geneid | 2247 |
---|---|
ensemblid | ENSG00000138685.18 |
hgncid | 3676 |
symbol | FGF2 |
name | fibroblast growth factor 2 |
refseq_nuc | NM_001361665.2 |
refseq_prot | NP_001348594.1 |
ensembl_nuc | ENST00000644866.2 |
ensembl_prot | ENSP00000494222.1 |
mane_status | MANE Select |
chr | chr4 |
start | 122826831 |
end | 122898236 |
strand | + |
ver | v1.2 |
region | chr4:122826831-122898236 |
region5000 | chr4:122821831-122903236 |
regionname0 | FGF2_chr4_122826831_122898236 |
regionname5000 | FGF2_chr4_122821831_122903236 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 155 | 256 | 90 | 58 | 60 | 10 | 36 | 42 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 6184 | 48 | 1 | 8 | 24 | 4 | 11 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
t0002 | 0/0 | 6185 | 47 | 4 | 19 | 14 | 4 | 6 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
t0003 | 0/0 | 6185 | 22 | 7 | 8 | 5 | 0 | 2 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
t0004 | 0/0 | 6185 | 13 | 8 | 4 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
t0005 | 0/1 | 6184 | 12 | 1 | 5 | 0 | 2 | 3 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
t0006 | 0/0 | 6185 | 11 | 0 | 2 | 7 | 0 | 2 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
t0007 | 0/0 | 6185 | 10 | 10 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
t0008 | 0/0 | 6185 | 8 | 2 | 1 | 0 | 0 | 5 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
t0009 | 0/0 | 6184 | 7 | 6 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
t0010 | 0/0 | 6184 | 7 | 7 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
t0011 | 0/0 | 6185 | 6 | 6 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
t0012 | 0/0 | 6185 | 5 | 0 | 0 | 4 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
t0013 | 0/0 | 6185 | 4 | 3 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
t0014 | 0/0 | 6185 | 4 | 4 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
t0015 | 0/0 | 6185 | 4 | 1 | 1 | 1 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
t0016 | 0/0 | 6184 | 4 | 0 | 0 | 3 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
t0017 | 0/0 | 6185 | 3 | 2 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
t0018 | 0/0 | 6185 | 3 | 2 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
t0019 | 0/0 | 6185 | 3 | 1 | 2 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
t0020 | 0/0 | 6185 | 3 | 3 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
t0021 | 0/0 | 6184 | 2 | 2 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
t0022 | 0/0 | 6185 | 2 | 2 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
t0023 | 0/0 | 6185 | 2 | 2 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
t0024 | 0/0 | 6184 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
t0025 | 0/0 | 6184 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
t0026 | 0/0 | 6185 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
t0027 | 0/0 | 6181 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
t0028 | 0/0 | 6185 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
t0029 | 0/0 | 6185 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
t0030 | 0/0 | 6185 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
t0031 | 0/0 | 6185 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
t0032 | 1/0 | 6185 | 1 | 0 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
t0033 | 0/0 | 6185 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
t0034 | 0/0 | 6185 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
t0035 | 0/0 | 6184 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
t0036 | 0/0 | 6185 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
t0037 | 0/0 | 6184 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
t0038 | 0/0 | 6185 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
t0039 | 0/0 | 6184 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
t0040 | 0/0 | 6185 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
t0041 | 0/0 | 6181 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
t0042 | 0/0 | 6185 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
t0043 | 0/0 | 6185 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
t0044 | 0/0 | 6185 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
t0045 | 0/0 | 6185 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
t0046 | 0/0 | 6185 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
t0047 | 0/0 | 6184 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
t0048 | 0/0 | 6184 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
t0049 | 0/0 | 6184 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0007 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0008 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0132 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0141 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 468 | 255 | 89 | 58 | 60 | 10 | 36 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
a0001c0002 | 0/0 | 468 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 6651 | 48 | 1 | 8 | 24 | 4 | 11 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
a0001c0001t0002 | 0/0 | 6652 | 47 | 4 | 19 | 14 | 4 | 6 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
a0001c0001t0003 | 0/0 | 6652 | 22 | 7 | 8 | 5 | 0 | 2 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
a0001c0001t0004 | 0/0 | 6652 | 13 | 8 | 4 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
a0001c0001t0005 | 0/1 | 6651 | 12 | 1 | 5 | 0 | 2 | 3 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
a0001c0001t0006 | 0/0 | 6652 | 11 | 0 | 2 | 7 | 0 | 2 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
a0001c0001t0007 | 0/0 | 6652 | 10 | 10 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
a0001c0001t0008 | 0/0 | 6652 | 8 | 2 | 1 | 0 | 0 | 5 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
a0001c0001t0009 | 0/0 | 6651 | 7 | 6 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
a0001c0001t0010 | 0/0 | 6651 | 7 | 7 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
a0001c0001t0011 | 0/0 | 6652 | 6 | 6 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
a0001c0001t0012 | 0/0 | 6652 | 5 | 0 | 0 | 4 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
a0001c0001t0013 | 0/0 | 6652 | 4 | 3 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
a0001c0001t0014 | 0/0 | 6652 | 4 | 4 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
a0001c0001t0015 | 0/0 | 6652 | 4 | 1 | 1 | 1 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
a0001c0001t0016 | 0/0 | 6651 | 4 | 0 | 0 | 3 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
a0001c0001t0017 | 0/0 | 6652 | 3 | 2 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
a0001c0001t0018 | 0/0 | 6652 | 3 | 2 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
a0001c0001t0019 | 0/0 | 6652 | 3 | 1 | 2 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
a0001c0001t0020 | 0/0 | 6652 | 3 | 3 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
a0001c0001t0021 | 0/0 | 6651 | 2 | 2 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
a0001c0001t0022 | 0/0 | 6652 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
a0001c0001t0023 | 0/0 | 6652 | 2 | 2 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
a0001c0001t0024 | 0/0 | 6651 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
a0001c0001t0025 | 0/0 | 6651 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
a0001c0001t0026 | 0/0 | 6652 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
a0001c0001t0027 | 0/0 | 6648 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
a0001c0001t0028 | 0/0 | 6652 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
a0001c0001t0029 | 0/0 | 6652 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
a0001c0001t0030 | 0/0 | 6652 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
a0001c0001t0031 | 0/0 | 6652 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
a0001c0001t0032 | 1/0 | 6652 | 1 | 0 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
a0001c0001t0033 | 0/0 | 6652 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
a0001c0001t0034 | 0/0 | 6652 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
a0001c0001t0035 | 0/0 | 6651 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
a0001c0001t0036 | 0/0 | 6652 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
a0001c0001t0037 | 0/0 | 6651 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
a0001c0001t0038 | 0/0 | 6652 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
a0001c0001t0039 | 0/0 | 6651 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
a0001c0001t0040 | 0/0 | 6652 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
a0001c0001t0041 | 0/0 | 6648 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
a0001c0001t0042 | 0/0 | 6652 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
a0001c0001t0043 | 0/0 | 6652 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
a0001c0001t0044 | 0/0 | 6652 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
a0001c0001t0045 | 0/0 | 6652 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
a0001c0001t0046 | 0/0 | 6652 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
a0001c0001t0047 | 0/0 | 6651 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
a0001c0001t0048 | 0/0 | 6651 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
a0001c0001t0049 | 0/0 | 6651 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
a0001c0002t0022 | 0/0 | 6652 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | copy fasta | chr4 | 122821831 | 122903236 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0003g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0003g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0003g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0003g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0003g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0003g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0003g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0003g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0003g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0003g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0003g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0003g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0003g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0003g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0004g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0004g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0004g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0004g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0004g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0004g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0004g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0004g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0004g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0004g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0004g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0004g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0004g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0005g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0005g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0005g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0005g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0005g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0005g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0005g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0005g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0005g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0005g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0005g0141 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0006g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0006g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0006g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0006g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0006g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0006g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0006g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0006g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0006g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0006g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0006g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0007g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0007g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0007g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0007g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0007g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0007g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0007g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0007g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0007g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0007g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0008g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0008g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0008g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0008g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0008g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0008g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0008g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0009g0007 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0009g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0009g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0009g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0009g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0009g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0010g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0010g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0010g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0010g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0010g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0010g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0010g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0011g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0011g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0011g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0011g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0011g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0011g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0012g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0012g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0012g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0012g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0012g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0013g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0013g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0013g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0013g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0014g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0014g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0014g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0014g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0015g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0015g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0015g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0015g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0016g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0016g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0016g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0016g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0017g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0017g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0017g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0018g0008 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0018g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0019g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0019g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0019g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0020g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0020g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0021g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0021g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0022g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0023g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0023g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0024g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0025g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0026g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0027g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0028g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0029g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0030g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0031g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0032g0132 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0033g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0034g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0035g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0036g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0037g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0038g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0039g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0040g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0041g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0042g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0043g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0044g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0045g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0046g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0047g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0048g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0001t0049g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
a0001c0002t0022g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0005 | g0106 | EUR | GBR | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0083 | EUR | GBR | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | CHS | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | CHS | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | CHS | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | CHS | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG00609 | hp1 | a0001 | c0001 | t0015 | g0144 | EAS | CHS | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG00609 | hp2 | a0001 | c0001 | t0006 | g0024 | EAS | CHS | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG00639 | hp1 | a0001 | c0001 | t0018 | g0008 | AMR | PUR | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0138 | AMR | PUR | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0214 | AMR | PUR | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0174 | AMR | PUR | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG00741 | hp2 | a0001 | c0001 | t0005 | g0134 | AMR | PUR | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0073 | AMR | PUR | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG01071 | hp1 | a0001 | c0001 | t0005 | g0131 | AMR | PUR | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0047 | AMR | PUR | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0044 | AMR | PUR | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0238 | AMR | PUR | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG01106 | hp1 | a0001 | c0001 | t0049 | g0233 | AMR | PUR | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0104 | AMR | PUR | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG01109 | hp1 | a0001 | c0001 | t0009 | g0007 | AMR | PUR | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG01109 | hp2 | a0001 | c0001 | t0015 | g0215 | AMR | PUR | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG01167 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0237 | AMR | PUR | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG01168 | hp1 | a0001 | c0001 | t0004 | g0196 | AMR | PUR | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0133 | AMR | PUR | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG01175 | hp1 | a0001 | c0001 | t0005 | g0105 | AMR | PUR | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG01175 | hp2 | a0001 | c0001 | t0004 | g0029 | AMR | PUR | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0135 | AMR | PUR | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG01192 | hp2 | a0001 | c0001 | t0013 | g0244 | AMR | PUR | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG01243 | hp1 | a0001 | c0001 | t0004 | g0229 | AMR | PUR | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0209 | AMR | PUR | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG01255 | hp1 | a0001 | c0001 | t0038 | g0030 | AMR | CLM | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG01255 | hp2 | a0001 | c0001 | t0019 | g0022 | AMR | CLM | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG01256 | hp1 | a0001 | c0001 | t0003 | g0175 | AMR | CLM | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG01256 | hp2 | a0001 | c0001 | t0005 | g0003 | AMR | CLM | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | CLM | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG01257 | hp2 | a0001 | c0001 | t0003 | g0172 | AMR | CLM | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG01258 | hp1 | a0001 | c0001 | t0005 | g0003 | AMR | CLM | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG01258 | hp2 | a0001 | c0001 | t0003 | g0173 | AMR | CLM | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG01261 | hp1 | a0001 | c0001 | t0006 | g0230 | AMR | CLM | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG01261 | hp2 | a0001 | c0001 | t0025 | g0107 | AMR | CLM | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | CLM | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG01346 | hp2 | a0001 | c0001 | t0019 | g0023 | AMR | CLM | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | CLM | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0054 | AMR | CLM | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG01361 | hp1 | a0001 | c0001 | t0046 | g0185 | AMR | CLM | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | CLM | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | CLM | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG01433 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | CLM | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0117 | EUR | IBS | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG01516 | hp2 | a0001 | c0001 | t0005 | g0057 | EUR | IBS | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG01517 | hp1 | a0001 | c0001 | t0002 | g0058 | EUR | IBS | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0042 | EUR | IBS | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG01884 | hp1 | a0001 | c0001 | t0009 | g0007 | AFR | ACB | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0076 | AFR | ACB | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG01891 | hp1 | a0001 | c0001 | t0011 | g0187 | AFR | ACB | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0211 | AFR | ACB | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG01928 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0053 | AMR | PEL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0142 | AMR | PEL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG01934 | hp2 | a0001 | c0001 | t0008 | g0116 | AMR | PEL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PEL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG01952 | hp2 | a0001 | c0001 | t0004 | g0028 | AMR | PEL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG01975 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PEL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG01975 | hp2 | a0001 | c0001 | t0017 | g0149 | AMR | PEL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0121 | AMR | PEL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG01978 | hp2 | a0001 | c0001 | t0003 | g0119 | AMR | PEL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0112 | AMR | PEL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0074 | AMR | PEL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG02004 | hp1 | a0001 | c0001 | t0006 | g0036 | AMR | PEL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0067 | AMR | PEL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG02015 | hp1 | a0001 | c0001 | t0012 | g0031 | EAS | KHV | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG02015 | hp2 | a0001 | c0001 | t0003 | g0098 | EAS | KHV | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG02040 | hp1 | a0001 | c0001 | t0006 | g0035 | EAS | KHV | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | KHV | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG02055 | hp1 | a0001 | c0001 | t0004 | g0228 | AFR | ACB | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG02055 | hp2 | a0001 | c0001 | t0029 | g0207 | AFR | ACB | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | KHV | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG02056 | hp2 | a0001 | c0001 | t0048 | g0019 | EAS | KHV | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG02074 | hp1 | a0001 | c0001 | t0003 | g0069 | EAS | KHV | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | KHV | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | KHV | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG02129 | hp2 | a0001 | c0001 | t0006 | g0018 | EAS | KHV | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | KHV | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | KHV | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG02145 | hp1 | a0001 | c0001 | t0017 | g0130 | AFR | ACB | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG02145 | hp2 | a0001 | c0001 | t0020 | g0239 | AFR | ACB | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG02257 | hp1 | a0001 | c0001 | t0022 | g0236 | AFR | ACB | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG02257 | hp2 | a0001 | c0001 | t0003 | g0171 | AFR | ACB | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG02258 | hp1 | a0001 | c0001 | t0003 | g0164 | AFR | ACB | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0213 | AFR | ACB | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG02280 | hp1 | a0001 | c0001 | t0019 | g0014 | AFR | ACB | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG02280 | hp2 | a0001 | c0001 | t0013 | g0243 | AFR | ACB | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG02572 | hp1 | a0001 | c0001 | t0010 | g0223 | AFR | GWD | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG02572 | hp2 | a0001 | c0001 | t0010 | g0206 | AFR | GWD | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG02602 | hp2 | a0001 | c0001 | t0005 | g0059 | SAS | PJL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG02615 | hp1 | a0001 | c0001 | t0007 | g0168 | AFR | GWD | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG02615 | hp2 | a0001 | c0001 | t0034 | g0217 | AFR | GWD | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG02622 | hp1 | a0001 | c0001 | t0010 | g0220 | AFR | GWD | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG02622 | hp2 | a0001 | c0001 | t0036 | g0200 | AFR | GWD | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG02630 | hp1 | a0001 | c0001 | t0009 | g0219 | AFR | GWD | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG02630 | hp2 | a0001 | c0001 | t0003 | g0241 | AFR | GWD | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG02698 | hp1 | a0001 | c0001 | t0005 | g0108 | SAS | PJL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG02698 | hp2 | a0001 | c0001 | t0035 | g0176 | SAS | PJL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG02717 | hp1 | a0001 | c0001 | t0039 | g0198 | AFR | GWD | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG02717 | hp2 | a0001 | c0001 | t0010 | g0224 | AFR | GWD | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG02723 | hp1 | a0001 | c0001 | t0003 | g0165 | AFR | GWD | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG02723 | hp2 | a0001 | c0001 | t0010 | g0167 | AFR | GWD | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0140 | SAS | PJL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG02735 | hp2 | a0001 | c0001 | t0016 | g0232 | SAS | PJL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG02738 | hp2 | a0001 | c0001 | t0003 | g0210 | SAS | PJL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG02809 | hp1 | a0001 | c0001 | t0007 | g0153 | AFR | GWD | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG02809 | hp2 | a0001 | c0001 | t0007 | g0179 | AFR | GWD | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG02818 | hp1 | a0001 | c0001 | t0004 | g0194 | AFR | GWD | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG02818 | hp2 | a0001 | c0001 | t0009 | g0201 | AFR | GWD | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG02886 | hp1 | a0001 | c0001 | t0005 | g0124 | AFR | GWD | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG02886 | hp2 | a0001 | c0001 | t0011 | g0192 | AFR | GWD | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG02896 | hp1 | a0001 | c0001 | t0020 | g0009 | AFR | GWD | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG02896 | hp2 | a0001 | c0001 | t0007 | g0148 | AFR | GWD | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG02897 | hp1 | a0001 | c0001 | t0004 | g0197 | AFR | GWD | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG02897 | hp2 | a0001 | c0001 | t0020 | g0009 | AFR | GWD | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG02922 | hp1 | a0001 | c0001 | t0018 | g0218 | AFR | ESN | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG02922 | hp2 | a0001 | c0001 | t0007 | g0147 | AFR | ESN | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG02965 | hp1 | a0001 | c0001 | t0023 | g0189 | AFR | ESN | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG02965 | hp2 | a0001 | c0001 | t0027 | g0204 | AFR | ESN | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG02970 | hp1 | a0001 | c0001 | t0011 | g0184 | AFR | ESN | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG02970 | hp2 | a0001 | c0001 | t0010 | g0221 | AFR | ESN | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG02976 | hp1 | a0001 | c0001 | t0021 | g0235 | AFR | ESN | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG02976 | hp2 | a0001 | c0001 | t0003 | g0118 | AFR | ESN | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG03041 | hp1 | a0001 | c0001 | t0007 | g0154 | AFR | GWD | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG03041 | hp2 | a0001 | c0001 | t0026 | g0202 | AFR | GWD | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG03098 | hp1 | a0001 | c0001 | t0004 | g0199 | AFR | MSL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG03098 | hp2 | a0001 | c0001 | t0008 | g0205 | AFR | MSL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG03130 | hp1 | a0001 | c0001 | t0015 | g0203 | AFR | ESN | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG03130 | hp2 | a0001 | c0001 | t0013 | g0246 | AFR | ESN | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG03139 | hp1 | a0001 | c0001 | t0010 | g0222 | AFR | ESN | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG03139 | hp2 | a0001 | c0001 | t0031 | g0247 | AFR | ESN | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG03195 | hp1 | a0001 | c0001 | t0014 | g0143 | AFR | ESN | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG03195 | hp2 | a0001 | c0001 | t0028 | g0216 | AFR | ESN | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG03209 | hp1 | a0001 | c0001 | t0041 | g0226 | AFR | MSL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG03209 | hp2 | a0001 | c0001 | t0043 | g0013 | AFR | MSL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG03225 | hp1 | a0001 | c0001 | t0047 | g0183 | AFR | MSL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG03225 | hp2 | a0001 | c0001 | t0003 | g0181 | AFR | MSL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0137 | SAS | PJL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG03239 | hp2 | a0001 | c0001 | t0003 | g0212 | SAS | PJL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | MSL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG03486 | hp2 | a0001 | c0001 | t0009 | g0225 | AFR | MSL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG03490 | hp1 | a0001 | c0001 | t0015 | g0136 | SAS | PJL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG03491 | hp1 | a0001 | c0001 | t0008 | g0006 | SAS | PJL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG03491 | hp2 | a0001 | c0001 | t0006 | g0034 | SAS | PJL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG03492 | hp2 | a0001 | c0001 | t0008 | g0006 | SAS | PJL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG03516 | hp1 | a0001 | c0001 | t0007 | g0152 | AFR | ESN | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG03516 | hp2 | a0001 | c0001 | t0004 | g0227 | AFR | ESN | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG03540 | hp1 | a0001 | c0001 | t0013 | g0245 | AFR | GWD | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG03540 | hp2 | a0001 | c0001 | t0007 | g0178 | AFR | GWD | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG03579 | hp1 | a0001 | c0001 | t0011 | g0190 | AFR | MSL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG03579 | hp2 | a0001 | c0001 | t0033 | g0150 | AFR | MSL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG03654 | hp2 | a0001 | c0001 | t0008 | g0160 | SAS | PJL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0061 | SAS | PJL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0045 | SAS | STU | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG03688 | hp2 | a0001 | c0001 | t0008 | g0166 | SAS | STU | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0177 | SAS | PJL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG03704 | hp2 | a0001 | c0001 | t0004 | g0231 | SAS | PJL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG03831 | hp1 | a0001 | c0001 | t0006 | g0033 | SAS | BEB | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0085 | SAS | BEB | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | BEB | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0158 | SAS | BEB | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0052 | SAS | STU | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG04115 | hp2 | a0001 | c0001 | t0012 | g0011 | SAS | STU | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG04199 | hp1 | a0001 | c0001 | t0040 | g0021 | SAS | STU | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG04199 | hp2 | a0001 | c0001 | t0024 | g0051 | SAS | STU | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG04204 | hp1 | a0001 | c0001 | t0005 | g0109 | SAS | STU | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | STU | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0041 | SAS | STU | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG04228 | hp2 | a0001 | c0001 | t0008 | g0159 | SAS | STU | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
