geneid | 51106 |
---|---|
ensemblid | ENSG00000029639.11 |
hgncid | 17037 |
symbol | TFB1M |
name | transcription factor B1, mitochondrial |
refseq_nuc | NM_016020.4 |
refseq_prot | NP_057104.2 |
ensembl_nuc | ENST00000367166.5 |
ensembl_prot | ENSP00000356134.4 |
mane_status | MANE Select |
chr | chr6 |
start | 155256134 |
end | 155314484 |
strand | - |
ver | v1.2 |
region | chr6:155256134-155314484 |
region5000 | chr6:155251134-155319484 |
regionname0 | TFB1M_chr6_155256134_155314484 |
regionname5000 | TFB1M_chr6_155251134_155319484 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 346 | 345 | 83 | 70 | 144 | 10 | 36 | 120 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
a0002 | 0/0 | 346 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
a0003 | 0/0 | 346 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
a0004 | 0/0 | 346 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 1041 | 232 | 50 | 43 | 108 | 5 | 26 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
c0002 | 1/1 | 1041 | 109 | 31 | 27 | 34 | 5 | 10 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
c0003 | 0/0 | 1041 | 2 | 0 | 0 | 2 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
c0004 | 0/0 | 1041 | 2 | 2 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
c0005 | 0/0 | 1041 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
c0006 | 0/0 | 1041 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
c0007 | 0/0 | 1041 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 1753 | 106 | 13 | 22 | 56 | 2 | 13 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
t0002 | 0/0 | 1756 | 45 | 1 | 2 | 36 | 0 | 6 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
t0003 | 0/0 | 1755 | 30 | 1 | 12 | 13 | 2 | 2 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
t0004 | 0/0 | 1755 | 26 | 14 | 7 | 1 | 2 | 2 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
t0005 | 1/1 | 1759 | 26 | 8 | 12 | 1 | 3 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
t0006 | 0/0 | 1755 | 16 | 9 | 5 | 1 | 1 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
t0007 | 0/0 | 1755 | 9 | 0 | 0 | 9 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
t0008 | 0/0 | 1753 | 8 | 0 | 0 | 8 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
t0009 | 0/0 | 1754 | 7 | 2 | 1 | 2 | 0 | 2 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
t0010 | 0/0 | 1759 | 7 | 2 | 0 | 2 | 0 | 3 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
t0011 | 0/0 | 1756 | 6 | 0 | 0 | 6 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
t0012 | 0/0 | 1756 | 6 | 6 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
t0013 | 0/0 | 1753 | 5 | 3 | 2 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
t0014 | 0/0 | 1756 | 5 | 4 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
t0015 | 0/0 | 1756 | 3 | 0 | 0 | 3 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
t0016 | 0/0 | 1757 | 3 | 1 | 0 | 2 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
t0017 | 0/0 | 1753 | 3 | 2 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
t0018 | 0/0 | 1755 | 3 | 2 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
t0019 | 0/0 | 1760 | 3 | 0 | 3 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
t0020 | 0/0 | 1754 | 2 | 2 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
t0021 | 0/0 | 1755 | 2 | 0 | 0 | 0 | 0 | 2 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
t0022 | 0/0 | 1760 | 2 | 0 | 0 | 1 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
t0023 | 0/0 | 1756 | 2 | 2 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
t0024 | 0/0 | 1753 | 2 | 2 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
t0025 | 0/0 | 1756 | 2 | 2 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
t0026 | 0/0 | 1754 | 2 | 2 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
t0027 | 0/0 | 1758 | 2 | 0 | 0 | 0 | 0 | 2 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
t0028 | 0/0 | 1753 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
t0029 | 0/0 | 1756 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
t0030 | 0/0 | 1755 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
t0031 | 0/0 | 1753 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
t0032 | 0/0 | 1754 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
t0033 | 0/0 | 1754 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
t0034 | 0/0 | 1753 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
t0035 | 0/0 | 1756 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
t0036 | 0/0 | 1755 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
t0037 | 0/0 | 1755 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
t0038 | 0/0 | 1756 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
t0039 | 0/0 | 1755 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
t0040 | 0/0 | 1756 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
t0041 | 0/0 | 1760 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
t0042 | 0/0 | 1754 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0002 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0004 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0006 | 0/1 | 3 | 0 | 1 | 0 | 1 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0008 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0011 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0014 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0015 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0022 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0243 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 1041 | 232 | 50 | 43 | 108 | 5 | 26 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
a0001c0002 | 1/1 | 1041 | 109 | 31 | 27 | 34 | 5 | 10 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
a0001c0003 | 0/0 | 1041 | 2 | 0 | 0 | 2 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
a0001c0004 | 0/0 | 1041 | 2 | 2 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
a0002c0005 | 0/0 | 1041 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
a0003c0006 | 0/0 | 1041 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
a0004c0007 | 0/0 | 1041 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2793 | 104 | 13 | 22 | 54 | 2 | 13 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
a0001c0001t0002 | 0/0 | 2796 | 45 | 1 | 2 | 36 | 0 | 6 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
a0001c0001t0004 | 0/0 | 2795 | 13 | 2 | 7 | 0 | 2 | 2 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
a0001c0001t0006 | 0/0 | 2795 | 13 | 6 | 5 | 1 | 1 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
a0001c0001t0008 | 0/0 | 2793 | 8 | 0 | 0 | 8 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
a0001c0001t0009 | 0/0 | 2794 | 7 | 2 | 1 | 2 | 0 | 2 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
a0001c0001t0012 | 0/0 | 2796 | 6 | 6 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
a0001c0001t0013 | 0/0 | 2793 | 5 | 3 | 2 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
a0001c0001t0014 | 0/0 | 2796 | 4 | 3 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
a0001c0001t0015 | 0/0 | 2796 | 3 | 0 | 0 | 3 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
a0001c0001t0016 | 0/0 | 2797 | 3 | 1 | 0 | 2 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
a0001c0001t0017 | 0/0 | 2793 | 3 | 2 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
a0001c0001t0018 | 0/0 | 2795 | 3 | 2 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
a0001c0001t0021 | 0/0 | 2795 | 2 | 0 | 0 | 0 | 0 | 2 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
a0001c0001t0024 | 0/0 | 2793 | 2 | 2 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
a0001c0001t0025 | 0/0 | 2796 | 2 | 2 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
a0001c0001t0026 | 0/0 | 2794 | 2 | 2 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
a0001c0001t0028 | 0/0 | 2793 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
a0001c0001t0030 | 0/0 | 2795 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
a0001c0001t0031 | 0/0 | 2793 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
a0001c0001t0033 | 0/0 | 2794 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
a0001c0001t0034 | 0/0 | 2793 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
a0001c0001t0040 | 0/0 | 2796 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
a0001c0001t0042 | 0/0 | 2794 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
a0001c0002t0003 | 0/0 | 2795 | 30 | 1 | 12 | 13 | 2 | 2 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
a0001c0002t0004 | 0/0 | 2795 | 13 | 12 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
a0001c0002t0005 | 1/1 | 2799 | 26 | 8 | 12 | 1 | 3 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
a0001c0002t0006 | 0/0 | 2795 | 3 | 3 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
a0001c0002t0007 | 0/0 | 2795 | 9 | 0 | 0 | 9 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
a0001c0002t0010 | 0/0 | 2799 | 7 | 2 | 0 | 2 | 0 | 3 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
a0001c0002t0011 | 0/0 | 2796 | 6 | 0 | 0 | 6 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
a0001c0002t0014 | 0/0 | 2796 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
a0001c0002t0019 | 0/0 | 2800 | 3 | 0 | 3 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
a0001c0002t0022 | 0/0 | 2800 | 2 | 0 | 0 | 1 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
a0001c0002t0023 | 0/0 | 2796 | 2 | 2 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
a0001c0002t0027 | 0/0 | 2798 | 2 | 0 | 0 | 0 | 0 | 2 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
a0001c0002t0029 | 0/0 | 2796 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
a0001c0002t0035 | 0/0 | 2796 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
a0001c0002t0036 | 0/0 | 2795 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
a0001c0002t0037 | 0/0 | 2795 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
a0001c0002t0041 | 0/0 | 2800 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
a0001c0003t0001 | 0/0 | 2793 | 2 | 0 | 0 | 2 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
a0001c0004t0020 | 0/0 | 2794 | 2 | 2 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
a0002c0005t0039 | 0/0 | 2795 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
a0003c0006t0038 | 0/0 | 2796 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
a0004c0007t0032 | 0/0 | 2794 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | copy fasta | chr6 | 155251134 | 155319484 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0002g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0002g0008 