geneid | 2395 |
---|---|
ensemblid | ENSG00000165060.15 |
hgncid | 3951 |
symbol | FXN |
name | frataxin |
refseq_nuc | NM_000144.5 |
refseq_prot | NP_000135.2 |
ensembl_nuc | ENST00000484259.3 |
ensembl_prot | ENSP00000419243.2 |
mane_status | MANE Select |
chr | chr9 |
start | 69035752 |
end | 69079076 |
strand | + |
ver | v1.2 |
region | chr9:69035752-69079076 |
region5000 | chr9:69030752-69084076 |
regionname0 | FXN_chr9_69035752_69079076 |
regionname5000 | FXN_chr9_69030752_69084076 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 210 | 418 | 85 | 70 | 200 | 18 | 43 | 159 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
a0002 | 0/0 | 210 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
a0003 | 0/0 | 210 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
a0004 | 0/0 | 210 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
a0005 | 0/0 | 210 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
a0006 | 0/0 | 210 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 633 | 403 | 75 | 70 | 197 | 18 | 42 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
c0002 | 1/0 | 633 | 11 | 10 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
c0003 | 0/0 | 633 | 7 | 7 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
c0004 | 0/0 | 633 | 4 | 4 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
c0005 | 0/0 | 633 | 3 | 0 | 0 | 3 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
c0006 | 0/0 | 633 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
c0007 | 0/0 | 633 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
c0008 | 0/0 | 633 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
c0009 | 0/0 | 633 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 6345 | 70 | 9 | 9 | 40 | 1 | 10 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
t0002 | 0/0 | 6351 | 70 | 2 | 18 | 47 | 0 | 3 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
t0003 | 0/0 | 6350 | 53 | 2 | 7 | 37 | 3 | 4 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
t0004 | 0/0 | 6346 | 31 | 0 | 6 | 25 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
t0005 | 0/0 | 6350 | 30 | 15 | 1 | 6 | 5 | 3 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
t0006 | 0/0 | 6351 | 27 | 11 | 7 | 2 | 3 | 4 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
t0007 | 0/0 | 6354 | 14 | 3 | 0 | 9 | 0 | 2 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
t0008 | 0/0 | 6346 | 12 | 3 | 5 | 0 | 2 | 2 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
t0009 | 0/0 | 6343 | 10 | 9 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
t0010 | 0/0 | 6344 | 6 | 0 | 2 | 2 | 0 | 2 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
t0011 | 1/0 | 6346 | 5 | 4 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
t0012 | 0/0 | 6351 | 5 | 1 | 0 | 0 | 2 | 2 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
t0013 | 0/0 | 6352 | 5 | 0 | 0 | 5 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
t0014 | 0/0 | 6359 | 4 | 3 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
t0015 | 0/0 | 6354 | 4 | 4 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
t0016 | 0/0 | 6354 | 4 | 0 | 0 | 4 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
t0017 | 0/0 | 6351 | 4 | 3 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
t0018 | 0/0 | 6345 | 3 | 0 | 1 | 0 | 2 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
t0019 | 0/0 | 6345 | 3 | 0 | 0 | 3 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
t0020 | 0/0 | 6345 | 3 | 3 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
t0021 | 0/0 | 6341 | 3 | 3 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
t0022 | 0/0 | 6345 | 3 | 0 | 3 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
t0023 | 0/0 | 6367 | 3 | 3 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
t0024 | 0/0 | 6353 | 3 | 0 | 0 | 3 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
t0025 | 0/0 | 6345 | 2 | 0 | 0 | 2 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
t0026 | 0/0 | 6344 | 2 | 0 | 0 | 0 | 0 | 2 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
t0027 | 0/0 | 6345 | 2 | 0 | 0 | 2 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
t0028 | 0/0 | 6350 | 2 | 0 | 0 | 0 | 0 | 2 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
t0029 | 0/0 | 6354 | 2 | 0 | 0 | 2 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
t0030 | 0/0 | 6347 | 2 | 0 | 0 | 0 | 0 | 2 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
t0031 | 0/0 | 6350 | 2 | 0 | 0 | 2 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
t0032 | 0/0 | 6352 | 2 | 2 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
t0033 | 0/0 | 6341 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
t0034 | 0/0 | 6346 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
t0035 | 0/0 | 6345 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
t0036 | 0/0 | 6345 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
t0037 | 0/0 | 6345 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
t0038 | 0/0 | 6345 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
t0039 | 0/0 | 6345 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
t0040 | 0/0 | 6345 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
t0041 | 0/0 | 6345 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
t0042 | 0/0 | 6345 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
t0043 | 0/0 | 6346 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
t0044 | 0/0 | 6345 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
t0045 | 0/0 | 6346 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
t0046 | 0/0 | 6346 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
t0047 | 0/0 | 6346 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
t0048 | 0/0 | 6343 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
t0049 | 0/0 | 6345 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
t0050 | 0/0 | 6346 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
t0051 | 0/0 | 6343 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
t0052 | 0/0 | 6354 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
t0053 | 0/0 | 6354 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
t0054 | 0/0 | 6354 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
t0055 | 0/0 | 6358 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
t0056 | 0/0 | 6355 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
t0057 | 0/0 | 6351 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
t0058 | 0/0 | 6351 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
t0059 | 0/0 | 6347 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
t0060 | 0/0 | 6351 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
t0061 | 0/0 | 6351 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
t0062 | 0/0 | 6350 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
t0063 | 0/0 | 6350 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
t0064 | 0/0 | 6351 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
t0065 | 0/0 | 6352 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
t0066 | 0/0 | 6351 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
t0067 | 0/0 | 6349 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
t0068 | 0/0 | 6349 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
t0069 | 0/0 | 6344 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
t0070 | 0/0 | 6350 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
t0071 | 0/0 | 6349 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
t0072 | 0/0 | 6348 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
t0073 | 0/0 | 6350 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 7 | 0 | 0 | 6 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0005 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0007 | 0/0 | 3 | 1 | 0 | 0 | 2 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0008 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0009 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0017 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0018 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0029 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0034 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0039 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0101 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0316 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0321 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0338 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0358 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0359 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0362 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0364 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0369 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 633 | 403 | 75 | 70 | 197 | 18 | 42 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
a0001c0002 | 1/0 | 633 | 11 | 10 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
a0001c0005 | 0/0 | 633 | 3 | 0 | 0 | 3 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
a0001c0008 | 0/0 | 633 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
a0002c0003 | 0/0 | 633 | 7 | 7 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
a0003c0004 | 0/0 | 633 | 4 | 4 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
a0004c0006 | 0/0 | 633 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
a0005c0007 | 0/0 | 633 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
a0006c0009 | 0/0 | 633 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 6977 | 66 | 9 | 9 | 36 | 1 | 10 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
a0001c0001t0002 | 0/0 | 6983 | 70 | 2 | 18 | 47 | 0 | 3 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
a0001c0001t0003 | 0/0 | 6982 | 53 | 2 | 7 | 37 | 3 | 4 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
a0001c0001t0004 | 0/0 | 6978 | 31 | 0 | 6 | 25 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
a0001c0001t0005 | 0/0 | 6982 | 28 | 14 | 1 | 5 | 5 | 3 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
a0001c0001t0006 | 0/0 | 6983 | 27 | 11 | 7 | 2 | 3 | 4 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
a0001c0001t0007 | 0/0 | 6986 | 14 | 3 | 0 | 9 | 0 | 2 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
a0001c0001t0008 | 0/0 | 6978 | 11 | 2 | 5 | 0 | 2 | 2 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
a0001c0001t0009 | 0/0 | 6975 | 10 | 9 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
a0001c0001t0010 | 0/0 | 6976 | 6 | 0 | 2 | 2 | 0 | 2 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
a0001c0001t0012 | 0/0 | 6983 | 5 | 1 | 0 | 0 | 2 | 2 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
a0001c0001t0013 | 0/0 | 6984 | 5 | 0 | 0 | 5 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
a0001c0001t0014 | 0/0 | 6991 | 4 | 3 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
a0001c0001t0015 | 0/0 | 6986 | 2 | 2 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
a0001c0001t0016 | 0/0 | 6986 | 4 | 0 | 0 | 4 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
a0001c0001t0017 | 0/0 | 6983 | 4 | 3 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
a0001c0001t0018 | 0/0 | 6977 | 3 | 0 | 1 | 0 | 2 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
a0001c0001t0019 | 0/0 | 6977 | 3 | 0 | 0 | 3 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
a0001c0001t0020 | 0/0 | 6977 | 3 | 3 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
a0001c0001t0022 | 0/0 | 6977 | 3 | 0 | 3 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
a0001c0001t0024 | 0/0 | 6985 | 3 | 0 | 0 | 3 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
a0001c0001t0025 | 0/0 | 6977 | 2 | 0 | 0 | 2 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
a0001c0001t0026 | 0/0 | 6976 | 2 | 0 | 0 | 0 | 0 | 2 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
a0001c0001t0027 | 0/0 | 6977 | 2 | 0 | 0 | 2 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
a0001c0001t0028 | 0/0 | 6982 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
a0001c0001t0029 | 0/0 | 6986 | 2 | 0 | 0 | 2 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
a0001c0001t0030 | 0/0 | 6979 | 2 | 0 | 0 | 0 | 0 | 2 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
a0001c0001t0031 | 0/0 | 6982 | 2 | 0 | 0 | 2 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
a0001c0001t0035 | 0/0 | 6977 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
a0001c0001t0036 | 0/0 | 6977 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
a0001c0001t0037 | 0/0 | 6977 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
a0001c0001t0038 | 0/0 | 6977 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
a0001c0001t0039 | 0/0 | 6977 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
a0001c0001t0040 | 0/0 | 6977 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
a0001c0001t0041 | 0/0 | 6977 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
a0001c0001t0042 | 0/0 | 6977 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
a0001c0001t0043 | 0/0 | 6978 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
a0001c0001t0044 | 0/0 | 6977 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
a0001c0001t0045 | 0/0 | 6978 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
a0001c0001t0046 | 0/0 | 6978 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
a0001c0001t0048 | 0/0 | 6975 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
a0001c0001t0049 | 0/0 | 6977 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
a0001c0001t0051 | 0/0 | 6975 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
a0001c0001t0052 | 0/0 | 6986 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
a0001c0001t0053 | 0/0 | 6986 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
a0001c0001t0054 | 0/0 | 6986 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
a0001c0001t0055 | 0/0 | 6990 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
a0001c0001t0056 | 0/0 | 6987 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
a0001c0001t0057 | 0/0 | 6983 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
a0001c0001t0058 | 0/0 | 6983 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
a0001c0001t0059 | 0/0 | 6979 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
a0001c0001t0060 | 0/0 | 6983 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
a0001c0001t0061 | 0/0 | 6983 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
a0001c0001t0062 | 0/0 | 6982 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
a0001c0001t0063 | 0/0 | 6982 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
a0001c0001t0064 | 0/0 | 6983 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
a0001c0001t0065 | 0/0 | 6984 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
a0001c0001t0066 | 0/0 | 6983 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
a0001c0001t0067 | 0/0 | 6981 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
a0001c0001t0068 | 0/0 | 6981 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
a0001c0001t0069 | 0/0 | 6976 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
a0001c0001t0070 | 0/0 | 6982 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
a0001c0001t0071 | 0/0 | 6981 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
a0001c0002t0005 | 0/0 | 6982 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
a0001c0002t0011 | 1/0 | 6978 | 5 | 4 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
a0001c0002t0023 | 0/0 | 6999 | 3 | 3 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
a0001c0002t0034 | 0/0 | 6978 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
a0001c0002t0047 | 0/0 | 6978 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
a0001c0005t0001 | 0/0 | 6977 | 3 | 0 | 0 | 3 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
a0001c0008t0073 | 0/0 | 6982 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
a0002c0003t0008 | 0/0 | 6978 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
a0002c0003t0015 | 0/0 | 6986 | 2 | 2 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
a0002c0003t0032 | 0/0 | 6984 | 2 | 2 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
a0002c0003t0050 | 0/0 | 6978 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
a0002c0003t0072 | 0/0 | 6980 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
a0003c0004t0021 | 0/0 | 6973 | 3 | 3 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
a0003c0004t0033 | 0/0 | 6973 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
a0004c0006t0001 | 0/0 | 6977 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
a0005c0007t0005 | 0/0 | 6982 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
a0006c0009t0028 | 0/0 | 6982 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | copy fasta | chr9 | 69030752 | 69084076 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0101 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0001g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0009 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0034 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0003g0001 | 0/0 | 7 | 0 | 0 | 6 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0003g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0003g0007 | 0/0 | 3 | 1 | 0 | 0 | 2 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0003g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0003g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0003g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0003g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0003g0029 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0003g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0003g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0003g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0003g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0003g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0003g0369 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0003g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0004g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0004g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0004g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0004g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0004g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0004g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0004g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0004g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0004g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0004g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0004g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0004g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0004g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0004g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0004g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0004g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0004g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0004g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0004g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0004g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0004g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0004g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0004g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0004g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0004g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0004g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0004g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0005g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0005g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0005g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0005g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0005g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0005g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0005g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0005g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0005g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0005g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0005g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0005g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0005g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0005g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0005g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0005g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0005g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0005g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0005g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0005g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0005g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0005g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0005g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0005g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0005g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0005g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0006g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0006g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0006g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0006g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0006g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0006g0321 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0006g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0006g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0006g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0006g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0006g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0006g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0006g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0006g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0006g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0006g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0006g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0006g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0006g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0006g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0006g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0006g0359 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0006g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0006g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0006g0364 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0006g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0006g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0007g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0007g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0007g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0007g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0007g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0007g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0007g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0007g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0007g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0007g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0007g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0007g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0008g0008 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0008g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0008g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0008g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0008g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0008g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0008g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0008g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0008g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0009g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0009g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0009g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0009g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0009g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0009g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0009g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0009g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0009g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0010g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0010g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0010g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0010g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0010g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0010g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0012g0338 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0012g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0012g0358 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0012g0362 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0012g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0013g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0013g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0013g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0013g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0013g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0014g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0014g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0014g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0014g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0015g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0015g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0016g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0016g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0016g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0016g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0017g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0017g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0017g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0018g0018 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0018g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0019g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0019g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0019g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0020g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0020g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0022g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0022g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0022g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0024g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0025g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0026g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0026g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0027g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0028g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0029g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0029g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0030g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0031g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0031g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0035g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0036g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0037g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0038g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0039g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0040g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0041g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0042g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0043g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0044g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0045g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0046g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0048g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0049g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0051g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0052g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0053g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0054g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0055g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0056g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0057g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0058g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0059g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0060g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0061g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0062g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0063g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0064g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0065g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0066g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0067g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0068g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0069g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0070g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0001t0071g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0002t0005g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0002t0011g0005 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0002t0011g0316 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0002t0023g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0002t0023g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0002t0034g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0002t0047g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0005t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0005t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0005t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0001c0008t0073g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0002c0003t0008g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0002c0003t0015g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0002c0003t0015g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0002c0003t0032g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0002c0003t0032g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0002c0003t0050g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0002c0003t0072g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0003c0004t0021g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0003c0004t0021g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0003c0004t0033g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0004c0006t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0005c0007t0005g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
