chr2 | 48377788 | |||||
chr2:48377839
|
C | T | 14 | a0001c0001t0002a0001c0001t0008a0001c0001t0012others(11): Show | 130 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(127): Show |
3_prime_UTR_variant | MODIFIER | c.*2396C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 7/7 | 2396 | chr2 | 48377839 | |||||
chr2:48378024
|
T | G | 1 | a0001c0001t0015 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2581T>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 7/7 | 2581 | chr2 | 48378024 | |||||
chr2:48378143
|
C | T | 1 | a0001c0002t0009 | 2 | HG02135.hp2 NA18982.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2700C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 7/7 | 2700 | chr2 | 48378143 | |||||
chr2:48378426
|
G | T | 1 | a0001c0003t0016 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2983G>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 7/7 | 2983 | chr2 | 48378426 | |||||
chr2:48378688
|
AT | A | 4 | a0001c0002t0003a0001c0002t0010a0001c0002t0022others(1): Show | 20 | HG00738.hp2 HG01070.hp2 HG01109.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*3260delT | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 7/7 | 3260 | INFO_REALIGN_3_PRIME | chr2 | 48378688 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:48314840
|
T | A | 2 | a0001c0003t0007g0011a0001c0003t0007g0012 | 2 | HG02055.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-157+26T>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48314840 | ||||||
chr2:48314906
|
C | T | 2 | a0001c0002t0002g0332a0001c0002t0002g0333 | 2 | HG01106.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.-157+92C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48314906 | ||||||
chr2:48314985
|
G | C | 1 | a0001c0001t0001g0013 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-157+171G>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48314985 | ||||||
chr2:48315003
|
C | A | 1 | a0001c0001t0001g0014 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-157+189C>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48315003 | ||||||
chr2:48315152
|
C | A | 1 | a0001c0001t0001g0015 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-157+338C>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48315152 | ||||||
chr2:48315201
|
C | T | 1 | a0001c0001t0017g0331 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-157+387C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48315201 | ||||||
chr2:48315391
|
C | T | 1 | a0001c0002t0023g0330 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-157+577C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48315391 | ||||||
chr2:48315526
|
C | G | 78 | a0001c0001t0001g0322a0001c0001t0001g0328a0001c0002t0002g0009others(75): Show | 80 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.-157+712C>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48315526 | ||||||
chr2:48315545
|
T | G | 1 | a0001c0002t0003g0016 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-157+731T>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48315545 | ||||||
chr2:48315598
|
C | A | 36 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0002g0023others(33): Show | 40 | HG01069.hp1 HG01123.hp1 HG01192.hp2 others(37): Show |
intron_variant | MODIFIER | c.-157+784C>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48315598 | ||||||
chr2:48315667
|
A | T | 3 | a0001c0002t0003g0016a0001c0002t0003g0255a0001c0002t0003g0256 | 3 | HG02717.hp2 HG03209.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-157+853A>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48315667 | ||||||
chr2:48315747
|
C | G | 1 | a0001c0001t0001g0254 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-157+933C>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48315747 | ||||||
chr2:48315793
|
C | G | 161 | a0001c0001t0001g0212a0001c0001t0001g0213a0001c0001t0001g0214others(158): Show | 167 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.-157+979C>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48315793 | ||||||
chr2:48315810
|
G | T | 2 | a0001c0001t0001g0210a0001c0001t0001g0211 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.-157+996G>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48315810 | ||||||
chr2:48316137
|
T | C | 1 | a0001c0002t0003g0016 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-157+1323T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48316137 | ||||||
chr2:48316323
|
A | G | 1 | a0001c0001t0001g0209 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-157+1509A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48316323 | ||||||
chr2:48316509
|
A | G | 1 | a0001c0001t0001g0208 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-157+1695A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48316509 | ||||||
chr2:48316590
|
G | A | 1 | a0001c0001t0001g0050 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-157+1776G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48316590 | ||||||
chr2:48316762
|
G | A | 1 | a0001c0001t0001g0051 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-157+1948G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48316762 | ||||||
chr2:48316778
|
G | A | 163 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(160): Show | 169 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.-157+1964G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48316778 | ||||||
chr2:48316893
|
C | T | 1 | a0001c0003t0001g0207 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-157+2079C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48316893 | ||||||
chr2:48316951
|
A | ATAG | 292 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0013others(289): Show | 300 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.-157+2137_-157+213 others(7): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48316951 | ||||||
chr2:48317121
|
G | A | 1 | a0001c0002t0003g0092 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-157+2307G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48317121 | ||||||
chr2:48317240
|
G | T | 1 | a0001c0001t0004g0091 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-157+2426G>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48317240 | ||||||
chr2:48317259
|
G | T | 2 | a0001c0002t0002g0048a0001c0002t0002g0049 | 2 | NA18944.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.-157+2445G>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48317259 | ||||||
chr2:48317418
|
C | T | 4 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205others(1): Show | 4 | HG00738.hp1 HG01106.hp1 HG01928.hp1 others(1): Show |
intron_variant | MODIFIER | c.-157+2604C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48317418 | ||||||
chr2:48317435
|
C | T | 1 | a0001c0001t0001g0252 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-157+2621C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48317435 | ||||||
chr2:48317448
|
C | CA | 65 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(62): Show | 69 | HG00099.hp1 HG00438.hp2 HG01069.hp1 others(66): Show |
intron_variant | MODIFIER | c.-157+2646dupA | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 48317448 | |||||
chr2:48317567
|
T | C | 1 | a0001c0002t0002g0258 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-157+2753T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48317567 | ||||||
chr2:48317584
|
C | T | 12 | a0001c0001t0005g0047a0001c0002t0003g0016a0001c0002t0003g0245others(9): Show | 12 | HG00738.hp2 HG01109.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.-157+2770C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48317584 | ||||||
chr2:48317595
|
C | CT | 9 | a0001c0001t0001g0090a0001c0001t0001g0202a0001c0001t0001g0206others(6): Show | 10 | HG01928.hp1 HG02056.hp1 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.-157+2811dupT | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 48317595 | |||||
chr2:48317595
|
C | CTT | 9 | a0001c0001t0005g0003a0001c0001t0005g0026a0001c0001t0005g0027others(6): Show | 10 | HG00738.hp2 HG01109.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.-157+2810_-157+281 others(6): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 48317595 | |||||
chr2:48317595
|
C | CTTT | 16 | a0001c0001t0001g0052a0001c0001t0001g0213a0001c0001t0001g0214others(13): Show | 16 | HG01070.hp1 HG01516.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.-157+2809_-157+281 others(7): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 48317595 | |||||
chr2:48317595
|
C | CTTTT | 25 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0220others(22): Show | 25 | HG00438.hp2 HG01069.hp1 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.-157+2808_-157+281 others(8): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 48317595 | |||||
chr2:48317595
|
C | CTTTTT | 9 | a0001c0001t0001g0230a0001c0001t0001g0231a0001c0001t0001g0232others(6): Show | 9 | HG00099.hp1 HG02145.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.-157+2807_-157+281 others(9): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 48317595 | |||||
chr2:48317595
|
C | CTTTTTTT others(1): Show |
7 | a0001c0001t0002g0046a0001c0001t0012g0044a0001c0002t0006g0240others(4): Show | 7 | HG00280.hp1 HG01081.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.-157+2804_-157+281 others(12): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 48317595 | |||||
chr2:48317595
|
CT | C | 139 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(136): Show | 145 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.-157+2811delT | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 48317595 | |||||
chr2:48317595
|
CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0002g0017 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-157+2799_-157+281 others(17): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 48317595 | |||||
chr2:48317595
|
CTTTTTTT others(9): Show |
C | 1 | a0001c0001t0001g0212 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-157+2796_-157+281 others(20): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 48317595 | |||||
chr2:48317595
|
CTTTTTTT others(10): Show |
C | 7 | a0001c0001t0001g0015a0001c0001t0001g0093a0001c0001t0001g0094others(4): Show | 7 | HG02723.hp1 HG02970.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.-157+2795_-157+281 others(21): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 48317595 | |||||
chr2:48317818
|
G | C | 2 | a0001c0002t0002g0298a0001c0002t0002g0299 | 2 | NA19004.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.-157+3004G>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48317818 | ||||||
chr2:48317854
|
G | A | 8 | a0001c0002t0006g0236a0001c0002t0006g0238a0001c0002t0006g0239others(5): Show | 8 | HG00280.hp1 HG01070.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.-157+3040G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48317854 | ||||||
chr2:48317858
|
C | G | 1 | a0001c0002t0023g0330 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-157+3044C>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48317858 | ||||||
chr2:48317869
|
A | G | 1 | a0001c0001t0002g0042 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-157+3055A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48317869 | ||||||
chr2:48317972
|
A | G | 102 | a0001c0001t0001g0160a0001c0001t0001g0235a0001c0001t0001g0322others(99): Show | 104 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.-157+3158A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48317972 | ||||||
chr2:48318009
|
C | T | 1 | a0001c0001t0004g0091 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-157+3195C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48318009 | ||||||
chr2:48318029
|
A | G | 63 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(60): Show | 67 | HG00099.hp1 HG00438.hp2 HG01069.hp1 others(64): Show |
intron_variant | MODIFIER | c.-157+3215A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48318029 | ||||||
chr2:48318126
|
C | T | 1 | a0001c0001t0001g0219 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-157+3312C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48318126 | ||||||
chr2:48318276
|
C | G | 1 | a0001c0001t0024g0201 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-157+3462C>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48318276 | ||||||
chr2:48318443
|
T | G | 165 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(162): Show | 171 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.-157+3629T>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48318443 | ||||||
chr2:48318448
|
A | G | 2 | a0001c0001t0001g0159a0001c0001t0001g0200 | 2 | HG02896.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-157+3634A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48318448 | ||||||
chr2:48318495
|
C | T | 3 | a0001c0002t0003g0016a0001c0002t0003g0255a0001c0002t0003g0256 | 3 | HG02717.hp2 HG03209.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-157+3681C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48318495 | ||||||
chr2:48318646
|
A | G | 1 | a0001c0002t0002g0229 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-157+3832A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48318646 | ||||||
chr2:48318847
|
T | A | 3 | a0001c0002t0003g0016a0001c0002t0003g0255a0001c0002t0003g0256 | 3 | HG02717.hp2 HG03209.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-157+4033T>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48318847 | ||||||
chr2:48318927
|
G | A | 11 | a0001c0002t0003g0016a0001c0002t0003g0245a0001c0002t0003g0247others(8): Show | 11 | HG00738.hp2 HG01109.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-157+4113G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48318927 | ||||||
chr2:48318930
|
T | G | 3 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054 | 3 | HG03704.hp1 HG04115.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.-157+4116T>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48318930 | ||||||
chr2:48319005
|
G | A | 1 | a0001c0002t0002g0300 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-157+4191G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48319005 | ||||||
chr2:48319042
|
A | C | 2 | a0001c0001t0011g0074a0001c0001t0011g0088 | 2 | HG02040.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.-157+4228A>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48319042 | ||||||
chr2:48319153
|
C | CT | 39 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0093others(36): Show | 40 | HG00642.hp1 HG00738.hp1 HG01106.hp1 others(37): Show |
intron_variant | MODIFIER | c.-157+4351dupT | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 48319153 | |||||
chr2:48319233
|
G | A | 164 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(161): Show | 170 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.-157+4419G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48319233 | ||||||
chr2:48319260
|
G | GA | 63 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(60): Show | 67 | HG00099.hp1 HG00438.hp2 HG01069.hp1 others(64): Show |
intron_variant | MODIFIER | c.-157+4455dupA | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 48319260 | |||||
chr2:48319372
|
T | C | 1 | a0001c0001t0001g0328 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-157+4558T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48319372 | ||||||
chr2:48319616
|
C | CT | 21 | a0001c0001t0001g0199a0001c0001t0002g0023a0001c0001t0005g0002others(18): Show | 23 | HG00280.hp1 HG01069.hp1 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.-157+4817dupT | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 48319616 | |||||
chr2:48319616
|
C | CTT | 144 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(141): Show | 148 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.-157+4816_-157+481 others(6): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 48319616 | |||||
chr2:48319655
|
G | T | 2 | a0001c0003t0007g0011a0001c0003t0007g0012 | 2 | HG02055.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-157+4841G>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48319655 | ||||||
chr2:48319666
|
G | A | 1 | a0001c0001t0014g0161 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-157+4852G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48319666 | ||||||
chr2:48319673
|
C | T | 1 | a0001c0001t0001g0153 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-157+4859C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48319673 | ||||||
chr2:48319757
|
C | T | 4 | a0001c0001t0001g0234a0001c0002t0003g0016a0001c0002t0003g0255others(1): Show | 4 | HG02717.hp2 HG03209.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-157+4943C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48319757 | ||||||
chr2:48319785
|
A | AT | 23 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0152others(20): Show | 23 | HG00733.hp1 HG00733.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.-157+4997dupT | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 48319785 | |||||
chr2:48319785
|
AT | A | 18 | a0001c0001t0001g0052a0001c0001t0001g0099a0001c0001t0001g0100others(15): Show | 18 | HG00280.hp2 HG01069.hp1 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.-157+4997delT | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 48319785 | |||||
chr2:48319785
|
ATT | A | 16 | a0001c0001t0001g0160a0001c0002t0002g0259a0001c0002t0003g0016others(13): Show | 16 | HG00280.hp1 HG00738.hp2 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.-157+4996_-157+499 others(6): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 48319785 | |||||
chr2:48320163
|
A | T | 90 | a0001c0001t0001g0160a0001c0001t0001g0235a0001c0001t0001g0322others(87): Show | 92 | HG00280.hp2 HG00408.hp1 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.-157+5349A>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48320163 | ||||||
chr2:48320190
|
A | G | 10 | a0001c0001t0001g0007a0001c0001t0001g0051a0001c0001t0001g0145others(7): Show | 11 | HG02109.hp2 HG02280.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.-157+5376A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48320190 | ||||||
chr2:48320247
|
A | T | 1 | a0001c0004t0003g0021 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-157+5433A>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48320247 | ||||||
chr2:48320304
|
A | T | 160 | a0001c0001t0001g0160a0001c0001t0001g0212a0001c0001t0001g0213others(157): Show | 166 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.-157+5490A>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48320304 | ||||||
chr2:48320327
|
G | C | 1 | a0001c0001t0001g0209 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-157+5513G>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48320327 | ||||||
chr2:48320369
|
C | T | 1 | a0001c0001t0021g0034 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-157+5555C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48320369 | ||||||
chr2:48320373
|
C | G | 2 | a0001c0003t0001g0149a0001c0003t0001g0207 | 2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-157+5559C>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48320373 | ||||||
chr2:48320438
|
A | C | 8 | a0001c0002t0006g0236a0001c0002t0006g0238a0001c0002t0006g0239others(5): Show | 8 | HG00280.hp1 HG01070.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.-157+5624A>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48320438 | ||||||
chr2:48320538
|
C | G | 1 | a0001c0001t0001g0073 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.-157+5724C>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48320538 | ||||||
chr2:48320608
|
A | G | 3 | a0001c0002t0002g0298a0001c0002t0002g0299a0001c0002t0002g0323 | 3 | NA18945.hp2 NA19004.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.-157+5794A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48320608 | ||||||