NA18522 | hp1 | a0001 | c0001 | t0014 | g0182 | AFR | YRI | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
NA18522 | hp2 | a0001 | c0001 | t0017 | g0123 | AFR | YRI | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
NA18906 | hp1 | a0001 | c0001 | t0023 | g0188 | AFR | YRI | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
NA18906 | hp2 | a0001 | c0001 | t0018 | g0008 | AFR | YRI | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
NA18945 | hp1 | a0001 | c0001 | t0012 | g0012 | EAS | JPT | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
NA18957 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
NA18957 | hp2 | a0001 | c0001 | t0016 | g0039 | EAS | JPT | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
NA18959 | hp1 | a0001 | c0001 | t0006 | g0026 | EAS | JPT | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
NA18961 | hp1 | a0001 | c0001 | t0012 | g0020 | EAS | JPT | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
NA18966 | hp1 | a0001 | c0001 | t0037 | g0101 | EAS | JPT | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
NA18972 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
NA18973 | hp1 | a0001 | c0001 | t0016 | g0025 | EAS | JPT | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
NA18974 | hp1 | a0001 | c0001 | t0003 | g0146 | EAS | JPT | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
NA19002 | hp2 | a0001 | c0001 | t0006 | g0032 | EAS | JPT | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
NA19003 | hp1 | a0001 | c0001 | t0003 | g0072 | EAS | JPT | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
NA19003 | hp2 | a0001 | c0001 | t0016 | g0038 | EAS | JPT | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
NA19030 | hp1 | a0001 | c0001 | t0004 | g0010 | AFR | LWK | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
NA19030 | hp2 | a0001 | c0001 | t0003 | g0242 | AFR | LWK | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
NA19043 | hp1 | a0001 | c0001 | t0011 | g0017 | AFR | LWK | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
NA19043 | hp2 | a0001 | c0001 | t0009 | g0169 | AFR | LWK | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
NA19059 | hp1 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
NA19059 | hp2 | a0001 | c0001 | t0006 | g0037 | EAS | JPT | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
NA19060 | hp1 | a0001 | c0001 | t0012 | g0027 | EAS | JPT | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
NA19070 | hp1 | a0001 | c0001 | t0006 | g0040 | EAS | JPT | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
NA19240 | hp1 | a0001 | c0001 | t0007 | g0151 | AFR | YRI | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
NA19240 | hp2 | a0001 | c0001 | t0030 | g0128 | AFR | YRI | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
NA20129 | hp1 | a0001 | c0001 | t0014 | g0127 | AFR | ASW | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
NA20129 | hp2 | a0001 | c0001 | t0042 | g0015 | AFR | ASW | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0125 | EUR | TSI | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0129 | EUR | TSI | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0060 | EUR | TSI | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0078 | EUR | TSI | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0139 | AFR | ACB | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG02109 | hp2 | a0001 | c0001 | t0004 | g0193 | AFR | ACB | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG02486 | hp1 | a0001 | c0001 | t0009 | g0180 | AFR | ACB | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG02486 | hp2 | a0001 | c0001 | t0011 | g0240 | AFR | ACB | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG02559 | hp1 | a0001 | c0002 | t0022 | g0016 | AFR | ACB | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG02559 | hp2 | a0001 | c0001 | t0007 | g0162 | AFR | ACB | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG03471 | hp1 | a0001 | c0001 | t0004 | g0195 | AFR | MSL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG03471 | hp2 | a0001 | c0001 | t0021 | g0234 | AFR | MSL | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG06807 | hp1 | a0001 | c0001 | t0008 | g0170 | AFR | USA | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
HG06807 | hp2 | a0001 | c0001 | t0045 | g0186 | AFR | USA | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
NA21309 | hp1 | a0001 | c0001 | t0014 | g0157 | AFR | LWK | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
NA21309 | hp2 | a0001 | c0001 | t0044 | g0191 | AFR | LWK | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0005 | g0141 | REF | REF | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0032 | g0132 | REF | REF | FGF2_chr4_122821831_122903236 | FGF2 | chr4 | 122821831 | 122903236 |
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:122876382
|
C | T | 1 | a0001c0002 | 1 | HG02559.hp1 | synonymous_variant | LOW | c.240C>T | p.Asn80Asn | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/3 | 584/6652 | 240/468 | 80/155 | chr4 | 122876382 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:122826931
|
C | T | 23 | a0001c0001t0004a0001c0001t0006a0001c0001t0011others(20): Show | 63 | HG00609.hp2 HG01106.hp1 HG01168.hp1 others(60): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-244C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/3 | chr4 | 122826931 | ||||||
chr4:122892421
|
T | C | 1 | a0001c0001t0024 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*25T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 25 | chr4 | 122892421 | |||||
chr4:122892564
|
A | C | 2 | a0001c0001t0037a0001c0001t0049 | 2 | HG01106.hp1 NA18966.hp1 |
3_prime_UTR_variant | MODIFIER | c.*168A>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 168 | chr4 | 122892564 | |||||
chr4:122892878
|
A | G | 1 | a0001c0001t0048 | 1 | HG02056.hp2 | 3_prime_UTR_variant | MODIFIER | c.*482A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 482 | chr4 | 122892878 | |||||
chr4:122892929
|
G | T | 1 | a0001c0001t0036 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*533G>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 533 | chr4 | 122892929 | |||||
chr4:122893080
|
T | C | 1 | a0001c0001t0038 | 1 | HG01255.hp1 | 3_prime_UTR_variant | MODIFIER | c.*684T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 684 | chr4 | 122893080 | |||||
chr4:122893153
|
C | T | 6 | a0001c0001t0001a0001c0001t0016a0001c0001t0024others(3): Show | 56 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*757C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 757 | chr4 | 122893153 | |||||
chr4:122893230
|
G | T | 6 | a0001c0001t0007a0001c0001t0011a0001c0001t0020others(3): Show | 22 | HG01361.hp1 HG01891.hp1 HG02145.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*834G>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 834 | chr4 | 122893230 | |||||
chr4:122893344
|
A | G | 1 | a0001c0001t0033 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*948A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 948 | chr4 | 122893344 | |||||
chr4:122893445
|
CT | C | 5 | a0001c0001t0005a0001c0001t0009a0001c0001t0021others(2): Show | 23 | HG00099.hp1 HG00741.hp2 HG01071.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*1052delT | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 1052 | INFO_REALIGN_3_PRIME | chr4 | 122893445 | ||||
chr4:122893745
|
G | A | 3 | a0001c0001t0002a0001c0001t0006a0001c0001t0038 | 59 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*1349G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 1349 | chr4 | 122893745 | |||||
chr4:122893765
|
C | T | 1 | a0001c0001t0023 | 2 | HG02965.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1369C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 1369 | chr4 | 122893765 | |||||
chr4:122893863
|
A | G | 2 | a0001c0001t0037a0001c0001t0049 | 2 | HG01106.hp1 NA18966.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1467A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 1467 | chr4 | 122893863 | |||||
chr4:122893926
|
A | G | 6 | a0001c0001t0007a0001c0001t0011a0001c0001t0020others(3): Show | 22 | HG01361.hp1 HG01891.hp1 HG02145.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*1530A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 1530 | chr4 | 122893926 | |||||
chr4:122894147
|
C | A | 6 | a0001c0001t0007a0001c0001t0011a0001c0001t0020others(3): Show | 22 | HG01361.hp1 HG01891.hp1 HG02145.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*1751C>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 1751 | chr4 | 122894147 | |||||
chr4:122894197
|
A | G | 2 | a0001c0001t0036a0001c0001t0044 | 2 | HG02622.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1801A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 1801 | chr4 | 122894197 | |||||
chr4:122894207
|
T | C | 45 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(42): Show | 217 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(214): Show |
3_prime_UTR_variant | MODIFIER | c.*1811T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 1811 | chr4 | 122894207 | |||||
chr4:122894208
|
G | A | 37 | a0001c0001t0001a0001c0001t0005a0001c0001t0007others(34): Show | 144 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(141): Show |
3_prime_UTR_variant | MODIFIER | c.*1812G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 1812 | chr4 | 122894208 | |||||
chr4:122894313
|
G | A | 3 | a0001c0001t0013a0001c0001t0022a0001c0002t0022 | 6 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1917G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 1917 | chr4 | 122894313 | |||||
chr4:122894343
|
C | A | 6 | a0001c0001t0007a0001c0001t0011a0001c0001t0020others(3): Show | 22 | HG01361.hp1 HG01891.hp1 HG02145.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*1947C>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 1947 | chr4 | 122894343 | |||||
chr4:122894480
|
G | A | 3 | a0001c0001t0013a0001c0001t0022a0001c0002t0022 | 6 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2084G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 2084 | chr4 | 122894480 | |||||
chr4:122894509
|
G | C | 1 | a0001c0001t0043 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2113G>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 2113 | chr4 | 122894509 | |||||
chr4:122894619
|
T | TA | 3 | a0001c0001t0013a0001c0001t0022a0001c0002t0022 | 6 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2225dupA | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 2226 | INFO_REALIGN_3_PRIME | chr4 | 122894619 | ||||
chr4:122894710
|
C | G | 2 | a0001c0001t0020a0001c0001t0034 | 4 | HG02145.hp2 HG02615.hp2 HG02896.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2314C>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 2314 | chr4 | 122894710 | |||||
chr4:122894867
|
T | C | 3 | a0001c0001t0008a0001c0001t0019a0001c0001t0040 | 12 | HG01255.hp2 HG01346.hp2 HG01934.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2471T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 2471 | chr4 | 122894867 | |||||
chr4:122894941
|
C | G | 1 | a0001c0001t0046 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2545C>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 2545 | chr4 | 122894941 | |||||
chr4:122894969
|
T | C | 49 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(46): Show | 255 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(252): Show |
3_prime_UTR_variant | MODIFIER | c.*2573T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 2573 | chr4 | 122894969 | |||||
chr4:122895136
|
T | C | 8 | a0001c0001t0005a0001c0001t0009a0001c0001t0021others(5): Show | 26 | HG00099.hp1 HG00741.hp2 HG01071.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*2740T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 2740 | chr4 | 122895136 | |||||
chr4:122895162
|
C | G | 1 | a0001c0001t0049 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2766C>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 2766 | chr4 | 122895162 | |||||
chr4:122895433
|
G | T | 1 | a0001c0001t0029 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3037G>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 3037 | chr4 | 122895433 | |||||
chr4:122895552
|
T | G | 8 | a0001c0001t0005a0001c0001t0009a0001c0001t0021others(5): Show | 26 | HG00099.hp1 HG00741.hp2 HG01071.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*3156T>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 3156 | chr4 | 122895552 | |||||
chr4:122895638
|
C | T | 3 | a0001c0001t0013a0001c0001t0022a0001c0002t0022 | 6 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3242C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 3242 | chr4 | 122895638 | |||||
chr4:122895737
|
ATTC | A | 2 | a0001c0001t0027a0001c0001t0041 | 2 | HG02965.hp2 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3345_*3347delTTC | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 3345 | INFO_REALIGN_3_PRIME | chr4 | 122895737 | ||||
chr4:122896020
|
T | C | 2 | a0001c0001t0037a0001c0001t0049 | 2 | HG01106.hp1 NA18966.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3624T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 3624 | chr4 | 122896020 | |||||
chr4:122896024
|
T | G | 1 | a0001c0001t0045 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3628T>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 3628 | chr4 | 122896024 | |||||
chr4:122896067
|
C | T | 45 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(42): Show | 217 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(214): Show |
3_prime_UTR_variant | MODIFIER | c.*3671C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 3671 | chr4 | 122896067 | |||||
chr4:122896098
|
C | T | 4 | a0001c0001t0013a0001c0001t0022a0001c0001t0025others(1): Show | 7 | HG01192.hp2 HG01261.hp2 HG02257.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3702C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 3702 | chr4 | 122896098 | |||||
chr4:122896181
|
CT | C | 14 | a0001c0001t0001a0001c0001t0010a0001c0001t0013others(11): Show | 73 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*3798delT | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 3798 | INFO_REALIGN_3_PRIME | chr4 | 122896181 | ||||
chr4:122896327
|
C | G | 1 | a0001c0001t0017 | 3 | HG01975.hp2 HG02145.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3931C>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 3931 | chr4 | 122896327 | |||||
chr4:122896373
|
T | C | 32 | a0001c0001t0001a0001c0001t0005a0001c0001t0007others(29): Show | 131 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(128): Show |
3_prime_UTR_variant | MODIFIER | c.*3977T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 3977 | chr4 | 122896373 | |||||
chr4:122896411
|
C | T | 1 | a0001c0001t0040 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4015C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 4015 | chr4 | 122896411 | |||||
chr4:122896590
|
A | G | 1 | a0001c0001t0025 | 1 | HG01261.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4194A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 4194 | chr4 | 122896590 | |||||
chr4:122896731
|
G | A | 2 | a0001c0001t0009a0001c0001t0039 | 8 | HG01109.hp1 HG01884.hp1 HG02486.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*4335G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 4335 | chr4 | 122896731 | |||||
chr4:122896919
|
T | C | 6 | a0001c0001t0002a0001c0001t0006a0001c0001t0012others(3): Show | 69 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*4523T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 4523 | chr4 | 122896919 | |||||
chr4:122896930
|
C | G | 3 | a0001c0001t0005a0001c0001t0021a0001c0001t0025 | 15 | HG00099.hp1 HG00741.hp2 HG01071.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*4534C>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 4534 | chr4 | 122896930 | |||||
chr4:122896975
|
G | A | 1 | a0001c0001t0047 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4579G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 4579 | chr4 | 122896975 | |||||
chr4:122896985
|
A | C | 2 | a0001c0001t0037a0001c0001t0049 | 2 | HG01106.hp1 NA18966.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4589A>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 4589 | chr4 | 122896985 | |||||
chr4:122897092
|
A | G | 2 | a0001c0001t0037a0001c0001t0049 | 2 | HG01106.hp1 NA18966.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4696A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 4696 | chr4 | 122897092 | |||||
chr4:122897116
|
A | T | 46 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(43): Show | 218 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(215): Show |
3_prime_UTR_variant | MODIFIER | c.*4720A>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 4720 | chr4 | 122897116 | |||||
chr4:122897117
|
C | T | 1 | a0001c0001t0030 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4721C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 4721 | chr4 | 122897117 | |||||
chr4:122897143
|
T | A | 11 | a0001c0001t0007a0001c0001t0008a0001c0001t0011others(8): Show | 39 | HG01255.hp2 HG01346.hp2 HG01361.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*4747T>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 4747 | chr4 | 122897143 | |||||
chr4:122897338
|
G | A | 1 | a0001c0001t0035 | 1 | HG02698.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4942G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 4942 | chr4 | 122897338 | |||||
chr4:122897350
|
C | G | 1 | a0001c0001t0045 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4954C>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 4954 | chr4 | 122897350 | |||||
chr4:122897356
|
A | C | 32 | a0001c0001t0001a0001c0001t0005a0001c0001t0007others(29): Show | 131 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(128): Show |
3_prime_UTR_variant | MODIFIER | c.*4960A>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 4960 | chr4 | 122897356 | |||||
chr4:122897401
|
G | A | 3 | a0001c0001t0005a0001c0001t0021a0001c0001t0025 | 15 | HG00099.hp1 HG00741.hp2 HG01071.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*5005G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 5005 | chr4 | 122897401 | |||||
chr4:122897745
|
C | T | 1 | a0001c0001t0026 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5349C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 5349 | chr4 | 122897745 | |||||
chr4:122897858
|
C | G | 6 | a0001c0001t0007a0001c0001t0011a0001c0001t0020others(3): Show | 22 | HG01361.hp1 HG01891.hp1 HG02145.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*5462C>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 5462 | chr4 | 122897858 | |||||
chr4:122897885
|
C | A | 1 | a0001c0001t0031 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5489C>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 3/3 | 5489 | chr4 | 122897885 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:122827369
|
T | C | 31 | a0001c0001t0004g0010a0001c0001t0004g0028a0001c0001t0004g0029others(28): Show | 31 | HG00609.hp2 HG01175.hp2 HG01255.hp1 others(28): Show |
intron_variant | MODIFIER | c.178+17T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122827369 | ||||||
chr4:122827460
|
G | T | 5 | a0001c0001t0013g0243a0001c0001t0013g0244a0001c0001t0013g0245others(2): Show | 5 | HG01192.hp2 HG02280.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.178+108G>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122827460 | ||||||
chr4:122827461
|
C | G | 136 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0163others(133): Show | 140 | HG00609.hp2 HG00639.hp1 HG00642.hp1 others(137): Show |
intron_variant | MODIFIER | c.178+109C>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122827461 | ||||||
chr4:122827579
|
C | T | 31 | a0001c0001t0004g0010a0001c0001t0004g0028a0001c0001t0004g0029others(28): Show | 31 | HG00609.hp2 HG01175.hp2 HG01255.hp1 others(28): Show |
intron_variant | MODIFIER | c.178+227C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122827579 | ||||||
chr4:122827639
|
G | C | 21 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0163others(18): Show | 22 | HG01975.hp2 HG02258.hp1 HG02559.hp2 others(19): Show |
intron_variant | MODIFIER | c.178+287G>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122827639 | ||||||
chr4:122827750
|
A | T | 2 | a0001c0001t0003g0241a0001c0001t0003g0242 | 2 | HG02630.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.178+398A>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122827750 | ||||||
chr4:122828039
|
T | A | 31 | a0001c0001t0004g0010a0001c0001t0004g0028a0001c0001t0004g0029others(28): Show | 31 | HG00609.hp2 HG01175.hp2 HG01255.hp1 others(28): Show |
intron_variant | MODIFIER | c.178+687T>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122828039 | ||||||
chr4:122828082
|
T | C | 21 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0163others(18): Show | 22 | HG01975.hp2 HG02258.hp1 HG02559.hp2 others(19): Show |
intron_variant | MODIFIER | c.178+730T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122828082 | ||||||
chr4:122828251
|
T | C | 6 | a0001c0001t0010g0167a0001c0001t0013g0243a0001c0001t0013g0244others(3): Show | 6 | HG01192.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.178+899T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122828251 | ||||||
chr4:122828273
|
C | T | 3 | a0001c0001t0011g0240a0001c0001t0020g0009a0001c0001t0020g0239 | 4 | HG02145.hp2 HG02486.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.178+921C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122828273 | ||||||
chr4:122828300
|
G | C | 1 | a0001c0001t0001g0041 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.178+948G>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122828300 | ||||||
chr4:122828345
|
C | T | 1 | a0001c0001t0003g0146 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.178+993C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122828345 | ||||||
chr4:122828397
|
C | T | 2 | a0001c0001t0002g0237a0001c0001t0002g0238 | 2 | HG01074.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.178+1045C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122828397 | ||||||
chr4:122828510
|
A | T | 21 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0163others(18): Show | 22 | HG01975.hp2 HG02258.hp1 HG02559.hp2 others(19): Show |
intron_variant | MODIFIER | c.178+1158A>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122828510 | ||||||
chr4:122828621
|
C | G | 1 | a0001c0001t0022g0236 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.178+1269C>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122828621 | ||||||
chr4:122828643
|
C | T | 2 | a0001c0001t0021g0234a0001c0001t0021g0235 | 2 | HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.178+1291C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122828643 | ||||||
chr4:122828796
|
G | C | 21 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0163others(18): Show | 22 | HG01975.hp2 HG02258.hp1 HG02559.hp2 others(19): Show |
intron_variant | MODIFIER | c.178+1444G>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122828796 | ||||||
chr4:122828832
|
AAC | A | 60 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0163others(57): Show | 61 | HG00609.hp2 HG01106.hp1 HG01175.hp2 others(58): Show |
intron_variant | MODIFIER | c.178+1481_178+1482d others(4): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122828832 | ||||||
chr4:122828835
|
T | G | 60 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0163others(57): Show | 61 | HG00609.hp2 HG01106.hp1 HG01175.hp2 others(58): Show |
intron_variant | MODIFIER | c.178+1483T>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122828835 | ||||||
chr4:122828836
|
C | T | 60 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0163others(57): Show | 61 | HG00609.hp2 HG01106.hp1 HG01175.hp2 others(58): Show |
intron_variant | MODIFIER | c.178+1484C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122828836 | ||||||
chr4:122829048
|
CT | C | 91 | a0001c0001t0001g0042a0001c0001t0001g0155a0001c0001t0001g0156others(88): Show | 93 | HG00609.hp2 HG00741.hp1 HG01074.hp2 others(90): Show |
intron_variant | MODIFIER | c.178+1705delT | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122829048 | |||||
chr4:122829088
|
C | G | 4 | a0001c0001t0011g0184a0001c0001t0045g0186a0001c0001t0046g0185others(1): Show | 4 | HG01361.hp1 HG02970.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.178+1736C>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122829088 | ||||||
chr4:122829112
|
C | T | 21 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0163others(18): Show | 22 | HG01975.hp2 HG02258.hp1 HG02559.hp2 others(19): Show |
intron_variant | MODIFIER | c.178+1760C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122829112 | ||||||
chr4:122829417
|
A | G | 39 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0163others(36): Show | 41 | HG00741.hp1 HG01074.hp2 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.178+2065A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122829417 | ||||||
chr4:122829531
|
C | T | 4 | a0001c0001t0004g0231a0001c0001t0006g0230a0001c0001t0016g0232others(1): Show | 4 | HG01106.hp1 HG01261.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.178+2179C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122829531 | ||||||
chr4:122829554
|
T | A | 1 | a0001c0001t0010g0167 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.178+2202T>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122829554 | ||||||
chr4:122829582
|
G | A | 15 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195others(12): Show | 15 | HG01168.hp1 HG01891.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.178+2230G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122829582 | ||||||
chr4:122829587
|
C | A | 1 | a0001c0001t0003g0043 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.178+2235C>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122829587 | ||||||
chr4:122829701
|
A | G | 8 | a0001c0001t0001g0163a0001c0001t0002g0161a0001c0001t0003g0164others(5): Show | 9 | HG02258.hp1 HG02559.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.178+2349A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122829701 | ||||||
chr4:122829909
|
G | A | 1 | a0001c0001t0002g0044 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.178+2557G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122829909 | ||||||
chr4:122830054
|
C | T | 2 | a0001c0001t0009g0225a0001c0001t0010g0224 | 2 | HG02717.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.178+2702C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122830054 | ||||||
chr4:122830101
|
A | T | 26 | a0001c0001t0002g0174a0001c0001t0002g0177a0001c0001t0002g0237others(23): Show | 27 | HG00741.hp1 HG01074.hp2 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.178+2749A>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122830101 | ||||||
chr4:122830232
|
G | T | 1 | a0001c0001t0001g0145 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.178+2880G>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122830232 | ||||||
chr4:122830304
|
G | A | 3 | a0001c0001t0003g0241a0001c0001t0003g0242a0001c0001t0007g0168 | 3 | HG02615.hp1 HG02630.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.178+2952G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122830304 | ||||||
chr4:122830365
|
