Item | Value |
---|---|
geneid | 119710 |
ensemblid | ENSG00000166352.18 |
hgncid | 25142 |
symbol | IFTAP |
name | intraflagellar transport associated protein |
refseq_nuc | NM_138787.4 |
refseq_prot | NP_620142.2 |
ensembl_nuc | ENST00000334307.10 |
ensembl_prot | ENSP00000334848.5 |
mane_status | MANE Select |
chr | chr11 |
start | 36594502 |
end | 36659272 |
strand | + |
ver | v1.2 |
region | chr11:36594502-36659272 |
region5000 | chr11:36589502-36664272 |
regionname0 | IFTAP_chr11_36594502_36659272 |
regionname5000 | IFTAP_chr11_36589502_36664272 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 221 | 351 | 89 | 67 | 150 | 12 | 31 | 112 | IFTAP_chr11_36589502_36664272 | IFTAP | copy fasta | chr11 | 36589502 | 36664272 |
a0002 | 0/0 | 221 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | copy fasta | chr11 | 36589502 | 36664272 |
a0003 | 0/0 | 221 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | copy fasta | chr11 | 36589502 | 36664272 |
a0004 | 0/0 | 221 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | copy fasta | chr11 | 36589502 | 36664272 |
a0005 | 0/0 | 221 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | copy fasta | chr11 | 36589502 | 36664272 |
chapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 666 | 345 | 83 | 67 | 150 | 12 | 31 | IFTAP_chr11_36589502_36664272 | IFTAP | copy fasta | chr11 | 36589502 | 36664272 | |
c0002 | 0/0 | 666 | 6 | 6 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | copy fasta | chr11 | 36589502 | 36664272 | |
c0003 | 0/0 | 666 | 2 | 2 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | copy fasta | chr11 | 36589502 | 36664272 | |
c0004 | 0/0 | 666 | 2 | 2 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | copy fasta | chr11 | 36589502 | 36664272 | |
c0005 | 0/0 | 666 | 1 | 0 | 0 | 0 | 0 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | copy fasta | chr11 | 36589502 | 36664272 | |
c0006 | 0/0 | 666 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | copy fasta | chr11 | 36589502 | 36664272 | |
c0007 | 0/0 | 666 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | copy fasta | chr11 | 36589502 | 36664272 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 201 | 297 | 62 | 58 | 138 | 8 | 29 | IFTAP_chr11_36589502_36664272 | IFTAP | copy fasta | chr11 | 36589502 | 36664272 |
t0002 | 0/0 | 201 | 53 | 26 | 10 | 12 | 3 | 2 | IFTAP_chr11_36589502_36664272 | IFTAP | copy fasta | chr11 | 36589502 | 36664272 |
t0003 | 0/0 | 201 | 6 | 6 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | copy fasta | chr11 | 36589502 | 36664272 |
t0004 | 0/0 | 201 | 2 | 0 | 0 | 0 | 1 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | copy fasta | chr11 | 36589502 | 36664272 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 12 | 1 | 0 | 10 | 0 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0002 | 0/0 | 11 | 0 | 2 | 8 | 0 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0003 | 0/0 | 10 | 0 | 0 | 9 | 0 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0004 | 0/0 | 6 | 1 | 1 | 4 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0005 | 0/0 | 5 | 1 | 2 | 2 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0006 | 0/0 | 5 | 0 | 3 | 0 | 1 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0007 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0015 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0016 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0018 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0038 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0042 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0045 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0078 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0193 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 666 | 345 | 83 | 67 | 150 | 12 | 31 | IFTAP_chr11_36589502_36664272 | IFTAP | copy fasta | chr11 | 36589502 | 36664272 | |
a0001c0002 | 0/0 | 666 | 6 | 6 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | copy fasta | chr11 | 36589502 | 36664272 | |
a0002c0003 | 0/0 | 666 | 2 | 2 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | copy fasta | chr11 | 36589502 | 36664272 | |
a0002c0004 | 0/0 | 666 | 2 | 2 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | copy fasta | chr11 | 36589502 | 36664272 | |
a0003c0007 | 0/0 | 666 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | copy fasta | chr11 | 36589502 | 36664272 | |
a0004c0006 | 0/0 | 666 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | copy fasta | chr11 | 36589502 | 36664272 | |
a0005c0005 | 0/0 | 666 | 1 | 0 | 0 | 0 | 0 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | copy fasta | chr11 | 36589502 | 36664272 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 866 | 295 | 61 | 57 | 138 | 8 | 29 | IFTAP_chr11_36589502_36664272 | IFTAP | copy fasta | chr11 | 36589502 | 36664272 |
a0001c0001t0002 | 0/0 | 866 | 48 | 22 | 10 | 12 | 3 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | copy fasta | chr11 | 36589502 | 36664272 |
a0001c0001t0004 | 0/0 | 866 | 2 | 0 | 0 | 0 | 1 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | copy fasta | chr11 | 36589502 | 36664272 |
a0001c0002t0003 | 0/0 | 866 | 6 | 6 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | copy fasta | chr11 | 36589502 | 36664272 |
a0002c0003t0002 | 0/0 | 866 | 2 | 2 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | copy fasta | chr11 | 36589502 | 36664272 |
a0002c0004t0002 | 0/0 | 866 | 2 | 2 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | copy fasta | chr11 | 36589502 | 36664272 |
a0003c0007t0001 | 0/0 | 866 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | copy fasta | chr11 | 36589502 | 36664272 |
a0004c0006t0001 | 0/0 | 866 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | copy fasta | chr11 | 36589502 | 36664272 |
a0005c0005t0002 | 0/0 | 866 | 1 | 0 | 0 | 0 | 0 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | copy fasta | chr11 | 36589502 | 36664272 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 12 | 1 | 0 | 10 | 0 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0002 | 0/0 | 11 | 0 | 2 | 8 | 0 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0003 | 0/0 | 10 | 0 | 0 | 9 | 0 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0004 | 0/0 | 6 | 1 | 1 | 4 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0005 | 0/0 | 5 | 1 | 2 | 2 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0006 | 0/0 | 5 | 0 | 3 | 0 | 1 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0007 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0015 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0038 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0045 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0078 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0193 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0002g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0002g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0002g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0002g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0002g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0002g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0004g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0001t0004g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0002t0003g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0002t0003g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0002t0003g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0001c0002t0003g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0002c0003t0002g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0002c0004t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0002c0004t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0003c0007t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0004c0006t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
a0005c0005t0002g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0163 | EUR | GBR | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0080 | EUR | GBR | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0076 | EUR | GBR | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG00140 | hp2 | a0001 | c0001 | t0004 | g0241 | EUR | GBR | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | CHS | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | CHS | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | CHS | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | CHS | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | CHS | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | CHS | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG00733 | hp2 | a0001 | c0001 | t0002 | g0032 | AMR | PUR | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0233 | AMR | PUR | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0033 | AMR | PUR | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0033 | AMR | PUR | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0227 | AMR | PUR | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0257 | AMR | PUR | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01243 | hp2 | a0004 | c0006 | t0001 | g0057 | AMR | PUR | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | CLM | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0032 | AMR | CLM | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | CLM | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0226 | AMR | CLM | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | CLM | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0229 | AMR | CLM | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | CLM | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0222 | AMR | CLM | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0217 | AMR | CLM | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | CLM | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0099 | EUR | IBS | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0101 | EUR | IBS | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0223 | EUR | IBS | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0018 | EUR | IBS | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0216 | EUR | IBS | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | ACB | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | ACB | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01891 | hp2 | a0003 | c0007 | t0001 | g0115 | AFR | ACB | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | PEL | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0262 | AMR | PEL | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PEL | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PEL | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PEL | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PEL | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | PEL | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PEL | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | ACB | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | KHV | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | KHV | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | KHV | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | KHV | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | KHV | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | KHV | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | KHV | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | KHV | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02145 | hp1 | a0001 | c0001 | t0002 | g0213 | AFR | ACB | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | ACB | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PEL | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PEL | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | CDX | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02257 | hp1 | a0001 | c0001 | t0002 | g0035 | AFR | ACB | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | ACB | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | ACB | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | ACB | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | ACB | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0034 | AFR | ACB | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0253 | AMR | PEL | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02451 | hp1 | a0001 | c0001 | t0002 | g0237 | AFR | ACB | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | ACB | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | KHV | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | KHV | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02572 | hp1 | a0001 | c0001 | t0002 | g0208 | AFR | GWD | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0242 | AFR | GWD | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | GWD | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02615 | hp2 | a0002 | c0004 | t0002 | g0236 | AFR | GWD | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | GWD | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0219 | AFR | GWD | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | GWD | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02723 | hp2 | a0001 | c0002 | t0003 | g0211 | AFR | GWD | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | GWD | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | GWD | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02886 | hp1 | a0001 | c0001 | t0002 | g0235 | AFR | GWD | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02886 | hp2 | a0001 | c0002 | t0003 | g0013 | AFR | GWD | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02895 | hp1 | a0001 | c0001 | t0002 | g0232 | AFR | GWD | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02896 | hp2 | a0001 | c0001 | t0002 | g0231 | AFR | GWD | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02897 | hp1 | a0001 | c0001 | t0002 | g0230 | AFR | GWD | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | ESN | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | ESN | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | ESN | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | ESN | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02970 | hp1 | a0002 | c0003 | t0002 | g0014 | AFR | ESN | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | ESN | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | ESN | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | ESN | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG03098 | hp1 | a0001 | c0001 | t0002 | g0218 | AFR | MSL | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0214 | AFR | MSL | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | ESN | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG03130 | hp2 | a0001 | c0001 | t0002 | g0207 | AFR | ESN | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0031 | AFR | ESN | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | ESN | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG03195 | hp1 | a0002 | c0004 | t0002 | g0014 | AFR | ESN | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG03195 | hp2 | a0001 | c0001 | t0002 | g0031 | AFR | ESN | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | MSL | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG03209 | hp2 | a0001 | c0001 | t0002 | g0224 | AFR | MSL | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0259 | AFR | MSL | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG03239 | hp1 | a0005 | c0005 | t0002 | g0016 | SAS | PJL | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | MSL | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG03453 | hp2 | a0001 | c0002 | t0003 | g0013 | AFR | MSL | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | MSL | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG03486 | hp2 | a0001 | c0002 | t0003 | g0209 | AFR | MSL | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0189 | SAS | PJL | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG03491 | hp2 | a0001 | c0001 | t0004 | g0240 | SAS | PJL | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG03516 | hp2 | a0001 | c0001 | t0002 | g0225 | AFR | ESN | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | GWD | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG03579 | hp1 | a0001 | c0001 | t0002 | g0215 | AFR | MSL | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG03579 | hp2 | a0001 | c0002 | t0003 | g0210 | AFR | MSL | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | PJL | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | STU | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | STU | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | BEB | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | BEB | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | BEB | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | BEB | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0079 | SAS | BEB | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0249 | SAS | BEB | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0150 | SAS | STU | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0264 | SAS | STU | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0081 | SAS | STU | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0131 | SAS | STU | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0250 | SAS | STU | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0177 | SAS | STU | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | YRI | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | YRI | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHB | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | CHB | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | CHB | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | CHB | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | YRI | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0034 | AFR | YRI | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18949 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18967 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA19030 | hp1 | a0001 | c0001 | t0002 | g0220 | AFR | LWK | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | LWK | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA19043 | hp1 | a0002 | c0003 | t0002 | g0014 | AFR | LWK | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | LWK | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0035 | AFR | YRI | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | YRI | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ASW | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ASW | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0228 | EUR | TSI | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0119 | EUR | TSI | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0165 | SAS | GIH | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0058 | SAS | GIH | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | CLM | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | CLM | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | MSL | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | USA | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | USA | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0258 | AFR | USA | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA20300 | hp2 | a0001 | c0002 | t0003 | g0013 | AFR | USA | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | LWK | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
NA21309 | hp2 | a0001 | c0001 | t0002 | g0221 | AFR | LWK | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0193 | REF | REF | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0078 | REF | REF | IFTAP_chr11_36589502_36664272 | IFTAP | chr11 | 36589502 | 36664272 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:36610161 | G | A | 1 | a0002 | 4 | HG02615.hp2 HG02970.hp1 HG03195.hp1 others(1): Show |
missense_variant | MODERATE | c.58G>A | p.Val20Ile | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/6 | 172/866 | 58/666 | 20/221 | chr11 | 36610161 | ||
chr11:36610171 | A | T | 1 | a0003 | 1 | HG01891.hp2 | missense_variant | MODERATE | c.68A>T | p.Lys23Ile | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/6 | 182/866 | 68/666 | 23/221 | chr11 | 36610171 | ||
chr11:36633338 | T | C | 1 | a0005 | 1 | HG03239.hp1 | missense_variant | MODERATE | c.191T>C | p.Phe64Ser | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 3/6 | 305/866 | 191/666 | 64/221 | chr11 | 36633338 | ||
chr11:36659169 | G | A | 1 | a0004 | 1 | HG01243.hp2 | missense_variant | MODERATE | c.649G>A | p.Glu217Lys | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 6/6 | 763/866 | 649/666 | 217/221 | chr11 | 36659169 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:36610160 | C | T | 1 | a0001c0002 | 6 | HG02723.hp2 HG02886.hp2 HG03453.hp2 others(3): Show |
synonymous_variant | LOW | c.57C>T | p.Asp19Asp | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/6 | 171/866 | 57/666 | 19/221 | chr11 | 36610160 | ||
chr11:36633354 | T | C | 1 | a0002c0003 | 2 | HG02970.hp1 NA19043.hp1 |
synonymous_variant | LOW | c.207T>C | p.Val69Val | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 3/6 | 321/866 | 207/666 | 69/221 | chr11 | 36633354 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:36594508 | G | C | 1 | a0001c0002t0003 | 6 | HG02723.hp2 HG02886.hp2 HG03453.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-108G>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/6 | 15596 | chr11 | 36594508 | |||||
chr11:36594562 | G | C | 5 | a0001c0001t0002a0001c0002t0003a0002c0003t0002others(2): Show | 59 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(56): Show |
5_prime_UTR_variant | MODIFIER | c.-54G>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/6 | 15542 | chr11 | 36594562 | |||||
chr11:36659215 | T | C | 1 | a0001c0001t0004 | 2 | HG00140.hp2 HG03491.hp2 |
3_prime_UTR_variant | MODIFIER | c.*29T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 6/6 | 29 | chr11 | 36659215 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:36595200 | G | A | 11 | a0001c0001t0002g0016a0001c0001t0002g0047a0001c0001t0002g0048others(8): Show | 11 | HG00438.hp1 HG02523.hp1 HG03239.hp1 others(8): Show |
intron_variant | MODIFIER | c.-24+608G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36595200 | ||||||
chr11:36595228 | C | T | 37 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0037others(34): Show | 59 | HG00140.hp2 HG00408.hp2 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.-24+636C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36595228 | ||||||
chr11:36595234 | A | G | 2 | a0001c0001t0001g0238a0001c0001t0001g0239 | 2 | HG01109.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-24+642A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36595234 | ||||||
chr11:36595317 | A | G | 136 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(133): Show | 173 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(170): Show |
intron_variant | MODIFIER | c.-24+725A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36595317 | ||||||
chr11:36595455 | G | A | 1 | a0001c0001t0001g0134 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-24+863G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36595455 | ||||||
chr11:36595503 | A | G | 1 | a0001c0001t0002g0237 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-24+911A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36595503 | ||||||
chr11:36595597 | T | G | 11 | a0001c0001t0002g0016a0001c0001t0002g0047a0001c0001t0002g0048others(8): Show | 11 | HG00438.hp1 HG02523.hp1 HG03239.hp1 others(8): Show |
intron_variant | MODIFIER | c.-24+1005T>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36595597 | ||||||
chr11:36595644 | T | C | 1 | a0001c0001t0002g0024 | 2 | NA18747.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.-24+1052T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36595644 | ||||||
chr11:36595718 | G | A | 11 | a0001c0001t0002g0016a0001c0001t0002g0047a0001c0001t0002g0048others(8): Show | 11 | HG00438.hp1 HG02523.hp1 HG03239.hp1 others(8): Show |
intron_variant | MODIFIER | c.-24+1126G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36595718 | ||||||
chr11:36595754 | C | T | 15 | a0001c0001t0002g0016a0001c0001t0002g0047a0001c0001t0002g0048others(12): Show | 16 | HG00438.hp1 HG02523.hp1 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.-24+1162C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36595754 | ||||||
chr11:36595761 | T | C | 6 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0002g0235others(3): Show | 7 | HG02615.hp2 HG02818.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-24+1169T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36595761 | ||||||
chr11:36595789 | A | T | 1 | a0001c0001t0001g0234 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.-24+1197A>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36595789 | ||||||
chr11:36595804 | C | T | 1 | a0001c0001t0001g0133 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-24+1212C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36595804 | ||||||
chr11:36595945 | A | G | 1 | a0001c0001t0001g0036 | 2 | HG00673.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.-24+1353A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36595945 | ||||||
chr11:36596026 | A | C | 52 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0212others(49): Show | 61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.-24+1434A>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36596026 | ||||||
chr11:36596065 | C | T | 1 | a0001c0001t0002g0233 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-24+1473C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36596065 | ||||||
chr11:36596211 | G | GT | 6 | a0001c0001t0002g0031a0001c0001t0002g0216a0001c0001t0002g0217others(3): Show | 7 | HG01496.hp1 HG01517.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.-24+1629dupT | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 36596211 | |||||
chr11:36596211 | G | GTT | 12 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0001g0204others(9): Show | 15 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.-24+1628_-24+1629d others(4): Show |
IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 36596211 | |||||
chr11:36596211 | G | GTTT | 11 | a0001c0001t0001g0030a0001c0001t0001g0206a0001c0001t0002g0035others(8): Show | 13 | HG01106.hp2 HG01258.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.-24+1627_-24+1629d others(5): Show |
IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 36596211 | |||||
chr11:36596211 | G | GTTTTTTT others(9): Show |
1 | a0001c0001t0002g0237 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-24+1629_-24+1630i others(18): Show |
IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 36596211 | |||||
chr11:36596218 | TTTTG | T | 10 | a0001c0001t0002g0016a0001c0001t0002g0048a0001c0001t0002g0049others(7): Show | 10 | HG00438.hp1 HG02523.hp1 HG03239.hp1 others(7): Show |
intron_variant | MODIFIER | c.-24+1630_-24+1633d others(6): Show |
IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 36596218 | |||||
chr11:36596222 | G | GT | 81 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(78): Show | 110 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.-24+1645dupT | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 36596222 | |||||
chr11:36596222 | G | GTT | 11 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0196others(8): Show | 12 | HG01074.hp2 HG01192.hp2 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.-24+1644_-24+1645d others(4): Show |
IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 36596222 | |||||
chr11:36596222 | G | T | 33 | a0001c0001t0001g0030a0001c0001t0001g0202a0001c0001t0001g0203others(30): Show | 39 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.-24+1630G>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36596222 | ||||||
chr11:36596233 | T | G | 1 | a0001c0001t0001g0056 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-24+1641T>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36596233 | ||||||
chr11:36596260 | C | T | 2 | a0001c0001t0001g0192a0001c0001t0001g0193 | 2 | HG01358.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-24+1668C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36596260 | ||||||
chr11:36596265 | G | A | 11 | a0001c0001t0002g0016a0001c0001t0002g0047a0001c0001t0002g0048others(8): Show | 11 | HG00438.hp1 HG02523.hp1 HG03239.hp1 others(8): Show |
intron_variant | MODIFIER | c.-24+1673G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36596265 | ||||||
chr11:36596308 | C | A | 2 | a0001c0001t0004g0240a0001c0001t0004g0241 | 2 | HG00140.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.-24+1716C>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36596308 | ||||||
chr11:36596323 | G | A | 1 | a0001c0001t0002g0024 | 2 | NA18747.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.-24+1731G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36596323 | ||||||
chr11:36596333 | G | T | 1 | a0001c0001t0001g0046 | 2 | HG02486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-24+1741G>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36596333 | ||||||
chr11:36596439 | T | C | 51 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0002g0016others(48): Show | 60 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.-24+1847T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36596439 | ||||||
chr11:36596446 | C | T | 1 | a0001c0001t0002g0215 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-24+1854C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36596446 | ||||||
chr11:36596475 | G | A | 12 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0002g0207others(9): Show | 15 | HG02572.hp1 HG02615.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.-24+1883G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36596475 | ||||||
chr11:36596695 | C | T | 6 | a0001c0001t0002g0207a0001c0001t0002g0208a0001c0002t0003g0013others(3): Show | 8 | HG02572.hp1 HG02723.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.-24+2103C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36596695 | ||||||
chr11:36596713 | A | C | 3 | a0001c0001t0001g0012a0001c0001t0001g0190a0001c0001t0001g0191 | 5 | HG00438.hp2 NA18944.hp1 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.-24+2121A>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36596713 | ||||||
chr11:36596839 | G | T | 51 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0002g0016others(48): Show | 60 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.-24+2247G>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36596839 | ||||||
chr11:36596904 | A | G | 51 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0002g0016others(48): Show | 60 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.-24+2312A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36596904 | ||||||
chr11:36596999 | T | A | 1 | a0004c0006t0001g0057 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-24+2407T>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36596999 | ||||||
chr11:36597100 | A | G | 6 | a0001c0001t0002g0207a0001c0001t0002g0208a0001c0002t0003g0013others(3): Show | 8 | HG02572.hp1 HG02723.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.-24+2508A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36597100 | ||||||
chr11:36597125 | A | G | 12 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0002g0207others(9): Show | 15 | HG02572.hp1 HG02615.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.-24+2533A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36597125 | ||||||
chr11:36597333 | A | C | 28 | a0001c0001t0002g0024a0001c0001t0002g0031a0001c0001t0002g0032others(25): Show | 34 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.-24+2741A>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36597333 | ||||||
chr11:36597633 | C | A | 2 | a0001c0001t0001g0135a0001c0001t0001g0136 | 2 | HG02818.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-24+3041C>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36597633 | ||||||
chr11:36597694 | G | A | 1 | a0001c0001t0001g0058 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-24+3102G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36597694 | ||||||
chr11:36597744 | G | A | 39 | a0001c0001t0002g0016a0001c0001t0002g0024a0001c0001t0002g0031others(36): Show | 45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.-24+3152G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36597744 | ||||||
chr11:36597745 | G | T | 1 | a0001c0001t0001g0128 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-24+3153G>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36597745 | ||||||
chr11:36597754 | G | A | 2 | a0001c0001t0002g0213a0001c0001t0002g0225 | 2 | HG02145.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-24+3162G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36597754 | ||||||
chr11:36597834 | T | C | 1 | a0001c0001t0001g0059 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-24+3242T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36597834 | ||||||
chr11:36597876 | C | G | 1 | a0001c0001t0001g0127 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-24+3284C>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36597876 | ||||||
chr11:36597917 | C | A | 11 | a0001c0001t0002g0016a0001c0001t0002g0047a0001c0001t0002g0048others(8): Show | 11 | HG00438.hp1 HG02523.hp1 HG03239.hp1 others(8): Show |
intron_variant | MODIFIER | c.-24+3325C>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36597917 | ||||||
chr11:36597938 | G | A | 2 | a0001c0001t0001g0135a0001c0001t0001g0136 | 2 | HG02818.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-24+3346G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36597938 | ||||||
chr11:36598211 | A | G | 37 | a0001c0001t0002g0016a0001c0001t0002g0031a0001c0001t0002g0032others(34): Show | 42 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.-24+3619A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36598211 | ||||||
chr11:36598299 | CT | C | 11 | a0001c0001t0002g0016a0001c0001t0002g0047a0001c0001t0002g0048others(8): Show | 11 | HG00438.hp1 HG02523.hp1 HG03239.hp1 others(8): Show |
intron_variant | MODIFIER | c.-24+3716delT | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 36598299 | |||||
chr11:36598542 | G | A | 132 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(129): Show | 169 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(166): Show |
intron_variant | MODIFIER | c.-24+3950G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36598542 | ||||||
chr11:36598545 | G | A | 1 | a0001c0001t0001g0015 | 3 | HG00642.hp1 HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-24+3953G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36598545 | ||||||
chr11:36598677 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-24+4085C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36598677 | ||||||
chr11:36598742 | G | A | 6 | a0001c0001t0001g0005a0001c0001t0001g0060a0001c0001t0001g0061others(3): Show | 10 | HG00544.hp1 HG01934.hp2 HG01978.hp2 others(7): Show |
intron_variant | MODIFIER | c.-24+4150G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36598742 | ||||||
chr11:36598837 | T | C | 1 | a0001c0001t0002g0235 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-24+4245T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36598837 | ||||||
chr11:36598852 | C | G | 26 | a0001c0001t0002g0031a0001c0001t0002g0032a0001c0001t0002g0033others(23): Show | 31 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.-24+4260C>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36598852 | ||||||
chr11:36599108 | C | G | 26 | a0001c0001t0002g0031a0001c0001t0002g0032a0001c0001t0002g0033others(23): Show | 31 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.-24+4516C>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36599108 | ||||||
chr11:36599215 | A | G | 1 | a0001c0001t0002g0024 | 2 | NA18747.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.-24+4623A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36599215 | ||||||
chr11:36599539 | A | G | 1 | a0001c0002t0003g0211 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-24+4947A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36599539 | ||||||
chr11:36599570 | C | A | 12 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0002g0207others(9): Show | 15 | HG02572.hp1 HG02615.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.-24+4978C>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36599570 | ||||||
chr11:36599642 | A | AT | 12 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0002g0207others(9): Show | 15 | HG02572.hp1 HG02615.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.-24+5059dupT | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 36599642 | |||||
chr11:36599642 | AT | A | 5 | a0001c0001t0001g0009a0001c0001t0001g0064a0001c0001t0001g0065others(2): Show | 7 | HG00609.hp1 HG00673.hp1 HG01993.hp1 others(4): Show |
intron_variant | MODIFIER | c.-24+5059delT | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 36599642 | |||||
chr11:36599705 | G | A | 6 | a0001c0001t0001g0005a0001c0001t0001g0060a0001c0001t0001g0061others(3): Show | 10 | HG00544.hp1 HG01261.hp1 HG01934.hp2 others(7): Show |
intron_variant | MODIFIER | c.-24+5113G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36599705 | ||||||
chr11:36599806 | T | A | 1 | a0001c0001t0001g0194 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-24+5214T>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36599806 | ||||||
chr11:36599883 | A | G | 37 | a0001c0001t0002g0016a0001c0001t0002g0031a0001c0001t0002g0032others(34): Show | 42 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.-24+5291A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36599883 | ||||||
chr11:36599884 | T | C | 4 | a0001c0001t0002g0048a0002c0003t0002g0014a0002c0004t0002g0014others(1): Show | 5 | HG02615.hp2 HG02970.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-24+5292T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36599884 | ||||||
chr11:36600009 | A | G | 1 | a0001c0001t0001g0205 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-24+5417A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36600009 | ||||||
chr11:36600045 | A | G | 6 | a0001c0001t0002g0207a0001c0001t0002g0208a0001c0002t0003g0013others(3): Show | 8 | HG02572.hp1 HG02723.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.-24+5453A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36600045 | ||||||
chr11:36600216 | A | G | 3 | a0001c0001t0001g0125a0001c0001t0001g0132a0001c0001t0001g0212 | 3 | HG02451.hp2 NA18522.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-24+5624A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36600216 | ||||||
chr11:36600232 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-24+5640G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36600232 | ||||||
chr11:36600237 | A | C | 6 | a0001c0001t0001g0005a0001c0001t0001g0060a0001c0001t0001g0061others(3): Show | 10 | HG00544.hp1 HG01261.hp1 HG01934.hp2 others(7): Show |
intron_variant | MODIFIER | c.-24+5645A>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36600237 | ||||||
chr11:36600308 | A | G | 39 | a0001c0001t0002g0016a0001c0001t0002g0024a0001c0001t0002g0031others(36): Show | 45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.-24+5716A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36600308 | ||||||
chr11:36600362 | C | T | 1 | a0001c0001t0002g0237 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-24+5770C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36600362 | ||||||
chr11:36600406 | A | G | 37 | a0001c0001t0002g0016a0001c0001t0002g0031a0001c0001t0002g0032others(34): Show | 42 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.-24+5814A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36600406 | ||||||
chr11:36600411 | G | A | 1 | a0001c0001t0002g0235 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-24+5819G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36600411 | ||||||
chr11:36600412 | C | T | 1 | a0001c0001t0002g0214 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-24+5820C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36600412 | ||||||
chr11:36600476 | A | C | 51 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0002g0016others(48): Show | 60 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.-24+5884A>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36600476 | ||||||
chr11:36600477 | G | A | 12 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0002g0207others(9): Show | 15 | HG02572.hp1 HG02615.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.-24+5885G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36600477 | ||||||
chr11:36600519 | C | A | 12 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0002g0207others(9): Show | 15 | HG02572.hp1 HG02615.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.-24+5927C>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36600519 | ||||||
chr11:36600564 | T | C | 1 | a0001c0001t0001g0132 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-24+5972T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36600564 | ||||||
chr11:36600578 | A | G | 10 | a0001c0001t0002g0207a0001c0001t0002g0208a0001c0001t0002g0235others(7): Show | 13 | HG02572.hp1 HG02615.hp2 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.-24+5986A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36600578 | ||||||
chr11:36600624 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-24+6032C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36600624 | ||||||
chr11:36600921 | C | T | 204 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(201): Show | 272 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(269): Show |
intron_variant | MODIFIER | c.-24+6329C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36600921 | ||||||
chr11:36601043 | C | T | 12 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0002g0207others(9): Show | 15 | HG02572.hp1 HG02615.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.-24+6451C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36601043 | ||||||
chr11:36601252 | G | A | 51 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0002g0016others(48): Show | 60 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.-24+6660G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36601252 | ||||||
chr11:36601504 | G | T | 3 | a0002c0003t0002g0014a0002c0004t0002g0014a0002c0004t0002g0236 | 4 | HG02615.hp2 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-24+6912G>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36601504 | ||||||
chr11:36601751 | C | T | 12 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0002g0207others(9): Show | 15 | HG02572.hp1 HG02615.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.-24+7159C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36601751 | ||||||
chr11:36601758 | A | G | 2 | a0001c0001t0001g0192a0001c0001t0001g0193 | 2 | HG01358.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-24+7166A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36601758 | ||||||
chr11:36601810 | T | G | 3 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0242 | 5 | HG01243.hp1 HG02257.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-24+7218T>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36601810 | ||||||
chr11:36601828 | A | AT | 12 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0002g0207others(9): Show | 15 | HG02572.hp1 HG02615.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.-24+7242dupT | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 36601828 | |||||
chr11:36601966 | A | G | 1 | a0001c0001t0002g0237 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-24+7374A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36601966 | ||||||
chr11:36602108 | A | G | 1 | a0001c0001t0001g0107 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-24+7516A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36602108 | ||||||
chr11:36602143 | A | T | 1 | a0001c0001t0001g0201 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.-24+7551A>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36602143 | ||||||
chr11:36602461 | T | G | 51 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0002g0016others(48): Show | 60 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.-23-7620T>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36602461 | ||||||
chr11:36602513 | A | C | 6 | a0001c0001t0002g0207a0001c0001t0002g0208a0001c0002t0003g0013others(3): Show | 8 | HG02572.hp1 HG02723.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.-23-7568A>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36602513 | ||||||
chr11:36602523 | G | A | 2 | a0001c0001t0001g0138a0001c0001t0001g0139 | 2 | NA19066.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.-23-7558G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36602523 | ||||||
chr11:36602576 | G | A | 1 | a0001c0001t0001g0019 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-23-7505G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36602576 | ||||||
chr11:36602633 | C | A | 2 | a0001c0001t0001g0135a0001c0001t0001g0136 | 2 | HG02818.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-23-7448C>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36602633 | ||||||
chr11:36602637 | G | A | 12 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0002g0207others(9): Show | 15 | HG02572.hp1 HG02615.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.-23-7444G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36602637 | ||||||
chr11:36602831 | TA | T | 80 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(77): Show | 107 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.-23-7240delA | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 36602831 | |||||
chr11:36602890 | T | G | 3 | a0002c0003t0002g0014a0002c0004t0002g0014a0002c0004t0002g0236 | 4 | HG02615.hp2 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-23-7191T>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36602890 | ||||||
chr11:36603024 | A | T | 39 | a0001c0001t0002g0016a0001c0001t0002g0024a0001c0001t0002g0031others(36): Show | 45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.-23-7057A>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36603024 | ||||||
chr11:36603489 | C | T | 3 | a0002c0003t0002g0014a0002c0004t0002g0014a0002c0004t0002g0236 | 4 | HG02615.hp2 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-23-6592C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36603489 | ||||||
chr11:36603511 | T | G | 1 | a0001c0001t0001g0026 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-23-6570T>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36603511 | ||||||
chr11:36603566 | A | C | 12 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0002g0207others(9): Show | 15 | HG02572.hp1 HG02615.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.-23-6515A>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36603566 | ||||||
chr11:36603645 | G | C | 3 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0243 | 5 | HG02129.hp1 NA18961.hp1 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.-23-6436G>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36603645 | ||||||
chr11:36603696 | C | T | 4 | a0001c0001t0001g0015a0001c0001t0001g0045a0001c0001t0001g0261others(1): Show | 7 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.-23-6385C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36603696 | ||||||
chr11:36603722 | G | T | 4 | a0001c0001t0002g0235a0002c0003t0002g0014a0002c0004t0002g0014others(1): Show | 5 | HG02615.hp2 HG02886.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-23-6359G>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36603722 | ||||||
chr11:36603802 | A | G | 1 | a0001c0001t0001g0185 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-23-6279A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36603802 | ||||||
chr11:36603922 | CA | C | 11 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0105others(8): Show | 11 | HG00621.hp1 HG01069.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.-23-6144delA | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 36603922 | |||||
chr11:36603922 | CAAA | C | 12 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0002g0207others(9): Show | 15 | HG02572.hp1 HG02615.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.-23-6146_-23-6144d others(5): Show |
IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 36603922 | |||||
chr11:36603954 | T | C | 1 | a0001c0001t0002g0024 | 2 | NA18747.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.-23-6127T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36603954 | ||||||
chr11:36603981 | C | G | 12 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0002g0207others(9): Show | 15 | HG02572.hp1 HG02615.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.-23-6100C>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36603981 | ||||||
chr11:36603994 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-23-6087G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36603994 | ||||||
chr11:36604054 | T | C | 26 | a0001c0001t0002g0031a0001c0001t0002g0032a0001c0001t0002g0033others(23): Show | 31 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.-23-6027T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36604054 | ||||||
chr11:36604077 | T | C | 1 | a0001c0001t0001g0244 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-23-6004T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36604077 | ||||||
chr11:36604155 | A | G | 2 | a0001c0001t0001g0182a0001c0001t0001g0183 | 2 | HG01884.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.-23-5926A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36604155 | ||||||
chr11:36604230 | T | TAATATTC others(354): Show |
1 | a0001c0001t0002g0232 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-23-5838_-23-5837i others(363): Show |
IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 36604230 | |||||
chr11:36604230 | T | TAATATTC others(355): Show |
2 | a0001c0001t0002g0230a0001c0001t0002g0231 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-23-5838_-23-5837i others(364): Show |
IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 36604230 | |||||
chr11:36604246 | G | A | 28 | a0001c0001t0002g0024a0001c0001t0002g0031a0001c0001t0002g0032others(25): Show | 34 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.-23-5835G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36604246 | ||||||
chr11:36604396 | A | G | 1 | a0001c0001t0001g0212 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-23-5685A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36604396 | ||||||
chr11:36604629 | A | C | 6 | a0001c0001t0002g0207a0001c0001t0002g0208a0001c0002t0003g0013others(3): Show | 8 | HG02572.hp1 HG02723.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.-23-5452A>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36604629 | ||||||
chr11:36604672 | T | C | 3 | a0002c0003t0002g0014a0002c0004t0002g0014a0002c0004t0002g0236 | 4 | HG02615.hp2 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-23-5409T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36604672 | ||||||
chr11:36604685 | C | T | 5 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0187others(2): Show | 5 | HG01358.hp2 HG01516.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.-23-5396C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36604685 | ||||||
chr11:36604707 | A | T | 1 | a0001c0001t0002g0024 | 2 | NA18747.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.-23-5374A>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36604707 | ||||||
chr11:36604725 | C | CT | 5 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0180others(2): Show | 5 | HG01981.hp1 HG02080.hp1 HG02083.hp2 others(2): Show |
intron_variant | MODIFIER | c.-23-5355dupT | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 36604725 | |||||
chr11:36604894 | C | A | 1 | a0001c0001t0001g0025 | 2 | HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-23-5187C>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36604894 | ||||||
chr11:36604930 | A | G | 1 | a0001c0001t0001g0177 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-23-5151A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36604930 | ||||||
chr11:36605032 | G | C | 11 | a0001c0001t0002g0016a0001c0001t0002g0047a0001c0001t0002g0048others(8): Show | 11 | HG00438.hp1 HG02523.hp1 HG03239.hp1 others(8): Show |
intron_variant | MODIFIER | c.-23-5049G>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36605032 | ||||||
chr11:36605055 | A | T | 2 | a0001c0001t0001g0135a0001c0001t0001g0136 | 2 | HG02818.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-23-5026A>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36605055 | ||||||
chr11:36605090 | C | T | 12 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0002g0207others(9): Show | 15 | HG02572.hp1 HG02615.hp2 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.-23-4991C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36605090 | ||||||
chr11:36605211 | T | A | 51 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0002g0016others(48): Show | 60 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.-23-4870T>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36605211 | ||||||
chr11:36605287 | C | A | 26 | a0001c0001t0002g0031a0001c0001t0002g0032a0001c0001t0002g0033others(23): Show | 31 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.-23-4794C>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36605287 | ||||||
chr11:36605289 | CT | C | 13 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(10): Show | 16 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.-23-4781delT | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 36605289 | |||||
chr11:36605309 | A | G | 3 | a0002c0003t0002g0014a0002c0004t0002g0014a0002c0004t0002g0236 | 4 | HG02615.hp2 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-23-4772A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36605309 | ||||||
chr11:36605588 | A | T | 13 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(10): Show | 16 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.-23-4493A>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36605588 | ||||||
chr11:36605643 | A | G | 13 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(10): Show | 16 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.-23-4438A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36605643 | ||||||
chr11:36605671 | T | G | 1 | a0001c0001t0001g0060 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-23-4410T>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36605671 | ||||||
chr11:36605672 | G | A | 1 | a0001c0001t0002g0049 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-23-4409G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36605672 | ||||||
chr11:36605807 | A | C | 1 | a0001c0001t0002g0024 | 2 | NA18747.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.-23-4274A>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36605807 | ||||||