chr2:48320612
|
C | T | 162 | a0001c0001t0001g0160a0001c0001t0001g0212a0001c0001t0001g0213others(159): Show | 168 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.-157+5798C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48320612 | ||||||
chr2:48320683
|
A | G | 1 | a0001c0001t0001g0144 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-157+5869A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48320683 | ||||||
chr2:48320716
|
T | C | 1 | a0001c0004t0003g0045 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-157+5902T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48320716 | ||||||
chr2:48320750
|
T | C | 1 | a0001c0001t0001g0234 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-157+5936T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48320750 | ||||||
chr2:48320767
|
C | T | 1 | a0001c0001t0001g0154 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-157+5953C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48320767 | ||||||
chr2:48320816
|
A | G | 1 | a0001c0002t0002g0294 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-157+6002A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48320816 | ||||||
chr2:48321009
|
T | C | 1 | a0001c0001t0001g0102 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-157+6195T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48321009 | ||||||
chr2:48321240
|
T | G | 8 | a0001c0002t0006g0236a0001c0002t0006g0238a0001c0002t0006g0239others(5): Show | 8 | HG00280.hp1 HG01070.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.-157+6426T>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48321240 | ||||||
chr2:48321303
|
G | A | 158 | a0001c0001t0001g0160a0001c0001t0001g0212a0001c0001t0001g0213others(155): Show | 164 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.-157+6489G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48321303 | ||||||
chr2:48321338
|
G | T | 2 | a0001c0002t0006g0239a0001c0002t0006g0243 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.-157+6524G>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48321338 | ||||||
chr2:48321350
|
C | T | 1 | a0001c0003t0001g0143 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-157+6536C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48321350 | ||||||
chr2:48321594
|
TTTTAGTA others(29): Show |
T | 2 | a0001c0002t0003g0249a0001c0002t0003g0250 | 2 | HG03225.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-157+6856_-156-685 others(40): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 48321594 | |||||
chr2:48321867
|
T | A | 1 | a0001c0001t0001g0075 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-156-6694T>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48321867 | ||||||
chr2:48321927
|
A | T | 1 | a0001c0001t0001g0098 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-156-6634A>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48321927 | ||||||
chr2:48322034
|
C | T | 1 | a0001c0002t0002g0041 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.-156-6527C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48322034 | ||||||
chr2:48322137
|
G | A | 10 | a0001c0001t0002g0023a0001c0001t0005g0002a0001c0001t0005g0003others(7): Show | 12 | HG01433.hp2 HG01891.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.-156-6424G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48322137 | ||||||
chr2:48322167
|
C | G | 1 | a0001c0001t0015g0184 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-156-6394C>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48322167 | ||||||
chr2:48322479
|
A | C | 1 | a0001c0002t0002g0293 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-156-6082A>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48322479 | ||||||
chr2:48322658
|
A | C | 1 | a0001c0002t0002g0321 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-156-5903A>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48322658 | ||||||
chr2:48323358
|
G | A | 99 | a0001c0001t0001g0160a0001c0001t0001g0213a0001c0001t0001g0230others(96): Show | 101 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.-156-5203G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48323358 | ||||||
chr2:48323439
|
G | A | 52 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(49): Show | 54 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.-156-5122G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48323439 | ||||||
chr2:48323493
|
G | T | 11 | a0001c0002t0003g0016a0001c0002t0003g0245a0001c0002t0003g0247others(8): Show | 11 | HG00738.hp2 HG01109.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-156-5068G>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48323493 | ||||||
chr2:48323549
|
C | T | 1 | a0001c0001t0001g0142 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-156-5012C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48323549 | ||||||
chr2:48323592
|
T | G | 1 | a0001c0002t0002g0303 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-156-4969T>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48323592 | ||||||
chr2:48323598
|
G | T | 5 | a0001c0004t0003g0001a0001c0004t0003g0019a0001c0004t0003g0020others(2): Show | 7 | HG01123.hp1 HG01192.hp2 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.-156-4963G>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48323598 | ||||||
chr2:48323631
|
G | C | 161 | a0001c0001t0001g0160a0001c0001t0001g0212a0001c0001t0001g0213others(158): Show | 167 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.-156-4930G>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48323631 | ||||||
chr2:48324194
|
A | AT | 63 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0093others(60): Show | 64 | HG00280.hp1 HG00642.hp1 HG00733.hp2 others(61): Show |
intron_variant | MODIFIER | c.-156-4349dupT | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 48324194 | |||||
chr2:48324194
|
A | ATTT | 11 | a0001c0001t0001g0234a0001c0001t0005g0002a0001c0001t0005g0003others(8): Show | 13 | HG01433.hp2 HG01891.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.-156-4351_-156-434 others(7): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 48324194 | |||||
chr2:48324194
|
A | ATTTT | 35 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0212others(32): Show | 37 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.-156-4352_-156-434 others(8): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 48324194 | |||||
chr2:48324194
|
A | ATTTTT | 16 | a0001c0001t0001g0054a0001c0001t0001g0217a0001c0001t0001g0218others(13): Show | 16 | HG01123.hp2 HG01358.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.-156-4353_-156-434 others(9): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 48324194 | |||||
chr2:48324227
|
C | T | 2 | a0001c0002t0002g0298a0001c0002t0002g0299 | 2 | NA19004.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.-156-4334C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48324227 | ||||||
chr2:48324240
|
GC | G | 162 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(159): Show | 168 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.-156-4319delC | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 48324240 | |||||
chr2:48324355
|
T | C | 2 | a0001c0003t0001g0134a0001c0003t0001g0135 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-156-4206T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48324355 | ||||||
chr2:48324413
|
C | T | 10 | a0001c0001t0002g0018a0001c0001t0002g0036a0001c0001t0002g0046others(7): Show | 12 | HG01123.hp1 HG01192.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.-156-4148C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48324413 | ||||||
chr2:48324555
|
T | G | 1 | a0001c0001t0001g0098 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-156-4006T>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48324555 | ||||||
chr2:48324783
|
A | G | 1 | a0001c0001t0001g0233 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-156-3778A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48324783 | ||||||
chr2:48324835
|
G | A | 1 | a0001c0002t0003g0255 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-156-3726G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48324835 | ||||||
chr2:48324990
|
C | T | 28 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(25): Show | 30 | HG01069.hp1 HG01123.hp1 HG01192.hp2 others(27): Show |
intron_variant | MODIFIER | c.-156-3571C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48324990 | ||||||
chr2:48325095
|
T | C | 1 | a0001c0001t0001g0150 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.-156-3466T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48325095 | ||||||
chr2:48325157
|
G | A | 1 | a0001c0001t0001g0191 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-156-3404G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48325157 | ||||||
chr2:48325407
|
ATG | A | 12 | a0001c0001t0002g0017a0001c0001t0002g0033a0001c0001t0002g0039others(9): Show | 12 | HG01069.hp1 HG02145.hp2 HG03239.hp1 others(9): Show |
intron_variant | MODIFIER | c.-156-3142_-156-314 others(6): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 48325407 | |||||
chr2:48325522
|
T | C | 1 | a0001c0001t0005g0027 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-156-3039T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48325522 | ||||||
chr2:48325708
|
T | C | 1 | a0001c0002t0003g0092 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-156-2853T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48325708 | ||||||
chr2:48325768
|
G | T | 2 | a0001c0003t0007g0011a0001c0003t0007g0012 | 2 | HG02055.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-156-2793G>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48325768 | ||||||
chr2:48325841
|
T | G | 8 | a0001c0001t0001g0013a0001c0001t0001g0103a0001c0001t0001g0104others(5): Show | 8 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(5): Show |
intron_variant | MODIFIER | c.-156-2720T>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48325841 | ||||||
chr2:48325844
|
C | CT | 55 | a0001c0001t0001g0097a0001c0001t0001g0131a0001c0001t0001g0132others(52): Show | 57 | HG00280.hp1 HG00738.hp2 HG01070.hp1 others(54): Show |
intron_variant | MODIFIER | c.-156-2695dupT | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 48325844 | |||||
chr2:48325844
|
CT | C | 13 | a0001c0001t0001g0050a0001c0001t0001g0055a0001c0001t0001g0057others(10): Show | 13 | HG01496.hp1 HG02897.hp2 HG03710.hp2 others(10): Show |
intron_variant | MODIFIER | c.-156-2695delT | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 48325844 | |||||
chr2:48326007
|
C | T | 1 | a0001c0002t0002g0288 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-156-2554C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48326007 | ||||||
chr2:48326069
|
C | T | 1 | a0001c0002t0002g0287 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-156-2492C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48326069 | ||||||
chr2:48326070
|
A | G | 135 | a0001c0001t0001g0160a0001c0001t0001g0212a0001c0001t0001g0213others(132): Show | 139 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.-156-2491A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48326070 | ||||||
chr2:48326094
|
C | T | 126 | a0001c0001t0001g0160a0001c0001t0001g0212a0001c0001t0001g0213others(123): Show | 130 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.-156-2467C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48326094 | ||||||
chr2:48326140
|
G | A | 1 | a0001c0002t0002g0298 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-156-2421G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48326140 | ||||||
chr2:48326165
|
C | T | 25 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0002g0031others(22): Show | 27 | HG01069.hp1 HG01123.hp1 HG01192.hp2 others(24): Show |
intron_variant | MODIFIER | c.-156-2396C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48326165 | ||||||
chr2:48326316
|
A | T | 25 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0002g0031others(22): Show | 27 | HG01069.hp1 HG01123.hp1 HG01192.hp2 others(24): Show |
intron_variant | MODIFIER | c.-156-2245A>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48326316 | ||||||
chr2:48326489
|
AAG | A | 26 | a0001c0001t0001g0223a0001c0001t0002g0017a0001c0001t0002g0018others(23): Show | 28 | HG01069.hp1 HG01123.hp1 HG01192.hp2 others(25): Show |
intron_variant | MODIFIER | c.-156-2065_-156-206 others(6): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 48326489 | |||||
chr2:48326893
|
C | A | 1 | a0001c0001t0018g0106 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-156-1668C>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48326893 | ||||||
chr2:48326906
|
A | G | 1 | a0001c0001t0001g0090 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-156-1655A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48326906 | ||||||
chr2:48327052
|
G | A | 159 | a0001c0001t0001g0160a0001c0001t0001g0212a0001c0001t0001g0213others(156): Show | 165 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.-156-1509G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48327052 | ||||||
chr2:48327060
|
G | T | 1 | a0001c0001t0001g0158 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-156-1501G>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48327060 | ||||||
chr2:48327111
|
T | A | 1 | a0001c0001t0001g0054 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-156-1450T>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48327111 | ||||||
chr2:48327118
|
C | T | 2 | a0001c0002t0003g0249a0001c0002t0003g0250 | 2 | HG03225.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-156-1443C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48327118 | ||||||
chr2:48327146
|
G | A | 1 | a0001c0001t0001g0224 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-156-1415G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48327146 | ||||||
chr2:48327299
|
A | T | 8 | a0001c0002t0006g0236a0001c0002t0006g0238a0001c0002t0006g0239others(5): Show | 8 | HG00280.hp1 HG01070.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.-156-1262A>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48327299 | ||||||
chr2:48327451
|
CT | C | 100 | a0001c0001t0001g0160a0001c0001t0001g0213a0001c0001t0001g0230others(97): Show | 102 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.-156-1099delT | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 48327451 | |||||
chr2:48327615
|
T | G | 5 | a0001c0001t0001g0099a0001c0001t0001g0151a0001c0001t0001g0166others(2): Show | 5 | HG00733.hp1 HG01981.hp2 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.-156-946T>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48327615 | ||||||
chr2:48327645
|
G | A | 159 | a0001c0001t0001g0160a0001c0001t0001g0212a0001c0001t0001g0213others(156): Show | 165 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.-156-916G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48327645 | ||||||
chr2:48327688
|
A | G | 1 | a0001c0001t0001g0105 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-156-873A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48327688 | ||||||
chr2:48327816
|
G | A | 5 | a0001c0001t0001g0050a0001c0001t0001g0107a0001c0001t0001g0167others(2): Show | 5 | HG00639.hp1 HG01123.hp2 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.-156-745G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48327816 | ||||||
chr2:48328056
|
A | G | 2 | a0001c0001t0001g0153a0001c0001t0024g0201 | 2 | HG01243.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-156-505A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48328056 | ||||||
chr2:48328153
|
G | A | 9 | a0001c0001t0001g0013a0001c0001t0001g0103a0001c0001t0001g0104others(6): Show | 9 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(6): Show |
intron_variant | MODIFIER | c.-156-408G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48328153 | ||||||
chr2:48328338
|
C | G | 129 | a0001c0001t0001g0160a0001c0001t0001g0212a0001c0001t0001g0213others(126): Show | 131 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.-156-223C>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48328338 | ||||||
chr2:48328446
|
A | G | 11 | a0001c0001t0002g0023a0001c0001t0005g0002a0001c0001t0005g0003others(8): Show | 13 | HG01433.hp2 HG01891.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.-156-115A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48328446 | ||||||
chr2:48328482
|
C | T | 109 | a0001c0001t0001g0160a0001c0001t0001g0213a0001c0001t0001g0230others(106): Show | 111 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.-156-79C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48328482 | ||||||
chr2:48328485
|
C | A | 12 | a0001c0002t0003g0016a0001c0002t0003g0092a0001c0002t0003g0245others(9): Show | 12 | HG00738.hp2 HG01109.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.-156-76C>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 1/6 | chr2 | 48328485 | ||||||
chr2:48328744
|
G | A | 1 | a0001c0001t0001g0073 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.-15+42G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48328744 | ||||||
chr2:48328758
|
C | A | 30 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0002g0023others(27): Show | 34 | HG01069.hp1 HG01123.hp1 HG01192.hp2 others(31): Show |
intron_variant | MODIFIER | c.-15+56C>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48328758 | ||||||
chr2:48328786
|
T | C | 1 | a0001c0003t0001g0149 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-15+84T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48328786 | ||||||
chr2:48328857
|
G | T | 14 | a0001c0002t0003g0016a0001c0002t0003g0092a0001c0002t0003g0245others(11): Show | 14 | HG00738.hp2 HG01109.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.-15+155G>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48328857 | ||||||
chr2:48329167
|
G | A | 1 | a0001c0001t0002g0036 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-15+465G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48329167 | ||||||
chr2:48329231
|
G | A | 1 | a0001c0001t0001g0220 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-15+529G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48329231 | ||||||
chr2:48329343
|
A | G | 166 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(163): Show | 172 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.-15+641A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48329343 | ||||||
chr2:48329550
|
G | A | 87 | a0001c0001t0001g0160a0001c0001t0001g0213a0001c0001t0001g0230others(84): Show | 89 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.-15+848G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48329550 | ||||||
chr2:48329616
|
A | C | 3 | a0001c0001t0001g0072a0001c0001t0001g0076a0001c0001t0001g0086 | 3 | NA18612.hp1 NA18994.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.-15+914A>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48329616 | ||||||
chr2:48329748
|
A | T | 1 | a0001c0001t0001g0076 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-15+1046A>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48329748 | ||||||
chr2:48329755
|
T | C | 3 | a0001c0001t0001g0013a0001c0001t0001g0103a0001c0001t0001g0104 | 3 | HG00099.hp2 HG00642.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.-15+1053T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48329755 | ||||||
chr2:48329831
|
A | G | 1 | a0001c0001t0001g0133 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.-15+1129A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48329831 | ||||||
chr2:48329846
|
