geneid | 2260 |
---|---|
ensemblid | ENSG00000077782.23 |
hgncid | 3688 |
symbol | FGFR1 |
name | fibroblast growth factor receptor 1 |
refseq_nuc | NM_023110.3 |
refseq_prot | NP_075598.2 |
ensembl_nuc | ENST00000447712.7 |
ensembl_prot | ENSP00000400162.2 |
mane_status | MANE Select |
chr | chr8 |
start | 38411143 |
end | 38468635 |
strand | - |
ver | v1.2 |
region | chr8:38411143-38468635 |
region5000 | chr8:38406143-38473635 |
regionname0 | FGFR1_chr8_38411143_38468635 |
regionname5000 | FGFR1_chr8_38406143_38473635 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 822 | 323 | 63 | 63 | 147 | 14 | 34 | 106 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
a0002 | 0/0 | 822 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
a0003 | 0/0 | 822 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
a0004 | 0/0 | 822 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
a0005 | 0/0 | 822 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
a0006 | 0/0 | 822 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
a0007 | 0/0 | 822 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
a0008 | 0/0 | 822 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 2469 | 316 | 61 | 60 | 146 | 14 | 33 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
c0002 | 0/0 | 2469 | 4 | 3 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
c0003 | 0/0 | 2469 | 3 | 0 | 3 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
c0004 | 0/0 | 2469 | 3 | 0 | 0 | 3 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
c0005 | 0/0 | 2469 | 2 | 0 | 0 | 0 | 0 | 2 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
c0006 | 0/0 | 2469 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
c0007 | 0/0 | 2469 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
c0008 | 0/0 | 2469 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
c0009 | 0/0 | 2469 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
c0010 | 0/0 | 2469 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
c0011 | 0/0 | 2469 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
c0012 | 0/0 | 2469 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
c0013 | 0/0 | 2469 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 3229 | 113 | 25 | 23 | 47 | 2 | 15 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
t0002 | 0/1 | 3229 | 87 | 9 | 14 | 42 | 5 | 16 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
t0003 | 0/0 | 3229 | 75 | 4 | 13 | 50 | 6 | 2 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
t0004 | 0/0 | 3229 | 19 | 3 | 7 | 8 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
t0005 | 0/0 | 3229 | 14 | 14 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
t0006 | 0/0 | 3229 | 3 | 0 | 3 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
t0007 | 0/0 | 3229 | 2 | 0 | 0 | 2 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
t0008 | 0/0 | 3229 | 2 | 2 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
t0009 | 0/0 | 3229 | 2 | 0 | 0 | 2 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
t0010 | 0/0 | 3229 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
t0011 | 0/0 | 3229 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
t0012 | 0/0 | 3229 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
t0013 | 0/0 | 3229 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
t0014 | 0/0 | 3229 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
t0015 | 0/0 | 3229 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
t0016 | 0/0 | 3229 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
t0017 | 0/0 | 3229 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
t0018 | 0/0 | 3229 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
t0019 | 0/0 | 3229 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
t0020 | 0/0 | 3229 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
t0021 | 0/0 | 3229 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
t0022 | 0/0 | 3229 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
t0023 | 0/0 | 3229 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
t0024 | 0/0 | 3229 | 1 | 0 | 0 | 0 | 1 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
t0025 | 0/0 | 3229 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
t0026 | 0/0 | 3229 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
t0027 | 0/0 | 3229 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
t0028 | 0/0 | 3229 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0009 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0292 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0308 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2469 | 316 | 61 | 60 | 146 | 14 | 33 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
a0001c0003 | 0/0 | 2469 | 3 | 0 | 3 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
a0001c0008 | 0/0 | 2469 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
a0001c0009 | 0/0 | 2469 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
a0001c0011 | 0/0 | 2469 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
a0001c0012 | 0/0 | 2469 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
a0002c0002 | 0/0 | 2469 | 4 | 3 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
a0003c0004 | 0/0 | 2469 | 3 | 0 | 0 | 3 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
a0004c0005 | 0/0 | 2469 | 2 | 0 | 0 | 0 | 0 | 2 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
a0005c0006 | 0/0 | 2469 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
a0006c0007 | 0/0 | 2469 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
a0007c0010 | 0/0 | 2469 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
a0008c0013 | 0/0 | 2469 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 5697 | 105 | 22 | 19 | 47 | 2 | 14 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
a0001c0001t0002 | 0/1 | 5697 | 83 | 9 | 14 | 40 | 5 | 14 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
a0001c0001t0003 | 0/0 | 5697 | 69 | 4 | 13 | 44 | 6 | 2 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
a0001c0001t0004 | 0/0 | 5697 | 19 | 3 | 7 | 8 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
a0001c0001t0005 | 0/0 | 5697 | 14 | 14 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
a0001c0001t0006 | 0/0 | 5697 | 3 | 0 | 3 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
a0001c0001t0007 | 0/0 | 5697 | 2 | 0 | 0 | 2 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
a0001c0001t0008 | 0/0 | 5697 | 2 | 2 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
a0001c0001t0009 | 0/0 | 5697 | 2 | 0 | 0 | 2 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
a0001c0001t0010 | 0/0 | 5697 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
a0001c0001t0011 | 0/0 | 5697 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
a0001c0001t0012 | 0/0 | 5697 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
a0001c0001t0014 | 0/0 | 5697 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
a0001c0001t0015 | 0/0 | 5697 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
a0001c0001t0016 | 0/0 | 5697 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
a0001c0001t0017 | 0/0 | 5697 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
a0001c0001t0018 | 0/0 | 5697 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
a0001c0001t0019 | 0/0 | 5697 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
a0001c0001t0021 | 0/0 | 5697 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
a0001c0001t0022 | 0/0 | 5697 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
a0001c0001t0023 | 0/0 | 5697 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
a0001c0001t0024 | 0/0 | 5697 | 1 | 0 | 0 | 0 | 1 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
a0001c0001t0025 | 0/0 | 5697 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
a0001c0001t0026 | 0/0 | 5697 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
a0001c0001t0027 | 0/0 | 5697 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
a0001c0001t0028 | 0/0 | 5697 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
a0001c0003t0001 | 0/0 | 5697 | 3 | 0 | 3 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
a0001c0008t0002 | 0/0 | 5697 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
a0001c0009t0013 | 0/0 | 5697 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
a0001c0011t0001 | 0/0 | 5697 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
a0001c0012t0020 | 0/0 | 5697 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
a0002c0002t0001 | 0/0 | 5697 | 4 | 3 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
a0003c0004t0003 | 0/0 | 5697 | 3 | 0 | 0 | 3 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
a0004c0005t0002 | 0/0 | 5697 | 2 | 0 | 0 | 0 | 0 | 2 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
a0005c0006t0003 | 0/0 | 5697 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
a0006c0007t0003 | 0/0 | 5697 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
a0007c0010t0002 | 0/0 | 5697 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
a0008c0013t0003 | 0/0 | 5697 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | copy fasta | chr8 | 38406143 | 38473635 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0009 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0002g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0002g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0002g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0002g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0002g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0002g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0002g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0002g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0002g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0002g0292 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0002g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0002g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0002g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0002g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0002g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0002g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0002g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0003g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0003g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0003g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0003g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0003g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0003g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0003g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0003g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0003g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0003g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0003g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0003g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0003g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0003g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0003g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0003g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0003g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0003g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0004g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0004g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0004g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0004g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0004g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0004g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0004g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0004g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0004g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0004g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0004g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0004g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0004g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0004g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0004g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0004g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0004g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0004g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0004g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0005g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0005g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0005g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0005g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0005g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0005g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0005g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0005g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0005g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0005g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0005g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0005g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0005g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0005g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0006g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0006g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0006g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0007g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0007g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0008g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0008g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0009g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0009g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0010g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0011g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0012g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0014g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0015g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0016g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0017g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0018g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0019g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0021g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0022g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0023g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0024g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0025g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0026g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0027g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0001t0028g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0003t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0003t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0003t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0008t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0009t0013g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0011t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0001c0012t0020g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0002c0002t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0002c0002t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0002c0002t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0002c0002t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0003c0004t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0003c0004t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0003c0004t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0004c0005t0002g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0004c0005t0002g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0005c0006t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0006c0007t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0007c0010t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
a0008c0013t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0003 | g0171 | EUR | GBR | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0300 | EUR | GBR | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG00140 | hp1 | a0001 | c0001 | t0003 | g0172 | EUR | GBR | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0308 | EUR | GBR | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0274 | EUR | FIN | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG00280 | hp2 | a0001 | c0001 | t0003 | g0165 | EUR | FIN | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0101 | EUR | FIN | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG00323 | hp2 | a0001 | c0001 | t0003 | g0174 | EUR | FIN | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG00408 | hp1 | a0001 | c0001 | t0007 | g0162 | EAS | CHS | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | CHS | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | CHS | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0314 | EAS | CHS | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG00438 | hp1 | a0001 | c0001 | t0003 | g0116 | EAS | CHS | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0225 | EAS | CHS | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0306 | EAS | CHS | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | CHS | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | CHS | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | CHS | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG00609 | hp1 | a0001 | c0001 | t0007 | g0193 | EAS | CHS | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0221 | EAS | CHS | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG00621 | hp1 | a0001 | c0001 | t0004 | g0232 | EAS | CHS | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG00621 | hp2 | a0001 | c0001 | t0003 | g0121 | EAS | CHS | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG00642 | hp1 | a0001 | c0003 | t0001 | g0198 | AMR | PUR | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG00642 | hp2 | a0001 | c0001 | t0003 | g0187 | AMR | PUR | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG00673 | hp1 | a0001 | c0001 | t0004 | g0286 | EAS | CHS | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | CHS | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG00735 | hp1 | a0001 | c0001 | t0023 | g0258 | AMR | PUR | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0257 | AMR | PUR | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG00738 | hp1 | a0001 | c0001 | t0003 | g0130 | AMR | PUR | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0298 | AMR | PUR | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG00741 | hp2 | a0001 | c0001 | t0003 | g0200 | AMR | PUR | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG01069 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG01070 | hp1 | a0001 | c0001 | t0004 | g0251 | AMR | PUR | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0294 | AMR | PUR | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG01071 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0295 | AMR | PUR | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG01074 | hp1 | a0001 | c0001 | t0022 | g0208 | AMR | PUR | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0285 | AMR | PUR | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG01081 | hp2 | a0001 | c0001 | t0003 | g0106 | AMR | PUR | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG01099 | hp2 | a0001 | c0001 | t0004 | g0246 | AMR | PUR | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0244 | AMR | PUR | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0239 | AMR | PUR | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG01167 | hp1 | a0001 | c0001 | t0004 | g0252 | AMR | PUR | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG01167 | hp2 | a0002 | c0002 | t0001 | g0205 | AMR | PUR | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0249 | AMR | PUR | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG01175 | hp2 | a0001 | c0003 | t0001 | g0197 | AMR | PUR | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG01192 | hp2 | a0001 | c0001 | t0004 | g0278 | AMR | PUR | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG01243 | hp1 | a0001 | c0001 | t0003 | g0204 | AMR | PUR | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG01243 | hp2 | a0001 | c0001 | t0004 | g0265 | AMR | PUR | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG01256 | hp1 | a0001 | c0001 | t0004 | g0264 | AMR | CLM | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0297 | AMR | CLM | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | CLM | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | CLM | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | CLM | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG01258 | hp2 | a0001 | c0001 | t0004 | g0266 | AMR | CLM | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | CLM | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG01261 | hp2 | a0001 | c0003 | t0001 | g0196 | AMR | CLM | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | CLM | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0250 | AMR | CLM | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | CLM | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0291 | AMR | CLM | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | CLM | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG01516 | hp1 | a0001 | c0001 | t0003 | g0176 | EUR | IBS | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0234 | EUR | IBS | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG01517 | hp1 | a0001 | c0001 | t0003 | g0173 | EUR | IBS | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0273 | EUR | IBS | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG01928 | hp1 | a0001 | c0001 | t0006 | g0160 | AMR | PEL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PEL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0276 | AMR | PEL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PEL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PEL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG01943 | hp2 | a0001 | c0001 | t0014 | g0006 | AMR | PEL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG01952 | hp1 | a0001 | c0001 | t0003 | g0024 | AMR | PEL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG01952 | hp2 | a0001 | c0001 | t0006 | g0052 | AMR | PEL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0287 | AMR | PEL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PEL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG01978 | hp1 | a0001 | c0001 | t0003 | g0190 | AMR | PEL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG01978 | hp2 | a0001 | c0001 | t0006 | g0035 | AMR | PEL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG01981 | hp1 | a0001 | c0001 | t0003 | g0030 | AMR | PEL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG01981 | hp2 | a0001 | c0001 | t0003 | g0163 | AMR | PEL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PEL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG01993 | hp2 | a0001 | c0001 | t0003 | g0031 | AMR | PEL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | KHV | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | KHV | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG02055 | hp1 | a0001 | c0001 | t0005 | g0325 | AFR | ACB | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | ACB | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | KHV | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | KHV | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG02071 | hp2 | a0007 | c0010 | t0002 | g0305 | EAS | KHV | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | KHV | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG02074 | hp2 | a0001 | c0001 | t0003 | g0159 | EAS | KHV | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG02080 | hp1 | a0001 | c0001 | t0003 | g0164 | EAS | KHV | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0304 | EAS | KHV | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | KHV | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0217 | EAS | KHV | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0242 | EAS | KHV | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | KHV | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG02155 | hp1 | a0001 | c0001 | t0003 | g0155 | EAS | CDX | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG02155 | hp2 | a0001 | c0001 | t0003 | g0166 | EAS | CDX | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG02165 | hp1 | a0001 | c0001 | t0003 | g0194 | EAS | CDX | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0270 | EAS | CDX | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG02258 | hp1 | a0001 | c0001 | t0004 | g0235 | AFR | ACB | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | ACB | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PEL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0240 | AMR | PEL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG02572 | hp1 | a0001 | c0001 | t0019 | g0100 | AFR | GWD | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | GWD | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0245 | SAS | PJL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG02615 | hp2 | a0001 | c0001 | t0003 | g0014 | AFR | GWD | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | GWD | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG02630 | hp1 | a0001 | c0001 | t0005 | g0327 | AFR | GWD | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG02647 | hp1 | a0001 | c0001 | t0005 | g0329 | AFR | GWD | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG02647 | hp2 | a0001 | c0001 | t0012 | g0004 | AFR | GWD | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | GWD | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG02723 | hp1 | a0001 | c0001 | t0004 | g0247 | AFR | GWD | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG02735 | hp2 | a0001 | c0001 | t0015 | g0084 | SAS | PJL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0195 | SAS | PJL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG02809 | hp1 | a0001 | c0001 | t0002 | g0301 | AFR | GWD | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG02818 | hp2 | a0001 | c0012 | t0020 | g0207 | AFR | GWD | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG02886 | hp1 | a0001 | c0001 | t0005 | g0333 | AFR | GWD | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG02895 | hp1 | a0001 | c0001 | t0005 | g0326 | AFR | GWD | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG02895 | hp2 | a0001 | c0001 | t0002 | g0313 | AFR | GWD | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG02922 | hp1 | a0001 | c0001 | t0005 | g0320 | AFR | ESN | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG02965 | hp1 | a0001 | c0001 | t0002 | g0262 | AFR | ESN | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG02965 | hp2 | a0001 | c0001 | t0005 | g0328 | AFR | ESN | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG02976 | hp1 | a0001 | c0001 | t0003 | g0202 | AFR | ESN | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG02976 | hp2 | a0001 | c0001 | t0008 | g0057 | AFR | ESN | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0241 | AFR | GWD | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | GWD | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG03130 | hp1 | a0001 | c0001 | t0002 | g0261 | AFR | ESN | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG03130 | hp2 | a0001 | c0001 | t0002 | g0282 | AFR | ESN | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG03139 | hp1 | a0002 | c0002 | t0001 | g0206 | AFR | ESN | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG03139 | hp2 | a0001 | c0001 | t0005 | g0324 | AFR | ESN | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG03195 | hp1 | a0002 | c0002 | t0001 | g0068 | AFR | ESN | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG03195 | hp2 | a0001 | c0001 | t0002 | g0281 | AFR | ESN | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG03225 | hp1 | a0001 | c0001 | t0005 | g0322 | AFR | MSL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG03239 | hp2 | a0001 | c0001 | t0003 | g0175 | SAS | PJL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG03453 | hp1 | a0001 | c0001 | t0011 | g0003 | AFR | MSL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | MSL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | MSL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG03486 | hp2 | a0001 | c0001 | t0005 | g0321 | AFR | MSL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0283 | SAS | PJL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0268 | SAS | PJL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0267 | SAS | PJL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0284 | SAS | PJL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG03540 | hp1 | a0001 | c0001 | t0005 | g0332 | AFR | GWD | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG03540 | hp2 | a0001 | c0001 | t0003 | g0016 | AFR | GWD | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG03579 | hp1 | a0002 | c0002 | t0001 | g0201 | AFR | MSL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG03579 | hp2 | a0001 | c0001 | t0008 | g0055 | AFR | MSL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0309 | SAS | PJL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG03654 | hp2 | a0001 | c0011 | t0001 | g0069 | SAS | PJL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG03688 | hp1 | a0001 | c0001 | t0003 | g0113 | SAS | STU | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0141 | SAS | STU | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0311 | SAS | PJL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0185 | SAS | PJL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | BEB | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0272 | SAS | BEB | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG03834 | hp1 | a0001 | c0001 | t0017 | g0095 | SAS | BEB | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG03834 | hp2 | a0004 | c0005 | t0002 | g0312 | SAS | BEB | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0310 | SAS | BEB | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0248 | SAS | BEB | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | BEB | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG03942 | hp2 | a0004 | c0005 | t0002 | g0279 | SAS | BEB | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0259 | SAS | STU | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0256 | SAS | STU | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0182 | SAS | STU | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0296 | SAS | STU | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA18522 | hp1 | a0001 | c0001 | t0004 | g0299 | AFR | YRI | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA18522 | hp2 | a0001 | c0001 | t0005 | g0334 | AFR | YRI | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA18612 | hp1 | a0001 | c0001 | t0003 | g0152 | EAS | CHB | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | CHB | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0277 | EAS | CHB | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA18747 | hp2 | a0001 | c0001 | t0018 | g0138 | EAS | CHB | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | YRI | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA18906 | hp2 | a0001 | c0001 | t0016 | g0072 | AFR | YRI | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA18939 | hp1 | a0001 | c0001 | t0003 | g0034 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA18941 | hp2 | a0003 | c0004 | t0003 | g0157 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA18942 | hp1 | a0001 | c0001 | t0003 | g0127 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA18942 | hp2 | a0001 | c0001 | t0021 | g0290 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA18943 | hp1 | a0001 | c0001 | t0004 | g0243 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA18943 | hp2 | a0003 | c0004 | t0003 | g0122 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA18944 | hp1 | a0001 | c0001 | t0003 | g0154 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA18952 | hp2 | a0001 | c0001 | t0003 | g0180 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA18953 | hp1 | a0001 | c0001 | t0003 | g0114 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA18956 | hp1 | a0001 | c0001 | t0009 | g0073 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA18956 | hp2 | a0001 | c0001 | t0003 | g0082 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA18957 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA18957 | hp2 | a0001 | c0001 | t0004 | g0238 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA18961 | hp1 | a0001 | c0001 | t0003 | g0109 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA18962 | hp2 | a0001 | c0001 | t0003 | g0137 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA18963 | hp1 | a0001 | c0001 | t0002 | g0303 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA18964 | hp1 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA18965 | hp1 | a0006 | c0007 | t0003 | g0178 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA18965 | hp2 | a0001 | c0001 | t0002 | g0280 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA18966 | hp2 | a0001 | c0001 | t0003 | g0188 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA18967 | hp2 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0302 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA18968 | hp2 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0315 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA18970 | hp1 | a0001 | c0001 | t0003 | g0132 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA18970 | hp2 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA18974 | hp1 | a0001 | c0001 | t0003 | g0168 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA18975 | hp1 | a0001 | c0001 | t0009 | g0149 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA18977 | hp1 | a0001 | c0001 | t0003 | g0169 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA18982 | hp1 | a0001 | c0001 | t0003 | g0032 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA18983 | hp2 | a0001 | c0001 | t0003 | g0177 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA18985 | hp1 | a0001 | c0001 | t0003 | g0128 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA18985 | hp2 | a0001 | c0001 | t0002 | g0255 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA18986 | hp1 | a0001 | c0001 | t0004 | g0307 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0289 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA18990 | hp1 | a0001 | c0001 | t0003 | g0126 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA18991 | hp2 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA18993 | hp1 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA18995 | hp2 | a0003 | c0004 | t0003 | g0158 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA18999 | hp2 | a0001 | c0001 | t0003 | g0112 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA19001 | hp1 | a0001 | c0001 | t0003 | g0077 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA19002 | hp1 | a0001 | c0008 | t0002 | g0275 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA19002 | hp2 | a0001 | c0001 | t0004 | g0226 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA19005 | hp2 | a0001 | c0001 | t0003 | g0170 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA19007 | hp1 | a0001 | c0001 | t0003 | g0131 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA19007 | hp2 | a0001 | c0001 | t0003 | g0191 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA19010 | hp2 | a0005 | c0006 | t0003 | g0029 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA19011 | hp2 | a0001 | c0001 | t0003 | g0033 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA19012 | hp1 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA19012 | hp2 | a0001 | c0001 | t0003 | g0153 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA19030 | hp1 | a0001 | c0001 | t0027 | g0331 | AFR | LWK | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | LWK | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA19056 | hp1 | a0001 | c0001 | t0003 | g0115 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA19056 | hp2 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA19060 | hp1 | a0001 | c0001 | t0004 | g0233 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA19060 | hp2 | a0001 | c0001 | t0003 | g0156 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA19062 | hp2 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA19063 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA19065 | hp2 | a0001 | c0001 | t0003 | g0103 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA19068 | hp1 | a0001 | c0001 | t0003 | g0151 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA19068 | hp2 | a0001 | c0001 | t0003 | g0023 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA19074 | hp1 | a0008 | c0013 | t0003 | g0181 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA19074 | hp2 | a0001 | c0001 | t0003 | g0124 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA19079 | hp1 | a0001 | c0001 | t0003 | g0161 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA19079 | hp2 | a0001 | c0001 | t0003 | g0051 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA19081 | hp2 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA19082 | hp2 | a0001 | c0001 | t0003 | g0110 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA19083 | hp1 | a0001 | c0001 | t0003 | g0125 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA19087 | hp1 | a0001 | c0001 | t0003 | g0119 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA19087 | hp2 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA19090 | hp1 | a0001 | c0001 | t0010 | g0002 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA19090 | hp2 | a0001 | c0001 | t0003 | g0167 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA19091 | hp2 | a0001 | c0001 | t0004 | g0316 | EAS | JPT | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA19240 | hp1 | a0001 | c0001 | t0005 | g0323 | AFR | YRI | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | YRI | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | ASW | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA20129 | hp2 | a0001 | c0001 | t0003 | g0064 | AFR | ASW | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA20752 | hp1 | a0001 | c0001 | t0024 | g0318 | EUR | TSI | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0099 | EUR | TSI | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0263 | SAS | GIH | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA20905 | hp2 | a0001 | c0001 | t0004 | g0269 | SAS | GIH | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG01123 | hp1 | a0001 | c0001 | t0003 | g0192 | AMR | CLM | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG01123 | hp2 | a0001 | c0001 | t0025 | g0317 | AMR | CLM | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG03471 | hp1 | a0001 | c0001 | t0002 | g0288 | AFR | MSL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG03471 | hp2 | a0001 | c0001 | t0028 | g0319 | AFR | MSL | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG06807 | hp1 | a0001 | c0001 | t0005 | g0330 | AFR | USA | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
HG06807 | hp2 | a0001 | c0001 | t0002 | g0293 | AFR | USA | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA21309 | hp1 | a0001 | c0009 | t0013 | g0005 | AFR | LWK | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
NA21309 | hp2 | a0001 | c0001 | t0026 | g0335 | AFR | LWK | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0292 | REF | REF | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0009 | REF | REF | FGFR1_chr8_38406143_38473635 | FGFR1 | chr8 | 38406143 | 38473635 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:38413783
|
G | A | 1 | a0002 | 4 | HG01167.hp2 HG03139.hp1 HG03195.hp1 others(1): Show |
missense_variant | MODERATE | c.2314C>T | p.Pro772Ser | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 18/18 | 3057/5697 | 2314/2469 | 772/822 | chr8 | 38413783 | ||
chr8:38414019
|
T | C | 1 | a0007 | 1 | HG02071.hp2 | missense_variant | MODERATE | c.2191A>G | p.Met731Val | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 17/18 | 2934/5697 | 2191/2469 | 731/822 | chr8 | 38414019 | ||
chr8:38429720
|
G | A | 1 | a0003 | 3 | NA18941.hp2 NA18943.hp2 NA18995.hp2 |
missense_variant | MODERATE | c.320C>T | p.Ser107Leu | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 3/18 | 1063/5697 | 320/2469 | 107/822 | chr8 | 38429720 | ||
chr8:38429736
|
C | T | 1 | a0006 | 1 | NA18965.hp1 | missense_variant | MODERATE | c.304G>A | p.Val102Ile | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 3/18 | 1047/5697 | 304/2469 | 102/822 | chr8 | 38429736 | ||
chr8:38429864
|
T | A | 1 | a0008 | 1 | NA19074.hp1 | missense_variant | MODERATE | c.176A>T | p.Asp59Val | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 3/18 | 919/5697 | 176/2469 | 59/822 | chr8 | 38429864 | ||
chr8:38429879
|
C | T | 1 | a0005 | 1 | NA19010.hp2 | missense_variant | MODERATE | c.161G>A | p.Arg54His | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 3/18 | 904/5697 | 161/2469 | 54/822 | chr8 | 38429879 | ||
chr8:38457381
|
C | G | 1 | a0004 | 2 | HG03834.hp2 HG03942.hp2 |
missense_variant | MODERATE | c.66G>C | p.Arg22Ser | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/18 | 809/5697 | 66/2469 | 22/822 | chr8 | 38457381 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:38413948
|
C | T | 1 | a0001c0003 | 3 | HG00642.hp1 HG01175.hp2 HG01261.hp2 |
synonymous_variant | LOW | c.2262G>A | p.Leu754Leu | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 17/18 | 3005/5697 | 2262/2469 | 754/822 | chr8 | 38413948 | ||
chr8:38419719
|
C | T | 1 | a0001c0009 | 1 | NA21309.hp1 | synonymous_variant | LOW | c.1098G>A | p.Pro366Pro | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 9/18 | 1841/5697 | 1098/2469 | 366/822 | chr8 | 38419719 | ||
chr8:38427942
|
G | A | 1 | a0001c0011 | 1 | HG03654.hp2 | synonymous_variant | LOW | c.600C>T | p.Asp200Asp | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 5/18 | 1343/5697 | 600/2469 | 200/822 | chr8 | 38427942 | ||
chr8:38429704
|
G | A | 1 | a0001c0012 | 1 | HG02818.hp2 | synonymous_variant | LOW | c.336C>T | p.Thr112Thr | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 3/18 | 1079/5697 | 336/2469 | 112/822 | chr8 | 38429704 | ||
chr8:38429719
|
C | T | 1 | a0001c0008 | 1 | NA19002.hp1 | synonymous_variant | LOW | c.321G>A | p.Ser107Ser | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 3/18 | 1064/5697 | 321/2469 | 107/822 | chr8 | 38429719 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:38411287
|
T | G | 1 | a0001c0001t0027 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2341A>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 18/18 | 2341 | chr8 | 38411287 | |||||
chr8:38411410
|
A | T | 1 | a0001c0001t0008 | 2 | HG02976.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2218T>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 18/18 | 2218 | chr8 | 38411410 | |||||
chr8:38411440
|
A | G | 1 | a0001c0001t0016 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2188T>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 18/18 | 2188 | chr8 | 38411440 | |||||
chr8:38411529
|
A | C | 1 | a0001c0001t0006 | 3 | HG01928.hp1 HG01952.hp2 HG01978.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2099T>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 18/18 | 2099 | chr8 | 38411529 | |||||
chr8:38411646
|
T | G | 1 | a0001c0001t0017 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1982A>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 18/18 | 1982 | chr8 | 38411646 | |||||
chr8:38411729
|
G | C | 1 | a0001c0001t0019 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1899C>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 18/18 | 1899 | chr8 | 38411729 | |||||
chr8:38411800
|
C | T | 1 | a0001c0001t0018 | 1 | NA18747.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1828G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 18/18 | 1828 | chr8 | 38411800 | |||||
chr8:38411996
|
T | C | 18 | a0001c0001t0003a0001c0001t0004a0001c0001t0007others(15): Show | 107 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(104): Show |
3_prime_UTR_variant | MODIFIER | c.*1632A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 18/18 | 1632 | chr8 | 38411996 | |||||
chr8:38412134
|
C | T | 1 | a0001c0001t0015 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1494G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 18/18 | 1494 | chr8 | 38412134 | |||||
chr8:38412204
|
C | T | 1 | a0001c0009t0013 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1424G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 18/18 | 1424 | chr8 | 38412204 | |||||
chr8:38412267
|
C | G | 1 | a0001c0001t0012 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1361G>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 18/18 | 1361 | chr8 | 38412267 | |||||
chr8:38412301
|
C | T | 1 | a0001c0001t0007 | 2 | HG00408.hp1 HG00609.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1327G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 18/18 | 1327 | chr8 | 38412301 | |||||
chr8:38412576
|
G | A | 1 | a0001c0001t0009 | 2 | NA18956.hp1 NA18975.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1052C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 18/18 | 1052 | chr8 | 38412576 | |||||
chr8:38412602
|
A | G | 1 | a0001c0001t0022 | 1 | HG01074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1026T>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 18/18 | 1026 | chr8 | 38412602 | |||||
chr8:38413008
|
G | A | 1 | a0001c0001t0023 | 1 | HG00735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*620C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 18/18 | 620 | chr8 | 38413008 | |||||