chr11:36605891 | C | T | 1 | a0001c0001t0001g0100 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-23-4190C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36605891 | ||||||
chr11:36605919 | G | A | 13 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(10): Show | 16 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.-23-4162G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36605919 | ||||||
chr11:36606000 | C | T | 1 | a0001c0001t0001g0029 | 2 | NA18964.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.-23-4081C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36606000 | ||||||
chr11:36606003 | T | C | 3 | a0001c0001t0002g0230a0001c0001t0002g0231a0001c0001t0002g0232 | 3 | HG02895.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-23-4078T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36606003 | ||||||
chr11:36606006 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-23-4075G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36606006 | ||||||
chr11:36606011 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-23-4070C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36606011 | ||||||
chr11:36606257 | G | C | 26 | a0001c0001t0002g0031a0001c0001t0002g0032a0001c0001t0002g0033others(23): Show | 31 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.-23-3824G>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36606257 | ||||||
chr11:36606304 | C | A | 1 | a0001c0001t0002g0207 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-23-3777C>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36606304 | ||||||
chr11:36606441 | C | CTAAA | 38 | a0001c0001t0002g0016a0001c0001t0002g0031a0001c0001t0002g0032others(35): Show | 43 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.-23-3621_-23-3618d others(6): Show |
IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 36606441 | |||||
chr11:36606485 | CTA | C | 13 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(10): Show | 16 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.-23-3592_-23-3591d others(4): Show |
IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 36606485 | |||||
chr11:36606625 | GA | G | 13 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(10): Show | 16 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.-23-3452delA | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 36606625 | |||||
chr11:36606690 | T | C | 1 | a0001c0001t0001g0126 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-23-3391T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36606690 | ||||||
chr11:36606824 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-23-3257C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36606824 | ||||||
chr11:36606963 | A | G | 2 | a0001c0001t0001g0135a0001c0001t0001g0136 | 2 | HG02818.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-23-3118A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36606963 | ||||||
chr11:36606990 | A | G | 13 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(10): Show | 16 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.-23-3091A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36606990 | ||||||
chr11:36606991 | G | A | 52 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(49): Show | 61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.-23-3090G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36606991 | ||||||
chr11:36607001 | G | A | 13 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(10): Show | 16 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.-23-3080G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36607001 | ||||||
chr11:36607054 | A | G | 39 | a0001c0001t0002g0016a0001c0001t0002g0024a0001c0001t0002g0031others(36): Show | 45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.-23-3027A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36607054 | ||||||
chr11:36607059 | A | G | 13 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(10): Show | 16 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.-23-3022A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36607059 | ||||||
chr11:36607283 | G | A | 13 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(10): Show | 16 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.-23-2798G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36607283 | ||||||
chr11:36607288 | C | T | 13 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(10): Show | 16 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.-23-2793C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36607288 | ||||||
chr11:36607350 | T | A | 27 | a0001c0001t0002g0024a0001c0001t0002g0031a0001c0001t0002g0032others(24): Show | 33 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.-23-2731T>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36607350 | ||||||
chr11:36607528 | A | G | 1 | a0001c0001t0002g0049 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-23-2553A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36607528 | ||||||
chr11:36607593 | AT | A | 14 | a0001c0001t0001g0132a0001c0001t0001g0135a0001c0001t0001g0136others(11): Show | 17 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(14): Show |
intron_variant | MODIFIER | c.-23-2477delT | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 36607593 | |||||
chr11:36607665 | T | TC | 52 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(49): Show | 61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.-23-2410dupC | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr11 | 36607665 | |||||
chr11:36607736 | T | C | 52 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(49): Show | 61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.-23-2345T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36607736 | ||||||
chr11:36607751 | G | A | 1 | a0001c0001t0002g0235 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-23-2330G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36607751 | ||||||
chr11:36607754 | A | C | 1 | a0001c0001t0001g0107 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-23-2327A>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36607754 | ||||||
chr11:36607818 | C | A | 2 | a0001c0001t0001g0020a0001c0001t0001g0109 | 3 | HG01074.hp1 HG01346.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.-23-2263C>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36607818 | ||||||
chr11:36608064 | G | T | 2 | a0001c0001t0001g0039a0001c0001t0001g0040 | 4 | NA18961.hp1 NA18970.hp2 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.-23-2017G>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36608064 | ||||||
chr11:36608477 | T | C | 13 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(10): Show | 16 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.-23-1604T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36608477 | ||||||
chr11:36608538 | G | A | 52 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(49): Show | 61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.-23-1543G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36608538 | ||||||
chr11:36608592 | A | G | 27 | a0001c0001t0002g0024a0001c0001t0002g0031a0001c0001t0002g0032others(24): Show | 33 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.-23-1489A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36608592 | ||||||
chr11:36608624 | CT | C | 5 | a0001c0001t0001g0137a0001c0001t0002g0235a0002c0003t0002g0014others(2): Show | 6 | HG02615.hp2 HG02630.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-23-1456delT | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36608624 | ||||||
chr11:36608704 | T | G | 1 | a0001c0001t0001g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-23-1377T>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36608704 | ||||||
chr11:36608729 | A | G | 2 | a0001c0001t0001g0137a0001c0001t0002g0235 | 2 | HG02630.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-23-1352A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36608729 | ||||||
chr11:36608817 | T | C | 11 | a0001c0001t0002g0016a0001c0001t0002g0047a0001c0001t0002g0048others(8): Show | 11 | HG00438.hp1 HG02523.hp1 HG03239.hp1 others(8): Show |
intron_variant | MODIFIER | c.-23-1264T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36608817 | ||||||
chr11:36608825 | A | T | 6 | a0001c0001t0002g0207a0001c0001t0002g0208a0001c0002t0003g0013others(3): Show | 8 | HG02572.hp1 HG02723.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.-23-1256A>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36608825 | ||||||
chr11:36608868 | T | C | 1 | a0001c0001t0001g0142 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-23-1213T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36608868 | ||||||
chr11:36608927 | TG | T | 13 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(10): Show | 16 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.-23-1153delG | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36608927 | ||||||
chr11:36608992 | T | G | 1 | a0001c0001t0001g0205 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-23-1089T>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36608992 | ||||||
chr11:36609204 | C | A | 3 | a0001c0001t0002g0230a0001c0001t0002g0231a0001c0001t0002g0232 | 3 | HG02895.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-23-877C>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36609204 | ||||||
chr11:36609231 | G | T | 1 | a0001c0001t0001g0176 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-23-850G>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36609231 | ||||||
chr11:36609335 | C | A | 1 | a0001c0001t0001g0238 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-23-746C>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36609335 | ||||||
chr11:36609442 | G | A | 1 | a0001c0001t0002g0237 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-23-639G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36609442 | ||||||
chr11:36609489 | A | C | 1 | a0001c0001t0001g0137 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-23-592A>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36609489 | ||||||
chr11:36609873 | G | A | 3 | a0001c0001t0001g0041a0001c0001t0001g0245a0001c0001t0001g0263 | 4 | NA18951.hp2 NA18978.hp2 NA19072.hp2 others(1): Show |
intron_variant | MODIFIER | c.-23-208G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 1/5 | chr11 | 36609873 | ||||||
chr11:36610317 | G | A | 52 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(49): Show | 61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.136+78G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36610317 | ||||||
chr11:36610327 | A | G | 4 | a0001c0002t0003g0013a0001c0002t0003g0209a0001c0002t0003g0210others(1): Show | 6 | HG02723.hp2 HG02886.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.136+88A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36610327 | ||||||
chr11:36610635 | C | G | 1 | a0001c0001t0001g0025 | 2 | HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.136+396C>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36610635 | ||||||
chr11:36610724 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.136+485G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36610724 | ||||||
chr11:36610816 | ATGC | A | 52 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(49): Show | 61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.136+598_136+600del others(3): Show |
IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 36610816 | |||||
chr11:36610833 | G | A | 71 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0011others(68): Show | 94 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.136+594G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36610833 | ||||||
chr11:36610850 | T | C | 1 | a0001c0001t0002g0024 | 2 | NA18747.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.136+611T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36610850 | ||||||
chr11:36610965 | G | A | 175 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(172): Show | 234 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(231): Show |
intron_variant | MODIFIER | c.136+726G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36610965 | ||||||
chr11:36610989 | C | T | 39 | a0001c0001t0002g0016a0001c0001t0002g0024a0001c0001t0002g0031others(36): Show | 45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.136+750C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36610989 | ||||||
chr11:36611006 | G | A | 1 | a0001c0001t0001g0042 | 2 | HG03688.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.136+767G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36611006 | ||||||
chr11:36611034 | A | T | 1 | a0001c0001t0001g0099 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.136+795A>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36611034 | ||||||
chr11:36611085 | A | G | 2 | a0001c0001t0001g0173a0001c0001t0001g0174 | 2 | NA18971.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.136+846A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36611085 | ||||||
chr11:36611228 | A | G | 21 | a0001c0001t0002g0031a0001c0001t0002g0032a0001c0001t0002g0033others(18): Show | 26 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.136+989A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36611228 | ||||||
chr11:36611236 | C | G | 11 | a0001c0001t0002g0016a0001c0001t0002g0047a0001c0001t0002g0048others(8): Show | 11 | HG00438.hp1 HG02523.hp1 HG03239.hp1 others(8): Show |
intron_variant | MODIFIER | c.136+997C>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36611236 | ||||||
chr11:36611255 | G | A | 1 | a0001c0001t0002g0024 | 2 | NA18747.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.136+1016G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36611255 | ||||||
chr11:36611392 | T | TA | 3 | a0002c0003t0002g0014a0002c0004t0002g0014a0002c0004t0002g0236 | 4 | HG02615.hp2 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.136+1160dupA | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 36611392 | |||||
chr11:36611558 | T | C | 1 | a0001c0001t0001g0070 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.136+1319T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36611558 | ||||||
chr11:36611581 | G | A | 5 | a0001c0001t0002g0214a0001c0001t0002g0215a0001c0001t0002g0230others(2): Show | 5 | HG02895.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.136+1342G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36611581 | ||||||
chr11:36611613 | T | G | 1 | a0001c0001t0001g0099 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.136+1374T>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36611613 | ||||||
chr11:36611752 | A | G | 89 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0037others(86): Show | 120 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.136+1513A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36611752 | ||||||
chr11:36611852 | A | C | 37 | a0001c0001t0002g0016a0001c0001t0002g0031a0001c0001t0002g0032others(34): Show | 42 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.136+1613A>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36611852 | ||||||
chr11:36612017 | C | T | 39 | a0001c0001t0002g0016a0001c0001t0002g0024a0001c0001t0002g0031others(36): Show | 45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.136+1778C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36612017 | ||||||
chr11:36612056 | A | G | 3 | a0002c0003t0002g0014a0002c0004t0002g0014a0002c0004t0002g0236 | 4 | HG02615.hp2 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.136+1817A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36612056 | ||||||
chr11:36612066 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.136+1827C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36612066 | ||||||
chr11:36612280 | G | GT | 40 | a0001c0001t0001g0172a0001c0001t0002g0016a0001c0001t0002g0024others(37): Show | 46 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.136+2052dupT | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 36612280 | |||||
chr11:36612528 | A | G | 5 | a0001c0001t0002g0031a0001c0001t0002g0217a0001c0001t0002g0218others(2): Show | 6 | HG01496.hp1 HG02647.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.136+2289A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36612528 | ||||||
chr11:36612547 | A | G | 1 | a0001c0001t0002g0024 | 2 | NA18747.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.136+2308A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36612547 | ||||||
chr11:36612561 | C | T | 1 | a0001c0001t0001g0171 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.136+2322C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36612561 | ||||||
chr11:36612669 | G | A | 3 | a0001c0001t0001g0025a0001c0001t0002g0207a0001c0001t0002g0208 | 4 | HG02572.hp1 HG02717.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.136+2430G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36612669 | ||||||
chr11:36612718 | T | A | 11 | a0001c0001t0002g0016a0001c0001t0002g0047a0001c0001t0002g0048others(8): Show | 11 | HG00438.hp1 HG02523.hp1 HG03239.hp1 others(8): Show |
intron_variant | MODIFIER | c.136+2479T>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36612718 | ||||||
chr11:36612842 | A | G | 39 | a0001c0001t0002g0016a0001c0001t0002g0024a0001c0001t0002g0031others(36): Show | 45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.136+2603A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36612842 | ||||||
chr11:36612995 | G | A | 1 | a0001c0001t0001g0144 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.136+2756G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36612995 | ||||||
chr11:36613069 | C | T | 1 | a0001c0001t0001g0260 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.136+2830C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36613069 | ||||||
chr11:36613070 | G | A | 1 | a0001c0001t0001g0015 | 3 | HG00642.hp1 HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.136+2831G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36613070 | ||||||
chr11:36613099 | C | T | 39 | a0001c0001t0002g0016a0001c0001t0002g0024a0001c0001t0002g0031others(36): Show | 45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.136+2860C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36613099 | ||||||
chr11:36613184 | T | C | 39 | a0001c0001t0002g0016a0001c0001t0002g0024a0001c0001t0002g0031others(36): Show | 45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.136+2945T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36613184 | ||||||
chr11:36613203 | T | C | 13 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(10): Show | 16 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.136+2964T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36613203 | ||||||
chr11:36613229 | A | T | 1 | a0001c0001t0002g0237 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.136+2990A>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36613229 | ||||||
chr11:36613239 | G | A | 52 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(49): Show | 61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.136+3000G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36613239 | ||||||
chr11:36613280 | C | T | 11 | a0001c0001t0002g0016a0001c0001t0002g0047a0001c0001t0002g0048others(8): Show | 11 | HG00438.hp1 HG02523.hp1 HG03239.hp1 others(8): Show |
intron_variant | MODIFIER | c.136+3041C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36613280 | ||||||
chr11:36613588 | A | T | 39 | a0001c0001t0002g0016a0001c0001t0002g0024a0001c0001t0002g0031others(36): Show | 45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.136+3349A>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36613588 | ||||||
chr11:36613599 | C | G | 1 | a0001c0001t0002g0237 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.136+3360C>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36613599 | ||||||
chr11:36613619 | C | G | 39 | a0001c0001t0002g0016a0001c0001t0002g0024a0001c0001t0002g0031others(36): Show | 45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.136+3380C>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36613619 | ||||||
chr11:36613667 | A | G | 1 | a0001c0002t0003g0211 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.136+3428A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36613667 | ||||||
chr11:36613853 | C | T | 5 | a0001c0001t0001g0030a0001c0001t0001g0203a0001c0001t0001g0204others(2): Show | 6 | HG02486.hp1 HG02622.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.136+3614C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36613853 | ||||||
chr11:36613879 | G | A | 1 | a0001c0001t0001g0192 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.136+3640G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36613879 | ||||||
chr11:36613890 | C | T | 2 | a0001c0001t0002g0031a0001c0001t0002g0220 | 3 | HG03139.hp1 HG03195.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.136+3651C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36613890 | ||||||
chr11:36613894 | T | C | 1 | a0001c0001t0001g0145 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.136+3655T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36613894 | ||||||
chr11:36613898 | TTTG | T | 70 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0011others(67): Show | 93 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.136+3669_136+3671d others(5): Show |
IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 36613898 | |||||
chr11:36613905 | T | A | 1 | a0001c0001t0001g0137 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.136+3666T>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36613905 | ||||||
chr11:36613916 | T | C | 1 | a0001c0001t0001g0173 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.136+3677T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36613916 | ||||||
chr11:36613917 | CT | C | 41 | a0001c0001t0001g0071a0001c0001t0001g0103a0001c0001t0002g0016others(38): Show | 47 | HG00438.hp1 HG00621.hp1 HG00733.hp2 others(44): Show |
intron_variant | MODIFIER | c.136+3690delT | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 36613917 | |||||
chr11:36613984 | G | T | 52 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(49): Show | 61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.136+3745G>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36613984 | ||||||
chr11:36614103 | A | G | 1 | a0001c0001t0001g0098 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.136+3864A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614103 | ||||||
chr11:36614119 | C | T | 2 | a0001c0001t0001g0135a0001c0001t0001g0136 | 2 | HG02818.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.136+3880C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614119 | ||||||
chr11:36614126 | A | T | 1 | a0001c0001t0001g0098 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.136+3887A>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614126 | ||||||
chr11:36614153 | T | G | 176 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(173): Show | 235 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(232): Show |
intron_variant | MODIFIER | c.136+3914T>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614153 | ||||||
chr11:36614160 | T | C | 1 | a0001c0001t0001g0098 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.136+3921T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614160 | ||||||
chr11:36614182 | T | C | 1 | a0001c0001t0001g0098 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.136+3943T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614182 | ||||||
chr11:36614236 | A | G | 1 | a0001c0001t0002g0237 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.136+3997A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614236 | ||||||
chr11:36614239 | G | C | 3 | a0001c0001t0001g0125a0001c0001t0001g0132a0001c0001t0001g0212 | 3 | HG02451.hp2 NA18522.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.136+4000G>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614239 | ||||||
chr11:36614242 | A | G | 5 | a0001c0001t0002g0214a0001c0001t0002g0215a0001c0001t0002g0230others(2): Show | 5 | HG02895.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.136+4003A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614242 | ||||||
chr11:36614344 | C | G | 39 | a0001c0001t0002g0016a0001c0001t0002g0024a0001c0001t0002g0031others(36): Show | 45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.136+4105C>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614344 | ||||||
chr11:36614353 | A | G | 1 | a0001c0001t0002g0131 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.136+4114A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614353 | ||||||
chr11:36614362 | A | G | 1 | a0001c0001t0001g0097 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.136+4123A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614362 | ||||||
chr11:36614415 | G | C | 1 | a0001c0001t0002g0050 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.136+4176G>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614415 | ||||||
chr11:36614418 | C | A | 1 | a0001c0001t0002g0050 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.136+4179C>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614418 | ||||||
chr11:36614572 | C | T | 39 | a0001c0001t0002g0016a0001c0001t0002g0024a0001c0001t0002g0031others(36): Show | 45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.136+4333C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614572 | ||||||
chr11:36614576 | G | A | 2 | a0001c0001t0002g0221a0001c0001t0002g0233 | 2 | HG00735.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.136+4337G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614576 | ||||||
chr11:36614651 | A | G | 52 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(49): Show | 61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.136+4412A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614651 | ||||||
chr11:36614675 | G | A | 39 | a0001c0001t0002g0016a0001c0001t0002g0024a0001c0001t0002g0031others(36): Show | 45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.136+4436G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614675 | ||||||
chr11:36614675 | G | C | 13 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(10): Show | 16 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.136+4436G>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614675 | ||||||
chr11:36614777 | C | T | 2 | a0001c0001t0001g0144a0001c0001t0001g0170 | 2 | NA18945.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.136+4538C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614777 | ||||||
chr11:36614809 | C | T | 1 | a0001c0001t0001g0139 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.136+4570C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614809 | ||||||
chr11:36614810 | T | A | 1 | a0001c0001t0001g0139 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.136+4571T>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614810 | ||||||
chr11:36614830 | G | T | 1 | a0001c0001t0001g0139 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.136+4591G>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614830 | ||||||
chr11:36614833 | G | C | 1 | a0001c0001t0001g0139 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.136+4594G>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614833 | ||||||
chr11:36614835 | G | A | 1 | a0001c0001t0001g0139 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.136+4596G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614835 | ||||||