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0002g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0002g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0004g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0004g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0004g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0004g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0004g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0004g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0004g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0004g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0004g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0004g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0004g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0004g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0004g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0006g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0006g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0006g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0006g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0006g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0006g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0006g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0006g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0006g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0006g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0006g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0008g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0008g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0008g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0008g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0008g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0009g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0009g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0009g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0009g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0009g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0009g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0009g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0012g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0012g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0012g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0012g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0012g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0013g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0013g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0013g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0013g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0013g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0014g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0014g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0014g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0014g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0015g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0015g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0015g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0016g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0016g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0016g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0017g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0017g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0017g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0018g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0018g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0018g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0021g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0021g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0024g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0024g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0025g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0025g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0026g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0028g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0030g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0031g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0033g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0034g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0040g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0001t0042g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0003g0002 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0003g0004 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0003g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0003g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0003g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0003g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0003g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0003g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0003g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0003g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0003g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0003g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0003g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0003g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0004g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0004g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0004g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0004g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0004g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0004g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0004g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0004g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0004g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0004g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0004g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0005g0006 | 0/1 | 3 | 0 | 1 | 0 | 1 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0005g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0005g0022 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0005g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0005g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0005g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0005g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0005g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0005g0243 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0005g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0005g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0005g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0005g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0005g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0005g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0005g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0005g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0005g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0005g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0005g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0005g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0005g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0006g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0006g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0006g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0007g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0007g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0007g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0007g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0007g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0007g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0007g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0007g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0010g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0010g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0010g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0010g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0010g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0010g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0010g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0011g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0011g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0011g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0011g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0011g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0011g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0014g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0019g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0019g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0022g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0022g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0023g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0023g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0027g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0027g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0029g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0035g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0036g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0037g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0002t0041g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0003t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0003t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0004t0020g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0001c0004t0020g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0002c0005t0039g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0003c0006t0038g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
a0004c0007t0032g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0006 | g0228 | EUR | GBR | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG00099 | hp2 | a0001 | c0002 | t0003 | g0004 | EUR | GBR | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG00280 | hp1 | a0001 | c0002 | t0005 | g0268 | EUR | FIN | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG00280 | hp2 | a0001 | c0002 | t0003 | g0192 | EUR | FIN | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | CHS | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0282 | EAS | CHS | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0278 | EAS | CHS | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | CHS | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0296 | EAS | CHS | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | CHS | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG00639 | hp1 | a0001 | c0001 | t0013 | g0035 | AMR | PUR | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG00642 | hp2 | a0001 | c0002 | t0005 | g0258 | AMR | PUR | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG00673 | hp1 | a0001 | c0002 | t0003 | g0214 | EAS | CHS | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | CHS | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG00733 | hp1 | a0001 | c0002 | t0003 | g0002 | AMR | PUR | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG00733 | hp2 | a0001 | c0001 | t0004 | g0174 | AMR | PUR | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0236 | AMR | PUR | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG00738 | hp1 | a0001 | c0001 | t0006 | g0227 | AMR | PUR | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG00738 | hp2 | a0001 | c0001 | t0040 | g0298 | AMR | PUR | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG00741 | hp1 | a0001 | c0002 | t0019 | g0270 | AMR | PUR | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG00741 | hp2 | a0001 | c0001 | t0017 | g0253 | AMR | PUR | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01069 | hp2 | a0001 | c0002 | t0005 | g0261 | AMR | PUR | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01070 | hp1 | a0001 | c0001 | t0018 | g0255 | AMR | PUR | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01070 | hp2 | a0001 | c0002 | t0003 | g0186 | AMR | PUR | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01071 | hp2 | a0001 | c0002 | t0003 | g0185 | AMR | PUR | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01074 | hp2 | a0001 | c0002 | t0005 | g0245 | AMR | PUR | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01081 | hp1 | a0001 | c0002 | t0005 | g0259 | AMR | PUR | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01099 | hp2 | a0001 | c0002 | t0003 | g0181 | AMR | PUR | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01106 | hp1 | a0001 | c0001 | t0006 | g0224 | AMR | PUR | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01109 | hp1 | a0001 | c0001 | t0013 | g0031 | AMR | PUR | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01109 | hp2 | a0001 | c0001 | t0004 | g0171 | AMR | PUR | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01167 | hp1 | a0001 | c0002 | t0003 | g0004 | AMR | PUR | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01167 | hp2 | a0001 | c0001 | t0004 | g0172 | AMR | PUR | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01168 | hp1 | a0001 | c0001 | t0006 | g0223 | AMR | PUR | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01169 | hp1 | a0001 | c0002 | t0003 | g0206 | AMR | PUR | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01169 | hp2 | a0001 | c0001 | t0006 | g0222 | AMR | PUR | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01175 | hp1 | a0001 | c0002 | t0003 | g0205 | AMR | PUR | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01175 | hp2 | a0001 | c0001 | t0009 | g0160 | AMR | PUR | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01192 | hp1 | a0001 | c0002 | t0003 | g0002 | AMR | PUR | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01243 | hp1 | a0001 | c0001 | t0004 | g0177 | AMR | PUR | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | CLM | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01255 | hp2 | a0001 | c0001 | t0014 | g0226 | AMR | CLM | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01256 | hp1 | a0001 | c0002 | t0019 | g0023 | AMR | CLM | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01257 | hp1 | a0001 | c0002 | t0003 | g0002 | AMR | CLM | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | CLM | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01258 | hp1 | a0001 | c0002 | t0003 | g0002 | AMR | CLM | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01261 | hp1 | a0001 | c0002 | t0005 | g0260 | AMR | CLM | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | CLM | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01346 | hp1 | a0001 | c0001 | t0004 | g0173 | AMR | CLM | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01346 | hp2 | a0001 | c0002 | t0005 | g0022 | AMR | CLM | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01358 | hp1 | a0001 | c0002 | t0005 | g0237 | AMR | CLM | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | CLM | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01361 | hp1 | a0001 | c0002 | t0005 | g0251 | AMR | CLM | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01361 | hp2 | a0001 | c0002 | t0003 | g0004 | AMR | CLM | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | CLM | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01433 | hp2 | a0001 | c0001 | t0004 | g0170 | AMR | CLM | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01496 | hp1 | a0001 | c0002 | t0019 | g0023 | AMR | CLM | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01496 | hp2 | a0001 | c0002 | t0005 | g0240 | AMR | CLM | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01515 | hp1 | a0001 | c0001 | t0004 | g0217 | EUR | IBS | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01515 | hp2 | a0001 | c0002 | t0005 | g0006 | EUR | IBS | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01516 | hp1 | a0001 | c0002 | t0005 | g0022 | EUR | IBS | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0015 | EUR | IBS | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01517 | hp1 | a0001 | c0001 | t0004 | g0216 | EUR | IBS | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0015 | EUR | IBS | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01884 | hp1 | a0001 | c0002 | t0005 | g0267 | AFR | ACB | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01884 | hp2 | a0001 | c0001 | t0012 | g0264 | AFR | ACB | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01891 | hp1 | a0002 | c0005 | t0039 | g0312 | AFR | ACB | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01891 | hp2 | a0001 | c0001 | t0012 | g0024 | AFR | ACB | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01934 | hp1 | a0001 | c0002 | t0005 | g0247 | AMR | PEL | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PEL | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01975 | hp1 | a0001 | c0002 | t0005 | g0006 | AMR | PEL | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PEL | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02040 | hp1 | a0001 | c0001 | t0015 | g0208 | EAS | KHV | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02055 | hp1 | a0001 | c0001 | t0009 | g0156 | AFR | ACB | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02055 | hp2 | a0001 | c0001 | t0018 | g0263 | AFR | ACB | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02056 | hp1 | a0001 | c0001 | t0009 | g0141 | EAS | KHV | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0280 | EAS | KHV | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02071 | hp1 | a0001 | c0002 | t0007 | g0212 | EAS | KHV | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02129 | hp1 | a0001 | c0002 | t0007 | g0165 | EAS | KHV | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | KHV | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | KHV | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | KHV | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02145 | hp1 | a0001 | c0004 | t0020 | g0167 | AFR | ACB | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02145 | hp2 | a0001 | c0002 | t0006 | g0219 | AFR | ACB | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | CDX | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02155 | hp2 | a0001 | c0001 | t0015 | g0102 | EAS | CDX | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | CDX | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | CDX | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ACB | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02257 | hp2 | a0001 | c0001 | t0018 | g0241 | AFR | ACB | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | ACB | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02258 | hp2 | a0001 | c0002 | t0005 | g0020 | AFR | ACB | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02273 | hp2 | a0001 | c0002 | t0003 | g0213 | AMR | PEL | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02280 | hp1 | a0001 | c0001 | t0006 | g0005 | AFR | ACB | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02280 | hp2 | a0001 | c0002 | t0003 | g0204 | AFR | ACB | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02300 | hp2 | a0001 | c0001 | t0004 | g0175 | AMR | PEL | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | ACB | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02451 | hp2 | a0001 | c0002 | t0004 | g0042 | AFR | ACB | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02523 | hp2 | a0001 | c0002 | t0007 | g0164 | EAS | KHV | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02572 | hp1 | a0001 | c0001 | t0016 | g0271 | AFR | GWD | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02602 | hp2 | a0001 | c0002 | t0027 | g0249 | SAS | PJL | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02622 | hp1 | a0004 | c0007 | t0032 | g0051 | AFR | GWD | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02622 | hp2 | a0001 | c0001 | t0028 | g0027 | AFR | GWD | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02647 | hp1 | a0001 | c0002 | t0010 | g0047 | AFR | GWD | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02647 | hp2 | a0001 | c0002 | t0004 | g0033 | AFR | GWD | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0297 | SAS | PJL | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02717 | hp1 | a0001 | c0002 | t0004 | g0043 | AFR | GWD | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | GWD | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02723 | hp1 | a0001 | c0001 | t0006 | g0232 | AFR | GWD | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02723 | hp2 | a0001 | c0001 | t0013 | g0030 | AFR | GWD | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02738 | hp1 | a0001 | c0001 | t0004 | g0168 | SAS | PJL | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0300 | SAS | PJL | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02809 | hp1 | a0001 | c0002 | t0004 | g0048 | AFR | GWD | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02809 | hp2 | a0001 | c0001 | t0026 | g0021 | AFR | GWD | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02818 | hp1 | a0001 | c0001 | t0012 | g0266 | AFR | GWD | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02818 | hp2 | a0001 | c0002 | t0004 | g0003 | AFR | GWD | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02886 | hp1 | a0001 | c0001 | t0012 | g0262 | AFR | GWD | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | GWD | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02895 | hp1 | a0001 | c0001 | t0024 | g0234 | AFR | GWD | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | GWD | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02896 | hp1 | a0001 | c0001 | t0017 | g0257 | AFR | GWD | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02896 | hp2 | a0001 | c0002 | t0004 | g0003 | AFR | GWD | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02897 | hp1 | a0001 | c0001 | t0024 | g0233 | AFR | GWD | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02897 | hp2 | a0001 | c0002 | t0004 | g0003 | AFR | GWD | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02922 | hp1 | a0001 | c0002 | t0014 | g0052 | AFR | ESN | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02922 | hp2 | a0001 | c0002 | t0005 | g0239 | AFR | ESN | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02965 | hp1 | a0001 | c0002 | t0004 | g0093 | AFR | ESN | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02965 | hp2 | a0001 | c0001 | t0014 | g0221 | AFR | ESN | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | ESN | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02970 | hp2 | a0001 | c0002 | t0023 | g0046 | AFR | ESN | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG03017 | hp1 | a0001 | c0002 | t0003 | g0195 | SAS | PJL | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG03041 | hp1 | a0001 | c0002 | t0004 | g0041 | AFR | GWD | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG03130 | hp1 | a0001 | c0001 | t0006 | g0230 | AFR | ESN | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG03130 | hp2 | a0001 | c0001 | t0012 | g0024 | AFR | ESN | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG03139 | hp1 | a0001 | c0002 | t0004 | g0045 | AFR | ESN | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG03139 | hp2 | a0001 | c0001 | t0025 | g0311 | AFR | ESN | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | ESN | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG03195 | hp2 | a0001 | c0002 | t0005 | g0238 | AFR | ESN | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0272 | AFR | MSL | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG03209 | hp2 | a0001 | c0002 | t0037 | g0049 | AFR | MSL | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG03225 | hp1 | a0001 | c0001 | t0006 | g0178 | AFR | MSL | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG03225 | hp2 | a0001 | c0002 | t0004 | g0038 | AFR | MSL | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG03239 | hp1 | a0001 | c0002 | t0003 | g0203 | SAS | PJL | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG03239 | hp2 | a0001 | c0002 | t0027 | g0248 | SAS | PJL | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG03453 | hp1 | a0001 | c0002 | t0010 | g0029 | AFR | MSL | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG03453 | hp2 | a0001 | c0001 | t0026 | g0021 | AFR | MSL | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG03486 | hp1 | a0001 | c0001 | t0004 | g0215 | AFR | MSL | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG03486 | hp2 | a0001 | c0001 | t0042 | g0313 | AFR | MSL | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG03490 | hp2 | a0001 | c0002 | t0010 | g0054 | SAS | PJL | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0008 | SAS | PJL | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG03491 | hp2 | a0001 | c0002 | t0010 | g0183 | SAS | PJL | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0008 | SAS | PJL | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG03540 | hp1 | a0001 | c0002 | t0029 | g0026 | AFR | GWD | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG03540 | hp2 | a0001 | c0001 | t0025 | g0310 | AFR | GWD | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG03579 | hp1 | a0001 | c0001 | t0009 | g0231 | AFR | MSL | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG03579 | hp2 | a0001 | c0001 | t0030 | g0050 | AFR | MSL | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG03688 | hp1 | a0001 | c0002 | t0041 | g0250 | SAS | STU | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG03688 | hp2 | a0001 | c0002 | t0022 | g0207 | SAS | STU | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0273 | SAS | PJL | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG03831 | hp1 | a0001 | c0002 | t0010 | g0184 | SAS | BEB | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG03831 | hp2 | a0001 | c0001 | t0009 | g0085 | SAS | BEB | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | BEB | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0299 | SAS | BEB | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG03927 | hp1 | a0001 | c0001 | t0009 | g0072 | SAS | BEB | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG03927 | hp2 | a0001 | c0002 | t0035 | g0182 | SAS | BEB | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG04115 | hp1 | a0001 | c0001 | t0034 | g0154 | SAS | STU | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | STU | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG04184 | hp1 | a0001 | c0001 | t0021 | g0034 | SAS | BEB | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | BEB | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | STU | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | STU | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG04204 | hp1 | a0001 | c0001 | t0021 | g0036 | SAS | STU | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0077 | SAS | STU | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18522 | hp1 | a0001 | c0002 | t0004 | g0040 | AFR | YRI | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18522 | hp2 | a0001 | c0002 | t0005 | g0254 | AFR | YRI | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18906 | hp1 | a0001 | c0001 | t0013 | g0028 | AFR | YRI | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18906 | hp2 | a0001 | c0001 | t0006 | g0005 | AFR | YRI | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18939 | hp1 | a0001 | c0001 | t0006 | g0064 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18939 | hp2 | a0001 | c0002 | t0003 | g0196 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18941 | hp1 | a0001 | c0001 | t0002 | g0306 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18941 | hp2 | a0001 | c0001 | t0008 | g0101 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18943 | hp1 | a0001 | c0002 | t0007 | g0209 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0274 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0291 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18948 | hp2 | a0001 | c0002 | t0011 | g0190 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0308 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18949 | hp2 | a0001 | c0001 | t0008 | g0001 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18951 | hp2 | a0001 | c0002 | t0011 | g0191 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0305 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18954 | hp1 | a0001 | c0002 | t0007 | g0163 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18956 | hp2 | a0001 | c0002 | t0004 | g0044 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18957 | hp1 | a0001 | c0001 | t0002 | g0307 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18965 | hp1 | a0001 | c0001 | t0002 | g0289 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18965 | hp2 | a0001 | c0002 | t0010 | g0057 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18967 | hp1 | a0001 | c0001 | t0002 | g0293 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18969 | hp1 | a0001 | c0003 | t0001 | g0099 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0294 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18970 | hp1 | a0001 | c0001 | t0016 | g0277 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18972 | hp1 | a0001 | c0001 | t0008 | g0097 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18972 | hp2 | a0001 | c0002 | t0011 | g0202 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18973 | hp2 | a0001 | c0001 | t0008 | g0137 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0279 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18977 | hp1 | a0001 | c0001 | t0008 | g0096 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18981 | hp2 | a0001 | c0002 | t0003 | g0201 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18982 | hp1 | a0001 | c0001 | t0008 | g0001 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18982 | hp2 | a0001 | c0002 | t0003 | g0197 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18983 | hp1 | a0001 | c0002 | t0003 | g0019 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18987 | hp2 | a0001 | c0002 | t0003 | g0211 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0290 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18994 | hp2 | a0001 | c0002 | t0003 | g0018 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18995 | hp1 | a0001 | c0001 | t0033 | g0100 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0269 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18998 | hp1 | a0001 | c0001 | t0002 | g0292 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19001 | hp2 | a0001 | c0002 | t0011 | g0198 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19002 | hp1 | a0001 | c0002 | t0007 | g0017 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19003 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19004 | hp1 | a0001 | c0001 | t0031 | g0083 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19004 | hp2 | a0001 | c0002 | t0003 | g0199 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19005 | hp1 | a0001 | c0002 | t0010 | g0055 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19006 | hp1 | a0001 | c0002 | t0036 | g0188 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19006 | hp2 | a0001 | c0001 | t0002 | g0304 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19007 | hp1 | a0001 | c0002 | t0007 | g0210 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0302 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19010 | hp1 | a0001 | c0002 | t0007 | g0017 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19012 | hp2 | a0001 | c0001 | t0016 | g0309 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19043 | hp1 | a0001 | c0002 | t0023 | g0037 | AFR | LWK | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19043 | hp2 | a0001 | c0004 | t0020 | g0166 | AFR | LWK | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19054 | hp1 | a0001 | c0001 | t0002 | g0281 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19055 | hp1 | a0001 | c0001 | t0002 | g0288 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19056 | hp1 | a0001 | c0002 | t0005 | g0246 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19056 | hp2 | a0001 | c0002 | t0011 | g0193 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0295 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19064 | hp1 | a0001 | c0001 | t0008 | g0001 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19065 | hp2 | a0001 | c0002 | t0003 | g0019 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19066 | hp1 | a0001 | c0002 | t0011 | g0187 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19067 | hp1 | a0001 | c0001 | t0009 | g0132 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19067 | hp2 | a0001 | c0002 | t0022 | g0056 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0286 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0303 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0284 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19079 | hp1 | a0001 | c0003 | t0001 | g0088 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19079 | hp2 | a0001 | c0002 | t0003 | g0194 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19081 | hp2 | a0001 | c0002 | t0007 | g0058 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19082 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19083 | hp1 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0283 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19084 | hp2 | a0001 | c0001 | t0008 | g0001 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19085 | hp2 | a0001 | c0002 | t0003 | g0200 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19090 | hp1 | a0001 | c0001 | t0015 | g0063 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19090 | hp2 | a0001 | c0002 | t0003 | g0018 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19240 | hp1 | a0001 | c0001 | t0006 | g0005 | AFR | YRI | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA19240 | hp2 | a0003 | c0006 | t0038 | g0235 | AFR | YRI | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA20129 | hp1 | a0001 | c0001 | t0017 | g0252 | AFR | ASW | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA20129 | hp2 | a0001 | c0001 | t0014 | g0229 | AFR | ASW | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA20905 | hp1 | a0001 | c0001 | t0004 | g0180 | SAS | GIH | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | GIH | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01123 | hp1 | a0001 | c0001 | t0006 | g0225 | AMR | CLM | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG01123 | hp2 | a0001 | c0002 | t0005 | g0242 | AMR | CLM | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02109 | hp1 | a0001 | c0002 | t0005 | g0244 | AFR | ACB | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02109 | hp2 | a0001 | c0001 | t0014 | g0179 | AFR | ACB | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02486 | hp1 | a0001 | c0002 | t0005 | g0256 | AFR | ACB | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02486 | hp2 | a0001 | c0002 | t0006 | g0220 | AFR | ACB | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | ACB | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG02559 | hp2 | a0001 | c0002 | t0005 | g0020 | AFR | ACB | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG03471 | hp1 | a0001 | c0002 | t0006 | g0053 | AFR | MSL | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
HG03471 | hp2 | a0001 | c0001 | t0012 | g0265 | AFR | MSL | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA18955 | hp2 | a0001 | c0002 | t0003 | g0189 | EAS | JPT | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | USA | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA20300 | hp2 | a0001 | c0001 | t0013 | g0032 | AFR | USA | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA21309 | hp1 | a0001 | c0001 | t0004 | g0176 | AFR | LWK | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | LWK | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0005 | g0006 | REF | REF | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
homoSapiens_grch38 | hp1 | a0001 | c0002 | t0005 | g0243 | REF | REF | TFB1M_chr6_155251134_155319484 | TFB1M | chr6 | 155251134 | 155319484 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:155260300
|
C | T | 1 | a0003 | 1 | NA19240.hp2 | missense_variant | MODERATE | c.767G>A | p.Arg256Gln | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 6/7 | 823/2799 | 767/1041 | 256/346 | chr6 | 155260300 | ||
chr6:155297084
|
T | C | 1 | a0004 | 1 | HG02622.hp1 | missense_variant | MODERATE | c.415A>G | p.Ile139Val | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/7 | 471/2799 | 415/1041 | 139/346 | chr6 | 155297084 | ||
chr6:155298554
|
C | T | 1 | a0002 | 1 | HG01891.hp1 | missense_variant | MODERATE | c.317G>A | p.Arg106Lys | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 3/7 | 373/2799 | 317/1041 | 106/346 | chr6 | 155298554 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:155257986
|
G | A | 1 | a0001c0003 | 2 | NA18969.hp1 NA19079.hp1 |
synonymous_variant | LOW | c.891C>T | p.Ile297Ile | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 7/7 | 947/2799 | 891/1041 | 297/346 | chr6 | 155257986 | ||
chr6:155285191
|
C | T | 5 | a0001c0001a0001c0003a0001c0004others(2): Show | 238 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(235): Show |
synonymous_variant | LOW | c.633G>A | p.Thr211Thr | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/7 | 689/2799 | 633/1041 | 211/346 | chr6 | 155285191 | ||
chr6:155311293
|
G | A | 1 | a0001c0004 | 2 | HG02145.hp1 NA19043.hp2 |
synonymous_variant | LOW | c.180C>T | p.Tyr60Tyr | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/7 | 236/2799 | 180/1041 | 60/346 | chr6 | 155311293 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:155256240
|
T | C | 37 | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(34): Show | 279 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(276): Show |
3_prime_UTR_variant | MODIFIER | c.*1596A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 7/7 | 1596 | chr6 | 155256240 | |||||
chr6:155256247
|
A | G | 1 | a0001c0004t0020 | 2 | HG02145.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1589T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 7/7 | 1589 | chr6 | 155256247 | |||||
chr6:155256580
|
G | C | 2 | a0001c0001t0013a0001c0001t0021 | 7 | HG00639.hp1 HG01109.hp1 HG02723.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1256C>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 7/7 | 1256 | chr6 | 155256580 | |||||
chr6:155256582
|
T | C | 2 | a0001c0001t0013a0001c0001t0021 | 7 | HG00639.hp1 HG01109.hp1 HG02723.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1254A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 7/7 | 1254 | chr6 | 155256582 | |||||
chr6:155256583
|
T | A | 2 | a0001c0001t0013a0001c0001t0021 | 7 | HG00639.hp1 HG01109.hp1 HG02723.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1253A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 7/7 | 1253 | chr6 | 155256583 | |||||
chr6:155256689
|
C | T | 35 | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(32): Show | 277 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(274): Show |