a0006c0009t0028g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0006 | g0321 | EUR | GBR | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG00099 | hp2 | a0001 | c0001 | t0003 | g0007 | EUR | GBR | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG00140 | hp1 | a0001 | c0001 | t0005 | g0301 | EUR | GBR | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG00140 | hp2 | a0001 | c0001 | t0012 | g0362 | EUR | GBR | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG00280 | hp1 | a0001 | c0001 | t0003 | g0195 | EUR | FIN | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG00280 | hp2 | a0001 | c0001 | t0006 | g0207 | EUR | FIN | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG00323 | hp1 | a0001 | c0001 | t0005 | g0226 | EUR | FIN | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0103 | EUR | FIN | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG00423 | hp1 | a0001 | c0001 | t0005 | g0281 | EAS | CHS | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG00423 | hp2 | a0001 | c0001 | t0003 | g0196 | EAS | CHS | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG00438 | hp1 | a0001 | c0001 | t0004 | g0112 | EAS | CHS | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0268 | EAS | CHS | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG00544 | hp1 | a0001 | c0001 | t0003 | g0205 | EAS | CHS | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | CHS | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0131 | EAS | CHS | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0261 | EAS | CHS | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0258 | AMR | PUR | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG00639 | hp2 | a0001 | c0001 | t0022 | g0169 | AMR | PUR | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG00642 | hp1 | a0001 | c0001 | t0054 | g0039 | AMR | PUR | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG00642 | hp2 | a0001 | c0001 | t0006 | g0365 | AMR | PUR | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG00673 | hp1 | a0001 | c0001 | t0019 | g0002 | EAS | CHS | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG00673 | hp2 | a0005 | c0007 | t0005 | g0305 | EAS | CHS | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0088 | AMR | PUR | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG00735 | hp2 | a0001 | c0001 | t0003 | g0232 | AMR | PUR | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG00738 | hp2 | a0001 | c0001 | t0044 | g0222 | AMR | PUR | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG00741 | hp1 | a0001 | c0001 | t0006 | g0361 | AMR | PUR | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01069 | hp2 | a0001 | c0001 | t0003 | g0027 | AMR | PUR | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0033 | AMR | PUR | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01070 | hp2 | a0001 | c0001 | t0006 | g0360 | AMR | PUR | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01071 | hp1 | a0001 | c0001 | t0003 | g0027 | AMR | PUR | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01081 | hp1 | a0001 | c0001 | t0008 | g0008 | AMR | PUR | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01081 | hp2 | a0001 | c0001 | t0006 | g0319 | AMR | PUR | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01099 | hp1 | a0001 | c0001 | t0004 | g0291 | AMR | PUR | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01099 | hp2 | a0001 | c0001 | t0006 | g0356 | AMR | PUR | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01106 | hp1 | a0001 | c0001 | t0003 | g0369 | AMR | PUR | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01106 | hp2 | a0001 | c0001 | t0003 | g0198 | AMR | PUR | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01109 | hp1 | a0001 | c0001 | t0008 | g0225 | AMR | PUR | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01109 | hp2 | a0001 | c0001 | t0042 | g0104 | AMR | PUR | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01167 | hp1 | a0001 | c0001 | t0010 | g0115 | AMR | PUR | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01167 | hp2 | a0001 | c0001 | t0049 | g0367 | AMR | PUR | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01168 | hp1 | a0001 | c0001 | t0058 | g0311 | AMR | PUR | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0341 | AMR | PUR | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01169 | hp1 | a0001 | c0001 | t0010 | g0017 | AMR | PUR | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0340 | AMR | PUR | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01175 | hp1 | a0001 | c0001 | t0005 | g0231 | AMR | PUR | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01192 | hp2 | a0001 | c0001 | t0006 | g0320 | AMR | PUR | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01243 | hp2 | a0001 | c0001 | t0060 | g0303 | AMR | PUR | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01255 | hp1 | a0001 | c0001 | t0008 | g0224 | AMR | CLM | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01255 | hp2 | a0001 | c0001 | t0009 | g0245 | AMR | CLM | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0047 | AMR | CLM | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | CLM | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01258 | hp1 | a0001 | c0001 | t0008 | g0008 | AMR | CLM | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | CLM | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01261 | hp1 | a0001 | c0001 | t0003 | g0159 | AMR | CLM | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0086 | AMR | CLM | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01346 | hp1 | a0001 | c0001 | t0045 | g0168 | AMR | CLM | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | CLM | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01358 | hp1 | a0001 | c0001 | t0018 | g0134 | AMR | CLM | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0084 | AMR | CLM | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01361 | hp1 | a0001 | c0001 | t0003 | g0029 | AMR | CLM | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0034 | AMR | CLM | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0288 | AMR | CLM | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01433 | hp2 | a0001 | c0001 | t0008 | g0221 | AMR | CLM | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01496 | hp1 | a0001 | c0001 | t0014 | g0219 | AMR | CLM | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01496 | hp2 | a0001 | c0001 | t0038 | g0119 | AMR | CLM | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01515 | hp1 | a0001 | c0001 | t0008 | g0213 | EUR | IBS | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01515 | hp2 | a0001 | c0001 | t0005 | g0211 | EUR | IBS | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01516 | hp1 | a0001 | c0001 | t0005 | g0212 | EUR | IBS | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01516 | hp2 | a0001 | c0001 | t0018 | g0018 | EUR | IBS | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01517 | hp1 | a0001 | c0001 | t0018 | g0018 | EUR | IBS | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01517 | hp2 | a0001 | c0001 | t0008 | g0214 | EUR | IBS | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01884 | hp1 | a0001 | c0001 | t0067 | g0230 | AFR | ACB | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01884 | hp2 | a0001 | c0002 | t0023 | g0048 | AFR | ACB | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | ACB | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01891 | hp2 | a0002 | c0003 | t0015 | g0042 | AFR | ACB | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PEL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01928 | hp2 | a0001 | c0001 | t0022 | g0105 | AMR | PEL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01943 | hp1 | a0001 | c0001 | t0061 | g0174 | AMR | PEL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01943 | hp2 | a0001 | c0001 | t0004 | g0015 | AMR | PEL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0285 | AMR | PEL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01975 | hp2 | a0001 | c0001 | t0022 | g0170 | AMR | PEL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01981 | hp1 | a0001 | c0001 | t0004 | g0163 | AMR | PEL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0045 | AMR | PEL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0279 | AMR | PEL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG01993 | hp2 | a0001 | c0001 | t0004 | g0161 | AMR | PEL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02004 | hp1 | a0001 | c0001 | t0004 | g0162 | AMR | PEL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0033 | AMR | PEL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02015 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02015 | hp2 | a0001 | c0001 | t0002 | g0240 | EAS | KHV | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02027 | hp1 | a0001 | c0001 | t0005 | g0304 | EAS | KHV | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02027 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02040 | hp1 | a0001 | c0001 | t0068 | g0188 | EAS | KHV | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02040 | hp2 | a0001 | c0001 | t0024 | g0010 | EAS | KHV | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02055 | hp1 | a0001 | c0001 | t0006 | g0350 | AFR | ACB | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02055 | hp2 | a0001 | c0001 | t0009 | g0246 | AFR | ACB | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02056 | hp1 | a0001 | c0001 | t0005 | g0035 | EAS | KHV | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02056 | hp2 | a0001 | c0001 | t0006 | g0357 | EAS | KHV | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02071 | hp1 | a0001 | c0001 | t0004 | g0092 | EAS | KHV | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02071 | hp2 | a0001 | c0001 | t0003 | g0054 | EAS | KHV | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0269 | EAS | KHV | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | KHV | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0294 | EAS | KHV | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02080 | hp2 | a0001 | c0001 | t0004 | g0014 | EAS | KHV | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02083 | hp1 | a0001 | c0001 | t0027 | g0023 | EAS | KHV | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02129 | hp1 | a0001 | c0001 | t0004 | g0080 | EAS | KHV | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02129 | hp2 | a0001 | c0001 | t0003 | g0189 | EAS | KHV | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02132 | hp1 | a0001 | c0001 | t0003 | g0055 | EAS | KHV | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | KHV | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02135 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02145 | hp1 | a0001 | c0001 | t0039 | g0122 | AFR | ACB | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02145 | hp2 | a0001 | c0001 | t0012 | g0363 | AFR | ACB | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0313 | EAS | CDX | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02155 | hp2 | a0001 | c0001 | t0003 | g0192 | EAS | CDX | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02165 | hp1 | a0001 | c0001 | t0004 | g0014 | EAS | CDX | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0293 | EAS | CDX | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02257 | hp1 | a0001 | c0001 | t0006 | g0348 | AFR | ACB | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02257 | hp2 | a0001 | c0001 | t0008 | g0325 | AFR | ACB | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02258 | hp1 | a0001 | c0001 | t0020 | g0031 | AFR | ACB | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02258 | hp2 | a0001 | c0001 | t0003 | g0029 | AFR | ACB | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02273 | hp1 | a0001 | c0001 | t0004 | g0015 | AMR | PEL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | PEL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02280 | hp1 | a0001 | c0001 | t0020 | g0031 | AFR | ACB | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | ACB | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0085 | AMR | PEL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02300 | hp2 | a0001 | c0001 | t0006 | g0352 | AMR | PEL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02451 | hp1 | a0002 | c0003 | t0015 | g0046 | AFR | ACB | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02451 | hp2 | a0001 | c0001 | t0008 | g0178 | AFR | ACB | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02523 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02572 | hp1 | a0001 | c0001 | t0014 | g0179 | AFR | GWD | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02572 | hp2 | a0001 | c0001 | t0009 | g0272 | AFR | GWD | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0254 | SAS | PJL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02602 | hp2 | a0001 | c0001 | t0026 | g0124 | SAS | PJL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02615 | hp1 | a0001 | c0001 | t0014 | g0183 | AFR | GWD | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02615 | hp2 | a0001 | c0001 | t0006 | g0351 | AFR | GWD | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02622 | hp1 | a0001 | c0002 | t0047 | g0049 | AFR | GWD | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02622 | hp2 | a0003 | c0004 | t0033 | g0322 | AFR | GWD | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02630 | hp1 | a0001 | c0001 | t0051 | g0244 | AFR | GWD | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02630 | hp2 | a0001 | c0001 | t0005 | g0216 | AFR | GWD | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02647 | hp1 | a0001 | c0001 | t0009 | g0032 | AFR | GWD | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02647 | hp2 | a0002 | c0003 | t0032 | g0043 | AFR | GWD | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0256 | SAS | PJL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02683 | hp2 | a0001 | c0001 | t0041 | g0117 | SAS | PJL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02698 | hp1 | a0001 | c0001 | t0008 | g0008 | SAS | PJL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02698 | hp2 | a0001 | c0008 | t0073 | g0237 | SAS | PJL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02717 | hp1 | a0001 | c0002 | t0023 | g0011 | AFR | GWD | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02717 | hp2 | a0001 | c0001 | t0017 | g0012 | AFR | GWD | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02723 | hp1 | a0001 | c0002 | t0023 | g0011 | AFR | GWD | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02723 | hp2 | a0002 | c0003 | t0050 | g0075 | AFR | GWD | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02735 | hp1 | a0001 | c0001 | t0005 | g0227 | SAS | PJL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02735 | hp2 | a0001 | c0001 | t0035 | g0140 | SAS | PJL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02738 | hp1 | a0001 | c0001 | t0071 | g0173 | SAS | PJL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0263 | SAS | PJL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02809 | hp1 | a0001 | c0001 | t0007 | g0368 | AFR | GWD | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02809 | hp2 | a0001 | c0001 | t0005 | g0220 | AFR | GWD | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02818 | hp1 | a0001 | c0001 | t0005 | g0229 | AFR | GWD | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02818 | hp2 | a0001 | c0001 | t0006 | g0345 | AFR | GWD | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02886 | hp1 | a0001 | c0001 | t0017 | g0012 | AFR | GWD | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02886 | hp2 | a0001 | c0001 | t0009 | g0243 | AFR | GWD | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02895 | hp1 | a0001 | c0001 | t0066 | g0057 | AFR | GWD | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02895 | hp2 | a0001 | c0001 | t0006 | g0343 | AFR | GWD | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02896 | hp1 | a0001 | c0002 | t0034 | g0315 | AFR | GWD | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02896 | hp2 | a0003 | c0004 | t0021 | g0037 | AFR | GWD | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02897 | hp1 | a0001 | c0001 | t0006 | g0366 | AFR | GWD | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02897 | hp2 | a0003 | c0004 | t0021 | g0037 | AFR | GWD | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02922 | hp1 | a0001 | c0001 | t0006 | g0347 | AFR | ESN | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | ESN | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02965 | hp1 | a0001 | c0001 | t0005 | g0030 | AFR | ESN | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02965 | hp2 | a0001 | c0001 | t0009 | g0241 | AFR | ESN | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02970 | hp1 | a0001 | c0001 | t0005 | g0210 | AFR | ESN | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02970 | hp2 | a0001 | c0001 | t0005 | g0215 | AFR | ESN | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02976 | hp1 | a0001 | c0002 | t0011 | g0005 | AFR | ESN | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02976 | hp2 | a0001 | c0001 | t0009 | g0206 | AFR | ESN | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03017 | hp1 | a0001 | c0001 | t0003 | g0001 | SAS | PJL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03017 | hp2 | a0001 | c0001 | t0006 | g0364 | SAS | PJL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03041 | hp1 | a0002 | c0003 | t0008 | g0071 | AFR | GWD | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03041 | hp2 | a0001 | c0001 | t0059 | g0160 | AFR | GWD | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03098 | hp1 | a0001 | c0001 | t0006 | g0349 | AFR | MSL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03098 | hp2 | a0001 | c0001 | t0015 | g0073 | AFR | MSL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03130 | hp1 | a0001 | c0001 | t0006 | g0354 | AFR | ESN | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | ESN | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03195 | hp1 | a0002 | c0003 | t0032 | g0044 | AFR | ESN | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03195 | hp2 | a0001 | c0002 | t0011 | g0005 | AFR | ESN | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03209 | hp1 | a0001 | c0001 | t0052 | g0074 | AFR | MSL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03209 | hp2 | a0001 | c0001 | t0005 | g0209 | AFR | MSL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03225 | hp1 | a0001 | c0001 | t0006 | g0346 | AFR | MSL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03225 | hp2 | a0001 | c0001 | t0014 | g0177 | AFR | MSL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03453 | hp1 | a0001 | c0001 | t0005 | g0217 | AFR | MSL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03453 | hp2 | a0001 | c0001 | t0009 | g0032 | AFR | MSL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03486 | hp1 | a0001 | c0001 | t0053 | g0052 | AFR | MSL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03486 | hp2 | a0003 | c0004 | t0021 | g0323 | AFR | MSL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03490 | hp1 | a0001 | c0001 | t0030 | g0028 | SAS | PJL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03490 | hp2 | a0001 | c0001 | t0006 | g0359 | SAS | PJL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03491 | hp1 | a0001 | c0001 | t0057 | g0239 | SAS | PJL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0307 | SAS | PJL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03492 | hp1 | a0001 | c0001 | t0030 | g0028 | SAS | PJL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0308 | SAS | PJL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03516 | hp1 | a0002 | c0003 | t0072 | g0041 | AFR | ESN | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03516 | hp2 | a0001 | c0001 | t0015 | g0072 | AFR | ESN | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03540 | hp1 | a0001 | c0001 | t0007 | g0038 | AFR | GWD | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03540 | hp2 | a0001 | c0001 | t0009 | g0271 | AFR | GWD | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | MSL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03579 | hp2 | a0001 | c0001 | t0007 | g0038 | AFR | MSL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0247 | SAS | PJL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03669 | hp1 | a0001 | c0001 | t0007 | g0332 | SAS | PJL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03669 | hp2 | a0001 | c0001 | t0007 | g0335 | SAS | PJL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03688 | hp1 | a0001 | c0001 | t0012 | g0342 | SAS | STU | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0060 | SAS | STU | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03704 | hp1 | a0001 | c0001 | t0070 | g0200 | SAS | PJL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03704 | hp2 | a0001 | c0001 | t0010 | g0082 | SAS | PJL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03710 | hp1 | a0006 | c0009 | t0028 | g0331 | SAS | PJL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03710 | hp2 | a0001 | c0001 | t0006 | g0136 | SAS | PJL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03831 | hp1 | a0001 | c0001 | t0003 | g0312 | SAS | BEB | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0310 | SAS | BEB | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03834 | hp1 | a0001 | c0001 | t0003 | g0238 | SAS | BEB | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03834 | hp2 | a0001 | c0001 | t0010 | g0083 | SAS | BEB | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | BEB | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03927 | hp2 | a0001 | c0001 | t0005 | g0228 | SAS | BEB | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03942 | hp1 | a0001 | c0001 | t0003 | g0199 | SAS | BEB | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03942 | hp2 | a0001 | c0001 | t0012 | g0358 | SAS | BEB | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG04184 | hp1 | a0001 | c0001 | t0028 | g0333 | SAS | BEB | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0137 | SAS | BEB | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG04199 | hp1 | a0001 | c0001 | t0008 | g0223 | SAS | STU | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG04199 | hp2 | a0001 | c0001 | t0005 | g0235 | SAS | STU | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | STU | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG04228 | hp2 | a0001 | c0001 | t0026 | g0121 | SAS | STU | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | CHB | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18612 | hp2 | a0001 | c0001 | t0004 | g0109 | EAS | CHB | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18747 | hp1 | a0001 | c0001 | t0027 | g0023 | EAS | CHB | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18747 | hp2 | a0001 | c0001 | t0004 | g0108 | EAS | CHB | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18906 | hp1 | a0001 | c0001 | t0005 | g0218 | AFR | YRI | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18906 | hp2 | a0001 | c0002 | t0011 | g0005 | AFR | YRI | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18939 | hp1 | a0001 | c0005 | t0001 | g0152 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18939 | hp2 | a0001 | c0001 | t0003 | g0187 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18940 | hp1 | a0001 | c0001 | t0003 | g0197 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18942 | hp1 | a0001 | c0001 | t0024 | g0010 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18942 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18943 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18943 | hp2 | a0001 | c0001 | t0003 | g0091 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18944 | hp1 | a0001 | c0001 | t0007 | g0251 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18944 | hp2 | a0001 | c0001 | t0004 | g0154 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18945 | hp1 | a0001 | c0001 | t0004 | g0094 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18945 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18946 | hp1 | a0001 | c0001 | t0007 | g0248 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18946 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18949 | hp1 | a0001 | c0001 | t0007 | g0330 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18949 | hp2 | a0001 | c0001 | t0036 | g0142 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18950 | hp1 | a0001 | c0001 | t0004 | g0078 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18951 | hp1 | a0004 | c0006 | t0001 | g0181 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18952 | hp2 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18953 | hp1 | a0001 | c0001 | t0069 | g0151 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18953 | hp2 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18954 | hp2 | a0001 | c0001 | t0003 | g0194 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18956 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18959 | hp2 | a0001 | c0001 | t0016 | g0324 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0284 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18962 | hp2 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18963 | hp2 | a0001 | c0001 | t0055 | g0252 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18964 | hp1 | a0001 | c0001 | t0002 | g0289 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18964 | hp2 | a0001 | c0001 | t0007 | g0040 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18965 | hp1 | a0001 | c0001 | t0064 | g0297 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18967 | hp1 | a0001 | c0001 | t0003 | g0172 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18967 | hp2 | a0001 | c0001 | t0065 | g0036 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18968 | hp2 | a0001 | c0001 | t0037 | g0016 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18969 | hp1 | a0001 | c0001 | t0007 | g0249 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18969 | hp2 | a0001 | c0001 | t0004 | g0114 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18971 | hp1 | a0001 | c0001 | t0024 | g0010 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18972 | hp1 | a0001 | c0001 | t0025 | g0021 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18972 | hp2 | a0001 | c0001 | t0003 | g0190 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18973 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18973 | hp2 | a0001 | c0001 | t0004 | g0077 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18974 | hp2 | a0001 | c0001 | t0004 | g0079 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18977 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18978 | hp1 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18978 | hp2 | a0001 | c0001 | t0029 | g0371 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0283 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18979 | hp2 | a0001 | c0001 | t0004 | g0106 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18980 | hp1 | a0001 | c0001 | t0003 | g0193 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18981 | hp1 | a0001 | c0001 | t0007 | g0039 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18981 | hp2 | a0001 | c0001 | t0004 | g0164 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18982 | hp1 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18984 | hp1 | a0001 | c0001 | t0031 | g0201 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18985 | hp2 | a0001 | c0001 | t0002 | g0317 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18986 | hp1 | a0001 | c0001 | t0005 | g0306 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18987 | hp1 | a0001 | c0001 | t0013 | g0157 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18988 | hp1 | a0001 | c0001 | t0002 | g0286 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18988 | hp2 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18989 | hp1 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18992 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18994 | hp2 | a0001 | c0001 | t0004 | g0107 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18997 | hp1 | a0001 | c0001 | t0040 | g0156 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18997 | hp2 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18998 | hp1 | a0001 | c0001 | t0004 | g0314 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18998 | hp2 | a0001 | c0001 | t0003 | g0203 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0290 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19000 | hp1 | a0001 | c0001 | t0003 | g0204 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19000 | hp2 | a0001 | c0001 | t0007 | g0040 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19001 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19002 | hp2 | a0001 | c0005 | t0001 | g0064 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0298 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19004 | hp1 | a0001 | c0001 | t0031 | g0166 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19004 | hp2 | a0001 | c0001 | t0002 | g0262 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19005 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19005 | hp2 | a0001 | c0001 | t0004 | g0113 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19007 | hp1 | a0001 | c0001 | t0003 | g0184 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19009 | hp1 | a0001 | c0001 | t0013 | g0176 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19010 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19011 | hp1 | a0001 | c0001 | t0016 | g0329 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19011 | hp2 | a0001 | c0001 | t0004 | g0095 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19012 | hp1 | a0001 | c0001 | t0010 | g0147 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19012 | hp2 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19030 | hp1 | a0001 | c0001 | t0009 | g0300 | AFR | LWK | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19030 | hp2 | a0001 | c0001 | t0005 | g0234 | AFR | LWK | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19043 | hp1 | a0001 | c0001 | t0005 | g0336 | AFR | LWK | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19043 | hp2 | a0001 | c0002 | t0005 | g0050 | AFR | LWK | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19055 | hp1 | a0001 | c0001 | t0003 | g0186 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19055 | hp2 | a0001 | c0001 | t0004 | g0111 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19056 | hp2 | a0001 | c0001 | t0006 | g0353 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19058 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19058 | hp2 | a0001 | c0001 | t0010 | g0063 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19060 | hp1 | a0001 | c0001 | t0004 | g0110 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19060 | hp2 | a0001 | c0001 | t0003 | g0370 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0296 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19065 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19066 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19066 | hp2 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19068 | hp1 | a0001 | c0001 | t0005 | g0035 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19068 | hp2 | a0001 | c0001 | t0004 | g0076 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19070 | hp1 | a0001 | c0001 | t0025 | g0021 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19070 | hp2 | a0001 | c0001 | t0013 | g0276 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0255 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19074 | hp2 | a0001 | c0001 | t0007 | g0250 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19075 | hp1 | a0001 | c0001 | t0019 | g0062 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19075 | hp2 | a0001 | c0001 | t0002 | g0278 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0295 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19078 | hp1 | a0001 | c0001 | t0017 | g0299 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19078 | hp2 | a0001 | c0001 | t0019 | g0061 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19079 | hp1 | a0001 | c0001 | t0029 | g0372 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19080 | hp1 | a0001 | c0001 | t0007 | g0334 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19080 | hp2 | a0001 | c0001 | t0062 | g0053 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19081 | hp1 | a0001 | c0001 | t0016 | g0328 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0292 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19082 | hp2 | a0001 | c0001 | t0063 | g0191 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19083 | hp1 | a0001 | c0001 | t0016 | g0327 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19083 | hp2 | a0001 | c0001 | t0003 | g0202 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19087 | hp1 | a0001 | c0001 | t0013 | g0277 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19089 | hp1 | a0001 | c0001 | t0003 | g0282 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19090 | hp1 | a0001 | c0005 | t0001 | g0153 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19090 | hp2 | a0001 | c0001 | t0013 | g0275 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19091 | hp2 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19240 | hp1 | a0001 | c0001 | t0043 | g0081 | AFR | YRI | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA19240 | hp2 | a0001 | c0001 | t0005 | g0030 | AFR | YRI | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA20129 | hp1 | a0001 | c0002 | t0011 | g0005 | AFR | ASW | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA20129 | hp2 | a0001 | c0001 | t0005 | g0208 | AFR | ASW | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA20752 | hp1 | a0001 | c0001 | t0005 | g0302 | EUR | TSI | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA20752 | hp2 | a0001 | c0001 | t0003 | g0007 | EUR | TSI | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA20805 | hp1 | a0001 | c0001 | t0012 | g0338 | EUR | TSI | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA20805 | hp2 | a0001 | c0001 | t0006 | g0318 | EUR | TSI | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA20905 | hp1 | a0001 | c0001 | t0006 | g0339 | SAS | GIH | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0102 | SAS | GIH | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0355 | AFR | ACB | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | ACB | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | ACB | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02486 | hp2 | a0001 | c0001 | t0056 | g0056 | AFR | ACB | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02559 | hp1 | a0001 | c0001 | t0017 | g0337 | AFR | ACB | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG02559 | hp2 | a0001 | c0001 | t0048 | g0242 | AFR | ACB | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03471 | hp1 | a0001 | c0001 | t0006 | g0344 | AFR | MSL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG03471 | hp2 | a0001 | c0001 | t0046 | g0326 | AFR | MSL | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG06807 | hp1 | a0001 | c0001 | t0003 | g0007 | AFR | USA | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
HG06807 | hp2 | a0001 | c0001 | t0002 | g0051 | AFR | USA | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0034 | AFR | USA | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA20300 | hp2 | a0001 | c0001 | t0005 | g0233 | AFR | USA | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA21309 | hp1 | a0001 | c0001 | t0020 | g0236 | AFR | LWK | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | LWK | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0101 | REF | REF | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
homoSapiens_grch38 | hp1 | a0001 | c0002 | t0011 | g0316 | REF | REF | FXN_chr9_69030752_69084076 | FXN | chr9 | 69030752 | 69084076 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:69035868
|
G | A | 1 | a0004 | 1 | NA18951.hp1 | missense_variant | MODERATE | c.86G>A | p.Arg29Gln | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/5 | 117/6978 | 86/633 | 29/210 | chr9 | 69035868 | ||
chr9:69046398
|
G | A | 1 | a0005 | 1 | HG00673.hp2 | missense_variant | MODERATE | c.179G>A | p.Arg60His | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/5 | 210/6978 | 179/633 | 60/210 | chr9 | 69046398 | ||
chr9:69046445
|
A | G | 1 | a0002 | 7 | HG01891.hp2 HG02451.hp1 HG02647.hp2 others(4): Show |
missense_variant | MODERATE | c.226A>G | p.Met76Val | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/5 | 257/6978 | 226/633 | 76/210 | chr9 | 69046445 | ||
chr9:69053175
|
A | C | 1 | a0006 | 1 | HG03710.hp1 | missense_variant | MODERATE | c.299A>C | p.Glu100Ala | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/5 | 330/6978 | 299/633 | 100/210 | chr9 | 69053175 | ||
chr9:69072755
|
A | G | 1 | a0003 | 4 | HG02622.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
missense_variant | MODERATE | c.626A>G | p.Asp209Gly | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 657/6978 | 626/633 | 209/210 | chr9 | 69072755 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:69035836
|
A | G | 8 | a0001c0001a0001c0005a0001c0008others(5): Show | 421 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(418): Show |
synonymous_variant | LOW | c.54A>G | p.Pro18Pro | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/5 | 85/6978 | 54/633 | 18/210 | chr9 | 69035836 | ||
chr9:69053233
|
G | A | 1 | a0001c0005 | 3 | NA18939.hp1 NA19002.hp2 NA19090.hp1 |
synonymous_variant | LOW | c.357G>A | p.Thr119Thr | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/5 | 388/6978 | 357/633 | 119/210 | chr9 | 69053233 | ||
chr9:69065021
|
A | G | 1 | a0001c0008 | 1 | HG02698.hp2 | synonymous_variant | LOW | c.468A>G | p.Leu156Leu | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/5 | 499/6978 | 468/633 | 156/210 | chr9 | 69065021 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:69035776
|
G | A | 1 | a0001c0001t0018 | 3 | HG01358.hp1 HG01516.hp2 HG01517.hp1 |
5_prime_UTR_variant | MODIFIER | c.-7G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/5 | 7 | chr9 | 69035776 | |||||
chr9:69072839
|
TTTG | T | 29 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(26): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
3_prime_UTR_variant | MODIFIER | c.*92_*94delGTT | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 92 | INFO_REALIGN_3_PRIME | chr9 | 69072839 | ||||
chr9:69073008
|
C | T | 44 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(41): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
3_prime_UTR_variant | MODIFIER | c.*246C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 246 | chr9 | 69073008 | |||||
chr9:69073156
|
G | A | 1 | a0003c0004t0033 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*394G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 394 | chr9 | 69073156 | |||||
chr9:69073185
|
A | G | 44 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(41): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
3_prime_UTR_variant | MODIFIER | c.*423A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 423 | chr9 | 69073185 | |||||
chr9:69073202
|
A | G | 1 | a0001c0001t0056 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*440A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 440 | chr9 | 69073202 | |||||
chr9:69073244
|
T | C | 15 | a0001c0001t0007a0001c0001t0014a0001c0001t0015others(12): Show | 41 | HG00642.hp1 HG01496.hp1 HG01884.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*482T>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 482 | chr9 | 69073244 | |||||
chr9:69073245
|
G | A | 1 | a0001c0001t0052 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*483G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 483 | chr9 | 69073245 | |||||
chr9:69073302
|
T | C | 44 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(41): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
3_prime_UTR_variant | MODIFIER | c.*540T>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 540 | chr9 | 69073302 | |||||
chr9:69073318
|
C | T | 12 | a0001c0001t0007a0001c0001t0015a0001c0001t0016others(9): Show | 33 | HG00642.hp1 HG01891.hp2 HG02040.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*556C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 556 | chr9 | 69073318 | |||||
chr9:69073384
|
A | G | 29 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(26): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
3_prime_UTR_variant | MODIFIER | c.*622A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 622 | chr9 | 69073384 | |||||
chr9:69073395
|
C | T | 44 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(41): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
3_prime_UTR_variant | MODIFIER | c.*633C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 633 | chr9 | 69073395 | |||||
chr9:69073402
|
G | C | 1 | a0001c0002t0034 | 1 | HG02896.hp1 | 3_prime_UTR_variant | MODIFIER | c.*640G>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 640 | chr9 | 69073402 | |||||
chr9:69073557
|
G | T | 2 | a0001c0001t0022a0001c0001t0027 | 5 | HG00639.hp2 HG01928.hp2 HG01975.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*795G>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 795 | chr9 | 69073557 | |||||
chr9:69073560
|
T | G | 20 | a0001c0001t0001a0001c0001t0004a0001c0001t0010others(17): Show | 133 | HG00323.hp2 HG00438.hp1 HG00639.hp2 others(130): Show |
3_prime_UTR_variant | MODIFIER | c.*798T>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 798 | chr9 | 69073560 | |||||
chr9:69073679
|
C | G | 1 | a0001c0001t0051 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*917C>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 917 | chr9 | 69073679 | |||||
chr9:69073760
|
A | G | 1 | a0001c0001t0042 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*998A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 998 | chr9 | 69073760 | |||||
chr9:69073830
|
T | A | 2 | a0003c0004t0021a0003c0004t0033 | 4 | HG02622.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1068T>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 1068 | chr9 | 69073830 | |||||
chr9:69073834
|
A | G | 2 | a0003c0004t0021a0003c0004t0033 | 4 | HG02622.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1072A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 1072 | chr9 | 69073834 | |||||
chr9:69073861
|
G | A | 15 | a0001c0001t0007a0001c0001t0014a0001c0001t0015others(12): Show | 41 | HG00642.hp1 HG01496.hp1 HG01884.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*1099G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 1099 | chr9 | 69073861 | |||||
chr9:69074037
|
T | A | 1 | a0001c0001t0057 | 1 | HG03491.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1275T>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 1275 | chr9 | 69074037 | |||||
chr9:69074042
|
G | A | 12 | a0001c0001t0007a0001c0001t0015a0001c0001t0016others(9): Show | 33 | HG00642.hp1 HG01891.hp2 HG02040.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*1280G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 1280 | chr9 | 69074042 | |||||
chr9:69074077
|
T | C | 44 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(41): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
3_prime_UTR_variant | MODIFIER | c.*1315T>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 1315 | chr9 | 69074077 | |||||
chr9:69074088
|
A | G | 44 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(41): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
3_prime_UTR_variant | MODIFIER | c.*1326A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 1326 | chr9 | 69074088 | |||||
chr9:69074129
|
A | G | 28 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(25): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
3_prime_UTR_variant | MODIFIER | c.*1367A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 1367 | chr9 | 69074129 | |||||
chr9:69074129
|
A | T | 1 | a0001c0008t0073 | 1 | HG02698.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1367A>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 1367 | chr9 | 69074129 | |||||
chr9:69074200
|
T | TAAA | 44 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(41): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
3_prime_UTR_variant | MODIFIER | c.*1439_*1440insAAA | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 1440 | INFO_REALIGN_3_PRIME | chr9 | 69074200 | ||||
chr9:69074261
|
A | G | 1 | a0001c0001t0041 | 1 | HG02683.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1499A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 1499 | chr9 | 69074261 | |||||
chr9:69074287
|
C | T | 1 | a0002c0003t0050 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1525C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 1525 | chr9 | 69074287 | |||||
chr9:69074295
|
T | G | 1 | a0001c0001t0012 | 5 | HG00140.hp2 HG02145.hp2 HG03688.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1533T>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 1533 | chr9 | 69074295 | |||||
chr9:69074352
|
A | T | 2 | a0002c0003t0032a0002c0003t0072 | 3 | HG02647.hp2 HG03195.hp1 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1590A>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 1590 | chr9 | 69074352 | |||||
chr9:69074439
|
C | T | 3 | a0001c0001t0016a0001c0001t0027a0001c0001t0031 | 8 | HG02083.hp1 NA18747.hp1 NA18959.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1677C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 1677 | chr9 | 69074439 | |||||
chr9:69074459
|
A | G | 44 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(41): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
3_prime_UTR_variant | MODIFIER | c.*1697A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 1697 | chr9 | 69074459 | |||||
chr9:69074470
|
G | T | 2 | a0001c0001t0070a0001c0001t0071 | 2 | HG02738.hp1 HG03704.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1708G>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 1708 | chr9 | 69074470 | |||||
chr9:69074497
|
G | A | 3 | a0001c0001t0006a0001c0001t0012a0001c0001t0058 | 33 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*1735G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 1735 | chr9 | 69074497 | |||||
chr9:69074499
|
G | A | 28 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(25): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
3_prime_UTR_variant | MODIFIER | c.*1737G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 1737 | chr9 | 69074499 | |||||
chr9:69074506
|
C | T | 1 | a0001c0001t0040 | 1 | NA18997.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1744C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 1744 | chr9 | 69074506 | |||||
chr9:69074519
|
CA | C | 3 | a0001c0001t0010a0001c0001t0026a0001c0001t0049 | 9 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1771delA | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 1771 | INFO_REALIGN_3_PRIME | chr9 | 69074519 | ||||
chr9:69074532
|
AAG | A | 44 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(41): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
3_prime_UTR_variant | MODIFIER | c.*1771_*1772delAG | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 1771 | chr9 | 69074532 | |||||
chr9:69074549
|
G | A | 44 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(41): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
3_prime_UTR_variant | MODIFIER | c.*1787G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 1787 | chr9 | 69074549 | |||||
chr9:69074594
|
A | G | 1 | a0001c0001t0058 | 1 | HG01168.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1832A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 1832 | chr9 | 69074594 | |||||
chr9:69074717
|
C | T | 44 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(41): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
3_prime_UTR_variant | MODIFIER | c.*1955C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 1955 | chr9 | 69074717 | |||||
chr9:69074743
|
G | GA | 27 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(24): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
3_prime_UTR_variant | MODIFIER | c.*1990dupA | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 1991 | INFO_REALIGN_3_PRIME | chr9 | 69074743 | ||||
chr9:69074789
|
T | G | 1 | a0001c0001t0056 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2027T>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 2027 | chr9 | 69074789 | |||||
chr9:69074840
|
T | C | 29 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(26): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
3_prime_UTR_variant | MODIFIER | c.*2078T>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 2078 | chr9 | 69074840 | |||||
chr9:69074964
|
G | A | 44 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(41): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
3_prime_UTR_variant | MODIFIER | c.*2202G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 2202 | chr9 | 69074964 | |||||
chr9:69075228
|
C | T | 44 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(41): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
3_prime_UTR_variant | MODIFIER | c.*2466C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 2466 | chr9 | 69075228 | |||||
chr9:69075229
|
A | G | 44 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(41): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
3_prime_UTR_variant | MODIFIER | c.*2467A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 2467 | chr9 | 69075229 | |||||
chr9:69075234
|
T | G | 79 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(76): Show | 427 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(424): Show |
3_prime_UTR_variant | MODIFIER | c.*2472T>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 2472 | chr9 | 69075234 | |||||
chr9:69075241
|
T | G | 1 | a0002c0003t0050 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2479T>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 2479 | chr9 | 69075241 | |||||
chr9:69075266
|
T | C | 44 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(41): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
3_prime_UTR_variant | MODIFIER | c.*2504T>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 2504 | chr9 | 69075266 | |||||
chr9:69075287
|
G | A | 1 | a0001c0001t0026 | 2 | HG02602.hp2 HG04228.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2525G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 2525 | chr9 | 69075287 | |||||
chr9:69075320
|
C | T | 1 | a0001c0001t0066 | 1 | HG02895.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2558C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 2558 | chr9 | 69075320 | |||||
chr9:69075327
|
G | A | 3 | a0001c0001t0015a0001c0001t0053a0002c0003t0015 | 5 | HG01891.hp2 HG02451.hp1 HG03098.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2565G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 2565 | chr9 | 69075327 | |||||
chr9:69075330
|
C | T | 44 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(41): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
3_prime_UTR_variant | MODIFIER | c.*2568C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 2568 | chr9 | 69075330 | |||||
chr9:69075454
|
C | T | 43 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(40): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
3_prime_UTR_variant | MODIFIER | c.*2692C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 2692 | chr9 | 69075454 | |||||
chr9:69075459
|
C | CAAAT | 37 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(34): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
3_prime_UTR_variant | MODIFIER | c.*2717_*2720dupTAAA | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 2721 | INFO_REALIGN_3_PRIME | chr9 | 69075459 | ||||
chr9:69075459
|
C | CAAATAAA others(1): Show |
3 | a0001c0001t0014a0001c0001t0055a0002c0003t0032 | 7 | HG01496.hp1 HG02572.hp1 HG02615.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2713_*2720dupTAAA others(4): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 2721 | INFO_REALIGN_3_PRIME | chr9 | 69075459 | ||||
chr9:69075459
|
C | CAAATAAA others(9): Show |
1 | a0001c0002t0023 | 3 | HG01884.hp2 HG02717.hp1 HG02723.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2705_*2720dupTAAA others(12): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 2721 | INFO_REALIGN_3_PRIME | chr9 | 69075459 | ||||
chr9:69075536
|
T | A | 57 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(54): Show | 292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
3_prime_UTR_variant | MODIFIER | c.*2774T>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 2774 | chr9 | 69075536 | |||||
chr9:69075566
|
T | G | 58 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(55): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
3_prime_UTR_variant | MODIFIER | c.*2804T>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 2804 | chr9 | 69075566 | |||||
chr9:69075585
|
A | G | 43 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(40): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
3_prime_UTR_variant | MODIFIER | c.*2823A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 2823 | chr9 | 69075585 | |||||
chr9:69075648
|
T | A | 1 | a0001c0001t0056 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2886T>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 2886 | chr9 | 69075648 | |||||
chr9:69075659
|
G | T | 1 | a0001c0001t0025 | 2 | NA18972.hp1 NA19070.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2897G>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 2897 | chr9 | 69075659 | |||||
chr9:69075768
|
G | T | 78 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(75): Show | 426 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(423): Show |
3_prime_UTR_variant | MODIFIER | c.*3006G>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 3006 | chr9 | 69075768 | |||||
chr9:69075797
|
C | CAA | 3 | a0001c0001t0014a0001c0001t0056a0001c0002t0023 | 8 | HG01496.hp1 HG01884.hp2 HG02486.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3037_*3038dupAA | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 3039 | INFO_REALIGN_3_PRIME | chr9 | 69075797 | ||||
chr9:69075822
|