C | T | 287 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0013others(284): Show | 295 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.-15+1144C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48329846 | ||||||
chr2:48330033
|
G | A | 1 | a0001c0002t0002g0265 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-15+1331G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48330033 | ||||||
chr2:48330037
|
C | A | 1 | a0001c0003t0016g0136 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-15+1335C>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48330037 | ||||||
chr2:48330608
|
G | C | 3 | a0001c0002t0003g0016a0001c0002t0003g0255a0001c0002t0003g0256 | 3 | HG02717.hp2 HG03209.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-15+1906G>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48330608 | ||||||
chr2:48330631
|
G | A | 1 | a0001c0002t0002g0266 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-15+1929G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48330631 | ||||||
chr2:48330657
|
T | G | 1 | a0001c0001t0001g0077 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-15+1955T>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48330657 | ||||||
chr2:48330732
|
C | T | 21 | a0001c0001t0001g0212a0001c0001t0001g0214a0001c0001t0001g0215others(18): Show | 21 | HG00099.hp1 HG00438.hp2 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.-15+2030C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48330732 | ||||||
chr2:48330756
|
CTTAAA | C | 21 | a0001c0001t0001g0212a0001c0001t0001g0214a0001c0001t0001g0215others(18): Show | 21 | HG00099.hp1 HG00438.hp2 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.-15+2059_-15+2063d others(7): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 48330756 | |||||
chr2:48330791
|
C | T | 158 | a0001c0001t0001g0212a0001c0001t0001g0213a0001c0001t0001g0214others(155): Show | 164 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.-15+2089C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48330791 | ||||||
chr2:48330947
|
C | T | 159 | a0001c0001t0001g0199a0001c0001t0001g0212a0001c0001t0001g0213others(156): Show | 165 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.-15+2245C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48330947 | ||||||
chr2:48331077
|
G | A | 1 | a0001c0002t0002g0294 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-15+2375G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48331077 | ||||||
chr2:48331118
|
A | G | 1 | a0001c0002t0002g0320 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-15+2416A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48331118 | ||||||
chr2:48331121
|
A | C | 33 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(30): Show | 37 | HG01069.hp1 HG01123.hp1 HG01192.hp2 others(34): Show |
intron_variant | MODIFIER | c.-15+2419A>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48331121 | ||||||
chr2:48331175
|
C | T | 11 | a0001c0001t0002g0023a0001c0001t0005g0002a0001c0001t0005g0003others(8): Show | 13 | HG01433.hp2 HG01891.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.-15+2473C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48331175 | ||||||
chr2:48331311
|
T | C | 33 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(30): Show | 37 | HG01069.hp1 HG01123.hp1 HG01192.hp2 others(34): Show |
intron_variant | MODIFIER | c.-15+2609T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48331311 | ||||||
chr2:48331343
|
CTATAG | C | 8 | a0001c0002t0006g0236a0001c0002t0006g0238a0001c0002t0006g0239others(5): Show | 8 | HG00280.hp1 HG01070.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.-15+2647_-15+2651d others(7): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 48331343 | |||||
chr2:48331356
|
A | G | 2 | a0001c0003t0007g0011a0001c0003t0007g0012 | 2 | HG02055.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-15+2654A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48331356 | ||||||
chr2:48331452
|
G | A | 21 | a0001c0001t0001g0212a0001c0001t0001g0214a0001c0001t0001g0215others(18): Show | 21 | HG00099.hp1 HG00438.hp2 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.-15+2750G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48331452 | ||||||
chr2:48331458
|
A | G | 1 | a0001c0001t0001g0198 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-15+2756A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48331458 | ||||||
chr2:48331480
|
T | G | 86 | a0001c0001t0001g0213a0001c0001t0001g0230a0001c0001t0001g0322others(83): Show | 88 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.-15+2778T>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48331480 | ||||||
chr2:48331545
|
C | G | 86 | a0001c0001t0001g0213a0001c0001t0001g0230a0001c0001t0001g0322others(83): Show | 88 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.-15+2843C>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48331545 | ||||||
chr2:48331631
|
A | G | 1 | a0001c0001t0001g0129 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-15+2929A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48331631 | ||||||
chr2:48331732
|
G | A | 1 | a0001c0003t0001g0137 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-15+3030G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48331732 | ||||||
chr2:48331792
|
C | T | 1 | a0001c0001t0001g0144 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-15+3090C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48331792 | ||||||
chr2:48331991
|
A | G | 1 | a0001c0001t0001g0212 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-15+3289A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48331991 | ||||||
chr2:48332408
|
A | G | 1 | a0001c0002t0002g0259 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-15+3706A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48332408 | ||||||
chr2:48332580
|
A | G | 1 | a0001c0001t0001g0015 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-15+3878A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48332580 | ||||||
chr2:48332722
|
T | C | 165 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(162): Show | 171 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.-15+4020T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48332722 | ||||||
chr2:48332913
|
C | A | 30 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0002g0023others(27): Show | 34 | HG01069.hp1 HG01123.hp1 HG01192.hp2 others(31): Show |
intron_variant | MODIFIER | c.-15+4211C>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48332913 | ||||||
chr2:48332981
|
A | G | 1 | a0001c0001t0001g0223 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-15+4279A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48332981 | ||||||
chr2:48332997
|
A | AT | 123 | a0001c0001t0001g0130a0001c0001t0001g0202a0001c0001t0001g0212others(120): Show | 125 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.-15+4300dupT | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 48332997 | |||||
chr2:48333088
|
T | G | 1 | a0001c0002t0002g0289 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-15+4386T>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48333088 | ||||||
chr2:48333094
|
T | C | 30 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0002g0023others(27): Show | 34 | HG01069.hp1 HG01123.hp1 HG01192.hp2 others(31): Show |
intron_variant | MODIFIER | c.-15+4392T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48333094 | ||||||
chr2:48333222
|
A | T | 2 | a0001c0001t0001g0052a0001c0001t0001g0053 | 2 | HG03704.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.-15+4520A>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48333222 | ||||||
chr2:48333246
|
A | G | 1 | a0001c0002t0002g0293 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-15+4544A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48333246 | ||||||
chr2:48333252
|
TATCTCTT others(4): Show |
T | 1 | a0001c0001t0002g0039 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-15+4558_-15+4568d others(13): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 48333252 | |||||
chr2:48333263
|
C | T | 1 | a0001c0002t0002g0293 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-15+4561C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48333263 | ||||||
chr2:48333406
|
A | G | 86 | a0001c0001t0001g0213a0001c0001t0001g0230a0001c0001t0001g0322others(83): Show | 88 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.-15+4704A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48333406 | ||||||
chr2:48333535
|
G | C | 1 | a0001c0001t0001g0109 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-15+4833G>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48333535 | ||||||
chr2:48333640
|
A | G | 1 | a0001c0001t0001g0109 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-15+4938A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48333640 | ||||||
chr2:48333848
|
G | C | 150 | a0001c0001t0001g0212a0001c0001t0001g0213a0001c0001t0001g0214others(147): Show | 156 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.-15+5146G>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48333848 | ||||||
chr2:48333888
|
G | GGT | 4 | a0001c0002t0002g0292a0001c0002t0002g0301a0001c0002t0002g0302others(1): Show | 4 | HG00558.hp2 HG01952.hp2 NA18956.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15+5203_-15+5204d others(4): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 48333888 | |||||
chr2:48334074
|
A | G | 1 | a0001c0001t0001g0128 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-15+5372A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48334074 | ||||||
chr2:48334095
|
G | C | 1 | a0001c0001t0001g0058 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-15+5393G>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48334095 | ||||||
chr2:48334171
|
T | C | 1 | a0001c0001t0001g0235 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-15+5469T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48334171 | ||||||
chr2:48334307
|
T | A | 9 | a0001c0001t0001g0007a0001c0001t0001g0051a0001c0001t0001g0145others(6): Show | 10 | HG02109.hp2 HG02280.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.-15+5605T>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48334307 | ||||||
chr2:48334482
|
ATC | A | 107 | a0001c0001t0001g0213a0001c0001t0001g0230a0001c0002t0002g0009others(104): Show | 109 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.-15+5782_-15+5783d others(4): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 48334482 | |||||
chr2:48334605
|
C | T | 1 | a0001c0001t0001g0254 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-15+5903C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48334605 | ||||||
chr2:48334709
|
C | T | 45 | a0001c0001t0001g0014a0001c0001t0001g0055a0001c0001t0001g0057others(42): Show | 48 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.-15+6007C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48334709 | ||||||
chr2:48334736
|
C | T | 1 | a0001c0001t0001g0127 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-15+6034C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48334736 | ||||||
chr2:48334793
|
A | T | 4 | a0001c0001t0001g0128a0001c0001t0001g0153a0001c0001t0001g0160others(1): Show | 4 | HG01243.hp2 HG02886.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-15+6091A>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48334793 | ||||||
chr2:48334829
|
A | G | 4 | a0001c0001t0001g0071a0001c0002t0002g0229a0001c0002t0002g0316others(1): Show | 4 | HG02056.hp1 NA18960.hp2 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15+6127A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48334829 | ||||||
chr2:48334857
|
C | T | 8 | a0001c0002t0006g0236a0001c0002t0006g0238a0001c0002t0006g0239others(5): Show | 8 | HG00280.hp1 HG01070.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.-15+6155C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48334857 | ||||||
chr2:48335021
|
C | T | 1 | a0001c0001t0001g0212 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-15+6319C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48335021 | ||||||
chr2:48335088
|
A | G | 1 | a0001c0002t0002g0289 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-15+6386A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48335088 | ||||||
chr2:48335161
|
T | G | 1 | a0001c0001t0001g0188 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-15+6459T>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48335161 | ||||||
chr2:48335165
|
G | A | 18 | a0001c0001t0001g0013a0001c0001t0001g0100a0001c0001t0001g0103others(15): Show | 18 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(15): Show |
intron_variant | MODIFIER | c.-15+6463G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48335165 | ||||||
chr2:48335173
|
A | G | 4 | a0001c0002t0006g0239a0001c0002t0006g0241a0001c0002t0006g0242others(1): Show | 4 | HG00280.hp1 HG01081.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15+6471A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48335173 | ||||||
chr2:48335291
|
A | C | 1 | a0001c0001t0002g0042 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-15+6589A>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48335291 | ||||||
chr2:48335334
|
TG | T | 8 | a0001c0002t0006g0236a0001c0002t0006g0238a0001c0002t0006g0239others(5): Show | 8 | HG00280.hp1 HG01070.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.-15+6633delG | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48335334 | ||||||
chr2:48335351
|
A | G | 1 | a0001c0001t0001g0126 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-15+6649A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48335351 | ||||||
chr2:48335526
|
A | G | 1 | a0001c0001t0014g0161 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-15+6824A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48335526 | ||||||
chr2:48335551
|
A | AGCAAAAA others(18): Show |
161 | a0001c0001t0001g0130a0001c0001t0001g0202a0001c0001t0001g0212others(158): Show | 167 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.-15+6859_-15+6860i others(27): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 48335551 | |||||
chr2:48335593
|
A | T | 1 | a0001c0001t0001g0180 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-15+6891A>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48335593 | ||||||
chr2:48335680
|
T | C | 54 | a0001c0001t0001g0130a0001c0001t0001g0202a0001c0001t0001g0212others(51): Show | 58 | HG00099.hp1 HG00438.hp2 HG01069.hp1 others(55): Show |
intron_variant | MODIFIER | c.-15+6978T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48335680 | ||||||
chr2:48335803
|
G | A | 3 | a0001c0002t0002g0267a0001c0002t0002g0318a0001c0002t0003g0092 | 3 | HG02080.hp2 HG03098.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.-15+7101G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48335803 | ||||||
chr2:48335826
|
G | C | 1 | a0001c0001t0001g0055 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-15+7124G>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48335826 | ||||||
chr2:48335915
|
C | T | 3 | a0001c0002t0003g0249a0001c0002t0003g0250a0001c0002t0003g0251 | 3 | HG03225.hp2 HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-15+7213C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48335915 | ||||||
chr2:48335958
|
G | A | 1 | a0001c0001t0001g0214 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-15+7256G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48335958 | ||||||
chr2:48335958
|
G | T | 1 | a0001c0002t0002g0315 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-15+7256G>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48335958 | ||||||
chr2:48336006
|
C | T | 1 | a0001c0002t0002g0294 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-15+7304C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48336006 | ||||||
chr2:48336033
|
A | AT | 125 | a0001c0001t0001g0130a0001c0001t0001g0202a0001c0001t0001g0212others(122): Show | 127 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.-15+7331_-15+7332i others(3): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48336033 | ||||||
chr2:48336036
|
A | AT | 8 | a0001c0002t0006g0236a0001c0002t0006g0238a0001c0002t0006g0239others(5): Show | 8 | HG00280.hp1 HG01070.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.-15+7334_-15+7335i others(3): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48336036 | ||||||
chr2:48336036
|
A | T | 125 | a0001c0001t0001g0130a0001c0001t0001g0202a0001c0001t0001g0212others(122): Show | 127 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.-15+7334A>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48336036 | ||||||
chr2:48336039
|
A | T | 163 | a0001c0001t0001g0130a0001c0001t0001g0202a0001c0001t0001g0212others(160): Show | 169 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.-15+7337A>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48336039 | ||||||
chr2:48336131
|
C | T | 1 | a0001c0001t0001g0197 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-15+7429C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48336131 | ||||||
chr2:48336142
|
G | A | 3 | a0001c0002t0003g0016a0001c0002t0003g0255a0001c0002t0003g0256 | 3 | HG02717.hp2 HG03209.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-15+7440G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48336142 | ||||||
chr2:48336202
|
A | G | 159 | a0001c0001t0001g0130a0001c0001t0001g0202a0001c0001t0001g0212others(156): Show | 165 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.-15+7500A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48336202 | ||||||
chr2:48336202
|
A | T | 3 | a0001c0002t0003g0016a0001c0002t0003g0255a0001c0002t0003g0256 | 3 | HG02717.hp2 HG03209.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-15+7500A>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48336202 | ||||||
chr2:48336225
|
G | GA | 10 | a0001c0001t0001g0007a0001c0001t0001g0051a0001c0001t0001g0145others(7): Show | 11 | HG02109.hp2 HG02280.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.-15+7526dupA | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 48336225 | |||||
chr2:48336347
|
G | T | 5 | a0001c0001t0001g0218a0001c0001t0001g0224a0001c0001t0001g0226others(2): Show | 5 | HG01358.hp1 HG02683.hp1 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.-15+7645G>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48336347 | ||||||
chr2:48336408
|
C | CAA | 9 | a0001c0002t0002g0257a0001c0002t0002g0268a0001c0002t0002g0269others(6): Show | 9 | HG03710.hp2 NA18972.hp2 NA18990.hp1 others(6): Show |
intron_variant | MODIFIER | c.-15+7716_-15+7717d others(4): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 48336408 | |||||
chr2:48336408
|
C | CAAAA | 50 | a0001c0001t0001g0130a0001c0001t0001g0202a0001c0001t0001g0212others(47): Show | 54 | HG00099.hp1 HG00438.hp2 HG01069.hp1 others(51): Show |
intron_variant | MODIFIER | c.-15+7714_-15+7717d others(6): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 48336408 | |||||
chr2:48336418
|
A | AAAAT | 88 | a0001c0001t0001g0322a0001c0001t0002g0033a0001c0001t0002g0043others(85): Show | 90 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.-15+7717_-15+7718i others(6): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 48336418 | |||||
chr2:48336418
|
A | T | 2 | a0001c0001t0001g0071a0001c0001t0001g0125 | 2 | NA19074.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.-15+7716A>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48336418 | ||||||
chr2:48336420
|
T | A | 6 | a0001c0001t0001g0213a0001c0001t0001g0230a0001c0001t0002g0040others(3): Show | 6 | HG01257.hp1 HG02602.hp2 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15+7718T>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48336420 | ||||||
chr2:48336431
|
G | A | 16 | a0001c0001t0001g0213a0001c0001t0001g0230a0001c0002t0002g0257others(13): Show | 16 | HG01257.hp1 HG02055.hp1 HG02602.hp2 others(13): Show |