3_prime_UTR_variant | MODIFIER | c.*1147G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 7/7 | 1147 | chr6 | 155256689 | |||||
chr6:155256731
|
T | A | 2 | a0001c0001t0008a0001c0001t0033 | 9 | NA18941.hp2 NA18949.hp2 NA18972.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1105A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 7/7 | 1105 | chr6 | 155256731 | |||||
chr6:155256738
|
C | T | 1 | a0001c0001t0021 | 2 | HG04184.hp1 HG04204.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1098G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 7/7 | 1098 | chr6 | 155256738 | |||||
chr6:155256831
|
G | A | 1 | a0001c0002t0041 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1005C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 7/7 | 1005 | chr6 | 155256831 | |||||
chr6:155256833
|
G | A | 1 | a0001c0001t0025 | 2 | HG03139.hp2 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1003C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 7/7 | 1003 | chr6 | 155256833 | |||||
chr6:155256876
|
G | A | 2 | a0001c0002t0007a0001c0002t0035 | 10 | HG02071.hp1 HG02129.hp1 HG02523.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*960C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 7/7 | 960 | chr6 | 155256876 | |||||
chr6:155256942
|
A | G | 1 | a0002c0005t0039 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*894T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 7/7 | 894 | chr6 | 155256942 | |||||
chr6:155257155
|
A | C | 2 | a0001c0004t0020a0004c0007t0032 | 3 | HG02145.hp1 HG02622.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*681T>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 7/7 | 681 | chr6 | 155257155 | |||||
chr6:155257190
|
C | CA | 11 | a0001c0001t0012a0001c0001t0014a0001c0002t0011others(8): Show | 28 | HG00741.hp1 HG01255.hp2 HG01256.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*645dupT | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 7/7 | 645 | chr6 | 155257190 | |||||
chr6:155257190
|
CA | C | 11 | a0001c0001t0002a0001c0001t0009a0001c0001t0015others(8): Show | 67 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*645delT | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 7/7 | 645 | chr6 | 155257190 | |||||
chr6:155257190
|
CAA | C | 11 | a0001c0001t0001a0001c0001t0008a0001c0001t0013others(8): Show | 129 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(126): Show |
3_prime_UTR_variant | MODIFIER | c.*644_*645delTT | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 7/7 | 644 | chr6 | 155257190 | |||||
chr6:155257206
|
A | C | 1 | a0001c0001t0031 | 1 | NA19004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*630T>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 7/7 | 630 | chr6 | 155257206 | |||||
chr6:155257214
|
G | A | 1 | a0001c0001t0034 | 1 | HG04115.hp1 | 3_prime_UTR_variant | MODIFIER | c.*622C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 7/7 | 622 | chr6 | 155257214 | |||||
chr6:155257384
|
A | ATT | 7 | a0001c0001t0002a0001c0001t0015a0001c0001t0016others(4): Show | 56 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*450_*451dupAA | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 7/7 | 451 | chr6 | 155257384 | |||||
chr6:155257432
|
T | C | 1 | a0001c0002t0036 | 1 | NA19006.hp1 | 3_prime_UTR_variant | MODIFIER | c.*404A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 7/7 | 404 | chr6 | 155257432 | |||||
chr6:155257465
|
A | T | 36 | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(33): Show | 278 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(275): Show |
3_prime_UTR_variant | MODIFIER | c.*371T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 7/7 | 371 | chr6 | 155257465 | |||||
chr6:155257550
|
G | A | 5 | a0001c0002t0003a0001c0002t0007a0001c0002t0011others(2): Show | 47 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*286C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 7/7 | 286 | chr6 | 155257550 | |||||
chr6:155257579
|
AAGAT | A | 40 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(37): Show | 307 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(304): Show |
3_prime_UTR_variant | MODIFIER | c.*253_*256delATCT | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 7/7 | 253 | chr6 | 155257579 | |||||
chr6:155257622
|
A | T | 36 | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(33): Show | 278 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(275): Show |
3_prime_UTR_variant | MODIFIER | c.*214T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 7/7 | 214 | chr6 | 155257622 | |||||
chr6:155314448
|
C | A | 2 | a0001c0001t0024a0003c0006t0038 | 3 | HG02895.hp1 HG02897.hp1 NA19240.hp2 |
5_prime_UTR_variant | MODIFIER | c.-20G>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 1/7 | 20 | chr6 | 155314448 | |||||
chr6:155314451
|
A | C | 32 | a0001c0001t0001a0001c0001t0004a0001c0001t0006others(29): Show | 249 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(246): Show |
5_prime_UTR_variant | MODIFIER | c.-23T>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 1/7 | 23 | chr6 | 155314451 | |||||
chr6:155314452
|
C | A | 1 | a0001c0001t0042 | 1 | HG03486.hp2 | 5_prime_UTR_variant | MODIFIER | c.-24G>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 1/7 | 24 | chr6 | 155314452 | |||||
chr6:155314461
|
A | C | 2 | a0001c0001t0028a0001c0002t0029 | 2 | HG02622.hp2 HG03540.hp1 |
5_prime_UTR_variant | MODIFIER | c.-33T>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 1/7 | 33 | chr6 | 155314461 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:155258112
|
A | C | 250 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(247): Show | 278 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(275): Show |
intron_variant | MODIFIER | c.795-30T>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 6/6 | chr6 | 155258112 | ||||||
chr6:155258158
|
A | G | 1 | a0001c0002t0027g0248 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.795-76T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 6/6 | chr6 | 155258158 | ||||||
chr6:155258244
|
A | G | 1 | a0001c0001t0030g0050 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.795-162T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 6/6 | chr6 | 155258244 | ||||||
chr6:155258249
|
C | T | 2 | a0001c0002t0005g0246a0001c0002t0005g0247 | 2 | HG01934.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.795-167G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 6/6 | chr6 | 155258249 | ||||||
chr6:155258266
|
A | G | 168 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(165): Show | 188 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(185): Show |
intron_variant | MODIFIER | c.795-184T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 6/6 | chr6 | 155258266 | ||||||
chr6:155258283
|
C | T | 1 | a0001c0002t0019g0023 | 2 | HG01256.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.795-201G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 6/6 | chr6 | 155258283 | ||||||
chr6:155258284
|
G | A | 1 | a0001c0001t0009g0085 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.795-202C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 6/6 | chr6 | 155258284 | ||||||
chr6:155258408
|
T | C | 3 | a0001c0001t0013g0035a0001c0001t0021g0034a0001c0001t0021g0036 | 3 | HG00639.hp1 HG04184.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.795-326A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 6/6 | chr6 | 155258408 | ||||||
chr6:155258423
|
A | G | 254 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(251): Show | 282 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.795-341T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 6/6 | chr6 | 155258423 | ||||||
chr6:155258510
|
C | T | 1 | a0001c0001t0001g0120 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.795-428G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 6/6 | chr6 | 155258510 | ||||||
chr6:155258547
|
A | AAT | 254 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(251): Show | 282 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.795-467_795-466dup others(2): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 6/6 | chr6 | 155258547 | ||||||
chr6:155258614
|
G | A | 9 | a0001c0001t0006g0222a0001c0001t0006g0223a0001c0001t0006g0224others(6): Show | 9 | HG00099.hp1 HG00738.hp1 HG01070.hp1 others(6): Show |
intron_variant | MODIFIER | c.795-532C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 6/6 | chr6 | 155258614 | ||||||
chr6:155258694
|
C | T | 2 | a0001c0001t0008g0096a0001c0001t0014g0229 | 2 | NA18977.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.795-612G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 6/6 | chr6 | 155258694 | ||||||
chr6:155258805
|
T | C | 1 | a0001c0001t0002g0300 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.795-723A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 6/6 | chr6 | 155258805 | ||||||
chr6:155258881
|
G | A | 1 | a0001c0002t0004g0033 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.795-799C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 6/6 | chr6 | 155258881 | ||||||
chr6:155258900
|
CTGA | C | 247 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(244): Show | 275 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.795-821_795-819del others(3): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 6/6 | chr6 | 155258900 | ||||||
chr6:155258962
|
C | A | 2 | a0001c0001t0001g0095a0001c0001t0001g0117 | 2 | HG01099.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.795-880G>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 6/6 | chr6 | 155258962 | ||||||
chr6:155259134
|
T | C | 250 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(247): Show | 278 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(275): Show |
intron_variant | MODIFIER | c.795-1052A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 6/6 | chr6 | 155259134 | ||||||
chr6:155259140
|
C | T | 2 | a0001c0001t0004g0168a0001c0001t0004g0180 | 2 | HG02738.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.795-1058G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 6/6 | chr6 | 155259140 | ||||||
chr6:155259207
|
A | G | 250 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(247): Show | 278 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(275): Show |
intron_variant | MODIFIER | c.794+1066T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 6/6 | chr6 | 155259207 | ||||||
chr6:155259213
|
C | T | 5 | a0001c0002t0003g0019a0001c0002t0003g0196a0001c0002t0003g0199others(2): Show | 6 | NA18939.hp2 NA18983.hp1 NA18987.hp2 others(3): Show |
intron_variant | MODIFIER | c.794+1060G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 6/6 | chr6 | 155259213 | ||||||
chr6:155259240
|
C | T | 1 | a0001c0002t0003g0019 | 2 | NA18983.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.794+1033G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 6/6 | chr6 | 155259240 | ||||||
chr6:155259442
|
T | C | 1 | a0001c0002t0005g0267 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.794+831A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 6/6 | chr6 | 155259442 | ||||||
chr6:155259504
|
G | A | 7 | a0001c0001t0013g0028a0001c0001t0013g0030a0001c0001t0013g0031others(4): Show | 7 | HG00639.hp1 HG01109.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.794+769C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 6/6 | chr6 | 155259504 | ||||||
chr6:155259620
|
A | AT | 3 | a0001c0002t0006g0053a0001c0002t0014g0052a0001c0002t0029g0026 | 3 | HG02922.hp1 HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.794+652dupA | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 6/6 | chr6 | 155259620 | ||||||
chr6:155259639
|
T | G | 13 | a0001c0001t0006g0005a0001c0001t0006g0222a0001c0001t0006g0223others(10): Show | 15 | HG00099.hp1 HG00738.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.794+634A>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 6/6 | chr6 | 155259639 | ||||||
chr6:155259749
|
T | G | 5 | a0001c0002t0003g0189a0001c0002t0003g0195a0001c0002t0011g0187others(2): Show | 5 | HG03017.hp1 NA18948.hp2 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.794+524A>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 6/6 | chr6 | 155259749 | ||||||
chr6:155259890
|
G | T | 170 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(167): Show | 190 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(187): Show |