C | T | 1 | a0001c0001t0053 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3060C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 3060 | chr9 | 69075822 | |||||
chr9:69075829
|
T | G | 1 | a0001c0001t0057 | 1 | HG03491.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3067T>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 3067 | chr9 | 69075829 | |||||
chr9:69076017
|
CTAT | C | 3 | a0001c0001t0009a0001c0001t0048a0001c0001t0051 | 12 | HG01255.hp2 HG02055.hp2 HG02559.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*3260_*3262delATT | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 3260 | INFO_REALIGN_3_PRIME | chr9 | 69076017 | ||||
chr9:69076047
|
A | C | 43 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(40): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
3_prime_UTR_variant | MODIFIER | c.*3285A>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 3285 | chr9 | 69076047 | |||||
chr9:69076058
|
A | G | 43 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(40): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
3_prime_UTR_variant | MODIFIER | c.*3296A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 3296 | chr9 | 69076058 | |||||
chr9:69076114
|
G | C | 43 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(40): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
3_prime_UTR_variant | MODIFIER | c.*3352G>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 3352 | chr9 | 69076114 | |||||
chr9:69076145
|
T | C | 3 | a0001c0001t0009a0001c0001t0048a0001c0001t0051 | 12 | HG01255.hp2 HG02055.hp2 HG02559.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*3383T>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 3383 | chr9 | 69076145 | |||||
chr9:69076217
|
GT | G | 21 | a0001c0001t0001a0001c0001t0004a0001c0001t0010others(18): Show | 134 | HG00323.hp2 HG00438.hp1 HG00639.hp2 others(131): Show |
3_prime_UTR_variant | MODIFIER | c.*3469delT | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 3469 | INFO_REALIGN_3_PRIME | chr9 | 69076217 | ||||
chr9:69076220
|
T | G | 1 | a0001c0001t0043 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3458T>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 3458 | chr9 | 69076220 | |||||
chr9:69076231
|
T | A | 1 | a0001c0001t0030 | 2 | HG03490.hp1 HG03492.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3469T>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 3469 | chr9 | 69076231 | |||||
chr9:69076231
|
T | TTTA | 25 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(22): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
3_prime_UTR_variant | MODIFIER | c.*3469_*3470insTTA | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 3470 | chr9 | 69076231 | |||||
chr9:69076231
|
T | TTTTA | 14 | a0001c0001t0007a0001c0001t0015a0001c0001t0016others(11): Show | 36 | HG00642.hp1 HG01891.hp2 HG02451.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*3469_*3470insTTTA | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 3470 | chr9 | 69076231 | |||||
chr9:69076323
|
G | A | 43 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(40): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
3_prime_UTR_variant | MODIFIER | c.*3561G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 3561 | chr9 | 69076323 | |||||
chr9:69076704
|
C | G | 1 | a0001c0001t0013 | 5 | NA18987.hp1 NA19009.hp1 NA19070.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3942C>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 3942 | chr9 | 69076704 | |||||
chr9:69076704
|
C | T | 4 | a0001c0001t0009a0001c0001t0048a0001c0001t0051others(1): Show | 13 | HG01255.hp2 HG02055.hp2 HG02559.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*3942C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 3942 | chr9 | 69076704 | |||||
chr9:69076752
|
G | A | 1 | a0001c0001t0019 | 3 | HG00673.hp1 NA19075.hp1 NA19078.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3990G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 3990 | chr9 | 69076752 | |||||
chr9:69076767
|
C | A | 1 | a0001c0001t0035 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4005C>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 4005 | chr9 | 69076767 | |||||
chr9:69076886
|
C | T | 2 | a0003c0004t0021a0003c0004t0033 | 4 | HG02622.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4124C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 4124 | chr9 | 69076886 | |||||
chr9:69077000
|
C | T | 1 | a0001c0001t0039 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4238C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 4238 | chr9 | 69077000 | |||||
chr9:69077001
|
G | A | 4 | a0001c0001t0016a0001c0001t0024a0001c0001t0029others(1): Show | 10 | HG02040.hp2 NA18942.hp1 NA18949.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*4239G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 4239 | chr9 | 69077001 | |||||
chr9:69077019
|
A | G | 9 | a0001c0001t0003a0001c0001t0030a0001c0001t0031others(6): Show | 63 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*4257A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 4257 | chr9 | 69077019 | |||||
chr9:69077164
|
C | G | 45 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(42): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
3_prime_UTR_variant | MODIFIER | c.*4402C>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 4402 | chr9 | 69077164 | |||||
chr9:69077192
|
G | A | 1 | a0001c0001t0062 | 1 | NA19080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4430G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 4430 | chr9 | 69077192 | |||||
chr9:69077221
|
T | G | 27 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(24): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
3_prime_UTR_variant | MODIFIER | c.*4459T>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 4459 | chr9 | 69077221 | |||||
chr9:69077469
|
A | G | 46 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(43): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
3_prime_UTR_variant | MODIFIER | c.*4707A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 4707 | chr9 | 69077469 | |||||
chr9:69077491
|
T | G | 1 | a0001c0001t0054 | 1 | HG00642.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4729T>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 4729 | chr9 | 69077491 | |||||
chr9:69077564
|
A | C | 5 | a0001c0001t0009a0001c0001t0048a0001c0001t0051others(2): Show | 14 | HG01255.hp2 HG02055.hp2 HG02559.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*4802A>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 4802 | chr9 | 69077564 | |||||
chr9:69077658
|
G | A | 2 | a0003c0004t0021a0003c0004t0033 | 4 | HG02622.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4896G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 4896 | chr9 | 69077658 | |||||
chr9:69077765
|
A | T | 2 | a0001c0001t0038a0001c0001t0039 | 2 | HG01496.hp2 HG02145.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5003A>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 5003 | chr9 | 69077765 | |||||
chr9:69077786
|
TGGCC | T | 2 | a0003c0004t0021a0003c0004t0033 | 4 | HG02622.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5026_*5029delGCCG | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 5026 | INFO_REALIGN_3_PRIME | chr9 | 69077786 | ||||
chr9:69077789
|
C | G | 76 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(73): Show | 422 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(419): Show |
3_prime_UTR_variant | MODIFIER | c.*5027C>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 5027 | chr9 | 69077789 | |||||
chr9:69077895
|
A | T | 29 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(26): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
3_prime_UTR_variant | MODIFIER | c.*5133A>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 5133 | chr9 | 69077895 | |||||
chr9:69077896
|
C | G | 5 | a0001c0001t0002a0001c0001t0057a0001c0001t0061others(2): Show | 74 | HG00438.hp2 HG00544.hp2 HG00558.hp1 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*5134C>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 5134 | chr9 | 69077896 | |||||
chr9:69077908
|
T | C | 43 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(40): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
3_prime_UTR_variant | MODIFIER | c.*5146T>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 5146 | chr9 | 69077908 | |||||
chr9:69077930
|
A | G | 29 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(26): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
3_prime_UTR_variant | MODIFIER | c.*5168A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 5168 | chr9 | 69077930 | |||||
chr9:69077946
|
G | A | 44 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(41): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
3_prime_UTR_variant | MODIFIER | c.*5184G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 5184 | chr9 | 69077946 | |||||
chr9:69077981
|
A | G | 1 | a0001c0002t0023 | 3 | HG01884.hp2 HG02717.hp1 HG02723.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5219A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 5219 | chr9 | 69077981 | |||||
chr9:69078028
|
A | C | 44 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(41): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
3_prime_UTR_variant | MODIFIER | c.*5266A>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 5266 | chr9 | 69078028 | |||||
chr9:69078163
|
C | G | 44 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(41): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
3_prime_UTR_variant | MODIFIER | c.*5401C>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 5401 | chr9 | 69078163 | |||||
chr9:69078212
|
G | C | 79 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(76): Show | 427 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(424): Show |
3_prime_UTR_variant | MODIFIER | c.*5450G>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 5450 | chr9 | 69078212 | |||||
chr9:69078227
|
T | A | 13 | a0001c0001t0007a0001c0001t0015a0001c0001t0016others(10): Show | 34 | HG00642.hp1 HG01891.hp2 HG02040.hp2 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*5465T>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 5465 | chr9 | 69078227 | |||||
chr9:69078351
|
C | T | 1 | a0001c0002t0023 | 3 | HG01884.hp2 HG02717.hp1 HG02723.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5589C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 5589 | chr9 | 69078351 | |||||
chr9:69078376
|
G | A | 44 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(41): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
3_prime_UTR_variant | MODIFIER | c.*5614G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 5614 | chr9 | 69078376 | |||||
chr9:69078500
|
AG | A | 16 | a0001c0001t0003a0001c0001t0005a0001c0001t0017others(13): Show | 100 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*5740delG | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 5740 | INFO_REALIGN_3_PRIME | chr9 | 69078500 | ||||
chr9:69078504
|
A | T | 17 | a0001c0001t0003a0001c0001t0005a0001c0001t0017others(14): Show | 101 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*5742A>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 5742 | chr9 | 69078504 | |||||
chr9:69078505
|
A | T | 17 | a0001c0001t0003a0001c0001t0005a0001c0001t0017others(14): Show | 101 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*5743A>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 5743 | chr9 | 69078505 | |||||
chr9:69078506
|
T | A | 17 | a0001c0001t0003a0001c0001t0005a0001c0001t0017others(14): Show | 101 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*5744T>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 5744 | chr9 | 69078506 | |||||
chr9:69078508
|
T | C | 17 | a0001c0001t0003a0001c0001t0005a0001c0001t0017others(14): Show | 101 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*5746T>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 5746 | chr9 | 69078508 | |||||
chr9:69078531
|
G | A | 1 | a0001c0001t0048 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5769G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 5769 | chr9 | 69078531 | |||||
chr9:69078565
|
C | T | 44 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(41): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
3_prime_UTR_variant | MODIFIER | c.*5803C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 5803 | chr9 | 69078565 | |||||
chr9:69078608
|
A | G | 1 | a0001c0001t0020 | 3 | HG02258.hp1 HG02280.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5846A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 5846 | chr9 | 69078608 | |||||
chr9:69078685
|
AT | A | 45 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(42): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
3_prime_UTR_variant | MODIFIER | c.*5927delT | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 5927 | INFO_REALIGN_3_PRIME | chr9 | 69078685 | ||||
chr9:69078693
|
G | A | 45 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(42): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
3_prime_UTR_variant | MODIFIER | c.*5931G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 5931 | chr9 | 69078693 | |||||
chr9:69078746
|
T | G | 1 | a0001c0002t0023 | 3 | HG01884.hp2 HG02717.hp1 HG02723.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5984T>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 5984 | chr9 | 69078746 | |||||
chr9:69078808
|
C | T | 2 | a0002c0003t0032a0002c0003t0072 | 3 | HG02647.hp2 HG03195.hp1 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6046C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 6046 | chr9 | 69078808 | |||||
chr9:69078861
|
C | T | 45 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(42): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
3_prime_UTR_variant | MODIFIER | c.*6099C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 6099 | chr9 | 69078861 | |||||
chr9:69078958
|
T | C | 2 | a0003c0004t0021a0003c0004t0033 | 4 | HG02622.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6196T>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 6196 | chr9 | 69078958 | |||||
chr9:69078977
|
A | T | 1 | a0001c0001t0037 | 1 | NA18968.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6215A>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 6215 | chr9 | 69078977 | |||||
chr9:69079050
|
G | T | 1 | a0001c0001t0045 | 1 | HG01346.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6288G>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 5/5 | 6288 | chr9 | 69079050 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:69035962
|
C | T | 2 | a0001c0001t0029g0371a0001c0001t0029g0372 | 2 | NA18978.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.165+15C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69035962 | ||||||
chr9:69035969
|
AGCCGCGG others(7): Show |
A | 11 | a0001c0001t0002g0045a0001c0001t0002g0047a0001c0002t0005g0050others(8): Show | 12 | HG01257.hp1 HG01884.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.165+42_165+55delGG others(12): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr9 | 69035969 | |||||
chr9:69036071
|
C | G | 2 | a0001c0001t0003g0369a0001c0001t0003g0370 | 2 | HG01106.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.165+124C>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69036071 | ||||||
chr9:69036130
|
C | T | 1 | a0001c0001t0007g0368 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.165+183C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69036130 | ||||||
chr9:69036170
|
G | A | 1 | a0001c0001t0002g0051 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.165+223G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69036170 | ||||||
chr9:69036325
|
G | A | 1 | a0001c0001t0053g0052 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.165+378G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69036325 | ||||||
chr9:69036453
|
G | A | 3 | a0001c0001t0003g0054a0001c0001t0003g0055a0001c0001t0062g0053 | 3 | HG02071.hp2 HG02132.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.165+506G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69036453 | ||||||
chr9:69036689
|
A | G | 59 | a0001c0001t0001g0340a0001c0001t0001g0341a0001c0001t0001g0355others(56): Show | 64 | HG00099.hp1 HG00140.hp2 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.165+742A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69036689 | ||||||
chr9:69036965
|
T | C | 4 | a0001c0001t0006g0318a0001c0001t0006g0319a0001c0001t0006g0320others(1): Show | 4 | HG00099.hp1 HG01081.hp2 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.165+1018T>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69036965 | ||||||
chr9:69036995
|
C | T | 1 | a0001c0001t0002g0317 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.165+1048C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69036995 | ||||||
chr9:69037043
|
G | A | 370 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(367): Show | 421 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(418): Show |
intron_variant | MODIFIER | c.165+1096G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69037043 | ||||||
chr9:69037045
|
A | G | 1 | a0001c0001t0004g0314 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.165+1098A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69037045 | ||||||
chr9:69037203
|
C | T | 1 | a0001c0001t0002g0313 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.165+1256C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69037203 | ||||||
chr9:69037284
|
A | AAAAAAGA others(2): Show |
6 | a0001c0001t0007g0368a0001c0001t0017g0012a0001c0001t0029g0371others(3): Show | 7 | HG02486.hp2 HG02717.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.165+1339_165+1340i others(11): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr9 | 69037284 | |||||
chr9:69037284
|
A | AAAAAAGA others(5): Show |
11 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0002g0058others(8): Show | 11 | HG02074.hp2 HG03688.hp2 NA18612.hp1 others(8): Show |
intron_variant | MODIFIER | c.165+1339_165+1340i others(14): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr9 | 69037284 | |||||
chr9:69037284
|
A | AAAAAGAA others(1): Show |
27 | a0001c0001t0005g0336a0001c0001t0007g0038a0001c0001t0007g0039others(24): Show | 31 | HG00642.hp1 HG01891.hp2 HG02040.hp2 others(28): Show |
intron_variant | MODIFIER | c.165+1339_165+1340i others(10): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr9 | 69037284 | |||||
chr9:69037284
|
A | AAAAAGAA others(4): Show |
111 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(108): Show | 127 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.165+1339_165+1340i others(13): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr9 | 69037284 | |||||
chr9:69037284
|
A | AAAAAGAA others(13): Show |
1 | a0001c0001t0012g0338 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.165+1339_165+1340i others(22): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr9 | 69037284 | |||||
chr9:69037284
|
A | AAAAAGAA others(31): Show |
1 | a0001c0001t0006g0339 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.165+1339_165+1340i others(40): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr9 | 69037284 | |||||
chr9:69037284
|
A | AAAAAGAA others(34): Show |
2 | a0001c0001t0001g0340a0001c0001t0001g0341 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.165+1339_165+1340i others(43): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr9 | 69037284 | |||||
chr9:69037284
|
A | AAAAAGAA others(37): Show |
1 | a0001c0001t0012g0342 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.165+1339_165+1340i others(46): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr9 | 69037284 | |||||
chr9:69037284
|
A | AAAAGAAG others(3): Show |
5 | a0001c0001t0001g0171a0001c0001t0002g0167a0001c0001t0022g0169others(2): Show | 5 | HG00639.hp2 HG01346.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.165+1339_165+1340i others(12): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr9 | 69037284 | |||||
chr9:69037284
|
A | AAAAGAAG others(18): Show |
5 | a0001c0001t0006g0343a0001c0001t0006g0344a0001c0001t0006g0345others(2): Show | 5 | HG02818.hp2 HG02895.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.165+1339_165+1340i others(27): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr9 | 69037284 | |||||
chr9:69037284
|
A | AAAAGAAG others(21): Show |
1 | a0001c0001t0006g0348 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.165+1339_165+1340i others(30): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr9 | 69037284 | |||||
chr9:69037284
|
A | AAAAGAAG others(24): Show |
1 | a0001c0001t0006g0349 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.165+1339_165+1340i others(33): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr9 | 69037284 | |||||
chr9:69037284
|
A | AAAAGAAG others(27): Show |
4 | a0001c0001t0006g0350a0001c0001t0006g0351a0001c0001t0006g0352others(1): Show | 4 | HG02055.hp1 HG02300.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.165+1339_165+1340i others(36): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr9 | 69037284 | |||||
chr9:69037284
|
A | AAAAGAAG others(30): Show |
2 | a0001c0001t0001g0355a0001c0001t0006g0354 | 2 | HG02109.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.165+1339_165+1340i others(39): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr9 | 69037284 | |||||
chr9:69037284
|
A | AAAAGAAG others(33): Show |
1 | a0001c0001t0006g0356 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.165+1339_165+1340i others(42): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr9 | 69037284 | |||||
chr9:69037284
|
A | AAAAGAAG others(36): Show |
3 | a0001c0001t0006g0318a0001c0001t0006g0357a0001c0001t0012g0358 | 3 | HG02056.hp2 HG03942.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.165+1339_165+1340i others(45): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr9 | 69037284 | |||||
chr9:69037284
|
A | AAAAGAAG others(39): Show |
3 | a0001c0001t0006g0319a0001c0001t0006g0320a0001c0001t0006g0359 | 3 | HG01081.hp2 HG01192.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.165+1339_165+1340i others(48): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr9 | 69037284 | |||||
chr9:69037284
|
A | AAAAGAAG others(42): Show |
3 | a0001c0001t0006g0321a0001c0001t0006g0360a0001c0001t0006g0361 | 3 | HG00099.hp1 HG00741.hp1 HG01070.hp2 |
intron_variant | MODIFIER | c.165+1339_165+1340i others(51): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr9 | 69037284 | |||||
chr9:69037284
|
A | AAAAGAAG others(45): Show |
2 | a0001c0001t0012g0362a0001c0001t0012g0363 | 2 | HG00140.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.165+1339_165+1340i others(54): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr9 | 69037284 | |||||
chr9:69037284
|
A | AAAAGAAG others(48): Show |
1 | a0001c0001t0006g0364 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.165+1339_165+1340i others(57): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr9 | 69037284 | |||||
chr9:69037284
|
A | AAAAGAAG others(69): Show |
1 | a0001c0001t0006g0365 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.165+1339_165+1340i others(78): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr9 | 69037284 | |||||
chr9:69037284
|
A | AAAGAAG | 73 | a0001c0001t0001g0185a0001c0001t0003g0001a0001c0001t0003g0003others(70): Show | 93 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.165+1352_165+1357d others(8): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr9 | 69037284 | |||||
chr9:69037284
|
A | AAAGAAGA others(2): Show |
73 | a0001c0001t0001g0254a0001c0001t0001g0274a0001c0001t0001g0280others(70): Show | 82 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.165+1349_165+1357d others(11): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr9 | 69037284 | |||||
chr9:69037284
|
A | AAAGAAGA others(5): Show |
1 | a0001c0001t0009g0300 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.165+1346_165+1357d others(14): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr9 | 69037284 | |||||
chr9:69037284
|
A | AAAGAAGA others(17): Show |
1 | a0001c0001t0006g0366 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.165+1357_165+1358i others(26): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr9 | 69037284 | |||||
chr9:69037284
|
A | AAAGAAGA others(38): Show |
1 | a0001c0001t0049g0367 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.165+1357_165+1358i others(47): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr9 | 69037284 | |||||
chr9:69037284
|
A | AAGAAG | 6 | a0001c0001t0005g0301a0001c0001t0005g0302a0001c0001t0005g0304others(3): Show | 6 | HG00140.hp1 HG00673.hp2 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.165+1338_165+1339i others(7): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr9 | 69037284 | |||||
chr9:69037284
|
A | AAGAAGAA others(4): Show |
6 | a0001c0001t0001g0307a0001c0001t0001g0308a0001c0001t0001g0309others(3): Show | 6 | HG01168.hp1 HG02132.hp2 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.165+1338_165+1339i others(13): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr9 | 69037284 | |||||
chr9:69037286
|
AG | A | 3 | a0001c0001t0001g0069a0001c0001t0001g0070a0002c0003t0008g0071 | 3 | HG02280.hp2 HG02922.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.165+1340delG | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69037286 | ||||||
chr9:69037287
|
G | A | 3 | a0003c0004t0021g0037a0003c0004t0021g0323a0003c0004t0033g0322 | 4 | HG02622.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.165+1340G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69037287 | ||||||
chr9:69037289
|
A | G | 1 | a0001c0001t0006g0365 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.165+1342A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69037289 | ||||||
chr9:69037334
|
C | T | 1 | a0002c0003t0050g0075 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.165+1387C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69037334 | ||||||
chr9:69037369
|
G | C | 3 | a0003c0004t0021g0037a0003c0004t0021g0323a0003c0004t0033g0322 | 4 | HG02622.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.165+1422G>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69037369 | ||||||
chr9:69037468
|
AAATAAT | A | 36 | a0001c0001t0001g0185a0001c0001t0003g0001a0001c0001t0003g0003others(33): Show | 51 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.165+1530_165+1535d others(8): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr9 | 69037468 | |||||
chr9:69037477
|
T | TA | 5 | a0001c0001t0001g0069a0001c0001t0001g0070a0003c0004t0021g0037others(2): Show | 6 | HG02280.hp2 HG02622.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.165+1532dupA | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr9 | 69037477 | |||||
chr9:69037517
|
C | T | 77 | a0001c0001t0001g0185a0001c0001t0003g0001a0001c0001t0003g0003others(74): Show | 96 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.165+1570C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69037517 | ||||||
chr9:69037572
|
GCAGACAT others(5): Show |
G | 1 | a0001c0001t0004g0076 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.165+1626_165+1637d others(14): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69037572 | ||||||
chr9:69037605
|
C | A | 1 | a0001c0001t0004g0076 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.165+1658C>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69037605 | ||||||
chr9:69037614
|
C | A | 1 | a0001c0001t0004g0076 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.165+1667C>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69037614 | ||||||
chr9:69037619
|
A | C | 1 | a0001c0001t0004g0076 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.165+1672A>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69037619 | ||||||
chr9:69037620
|
T | A | 1 | a0001c0001t0004g0076 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.165+1673T>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69037620 | ||||||
chr9:69037632
|
C | A | 1 | a0001c0001t0004g0076 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.165+1685C>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69037632 | ||||||
chr9:69037634
|
C | T | 1 | a0001c0001t0004g0076 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.165+1687C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69037634 | ||||||
chr9:69037642
|
G | T | 1 | a0001c0001t0004g0076 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.165+1695G>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69037642 | ||||||