chr11:36614839 | A | G | 39 | a0001c0001t0002g0016a0001c0001t0002g0024a0001c0001t0002g0031others(36): Show | 45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.136+4600A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614839 | ||||||
chr11:36614840 | T | G | 1 | a0001c0001t0001g0139 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.136+4601T>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614840 | ||||||
chr11:36614851 | T | A | 1 | a0001c0001t0001g0139 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.136+4612T>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614851 | ||||||
chr11:36614872 | C | T | 1 | a0001c0001t0001g0139 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.136+4633C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614872 | ||||||
chr11:36614874 | G | A | 1 | a0001c0001t0001g0139 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.136+4635G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614874 | ||||||
chr11:36614875 | T | C | 1 | a0001c0001t0001g0139 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.136+4636T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614875 | ||||||
chr11:36614886 | G | C | 1 | a0001c0001t0001g0139 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.136+4647G>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614886 | ||||||
chr11:36614887 | G | T | 1 | a0001c0001t0001g0139 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.136+4648G>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614887 | ||||||
chr11:36614898 | A | T | 52 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(49): Show | 61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.136+4659A>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614898 | ||||||
chr11:36614900 | C | A | 1 | a0001c0001t0001g0139 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.136+4661C>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614900 | ||||||
chr11:36614912 | T | A | 1 | a0001c0001t0001g0139 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.136+4673T>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614912 | ||||||
chr11:36614925 | T | G | 1 | a0001c0001t0002g0237 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.136+4686T>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614925 | ||||||
chr11:36614950 | T | A | 1 | a0001c0001t0001g0139 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.136+4711T>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614950 | ||||||
chr11:36614962 | G | T | 1 | a0001c0001t0001g0139 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.136+4723G>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614962 | ||||||
chr11:36614966 | T | G | 1 | a0001c0001t0001g0139 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.136+4727T>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614966 | ||||||
chr11:36614967 | T | A | 1 | a0001c0001t0001g0139 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.136+4728T>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614967 | ||||||
chr11:36614969 | G | T | 1 | a0001c0001t0001g0139 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.136+4730G>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614969 | ||||||
chr11:36614970 | T | C | 1 | a0001c0001t0001g0139 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.136+4731T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614970 | ||||||
chr11:36614971 | G | C | 1 | a0001c0001t0001g0139 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.136+4732G>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614971 | ||||||
chr11:36614972 | T | C | 1 | a0001c0001t0001g0139 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.136+4733T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614972 | ||||||
chr11:36614975 | C | T | 26 | a0001c0001t0002g0031a0001c0001t0002g0032a0001c0001t0002g0033others(23): Show | 31 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.136+4736C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614975 | ||||||
chr11:36614976 | A | C | 1 | a0001c0001t0001g0139 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.136+4737A>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614976 | ||||||
chr11:36614976 | A | G | 26 | a0001c0001t0002g0031a0001c0001t0002g0032a0001c0001t0002g0033others(23): Show | 31 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.136+4737A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614976 | ||||||
chr11:36614977 | G | A | 1 | a0001c0001t0001g0139 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.136+4738G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614977 | ||||||
chr11:36614984 | A | C | 1 | a0001c0001t0001g0139 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.136+4745A>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614984 | ||||||
chr11:36614985 | G | T | 1 | a0001c0001t0001g0139 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.136+4746G>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614985 | ||||||
chr11:36614989 | T | A | 1 | a0001c0001t0001g0139 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.136+4750T>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614989 | ||||||
chr11:36614992 | C | G | 1 | a0001c0001t0001g0139 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.136+4753C>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36614992 | ||||||
chr11:36615066 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.136+4827G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36615066 | ||||||
chr11:36615137 | T | G | 1 | a0001c0001t0002g0222 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.136+4898T>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36615137 | ||||||
chr11:36615238 | A | G | 53 | a0001c0001t0001g0025a0001c0001t0001g0135a0001c0001t0001g0136others(50): Show | 63 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.136+4999A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36615238 | ||||||
chr11:36615240 | C | T | 29 | a0001c0001t0001g0025a0001c0001t0002g0024a0001c0001t0002g0031others(26): Show | 36 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.136+5001C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36615240 | ||||||
chr11:36615351 | T | C | 1 | a0001c0001t0001g0246 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.136+5112T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36615351 | ||||||
chr11:36615389 | C | A | 3 | a0001c0001t0001g0175a0001c0001t0001g0182a0001c0001t0001g0183 | 3 | HG01884.hp1 HG02896.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.136+5150C>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36615389 | ||||||
chr11:36615395 | C | T | 3 | a0002c0003t0002g0014a0002c0004t0002g0014a0002c0004t0002g0236 | 4 | HG02615.hp2 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.136+5156C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36615395 | ||||||
chr11:36615424 | A | T | 1 | a0001c0001t0001g0130 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.136+5185A>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36615424 | ||||||
chr11:36615579 | A | G | 39 | a0001c0001t0002g0016a0001c0001t0002g0024a0001c0001t0002g0031others(36): Show | 45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.136+5340A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36615579 | ||||||
chr11:36615581 | G | C | 40 | a0001c0001t0001g0170a0001c0001t0002g0016a0001c0001t0002g0024others(37): Show | 46 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.136+5342G>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36615581 | ||||||
chr11:36615765 | T | C | 39 | a0001c0001t0002g0016a0001c0001t0002g0024a0001c0001t0002g0031others(36): Show | 45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.136+5526T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36615765 | ||||||
chr11:36615767 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.136+5528G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36615767 | ||||||
chr11:36615854 | G | A | 1 | a0001c0001t0001g0147 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.136+5615G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36615854 | ||||||
chr11:36615883 | T | C | 139 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(136): Show | 176 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(173): Show |
intron_variant | MODIFIER | c.136+5644T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36615883 | ||||||
chr11:36616006 | G | A | 6 | a0001c0001t0002g0207a0001c0001t0002g0208a0001c0002t0003g0013others(3): Show | 8 | HG02572.hp1 HG02723.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.136+5767G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36616006 | ||||||
chr11:36616007 | T | G | 4 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0180others(1): Show | 4 | HG01981.hp1 HG02080.hp1 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.136+5768T>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36616007 | ||||||
chr11:36616016 | C | G | 4 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0180others(1): Show | 4 | HG01981.hp1 HG02080.hp1 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.136+5777C>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36616016 | ||||||
chr11:36616024 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.136+5785G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36616024 | ||||||
chr11:36616057 | A | T | 4 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0213others(1): Show | 6 | HG02145.hp1 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.136+5818A>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36616057 | ||||||
chr11:36616138 | C | A | 2 | a0001c0001t0001g0144a0001c0001t0001g0170 | 2 | NA18945.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.136+5899C>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36616138 | ||||||
chr11:36616497 | A | G | 1 | a0001c0001t0002g0024 | 2 | NA18747.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.136+6258A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36616497 | ||||||
chr11:36616563 | C | G | 38 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0037others(35): Show | 60 | HG00140.hp2 HG00408.hp2 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.136+6324C>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36616563 | ||||||
chr11:36616617 | A | G | 1 | a0001c0001t0001g0212 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.136+6378A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36616617 | ||||||
chr11:36616627 | C | A | 5 | a0001c0001t0001g0005a0001c0001t0001g0060a0001c0001t0001g0061others(2): Show | 9 | HG00544.hp1 HG01934.hp2 HG01978.hp2 others(6): Show |
intron_variant | MODIFIER | c.136+6388C>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36616627 | ||||||
chr11:36616645 | A | G | 39 | a0001c0001t0002g0016a0001c0001t0002g0024a0001c0001t0002g0031others(36): Show | 45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.136+6406A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36616645 | ||||||
chr11:36616677 | G | A | 1 | a0001c0001t0001g0046 | 2 | HG02486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.136+6438G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36616677 | ||||||
chr11:36616784 | G | A | 6 | a0001c0001t0002g0207a0001c0001t0002g0208a0001c0002t0003g0013others(3): Show | 8 | HG02572.hp1 HG02723.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.136+6545G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36616784 | ||||||
chr11:36616785 | T | C | 52 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(49): Show | 61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.136+6546T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36616785 | ||||||
chr11:36616813 | G | C | 1 | a0001c0001t0001g0247 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.136+6574G>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36616813 | ||||||
chr11:36616817 | T | C | 1 | a0001c0001t0001g0196 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.136+6578T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36616817 | ||||||
chr11:36616871 | TA | T | 39 | a0001c0001t0002g0016a0001c0001t0002g0024a0001c0001t0002g0031others(36): Show | 45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.136+6639delA | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 36616871 | |||||
chr11:36616887 | C | T | 1 | a0001c0001t0002g0237 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.136+6648C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36616887 | ||||||
chr11:36616949 | C | T | 39 | a0001c0001t0002g0016a0001c0001t0002g0024a0001c0001t0002g0031others(36): Show | 45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.136+6710C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36616949 | ||||||
chr11:36617047 | A | G | 3 | a0002c0003t0002g0014a0002c0004t0002g0014a0002c0004t0002g0236 | 4 | HG02615.hp2 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.136+6808A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36617047 | ||||||
chr11:36617138 | T | C | 1 | a0001c0001t0002g0024 | 2 | NA18747.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.136+6899T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36617138 | ||||||
chr11:36617158 | C | T | 39 | a0001c0001t0002g0016a0001c0001t0002g0024a0001c0001t0002g0031others(36): Show | 45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.136+6919C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36617158 | ||||||
chr11:36617160 | T | C | 1 | a0001c0001t0001g0074 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.136+6921T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36617160 | ||||||
chr11:36617165 | AATG | A | 2 | a0001c0001t0002g0032a0001c0001t0002g0226 | 3 | HG00733.hp2 HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.136+6929_136+6931d others(5): Show |
IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 36617165 | |||||
chr11:36617198 | T | G | 1 | a0001c0001t0002g0237 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.136+6959T>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36617198 | ||||||
chr11:36617351 | C | G | 13 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(10): Show | 16 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.136+7112C>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36617351 | ||||||
chr11:36617360 | TG | T | 29 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0039others(26): Show | 46 | HG00140.hp2 HG00408.hp2 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.136+7123delG | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 36617360 | |||||
chr11:36617382 | A | G | 39 | a0001c0001t0002g0016a0001c0001t0002g0024a0001c0001t0002g0031others(36): Show | 45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.136+7143A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36617382 | ||||||
chr11:36617477 | G | A | 1 | a0001c0001t0002g0024 | 2 | NA18747.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.136+7238G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36617477 | ||||||
chr11:36617512 | G | A | 1 | a0001c0001t0001g0075 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.136+7273G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36617512 | ||||||
chr11:36617530 | T | C | 1 | a0001c0001t0001g0260 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.136+7291T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36617530 | ||||||
chr11:36617549 | T | C | 7 | a0001c0001t0001g0015a0001c0001t0001g0045a0001c0001t0001g0248others(4): Show | 10 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(7): Show |
intron_variant | MODIFIER | c.136+7310T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36617549 | ||||||
chr11:36617650 | T | C | 1 | a0004c0006t0001g0057 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.136+7411T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36617650 | ||||||
chr11:36617709 | G | A | 39 | a0001c0001t0002g0016a0001c0001t0002g0024a0001c0001t0002g0031others(36): Show | 45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.136+7470G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36617709 | ||||||
chr11:36617725 | G | C | 1 | a0001c0001t0001g0135 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.136+7486G>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36617725 | ||||||
chr11:36617814 | T | A | 39 | a0001c0001t0002g0016a0001c0001t0002g0024a0001c0001t0002g0031others(36): Show | 45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.136+7575T>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36617814 | ||||||
chr11:36617891 | G | C | 39 | a0001c0001t0002g0016a0001c0001t0002g0024a0001c0001t0002g0031others(36): Show | 45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.136+7652G>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36617891 | ||||||
chr11:36618041 | G | T | 52 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(49): Show | 61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.136+7802G>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36618041 | ||||||
chr11:36618134 | G | T | 71 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0011others(68): Show | 94 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.136+7895G>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36618134 | ||||||
chr11:36618174 | A | G | 1 | a0001c0001t0001g0169 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.136+7935A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36618174 | ||||||
chr11:36618237 | G | C | 3 | a0001c0001t0001g0175a0001c0001t0001g0182a0001c0001t0001g0183 | 3 | HG01884.hp1 HG02896.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.136+7998G>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36618237 | ||||||
chr11:36618246 | C | T | 39 | a0001c0001t0002g0016a0001c0001t0002g0024a0001c0001t0002g0031others(36): Show | 45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.136+8007C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36618246 | ||||||
chr11:36618630 | G | C | 1 | a0001c0001t0001g0025 | 2 | HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.136+8391G>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36618630 | ||||||
chr11:36618696 | G | A | 39 | a0001c0001t0002g0016a0001c0001t0002g0024a0001c0001t0002g0031others(36): Show | 45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.136+8457G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36618696 | ||||||
chr11:36618716 | C | T | 1 | a0001c0001t0002g0131 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.136+8477C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36618716 | ||||||
chr11:36618923 | G | A | 39 | a0001c0001t0002g0016a0001c0001t0002g0024a0001c0001t0002g0031others(36): Show | 45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.136+8684G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36618923 | ||||||
chr11:36618931 | A | G | 1 | a0001c0001t0001g0183 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.136+8692A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36618931 | ||||||
chr11:36618994 | C | A | 3 | a0001c0001t0001g0175a0001c0001t0001g0182a0001c0001t0001g0183 | 3 | HG01884.hp1 HG02896.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.136+8755C>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36618994 | ||||||
chr11:36619044 | C | T | 3 | a0001c0001t0001g0041a0001c0001t0001g0245a0001c0001t0001g0263 | 4 | NA18951.hp2 NA18978.hp2 NA19072.hp2 others(1): Show |
intron_variant | MODIFIER | c.136+8805C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36619044 | ||||||
chr11:36619234 | A | G | 2 | a0001c0001t0001g0095a0001c0001t0001g0096 | 2 | NA18943.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.136+8995A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36619234 | ||||||
chr11:36619267 | G | C | 13 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(10): Show | 16 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.136+9028G>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36619267 | ||||||
chr11:36619307 | C | G | 1 | a0001c0001t0001g0125 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.136+9068C>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36619307 | ||||||
chr11:36619313 | C | T | 1 | a0001c0001t0001g0063 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.136+9074C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36619313 | ||||||
chr11:36619314 | G | A | 1 | a0001c0001t0001g0148 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.136+9075G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36619314 | ||||||
chr11:36619325 | A | G | 1 | a0001c0001t0001g0200 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.136+9086A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36619325 | ||||||
chr11:36619427 | A | G | 2 | a0001c0001t0001g0173a0001c0001t0001g0174 | 2 | NA18971.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.136+9188A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36619427 | ||||||
chr11:36619432 | A | G | 13 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(10): Show | 16 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.136+9193A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36619432 | ||||||
chr11:36619455 | G | C | 52 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(49): Show | 61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.136+9216G>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36619455 | ||||||
chr11:36619558 | A | G | 1 | a0001c0001t0001g0019 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.136+9319A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36619558 | ||||||
chr11:36619899 | A | G | 39 | a0001c0001t0002g0016a0001c0001t0002g0024a0001c0001t0002g0031others(36): Show | 45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.136+9660A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36619899 | ||||||
chr11:36619955 | A | AGACATAG others(7): Show |
174 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(171): Show | 233 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(230): Show |
intron_variant | MODIFIER | c.136+9718_136+9731d others(16): Show |
IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 36619955 | |||||
chr11:36620034 | C | T | 1 | a0001c0001t0001g0025 | 2 | HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.136+9795C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36620034 | ||||||
chr11:36620204 | A | G | 1 | a0001c0001t0001g0094 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.136+9965A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36620204 | ||||||
chr11:36620217 | A | G | 13 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(10): Show | 16 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.136+9978A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36620217 | ||||||
chr11:36620256 | G | A | 2 | a0001c0001t0001g0192a0001c0001t0001g0193 | 2 | HG01358.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.136+10017G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36620256 | ||||||
chr11:36620273 | A | G | 1 | a0001c0001t0001g0212 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.136+10034A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36620273 | ||||||
chr11:36620280 | C | G | 39 | a0001c0001t0002g0016a0001c0001t0002g0024a0001c0001t0002g0031others(36): Show | 45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.136+10041C>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36620280 | ||||||
chr11:36620283 | A | G | 1 | a0001c0001t0001g0168 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.136+10044A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36620283 | ||||||
chr11:36620427 | G | C | 1 | a0001c0001t0001g0187 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.136+10188G>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36620427 | ||||||
chr11:36620639 | G | T | 41 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0002g0016others(38): Show | 47 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.136+10400G>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36620639 | ||||||
chr11:36620652 | A | G | 16 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0023others(13): Show | 19 | HG00741.hp1 HG01074.hp1 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.136+10413A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36620652 | ||||||
chr11:36620740 | C | T | 52 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(49): Show | 61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.136+10501C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36620740 | ||||||
chr11:36620812 | T | A | 1 | a0001c0001t0001g0107 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.136+10573T>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36620812 | ||||||
chr11:36620823 | C | T | 135 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(132): Show | 172 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(169): Show |
intron_variant | MODIFIER | c.136+10584C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36620823 | ||||||
chr11:36620864 | ATTGT | A | 39 | a0001c0001t0002g0016a0001c0001t0002g0024a0001c0001t0002g0031others(36): Show | 45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.136+10629_136+1063 others(8): Show |
IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 36620864 | |||||
chr11:36620935 | ATAAAT | A | 39 | a0001c0001t0002g0016a0001c0001t0002g0024a0001c0001t0002g0031others(36): Show | 45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.136+10699_136+1070 others(9): Show |
IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 36620935 | |||||
chr11:36620954 | T | G | 1 | a0001c0001t0001g0076 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.136+10715T>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36620954 | ||||||
chr11:36620969 | G | A | 39 | a0001c0001t0002g0016a0001c0001t0002g0024a0001c0001t0002g0031others(36): Show | 45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.136+10730G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36620969 | ||||||
chr11:36621009 | G | C | 39 | a0001c0001t0002g0016a0001c0001t0002g0024a0001c0001t0002g0031others(36): Show | 45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.136+10770G>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36621009 | ||||||
chr11:36621010 | T | C | 39 | a0001c0001t0002g0016a0001c0001t0002g0024a0001c0001t0002g0031others(36): Show | 45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.136+10771T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36621010 | ||||||
chr11:36621013 | A | G | 11 | a0001c0001t0002g0016a0001c0001t0002g0047a0001c0001t0002g0048others(8): Show | 11 | HG00438.hp1 HG02523.hp1 HG03239.hp1 others(8): Show |
intron_variant | MODIFIER | c.136+10774A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36621013 | ||||||
chr11:36621014 | A | G | 39 | a0001c0001t0002g0016a0001c0001t0002g0024a0001c0001t0002g0031others(36): Show | 45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.136+10775A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36621014 | ||||||
chr11:36621140 | G | A | 39 | a0001c0001t0002g0016a0001c0001t0002g0024a0001c0001t0002g0031others(36): Show | 45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.136+10901G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36621140 | ||||||
chr11:36621251 | TTAGCAA | T | 3 | a0002c0003t0002g0014a0002c0004t0002g0014a0002c0004t0002g0236 | 4 | HG02615.hp2 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.136+11013_136+1101 others(10): Show |
IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36621251 | ||||||