T | C | 2 | a0001c0001t0020g0009a0001c0001t0020g0239 | 3 | HG02145.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.178+3013T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122830365 | ||||||
chr4:122830406
|
T | TGGAAACA | 12 | a0001c0001t0004g0227a0001c0001t0004g0228a0001c0001t0004g0229others(9): Show | 12 | HG01106.hp1 HG01243.hp1 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.178+3055_178+3056i others(9): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122830406 | |||||
chr4:122830419
|
C | T | 1 | a0001c0001t0045g0186 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.178+3067C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122830419 | ||||||
chr4:122830444
|
C | T | 23 | a0001c0001t0004g0028a0001c0001t0004g0029a0001c0001t0006g0018others(20): Show | 23 | HG00609.hp2 HG01175.hp2 HG01255.hp1 others(20): Show |
intron_variant | MODIFIER | c.178+3092C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122830444 | ||||||
chr4:122830580
|
T | C | 1 | a0001c0001t0036g0200 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.178+3228T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122830580 | ||||||
chr4:122830582
|
C | T | 26 | a0001c0001t0002g0174a0001c0001t0002g0177a0001c0001t0002g0237others(23): Show | 27 | HG00741.hp1 HG01074.hp2 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.178+3230C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122830582 | ||||||
chr4:122830672
|
A | G | 1 | a0001c0001t0015g0144 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.178+3320A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122830672 | ||||||
chr4:122830816
|
C | CA | 22 | a0001c0001t0001g0122a0001c0001t0001g0129a0001c0001t0002g0125others(19): Show | 23 | HG00639.hp1 HG00642.hp1 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.178+3488dupA | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122830816 | |||||
chr4:122830816
|
C | CAA | 26 | a0001c0001t0001g0120a0001c0001t0001g0155a0001c0001t0001g0156others(23): Show | 27 | HG01074.hp1 HG01243.hp2 HG01516.hp1 others(24): Show |
intron_variant | MODIFIER | c.178+3487_178+3488d others(4): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122830816 | |||||
chr4:122830816
|
C | CAAA | 82 | a0001c0001t0001g0004a0001c0001t0001g0041a0001c0001t0001g0042others(79): Show | 86 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.178+3486_178+3488d others(5): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122830816 | |||||
chr4:122830816
|
C | CAAAA | 23 | a0001c0001t0001g0046a0001c0001t0001g0048a0001c0001t0001g0049others(20): Show | 24 | HG00642.hp2 HG01071.hp2 HG01358.hp1 others(21): Show |
intron_variant | MODIFIER | c.178+3485_178+3488d others(6): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122830816 | |||||
chr4:122830816
|
C | CAAAAA | 5 | a0001c0001t0006g0036a0001c0001t0006g0037a0001c0001t0006g0040others(2): Show | 5 | HG02004.hp1 NA18957.hp2 NA19003.hp2 others(2): Show |
intron_variant | MODIFIER | c.178+3484_178+3488d others(7): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122830816 | |||||
chr4:122830816
|
C | CAAAAAA | 13 | a0001c0001t0004g0028a0001c0001t0004g0029a0001c0001t0006g0024others(10): Show | 13 | HG00609.hp2 HG01175.hp2 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.178+3483_178+3488d others(8): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122830816 | |||||
chr4:122830816
|
C | CAAAAAAA | 7 | a0001c0001t0012g0020a0001c0001t0019g0014a0001c0001t0019g0022others(4): Show | 7 | HG01255.hp2 HG01346.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.178+3482_178+3488d others(9): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122830816 | |||||
chr4:122830816
|
C | CAAAAAAA others(1): Show |
6 | a0001c0001t0004g0010a0001c0001t0006g0018a0001c0001t0012g0011others(3): Show | 6 | HG02056.hp2 HG02129.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.178+3481_178+3488d others(10): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122830816 | |||||
chr4:122830816
|
CAAAAAA | C | 10 | a0001c0001t0004g0227a0001c0001t0004g0228a0001c0001t0004g0229others(7): Show | 10 | HG01243.hp1 HG02055.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.178+3483_178+3488d others(8): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122830816 | |||||
chr4:122830816
|
CAAAAAAA others(1): Show |
C | 8 | a0001c0001t0003g0181a0001c0001t0009g0007a0001c0001t0009g0180others(5): Show | 9 | HG01109.hp1 HG01361.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.178+3481_178+3488d others(10): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122830816 | |||||
chr4:122830841
|
T | C | 52 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0163others(49): Show | 53 | HG00609.hp2 HG01175.hp2 HG01255.hp1 others(50): Show |
intron_variant | MODIFIER | c.178+3489T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122830841 | ||||||
chr4:122830862
|
T | G | 109 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0163others(106): Show | 112 | HG00609.hp2 HG00741.hp1 HG01074.hp2 others(109): Show |
intron_variant | MODIFIER | c.178+3510T>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122830862 | ||||||
chr4:122830873
|
G | T | 1 | a0001c0001t0003g0043 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.178+3521G>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122830873 | ||||||
chr4:122831120
|
G | T | 1 | a0001c0001t0008g0116 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.178+3768G>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122831120 | ||||||
chr4:122831180
|
T | C | 3 | a0001c0001t0009g0201a0001c0001t0015g0203a0001c0001t0026g0202 | 3 | HG02818.hp2 HG03041.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.178+3828T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122831180 | ||||||
chr4:122831192
|
A | G | 52 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0163others(49): Show | 53 | HG00609.hp2 HG01175.hp2 HG01255.hp1 others(50): Show |
intron_variant | MODIFIER | c.178+3840A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122831192 | ||||||
chr4:122831385
|
G | C | 15 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195others(12): Show | 15 | HG01168.hp1 HG01891.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.178+4033G>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122831385 | ||||||
chr4:122831438
|
T | C | 52 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0163others(49): Show | 53 | HG00609.hp2 HG01175.hp2 HG01255.hp1 others(50): Show |
intron_variant | MODIFIER | c.178+4086T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122831438 | ||||||
chr4:122831505
|
C | T | 52 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0163others(49): Show | 53 | HG00609.hp2 HG01175.hp2 HG01255.hp1 others(50): Show |
intron_variant | MODIFIER | c.178+4153C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122831505 | ||||||
chr4:122831508
|
G | A | 52 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0163others(49): Show | 53 | HG00609.hp2 HG01175.hp2 HG01255.hp1 others(50): Show |
intron_variant | MODIFIER | c.178+4156G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122831508 | ||||||
chr4:122831537
|
G | T | 52 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0163others(49): Show | 53 | HG00609.hp2 HG01175.hp2 HG01255.hp1 others(50): Show |
intron_variant | MODIFIER | c.178+4185G>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122831537 | ||||||
chr4:122831545
|
T | G | 6 | a0001c0001t0010g0167a0001c0001t0013g0243a0001c0001t0013g0244others(3): Show | 6 | HG01192.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.178+4193T>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122831545 | ||||||
chr4:122831585
|
G | C | 7 | a0001c0001t0004g0193a0001c0001t0011g0187a0001c0001t0011g0190others(4): Show | 7 | HG01891.hp1 HG02109.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.178+4233G>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122831585 | ||||||
chr4:122831659
|
A | G | 1 | a0001c0001t0034g0217 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.178+4307A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122831659 | ||||||
chr4:122831846
|
G | A | 1 | a0001c0001t0007g0148 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.178+4494G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122831846 | ||||||
chr4:122831904
|
A | G | 1 | a0001c0001t0001g0056 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.178+4552A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122831904 | ||||||
chr4:122832102
|
CTTG | C | 4 | a0001c0001t0011g0184a0001c0001t0045g0186a0001c0001t0046g0185others(1): Show | 4 | HG01361.hp1 HG02970.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.178+4753_178+4755d others(5): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122832102 | |||||
chr4:122832409
|
T | A | 1 | a0001c0001t0001g0041 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.178+5057T>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122832409 | ||||||
chr4:122832447
|
GAA | G | 127 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0163others(124): Show | 131 | HG00609.hp2 HG00639.hp1 HG00741.hp1 others(128): Show |
intron_variant | MODIFIER | c.178+5096_178+5097d others(4): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122832447 | ||||||
chr4:122832609
|
T | C | 13 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195others(10): Show | 13 | HG01168.hp1 HG01891.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.178+5257T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122832609 | ||||||
chr4:122832742
|
G | A | 1 | a0001c0001t0005g0057 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.178+5390G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122832742 | ||||||
chr4:122832960
|
C | A | 5 | a0001c0001t0002g0045a0001c0001t0002g0058a0001c0001t0002g0060others(2): Show | 5 | HG01516.hp1 HG01517.hp1 HG02602.hp2 others(2): Show |
intron_variant | MODIFIER | c.178+5608C>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122832960 | ||||||
chr4:122833074
|
T | A | 50 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0163others(47): Show | 52 | HG00609.hp2 HG01109.hp1 HG01175.hp2 others(49): Show |
intron_variant | MODIFIER | c.178+5722T>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122833074 | ||||||
chr4:122833179
|
A | ATG | 3 | a0001c0001t0001g0041a0001c0001t0001g0115a0001c0001t0017g0130 | 3 | HG02145.hp1 HG03654.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.178+5849_178+5850d others(4): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122833179 | |||||
chr4:122833179
|
A | ATGTG | 3 | a0001c0001t0003g0241a0001c0001t0003g0242a0001c0001t0007g0168 | 3 | HG02615.hp1 HG02630.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.178+5847_178+5850d others(6): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122833179 | |||||
chr4:122833179
|
A | ATGTGTG | 16 | a0001c0001t0003g0181a0001c0001t0004g0227a0001c0001t0004g0228others(13): Show | 17 | HG01106.hp1 HG01109.hp1 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.178+5845_178+5850d others(8): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122833179 | |||||
chr4:122833179
|
A | ATGTGTGT others(3): Show |
15 | a0001c0001t0001g0163a0001c0001t0002g0161a0001c0001t0003g0164others(12): Show | 16 | HG00609.hp2 HG02258.hp1 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.178+5841_178+5850d others(12): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122833179 | |||||
chr4:122833179
|
A | ATGTGTGT others(5): Show |
2 | a0001c0001t0042g0015a0001c0002t0022g0016 | 2 | HG02559.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.178+5839_178+5850d others(14): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122833179 | |||||
chr4:122833179
|
A | ATGTGTGT others(7): Show |
25 | a0001c0001t0002g0158a0001c0001t0004g0010a0001c0001t0004g0028others(22): Show | 25 | HG01175.hp2 HG01255.hp1 HG01255.hp2 others(22): Show |
intron_variant | MODIFIER | c.178+5837_178+5850d others(16): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122833179 | |||||
chr4:122833179
|
A | ATGTGTGT others(9): Show |
2 | a0001c0001t0001g0155a0001c0001t0001g0156 | 2 | HG03669.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.178+5835_178+5850d others(18): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122833179 | |||||
chr4:122833201
|
G | A | 4 | a0001c0001t0009g0225a0001c0001t0010g0224a0001c0001t0018g0008others(1): Show | 5 | HG00639.hp1 HG02717.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.178+5849G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122833201 | ||||||
chr4:122833203
|
A | G | 8 | a0001c0001t0003g0181a0001c0001t0009g0007a0001c0001t0009g0180others(5): Show | 10 | HG00639.hp1 HG01109.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.178+5851A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122833203 | ||||||
chr4:122833444
|
TAATTA | T | 15 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195others(12): Show | 15 | HG01168.hp1 HG01891.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.178+6096_178+6100d others(7): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122833444 | |||||
chr4:122833598
|
G | T | 4 | a0001c0001t0008g0205a0001c0001t0010g0206a0001c0001t0027g0204others(1): Show | 4 | HG02055.hp2 HG02572.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.178+6246G>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122833598 | ||||||
chr4:122833723
|
G | C | 103 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0163others(100): Show | 106 | HG00609.hp2 HG00741.hp1 HG01074.hp2 others(103): Show |
intron_variant | MODIFIER | c.178+6371G>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122833723 | ||||||
chr4:122834021
|
C | T | 12 | a0001c0001t0004g0227a0001c0001t0004g0228a0001c0001t0004g0229others(9): Show | 12 | HG01106.hp1 HG01243.hp1 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.178+6669C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122834021 | ||||||
chr4:122834274
|
C | T | 8 | a0001c0001t0004g0227a0001c0001t0004g0228a0001c0001t0004g0229others(5): Show | 8 | HG01106.hp1 HG01243.hp1 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.178+6922C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122834274 | ||||||
chr4:122834346
|
C | T | 1 | a0001c0001t0014g0143 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.178+6994C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122834346 | ||||||
chr4:122834775
|
G | A | 4 | a0001c0001t0004g0231a0001c0001t0006g0230a0001c0001t0016g0232others(1): Show | 4 | HG01106.hp1 HG01261.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.178+7423G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122834775 | ||||||
chr4:122834787
|
A | G | 2 | a0001c0001t0021g0234a0001c0001t0021g0235 | 2 | HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.178+7435A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122834787 | ||||||
chr4:122834801
|
A | G | 4 | a0001c0001t0003g0181a0001c0001t0009g0007a0001c0001t0009g0180others(1): Show | 5 | HG01109.hp1 HG01884.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.178+7449A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122834801 | ||||||
chr4:122834825
|
G | T | 1 | a0001c0001t0007g0168 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.178+7473G>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122834825 | ||||||
chr4:122834905
|
G | A | 4 | a0001c0001t0004g0227a0001c0001t0004g0228a0001c0001t0004g0229others(1): Show | 4 | HG01243.hp1 HG02055.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.178+7553G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122834905 | ||||||
chr4:122835077
|
A | G | 1 | a0001c0001t0002g0005 | 2 | NA18984.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.178+7725A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122835077 | ||||||
chr4:122835191
|
A | G | 1 | a0001c0001t0002g0142 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.178+7839A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122835191 | ||||||
chr4:122835292
|
G | A | 4 | a0001c0001t0004g0231a0001c0001t0006g0230a0001c0001t0016g0232others(1): Show | 4 | HG01106.hp1 HG01261.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.178+7940G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122835292 | ||||||
chr4:122835338
|
G | GT | 11 | a0001c0001t0001g0163a0001c0001t0002g0140a0001c0001t0002g0161others(8): Show | 12 | HG02258.hp1 HG02559.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.178+7996dupT | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122835338 | |||||
chr4:122835382
|
C | T | 46 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0163others(43): Show | 47 | HG00609.hp2 HG01175.hp2 HG01255.hp1 others(44): Show |
intron_variant | MODIFIER | c.178+8030C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122835382 | ||||||
chr4:122835607
|
T | C | 1 | a0001c0001t0041g0226 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.178+8255T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122835607 | ||||||
chr4:122835790
|
T | A | 1 | a0001c0001t0008g0006 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.178+8438T>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122835790 | ||||||
chr4:122835876
|
T | C | 11 | a0001c0001t0002g0174a0001c0001t0002g0177a0001c0001t0002g0237others(8): Show | 11 | HG00741.hp1 HG01074.hp2 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.178+8524T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122835876 | ||||||
chr4:122835879
|
C | T | 2 | a0001c0001t0001g0055a0001c0001t0001g0114 | 2 | HG01257.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.178+8527C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122835879 | ||||||
chr4:122836141
|
G | A | 46 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0163others(43): Show | 47 | HG00609.hp2 HG01175.hp2 HG01255.hp1 others(44): Show |
intron_variant | MODIFIER | c.178+8789G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122836141 | ||||||
chr4:122836202
|
A | C | 6 | a0001c0001t0009g0219a0001c0001t0010g0220a0001c0001t0010g0221others(3): Show | 6 | HG02572.hp1 HG02622.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.178+8850A>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122836202 | ||||||
chr4:122836377
|
G | A | 50 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0163others(47): Show | 52 | HG00609.hp2 HG01109.hp1 HG01175.hp2 others(49): Show |
intron_variant | MODIFIER | c.178+9025G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122836377 | ||||||
chr4:122836537
|
G | T | 4 | a0001c0001t0004g0227a0001c0001t0004g0228a0001c0001t0004g0229others(1): Show | 4 | HG01243.hp1 HG02055.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.178+9185G>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122836537 | ||||||
chr4:122836593
|
C | T | 135 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0163others(132): Show | 139 | HG00609.hp2 HG00639.hp1 HG00642.hp1 others(136): Show |
intron_variant | MODIFIER | c.178+9241C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122836593 | ||||||
chr4:122836595
|
T | G | 1 | a0001c0001t0001g0208 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.178+9243T>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122836595 | ||||||
chr4:122836730
|
A | C | 1 | a0001c0001t0043g0013 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.178+9378A>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122836730 | ||||||
chr4:122836734
|
A | G | 22 | a0001c0001t0002g0174a0001c0001t0002g0177a0001c0001t0002g0237others(19): Show | 22 | HG00741.hp1 HG01074.hp2 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.178+9382A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122836734 | ||||||
chr4:122836833
|
C | T | 50 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0163others(47): Show | 52 | HG00609.hp2 HG01109.hp1 HG01175.hp2 others(49): Show |
intron_variant | MODIFIER | c.178+9481C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122836833 | ||||||
chr4:122836839
|
G | A | 1 | a0001c0001t0019g0022 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.178+9487G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122836839 | ||||||
chr4:122836978
|
A | C | 1 | a0001c0001t0002g0177 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.178+9626A>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122836978 | ||||||
chr4:122837066
|
T | C | 4 | a0001c0001t0004g0227a0001c0001t0004g0228a0001c0001t0004g0229others(1): Show | 4 | HG01243.hp1 HG02055.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.178+9714T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122837066 | ||||||
chr4:122837184
|
C | T | 4 | a0001c0001t0004g0227a0001c0001t0004g0228a0001c0001t0004g0229others(1): Show | 4 | HG01243.hp1 HG02055.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.178+9832C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122837184 | ||||||
chr4:122837187
|
T | A | 1 | a0001c0001t0002g0061 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.178+9835T>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122837187 | ||||||
chr4:122837343
|
G | A | 1 | a0001c0001t0001g0062 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.178+9991G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122837343 | ||||||
chr4:122837378
|
A | G | 1 | a0001c0001t0001g0062 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.178+10026A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122837378 | ||||||
chr4:122837466
|
A | G | 50 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0163others(47): Show | 52 | HG00609.hp2 HG01109.hp1 HG01175.hp2 others(49): Show |
intron_variant | MODIFIER | c.178+10114A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122837466 | ||||||
chr4:122837830
|
C | T | 1 | a0001c0001t0007g0154 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.178+10478C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122837830 | ||||||
chr4:122837831
|
G | A | 1 | a0001c0001t0001g0063 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.178+10479G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122837831 | ||||||
chr4:122837983
|
A | G | 1 | a0001c0001t0002g0054 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.178+10631A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122837983 | ||||||
chr4:122838023
|
G | C | 84 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0163others(81): Show | 86 | HG00609.hp2 HG00741.hp1 HG01074.hp2 others(83): Show |
intron_variant | MODIFIER | c.178+10671G>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122838023 | ||||||
chr4:122838596
|
C | T | 50 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0163others(47): Show | 52 | HG00609.hp2 HG01109.hp1 HG01175.hp2 others(49): Show |
intron_variant | MODIFIER | c.178+11244C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122838596 | ||||||
chr4:122838643
|
A | C | 1 | a0001c0001t0006g0035 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.178+11291A>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122838643 | ||||||
chr4:122838701
|
A | G | 4 | a0001c0001t0003g0181a0001c0001t0009g0007a0001c0001t0009g0180others(1): Show | 5 | HG01109.hp1 HG01884.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.178+11349A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122838701 | ||||||
chr4:122838827
|
C | G | 7 | a0001c0001t0004g0193a0001c0001t0011g0187a0001c0001t0011g0190others(4): Show | 7 | HG01891.hp1 HG02109.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.178+11475C>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122838827 | ||||||
chr4:122838836
|
C | T | 8 | a0001c0001t0004g0227a0001c0001t0004g0228a0001c0001t0004g0229others(5): Show | 8 | HG01106.hp1 HG01243.hp1 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.178+11484C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122838836 | ||||||
chr4:122838847
|
A | T | 4 | a0001c0001t0011g0240a0001c0001t0020g0009a0001c0001t0020g0239others(1): Show | 5 | HG02145.hp2 HG02257.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.178+11495A>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122838847 | ||||||
chr4:122838863
|
A | T | 1 | a0001c0001t0008g0166 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.178+11511A>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122838863 | ||||||
chr4:122839178
|
T | A | 1 | a0001c0001t0002g0213 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.178+11826T>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122839178 | ||||||
chr4:122839221
|
G | A | 1 | a0001c0001t0001g0064 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.178+11869G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122839221 | ||||||
chr4:122839350
|
G | C | 4 | a0001c0001t0004g0227a0001c0001t0004g0228a0001c0001t0004g0229others(1): Show | 4 | HG01243.hp1 HG02055.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.178+11998G>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122839350 | ||||||
chr4:122839372
|
A | AAAC | 21 | a0001c0001t0002g0174a0001c0001t0002g0177a0001c0001t0002g0237others(18): Show | 21 | HG00741.hp1 HG01074.hp2 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.178+12038_178+1204 others(7): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122839372 | |||||
chr4:122839534
|
G | A | 12 | a0001c0001t0004g0227a0001c0001t0004g0228a0001c0001t0004g0229others(9): Show | 12 | HG01106.hp1 HG01243.hp1 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.178+12182G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122839534 | ||||||
chr4:122839614
|
C | T | 1 | a0001c0001t0001g0113 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.178+12262C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122839614 | ||||||
chr4:122839632
|
A | G | 53 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0163others(50): Show | 55 | HG00609.hp2 HG01109.hp1 HG01175.hp2 others(52): Show |
intron_variant | MODIFIER | c.178+12280A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122839632 | ||||||
chr4:122839647
|
T | C | 23 | a0001c0001t0004g0028a0001c0001t0004g0029a0001c0001t0006g0018others(20): Show | 23 | HG00609.hp2 HG01175.hp2 HG01255.hp1 others(20): Show |
intron_variant | MODIFIER | c.178+12295T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122839647 | ||||||
chr4:122839731
|
T | C | 1 | a0001c0001t0001g0065 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.178+12379T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122839731 | ||||||
chr4:122839891
|
G | C | 1 | a0001c0001t0001g0046 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.178+12539G>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122839891 | ||||||
chr4:122840061
|
T | C | 1 | a0001c0001t0002g0066 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.178+12709T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122840061 | ||||||
chr4:122840098
|
T | G | 4 | a0001c0001t0003g0181a0001c0001t0009g0007a0001c0001t0009g0180others(1): Show | 5 | HG01109.hp1 HG01884.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.178+12746T>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122840098 | ||||||
chr4:122840486
|
A | C | 5 | a0001c0001t0009g0225a0001c0001t0010g0224a0001c0001t0018g0008others(2): Show | 6 | HG00639.hp1 HG02615.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.178+13134A>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122840486 | ||||||
chr4:122840531
|
G | C | 8 | a0001c0001t0004g0227a0001c0001t0004g0228a0001c0001t0004g0229others(5): Show | 8 | HG01106.hp1 HG01243.hp1 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.178+13179G>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122840531 | ||||||
chr4:122840668
|
G | A | 1 | a0001c0001t0002g0140 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.178+13316G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122840668 | ||||||
chr4:122840817
|
C | T | 1 | a0001c0001t0031g0247 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.178+13465C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122840817 | ||||||
chr4:122840875
|
A | G | 15 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195others(12): Show | 15 | HG01168.hp1 HG01891.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.178+13523A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122840875 | ||||||
chr4:122841098
|
G | A | 1 | a0001c0001t0021g0235 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.178+13746G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122841098 | ||||||
chr4:122841139
|
T | A | 1 | a0001c0001t0002g0067 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.178+13787T>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122841139 | ||||||
chr4:122841366
|
A | G | 4 | a0001c0001t0002g0053a0001c0001t0002g0110a0001c0001t0002g0111others(1): Show | 4 | HG01928.hp2 HG01981.hp1 NA18950.hp1 others(1): Show |
intron_variant | MODIFIER | c.178+14014A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122841366 | ||||||
chr4:122841593
|
G | C | 5 | a0001c0001t0009g0225a0001c0001t0010g0224a0001c0001t0018g0008others(2): Show | 6 | HG00639.hp1 HG02615.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.178+14241G>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122841593 | ||||||
chr4:122841742
|
A | G | 11 | a0001c0001t0002g0174a0001c0001t0002g0177a0001c0001t0002g0237others(8): Show | 11 | HG00741.hp1 HG01074.hp2 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.178+14390A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122841742 | ||||||
chr4:122841789
|
C | T | 49 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0163others(46): Show | 50 | HG00609.hp2 HG01175.hp2 HG01255.hp1 others(47): Show |
intron_variant | MODIFIER | c.178+14437C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122841789 | ||||||
chr4:122841926
|
A | G | 1 | a0001c0001t0010g0167 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.178+14574A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122841926 | ||||||
chr4:122842037
|
G | A | 1 | a0001c0001t0008g0170 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.178+14685G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122842037 | ||||||
chr4:122842092
|
G | T | 1 | a0001c0001t0043g0013 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.178+14740G>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122842092 | ||||||
chr4:122842471
|
A | T | 4 | a0001c0001t0004g0231a0001c0001t0006g0230a0001c0001t0016g0232others(1): Show | 4 | HG01106.hp1 HG01261.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.178+15119A>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122842471 | ||||||
chr4:122842564
|
C | G | 1 | a0001c0001t0001g0208 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.178+15212C>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122842564 | ||||||
chr4:122842746
|
C | T | 17 | a0001c0001t0001g0052a0001c0001t0001g0129a0001c0001t0002g0044others(14): Show | 17 | HG00099.hp1 HG01074.hp1 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.178+15394C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122842746 | ||||||
chr4:122842972
|
C | T | 127 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0163others(124): Show | 131 | HG00609.hp2 HG00639.hp1 HG00741.hp1 others(128): Show |
intron_variant | MODIFIER | c.178+15620C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122842972 | ||||||
chr4:122843303
|
G | T | 49 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0163others(46): Show | 50 | HG00609.hp2 HG01175.hp2 HG01255.hp1 others(47): Show |