chr9:69037646
|
A | C | 1 | a0001c0001t0004g0076 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.165+1699A>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69037646 | ||||||
chr9:69037652
|
T | G | 1 | a0001c0001t0004g0076 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.165+1705T>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69037652 | ||||||
chr9:69037653
|
G | A | 1 | a0001c0001t0004g0076 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.165+1706G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69037653 | ||||||
chr9:69037654
|
G | T | 1 | a0001c0001t0004g0076 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.165+1707G>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69037654 | ||||||
chr9:69037656
|
T | C | 1 | a0001c0001t0004g0076 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.165+1709T>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69037656 | ||||||
chr9:69037659
|
T | G | 1 | a0001c0001t0004g0076 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.165+1712T>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69037659 | ||||||
chr9:69037660
|
C | T | 1 | a0001c0001t0004g0076 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.165+1713C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69037660 | ||||||
chr9:69037672
|
G | T | 1 | a0001c0001t0004g0076 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.165+1725G>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69037672 | ||||||
chr9:69037673
|
T | A | 1 | a0001c0001t0004g0076 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.165+1726T>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69037673 | ||||||
chr9:69037677
|
G | T | 1 | a0001c0001t0004g0076 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.165+1730G>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69037677 | ||||||
chr9:69037682
|
G | A | 1 | a0001c0001t0004g0076 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.165+1735G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69037682 | ||||||
chr9:69037695
|
A | G | 1 | a0001c0001t0004g0076 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.165+1748A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69037695 | ||||||
chr9:69037700
|
T | C | 1 | a0001c0001t0004g0076 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.165+1753T>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69037700 | ||||||
chr9:69037702
|
C | T | 1 | a0001c0001t0004g0076 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.165+1755C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69037702 | ||||||
chr9:69037711
|
T | C | 1 | a0001c0001t0004g0076 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.165+1764T>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69037711 | ||||||
chr9:69037729
|
G | T | 1 | a0001c0001t0004g0076 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.165+1782G>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69037729 | ||||||
chr9:69037733
|
C | G | 1 | a0001c0001t0004g0076 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.165+1786C>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69037733 | ||||||
chr9:69037734
|
T | C | 1 | a0001c0001t0004g0076 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.165+1787T>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69037734 | ||||||
chr9:69037735
|
C | G | 1 | a0001c0001t0004g0076 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.165+1788C>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69037735 | ||||||
chr9:69037741
|
C | T | 1 | a0001c0001t0004g0076 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.165+1794C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69037741 | ||||||
chr9:69037742
|
A | G | 1 | a0001c0001t0004g0076 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.165+1795A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69037742 | ||||||
chr9:69037746
|
C | T | 1 | a0001c0001t0004g0076 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.165+1799C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69037746 | ||||||
chr9:69037748
|
C | A | 1 | a0001c0001t0004g0076 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.165+1801C>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69037748 | ||||||
chr9:69038062
|
G | C | 1 | a0001c0001t0002g0058 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.165+2115G>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69038062 | ||||||
chr9:69038125
|
G | T | 1 | a0001c0001t0003g0205 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.165+2178G>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69038125 | ||||||
chr9:69038228
|
G | A | 4 | a0001c0001t0004g0076a0001c0001t0004g0077a0001c0001t0004g0078others(1): Show | 4 | NA18950.hp1 NA18973.hp2 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.165+2281G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69038228 | ||||||
chr9:69038281
|
T | A | 2 | a0001c0001t0005g0208a0001c0001t0005g0209 | 2 | HG03209.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.165+2334T>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69038281 | ||||||
chr9:69038667
|
A | C | 169 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(166): Show | 191 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(188): Show |
intron_variant | MODIFIER | c.165+2720A>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69038667 | ||||||
chr9:69038813
|
A | G | 1 | a0001c0001t0005g0306 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.165+2866A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69038813 | ||||||
chr9:69038836
|
C | A | 1 | a0001c0001t0004g0080 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.165+2889C>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69038836 | ||||||
chr9:69038999
|
T | A | 1 | a0001c0001t0016g0324 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.165+3052T>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69038999 | ||||||
chr9:69039039
|
G | A | 156 | a0001c0001t0001g0185a0001c0001t0001g0254a0001c0001t0001g0274others(153): Show | 184 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.165+3092G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69039039 | ||||||
chr9:69039128
|
C | A | 164 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(161): Show | 185 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(182): Show |
intron_variant | MODIFIER | c.165+3181C>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69039128 | ||||||
chr9:69039231
|
G | A | 1 | a0001c0001t0014g0177 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.165+3284G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69039231 | ||||||
chr9:69039401
|
A | G | 1 | a0001c0001t0053g0052 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.165+3454A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69039401 | ||||||
chr9:69039519
|
AC | A | 133 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(130): Show | 150 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.165+3574delC | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr9 | 69039519 | |||||
chr9:69039595
|
T | A | 2 | a0001c0001t0010g0082a0001c0001t0010g0083 | 2 | HG03704.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.165+3648T>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69039595 | ||||||
chr9:69039721
|
G | A | 1 | a0001c0001t0015g0072 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.165+3774G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69039721 | ||||||
chr9:69039723
|
A | G | 157 | a0001c0001t0001g0185a0001c0001t0001g0254a0001c0001t0001g0274others(154): Show | 185 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.165+3776A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69039723 | ||||||
chr9:69039745
|
A | G | 1 | a0002c0003t0008g0071 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.165+3798A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69039745 | ||||||
chr9:69039765
|
T | C | 133 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(130): Show | 150 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.165+3818T>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69039765 | ||||||
chr9:69040008
|
T | C | 1 | a0001c0002t0023g0048 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.165+4061T>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69040008 | ||||||
chr9:69040050
|
C | A | 1 | a0002c0003t0015g0042 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.165+4103C>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69040050 | ||||||
chr9:69040057
|
C | T | 1 | a0001c0001t0002g0298 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.165+4110C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69040057 | ||||||
chr9:69040194
|
A | G | 1 | a0001c0001t0006g0347 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.165+4247A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69040194 | ||||||
chr9:69040565
|
C | T | 2 | a0001c0001t0003g0238a0001c0008t0073g0237 | 2 | HG02698.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.165+4618C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69040565 | ||||||
chr9:69040602
|
A | G | 157 | a0001c0001t0001g0185a0001c0001t0001g0254a0001c0001t0001g0274others(154): Show | 185 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.165+4655A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69040602 | ||||||
chr9:69040668
|
A | G | 5 | a0001c0001t0001g0069a0001c0001t0001g0070a0003c0004t0021g0037others(2): Show | 6 | HG02280.hp2 HG02622.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.165+4721A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69040668 | ||||||
chr9:69040672
|
A | G | 22 | a0001c0001t0001g0340a0001c0001t0001g0341a0001c0001t0006g0318others(19): Show | 22 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.165+4725A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69040672 | ||||||
chr9:69040678
|
AT | A | 6 | a0001c0001t0001g0274a0001c0001t0002g0247a0001c0001t0013g0176others(3): Show | 6 | HG03654.hp1 NA18987.hp2 NA19009.hp1 others(3): Show |
intron_variant | MODIFIER | c.165+4732delT | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69040678 | ||||||
chr9:69040679
|
T | A | 76 | a0001c0001t0001g0254a0001c0001t0001g0340a0001c0001t0001g0341others(73): Show | 81 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.165+4732T>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69040679 | ||||||
chr9:69040683
|
T | A | 12 | a0001c0001t0002g0240a0001c0001t0002g0247a0001c0001t0009g0032others(9): Show | 13 | HG01255.hp2 HG02015.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.165+4736T>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69040683 | ||||||
chr9:69040750
|
C | T | 1 | a0001c0001t0027g0023 | 2 | HG02083.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.165+4803C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69040750 | ||||||
chr9:69040968
|
C | G | 5 | a0001c0001t0001g0069a0001c0001t0001g0070a0003c0004t0021g0037others(2): Show | 6 | HG02280.hp2 HG02622.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.165+5021C>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69040968 | ||||||
chr9:69041238
|
A | G | 1 | a0001c0001t0020g0031 | 2 | HG02258.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.166-5147A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69041238 | ||||||
chr9:69041309
|
T | A | 1 | a0001c0001t0002g0278 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.166-5076T>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69041309 | ||||||
chr9:69041411
|
A | C | 1 | a0001c0001t0004g0080 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.166-4974A>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69041411 | ||||||
chr9:69041416
|
C | G | 1 | a0001c0001t0031g0166 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.166-4969C>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69041416 | ||||||
chr9:69041672
|
G | T | 1 | a0001c0001t0001g0165 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.166-4713G>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69041672 | ||||||
chr9:69041822
|
G | T | 4 | a0001c0001t0004g0161a0001c0001t0004g0162a0001c0001t0004g0163others(1): Show | 4 | HG01981.hp1 HG01993.hp2 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.166-4563G>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69041822 | ||||||
chr9:69041899
|
G | A | 7 | a0001c0001t0002g0013a0001c0001t0002g0045a0001c0001t0002g0084others(4): Show | 8 | HG00544.hp2 HG00735.hp1 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.166-4486G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69041899 | ||||||
chr9:69041945
|
A | G | 2 | a0001c0001t0002g0273a0001c0001t0064g0297 | 2 | NA18965.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.166-4440A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69041945 | ||||||
chr9:69041971
|
G | A | 1 | a0001c0001t0002g0279 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.166-4414G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69041971 | ||||||
chr9:69042205
|
T | A | 159 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(156): Show | 180 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(177): Show |
intron_variant | MODIFIER | c.166-4180T>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69042205 | ||||||
chr9:69042206
|
C | T | 159 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(156): Show | 180 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(177): Show |
intron_variant | MODIFIER | c.166-4179C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69042206 | ||||||
chr9:69042239
|
G | GA | 188 | a0001c0001t0001g0089a0001c0001t0001g0185a0001c0001t0001g0254others(185): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.166-4131dupA | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr9 | 69042239 | |||||
chr9:69042264
|
C | T | 2 | a0001c0001t0004g0154a0001c0001t0025g0021 | 3 | NA18944.hp2 NA18972.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.166-4121C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69042264 | ||||||
chr9:69042302
|
C | G | 1 | a0001c0001t0053g0052 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.166-4083C>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69042302 | ||||||
chr9:69042481
|
G | A | 161 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(158): Show | 181 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(178): Show |
intron_variant | MODIFIER | c.166-3904G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69042481 | ||||||
chr9:69042568
|
A | G | 3 | a0001c0005t0001g0064a0001c0005t0001g0152a0001c0005t0001g0153 | 3 | NA18939.hp1 NA19002.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.166-3817A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69042568 | ||||||
chr9:69042637
|
G | A | 1 | a0001c0001t0001g0090 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.166-3748G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69042637 | ||||||
chr9:69042641
|
C | T | 3 | a0003c0004t0021g0037a0003c0004t0021g0323a0003c0004t0033g0322 | 4 | HG02622.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.166-3744C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69042641 | ||||||
chr9:69042691
|
A | AAC | 31 | a0001c0001t0001g0165a0001c0001t0007g0038a0001c0001t0007g0039others(28): Show | 36 | HG00642.hp1 HG02040.hp2 HG02486.hp2 others(33): Show |
intron_variant | MODIFIER | c.166-3680_166-3679d others(4): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr9 | 69042691 | |||||
chr9:69042854
|
T | C | 1 | a0001c0001t0002g0047 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.166-3531T>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69042854 | ||||||
chr9:69043095
|
G | A | 1 | a0001c0001t0003g0091 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.166-3290G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69043095 | ||||||
chr9:69043222
|
T | A | 1 | a0001c0001t0003g0184 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.166-3163T>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69043222 | ||||||
chr9:69043231
|
G | A | 3 | a0003c0004t0021g0037a0003c0004t0021g0323a0003c0004t0033g0322 | 4 | HG02622.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.166-3154G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69043231 | ||||||
chr9:69043279
|
C | G | 41 | a0001c0001t0001g0185a0001c0001t0003g0001a0001c0001t0003g0003others(38): Show | 59 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.166-3106C>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69043279 | ||||||
chr9:69043520
|
G | A | 32 | a0001c0001t0001g0355a0001c0001t0006g0318a0001c0001t0006g0319others(29): Show | 32 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.166-2865G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69043520 | ||||||
chr9:69043565
|
C | T | 1 | a0001c0001t0069g0151 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.166-2820C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69043565 | ||||||
chr9:69043591
|
T | C | 6 | a0001c0001t0014g0183a0002c0003t0015g0042a0002c0003t0015g0046others(3): Show | 6 | HG01891.hp2 HG02451.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.166-2794T>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69043591 | ||||||
chr9:69043646
|
C | T | 1 | a0001c0001t0002g0270 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.166-2739C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69043646 | ||||||
chr9:69043647
|
G | A | 1 | a0001c0001t0017g0299 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.166-2738G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69043647 | ||||||
chr9:69043679
|
A | G | 1 | a0001c0001t0002g0058 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.166-2706A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69043679 | ||||||
chr9:69043772
|
C | T | 1 | a0001c0001t0002g0295 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.166-2613C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69043772 | ||||||
chr9:69043773
|
G | A | 1 | a0001c0001t0005g0211 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.166-2612G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69043773 | ||||||
chr9:69043877
|
C | G | 1 | a0001c0001t0002g0278 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.166-2508C>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69043877 | ||||||
chr9:69044030
|
G | A | 2 | a0001c0001t0004g0014a0001c0001t0004g0092 | 3 | HG02071.hp1 HG02080.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.166-2355G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69044030 | ||||||
chr9:69044172
|
T | A | 2 | a0001c0001t0005g0301a0001c0001t0005g0302 | 2 | HG00140.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.166-2213T>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69044172 | ||||||
chr9:69044176
|
G | C | 186 | a0001c0001t0001g0185a0001c0001t0001g0254a0001c0001t0001g0274others(183): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.166-2209G>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69044176 | ||||||
chr9:69044364
|
C | T | 66 | a0001c0001t0001g0254a0001c0001t0001g0274a0001c0001t0002g0004others(63): Show | 73 | HG00438.hp2 HG00558.hp2 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.166-2021C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69044364 | ||||||
chr9:69044655
|
C | T | 2 | a0001c0001t0001g0149a0001c0001t0001g0150 | 2 | HG01891.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.166-1730C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69044655 | ||||||
chr9:69044691
|
C | G | 1 | a0001c0001t0001g0148 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.166-1694C>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69044691 | ||||||
chr9:69044694
|
C | T | 28 | a0001c0001t0002g0004a0001c0001t0002g0036a0001c0001t0002g0047others(25): Show | 31 | HG00438.hp2 HG01099.hp1 HG01257.hp1 others(28): Show |
intron_variant | MODIFIER | c.166-1691C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69044694 | ||||||
chr9:69044704
|
C | T | 10 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0144others(7): Show | 12 | HG02083.hp2 NA18939.hp1 NA18965.hp2 others(9): Show |
intron_variant | MODIFIER | c.166-1681C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69044704 | ||||||
chr9:69045193
|
G | A | 152 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(149): Show | 170 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(167): Show |
intron_variant | MODIFIER | c.166-1192G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69045193 | ||||||
chr9:69045249
|
A | AC | 375 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(372): Show | 427 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(424): Show |
intron_variant | MODIFIER | c.166-1136_166-1135i others(3): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69045249 | ||||||
chr9:69045274
|
TA | T | 21 | a0001c0001t0002g0167a0001c0001t0002g0278a0001c0001t0009g0032others(18): Show | 24 | HG01255.hp2 HG01884.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.166-1098delA | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr9 | 69045274 | |||||
chr9:69045317
|
T | C | 350 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(347): Show | 399 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(396): Show |
intron_variant | MODIFIER | c.166-1068T>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69045317 | ||||||
chr9:69045464
|
G | T | 7 | a0002c0003t0008g0071a0002c0003t0015g0042a0002c0003t0015g0046others(4): Show | 7 | HG01891.hp2 HG02451.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.166-921G>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69045464 | ||||||
chr9:69045474
|
T | A | 1 | a0001c0001t0003g0282 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.166-911T>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69045474 | ||||||
chr9:69045475
|
C | T | 1 | a0001c0001t0003g0282 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.166-910C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69045475 | ||||||
chr9:69045517
|
C | T | 2 | a0001c0001t0005g0235a0001c0001t0017g0299 | 2 | HG04199.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.166-868C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69045517 | ||||||
chr9:69045547
|
C | T | 2 | a0001c0001t0005g0035a0001c0001t0060g0303 | 3 | HG01243.hp2 HG02056.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.166-838C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69045547 | ||||||
chr9:69045548
|
G | A | 2 | a0001c0001t0020g0031a0001c0001t0020g0236 | 3 | HG02258.hp1 HG02280.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.166-837G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69045548 | ||||||
chr9:69045549
|
T | C | 375 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(372): Show | 427 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(424): Show |
intron_variant | MODIFIER | c.166-836T>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69045549 | ||||||
chr9:69045611
|
C | T | 5 | a0001c0001t0006g0318a0001c0001t0006g0319a0001c0001t0006g0320others(2): Show | 5 | HG00099.hp1 HG00642.hp2 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.166-774C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69045611 | ||||||
chr9:69045612
|
C | A | 1 | a0001c0001t0002g0278 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.166-773C>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69045612 | ||||||
chr9:69045612
|
C | CA | 8 | a0001c0001t0004g0076a0002c0003t0008g0071a0002c0003t0015g0042others(5): Show | 8 | HG01891.hp2 HG02451.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.166-762dupA | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr9 | 69045612 | |||||
chr9:69045622
|
A | C | 187 | a0001c0001t0001g0274a0001c0001t0001g0355a0001c0001t0002g0004others(184): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.166-763A>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69045622 | ||||||
chr9:69045650
|
G | A | 1 | a0001c0001t0020g0236 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.166-735G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69045650 | ||||||
chr9:69045869
|
G | A | 1 | a0001c0001t0003g0369 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.166-516G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69045869 | ||||||
chr9:69046200
|
G | A | 88 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0007others(85): Show | 111 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.166-185G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 1/4 | chr9 | 69046200 | ||||||
chr9:69046540
|
C | G | 2 | a0001c0001t0005g0233a0001c0001t0005g0234 | 2 | NA19030.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.263+58C>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69046540 | ||||||
chr9:69046625
|
G | C | 1 | a0001c0001t0003g0282 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.263+143G>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69046625 | ||||||
chr9:69046626
|
A | C | 1 | a0001c0001t0003g0282 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.263+144A>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69046626 | ||||||
chr9:69046627
|
A | C | 1 | a0001c0001t0003g0282 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.263+145A>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69046627 | ||||||
chr9:69046628
|
A | C | 1 | a0001c0001t0003g0282 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.263+146A>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69046628 | ||||||
chr9:69046629
|
T | G | 1 | a0001c0001t0003g0282 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.263+147T>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69046629 | ||||||
chr9:69046667
|
C | T | 1 | a0001c0001t0056g0056 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.263+185C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69046667 | ||||||
chr9:69046743
|
G | A | 4 | a0001c0001t0006g0352a0001c0001t0006g0359a0001c0001t0006g0360others(1): Show | 4 | HG01070.hp2 HG02300.hp2 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.263+261G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69046743 | ||||||
chr9:69046753
|
C | T | 1 | a0002c0003t0008g0071 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.263+271C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69046753 | ||||||
chr9:69046880
|
A | T | 1 | a0001c0001t0003g0282 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.263+398A>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69046880 | ||||||
chr9:69046973
|
G | A | 2 | a0001c0001t0005g0304a0005c0007t0005g0305 | 2 | HG00673.hp2 HG02027.hp1 |
intron_variant | MODIFIER | c.263+491G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69046973 | ||||||
chr9:69047106
|
G | A | 188 | a0001c0001t0001g0274a0001c0001t0001g0355a0001c0001t0002g0004others(185): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.263+624G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69047106 | ||||||
chr9:69047116
|
A | T | 2 | a0001c0001t0004g0154a0001c0001t0025g0021 | 3 | NA18944.hp2 NA18972.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.263+634A>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69047116 | ||||||
chr9:69047117
|
T | G | 2 | a0001c0001t0004g0154a0001c0001t0025g0021 | 3 | NA18944.hp2 NA18972.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.263+635T>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69047117 | ||||||
chr9:69047139
|
A | G | 3 | a0003c0004t0021g0037a0003c0004t0021g0323a0003c0004t0033g0322 | 4 | HG02622.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.263+657A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69047139 | ||||||
chr9:69047224
|
C | T | 161 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(158): Show | 180 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(177): Show |
intron_variant | MODIFIER | c.263+742C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69047224 | ||||||
chr9:69047262
|
A | C | 28 | a0001c0001t0007g0038a0001c0001t0007g0039a0001c0001t0007g0040others(25): Show | 32 | HG00642.hp1 HG02040.hp2 HG02486.hp2 others(29): Show |
intron_variant | MODIFIER | c.263+780A>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69047262 | ||||||
chr9:69047301
|
T | C | 188 | a0001c0001t0001g0274a0001c0001t0001g0355a0001c0001t0002g0004others(185): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.263+819T>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69047301 | ||||||
chr9:69047330
|