chr8:38413059
|
G | A | 1 | a0001c0001t0028 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*569C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 18/18 | 569 | chr8 | 38413059 | |||||
chr8:38413408
|
A | G | 1 | a0001c0001t0021 | 1 | NA18942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*220T>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 18/18 | 220 | chr8 | 38413408 | |||||
chr8:38468016
|
C | T | 1 | a0001c0001t0014 | 1 | HG01943.hp2 | 5_prime_UTR_variant | MODIFIER | c.-124G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/18 | 10570 | chr8 | 38468016 | |||||
chr8:38468140
|
C | T | 1 | a0001c0009t0013 | 1 | NA21309.hp1 | 5_prime_UTR_variant | MODIFIER | c.-248G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/18 | 10694 | chr8 | 38468140 | |||||
chr8:38468230
|
A | C | 1 | a0001c0001t0012 | 1 | HG02647.hp2 | 5_prime_UTR_variant | MODIFIER | c.-338T>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/18 | 10784 | chr8 | 38468230 | |||||
chr8:38468249
|
T | C | 1 | a0001c0012t0020 | 1 | HG02818.hp2 | 5_prime_UTR_variant | MODIFIER | c.-357A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/18 | 10803 | chr8 | 38468249 | |||||
chr8:38468250
|
G | A | 2 | a0001c0001t0024a0001c0001t0025 | 2 | HG01123.hp2 NA20752.hp1 |
5_prime_UTR_variant | MODIFIER | c.-358C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/18 | 10804 | chr8 | 38468250 | |||||
chr8:38468277
|
C | T | 5 | a0001c0001t0005a0001c0001t0011a0001c0001t0026others(2): Show | 18 | HG02055.hp1 HG02630.hp1 HG02647.hp1 others(15): Show |
5_prime_UTR_variant | MODIFIER | c.-385G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/18 | 10831 | chr8 | 38468277 | |||||
chr8:38468528
|
G | A | 10 | a0001c0001t0002a0001c0001t0004a0001c0001t0021others(7): Show | 111 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(108): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-636C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/18 | chr8 | 38468528 | ||||||
chr8:38468591
|
G | A | 4 | a0001c0001t0005a0001c0001t0026a0001c0001t0027others(1): Show | 17 | HG02055.hp1 HG02630.hp1 HG02647.hp1 others(14): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-699C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/18 | chr8 | 38468591 | ||||||
chr8:38468596
|
C | G | 1 | a0001c0001t0010 | 1 | NA19090.hp1 | 5_prime_UTR_variant | MODIFIER | c.-704G>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/18 | 11150 | chr8 | 38468596 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:38413882
|
C | T | 1 | a0001c0001t0002g0281 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2292+36G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 17/17 | chr8 | 38413882 | ||||||
chr8:38414331
|
G | A | 2 | a0001c0001t0003g0188a0001c0001t0004g0316 | 2 | NA18966.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2049-42C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 15/17 | chr8 | 38414331 | ||||||
chr8:38414344
|
C | T | 1 | a0001c0001t0003g0016 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2049-55G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 15/17 | chr8 | 38414344 | ||||||
chr8:38415024
|
C | G | 86 | a0001c0001t0003g0001a0001c0001t0003g0014a0001c0001t0003g0016others(83): Show | 87 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.1855-123G>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 13/17 | chr8 | 38415024 | ||||||
chr8:38415064
|
C | A | 84 | a0001c0001t0003g0001a0001c0001t0003g0014a0001c0001t0003g0024others(81): Show | 85 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.1855-163G>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 13/17 | chr8 | 38415064 | ||||||
chr8:38415066
|
C | G | 1 | a0001c0001t0002g0242 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1855-165G>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 13/17 | chr8 | 38415066 | ||||||
chr8:38415136
|
G | A | 1 | a0001c0001t0004g0307 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1855-235C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 13/17 | chr8 | 38415136 | ||||||
chr8:38415269
|
A | C | 1 | a0001c0001t0004g0269 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1855-368T>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 13/17 | chr8 | 38415269 | ||||||
chr8:38415296
|
T | C | 52 | a0001c0001t0001g0028a0001c0001t0001g0047a0001c0001t0001g0048others(49): Show | 52 | HG00423.hp1 HG00558.hp1 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.1855-395A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 13/17 | chr8 | 38415296 | ||||||
chr8:38415400
|
C | T | 1 | a0001c0001t0001g0011 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1854+470G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 13/17 | chr8 | 38415400 | ||||||
chr8:38415434
|
T | C | 90 | a0001c0001t0003g0001a0001c0001t0003g0014a0001c0001t0003g0016others(87): Show | 91 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.1854+436A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 13/17 | chr8 | 38415434 | ||||||
chr8:38415441
|
G | A | 1 | a0001c0001t0001g0049 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1854+429C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 13/17 | chr8 | 38415441 | ||||||
chr8:38415468
|
A | AT | 42 | a0001c0001t0001g0020a0001c0001t0001g0025a0001c0001t0001g0026others(39): Show | 42 | HG00438.hp2 HG00558.hp2 HG01069.hp2 others(39): Show |
intron_variant | MODIFIER | c.1854+401dupA | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 13/17 | chr8 | 38415468 | ||||||
chr8:38415468
|
A | T | 1 | a0001c0001t0001g0022 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1854+402T>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 13/17 | chr8 | 38415468 | ||||||
chr8:38415468
|
AT | A | 12 | a0001c0001t0001g0042a0001c0001t0001g0148a0001c0001t0002g0253others(9): Show | 12 | HG00099.hp2 HG01081.hp2 HG02735.hp1 others(9): Show |
intron_variant | MODIFIER | c.1854+401delA | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 13/17 | chr8 | 38415468 | ||||||
chr8:38415568
|
G | A | 1 | a0001c0001t0001g0036 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1854+302C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 13/17 | chr8 | 38415568 | ||||||
chr8:38415747
|
C | T | 1 | a0001c0001t0001g0015 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1854+123G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 13/17 | chr8 | 38415747 | ||||||
chr8:38416212
|
A | C | 1 | a0001c0001t0012g0004 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1664-152T>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 12/17 | chr8 | 38416212 | ||||||
chr8:38416429
|
C | G | 3 | a0001c0001t0002g0313a0001c0001t0008g0055a0001c0001t0008g0057 | 3 | HG02895.hp2 HG02976.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1664-369G>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 12/17 | chr8 | 38416429 | ||||||
chr8:38416448
|
A | AT | 183 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0011others(180): Show | 183 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(180): Show |
intron_variant | MODIFIER | c.1664-389dupA | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 12/17 | chr8 | 38416448 | ||||||
chr8:38416448
|
A | ATT | 15 | a0001c0001t0001g0038a0001c0001t0001g0054a0001c0001t0001g0071others(12): Show | 15 | HG00735.hp2 HG00741.hp1 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.1664-390_1664-389d others(4): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 12/17 | chr8 | 38416448 | ||||||
chr8:38416448
|
ATT | A | 11 | a0001c0001t0003g0016a0001c0001t0003g0114a0001c0001t0003g0127others(8): Show | 11 | HG02572.hp1 HG02723.hp1 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.1664-390_1664-389d others(4): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 12/17 | chr8 | 38416448 | ||||||
chr8:38416448
|
ATTT | A | 74 | a0001c0001t0003g0001a0001c0001t0003g0014a0001c0001t0003g0024others(71): Show | 75 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.1664-391_1664-389d others(5): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 12/17 | chr8 | 38416448 | ||||||
chr8:38416448
|
ATTTTTTT others(6): Show |
A | 1 | a0001c0001t0012g0004 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1664-401_1664-389d others(15): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 12/17 | chr8 | 38416448 | ||||||
chr8:38416541
|
C | T | 2 | a0001c0001t0003g0064a0001c0001t0003g0204 | 2 | HG01243.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1664-481G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 12/17 | chr8 | 38416541 | ||||||
chr8:38416551
|
G | A | 1 | a0001c0001t0004g0243 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1664-491C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 12/17 | chr8 | 38416551 | ||||||
chr8:38416604
|
C | T | 1 | a0001c0001t0012g0004 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1664-544G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 12/17 | chr8 | 38416604 | ||||||
chr8:38416613
|
G | A | 1 | a0001c0001t0012g0004 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1664-553C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 12/17 | chr8 | 38416613 | ||||||
chr8:38416657
|
G | C | 1 | a0001c0001t0001g0013 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1664-597C>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 12/17 | chr8 | 38416657 | ||||||
chr8:38416672
|
C | G | 1 | a0001c0009t0013g0005 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1664-612G>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 12/17 | chr8 | 38416672 | ||||||
chr8:38416675
|
C | G | 101 | a0001c0001t0003g0001a0001c0001t0003g0014a0001c0001t0003g0016others(98): Show | 102 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.1664-615G>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 12/17 | chr8 | 38416675 | ||||||
chr8:38416718
|
G | T | 3 | a0001c0001t0001g0078a0001c0001t0002g0222a0008c0013t0003g0181 | 3 | NA19011.hp1 NA19074.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.1663+588C>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 12/17 | chr8 | 38416718 | ||||||
chr8:38416840
|
C | T | 8 | a0001c0001t0001g0075a0001c0001t0001g0086a0001c0001t0001g0102others(5): Show | 8 | HG00423.hp2 HG02074.hp1 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.1663+466G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 12/17 | chr8 | 38416840 | ||||||
chr8:38416901
|
C | T | 2 | a0001c0001t0003g0173a0001c0001t0003g0176 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1663+405G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 12/17 | chr8 | 38416901 | ||||||
chr8:38416965
|
A | G | 1 | a0001c0001t0003g0016 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1663+341T>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 12/17 | chr8 | 38416965 | ||||||
chr8:38417241
|
G | T | 1 | a0001c0001t0028g0319 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1663+65C>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 12/17 | chr8 | 38417241 | ||||||
chr8:38417268
|
C | G | 2 | a0001c0001t0001g0043a0001c0001t0002g0284 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1663+38G>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 12/17 | chr8 | 38417268 | ||||||
chr8:38417637
|
G | A | 1 | a0001c0001t0003g0103 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1553-221C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 11/17 | chr8 | 38417637 | ||||||
chr8:38418520
|
A | G | 2 | a0001c0001t0002g0253a0001c0001t0002g0254 | 2 | NA19012.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.1285-147T>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 9/17 | chr8 | 38418520 | ||||||
chr8:38418735
|
G | C | 2 | a0001c0001t0001g0142a0001c0001t0001g0143 | 2 | NA18952.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1285-362C>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 9/17 | chr8 | 38418735 | ||||||
chr8:38418929
|
G | A | 1 | a0006c0007t0003g0178 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1285-556C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 9/17 | chr8 | 38418929 | ||||||
chr8:38419027
|
T | C | 1 | a0001c0001t0001g0013 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1284+506A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 9/17 | chr8 | 38419027 | ||||||
chr8:38419084
|
C | T | 1 | a0001c0001t0026g0335 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1284+449G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 9/17 | chr8 | 38419084 | ||||||
chr8:38419230
|
C | T | 3 | a0001c0001t0003g0001a0001c0001t0003g0172a0001c0001t0004g0278 | 4 | HG00140.hp1 HG01069.hp1 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.1284+303G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 9/17 | chr8 | 38419230 | ||||||
chr8:38419276
|
CA | C | 8 | a0001c0001t0001g0025a0001c0001t0001g0038a0001c0001t0001g0039others(5): Show | 8 | HG01257.hp1 HG01361.hp2 HG01943.hp1 others(5): Show |
intron_variant | MODIFIER | c.1284+256delT | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 9/17 | chr8 | 38419276 | ||||||
chr8:38419779
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1082-44C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 8/17 | chr8 | 38419779 | ||||||
chr8:38419786
|
C | T | 1 | a0001c0001t0001g0070 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1082-51G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 8/17 | chr8 | 38419786 | ||||||
chr8:38419971
|
C | T | 1 | a0001c0001t0001g0059 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1082-236G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 8/17 | chr8 | 38419971 | ||||||
chr8:38420156
|
C | A | 1 | a0001c0001t0001g0071 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1082-421G>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 8/17 | chr8 | 38420156 | ||||||
chr8:38420292
|
G | A | 1 | a0001c0001t0001g0099 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1082-557C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 8/17 | chr8 | 38420292 | ||||||
chr8:38420750
|
C | T | 1 | a0001c0001t0012g0004 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1082-1015G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 8/17 | chr8 | 38420750 | ||||||
chr8:38420920
|
G | A | 2 | a0001c0001t0002g0304a0007c0010t0002g0305 | 2 | HG02071.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.1081+877C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 8/17 | chr8 | 38420920 | ||||||
chr8:38420929
|
G | A | 1 | a0001c0001t0003g0016 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1081+868C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 8/17 | chr8 | 38420929 | ||||||
chr8:38421006
|
C | G | 1 | a0001c0001t0002g0281 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1081+791G>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 8/17 | chr8 | 38421006 | ||||||
chr8:38421176
|
C | G | 1 | a0001c0001t0012g0004 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1081+621G>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 8/17 | chr8 | 38421176 | ||||||
chr8:38421211
|
C | T | 22 | a0001c0001t0001g0107a0001c0001t0001g0118a0001c0001t0001g0120others(19): Show | 22 | HG00597.hp1 HG00609.hp2 HG02056.hp2 others(19): Show |
intron_variant | MODIFIER | c.1081+586G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 8/17 | chr8 | 38421211 | ||||||
chr8:38421219
|
G | A | 1 | a0001c0012t0020g0207 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1081+578C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 8/17 | chr8 | 38421219 | ||||||
chr8:38421461
|
G | C | 1 | a0001c0001t0003g0082 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1081+336C>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 8/17 | chr8 | 38421461 | ||||||
chr8:38421461
|
G | T | 1 | a0001c0001t0002g0301 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1081+336C>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 8/17 | chr8 | 38421461 | ||||||
chr8:38421547
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1081+250C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 8/17 | chr8 | 38421547 | ||||||
chr8:38421730
|
G | A | 3 | a0001c0001t0003g0016a0001c0001t0019g0100a0001c0009t0013g0005 | 3 | HG02572.hp1 HG03540.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1081+67C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 8/17 | chr8 | 38421730 | ||||||
chr8:38421746
|
C | T | 1 | a0001c0012t0020g0207 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1081+51G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 8/17 | chr8 | 38421746 | ||||||
chr8:38421777
|
G | A | 1 | a0001c0001t0001g0059 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1081+20C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 8/17 | chr8 | 38421777 | ||||||
chr8:38422000
|
G | A | 2 | a0001c0001t0002g0291a0001c0001t0002g0300 | 2 | HG00099.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.937-59C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 7/17 | chr8 | 38422000 | ||||||
chr8:38422123
|
G | A | 1 | a0001c0001t0001g0195 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.937-182C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 7/17 | chr8 | 38422123 | ||||||
chr8:38422223
|
C | T | 1 | a0001c0001t0001g0070 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.937-282G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 7/17 | chr8 | 38422223 | ||||||
chr8:38422231
|
G | A | 2 | a0001c0001t0001g0085a0001c0001t0001g0090 | 2 | HG02040.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.937-290C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 7/17 | chr8 | 38422231 | ||||||
chr8:38422255
|
G | A | 3 | a0001c0001t0003g0016a0001c0001t0019g0100a0001c0009t0013g0005 | 3 | HG02572.hp1 HG03540.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.937-314C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 7/17 | chr8 | 38422255 | ||||||
chr8:38422312
|
C | T | 2 | a0001c0001t0003g0064a0001c0001t0003g0204 | 2 | HG01243.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.937-371G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 7/17 | chr8 | 38422312 | ||||||
chr8:38422351
|
C | T | 8 | a0001c0001t0001g0099a0001c0001t0002g0244a0001c0001t0002g0249others(5): Show | 8 | HG01070.hp2 HG01071.hp2 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.937-410G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 7/17 | chr8 | 38422351 | ||||||
chr8:38422380
|
C | T | 1 | a0001c0001t0012g0004 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.937-439G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 7/17 | chr8 | 38422380 | ||||||
chr8:38422459
|
T | C | 3 | a0001c0001t0003g0016a0001c0001t0019g0100a0001c0009t0013g0005 | 3 | HG02572.hp1 HG03540.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.937-518A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 7/17 | chr8 | 38422459 | ||||||
chr8:38422646
|
C | T | 1 | a0001c0001t0009g0073 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.937-705G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 7/17 | chr8 | 38422646 | ||||||
chr8:38422995
|
A | T | 2 | a0001c0001t0001g0094a0001c0001t0001g0150 | 2 | HG01358.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.937-1054T>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 7/17 | chr8 | 38422995 | ||||||
chr8:38423233
|
C | G | 1 | a0001c0001t0001g0013 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.936+1276G>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 7/17 | chr8 | 38423233 | ||||||
chr8:38423312
|
G | GT | 26 | a0001c0001t0001g0058a0001c0001t0001g0075a0001c0001t0001g0083others(23): Show | 27 | HG00140.hp1 HG00438.hp1 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.936+1196dupA | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 7/17 | chr8 | 38423312 | ||||||
chr8:38423312
|
G | GTT | 88 | a0001c0001t0001g0063a0001c0001t0001g0079a0001c0001t0003g0019others(85): Show | 88 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.936+1195_936+1196d others(4): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 7/17 | chr8 | 38423312 | ||||||
chr8:38423356
|
C | T | 4 | a0001c0001t0001g0075a0001c0001t0001g0102a0001c0001t0002g0212others(1): Show | 4 | NA18939.hp2 NA18968.hp2 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.936+1153G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 7/17 | chr8 | 38423356 | ||||||
chr8:38423530
|
C | T | 4 | a0001c0001t0003g0109a0001c0001t0003g0188a0001c0001t0004g0238others(1): Show | 4 | NA18957.hp2 NA18961.hp1 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.936+979G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 7/17 | chr8 | 38423530 | ||||||
chr8:38423552
|
C | A | 3 | a0001c0001t0003g0114a0001c0001t0003g0115a0001c0001t0003g0151 | 3 | NA18953.hp1 NA19056.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.936+957G>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 7/17 | chr8 | 38423552 | ||||||
chr8:38423573
|
G | A | 3 | a0001c0001t0002g0313a0001c0001t0008g0055a0001c0001t0008g0057 | 3 | HG02895.hp2 HG02976.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.936+936C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 7/17 | chr8 | 38423573 | ||||||
chr8:38423603
|
C | T | 2 | a0001c0001t0004g0247a0001c0001t0012g0004 | 2 | HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.936+906G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 7/17 | chr8 | 38423603 | ||||||
chr8:38423662
|
T | TA | 41 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0046others(38): Show | 41 | HG00423.hp1 HG00558.hp1 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.936+846dupT | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 7/17 | chr8 | 38423662 | ||||||
chr8:38423662
|
TA | T | 26 | a0001c0001t0001g0022a0001c0001t0001g0028a0001c0001t0001g0087others(23): Show | 26 | HG00408.hp1 HG00609.hp2 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.936+846delT | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 7/17 | chr8 | 38423662 | ||||||
chr8:38423739
|
C | A | 1 | a0001c0001t0004g0247 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.936+770G>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 7/17 | chr8 | 38423739 | ||||||
chr8:38423854
|
G | A | 1 | a0001c0001t0001g0184 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.936+655C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 7/17 | chr8 | 38423854 | ||||||
chr8:38424057
|
A | C | 2 | a0001c0001t0004g0264a0001c0001t0004g0266 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.936+452T>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 7/17 | chr8 | 38424057 | ||||||
chr8:38424131
|
G | A | 2 | a0001c0001t0001g0067a0001c0001t0001g0083 | 2 | HG02055.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.936+378C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 7/17 | chr8 | 38424131 | ||||||
chr8:38424140
|