intron_variant | MODIFIER | c.178+15951G>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122843303 | ||||||
chr4:122843353
|
A | G | 99 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0163others(96): Show | 101 | HG00609.hp2 HG00741.hp1 HG01074.hp2 others(98): Show |
intron_variant | MODIFIER | c.178+16001A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122843353 | ||||||
chr4:122843636
|
A | G | 49 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0163others(46): Show | 50 | HG00609.hp2 HG01175.hp2 HG01255.hp1 others(47): Show |
intron_variant | MODIFIER | c.178+16284A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122843636 | ||||||
chr4:122843690
|
A | G | 103 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0163others(100): Show | 106 | HG00609.hp2 HG00741.hp1 HG01074.hp2 others(103): Show |
intron_variant | MODIFIER | c.178+16338A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122843690 | ||||||
chr4:122843758
|
T | C | 12 | a0001c0001t0007g0147a0001c0001t0007g0148a0001c0001t0007g0151others(9): Show | 12 | HG02572.hp1 HG02622.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.178+16406T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122843758 | ||||||
chr4:122843823
|
G | A | 1 | a0001c0001t0001g0068 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.178+16471G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122843823 | ||||||
chr4:122843917
|
G | A | 1 | a0001c0001t0003g0118 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.178+16565G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122843917 | ||||||
chr4:122844047
|
A | G | 4 | a0001c0001t0011g0184a0001c0001t0045g0186a0001c0001t0046g0185others(1): Show | 4 | HG01361.hp1 HG02970.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.178+16695A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122844047 | ||||||
chr4:122844282
|
A | G | 12 | a0001c0001t0007g0147a0001c0001t0007g0148a0001c0001t0007g0151others(9): Show | 12 | HG02572.hp1 HG02622.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.178+16930A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122844282 | ||||||
chr4:122844537
|
T | C | 1 | a0001c0001t0005g0057 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.178+17185T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122844537 | ||||||
chr4:122844557
|
TTTTCTTT others(11): Show |
T | 4 | a0001c0001t0004g0227a0001c0001t0004g0228a0001c0001t0004g0229others(1): Show | 4 | HG01243.hp1 HG02055.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.178+17220_178+1723 others(22): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122844557 | |||||
chr4:122844565
|
CTTTCTT | C | 9 | a0001c0001t0004g0231a0001c0001t0006g0230a0001c0001t0007g0147others(6): Show | 9 | HG01261.hp1 HG02735.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.178+17221_178+1722 others(10): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122844565 | |||||
chr4:122844568
|
T | C | 1 | a0001c0001t0049g0233 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.178+17216T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122844568 | ||||||
chr4:122844569
|
C | T | 29 | a0001c0001t0004g0010a0001c0001t0004g0028a0001c0001t0004g0029others(26): Show | 29 | HG00609.hp2 HG01175.hp2 HG01255.hp1 others(26): Show |
intron_variant | MODIFIER | c.178+17217C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122844569 | ||||||
chr4:122844571
|
T | C | 29 | a0001c0001t0004g0010a0001c0001t0004g0028a0001c0001t0004g0029others(26): Show | 29 | HG00609.hp2 HG01175.hp2 HG01255.hp1 others(26): Show |
intron_variant | MODIFIER | c.178+17219T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122844571 | ||||||
chr4:122844571
|
T | TCCTTCC | 5 | a0001c0001t0013g0243a0001c0001t0013g0244a0001c0001t0013g0245others(2): Show | 5 | HG01192.hp2 HG02280.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.178+17219_178+1722 others(10): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122844571 | ||||||
chr4:122844571
|
T | TCCTTCCT others(3): Show |
1 | a0001c0001t0010g0167 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.178+17219_178+1722 others(14): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122844571 | ||||||
chr4:122844574
|
T | C | 10 | a0001c0001t0004g0231a0001c0001t0006g0230a0001c0001t0010g0167others(7): Show | 10 | HG01106.hp1 HG01192.hp2 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.178+17222T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122844574 | ||||||
chr4:122844578
|
T | C | 10 | a0001c0001t0004g0231a0001c0001t0006g0230a0001c0001t0010g0167others(7): Show | 10 | HG01106.hp1 HG01192.hp2 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.178+17226T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122844578 | ||||||
chr4:122844582
|
T | C | 16 | a0001c0001t0004g0231a0001c0001t0006g0230a0001c0001t0007g0147others(13): Show | 16 | HG01106.hp1 HG01192.hp2 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.178+17230T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122844582 | ||||||
chr4:122844582
|
T | TCTTC | 13 | a0001c0001t0006g0018a0001c0001t0006g0032a0001c0001t0006g0033others(10): Show | 13 | HG01346.hp2 HG02015.hp1 HG02056.hp2 others(10): Show |
intron_variant | MODIFIER | c.178+17233_178+1723 others(8): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122844582 | |||||
chr4:122844582
|
T | TCTTCCTT others(1): Show |
17 | a0001c0001t0004g0010a0001c0001t0004g0028a0001c0001t0004g0029others(14): Show | 17 | HG01175.hp2 HG01255.hp1 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.178+17233_178+1723 others(12): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122844582 | |||||
chr4:122844582
|
T | TCTTCCTT others(5): Show |
3 | a0001c0001t0002g0174a0001c0001t0003g0175a0001c0001t0035g0176 | 3 | HG00741.hp1 HG01256.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.178+17233_178+1723 others(16): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122844582 | |||||
chr4:122844582
|
T | TCTTCCTT others(9): Show |
7 | a0001c0001t0003g0172a0001c0001t0003g0173a0001c0001t0008g0170others(4): Show | 7 | HG01257.hp2 HG01258.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.178+17233_178+1723 others(20): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122844582 | |||||
chr4:122844582
|
T | TCTTCCTT others(13): Show |
4 | a0001c0001t0002g0238a0001c0001t0003g0171a0001c0001t0018g0008others(1): Show | 5 | HG00639.hp1 HG01074.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.178+17233_178+1723 others(24): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122844582 | |||||
chr4:122844582
|
T | TCTTCCTT others(17): Show |
2 | a0001c0001t0002g0237a0001c0001t0006g0024 | 2 | HG00609.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.178+17233_178+1723 others(28): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122844582 | |||||
chr4:122844582
|
T | TCTTCCTT others(21): Show |
2 | a0001c0001t0002g0177a0001c0001t0007g0178 | 2 | HG03540.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.178+17233_178+1723 others(32): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122844582 | |||||
chr4:122844586
|
T | C | 68 | a0001c0001t0002g0174a0001c0001t0002g0177a0001c0001t0002g0237others(65): Show | 69 | HG00609.hp2 HG00639.hp1 HG00741.hp1 others(66): Show |
intron_variant | MODIFIER | c.178+17234T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122844586 | ||||||
chr4:122844586
|
T | TCTTC | 22 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0122others(19): Show | 22 | HG01891.hp1 HG01934.hp1 HG02074.hp1 others(19): Show |
intron_variant | MODIFIER | c.178+17262_178+1726 others(8): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122844586 | |||||
chr4:122844586
|
T | TCTTCCTT others(1): Show |
8 | a0001c0001t0001g0163a0001c0001t0002g0158a0001c0001t0003g0164others(5): Show | 8 | HG02258.hp1 HG02615.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.178+17258_178+1726 others(12): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122844586 | |||||
chr4:122844586
|
T | TCTTCCTT others(5): Show |
7 | a0001c0001t0002g0161a0001c0001t0007g0162a0001c0001t0008g0160others(4): Show | 7 | HG01975.hp2 HG02257.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.178+17254_178+1726 others(16): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122844586 | |||||
chr4:122844586
|
T | TCTTCCTT others(9): Show |
3 | a0001c0001t0008g0006a0001c0001t0020g0009a0001c0001t0020g0239 | 5 | HG02145.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.178+17250_178+1726 others(20): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122844586 | |||||
chr4:122844586
|
T | TCTTCCTT others(13): Show |
6 | a0001c0001t0003g0181a0001c0001t0009g0007a0001c0001t0009g0180others(3): Show | 7 | HG01109.hp1 HG01884.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.178+17246_178+1726 others(24): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122844586 | |||||
chr4:122844586
|
T | TCTTCCTT others(17): Show |
4 | a0001c0001t0004g0196a0001c0001t0004g0197a0001c0001t0004g0199others(1): Show | 4 | HG01168.hp1 HG02486.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.178+17242_178+1726 others(28): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122844586 | |||||
chr4:122844586
|
T | TCTTCCTT others(21): Show |
2 | a0001c0001t0004g0194a0001c0001t0004g0195 | 2 | HG02818.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.178+17238_178+1726 others(32): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122844586 | |||||
chr4:122844586
|
T | TCTTCCTT others(25): Show |
1 | a0001c0001t0007g0179 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.178+17265_178+1726 others(36): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122844586 | |||||
chr4:122844586
|
T | TCTTTCTT others(25): Show |
1 | a0001c0001t0047g0183 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.178+17237_178+1723 others(36): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122844586 | |||||
chr4:122844586
|
T | TCTTTCTT others(25): Show |
1 | a0001c0001t0046g0185 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.178+17237_178+1723 others(36): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122844586 | |||||
chr4:122844586
|
T | TCTTTCTT others(29): Show |
1 | a0001c0001t0011g0184 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.178+17237_178+1723 others(40): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122844586 | |||||
chr4:122844586
|
T | TCTTTCTT others(37): Show |
1 | a0001c0001t0045g0186 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.178+17237_178+1723 others(48): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122844586 | |||||
chr4:122844586
|
TCTTCCTT others(5): Show |
T | 17 | a0001c0001t0001g0052a0001c0001t0001g0129a0001c0001t0002g0044others(14): Show | 17 | HG00099.hp1 HG01074.hp1 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.178+17254_178+1726 others(16): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122844586 | |||||
chr4:122844601
|
T | C | 4 | a0001c0001t0004g0227a0001c0001t0004g0228a0001c0001t0004g0229others(1): Show | 4 | HG01243.hp1 HG02055.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.178+17249T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122844601 | ||||||
chr4:122844618
|
T | C | 5 | a0001c0001t0004g0231a0001c0001t0006g0230a0001c0001t0011g0240others(2): Show | 5 | HG01106.hp1 HG01261.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.178+17266T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122844618 | ||||||
chr4:122844711
|
C | A | 4 | a0001c0001t0003g0181a0001c0001t0009g0007a0001c0001t0009g0180others(1): Show | 5 | HG01109.hp1 HG01884.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.178+17359C>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122844711 | ||||||
chr4:122844727
|
C | T | 13 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195others(10): Show | 13 | HG01168.hp1 HG01891.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.178+17375C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122844727 | ||||||
chr4:122844829
|
G | T | 11 | a0001c0001t0002g0174a0001c0001t0002g0177a0001c0001t0002g0237others(8): Show | 11 | HG00741.hp1 HG01074.hp2 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.178+17477G>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122844829 | ||||||
chr4:122844892
|
T | A | 11 | a0001c0001t0009g0225a0001c0001t0010g0167a0001c0001t0010g0224others(8): Show | 12 | HG00639.hp1 HG01192.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.178+17540T>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122844892 | ||||||
chr4:122844921
|
G | A | 4 | a0001c0001t0004g0231a0001c0001t0006g0230a0001c0001t0016g0232others(1): Show | 4 | HG01106.hp1 HG01261.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.178+17569G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122844921 | ||||||
chr4:122844944
|
G | T | 11 | a0001c0001t0009g0225a0001c0001t0010g0167a0001c0001t0010g0224others(8): Show | 12 | HG00639.hp1 HG01192.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.178+17592G>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122844944 | ||||||
chr4:122844988
|
C | G | 2 | a0001c0001t0020g0009a0001c0001t0020g0239 | 3 | HG02145.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.178+17636C>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122844988 | ||||||
chr4:122845064
|
G | A | 55 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0163others(52): Show | 56 | HG00609.hp2 HG01106.hp1 HG01175.hp2 others(53): Show |
intron_variant | MODIFIER | c.178+17712G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122845064 | ||||||
chr4:122845281
|
G | A | 66 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0163others(63): Show | 68 | HG00609.hp2 HG00639.hp1 HG01106.hp1 others(65): Show |
intron_variant | MODIFIER | c.178+17929G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122845281 | ||||||
chr4:122845484
|
G | A | 4 | a0001c0001t0004g0227a0001c0001t0004g0228a0001c0001t0004g0229others(1): Show | 4 | HG01243.hp1 HG02055.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.178+18132G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122845484 | ||||||
chr4:122845566
|
G | A | 4 | a0001c0001t0002g0174a0001c0001t0002g0177a0001c0001t0002g0237others(1): Show | 4 | HG00741.hp1 HG01074.hp2 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.178+18214G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122845566 | ||||||
chr4:122845588
|
T | G | 120 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0163others(117): Show | 124 | HG00609.hp2 HG00639.hp1 HG00741.hp1 others(121): Show |
intron_variant | MODIFIER | c.178+18236T>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122845588 | ||||||
chr4:122845654
|
C | T | 11 | a0001c0001t0002g0174a0001c0001t0002g0177a0001c0001t0002g0237others(8): Show | 11 | HG00741.hp1 HG01074.hp2 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.178+18302C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122845654 | ||||||
chr4:122845751
|
G | A | 11 | a0001c0001t0009g0225a0001c0001t0010g0167a0001c0001t0010g0224others(8): Show | 12 | HG00639.hp1 HG01192.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.178+18399G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122845751 | ||||||
chr4:122845829
|
T | C | 1 | a0001c0001t0010g0223 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.178+18477T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122845829 | ||||||
chr4:122845865
|
T | C | 1 | a0001c0001t0019g0023 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.178+18513T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122845865 | ||||||
chr4:122845944
|
G | A | 1 | a0001c0001t0049g0233 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.178+18592G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122845944 | ||||||
chr4:122846085
|
G | A | 66 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0163others(63): Show | 68 | HG00609.hp2 HG00639.hp1 HG01106.hp1 others(65): Show |
intron_variant | MODIFIER | c.178+18733G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122846085 | ||||||
chr4:122846097
|
A | G | 58 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0163others(55): Show | 60 | HG00609.hp2 HG00639.hp1 HG01175.hp2 others(57): Show |
intron_variant | MODIFIER | c.178+18745A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122846097 | ||||||
chr4:122846364
|
G | A | 4 | a0001c0001t0004g0227a0001c0001t0004g0228a0001c0001t0004g0229others(1): Show | 4 | HG01243.hp1 HG02055.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.178+19012G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122846364 | ||||||
chr4:122846603
|
A | G | 11 | a0001c0001t0009g0225a0001c0001t0010g0167a0001c0001t0010g0224others(8): Show | 12 | HG00639.hp1 HG01192.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.178+19251A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122846603 | ||||||
chr4:122846669
|
A | G | 11 | a0001c0001t0009g0225a0001c0001t0010g0167a0001c0001t0010g0224others(8): Show | 12 | HG00639.hp1 HG01192.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.178+19317A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122846669 | ||||||
chr4:122846753
|
T | C | 2 | a0001c0001t0002g0237a0001c0001t0002g0238 | 2 | HG01074.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.178+19401T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122846753 | ||||||
chr4:122846788
|
G | A | 55 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0163others(52): Show | 56 | HG00609.hp2 HG01106.hp1 HG01175.hp2 others(53): Show |
intron_variant | MODIFIER | c.178+19436G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122846788 | ||||||
chr4:122846965
|
G | C | 66 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0163others(63): Show | 68 | HG00609.hp2 HG00639.hp1 HG01106.hp1 others(65): Show |
intron_variant | MODIFIER | c.178+19613G>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122846965 | ||||||
chr4:122847108
|
A | G | 123 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0163others(120): Show | 126 | HG00609.hp2 HG00639.hp1 HG00741.hp1 others(123): Show |
intron_variant | MODIFIER | c.178+19756A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122847108 | ||||||
chr4:122847182
|
A | C | 61 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0163others(58): Show | 62 | HG00609.hp2 HG01106.hp1 HG01175.hp2 others(59): Show |
intron_variant | MODIFIER | c.178+19830A>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122847182 | ||||||
chr4:122847205
|
A | G | 11 | a0001c0001t0009g0225a0001c0001t0010g0167a0001c0001t0010g0224others(8): Show | 12 | HG00639.hp1 HG01192.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.178+19853A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122847205 | ||||||
chr4:122847297
|
G | A | 4 | a0001c0001t0004g0227a0001c0001t0004g0228a0001c0001t0004g0229others(1): Show | 4 | HG01243.hp1 HG02055.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.178+19945G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122847297 | ||||||
chr4:122847471
|
C | T | 47 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0163others(44): Show | 48 | HG00609.hp2 HG01175.hp2 HG01255.hp1 others(45): Show |
intron_variant | MODIFIER | c.178+20119C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122847471 | ||||||
chr4:122847603
|
C | CTCTA | 25 | a0001c0001t0001g0046a0001c0001t0001g0048a0001c0001t0001g0052others(22): Show | 25 | HG00099.hp1 HG00609.hp1 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.178+20287_178+2029 others(8): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122847603 | |||||
chr4:122847603
|
C | CTCTATCT others(1): Show |
8 | a0001c0001t0001g0114a0001c0001t0002g0047a0001c0001t0002g0067others(5): Show | 8 | HG01070.hp1 HG01071.hp2 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.178+20283_178+2029 others(12): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122847603 | |||||
chr4:122847603
|
C | CTCTATCT others(5): Show |
3 | a0001c0001t0001g0065a0001c0001t0002g0104a0001c0001t0002g0214 | 3 | HG00438.hp2 HG00642.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.178+20279_178+2029 others(16): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122847603 | |||||
chr4:122847603
|
C | CTCTATTA others(4): Show |
1 | a0001c0001t0001g0103 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.178+20256_178+2025 others(15): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122847603 | |||||
chr4:122847603
|
CTCTA | C | 45 | a0001c0001t0001g0004a0001c0001t0001g0042a0001c0001t0001g0063others(42): Show | 46 | HG00408.hp1 HG00408.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.178+20287_178+2029 others(8): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122847603 | |||||
chr4:122847606
|
T | C | 53 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0163others(50): Show | 54 | HG00609.hp2 HG01106.hp1 HG01175.hp2 others(51): Show |
intron_variant | MODIFIER | c.178+20254T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122847606 | ||||||
chr4:122847623
|
ATCTATCT others(13): Show |
A | 12 | a0001c0001t0007g0147a0001c0001t0007g0148a0001c0001t0007g0151others(9): Show | 12 | HG02572.hp1 HG02622.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.178+20280_178+2029 others(24): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122847623 | |||||
chr4:122847627
|
ATCTATCT others(9): Show |
A | 4 | a0001c0001t0003g0181a0001c0001t0009g0007a0001c0001t0009g0180others(1): Show | 5 | HG01109.hp1 HG01884.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.178+20284_178+2029 others(20): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122847627 | |||||
chr4:122847635
|
ATCTATCT others(1): Show |
A | 8 | a0001c0001t0008g0170a0001c0001t0009g0169a0001c0001t0009g0201others(5): Show | 8 | HG02717.hp1 HG02818.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.178+20291_178+2029 others(12): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122847635 | |||||
chr4:122847638
|
TATCTGTC others(6): Show |
T | 1 | a0001c0001t0031g0247 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.178+20291_178+2030 others(17): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122847638 | |||||
chr4:122847639
|
ATCTG | A | 57 | a0001c0001t0001g0115a0001c0001t0001g0155a0001c0001t0001g0163others(54): Show | 58 | HG00609.hp2 HG00741.hp1 HG01074.hp2 others(55): Show |
intron_variant | MODIFIER | c.178+20291_178+2029 others(8): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122847639 | |||||
chr4:122847642
|
TGTCTATC others(2): Show |
T | 6 | a0001c0001t0010g0167a0001c0001t0010g0224a0001c0001t0013g0243others(3): Show | 7 | HG00639.hp1 HG01192.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.178+20291_178+2029 others(13): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122847642 | ||||||
chr4:122847643
|
G | A | 41 | a0001c0001t0001g0041a0001c0001t0001g0156a0001c0001t0002g0177others(38): Show | 42 | HG01106.hp1 HG01243.hp1 HG01346.hp2 others(39): Show |
intron_variant | MODIFIER | c.178+20291G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122847643 | ||||||
chr4:122847646
|
TATCTA | T | 4 | a0001c0001t0009g0225a0001c0001t0013g0245a0001c0001t0013g0246others(1): Show | 4 | HG02615.hp2 HG03130.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.178+20300_178+2030 others(9): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122847646 | |||||
chr4:122847653
|
T | C | 10 | a0001c0001t0009g0225a0001c0001t0010g0167a0001c0001t0013g0243others(7): Show | 11 | HG00639.hp1 HG01192.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.178+20301T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122847653 | ||||||
chr4:122847657
|
T | C | 11 | a0001c0001t0009g0225a0001c0001t0010g0167a0001c0001t0010g0224others(8): Show | 12 | HG00639.hp1 HG01192.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.178+20305T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122847657 | ||||||
chr4:122847661
|
T | C | 11 | a0001c0001t0009g0225a0001c0001t0010g0167a0001c0001t0010g0224others(8): Show | 12 | HG00639.hp1 HG01192.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.178+20309T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122847661 | ||||||
chr4:122847802
|
G | T | 1 | a0001c0001t0001g0048 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.178+20450G>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122847802 | ||||||
chr4:122847872
|
C | T | 4 | a0001c0001t0003g0241a0001c0001t0003g0242a0001c0001t0007g0168others(1): Show | 4 | HG02615.hp1 HG02630.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.178+20520C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122847872 | ||||||
chr4:122847881
|
A | G | 11 | a0001c0001t0009g0225a0001c0001t0010g0167a0001c0001t0010g0224others(8): Show | 12 | HG00639.hp1 HG01192.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.178+20529A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122847881 | ||||||
chr4:122847898
|
C | T | 1 | a0001c0001t0002g0121 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.178+20546C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122847898 | ||||||
chr4:122847974
|
G | A | 55 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0163others(52): Show | 56 | HG00609.hp2 HG01106.hp1 HG01175.hp2 others(53): Show |
intron_variant | MODIFIER | c.178+20622G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122847974 | ||||||
chr4:122848013
|
C | T | 11 | a0001c0001t0002g0174a0001c0001t0002g0177a0001c0001t0002g0237others(8): Show | 11 | HG00741.hp1 HG01074.hp2 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.178+20661C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122848013 | ||||||
chr4:122848094
|
C | G | 13 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195others(10): Show | 13 | HG01168.hp1 HG01891.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.178+20742C>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122848094 | ||||||
chr4:122848103
|
G | A | 11 | a0001c0001t0009g0225a0001c0001t0010g0167a0001c0001t0010g0224others(8): Show | 12 | HG00639.hp1 HG01192.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.178+20751G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122848103 | ||||||
chr4:122848130
|
C | T | 2 | a0001c0001t0010g0222a0001c0001t0010g0223 | 2 | HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.178+20778C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122848130 | ||||||
chr4:122848228
|
T | C | 1 | a0001c0001t0002g0161 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.178+20876T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122848228 | ||||||
chr4:122848291
|
T | C | 1 | a0001c0001t0002g0086 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.178+20939T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122848291 | ||||||
chr4:122848354
|
A | G | 1 | a0001c0001t0030g0128 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.178+21002A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122848354 | ||||||
chr4:122848379
|
T | C | 1 | a0001c0001t0003g0242 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.178+21027T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122848379 | ||||||
chr4:122848400
|
A | G | 11 | a0001c0001t0009g0225a0001c0001t0010g0167a0001c0001t0010g0224others(8): Show | 12 | HG00639.hp1 HG01192.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.178+21048A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122848400 | ||||||
chr4:122848434
|
T | A | 123 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0163others(120): Show | 126 | HG00609.hp2 HG00639.hp1 HG00741.hp1 others(123): Show |
intron_variant | MODIFIER | c.178+21082T>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122848434 | ||||||
chr4:122848661
|
A | G | 11 | a0001c0001t0009g0225a0001c0001t0010g0167a0001c0001t0010g0224others(8): Show | 12 | HG00639.hp1 HG01192.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.178+21309A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122848661 | ||||||
chr4:122848699
|
A | C | 4 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0002g0158others(1): Show | 4 | HG03669.hp2 HG03834.hp2 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.178+21347A>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122848699 | ||||||
chr4:122848793
|
G | A | 4 | a0001c0001t0019g0014a0001c0001t0021g0234a0001c0001t0021g0235others(1): Show | 4 | HG02280.hp1 HG02976.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.178+21441G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122848793 | ||||||
chr4:122848967
|
C | CAG | 5 | a0001c0001t0009g0225a0001c0001t0010g0224a0001c0001t0018g0008others(2): Show | 6 | HG00639.hp1 HG02615.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.178+21620_178+2162 others(6): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122848967 | |||||
chr4:122848983
|
T | C | 11 | a0001c0001t0009g0225a0001c0001t0010g0167a0001c0001t0010g0224others(8): Show | 12 | HG00639.hp1 HG01192.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.178+21631T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122848983 | ||||||
chr4:122849027
|
C | T | 5 | a0001c0001t0009g0219a0001c0001t0010g0220a0001c0001t0010g0221others(2): Show | 5 | HG02572.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.178+21675C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122849027 | ||||||
chr4:122849455
|
G | T | 6 | a0001c0001t0010g0167a0001c0001t0013g0243a0001c0001t0013g0244others(3): Show | 6 | HG01192.hp2 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.178+22103G>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122849455 | ||||||
chr4:122849530
|
C | T | 8 | a0001c0001t0003g0181a0001c0001t0009g0007a0001c0001t0009g0180others(5): Show | 9 | HG01109.hp1 HG01884.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.178+22178C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122849530 | ||||||
chr4:122849654
|
A | G | 2 | a0001c0001t0019g0014a0001c0001t0042g0015 | 2 | HG02280.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.178+22302A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122849654 | ||||||
chr4:122849880
|
T | A | 1 | a0001c0001t0006g0036 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.178+22528T>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122849880 | ||||||
chr4:122849987
|
C | T | 11 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195others(8): Show | 11 | HG01168.hp1 HG01891.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.178+22635C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122849987 | ||||||
chr4:122849990
|
G | A | 7 | a0001c0001t0001g0079a0001c0001t0010g0167a0001c0001t0013g0243others(4): Show | 7 | HG01192.hp2 HG02280.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.178+22638G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122849990 | ||||||
chr4:122850090
|
C | T | 55 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0163others(52): Show | 56 | HG00609.hp2 HG01106.hp1 HG01175.hp2 others(53): Show |
intron_variant | MODIFIER | c.178+22738C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122850090 | ||||||
chr4:122850238
|
G | T | 54 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0163others(51): Show | 55 | HG00609.hp2 HG01175.hp2 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.178+22886G>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122850238 | ||||||
chr4:122850247
|