G | GACACAGA others(7): Show |
1 | a0001c0001t0001g0143 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.263+868_263+881dup others(14): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr9 | 69047330 | |||||
chr9:69047344
|
C | T | 17 | a0001c0001t0009g0032a0001c0001t0009g0206a0001c0001t0009g0241others(14): Show | 19 | HG01255.hp2 HG01884.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.263+862C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69047344 | ||||||
chr9:69047350
|
G | C | 1 | a0001c0001t0007g0038 | 2 | HG03540.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.263+868G>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69047350 | ||||||
chr9:69047350
|
G | GAC | 34 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0096others(31): Show | 39 | HG01257.hp2 HG01258.hp2 HG01515.hp1 others(36): Show |
intron_variant | MODIFIER | c.263+897_263+898dup others(2): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr9 | 69047350 | |||||
chr9:69047350
|
G | GACAC | 6 | a0001c0001t0001g0093a0001c0001t0014g0177a0001c0001t0014g0179others(3): Show | 6 | HG01243.hp1 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.263+895_263+898dup others(4): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr9 | 69047350 | |||||
chr9:69047350
|
GAC | G | 37 | a0001c0001t0001g0310a0001c0001t0002g0004a0001c0001t0002g0036others(34): Show | 40 | HG00438.hp2 HG01099.hp1 HG01257.hp1 others(37): Show |
intron_variant | MODIFIER | c.263+897_263+898del others(2): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr9 | 69047350 | |||||
chr9:69047433
|
C | T | 3 | a0001c0001t0002g0264a0001c0001t0002g0265a0001c0001t0002g0266 | 3 | NA18947.hp2 NA18994.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.263+951C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69047433 | ||||||
chr9:69047712
|
C | T | 1 | a0001c0001t0007g0335 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.263+1230C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69047712 | ||||||
chr9:69047781
|
G | A | 2 | a0001c0001t0001g0103a0001c0001t0042g0104 | 2 | HG00323.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.263+1299G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69047781 | ||||||
chr9:69047863
|
G | A | 17 | a0001c0001t0009g0032a0001c0001t0009g0206a0001c0001t0009g0241others(14): Show | 19 | HG01255.hp2 HG01884.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.263+1381G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69047863 | ||||||
chr9:69047933
|
G | A | 1 | a0001c0001t0005g0211 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.263+1451G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69047933 | ||||||
chr9:69047960
|
C | T | 1 | a0001c0001t0003g0232 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.263+1478C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69047960 | ||||||
chr9:69047961
|
G | A | 1 | a0001c0001t0022g0105 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.263+1479G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69047961 | ||||||
chr9:69047983
|
G | C | 1 | a0002c0003t0050g0075 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.263+1501G>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69047983 | ||||||
chr9:69048288
|
G | A | 1 | a0001c0001t0012g0342 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.263+1806G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69048288 | ||||||
chr9:69048343
|
G | A | 3 | a0003c0004t0021g0037a0003c0004t0021g0323a0003c0004t0033g0322 | 4 | HG02622.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.263+1861G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69048343 | ||||||
chr9:69048465
|
C | T | 1 | a0002c0003t0050g0075 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.263+1983C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69048465 | ||||||
chr9:69048590
|
C | T | 3 | a0001c0001t0005g0229a0001c0001t0005g0231a0001c0001t0067g0230 | 3 | HG01175.hp1 HG01884.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.263+2108C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69048590 | ||||||
chr9:69048773
|
C | T | 3 | a0001c0001t0002g0068a0001c0001t0002g0158a0001c0001t0002g0175 | 3 | NA18950.hp2 NA19065.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.263+2291C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69048773 | ||||||
chr9:69048973
|
T | C | 1 | a0001c0001t0001g0144 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.263+2491T>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69048973 | ||||||
chr9:69049146
|
C | T | 1 | a0001c0001t0006g0353 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.263+2664C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69049146 | ||||||
chr9:69049245
|
G | A | 1 | a0001c0001t0002g0283 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.263+2763G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69049245 | ||||||
chr9:69049290
|
T | C | 2 | a0001c0001t0005g0215a0001c0001t0005g0216 | 2 | HG02630.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.263+2808T>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69049290 | ||||||
chr9:69049812
|
C | G | 3 | a0003c0004t0021g0037a0003c0004t0021g0323a0003c0004t0033g0322 | 4 | HG02622.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.264-3328C>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69049812 | ||||||
chr9:69049838
|
C | T | 6 | a0001c0001t0005g0211a0001c0001t0005g0212a0001c0001t0005g0226others(3): Show | 6 | HG00323.hp1 HG01515.hp2 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.264-3302C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69049838 | ||||||
chr9:69049844
|
G | T | 1 | a0001c0001t0002g0263 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.264-3296G>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69049844 | ||||||
chr9:69049864
|
A | T | 1 | a0001c0001t0003g0282 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.264-3276A>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69049864 | ||||||
chr9:69050181
|
A | T | 89 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0007others(86): Show | 112 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.264-2959A>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69050181 | ||||||
chr9:69050220
|
A | G | 33 | a0001c0001t0001g0355a0001c0001t0006g0207a0001c0001t0006g0318others(30): Show | 33 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(30): Show |
intron_variant | MODIFIER | c.264-2920A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69050220 | ||||||
chr9:69050259
|
G | C | 29 | a0001c0001t0002g0253a0001c0001t0007g0038a0001c0001t0007g0039others(26): Show | 33 | HG00642.hp1 HG02040.hp2 HG02486.hp2 others(30): Show |
intron_variant | MODIFIER | c.264-2881G>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69050259 | ||||||
chr9:69050407
|
TAAGAGTG others(227): Show |
T | 370 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(367): Show | 422 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(419): Show |
intron_variant | MODIFIER | c.264-2716_264-2483d others(2): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr9 | 69050407 | |||||
chr9:69050783
|
T | C | 2 | a0001c0001t0005g0217a0001c0001t0005g0218 | 2 | HG03453.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.264-2357T>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69050783 | ||||||
chr9:69050784
|
C | CT | 211 | a0001c0001t0001g0274a0001c0001t0001g0355a0001c0001t0002g0004others(208): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.264-2343dupT | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr9 | 69050784 | |||||
chr9:69050834
|
G | A | 1 | a0001c0001t0004g0106 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.264-2306G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69050834 | ||||||
chr9:69050844
|
G | A | 2 | a0001c0001t0003g0370a0001c0002t0034g0315 | 2 | HG02896.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.264-2296G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69050844 | ||||||
chr9:69050905
|
C | T | 1 | a0001c0001t0024g0010 | 3 | HG02040.hp2 NA18942.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.264-2235C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69050905 | ||||||
chr9:69051000
|
G | A | 3 | a0003c0004t0021g0037a0003c0004t0021g0323a0003c0004t0033g0322 | 4 | HG02622.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.264-2140G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69051000 | ||||||
chr9:69051023
|
G | A | 1 | a0002c0003t0050g0075 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.264-2117G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69051023 | ||||||
chr9:69051026
|
C | T | 28 | a0001c0001t0002g0253a0001c0001t0007g0038a0001c0001t0007g0039others(25): Show | 32 | HG00642.hp1 HG02040.hp2 HG02809.hp1 others(29): Show |
intron_variant | MODIFIER | c.264-2114C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69051026 | ||||||
chr9:69051040
|
G | A | 79 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0007others(76): Show | 100 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.264-2100G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69051040 | ||||||
chr9:69051081
|
G | A | 18 | a0001c0001t0004g0006a0001c0001t0004g0015a0001c0001t0004g0094others(15): Show | 21 | HG00438.hp1 HG01943.hp2 HG01981.hp1 others(18): Show |
intron_variant | MODIFIER | c.264-2059G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69051081 | ||||||
chr9:69051161
|
G | A | 1 | a0001c0001t0002g0084 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.264-1979G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69051161 | ||||||
chr9:69051419
|
CT | C | 9 | a0001c0001t0002g0065a0001c0001t0002g0256a0001c0001t0002g0284others(6): Show | 9 | HG00639.hp2 HG01515.hp1 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.264-1708delT | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr9 | 69051419 | |||||
chr9:69051420
|
T | C | 1 | a0001c0001t0003g0282 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.264-1720T>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69051420 | ||||||
chr9:69051638
|
C | T | 1 | a0001c0001t0008g0325 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.264-1502C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69051638 | ||||||
chr9:69051772
|
G | A | 1 | a0001c0001t0007g0368 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.264-1368G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69051772 | ||||||
chr9:69051869
|
C | T | 17 | a0001c0001t0009g0032a0001c0001t0009g0206a0001c0001t0009g0241others(14): Show | 19 | HG01255.hp2 HG01884.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.264-1271C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69051869 | ||||||
chr9:69051935
|
C | T | 188 | a0001c0001t0001g0274a0001c0001t0001g0355a0001c0001t0002g0004others(185): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.264-1205C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69051935 | ||||||
chr9:69052007
|
C | T | 1 | a0001c0001t0008g0325 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.264-1133C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69052007 | ||||||
chr9:69052036
|
C | T | 1 | a0001c0002t0034g0315 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.264-1104C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69052036 | ||||||
chr9:69052149
|
A | AT | 10 | a0001c0001t0003g0202a0001c0001t0003g0203a0001c0001t0003g0204others(7): Show | 11 | HG01109.hp1 HG01255.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.264-977dupT | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr9 | 69052149 | |||||
chr9:69052149
|
A | T | 1 | a0001c0001t0056g0056 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.264-991A>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69052149 | ||||||
chr9:69052149
|
AT | A | 21 | a0001c0001t0001g0141a0001c0001t0008g0178a0001c0001t0008g0325others(18): Show | 23 | HG01255.hp2 HG01884.hp2 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.264-977delT | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr9 | 69052149 | |||||
chr9:69052149
|
ATT | A | 121 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(118): Show | 135 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(132): Show |
intron_variant | MODIFIER | c.264-978_264-977del others(2): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr9 | 69052149 | |||||
chr9:69052537
|
AT | A | 302 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(299): Show | 348 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(345): Show |
intron_variant | MODIFIER | c.264-580delT | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr9 | 69052537 | |||||
chr9:69052537
|
ATT | A | 50 | a0001c0001t0001g0096a0001c0001t0001g0116a0001c0001t0001g0307others(47): Show | 56 | HG00642.hp1 HG01070.hp1 HG01081.hp2 others(53): Show |
intron_variant | MODIFIER | c.264-581_264-580del others(2): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr9 | 69052537 | |||||
chr9:69052582
|
G | T | 3 | a0003c0004t0021g0037a0003c0004t0021g0323a0003c0004t0033g0322 | 4 | HG02622.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.264-558G>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69052582 | ||||||
chr9:69052605
|
C | T | 5 | a0002c0003t0015g0042a0002c0003t0015g0046a0002c0003t0032g0043others(2): Show | 5 | HG01891.hp2 HG02451.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.264-535C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69052605 | ||||||
chr9:69052612
|
G | A | 1 | a0001c0001t0002g0258 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.264-528G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69052612 | ||||||
chr9:69052734
|
G | T | 2 | a0002c0003t0015g0046a0002c0003t0072g0041 | 2 | HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.264-406G>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69052734 | ||||||
chr9:69052755
|
G | C | 2 | a0001c0001t0001g0096a0001c0001t0001g0097 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.264-385G>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69052755 | ||||||
chr9:69052807
|
G | A | 2 | a0001c0001t0020g0031a0001c0001t0020g0236 | 3 | HG02258.hp1 HG02280.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.264-333G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69052807 | ||||||
chr9:69052873
|
C | A | 3 | a0003c0004t0021g0037a0003c0004t0021g0323a0003c0004t0033g0322 | 4 | HG02622.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.264-267C>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69052873 | ||||||
chr9:69053070
|
G | A | 132 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(129): Show | 147 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(144): Show |
intron_variant | MODIFIER | c.264-70G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 2/4 | chr9 | 69053070 | ||||||
chr9:69053281
|
T | C | 189 | a0001c0001t0001g0274a0001c0001t0001g0355a0001c0001t0002g0004others(186): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.384+21T>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69053281 | ||||||
chr9:69053368
|
GT | G | 5 | a0001c0001t0004g0107a0001c0001t0004g0109a0001c0001t0004g0110others(2): Show | 5 | NA18612.hp2 NA18994.hp2 NA18998.hp1 others(2): Show |
intron_variant | MODIFIER | c.384+109delT | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69053368 | ||||||
chr9:69053371
|
G | A | 1 | a0001c0001t0056g0056 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.384+111G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69053371 | ||||||
chr9:69053419
|
C | A | 17 | a0001c0001t0009g0032a0001c0001t0009g0206a0001c0001t0009g0241others(14): Show | 19 | HG01255.hp2 HG01884.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.384+159C>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69053419 | ||||||
chr9:69053458
|
G | A | 64 | a0001c0001t0001g0274a0001c0001t0002g0004a0001c0001t0002g0009others(61): Show | 71 | HG00438.hp2 HG00558.hp2 HG00639.hp1 others(68): Show |
intron_variant | MODIFIER | c.384+198G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69053458 | ||||||
chr9:69053471
|
A | AGATG | 155 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0060others(152): Show | 191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.384+247_384+250dup others(4): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr9 | 69053471 | |||||
chr9:69053471
|
A | AGATGGAT others(1): Show |
82 | a0001c0001t0001g0182a0001c0001t0001g0274a0001c0001t0001g0307others(79): Show | 89 | HG00323.hp1 HG00423.hp1 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.384+243_384+250dup others(8): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr9 | 69053471 | |||||
chr9:69053471
|
A | AGATGGAT others(5): Show |
12 | a0001c0001t0001g0309a0001c0001t0002g0247a0001c0001t0002g0266others(9): Show | 12 | HG00438.hp2 HG00735.hp2 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.384+239_384+250dup others(12): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr9 | 69053471 | |||||
chr9:69053471
|
A | AGATGGAT others(9): Show |
2 | a0001c0001t0005g0301a0001c0001t0005g0302 | 2 | HG00140.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.384+235_384+250dup others(16): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr9 | 69053471 | |||||
chr9:69053471
|
A | G | 16 | a0001c0001t0003g0238a0001c0001t0009g0032a0001c0001t0009g0206others(13): Show | 18 | HG01255.hp2 HG01884.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.384+211A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69053471 | ||||||
chr9:69053499
|
GGATGGAT others(9): Show |
G | 1 | a0001c0001t0001g0100 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.384+243_384+258del others(16): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr9 | 69053499 | |||||
chr9:69053507
|
GGATA | G | 7 | a0001c0001t0006g0352a0001c0001t0046g0326a0002c0003t0015g0042others(4): Show | 7 | HG01891.hp2 HG02300.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.384+273_384+276del others(4): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr9 | 69053507 | |||||
chr9:69053511
|
A | G | 362 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(359): Show | 414 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(411): Show |
intron_variant | MODIFIER | c.384+251A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69053511 | ||||||
chr9:69053515
|
A | G | 136 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(133): Show | 151 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(148): Show |
intron_variant | MODIFIER | c.384+255A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69053515 | ||||||
chr9:69053519
|
A | G | 8 | a0001c0001t0002g0088a0001c0001t0002g0294a0001c0001t0014g0177others(5): Show | 8 | HG00735.hp1 HG02080.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.384+259A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69053519 | ||||||
chr9:69053523
|
A | G | 1 | a0002c0003t0008g0071 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.384+263A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69053523 | ||||||
chr9:69053529
|
A | G | 4 | a0001c0001t0014g0177a0001c0001t0014g0179a0001c0001t0014g0183others(1): Show | 4 | HG02572.hp1 HG02615.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.384+269A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69053529 | ||||||
chr9:69053559
|
TAAGAC | T | 3 | a0001c0001t0001g0307a0001c0001t0001g0308a0001c0001t0001g0310 | 3 | HG03491.hp2 HG03492.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.384+305_384+309del others(5): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr9 | 69053559 | |||||
chr9:69053856
|
C | A | 1 | a0001c0001t0002g0258 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.384+596C>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69053856 | ||||||
chr9:69053926
|
C | T | 1 | a0001c0001t0006g0318 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.384+666C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69053926 | ||||||
chr9:69054159
|
C | T | 5 | a0001c0001t0006g0318a0001c0001t0006g0319a0001c0001t0006g0320others(2): Show | 5 | HG00099.hp1 HG00642.hp2 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.384+899C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69054159 | ||||||
chr9:69054173
|
G | C | 1 | a0001c0001t0001g0165 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.384+913G>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69054173 | ||||||
chr9:69054200
|
A | G | 1 | a0001c0001t0001g0149 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.384+940A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69054200 | ||||||
chr9:69054219
|
C | T | 1 | a0001c0001t0043g0081 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.384+959C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69054219 | ||||||
chr9:69054242
|
C | G | 17 | a0001c0001t0009g0032a0001c0001t0009g0206a0001c0001t0009g0241others(14): Show | 19 | HG01255.hp2 HG01884.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.384+982C>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69054242 | ||||||
chr9:69054441
|
T | TAAAGTAG others(344): Show |
1 | a0002c0003t0008g0071 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.384+1197_384+1198i others(353): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr9 | 69054441 | |||||
chr9:69054581
|
A | G | 1 | a0001c0001t0031g0201 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.384+1321A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69054581 | ||||||
chr9:69054797
|
G | A | 1 | a0002c0003t0050g0075 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.384+1537G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69054797 | ||||||
chr9:69054839
|
G | A | 5 | a0001c0001t0014g0177a0001c0001t0014g0179a0001c0001t0014g0183others(2): Show | 5 | HG02572.hp1 HG02615.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.384+1579G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69054839 | ||||||
chr9:69054866
|
G | A | 1 | a0001c0001t0005g0233 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.384+1606G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69054866 | ||||||
chr9:69054881
|
A | T | 1 | a0001c0001t0004g0076 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.384+1621A>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69054881 | ||||||
chr9:69055096
|
A | C | 17 | a0001c0001t0009g0032a0001c0001t0009g0206a0001c0001t0009g0241others(14): Show | 19 | HG01255.hp2 HG01884.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.384+1836A>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69055096 | ||||||
chr9:69055272
|
C | A | 2 | a0001c0001t0020g0031a0001c0001t0020g0236 | 3 | HG02258.hp1 HG02280.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.384+2012C>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69055272 | ||||||
chr9:69055370
|
G | C | 1 | a0001c0001t0046g0326 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.384+2110G>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69055370 | ||||||
chr9:69055491
|
T | A | 5 | a0001c0001t0014g0177a0001c0001t0014g0179a0001c0001t0014g0183others(2): Show | 5 | HG02572.hp1 HG02615.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.384+2231T>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69055491 | ||||||
chr9:69055496
|
C | CT | 24 | a0001c0001t0001g0125a0001c0001t0001g0171a0001c0001t0006g0345others(21): Show | 26 | HG01255.hp2 HG01884.hp2 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.384+2251dupT | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr9 | 69055496 | |||||
chr9:69055571
|
G | A | 2 | a0001c0001t0005g0301a0001c0001t0005g0302 | 2 | HG00140.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.384+2311G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69055571 | ||||||
chr9:69055590
|
T | G | 1 | a0001c0001t0001g0180 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.384+2330T>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69055590 | ||||||
chr9:69055594
|
A | C | 1 | a0001c0001t0003g0029 | 2 | HG01361.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.384+2334A>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69055594 | ||||||
chr9:69055646
|
ACAATACA others(494): Show |
A | 1 | a0001c0001t0001g0185 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.384+2387_384+2887d others(2): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69055646 | ||||||
chr9:69055649
|
A | G | 122 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(119): Show | 136 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(133): Show |
intron_variant | MODIFIER | c.384+2389A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69055649 | ||||||
chr9:69055862
|
T | C | 1 | a0001c0001t0001g0165 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.384+2602T>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69055862 | ||||||
chr9:69056117
|
G | A | 1 | a0001c0001t0008g0178 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.384+2857G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69056117 | ||||||
chr9:69056147
|
G | A | 374 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(371): Show | 426 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(423): Show |
intron_variant | MODIFIER | c.384+2887G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69056147 | ||||||
chr9:69056174
|
C | T | 27 | a0001c0001t0007g0038a0001c0001t0007g0039a0001c0001t0007g0040others(24): Show | 31 | HG00642.hp1 HG02040.hp2 HG02809.hp1 others(28): Show |
intron_variant | MODIFIER | c.384+2914C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69056174 | ||||||
chr9:69056196
|
G | A | 1 | a0001c0001t0005g0226 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.384+2936G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69056196 | ||||||
chr9:69056200
|
G | A | 162 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(159): Show | 182 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(179): Show |
intron_variant | MODIFIER | c.384+2940G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69056200 | ||||||
chr9:69056330
|
C | T | 31 | a0001c0001t0007g0038a0001c0001t0007g0039a0001c0001t0007g0040others(28): Show | 36 | HG00642.hp1 HG02040.hp2 HG02486.hp2 others(33): Show |
intron_variant | MODIFIER | c.384+3070C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69056330 | ||||||
chr9:69056404
|
G | A | 2 | a0001c0001t0007g0248a0001c0001t0007g0249 | 2 | NA18946.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.384+3144G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69056404 | ||||||
chr9:69056617
|
A | G | 1 | a0001c0001t0016g0324 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.384+3357A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69056617 | ||||||
chr9:69056713
|
T | G | 17 | a0001c0001t0009g0032a0001c0001t0009g0206a0001c0001t0009g0241others(14): Show | 19 | HG01255.hp2 HG01884.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.384+3453T>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69056713 | ||||||
chr9:69056740
|
CT | C | 5 | a0001c0001t0003g0282a0001c0001t0010g0063a0003c0004t0021g0037others(2): Show | 6 | HG02622.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.384+3494delT | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr9 | 69056740 | |||||
chr9:69056773
|
TGCTCTGT others(202): Show |
T | 1 | a0001c0001t0001g0118 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.384+3514_384+3722d others(2): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69056773 | ||||||
chr9:69056795
|
T | C | 33 | a0001c0001t0002g0253a0001c0001t0005g0215a0001c0001t0007g0038others(30): Show | 38 | HG00642.hp1 HG02040.hp2 HG02486.hp2 others(35): Show |
intron_variant | MODIFIER | c.384+3535T>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69056795 | ||||||
chr9:69056820
|
G | A | 1 | a0002c0003t0008g0071 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.384+3560G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69056820 | ||||||
chr9:69056823
|
A | T | 17 | a0001c0001t0009g0032a0001c0001t0009g0206a0001c0001t0009g0241others(14): Show | 19 | HG01255.hp2 HG01884.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.384+3563A>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69056823 | ||||||
chr9:69056830
|
C | T | 1 | a0001c0001t0003g0189 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.384+3570C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69056830 | ||||||
chr9:69056916
|
T | A | 1 | a0003c0004t0033g0322 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.384+3656T>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69056916 | ||||||