G | A | 84 | a0001c0001t0001g0063a0001c0001t0001g0079a0001c0001t0003g0001others(81): Show | 85 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.936+369C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 7/17 | chr8 | 38424140 | ||||||
chr8:38424366
|
C | T | 1 | a0001c0001t0002g0221 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.936+143G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 7/17 | chr8 | 38424366 | ||||||
chr8:38424396
|
G | A | 5 | a0001c0001t0003g0121a0001c0001t0003g0137a0001c0001t0003g0155others(2): Show | 5 | HG00621.hp2 HG02155.hp1 NA18747.hp2 others(2): Show |
intron_variant | MODIFIER | c.936+113C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 7/17 | chr8 | 38424396 | ||||||
chr8:38424776
|
C | T | 50 | a0001c0001t0001g0028a0001c0001t0001g0047a0001c0001t0001g0048others(47): Show | 50 | HG00423.hp1 HG00558.hp1 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.746-77G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 6/17 | chr8 | 38424776 | ||||||
chr8:38424875
|
G | A | 3 | a0001c0001t0003g0194a0001c0001t0004g0232a0001c0001t0004g0235 | 3 | HG00621.hp1 HG02165.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.746-176C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 6/17 | chr8 | 38424875 | ||||||
chr8:38424971
|
T | G | 5 | a0001c0001t0003g0016a0001c0001t0003g0064a0001c0001t0003g0204others(2): Show | 5 | HG01243.hp1 HG02572.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.746-272A>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 6/17 | chr8 | 38424971 | ||||||
chr8:38425054
|
G | A | 2 | a0001c0001t0008g0055a0001c0001t0008g0057 | 2 | HG02976.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.746-355C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 6/17 | chr8 | 38425054 | ||||||
chr8:38425136
|
C | T | 1 | a0001c0001t0003g0016 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.746-437G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 6/17 | chr8 | 38425136 | ||||||
chr8:38425145
|
CT | C | 81 | a0001c0001t0001g0063a0001c0001t0001g0079a0001c0001t0003g0001others(78): Show | 82 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.746-447delA | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 6/17 | chr8 | 38425145 | ||||||
chr8:38425428
|
G | T | 2 | a0001c0001t0019g0100a0001c0009t0013g0005 | 2 | HG02572.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.745+694C>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 6/17 | chr8 | 38425428 | ||||||
chr8:38425541
|
C | A | 1 | a0001c0012t0020g0207 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.745+581G>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 6/17 | chr8 | 38425541 | ||||||
chr8:38425586
|
A | T | 1 | a0001c0001t0001g0142 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.745+536T>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 6/17 | chr8 | 38425586 | ||||||
chr8:38425656
|
C | T | 2 | a0001c0001t0002g0282a0001c0001t0005g0323 | 2 | HG03130.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.745+466G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 6/17 | chr8 | 38425656 | ||||||
chr8:38425690
|
C | A | 83 | a0001c0001t0001g0063a0001c0001t0001g0079a0001c0001t0003g0001others(80): Show | 84 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.745+432G>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 6/17 | chr8 | 38425690 | ||||||
chr8:38425828
|
C | T | 2 | a0001c0001t0003g0103a0001c0001t0009g0149 | 2 | NA18975.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.745+294G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 6/17 | chr8 | 38425828 | ||||||
chr8:38425851
|
C | A | 1 | a0001c0001t0028g0319 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.745+271G>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 6/17 | chr8 | 38425851 | ||||||
chr8:38425916
|
C | T | 3 | a0001c0001t0003g0119a0001c0001t0003g0131a0001c0001t0003g0132 | 3 | NA18970.hp1 NA19007.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.745+206G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 6/17 | chr8 | 38425916 | ||||||
chr8:38426493
|
C | T | 81 | a0001c0001t0001g0063a0001c0001t0001g0079a0001c0001t0003g0001others(78): Show | 82 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.622-248G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 5/17 | chr8 | 38426493 | ||||||
chr8:38426545
|
A | G | 1 | a0001c0001t0003g0016 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.622-300T>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 5/17 | chr8 | 38426545 | ||||||
chr8:38426598
|
C | T | 2 | a0001c0001t0019g0100a0001c0009t0013g0005 | 2 | HG02572.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.622-353G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 5/17 | chr8 | 38426598 | ||||||
chr8:38426871
|
G | A | 1 | a0001c0001t0002g0256 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.622-626C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 5/17 | chr8 | 38426871 | ||||||
chr8:38426934
|
G | A | 2 | a0001c0001t0002g0309a0001c0001t0002g0310 | 2 | HG03654.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.622-689C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 5/17 | chr8 | 38426934 | ||||||
chr8:38427028
|
A | G | 2 | a0001c0001t0001g0045a0001c0001t0001g0050 | 2 | HG01928.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.622-783T>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 5/17 | chr8 | 38427028 | ||||||
chr8:38427063
|
C | T | 81 | a0001c0001t0001g0063a0001c0001t0001g0079a0001c0001t0003g0001others(78): Show | 82 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.622-818G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 5/17 | chr8 | 38427063 | ||||||
chr8:38427088
|
CAG | C | 79 | a0001c0001t0001g0063a0001c0001t0001g0079a0001c0001t0003g0001others(76): Show | 80 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.621+831_621+832del others(2): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 5/17 | chr8 | 38427088 | ||||||
chr8:38427105
|
T | TA | 92 | a0001c0001t0001g0063a0001c0001t0001g0075a0001c0001t0001g0079others(89): Show | 93 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.621+815dupT | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 5/17 | chr8 | 38427105 | ||||||
chr8:38427122
|
T | A | 2 | a0001c0001t0001g0056a0001c0001t0001g0081 | 2 | HG02258.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.621+799A>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 5/17 | chr8 | 38427122 | ||||||
chr8:38427476
|
C | T | 19 | a0001c0001t0003g0024a0001c0001t0003g0034a0001c0001t0003g0114others(16): Show | 19 | HG00673.hp1 HG01928.hp1 HG01952.hp1 others(16): Show |
intron_variant | MODIFIER | c.621+445G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 5/17 | chr8 | 38427476 | ||||||
chr8:38427477
|
G | A | 2 | a0001c0001t0004g0247a0001c0001t0012g0004 | 2 | HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.621+444C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 5/17 | chr8 | 38427477 | ||||||
chr8:38427777
|
A | G | 1 | a0001c0001t0012g0004 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.621+144T>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 5/17 | chr8 | 38427777 | ||||||
chr8:38427894
|
C | G | 1 | a0001c0001t0027g0331 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.621+27G>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 5/17 | chr8 | 38427894 | ||||||
chr8:38428101
|
G | T | 1 | a0001c0001t0001g0117 | 1 | HG00408.hp2 | splice_region_variant&intron_variant | LOW | c.449-8C>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 4/17 | chr8 | 38428101 | ||||||
chr8:38428175
|
C | G | 2 | a0001c0001t0003g0016a0001c0001t0005g0327 | 2 | HG02630.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.449-82G>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 4/17 | chr8 | 38428175 | ||||||
chr8:38428216
|
G | A | 1 | a0001c0001t0001g0060 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.449-123C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 4/17 | chr8 | 38428216 | ||||||
chr8:38428439
|
T | C | 1 | a0001c0003t0001g0197 | 1 | HG01175.hp2 | splice_region_variant&intron_variant | LOW | c.359-4A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 3/17 | chr8 | 38428439 | ||||||
chr8:38428707
|
G | A | 46 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0025others(43): Show | 46 | HG00323.hp1 HG00438.hp2 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.359-272C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 3/17 | chr8 | 38428707 | ||||||
chr8:38428805
|
A | G | 4 | a0001c0001t0001g0010a0001c0001t0002g0282a0001c0001t0005g0323others(1): Show | 4 | HG03130.hp2 HG03225.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.359-370T>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 3/17 | chr8 | 38428805 | ||||||
chr8:38428955
|
A | T | 1 | a0001c0001t0001g0120 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.359-520T>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 3/17 | chr8 | 38428955 | ||||||
chr8:38429017
|
T | C | 1 | a0001c0001t0002g0308 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.359-582A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 3/17 | chr8 | 38429017 | ||||||
chr8:38429119
|
A | G | 1 | a0001c0001t0001g0135 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.358+563T>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 3/17 | chr8 | 38429119 | ||||||
chr8:38429293
|
C | G | 85 | a0001c0001t0001g0079a0001c0001t0003g0001a0001c0001t0003g0016others(82): Show | 86 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.358+389G>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 3/17 | chr8 | 38429293 | ||||||
chr8:38429384
|
G | A | 2 | a0002c0002t0001g0205a0002c0002t0001g0206 | 2 | HG01167.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.358+298C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 3/17 | chr8 | 38429384 | ||||||
chr8:38429469
|
C | A | 1 | a0001c0001t0002g0285 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.358+213G>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 3/17 | chr8 | 38429469 | ||||||
chr8:38429496
|
A | G | 3 | a0001c0001t0001g0007a0001c0001t0005g0333a0001c0001t0005g0334 | 3 | HG02622.hp1 HG02886.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.358+186T>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 3/17 | chr8 | 38429496 | ||||||
chr8:38429962
|
G | A | 1 | a0001c0001t0003g0194 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.92-14C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38429962 | ||||||
chr8:38430037
|
C | T | 82 | a0001c0001t0001g0079a0001c0001t0003g0001a0001c0001t0003g0016others(79): Show | 83 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.92-89G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38430037 | ||||||
chr8:38430234
|
G | GGATCA | 332 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(329): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.92-287_92-286insTG others(3): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38430234 | ||||||
chr8:38430295
|
G | A | 1 | a0001c0001t0001g0026 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.92-347C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38430295 | ||||||
chr8:38430415
|
C | T | 1 | a0001c0001t0003g0188 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.92-467G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38430415 | ||||||
chr8:38430449
|
C | T | 2 | a0001c0001t0003g0171a0001c0001t0003g0187 | 2 | HG00099.hp1 HG00642.hp2 |
intron_variant | MODIFIER | c.92-501G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38430449 | ||||||
chr8:38430688
|
G | A | 2 | a0001c0001t0001g0140a0001c0001t0022g0208 | 2 | HG01074.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.92-740C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38430688 | ||||||
chr8:38430764
|
G | A | 2 | a0001c0001t0001g0071a0001c0001t0005g0322 | 2 | HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.92-816C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38430764 | ||||||
chr8:38431048
|
C | G | 80 | a0001c0001t0001g0079a0001c0001t0003g0001a0001c0001t0003g0024others(77): Show | 81 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.92-1100G>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38431048 | ||||||
chr8:38431054
|
T | G | 1 | a0001c0001t0024g0318 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.92-1106A>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38431054 | ||||||
chr8:38431285
|
G | A | 1 | a0001c0001t0003g0019 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.92-1337C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38431285 | ||||||
chr8:38431312
|
G | A | 1 | a0001c0001t0004g0247 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.92-1364C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38431312 | ||||||
chr8:38431326
|
G | A | 1 | a0001c0001t0001g0013 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.92-1378C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38431326 | ||||||
chr8:38431384
|
T | C | 2 | a0001c0001t0019g0100a0001c0009t0013g0005 | 2 | HG02572.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.92-1436A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38431384 | ||||||
chr8:38431415
|
G | A | 1 | a0001c0012t0020g0207 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.92-1467C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38431415 | ||||||
chr8:38431419
|
C | T | 1 | a0001c0001t0002g0248 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.92-1471G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38431419 | ||||||
chr8:38431712
|
G | A | 14 | a0001c0001t0001g0107a0001c0001t0001g0118a0001c0001t0001g0183others(11): Show | 14 | HG00597.hp1 HG00609.hp2 NA18944.hp2 others(11): Show |
intron_variant | MODIFIER | c.92-1764C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38431712 | ||||||
chr8:38431790
|
G | A | 1 | a0001c0012t0020g0207 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.92-1842C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38431790 | ||||||
chr8:38431854
|
C | T | 2 | a0001c0001t0004g0247a0001c0001t0012g0004 | 2 | HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.92-1906G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38431854 | ||||||
chr8:38431928
|
T | C | 1 | a0001c0012t0020g0207 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.92-1980A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38431928 | ||||||
chr8:38432232
|
C | T | 1 | a0001c0001t0002g0239 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.92-2284G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38432232 | ||||||
chr8:38432357
|
C | A | 1 | a0001c0001t0003g0016 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.92-2409G>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38432357 | ||||||
chr8:38432410
|
A | AT | 27 | a0001c0001t0001g0056a0001c0001t0001g0081a0001c0001t0001g0123others(24): Show | 27 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(24): Show |
intron_variant | MODIFIER | c.92-2463dupA | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38432410 | ||||||
chr8:38432410
|
AT | A | 19 | a0001c0001t0001g0062a0001c0001t0001g0089a0001c0001t0001g0097others(16): Show | 19 | HG00099.hp2 HG00140.hp2 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.92-2463delA | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38432410 | ||||||
chr8:38432769
|
T | C | 1 | a0001c0001t0001g0015 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.92-2821A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38432769 | ||||||
chr8:38432891
|
C | T | 1 | a0001c0001t0003g0016 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.92-2943G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38432891 | ||||||
chr8:38432904
|
C | CCA | 18 | a0001c0001t0003g0001a0001c0001t0003g0016a0001c0001t0003g0082others(15): Show | 19 | HG00140.hp1 HG00735.hp1 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.92-2957_92-2956ins others(2): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38432904 | ||||||
chr8:38432906
|
G | A | 65 | a0001c0001t0001g0079a0001c0001t0003g0024a0001c0001t0003g0034others(62): Show | 65 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.92-2958C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38432906 | ||||||
chr8:38432908
|
G | C | 18 | a0001c0001t0003g0001a0001c0001t0003g0016a0001c0001t0003g0082others(15): Show | 19 | HG00140.hp1 HG00735.hp1 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.92-2960C>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38432908 | ||||||
chr8:38432908
|
G | GC | 169 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0015others(166): Show | 169 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.92-2961dupG | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38432908 | ||||||
chr8:38432916
|
C | G | 1 | a0001c0001t0003g0161 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.92-2968G>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38432916 | ||||||
chr8:38432919
|
T | A | 4 | a0001c0001t0004g0247a0001c0001t0012g0004a0001c0001t0019g0100others(1): Show | 4 | HG02572.hp1 HG02647.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.92-2971A>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38432919 | ||||||
chr8:38432919
|
T | C | 98 | a0001c0001t0001g0079a0001c0001t0003g0001a0001c0001t0003g0016others(95): Show | 99 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.92-2971A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38432919 | ||||||
chr8:38432921
|
C | T | 1 | a0001c0001t0003g0180 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.92-2973G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38432921 | ||||||
chr8:38433163
|
C | T | 2 | a0001c0001t0004g0247a0001c0001t0012g0004 | 2 | HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.92-3215G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38433163 | ||||||
chr8:38433294
|
C | T | 1 | a0001c0012t0020g0207 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.92-3346G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38433294 | ||||||
chr8:38433413
|
C | G | 3 | a0001c0001t0003g0024a0001c0001t0003g0163a0001c0001t0006g0160 | 3 | HG01928.hp1 HG01952.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.92-3465G>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38433413 | ||||||
chr8:38433562
|
G | A | 1 | a0001c0012t0020g0207 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.92-3614C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38433562 | ||||||
chr8:38433582
|
G | T | 2 | a0001c0001t0002g0273a0001c0001t0002g0274 | 2 | HG00280.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.92-3634C>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38433582 | ||||||
chr8:38433583
|
C | T | 2 | a0001c0001t0002g0273a0001c0001t0002g0274 | 2 | HG00280.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.92-3635G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38433583 | ||||||
chr8:38433601
|
G | A | 1 | a0001c0001t0004g0269 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.92-3653C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38433601 | ||||||
chr8:38433670
|
T | C | 1 | a0001c0012t0020g0207 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.92-3722A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38433670 | ||||||
chr8:38433694
|
G | A | 10 | a0001c0001t0001g0011a0001c0001t0001g0018a0001c0001t0005g0320others(7): Show | 10 | HG02055.hp1 HG02615.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.92-3746C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38433694 | ||||||
chr8:38433910
|
T | C | 4 | a0001c0001t0001g0179a0001c0001t0002g0210a0001c0001t0002g0260others(1): Show | 4 | NA18947.hp1 NA18953.hp2 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.92-3962A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38433910 | ||||||
chr8:38433965
|
C | G | 1 | a0001c0001t0001g0088 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.92-4017G>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38433965 | ||||||
chr8:38434030
|
G | C | 2 | a0001c0001t0002g0267a0001c0001t0002g0268 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.92-4082C>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38434030 | ||||||
chr8:38434168
|
T | C | 2 | a0001c0001t0002g0256a0001c0001t0002g0272 | 2 | HG03831.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.92-4220A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38434168 | ||||||
chr8:38434318
|
T | C | 88 | a0001c0001t0001g0079a0001c0001t0003g0001a0001c0001t0003g0019others(85): Show | 89 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.92-4370A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38434318 | ||||||
chr8:38434320
|
TTGC | T | 6 | a0001c0001t0003g0034a0001c0001t0003g0106a0001c0001t0003g0115others(3): Show | 6 | HG01081.hp2 HG01167.hp1 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.92-4375_92-4373del others(3): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38434320 | ||||||
chr8:38434327
|
TG | T | 5 | a0001c0001t0003g0001a0001c0001t0003g0159a0001c0001t0003g0169others(2): Show | 6 | HG00140.hp1 HG01069.hp1 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.92-4380delC | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38434327 | ||||||
chr8:38434327
|
TGC | T | 77 | a0001c0001t0001g0079a0001c0001t0003g0019a0001c0001t0003g0023others(74): Show | 77 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.92-4381_92-4380del others(2): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38434327 | ||||||
chr8:38434329
|
C | T | 5 | a0001c0001t0003g0001a0001c0001t0003g0159a0001c0001t0003g0169others(2): Show | 6 | HG00140.hp1 HG01069.hp1 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.92-4381G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38434329 | ||||||
chr8:38434329
|
CT | C | 6 | a0001c0001t0001g0046a0001c0001t0001g0070a0001c0001t0001g0120others(3): Show | 6 | HG02683.hp2 HG02818.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.92-4382delA | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38434329 | ||||||
chr8:38434346
|
T | A | 1 | a0001c0001t0001g0117 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.92-4398A>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38434346 | ||||||
chr8:38434487
|
T | C | 1 | a0001c0001t0003g0116 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.92-4539A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38434487 | ||||||
chr8:38434629
|
A | C | 92 | a0001c0001t0001g0079a0001c0001t0003g0001a0001c0001t0003g0016others(89): Show | 93 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.92-4681T>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38434629 | ||||||
chr8:38434697
|
G | C | 1 | a0001c0001t0001g0007 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.92-4749C>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38434697 | ||||||
chr8:38434748
|
C | A | 51 | a0001c0001t0001g0028a0001c0001t0001g0047a0001c0001t0001g0048others(48): Show | 51 | HG00423.hp1 HG00558.hp1 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.92-4800G>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38434748 | ||||||