G | A | 5 | a0001c0001t0009g0225a0001c0001t0010g0224a0001c0001t0018g0008others(2): Show | 6 | HG00639.hp1 HG02615.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.178+22895G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122850247 | ||||||
chr4:122850261
|
CA | C | 24 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195others(21): Show | 25 | HG00639.hp1 HG01168.hp1 HG01192.hp2 others(22): Show |
intron_variant | MODIFIER | c.178+22920delA | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122850261 | |||||
chr4:122850371
|
C | T | 1 | a0001c0001t0026g0202 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.178+23019C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122850371 | ||||||
chr4:122850393
|
C | T | 5 | a0001c0001t0013g0243a0001c0001t0013g0244a0001c0001t0013g0245others(2): Show | 5 | HG01192.hp2 HG02280.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.178+23041C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122850393 | ||||||
chr4:122850673
|
C | T | 81 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0002g0158others(78): Show | 84 | HG00741.hp1 HG01074.hp2 HG01109.hp1 others(81): Show |
intron_variant | MODIFIER | c.178+23321C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122850673 | ||||||
chr4:122850804
|
G | C | 5 | a0001c0001t0007g0147a0001c0001t0007g0151a0001c0001t0007g0152others(2): Show | 5 | HG02809.hp1 HG02922.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.178+23452G>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122850804 | ||||||
chr4:122850863
|
C | A | 90 | a0001c0001t0002g0125a0001c0001t0002g0133a0001c0001t0002g0135others(87): Show | 94 | HG00639.hp1 HG00741.hp1 HG00741.hp2 others(91): Show |
intron_variant | MODIFIER | c.178+23511C>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122850863 | ||||||
chr4:122850999
|
C | T | 2 | a0001c0001t0002g0047a0001c0001t0002g0073 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.178+23647C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122850999 | ||||||
chr4:122851050
|
T | C | 246 | a0001c0001t0001g0004a0001c0001t0001g0041a0001c0001t0001g0042others(243): Show | 255 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.178+23698T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122851050 | ||||||
chr4:122851149
|
A | G | 18 | a0001c0001t0001g0041a0001c0001t0001g0115a0001c0001t0003g0164others(15): Show | 19 | HG01192.hp2 HG02258.hp1 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.178+23797A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122851149 | ||||||
chr4:122851459
|
C | G | 95 | a0001c0001t0001g0041a0001c0001t0001g0052a0001c0001t0001g0102others(92): Show | 98 | HG00639.hp1 HG01109.hp1 HG01175.hp2 others(95): Show |
intron_variant | MODIFIER | c.178+24107C>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122851459 | ||||||
chr4:122851544
|
G | A | 2 | a0001c0001t0019g0014a0001c0001t0042g0015 | 2 | HG02280.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.178+24192G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122851544 | ||||||
chr4:122851732
|
C | T | 21 | a0001c0001t0001g0052a0001c0001t0003g0241a0001c0001t0003g0242others(18): Show | 22 | HG01192.hp2 HG02280.hp2 HG02559.hp2 others(19): Show |
intron_variant | MODIFIER | c.178+24380C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122851732 | ||||||
chr4:122851862
|
A | T | 3 | a0001c0001t0011g0184a0001c0001t0045g0186a0001c0001t0046g0185 | 3 | HG01361.hp1 HG02970.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.179-24459A>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122851862 | ||||||
chr4:122851917
|
T | C | 2 | a0001c0001t0004g0193a0001c0001t0044g0191 | 2 | HG02109.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.179-24404T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122851917 | ||||||
chr4:122852029
|
ACTGTTAT others(8): Show |
A | 2 | a0001c0001t0001g0042a0001c0001t0001g0068 | 2 | HG01361.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.179-24290_179-2427 others(19): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122852029 | |||||
chr4:122852057
|
A | G | 1 | a0001c0001t0024g0051 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.179-24264A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122852057 | ||||||
chr4:122852111
|
A | G | 1 | a0001c0001t0003g0212 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.179-24210A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122852111 | ||||||
chr4:122852284
|
T | C | 116 | a0001c0001t0001g0049a0001c0001t0001g0052a0001c0001t0001g0062others(113): Show | 121 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(118): Show |
intron_variant | MODIFIER | c.179-24037T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122852284 | ||||||
chr4:122852347
|
T | C | 28 | a0001c0001t0003g0181a0001c0001t0004g0194a0001c0001t0004g0195others(25): Show | 29 | HG01109.hp1 HG01168.hp1 HG01192.hp2 others(26): Show |
intron_variant | MODIFIER | c.179-23974T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122852347 | ||||||
chr4:122852381
|
G | A | 2 | a0001c0001t0018g0008a0001c0001t0018g0218 | 3 | HG00639.hp1 HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.179-23940G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122852381 | ||||||
chr4:122852424
|
T | G | 27 | a0001c0001t0001g0052a0001c0001t0004g0194a0001c0001t0004g0195others(24): Show | 28 | HG01168.hp1 HG01891.hp1 HG02717.hp1 others(25): Show |
intron_variant | MODIFIER | c.179-23897T>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122852424 | ||||||
chr4:122852532
|
G | A | 2 | a0001c0001t0018g0008a0001c0001t0018g0218 | 3 | HG00639.hp1 HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.179-23789G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122852532 | ||||||
chr4:122852652
|
C | G | 7 | a0001c0001t0001g0052a0001c0001t0005g0124a0001c0001t0008g0006others(4): Show | 8 | HG02886.hp1 HG03098.hp2 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.179-23669C>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122852652 | ||||||
chr4:122852659
|
G | A | 21 | a0001c0001t0007g0148a0001c0001t0007g0162a0001c0001t0007g0178others(18): Show | 22 | HG00639.hp1 HG01106.hp1 HG01361.hp1 others(19): Show |
intron_variant | MODIFIER | c.179-23662G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122852659 | ||||||
chr4:122852910
|
C | T | 91 | a0001c0001t0001g0049a0001c0001t0001g0052a0001c0001t0001g0062others(88): Show | 96 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(93): Show |
intron_variant | MODIFIER | c.179-23411C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122852910 | ||||||
chr4:122852955
|
A | T | 16 | a0001c0001t0007g0147a0001c0001t0007g0148a0001c0001t0007g0151others(13): Show | 16 | HG01361.hp1 HG02055.hp2 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.179-23366A>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122852955 | ||||||
chr4:122852973
|
G | GC | 246 | a0001c0001t0001g0004a0001c0001t0001g0041a0001c0001t0001g0042others(243): Show | 255 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.179-23346dupC | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122852973 | |||||
chr4:122853042
|
A | T | 1 | a0001c0001t0005g0124 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.179-23279A>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122853042 | ||||||
chr4:122853109
|
G | A | 28 | a0001c0001t0001g0049a0001c0001t0001g0062a0001c0001t0001g0087others(25): Show | 30 | HG00741.hp2 HG01070.hp2 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.179-23212G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122853109 | ||||||
chr4:122853183
|
A | C | 22 | a0001c0001t0007g0147a0001c0001t0007g0148a0001c0001t0007g0151others(19): Show | 22 | HG01361.hp1 HG02015.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.179-23138A>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122853183 | ||||||
chr4:122853217
|
G | A | 7 | a0001c0001t0013g0243a0001c0001t0013g0244a0001c0001t0013g0245others(4): Show | 7 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.179-23104G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122853217 | ||||||
chr4:122853289
|
T | A | 2 | a0001c0001t0009g0201a0001c0001t0026g0202 | 2 | HG02818.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.179-23032T>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122853289 | ||||||
chr4:122853655
|
ACTC | A | 114 | a0001c0001t0001g0049a0001c0001t0001g0052a0001c0001t0001g0062others(111): Show | 119 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(116): Show |
intron_variant | MODIFIER | c.179-22663_179-2266 others(7): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122853655 | |||||
chr4:122853677
|
G | A | 30 | a0001c0001t0001g0049a0001c0001t0001g0062a0001c0001t0001g0087others(27): Show | 32 | HG00741.hp2 HG01070.hp2 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.179-22644G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122853677 | ||||||
chr4:122853726
|
G | T | 14 | a0001c0001t0003g0241a0001c0001t0003g0242a0001c0001t0008g0170others(11): Show | 14 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.179-22595G>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122853726 | ||||||
chr4:122853758
|
T | A | 138 | a0001c0001t0001g0049a0001c0001t0001g0052a0001c0001t0001g0062others(135): Show | 144 | HG00639.hp1 HG00741.hp2 HG01070.hp2 others(141): Show |
intron_variant | MODIFIER | c.179-22563T>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122853758 | ||||||
chr4:122853801
|
C | A | 33 | a0001c0001t0001g0052a0001c0001t0003g0241a0001c0001t0003g0242others(30): Show | 34 | HG01192.hp2 HG01361.hp1 HG02257.hp1 others(31): Show |
intron_variant | MODIFIER | c.179-22520C>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122853801 | ||||||
chr4:122853942
|
T | C | 8 | a0001c0001t0009g0201a0001c0001t0010g0167a0001c0001t0011g0240others(5): Show | 8 | HG02015.hp1 HG02486.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.179-22379T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122853942 | ||||||
chr4:122853961
|
A | C | 1 | a0001c0001t0005g0124 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.179-22360A>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122853961 | ||||||
chr4:122853984
|
G | A | 1 | a0001c0001t0005g0106 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.179-22337G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122853984 | ||||||
chr4:122854129
|
C | A | 1 | a0001c0001t0036g0200 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.179-22192C>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122854129 | ||||||
chr4:122854186
|
ATAAGGAT others(9): Show |
A | 1 | a0001c0001t0019g0023 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.179-22131_179-2211 others(20): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122854186 | |||||
chr4:122854222
|
A | G | 12 | a0001c0001t0009g0201a0001c0001t0010g0167a0001c0001t0010g0206others(9): Show | 12 | HG02015.hp1 HG02055.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.179-22099A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122854222 | ||||||
chr4:122854278
|
G | A | 67 | a0001c0001t0001g0049a0001c0001t0001g0062a0001c0001t0001g0087others(64): Show | 70 | HG00741.hp2 HG01070.hp2 HG01106.hp2 others(67): Show |
intron_variant | MODIFIER | c.179-22043G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122854278 | ||||||
chr4:122854341
|
C | T | 1 | a0001c0001t0049g0233 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.179-21980C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122854341 | ||||||
chr4:122854439
|
T | G | 3 | a0001c0001t0001g0042a0001c0001t0001g0068a0001c0001t0005g0003 | 4 | HG01256.hp2 HG01258.hp1 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.179-21882T>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122854439 | ||||||
chr4:122854494
|
T | C | 14 | a0001c0001t0003g0241a0001c0001t0003g0242a0001c0001t0008g0170others(11): Show | 14 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.179-21827T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122854494 | ||||||
chr4:122854612
|
G | A | 33 | a0001c0001t0001g0052a0001c0001t0003g0241a0001c0001t0003g0242others(30): Show | 34 | HG01192.hp2 HG01361.hp1 HG02257.hp1 others(31): Show |
intron_variant | MODIFIER | c.179-21709G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122854612 | ||||||
chr4:122854668
|
G | A | 1 | a0001c0001t0005g0124 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.179-21653G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122854668 | ||||||
chr4:122854920
|
A | G | 1 | a0001c0001t0005g0124 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.179-21401A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122854920 | ||||||
chr4:122854985
|
C | T | 1 | a0001c0001t0002g0213 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.179-21336C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122854985 | ||||||
chr4:122855207
|
C | T | 1 | a0001c0001t0007g0178 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.179-21114C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122855207 | ||||||
chr4:122855243
|
A | G | 2 | a0001c0001t0018g0008a0001c0001t0018g0218 | 3 | HG00639.hp1 HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.179-21078A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122855243 | ||||||
chr4:122855245
|
A | G | 10 | a0001c0001t0009g0201a0001c0001t0010g0167a0001c0001t0011g0240others(7): Show | 10 | HG00609.hp1 HG02015.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.179-21076A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122855245 | ||||||
chr4:122855254
|
A | G | 1 | a0001c0001t0003g0119 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.179-21067A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122855254 | ||||||
chr4:122855376
|
G | A | 26 | a0001c0001t0001g0049a0001c0001t0001g0062a0001c0001t0001g0087others(23): Show | 28 | HG00741.hp2 HG01070.hp2 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.179-20945G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122855376 | ||||||
chr4:122855639
|
A | T | 9 | a0001c0001t0003g0181a0001c0001t0007g0168a0001c0001t0009g0007others(6): Show | 10 | HG01109.hp1 HG01884.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.179-20682A>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122855639 | ||||||
chr4:122855667
|
C | G | 2 | a0001c0001t0011g0184a0001c0001t0046g0185 | 2 | HG01361.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.179-20654C>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122855667 | ||||||
chr4:122855908
|
T | C | 28 | a0001c0001t0003g0241a0001c0001t0003g0242a0001c0001t0004g0194others(25): Show | 28 | HG01192.hp2 HG01361.hp1 HG01975.hp2 others(25): Show |
intron_variant | MODIFIER | c.179-20413T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122855908 | ||||||
chr4:122855991
|
T | C | 1 | a0001c0001t0002g0133 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.179-20330T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122855991 | ||||||
chr4:122856084
|
A | T | 6 | a0001c0001t0003g0181a0001c0001t0009g0007a0001c0001t0009g0169others(3): Show | 7 | HG01109.hp1 HG01884.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.179-20237A>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122856084 | ||||||
chr4:122856412
|
G | A | 1 | a0001c0001t0006g0230 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.179-19909G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122856412 | ||||||
chr4:122856705
|
C | G | 5 | a0001c0001t0010g0220a0001c0001t0010g0221a0001c0001t0010g0222others(2): Show | 5 | HG02572.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.179-19616C>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122856705 | ||||||
chr4:122856714
|
A | G | 4 | a0001c0001t0005g0003a0001c0001t0016g0232a0001c0001t0037g0101others(1): Show | 5 | HG01106.hp1 HG01256.hp2 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.179-19607A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122856714 | ||||||
chr4:122856812
|
C | T | 4 | a0001c0001t0014g0127a0001c0001t0017g0123a0001c0001t0017g0130others(1): Show | 4 | HG01975.hp2 HG02145.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.179-19509C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122856812 | ||||||
chr4:122856897
|
A | G | 12 | a0001c0001t0002g0213a0001c0001t0003g0181a0001c0001t0005g0108others(9): Show | 13 | HG01109.hp1 HG01884.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.179-19424A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122856897 | ||||||
chr4:122857017
|
G | C | 13 | a0001c0001t0003g0241a0001c0001t0003g0242a0001c0001t0013g0243others(10): Show | 13 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.179-19304G>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122857017 | ||||||
chr4:122857118
|
A | G | 7 | a0001c0001t0010g0167a0001c0001t0011g0240a0001c0001t0012g0011others(4): Show | 7 | HG02015.hp1 HG02486.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.179-19203A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122857118 | ||||||
chr4:122857219
|
C | G | 2 | a0001c0001t0011g0184a0001c0001t0046g0185 | 2 | HG01361.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.179-19102C>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122857219 | ||||||
chr4:122857220
|
CT | C | 16 | a0001c0001t0004g0194a0001c0001t0004g0195a0001c0001t0004g0196others(13): Show | 16 | HG01168.hp1 HG02015.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.179-19098delT | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122857220 | |||||
chr4:122857222
|
T | C | 16 | a0001c0001t0004g0194a0001c0001t0004g0195a0001c0001t0004g0196others(13): Show | 16 | HG01168.hp1 HG02015.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.179-19099T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122857222 | ||||||
chr4:122857391
|
A | G | 5 | a0001c0001t0003g0118a0001c0001t0004g0010a0001c0001t0004g0193others(2): Show | 5 | HG02109.hp2 HG02965.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.179-18930A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122857391 | ||||||
chr4:122857917
|
C | A | 2 | a0001c0001t0018g0008a0001c0001t0018g0218 | 3 | HG00639.hp1 HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.179-18404C>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122857917 | ||||||
chr4:122858186
|
T | C | 2 | a0001c0001t0005g0124a0001c0001t0005g0131 | 2 | HG01071.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.179-18135T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122858186 | ||||||
chr4:122858246
|
G | A | 2 | a0001c0001t0001g0122a0001c0001t0016g0039 | 2 | HG02132.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.179-18075G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122858246 | ||||||
chr4:122858429
|
G | A | 3 | a0001c0001t0016g0232a0001c0001t0037g0101a0001c0001t0049g0233 | 3 | HG01106.hp1 HG02735.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.179-17892G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122858429 | ||||||
chr4:122858811
|
A | C | 5 | a0001c0001t0010g0220a0001c0001t0010g0221a0001c0001t0010g0222others(2): Show | 5 | HG02572.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.179-17510A>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122858811 | ||||||
chr4:122858912
|
AT | A | 7 | a0001c0001t0010g0220a0001c0001t0010g0221a0001c0001t0010g0222others(4): Show | 8 | HG00639.hp1 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.179-17405delT | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122858912 | |||||
chr4:122858936
|
C | CT | 24 | a0001c0001t0003g0181a0001c0001t0003g0241a0001c0001t0003g0242others(21): Show | 25 | HG01109.hp1 HG01192.hp2 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.179-17384dupT | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122858936 | |||||
chr4:122858954
|
T | TA | 24 | a0001c0001t0003g0181a0001c0001t0003g0241a0001c0001t0003g0242others(21): Show | 25 | HG01109.hp1 HG01192.hp2 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.179-17361dupA | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122858954 | |||||
chr4:122859108
|
C | G | 26 | a0001c0001t0003g0181a0001c0001t0003g0241a0001c0001t0003g0242others(23): Show | 27 | HG01071.hp1 HG01109.hp1 HG01192.hp2 others(24): Show |
intron_variant | MODIFIER | c.179-17213C>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122859108 | ||||||
chr4:122859306
|
C | CTGAA | 13 | a0001c0001t0003g0241a0001c0001t0003g0242a0001c0001t0013g0243others(10): Show | 13 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.179-17005_179-1700 others(8): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122859306 | |||||
chr4:122859398
|
AATTT | A | 3 | a0001c0001t0001g0050a0001c0001t0001g0063a0001c0001t0001g0090 | 3 | HG02040.hp2 HG02129.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.179-16915_179-1691 others(8): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122859398 | |||||
chr4:122859432
|
G | A | 1 | a0001c0001t0005g0131 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.179-16889G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122859432 | ||||||
chr4:122859559
|
T | C | 3 | a0001c0001t0010g0206a0001c0001t0028g0216a0001c0001t0029g0207 | 3 | HG02055.hp2 HG02572.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.179-16762T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122859559 | ||||||
chr4:122859590
|
CA | C | 3 | a0001c0001t0016g0232a0001c0001t0037g0101a0001c0001t0049g0233 | 3 | HG01106.hp1 HG02735.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.179-16728delA | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122859590 | |||||
chr4:122859650
|
A | G | 1 | a0001c0001t0013g0245 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.179-16671A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122859650 | ||||||
chr4:122859653
|
T | TAC | 12 | a0001c0001t0003g0181a0001c0001t0005g0108a0001c0001t0005g0124others(9): Show | 13 | HG01109.hp1 HG01884.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.179-16646_179-1664 others(6): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122859653 | |||||
chr4:122859653
|
TAC | T | 174 | a0001c0001t0001g0004a0001c0001t0001g0041a0001c0001t0001g0042others(171): Show | 180 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.179-16646_179-1664 others(6): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122859653 | |||||
chr4:122859653
|
TACAC | T | 18 | a0001c0001t0004g0194a0001c0001t0004g0195a0001c0001t0004g0196others(15): Show | 18 | HG01168.hp1 HG02015.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.179-16648_179-1664 others(8): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122859653 | |||||
chr4:122859655
|
C | T | 3 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0163 | 3 | NA18953.hp2 NA18968.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.179-16666C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122859655 | ||||||
chr4:122859660
|
A | ACACACAC others(5): Show |
13 | a0001c0001t0003g0241a0001c0001t0003g0242a0001c0001t0013g0243others(10): Show | 13 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.179-16650_179-1664 others(16): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122859660 | |||||
chr4:122859677
|
A | C | 13 | a0001c0001t0003g0241a0001c0001t0003g0242a0001c0001t0013g0243others(10): Show | 13 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.179-16644A>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122859677 | ||||||
chr4:122859704
|
G | T | 2 | a0001c0001t0005g0124a0001c0001t0005g0131 | 2 | HG01071.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.179-16617G>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122859704 | ||||||
chr4:122860263
|
T | G | 27 | a0001c0001t0003g0181a0001c0001t0003g0241a0001c0001t0003g0242others(24): Show | 28 | HG01071.hp1 HG01109.hp1 HG01192.hp2 others(25): Show |
intron_variant | MODIFIER | c.179-16058T>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122860263 | ||||||
chr4:122860447
|
C | CT | 23 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0114others(20): Show | 24 | HG01070.hp2 HG01167.hp2 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.179-15849dupT | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122860447 | |||||
chr4:122860447
|
C | CTT | 108 | a0001c0001t0001g0004a0001c0001t0001g0041a0001c0001t0001g0042others(105): Show | 111 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.179-15850_179-1584 others(6): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122860447 | |||||
chr4:122860447
|
C | CTTT | 16 | a0001c0001t0001g0048a0001c0001t0001g0078a0001c0001t0001g0085others(13): Show | 16 | HG00642.hp2 HG01358.hp2 HG01928.hp2 others(13): Show |
intron_variant | MODIFIER | c.179-15851_179-1584 others(7): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122860447 | |||||
chr4:122860447
|
CT | C | 16 | a0001c0001t0003g0175a0001c0001t0004g0010a0001c0001t0004g0193others(13): Show | 18 | HG00639.hp1 HG01168.hp1 HG01256.hp1 others(15): Show |
intron_variant | MODIFIER | c.179-15849delT | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122860447 | |||||
chr4:122860525
|
G | A | 1 | a0001c0001t0002g0086 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.179-15796G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122860525 | ||||||
chr4:122860544
|
C | T | 37 | a0001c0001t0003g0118a0001c0001t0004g0010a0001c0001t0004g0029others(34): Show | 39 | HG01175.hp2 HG01255.hp2 HG01346.hp2 others(36): Show |
intron_variant | MODIFIER | c.179-15777C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122860544 | ||||||
chr4:122860583
|
G | A | 2 | a0001c0001t0018g0008a0001c0001t0018g0218 | 3 | HG00639.hp1 HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.179-15738G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122860583 | ||||||
chr4:122860611
|
A | G | 11 | a0001c0001t0003g0181a0001c0001t0005g0108a0001c0001t0009g0007others(8): Show | 12 | HG01109.hp1 HG01884.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.179-15710A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122860611 | ||||||
chr4:122860662
|
G | A | 2 | a0001c0001t0003g0164a0001c0001t0003g0165 | 2 | HG02258.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.179-15659G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122860662 | ||||||
chr4:122860677
|
G | A | 2 | a0001c0001t0005g0124a0001c0001t0005g0131 | 2 | HG01071.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.179-15644G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122860677 | ||||||
chr4:122860702
|
C | T | 1 | a0001c0001t0003g0165 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.179-15619C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122860702 | ||||||
chr4:122860716
|
C | T | 3 | a0001c0001t0016g0232a0001c0001t0037g0101a0001c0001t0049g0233 | 3 | HG01106.hp1 HG02735.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.179-15605C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122860716 | ||||||
chr4:122860717
|
G | A | 52 | a0001c0001t0003g0181a0001c0001t0003g0241a0001c0001t0003g0242others(49): Show | 54 | HG00639.hp1 HG01071.hp1 HG01109.hp1 others(51): Show |
intron_variant | MODIFIER | c.179-15604G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122860717 | ||||||
chr4:122860754
|
C | T | 11 | a0001c0001t0003g0181a0001c0001t0005g0108a0001c0001t0009g0007others(8): Show | 12 | HG01109.hp1 HG01884.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.179-15567C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122860754 | ||||||
chr4:122860798
|
A | G | 2 | a0001c0001t0016g0232a0001c0001t0049g0233 | 2 | HG01106.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.179-15523A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122860798 | ||||||
chr4:122860851
|
C | T | 24 | a0001c0001t0004g0194a0001c0001t0004g0195a0001c0001t0004g0196others(21): Show | 24 | HG01168.hp1 HG02015.hp1 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.179-15470C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122860851 | ||||||
chr4:122860890
|
A | C | 1 | a0001c0001t0001g0155 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.179-15431A>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122860890 | ||||||
chr4:122860928
|
T | C | 19 | a0001c0001t0004g0194a0001c0001t0004g0195a0001c0001t0004g0196others(16): Show | 19 | HG01168.hp1 HG02015.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.179-15393T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122860928 | ||||||
chr4:122861041
|
C | T | 5 | a0001c0001t0004g0194a0001c0001t0004g0195a0001c0001t0004g0196others(2): Show | 5 | HG01168.hp1 HG02818.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.179-15280C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122861041 | ||||||
chr4:122861186
|
C | T | 1 | a0001c0001t0004g0029 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.179-15135C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122861186 | ||||||
chr4:122861289
|
T | C | 12 | a0001c0001t0003g0241a0001c0001t0003g0242a0001c0001t0013g0243others(9): Show | 12 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.179-15032T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122861289 | ||||||
chr4:122861337
|
T | C | 1 | a0001c0001t0002g0126 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.179-14984T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122861337 | ||||||
chr4:122861368
|
T | C | 4 | a0001c0001t0010g0206a0001c0001t0028g0216a0001c0001t0029g0207others(1): Show | 4 | HG02055.hp2 HG02572.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.179-14953T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122861368 | ||||||
chr4:122861413
|
C | A | 23 | a0001c0001t0003g0181a0001c0001t0004g0194a0001c0001t0004g0195others(20): Show | 24 | HG01071.hp1 HG01106.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.179-14908C>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122861413 | ||||||
chr4:122861540
|
A | T | 1 | a0001c0001t0017g0149 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.179-14781A>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122861540 | ||||||
chr4:122861631
|
GT | G | 34 | a0001c0001t0001g0004a0001c0001t0001g0090a0001c0001t0001g0092others(31): Show | 35 | HG00408.hp2 HG01074.hp1 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.179-14689delT | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122861631 | ||||||
chr4:122861667
|
T | A | 4 | a0001c0001t0009g0169a0001c0001t0009g0225a0001c0001t0018g0008others(1): Show | 5 | HG00639.hp1 HG02922.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.179-14654T>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122861667 | ||||||
chr4:122861671
|
A | G | 5 | a0001c0001t0010g0206a0001c0001t0013g0243a0001c0001t0013g0244others(2): Show | 5 | HG01192.hp2 HG02055.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.179-14650A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122861671 | ||||||
chr4:122861741
|
A | T | 187 | a0001c0001t0001g0004a0001c0001t0001g0041a0001c0001t0001g0046others(184): Show | 195 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(192): Show |
intron_variant | MODIFIER | c.179-14580A>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122861741 | ||||||
chr4:122861747
|
C | G | 5 | a0001c0001t0003g0118a0001c0001t0004g0010a0001c0001t0004g0193others(2): Show | 5 | HG02109.hp2 HG02965.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.179-14574C>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122861747 | ||||||