chr9:69057109
|
C | G | 1 | a0001c0001t0013g0176 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.384+3849C>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69057109 | ||||||
chr9:69057153
|
G | A | 1 | a0001c0001t0006g0339 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.384+3893G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69057153 | ||||||
chr9:69057309
|
C | T | 17 | a0001c0001t0009g0032a0001c0001t0009g0206a0001c0001t0009g0241others(14): Show | 19 | HG01255.hp2 HG01884.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.384+4049C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69057309 | ||||||
chr9:69057515
|
A | G | 1 | a0001c0001t0003g0199 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.384+4255A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69057515 | ||||||
chr9:69057535
|
G | A | 1 | a0001c0001t0002g0051 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.384+4275G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69057535 | ||||||
chr9:69057579
|
A | G | 90 | a0001c0001t0003g0001a0001c0001t0003g0003a0001c0001t0003g0007others(87): Show | 113 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.384+4319A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69057579 | ||||||
chr9:69057837
|
G | C | 1 | a0001c0001t0003g0205 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.384+4577G>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69057837 | ||||||
chr9:69057942
|
C | T | 31 | a0001c0001t0007g0038a0001c0001t0007g0039a0001c0001t0007g0040others(28): Show | 36 | HG00642.hp1 HG02040.hp2 HG02486.hp2 others(33): Show |
intron_variant | MODIFIER | c.384+4682C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69057942 | ||||||
chr9:69058031
|
T | C | 1 | a0001c0001t0006g0357 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.384+4771T>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69058031 | ||||||
chr9:69058077
|
C | T | 2 | a0001c0001t0046g0326a0002c0003t0050g0075 | 2 | HG02723.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.384+4817C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69058077 | ||||||
chr9:69058114
|
C | T | 31 | a0001c0001t0007g0038a0001c0001t0007g0039a0001c0001t0007g0040others(28): Show | 36 | HG00642.hp1 HG02040.hp2 HG02486.hp2 others(33): Show |
intron_variant | MODIFIER | c.384+4854C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69058114 | ||||||
chr9:69058117
|
G | A | 128 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(125): Show | 142 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(139): Show |
intron_variant | MODIFIER | c.384+4857G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69058117 | ||||||
chr9:69058369
|
C | A | 17 | a0001c0001t0009g0032a0001c0001t0009g0206a0001c0001t0009g0241others(14): Show | 19 | HG01255.hp2 HG01884.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.384+5109C>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69058369 | ||||||
chr9:69058397
|
C | CT | 31 | a0001c0001t0006g0318a0001c0001t0006g0319a0001c0001t0006g0320others(28): Show | 31 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.384+5145dupT | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr9 | 69058397 | |||||
chr9:69058407
|
C | A | 1 | a0001c0002t0047g0049 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.384+5147C>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69058407 | ||||||
chr9:69058490
|
T | A | 2 | a0001c0001t0017g0012a0001c0001t0066g0057 | 3 | HG02717.hp2 HG02886.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.384+5230T>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69058490 | ||||||
chr9:69058600
|
T | TA | 101 | a0001c0001t0001g0141a0001c0001t0001g0274a0001c0001t0002g0004others(98): Show | 108 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.384+5354dupA | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr9 | 69058600 | |||||
chr9:69058704
|
G | A | 17 | a0001c0001t0009g0032a0001c0001t0009g0206a0001c0001t0009g0241others(14): Show | 19 | HG01255.hp2 HG01884.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.384+5444G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69058704 | ||||||
chr9:69058796
|
C | T | 7 | a0001c0001t0001g0116a0001c0001t0001g0138a0001c0001t0001g0139others(4): Show | 8 | HG00639.hp2 HG01928.hp2 HG01975.hp2 others(5): Show |
intron_variant | MODIFIER | c.384+5536C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69058796 | ||||||
chr9:69058801
|
C | G | 1 | a0001c0001t0005g0216 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.384+5541C>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69058801 | ||||||
chr9:69058806
|
C | T | 2 | a0001c0001t0020g0031a0001c0001t0020g0236 | 3 | HG02258.hp1 HG02280.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.384+5546C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69058806 | ||||||
chr9:69058840
|
G | A | 28 | a0001c0001t0007g0038a0001c0001t0007g0039a0001c0001t0007g0040others(25): Show | 32 | HG00642.hp1 HG02040.hp2 HG02486.hp2 others(29): Show |
intron_variant | MODIFIER | c.384+5580G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69058840 | ||||||
chr9:69058871
|
A | G | 5 | a0002c0003t0015g0042a0002c0003t0015g0046a0002c0003t0032g0043others(2): Show | 5 | HG01891.hp2 HG02451.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.384+5611A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69058871 | ||||||
chr9:69058929
|
G | A | 28 | a0001c0001t0007g0038a0001c0001t0007g0039a0001c0001t0007g0040others(25): Show | 32 | HG00642.hp1 HG02040.hp2 HG02486.hp2 others(29): Show |
intron_variant | MODIFIER | c.384+5669G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69058929 | ||||||
chr9:69058954
|
G | A | 16 | a0001c0001t0009g0032a0001c0001t0009g0206a0001c0001t0009g0241others(13): Show | 18 | HG01255.hp2 HG01884.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.384+5694G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69058954 | ||||||
chr9:69059000
|
G | A | 31 | a0001c0001t0006g0318a0001c0001t0006g0319a0001c0001t0006g0320others(28): Show | 31 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.384+5740G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69059000 | ||||||
chr9:69059055
|
G | C | 4 | a0001c0001t0005g0336a0001c0001t0017g0012a0001c0001t0017g0337others(1): Show | 5 | HG02559.hp1 HG02717.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.384+5795G>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69059055 | ||||||
chr9:69059063
|
A | G | 1 | a0001c0001t0001g0182 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.384+5803A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69059063 | ||||||
chr9:69059152
|
G | A | 1 | a0002c0003t0008g0071 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.385-5786G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69059152 | ||||||
chr9:69059209
|
G | A | 126 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(123): Show | 140 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(137): Show |
intron_variant | MODIFIER | c.385-5729G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69059209 | ||||||
chr9:69059218
|
T | A | 1 | a0001c0001t0008g0224 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.385-5720T>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69059218 | ||||||
chr9:69059224
|
T | C | 16 | a0001c0001t0009g0032a0001c0001t0009g0206a0001c0001t0009g0241others(13): Show | 18 | HG01255.hp2 HG01884.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.385-5714T>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69059224 | ||||||
chr9:69059391
|
C | CT | 46 | a0001c0001t0005g0208a0001c0001t0006g0318a0001c0001t0006g0319others(43): Show | 48 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.385-5520dupT | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr9 | 69059391 | |||||
chr9:69059391
|
C | CTT | 55 | a0001c0001t0002g0240a0001c0001t0002g0257a0001c0001t0002g0258others(52): Show | 61 | HG00140.hp1 HG00423.hp1 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.385-5521_385-5520d others(4): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr9 | 69059391 | |||||
chr9:69059391
|
C | CTTT | 89 | a0001c0001t0001g0274a0001c0001t0002g0004a0001c0001t0002g0009others(86): Show | 107 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.385-5522_385-5520d others(5): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr9 | 69059391 | |||||
chr9:69059391
|
C | CTTTT | 37 | a0001c0001t0001g0016a0001c0001t0001g0126a0001c0001t0001g0127others(34): Show | 46 | HG00099.hp2 HG00280.hp2 HG01106.hp1 others(43): Show |
intron_variant | MODIFIER | c.385-5523_385-5520d others(6): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr9 | 69059391 | |||||
chr9:69059391
|
C | CTTTTT | 71 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0019others(68): Show | 80 | HG00323.hp2 HG00558.hp1 HG00639.hp2 others(77): Show |
intron_variant | MODIFIER | c.385-5524_385-5520d others(7): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr9 | 69059391 | |||||
chr9:69059391
|
C | CTTTTTT | 33 | a0001c0001t0001g0020a0001c0001t0001g0024a0001c0001t0001g0060others(30): Show | 37 | HG00438.hp1 HG00544.hp2 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.385-5525_385-5520d others(8): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr9 | 69059391 | |||||
chr9:69059391
|
C | CTTTTTTT | 8 | a0001c0001t0001g0102a0001c0001t0001g0137a0001c0001t0001g0171others(5): Show | 8 | HG03710.hp2 HG04184.hp2 NA18951.hp1 others(5): Show |
intron_variant | MODIFIER | c.385-5526_385-5520d others(9): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr9 | 69059391 | |||||
chr9:69059391
|
CT | C | 7 | a0001c0001t0014g0177a0001c0001t0014g0179a0001c0001t0014g0183others(4): Show | 8 | HG02572.hp1 HG02615.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.385-5520delT | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr9 | 69059391 | |||||
chr9:69059391
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0005g0226 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.385-5529_385-5520d others(12): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr9 | 69059391 | |||||
chr9:69059462
|
C | T | 1 | a0001c0001t0062g0053 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.385-5476C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69059462 | ||||||
chr9:69059547
|
G | A | 1 | a0001c0001t0003g0199 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.385-5391G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69059547 | ||||||
chr9:69059566
|
AT | A | 366 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(363): Show | 417 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(414): Show |
intron_variant | MODIFIER | c.385-5361delT | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr9 | 69059566 | |||||
chr9:69059669
|
G | A | 3 | a0001c0001t0014g0177a0001c0001t0014g0179a0001c0001t0014g0183 | 3 | HG02572.hp1 HG02615.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.385-5269G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69059669 | ||||||
chr9:69059714
|
C | T | 1 | a0002c0003t0008g0071 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.385-5224C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69059714 | ||||||
chr9:69059722
|
C | T | 1 | a0001c0001t0038g0119 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.385-5216C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69059722 | ||||||
chr9:69059785
|
C | A | 3 | a0003c0004t0021g0037a0003c0004t0021g0323a0003c0004t0033g0322 | 4 | HG02622.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.385-5153C>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69059785 | ||||||
chr9:69059873
|
G | A | 1 | a0001c0001t0002g0263 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.385-5065G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69059873 | ||||||
chr9:69060045
|
G | A | 188 | a0001c0001t0001g0274a0001c0001t0002g0004a0001c0001t0002g0009others(185): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.385-4893G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69060045 | ||||||
chr9:69060046
|
G | T | 1 | a0001c0001t0052g0074 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.385-4892G>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69060046 | ||||||
chr9:69060096
|
T | C | 5 | a0001c0001t0002g0045a0001c0001t0002g0084a0001c0001t0002g0086others(2): Show | 5 | HG00735.hp1 HG01261.hp2 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.385-4842T>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69060096 | ||||||
chr9:69060106
|
C | T | 2 | a0001c0002t0023g0011a0001c0002t0023g0048 | 3 | HG01884.hp2 HG02717.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.385-4832C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69060106 | ||||||
chr9:69060107
|
G | A | 1 | a0001c0001t0043g0081 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.385-4831G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69060107 | ||||||
chr9:69060135
|
A | G | 4 | a0001c0001t0002g0065a0001c0001t0002g0066a0001c0001t0002g0067others(1): Show | 4 | NA18612.hp1 NA18942.hp2 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.385-4803A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69060135 | ||||||
chr9:69060154
|
G | A | 5 | a0002c0003t0015g0042a0002c0003t0015g0046a0002c0003t0032g0043others(2): Show | 5 | HG01891.hp2 HG02451.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.385-4784G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69060154 | ||||||
chr9:69060164
|
C | G | 5 | a0002c0003t0015g0042a0002c0003t0015g0046a0002c0003t0032g0043others(2): Show | 5 | HG01891.hp2 HG02451.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.385-4774C>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69060164 | ||||||
chr9:69060173
|
T | C | 45 | a0001c0001t0002g0257a0001c0001t0003g0232a0001c0001t0005g0211others(42): Show | 45 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(42): Show |
intron_variant | MODIFIER | c.385-4765T>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69060173 | ||||||
chr9:69060196
|
G | A | 110 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0019others(107): Show | 123 | HG00323.hp2 HG00438.hp1 HG00639.hp2 others(120): Show |
intron_variant | MODIFIER | c.385-4742G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69060196 | ||||||
chr9:69060231
|
C | T | 1 | a0001c0001t0035g0140 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.385-4707C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69060231 | ||||||
chr9:69060238
|
G | T | 2 | a0001c0001t0020g0031a0001c0001t0020g0236 | 3 | HG02258.hp1 HG02280.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.385-4700G>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69060238 | ||||||
chr9:69060244
|
G | A | 2 | a0001c0001t0001g0340a0001c0001t0001g0341 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.385-4694G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69060244 | ||||||
chr9:69060263
|
C | T | 2 | a0001c0001t0001g0340a0001c0001t0001g0341 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.385-4675C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69060263 | ||||||
chr9:69060295
|
C | G | 186 | a0001c0001t0001g0274a0001c0001t0002g0004a0001c0001t0002g0009others(183): Show | 215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.385-4643C>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69060295 | ||||||
chr9:69060303
|
A | G | 20 | a0001c0001t0007g0039a0001c0001t0007g0040a0001c0001t0007g0248others(17): Show | 23 | HG00642.hp1 HG02040.hp2 HG03669.hp1 others(20): Show |
intron_variant | MODIFIER | c.385-4635A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69060303 | ||||||
chr9:69060304
|
G | C | 191 | a0001c0001t0001g0274a0001c0001t0002g0004a0001c0001t0002g0009others(188): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.385-4634G>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69060304 | ||||||
chr9:69060373
|
A | G | 3 | a0001c0001t0014g0177a0001c0001t0014g0179a0001c0001t0014g0183 | 3 | HG02572.hp1 HG02615.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.385-4565A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69060373 | ||||||
chr9:69060548
|
T | G | 118 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(115): Show | 131 | HG00323.hp2 HG00438.hp1 HG00639.hp2 others(128): Show |
intron_variant | MODIFIER | c.385-4390T>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69060548 | ||||||
chr9:69060644
|
T | C | 1 | a0001c0001t0002g0270 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.385-4294T>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69060644 | ||||||
chr9:69060659
|
TG | T | 6 | a0001c0001t0002g0009a0001c0001t0002g0033a0001c0001t0002g0034others(3): Show | 10 | HG00639.hp1 HG01070.hp1 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.385-4274delG | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr9 | 69060659 | |||||
chr9:69060674
|
A | G | 1 | a0001c0001t0001g0171 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.385-4264A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69060674 | ||||||
chr9:69060827
|
T | C | 1 | a0001c0001t0052g0074 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.385-4111T>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69060827 | ||||||
chr9:69060892
|
G | A | 3 | a0001c0001t0014g0177a0001c0001t0014g0179a0001c0001t0014g0183 | 3 | HG02572.hp1 HG02615.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.385-4046G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69060892 | ||||||
chr9:69061022
|
A | G | 1 | a0001c0001t0035g0140 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.385-3916A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69061022 | ||||||
chr9:69061135
|
A | G | 194 | a0001c0001t0002g0004a0001c0001t0002g0009a0001c0001t0002g0013others(191): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.385-3803A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69061135 | ||||||
chr9:69061172
|
C | T | 118 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(115): Show | 131 | HG00323.hp2 HG00438.hp1 HG00639.hp2 others(128): Show |
intron_variant | MODIFIER | c.385-3766C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69061172 | ||||||
chr9:69061178
|
C | T | 1 | a0001c0002t0005g0050 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.385-3760C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69061178 | ||||||
chr9:69061270
|
G | A | 2 | a0001c0001t0020g0031a0001c0001t0020g0236 | 3 | HG02258.hp1 HG02280.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.385-3668G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69061270 | ||||||
chr9:69061276
|
C | G | 1 | a0001c0001t0003g0186 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.385-3662C>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69061276 | ||||||
chr9:69061317
|
G | A | 4 | a0001c0001t0016g0324a0001c0001t0016g0327a0001c0001t0016g0328others(1): Show | 4 | NA18959.hp2 NA19011.hp1 NA19081.hp1 others(1): Show |
intron_variant | MODIFIER | c.385-3621G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69061317 | ||||||
chr9:69061365
|
A | C | 1 | a0001c0001t0003g0199 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.385-3573A>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69061365 | ||||||
chr9:69061428
|
C | A | 4 | a0001c0001t0008g0178a0001c0001t0008g0325a0001c0001t0043g0081others(1): Show | 4 | HG02257.hp2 HG02451.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.385-3510C>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69061428 | ||||||
chr9:69061440
|
G | A | 118 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(115): Show | 131 | HG00323.hp2 HG00438.hp1 HG00639.hp2 others(128): Show |
intron_variant | MODIFIER | c.385-3498G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69061440 | ||||||
chr9:69061448
|
C | T | 2 | a0001c0001t0002g0036a0001c0001t0065g0036 | 2 | NA18967.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.385-3490C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69061448 | ||||||
chr9:69061517
|
C | A | 1 | a0001c0001t0002g0288 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.385-3421C>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69061517 | ||||||
chr9:69061529
|
A | T | 2 | a0001c0001t0046g0326a0002c0003t0050g0075 | 2 | HG02723.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.385-3409A>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69061529 | ||||||
chr9:69061555
|
C | G | 14 | a0001c0001t0009g0032a0001c0001t0009g0206a0001c0001t0009g0241others(11): Show | 15 | HG01255.hp2 HG02055.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.385-3383C>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69061555 | ||||||
chr9:69061646
|
G | T | 255 | a0001c0001t0002g0004a0001c0001t0002g0009a0001c0001t0002g0013others(252): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.385-3292G>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69061646 | ||||||
chr9:69061668
|
C | T | 1 | a0001c0001t0024g0010 | 3 | HG02040.hp2 NA18942.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.385-3270C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69061668 | ||||||
chr9:69061721
|
C | T | 3 | a0001c0001t0002g0264a0001c0001t0002g0265a0001c0001t0002g0266 | 3 | NA18947.hp2 NA18994.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.385-3217C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69061721 | ||||||
chr9:69062008
|
C | T | 2 | a0001c0002t0023g0011a0001c0002t0023g0048 | 3 | HG01884.hp2 HG02717.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.385-2930C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69062008 | ||||||
chr9:69062149
|
T | C | 1 | a0001c0001t0001g0090 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.385-2789T>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69062149 | ||||||
chr9:69062182
|
G | A | 2 | a0001c0001t0001g0016a0001c0001t0037g0016 | 2 | NA18968.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.385-2756G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69062182 | ||||||
chr9:69062502
|
T | C | 1 | a0001c0001t0039g0122 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.385-2436T>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69062502 | ||||||
chr9:69062594
|
GAAGTAGT others(3): Show |
G | 1 | a0001c0001t0059g0160 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.385-2331_385-2322d others(12): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr9 | 69062594 | |||||
chr9:69062720
|
A | C | 1 | a0001c0001t0002g0287 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.385-2218A>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69062720 | ||||||
chr9:69062727
|
A | G | 1 | a0001c0001t0030g0028 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.385-2211A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69062727 | ||||||
chr9:69062745
|
T | C | 1 | a0001c0001t0015g0072 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.385-2193T>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69062745 | ||||||
chr9:69062791
|
G | C | 5 | a0002c0003t0015g0042a0002c0003t0015g0046a0002c0003t0032g0043others(2): Show | 5 | HG01891.hp2 HG02451.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.385-2147G>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69062791 | ||||||
chr9:69062811
|
G | A | 2 | a0001c0001t0046g0326a0002c0003t0050g0075 | 2 | HG02723.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.385-2127G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69062811 | ||||||
chr9:69062893
|
TA | T | 46 | a0001c0001t0001g0069a0001c0001t0001g0171a0001c0001t0001g0341others(43): Show | 52 | HG00642.hp1 HG01168.hp2 HG01255.hp2 others(49): Show |
intron_variant | MODIFIER | c.385-2031delA | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr9 | 69062893 | |||||
chr9:69062960
|
G | A | 1 | a0001c0001t0015g0072 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.385-1978G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69062960 | ||||||
chr9:69063023
|
C | A | 1 | a0001c0001t0002g0292 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.385-1915C>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69063023 | ||||||
chr9:69063077
|
C | T | 1 | a0001c0001t0002g0283 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.385-1861C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69063077 | ||||||
chr9:69063412
|
C | T | 5 | a0002c0003t0015g0042a0002c0003t0015g0046a0002c0003t0032g0043others(2): Show | 5 | HG01891.hp2 HG02451.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.385-1526C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69063412 | ||||||
chr9:69063529
|
C | T | 37 | a0001c0001t0005g0210a0001c0001t0005g0217a0001c0001t0005g0218others(34): Show | 42 | HG00642.hp1 HG02040.hp2 HG02486.hp2 others(39): Show |
intron_variant | MODIFIER | c.385-1409C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69063529 | ||||||
chr9:69063550
|
T | C | 208 | a0001c0001t0001g0016a0001c0001t0002g0004a0001c0001t0002g0009others(205): Show | 240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.385-1388T>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69063550 | ||||||
chr9:69063720
|
G | GT | 92 | a0001c0001t0002g0262a0001c0001t0003g0001a0001c0001t0003g0003others(89): Show | 114 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.385-1217dupT | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr9 | 69063720 | |||||
chr9:69063723
|
G | A | 2 | a0001c0001t0001g0126a0001c0001t0001g0141 | 2 | NA18956.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.385-1215G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69063723 | ||||||
chr9:69063733
|
G | T | 3 | a0001c0001t0014g0177a0001c0001t0014g0179a0001c0001t0014g0183 | 3 | HG02572.hp1 HG02615.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.385-1205G>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69063733 | ||||||
chr9:69063743
|
G | A | 27 | a0001c0001t0007g0038a0001c0001t0007g0039a0001c0001t0007g0040others(24): Show | 31 | HG00642.hp1 HG02040.hp2 HG02809.hp1 others(28): Show |
intron_variant | MODIFIER | c.385-1195G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69063743 | ||||||
chr9:69063828
|
C | T | 2 | a0001c0001t0005g0301a0001c0001t0005g0302 | 2 | HG00140.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.385-1110C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69063828 | ||||||
chr9:69063875
|
G | A | 1 | a0001c0001t0004g0113 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.385-1063G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69063875 | ||||||
chr9:69063890
|
C | T | 1 | a0002c0003t0008g0071 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.385-1048C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69063890 | ||||||
chr9:69064046
|
A | G | 3 | a0001c0001t0008g0178a0001c0001t0008g0325a0002c0003t0008g0071 | 3 | HG02257.hp2 HG02451.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.385-892A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69064046 | ||||||
chr9:69064079
|
G | A | 2 | a0001c0001t0019g0061a0001c0001t0019g0062 | 2 | NA19075.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.385-859G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69064079 | ||||||
chr9:69064100
|
A | G | 1 | a0001c0001t0008g0178 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.385-838A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69064100 | ||||||
chr9:69064157
|
C | A | 3 | a0001c0001t0014g0177a0001c0001t0014g0179a0001c0001t0014g0183 | 3 | HG02572.hp1 HG02615.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.385-781C>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69064157 | ||||||
chr9:69064249
|
T | A | 2 | a0001c0001t0002g0278a0001c0001t0002g0289 | 2 | NA18964.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.385-689T>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69064249 | ||||||
chr9:69064341
|
C | T | 1 | a0001c0001t0003g0196 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.385-597C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69064341 | ||||||
chr9:69064432
|
C | A | 1 | a0001c0001t0002g0131 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.385-506C>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69064432 | ||||||
chr9:69064522
|
A | G | 256 | a0001c0001t0002g0004a0001c0001t0002g0009a0001c0001t0002g0013others(253): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.385-416A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69064522 | ||||||
chr9:69064529
|
G | A | 1 | a0001c0001t0053g0052 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.385-409G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69064529 | ||||||