intron_variant | MODIFIER | c.794+383C>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 6/6 | chr6 | 155259890 | ||||||
chr6:155260018
|
G | C | 1 | a0001c0001t0002g0306 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.794+255C>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 6/6 | chr6 | 155260018 | ||||||
chr6:155260052
|
C | T | 250 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(247): Show | 278 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(275): Show |
intron_variant | MODIFIER | c.794+221G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 6/6 | chr6 | 155260052 | ||||||
chr6:155260083
|
G | A | 1 | a0001c0001t0002g0273 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.794+190C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 6/6 | chr6 | 155260083 | ||||||
chr6:155260155
|
C | A | 250 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(247): Show | 278 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(275): Show |
intron_variant | MODIFIER | c.794+118G>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 6/6 | chr6 | 155260155 | ||||||
chr6:155260237
|
A | G | 1 | a0001c0002t0029g0026 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.794+36T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 6/6 | chr6 | 155260237 | ||||||
chr6:155260254
|
G | C | 3 | a0001c0002t0006g0053a0001c0002t0014g0052a0001c0002t0029g0026 | 3 | HG02922.hp1 HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.794+19C>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 6/6 | chr6 | 155260254 | ||||||
chr6:155260485
|
G | A | 250 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(247): Show | 278 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(275): Show |
intron_variant | MODIFIER | c.667-85C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155260485 | ||||||
chr6:155260589
|
G | A | 1 | a0001c0001t0002g0280 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.667-189C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155260589 | ||||||
chr6:155260601
|
G | A | 11 | a0001c0001t0004g0168a0001c0001t0004g0170a0001c0001t0004g0171others(8): Show | 11 | HG00733.hp2 HG01109.hp2 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.667-201C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155260601 | ||||||
chr6:155260701
|
T | G | 247 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(244): Show | 275 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.667-301A>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155260701 | ||||||
chr6:155260763
|
A | G | 48 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0025others(45): Show | 53 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.667-363T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155260763 | ||||||
chr6:155260770
|
C | T | 250 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(247): Show | 278 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(275): Show |
intron_variant | MODIFIER | c.667-370G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155260770 | ||||||
chr6:155261081
|
T | G | 250 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(247): Show | 278 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(275): Show |
intron_variant | MODIFIER | c.667-681A>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155261081 | ||||||
chr6:155261122
|
A | C | 1 | a0001c0001t0009g0231 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.667-722T>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155261122 | ||||||
chr6:155261216
|
G | A | 51 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0025others(48): Show | 56 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.667-816C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155261216 | ||||||
chr6:155261331
|
C | T | 3 | a0001c0002t0006g0053a0001c0002t0014g0052a0001c0002t0029g0026 | 3 | HG02922.hp1 HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.667-931G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155261331 | ||||||
chr6:155261342
|
C | T | 6 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0113others(3): Show | 8 | HG00642.hp1 HG01081.hp2 HG01516.hp2 others(5): Show |
intron_variant | MODIFIER | c.667-942G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155261342 | ||||||
chr6:155261393
|
T | C | 3 | a0001c0002t0006g0053a0001c0002t0014g0052a0001c0002t0029g0026 | 3 | HG02922.hp1 HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.667-993A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155261393 | ||||||
chr6:155261611
|
T | G | 25 | a0001c0001t0006g0005a0001c0001t0006g0178a0001c0001t0006g0222others(22): Show | 28 | HG00099.hp1 HG00738.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.667-1211A>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155261611 | ||||||
chr6:155261617
|
AGGTGCCT others(2): Show |
A | 3 | a0001c0002t0006g0053a0001c0002t0014g0052a0001c0002t0029g0026 | 3 | HG02922.hp1 HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.667-1226_667-1218d others(11): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155261617 | ||||||
chr6:155261670
|
T | C | 2 | a0001c0001t0001g0066a0001c0001t0001g0067 | 2 | NA18973.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.667-1270A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155261670 | ||||||
chr6:155261704
|
C | T | 3 | a0001c0002t0006g0053a0001c0002t0014g0052a0001c0002t0029g0026 | 3 | HG02922.hp1 HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.667-1304G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155261704 | ||||||
chr6:155261708
|
G | A | 6 | a0001c0002t0005g0020a0001c0002t0005g0238a0001c0002t0005g0239others(3): Show | 7 | HG01496.hp2 HG02258.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.667-1308C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155261708 | ||||||
chr6:155261814
|
C | G | 54 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0025others(51): Show | 59 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.667-1414G>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155261814 | ||||||
chr6:155262132
|
G | C | 1 | a0001c0002t0005g0260 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.667-1732C>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155262132 | ||||||
chr6:155262155
|
G | A | 3 | a0001c0001t0006g0178a0001c0001t0014g0179a0001c0001t0014g0221 | 3 | HG02109.hp2 HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.667-1755C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155262155 | ||||||
chr6:155262156
|
T | C | 1 | a0001c0001t0004g0175 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.667-1756A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155262156 | ||||||
chr6:155262163
|
G | A | 1 | a0001c0001t0030g0050 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.667-1763C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155262163 | ||||||
chr6:155262252
|
G | A | 7 | a0001c0001t0013g0028a0001c0001t0013g0030a0001c0001t0013g0031others(4): Show | 7 | HG00639.hp1 HG01109.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.667-1852C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155262252 | ||||||
chr6:155262405
|
C | T | 4 | a0001c0001t0001g0071a0001c0001t0001g0080a0001c0001t0001g0108others(1): Show | 4 | HG01257.hp2 HG02683.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.667-2005G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155262405 | ||||||
chr6:155262411
|
G | A | 224 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(221): Show | 249 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(246): Show |
intron_variant | MODIFIER | c.667-2011C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155262411 | ||||||
chr6:155262452
|
C | T | 1 | a0001c0001t0001g0138 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.667-2052G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155262452 | ||||||
chr6:155262457
|
G | T | 1 | a0001c0001t0014g0226 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.667-2057C>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155262457 | ||||||
chr6:155262470
|
C | G | 1 | a0001c0001t0030g0050 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.667-2070G>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155262470 | ||||||
chr6:155262486
|
G | C | 225 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(222): Show | 250 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(247): Show |
intron_variant | MODIFIER | c.667-2086C>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155262486 | ||||||
chr6:155262524
|
G | A | 1 | a0001c0001t0001g0129 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.667-2124C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155262524 | ||||||
chr6:155262539
|
A | C | 250 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(247): Show | 278 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(275): Show |
intron_variant | MODIFIER | c.667-2139T>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155262539 | ||||||
chr6:155262733
|
G | GA | 23 | a0001c0001t0006g0005a0001c0001t0006g0178a0001c0001t0006g0222others(20): Show | 26 | HG00099.hp1 HG00738.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.667-2334dupT | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155262733 | ||||||
chr6:155262862
|
A | T | 1 | a0001c0002t0035g0182 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.667-2462T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155262862 | ||||||
chr6:155262949
|
T | C | 1 | a0001c0001t0006g0225 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.667-2549A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155262949 | ||||||
chr6:155263030
|
A | C | 3 | a0001c0002t0006g0053a0001c0002t0014g0052a0001c0002t0029g0026 | 3 | HG02922.hp1 HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.667-2630T>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155263030 | ||||||
chr6:155263222
|
T | C | 253 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(250): Show | 281 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(278): Show |
intron_variant | MODIFIER | c.667-2822A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155263222 | ||||||
chr6:155263535
|
C | T | 1 | a0001c0001t0001g0140 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.667-3135G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155263535 | ||||||
chr6:155263576
|
G | A | 1 | a0001c0001t0013g0035 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.667-3176C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155263576 | ||||||
chr6:155263610
|
C | A | 1 | a0001c0001t0001g0109 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.667-3210G>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155263610 | ||||||
chr6:155263619
|
G | C | 1 | a0001c0001t0018g0255 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.667-3219C>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155263619 | ||||||
chr6:155263742
|
CAT | C | 3 | a0001c0001t0006g0178a0001c0001t0014g0179a0001c0001t0014g0221 | 3 | HG02109.hp2 HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.667-3344_667-3343d others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155263742 | ||||||
chr6:155263746
|
T | C | 1 | a0001c0001t0009g0231 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.667-3346A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155263746 | ||||||
chr6:155263944
|
T | TG | 22 | a0001c0001t0006g0005a0001c0001t0006g0178a0001c0001t0006g0222others(19): Show | 25 | HG00099.hp1 HG00738.hp1 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.667-3545dupC | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155263944 | ||||||
chr6:155263946
|
A | G | 254 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(251): Show | 281 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(278): Show |
intron_variant | MODIFIER | c.667-3546T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155263946 | ||||||
chr6:155264020
|
G | A | 13 | a0001c0001t0006g0005a0001c0001t0006g0222a0001c0001t0006g0223others(10): Show | 15 | HG00099.hp1 HG00738.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.667-3620C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155264020 | ||||||
chr6:155264099
|
A | G | 292 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(289): Show | 323 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(320): Show |
intron_variant | MODIFIER | c.667-3699T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155264099 | ||||||
chr6:155264144
|