chr11:36621380 | C | A | 1 | a0001c0001t0001g0143 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.136+11141C>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36621380 | ||||||
chr11:36621660 | T | G | 4 | a0001c0002t0003g0013a0001c0002t0003g0209a0001c0002t0003g0210others(1): Show | 6 | HG02723.hp2 HG02886.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.136+11421T>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36621660 | ||||||
chr11:36621695 | C | G | 2 | a0001c0001t0002g0207a0001c0001t0002g0208 | 2 | HG02572.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.136+11456C>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36621695 | ||||||
chr11:36621724 | G | T | 2 | a0001c0001t0001g0135a0001c0001t0001g0136 | 2 | HG02818.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.136+11485G>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36621724 | ||||||
chr11:36622061 | T | G | 2 | a0001c0001t0001g0135a0001c0001t0001g0136 | 2 | HG02818.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.137-11223T>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36622061 | ||||||
chr11:36622069 | T | C | 2 | a0001c0001t0001g0251a0001c0001t0001g0260 | 2 | NA18964.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.137-11215T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36622069 | ||||||
chr11:36622083 | A | ATTTTTTT | 26 | a0001c0001t0002g0016a0001c0001t0002g0031a0001c0001t0002g0032others(23): Show | 31 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.137-11195_137-1119 others(11): Show |
IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 36622083 | |||||
chr11:36622083 | A | ATTTTTTT others(1): Show |
7 | a0001c0001t0002g0048a0001c0001t0002g0055a0001c0001t0002g0214others(4): Show | 7 | HG01517.hp2 HG02523.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.137-11195_137-1119 others(12): Show |
IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 36622083 | |||||
chr11:36622088 | TTA | T | 8 | a0001c0001t0001g0137a0001c0001t0001g0194a0001c0001t0001g0197others(5): Show | 8 | HG01074.hp2 HG01192.hp2 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.137-11194_137-1119 others(6): Show |
IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 36622088 | |||||
chr11:36622089 | TA | T | 62 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0011others(59): Show | 86 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.137-11194delA | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36622089 | ||||||
chr11:36622090 | A | T | 59 | a0001c0001t0001g0008a0001c0001t0001g0030a0001c0001t0001g0138others(56): Show | 71 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(68): Show |
intron_variant | MODIFIER | c.137-11194A>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36622090 | ||||||
chr11:36622168 | C | T | 1 | a0001c0001t0001g0105 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.137-11116C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36622168 | ||||||
chr11:36622401 | G | A | 39 | a0001c0001t0002g0016a0001c0001t0002g0024a0001c0001t0002g0031others(36): Show | 45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.137-10883G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36622401 | ||||||
chr11:36622483 | C | T | 1 | a0001c0001t0001g0132 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.137-10801C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36622483 | ||||||
chr11:36622526 | A | G | 39 | a0001c0001t0002g0016a0001c0001t0002g0024a0001c0001t0002g0031others(36): Show | 45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.137-10758A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36622526 | ||||||
chr11:36622549 | C | G | 1 | a0001c0001t0002g0235 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.137-10735C>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36622549 | ||||||
chr11:36622596 | C | G | 5 | a0001c0001t0002g0214a0001c0001t0002g0215a0001c0001t0002g0230others(2): Show | 5 | HG02895.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.137-10688C>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36622596 | ||||||
chr11:36622707 | CAT | C | 2 | a0001c0001t0001g0025a0001c0001t0001g0098 | 3 | HG02523.hp2 HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.137-10576_137-1057 others(6): Show |
IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36622707 | ||||||
chr11:36622712 | G | A | 1 | a0001c0001t0002g0237 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.137-10572G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36622712 | ||||||
chr11:36622719 | T | G | 11 | a0001c0001t0002g0016a0001c0001t0002g0047a0001c0001t0002g0048others(8): Show | 11 | HG00438.hp1 HG02523.hp1 HG03239.hp1 others(8): Show |
intron_variant | MODIFIER | c.137-10565T>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36622719 | ||||||
chr11:36622748 | C | T | 39 | a0001c0001t0002g0016a0001c0001t0002g0024a0001c0001t0002g0031others(36): Show | 45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.137-10536C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36622748 | ||||||
chr11:36622800 | T | C | 3 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0242 | 5 | HG01243.hp1 HG02257.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.137-10484T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36622800 | ||||||
chr11:36623004 | A | C | 1 | a0001c0001t0001g0194 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.137-10280A>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36623004 | ||||||
chr11:36623031 | T | C | 39 | a0001c0001t0002g0016a0001c0001t0002g0024a0001c0001t0002g0031others(36): Show | 45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.137-10253T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36623031 | ||||||
chr11:36623100 | T | G | 1 | a0001c0001t0001g0181 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.137-10184T>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36623100 | ||||||
chr11:36623128 | G | C | 1 | a0001c0001t0001g0077 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.137-10156G>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36623128 | ||||||
chr11:36623143 | T | C | 39 | a0001c0001t0002g0016a0001c0001t0002g0024a0001c0001t0002g0031others(36): Show | 45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.137-10141T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36623143 | ||||||
chr11:36623172 | C | T | 13 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(10): Show | 16 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.137-10112C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36623172 | ||||||
chr11:36623317 | T | TC | 39 | a0001c0001t0002g0016a0001c0001t0002g0024a0001c0001t0002g0031others(36): Show | 45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.137-9967_137-9966i others(3): Show |
IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36623317 | ||||||
chr11:36623353 | T | C | 39 | a0001c0001t0002g0016a0001c0001t0002g0024a0001c0001t0002g0031others(36): Show | 45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.137-9931T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36623353 | ||||||
chr11:36623356 | T | TC | 78 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0011others(75): Show | 104 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.137-9919dupC | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 36623356 | |||||
chr11:36623490 | C | T | 3 | a0002c0003t0002g0014a0002c0004t0002g0014a0002c0004t0002g0236 | 4 | HG02615.hp2 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.137-9794C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36623490 | ||||||
chr11:36623657 | C | T | 39 | a0001c0001t0002g0016a0001c0001t0002g0024a0001c0001t0002g0031others(36): Show | 45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.137-9627C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36623657 | ||||||
chr11:36623681 | C | T | 39 | a0001c0001t0002g0016a0001c0001t0002g0024a0001c0001t0002g0031others(36): Show | 45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.137-9603C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36623681 | ||||||
chr11:36623707 | A | G | 39 | a0001c0001t0002g0016a0001c0001t0002g0024a0001c0001t0002g0031others(36): Show | 45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.137-9577A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36623707 | ||||||
chr11:36623745 | A | G | 1 | a0001c0001t0001g0137 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.137-9539A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36623745 | ||||||
chr11:36623826 | G | A | 39 | a0001c0001t0002g0016a0001c0001t0002g0024a0001c0001t0002g0031others(36): Show | 45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.137-9458G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36623826 | ||||||
chr11:36623853 | AG | A | 39 | a0001c0001t0002g0016a0001c0001t0002g0024a0001c0001t0002g0031others(36): Show | 45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.137-9430delG | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36623853 | ||||||
chr11:36623860 | C | T | 1 | a0001c0001t0001g0165 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.137-9424C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36623860 | ||||||
chr11:36623861 | G | A | 47 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0109others(44): Show | 55 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.137-9423G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36623861 | ||||||
chr11:36623863 | A | G | 1 | a0001c0001t0002g0131 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.137-9421A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36623863 | ||||||
chr11:36623967 | TTATATAT others(7): Show |
T | 1 | a0001c0001t0001g0178 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.137-9293_137-9280d others(16): Show |
IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 36623967 | |||||
chr11:36623995 | G | GTA | 14 | a0001c0001t0002g0016a0001c0001t0002g0024a0001c0001t0002g0047others(11): Show | 15 | HG01516.hp2 HG01517.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.137-9279_137-9278d others(4): Show |
IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 36623995 | |||||
chr11:36624005 | A | ATT | 23 | a0001c0001t0002g0031a0001c0001t0002g0032a0001c0001t0002g0033others(20): Show | 28 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.137-9273_137-9272d others(4): Show |
IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 36624005 | |||||
chr11:36624005 | A | T | 11 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0056others(8): Show | 16 | HG01069.hp2 HG01071.hp1 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.137-9279A>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36624005 | ||||||
chr11:36624043 | C | T | 263 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(260): Show | 355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.137-9241C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36624043 | ||||||
chr11:36624079 | C | T | 1 | a0001c0001t0002g0237 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.137-9205C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36624079 | ||||||
chr11:36624176 | A | T | 1 | a0001c0001t0001g0168 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.137-9108A>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36624176 | ||||||
chr11:36624335 | G | A | 1 | a0001c0001t0001g0248 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.137-8949G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36624335 | ||||||
chr11:36624337 | G | A | 39 | a0001c0001t0002g0016a0001c0001t0002g0024a0001c0001t0002g0031others(36): Show | 45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.137-8947G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36624337 | ||||||
chr11:36624389 | G | A | 13 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(10): Show | 16 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.137-8895G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36624389 | ||||||
chr11:36624490 | C | T | 39 | a0001c0001t0002g0016a0001c0001t0002g0024a0001c0001t0002g0031others(36): Show | 45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.137-8794C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36624490 | ||||||
chr11:36624514 | C | T | 39 | a0001c0001t0002g0016a0001c0001t0002g0024a0001c0001t0002g0031others(36): Show | 45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.137-8770C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36624514 | ||||||
chr11:36624576 | C | G | 27 | a0001c0001t0002g0024a0001c0001t0002g0031a0001c0001t0002g0032others(24): Show | 33 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.137-8708C>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36624576 | ||||||
chr11:36624680 | C | T | 26 | a0001c0001t0002g0031a0001c0001t0002g0032a0001c0001t0002g0033others(23): Show | 31 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.137-8604C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36624680 | ||||||
chr11:36624692 | G | T | 11 | a0001c0001t0002g0016a0001c0001t0002g0047a0001c0001t0002g0048others(8): Show | 11 | HG00438.hp1 HG02523.hp1 HG03239.hp1 others(8): Show |
intron_variant | MODIFIER | c.137-8592G>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36624692 | ||||||
chr11:36624727 | G | A | 1 | a0001c0001t0001g0025 | 2 | HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.137-8557G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36624727 | ||||||
chr11:36624766 | T | C | 11 | a0001c0001t0002g0016a0001c0001t0002g0047a0001c0001t0002g0048others(8): Show | 11 | HG00438.hp1 HG02523.hp1 HG03239.hp1 others(8): Show |
intron_variant | MODIFIER | c.137-8518T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36624766 | ||||||
chr11:36624772 | G | A | 2 | a0001c0001t0001g0135a0001c0001t0001g0136 | 2 | HG02818.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.137-8512G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36624772 | ||||||
chr11:36624800 | C | T | 52 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(49): Show | 61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.137-8484C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36624800 | ||||||
chr11:36624808 | T | C | 1 | a0001c0001t0001g0079 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.137-8476T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36624808 | ||||||
chr11:36624840 | A | AAAC | 39 | a0001c0001t0002g0016a0001c0001t0002g0024a0001c0001t0002g0031others(36): Show | 45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.137-8444_137-8443i others(5): Show |
IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36624840 | ||||||
chr11:36624841 | G | A | 39 | a0001c0001t0002g0016a0001c0001t0002g0024a0001c0001t0002g0031others(36): Show | 45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.137-8443G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36624841 | ||||||
chr11:36624842 | G | A | 39 | a0001c0001t0002g0016a0001c0001t0002g0024a0001c0001t0002g0031others(36): Show | 45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.137-8442G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36624842 | ||||||
chr11:36625013 | A | G | 52 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(49): Show | 61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.137-8271A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36625013 | ||||||
chr11:36625040 | A | G | 1 | a0001c0001t0002g0235 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.137-8244A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36625040 | ||||||
chr11:36625178 | T | C | 6 | a0001c0001t0002g0207a0001c0001t0002g0208a0001c0002t0003g0013others(3): Show | 8 | HG02572.hp1 HG02723.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.137-8106T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36625178 | ||||||
chr11:36625289 | A | C | 1 | a0001c0001t0001g0067 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.137-7995A>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36625289 | ||||||
chr11:36625295 | T | G | 52 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(49): Show | 61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.137-7989T>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36625295 | ||||||
chr11:36625319 | A | C | 39 | a0001c0001t0002g0016a0001c0001t0002g0024a0001c0001t0002g0031others(36): Show | 45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.137-7965A>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36625319 | ||||||
chr11:36625460 | A | G | 26 | a0001c0001t0002g0031a0001c0001t0002g0032a0001c0001t0002g0033others(23): Show | 31 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.137-7824A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36625460 | ||||||
chr11:36625611 | G | A | 2 | a0001c0001t0002g0207a0001c0001t0002g0208 | 2 | HG02572.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.137-7673G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36625611 | ||||||
chr11:36625756 | G | A | 2 | a0001c0001t0001g0017a0001c0001t0001g0080 | 3 | HG00099.hp2 HG00741.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.137-7528G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36625756 | ||||||
chr11:36625794 | G | A | 1 | a0001c0001t0001g0025 | 2 | HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.137-7490G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36625794 | ||||||
chr11:36625905 | C | T | 1 | a0001c0001t0002g0054 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.137-7379C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36625905 | ||||||
chr11:36625907 | AGTGCAAA others(7347): Show |
A | 6 | a0001c0001t0001g0008a0001c0001t0001g0030a0001c0001t0001g0203others(3): Show | 10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.137-7376_137-23del | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36625907 | ||||||
chr11:36626241 | T | C | 13 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(10): Show | 16 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.137-7043T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36626241 | ||||||
chr11:36626482 | G | A | 1 | a0001c0001t0002g0235 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.137-6802G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36626482 | ||||||
chr11:36626528 | C | A | 11 | a0001c0001t0002g0016a0001c0001t0002g0047a0001c0001t0002g0048others(8): Show | 11 | HG00438.hp1 HG02523.hp1 HG03239.hp1 others(8): Show |
intron_variant | MODIFIER | c.137-6756C>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36626528 | ||||||
chr11:36626570 | C | T | 2 | a0001c0001t0002g0024a0001c0001t0002g0237 | 3 | HG02451.hp1 NA18747.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.137-6714C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36626570 | ||||||
chr11:36626635 | C | G | 11 | a0001c0001t0002g0016a0001c0001t0002g0047a0001c0001t0002g0048others(8): Show | 11 | HG00438.hp1 HG02523.hp1 HG03239.hp1 others(8): Show |
intron_variant | MODIFIER | c.137-6649C>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36626635 | ||||||
chr11:36626722 | C | T | 1 | a0001c0001t0001g0242 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.137-6562C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36626722 | ||||||
chr11:36626882 | G | A | 3 | a0001c0001t0001g0125a0001c0001t0001g0132a0001c0001t0001g0212 | 3 | HG02451.hp2 NA18522.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.137-6402G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36626882 | ||||||
chr11:36626896 | C | T | 1 | a0001c0001t0001g0132 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.137-6388C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36626896 | ||||||
chr11:36627091 | C | T | 5 | a0001c0001t0002g0214a0001c0001t0002g0215a0001c0001t0002g0230others(2): Show | 5 | HG02895.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.137-6193C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36627091 | ||||||
chr11:36627343 | C | T | 1 | a0001c0001t0001g0185 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.137-5941C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36627343 | ||||||
chr11:36627345 | C | A | 1 | a0001c0001t0001g0046 | 2 | HG02486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.137-5939C>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36627345 | ||||||
chr11:36627425 | T | A | 1 | a0001c0001t0001g0025 | 2 | HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.137-5859T>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36627425 | ||||||
chr11:36627631 | G | T | 1 | a0001c0001t0001g0028 | 2 | HG01891.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.137-5653G>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36627631 | ||||||
chr11:36627648 | C | T | 2 | a0001c0001t0002g0207a0001c0001t0002g0208 | 2 | HG02572.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.137-5636C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36627648 | ||||||
chr11:36627813 | A | C | 3 | a0002c0003t0002g0014a0002c0004t0002g0014a0002c0004t0002g0236 | 4 | HG02615.hp2 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.137-5471A>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36627813 | ||||||
chr11:36628001 | T | C | 37 | a0001c0001t0002g0016a0001c0001t0002g0031a0001c0001t0002g0032others(34): Show | 42 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.137-5283T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36628001 | ||||||
chr11:36628004 | G | T | 4 | a0001c0001t0001g0077a0001c0001t0001g0090a0001c0001t0001g0091others(1): Show | 4 | HG01099.hp2 HG01106.hp1 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.137-5280G>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36628004 | ||||||
chr11:36628009 | C | CT | 10 | a0001c0001t0001g0110a0001c0001t0001g0135a0001c0001t0001g0136others(7): Show | 11 | HG01109.hp1 HG01109.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.137-5262dupT | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 36628009 | |||||
chr11:36628009 | C | CTT | 6 | a0001c0001t0002g0207a0001c0001t0002g0208a0001c0002t0003g0013others(3): Show | 8 | HG02572.hp1 HG02723.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.137-5263_137-5262d others(4): Show |
IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 36628009 | |||||
chr11:36628009 | CT | C | 27 | a0001c0001t0001g0195a0001c0001t0002g0031a0001c0001t0002g0032others(24): Show | 32 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.137-5262delT | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 36628009 | |||||
chr11:36628054 | T | C | 1 | a0001c0001t0002g0237 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.137-5230T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36628054 | ||||||
chr11:36628172 | T | G | 2 | a0001c0001t0001g0135a0001c0001t0001g0136 | 2 | HG02818.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.137-5112T>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36628172 | ||||||
chr11:36628425 | G | A | 3 | a0001c0001t0001g0125a0001c0001t0001g0132a0001c0001t0001g0212 | 3 | HG02451.hp2 NA18522.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.137-4859G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36628425 | ||||||
chr11:36628616 | T | C | 1 | a0001c0001t0001g0090 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.137-4668T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36628616 | ||||||
chr11:36628634 | C | T | 2 | a0001c0001t0002g0207a0001c0001t0002g0208 | 2 | HG02572.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.137-4650C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36628634 | ||||||
chr11:36628703 | T | G | 13 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(10): Show | 16 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.137-4581T>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36628703 | ||||||
chr11:36628807 | A | G | 52 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(49): Show | 61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.137-4477A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36628807 | ||||||
chr11:36628998 | G | C | 1 | a0001c0001t0001g0025 | 2 | HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.137-4286G>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36628998 | ||||||
chr11:36629244 | A | C | 1 | a0001c0001t0001g0164 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.137-4040A>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36629244 | ||||||
chr11:36629287 | T | A | 1 | a0001c0001t0001g0179 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.137-3997T>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36629287 | ||||||
chr11:36629366 | A | G | 26 | a0001c0001t0002g0031a0001c0001t0002g0032a0001c0001t0002g0033others(23): Show | 31 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.137-3918A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36629366 | ||||||
chr11:36629743 | G | T | 3 | a0002c0003t0002g0014a0002c0004t0002g0014a0002c0004t0002g0236 | 4 | HG02615.hp2 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.137-3541G>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36629743 | ||||||
chr11:36629910 | C | T | 2 | a0001c0001t0001g0137a0001c0001t0002g0235 | 2 | HG02630.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.137-3374C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36629910 | ||||||
chr11:36629957 | T | G | 4 | a0001c0002t0003g0013a0001c0002t0003g0209a0001c0002t0003g0210others(1): Show | 6 | HG02723.hp2 HG02886.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.137-3327T>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36629957 | ||||||
chr11:36630001 | A | G | 2 | a0001c0001t0001g0173a0001c0001t0001g0174 | 2 | NA18971.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.137-3283A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36630001 | ||||||
chr11:36630354 | G | A | 52 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(49): Show | 61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.137-2930G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36630354 | ||||||
chr11:36630590 | A | G | 6 | a0001c0001t0002g0207a0001c0001t0002g0208a0001c0002t0003g0013others(3): Show | 8 | HG02572.hp1 HG02723.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.137-2694A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36630590 | ||||||
chr11:36630655 | T | C | 1 | a0001c0001t0001g0181 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.137-2629T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36630655 | ||||||
chr11:36630669 | C | T | 4 | a0001c0001t0001g0088a0001c0001t0001g0103a0001c0001t0001g0106others(1): Show | 4 | HG00621.hp1 HG02155.hp1 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.137-2615C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36630669 | ||||||
chr11:36630765 | A | G | 26 | a0001c0001t0002g0031a0001c0001t0002g0032a0001c0001t0002g0033others(23): Show | 31 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.137-2519A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36630765 | ||||||
chr11:36630886 | G | C | 1 | a0001c0001t0001g0146 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.137-2398G>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36630886 | ||||||
chr11:36630956 | A | G | 1 | a0001c0001t0001g0179 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.137-2328A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36630956 | ||||||
chr11:36630989 | C | G | 26 | a0001c0001t0002g0031a0001c0001t0002g0032a0001c0001t0002g0033others(23): Show | 31 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.137-2295C>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36630989 | ||||||