chr8:38434807
|
A | G | 1 | a0001c0012t0020g0207 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.92-4859T>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38434807 | ||||||
chr8:38434821
|
C | T | 2 | a0001c0001t0001g0142a0001c0001t0001g0143 | 2 | NA18952.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.92-4873G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38434821 | ||||||
chr8:38434948
|
A | T | 90 | a0001c0001t0001g0079a0001c0001t0003g0001a0001c0001t0003g0019others(87): Show | 91 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.92-5000T>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38434948 | ||||||
chr8:38435090
|
G | A | 1 | a0001c0001t0001g0053 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.92-5142C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38435090 | ||||||
chr8:38435166
|
G | A | 2 | a0001c0001t0003g0064a0001c0001t0003g0204 | 2 | HG01243.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.92-5218C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38435166 | ||||||
chr8:38435295
|
C | A | 1 | a0001c0001t0001g0134 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.92-5347G>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38435295 | ||||||
chr8:38435304
|
C | T | 1 | a0001c0003t0001g0197 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.92-5356G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38435304 | ||||||
chr8:38435320
|
A | G | 3 | a0001c0001t0003g0119a0001c0001t0003g0131a0001c0001t0003g0132 | 3 | NA18970.hp1 NA19007.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.92-5372T>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38435320 | ||||||
chr8:38435376
|
G | A | 23 | a0001c0001t0001g0028a0001c0001t0001g0049a0001c0001t0001g0058others(20): Show | 23 | HG02015.hp2 HG02040.hp1 HG02040.hp2 others(20): Show |
intron_variant | MODIFIER | c.92-5428C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38435376 | ||||||
chr8:38435384
|
T | G | 2 | a0001c0001t0003g0064a0001c0001t0003g0204 | 2 | HG01243.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.92-5436A>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38435384 | ||||||
chr8:38435700
|
T | G | 2 | a0004c0005t0002g0279a0004c0005t0002g0312 | 2 | HG03834.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.92-5752A>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38435700 | ||||||
chr8:38435735
|
G | A | 1 | a0001c0001t0003g0016 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.92-5787C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38435735 | ||||||
chr8:38435903
|
A | G | 1 | a0001c0001t0028g0319 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.92-5955T>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38435903 | ||||||
chr8:38435945
|
G | A | 89 | a0001c0001t0001g0049a0001c0001t0001g0079a0001c0001t0001g0087others(86): Show | 90 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.92-5997C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38435945 | ||||||
chr8:38435959
|
T | C | 97 | a0001c0001t0001g0049a0001c0001t0001g0079a0001c0001t0001g0087others(94): Show | 98 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.92-6011A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38435959 | ||||||
chr8:38435998
|
G | A | 1 | a0001c0001t0004g0247 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.92-6050C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38435998 | ||||||
chr8:38436269
|
G | A | 1 | a0001c0001t0001g0120 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.92-6321C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38436269 | ||||||
chr8:38436280
|
G | A | 4 | a0001c0001t0003g0121a0001c0001t0003g0137a0001c0001t0003g0155others(1): Show | 4 | HG00621.hp2 HG02155.hp1 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.92-6332C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38436280 | ||||||
chr8:38436409
|
C | A | 9 | a0001c0001t0001g0028a0001c0001t0001g0058a0001c0001t0001g0065others(6): Show | 9 | HG02040.hp1 NA18947.hp2 NA18964.hp2 others(6): Show |
intron_variant | MODIFIER | c.92-6461G>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38436409 | ||||||
chr8:38436416
|
C | T | 1 | a0001c0001t0001g0025 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.92-6468G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38436416 | ||||||
chr8:38437616
|
A | G | 1 | a0001c0001t0001g0107 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.92-7668T>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38437616 | ||||||
chr8:38437735
|
G | T | 2 | a0001c0001t0002g0292a0001c0001t0002g0297 | 2 | HG01256.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.92-7787C>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38437735 | ||||||
chr8:38437824
|
A | G | 1 | a0001c0001t0001g0026 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.92-7876T>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38437824 | ||||||
chr8:38438024
|
G | A | 51 | a0001c0001t0001g0028a0001c0001t0001g0047a0001c0001t0001g0048others(48): Show | 51 | HG00423.hp1 HG00558.hp1 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.92-8076C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38438024 | ||||||
chr8:38438172
|
C | T | 2 | a0001c0001t0002g0253a0001c0001t0002g0254 | 2 | NA19012.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.92-8224G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38438172 | ||||||
chr8:38438201
|
T | TCA | 28 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0060others(25): Show | 28 | HG00423.hp1 HG00558.hp1 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.92-8255_92-8254dup others(2): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38438201 | ||||||
chr8:38438225
|
T | C | 94 | a0001c0001t0001g0079a0001c0001t0002g0242a0001c0001t0003g0001others(91): Show | 95 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.92-8277A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38438225 | ||||||
chr8:38438286
|
A | G | 1 | a0001c0001t0001g0046 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.92-8338T>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38438286 | ||||||
chr8:38438384
|
A | G | 2 | a0001c0001t0003g0016a0001c0001t0003g0064 | 2 | HG03540.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.92-8436T>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38438384 | ||||||
chr8:38438410
|
A | G | 101 | a0001c0001t0001g0015a0001c0001t0001g0079a0001c0001t0002g0242others(98): Show | 102 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.92-8462T>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38438410 | ||||||
chr8:38438542
|
C | CA | 16 | a0001c0001t0001g0010a0001c0001t0001g0037a0001c0001t0001g0046others(13): Show | 16 | HG01074.hp1 HG01192.hp1 HG02602.hp1 others(13): Show |
intron_variant | MODIFIER | c.92-8595dupT | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38438542 | ||||||
chr8:38438560
|
G | A | 1 | a0001c0001t0004g0307 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.92-8612C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38438560 | ||||||
chr8:38438690
|
A | G | 1 | a0001c0001t0002g0285 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.92-8742T>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38438690 | ||||||
chr8:38438813
|
C | A | 2 | a0001c0001t0001g0104a0001c0001t0001g0105 | 2 | NA18969.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.92-8865G>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38438813 | ||||||
chr8:38438816
|
C | T | 1 | a0001c0001t0004g0252 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.92-8868G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38438816 | ||||||
chr8:38438901
|
T | C | 1 | a0001c0001t0002g0291 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.92-8953A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38438901 | ||||||
chr8:38438907
|
A | G | 1 | a0001c0012t0020g0207 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.92-8959T>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38438907 | ||||||
chr8:38438984
|
G | A | 1 | a0001c0001t0027g0331 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.92-9036C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38438984 | ||||||
chr8:38439253
|
C | T | 1 | a0001c0001t0003g0187 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.92-9305G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38439253 | ||||||
chr8:38439299
|
G | T | 3 | a0001c0001t0001g0054a0001c0001t0001g0135a0001c0001t0002g0231 | 3 | HG01361.hp1 NA18973.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.92-9351C>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38439299 | ||||||
chr8:38439469
|
A | C | 1 | a0001c0001t0002g0248 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.92-9521T>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38439469 | ||||||
chr8:38439571
|
C | A | 1 | a0001c0001t0002g0241 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.92-9623G>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38439571 | ||||||
chr8:38439596
|
G | A | 1 | a0003c0004t0003g0122 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.92-9648C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38439596 | ||||||
chr8:38439863
|
T | TCTCGCAC others(3): Show |
1 | a0001c0001t0001g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.92-9916_92-9915ins others(10): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38439863 | ||||||
chr8:38439866
|
T | C | 1 | a0001c0001t0001g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.92-9918A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38439866 | ||||||
chr8:38439905
|
G | A | 4 | a0001c0001t0003g0119a0001c0001t0003g0131a0001c0001t0003g0132others(1): Show | 4 | NA18970.hp1 NA18986.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.92-9957C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38439905 | ||||||
chr8:38440242
|
G | A | 1 | a0001c0001t0003g0064 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.92-10294C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38440242 | ||||||
chr8:38440566
|
G | A | 1 | a0001c0001t0001g0089 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.92-10618C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38440566 | ||||||
chr8:38441029
|
C | G | 1 | a0001c0001t0001g0015 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.92-11081G>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38441029 | ||||||
chr8:38441048
|
C | A | 1 | a0001c0001t0019g0100 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.92-11100G>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38441048 | ||||||
chr8:38441129
|
C | T | 78 | a0001c0001t0001g0079a0001c0001t0002g0242a0001c0001t0003g0001others(75): Show | 79 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.92-11181G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38441129 | ||||||
chr8:38441304
|
T | C | 1 | a0001c0001t0004g0252 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.92-11356A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38441304 | ||||||
chr8:38441901
|
G | A | 167 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0015others(164): Show | 168 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.92-11953C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38441901 | ||||||
chr8:38442106
|
T | C | 78 | a0001c0001t0001g0079a0001c0001t0002g0242a0001c0001t0003g0001others(75): Show | 79 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.92-12158A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38442106 | ||||||
chr8:38442192
|
G | A | 1 | a0001c0001t0003g0064 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.92-12244C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38442192 | ||||||
chr8:38442197
|
G | C | 168 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0018others(165): Show | 169 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.92-12249C>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38442197 | ||||||
chr8:38442362
|
G | GGTGTGGG others(7): Show |
1 | a0001c0001t0001g0015 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.92-12415_92-12414i others(16): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38442362 | ||||||
chr8:38442362
|
G | GGTGTGT | 4 | a0001c0001t0002g0304a0001c0001t0003g0168a0001c0001t0003g0187others(1): Show | 4 | HG00642.hp2 HG02071.hp2 HG02083.hp2 others(1): Show |
intron_variant | MODIFIER | c.92-12420_92-12415d others(8): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38442362 | ||||||
chr8:38442362
|
G | GGTGTGTG others(1): Show |
13 | a0001c0001t0001g0058a0001c0001t0001g0092a0001c0001t0001g0098others(10): Show | 13 | HG00642.hp1 HG02809.hp1 NA18953.hp1 others(10): Show |
intron_variant | MODIFIER | c.92-12422_92-12415d others(10): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38442362 | ||||||
chr8:38442362
|
G | GGTGTGTG others(3): Show |
64 | a0001c0001t0001g0028a0001c0001t0001g0049a0001c0001t0001g0056others(61): Show | 64 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(61): Show |
intron_variant | MODIFIER | c.92-12424_92-12415d others(12): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38442362 | ||||||
chr8:38442362
|
G | GGTGTGTG others(5): Show |
43 | a0001c0001t0001g0060a0001c0001t0001g0065a0001c0001t0001g0078others(40): Show | 44 | HG00738.hp1 HG00738.hp2 HG00741.hp1 others(41): Show |
intron_variant | MODIFIER | c.92-12426_92-12415d others(14): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38442362 | ||||||
chr8:38442362
|
G | GGTGTGTG others(7): Show |
16 | a0001c0001t0001g0066a0001c0001t0001g0081a0001c0001t0001g0094others(13): Show | 16 | HG00423.hp1 HG00558.hp1 HG00673.hp2 others(13): Show |
intron_variant | MODIFIER | c.92-12428_92-12415d others(16): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38442362 | ||||||
chr8:38442362
|
G | GGTGTGTG others(9): Show |
7 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0063others(4): Show | 7 | HG01934.hp2 HG01993.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.92-12430_92-12415d others(18): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38442362 | ||||||
chr8:38442362
|
G | GGTGTGTG others(13): Show |
3 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0076 | 3 | HG01257.hp2 HG01258.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.92-12434_92-12415d others(22): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38442362 | ||||||
chr8:38442362
|
G | GGTGTGTG others(15): Show |
1 | a0001c0009t0013g0005 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.92-12436_92-12415d others(24): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38442362 | ||||||
chr8:38442362
|
GGT | G | 149 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0013others(146): Show | 149 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.92-12416_92-12415d others(4): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38442362 | ||||||
chr8:38442383
|
G | GTGTGTGT others(6): Show |
1 | a0001c0001t0003g0153 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.92-12448_92-12436d others(15): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38442383 | ||||||
chr8:38442727
|
G | A | 1 | a0001c0001t0001g0028 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.92-12779C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38442727 | ||||||
chr8:38442792
|
C | T | 1 | a0001c0001t0005g0330 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.92-12844G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38442792 | ||||||
chr8:38442920
|
A | G | 1 | a0001c0001t0019g0100 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.92-12972T>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38442920 | ||||||
chr8:38442929
|
C | T | 1 | a0001c0001t0003g0024 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.92-12981G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38442929 | ||||||
chr8:38443133
|
G | A | 1 | a0001c0001t0003g0170 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.92-13185C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38443133 | ||||||
chr8:38443173
|
C | A | 2 | a0001c0001t0003g0153a0001c0001t0003g0154 | 2 | NA18944.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.92-13225G>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38443173 | ||||||
chr8:38443212
|
T | A | 170 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0015others(167): Show | 171 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.92-13264A>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38443212 | ||||||
chr8:38443496
|
C | CA | 7 | a0001c0001t0001g0007a0001c0001t0001g0017a0001c0001t0001g0102others(4): Show | 7 | HG02622.hp1 HG02886.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.92-13549dupT | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38443496 | ||||||
chr8:38443496
|
CA | C | 167 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0015others(164): Show | 168 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.92-13549delT | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38443496 | ||||||
chr8:38443564
|
T | C | 73 | a0001c0001t0001g0028a0001c0001t0001g0047a0001c0001t0001g0048others(70): Show | 73 | HG00423.hp1 HG00558.hp1 HG00642.hp1 others(70): Show |
intron_variant | MODIFIER | c.92-13616A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38443564 | ||||||
chr8:38443594
|
G | C | 1 | a0001c0001t0003g0016 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.92-13646C>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38443594 | ||||||
chr8:38443617
|
G | A | 1 | a0001c0001t0002g0280 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.92-13669C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38443617 | ||||||
chr8:38443851
|
C | T | 1 | a0001c0001t0003g0180 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.91+13505G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38443851 | ||||||
chr8:38443921
|
C | T | 1 | a0001c0001t0002g0301 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.91+13435G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38443921 | ||||||
chr8:38443970
|
G | A | 1 | a0001c0001t0014g0006 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.91+13386C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38443970 | ||||||
chr8:38444051
|
C | CA | 46 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0018others(43): Show | 46 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.91+13304dupT | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444051 | ||||||
chr8:38444051
|
CA | C | 102 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0020others(99): Show | 102 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.91+13304delT | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444051 | ||||||
chr8:38444051
|
CAA | C | 6 | a0001c0001t0001g0075a0001c0001t0001g0089a0001c0001t0002g0210others(3): Show | 6 | HG01069.hp2 HG03492.hp1 HG03834.hp1 others(3): Show |
intron_variant | MODIFIER | c.91+13303_91+13304d others(4): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444051 | ||||||
chr8:38444051
|
CAAAAAAA | C | 56 | a0001c0001t0001g0010a0001c0001t0001g0047a0001c0001t0001g0048others(53): Show | 56 | HG00642.hp1 HG00738.hp2 HG00741.hp1 others(53): Show |
intron_variant | MODIFIER | c.91+13298_91+13304d others(9): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444051 | ||||||
chr8:38444051
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0003g0169 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.91+13293_91+13304d others(14): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444051 | ||||||
chr8:38444231
|
C | G | 1 | a0001c0001t0003g0153 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+13125G>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444231 | ||||||
chr8:38444242
|
G | A | 1 | a0001c0001t0003g0153 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+13114C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444242 | ||||||
chr8:38444243
|
A | C | 1 | a0001c0001t0003g0153 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+13113T>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444243 | ||||||
chr8:38444244
|
G | C | 1 | a0001c0001t0003g0153 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+13112C>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444244 | ||||||
chr8:38444252
|
A | T | 1 | a0001c0001t0003g0153 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+13104T>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444252 | ||||||
chr8:38444261
|
C | T | 1 | a0001c0001t0003g0153 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+13095G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444261 | ||||||
chr8:38444263
|
G | T | 1 | a0001c0001t0003g0153 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+13093C>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444263 | ||||||
chr8:38444265
|
T | A | 1 | a0001c0001t0003g0153 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+13091A>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444265 | ||||||
chr8:38444269
|
T | G | 1 | a0001c0001t0003g0153 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+13087A>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444269 | ||||||
chr8:38444271
|
C | A | 1 | a0001c0001t0003g0153 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+13085G>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444271 | ||||||
chr8:38444281
|
C | T | 1 | a0001c0001t0003g0153 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+13075G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444281 | ||||||
chr8:38444283
|
A | T | 1 | a0001c0001t0003g0153 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+13073T>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444283 | ||||||
chr8:38444285
|
C | G | 1 | a0001c0001t0003g0153 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+13071G>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444285 | ||||||
chr8:38444286
|
C | G | 1 | a0001c0001t0003g0153 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+13070G>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444286 | ||||||
chr8:38444293
|
C | A | 1 | a0001c0001t0003g0153 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+13063G>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444293 | ||||||
chr8:38444297
|
C | A | 1 | a0001c0001t0003g0153 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+13059G>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444297 | ||||||
chr8:38444299
|
T | A | 1 | a0001c0001t0003g0153 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+13057A>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444299 | ||||||
chr8:38444314
|
C | A | 1 | a0001c0001t0003g0153 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+13042G>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444314 | ||||||
chr8:38444331
|
C | T | 1 | a0001c0001t0003g0153 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+13025G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444331 | ||||||