C | T | 224 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(221): Show | 249 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(246): Show |
intron_variant | MODIFIER | c.667-3744G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155264144 | ||||||
chr6:155264164
|
G | A | 3 | a0001c0001t0006g0178a0001c0001t0014g0179a0001c0001t0014g0221 | 3 | HG02109.hp2 HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.667-3764C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155264164 | ||||||
chr6:155264177
|
G | A | 1 | a0001c0001t0001g0117 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.667-3777C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155264177 | ||||||
chr6:155264191
|
C | T | 127 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(124): Show | 139 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(136): Show |
intron_variant | MODIFIER | c.667-3791G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155264191 | ||||||
chr6:155264531
|
C | T | 6 | a0001c0002t0005g0020a0001c0002t0005g0238a0001c0002t0005g0239others(3): Show | 7 | HG01496.hp2 HG02258.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.667-4131G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155264531 | ||||||
chr6:155264600
|
TC | T | 6 | a0001c0002t0005g0020a0001c0002t0005g0238a0001c0002t0005g0239others(3): Show | 7 | HG01496.hp2 HG02258.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.667-4201delG | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155264600 | ||||||
chr6:155264734
|
G | A | 51 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0025others(48): Show | 56 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.667-4334C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155264734 | ||||||
chr6:155264784
|
G | T | 1 | a0001c0002t0004g0003 | 3 | HG02818.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.667-4384C>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155264784 | ||||||
chr6:155264817
|
A | C | 1 | a0001c0001t0001g0094 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.667-4417T>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155264817 | ||||||
chr6:155264930
|
C | T | 6 | a0001c0002t0005g0020a0001c0002t0005g0238a0001c0002t0005g0239others(3): Show | 7 | HG01496.hp2 HG02258.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.667-4530G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155264930 | ||||||
chr6:155264997
|
C | T | 302 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(299): Show | 335 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.667-4597G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155264997 | ||||||
chr6:155264998
|
A | G | 13 | a0001c0001t0006g0005a0001c0001t0006g0222a0001c0001t0006g0223others(10): Show | 15 | HG00099.hp1 HG00738.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.667-4598T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155264998 | ||||||
chr6:155265355
|
T | C | 2 | a0001c0002t0007g0017a0001c0002t0007g0058 | 3 | NA19002.hp1 NA19010.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.667-4955A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155265355 | ||||||
chr6:155265442
|
G | A | 1 | a0001c0001t0001g0039 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.667-5042C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155265442 | ||||||
chr6:155265462
|
G | A | 53 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0025others(50): Show | 58 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.667-5062C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155265462 | ||||||
chr6:155265464
|
A | C | 247 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(244): Show | 275 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.667-5064T>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155265464 | ||||||
chr6:155265487
|
T | C | 6 | a0001c0001t0012g0024a0001c0001t0012g0262a0001c0001t0012g0264others(3): Show | 7 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.667-5087A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155265487 | ||||||
chr6:155265503
|
CAGA | C | 250 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(247): Show | 278 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(275): Show |
intron_variant | MODIFIER | c.667-5106_667-5104d others(5): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155265503 | ||||||
chr6:155265671
|
G | A | 2 | a0001c0002t0006g0053a0001c0002t0014g0052 | 2 | HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.667-5271C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155265671 | ||||||
chr6:155265706
|
T | A | 1 | a0001c0002t0019g0270 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.667-5306A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155265706 | ||||||
chr6:155265729
|
A | AATATATA others(22): Show |
1 | a0001c0001t0001g0073 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.667-5358_667-5330d others(31): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155265729 | ||||||
chr6:155265730
|
ATATATAT | A | 7 | a0001c0001t0013g0028a0001c0001t0013g0030a0001c0001t0013g0031others(4): Show | 7 | HG00639.hp1 HG01109.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.667-5337_667-5331d others(9): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155265730 | ||||||
chr6:155265735
|
T | C | 1 | a0004c0007t0032g0051 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.667-5335A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155265735 | ||||||
chr6:155265736
|
A | T | 1 | a0001c0001t0009g0231 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.667-5336T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155265736 | ||||||
chr6:155265738
|
T | A | 8 | a0001c0001t0001g0039a0001c0001t0002g0269a0001c0001t0004g0176others(5): Show | 8 | HG02257.hp1 HG02723.hp1 HG03139.hp2 others(5): Show |
intron_variant | MODIFIER | c.667-5338A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155265738 | ||||||
chr6:155266001
|
C | T | 9 | a0001c0001t0012g0024a0001c0001t0012g0262a0001c0001t0012g0264others(6): Show | 10 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.667-5601G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155266001 | ||||||
chr6:155266063
|
C | A | 222 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(219): Show | 247 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(244): Show |
intron_variant | MODIFIER | c.667-5663G>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155266063 | ||||||
chr6:155266111
|
C | A | 3 | a0001c0002t0006g0053a0001c0002t0014g0052a0001c0002t0029g0026 | 3 | HG02922.hp1 HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.667-5711G>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155266111 | ||||||
chr6:155266288
|
A | G | 250 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(247): Show | 278 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(275): Show |
intron_variant | MODIFIER | c.667-5888T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155266288 | ||||||
chr6:155266333
|
C | G | 2 | a0001c0004t0020g0166a0001c0004t0020g0167 | 2 | HG02145.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.667-5933G>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155266333 | ||||||
chr6:155266462
|
A | C | 250 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(247): Show | 278 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(275): Show |
intron_variant | MODIFIER | c.667-6062T>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155266462 | ||||||
chr6:155266568
|
T | C | 247 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(244): Show | 275 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.667-6168A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155266568 | ||||||
chr6:155266575
|
T | A | 1 | a0001c0002t0011g0191 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.667-6175A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155266575 | ||||||
chr6:155266575
|
T | G | 246 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(243): Show | 274 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(271): Show |
intron_variant | MODIFIER | c.667-6175A>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155266575 | ||||||
chr6:155266613
|
A | G | 250 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(247): Show | 278 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(275): Show |
intron_variant | MODIFIER | c.667-6213T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155266613 | ||||||
chr6:155266642
|
C | T | 118 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(115): Show | 130 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(127): Show |
intron_variant | MODIFIER | c.667-6242G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155266642 | ||||||
chr6:155266708
|
G | A | 1 | a0001c0001t0009g0231 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.667-6308C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155266708 | ||||||
chr6:155266771
|
T | C | 250 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(247): Show | 278 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(275): Show |
intron_variant | MODIFIER | c.667-6371A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155266771 | ||||||
chr6:155266778
|
C | T | 2 | a0001c0001t0001g0104a0001c0001t0001g0105 | 2 | HG00673.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.667-6378G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155266778 | ||||||
chr6:155266841
|
C | T | 53 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0025others(50): Show | 58 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.667-6441G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155266841 | ||||||
chr6:155266846
|
C | CA | 18 | a0001c0001t0004g0168a0001c0001t0004g0171a0001c0001t0004g0173others(15): Show | 18 | HG01109.hp2 HG01243.hp1 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.667-6447dupT | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155266846 | ||||||
chr6:155266846
|
CAA | C | 16 | a0001c0001t0001g0111a0001c0001t0009g0231a0001c0001t0012g0024others(13): Show | 17 | HG00741.hp2 HG01175.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.667-6448_667-6447d others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155266846 | ||||||
chr6:155266846
|
CAAA | C | 73 | a0001c0001t0001g0039a0001c0001t0001g0074a0001c0001t0001g0089others(70): Show | 81 | HG00099.hp2 HG00280.hp2 HG00621.hp2 others(78): Show |
intron_variant | MODIFIER | c.667-6449_667-6447d others(5): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155266846 | ||||||
chr6:155266846
|
CAAAA | C | 156 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(153): Show | 175 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(172): Show |
intron_variant | MODIFIER | c.667-6450_667-6447d others(6): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155266846 | ||||||
chr6:155266970
|
C | CT | 26 | a0001c0001t0001g0039a0001c0001t0004g0168a0001c0001t0004g0170others(23): Show | 26 | HG00733.hp2 HG00738.hp1 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.667-6571dupA | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155266970 | ||||||
chr6:155266970
|
C | CTTT | 8 | a0001c0001t0012g0024a0001c0001t0012g0264a0001c0001t0012g0265others(5): Show | 9 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.667-6573_667-6571d others(5): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155266970 | ||||||
chr6:155266970
|
CT | C | 116 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(113): Show | 128 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(125): Show |
intron_variant | MODIFIER | c.667-6571delA | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155266970 | ||||||
chr6:155267024
|
C | T | 3 | a0001c0002t0006g0053a0001c0002t0014g0052a0001c0002t0029g0026 | 3 | HG02922.hp1 HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.667-6624G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155267024 | ||||||
chr6:155267037
|
T | C | 1 | a0001c0001t0001g0080 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.667-6637A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155267037 | ||||||
chr6:155267134
|
C | T | 51 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0025others(48): Show | 56 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.667-6734G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155267134 | ||||||
chr6:155267223
|
C | T | 4 | a0001c0002t0004g0040a0001c0002t0004g0041a0001c0002t0004g0042others(1): Show | 4 | HG02451.hp2 HG02717.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.667-6823G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155267223 | ||||||