intron_variant | MODIFIER | c.-15+7729G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48336431 | ||||||
chr2:48336433
|
A | G | 9 | a0001c0002t0002g0257a0001c0002t0002g0268a0001c0002t0002g0269others(6): Show | 9 | HG03710.hp2 NA18972.hp2 NA18990.hp1 others(6): Show |
intron_variant | MODIFIER | c.-15+7731A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48336433 | ||||||
chr2:48336433
|
ATATGTG | A | 4 | a0001c0001t0001g0213a0001c0001t0001g0230a0001c0002t0002g0287others(1): Show | 4 | HG02602.hp2 HG03492.hp1 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15+7733_-15+7738d others(8): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 48336433 | |||||
chr2:48336435
|
A | ATG | 44 | a0001c0001t0001g0053a0001c0001t0001g0099a0001c0001t0001g0102others(41): Show | 44 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.-15+7755_-15+7756d others(4): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 48336435 | |||||
chr2:48336435
|
A | ATGTG | 5 | a0001c0002t0003g0245a0001c0002t0003g0247a0001c0002t0003g0248others(2): Show | 5 | HG00738.hp2 HG01109.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.-15+7753_-15+7756d others(6): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 48336435 | |||||
chr2:48336435
|
A | G | 1 | a0001c0002t0006g0238 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-15+7733A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48336435 | ||||||
chr2:48336437
|
G | A | 12 | a0001c0002t0002g0257a0001c0002t0002g0268a0001c0002t0002g0269others(9): Show | 12 | HG01257.hp1 HG02055.hp1 HG03098.hp2 others(9): Show |
intron_variant | MODIFIER | c.-15+7735G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48336437 | ||||||
chr2:48336439
|
G | A | 2 | a0001c0001t0002g0040a0001c0002t0006g0238 | 2 | HG01257.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.-15+7737G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48336439 | ||||||
chr2:48336441
|
G | A | 1 | a0001c0001t0002g0040 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-15+7739G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48336441 | ||||||
chr2:48336443
|
G | A | 4 | a0001c0001t0001g0213a0001c0001t0001g0230a0001c0002t0002g0287others(1): Show | 4 | HG02602.hp2 HG03492.hp1 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15+7741G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48336443 | ||||||
chr2:48336445
|
G | A | 4 | a0001c0001t0001g0213a0001c0001t0001g0230a0001c0002t0002g0287others(1): Show | 4 | HG02602.hp2 HG03492.hp1 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15+7743G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48336445 | ||||||
chr2:48336457
|
G | A | 1 | a0001c0001t0001g0167 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-15+7755G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48336457 | ||||||
chr2:48336457
|
GTA | G | 19 | a0001c0001t0001g0224a0001c0001t0002g0023a0001c0001t0005g0002others(16): Show | 21 | HG00280.hp1 HG01070.hp2 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.-15+7763_-15+7764d others(4): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 48336457 | |||||
chr2:48336459
|
A | G | 45 | a0001c0001t0001g0104a0001c0001t0001g0124a0001c0001t0001g0130others(42): Show | 47 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(44): Show |
intron_variant | MODIFIER | c.-15+7757A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48336459 | ||||||
chr2:48336567
|
C | G | 1 | a0001c0001t0021g0034 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-15+7865C>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48336567 | ||||||
chr2:48336571
|
C | T | 101 | a0001c0001t0001g0213a0001c0001t0001g0230a0001c0001t0001g0322others(98): Show | 103 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.-15+7869C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48336571 | ||||||
chr2:48336702
|
T | C | 163 | a0001c0001t0001g0130a0001c0001t0001g0202a0001c0001t0001g0212others(160): Show | 169 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.-15+8000T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48336702 | ||||||
chr2:48336861
|
C | T | 5 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0069others(2): Show | 5 | HG02080.hp1 NA18949.hp1 NA19000.hp1 others(2): Show |
intron_variant | MODIFIER | c.-15+8159C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48336861 | ||||||
chr2:48336956
|
A | G | 1 | a0001c0001t0001g0071 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-15+8254A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48336956 | ||||||
chr2:48337055
|
CT | C | 116 | a0001c0001t0001g0051a0001c0001t0001g0059a0001c0001t0001g0079others(113): Show | 118 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(115): Show |
intron_variant | MODIFIER | c.-15+8367delT | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 48337055 | |||||
chr2:48337291
|
C | CT | 53 | a0001c0001t0001g0080a0001c0001t0001g0196a0001c0001t0001g0212others(50): Show | 57 | HG00099.hp1 HG00438.hp2 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.-15+8605dupT | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 48337291 | |||||
chr2:48337319
|
G | A | 1 | a0001c0002t0006g0241 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-15+8617G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48337319 | ||||||
chr2:48337420
|
C | G | 2 | a0001c0001t0001g0228a0001c0001t0001g0232 | 2 | HG00099.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.-15+8718C>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48337420 | ||||||
chr2:48337623
|
G | A | 2 | a0001c0002t0003g0247a0001c0002t0003g0248 | 2 | HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-14-8578G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48337623 | ||||||
chr2:48337648
|
C | A | 2 | a0001c0001t0002g0031a0001c0001t0002g0035 | 2 | HG01891.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.-14-8553C>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48337648 | ||||||
chr2:48337686
|
A | G | 1 | a0001c0001t0024g0201 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-14-8515A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48337686 | ||||||
chr2:48337859
|
T | A | 50 | a0001c0001t0001g0130a0001c0001t0001g0202a0001c0001t0001g0212others(47): Show | 54 | HG00099.hp1 HG00438.hp2 HG01069.hp1 others(51): Show |
intron_variant | MODIFIER | c.-14-8342T>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48337859 | ||||||
chr2:48337866
|
G | A | 160 | a0001c0001t0001g0130a0001c0001t0001g0202a0001c0001t0001g0212others(157): Show | 166 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.-14-8335G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48337866 | ||||||
chr2:48338080
|
A | G | 2 | a0001c0003t0007g0011a0001c0003t0007g0012 | 2 | HG02055.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-14-8121A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48338080 | ||||||
chr2:48338141
|
A | G | 3 | a0001c0002t0003g0016a0001c0002t0003g0255a0001c0002t0003g0256 | 3 | HG02717.hp2 HG03209.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-14-8060A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48338141 | ||||||
chr2:48338196
|
G | A | 161 | a0001c0001t0001g0130a0001c0001t0001g0202a0001c0001t0001g0212others(158): Show | 167 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.-14-8005G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48338196 | ||||||
chr2:48338203
|
C | A | 1 | a0001c0001t0001g0013 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-14-7998C>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48338203 | ||||||
chr2:48338238
|
T | G | 1 | a0001c0001t0005g0030 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-14-7963T>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48338238 | ||||||
chr2:48338385
|
C | A | 11 | a0001c0001t0002g0023a0001c0001t0005g0002a0001c0001t0005g0003others(8): Show | 13 | HG01433.hp2 HG01891.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.-14-7816C>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48338385 | ||||||
chr2:48338386
|
A | T | 11 | a0001c0001t0002g0023a0001c0001t0005g0002a0001c0001t0005g0003others(8): Show | 13 | HG01433.hp2 HG01891.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.-14-7815A>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48338386 | ||||||
chr2:48338396
|
C | A | 161 | a0001c0001t0001g0130a0001c0001t0001g0202a0001c0001t0001g0212others(158): Show | 167 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.-14-7805C>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48338396 | ||||||
chr2:48338398
|
A | AT | 160 | a0001c0001t0001g0055a0001c0001t0001g0130a0001c0001t0001g0202others(157): Show | 166 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.-14-7790dupT | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 48338398 | |||||
chr2:48338555
|
C | T | 1 | a0001c0001t0001g0185 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-14-7646C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48338555 | ||||||
chr2:48338643
|
C | T | 130 | a0001c0001t0001g0130a0001c0001t0001g0202a0001c0001t0001g0212others(127): Show | 132 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.-14-7558C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48338643 | ||||||
chr2:48338840
|
A | G | 2 | a0001c0002t0002g0267a0001c0002t0002g0318 | 2 | HG02080.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.-14-7361A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48338840 | ||||||
chr2:48338892
|
C | T | 212 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0015others(209): Show | 220 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.-14-7309C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48338892 | ||||||
chr2:48339073
|
T | C | 3 | a0001c0001t0001g0153a0001c0001t0001g0160a0001c0001t0024g0201 | 3 | HG01243.hp2 HG02976.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-14-7128T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48339073 | ||||||
chr2:48339277
|
C | G | 30 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0002g0023others(27): Show | 34 | HG01069.hp1 HG01123.hp1 HG01192.hp2 others(31): Show |
intron_variant | MODIFIER | c.-14-6924C>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48339277 | ||||||
chr2:48339796
|
C | T | 159 | a0001c0001t0001g0130a0001c0001t0001g0202a0001c0001t0001g0212others(156): Show | 165 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.-14-6405C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48339796 | ||||||
chr2:48339799
|
A | G | 159 | a0001c0001t0001g0130a0001c0001t0001g0202a0001c0001t0001g0212others(156): Show | 165 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.-14-6402A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48339799 | ||||||
chr2:48339887
|
A | G | 2 | a0001c0001t0001g0213a0001c0001t0001g0230 | 2 | HG02602.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-14-6314A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48339887 | ||||||
chr2:48340305
|
T | C | 10 | a0001c0001t0001g0007a0001c0001t0001g0051a0001c0001t0001g0145others(7): Show | 11 | HG02109.hp2 HG02280.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.-14-5896T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48340305 | ||||||
chr2:48340468
|
G | A | 1 | a0001c0001t0001g0173 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-14-5733G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48340468 | ||||||
chr2:48340545
|
G | A | 1 | a0001c0001t0001g0208 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-14-5656G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48340545 | ||||||
chr2:48340574
|
C | T | 1 | a0001c0001t0001g0198 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-14-5627C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48340574 | ||||||
chr2:48340666
|
T | G | 2 | a0001c0003t0007g0011a0001c0003t0007g0012 | 2 | HG02055.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-14-5535T>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48340666 | ||||||
chr2:48340711
|
G | A | 1 | a0001c0002t0003g0092 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-14-5490G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48340711 | ||||||
chr2:48340825
|
C | G | 53 | a0001c0001t0001g0130a0001c0001t0001g0202a0001c0001t0001g0212others(50): Show | 57 | HG00099.hp1 HG00438.hp2 HG01069.hp1 others(54): Show |
intron_variant | MODIFIER | c.-14-5376C>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48340825 | ||||||
chr2:48340871
|
C | A | 101 | a0001c0001t0001g0213a0001c0001t0001g0230a0001c0001t0001g0322others(98): Show | 103 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.-14-5330C>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48340871 | ||||||
chr2:48340922
|
A | G | 2 | a0001c0002t0002g0300a0001c0002t0002g0306 | 2 | NA18990.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.-14-5279A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48340922 | ||||||
chr2:48340944
|
A | G | 2 | a0001c0001t0001g0096a0001c0001t0001g0097 | 2 | HG02970.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-14-5257A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48340944 | ||||||
chr2:48340969
|
C | T | 2 | a0001c0003t0007g0011a0001c0003t0007g0012 | 2 | HG02055.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-14-5232C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48340969 | ||||||
chr2:48341226
|
A | G | 124 | a0001c0001t0001g0130a0001c0001t0001g0202a0001c0001t0001g0212others(121): Show | 126 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.-14-4975A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48341226 | ||||||
chr2:48341441
|
A | G | 1 | a0001c0001t0001g0099 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-14-4760A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48341441 | ||||||
chr2:48341580
|
G | A | 3 | a0001c0001t0001g0322a0001c0002t0002g0272a0001c0002t0002g0273 | 3 | HG02132.hp2 HG02135.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.-14-4621G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48341580 | ||||||
chr2:48341726
|
G | A | 161 | a0001c0001t0001g0130a0001c0001t0001g0202a0001c0001t0001g0212others(158): Show | 167 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.-14-4475G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48341726 | ||||||
chr2:48341766
|
G | T | 30 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0002g0023others(27): Show | 34 | HG01069.hp1 HG01123.hp1 HG01192.hp2 others(31): Show |
intron_variant | MODIFIER | c.-14-4435G>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48341766 | ||||||
chr2:48341920
|
A | G | 162 | a0001c0001t0001g0130a0001c0001t0001g0202a0001c0001t0001g0212others(159): Show | 168 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.-14-4281A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48341920 | ||||||
chr2:48342047
|
A | T | 19 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0002g0031others(16): Show | 21 | HG01069.hp1 HG01123.hp1 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.-14-4154A>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48342047 | ||||||
chr2:48342176
|
A | G | 8 | a0001c0002t0006g0236a0001c0002t0006g0238a0001c0002t0006g0239others(5): Show | 8 | HG00280.hp1 HG01070.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.-14-4025A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48342176 | ||||||
chr2:48342396
|
AG | A | 29 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0002g0023others(26): Show | 33 | HG01069.hp1 HG01123.hp1 HG01192.hp2 others(30): Show |
intron_variant | MODIFIER | c.-14-3802delG | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 48342396 | |||||
chr2:48342443
|
A | G | 31 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0052others(28): Show | 32 | HG00642.hp1 HG00733.hp2 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.-14-3758A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48342443 | ||||||
chr2:48342503
|
T | G | 3 | a0001c0002t0002g0266a0001c0002t0002g0315a0001c0002t0002g0324 | 3 | NA18994.hp2 NA19005.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.-14-3698T>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48342503 | ||||||
chr2:48342518
|
G | A | 1 | a0001c0001t0001g0145 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-14-3683G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48342518 | ||||||
chr2:48342553
|
T | A | 1 | a0001c0002t0003g0016 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-14-3648T>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48342553 | ||||||
chr2:48342728
|
A | G | 1 | a0001c0001t0001g0254 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-14-3473A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48342728 | ||||||
chr2:48342732
|
G | A | 2 | a0001c0003t0007g0011a0001c0003t0007g0012 | 2 | HG02055.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-14-3469G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48342732 | ||||||
chr2:48342765
|
T | G | 2 | a0001c0002t0006g0239a0001c0002t0006g0243 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.-14-3436T>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48342765 | ||||||
chr2:48342818
|
A | G | 2 | a0001c0001t0001g0228a0001c0001t0001g0232 | 2 | HG00099.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.-14-3383A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48342818 | ||||||
chr2:48342997
|
A | C | 4 | a0001c0003t0001g0137a0001c0003t0001g0138a0001c0003t0001g0149others(1): Show | 4 | HG02109.hp1 HG02451.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.-14-3204A>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48342997 | ||||||
chr2:48343109
|
T | G | 1 | a0001c0004t0002g0022 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-14-3092T>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48343109 | ||||||
chr2:48343161
|
C | T | 1 | a0001c0001t0001g0071 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-14-3040C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48343161 | ||||||
chr2:48343180
|
C | T | 2 | a0001c0002t0002g0285a0001c0002t0002g0314 | 2 | HG00621.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.-14-3021C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48343180 | ||||||
chr2:48343239
|
T | A | 1 | a0001c0001t0001g0125 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-14-2962T>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48343239 | ||||||
chr2:48343369
|
G | T | 130 | a0001c0001t0001g0130a0001c0001t0001g0202a0001c0001t0001g0212others(127): Show | 132 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.-14-2832G>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48343369 | ||||||
chr2:48343761
|
T | TA | 32 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0002g0023others(29): Show | 36 | HG01069.hp1 HG01123.hp1 HG01192.hp2 others(33): Show |
intron_variant | MODIFIER | c.-14-2427dupA | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 48343761 | |||||
chr2:48343937
|
T | G | 1 | a0001c0002t0006g0242 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-14-2264T>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48343937 | ||||||
chr2:48343940
|
A | G | 2 | a0001c0001t0001g0068a0001c0001t0001g0085 | 2 | NA18941.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.-14-2261A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48343940 | ||||||
chr2:48343950
|
T | A | 1 | a0001c0004t0002g0022 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-14-2251T>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48343950 | ||||||
chr2:48344040
|
C | T | 1 | a0001c0001t0002g0040 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-14-2161C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48344040 | ||||||