chr4:122861821
|
G | T | 1 | a0001c0001t0002g0126 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.179-14500G>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122861821 | ||||||
chr4:122861876
|
G | A | 50 | a0001c0001t0003g0210a0001c0001t0003g0241a0001c0001t0003g0242others(47): Show | 53 | HG00639.hp1 HG01192.hp2 HG01255.hp2 others(50): Show |
intron_variant | MODIFIER | c.179-14445G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122861876 | ||||||
chr4:122861950
|
G | A | 217 | a0001c0001t0001g0004a0001c0001t0001g0041a0001c0001t0001g0042others(214): Show | 224 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(221): Show |
intron_variant | MODIFIER | c.179-14371G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122861950 | ||||||
chr4:122861989
|
A | C | 14 | a0001c0001t0003g0241a0001c0001t0003g0242a0001c0001t0013g0243others(11): Show | 14 | HG01192.hp2 HG02055.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.179-14332A>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122861989 | ||||||
chr4:122862039
|
T | C | 28 | a0001c0001t0004g0194a0001c0001t0004g0195a0001c0001t0004g0196others(25): Show | 30 | HG00099.hp1 HG01071.hp1 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.179-14282T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122862039 | ||||||
chr4:122862061
|
G | A | 10 | a0001c0001t0008g0006a0001c0001t0008g0116a0001c0001t0008g0159others(7): Show | 11 | HG01346.hp2 HG01934.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.179-14260G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122862061 | ||||||
chr4:122862104
|
T | C | 5 | a0001c0001t0003g0118a0001c0001t0004g0010a0001c0001t0004g0193others(2): Show | 5 | HG02109.hp2 HG02965.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.179-14217T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122862104 | ||||||
chr4:122862232
|
A | G | 57 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0046others(54): Show | 58 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.179-14089A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122862232 | ||||||
chr4:122862240
|
A | G | 11 | a0001c0001t0008g0006a0001c0001t0008g0116a0001c0001t0008g0159others(8): Show | 12 | HG01255.hp2 HG01346.hp2 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.179-14081A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122862240 | ||||||
chr4:122862257
|
A | G | 6 | a0001c0001t0013g0243a0001c0001t0013g0244a0001c0001t0013g0245others(3): Show | 6 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.179-14064A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122862257 | ||||||
chr4:122862292
|
T | C | 1 | a0001c0001t0005g0124 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.179-14029T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122862292 | ||||||
chr4:122862655
|
C | T | 2 | a0001c0001t0002g0089a0001c0001t0002g0091 | 2 | NA18953.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.179-13666C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122862655 | ||||||
chr4:122862681
|
A | G | 1 | a0001c0001t0002g0174 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.179-13640A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122862681 | ||||||
chr4:122862849
|
G | A | 6 | a0001c0001t0013g0243a0001c0001t0013g0244a0001c0001t0013g0245others(3): Show | 6 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.179-13472G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122862849 | ||||||
chr4:122863140
|
G | A | 55 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0046others(52): Show | 55 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.179-13181G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122863140 | ||||||
chr4:122863209
|
C | T | 1 | a0001c0001t0001g0056 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.179-13112C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122863209 | ||||||
chr4:122863248
|
G | A | 211 | a0001c0001t0001g0004a0001c0001t0001g0041a0001c0001t0001g0042others(208): Show | 218 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(215): Show |
intron_variant | MODIFIER | c.179-13073G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122863248 | ||||||
chr4:122863566
|
A | G | 70 | a0001c0001t0001g0004a0001c0001t0002g0005a0001c0001t0002g0044others(67): Show | 72 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.179-12755A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122863566 | ||||||
chr4:122863766
|
T | C | 6 | a0001c0001t0013g0243a0001c0001t0013g0244a0001c0001t0013g0245others(3): Show | 6 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.179-12555T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122863766 | ||||||
chr4:122863770
|
G | T | 6 | a0001c0001t0013g0243a0001c0001t0013g0244a0001c0001t0013g0245others(3): Show | 6 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.179-12551G>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122863770 | ||||||
chr4:122863903
|
C | A | 3 | a0001c0001t0004g0227a0001c0001t0004g0228a0001c0001t0004g0229 | 3 | HG01243.hp1 HG02055.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.179-12418C>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122863903 | ||||||
chr4:122863931
|
A | G | 26 | a0001c0001t0005g0003a0001c0001t0005g0057a0001c0001t0005g0059others(23): Show | 28 | HG00099.hp1 HG00741.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.179-12390A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122863931 | ||||||
chr4:122863948
|
GTTCTTTA others(48): Show |
G | 6 | a0001c0001t0013g0243a0001c0001t0013g0244a0001c0001t0013g0245others(3): Show | 6 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.179-12363_179-1230 others(59): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122863948 | |||||
chr4:122864021
|
A | G | 4 | a0001c0001t0014g0127a0001c0001t0014g0143a0001c0001t0014g0157others(1): Show | 4 | HG03195.hp1 NA18522.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.179-12300A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122864021 | ||||||
chr4:122864029
|
T | C | 2 | a0001c0001t0037g0101a0001c0001t0049g0233 | 2 | HG01106.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.179-12292T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122864029 | ||||||
chr4:122864105
|
A | T | 12 | a0001c0001t0008g0006a0001c0001t0008g0116a0001c0001t0008g0159others(9): Show | 13 | HG01255.hp2 HG01346.hp2 HG01934.hp2 others(10): Show |
intron_variant | MODIFIER | c.179-12216A>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122864105 | ||||||
chr4:122864159
|
T | C | 26 | a0001c0001t0005g0003a0001c0001t0005g0057a0001c0001t0005g0059others(23): Show | 28 | HG00099.hp1 HG00741.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.179-12162T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122864159 | ||||||
chr4:122864293
|
C | T | 87 | a0001c0001t0001g0004a0001c0001t0001g0041a0001c0001t0001g0042others(84): Show | 90 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.179-12028C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122864293 | ||||||
chr4:122864297
|
T | C | 21 | a0001c0001t0007g0147a0001c0001t0007g0148a0001c0001t0007g0151others(18): Show | 22 | HG01361.hp1 HG01891.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.179-12024T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122864297 | ||||||
chr4:122864377
|
G | A | 1 | a0001c0001t0028g0216 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.179-11944G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122864377 | ||||||
chr4:122864475
|
T | C | 2 | a0001c0001t0018g0008a0001c0001t0018g0218 | 3 | HG00639.hp1 HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.179-11846T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122864475 | ||||||
chr4:122864553
|
C | T | 6 | a0001c0001t0013g0243a0001c0001t0013g0244a0001c0001t0013g0245others(3): Show | 6 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.179-11768C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122864553 | ||||||
chr4:122864623
|
G | A | 2 | a0001c0001t0036g0200a0001c0001t0044g0191 | 2 | HG02622.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.179-11698G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122864623 | ||||||
chr4:122864739
|
A | G | 1 | a0001c0001t0028g0216 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.179-11582A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122864739 | ||||||
chr4:122864959
|
A | G | 32 | a0001c0001t0005g0003a0001c0001t0005g0057a0001c0001t0005g0059others(29): Show | 34 | HG00099.hp1 HG00741.hp2 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.179-11362A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122864959 | ||||||
chr4:122865050
|
A | G | 4 | a0001c0001t0014g0127a0001c0001t0014g0143a0001c0001t0014g0157others(1): Show | 4 | HG03195.hp1 NA18522.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.179-11271A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122865050 | ||||||
chr4:122865125
|
A | G | 1 | a0001c0001t0029g0207 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.179-11196A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122865125 | ||||||
chr4:122865160
|
G | A | 13 | a0001c0001t0010g0167a0001c0001t0010g0206a0001c0001t0010g0220others(10): Show | 13 | HG01975.hp2 HG02055.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.179-11161G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122865160 | ||||||
chr4:122865269
|
C | T | 72 | a0001c0001t0001g0004a0001c0001t0002g0005a0001c0001t0002g0044others(69): Show | 75 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(72): Show |
intron_variant | MODIFIER | c.179-11052C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122865269 | ||||||
chr4:122865277
|
T | G | 88 | a0001c0001t0001g0004a0001c0001t0002g0005a0001c0001t0002g0044others(85): Show | 92 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.179-11044T>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122865277 | ||||||
chr4:122865277
|
TTTTG | T | 54 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0046others(51): Show | 54 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.179-11028_179-1102 others(8): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122865277 | |||||
chr4:122865376
|
C | T | 26 | a0001c0001t0005g0003a0001c0001t0005g0057a0001c0001t0005g0059others(23): Show | 28 | HG00099.hp1 HG00741.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.179-10945C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122865376 | ||||||
chr4:122865475
|
A | G | 3 | a0001c0001t0017g0123a0001c0001t0017g0130a0001c0001t0017g0149 | 3 | HG01975.hp2 HG02145.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.179-10846A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122865475 | ||||||
chr4:122865552
|
T | C | 6 | a0001c0001t0013g0243a0001c0001t0013g0244a0001c0001t0013g0245others(3): Show | 6 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.179-10769T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122865552 | ||||||
chr4:122865677
|
A | G | 211 | a0001c0001t0001g0004a0001c0001t0001g0041a0001c0001t0001g0042others(208): Show | 218 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(215): Show |
intron_variant | MODIFIER | c.179-10644A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122865677 | ||||||
chr4:122865706
|
T | C | 1 | a0001c0001t0045g0186 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.179-10615T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122865706 | ||||||
chr4:122865742
|
C | A | 1 | a0001c0001t0002g0074 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.179-10579C>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122865742 | ||||||
chr4:122865862
|
C | G | 1 | a0001c0001t0002g0076 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.179-10459C>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122865862 | ||||||
chr4:122865879
|
T | A | 2 | a0001c0001t0001g0155a0001c0001t0001g0156 | 2 | HG03669.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.179-10442T>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122865879 | ||||||
chr4:122865924
|
G | A | 123 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0046others(120): Show | 127 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.179-10397G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122865924 | ||||||
chr4:122865972
|
T | A | 2 | a0001c0001t0037g0101a0001c0001t0049g0233 | 2 | HG01106.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.179-10349T>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122865972 | ||||||
chr4:122866096
|
G | A | 1 | a0001c0001t0011g0240 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.179-10225G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122866096 | ||||||
chr4:122866165
|
C | G | 1 | a0001c0001t0034g0217 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.179-10156C>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122866165 | ||||||
chr4:122866165
|
C | T | 50 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0046others(47): Show | 50 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.179-10156C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122866165 | ||||||
chr4:122866186
|
A | G | 211 | a0001c0001t0001g0004a0001c0001t0001g0041a0001c0001t0001g0042others(208): Show | 218 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(215): Show |
intron_variant | MODIFIER | c.179-10135A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122866186 | ||||||
chr4:122866249
|
T | C | 1 | a0001c0001t0044g0191 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.179-10072T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122866249 | ||||||
chr4:122866294
|
G | A | 2 | a0001c0001t0001g0122a0001c0001t0016g0039 | 2 | HG02132.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.179-10027G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122866294 | ||||||
chr4:122866299
|
C | T | 1 | a0001c0001t0031g0247 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.179-10022C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122866299 | ||||||
chr4:122866325
|
G | A | 1 | a0001c0001t0029g0207 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.179-9996G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122866325 | ||||||
chr4:122866363
|
G | A | 1 | a0001c0001t0003g0119 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.179-9958G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122866363 | ||||||
chr4:122866367
|
C | CA | 106 | a0001c0001t0001g0004a0001c0001t0002g0005a0001c0001t0002g0044others(103): Show | 110 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.179-9940dupA | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122866367 | |||||
chr4:122866378
|
A | AT | 76 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0046others(73): Show | 76 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.179-9943_179-9942i others(3): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122866378 | ||||||
chr4:122866378
|
A | T | 3 | a0001c0001t0004g0197a0001c0001t0027g0204a0001c0001t0041g0226 | 3 | HG02897.hp1 HG02965.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.179-9943A>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122866378 | ||||||
chr4:122866392
|
T | A | 86 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0046others(83): Show | 88 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.179-9929T>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122866392 | ||||||
chr4:122866502
|
A | G | 4 | a0001c0001t0002g0076a0001c0001t0002g0081a0001c0001t0002g0082others(1): Show | 4 | HG00438.hp1 HG01884.hp2 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.179-9819A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122866502 | ||||||
chr4:122866537
|
G | T | 32 | a0001c0001t0005g0003a0001c0001t0005g0057a0001c0001t0005g0059others(29): Show | 34 | HG00099.hp1 HG00741.hp2 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.179-9784G>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122866537 | ||||||
chr4:122866572
|
A | G | 208 | a0001c0001t0001g0004a0001c0001t0001g0041a0001c0001t0001g0042others(205): Show | 214 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(211): Show |
intron_variant | MODIFIER | c.179-9749A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122866572 | ||||||
chr4:122866600
|
C | A | 1 | a0001c0001t0002g0133 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.179-9721C>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122866600 | ||||||
chr4:122866855
|
A | G | 13 | a0001c0001t0010g0167a0001c0001t0010g0206a0001c0001t0010g0220others(10): Show | 13 | HG01975.hp2 HG02055.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.179-9466A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122866855 | ||||||
chr4:122866872
|
T | C | 26 | a0001c0001t0005g0003a0001c0001t0005g0057a0001c0001t0005g0059others(23): Show | 28 | HG00099.hp1 HG00741.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.179-9449T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122866872 | ||||||
chr4:122867220
|
C | A | 211 | a0001c0001t0001g0004a0001c0001t0001g0041a0001c0001t0001g0042others(208): Show | 218 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(215): Show |
intron_variant | MODIFIER | c.179-9101C>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122867220 | ||||||
chr4:122867223
|
A | G | 1 | a0001c0001t0006g0034 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.179-9098A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122867223 | ||||||
chr4:122867340
|
T | C | 26 | a0001c0001t0005g0003a0001c0001t0005g0057a0001c0001t0005g0059others(23): Show | 28 | HG00099.hp1 HG00741.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.179-8981T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122867340 | ||||||
chr4:122867387
|
A | G | 1 | a0001c0001t0049g0233 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.179-8934A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122867387 | ||||||
chr4:122867486
|
G | T | 1 | a0001c0001t0049g0233 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.179-8835G>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122867486 | ||||||
chr4:122867513
|
A | T | 1 | a0001c0001t0015g0144 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.179-8808A>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122867513 | ||||||
chr4:122867536
|
G | C | 26 | a0001c0001t0005g0003a0001c0001t0005g0057a0001c0001t0005g0059others(23): Show | 28 | HG00099.hp1 HG00741.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.179-8785G>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122867536 | ||||||
chr4:122867586
|
C | G | 1 | a0001c0001t0031g0247 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.179-8735C>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122867586 | ||||||
chr4:122867793
|
T | C | 1 | a0001c0001t0049g0233 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.179-8528T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122867793 | ||||||
chr4:122867870
|
C | G | 1 | a0001c0001t0049g0233 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.179-8451C>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122867870 | ||||||
chr4:122867938
|
G | C | 4 | a0001c0001t0014g0127a0001c0001t0014g0143a0001c0001t0014g0157others(1): Show | 4 | HG03195.hp1 NA18522.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.179-8383G>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122867938 | ||||||
chr4:122867956
|
T | G | 6 | a0001c0001t0013g0243a0001c0001t0013g0244a0001c0001t0013g0245others(3): Show | 6 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.179-8365T>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122867956 | ||||||
chr4:122868083
|
G | A | 16 | a0001c0001t0008g0006a0001c0001t0008g0116a0001c0001t0008g0159others(13): Show | 17 | HG01255.hp2 HG01346.hp2 HG01934.hp2 others(14): Show |
intron_variant | MODIFIER | c.179-8238G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122868083 | ||||||
chr4:122868214
|
C | T | 16 | a0001c0001t0008g0006a0001c0001t0008g0116a0001c0001t0008g0159others(13): Show | 17 | HG01255.hp2 HG01346.hp2 HG01934.hp2 others(14): Show |
intron_variant | MODIFIER | c.179-8107C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122868214 | ||||||
chr4:122868252
|
C | T | 1 | a0001c0001t0001g0085 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.179-8069C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122868252 | ||||||
chr4:122868298
|
G | A | 16 | a0001c0001t0008g0006a0001c0001t0008g0116a0001c0001t0008g0159others(13): Show | 17 | HG01255.hp2 HG01346.hp2 HG01934.hp2 others(14): Show |
intron_variant | MODIFIER | c.179-8023G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122868298 | ||||||
chr4:122868428
|
T | C | 55 | a0001c0001t0001g0004a0001c0001t0001g0041a0001c0001t0001g0042others(52): Show | 56 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.179-7893T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122868428 | ||||||
chr4:122868481
|
C | T | 5 | a0001c0001t0010g0220a0001c0001t0010g0221a0001c0001t0010g0222others(2): Show | 5 | HG02572.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.179-7840C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122868481 | ||||||
chr4:122868543
|
C | T | 1 | a0001c0001t0013g0246 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.179-7778C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122868543 | ||||||
chr4:122868667
|
C | T | 55 | a0001c0001t0001g0004a0001c0001t0001g0041a0001c0001t0001g0042others(52): Show | 56 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.179-7654C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122868667 | ||||||
chr4:122868781
|
T | C | 24 | a0001c0001t0005g0003a0001c0001t0005g0057a0001c0001t0005g0059others(21): Show | 26 | HG00099.hp1 HG00741.hp2 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.179-7540T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122868781 | ||||||
chr4:122868912
|
T | C | 26 | a0001c0001t0005g0003a0001c0001t0005g0057a0001c0001t0005g0059others(23): Show | 28 | HG00099.hp1 HG00741.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.179-7409T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122868912 | ||||||
chr4:122868976
|
G | C | 2 | a0001c0001t0027g0204a0001c0001t0041g0226 | 2 | HG02965.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.179-7345G>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122868976 | ||||||
chr4:122869085
|
G | A | 1 | a0001c0001t0006g0040 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.179-7236G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122869085 | ||||||
chr4:122869281
|
C | T | 7 | a0001c0001t0010g0167a0001c0001t0010g0206a0001c0001t0010g0220others(4): Show | 7 | HG02572.hp1 HG02572.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.179-7040C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122869281 | ||||||
chr4:122869336
|
T | C | 55 | a0001c0001t0001g0004a0001c0001t0001g0041a0001c0001t0001g0042others(52): Show | 56 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.179-6985T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122869336 | ||||||
chr4:122869430
|
A | G | 6 | a0001c0001t0013g0243a0001c0001t0013g0244a0001c0001t0013g0245others(3): Show | 6 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.179-6891A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122869430 | ||||||
chr4:122869444
|
G | A | 6 | a0001c0001t0013g0243a0001c0001t0013g0244a0001c0001t0013g0245others(3): Show | 6 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.179-6877G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122869444 | ||||||
chr4:122869606
|
C | T | 2 | a0001c0001t0019g0022a0001c0001t0019g0023 | 2 | HG01255.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.179-6715C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122869606 | ||||||
chr4:122869774
|
A | G | 1 | a0001c0001t0008g0205 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.179-6547A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122869774 | ||||||
chr4:122869821
|
C | G | 68 | a0001c0001t0002g0005a0001c0001t0002g0044a0001c0001t0002g0045others(65): Show | 69 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.179-6500C>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122869821 | ||||||
chr4:122869897
|
C | A | 2 | a0001c0001t0002g0005a0001c0001t0002g0084 | 3 | NA18972.hp1 NA18984.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.179-6424C>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122869897 | ||||||
chr4:122869914
|
A | G | 124 | a0001c0001t0001g0004a0001c0001t0001g0041a0001c0001t0001g0042others(121): Show | 129 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.179-6407A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122869914 | ||||||
chr4:122869960
|
G | A | 6 | a0001c0001t0013g0243a0001c0001t0013g0244a0001c0001t0013g0245others(3): Show | 6 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.179-6361G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122869960 | ||||||
chr4:122870019
|
T | C | 3 | a0001c0001t0017g0123a0001c0001t0017g0130a0001c0001t0017g0149 | 3 | HG01975.hp2 HG02145.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.179-6302T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122870019 | ||||||
chr4:122870093
|
C | T | 1 | a0001c0001t0004g0029 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.179-6228C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122870093 | ||||||
chr4:122870170
|
C | T | 6 | a0001c0001t0013g0243a0001c0001t0013g0244a0001c0001t0013g0245others(3): Show | 6 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.179-6151C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122870170 | ||||||
chr4:122870198
|
G | A | 1 | a0001c0001t0002g0161 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.179-6123G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122870198 | ||||||
chr4:122870237
|
G | T | 1 | a0001c0001t0003g0043 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.179-6084G>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122870237 | ||||||
chr4:122870329
|
G | A | 54 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0046others(51): Show | 54 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.179-5992G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122870329 | ||||||
chr4:122870555
|
A | G | 26 | a0001c0001t0005g0003a0001c0001t0005g0057a0001c0001t0005g0059others(23): Show | 28 | HG00099.hp1 HG00741.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.179-5766A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122870555 | ||||||
chr4:122870556
|
C | T | 68 | a0001c0001t0002g0005a0001c0001t0002g0044a0001c0001t0002g0045others(65): Show | 69 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.179-5765C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122870556 | ||||||
chr4:122870882
|
T | G | 11 | a0001c0001t0008g0006a0001c0001t0008g0116a0001c0001t0008g0159others(8): Show | 12 | HG01255.hp2 HG01346.hp2 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.179-5439T>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122870882 | ||||||
chr4:122870911
|
T | C | 1 | a0001c0001t0002g0053 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.179-5410T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122870911 | ||||||
chr4:122870991
|
T | C | 1 | a0001c0001t0042g0015 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.179-5330T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122870991 | ||||||
chr4:122871064
|
C | T | 26 | a0001c0001t0005g0003a0001c0001t0005g0057a0001c0001t0005g0059others(23): Show | 28 | HG00099.hp1 HG00741.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.179-5257C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122871064 | ||||||
chr4:122871173
|
C | T | 6 | a0001c0001t0013g0243a0001c0001t0013g0244a0001c0001t0013g0245others(3): Show | 6 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.179-5148C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122871173 | ||||||
chr4:122871188
|
C | CTGTT | 32 | a0001c0001t0005g0003a0001c0001t0005g0057a0001c0001t0005g0059others(29): Show | 34 | HG00099.hp1 HG00741.hp2 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.179-5132_179-5129d others(6): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122871188 | |||||
chr4:122871209
|
T | C | 6 | a0001c0001t0013g0243a0001c0001t0013g0244a0001c0001t0013g0245others(3): Show | 6 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.179-5112T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122871209 | ||||||
chr4:122871277
|
G | A | 1 | a0001c0001t0049g0233 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.179-5044G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122871277 | ||||||
chr4:122871302
|
T | TGGGGTC | 3 | a0001c0001t0004g0227a0001c0001t0004g0228a0001c0001t0004g0229 | 3 | HG01243.hp1 HG02055.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.179-5014_179-5013i others(8): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122871302 | |||||
chr4:122871465
|
T | A | 2 | a0001c0001t0037g0101a0001c0001t0049g0233 | 2 | HG01106.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.179-4856T>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122871465 | ||||||
chr4:122871528
|
C | T | 1 | a0001c0001t0031g0247 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.179-4793C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122871528 | ||||||
chr4:122871673
|
C | T | 1 | a0001c0001t0010g0167 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.179-4648C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122871673 | ||||||
chr4:122871692
|
T | A | 16 | a0001c0001t0008g0006a0001c0001t0008g0116a0001c0001t0008g0159others(13): Show | 17 | HG01255.hp2 HG01346.hp2 HG01934.hp2 others(14): Show |
intron_variant | MODIFIER | c.179-4629T>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122871692 | ||||||
chr4:122871781
|
C | CA | 13 | a0001c0001t0001g0056a0001c0001t0001g0092a0001c0001t0002g0061others(10): Show | 13 | HG00741.hp1 HG01167.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.179-4523dupA | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122871781 | |||||
chr4:122871781
|
C | CAA | 44 | a0001c0001t0005g0003a0001c0001t0005g0057a0001c0001t0005g0059others(41): Show | 47 | HG00099.hp1 HG00741.hp2 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.179-4524_179-4523d others(4): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122871781 | |||||
chr4:122871781
|
C | CAAA | 9 | a0001c0001t0005g0105a0001c0001t0005g0141a0001c0001t0010g0220others(6): Show | 9 | HG01175.hp1 HG02572.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.179-4525_179-4523d others(5): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122871781 | |||||
chr4:122871781
|
C | CAAAA | 6 | a0001c0001t0013g0243a0001c0001t0013g0244a0001c0001t0013g0245others(3): Show | 6 | HG01106.hp1 HG01192.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.179-4526_179-4523d others(6): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122871781 | |||||
chr4:122871781
|
CA | C | 8 | a0001c0001t0001g0042a0001c0001t0001g0068a0001c0001t0001g0080others(5): Show | 8 | HG01346.hp1 HG01361.hp2 HG01517.hp2 others(5): Show |
intron_variant | MODIFIER | c.179-4523delA | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122871781 | |||||
chr4:122871781
|