chr11:36631019 | C | T | 39 | a0001c0001t0002g0016a0001c0001t0002g0024a0001c0001t0002g0031others(36): Show | 45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.137-2265C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36631019 | ||||||
chr11:36631247 | T | C | 11 | a0001c0001t0002g0016a0001c0001t0002g0047a0001c0001t0002g0048others(8): Show | 11 | HG00438.hp1 HG02523.hp1 HG03239.hp1 others(8): Show |
intron_variant | MODIFIER | c.137-2037T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36631247 | ||||||
chr11:36631267 | TGGTG | T | 3 | a0002c0003t0002g0014a0002c0004t0002g0014a0002c0004t0002g0236 | 4 | HG02615.hp2 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.137-2016_137-2013d others(6): Show |
IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36631267 | ||||||
chr11:36631336 | G | A | 3 | a0002c0003t0002g0014a0002c0004t0002g0014a0002c0004t0002g0236 | 4 | HG02615.hp2 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.137-1948G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36631336 | ||||||
chr11:36631434 | G | A | 13 | a0001c0001t0002g0016a0001c0001t0002g0024a0001c0001t0002g0047others(10): Show | 14 | HG00438.hp1 HG02451.hp1 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.137-1850G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36631434 | ||||||
chr11:36631645 | A | G | 259 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(256): Show | 347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.137-1639A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36631645 | ||||||
chr11:36631723 | T | G | 3 | a0002c0003t0002g0014a0002c0004t0002g0014a0002c0004t0002g0236 | 4 | HG02615.hp2 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.137-1561T>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36631723 | ||||||
chr11:36631726 | A | G | 3 | a0002c0003t0002g0014a0002c0004t0002g0014a0002c0004t0002g0236 | 4 | HG02615.hp2 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.137-1558A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36631726 | ||||||
chr11:36631766 | C | G | 1 | a0001c0001t0002g0237 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.137-1518C>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36631766 | ||||||
chr11:36631793 | C | G | 2 | a0001c0001t0001g0135a0001c0001t0001g0136 | 2 | HG02818.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.137-1491C>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36631793 | ||||||
chr11:36631799 | T | C | 37 | a0001c0001t0002g0016a0001c0001t0002g0031a0001c0001t0002g0032others(34): Show | 42 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.137-1485T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36631799 | ||||||
chr11:36631913 | ATTC | A | 2 | a0001c0001t0002g0024a0001c0001t0002g0237 | 3 | HG02451.hp1 NA18747.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.137-1365_137-1363d others(5): Show |
IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr11 | 36631913 | |||||
chr11:36632028 | G | A | 2 | a0001c0001t0001g0135a0001c0001t0001g0136 | 2 | HG02818.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.137-1256G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36632028 | ||||||
chr11:36632179 | T | G | 4 | a0001c0001t0001g0028a0001c0001t0001g0152a0001c0001t0001g0153others(1): Show | 5 | HG01891.hp1 HG02615.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.137-1105T>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36632179 | ||||||
chr11:36632181 | T | A | 1 | a0001c0001t0001g0081 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.137-1103T>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36632181 | ||||||
chr11:36632299 | G | T | 1 | a0001c0001t0001g0133 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.137-985G>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36632299 | ||||||
chr11:36632412 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.137-872C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36632412 | ||||||
chr11:36632609 | A | G | 1 | a0001c0001t0002g0024 | 2 | NA18747.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.137-675A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36632609 | ||||||
chr11:36632786 | C | T | 52 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(49): Show | 61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.137-498C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36632786 | ||||||
chr11:36632920 | G | A | 52 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(49): Show | 61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.137-364G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36632920 | ||||||
chr11:36632953 | A | C | 1 | a0001c0001t0001g0250 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.137-331A>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36632953 | ||||||
chr11:36633072 | T | G | 26 | a0001c0001t0002g0031a0001c0001t0002g0032a0001c0001t0002g0033others(23): Show | 31 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.137-212T>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36633072 | ||||||
chr11:36633086 | G | A | 11 | a0001c0001t0002g0016a0001c0001t0002g0047a0001c0001t0002g0048others(8): Show | 11 | HG00438.hp1 HG02523.hp1 HG03239.hp1 others(8): Show |
intron_variant | MODIFIER | c.137-198G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36633086 | ||||||
chr11:36633162 | C | T | 1 | a0001c0001t0001g0062 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.137-122C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36633162 | ||||||
chr11:36633164 | G | A | 2 | a0001c0001t0002g0221a0001c0001t0002g0233 | 2 | HG00735.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.137-120G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36633164 | ||||||
chr11:36633263 | G | C | 6 | a0001c0001t0001g0008a0001c0001t0001g0030a0001c0001t0001g0203others(3): Show | 10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.137-21G>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36633263 | ||||||
chr11:36633265 | G | A | 6 | a0001c0001t0001g0008a0001c0001t0001g0030a0001c0001t0001g0203others(3): Show | 10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.137-19G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36633265 | ||||||
chr11:36633266 | C | A | 6 | a0001c0001t0001g0008a0001c0001t0001g0030a0001c0001t0001g0203others(3): Show | 10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.137-18C>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36633266 | ||||||
chr11:36633270 | AC | A | 6 | a0001c0001t0001g0008a0001c0001t0001g0030a0001c0001t0001g0203others(3): Show | 10 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.137-13delC | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 2/5 | chr11 | 36633270 | ||||||
chr11:36633499 | C | CA | 52 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(49): Show | 61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.291+69dupA | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr11 | 36633499 | |||||
chr11:36633539 | A | G | 74 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0011others(71): Show | 97 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.291+101A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 3/5 | chr11 | 36633539 | ||||||
chr11:36633738 | A | G | 52 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(49): Show | 61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.291+300A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 3/5 | chr11 | 36633738 | ||||||
chr11:36633816 | G | A | 1 | a0001c0002t0003g0211 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.291+378G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 3/5 | chr11 | 36633816 | ||||||
chr11:36633825 | G | A | 1 | a0001c0001t0001g0130 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.291+387G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 3/5 | chr11 | 36633825 | ||||||
chr11:36633849 | C | T | 52 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(49): Show | 61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.291+411C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 3/5 | chr11 | 36633849 | ||||||
chr11:36634026 | A | G | 52 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(49): Show | 61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.291+588A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 3/5 | chr11 | 36634026 | ||||||
chr11:36634201 | T | C | 83 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(80): Show | 110 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.291+763T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 3/5 | chr11 | 36634201 | ||||||
chr11:36634234 | G | A | 178 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(175): Show | 237 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(234): Show |
intron_variant | MODIFIER | c.291+796G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 3/5 | chr11 | 36634234 | ||||||
chr11:36634256 | A | G | 1 | a0004c0006t0001g0057 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.291+818A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 3/5 | chr11 | 36634256 | ||||||
chr11:36634314 | G | T | 13 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(10): Show | 16 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.291+876G>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 3/5 | chr11 | 36634314 | ||||||
chr11:36634336 | T | C | 11 | a0001c0001t0002g0016a0001c0001t0002g0047a0001c0001t0002g0048others(8): Show | 11 | HG00438.hp1 HG02523.hp1 HG03239.hp1 others(8): Show |
intron_variant | MODIFIER | c.291+898T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 3/5 | chr11 | 36634336 | ||||||
chr11:36634339 | A | G | 139 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(136): Show | 176 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(173): Show |
intron_variant | MODIFIER | c.291+901A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 3/5 | chr11 | 36634339 | ||||||
chr11:36634383 | C | G | 1 | a0001c0001t0002g0024 | 2 | NA18747.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.291+945C>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 3/5 | chr11 | 36634383 | ||||||
chr11:36634461 | G | A | 16 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0023others(13): Show | 19 | HG00741.hp1 HG01074.hp1 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.291+1023G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 3/5 | chr11 | 36634461 | ||||||
chr11:36634544 | A | G | 2 | a0001c0001t0001g0020a0001c0001t0001g0109 | 3 | HG01074.hp1 HG01346.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.291+1106A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 3/5 | chr11 | 36634544 | ||||||
chr11:36634814 | AT | A | 52 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(49): Show | 61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.292-1228delT | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr11 | 36634814 | |||||
chr11:36634889 | G | C | 2 | a0001c0001t0001g0137a0001c0001t0002g0235 | 2 | HG02630.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.292-1162G>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 3/5 | chr11 | 36634889 | ||||||
chr11:36634946 | G | C | 3 | a0002c0003t0002g0014a0002c0004t0002g0014a0002c0004t0002g0236 | 4 | HG02615.hp2 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.292-1105G>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 3/5 | chr11 | 36634946 | ||||||
chr11:36634949 | TACACCAC others(23): Show |
T | 2 | a0001c0001t0002g0034a0001c0001t0002g0035 | 4 | HG02257.hp1 HG02280.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.292-1098_292-1069d others(32): Show |
IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr11 | 36634949 | |||||
chr11:36634990 | A | T | 1 | a0001c0001t0002g0215 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.292-1061A>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 3/5 | chr11 | 36634990 | ||||||
chr11:36635063 | G | A | 11 | a0001c0001t0002g0016a0001c0001t0002g0047a0001c0001t0002g0048others(8): Show | 11 | HG00438.hp1 HG02523.hp1 HG03239.hp1 others(8): Show |
intron_variant | MODIFIER | c.292-988G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 3/5 | chr11 | 36635063 | ||||||
chr11:36635066 | T | A | 11 | a0001c0001t0002g0016a0001c0001t0002g0047a0001c0001t0002g0048others(8): Show | 11 | HG00438.hp1 HG02523.hp1 HG03239.hp1 others(8): Show |
intron_variant | MODIFIER | c.292-985T>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 3/5 | chr11 | 36635066 | ||||||
chr11:36635067 | G | T | 11 | a0001c0001t0002g0016a0001c0001t0002g0047a0001c0001t0002g0048others(8): Show | 11 | HG00438.hp1 HG02523.hp1 HG03239.hp1 others(8): Show |
intron_variant | MODIFIER | c.292-984G>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 3/5 | chr11 | 36635067 | ||||||
chr11:36635068 | T | A | 11 | a0001c0001t0002g0016a0001c0001t0002g0047a0001c0001t0002g0048others(8): Show | 11 | HG00438.hp1 HG02523.hp1 HG03239.hp1 others(8): Show |
intron_variant | MODIFIER | c.292-983T>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 3/5 | chr11 | 36635068 | ||||||
chr11:36635106 | G | A | 52 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(49): Show | 61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.292-945G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 3/5 | chr11 | 36635106 | ||||||
chr11:36635207 | A | G | 52 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(49): Show | 61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.292-844A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 3/5 | chr11 | 36635207 | ||||||
chr11:36635257 | C | G | 13 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(10): Show | 16 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.292-794C>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 3/5 | chr11 | 36635257 | ||||||
chr11:36635304 | A | G | 52 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(49): Show | 61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.292-747A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 3/5 | chr11 | 36635304 | ||||||
chr11:36635395 | G | C | 2 | a0001c0001t0001g0121a0001c0001t0001g0129 | 2 | HG01123.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.292-656G>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 3/5 | chr11 | 36635395 | ||||||
chr11:36635409 | A | C | 52 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(49): Show | 61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.292-642A>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 3/5 | chr11 | 36635409 | ||||||
chr11:36635440 | A | G | 52 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(49): Show | 61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.292-611A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 3/5 | chr11 | 36635440 | ||||||
chr11:36635505 | C | T | 1 | a0001c0001t0002g0237 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.292-546C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 3/5 | chr11 | 36635505 | ||||||
chr11:36635668 | G | A | 1 | a0001c0001t0002g0224 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.292-383G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 3/5 | chr11 | 36635668 | ||||||
chr11:36635692 | G | T | 173 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(170): Show | 232 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(229): Show |
intron_variant | MODIFIER | c.292-359G>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 3/5 | chr11 | 36635692 | ||||||
chr11:36635722 | A | G | 52 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(49): Show | 61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.292-329A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 3/5 | chr11 | 36635722 | ||||||
chr11:36635808 | A | G | 52 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(49): Show | 61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.292-243A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 3/5 | chr11 | 36635808 | ||||||
chr11:36635827 | G | A | 1 | a0001c0001t0001g0252 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.292-224G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 3/5 | chr11 | 36635827 | ||||||
chr11:36635863 | T | A | 1 | a0001c0001t0001g0125 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.292-188T>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 3/5 | chr11 | 36635863 | ||||||
chr11:36635987 | CTT | C | 3 | a0002c0003t0002g0014a0002c0004t0002g0014a0002c0004t0002g0236 | 4 | HG02615.hp2 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.292-61_292-60delTT | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr11 | 36635987 | |||||
chr11:36636225 | A | G | 28 | a0001c0001t0002g0024a0001c0001t0002g0031a0001c0001t0002g0032others(25): Show | 34 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.358+108A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36636225 | ||||||
chr11:36636361 | T | A | 1 | a0001c0001t0001g0091 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.358+244T>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36636361 | ||||||
chr11:36636598 | G | A | 52 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(49): Show | 61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.358+481G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36636598 | ||||||
chr11:36636604 | C | T | 52 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(49): Show | 61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.358+487C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36636604 | ||||||
chr11:36636732 | T | C | 11 | a0001c0001t0002g0016a0001c0001t0002g0047a0001c0001t0002g0048others(8): Show | 11 | HG00438.hp1 HG02523.hp1 HG03239.hp1 others(8): Show |
intron_variant | MODIFIER | c.358+615T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36636732 | ||||||
chr11:36636770 | A | AT | 52 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(49): Show | 61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.358+657dupT | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr11 | 36636770 | |||||
chr11:36636836 | C | G | 11 | a0001c0001t0002g0016a0001c0001t0002g0047a0001c0001t0002g0048others(8): Show | 11 | HG00438.hp1 HG02523.hp1 HG03239.hp1 others(8): Show |
intron_variant | MODIFIER | c.358+719C>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36636836 | ||||||
chr11:36636889 | C | T | 39 | a0001c0001t0002g0016a0001c0001t0002g0024a0001c0001t0002g0031others(36): Show | 45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.358+772C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36636889 | ||||||
chr11:36636922 | A | G | 52 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(49): Show | 61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.358+805A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36636922 | ||||||
chr11:36636923 | GT | G | 13 | a0001c0001t0001g0080a0001c0001t0001g0082a0001c0001t0001g0104others(10): Show | 13 | HG00099.hp2 HG01074.hp2 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.358+824delT | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr11 | 36636923 | |||||
chr11:36636923 | GTT | G | 46 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(43): Show | 53 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.358+823_358+824del others(2): Show |
IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr11 | 36636923 | |||||
chr11:36636923 | GTTT | G | 6 | a0001c0001t0002g0207a0001c0001t0002g0208a0001c0002t0003g0013others(3): Show | 8 | HG02572.hp1 HG02723.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.358+822_358+824del others(3): Show |
IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr11 | 36636923 | |||||
chr11:36636930 | T | G | 39 | a0001c0001t0002g0016a0001c0001t0002g0024a0001c0001t0002g0031others(36): Show | 45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.358+813T>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36636930 | ||||||
chr11:36636946 | A | T | 1 | a0001c0001t0001g0086 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.358+829A>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36636946 | ||||||
chr11:36637023 | T | C | 27 | a0001c0001t0002g0024a0001c0001t0002g0031a0001c0001t0002g0032others(24): Show | 33 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.358+906T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36637023 | ||||||
chr11:36637064 | G | A | 52 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(49): Show | 61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.358+947G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36637064 | ||||||
chr11:36637272 | A | G | 11 | a0001c0001t0002g0016a0001c0001t0002g0047a0001c0001t0002g0048others(8): Show | 11 | HG00438.hp1 HG02523.hp1 HG03239.hp1 others(8): Show |
intron_variant | MODIFIER | c.358+1155A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36637272 | ||||||
chr11:36637273 | G | A | 52 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(49): Show | 61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.358+1156G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36637273 | ||||||
chr11:36637324 | C | T | 52 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(49): Show | 61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.358+1207C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36637324 | ||||||
chr11:36637549 | G | C | 1 | a0001c0001t0001g0253 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.358+1432G>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36637549 | ||||||
chr11:36637651 | C | G | 52 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(49): Show | 61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.358+1534C>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36637651 | ||||||
chr11:36637651 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.358+1534C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36637651 | ||||||
chr11:36637661 | A | G | 52 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(49): Show | 61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.358+1544A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36637661 | ||||||
chr11:36637885 | C | CTT | 38 | a0001c0001t0002g0016a0001c0001t0002g0024a0001c0001t0002g0031others(35): Show | 44 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.358+1780_358+1781d others(4): Show |
IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr11 | 36637885 | |||||
chr11:36637885 | C | CTTT | 14 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(11): Show | 17 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(14): Show |
intron_variant | MODIFIER | c.358+1779_358+1781d others(5): Show |
IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr11 | 36637885 | |||||
chr11:36637885 | CT | C | 39 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0037others(36): Show | 61 | HG00140.hp2 HG00408.hp2 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.358+1781delT | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr11 | 36637885 | |||||
chr11:36637902 | A | G | 13 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(10): Show | 16 | HG02572.hp1 HG02615.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.358+1785A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36637902 | ||||||
chr11:36638037 | T | C | 138 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(135): Show | 175 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(172): Show |
intron_variant | MODIFIER | c.358+1920T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36638037 | ||||||
chr11:36638134 | G | A | 1 | a0001c0001t0001g0179 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.358+2017G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36638134 | ||||||
chr11:36638153 | G | C | 52 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(49): Show | 61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.358+2036G>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36638153 | ||||||
chr11:36638156 | C | T | 39 | a0001c0001t0002g0016a0001c0001t0002g0024a0001c0001t0002g0031others(36): Show | 45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.358+2039C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36638156 | ||||||
chr11:36638216 | C | T | 265 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(262): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.358+2099C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36638216 | ||||||
chr11:36638221 | T | G | 1 | a0001c0001t0001g0037 | 2 | HG02922.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.358+2104T>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36638221 | ||||||
chr11:36638344 | A | C | 11 | a0001c0001t0002g0016a0001c0001t0002g0047a0001c0001t0002g0048others(8): Show | 11 | HG00438.hp1 HG02523.hp1 HG03239.hp1 others(8): Show |
intron_variant | MODIFIER | c.358+2227A>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36638344 | ||||||
chr11:36638415 | C | A | 26 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(23): Show | 30 | HG00438.hp1 HG02451.hp1 HG02523.hp1 others(27): Show |
intron_variant | MODIFIER | c.358+2298C>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36638415 | ||||||
chr11:36638446 | G | T | 52 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(49): Show | 61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.358+2329G>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36638446 | ||||||
chr11:36638468 | A | G | 52 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(49): Show | 61 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.358+2351A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36638468 | ||||||
chr11:36638584 | G | A | 5 | a0001c0001t0002g0214a0001c0001t0002g0215a0001c0001t0002g0230others(2): Show | 5 | HG02895.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.358+2467G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36638584 | ||||||
chr11:36638819 | C | G | 1 | a0001c0001t0001g0019 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.358+2702C>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36638819 | ||||||
chr11:36638941 | T | C | 2 | a0001c0001t0001g0132a0001c0001t0001g0212 | 2 | HG02451.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.358+2824T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36638941 | ||||||
chr11:36639018 | A | G | 4 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0213others(1): Show | 6 | HG02145.hp1 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.358+2901A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36639018 | ||||||
chr11:36639082 | C | T | 6 | a0001c0001t0002g0207a0001c0001t0002g0208a0001c0002t0003g0013others(3): Show | 8 | HG02572.hp1 HG02723.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.358+2965C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36639082 | ||||||
chr11:36639156 | TTAGAA | T | 5 | a0001c0001t0002g0214a0001c0001t0002g0215a0001c0001t0002g0230others(2): Show | 5 | HG02895.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.358+3043_358+3047d others(7): Show |
IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr11 | 36639156 | |||||
chr11:36639169 | A | G | 2 | a0001c0001t0001g0144a0001c0001t0001g0170 | 2 | NA18945.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.358+3052A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36639169 | ||||||
chr11:36639253 | C | CT | 50 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(47): Show | 58 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(55): Show |
intron_variant | MODIFIER | c.358+3150dupT | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr11 | 36639253 | |||||
chr11:36639409 | GTTCTCCA others(9): Show |