chr2:48344044
|
A | G | 1 | a0001c0001t0001g0126 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-14-2157A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48344044 | ||||||
chr2:48344072
|
G | A | 1 | a0001c0001t0001g0228 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-14-2129G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48344072 | ||||||
chr2:48344277
|
C | T | 122 | a0001c0001t0001g0130a0001c0001t0001g0202a0001c0001t0001g0212others(119): Show | 124 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.-14-1924C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48344277 | ||||||
chr2:48344497
|
C | T | 30 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0002g0023others(27): Show | 34 | HG01069.hp1 HG01123.hp1 HG01192.hp2 others(31): Show |
intron_variant | MODIFIER | c.-14-1704C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48344497 | ||||||
chr2:48344685
|
A | T | 30 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0002g0023others(27): Show | 34 | HG01069.hp1 HG01123.hp1 HG01192.hp2 others(31): Show |
intron_variant | MODIFIER | c.-14-1516A>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48344685 | ||||||
chr2:48344712
|
T | A | 89 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0219others(86): Show | 91 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.-14-1489T>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48344712 | ||||||
chr2:48344778
|
G | A | 1 | a0001c0001t0001g0235 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-14-1423G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48344778 | ||||||
chr2:48344779
|
G | T | 1 | a0001c0001t0001g0140 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-14-1422G>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48344779 | ||||||
chr2:48344840
|
A | AC | 39 | a0001c0001t0001g0080a0001c0001t0001g0086a0001c0001t0001g0090others(36): Show | 40 | HG00099.hp2 HG00621.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.-14-1349dupC | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 48344840 | |||||
chr2:48344840
|
A | ACC | 19 | a0001c0001t0001g0013a0001c0001t0001g0054a0001c0001t0001g0059others(16): Show | 19 | HG00642.hp2 HG01081.hp1 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.-14-1350_-14-1349d others(4): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 48344840 | |||||
chr2:48344840
|
AC | A | 42 | a0001c0001t0001g0071a0001c0001t0001g0093a0001c0001t0001g0116others(39): Show | 46 | HG00408.hp2 HG00738.hp2 HG01069.hp1 others(43): Show |
intron_variant | MODIFIER | c.-14-1349delC | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 48344840 | |||||
chr2:48344840
|
ACC | A | 99 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0219others(96): Show | 101 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.-14-1350_-14-1349d others(4): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 48344840 | |||||
chr2:48344840
|
ACCC | A | 20 | a0001c0001t0001g0130a0001c0001t0001g0202a0001c0001t0001g0212others(17): Show | 20 | HG00099.hp1 HG00438.hp2 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.-14-1351_-14-1349d others(5): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 48344840 | |||||
chr2:48345201
|
T | C | 1 | a0001c0001t0001g0153 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-14-1000T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48345201 | ||||||
chr2:48345278
|
T | C | 132 | a0001c0001t0001g0130a0001c0001t0001g0202a0001c0001t0001g0212others(129): Show | 134 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.-14-923T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48345278 | ||||||
chr2:48345361
|
G | C | 21 | a0001c0001t0001g0130a0001c0001t0001g0202a0001c0001t0001g0212others(18): Show | 21 | HG00099.hp1 HG00438.hp2 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.-14-840G>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48345361 | ||||||
chr2:48345514
|
T | G | 35 | a0001c0001t0001g0130a0001c0001t0001g0202a0001c0001t0001g0212others(32): Show | 35 | HG00099.hp1 HG00438.hp2 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.-14-687T>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48345514 | ||||||
chr2:48345581
|
A | G | 30 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0002g0023others(27): Show | 34 | HG01069.hp1 HG01123.hp1 HG01192.hp2 others(31): Show |
intron_variant | MODIFIER | c.-14-620A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48345581 | ||||||
chr2:48345683
|
A | C | 132 | a0001c0001t0001g0130a0001c0001t0001g0202a0001c0001t0001g0212others(129): Show | 134 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.-14-518A>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48345683 | ||||||
chr2:48345770
|
A | G | 132 | a0001c0001t0001g0130a0001c0001t0001g0202a0001c0001t0001g0212others(129): Show | 134 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.-14-431A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48345770 | ||||||
chr2:48345842
|
A | G | 2 | a0001c0001t0001g0232a0001c0002t0002g0273 | 2 | HG00099.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.-14-359A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48345842 | ||||||
chr2:48345909
|
G | A | 30 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0002g0023others(27): Show | 34 | HG01069.hp1 HG01123.hp1 HG01192.hp2 others(31): Show |
intron_variant | MODIFIER | c.-14-292G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48345909 | ||||||
chr2:48345936
|
A | G | 4 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0188others(1): Show | 4 | HG02683.hp2 HG03669.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.-14-265A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48345936 | ||||||
chr2:48346062
|
C | G | 1 | a0001c0001t0018g0106 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-14-139C>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48346062 | ||||||
chr2:48346145
|
T | C | 1 | a0001c0004t0003g0045 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-14-56T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 2/6 | chr2 | 48346145 | ||||||
chr2:48346756
|
G | C | 10 | a0001c0001t0001g0050a0001c0001t0001g0107a0001c0001t0001g0142others(7): Show | 10 | HG00639.hp1 HG01123.hp2 HG01346.hp1 others(7): Show |
splice_region_variant&intron_variant | LOW | c.537+5G>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48346756 | ||||||
chr2:48346767
|
C | T | 6 | a0001c0003t0001g0134a0001c0003t0001g0135a0001c0003t0001g0137others(3): Show | 6 | HG01884.hp2 HG02109.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.537+16C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48346767 | ||||||
chr2:48346845
|
T | G | 1 | a0001c0001t0001g0221 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.537+94T>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48346845 | ||||||
chr2:48346896
|
C | G | 1 | a0001c0002t0002g0259 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.537+145C>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48346896 | ||||||
chr2:48347025
|
T | C | 135 | a0001c0001t0001g0014a0001c0001t0001g0069a0001c0001t0001g0090others(132): Show | 137 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.537+274T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48347025 | ||||||
chr2:48347172
|
C | A | 2 | a0001c0001t0002g0031a0001c0001t0002g0035 | 2 | HG01891.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.537+421C>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48347172 | ||||||
chr2:48347187
|
G | T | 2 | a0001c0001t0002g0031a0001c0001t0002g0035 | 2 | HG01891.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.537+436G>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48347187 | ||||||
chr2:48347220
|
C | CT | 70 | a0001c0001t0001g0050a0001c0001t0001g0057a0001c0001t0001g0070others(67): Show | 71 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.537+493dupT | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 48347220 | |||||
chr2:48347220
|
C | CTT | 23 | a0001c0001t0001g0130a0001c0001t0001g0202a0001c0001t0001g0215others(20): Show | 23 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(20): Show |
intron_variant | MODIFIER | c.537+492_537+493dup others(2): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 48347220 | |||||
chr2:48347220
|
C | CTTT | 7 | a0001c0001t0001g0212a0001c0001t0001g0222a0001c0001t0001g0223others(4): Show | 7 | HG01358.hp1 HG02056.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.537+491_537+493dup others(3): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 48347220 | |||||
chr2:48347220
|
CT | C | 31 | a0001c0001t0001g0131a0001c0001t0001g0203a0001c0001t0002g0017others(28): Show | 35 | HG00738.hp1 HG01069.hp1 HG01123.hp1 others(32): Show |
intron_variant | MODIFIER | c.537+493delT | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 48347220 | |||||
chr2:48347232
|
T | G | 19 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0002g0031others(16): Show | 21 | HG01069.hp1 HG01123.hp1 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.537+481T>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48347232 | ||||||
chr2:48347253
|
G | A | 1 | a0001c0002t0002g0265 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.537+502G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48347253 | ||||||
chr2:48347288
|
G | C | 1 | a0001c0001t0001g0140 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.537+537G>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48347288 | ||||||
chr2:48347290
|
G | A | 8 | a0001c0002t0006g0236a0001c0002t0006g0238a0001c0002t0006g0239others(5): Show | 8 | HG00280.hp1 HG01070.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.537+539G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48347290 | ||||||
chr2:48347352
|
A | C | 1 | a0001c0002t0002g0264 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.537+601A>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48347352 | ||||||
chr2:48347381
|
C | T | 30 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0002g0023others(27): Show | 34 | HG01069.hp1 HG01123.hp1 HG01192.hp2 others(31): Show |
intron_variant | MODIFIER | c.537+630C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48347381 | ||||||
chr2:48347533
|
T | TTG | 21 | a0001c0001t0001g0051a0001c0001t0001g0108a0001c0001t0001g0109others(18): Show | 21 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(18): Show |
intron_variant | MODIFIER | c.537+808_537+809dup others(2): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 48347533 | |||||
chr2:48347533
|
T | TTGTG | 28 | a0001c0001t0001g0130a0001c0001t0001g0202a0001c0001t0001g0212others(25): Show | 28 | HG00099.hp1 HG00438.hp2 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.537+806_537+809dup others(4): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 48347533 | |||||
chr2:48347533
|
T | TTGTGTG | 91 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0219others(88): Show | 93 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.537+804_537+809dup others(6): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 48347533 | |||||
chr2:48347533
|
T | TTGTGTGT others(1): Show |
7 | a0001c0002t0002g0265a0001c0002t0002g0295a0001c0002t0002g0318others(4): Show | 7 | HG01106.hp2 HG01109.hp1 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.537+802_537+809dup others(8): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 48347533 | |||||
chr2:48347902
|
T | C | 2 | a0001c0002t0002g0264a0001c0002t0002g0290 | 2 | NA18954.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.537+1151T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48347902 | ||||||
chr2:48347936
|
T | A | 1 | a0001c0002t0002g0288 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.537+1185T>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48347936 | ||||||
chr2:48348236
|
C | T | 1 | a0001c0002t0002g0263 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.537+1485C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48348236 | ||||||
chr2:48348346
|
A | C | 8 | a0001c0002t0006g0236a0001c0002t0006g0238a0001c0002t0006g0239others(5): Show | 8 | HG00280.hp1 HG01070.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.537+1595A>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48348346 | ||||||
chr2:48348427
|
A | G | 1 | a0001c0001t0001g0167 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.537+1676A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48348427 | ||||||
chr2:48348523
|
A | T | 161 | a0001c0001t0001g0130a0001c0001t0001g0202a0001c0001t0001g0212others(158): Show | 167 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.537+1772A>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48348523 | ||||||
chr2:48348559
|
G | A | 88 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0219others(85): Show | 90 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.537+1808G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48348559 | ||||||
chr2:48348628
|
G | C | 102 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0219others(99): Show | 104 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.537+1877G>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48348628 | ||||||
chr2:48348636
|
G | A | 30 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0002g0023others(27): Show | 34 | HG01069.hp1 HG01123.hp1 HG01192.hp2 others(31): Show |
intron_variant | MODIFIER | c.537+1885G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48348636 | ||||||
chr2:48348649
|
T | C | 1 | a0001c0001t0001g0015 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.537+1898T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48348649 | ||||||
chr2:48348708
|
C | G | 8 | a0001c0002t0006g0236a0001c0002t0006g0238a0001c0002t0006g0239others(5): Show | 8 | HG00280.hp1 HG01070.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.537+1957C>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48348708 | ||||||
chr2:48348760
|
T | G | 1 | a0001c0001t0001g0015 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.537+2009T>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48348760 | ||||||
chr2:48348785
|
A | G | 1 | a0001c0001t0001g0167 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.537+2034A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48348785 | ||||||
chr2:48348791
|
G | C | 3 | a0001c0001t0001g0155a0001c0001t0001g0158a0001c0001t0001g0198 | 3 | HG02717.hp1 HG03225.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.537+2040G>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48348791 | ||||||
chr2:48349312
|
C | T | 1 | a0001c0002t0006g0242 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.537+2561C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48349312 | ||||||
chr2:48349324
|
A | G | 6 | a0001c0001t0002g0017a0001c0001t0002g0033a0001c0001t0002g0039others(3): Show | 6 | HG01069.hp1 HG02145.hp2 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.537+2573A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48349324 | ||||||
chr2:48349409
|
C | T | 107 | a0001c0001t0001g0213a0001c0001t0001g0230a0001c0001t0001g0322others(104): Show | 109 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.537+2658C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48349409 | ||||||
chr2:48349522
|
C | T | 138 | a0001c0001t0001g0213a0001c0001t0001g0230a0001c0001t0001g0322others(135): Show | 144 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.537+2771C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48349522 | ||||||
chr2:48349548
|
C | T | 108 | a0001c0001t0001g0213a0001c0001t0001g0230a0001c0001t0001g0322others(105): Show | 110 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.537+2797C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48349548 | ||||||
chr2:48349610
|
C | T | 1 | a0001c0001t0001g0121 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.537+2859C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48349610 | ||||||
chr2:48349681
|
A | G | 5 | a0001c0001t0001g0105a0001c0001t0001g0162a0001c0001t0001g0165others(2): Show | 5 | HG00639.hp2 HG01261.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.537+2930A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48349681 | ||||||
chr2:48349830
|
C | T | 1 | a0001c0001t0014g0161 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.537+3079C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48349830 | ||||||
chr2:48349835
|
A | G | 1 | a0001c0001t0014g0161 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.537+3084A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48349835 | ||||||
chr2:48349840
|
G | A | 2 | a0001c0001t0001g0107a0001c0001t0001g0253 | 2 | HG00639.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.537+3089G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48349840 | ||||||
chr2:48349964
|
A | G | 100 | a0001c0001t0001g0213a0001c0001t0001g0230a0001c0001t0001g0322others(97): Show | 102 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.537+3213A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48349964 | ||||||
chr2:48350084
|
G | C | 2 | a0001c0002t0003g0249a0001c0002t0003g0250 | 2 | HG03225.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.537+3333G>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48350084 | ||||||
chr2:48350108
|
A | T | 1 | a0001c0001t0001g0144 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.537+3357A>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48350108 | ||||||
chr2:48350664
|
A | G | 2 | a0001c0001t0001g0213a0001c0001t0001g0230 | 2 | HG02602.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.537+3913A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48350664 | ||||||
chr2:48350758
|
C | G | 2 | a0001c0001t0001g0228a0001c0001t0001g0232 | 2 | HG00099.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.537+4007C>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48350758 | ||||||
chr2:48350987
|
A | G | 1 | a0001c0001t0005g0002 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.537+4236A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48350987 | ||||||
chr2:48351007
|
C | T | 2 | a0001c0002t0002g0296a0001c0002t0002g0312 | 2 | NA18991.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.537+4256C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48351007 | ||||||
chr2:48351191
|
G | A | 5 | a0001c0001t0001g0322a0001c0002t0002g0264a0001c0002t0002g0272others(2): Show | 5 | HG02132.hp2 HG02135.hp1 HG02155.hp1 others(2): Show |
intron_variant | MODIFIER | c.537+4440G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48351191 | ||||||
chr2:48351258
|
G | A | 11 | a0001c0001t0001g0142a0001c0001t0001g0157a0001c0001t0001g0163others(8): Show | 11 | HG02145.hp1 HG02809.hp1 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.537+4507G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48351258 | ||||||
chr2:48351317
|
G | T | 1 | a0001c0003t0001g0137 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.537+4566G>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48351317 | ||||||
chr2:48351500
|
G | A | 3 | a0001c0002t0003g0016a0001c0002t0003g0255a0001c0002t0003g0256 | 3 | HG02717.hp2 HG03209.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.537+4749G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48351500 | ||||||
chr2:48351660
|
G | A | 101 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0219others(98): Show | 103 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.537+4909G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48351660 | ||||||
chr2:48351783
|
C | G | 1 | a0001c0002t0003g0092 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.537+5032C>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48351783 | ||||||
chr2:48352049
|
T | TTTTGTGC others(8): Show |