CAA | C | 18 | a0001c0001t0007g0147a0001c0001t0007g0148a0001c0001t0007g0151others(15): Show | 18 | HG01361.hp1 HG01891.hp1 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.179-4524_179-4523d others(4): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122871781 | |||||
chr4:122871809
|
GCAA | G | 16 | a0001c0001t0008g0006a0001c0001t0008g0116a0001c0001t0008g0159others(13): Show | 17 | HG01255.hp2 HG01346.hp2 HG01934.hp2 others(14): Show |
intron_variant | MODIFIER | c.179-4503_179-4501d others(5): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122871809 | |||||
chr4:122871915
|
GA | G | 230 | a0001c0001t0001g0004a0001c0001t0001g0041a0001c0001t0001g0042others(227): Show | 237 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(234): Show |
intron_variant | MODIFIER | c.179-4403delA | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122871915 | |||||
chr4:122871923
|
C | T | 1 | a0001c0001t0033g0150 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.179-4398C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122871923 | ||||||
chr4:122871932
|
G | T | 71 | a0001c0001t0002g0005a0001c0001t0002g0044a0001c0001t0002g0045others(68): Show | 73 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.179-4389G>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122871932 | ||||||
chr4:122872010
|
A | G | 1 | a0001c0001t0003g0069 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.179-4311A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122872010 | ||||||
chr4:122872258
|
T | C | 21 | a0001c0001t0007g0147a0001c0001t0007g0148a0001c0001t0007g0151others(18): Show | 22 | HG01361.hp1 HG01891.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.179-4063T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122872258 | ||||||
chr4:122872294
|
C | T | 1 | a0001c0001t0012g0011 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.179-4027C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122872294 | ||||||
chr4:122872335
|
T | G | 2 | a0001c0001t0008g0205a0001c0001t0019g0014 | 2 | HG02280.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.179-3986T>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122872335 | ||||||
chr4:122872385
|
G | A | 21 | a0001c0001t0007g0147a0001c0001t0007g0148a0001c0001t0007g0151others(18): Show | 22 | HG01361.hp1 HG01891.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.179-3936G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122872385 | ||||||
chr4:122872396
|
C | T | 1 | a0001c0001t0003g0171 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.179-3925C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122872396 | ||||||
chr4:122872691
|
A | G | 2 | a0001c0001t0020g0009a0001c0001t0020g0239 | 3 | HG02145.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.179-3630A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122872691 | ||||||
chr4:122872718
|
A | C | 13 | a0001c0001t0010g0167a0001c0001t0010g0206a0001c0001t0010g0220others(10): Show | 13 | HG01975.hp2 HG02055.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.179-3603A>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122872718 | ||||||
chr4:122872813
|
A | G | 6 | a0001c0001t0013g0243a0001c0001t0013g0244a0001c0001t0013g0245others(3): Show | 6 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.179-3508A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122872813 | ||||||
chr4:122872829
|
G | A | 1 | a0001c0001t0028g0216 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.179-3492G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122872829 | ||||||
chr4:122872858
|
C | A | 123 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0046others(120): Show | 127 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.179-3463C>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122872858 | ||||||
chr4:122872858
|
C | T | 1 | a0001c0001t0031g0247 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.179-3463C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122872858 | ||||||
chr4:122872972
|
T | C | 55 | a0001c0001t0001g0004a0001c0001t0001g0041a0001c0001t0001g0042others(52): Show | 56 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.179-3349T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122872972 | ||||||
chr4:122873015
|
C | A | 71 | a0001c0001t0002g0005a0001c0001t0002g0044a0001c0001t0002g0045others(68): Show | 73 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.179-3306C>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122873015 | ||||||
chr4:122873297
|
C | G | 1 | a0001c0001t0015g0144 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.179-3024C>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122873297 | ||||||
chr4:122873556
|
CA | C | 6 | a0001c0001t0013g0243a0001c0001t0013g0244a0001c0001t0013g0245others(3): Show | 6 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.179-2763delA | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122873556 | |||||
chr4:122873597
|
A | G | 12 | a0001c0001t0008g0006a0001c0001t0008g0116a0001c0001t0008g0159others(9): Show | 13 | HG01255.hp2 HG01346.hp2 HG01934.hp2 others(10): Show |
intron_variant | MODIFIER | c.179-2724A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122873597 | ||||||
chr4:122873807
|
T | A | 6 | a0001c0001t0013g0243a0001c0001t0013g0244a0001c0001t0013g0245others(3): Show | 6 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.179-2514T>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122873807 | ||||||
chr4:122873830
|
AATGGAAA others(1): Show |
A | 15 | a0001c0001t0010g0167a0001c0001t0010g0206a0001c0001t0010g0220others(12): Show | 15 | HG01975.hp2 HG02055.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.179-2489_179-2482d others(10): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122873830 | |||||
chr4:122873952
|
A | G | 5 | a0001c0001t0004g0194a0001c0001t0004g0195a0001c0001t0004g0196others(2): Show | 5 | HG01168.hp1 HG02818.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.179-2369A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122873952 | ||||||
chr4:122874120
|
C | G | 1 | a0001c0001t0026g0202 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.179-2201C>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122874120 | ||||||
chr4:122874182
|
A | T | 26 | a0001c0001t0005g0003a0001c0001t0005g0057a0001c0001t0005g0059others(23): Show | 28 | HG00099.hp1 HG00741.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.179-2139A>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122874182 | ||||||
chr4:122874253
|
G | A | 26 | a0001c0001t0005g0003a0001c0001t0005g0057a0001c0001t0005g0059others(23): Show | 28 | HG00099.hp1 HG00741.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.179-2068G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122874253 | ||||||
chr4:122874288
|
C | T | 3 | a0001c0001t0026g0202a0001c0001t0036g0200a0001c0001t0044g0191 | 3 | HG02622.hp2 HG03041.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.179-2033C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122874288 | ||||||
chr4:122874353
|
T | C | 16 | a0001c0001t0008g0006a0001c0001t0008g0116a0001c0001t0008g0159others(13): Show | 17 | HG01255.hp2 HG01346.hp2 HG01934.hp2 others(14): Show |
intron_variant | MODIFIER | c.179-1968T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122874353 | ||||||
chr4:122874498
|
A | G | 26 | a0001c0001t0005g0003a0001c0001t0005g0057a0001c0001t0005g0059others(23): Show | 28 | HG00099.hp1 HG00741.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.179-1823A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122874498 | ||||||
chr4:122874663
|
T | C | 1 | a0001c0001t0003g0171 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.179-1658T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122874663 | ||||||
chr4:122874729
|
A | T | 211 | a0001c0001t0001g0004a0001c0001t0001g0041a0001c0001t0001g0042others(208): Show | 218 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(215): Show |
intron_variant | MODIFIER | c.179-1592A>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122874729 | ||||||
chr4:122874749
|
A | G | 1 | a0001c0001t0049g0233 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.179-1572A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122874749 | ||||||
chr4:122874813
|
C | T | 6 | a0001c0001t0013g0243a0001c0001t0013g0244a0001c0001t0013g0245others(3): Show | 6 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.179-1508C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122874813 | ||||||
chr4:122874952
|
T | G | 55 | a0001c0001t0001g0004a0001c0001t0001g0041a0001c0001t0001g0042others(52): Show | 56 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.179-1369T>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122874952 | ||||||
chr4:122875107
|
C | A | 1 | a0001c0001t0015g0144 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.179-1214C>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122875107 | ||||||
chr4:122875308
|
C | G | 24 | a0001c0001t0005g0003a0001c0001t0005g0057a0001c0001t0005g0059others(21): Show | 26 | HG00099.hp1 HG00741.hp2 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.179-1013C>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122875308 | ||||||
chr4:122875386
|
G | A | 68 | a0001c0001t0002g0005a0001c0001t0002g0044a0001c0001t0002g0045others(65): Show | 69 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.179-935G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122875386 | ||||||
chr4:122875427
|
C | CAAAAAAA others(270): Show |
1 | a0001c0001t0001g0080 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.179-877_179-876ins others(277): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122875427 | |||||
chr4:122875427
|
C | CAAAAAAA others(271): Show |
47 | a0001c0001t0001g0004a0001c0001t0001g0041a0001c0001t0001g0046others(44): Show | 48 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.179-877_179-876ins others(278): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122875427 | |||||
chr4:122875427
|
C | CAAAAAAA others(272): Show |
7 | a0001c0001t0001g0042a0001c0001t0001g0049a0001c0001t0001g0102others(4): Show | 7 | HG01358.hp1 HG01517.hp2 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.179-877_179-876ins others(279): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr4 | 122875427 | |||||
chr4:122875580
|
A | G | 32 | a0001c0001t0005g0003a0001c0001t0005g0057a0001c0001t0005g0059others(29): Show | 34 | HG00099.hp1 HG00741.hp2 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.179-741A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122875580 | ||||||
chr4:122875590
|
C | T | 6 | a0001c0001t0013g0243a0001c0001t0013g0244a0001c0001t0013g0245others(3): Show | 6 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.179-731C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122875590 | ||||||
chr4:122875633
|
G | A | 1 | a0001c0001t0003g0146 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.179-688G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122875633 | ||||||
chr4:122875635
|
G | A | 1 | a0001c0001t0034g0217 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.179-686G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122875635 | ||||||
chr4:122875697
|
C | T | 6 | a0001c0001t0013g0243a0001c0001t0013g0244a0001c0001t0013g0245others(3): Show | 6 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.179-624C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122875697 | ||||||
chr4:122875801
|
C | T | 1 | a0001c0001t0039g0198 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.179-520C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122875801 | ||||||
chr4:122875843
|
G | C | 1 | a0001c0001t0001g0094 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.179-478G>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122875843 | ||||||
chr4:122875944
|
C | T | 1 | a0001c0001t0009g0169 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.179-377C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122875944 | ||||||
chr4:122876028
|
C | T | 6 | a0001c0001t0013g0243a0001c0001t0013g0244a0001c0001t0013g0245others(3): Show | 6 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.179-293C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122876028 | ||||||
chr4:122876099
|
A | T | 2 | a0001c0001t0002g0075a0001c0001t0006g0026 | 2 | NA18957.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.179-222A>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122876099 | ||||||
chr4:122876273
|
G | T | 11 | a0001c0001t0008g0006a0001c0001t0008g0116a0001c0001t0008g0159others(8): Show | 12 | HG01255.hp2 HG01346.hp2 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.179-48G>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122876273 | ||||||
chr4:122876313
|
C | T | 1 | a0001c0001t0037g0101 | 1 | NA18966.hp1 | splice_region_variant&intron_variant | LOW | c.179-8C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 1/2 | chr4 | 122876313 | ||||||
chr4:122876449
|
C | T | 6 | a0001c0001t0013g0243a0001c0001t0013g0244a0001c0001t0013g0245others(3): Show | 6 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.282+25C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122876449 | ||||||
chr4:122876700
|
T | G | 2 | a0001c0001t0003g0172a0001c0001t0003g0173 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.282+276T>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122876700 | ||||||
chr4:122876756
|
T | C | 1 | a0001c0001t0037g0101 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.282+332T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122876756 | ||||||
chr4:122876768
|
G | A | 24 | a0001c0001t0005g0003a0001c0001t0005g0057a0001c0001t0005g0059others(21): Show | 26 | HG00099.hp1 HG00741.hp2 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.282+344G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122876768 | ||||||
chr4:122876787
|
A | G | 211 | a0001c0001t0001g0004a0001c0001t0001g0041a0001c0001t0001g0042others(208): Show | 218 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(215): Show |
intron_variant | MODIFIER | c.282+363A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122876787 | ||||||
chr4:122876796
|
G | A | 2 | a0001c0001t0002g0133a0001c0001t0002g0213 | 2 | HG01168.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.282+372G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122876796 | ||||||
chr4:122877028
|
C | T | 26 | a0001c0001t0005g0003a0001c0001t0005g0057a0001c0001t0005g0059others(23): Show | 28 | HG00099.hp1 HG00741.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.282+604C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122877028 | ||||||
chr4:122877105
|
CT | C | 6 | a0001c0001t0003g0172a0001c0001t0010g0220a0001c0001t0010g0221others(3): Show | 6 | HG01257.hp2 HG02572.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.282+691delT | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr4 | 122877105 | |||||
chr4:122877115
|
T | C | 2 | a0001c0001t0026g0202a0001c0001t0049g0233 | 2 | HG01106.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.282+691T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122877115 | ||||||
chr4:122877116
|
C | CT | 35 | a0001c0001t0005g0003a0001c0001t0005g0057a0001c0001t0005g0059others(32): Show | 38 | HG00099.hp1 HG00609.hp2 HG00741.hp2 others(35): Show |
intron_variant | MODIFIER | c.282+703dupT | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr4 | 122877116 | |||||
chr4:122877116
|
C | T | 2 | a0001c0001t0026g0202a0001c0001t0049g0233 | 2 | HG01106.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.282+692C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122877116 | ||||||
chr4:122877150
|
C | T | 1 | a0001c0001t0015g0203 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.282+726C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122877150 | ||||||
chr4:122877151
|
G | A | 1 | a0001c0001t0012g0031 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.282+727G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122877151 | ||||||
chr4:122877211
|
G | A | 21 | a0001c0001t0007g0147a0001c0001t0007g0148a0001c0001t0007g0151others(18): Show | 22 | HG01361.hp1 HG01891.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.282+787G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122877211 | ||||||
chr4:122877273
|
T | C | 87 | a0001c0001t0001g0004a0001c0001t0001g0041a0001c0001t0001g0042others(84): Show | 90 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.282+849T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122877273 | ||||||
chr4:122877310
|
G | A | 1 | a0001c0001t0026g0202 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.282+886G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122877310 | ||||||
chr4:122877532
|
G | A | 1 | a0001c0001t0002g0081 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.282+1108G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122877532 | ||||||
chr4:122877556
|
T | C | 26 | a0001c0001t0005g0003a0001c0001t0005g0057a0001c0001t0005g0059others(23): Show | 28 | HG00099.hp1 HG00741.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.282+1132T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122877556 | ||||||
chr4:122877628
|
A | G | 1 | a0001c0001t0001g0085 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.282+1204A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122877628 | ||||||
chr4:122877695
|
A | C | 1 | a0001c0001t0047g0183 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.282+1271A>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122877695 | ||||||
chr4:122877719
|
C | T | 2 | a0001c0001t0037g0101a0001c0001t0049g0233 | 2 | HG01106.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.282+1295C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122877719 | ||||||
chr4:122877838
|
A | C | 55 | a0001c0001t0001g0004a0001c0001t0001g0041a0001c0001t0001g0042others(52): Show | 56 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.282+1414A>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122877838 | ||||||
chr4:122877846
|
A | C | 18 | a0001c0001t0007g0147a0001c0001t0007g0148a0001c0001t0007g0151others(15): Show | 18 | HG01361.hp1 HG01891.hp1 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.282+1422A>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122877846 | ||||||
chr4:122877875
|
A | T | 1 | a0001c0001t0009g0201 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.282+1451A>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122877875 | ||||||
chr4:122878092
|
C | A | 1 | a0001c0001t0002g0074 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.282+1668C>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122878092 | ||||||
chr4:122878170
|
A | G | 26 | a0001c0001t0005g0003a0001c0001t0005g0057a0001c0001t0005g0059others(23): Show | 28 | HG00099.hp1 HG00741.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.282+1746A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122878170 | ||||||
chr4:122878320
|
G | T | 2 | a0001c0001t0027g0204a0001c0001t0041g0226 | 2 | HG02965.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.282+1896G>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122878320 | ||||||
chr4:122878342
|
T | A | 1 | a0001c0001t0008g0160 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.282+1918T>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122878342 | ||||||
chr4:122878499
|
G | A | 2 | a0001c0001t0037g0101a0001c0001t0049g0233 | 2 | HG01106.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.282+2075G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122878499 | ||||||
chr4:122878651
|
G | A | 21 | a0001c0001t0007g0147a0001c0001t0007g0148a0001c0001t0007g0151others(18): Show | 22 | HG01361.hp1 HG01891.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.282+2227G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122878651 | ||||||
chr4:122878752
|
G | C | 1 | a0001c0001t0001g0085 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.282+2328G>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122878752 | ||||||
chr4:122878832
|
A | G | 210 | a0001c0001t0001g0004a0001c0001t0001g0041a0001c0001t0001g0042others(207): Show | 217 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.282+2408A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122878832 | ||||||
chr4:122878893
|
G | A | 16 | a0001c0001t0008g0006a0001c0001t0008g0116a0001c0001t0008g0159others(13): Show | 17 | HG01255.hp2 HG01346.hp2 HG01934.hp2 others(14): Show |
intron_variant | MODIFIER | c.282+2469G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122878893 | ||||||
chr4:122879126
|
C | A | 1 | a0001c0001t0007g0162 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.282+2702C>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122879126 | ||||||
chr4:122879177
|
A | G | 1 | a0001c0001t0002g0112 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.282+2753A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122879177 | ||||||
chr4:122879251
|
A | C | 211 | a0001c0001t0001g0004a0001c0001t0001g0041a0001c0001t0001g0042others(208): Show | 218 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(215): Show |
intron_variant | MODIFIER | c.282+2827A>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122879251 | ||||||
chr4:122879389
|
A | G | 1 | a0001c0001t0001g0041 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.282+2965A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122879389 | ||||||
chr4:122879462
|
A | G | 21 | a0001c0001t0005g0003a0001c0001t0005g0057a0001c0001t0005g0059others(18): Show | 23 | HG00099.hp1 HG00741.hp2 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.282+3038A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122879462 | ||||||
chr4:122879581
|
A | G | 1 | a0001c0001t0012g0011 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.282+3157A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122879581 | ||||||
chr4:122879613
|
A | C | 71 | a0001c0001t0002g0005a0001c0001t0002g0044a0001c0001t0002g0045others(68): Show | 73 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.282+3189A>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122879613 | ||||||
chr4:122879614
|
T | A | 2 | a0001c0001t0027g0204a0001c0001t0041g0226 | 2 | HG02965.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.282+3190T>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122879614 | ||||||
chr4:122879731
|
A | G | 1 | a0001c0001t0031g0247 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.282+3307A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122879731 | ||||||
chr4:122879752
|
G | A | 2 | a0001c0001t0037g0101a0001c0001t0049g0233 | 2 | HG01106.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.282+3328G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122879752 | ||||||
chr4:122879777
|
G | T | 211 | a0001c0001t0001g0004a0001c0001t0001g0041a0001c0001t0001g0042others(208): Show | 218 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(215): Show |
intron_variant | MODIFIER | c.282+3353G>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122879777 | ||||||
chr4:122879935
|
A | T | 1 | a0001c0001t0033g0150 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.282+3511A>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122879935 | ||||||
chr4:122880075
|
A | C | 1 | a0001c0001t0031g0247 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.282+3651A>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122880075 | ||||||
chr4:122880201
|
C | T | 11 | a0001c0001t0008g0006a0001c0001t0008g0116a0001c0001t0008g0159others(8): Show | 12 | HG01255.hp2 HG01346.hp2 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.282+3777C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122880201 | ||||||
chr4:122880245
|
C | CT | 40 | a0001c0001t0001g0052a0001c0001t0001g0103a0001c0001t0004g0227others(37): Show | 42 | HG01109.hp1 HG01192.hp2 HG01255.hp2 others(39): Show |
intron_variant | MODIFIER | c.282+3840dupT | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr4 | 122880245 | |||||
chr4:122880245
|
C | CTT | 5 | a0001c0001t0005g0003a0001c0001t0005g0105a0001c0001t0008g0116others(2): Show | 6 | HG01106.hp1 HG01175.hp1 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.282+3839_282+3840d others(4): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr4 | 122880245 | |||||
chr4:122880278
|
G | A | 14 | a0001c0001t0010g0167a0001c0001t0010g0206a0001c0001t0010g0220others(11): Show | 14 | HG01975.hp2 HG02055.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.282+3854G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122880278 | ||||||
chr4:122880339
|
C | T | 2 | a0001c0001t0037g0101a0001c0001t0049g0233 | 2 | HG01106.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.282+3915C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122880339 | ||||||
chr4:122880347
|
C | T | 17 | a0001c0001t0008g0006a0001c0001t0008g0116a0001c0001t0008g0159others(14): Show | 18 | HG01255.hp2 HG01346.hp2 HG01934.hp2 others(15): Show |
intron_variant | MODIFIER | c.282+3923C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122880347 | ||||||
chr4:122880373
|
A | G | 1 | a0001c0001t0010g0224 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.282+3949A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122880373 | ||||||
chr4:122880407
|
C | T | 24 | a0001c0001t0005g0003a0001c0001t0005g0057a0001c0001t0005g0059others(21): Show | 26 | HG00099.hp1 HG00741.hp2 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.282+3983C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122880407 | ||||||
chr4:122880528
|
G | A | 13 | a0001c0001t0010g0167a0001c0001t0010g0206a0001c0001t0010g0220others(10): Show | 13 | HG01975.hp2 HG02055.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.282+4104G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122880528 | ||||||
chr4:122880737
|
T | C | 2 | a0001c0001t0003g0241a0001c0001t0003g0242 | 2 | HG02630.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.282+4313T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122880737 | ||||||
chr4:122880757
|
T | A | 1 | a0001c0001t0009g0201 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.282+4333T>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122880757 | ||||||
chr4:122880803
|
C | T | 1 | a0001c0001t0008g0116 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.282+4379C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122880803 | ||||||
chr4:122880848
|
C | T | 2 | a0001c0001t0006g0036a0001c0001t0038g0030 | 2 | HG01255.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.282+4424C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122880848 | ||||||
chr4:122881009
|
C | T | 3 | a0001c0001t0011g0187a0001c0001t0011g0190a0001c0001t0011g0192 | 3 | HG01891.hp1 HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.282+4585C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122881009 | ||||||
chr4:122881015
|
GA | G | 6 | a0001c0001t0013g0243a0001c0001t0013g0244a0001c0001t0013g0245others(3): Show | 6 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.282+4593delA | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr4 | 122881015 | |||||
chr4:122881060
|
G | A | 1 | a0001c0001t0007g0168 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.282+4636G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122881060 | ||||||
chr4:122881164
|
A | T | 5 | a0001c0001t0010g0220a0001c0001t0010g0221a0001c0001t0010g0222others(2): Show | 5 | HG02572.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.282+4740A>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122881164 | ||||||
chr4:122881277
|
C | T | 1 | a0001c0001t0047g0183 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.282+4853C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122881277 | ||||||
chr4:122881537
|
G | A | 2 | a0001c0001t0027g0204a0001c0001t0041g0226 | 2 | HG02965.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.282+5113G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122881537 | ||||||
chr4:122881576
|
G | A | 1 | a0001c0001t0028g0216 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.282+5152G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122881576 | ||||||
chr4:122881600
|
A | G | 1 | a0001c0001t0031g0247 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.282+5176A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122881600 | ||||||
chr4:122881620
|
G | A | 1 | a0001c0001t0005g0134 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.282+5196G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122881620 | ||||||
chr4:122881624
|
TTCATTGT others(5): Show |
T | 1 | a0001c0001t0031g0247 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.282+5206_282+5217d others(14): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr4 | 122881624 | |||||
chr4:122881710
|
C | T | 2 | a0001c0001t0037g0101a0001c0001t0049g0233 | 2 | HG01106.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.282+5286C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122881710 | ||||||
chr4:122881774
|
C | T | 55 | a0001c0001t0001g0004a0001c0001t0001g0041a0001c0001t0001g0042others(52): Show | 56 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.282+5350C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122881774 | ||||||
chr4:122881775
|
G | A | 7 | a0001c0001t0009g0007a0001c0001t0009g0169a0001c0001t0009g0180others(4): Show | 8 | HG01109.hp1 HG01884.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.282+5351G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122881775 | ||||||
chr4:122881813
|
C | A | 1 | a0001c0001t0049g0233 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.282+5389C>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122881813 | ||||||
chr4:122881939
|
G | A | 21 | a0001c0001t0007g0147a0001c0001t0007g0148a0001c0001t0007g0151others(18): Show | 22 | HG01361.hp1 HG01891.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.282+5515G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122881939 | ||||||
chr4:122881977
|
A | G | 1 | a0001c0001t0031g0247 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.282+5553A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122881977 | ||||||
chr4:122882124
|
C | T | 2 | a0001c0001t0037g0101a0001c0001t0049g0233 | 2 | HG01106.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.282+5700C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122882124 | ||||||
chr4:122882215
|
C | T | 55 | a0001c0001t0001g0004a0001c0001t0001g0041a0001c0001t0001g0042others(52): Show | 56 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.282+5791C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122882215 | ||||||
chr4:122882518
|
A | G | 21 | a0001c0001t0007g0147a0001c0001t0007g0148a0001c0001t0007g0151others(18): Show | 22 | HG01361.hp1 HG01891.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.282+6094A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122882518 | ||||||
chr4:122882573
|
T | C | 5 | a0001c0001t0007g0147a0001c0001t0007g0151a0001c0001t0007g0152others(2): Show | 5 | HG02809.hp1 HG02922.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.282+6149T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122882573 | ||||||
chr4:122882716
|
G | A | 1 | a0001c0001t0001g0092 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.282+6292G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122882716 | ||||||
chr4:122882829
|
C | T | 1 | a0001c0001t0031g0247 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.282+6405C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122882829 | ||||||
chr4:122883207
|