chr8:38444341
|
G | T | 1 | a0001c0001t0003g0153 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+13015C>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444341 | ||||||
chr8:38444343
|
G | T | 1 | a0001c0001t0003g0153 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+13013C>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444343 | ||||||
chr8:38444350
|
G | C | 1 | a0001c0001t0003g0153 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+13006C>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444350 | ||||||
chr8:38444352
|
A | G | 1 | a0001c0001t0003g0153 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+13004T>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444352 | ||||||
chr8:38444355
|
C | G | 1 | a0001c0001t0003g0153 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+13001G>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444355 | ||||||
chr8:38444356
|
T | C | 1 | a0001c0001t0003g0153 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+13000A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444356 | ||||||
chr8:38444358
|
A | T | 1 | a0001c0001t0003g0153 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+12998T>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444358 | ||||||
chr8:38444369
|
A | C | 1 | a0001c0001t0003g0153 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+12987T>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444369 | ||||||
chr8:38444370
|
T | A | 1 | a0001c0001t0003g0153 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+12986A>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444370 | ||||||
chr8:38444372
|
A | T | 1 | a0001c0001t0003g0153 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+12984T>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444372 | ||||||
chr8:38444379
|
T | C | 1 | a0001c0001t0005g0332 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.91+12977A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444379 | ||||||
chr8:38444385
|
G | T | 1 | a0001c0001t0003g0153 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+12971C>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444385 | ||||||
chr8:38444387
|
G | GT | 24 | a0001c0001t0001g0015a0001c0001t0001g0040a0001c0001t0001g0071others(21): Show | 24 | HG00438.hp1 HG00738.hp1 HG01981.hp1 others(21): Show |
intron_variant | MODIFIER | c.91+12968dupA | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444387 | ||||||
chr8:38444387
|
G | T | 1 | a0001c0001t0003g0153 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+12969C>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444387 | ||||||
chr8:38444387
|
GT | G | 7 | a0001c0001t0001g0099a0001c0001t0001g0182a0001c0001t0002g0293others(4): Show | 7 | HG01070.hp2 HG01071.hp2 HG04228.hp1 others(4): Show |
intron_variant | MODIFIER | c.91+12968delA | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444387 | ||||||
chr8:38444391
|
T | TG | 55 | a0001c0001t0001g0028a0001c0001t0001g0047a0001c0001t0001g0048others(52): Show | 55 | HG00642.hp1 HG00738.hp2 HG00741.hp1 others(52): Show |
intron_variant | MODIFIER | c.91+12964_91+12965i others(3): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444391 | ||||||
chr8:38444403
|
C | T | 1 | a0001c0001t0003g0153 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+12953G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444403 | ||||||
chr8:38444415
|
G | T | 1 | a0001c0001t0003g0153 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+12941C>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444415 | ||||||
chr8:38444439
|
A | G | 1 | a0001c0001t0003g0153 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+12917T>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444439 | ||||||
chr8:38444442
|
A | G | 1 | a0001c0001t0003g0153 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+12914T>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444442 | ||||||
chr8:38444449
|
C | A | 1 | a0001c0001t0003g0153 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+12907G>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444449 | ||||||
chr8:38444453
|
A | G | 1 | a0001c0001t0003g0153 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+12903T>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444453 | ||||||
chr8:38444454
|
T | A | 1 | a0001c0001t0003g0153 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+12902A>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444454 | ||||||
chr8:38444485
|
C | T | 1 | a0001c0001t0003g0153 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+12871G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444485 | ||||||
chr8:38444489
|
A | C | 1 | a0001c0001t0003g0153 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+12867T>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444489 | ||||||
chr8:38444491
|
T | A | 1 | a0001c0001t0003g0153 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+12865A>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444491 | ||||||
chr8:38444493
|
A | T | 1 | a0001c0001t0003g0153 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+12863T>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444493 | ||||||
chr8:38444496
|
C | T | 1 | a0001c0001t0003g0153 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+12860G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444496 | ||||||
chr8:38444510
|
C | T | 1 | a0001c0001t0003g0153 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+12846G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444510 | ||||||
chr8:38444512
|
C | A | 2 | a0001c0001t0012g0004a0001c0012t0020g0207 | 2 | HG02647.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.91+12844G>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444512 | ||||||
chr8:38444526
|
G | T | 1 | a0001c0001t0003g0153 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+12830C>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444526 | ||||||
chr8:38444529
|
T | C | 1 | a0001c0001t0003g0153 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+12827A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444529 | ||||||
chr8:38444546
|
G | A | 1 | a0001c0001t0003g0153 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+12810C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444546 | ||||||
chr8:38444548
|
G | C | 1 | a0001c0001t0003g0153 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+12808C>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444548 | ||||||
chr8:38444556
|
A | AT | 6 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0002g0227others(3): Show | 6 | HG02615.hp1 HG03225.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.91+12799dupA | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444556 | ||||||
chr8:38444556
|
A | ATTTTTTT | 123 | a0001c0001t0001g0028a0001c0001t0001g0047a0001c0001t0001g0048others(120): Show | 124 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.91+12793_91+12799d others(9): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444556 | ||||||
chr8:38444556
|
A | ATTTTTTT others(1): Show |
20 | a0001c0001t0001g0059a0001c0001t0001g0065a0001c0001t0001g0080others(17): Show | 20 | HG01175.hp2 HG01261.hp1 HG01261.hp2 others(17): Show |
intron_variant | MODIFIER | c.91+12792_91+12799d others(10): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444556 | ||||||
chr8:38444585
|
T | A | 1 | a0001c0001t0003g0016 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.91+12771A>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444585 | ||||||
chr8:38444588
|
T | A | 1 | a0001c0001t0003g0153 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+12768A>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444588 | ||||||
chr8:38444589
|
A | T | 1 | a0001c0001t0003g0153 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.91+12767T>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444589 | ||||||
chr8:38444591
|
C | T | 3 | a0001c0001t0001g0015a0001c0001t0019g0100a0001c0009t0013g0005 | 3 | HG02572.hp1 HG02630.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.91+12765G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444591 | ||||||
chr8:38444603
|
G | A | 1 | a0001c0001t0003g0024 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.91+12753C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444603 | ||||||
chr8:38444710
|
C | A | 1 | a0001c0001t0001g0028 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.91+12646G>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38444710 | ||||||
chr8:38445125
|
G | A | 1 | a0001c0001t0001g0063 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.91+12231C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38445125 | ||||||
chr8:38445126
|
C | A | 1 | a0001c0001t0001g0063 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.91+12230G>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38445126 | ||||||
chr8:38445199
|
C | G | 2 | a0001c0001t0001g0108a0001c0001t0001g0144 | 2 | HG00673.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.91+12157G>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38445199 | ||||||
chr8:38445234
|
C | A | 1 | a0001c0001t0003g0016 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.91+12122G>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38445234 | ||||||
chr8:38445447
|
C | T | 61 | a0001c0001t0001g0015a0001c0001t0001g0028a0001c0001t0001g0047others(58): Show | 61 | HG00642.hp1 HG00738.hp2 HG00741.hp1 others(58): Show |
intron_variant | MODIFIER | c.91+11909G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38445447 | ||||||
chr8:38445510
|
G | T | 1 | a0001c0001t0001g0028 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.91+11846C>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38445510 | ||||||
chr8:38445608
|
G | A | 1 | a0001c0001t0003g0016 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.91+11748C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38445608 | ||||||
chr8:38445702
|
T | C | 8 | a0001c0001t0005g0320a0001c0001t0005g0321a0001c0001t0005g0324others(5): Show | 8 | HG02055.hp1 HG02630.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.91+11654A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38445702 | ||||||
chr8:38445707
|
T | A | 4 | a0001c0001t0003g0016a0001c0001t0003g0064a0001c0001t0012g0004others(1): Show | 4 | HG02647.hp2 HG02818.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.91+11649A>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38445707 | ||||||
chr8:38445710
|
T | A | 1 | a0001c0012t0020g0207 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.91+11646A>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38445710 | ||||||
chr8:38445981
|
C | T | 3 | a0001c0001t0001g0015a0001c0001t0019g0100a0001c0009t0013g0005 | 3 | HG02572.hp1 HG02630.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.91+11375G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38445981 | ||||||
chr8:38446205
|
C | CT | 20 | a0001c0001t0001g0050a0001c0001t0001g0056a0001c0001t0001g0067others(17): Show | 20 | HG00438.hp1 HG01123.hp1 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.91+11150dupA | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38446205 | ||||||
chr8:38446205
|
CT | C | 10 | a0001c0001t0001g0008a0001c0001t0002g0224a0001c0001t0002g0270others(7): Show | 10 | HG01070.hp1 HG01070.hp2 HG02165.hp2 others(7): Show |
intron_variant | MODIFIER | c.91+11150delA | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38446205 | ||||||
chr8:38446228
|
TA | T | 4 | a0001c0001t0001g0015a0001c0001t0015g0084a0001c0001t0019g0100others(1): Show | 4 | HG02572.hp1 HG02630.hp2 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.91+11127delT | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38446228 | ||||||
chr8:38446229
|
A | T | 56 | a0001c0001t0001g0028a0001c0001t0001g0047a0001c0001t0001g0048others(53): Show | 56 | HG00642.hp1 HG00738.hp2 HG00741.hp1 others(53): Show |
intron_variant | MODIFIER | c.91+11127T>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38446229 | ||||||
chr8:38446336
|
G | A | 1 | a0001c0001t0003g0016 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.91+11020C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38446336 | ||||||
chr8:38446371
|
C | T | 4 | a0001c0001t0001g0015a0001c0001t0002g0301a0001c0001t0019g0100others(1): Show | 4 | HG02572.hp1 HG02630.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.91+10985G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38446371 | ||||||
chr8:38446372
|
G | A | 1 | a0001c0001t0017g0095 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.91+10984C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38446372 | ||||||
chr8:38446400
|
A | G | 334 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(331): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.91+10956T>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38446400 | ||||||
chr8:38446461
|
T | A | 55 | a0001c0001t0001g0028a0001c0001t0001g0047a0001c0001t0001g0048others(52): Show | 55 | HG00642.hp1 HG00738.hp2 HG00741.hp1 others(52): Show |
intron_variant | MODIFIER | c.91+10895A>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38446461 | ||||||
chr8:38446471
|
A | G | 3 | a0001c0001t0001g0015a0001c0001t0019g0100a0001c0009t0013g0005 | 3 | HG02572.hp1 HG02630.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.91+10885T>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38446471 | ||||||
chr8:38446606
|
G | T | 1 | a0001c0001t0003g0174 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.91+10750C>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38446606 | ||||||
chr8:38446716
|
A | G | 1 | a0001c0001t0004g0246 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.91+10640T>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38446716 | ||||||
chr8:38446816
|
A | G | 1 | a0001c0001t0004g0299 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.91+10540T>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38446816 | ||||||
chr8:38446907
|
G | A | 1 | a0001c0001t0002g0241 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.91+10449C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38446907 | ||||||
chr8:38446926
|
G | A | 3 | a0001c0001t0001g0015a0001c0001t0019g0100a0001c0009t0013g0005 | 3 | HG02572.hp1 HG02630.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.91+10430C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38446926 | ||||||
chr8:38447094
|
A | C | 1 | a0001c0001t0002g0234 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.91+10262T>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38447094 | ||||||
chr8:38447096
|
CA | C | 3 | a0001c0001t0001g0054a0001c0001t0021g0290a0001c0008t0002g0275 | 3 | HG01361.hp1 NA18942.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.91+10259delT | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38447096 | ||||||
chr8:38447097
|
AAAC | A | 3 | a0001c0001t0001g0088a0001c0001t0001g0111a0001c0001t0002g0294 | 3 | HG01070.hp2 HG01099.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.91+10256_91+10258d others(5): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38447097 | ||||||
chr8:38447097
|
AAACACAC others(4): Show |
A | 1 | a0001c0001t0003g0124 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.91+10248_91+10258d others(13): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38447097 | ||||||
chr8:38447098
|
A | AAC | 7 | a0001c0001t0001g0053a0001c0001t0001g0133a0001c0001t0001g0143others(4): Show | 7 | HG01975.hp2 HG02135.hp2 HG03942.hp2 others(4): Show |
intron_variant | MODIFIER | c.91+10256_91+10257d others(4): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38447098 | ||||||
chr8:38447098
|
A | AACAC | 7 | a0001c0001t0001g0036a0001c0001t0001g0074a0001c0001t0001g0101others(4): Show | 7 | HG00323.hp1 HG00438.hp2 HG00558.hp2 others(4): Show |
intron_variant | MODIFIER | c.91+10254_91+10257d others(6): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38447098 | ||||||
chr8:38447098
|
A | AACACACA others(3): Show |
2 | a0001c0001t0001g0045a0001c0001t0002g0240 | 2 | HG02293.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.91+10248_91+10257d others(12): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38447098 | ||||||
chr8:38447098
|
AAC | A | 46 | a0001c0001t0001g0022a0001c0001t0001g0025a0001c0001t0001g0037others(43): Show | 46 | HG00323.hp2 HG00423.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.91+10256_91+10257d others(4): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38447098 | ||||||
chr8:38447098
|
AACAC | A | 58 | a0001c0001t0001g0013a0001c0001t0001g0026a0001c0001t0001g0027others(55): Show | 58 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.91+10254_91+10257d others(6): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38447098 | ||||||
chr8:38447098
|
AACACAC | A | 43 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0017others(40): Show | 43 | HG00280.hp2 HG00438.hp1 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.91+10252_91+10257d others(8): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38447098 | ||||||
chr8:38447098
|
AACACACA others(1): Show |
A | 36 | a0001c0001t0001g0018a0001c0001t0001g0047a0001c0001t0001g0117others(33): Show | 37 | HG00408.hp2 HG00642.hp2 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.91+10250_91+10257d others(10): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38447098 | ||||||
chr8:38447098
|
AACACACA others(3): Show |
A | 11 | a0001c0001t0001g0048a0001c0001t0001g0059a0001c0001t0001g0079others(8): Show | 11 | HG00140.hp1 HG00621.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.91+10248_91+10257d others(12): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38447098 | ||||||
chr8:38447098
|
AACACACA others(5): Show |
A | 51 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0049others(48): Show | 51 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.91+10246_91+10257d others(14): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38447098 | ||||||
chr8:38447098
|
AACACACA others(7): Show |
A | 11 | a0001c0001t0001g0021a0001c0001t0001g0058a0001c0001t0001g0071others(8): Show | 11 | HG00597.hp2 HG01261.hp2 HG02040.hp1 others(8): Show |
intron_variant | MODIFIER | c.91+10244_91+10257d others(16): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38447098 | ||||||
chr8:38447098
|
AACACACA others(9): Show |
A | 2 | a0001c0001t0001g0066a0001c0001t0002g0230 | 2 | NA19087.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.91+10242_91+10257d others(18): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38447098 | ||||||
chr8:38447098
|
AACACACA others(11): Show |
A | 2 | a0001c0001t0002g0300a0001c0001t0003g0016 | 2 | HG00099.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.91+10240_91+10257d others(20): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38447098 | ||||||
chr8:38447098
|
AACACACA others(13): Show |
A | 1 | a0001c0012t0020g0207 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.91+10238_91+10257d others(22): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38447098 | ||||||
chr8:38447098
|
AACACACA others(17): Show |
A | 1 | a0001c0001t0015g0084 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.91+10234_91+10257d others(26): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38447098 | ||||||
chr8:38447098
|
AACACACA others(21): Show |
A | 1 | a0001c0001t0002g0263 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.91+10230_91+10257d others(30): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38447098 | ||||||
chr8:38447116
|
C | T | 9 | a0001c0001t0001g0123a0001c0001t0001g0184a0001c0001t0001g0185others(6): Show | 9 | HG00642.hp1 HG00738.hp2 HG00741.hp1 others(6): Show |
intron_variant | MODIFIER | c.91+10240G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38447116 | ||||||
chr8:38447118
|
C | T | 1 | a0001c0003t0001g0196 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.91+10238G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38447118 | ||||||
chr8:38447141
|
ACACACAC others(4): Show |
A | 2 | a0001c0001t0001g0028a0008c0013t0003g0181 | 2 | NA19063.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.91+10204_91+10214d others(13): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38447141 | ||||||
chr8:38447151
|
A | C | 6 | a0001c0001t0002g0253a0001c0001t0002g0254a0001c0001t0002g0289others(3): Show | 6 | HG03710.hp1 NA18942.hp2 NA18986.hp2 others(3): Show |
intron_variant | MODIFIER | c.91+10205T>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38447151 | ||||||
chr8:38447153
|
C | A | 2 | a0001c0001t0001g0054a0001c0001t0005g0322 | 2 | HG01361.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.91+10203G>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38447153 | ||||||
chr8:38447376
|
C | A | 3 | a0001c0003t0001g0196a0001c0003t0001g0197a0001c0003t0001g0198 | 3 | HG00642.hp1 HG01175.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.91+9980G>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38447376 | ||||||
chr8:38447640
|
A | G | 1 | a0001c0001t0001g0065 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.91+9716T>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38447640 | ||||||
chr8:38447677
|
T | C | 62 | a0001c0001t0001g0015a0001c0001t0001g0028a0001c0001t0001g0047others(59): Show | 62 | HG00642.hp1 HG00738.hp2 HG00741.hp1 others(59): Show |
intron_variant | MODIFIER | c.91+9679A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38447677 | ||||||
chr8:38447769
|
C | T | 1 | a0001c0001t0002g0219 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.91+9587G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38447769 | ||||||
chr8:38447776
|
C | T | 62 | a0001c0001t0001g0015a0001c0001t0001g0028a0001c0001t0001g0047others(59): Show | 62 | HG00642.hp1 HG00738.hp2 HG00741.hp1 others(59): Show |
intron_variant | MODIFIER | c.91+9580G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38447776 | ||||||
chr8:38447966
|
C | G | 1 | a0001c0001t0001g0199 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.91+9390G>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38447966 | ||||||
chr8:38447968
|
C | A | 3 | a0001c0001t0003g0001a0001c0001t0003g0172a0001c0001t0004g0278 | 4 | HG00140.hp1 HG01069.hp1 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.91+9388G>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38447968 | ||||||
chr8:38448006
|
A | G | 1 | a0001c0001t0003g0016 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.91+9350T>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38448006 | ||||||
chr8:38448278
|
AT | A | 58 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0049others(55): Show | 58 | HG00140.hp2 HG00642.hp1 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.91+9077delA | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38448278 | ||||||
chr8:38448331
|
G | A | 1 | a0001c0001t0001g0081 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.91+9025C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38448331 | ||||||