chr9:69064550
|
A | C | 4 | a0001c0001t0003g0027a0001c0001t0003g0029a0001c0001t0003g0195others(1): Show | 6 | HG00280.hp1 HG01069.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.385-388A>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69064550 | ||||||
chr9:69064710
|
G | A | 1 | a0001c0001t0005g0229 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.385-228G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69064710 | ||||||
chr9:69064725
|
A | T | 5 | a0002c0003t0015g0042a0002c0003t0015g0046a0002c0003t0032g0043others(2): Show | 5 | HG01891.hp2 HG02451.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.385-213A>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69064725 | ||||||
chr9:69064858
|
A | G | 3 | a0001c0001t0014g0177a0001c0001t0014g0179a0001c0001t0014g0183 | 3 | HG02572.hp1 HG02615.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.385-80A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 3/4 | chr9 | 69064858 | ||||||
chr9:69065077
|
A | G | 5 | a0001c0001t0046g0326a0002c0003t0050g0075a0003c0004t0021g0037others(2): Show | 6 | HG02622.hp2 HG02723.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.482+42A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69065077 | ||||||
chr9:69065223
|
A | G | 2 | a0001c0001t0006g0345a0001c0001t0006g0346 | 2 | HG02818.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.482+188A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69065223 | ||||||
chr9:69065476
|
G | C | 3 | a0003c0004t0021g0037a0003c0004t0021g0323a0003c0004t0033g0322 | 4 | HG02622.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.482+441G>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69065476 | ||||||
chr9:69065498
|
G | A | 1 | a0001c0001t0006g0347 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.482+463G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69065498 | ||||||
chr9:69065540
|
C | CAA | 120 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(117): Show | 137 | HG00323.hp2 HG00438.hp1 HG00639.hp2 others(134): Show |
intron_variant | MODIFIER | c.482+519_482+520dup others(2): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr9 | 69065540 | |||||
chr9:69065540
|
C | CAAA | 233 | a0001c0001t0001g0090a0001c0001t0001g0128a0001c0001t0002g0004others(230): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.482+518_482+520dup others(3): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr9 | 69065540 | |||||
chr9:69065540
|
C | CAAAA | 21 | a0001c0001t0002g0045a0001c0001t0002g0266a0001c0001t0002g0268others(18): Show | 21 | HG00323.hp1 HG00438.hp2 HG01515.hp2 others(18): Show |
intron_variant | MODIFIER | c.482+517_482+520dup others(4): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr9 | 69065540 | |||||
chr9:69065561
|
C | T | 1 | a0001c0002t0034g0315 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.482+526C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69065561 | ||||||
chr9:69065642
|
A | G | 14 | a0001c0001t0009g0032a0001c0001t0009g0206a0001c0001t0009g0241others(11): Show | 15 | HG01255.hp2 HG02055.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.482+607A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69065642 | ||||||
chr9:69066167
|
C | T | 1 | a0001c0001t0004g0108 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.482+1132C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69066167 | ||||||
chr9:69066253
|
G | A | 1 | a0001c0001t0015g0072 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.482+1218G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69066253 | ||||||
chr9:69066324
|
T | C | 255 | a0001c0001t0002g0004a0001c0001t0002g0009a0001c0001t0002g0013others(252): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.482+1289T>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69066324 | ||||||
chr9:69066337
|
C | A | 236 | a0001c0001t0002g0004a0001c0001t0002g0009a0001c0001t0002g0013others(233): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.482+1302C>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69066337 | ||||||
chr9:69066425
|
G | C | 1 | a0001c0001t0004g0094 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.482+1390G>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69066425 | ||||||
chr9:69066858
|
C | CA | 7 | a0001c0001t0008g0178a0001c0001t0008g0325a0001c0001t0009g0243others(4): Show | 7 | HG01255.hp2 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.482+1835dupA | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr9 | 69066858 | |||||
chr9:69066867
|
A | AT | 31 | a0001c0001t0003g0232a0001c0001t0005g0030a0001c0001t0005g0035others(28): Show | 34 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(31): Show |
intron_variant | MODIFIER | c.482+1832_482+1833i others(3): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69066867 | ||||||
chr9:69066867
|
A | ATAT | 4 | a0001c0001t0001g0127a0001c0001t0001g0135a0001c0001t0001g0254others(1): Show | 4 | HG01109.hp2 HG02602.hp1 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.482+1832_482+1833i others(5): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69066867 | ||||||
chr9:69066867
|
A | T | 4 | a0001c0001t0007g0335a0003c0004t0021g0037a0003c0004t0021g0323others(1): Show | 5 | HG02622.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.482+1832A>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69066867 | ||||||
chr9:69066869
|
A | AAAT | 12 | a0001c0001t0001g0020a0001c0001t0001g0089a0001c0001t0001g0120others(9): Show | 13 | HG00741.hp2 HG01175.hp2 HG03130.hp2 others(10): Show |
intron_variant | MODIFIER | c.482+1835_482+1836i others(5): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr9 | 69066869 | |||||
chr9:69066869
|
A | AT | 10 | a0001c0001t0005g0306a0001c0001t0009g0032a0001c0001t0009g0206others(7): Show | 11 | HG02055.hp2 HG02559.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.482+1834_482+1835i others(3): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69066869 | ||||||
chr9:69066869
|
A | ATAT | 90 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0019others(87): Show | 102 | HG00323.hp2 HG00438.hp1 HG00639.hp2 others(99): Show |
intron_variant | MODIFIER | c.482+1834_482+1835i others(5): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69066869 | ||||||
chr9:69066869
|
A | ATATAT | 3 | a0001c0001t0004g0161a0001c0001t0004g0162a0001c0001t0004g0163 | 3 | HG01981.hp1 HG01993.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.482+1834_482+1835i others(7): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69066869 | ||||||
chr9:69066869
|
A | T | 205 | a0001c0001t0001g0016a0001c0001t0001g0096a0001c0001t0001g0097others(202): Show | 240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.482+1834A>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69066869 | ||||||
chr9:69066870
|
AT | A | 3 | a0001c0001t0014g0177a0001c0001t0014g0179a0001c0001t0014g0183 | 3 | HG02572.hp1 HG02615.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.482+1836delT | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69066870 | ||||||
chr9:69066871
|
T | A | 1 | a0001c0001t0008g0325 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.482+1836T>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69066871 | ||||||
chr9:69066959
|
A | G | 6 | a0001c0001t0005g0030a0001c0001t0005g0208a0001c0001t0005g0209others(3): Show | 7 | HG01175.hp1 HG01884.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.482+1924A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69066959 | ||||||
chr9:69066966
|
C | T | 2 | a0001c0001t0001g0123a0001c0001t0001g0355 | 2 | HG02109.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.482+1931C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69066966 | ||||||
chr9:69066970
|
G | A | 4 | a0001c0001t0008g0178a0001c0001t0008g0325a0001c0001t0043g0081others(1): Show | 4 | HG02257.hp2 HG02451.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.482+1935G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69066970 | ||||||
chr9:69066989
|
C | T | 1 | a0001c0001t0006g0346 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.482+1954C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69066989 | ||||||
chr9:69067008
|
G | A | 2 | a0001c0001t0005g0235a0001c0001t0017g0299 | 2 | HG04199.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.482+1973G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69067008 | ||||||
chr9:69067070
|
C | T | 207 | a0001c0001t0001g0118a0001c0001t0002g0004a0001c0001t0002g0009others(204): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.482+2035C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69067070 | ||||||
chr9:69067199
|
C | T | 8 | a0001c0001t0005g0035a0001c0001t0005g0281a0001c0001t0005g0301others(5): Show | 9 | HG00140.hp1 HG00423.hp1 HG00673.hp2 others(6): Show |
intron_variant | MODIFIER | c.482+2164C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69067199 | ||||||
chr9:69067249
|
C | G | 1 | a0001c0001t0001g0120 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.482+2214C>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69067249 | ||||||
chr9:69067298
|
C | A | 1 | a0001c0001t0053g0052 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.482+2263C>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69067298 | ||||||
chr9:69067366
|
G | A | 118 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(115): Show | 131 | HG00323.hp2 HG00438.hp1 HG00639.hp2 others(128): Show |
intron_variant | MODIFIER | c.482+2331G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69067366 | ||||||
chr9:69067479
|
G | A | 3 | a0003c0004t0021g0037a0003c0004t0021g0323a0003c0004t0033g0322 | 4 | HG02622.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.482+2444G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69067479 | ||||||
chr9:69067606
|
C | A | 1 | a0001c0001t0003g0238 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.482+2571C>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69067606 | ||||||
chr9:69067611
|
A | AAAC | 6 | a0001c0001t0043g0081a0002c0003t0015g0042a0002c0003t0015g0046others(3): Show | 6 | HG01891.hp2 HG02451.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.482+2594_482+2596d others(5): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr9 | 69067611 | |||||
chr9:69067629
|
C | A | 1 | a0001c0001t0004g0080 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.482+2594C>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69067629 | ||||||
chr9:69067815
|
T | C | 1 | a0001c0001t0051g0244 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.482+2780T>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69067815 | ||||||
chr9:69067895
|
G | A | 2 | a0001c0001t0005g0217a0001c0001t0005g0218 | 2 | HG03453.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.482+2860G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69067895 | ||||||
chr9:69067951
|
A | C | 1 | a0001c0001t0005g0306 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.482+2916A>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69067951 | ||||||
chr9:69068053
|
GAGAC | G | 118 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(115): Show | 131 | HG00323.hp2 HG00438.hp1 HG00639.hp2 others(128): Show |
intron_variant | MODIFIER | c.482+3023_482+3026d others(6): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr9 | 69068053 | |||||
chr9:69068199
|
C | T | 1 | a0001c0001t0022g0169 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.482+3164C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69068199 | ||||||
chr9:69068258
|
G | A | 2 | a0001c0001t0046g0326a0002c0003t0050g0075 | 2 | HG02723.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.482+3223G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69068258 | ||||||
chr9:69068371
|
C | T | 4 | a0001c0001t0015g0072a0001c0001t0015g0073a0001c0001t0053g0052others(1): Show | 4 | HG01891.hp2 HG03098.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.482+3336C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69068371 | ||||||
chr9:69068373
|
C | G | 2 | a0001c0001t0001g0129a0001c0001t0001g0137 | 2 | HG04184.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.482+3338C>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69068373 | ||||||
chr9:69068396
|
T | C | 3 | a0003c0004t0021g0037a0003c0004t0021g0323a0003c0004t0033g0322 | 4 | HG02622.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.482+3361T>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69068396 | ||||||
chr9:69068490
|
G | C | 1 | a0003c0004t0021g0323 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.482+3455G>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69068490 | ||||||
chr9:69068505
|
C | T | 1 | a0001c0001t0001g0123 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.482+3470C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69068505 | ||||||
chr9:69068574
|
G | A | 1 | a0001c0001t0001g0132 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.482+3539G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69068574 | ||||||
chr9:69068773
|
T | TA | 4 | a0001c0001t0006g0344a0001c0001t0006g0348a0001c0001t0006g0349others(1): Show | 4 | HG02257.hp1 HG03098.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.482+3739dupA | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr9 | 69068773 | |||||
chr9:69068776
|
G | A | 5 | a0001c0001t0015g0072a0001c0001t0015g0073a0001c0001t0018g0018others(2): Show | 6 | HG01516.hp2 HG01517.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.482+3741G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69068776 | ||||||
chr9:69068824
|
G | A | 3 | a0001c0001t0001g0340a0001c0001t0001g0341a0001c0001t0041g0117 | 3 | HG01168.hp2 HG01169.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.483-3788G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69068824 | ||||||
chr9:69068913
|
C | T | 1 | a0001c0001t0004g0077 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.483-3699C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69068913 | ||||||
chr9:69069020
|
C | T | 1 | a0001c0001t0003g0312 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.483-3592C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69069020 | ||||||
chr9:69069046
|
C | T | 1 | a0001c0001t0015g0072 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.483-3566C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69069046 | ||||||
chr9:69069222
|
A | G | 29 | a0001c0001t0007g0038a0001c0001t0007g0039a0001c0001t0007g0040others(26): Show | 33 | HG00642.hp1 HG01891.hp2 HG02040.hp2 others(30): Show |
intron_variant | MODIFIER | c.483-3390A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69069222 | ||||||
chr9:69069254
|
G | A | 226 | a0001c0001t0002g0004a0001c0001t0002g0009a0001c0001t0002g0013others(223): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.483-3358G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69069254 | ||||||
chr9:69069304
|
G | A | 3 | a0003c0004t0021g0037a0003c0004t0021g0323a0003c0004t0033g0322 | 4 | HG02622.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.483-3308G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69069304 | ||||||
chr9:69069320
|
G | A | 2 | a0001c0002t0023g0011a0001c0002t0023g0048 | 3 | HG01884.hp2 HG02717.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.483-3292G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69069320 | ||||||
chr9:69069343
|
C | T | 208 | a0001c0001t0002g0004a0001c0001t0002g0009a0001c0001t0002g0013others(205): Show | 240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.483-3269C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69069343 | ||||||
chr9:69069367
|
AAAG | A | 5 | a0001c0001t0014g0177a0001c0001t0014g0179a0001c0001t0014g0183others(2): Show | 6 | HG01884.hp2 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.483-3244_483-3242d others(5): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69069367 | ||||||
chr9:69069453
|
G | A | 10 | a0001c0001t0008g0008a0001c0001t0008g0213a0001c0001t0008g0214others(7): Show | 12 | HG00738.hp2 HG01081.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.483-3159G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69069453 | ||||||
chr9:69069471
|
C | G | 1 | a0001c0008t0073g0237 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.483-3141C>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69069471 | ||||||
chr9:69069511
|
ACACT | A | 11 | a0001c0001t0008g0008a0001c0001t0008g0213a0001c0001t0008g0214others(8): Show | 13 | HG00738.hp2 HG01081.hp1 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.483-3097_483-3094d others(6): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr9 | 69069511 | |||||
chr9:69069675
|
T | C | 226 | a0001c0001t0002g0004a0001c0001t0002g0009a0001c0001t0002g0013others(223): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.483-2937T>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69069675 | ||||||
chr9:69069783
|
G | A | 3 | a0001c0001t0003g0172a0001c0001t0003g0194a0001c0001t0003g0197 | 3 | NA18940.hp1 NA18954.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.483-2829G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69069783 | ||||||
chr9:69069786
|
G | A | 202 | a0001c0001t0002g0004a0001c0001t0002g0009a0001c0001t0002g0013others(199): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.483-2826G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69069786 | ||||||
chr9:69069879
|
A | G | 1 | a0001c0002t0034g0315 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.483-2733A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69069879 | ||||||
chr9:69069985
|
T | G | 2 | a0001c0001t0046g0326a0002c0003t0050g0075 | 2 | HG02723.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.483-2627T>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69069985 | ||||||
chr9:69069989
|
G | A | 3 | a0001c0001t0005g0211a0001c0001t0005g0212a0001c0001t0005g0227 | 3 | HG01515.hp2 HG01516.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.483-2623G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69069989 | ||||||
chr9:69070045
|
A | G | 13 | a0001c0001t0009g0032a0001c0001t0009g0206a0001c0001t0009g0241others(10): Show | 14 | HG01255.hp2 HG02055.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.483-2567A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69070045 | ||||||
chr9:69070096
|
A | G | 19 | a0001c0001t0009g0032a0001c0001t0009g0206a0001c0001t0009g0241others(16): Show | 21 | HG01255.hp2 HG01496.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.483-2516A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69070096 | ||||||
chr9:69070118
|
A | G | 1 | a0001c0001t0001g0123 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.483-2494A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69070118 | ||||||
chr9:69070208
|
G | A | 1 | a0001c0001t0003g0159 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.483-2404G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69070208 | ||||||
chr9:69070236
|
A | G | 1 | a0001c0002t0034g0315 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.483-2376A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69070236 | ||||||
chr9:69070242
|
A | G | 1 | a0001c0001t0059g0160 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.483-2370A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69070242 | ||||||
chr9:69070275
|
G | A | 5 | a0001c0001t0004g0092a0002c0003t0015g0046a0002c0003t0032g0043others(2): Show | 5 | HG02071.hp1 HG02451.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.483-2337G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69070275 | ||||||
chr9:69070399
|
G | A | 1 | a0001c0001t0002g0295 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.483-2213G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69070399 | ||||||
chr9:69070400
|
C | G | 1 | a0001c0001t0001g0141 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.483-2212C>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69070400 | ||||||
chr9:69070516
|
T | G | 2 | a0001c0002t0023g0011a0001c0002t0023g0048 | 3 | HG01884.hp2 HG02717.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.483-2096T>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69070516 | ||||||
chr9:69070598
|
C | T | 36 | a0001c0001t0008g0008a0001c0001t0008g0178a0001c0001t0008g0213others(33): Show | 40 | HG00738.hp2 HG01081.hp1 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.483-2014C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69070598 | ||||||
chr9:69070728
|
T | A | 2 | a0001c0001t0006g0343a0001c0001t0006g0366 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.483-1884T>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69070728 | ||||||
chr9:69070729
|
G | GT | 17 | a0001c0001t0002g0295a0001c0001t0003g0190a0001c0001t0009g0032others(14): Show | 18 | HG01255.hp2 HG02055.hp2 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.483-1874dupT | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr9 | 69070729 | |||||
chr9:69070802
|
GT | G | 225 | a0001c0001t0002g0004a0001c0001t0002g0009a0001c0001t0002g0013others(222): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.483-1800delT | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr9 | 69070802 | |||||
chr9:69070883
|
TTGGTCTG others(7): Show |
T | 36 | a0001c0001t0008g0008a0001c0001t0008g0178a0001c0001t0008g0213others(33): Show | 40 | HG00738.hp2 HG01081.hp1 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.483-1725_483-1712d others(16): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr9 | 69070883 | |||||
chr9:69070946
|
T | TG | 4 | a0001c0001t0014g0177a0001c0001t0014g0179a0001c0001t0014g0183others(1): Show | 4 | HG01496.hp1 HG02572.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.483-1663dupG | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr9 | 69070946 | |||||
chr9:69070980
|
G | T | 1 | a0001c0001t0004g0107 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.483-1632G>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69070980 | ||||||
chr9:69070992
|
T | G | 251 | a0001c0001t0002g0004a0001c0001t0002g0009a0001c0001t0002g0013others(248): Show | 288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.483-1620T>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69070992 | ||||||
chr9:69071088
|
GGGA | G | 2 | a0001c0001t0020g0031a0001c0001t0020g0236 | 3 | HG02258.hp1 HG02280.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.483-1523_483-1521d others(5): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69071088 | ||||||
chr9:69071265
|
T | C | 242 | a0001c0001t0002g0004a0001c0001t0002g0009a0001c0001t0002g0013others(239): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.483-1347T>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69071265 | ||||||
chr9:69071499
|
T | C | 1 | a0001c0001t0043g0081 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.483-1113T>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69071499 | ||||||
chr9:69071560
|
G | A | 185 | a0001c0001t0002g0004a0001c0001t0002g0009a0001c0001t0002g0013others(182): Show | 214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.483-1052G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69071560 | ||||||
chr9:69071585
|
G | A | 1 | a0001c0001t0001g0120 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.483-1027G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69071585 | ||||||
chr9:69071597
|
C | T | 1 | a0001c0001t0007g0335 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.483-1015C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69071597 | ||||||
chr9:69071604
|
A | G | 237 | a0001c0001t0002g0004a0001c0001t0002g0009a0001c0001t0002g0013others(234): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.483-1008A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69071604 | ||||||
chr9:69071641
|
T | G | 188 | a0001c0001t0002g0004a0001c0001t0002g0009a0001c0001t0002g0013others(185): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.483-971T>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69071641 | ||||||
chr9:69071649
|
C | A | 29 | a0001c0001t0007g0038a0001c0001t0007g0039a0001c0001t0007g0040others(26): Show | 33 | HG00642.hp1 HG01891.hp2 HG02040.hp2 others(30): Show |
intron_variant | MODIFIER | c.483-963C>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69071649 | ||||||
chr9:69071716
|
A | G | 1 | a0001c0001t0005g0220 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.483-896A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69071716 | ||||||
chr9:69071786
|
A | G | 224 | a0001c0001t0002g0004a0001c0001t0002g0009a0001c0001t0002g0013others(221): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.483-826A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69071786 | ||||||
chr9:69071803
|
T | C | 36 | a0001c0001t0007g0038a0001c0001t0007g0039a0001c0001t0007g0040others(33): Show | 41 | HG00642.hp1 HG01496.hp1 HG01884.hp2 others(38): Show |
intron_variant | MODIFIER | c.483-809T>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69071803 | ||||||
chr9:69071809
|
A | G | 36 | a0001c0001t0007g0038a0001c0001t0007g0039a0001c0001t0007g0040others(33): Show | 41 | HG00642.hp1 HG01496.hp1 HG01884.hp2 others(38): Show |
intron_variant | MODIFIER | c.483-803A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69071809 | ||||||
chr9:69071950
|
G | A | 224 | a0001c0001t0002g0004a0001c0001t0002g0009a0001c0001t0002g0013others(221): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.483-662G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69071950 | ||||||
chr9:69072002
|
G | A | 224 | a0001c0001t0002g0004a0001c0001t0002g0009a0001c0001t0002g0013others(221): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.483-610G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69072002 | ||||||
chr9:69072136
|
G | A | 224 | a0001c0001t0002g0004a0001c0001t0002g0009a0001c0001t0002g0013others(221): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.483-476G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69072136 | ||||||
chr9:69072254
|
G | T | 1 | a0001c0001t0002g0084 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.483-358G>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69072254 | ||||||
chr9:69072274
|
A | G | 2 | a0001c0002t0023g0011a0001c0002t0023g0048 | 3 | HG01884.hp2 HG02717.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.483-338A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69072274 | ||||||
chr9:69072275
|
C | T | 12 | a0001c0001t0009g0032a0001c0001t0009g0206a0001c0001t0009g0241others(9): Show | 13 | HG01255.hp2 HG02055.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.483-337C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69072275 | ||||||
chr9:69072285
|
C | A | 1 | a0001c0001t0009g0245 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.483-327C>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69072285 | ||||||
chr9:69072307
|
C | A | 4 | a0001c0001t0014g0177a0001c0001t0014g0179a0001c0001t0014g0183others(1): Show | 4 | HG01496.hp1 HG02572.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.483-305C>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69072307 | ||||||
chr9:69072381
|
G | A | 1 | a0001c0001t0001g0120 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.483-231G>A | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69072381 | ||||||
chr9:69072413
|
T | C | 5 | a0001c0001t0005g0035a0001c0001t0005g0281a0001c0001t0005g0304others(2): Show | 6 | HG00423.hp1 HG00673.hp2 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.483-199T>C | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69072413 | ||||||
chr9:69072437
|
T | G | 30 | a0001c0001t0007g0038a0001c0001t0007g0039a0001c0001t0007g0040others(27): Show | 34 | HG00642.hp1 HG01891.hp2 HG02040.hp2 others(31): Show |
intron_variant | MODIFIER | c.483-175T>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69072437 | ||||||
chr9:69072443
|
A | G | 1 | a0001c0001t0053g0052 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.483-169A>G | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69072443 | ||||||
chr9:69072484
|
C | CTG | 224 | a0001c0001t0002g0004a0001c0001t0002g0009a0001c0001t0002g0013others(221): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.483-127_483-126ins others(2): Show |
FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr9 | 69072484 | |||||
chr9:69072524
|
C | T | 188 | a0001c0001t0002g0004a0001c0001t0002g0009a0001c0001t0002g0013others(185): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.483-88C>T | FXN | ENSG00000165060.15 | transcript | ENST00000484259.3 | protein_coding | 4/4 | chr9 | 69072524 |