C | T | 6 | a0001c0001t0013g0243a0001c0001t0013g0244a0001c0001t0013g0245others(3): Show | 6 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.282+6783C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122883207 | ||||||
chr4:122883366
|
C | G | 15 | a0001c0001t0010g0167a0001c0001t0010g0206a0001c0001t0010g0220others(12): Show | 15 | HG01975.hp2 HG02055.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.282+6942C>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122883366 | ||||||
chr4:122883394
|
G | T | 1 | a0001c0001t0002g0238 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.282+6970G>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122883394 | ||||||
chr4:122883487
|
T | C | 1 | a0001c0001t0002g0133 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.282+7063T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122883487 | ||||||
chr4:122883553
|
G | A | 1 | a0001c0001t0019g0022 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.282+7129G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122883553 | ||||||
chr4:122883666
|
G | A | 6 | a0001c0001t0013g0243a0001c0001t0013g0244a0001c0001t0013g0245others(3): Show | 6 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.282+7242G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122883666 | ||||||
chr4:122883794
|
C | A | 18 | a0001c0001t0007g0147a0001c0001t0007g0148a0001c0001t0007g0151others(15): Show | 18 | HG01361.hp1 HG01891.hp1 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.282+7370C>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122883794 | ||||||
chr4:122884009
|
C | G | 1 | a0001c0001t0003g0043 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.282+7585C>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122884009 | ||||||
chr4:122884073
|
G | A | 1 | a0001c0001t0002g0139 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.282+7649G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122884073 | ||||||
chr4:122884226
|
G | A | 6 | a0001c0001t0013g0243a0001c0001t0013g0244a0001c0001t0013g0245others(3): Show | 6 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.282+7802G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122884226 | ||||||
chr4:122884276
|
T | C | 6 | a0001c0001t0008g0006a0001c0001t0008g0159a0001c0001t0008g0160others(3): Show | 7 | HG02280.hp1 HG03098.hp2 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.282+7852T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122884276 | ||||||
chr4:122884314
|
C | T | 15 | a0001c0001t0010g0167a0001c0001t0010g0206a0001c0001t0010g0220others(12): Show | 15 | HG01975.hp2 HG02055.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.282+7890C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122884314 | ||||||
chr4:122884422
|
G | A | 16 | a0001c0001t0008g0006a0001c0001t0008g0116a0001c0001t0008g0159others(13): Show | 17 | HG01255.hp2 HG01346.hp2 HG01934.hp2 others(14): Show |
intron_variant | MODIFIER | c.283-7789G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122884422 | ||||||
chr4:122884710
|
C | T | 2 | a0001c0001t0037g0101a0001c0001t0049g0233 | 2 | HG01106.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.283-7501C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122884710 | ||||||
chr4:122884757
|
TAGGAGTG others(34): Show |
T | 1 | a0001c0001t0015g0203 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.283-7451_283-7411d others(43): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr4 | 122884757 | |||||
chr4:122884776
|
T | C | 1 | a0001c0001t0003g0098 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.283-7435T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122884776 | ||||||
chr4:122884796
|
G | A | 1 | a0001c0001t0031g0247 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.283-7415G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122884796 | ||||||
chr4:122884853
|
G | A | 1 | a0001c0001t0002g0237 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.283-7358G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122884853 | ||||||
chr4:122884914
|
A | T | 55 | a0001c0001t0001g0004a0001c0001t0001g0041a0001c0001t0001g0042others(52): Show | 56 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.283-7297A>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122884914 | ||||||
chr4:122884940
|
G | C | 2 | a0001c0001t0027g0204a0001c0001t0041g0226 | 2 | HG02965.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.283-7271G>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122884940 | ||||||
chr4:122885233
|
G | C | 2 | a0001c0001t0027g0204a0001c0001t0041g0226 | 2 | HG02965.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.283-6978G>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122885233 | ||||||
chr4:122885383
|
T | C | 1 | a0001c0001t0049g0233 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.283-6828T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122885383 | ||||||
chr4:122885722
|
A | T | 2 | a0001c0001t0005g0003a0001c0001t0005g0105 | 3 | HG01175.hp1 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.283-6489A>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122885722 | ||||||
chr4:122885913
|
C | CT | 39 | a0001c0001t0002g0045a0001c0001t0002g0053a0001c0001t0003g0119others(36): Show | 40 | HG01175.hp2 HG01243.hp1 HG01255.hp2 others(37): Show |
intron_variant | MODIFIER | c.283-6275dupT | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr4 | 122885913 | |||||
chr4:122885913
|
C | CTT | 7 | a0001c0001t0004g0199a0001c0001t0007g0168a0001c0001t0011g0184others(4): Show | 7 | HG01106.hp1 HG01361.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.283-6276_283-6275d others(4): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr4 | 122885913 | |||||
chr4:122885913
|
CT | C | 44 | a0001c0001t0002g0137a0001c0001t0002g0177a0001c0001t0003g0002others(41): Show | 47 | HG00099.hp1 HG00741.hp2 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.283-6275delT | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr4 | 122885913 | |||||
chr4:122885913
|
CTTTTTTT others(1): Show |
C | 57 | a0001c0001t0001g0004a0001c0001t0001g0041a0001c0001t0001g0042others(54): Show | 59 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.283-6282_283-6275d others(10): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr4 | 122885913 | |||||
chr4:122885914
|
T | C | 5 | a0001c0001t0013g0243a0001c0001t0013g0244a0001c0001t0013g0245others(2): Show | 5 | HG01192.hp2 HG02280.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.283-6297T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122885914 | ||||||
chr4:122885995
|
C | T | 2 | a0001c0001t0017g0130a0001c0001t0017g0149 | 2 | HG01975.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.283-6216C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122885995 | ||||||
chr4:122886005
|
A | G | 6 | a0001c0001t0013g0243a0001c0001t0013g0244a0001c0001t0013g0245others(3): Show | 6 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.283-6206A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122886005 | ||||||
chr4:122886039
|
C | T | 1 | a0001c0001t0007g0147 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.283-6172C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122886039 | ||||||
chr4:122886107
|
G | A | 69 | a0001c0001t0002g0005a0001c0001t0002g0044a0001c0001t0002g0045others(66): Show | 70 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.283-6104G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122886107 | ||||||
chr4:122886124
|
T | C | 55 | a0001c0001t0001g0004a0001c0001t0001g0041a0001c0001t0001g0042others(52): Show | 56 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.283-6087T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122886124 | ||||||
chr4:122886217
|
A | G | 210 | a0001c0001t0001g0004a0001c0001t0001g0041a0001c0001t0001g0042others(207): Show | 217 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.283-5994A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122886217 | ||||||
chr4:122886348
|
T | C | 6 | a0001c0001t0013g0243a0001c0001t0013g0244a0001c0001t0013g0245others(3): Show | 6 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.283-5863T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122886348 | ||||||
chr4:122886562
|
A | G | 4 | a0001c0001t0014g0127a0001c0001t0014g0143a0001c0001t0014g0157others(1): Show | 4 | HG03195.hp1 NA18522.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.283-5649A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122886562 | ||||||
chr4:122886581
|
T | A | 6 | a0001c0001t0013g0243a0001c0001t0013g0244a0001c0001t0013g0245others(3): Show | 6 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.283-5630T>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122886581 | ||||||
chr4:122886622
|
C | G | 6 | a0001c0001t0013g0243a0001c0001t0013g0244a0001c0001t0013g0245others(3): Show | 6 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.283-5589C>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122886622 | ||||||
chr4:122886623
|
C | T | 55 | a0001c0001t0001g0004a0001c0001t0001g0041a0001c0001t0001g0042others(52): Show | 56 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.283-5588C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122886623 | ||||||
chr4:122886677
|
A | C | 6 | a0001c0001t0013g0243a0001c0001t0013g0244a0001c0001t0013g0245others(3): Show | 6 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.283-5534A>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122886677 | ||||||
chr4:122886926
|
CTAAGCT | C | 8 | a0001c0001t0013g0243a0001c0001t0013g0244a0001c0001t0013g0245others(5): Show | 8 | HG01106.hp1 HG01192.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.283-5278_283-5273d others(8): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr4 | 122886926 | |||||
chr4:122886973
|
G | A | 12 | a0001c0001t0008g0006a0001c0001t0008g0116a0001c0001t0008g0159others(9): Show | 13 | HG01255.hp2 HG01346.hp2 HG01934.hp2 others(10): Show |
intron_variant | MODIFIER | c.283-5238G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122886973 | ||||||
chr4:122887111
|
C | T | 59 | a0001c0001t0001g0004a0001c0001t0001g0041a0001c0001t0001g0042others(56): Show | 60 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.283-5100C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122887111 | ||||||
chr4:122887230
|
C | T | 6 | a0001c0001t0013g0243a0001c0001t0013g0244a0001c0001t0013g0245others(3): Show | 6 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.283-4981C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122887230 | ||||||
chr4:122887291
|
G | T | 24 | a0001c0001t0005g0003a0001c0001t0005g0057a0001c0001t0005g0059others(21): Show | 26 | HG00099.hp1 HG00741.hp2 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.283-4920G>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122887291 | ||||||
chr4:122887350
|
G | A | 2 | a0001c0001t0037g0101a0001c0001t0049g0233 | 2 | HG01106.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.283-4861G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122887350 | ||||||
chr4:122887395
|
A | G | 15 | a0001c0001t0010g0167a0001c0001t0010g0206a0001c0001t0010g0220others(12): Show | 15 | HG01975.hp2 HG02055.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.283-4816A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122887395 | ||||||
chr4:122887470
|
G | A | 1 | a0001c0001t0020g0009 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.283-4741G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122887470 | ||||||
chr4:122887801
|
A | C | 1 | a0001c0001t0001g0115 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.283-4410A>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122887801 | ||||||
chr4:122887841
|
T | G | 2 | a0001c0001t0005g0106a0001c0001t0025g0107 | 2 | HG00099.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.283-4370T>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122887841 | ||||||
chr4:122887921
|
AAAT | A | 6 | a0001c0001t0013g0243a0001c0001t0013g0244a0001c0001t0013g0245others(3): Show | 6 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.283-4289_283-4287d others(5): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122887921 | ||||||
chr4:122887967
|
A | G | 2 | a0001c0001t0037g0101a0001c0001t0049g0233 | 2 | HG01106.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.283-4244A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122887967 | ||||||
chr4:122888123
|
C | T | 21 | a0001c0001t0007g0147a0001c0001t0007g0148a0001c0001t0007g0151others(18): Show | 22 | HG01361.hp1 HG01891.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.283-4088C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122888123 | ||||||
chr4:122888466
|
G | C | 1 | a0001c0002t0022g0016 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.283-3745G>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122888466 | ||||||
chr4:122888550
|
C | T | 2 | a0001c0001t0022g0236a0001c0002t0022g0016 | 2 | HG02257.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.283-3661C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122888550 | ||||||
chr4:122888804
|
G | A | 1 | a0001c0001t0005g0057 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.283-3407G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122888804 | ||||||
chr4:122888843
|
A | G | 1 | a0001c0001t0048g0019 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.283-3368A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122888843 | ||||||
chr4:122888987
|
G | T | 2 | a0001c0001t0027g0204a0001c0001t0041g0226 | 2 | HG02965.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.283-3224G>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122888987 | ||||||
chr4:122889173
|
T | C | 24 | a0001c0001t0005g0003a0001c0001t0005g0057a0001c0001t0005g0059others(21): Show | 26 | HG00099.hp1 HG00741.hp2 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.283-3038T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122889173 | ||||||
chr4:122889212
|
A | G | 21 | a0001c0001t0007g0147a0001c0001t0007g0148a0001c0001t0007g0151others(18): Show | 22 | HG01361.hp1 HG01891.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.283-2999A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122889212 | ||||||
chr4:122889281
|
T | C | 6 | a0001c0001t0013g0243a0001c0001t0013g0244a0001c0001t0013g0245others(3): Show | 6 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.283-2930T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122889281 | ||||||
chr4:122889302
|
G | A | 1 | a0001c0001t0037g0101 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.283-2909G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122889302 | ||||||
chr4:122889457
|
T | A | 1 | a0001c0001t0037g0101 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.283-2754T>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122889457 | ||||||
chr4:122889467
|
A | G | 2 | a0001c0001t0037g0101a0001c0001t0049g0233 | 2 | HG01106.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.283-2744A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122889467 | ||||||
chr4:122889513
|
AC | A | 86 | a0001c0001t0001g0004a0001c0001t0001g0041a0001c0001t0001g0042others(83): Show | 88 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.283-2697delC | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122889513 | ||||||
chr4:122889579
|
C | G | 57 | a0001c0001t0001g0004a0001c0001t0001g0041a0001c0001t0001g0042others(54): Show | 58 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.283-2632C>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122889579 | ||||||
chr4:122889660
|
T | A | 1 | a0001c0001t0029g0207 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.283-2551T>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122889660 | ||||||
chr4:122889845
|
T | A | 7 | a0001c0001t0009g0007a0001c0001t0009g0169a0001c0001t0009g0180others(4): Show | 8 | HG01109.hp1 HG01884.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.283-2366T>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122889845 | ||||||
chr4:122889848
|
A | C | 6 | a0001c0001t0013g0243a0001c0001t0013g0244a0001c0001t0013g0245others(3): Show | 6 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.283-2363A>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122889848 | ||||||
chr4:122889861
|
C | A | 2 | a0001c0001t0027g0204a0001c0001t0041g0226 | 2 | HG02965.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.283-2350C>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122889861 | ||||||
chr4:122889911
|
G | A | 2 | a0001c0001t0003g0241a0001c0001t0003g0242 | 2 | HG02630.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.283-2300G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122889911 | ||||||
chr4:122889956
|
G | A | 6 | a0001c0001t0013g0243a0001c0001t0013g0244a0001c0001t0013g0245others(3): Show | 6 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.283-2255G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122889956 | ||||||
chr4:122890272
|
C | T | 4 | a0001c0001t0022g0236a0001c0001t0027g0204a0001c0001t0041g0226others(1): Show | 4 | HG02257.hp1 HG02559.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.283-1939C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122890272 | ||||||
chr4:122890316
|
A | G | 1 | a0001c0001t0009g0201 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.283-1895A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122890316 | ||||||
chr4:122890317
|
T | C | 24 | a0001c0001t0005g0003a0001c0001t0005g0057a0001c0001t0005g0059others(21): Show | 26 | HG00099.hp1 HG00741.hp2 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.283-1894T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122890317 | ||||||
chr4:122890452
|
T | C | 55 | a0001c0001t0001g0004a0001c0001t0001g0041a0001c0001t0001g0042others(52): Show | 56 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.283-1759T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122890452 | ||||||
chr4:122890537
|
C | A | 1 | a0001c0001t0002g0067 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.283-1674C>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122890537 | ||||||
chr4:122890543
|
T | A | 1 | a0001c0001t0002g0067 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.283-1668T>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122890543 | ||||||
chr4:122890545
|
C | A | 1 | a0001c0001t0002g0067 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.283-1666C>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122890545 | ||||||
chr4:122890548
|
T | A | 1 | a0001c0001t0002g0067 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.283-1663T>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122890548 | ||||||
chr4:122890550
|
G | C | 1 | a0001c0001t0002g0067 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.283-1661G>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122890550 | ||||||
chr4:122890554
|
G | A | 1 | a0001c0001t0002g0067 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.283-1657G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122890554 | ||||||
chr4:122890556
|
T | A | 1 | a0001c0001t0002g0067 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.283-1655T>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122890556 | ||||||
chr4:122890557
|
G | T | 1 | a0001c0001t0002g0067 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.283-1654G>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122890557 | ||||||
chr4:122890559
|
G | A | 1 | a0001c0001t0002g0067 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.283-1652G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122890559 | ||||||
chr4:122890561
|
C | T | 1 | a0001c0001t0002g0067 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.283-1650C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122890561 | ||||||
chr4:122890565
|
T | C | 1 | a0001c0001t0002g0067 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.283-1646T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122890565 | ||||||
chr4:122890579
|
T | A | 1 | a0001c0001t0002g0067 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.283-1632T>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122890579 | ||||||
chr4:122890581
|
C | T | 1 | a0001c0001t0002g0067 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.283-1630C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122890581 | ||||||
chr4:122890582
|
T | G | 1 | a0001c0001t0002g0067 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.283-1629T>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122890582 | ||||||
chr4:122890583
|
T | C | 1 | a0001c0001t0002g0067 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.283-1628T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122890583 | ||||||
chr4:122890587
|
C | T | 1 | a0001c0001t0012g0031 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.283-1624C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122890587 | ||||||
chr4:122890592
|
T | G | 1 | a0001c0001t0002g0067 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.283-1619T>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122890592 | ||||||
chr4:122890593
|
T | A | 1 | a0001c0001t0002g0067 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.283-1618T>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122890593 | ||||||
chr4:122890594
|
T | C | 1 | a0001c0001t0002g0067 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.283-1617T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122890594 | ||||||
chr4:122890597
|
T | A | 1 | a0001c0001t0002g0067 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.283-1614T>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122890597 | ||||||
chr4:122890601
|
C | G | 1 | a0001c0001t0002g0067 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.283-1610C>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122890601 | ||||||
chr4:122890604
|
TTTTGTTA others(3): Show |
T | 1 | a0001c0001t0002g0067 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.283-1605_283-1596d others(12): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr4 | 122890604 | |||||
chr4:122890620
|
G | C | 1 | a0001c0001t0002g0067 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.283-1591G>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122890620 | ||||||
chr4:122890622
|
T | A | 1 | a0001c0001t0002g0067 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.283-1589T>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122890622 | ||||||
chr4:122890624
|
T | C | 1 | a0001c0001t0002g0067 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.283-1587T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122890624 | ||||||
chr4:122890625
|
T | C | 1 | a0001c0001t0002g0067 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.283-1586T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122890625 | ||||||
chr4:122890630
|
T | G | 1 | a0001c0001t0002g0067 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.283-1581T>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122890630 | ||||||
chr4:122890631
|
T | TCTCCCCC others(6): Show |
1 | a0001c0001t0002g0067 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.283-1580_283-1579i others(15): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122890631 | ||||||
chr4:122890632
|
G | C | 1 | a0001c0001t0002g0067 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.283-1579G>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122890632 | ||||||
chr4:122890634
|
T | G | 1 | a0001c0001t0002g0067 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.283-1577T>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122890634 | ||||||
chr4:122890859
|
C | T | 21 | a0001c0001t0007g0147a0001c0001t0007g0148a0001c0001t0007g0151others(18): Show | 22 | HG01361.hp1 HG01891.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.283-1352C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122890859 | ||||||
chr4:122890888
|
G | A | 8 | a0001c0001t0013g0243a0001c0001t0013g0244a0001c0001t0013g0245others(5): Show | 8 | HG01106.hp1 HG01192.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.283-1323G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122890888 | ||||||
chr4:122891013
|
CA | C | 102 | a0001c0001t0001g0004a0001c0001t0001g0041a0001c0001t0001g0042others(99): Show | 105 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.283-1196delA | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr4 | 122891013 | |||||
chr4:122891017
|
T | C | 11 | a0001c0001t0008g0006a0001c0001t0008g0116a0001c0001t0008g0159others(8): Show | 12 | HG01255.hp2 HG01346.hp2 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.283-1194T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122891017 | ||||||
chr4:122891021
|
C | CT | 52 | a0001c0001t0001g0004a0001c0001t0001g0041a0001c0001t0001g0042others(49): Show | 53 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.283-1176dupT | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr4 | 122891021 | |||||
chr4:122891021
|
CT | C | 23 | a0001c0001t0003g0043a0001c0001t0004g0231a0001c0001t0007g0147others(20): Show | 24 | HG01361.hp1 HG01891.hp1 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.283-1176delT | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr4 | 122891021 | |||||
chr4:122891031
|
T | G | 29 | a0001c0001t0003g0181a0001c0001t0005g0003a0001c0001t0005g0057others(26): Show | 31 | HG00099.hp1 HG00741.hp2 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.283-1180T>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122891031 | ||||||
chr4:122891032
|
T | G | 7 | a0001c0001t0006g0018a0001c0001t0006g0034a0001c0001t0006g0035others(4): Show | 8 | HG00639.hp1 HG01106.hp1 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.283-1179T>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122891032 | ||||||
chr4:122891032
|
TTTTG | T | 14 | a0001c0001t0008g0006a0001c0001t0008g0116a0001c0001t0008g0159others(11): Show | 15 | HG01255.hp2 HG01346.hp2 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.283-1175_283-1172d others(6): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr4 | 122891032 | |||||
chr4:122891035
|
TG | T | 5 | a0001c0001t0002g0066a0001c0001t0002g0110a0001c0001t0006g0037others(2): Show | 5 | HG00408.hp2 HG02723.hp2 NA18950.hp1 others(2): Show |
intron_variant | MODIFIER | c.283-1175delG | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122891035 | ||||||
chr4:122891036
|
G | T | 134 | a0001c0001t0001g0004a0001c0001t0001g0041a0001c0001t0001g0042others(131): Show | 136 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(133): Show |
intron_variant | MODIFIER | c.283-1175G>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122891036 | ||||||
chr4:122891037
|
T | G | 1 | a0001c0001t0010g0206 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.283-1174T>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122891037 | ||||||
chr4:122891041
|
G | T | 74 | a0001c0001t0001g0004a0001c0001t0001g0041a0001c0001t0001g0042others(71): Show | 76 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.283-1170G>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122891041 | ||||||
chr4:122891044
|
T | G | 2 | a0001c0001t0037g0101a0001c0001t0049g0233 | 2 | HG01106.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.283-1167T>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122891044 | ||||||
chr4:122891046
|
G | T | 2 | a0001c0001t0037g0101a0001c0001t0049g0233 | 2 | HG01106.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.283-1165G>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122891046 | ||||||
chr4:122891053
|
T | A | 57 | a0001c0001t0001g0004a0001c0001t0001g0041a0001c0001t0001g0042others(54): Show | 58 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.283-1158T>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122891053 | ||||||
chr4:122891054
|
T | G | 4 | a0001c0001t0008g0116a0001c0001t0019g0022a0001c0001t0019g0023others(1): Show | 4 | HG01255.hp2 HG01346.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.283-1157T>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122891054 | ||||||
chr4:122891129
|
C | T | 18 | a0001c0001t0007g0147a0001c0001t0007g0148a0001c0001t0007g0151others(15): Show | 18 | HG01361.hp1 HG01891.hp1 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.283-1082C>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122891129 | ||||||
chr4:122891134
|
A | G | 18 | a0001c0001t0007g0147a0001c0001t0007g0148a0001c0001t0007g0151others(15): Show | 18 | HG01361.hp1 HG01891.hp1 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.283-1077A>G | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122891134 | ||||||
chr4:122891202
|
G | A | 2 | a0001c0001t0008g0006a0001c0001t0008g0160 | 3 | HG03491.hp1 HG03492.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.283-1009G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122891202 | ||||||
chr4:122891283
|
G | T | 6 | a0001c0001t0013g0243a0001c0001t0013g0244a0001c0001t0013g0245others(3): Show | 6 | HG01192.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.283-928G>T | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122891283 | ||||||
chr4:122891424
|
C | CT | 11 | a0001c0001t0013g0243a0001c0001t0013g0244a0001c0001t0013g0245others(8): Show | 12 | HG01106.hp1 HG01192.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.283-771dupT | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr4 | 122891424 | |||||
chr4:122891424
|
C | CTT | 20 | a0001c0001t0001g0078a0001c0001t0007g0147a0001c0001t0007g0148others(17): Show | 20 | HG01361.hp1 HG01891.hp1 HG02486.hp2 others(17): Show |
intron_variant | MODIFIER | c.283-772_283-771dup others(2): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr4 | 122891424 | |||||
chr4:122891424
|
C | CTTT | 54 | a0001c0001t0001g0004a0001c0001t0001g0041a0001c0001t0001g0042others(51): Show | 55 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.283-773_283-771dup others(3): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr4 | 122891424 | |||||
chr4:122891424
|
CT | C | 13 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0043others(10): Show | 15 | HG01167.hp1 HG01257.hp2 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.283-771delT | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr4 | 122891424 | |||||
chr4:122891583
|
T | A | 1 | a0001c0001t0010g0206 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.283-628T>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122891583 | ||||||
chr4:122891642
|
G | C | 24 | a0001c0001t0005g0003a0001c0001t0005g0057a0001c0001t0005g0059others(21): Show | 26 | HG00099.hp1 HG00741.hp2 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.283-569G>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122891642 | ||||||
chr4:122891726
|
C | CCTT | 65 | a0001c0001t0001g0004a0001c0001t0001g0041a0001c0001t0001g0042others(62): Show | 66 | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.283-482_283-480dup others(3): Show |
FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr4 | 122891726 | |||||
chr4:122891854
|
G | A | 139 | a0001c0001t0001g0004a0001c0001t0001g0041a0001c0001t0001g0042others(136): Show | 144 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.283-357G>A | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122891854 | ||||||
chr4:122892002
|
T | C | 1 | a0001c0001t0031g0247 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.283-209T>C | FGF2 | ENSG00000138685.18 | transcript | ENST00000644866.2 | protein_coding | 2/2 | chr4 | 122892002 |