1 | a0001c0002t0002g0302 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.537+5302_537+5303i others(17): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 48352049 | |||||
chr2:48352055
|
G | A | 1 | a0001c0002t0002g0302 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.537+5304G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48352055 | ||||||
chr2:48352055
|
G | GCTTCAGT others(8): Show |
108 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0219others(105): Show | 110 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.537+5313_537+5327d others(17): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 48352055 | |||||
chr2:48352220
|
G | C | 11 | a0001c0001t0002g0023a0001c0001t0005g0002a0001c0001t0005g0003others(8): Show | 13 | HG01433.hp2 HG01891.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.537+5469G>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48352220 | ||||||
chr2:48352303
|
C | T | 2 | a0001c0001t0001g0228a0001c0001t0001g0232 | 2 | HG00099.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.537+5552C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48352303 | ||||||
chr2:48352332
|
C | G | 4 | a0001c0001t0002g0031a0001c0001t0002g0035a0001c0001t0002g0040others(1): Show | 4 | HG01884.hp1 HG01891.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.537+5581C>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48352332 | ||||||
chr2:48352585
|
C | T | 2 | a0001c0001t0002g0031a0001c0001t0002g0035 | 2 | HG01891.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.537+5834C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48352585 | ||||||
chr2:48352639
|
G | A | 150 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0215others(147): Show | 156 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.537+5888G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48352639 | ||||||
chr2:48352647
|
A | T | 8 | a0001c0002t0006g0236a0001c0002t0006g0238a0001c0002t0006g0239others(5): Show | 8 | HG00280.hp1 HG01070.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.537+5896A>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48352647 | ||||||
chr2:48352655
|
C | T | 1 | a0001c0001t0001g0124 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.537+5904C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48352655 | ||||||
chr2:48352916
|
G | T | 1 | a0001c0002t0002g0271 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.538-6131G>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48352916 | ||||||
chr2:48353045
|
G | T | 1 | a0001c0003t0016g0136 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.538-6002G>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48353045 | ||||||
chr2:48353066
|
G | C | 5 | a0001c0001t0001g0142a0001c0001t0001g0163a0001c0001t0001g0189others(2): Show | 5 | HG02145.hp1 HG02809.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.538-5981G>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48353066 | ||||||
chr2:48353156
|
A | T | 1 | a0001c0001t0001g0121 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.538-5891A>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48353156 | ||||||
chr2:48353157
|
T | A | 1 | a0001c0001t0001g0121 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.538-5890T>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48353157 | ||||||
chr2:48353221
|
C | A | 1 | a0001c0002t0002g0294 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.538-5826C>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48353221 | ||||||
chr2:48353378
|
G | A | 1 | a0001c0002t0002g0307 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.538-5669G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48353378 | ||||||
chr2:48353416
|
A | G | 6 | a0001c0002t0002g0010a0001c0002t0002g0286a0001c0002t0002g0316others(3): Show | 7 | HG02056.hp1 HG02135.hp2 NA18950.hp2 others(4): Show |
intron_variant | MODIFIER | c.538-5631A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48353416 | ||||||
chr2:48353506
|
T | G | 113 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0215others(110): Show | 115 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.538-5541T>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48353506 | ||||||
chr2:48353552
|
CTG | C | 33 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0080others(30): Show | 34 | HG00408.hp1 HG00438.hp1 HG00621.hp1 others(31): Show |
intron_variant | MODIFIER | c.538-5442_538-5441d others(4): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 48353552 | |||||
chr2:48353552
|
CTGTG | C | 53 | a0001c0001t0001g0051a0001c0001t0001g0059a0001c0001t0001g0065others(50): Show | 53 | HG00408.hp2 HG00558.hp1 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.538-5444_538-5441d others(6): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 48353552 | |||||
chr2:48353552
|
CTGTGTG | C | 107 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0050others(104): Show | 114 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.538-5446_538-5441d others(8): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 48353552 | |||||
chr2:48353552
|
CTGTGTGT others(1): Show |
C | 55 | a0001c0001t0001g0013a0001c0001t0001g0052a0001c0001t0001g0054others(52): Show | 55 | HG00280.hp2 HG00639.hp2 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.538-5448_538-5441d others(10): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 48353552 | |||||
chr2:48353552
|
CTGTGTGT others(3): Show |
C | 35 | a0001c0001t0001g0077a0001c0001t0001g0094a0001c0001t0001g0162others(32): Show | 37 | HG01069.hp1 HG01109.hp2 HG01123.hp1 others(34): Show |
intron_variant | MODIFIER | c.538-5450_538-5441d others(12): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 48353552 | |||||
chr2:48353552
|
CTGTGTGT others(5): Show |
C | 13 | a0001c0001t0001g0015a0001c0001t0001g0093a0001c0001t0001g0098others(10): Show | 13 | HG00099.hp2 HG00738.hp2 HG01346.hp2 others(10): Show |
intron_variant | MODIFIER | c.538-5452_538-5441d others(14): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 48353552 | |||||
chr2:48353552
|
CTGTGTGT others(7): Show |
C | 3 | a0001c0001t0001g0158a0001c0002t0002g0259a0001c0003t0007g0011 | 3 | HG02717.hp1 HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.538-5454_538-5441d others(16): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 48353552 | |||||
chr2:48353552
|
CTGTGTGT others(9): Show |
C | 9 | a0001c0002t0006g0236a0001c0002t0006g0238a0001c0002t0006g0239others(6): Show | 9 | HG00280.hp1 HG01070.hp2 HG01081.hp2 others(6): Show |
intron_variant | MODIFIER | c.538-5456_538-5441d others(18): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 48353552 | |||||
chr2:48353552
|
CTGTGTGT others(15): Show |
C | 1 | a0001c0001t0001g0061 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.538-5462_538-5441d others(24): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 48353552 | |||||
chr2:48353552
|
CTGTGTGT others(19): Show |
C | 1 | a0001c0001t0001g0231 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.538-5466_538-5441d others(28): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 48353552 | |||||
chr2:48353605
|
T | A | 27 | a0001c0001t0002g0018a0001c0001t0002g0031a0001c0001t0002g0035others(24): Show | 30 | HG00280.hp1 HG01070.hp2 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.538-5442T>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48353605 | ||||||
chr2:48353605
|
T | TGA | 5 | a0001c0001t0002g0023a0001c0001t0005g0003a0001c0001t0005g0027others(2): Show | 6 | HG01433.hp2 HG01891.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.538-5441_538-5440d others(4): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 48353605 | |||||
chr2:48353619
|
G | C | 1 | a0001c0001t0004g0082 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.538-5428G>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48353619 | ||||||
chr2:48353855
|
T | A | 1 | a0001c0001t0002g0039 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.538-5192T>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48353855 | ||||||
chr2:48354219
|
C | G | 1 | a0001c0002t0003g0255 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.538-4828C>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48354219 | ||||||
chr2:48354335
|
C | A | 1 | a0001c0001t0014g0161 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.538-4712C>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48354335 | ||||||
chr2:48354339
|
C | T | 2 | a0001c0001t0001g0228a0001c0001t0001g0232 | 2 | HG00099.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.538-4708C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48354339 | ||||||
chr2:48354367
|
T | C | 206 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0052others(203): Show | 213 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.538-4680T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48354367 | ||||||
chr2:48354367
|
T | G | 7 | a0001c0001t0001g0007a0001c0001t0001g0051a0001c0001t0001g0145others(4): Show | 8 | HG02109.hp2 HG02280.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.538-4680T>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48354367 | ||||||
chr2:48354585
|
C | T | 1 | a0001c0001t0001g0227 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.538-4462C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48354585 | ||||||
chr2:48354593
|
C | T | 1 | a0001c0001t0001g0170 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.538-4454C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48354593 | ||||||
chr2:48354649
|
A | G | 2 | a0001c0001t0001g0014a0001c0001t0004g0006 | 3 | NA18960.hp1 NA18998.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.538-4398A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48354649 | ||||||
chr2:48354737
|
T | C | 150 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0215others(147): Show | 156 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.538-4310T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48354737 | ||||||
chr2:48354805
|
A | G | 1 | a0001c0001t0001g0140 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.538-4242A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48354805 | ||||||
chr2:48354999
|
G | A | 2 | a0001c0002t0003g0016a0001c0002t0003g0256 | 2 | HG02717.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.538-4048G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48354999 | ||||||
chr2:48355159
|
A | G | 11 | a0001c0001t0002g0023a0001c0001t0005g0002a0001c0001t0005g0003others(8): Show | 13 | HG01433.hp2 HG01891.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.538-3888A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48355159 | ||||||
chr2:48355171
|
G | A | 1 | a0001c0002t0002g0269 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.538-3876G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48355171 | ||||||
chr2:48355189
|
G | T | 1 | a0001c0002t0002g0326 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.538-3858G>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48355189 | ||||||
chr2:48355201
|
T | C | 1 | a0001c0001t0001g0130 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.538-3846T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48355201 | ||||||
chr2:48355401
|
T | C | 10 | a0001c0002t0003g0016a0001c0002t0003g0245a0001c0002t0003g0247others(7): Show | 10 | HG00738.hp2 HG01109.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.538-3646T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48355401 | ||||||
chr2:48355430
|
C | T | 1 | a0001c0001t0001g0179 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.538-3617C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48355430 | ||||||
chr2:48355511
|
G | A | 88 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0219others(85): Show | 90 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.538-3536G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48355511 | ||||||
chr2:48355566
|
T | A | 3 | a0001c0001t0001g0204a0001c0003t0007g0011a0001c0003t0007g0012 | 3 | HG01106.hp1 HG02055.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.538-3481T>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48355566 | ||||||
chr2:48355606
|
G | A | 98 | a0001c0001t0001g0213a0001c0001t0001g0230a0001c0001t0001g0322others(95): Show | 100 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.538-3441G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48355606 | ||||||
chr2:48355815
|
C | G | 11 | a0001c0001t0002g0023a0001c0001t0005g0002a0001c0001t0005g0003others(8): Show | 13 | HG01433.hp2 HG01891.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.538-3232C>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48355815 | ||||||
chr2:48355818
|
TATC | T | 3 | a0001c0002t0003g0249a0001c0002t0003g0250a0001c0002t0003g0251 | 3 | HG03225.hp2 HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.538-3223_538-3221d others(5): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 48355818 | |||||
chr2:48356283
|
A | G | 1 | a0001c0001t0001g0157 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.538-2764A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48356283 | ||||||
chr2:48356324
|
C | T | 6 | a0001c0003t0001g0134a0001c0003t0001g0135a0001c0003t0001g0137others(3): Show | 6 | HG01884.hp2 HG02109.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.538-2723C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48356324 | ||||||
chr2:48356325
|
C | A | 1 | a0001c0002t0002g0274 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.538-2722C>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48356325 | ||||||
chr2:48356406
|
A | G | 150 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0215others(147): Show | 156 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.538-2641A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48356406 | ||||||
chr2:48356460
|
C | T | 86 | a0001c0001t0001g0213a0001c0001t0001g0230a0001c0001t0001g0322others(83): Show | 88 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.538-2587C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48356460 | ||||||
chr2:48356582
|
AATT | A | 98 | a0001c0001t0001g0213a0001c0001t0001g0230a0001c0001t0001g0322others(95): Show | 100 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.538-2461_538-2459d others(5): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 48356582 | |||||
chr2:48356703
|
A | C | 1 | a0001c0002t0002g0319 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.538-2344A>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48356703 | ||||||
chr2:48356852
|
C | T | 41 | a0001c0001t0001g0215a0001c0001t0001g0216a0001c0001t0001g0218others(38): Show | 45 | HG00099.hp1 HG01069.hp1 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.538-2195C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48356852 | ||||||
chr2:48356855
|
C | T | 1 | a0001c0001t0001g0163 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.538-2192C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48356855 | ||||||
chr2:48357020
|
A | G | 8 | a0001c0002t0006g0236a0001c0002t0006g0238a0001c0002t0006g0239others(5): Show | 8 | HG00280.hp1 HG01070.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.538-2027A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48357020 | ||||||
chr2:48357163
|
G | A | 149 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0215others(146): Show | 155 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.538-1884G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48357163 | ||||||
chr2:48357335
|
A | G | 98 | a0001c0001t0001g0213a0001c0001t0001g0230a0001c0001t0001g0322others(95): Show | 100 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.538-1712A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48357335 | ||||||
chr2:48357436
|
C | G | 120 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0215others(117): Show | 122 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.538-1611C>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48357436 | ||||||
chr2:48357453
|
G | C | 1 | a0001c0001t0001g0157 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.538-1594G>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48357453 | ||||||
chr2:48357504
|
C | CT | 8 | a0001c0002t0006g0236a0001c0002t0006g0238a0001c0002t0006g0239others(5): Show | 8 | HG00280.hp1 HG01070.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.538-1530dupT | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 48357504 | |||||
chr2:48357687
|
C | T | 106 | a0001c0001t0001g0213a0001c0001t0001g0230a0001c0001t0001g0322others(103): Show | 108 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.538-1360C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48357687 | ||||||
chr2:48357705
|
G | A | 1 | a0001c0002t0002g0294 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.538-1342G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48357705 | ||||||
chr2:48357802
|
T | C | 10 | a0001c0002t0003g0016a0001c0002t0003g0245a0001c0002t0003g0247others(7): Show | 10 | HG00738.hp2 HG01109.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.538-1245T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48357802 | ||||||
chr2:48357862
|
GA | G | 7 | a0001c0001t0001g0055a0001c0001t0001g0121a0001c0001t0001g0160others(4): Show | 7 | HG02738.hp2 HG02965.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.538-1166delA | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 48357862 | |||||
chr2:48357862
|
GAA | G | 29 | a0001c0001t0001g0215a0001c0001t0001g0216a0001c0001t0001g0218others(26): Show | 31 | HG00099.hp1 HG01069.hp1 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.538-1167_538-1166d others(4): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 48357862 | |||||
chr2:48357862
|
GAAA | G | 109 | a0001c0001t0001g0213a0001c0001t0001g0230a0001c0001t0001g0322others(106): Show | 113 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(110): Show |
intron_variant | MODIFIER | c.538-1168_538-1166d others(5): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 48357862 | |||||
chr2:48357862
|
GAAAA | G | 8 | a0001c0002t0006g0236a0001c0002t0006g0238a0001c0002t0006g0239others(5): Show | 8 | HG00280.hp1 HG01070.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.538-1169_538-1166d others(6): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 48357862 | |||||
chr2:48357906
|
A | G | 8 | a0001c0002t0006g0236a0001c0002t0006g0238a0001c0002t0006g0239others(5): Show | 8 | HG00280.hp1 HG01070.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.538-1141A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48357906 | ||||||
chr2:48357958
|
A | G | 1 | a0001c0002t0002g0037 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.538-1089A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48357958 | ||||||
chr2:48358019
|
A | G | 98 | a0001c0001t0001g0213a0001c0001t0001g0230a0001c0001t0001g0322others(95): Show | 100 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.538-1028A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48358019 | ||||||
chr2:48358036
|
T | G | 4 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205others(1): Show | 4 | HG00738.hp1 HG01106.hp1 HG01928.hp1 others(1): Show |
intron_variant | MODIFIER | c.538-1011T>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48358036 | ||||||
chr2:48358312
|
G | A | 3 | a0001c0002t0002g0265a0001c0002t0002g0332a0001c0002t0002g0333 | 3 | HG01106.hp2 HG01109.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.538-735G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48358312 | ||||||
chr2:48358367
|
C | T | 107 | a0001c0001t0001g0213a0001c0001t0001g0230a0001c0001t0001g0322others(104): Show | 109 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.538-680C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48358367 | ||||||