chr8:38448348
|
C | T | 1 | a0001c0001t0003g0064 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.91+9008G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38448348 | ||||||
chr8:38448432
|
A | G | 1 | a0001c0001t0003g0064 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.91+8924T>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38448432 | ||||||
chr8:38448478
|
C | G | 1 | a0001c0001t0003g0130 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.91+8878G>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38448478 | ||||||
chr8:38448659
|
G | A | 1 | a0001c0001t0002g0301 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.91+8697C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38448659 | ||||||
chr8:38448785
|
T | C | 1 | a0001c0001t0006g0035 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.91+8571A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38448785 | ||||||
chr8:38448838
|
C | A | 1 | a0001c0001t0003g0016 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.91+8518G>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38448838 | ||||||
chr8:38448904
|
G | A | 1 | a0001c0001t0003g0064 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.91+8452C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38448904 | ||||||
chr8:38448909
|
C | T | 1 | a0001c0001t0002g0280 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.91+8447G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38448909 | ||||||
chr8:38448918
|
G | A | 1 | a0001c0001t0001g0076 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.91+8438C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38448918 | ||||||
chr8:38449089
|
G | A | 1 | a0001c0001t0003g0191 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.91+8267C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38449089 | ||||||
chr8:38449136
|
G | GA | 4 | a0001c0001t0001g0012a0001c0001t0001g0097a0001c0001t0002g0261others(1): Show | 4 | HG02809.hp2 HG02965.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.91+8219dupT | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38449136 | ||||||
chr8:38449156
|
T | A | 1 | a0001c0001t0002g0301 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.91+8200A>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38449156 | ||||||
chr8:38449320
|
T | C | 1 | a0001c0001t0001g0186 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.91+8036A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38449320 | ||||||
chr8:38449335
|
T | C | 1 | a0001c0001t0001g0028 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.91+8021A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38449335 | ||||||
chr8:38449344
|
C | T | 3 | a0001c0001t0001g0015a0001c0001t0019g0100a0001c0009t0013g0005 | 3 | HG02572.hp1 HG02630.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.91+8012G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38449344 | ||||||
chr8:38449409
|
C | G | 63 | a0001c0001t0001g0015a0001c0001t0001g0028a0001c0001t0001g0047others(60): Show | 63 | HG00642.hp1 HG00738.hp2 HG00741.hp1 others(60): Show |
intron_variant | MODIFIER | c.91+7947G>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38449409 | ||||||
chr8:38449553
|
C | T | 1 | a0001c0001t0004g0251 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.91+7803G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38449553 | ||||||
chr8:38449625
|
G | A | 2 | a0001c0001t0004g0247a0001c0001t0027g0331 | 2 | HG02723.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.91+7731C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38449625 | ||||||
chr8:38449656
|
C | A | 1 | a0001c0001t0002g0250 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.91+7700G>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38449656 | ||||||
chr8:38449665
|
A | ACCATTCT | 64 | a0001c0001t0001g0015a0001c0001t0001g0047a0001c0001t0001g0048others(61): Show | 64 | HG00642.hp1 HG00738.hp2 HG00741.hp1 others(61): Show |
intron_variant | MODIFIER | c.91+7690_91+7691ins others(7): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38449665 | ||||||
chr8:38449665
|
A | T | 1 | a0001c0001t0001g0028 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.91+7691T>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38449665 | ||||||
chr8:38449685
|
C | T | 9 | a0001c0001t0003g0019a0001c0001t0003g0023a0001c0001t0003g0032others(6): Show | 9 | NA18982.hp1 NA19001.hp1 NA19007.hp2 others(6): Show |
intron_variant | MODIFIER | c.91+7671G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38449685 | ||||||
chr8:38449725
|
G | C | 1 | a0001c0001t0003g0202 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.91+7631C>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38449725 | ||||||
chr8:38449728
|
G | A | 1 | a0001c0001t0001g0070 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.91+7628C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38449728 | ||||||
chr8:38450097
|
C | T | 3 | a0001c0001t0001g0097a0001c0001t0002g0261a0001c0001t0002g0262 | 3 | HG02965.hp1 HG03041.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.91+7259G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38450097 | ||||||
chr8:38450213
|
G | A | 2 | a0001c0001t0012g0004a0001c0012t0020g0207 | 2 | HG02647.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.91+7143C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38450213 | ||||||
chr8:38450218
|
C | A | 1 | a0001c0001t0003g0016 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.91+7138G>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38450218 | ||||||
chr8:38450352
|
G | T | 1 | a0001c0001t0003g0064 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.91+7004C>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38450352 | ||||||
chr8:38450353
|
A | T | 1 | a0001c0001t0003g0064 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.91+7003T>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38450353 | ||||||
chr8:38450427
|
T | G | 2 | a0001c0001t0004g0247a0001c0001t0027g0331 | 2 | HG02723.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.91+6929A>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38450427 | ||||||
chr8:38450449
|
T | G | 1 | a0001c0001t0001g0022 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.91+6907A>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38450449 | ||||||
chr8:38450467
|
G | A | 2 | a0001c0001t0003g0177a0006c0007t0003g0178 | 2 | NA18965.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.91+6889C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38450467 | ||||||
chr8:38450517
|
T | C | 1 | a0001c0001t0002g0301 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.91+6839A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38450517 | ||||||
chr8:38450649
|
T | C | 11 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0044others(8): Show | 11 | HG01243.hp2 HG01256.hp1 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.91+6707A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38450649 | ||||||
chr8:38450869
|
T | C | 12 | a0001c0001t0001g0107a0001c0001t0001g0118a0001c0001t0001g0183others(9): Show | 12 | HG00597.hp1 HG00609.hp2 NA18944.hp2 others(9): Show |
intron_variant | MODIFIER | c.91+6487A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38450869 | ||||||
chr8:38451064
|
C | A | 1 | a0001c0001t0012g0004 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.91+6292G>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38451064 | ||||||
chr8:38451339
|
T | C | 1 | a0001c0001t0003g0016 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.91+6017A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38451339 | ||||||
chr8:38451510
|
G | A | 1 | a0001c0001t0003g0112 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.91+5846C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38451510 | ||||||
chr8:38451717
|
A | C | 4 | a0001c0001t0001g0012a0001c0001t0001g0097a0001c0001t0002g0261others(1): Show | 4 | HG02809.hp2 HG02965.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.91+5639T>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38451717 | ||||||
chr8:38451916
|
G | T | 2 | a0001c0001t0003g0016a0001c0001t0003g0064 | 2 | HG03540.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.91+5440C>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38451916 | ||||||
chr8:38451919
|
T | C | 1 | a0001c0001t0001g0079 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.91+5437A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38451919 | ||||||
chr8:38451943
|
C | G | 1 | a0001c0001t0001g0089 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.91+5413G>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38451943 | ||||||
chr8:38452148
|
G | A | 4 | a0001c0001t0003g0121a0001c0001t0003g0137a0001c0001t0003g0155others(1): Show | 4 | HG00621.hp2 HG02155.hp1 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.91+5208C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38452148 | ||||||
chr8:38452192
|
GACACACA others(13): Show |
G | 1 | a0001c0009t0013g0005 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.91+5144_91+5163del others(20): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38452192 | ||||||
chr8:38452200
|
G | GAC | 4 | a0001c0001t0001g0054a0001c0001t0001g0083a0001c0001t0021g0290others(1): Show | 4 | HG01361.hp1 HG02055.hp2 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.91+5154_91+5155dup others(2): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38452200 | ||||||
chr8:38452200
|
GAC | G | 28 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0018others(25): Show | 28 | HG00597.hp2 HG01070.hp2 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.91+5154_91+5155del others(2): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38452200 | ||||||
chr8:38452200
|
GACAC | G | 77 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0017others(74): Show | 77 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.91+5152_91+5155del others(4): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38452200 | ||||||
chr8:38452200
|
GACACAC | G | 46 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0047others(43): Show | 46 | HG00423.hp2 HG00438.hp2 HG01243.hp2 others(43): Show |
intron_variant | MODIFIER | c.91+5150_91+5155del others(6): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38452200 | ||||||
chr8:38452200
|
GACACACA others(1): Show |
G | 51 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0046others(48): Show | 51 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.91+5148_91+5155del others(8): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38452200 | ||||||
chr8:38452200
|
GACACACA others(3): Show |
G | 89 | a0001c0001t0001g0060a0001c0001t0001g0078a0001c0001t0001g0079others(86): Show | 90 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.91+5146_91+5155del others(10): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38452200 | ||||||
chr8:38452200
|
GACACACA others(5): Show |
G | 6 | a0001c0001t0003g0121a0001c0001t0003g0137a0001c0001t0003g0155others(3): Show | 6 | HG00621.hp2 HG02155.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.91+5144_91+5155del others(12): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38452200 | ||||||
chr8:38452200
|
GACACACA others(7): Show |
G | 6 | a0001c0001t0001g0027a0001c0001t0002g0211a0001c0001t0002g0263others(3): Show | 6 | NA18944.hp1 NA18962.hp1 NA19012.hp2 others(3): Show |
intron_variant | MODIFIER | c.91+5142_91+5155del others(14): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38452200 | ||||||
chr8:38452200
|
GACACACA others(9): Show |
G | 5 | a0001c0001t0003g0114a0001c0001t0003g0115a0001c0001t0003g0151others(2): Show | 5 | HG00673.hp1 NA18612.hp1 NA18953.hp1 others(2): Show |
intron_variant | MODIFIER | c.91+5140_91+5155del others(16): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38452200 | ||||||
chr8:38452200
|
GACACACA others(13): Show |
G | 3 | a0001c0001t0003g0016a0001c0001t0004g0251a0001c0001t0004g0252 | 3 | HG01070.hp1 HG01167.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.91+5136_91+5155del others(20): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38452200 | ||||||
chr8:38452210
|
C | G | 3 | a0001c0001t0001g0007a0001c0001t0001g0028a0001c0001t0005g0334 | 3 | HG02622.hp1 NA18522.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.91+5146G>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38452210 | ||||||
chr8:38452212
|
C | G | 2 | a0001c0001t0002g0237a0001c0001t0004g0238 | 2 | NA18957.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.91+5144G>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38452212 | ||||||
chr8:38452214
|
C | G | 1 | a0001c0001t0005g0333 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.91+5142G>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38452214 | ||||||
chr8:38452216
|
C | G | 1 | a0001c0001t0001g0085 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.91+5140G>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38452216 | ||||||
chr8:38452218
|
C | G | 1 | a0001c0001t0012g0004 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.91+5138G>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38452218 | ||||||
chr8:38452220
|
C | G | 1 | a0001c0012t0020g0207 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.91+5136G>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38452220 | ||||||
chr8:38452727
|
A | T | 1 | a0001c0001t0003g0014 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.91+4629T>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38452727 | ||||||
chr8:38452739
|
G | A | 1 | a0003c0004t0003g0122 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.91+4617C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38452739 | ||||||
chr8:38452849
|
C | T | 1 | a0001c0001t0002g0245 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.91+4507G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38452849 | ||||||
chr8:38452980
|
A | T | 2 | a0001c0001t0001g0186a0001c0001t0004g0232 | 2 | HG00621.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.91+4376T>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38452980 | ||||||
chr8:38452980
|
AAATT | A | 9 | a0001c0001t0003g0019a0001c0001t0003g0023a0001c0001t0003g0032others(6): Show | 9 | NA18982.hp1 NA19001.hp1 NA19007.hp2 others(6): Show |
intron_variant | MODIFIER | c.91+4372_91+4375del others(4): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38452980 | ||||||
chr8:38452984
|
T | A | 3 | a0001c0001t0002g0223a0001c0001t0002g0227a0001c0001t0002g0228 | 3 | NA18964.hp1 NA18991.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.91+4372A>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38452984 | ||||||
chr8:38453112
|
T | C | 1 | a0001c0001t0001g0186 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.91+4244A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38453112 | ||||||
chr8:38453215
|
A | G | 1 | a0001c0001t0002g0301 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.91+4141T>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38453215 | ||||||
chr8:38453285
|
C | T | 1 | a0001c0001t0001g0021 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.91+4071G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38453285 | ||||||
chr8:38453392
|
T | G | 84 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0002g0209others(81): Show | 85 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.91+3964A>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38453392 | ||||||
chr8:38453483
|
C | T | 124 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0013others(121): Show | 124 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.91+3873G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38453483 | ||||||
chr8:38453720
|
C | G | 1 | a0001c0001t0012g0004 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.91+3636G>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38453720 | ||||||
chr8:38453875
|
G | A | 1 | a0001c0001t0005g0322 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.91+3481C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38453875 | ||||||
chr8:38453903
|
C | A | 8 | a0001c0001t0001g0015a0001c0001t0002g0301a0001c0001t0003g0016others(5): Show | 8 | HG02572.hp1 HG02630.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.91+3453G>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38453903 | ||||||
chr8:38453907
|
C | A | 323 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0011others(320): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.91+3449G>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38453907 | ||||||
chr8:38454052
|
C | T | 1 | a0001c0001t0003g0016 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.91+3304G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38454052 | ||||||
chr8:38454076
|
T | A | 1 | a0004c0005t0002g0279 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.91+3280A>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38454076 | ||||||
chr8:38454119
|
A | T | 1 | a0001c0001t0001g0028 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.91+3237T>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38454119 | ||||||
chr8:38454124
|
C | T | 1 | a0001c0001t0004g0269 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.91+3232G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38454124 | ||||||
chr8:38454155
|
C | T | 4 | a0001c0001t0003g0119a0001c0001t0003g0131a0001c0001t0003g0132others(1): Show | 4 | NA18970.hp1 NA18986.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.91+3201G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38454155 | ||||||
chr8:38454289
|
A | C | 3 | a0001c0001t0001g0007a0001c0001t0005g0333a0001c0001t0005g0334 | 3 | HG02622.hp1 HG02886.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.91+3067T>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38454289 | ||||||
chr8:38454788
|
A | G | 1 | a0001c0001t0001g0123 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.91+2568T>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38454788 | ||||||
chr8:38454820
|
A | G | 1 | a0001c0001t0001g0008 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.91+2536T>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38454820 | ||||||
chr8:38454973
|
C | CT | 124 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0017others(121): Show | 124 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.91+2382dupA | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38454973 | ||||||
chr8:38454973
|
C | CTT | 9 | a0001c0001t0001g0011a0001c0001t0001g0086a0001c0001t0001g0118others(6): Show | 9 | HG01952.hp2 HG02080.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.91+2381_91+2382dup others(2): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38454973 | ||||||
chr8:38454973
|
CT | C | 7 | a0001c0001t0001g0007a0001c0001t0001g0094a0001c0001t0003g0016others(4): Show | 7 | HG01496.hp2 HG02622.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.91+2382delA | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38454973 | ||||||
chr8:38455017
|
C | T | 1 | a0001c0001t0002g0281 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.91+2339G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38455017 | ||||||
chr8:38455049
|
C | T | 3 | a0001c0001t0001g0028a0001c0001t0002g0230a0001c0001t0002g0280 | 3 | NA18965.hp2 NA19063.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.91+2307G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38455049 | ||||||
chr8:38455330
|
G | A | 1 | a0001c0001t0002g0302 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.91+2026C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38455330 | ||||||
chr8:38455382
|
G | A | 3 | a0001c0001t0002g0223a0001c0001t0002g0227a0001c0001t0002g0228 | 3 | NA18964.hp1 NA18991.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.91+1974C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38455382 | ||||||
chr8:38455550
|
C | T | 1 | a0001c0001t0003g0014 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.91+1806G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38455550 | ||||||
chr8:38455824
|
C | T | 1 | a0001c0001t0003g0128 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.91+1532G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38455824 | ||||||
chr8:38456122
|
C | T | 1 | a0001c0012t0020g0207 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.91+1234G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38456122 | ||||||
chr8:38456286
|
A | G | 1 | a0001c0001t0003g0016 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.91+1070T>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38456286 | ||||||
chr8:38456394
|
G | T | 2 | a0001c0001t0012g0004a0001c0012t0020g0207 | 2 | HG02647.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.91+962C>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38456394 | ||||||
chr8:38456415
|
C | A | 1 | a0001c0001t0001g0022 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.91+941G>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38456415 | ||||||
chr8:38456432
|
C | T | 3 | a0001c0001t0002g0304a0001c0001t0003g0194a0007c0010t0002g0305 | 3 | HG02071.hp2 HG02083.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.91+924G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38456432 | ||||||
chr8:38456625
|
T | C | 1 | a0001c0001t0017g0095 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.91+731A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38456625 | ||||||
chr8:38456709
|
T | A | 2 | a0001c0001t0012g0004a0001c0012t0020g0207 | 2 | HG02647.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.91+647A>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38456709 | ||||||
chr8:38456716
|
G | A | 1 | a0001c0001t0003g0194 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.91+640C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38456716 | ||||||
chr8:38456768
|
G | A | 3 | a0001c0001t0001g0015a0001c0001t0019g0100a0001c0009t0013g0005 | 3 | HG02572.hp1 HG02630.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.91+588C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38456768 | ||||||
chr8:38456906
|
A | G | 1 | a0001c0001t0006g0035 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.91+450T>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38456906 | ||||||
chr8:38457146
|
C | T | 1 | a0001c0001t0003g0204 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.91+210G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38457146 | ||||||
chr8:38457299
|
C | T | 3 | a0001c0001t0001g0007a0001c0001t0005g0333a0001c0001t0005g0334 | 3 | HG02622.hp1 HG02886.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.91+57G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38457299 | ||||||
chr8:38457306
|
T | A | 1 | a0001c0001t0012g0004 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.91+50A>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 2/17 | chr8 | 38457306 | ||||||
chr8:38457553
|