G | 1 | a0001c0001t0001g0027 | 2 | NA18970.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.358+3297_358+3312d others(18): Show |
IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr11 | 36639409 | |||||
chr11:36639454 | A | G | 1 | a0001c0001t0001g0042 | 2 | HG03688.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.358+3337A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36639454 | ||||||
chr11:36639500 | A | G | 38 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(35): Show | 46 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.358+3383A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36639500 | ||||||
chr11:36639537 | G | A | 4 | a0001c0002t0003g0013a0001c0002t0003g0209a0001c0002t0003g0210others(1): Show | 6 | HG02723.hp2 HG02886.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.358+3420G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36639537 | ||||||
chr11:36639569 | A | G | 1 | a0001c0001t0002g0024 | 2 | NA18747.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.358+3452A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36639569 | ||||||
chr11:36639600 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.358+3483C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36639600 | ||||||
chr11:36639674 | G | A | 5 | a0001c0001t0001g0023a0001c0001t0001g0117a0001c0001t0001g0118others(2): Show | 6 | HG00741.hp1 HG01081.hp2 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.358+3557G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36639674 | ||||||
chr11:36639711 | G | A | 40 | a0001c0001t0001g0008a0001c0001t0001g0135a0001c0001t0001g0136others(37): Show | 51 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.358+3594G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36639711 | ||||||
chr11:36639731 | G | C | 39 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(36): Show | 47 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.358+3614G>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36639731 | ||||||
chr11:36639775 | C | T | 262 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(259): Show | 354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.358+3658C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36639775 | ||||||
chr11:36639852 | G | A | 133 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(130): Show | 170 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(167): Show |
intron_variant | MODIFIER | c.358+3735G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36639852 | ||||||
chr11:36639893 | C | T | 39 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(36): Show | 47 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.358+3776C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36639893 | ||||||
chr11:36639897 | T | C | 1 | a0001c0002t0003g0209 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.358+3780T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36639897 | ||||||
chr11:36639956 | C | T | 1 | a0001c0001t0001g0199 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.358+3839C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36639956 | ||||||
chr11:36640046 | A | G | 2 | a0001c0001t0001g0137a0001c0001t0002g0235 | 2 | HG02630.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.358+3929A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36640046 | ||||||
chr11:36640117 | A | T | 1 | a0001c0001t0001g0246 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.358+4000A>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36640117 | ||||||
chr11:36640173 | A | G | 39 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(36): Show | 47 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.358+4056A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36640173 | ||||||
chr11:36640286 | TTG | T | 39 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(36): Show | 47 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.358+4173_358+4174d others(4): Show |
IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr11 | 36640286 | |||||
chr11:36640338 | C | T | 1 | a0001c0001t0001g0247 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.358+4221C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36640338 | ||||||
chr11:36640383 | T | C | 2 | a0001c0001t0001g0135a0001c0001t0001g0136 | 2 | HG02818.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.358+4266T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36640383 | ||||||
chr11:36640399 | T | C | 1 | a0001c0001t0002g0237 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.358+4282T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36640399 | ||||||
chr11:36640450 | A | C | 1 | a0001c0001t0001g0100 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.358+4333A>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36640450 | ||||||
chr11:36640667 | G | A | 39 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(36): Show | 47 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.358+4550G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36640667 | ||||||
chr11:36640966 | G | T | 1 | a0001c0001t0001g0008 | 4 | HG02055.hp2 HG03225.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.358+4849G>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36640966 | ||||||
chr11:36641014 | C | T | 5 | a0001c0001t0001g0030a0001c0001t0001g0203a0001c0001t0001g0204others(2): Show | 6 | HG02486.hp1 HG02622.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.358+4897C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36641014 | ||||||
chr11:36641053 | A | G | 5 | a0001c0001t0001g0137a0001c0001t0002g0235a0002c0003t0002g0014others(2): Show | 6 | HG02615.hp2 HG02630.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.358+4936A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36641053 | ||||||
chr11:36641660 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.358+5543C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36641660 | ||||||
chr11:36641756 | T | A | 1 | a0001c0001t0002g0235 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.358+5639T>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36641756 | ||||||
chr11:36641790 | C | A | 1 | a0001c0001t0001g0043 | 2 | HG02622.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.358+5673C>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36641790 | ||||||
chr11:36642052 | C | G | 1 | a0001c0001t0001g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.358+5935C>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36642052 | ||||||
chr11:36642053 | T | G | 1 | a0001c0001t0002g0052 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.358+5936T>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36642053 | ||||||
chr11:36642089 | A | T | 2 | a0001c0001t0001g0163a0001c0001t0001g0165 | 2 | HG00099.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.359-5927A>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36642089 | ||||||
chr11:36642103 | C | A | 1 | a0001c0001t0001g0008 | 4 | HG02055.hp2 HG03225.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.359-5913C>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36642103 | ||||||
chr11:36642103 | C | G | 1 | a0001c0001t0002g0237 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.359-5913C>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36642103 | ||||||
chr11:36642104 | C | T | 1 | a0001c0001t0001g0058 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.359-5912C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36642104 | ||||||
chr11:36642172 | G | C | 1 | a0001c0001t0002g0237 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.359-5844G>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36642172 | ||||||
chr11:36642235 | A | G | 1 | a0001c0001t0001g0083 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.359-5781A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36642235 | ||||||
chr11:36642255 | A | G | 1 | a0001c0001t0001g0234 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.359-5761A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36642255 | ||||||
chr11:36642281 | C | G | 83 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(80): Show | 110 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.359-5735C>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36642281 | ||||||
chr11:36642282 | A | G | 39 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(36): Show | 47 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.359-5734A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36642282 | ||||||
chr11:36642414 | A | C | 5 | a0001c0001t0001g0137a0001c0001t0002g0235a0002c0003t0002g0014others(2): Show | 6 | HG02615.hp2 HG02630.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.359-5602A>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36642414 | ||||||
chr11:36642429 | C | T | 1 | a0001c0001t0001g0096 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.359-5587C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36642429 | ||||||
chr11:36642470 | G | C | 39 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(36): Show | 47 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.359-5546G>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36642470 | ||||||
chr11:36642591 | C | T | 26 | a0001c0001t0002g0031a0001c0001t0002g0032a0001c0001t0002g0033others(23): Show | 31 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.359-5425C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36642591 | ||||||
chr11:36642715 | A | G | 39 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(36): Show | 47 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.359-5301A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36642715 | ||||||
chr11:36642742 | A | G | 1 | a0001c0001t0001g0061 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.359-5274A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36642742 | ||||||
chr11:36643070 | C | T | 1 | a0001c0001t0002g0235 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.359-4946C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36643070 | ||||||
chr11:36643095 | A | G | 1 | a0001c0001t0002g0024 | 2 | NA18747.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.359-4921A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36643095 | ||||||
chr11:36643152 | G | C | 18 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0076others(15): Show | 24 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.359-4864G>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36643152 | ||||||
chr11:36643159 | G | T | 3 | a0001c0001t0001g0175a0001c0001t0001g0182a0001c0001t0001g0183 | 3 | HG01884.hp1 HG02896.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.359-4857G>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36643159 | ||||||
chr11:36643162 | A | G | 39 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(36): Show | 47 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.359-4854A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36643162 | ||||||
chr11:36643180 | A | T | 4 | a0001c0001t0001g0012a0001c0001t0001g0162a0001c0001t0001g0190others(1): Show | 6 | HG00438.hp2 NA18944.hp1 NA18954.hp1 others(3): Show |
intron_variant | MODIFIER | c.359-4836A>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36643180 | ||||||
chr11:36643338 | G | T | 1 | a0001c0001t0001g0022 | 2 | HG03453.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.359-4678G>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36643338 | ||||||
chr11:36643357 | A | G | 1 | a0001c0002t0003g0210 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.359-4659A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36643357 | ||||||
chr11:36643379 | C | T | 11 | a0001c0001t0002g0016a0001c0001t0002g0047a0001c0001t0002g0048others(8): Show | 11 | HG00438.hp1 HG02523.hp1 HG03239.hp1 others(8): Show |
intron_variant | MODIFIER | c.359-4637C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36643379 | ||||||
chr11:36643383 | A | T | 11 | a0001c0001t0002g0016a0001c0001t0002g0047a0001c0001t0002g0048others(8): Show | 11 | HG00438.hp1 HG02523.hp1 HG03239.hp1 others(8): Show |
intron_variant | MODIFIER | c.359-4633A>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36643383 | ||||||
chr11:36643469 | A | C | 39 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(36): Show | 47 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.359-4547A>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36643469 | ||||||
chr11:36643469 | A | G | 1 | a0001c0001t0002g0024 | 2 | NA18747.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.359-4547A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36643469 | ||||||
chr11:36643493 | A | G | 1 | a0001c0001t0001g0089 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.359-4523A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36643493 | ||||||
chr11:36643545 | T | A | 1 | a0001c0001t0001g0025 | 2 | HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.359-4471T>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36643545 | ||||||
chr11:36643600 | G | C | 2 | a0001c0001t0001g0020a0001c0001t0001g0109 | 3 | HG01074.hp1 HG01346.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.359-4416G>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36643600 | ||||||
chr11:36643605 | A | G | 11 | a0001c0001t0002g0016a0001c0001t0002g0047a0001c0001t0002g0048others(8): Show | 11 | HG00438.hp1 HG02523.hp1 HG03239.hp1 others(8): Show |
intron_variant | MODIFIER | c.359-4411A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36643605 | ||||||
chr11:36643636 | G | C | 26 | a0001c0001t0002g0031a0001c0001t0002g0032a0001c0001t0002g0033others(23): Show | 31 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.359-4380G>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36643636 | ||||||
chr11:36643802 | A | G | 1 | a0001c0001t0001g0025 | 2 | HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.359-4214A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36643802 | ||||||
chr11:36643893 | C | A | 2 | a0001c0001t0002g0033a0001c0001t0002g0227 | 3 | HG00738.hp2 HG01099.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.359-4123C>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36643893 | ||||||
chr11:36644002 | T | A | 1 | a0001c0001t0001g0249 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.359-4014T>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36644002 | ||||||
chr11:36644021 | G | T | 34 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0002g0031others(31): Show | 41 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.359-3995G>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36644021 | ||||||
chr11:36644041 | T | C | 6 | a0001c0001t0002g0207a0001c0001t0002g0208a0001c0002t0003g0013others(3): Show | 8 | HG02572.hp1 HG02723.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.359-3975T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36644041 | ||||||
chr11:36644045 | A | C | 45 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(42): Show | 51 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.359-3971A>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36644045 | ||||||
chr11:36644099 | A | T | 208 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(205): Show | 276 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(273): Show |
intron_variant | MODIFIER | c.359-3917A>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36644099 | ||||||
chr11:36644103 | A | C | 4 | a0001c0001t0001g0148a0001c0001t0001g0161a0001c0001t0001g0166others(1): Show | 4 | HG00735.hp2 NA18966.hp1 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.359-3913A>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36644103 | ||||||
chr11:36644233 | C | A | 11 | a0001c0001t0002g0016a0001c0001t0002g0047a0001c0001t0002g0048others(8): Show | 11 | HG00438.hp1 HG02523.hp1 HG03239.hp1 others(8): Show |
intron_variant | MODIFIER | c.359-3783C>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36644233 | ||||||
chr11:36644234 | G | A | 13 | a0001c0001t0001g0102a0001c0001t0001g0125a0001c0001t0002g0016others(10): Show | 13 | HG00438.hp1 HG01358.hp2 HG02523.hp1 others(10): Show |
intron_variant | MODIFIER | c.359-3782G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36644234 | ||||||
chr11:36644235 | G | A | 11 | a0001c0001t0002g0016a0001c0001t0002g0047a0001c0001t0002g0048others(8): Show | 11 | HG00438.hp1 HG02523.hp1 HG03239.hp1 others(8): Show |
intron_variant | MODIFIER | c.359-3781G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36644235 | ||||||
chr11:36644236 | G | A | 11 | a0001c0001t0002g0016a0001c0001t0002g0047a0001c0001t0002g0048others(8): Show | 11 | HG00438.hp1 HG02523.hp1 HG03239.hp1 others(8): Show |
intron_variant | MODIFIER | c.359-3780G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36644236 | ||||||
chr11:36644237 | C | T | 3 | a0001c0001t0001g0175a0001c0001t0001g0182a0001c0001t0001g0183 | 3 | HG01884.hp1 HG02896.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.359-3779C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36644237 | ||||||
chr11:36644394 | G | A | 2 | a0001c0001t0001g0137a0001c0001t0002g0235 | 2 | HG02630.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.359-3622G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36644394 | ||||||
chr11:36644405 | T | C | 5 | a0001c0001t0001g0146a0001c0001t0001g0148a0001c0001t0001g0161others(2): Show | 5 | HG00735.hp2 HG03654.hp2 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.359-3611T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36644405 | ||||||
chr11:36644564 | G | A | 1 | a0001c0001t0001g0212 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.359-3452G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36644564 | ||||||
chr11:36644766 | T | C | 39 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(36): Show | 47 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.359-3250T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36644766 | ||||||
chr11:36644767 | G | T | 3 | a0002c0003t0002g0014a0002c0004t0002g0014a0002c0004t0002g0236 | 4 | HG02615.hp2 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.359-3249G>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36644767 | ||||||
chr11:36644768 | A | C | 39 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(36): Show | 47 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.359-3248A>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36644768 | ||||||
chr11:36644782 | T | C | 1 | a0001c0001t0001g0090 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.359-3234T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36644782 | ||||||
chr11:36644855 | T | TG | 56 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0018others(53): Show | 66 | HG00408.hp2 HG00544.hp2 HG00733.hp1 others(63): Show |
intron_variant | MODIFIER | c.359-3155dupG | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr11 | 36644855 | |||||
chr11:36644862 | A | G | 1 | a0001c0001t0001g0069 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.359-3154A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36644862 | ||||||
chr11:36644880 | A | G | 1 | a0001c0001t0002g0024 | 2 | NA18747.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.359-3136A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36644880 | ||||||
chr11:36644905 | A | G | 11 | a0001c0001t0002g0016a0001c0001t0002g0047a0001c0001t0002g0048others(8): Show | 11 | HG00438.hp1 HG02523.hp1 HG03239.hp1 others(8): Show |
intron_variant | MODIFIER | c.359-3111A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36644905 | ||||||
chr11:36644906 | G | A | 11 | a0001c0001t0002g0016a0001c0001t0002g0047a0001c0001t0002g0048others(8): Show | 11 | HG00438.hp1 HG02523.hp1 HG03239.hp1 others(8): Show |
intron_variant | MODIFIER | c.359-3110G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36644906 | ||||||
chr11:36644993 | T | TATA | 10 | a0001c0001t0001g0008a0001c0001t0001g0030a0001c0001t0001g0132others(7): Show | 14 | HG02055.hp2 HG02451.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.359-3000_359-2998d others(5): Show |
IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr11 | 36644993 | |||||
chr11:36644993 | TATA | T | 79 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0037others(76): Show | 109 | HG00140.hp2 HG00408.hp2 HG00597.hp1 others(106): Show |
intron_variant | MODIFIER | c.359-3000_359-2998d others(5): Show |
IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr11 | 36644993 | |||||
chr11:36645054 | A | G | 39 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(36): Show | 47 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.359-2962A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36645054 | ||||||
chr11:36645160 | A | C | 2 | a0001c0001t0002g0216a0001c0001t0002g0223 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.359-2856A>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36645160 | ||||||
chr11:36645381 | A | G | 2 | a0001c0001t0002g0207a0001c0001t0002g0208 | 2 | HG02572.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.359-2635A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36645381 | ||||||
chr11:36645391 | G | A | 1 | a0001c0001t0002g0024 | 2 | NA18747.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.359-2625G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36645391 | ||||||
chr11:36645396 | C | T | 1 | a0001c0001t0004g0241 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.359-2620C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36645396 | ||||||
chr11:36645456 | G | A | 1 | a0001c0001t0001g0201 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.359-2560G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36645456 | ||||||
chr11:36645485 | T | C | 11 | a0001c0001t0002g0016a0001c0001t0002g0047a0001c0001t0002g0048others(8): Show | 11 | HG00438.hp1 HG02523.hp1 HG03239.hp1 others(8): Show |
intron_variant | MODIFIER | c.359-2531T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36645485 | ||||||
chr11:36645544 | T | C | 1 | a0001c0001t0001g0253 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.359-2472T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36645544 | ||||||
chr11:36645649 | T | C | 3 | a0002c0003t0002g0014a0002c0004t0002g0014a0002c0004t0002g0236 | 4 | HG02615.hp2 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.359-2367T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36645649 | ||||||
chr11:36645689 | T | C | 1 | a0001c0001t0002g0024 | 2 | NA18747.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.359-2327T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36645689 | ||||||
chr11:36645949 | A | T | 3 | a0002c0003t0002g0014a0002c0004t0002g0014a0002c0004t0002g0236 | 4 | HG02615.hp2 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.359-2067A>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36645949 | ||||||
chr11:36646000 | T | C | 39 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(36): Show | 47 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.359-2016T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36646000 | ||||||
chr11:36646031 | C | T | 70 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0011others(67): Show | 93 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.359-1985C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36646031 | ||||||
chr11:36646044 | G | A | 1 | a0001c0001t0002g0237 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.359-1972G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36646044 | ||||||
chr11:36646088 | A | G | 1 | a0001c0001t0001g0065 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.359-1928A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36646088 | ||||||
chr11:36646340 | T | C | 1 | a0001c0001t0002g0215 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.359-1676T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36646340 | ||||||
chr11:36646436 | G | T | 6 | a0001c0001t0002g0207a0001c0001t0002g0208a0001c0002t0003g0013others(3): Show | 8 | HG02572.hp1 HG02723.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.359-1580G>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36646436 | ||||||
chr11:36646628 | AT | A | 4 | a0001c0002t0003g0013a0001c0002t0003g0209a0001c0002t0003g0210others(1): Show | 6 | HG02723.hp2 HG02886.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.359-1385delT | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr11 | 36646628 | |||||
chr11:36646708 | T | G | 1 | a0001c0001t0001g0190 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.359-1308T>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36646708 | ||||||
chr11:36646848 | T | C | 1 | a0001c0001t0001g0008 | 4 | HG02055.hp2 HG03225.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.359-1168T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36646848 | ||||||
chr11:36647171 | G | A | 3 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189 | 3 | HG02258.hp1 HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.359-845G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36647171 | ||||||
chr11:36647462 | T | C | 53 | a0001c0001t0001g0036a0001c0001t0001g0135a0001c0001t0001g0136others(50): Show | 63 | HG00438.hp1 HG00673.hp2 HG00733.hp2 others(60): Show |
intron_variant | MODIFIER | c.359-554T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36647462 | ||||||
chr11:36647468 | T | G | 1 | a0001c0001t0001g0125 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.359-548T>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36647468 | ||||||
chr11:36647580 | C | T | 131 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(128): Show | 167 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(164): Show |
intron_variant | MODIFIER | c.359-436C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36647580 | ||||||
chr11:36647660 | A | G | 27 | a0001c0001t0001g0036a0001c0001t0002g0031a0001c0001t0002g0032others(24): Show | 33 | HG00673.hp2 HG00733.hp2 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.359-356A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36647660 | ||||||
chr11:36647691 | A | G | 1 | a0001c0001t0001g0084 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.359-325A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36647691 | ||||||
chr11:36647804 | C | T | 4 | a0001c0001t0001g0011a0001c0001t0001g0138a0001c0001t0001g0139others(1): Show | 6 | HG00597.hp2 HG00609.hp2 HG02129.hp2 others(3): Show |
intron_variant | MODIFIER | c.359-212C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36647804 | ||||||
chr11:36647828 | A | G | 1 | a0001c0001t0001g0184 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.359-188A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36647828 | ||||||
chr11:36647887 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.359-129G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 4/5 | chr11 | 36647887 | ||||||
chr11:36648228 | C | T | 174 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(171): Show | 233 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(230): Show |
intron_variant | MODIFIER | c.498+73C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36648228 | ||||||
chr11:36648380 | T | C | 2 | a0001c0001t0001g0098a0001c0001t0001g0133 | 2 | HG02523.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.498+225T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36648380 | ||||||
chr11:36648432 | C | T | 39 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(36): Show | 47 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.498+277C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36648432 | ||||||