chr2:48358443
|
A | G | 10 | a0001c0001t0001g0007a0001c0001t0001g0051a0001c0001t0001g0145others(7): Show | 11 | HG02109.hp2 HG02280.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.538-604A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48358443 | ||||||
chr2:48358449
|
T | C | 2 | a0001c0001t0001g0096a0001c0001t0001g0097 | 2 | HG02970.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.538-598T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48358449 | ||||||
chr2:48358499
|
C | T | 1 | a0001c0001t0001g0216 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.538-548C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48358499 | ||||||
chr2:48358673
|
A | G | 5 | a0001c0002t0003g0245a0001c0002t0003g0247a0001c0002t0003g0248others(2): Show | 5 | HG00738.hp2 HG01109.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.538-374A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48358673 | ||||||
chr2:48358824
|
A | C | 41 | a0001c0001t0001g0215a0001c0001t0001g0216a0001c0001t0001g0218others(38): Show | 45 | HG00099.hp1 HG01069.hp1 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.538-223A>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48358824 | ||||||
chr2:48358880
|
AATCC | A | 146 | a0001c0001t0001g0215a0001c0001t0001g0216a0001c0001t0001g0218others(143): Show | 152 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.538-166_538-163del others(4): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48358880 | ||||||
chr2:48358883
|
C | A | 1 | a0001c0001t0001g0090 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.538-164C>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48358883 | ||||||
chr2:48358884
|
C | T | 1 | a0001c0001t0001g0192 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.538-163C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48358884 | ||||||
chr2:48358895
|
C | G | 116 | a0001c0001t0001g0215a0001c0001t0001g0216a0001c0001t0001g0218others(113): Show | 118 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.538-152C>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48358895 | ||||||
chr2:48358926
|
C | T | 11 | a0001c0002t0003g0016a0001c0002t0003g0245a0001c0002t0003g0247others(8): Show | 11 | HG00738.hp2 HG01109.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.538-121C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48358926 | ||||||
chr2:48359001
|
G | C | 1 | a0001c0002t0002g0293 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.538-46G>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 3/6 | chr2 | 48359001 | ||||||
chr2:48359225
|
G | A | 1 | a0001c0002t0002g0294 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.638+78G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 4/6 | chr2 | 48359225 | ||||||
chr2:48359226
|
G | A | 4 | a0001c0001t0001g0111a0001c0001t0001g0113a0001c0001t0001g0171others(1): Show | 4 | HG01099.hp1 HG01175.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.638+79G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 4/6 | chr2 | 48359226 | ||||||
chr2:48359264
|
T | C | 3 | a0001c0002t0003g0016a0001c0002t0003g0255a0001c0002t0003g0256 | 3 | HG02717.hp2 HG03209.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.638+117T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 4/6 | chr2 | 48359264 | ||||||
chr2:48359270
|
ATTTAGTT | A | 105 | a0001c0001t0001g0322a0001c0002t0002g0009a0001c0002t0002g0010others(102): Show | 107 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.638+141_638+147del others(7): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 48359270 | |||||
chr2:48359355
|
G | C | 1 | a0001c0001t0001g0129 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.638+208G>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 4/6 | chr2 | 48359355 | ||||||
chr2:48359358
|
A | T | 1 | a0001c0002t0002g0324 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.638+211A>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 4/6 | chr2 | 48359358 | ||||||
chr2:48359403
|
C | T | 1 | a0001c0001t0001g0212 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.638+256C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 4/6 | chr2 | 48359403 | ||||||
chr2:48359499
|
G | A | 1 | a0001c0001t0001g0065 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.638+352G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 4/6 | chr2 | 48359499 | ||||||
chr2:48359549
|
C | T | 1 | a0001c0002t0003g0256 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.638+402C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 4/6 | chr2 | 48359549 | ||||||
chr2:48359563
|
G | A | 1 | a0001c0001t0001g0199 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.638+416G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 4/6 | chr2 | 48359563 | ||||||
chr2:48359574
|
G | A | 8 | a0001c0002t0006g0236a0001c0002t0006g0238a0001c0002t0006g0239others(5): Show | 8 | HG00280.hp1 HG01070.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.638+427G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 4/6 | chr2 | 48359574 | ||||||
chr2:48359586
|
C | A | 7 | a0001c0003t0001g0134a0001c0003t0001g0135a0001c0003t0001g0137others(4): Show | 7 | HG01884.hp2 HG02109.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.638+439C>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 4/6 | chr2 | 48359586 | ||||||
chr2:48359597
|
TTTTTCTT others(3): Show |
T | 2 | a0001c0003t0016g0136a0002c0006t0001g0064 | 2 | HG03130.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.638+470_638+479del others(10): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 48359597 | |||||
chr2:48359622
|
C | CTTTTT | 94 | a0001c0001t0001g0322a0001c0002t0002g0009a0001c0002t0002g0010others(91): Show | 96 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.638+478_638+482dup others(5): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 48359622 | |||||
chr2:48359622
|
C | T | 49 | a0001c0001t0001g0215a0001c0001t0001g0216a0001c0001t0001g0218others(46): Show | 53 | HG00099.hp1 HG00280.hp1 HG01069.hp1 others(50): Show |
intron_variant | MODIFIER | c.638+475C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 4/6 | chr2 | 48359622 | ||||||
chr2:48359925
|
T | A | 1 | a0001c0001t0001g0178 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.638+778T>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 4/6 | chr2 | 48359925 | ||||||
chr2:48360015
|
A | G | 1 | a0001c0001t0001g0124 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.638+868A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 4/6 | chr2 | 48360015 | ||||||
chr2:48360059
|
A | G | 106 | a0001c0001t0001g0214a0001c0001t0001g0219a0001c0002t0002g0009others(103): Show | 108 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.638+912A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 4/6 | chr2 | 48360059 | ||||||
chr2:48360200
|
C | G | 1 | a0001c0001t0002g0023 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.638+1053C>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 4/6 | chr2 | 48360200 | ||||||
chr2:48360547
|
C | G | 44 | a0001c0001t0001g0155a0001c0001t0001g0158a0001c0001t0001g0198others(41): Show | 48 | HG00099.hp1 HG01069.hp1 HG01069.hp2 others(45): Show |
intron_variant | MODIFIER | c.638+1400C>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 4/6 | chr2 | 48360547 | ||||||
chr2:48360602
|
A | G | 85 | a0001c0001t0001g0214a0001c0001t0001g0219a0001c0002t0002g0009others(82): Show | 87 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.638+1455A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 4/6 | chr2 | 48360602 | ||||||
chr2:48360680
|
A | G | 13 | a0001c0002t0003g0016a0001c0002t0003g0245a0001c0002t0003g0247others(10): Show | 13 | HG00738.hp2 HG01109.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.638+1533A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 4/6 | chr2 | 48360680 | ||||||
chr2:48360776
|
C | T | 1 | a0001c0001t0005g0030 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.638+1629C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 4/6 | chr2 | 48360776 | ||||||
chr2:48360790
|
G | GT | 16 | a0001c0001t0001g0116a0001c0001t0001g0121a0001c0001t0001g0177others(13): Show | 16 | HG00408.hp2 HG00438.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.638+1658dupT | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 48360790 | |||||
chr2:48360824
|
A | T | 32 | a0001c0001t0001g0099a0001c0001t0001g0102a0001c0001t0001g0109others(29): Show | 32 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.638+1677A>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 4/6 | chr2 | 48360824 | ||||||
chr2:48360918
|
G | A | 8 | a0001c0002t0003g0245a0001c0002t0003g0247a0001c0002t0003g0248others(5): Show | 8 | HG00738.hp2 HG01109.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.639-1725G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 4/6 | chr2 | 48360918 | ||||||
chr2:48361013
|
CA | C | 146 | a0001c0001t0001g0215a0001c0001t0001g0216a0001c0001t0001g0218others(143): Show | 152 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.639-1616delA | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | 48361013 | |||||
chr2:48361058
|
G | C | 146 | a0001c0001t0001g0215a0001c0001t0001g0216a0001c0001t0001g0218others(143): Show | 152 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.639-1585G>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 4/6 | chr2 | 48361058 | ||||||
chr2:48361128
|
A | C | 1 | a0001c0001t0001g0163 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.639-1515A>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 4/6 | chr2 | 48361128 | ||||||
chr2:48361416
|
G | A | 3 | a0001c0002t0003g0016a0001c0002t0003g0255a0001c0002t0003g0256 | 3 | HG02717.hp2 HG03209.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.639-1227G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 4/6 | chr2 | 48361416 | ||||||
chr2:48361438
|
G | A | 10 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0003t0001g0134others(7): Show | 10 | HG01074.hp1 HG01884.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.639-1205G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 4/6 | chr2 | 48361438 | ||||||
chr2:48361826
|
A | C | 1 | a0001c0003t0001g0138 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.639-817A>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 4/6 | chr2 | 48361826 | ||||||
chr2:48361841
|
A | G | 1 | a0001c0002t0003g0256 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.639-802A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 4/6 | chr2 | 48361841 | ||||||
chr2:48362027
|
A | C | 150 | a0001c0001t0001g0173a0001c0001t0001g0214a0001c0001t0001g0215others(147): Show | 156 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.639-616A>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 4/6 | chr2 | 48362027 | ||||||
chr2:48362165
|
C | A | 1 | a0001c0001t0001g0217 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.639-478C>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 4/6 | chr2 | 48362165 | ||||||
chr2:48362259
|
A | G | 1 | a0001c0002t0002g0270 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.639-384A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 4/6 | chr2 | 48362259 | ||||||
chr2:48362287
|
G | C | 1 | a0001c0002t0002g0257 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.639-356G>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 4/6 | chr2 | 48362287 | ||||||
chr2:48362511
|
G | C | 1 | a0001c0002t0003g0092 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.639-132G>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 4/6 | chr2 | 48362511 | ||||||
chr2:48362544
|
G | A | 17 | a0001c0001t0001g0013a0001c0001t0001g0100a0001c0001t0001g0103others(14): Show | 17 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(14): Show |
intron_variant | MODIFIER | c.639-99G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 4/6 | chr2 | 48362544 | ||||||
chr2:48362570
|
C | A | 1 | a0001c0002t0002g0294 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.639-73C>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 4/6 | chr2 | 48362570 | ||||||
chr2:48362782
|
G | T | 1 | a0001c0001t0001g0108 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.703+75G>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48362782 | ||||||
chr2:48362790
|
C | A | 1 | a0001c0001t0001g0094 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.703+83C>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48362790 | ||||||
chr2:48362852
|
T | C | 1 | a0001c0001t0014g0161 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.703+145T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48362852 | ||||||
chr2:48362879
|
T | A | 1 | a0001c0003t0001g0138 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.703+172T>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48362879 | ||||||
chr2:48363028
|
G | A | 2 | a0001c0002t0002g0278a0001c0002t0002g0287 | 2 | HG03834.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.703+321G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48363028 | ||||||
chr2:48363074
|
C | T | 1 | a0001c0001t0001g0104 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.703+367C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48363074 | ||||||
chr2:48363131
|
T | C | 293 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0013others(290): Show | 301 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.703+424T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48363131 | ||||||
chr2:48363210
|
G | T | 2 | a0001c0001t0001g0122a0001c0001t0020g0117 | 2 | HG01952.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.703+503G>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48363210 | ||||||
chr2:48363238
|
G | A | 1 | a0001c0001t0004g0056 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.703+531G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48363238 | ||||||
chr2:48363385
|
AG | A | 38 | a0001c0001t0001g0099a0001c0001t0001g0102a0001c0001t0001g0109others(35): Show | 38 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.703+679delG | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48363385 | ||||||
chr2:48363423
|
T | C | 1 | a0001c0001t0001g0202 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.703+716T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48363423 | ||||||
chr2:48363987
|
A | G | 2 | a0001c0001t0001g0213a0001c0001t0001g0230 | 2 | HG02602.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.703+1280A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48363987 | ||||||
chr2:48364071
|
A | C | 1 | a0001c0001t0001g0133 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.703+1364A>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48364071 | ||||||
chr2:48364162
|
G | A | 1 | a0001c0001t0001g0054 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.703+1455G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48364162 | ||||||
chr2:48364290
|
C | G | 1 | a0001c0002t0002g0259 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.703+1583C>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48364290 | ||||||
chr2:48364468
|
G | A | 98 | a0001c0001t0018g0106a0001c0002t0002g0009a0001c0002t0002g0010others(95): Show | 100 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.703+1761G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48364468 | ||||||
chr2:48364553
|
C | T | 10 | a0001c0001t0005g0002a0001c0001t0005g0003a0001c0001t0005g0024others(7): Show | 12 | HG01433.hp2 HG01891.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.703+1846C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48364553 | ||||||
chr2:48364619
|
A | G | 1 | a0001c0001t0002g0040 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.703+1912A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48364619 | ||||||
chr2:48364637
|
G | C | 3 | a0001c0002t0002g0263a0001c0002t0002g0279a0001c0002t0002g0319 | 3 | NA18942.hp1 NA19000.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.703+1930G>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48364637 | ||||||
chr2:48364750
|
G | C | 40 | a0001c0001t0001g0215a0001c0001t0001g0216a0001c0001t0001g0218others(37): Show | 42 | HG00099.hp1 HG01069.hp1 HG01069.hp2 others(39): Show |
intron_variant | MODIFIER | c.703+2043G>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48364750 | ||||||
chr2:48364830
|
C | T | 1 | a0001c0001t0012g0044 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.703+2123C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48364830 | ||||||
chr2:48364871
|
C | A | 2 | a0001c0001t0001g0096a0001c0001t0001g0097 | 2 | HG02970.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.703+2164C>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48364871 | ||||||
chr2:48364947
|
T | C | 1 | a0001c0001t0002g0023 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.703+2240T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48364947 | ||||||
chr2:48365002
|
A | G | 1 | a0001c0001t0001g0166 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.703+2295A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48365002 | ||||||
chr2:48365010
|
T | C | 1 | a0001c0001t0004g0062 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.703+2303T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48365010 | ||||||
chr2:48365023
|
G | A | 2 | a0001c0002t0010g0244a0001c0002t0010g0246 | 2 | HG01109.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.703+2316G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48365023 | ||||||
chr2:48365028
|
T | G | 1 | a0001c0004t0003g0045 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.703+2321T>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48365028 | ||||||
chr2:48365063
|
T | C | 97 | a0001c0001t0018g0106a0001c0002t0002g0009a0001c0002t0002g0010others(94): Show | 99 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.703+2356T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48365063 | ||||||
chr2:48365085
|
G | A | 138 | a0001c0001t0001g0215a0001c0001t0001g0216a0001c0001t0001g0218others(135): Show | 142 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.703+2378G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48365085 | ||||||
chr2:48365102
|
C | T | 85 | a0001c0001t0018g0106a0001c0002t0002g0009a0001c0002t0002g0010others(82): Show | 87 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.703+2395C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48365102 | ||||||
chr2:48365430
|
T | C | 39 | a0001c0001t0001g0215a0001c0001t0001g0216a0001c0001t0001g0218others(36): Show | 41 | HG00099.hp1 HG01069.hp1 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.703+2723T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48365430 | ||||||
chr2:48365469
|
T | A | 1 | a0001c0001t0001g0198 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.703+2762T>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48365469 | ||||||
chr2:48365574
|
G | C | 1 | a0001c0001t0001g0254 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.703+2867G>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48365574 | ||||||
chr2:48365615
|
T | C | 13 | a0001c0001t0002g0017a0001c0001t0002g0033a0001c0001t0002g0039others(10): Show | 13 | HG01069.hp1 HG01167.hp2 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.703+2908T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48365615 | ||||||
chr2:48365627
|
A | G | 1 | a0001c0002t0002g0259 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.703+2920A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48365627 | ||||||
chr2:48365639
|
G | A | 1 | a0001c0003t0016g0136 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.703+2932G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48365639 | ||||||
chr2:48365658