C | A | 1 | a0001c0001t0001g0203 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-88-19G>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38457553 | ||||||
chr8:38457756
|
C | T | 1 | a0001c0001t0003g0194 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-88-222G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38457756 | ||||||
chr8:38457882
|
C | G | 1 | a0001c0001t0004g0235 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-88-348G>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38457882 | ||||||
chr8:38457883
|
T | C | 18 | a0001c0001t0001g0099a0001c0001t0001g0111a0001c0001t0001g0179others(15): Show | 18 | HG00099.hp2 HG00140.hp2 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.-88-349A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38457883 | ||||||
chr8:38457903
|
A | C | 2 | a0001c0001t0004g0247a0001c0001t0027g0331 | 2 | HG02723.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-88-369T>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38457903 | ||||||
chr8:38458062
|
C | T | 1 | a0001c0001t0003g0064 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-88-528G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38458062 | ||||||
chr8:38458265
|
G | A | 1 | a0001c0001t0019g0100 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-88-731C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38458265 | ||||||
chr8:38458349
|
T | C | 26 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0056others(23): Show | 26 | HG00099.hp2 HG00642.hp1 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.-88-815A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38458349 | ||||||
chr8:38458362
|
G | A | 4 | a0001c0001t0001g0015a0001c0001t0002g0301a0001c0001t0019g0100others(1): Show | 4 | HG02572.hp1 HG02630.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.-88-828C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38458362 | ||||||
chr8:38458420
|
A | G | 1 | a0001c0001t0002g0255 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.-88-886T>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38458420 | ||||||
chr8:38458489
|
C | A | 2 | a0001c0001t0003g0180a0008c0013t0003g0181 | 2 | NA18952.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.-88-955G>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38458489 | ||||||
chr8:38458682
|
A | G | 4 | a0001c0001t0001g0182a0001c0001t0004g0264a0001c0001t0004g0265others(1): Show | 4 | HG01243.hp2 HG01256.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.-88-1148T>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38458682 | ||||||
chr8:38458942
|
G | C | 2 | a0004c0005t0002g0279a0004c0005t0002g0312 | 2 | HG03834.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-88-1408C>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38458942 | ||||||
chr8:38458992
|
AAGCACTG others(17): Show |
A | 1 | a0001c0001t0002g0224 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.-88-1482_-88-1459d others(26): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38458992 | ||||||
chr8:38459146
|
T | C | 2 | a0001c0001t0005g0332a0001c0001t0027g0331 | 2 | HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-88-1612A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38459146 | ||||||
chr8:38459316
|
G | A | 4 | a0001c0001t0002g0210a0001c0001t0002g0260a0001c0001t0002g0302others(1): Show | 4 | NA18947.hp1 NA18963.hp1 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.-88-1782C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38459316 | ||||||
chr8:38459331
|
C | T | 84 | a0001c0001t0001g0060a0001c0001t0001g0107a0001c0001t0001g0108others(81): Show | 85 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.-88-1797G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38459331 | ||||||
chr8:38459427
|
A | C | 1 | a0001c0001t0004g0316 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-88-1893T>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38459427 | ||||||
chr8:38459437
|
T | C | 1 | a0001c0001t0001g0096 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-88-1903A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38459437 | ||||||
chr8:38459712
|
A | C | 3 | a0002c0002t0001g0068a0002c0002t0001g0205a0002c0002t0001g0206 | 3 | HG01167.hp2 HG03139.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-88-2178T>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38459712 | ||||||
chr8:38459880
|
T | C | 195 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0028others(192): Show | 196 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.-88-2346A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38459880 | ||||||
chr8:38459891
|
T | C | 40 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(37): Show | 40 | HG00597.hp2 HG01257.hp1 HG01361.hp2 others(37): Show |
intron_variant | MODIFIER | c.-88-2357A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38459891 | ||||||
chr8:38459958
|
A | C | 234 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(231): Show | 235 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.-88-2424T>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38459958 | ||||||
chr8:38460136
|
T | C | 2 | a0001c0001t0003g0109a0001c0001t0003g0188 | 2 | NA18961.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.-88-2602A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38460136 | ||||||
chr8:38460145
|
T | C | 1 | a0001c0001t0003g0014 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-88-2611A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38460145 | ||||||
chr8:38460165
|
G | A | 1 | a0001c0001t0003g0082 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-88-2631C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38460165 | ||||||
chr8:38460457
|
T | C | 1 | a0001c0012t0020g0207 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-88-2923A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38460457 | ||||||
chr8:38460553
|
C | T | 1 | a0001c0001t0002g0263 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-88-3019G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38460553 | ||||||
chr8:38460649
|
T | C | 39 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(36): Show | 39 | HG00597.hp2 HG01167.hp2 HG01257.hp1 others(36): Show |
intron_variant | MODIFIER | c.-88-3115A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38460649 | ||||||
chr8:38460819
|
G | C | 145 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(142): Show | 146 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.-88-3285C>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38460819 | ||||||
chr8:38460903
|
T | C | 1 | a0001c0001t0019g0100 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-88-3369A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38460903 | ||||||
chr8:38461197
|
A | G | 3 | a0001c0001t0001g0203a0001c0001t0003g0202a0002c0002t0001g0201 | 3 | HG02717.hp2 HG02976.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-88-3663T>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38461197 | ||||||
chr8:38461263
|
A | C | 2 | a0001c0001t0002g0253a0001c0001t0002g0254 | 2 | NA19012.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.-88-3729T>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38461263 | ||||||
chr8:38461321
|
C | T | 1 | a0001c0001t0001g0015 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-88-3787G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38461321 | ||||||
chr8:38461363
|
G | A | 6 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(3): Show | 6 | HG02615.hp1 HG02615.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-88-3829C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38461363 | ||||||
chr8:38461420
|
C | T | 1 | a0001c0001t0026g0335 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-88-3886G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38461420 | ||||||
chr8:38461456
|
T | G | 1 | a0001c0003t0001g0198 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-88-3922A>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38461456 | ||||||
chr8:38461696
|
C | T | 2 | a0001c0001t0002g0261a0001c0001t0002g0262 | 2 | HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-88-4162G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38461696 | ||||||
chr8:38461733
|
A | AT | 9 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(6): Show | 9 | HG02615.hp1 HG02615.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.-88-4200dupA | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38461733 | ||||||
chr8:38461740
|
G | C | 2 | a0001c0001t0002g0304a0007c0010t0002g0305 | 2 | HG02071.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.-88-4206C>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38461740 | ||||||
chr8:38461831
|
G | T | 41 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(38): Show | 41 | HG00597.hp2 HG01257.hp1 HG01361.hp1 others(38): Show |
intron_variant | MODIFIER | c.-88-4297C>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38461831 | ||||||
chr8:38462187
|
A | G | 1 | a0001c0001t0002g0314 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-88-4653T>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38462187 | ||||||
chr8:38462211
|
A | G | 41 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(38): Show | 41 | HG00597.hp2 HG01257.hp1 HG01361.hp1 others(38): Show |
intron_variant | MODIFIER | c.-88-4677T>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38462211 | ||||||
chr8:38462238
|
G | T | 1 | a0001c0001t0003g0103 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-88-4704C>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38462238 | ||||||
chr8:38462504
|
A | C | 1 | a0001c0001t0002g0234 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-88-4970T>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38462504 | ||||||
chr8:38462513
|
A | AT | 7 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(4): Show | 7 | HG02615.hp1 HG02615.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.-88-4980dupA | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38462513 | ||||||
chr8:38462513
|
A | T | 2 | a0001c0001t0001g0050a0001c0001t0004g0251 | 2 | HG01070.hp1 HG01928.hp2 |
intron_variant | MODIFIER | c.-88-4979T>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38462513 | ||||||
chr8:38462765
|
G | A | 1 | a0001c0001t0002g0306 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-89+5216C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38462765 | ||||||
chr8:38462855
|
T | G | 1 | a0001c0001t0004g0246 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-89+5126A>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38462855 | ||||||
chr8:38462902
|
C | CT | 35 | a0001c0001t0002g0211a0001c0001t0002g0212a0001c0001t0002g0213others(32): Show | 35 | HG00597.hp1 HG00609.hp2 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.-89+5078dupA | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38462902 | ||||||
chr8:38462902
|
CT | C | 167 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(164): Show | 168 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.-89+5078delA | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38462902 | ||||||
chr8:38462980
|
T | C | 1 | a0001c0001t0001g0101 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-89+5001A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38462980 | ||||||
chr8:38463056
|
G | A | 1 | a0001c0001t0001g0107 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-89+4925C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38463056 | ||||||
chr8:38463371
|
T | C | 4 | a0001c0001t0001g0067a0001c0001t0001g0083a0001c0001t0001g0097others(1): Show | 4 | HG02055.hp2 HG02572.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-89+4610A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38463371 | ||||||
chr8:38463395
|
A | C | 9 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(6): Show | 9 | HG02615.hp1 HG02615.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.-89+4586T>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38463395 | ||||||
chr8:38463458
|
T | C | 1 | a0001c0001t0002g0308 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-89+4523A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38463458 | ||||||
chr8:38463558
|
T | G | 3 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0009t0013g0005 | 3 | HG02622.hp1 HG02922.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-89+4423A>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38463558 | ||||||
chr8:38463861
|
G | T | 1 | a0001c0001t0002g0253 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-89+4120C>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38463861 | ||||||
chr8:38464035
|
T | C | 317 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(314): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.-89+3946A>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38464035 | ||||||
chr8:38464081
|
G | A | 2 | a0001c0001t0005g0333a0001c0001t0005g0334 | 2 | HG02886.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-89+3900C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38464081 | ||||||
chr8:38464089
|
C | T | 109 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0002g0209others(106): Show | 109 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.-89+3892G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38464089 | ||||||
chr8:38464179
|
G | T | 1 | a0001c0001t0026g0335 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-89+3802C>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38464179 | ||||||
chr8:38464312
|
C | CA | 16 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0050others(13): Show | 16 | HG00597.hp2 HG00741.hp2 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.-89+3668dupT | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38464312 | ||||||
chr8:38464312
|
CA | C | 88 | a0001c0001t0001g0022a0001c0001t0001g0107a0001c0001t0001g0108others(85): Show | 89 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.-89+3668delT | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38464312 | ||||||
chr8:38464312
|
CAA | C | 31 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0065others(28): Show | 31 | HG01175.hp1 HG02055.hp1 HG02055.hp2 others(28): Show |
intron_variant | MODIFIER | c.-89+3667_-89+3668d others(4): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38464312 | ||||||
chr8:38464312
|
CAAA | C | 148 | a0001c0001t0001g0056a0001c0001t0001g0058a0001c0001t0001g0059others(145): Show | 148 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.-89+3666_-89+3668d others(5): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38464312 | ||||||
chr8:38464572
|
C | T | 6 | a0001c0001t0001g0203a0001c0001t0003g0202a0001c0001t0003g0204others(3): Show | 6 | HG01167.hp2 HG01243.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-89+3409G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38464572 | ||||||
chr8:38464713
|
C | T | 2 | a0001c0001t0003g0114a0001c0001t0003g0115 | 2 | NA18953.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.-89+3268G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38464713 | ||||||
chr8:38464828
|
A | G | 210 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0020others(207): Show | 210 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.-89+3153T>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38464828 | ||||||
chr8:38464917
|
C | A | 1 | a0001c0001t0001g0101 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-89+3064G>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38464917 | ||||||
chr8:38465102
|
G | A | 37 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(34): Show | 37 | HG00597.hp2 HG01257.hp1 HG01361.hp1 others(34): Show |
intron_variant | MODIFIER | c.-89+2879C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38465102 | ||||||
chr8:38465118
|
T | G | 3 | a0001c0003t0001g0196a0001c0003t0001g0197a0001c0003t0001g0198 | 3 | HG00642.hp1 HG01175.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.-89+2863A>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38465118 | ||||||
chr8:38465148
|
C | G | 19 | a0001c0001t0002g0211a0001c0001t0002g0212a0001c0001t0002g0213others(16): Show | 19 | HG00438.hp2 HG00597.hp1 HG00609.hp2 others(16): Show |
intron_variant | MODIFIER | c.-89+2833G>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38465148 | ||||||
chr8:38465196
|
C | A | 1 | a0001c0001t0026g0335 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-89+2785G>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38465196 | ||||||
chr8:38465685
|
C | T | 1 | a0001c0001t0001g0107 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-89+2296G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38465685 | ||||||
chr8:38465692
|
G | T | 1 | a0001c0001t0003g0113 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-89+2289C>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38465692 | ||||||
chr8:38465874
|
T | A | 1 | a0001c0001t0001g0199 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-89+2107A>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38465874 | ||||||
chr8:38466006
|
G | GT | 4 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0011g0003others(1): Show | 4 | HG02622.hp1 HG02922.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-89+1974dupA | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38466006 | ||||||
chr8:38466175
|
A | G | 5 | a0001c0001t0002g0250a0001c0001t0004g0251a0001c0001t0004g0252others(2): Show | 5 | HG01070.hp1 HG01123.hp2 HG01167.hp1 others(2): Show |
intron_variant | MODIFIER | c.-89+1806T>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38466175 | ||||||
chr8:38466240
|
C | T | 1 | a0001c0001t0003g0112 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-89+1741G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38466240 | ||||||
chr8:38466247
|
C | G | 115 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0002g0209others(112): Show | 115 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.-89+1734G>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38466247 | ||||||
chr8:38466255
|
G | C | 1 | a0001c0001t0012g0004 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-89+1726C>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38466255 | ||||||
chr8:38466758
|
T | A | 3 | a0001c0001t0002g0314a0001c0001t0002g0315a0001c0001t0004g0316 | 3 | HG00423.hp2 NA18969.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.-89+1223A>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38466758 | ||||||
chr8:38466763
|
C | A | 44 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(41): Show | 44 | HG00597.hp2 HG01167.hp2 HG01243.hp1 others(41): Show |
intron_variant | MODIFIER | c.-89+1218G>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38466763 | ||||||
chr8:38466823
|
G | A | 52 | a0001c0001t0001g0056a0001c0001t0001g0058a0001c0001t0001g0059others(49): Show | 52 | HG00323.hp1 HG00558.hp2 HG01069.hp2 others(49): Show |
intron_variant | MODIFIER | c.-89+1158C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38466823 | ||||||
chr8:38466888
|
ACACCC | A | 17 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0087others(14): Show | 17 | HG00323.hp1 HG01069.hp2 HG01496.hp2 others(14): Show |
intron_variant | MODIFIER | c.-89+1088_-89+1092d others(7): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38466888 | ||||||
chr8:38466891
|
CCCCA | C | 14 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(11): Show | 14 | HG01257.hp2 HG01258.hp1 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.-89+1086_-89+1089d others(6): Show |
FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38466891 | ||||||
chr8:38466895
|
A | C | 3 | a0001c0001t0001g0056a0001c0001t0008g0055a0001c0001t0008g0057 | 3 | HG02976.hp2 HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-89+1086T>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38466895 | ||||||
chr8:38466895
|
A | G | 1 | a0001c0001t0001g0102 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-89+1086T>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38466895 | ||||||
chr8:38466895
|
AC | A | 223 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0022others(220): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.-89+1085delG | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38466895 | ||||||
chr8:38466900
|
C | G | 2 | a0001c0001t0002g0209a0001c0001t0002g0210 | 2 | NA18947.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.-89+1081G>C | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38466900 | ||||||
chr8:38466906
|
A | C | 48 | a0001c0001t0001g0056a0001c0001t0001g0058a0001c0001t0001g0059others(45): Show | 48 | HG00323.hp1 HG00558.hp2 HG01069.hp2 others(45): Show |
intron_variant | MODIFIER | c.-89+1075T>G | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38466906 | ||||||
chr8:38466908
|
C | A | 112 | a0001c0001t0002g0209a0001c0001t0002g0210a0001c0001t0002g0211others(109): Show | 112 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.-89+1073G>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38466908 | ||||||
chr8:38467001
|
G | A | 1 | a0001c0001t0003g0200 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-89+980C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38467001 | ||||||
chr8:38467098
|
G | A | 148 | a0001c0001t0001g0056a0001c0001t0001g0058a0001c0001t0001g0059others(145): Show | 149 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.-89+883C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38467098 | ||||||
chr8:38467120
|
C | T | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG02622.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-89+861G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38467120 | ||||||
chr8:38467298
|
C | T | 1 | a0001c0001t0028g0319 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-89+683G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38467298 | ||||||
chr8:38467613
|
G | A | 97 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0111others(94): Show | 98 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.-89+368C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38467613 | ||||||
chr8:38467650
|
G | T | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | HG02622.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-89+331C>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38467650 | ||||||
chr8:38467753
|
G | A | 7 | a0001c0001t0001g0203a0001c0001t0003g0202a0001c0001t0003g0204others(4): Show | 7 | HG01167.hp2 HG01243.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.-89+228C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38467753 | ||||||
chr8:38467767
|
C | T | 1 | a0001c0001t0022g0208 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-89+214G>A | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38467767 | ||||||
chr8:38467893
|
G | A | 111 | a0001c0001t0002g0209a0001c0001t0002g0210a0001c0001t0002g0211others(108): Show | 111 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.-89+88C>T | FGFR1 | ENSG00000077782.23 | transcript | ENST00000447712.7 | protein_coding | 1/17 | chr8 | 38467893 |