chr11:36648523 | C | T | 1 | a0001c0001t0001g0239 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.498+368C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36648523 | ||||||
chr11:36648622 | G | A | 1 | a0001c0001t0001g0092 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.498+467G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36648622 | ||||||
chr11:36648811 | C | T | 1 | a0001c0001t0002g0237 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.498+656C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36648811 | ||||||
chr11:36648812 | G | A | 2 | a0001c0001t0001g0025a0001c0001t0001g0234 | 3 | HG02717.hp1 HG03486.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.498+657G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36648812 | ||||||
chr11:36648825 | T | C | 2 | a0001c0001t0001g0135a0001c0001t0001g0136 | 2 | HG02818.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.498+670T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36648825 | ||||||
chr11:36649005 | A | G | 39 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(36): Show | 47 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.498+850A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36649005 | ||||||
chr11:36649119 | A | G | 1 | a0001c0001t0001g0099 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.498+964A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36649119 | ||||||
chr11:36649173 | T | G | 26 | a0001c0001t0002g0031a0001c0001t0002g0032a0001c0001t0002g0033others(23): Show | 31 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.498+1018T>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36649173 | ||||||
chr11:36649199 | CA | C | 6 | a0001c0001t0002g0207a0001c0001t0002g0208a0001c0002t0003g0013others(3): Show | 8 | HG02572.hp1 HG02723.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.498+1045delA | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36649199 | ||||||
chr11:36649249 | C | T | 1 | a0001c0001t0001g0026 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.498+1094C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36649249 | ||||||
chr11:36649354 | T | C | 3 | a0002c0003t0002g0014a0002c0004t0002g0014a0002c0004t0002g0236 | 4 | HG02615.hp2 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.498+1199T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36649354 | ||||||
chr11:36649487 | T | C | 11 | a0001c0001t0002g0016a0001c0001t0002g0047a0001c0001t0002g0048others(8): Show | 11 | HG00438.hp1 HG02523.hp1 HG03239.hp1 others(8): Show |
intron_variant | MODIFIER | c.498+1332T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36649487 | ||||||
chr11:36649699 | G | A | 3 | a0001c0001t0001g0175a0001c0001t0001g0182a0001c0001t0001g0183 | 3 | HG01884.hp1 HG02896.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.498+1544G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36649699 | ||||||
chr11:36649721 | C | T | 1 | a0001c0001t0001g0212 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.498+1566C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36649721 | ||||||
chr11:36649724 | G | C | 1 | a0001c0001t0001g0137 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.498+1569G>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36649724 | ||||||
chr11:36650111 | C | A | 1 | a0001c0001t0001g0156 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.498+1956C>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36650111 | ||||||
chr11:36650119 | G | A | 26 | a0001c0001t0002g0031a0001c0001t0002g0032a0001c0001t0002g0033others(23): Show | 31 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.498+1964G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36650119 | ||||||
chr11:36650327 | C | T | 1 | a0001c0001t0001g0251 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.498+2172C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36650327 | ||||||
chr11:36650328 | T | C | 1 | a0001c0001t0001g0251 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.498+2173T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36650328 | ||||||
chr11:36650421 | G | A | 26 | a0001c0001t0002g0031a0001c0001t0002g0032a0001c0001t0002g0033others(23): Show | 31 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.498+2266G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36650421 | ||||||
chr11:36650477 | A | G | 2 | a0001c0001t0001g0137a0001c0001t0002g0235 | 2 | HG02630.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.498+2322A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36650477 | ||||||
chr11:36650544 | C | CT | 216 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(213): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.498+2401dupT | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr11 | 36650544 | |||||
chr11:36650557 | C | T | 3 | a0001c0001t0001g0081a0001c0001t0001g0132a0001c0001t0001g0150 | 3 | HG04115.hp1 HG04204.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.498+2402C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36650557 | ||||||
chr11:36650558 | C | A | 1 | a0001c0001t0002g0024 | 2 | NA18747.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.498+2403C>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36650558 | ||||||
chr11:36650559 | A | C | 3 | a0001c0001t0001g0081a0001c0001t0001g0132a0001c0001t0001g0150 | 3 | HG04115.hp1 HG04204.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.498+2404A>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36650559 | ||||||
chr11:36650613 | G | A | 1 | a0001c0001t0002g0235 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.498+2458G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36650613 | ||||||
chr11:36650726 | C | T | 1 | a0001c0001t0001g0119 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.498+2571C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36650726 | ||||||
chr11:36650743 | C | G | 6 | a0001c0001t0002g0207a0001c0001t0002g0208a0001c0002t0003g0013others(3): Show | 8 | HG02572.hp1 HG02723.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.498+2588C>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36650743 | ||||||
chr11:36650768 | A | C | 5 | a0001c0001t0001g0030a0001c0001t0001g0203a0001c0001t0001g0204others(2): Show | 6 | HG02486.hp1 HG02622.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.498+2613A>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36650768 | ||||||
chr11:36650856 | T | G | 1 | a0001c0001t0001g0085 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.498+2701T>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36650856 | ||||||
chr11:36650890 | A | C | 2 | a0001c0001t0001g0135a0001c0001t0001g0136 | 2 | HG02818.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.498+2735A>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36650890 | ||||||
chr11:36650930 | C | T | 1 | a0001c0001t0001g0132 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.498+2775C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36650930 | ||||||
chr11:36650969 | G | T | 1 | a0001c0001t0001g0142 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.498+2814G>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36650969 | ||||||
chr11:36651005 | G | A | 3 | a0001c0001t0001g0175a0001c0001t0001g0182a0001c0001t0001g0183 | 3 | HG01884.hp1 HG02896.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.498+2850G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36651005 | ||||||
chr11:36651117 | T | C | 3 | a0002c0003t0002g0014a0002c0004t0002g0014a0002c0004t0002g0236 | 4 | HG02615.hp2 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.498+2962T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36651117 | ||||||
chr11:36651125 | C | T | 73 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0011others(70): Show | 96 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(93): Show |
intron_variant | MODIFIER | c.498+2970C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36651125 | ||||||
chr11:36651150 | G | C | 6 | a0001c0001t0002g0207a0001c0001t0002g0208a0001c0002t0003g0013others(3): Show | 8 | HG02572.hp1 HG02723.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.498+2995G>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36651150 | ||||||
chr11:36651319 | G | T | 1 | a0001c0001t0001g0132 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.498+3164G>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36651319 | ||||||
chr11:36651331 | T | C | 1 | a0001c0001t0001g0132 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.498+3176T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36651331 | ||||||
chr11:36651333 | T | C | 1 | a0001c0001t0001g0132 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.498+3178T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36651333 | ||||||
chr11:36651376 | G | A | 39 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(36): Show | 47 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.498+3221G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36651376 | ||||||
chr11:36651438 | G | A | 2 | a0001c0001t0001g0137a0001c0001t0002g0235 | 2 | HG02630.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.498+3283G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36651438 | ||||||
chr11:36651518 | G | T | 3 | a0001c0001t0001g0244a0001c0001t0001g0254a0001c0001t0001g0256 | 3 | NA18954.hp2 NA18969.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.498+3363G>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36651518 | ||||||
chr11:36651687 | T | C | 2 | a0001c0001t0001g0137a0001c0001t0002g0235 | 2 | HG02630.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.498+3532T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36651687 | ||||||
chr11:36651770 | T | G | 39 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(36): Show | 47 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.498+3615T>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36651770 | ||||||
chr11:36651786 | C | A | 2 | a0001c0001t0001g0117a0001c0001t0001g0118 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.498+3631C>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36651786 | ||||||
chr11:36651798 | A | T | 11 | a0001c0001t0002g0016a0001c0001t0002g0047a0001c0001t0002g0048others(8): Show | 11 | HG00438.hp1 HG02523.hp1 HG03239.hp1 others(8): Show |
intron_variant | MODIFIER | c.498+3643A>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36651798 | ||||||
chr11:36651801 | T | A | 18 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0076others(15): Show | 24 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.498+3646T>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36651801 | ||||||
chr11:36651985 | G | A | 2 | a0001c0001t0001g0137a0001c0001t0002g0235 | 2 | HG02630.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.498+3830G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36651985 | ||||||
chr11:36652018 | T | A | 1 | a0001c0001t0001g0113 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.498+3863T>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36652018 | ||||||
chr11:36652035 | G | A | 1 | a0001c0001t0002g0024 | 2 | NA18747.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.498+3880G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36652035 | ||||||
chr11:36652123 | A | G | 1 | a0001c0001t0001g0126 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.498+3968A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36652123 | ||||||
chr11:36652169 | T | C | 4 | a0001c0001t0001g0154a0001c0001t0001g0157a0001c0001t0001g0164others(1): Show | 4 | NA18942.hp2 NA18948.hp1 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.498+4014T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36652169 | ||||||
chr11:36652324 | G | T | 39 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137others(36): Show | 47 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.498+4169G>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36652324 | ||||||
chr11:36652381 | C | G | 1 | a0001c0001t0002g0237 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.498+4226C>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36652381 | ||||||
chr11:36652381 | C | T | 1 | a0001c0001t0002g0024 | 2 | NA18747.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.498+4226C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36652381 | ||||||
chr11:36652632 | G | C | 3 | a0001c0001t0001g0175a0001c0001t0001g0182a0001c0001t0001g0183 | 3 | HG01884.hp1 HG02896.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.498+4477G>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36652632 | ||||||
chr11:36652782 | A | G | 1 | a0001c0001t0002g0131 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.498+4627A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36652782 | ||||||
chr11:36652857 | A | G | 1 | a0001c0001t0001g0026 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.498+4702A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36652857 | ||||||
chr11:36653198 | G | A | 13 | a0001c0001t0002g0016a0001c0001t0002g0024a0001c0001t0002g0047others(10): Show | 14 | HG00438.hp1 HG02451.hp1 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.498+5043G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36653198 | ||||||
chr11:36653258 | A | G | 1 | a0001c0001t0001g0137 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.498+5103A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36653258 | ||||||
chr11:36653270 | A | G | 1 | a0004c0006t0001g0057 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.498+5115A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36653270 | ||||||
chr11:36653283 | G | C | 3 | a0002c0003t0002g0014a0002c0004t0002g0014a0002c0004t0002g0236 | 4 | HG02615.hp2 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.498+5128G>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36653283 | ||||||
chr11:36653285 | A | T | 1 | a0001c0001t0001g0103 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.498+5130A>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36653285 | ||||||
chr11:36653408 | C | G | 1 | a0001c0001t0002g0053 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.498+5253C>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36653408 | ||||||
chr11:36653554 | A | G | 1 | a0001c0001t0001g0064 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.498+5399A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36653554 | ||||||
chr11:36653613 | A | G | 1 | a0001c0001t0001g0111 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.499-5406A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36653613 | ||||||
chr11:36653665 | G | A | 1 | a0001c0001t0002g0207 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.499-5354G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36653665 | ||||||
chr11:36653718 | A | G | 26 | a0001c0001t0002g0031a0001c0001t0002g0032a0001c0001t0002g0033others(23): Show | 31 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.499-5301A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36653718 | ||||||
chr11:36653864 | A | G | 5 | a0001c0001t0001g0030a0001c0001t0001g0203a0001c0001t0001g0204others(2): Show | 6 | HG02486.hp1 HG02622.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.499-5155A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36653864 | ||||||
chr11:36653924 | G | A | 1 | a0001c0001t0002g0024 | 2 | NA18747.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.499-5095G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36653924 | ||||||
chr11:36653963 | C | T | 1 | a0001c0001t0002g0237 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.499-5056C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36653963 | ||||||
chr11:36654204 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.499-4815C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36654204 | ||||||
chr11:36654343 | T | A | 1 | a0001c0001t0001g0145 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.499-4676T>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36654343 | ||||||
chr11:36654347 | T | C | 11 | a0001c0001t0002g0016a0001c0001t0002g0047a0001c0001t0002g0048others(8): Show | 11 | HG00438.hp1 HG02523.hp1 HG03239.hp1 others(8): Show |
intron_variant | MODIFIER | c.499-4672T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36654347 | ||||||
chr11:36654353 | A | T | 11 | a0001c0001t0002g0016a0001c0001t0002g0047a0001c0001t0002g0048others(8): Show | 11 | HG00438.hp1 HG02523.hp1 HG03239.hp1 others(8): Show |
intron_variant | MODIFIER | c.499-4666A>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36654353 | ||||||
chr11:36654387 | T | C | 1 | a0001c0001t0001g0175 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.499-4632T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36654387 | ||||||
chr11:36654442 | C | A | 1 | a0001c0001t0002g0024 | 2 | NA18747.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.499-4577C>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36654442 | ||||||
chr11:36654628 | C | A | 1 | a0001c0001t0002g0052 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.499-4391C>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36654628 | ||||||
chr11:36654669 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.499-4350C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36654669 | ||||||
chr11:36654720 | T | C | 1 | a0001c0001t0001g0025 | 2 | HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.499-4299T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36654720 | ||||||
chr11:36654859 | C | T | 13 | a0001c0001t0002g0016a0001c0001t0002g0024a0001c0001t0002g0047others(10): Show | 14 | HG00438.hp1 HG02451.hp1 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.499-4160C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36654859 | ||||||
chr11:36654903 | C | T | 4 | a0001c0002t0003g0013a0001c0002t0003g0209a0001c0002t0003g0210others(1): Show | 6 | HG02723.hp2 HG02886.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.499-4116C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36654903 | ||||||
chr11:36655106 | CTT | C | 1 | a0001c0001t0001g0008 | 4 | HG02055.hp2 HG03225.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.499-3910_499-3909d others(4): Show |
IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr11 | 36655106 | |||||
chr11:36655367 | C | A | 1 | a0001c0001t0002g0131 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.499-3652C>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36655367 | ||||||
chr11:36655504 | C | G | 1 | a0001c0001t0002g0131 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.499-3515C>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36655504 | ||||||
chr11:36655635 | T | C | 13 | a0001c0001t0002g0016a0001c0001t0002g0024a0001c0001t0002g0047others(10): Show | 14 | HG00438.hp1 HG02451.hp1 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.499-3384T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36655635 | ||||||
chr11:36655689 | G | A | 3 | a0001c0001t0001g0125a0001c0001t0001g0132a0001c0001t0001g0212 | 3 | HG02451.hp2 NA18522.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.499-3330G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36655689 | ||||||
chr11:36655701 | T | C | 51 | a0001c0001t0001g0030a0001c0001t0001g0135a0001c0001t0001g0136others(48): Show | 59 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(56): Show |
intron_variant | MODIFIER | c.499-3318T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36655701 | ||||||
chr11:36655734 | C | T | 5 | a0001c0001t0002g0033a0001c0001t0002g0216a0001c0001t0002g0223others(2): Show | 6 | HG00738.hp2 HG01099.hp1 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.499-3285C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36655734 | ||||||
chr11:36655782 | T | G | 1 | a0001c0001t0002g0235 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.499-3237T>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36655782 | ||||||
chr11:36655971 | A | T | 74 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0011others(71): Show | 97 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.499-3048A>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36655971 | ||||||
chr11:36655995 | A | G | 21 | a0001c0001t0002g0031a0001c0001t0002g0032a0001c0001t0002g0033others(18): Show | 26 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.499-3024A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36655995 | ||||||
chr11:36655996 | T | C | 1 | a0001c0001t0001g0152 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.499-3023T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36655996 | ||||||
chr11:36656032 | G | A | 3 | a0001c0001t0001g0175a0001c0001t0001g0182a0001c0001t0001g0183 | 3 | HG01884.hp1 HG02896.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.499-2987G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36656032 | ||||||
chr11:36656137 | G | A | 1 | a0002c0004t0002g0236 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.499-2882G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36656137 | ||||||
chr11:36656182 | C | G | 1 | a0001c0001t0002g0237 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.499-2837C>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36656182 | ||||||
chr11:36656398 | T | C | 11 | a0001c0001t0002g0016a0001c0001t0002g0047a0001c0001t0002g0048others(8): Show | 11 | HG00438.hp1 HG02523.hp1 HG03239.hp1 others(8): Show |
intron_variant | MODIFIER | c.499-2621T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36656398 | ||||||
chr11:36656412 | A | C | 26 | a0001c0001t0002g0031a0001c0001t0002g0032a0001c0001t0002g0033others(23): Show | 31 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.499-2607A>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36656412 | ||||||
chr11:36656498 | A | C | 3 | a0001c0001t0001g0125a0001c0001t0001g0132a0001c0001t0001g0212 | 3 | HG02451.hp2 NA18522.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.499-2521A>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36656498 | ||||||
chr11:36656568 | TA | T | 39 | a0001c0001t0002g0016a0001c0001t0002g0024a0001c0001t0002g0031others(36): Show | 45 | HG00438.hp1 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.499-2440delA | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr11 | 36656568 | |||||
chr11:36656632 | T | G | 1 | a0001c0001t0001g0114 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.499-2387T>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36656632 | ||||||
chr11:36656650 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.499-2369G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36656650 | ||||||
chr11:36656767 | T | C | 11 | a0001c0001t0001g0008a0001c0001t0001g0030a0001c0001t0001g0137others(8): Show | 16 | HG02055.hp2 HG02486.hp1 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.499-2252T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36656767 | ||||||
chr11:36656930 | G | C | 3 | a0001c0001t0001g0147a0001c0001t0001g0158a0001c0001t0001g0160 | 3 | HG02135.hp1 NA18943.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.499-2089G>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36656930 | ||||||
chr11:36657112 | A | T | 1 | a0001c0001t0002g0215 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.499-1907A>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36657112 | ||||||
chr11:36657118 | A | G | 2 | a0001c0001t0001g0238a0001c0001t0001g0239 | 2 | HG01109.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.499-1901A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36657118 | ||||||
chr11:36657209 | C | G | 1 | a0001c0001t0001g0159 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.499-1810C>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36657209 | ||||||
chr11:36657260 | G | C | 136 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(133): Show | 173 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(170): Show |
intron_variant | MODIFIER | c.499-1759G>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36657260 | ||||||
chr11:36657391 | A | G | 1 | a0001c0001t0001g0212 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.499-1628A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36657391 | ||||||
chr11:36657416 | G | C | 1 | a0001c0001t0001g0081 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.499-1603G>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36657416 | ||||||
chr11:36657423 | T | A | 1 | a0001c0001t0002g0237 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.499-1596T>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36657423 | ||||||
chr11:36657454 | A | G | 1 | a0003c0007t0001g0115 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.499-1565A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36657454 | ||||||
chr11:36657528 | G | A | 1 | a0001c0001t0001g0008 | 4 | HG02055.hp2 HG03225.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.499-1491G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36657528 | ||||||
chr11:36657580 | C | T | 1 | a0001c0001t0002g0235 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.499-1439C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36657580 | ||||||
chr11:36657613 | T | C | 1 | a0001c0001t0001g0125 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.499-1406T>C | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36657613 | ||||||
chr11:36657655 | C | T | 1 | a0001c0001t0002g0047 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.499-1364C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36657655 | ||||||
chr11:36657656 | C | G | 1 | a0001c0001t0002g0237 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.499-1363C>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36657656 | ||||||
chr11:36657885 | C | T | 2 | a0001c0001t0001g0238a0001c0001t0001g0239 | 2 | HG01109.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.499-1134C>T | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36657885 | ||||||
chr11:36658100 | G | A | 1 | a0001c0001t0001g0212 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.499-919G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36658100 | ||||||
chr11:36658185 | T | G | 1 | a0001c0001t0002g0131 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.499-834T>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36658185 | ||||||
chr11:36658330 | C | CT | 74 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0011others(71): Show | 97 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.499-683dupT | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr11 | 36658330 | |||||
chr11:36658356 | G | A | 1 | a0001c0001t0001g0025 | 2 | HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.499-663G>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36658356 | ||||||
chr11:36658644 | A | G | 1 | a0001c0001t0002g0237 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.499-375A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36658644 | ||||||
chr11:36658675 | A | G | 5 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0112others(2): Show | 7 | HG01884.hp2 HG02258.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.499-344A>G | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36658675 | ||||||
chr11:36658908 | C | A | 1 | a0001c0001t0001g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.499-111C>A | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | chr11 | 36658908 | ||||||
chr11:36658917 | G | GA | 13 | a0001c0001t0002g0016a0001c0001t0002g0024a0001c0001t0002g0047others(10): Show | 14 | HG00438.hp1 HG02451.hp1 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.499-96dupA | IFTAP | ENSG00000166352.18 | transcript | ENST00000334307.10 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr11 | 36658917 |