|
T | C | 1 | a0001c0001t0001g0014 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.703+2951T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48365658 | ||||||
chr2:48365663
|
C | G | 8 | a0001c0002t0006g0236a0001c0002t0006g0238a0001c0002t0006g0239others(5): Show | 8 | HG00280.hp1 HG01070.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.703+2956C>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48365663 | ||||||
chr2:48365693
|
C | T | 1 | a0001c0001t0001g0076 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.703+2986C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48365693 | ||||||
chr2:48365938
|
A | G | 56 | a0001c0001t0018g0106a0001c0002t0002g0009a0001c0002t0002g0010others(53): Show | 58 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.703+3231A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48365938 | ||||||
chr2:48366025
|
A | G | 1 | a0001c0001t0002g0031 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.703+3318A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48366025 | ||||||
chr2:48366080
|
G | A | 40 | a0001c0001t0001g0215a0001c0001t0001g0216a0001c0001t0001g0218others(37): Show | 42 | HG00099.hp1 HG01069.hp1 HG01069.hp2 others(39): Show |
intron_variant | MODIFIER | c.703+3373G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48366080 | ||||||
chr2:48366085
|
A | G | 140 | a0001c0001t0001g0214a0001c0001t0001g0215a0001c0001t0001g0216others(137): Show | 144 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.703+3378A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48366085 | ||||||
chr2:48366108
|
G | A | 1 | a0001c0002t0003g0092 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.703+3401G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48366108 | ||||||
chr2:48366134
|
A | G | 8 | a0001c0002t0006g0236a0001c0002t0006g0238a0001c0002t0006g0239others(5): Show | 8 | HG00280.hp1 HG01070.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.703+3427A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48366134 | ||||||
chr2:48366353
|
C | CA | 10 | a0001c0001t0001g0086a0001c0001t0001g0090a0001c0001t0001g0121others(7): Show | 10 | HG00099.hp1 HG00733.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.703+3664dupA | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 48366353 | |||||
chr2:48366353
|
CA | C | 100 | a0001c0001t0018g0106a0001c0002t0002g0009a0001c0002t0002g0010others(97): Show | 102 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.703+3664delA | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 48366353 | |||||
chr2:48366577
|
A | G | 1 | a0001c0002t0002g0294 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.703+3870A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48366577 | ||||||
chr2:48366608
|
C | A | 1 | a0001c0001t0001g0208 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.703+3901C>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48366608 | ||||||
chr2:48366662
|
A | G | 40 | a0001c0001t0001g0215a0001c0001t0001g0216a0001c0001t0001g0218others(37): Show | 42 | HG00099.hp1 HG01069.hp1 HG01069.hp2 others(39): Show |
intron_variant | MODIFIER | c.703+3955A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48366662 | ||||||
chr2:48367171
|
C | G | 80 | a0001c0001t0001g0214a0001c0001t0001g0219a0001c0001t0018g0106others(77): Show | 82 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.703+4464C>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48367171 | ||||||
chr2:48367198
|
C | T | 1 | a0001c0001t0001g0163 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.703+4491C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48367198 | ||||||
chr2:48367216
|
A | G | 41 | a0001c0001t0001g0154a0001c0001t0001g0215a0001c0001t0001g0216others(38): Show | 43 | HG00099.hp1 HG01069.hp1 HG01069.hp2 others(40): Show |
intron_variant | MODIFIER | c.703+4509A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48367216 | ||||||
chr2:48367456
|
C | T | 141 | a0001c0001t0001g0154a0001c0001t0001g0214a0001c0001t0001g0215others(138): Show | 145 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.703+4749C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48367456 | ||||||
chr2:48367728
|
A | T | 1 | a0001c0003t0001g0138 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.703+5021A>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48367728 | ||||||
chr2:48367748
|
T | C | 87 | a0001c0001t0001g0214a0001c0001t0001g0219a0001c0001t0018g0106others(84): Show | 89 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.703+5041T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48367748 | ||||||
chr2:48367826
|
A | G | 141 | a0001c0001t0001g0154a0001c0001t0001g0214a0001c0001t0001g0215others(138): Show | 145 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.703+5119A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48367826 | ||||||
chr2:48368158
|
C | T | 1 | a0001c0002t0003g0255 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.704-5134C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48368158 | ||||||
chr2:48368253
|
A | AAT | 28 | a0001c0002t0003g0016a0001c0002t0003g0092a0001c0002t0003g0245others(25): Show | 30 | HG00280.hp1 HG00738.hp2 HG01070.hp2 others(27): Show |
intron_variant | MODIFIER | c.704-5037_704-5036d others(4): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 48368253 | |||||
chr2:48368292
|
A | G | 1 | a0001c0001t0001g0015 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.704-5000A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48368292 | ||||||
chr2:48368296
|
A | C | 332 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0013others(329): Show | 343 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(340): Show |
intron_variant | MODIFIER | c.704-4996A>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48368296 | ||||||
chr2:48368351
|
A | G | 1 | a0001c0001t0001g0151 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.704-4941A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48368351 | ||||||
chr2:48368767
|
A | T | 1 | a0001c0001t0001g0063 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.704-4525A>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48368767 | ||||||
chr2:48368779
|
C | A | 8 | a0001c0002t0006g0236a0001c0002t0006g0238a0001c0002t0006g0239others(5): Show | 8 | HG00280.hp1 HG01070.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.704-4513C>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48368779 | ||||||
chr2:48368797
|
T | A | 1 | a0001c0001t0001g0105 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.704-4495T>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48368797 | ||||||
chr2:48368843
|
T | G | 2 | a0001c0002t0002g0298a0001c0002t0002g0299 | 2 | NA19004.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.704-4449T>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48368843 | ||||||
chr2:48369034
|
A | G | 2 | a0001c0001t0008g0101a0001c0001t0008g0112 | 2 | HG02809.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.704-4258A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48369034 | ||||||
chr2:48369082
|
C | T | 1 | a0001c0002t0002g0288 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.704-4210C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48369082 | ||||||
chr2:48369097
|
G | A | 1 | a0004c0005t0001g0095 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.704-4195G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48369097 | ||||||
chr2:48369373
|
A | C | 1 | a0001c0001t0001g0192 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.704-3919A>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48369373 | ||||||
chr2:48369395
|
G | A | 1 | a0001c0001t0002g0036 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.704-3897G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48369395 | ||||||
chr2:48369434
|
A | C | 17 | a0001c0001t0001g0102a0001c0001t0001g0109a0001c0001t0001g0115others(14): Show | 17 | HG00408.hp2 HG00423.hp2 HG00558.hp1 others(14): Show |
intron_variant | MODIFIER | c.704-3858A>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48369434 | ||||||
chr2:48369504
|
C | T | 1 | a0001c0002t0002g0314 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.704-3788C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48369504 | ||||||
chr2:48369517
|
G | C | 1 | a0001c0001t0001g0177 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.704-3775G>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48369517 | ||||||
chr2:48369696
|
A | G | 1 | a0001c0002t0002g0274 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.704-3596A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48369696 | ||||||
chr2:48369710
|
C | T | 2 | a0001c0001t0001g0139a0001c0001t0001g0148 | 2 | HG02886.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.704-3582C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48369710 | ||||||
chr2:48369811
|
C | G | 84 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0032others(81): Show | 86 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.704-3481C>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48369811 | ||||||
chr2:48369813
|
C | T | 1 | a0001c0002t0022g0237 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.704-3479C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48369813 | ||||||
chr2:48369823
|
A | G | 84 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0032others(81): Show | 86 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.704-3469A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48369823 | ||||||
chr2:48369848
|
A | G | 1 | a0001c0002t0002g0304 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.704-3444A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48369848 | ||||||
chr2:48369862
|
C | T | 1 | a0001c0002t0002g0271 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.704-3430C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48369862 | ||||||
chr2:48369880
|
G | A | 1 | a0001c0002t0002g0299 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.704-3412G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48369880 | ||||||
chr2:48369906
|
T | G | 112 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0032others(109): Show | 116 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.704-3386T>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48369906 | ||||||
chr2:48370156
|
C | T | 84 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0032others(81): Show | 86 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.704-3136C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48370156 | ||||||
chr2:48370244
|
A | G | 1 | a0001c0001t0002g0036 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.704-3048A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48370244 | ||||||
chr2:48370328
|
ATTGGAGA others(10): Show |
A | 2 | a0001c0001t0001g0151a0001c0001t0001g0235 | 2 | HG00733.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.704-2961_704-2945d others(19): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 48370328 | |||||
chr2:48370417
|
C | A | 4 | a0001c0001t0001g0152a0001c0001t0001g0156a0001c0001t0001g0183others(1): Show | 4 | HG00733.hp2 HG01167.hp1 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.704-2875C>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48370417 | ||||||
chr2:48370420
|
G | A | 136 | a0001c0001t0001g0154a0001c0001t0001g0215a0001c0001t0001g0216others(133): Show | 140 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.704-2872G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48370420 | ||||||
chr2:48370660
|
G | C | 95 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0032others(92): Show | 99 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.704-2632G>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48370660 | ||||||
chr2:48370812
|
G | A | 1 | a0003c0007t0013g0146 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.704-2480G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48370812 | ||||||
chr2:48371362
|
C | T | 1 | a0001c0001t0001g0216 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.704-1930C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48371362 | ||||||
chr2:48371429
|
T | C | 1 | a0001c0002t0003g0092 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.704-1863T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48371429 | ||||||
chr2:48371431
|
A | G | 12 | a0001c0002t0003g0016a0001c0002t0003g0092a0001c0002t0003g0245others(9): Show | 12 | HG00738.hp2 HG01109.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.704-1861A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48371431 | ||||||
chr2:48371538
|
T | C | 146 | a0001c0001t0001g0154a0001c0001t0001g0215a0001c0001t0001g0216others(143): Show | 152 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.704-1754T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48371538 | ||||||
chr2:48371710
|
C | G | 77 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0032others(74): Show | 79 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.704-1582C>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48371710 | ||||||
chr2:48371743
|
G | A | 134 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0002g0023others(131): Show | 140 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.704-1549G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48371743 | ||||||
chr2:48372120
|
A | C | 1 | a0001c0002t0002g0316 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.704-1172A>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48372120 | ||||||
chr2:48372123
|
C | T | 2 | a0001c0002t0002g0295a0001c0002t0002g0326 | 2 | NA18975.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.704-1169C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48372123 | ||||||
chr2:48372249
|
C | T | 8 | a0001c0002t0006g0236a0001c0002t0006g0238a0001c0002t0006g0239others(5): Show | 8 | HG00280.hp1 HG01070.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.704-1043C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48372249 | ||||||
chr2:48372263
|
A | C | 3 | a0001c0001t0004g0005a0001c0001t0004g0081a0001c0001t0004g0087 | 4 | NA19004.hp2 NA19064.hp1 NA19083.hp1 others(1): Show |
intron_variant | MODIFIER | c.704-1029A>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48372263 | ||||||
chr2:48372484
|
A | G | 2 | a0001c0001t0001g0107a0001c0001t0001g0253 | 2 | HG00639.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.704-808A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48372484 | ||||||
chr2:48372512
|
A | G | 1 | a0001c0004t0003g0020 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.704-780A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48372512 | ||||||
chr2:48372892
|
A | G | 11 | a0001c0001t0001g0007a0001c0001t0001g0051a0001c0001t0001g0145others(8): Show | 12 | HG01346.hp1 HG02109.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.704-400A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48372892 | ||||||
chr2:48372922
|
CA | C | 27 | a0001c0001t0001g0154a0001c0001t0001g0215a0001c0001t0001g0216others(24): Show | 27 | HG00099.hp1 HG01069.hp1 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.704-356delA | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 48372922 | |||||
chr2:48373012
|
G | A | 1 | a0001c0001t0001g0129 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.704-280G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48373012 | ||||||
chr2:48373073
|
T | C | 2 | a0001c0002t0002g0332a0001c0002t0002g0333 | 2 | HG01106.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.704-219T>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48373073 | ||||||
chr2:48373103
|
G | A | 1 | a0001c0001t0001g0208 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.704-189G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48373103 | ||||||
chr2:48373190
|
A | G | 1 | a0001c0001t0004g0066 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.704-102A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 5/6 | chr2 | 48373190 | ||||||
chr2:48373381
|
T | A | 1 | a0001c0001t0002g0031 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.772+21T>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 6/6 | chr2 | 48373381 | ||||||
chr2:48373390
|
A | T | 1 | a0001c0001t0002g0036 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.772+30A>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 6/6 | chr2 | 48373390 | ||||||
chr2:48373494
|
CTGTTT | C | 3 | a0001c0002t0003g0016a0001c0002t0003g0255a0001c0002t0003g0256 | 3 | HG02717.hp2 HG03209.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.772+136_772+140del others(5): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | 48373494 | |||||
chr2:48373552
|
T | G | 134 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0002g0023others(131): Show | 140 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.772+192T>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 6/6 | chr2 | 48373552 | ||||||
chr2:48373553
|
C | T | 134 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0002g0023others(131): Show | 140 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.772+193C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 6/6 | chr2 | 48373553 | ||||||
chr2:48373918
|
G | A | 1 | a0001c0002t0009g0283 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.772+558G>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 6/6 | chr2 | 48373918 | ||||||
chr2:48373947
|
C | G | 1 | a0001c0001t0001g0162 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.772+587C>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 6/6 | chr2 | 48373947 | ||||||
chr2:48373992
|
TTGCAGTG others(12): Show |
T | 2 | a0001c0001t0001g0139a0001c0001t0001g0148 | 2 | HG02886.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.772+643_772+661del others(19): Show |
FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | 48373992 | |||||
chr2:48374166
|
A | G | 6 | a0001c0001t0001g0099a0001c0001t0001g0151a0001c0001t0001g0166others(3): Show | 6 | HG00733.hp1 HG01981.hp2 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.773-754A>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 6/6 | chr2 | 48374166 | ||||||
chr2:48374309
|
G | T | 134 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0002g0023others(131): Show | 140 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.773-611G>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 6/6 | chr2 | 48374309 | ||||||
chr2:48374359
|
G | C | 1 | a0001c0002t0003g0092 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.773-561G>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 6/6 | chr2 | 48374359 | ||||||
chr2:48374381
|
T | A | 2 | a0001c0002t0002g0296a0001c0002t0002g0312 | 2 | NA18991.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.773-539T>A | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 6/6 | chr2 | 48374381 | ||||||
chr2:48374589
|
G | C | 1 | a0001c0001t0001g0231 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.773-331G>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 6/6 | chr2 | 48374589 | ||||||
chr2:48374677
|
C | T | 134 | a0001c0001t0002g0017a0001c0001t0002g0018a0001c0001t0002g0023others(131): Show | 140 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.773-243C>T | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 6/6 | chr2 | 48374677 | ||||||
chr2:48374702
|
A | C | 1 | a0001c0002t0002g0259 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.773-218A>C | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 6/6 | chr2 | 48374702 | ||||||
chr2:48374719
|
C | G | 1 | a0001c0001t0019g0169 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.773-201C>G | FOXN2 | ENSG00000170802.17 | transcript | ENST00000340553.8 | protein_coding | 6/6 | chr2 | 48374719 |