chr6:155267241
|
T | C | 250 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(247): Show | 278 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(275): Show |
intron_variant | MODIFIER | c.667-6841A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155267241 | ||||||
chr6:155267254
|
C | T | 4 | a0001c0001t0002g0269a0001c0002t0006g0053a0001c0002t0014g0052others(1): Show | 4 | HG02922.hp1 HG03471.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.667-6854G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155267254 | ||||||
chr6:155267255
|
A | G | 250 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(247): Show | 278 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(275): Show |
intron_variant | MODIFIER | c.667-6855T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155267255 | ||||||
chr6:155267321
|
C | T | 3 | a0001c0002t0006g0053a0001c0002t0014g0052a0001c0002t0029g0026 | 3 | HG02922.hp1 HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.667-6921G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155267321 | ||||||
chr6:155267327
|
G | A | 250 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(247): Show | 278 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(275): Show |
intron_variant | MODIFIER | c.667-6927C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155267327 | ||||||
chr6:155267350
|
T | C | 41 | a0001c0002t0003g0002a0001c0002t0003g0004a0001c0002t0003g0018others(38): Show | 49 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.667-6950A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155267350 | ||||||
chr6:155267424
|
G | C | 1 | a0001c0001t0002g0291 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.667-7024C>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155267424 | ||||||
chr6:155267548
|
T | C | 118 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(115): Show | 130 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(127): Show |
intron_variant | MODIFIER | c.667-7148A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155267548 | ||||||
chr6:155267752
|
G | A | 1 | a0001c0001t0001g0073 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.667-7352C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155267752 | ||||||
chr6:155267781
|
T | A | 7 | a0001c0001t0013g0028a0001c0001t0013g0030a0001c0001t0013g0031others(4): Show | 7 | HG00639.hp1 HG01109.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.667-7381A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155267781 | ||||||
chr6:155267793
|
C | G | 1 | a0001c0002t0007g0209 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.667-7393G>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155267793 | ||||||
chr6:155268639
|
G | A | 247 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(244): Show | 275 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.667-8239C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155268639 | ||||||
chr6:155268698
|
G | A | 118 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(115): Show | 130 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(127): Show |
intron_variant | MODIFIER | c.667-8298C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155268698 | ||||||
chr6:155268736
|
G | A | 41 | a0001c0002t0003g0002a0001c0002t0003g0004a0001c0002t0003g0018others(38): Show | 49 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.667-8336C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155268736 | ||||||
chr6:155268757
|
T | C | 122 | a0001c0001t0001g0039a0001c0001t0002g0007a0001c0001t0002g0008others(119): Show | 138 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.667-8357A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155268757 | ||||||
chr6:155268757
|
T | G | 7 | a0001c0001t0013g0028a0001c0001t0013g0030a0001c0001t0013g0031others(4): Show | 7 | HG00639.hp1 HG01109.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.667-8357A>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155268757 | ||||||
chr6:155268759
|
C | T | 129 | a0001c0001t0001g0039a0001c0001t0002g0007a0001c0001t0002g0008others(126): Show | 145 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.667-8359G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155268759 | ||||||
chr6:155268800
|
CACAA | C | 4 | a0001c0001t0002g0285a0001c0001t0002g0288a0001c0001t0002g0295others(1): Show | 4 | NA18941.hp1 NA18975.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.667-8404_667-8401d others(6): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155268800 | ||||||
chr6:155268811
|
C | T | 3 | a0001c0002t0006g0053a0001c0002t0014g0052a0001c0002t0029g0026 | 3 | HG02922.hp1 HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.667-8411G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155268811 | ||||||
chr6:155268820
|
G | C | 7 | a0001c0001t0013g0028a0001c0001t0013g0030a0001c0001t0013g0031others(4): Show | 7 | HG00639.hp1 HG01109.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.667-8420C>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155268820 | ||||||
chr6:155268897
|
A | G | 41 | a0001c0002t0003g0002a0001c0002t0003g0004a0001c0002t0003g0018others(38): Show | 49 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.667-8497T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155268897 | ||||||
chr6:155268954
|
A | G | 4 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0001t0001g0128others(1): Show | 4 | HG02559.hp1 HG02572.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.667-8554T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155268954 | ||||||
chr6:155268986
|
TA | T | 244 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(241): Show | 274 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(271): Show |
intron_variant | MODIFIER | c.667-8587delT | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155268986 | ||||||
chr6:155268986
|
TAA | T | 12 | a0001c0001t0001g0039a0001c0001t0001g0119a0001c0001t0002g0289others(9): Show | 12 | HG00639.hp1 HG01109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.667-8588_667-8587d others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155268986 | ||||||
chr6:155269065
|
C | T | 1 | a0001c0002t0006g0219 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.667-8665G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155269065 | ||||||
chr6:155269098
|
T | C | 3 | a0001c0002t0006g0053a0001c0002t0014g0052a0001c0002t0029g0026 | 3 | HG02922.hp1 HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.667-8698A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155269098 | ||||||
chr6:155269140
|
T | C | 1 | a0004c0007t0032g0051 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.667-8740A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155269140 | ||||||
chr6:155269154
|
G | C | 2 | a0001c0002t0003g0185a0001c0002t0003g0186 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.667-8754C>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155269154 | ||||||
chr6:155269304
|
G | C | 1 | a0001c0001t0001g0144 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.667-8904C>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155269304 | ||||||
chr6:155269304
|
GTTTTC | G | 5 | a0001c0002t0004g0040a0001c0002t0004g0041a0001c0002t0004g0042others(2): Show | 5 | HG02451.hp2 HG02717.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.667-8909_667-8905d others(7): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155269304 | ||||||
chr6:155269324
|
C | CTT | 8 | a0001c0001t0001g0155a0001c0001t0013g0028a0001c0001t0013g0030others(5): Show | 8 | HG00639.hp1 HG01109.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.667-8926_667-8925d others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155269324 | ||||||
chr6:155269324
|
C | CTTT | 139 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(136): Show | 154 | HG00099.hp1 HG00558.hp1 HG00609.hp2 others(151): Show |
intron_variant | MODIFIER | c.667-8927_667-8925d others(5): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155269324 | ||||||
chr6:155269324
|
C | CTTTT | 95 | a0001c0001t0001g0039a0001c0001t0001g0092a0001c0001t0002g0007others(92): Show | 108 | HG00099.hp2 HG00280.hp2 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.667-8928_667-8925d others(6): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155269324 | ||||||
chr6:155269329
|
T | C | 1 | a0001c0002t0037g0049 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.667-8929A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155269329 | ||||||
chr6:155269384
|
C | T | 41 | a0001c0002t0003g0002a0001c0002t0003g0004a0001c0002t0003g0018others(38): Show | 49 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.667-8984G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155269384 | ||||||
chr6:155269408
|
G | A | 1 | a0002c0005t0039g0312 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.667-9008C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155269408 | ||||||
chr6:155269447
|
G | A | 1 | a0001c0001t0006g0228 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.667-9047C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155269447 | ||||||
chr6:155269455
|
G | A | 9 | a0001c0001t0012g0024a0001c0001t0012g0262a0001c0001t0012g0264others(6): Show | 10 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.667-9055C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155269455 | ||||||
chr6:155269559
|
C | T | 250 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(247): Show | 278 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(275): Show |
intron_variant | MODIFIER | c.667-9159G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155269559 | ||||||
chr6:155269564
|
C | T | 1 | a0001c0002t0003g0199 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.667-9164G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155269564 | ||||||
chr6:155269675
|
A | T | 186 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(183): Show | 209 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.667-9275T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155269675 | ||||||
chr6:155269950
|
C | T | 184 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(181): Show | 207 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.667-9550G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155269950 | ||||||
chr6:155269952
|
A | G | 1 | a0001c0001t0040g0298 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.667-9552T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155269952 | ||||||
chr6:155269990
|
T | A | 1 | a0001c0001t0001g0078 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.667-9590A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155269990 | ||||||
chr6:155270265
|
C | G | 2 | a0001c0002t0003g0185a0001c0002t0003g0186 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.667-9865G>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155270265 | ||||||
chr6:155270270
|
G | A | 39 | a0001c0002t0003g0002a0001c0002t0003g0004a0001c0002t0003g0018others(36): Show | 47 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(44): Show |
intron_variant | MODIFIER | c.667-9870C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155270270 | ||||||
chr6:155270283
|
C | G | 1 | a0001c0001t0034g0154 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.667-9883G>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155270283 | ||||||
chr6:155270417
|
A | G | 41 | a0001c0002t0003g0002a0001c0002t0003g0004a0001c0002t0003g0018others(38): Show | 49 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.667-10017T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155270417 | ||||||
chr6:155270501
|
C | T | 17 | a0001c0001t0006g0222a0001c0001t0006g0223a0001c0001t0006g0224others(14): Show | 18 | HG00099.hp1 HG00738.hp1 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.667-10101G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155270501 | ||||||
chr6:155270565
|
T | C | 1 | a0001c0001t0001g0109 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.667-10165A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155270565 | ||||||
chr6:155270705
|
C | G | 10 | a0001c0001t0006g0178a0001c0001t0012g0024a0001c0001t0012g0262others(7): Show | 11 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.667-10305G>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155270705 | ||||||
chr6:155270950
|
T | G | 64 | a0001c0001t0001g0039a0001c0001t0002g0007a0001c0001t0002g0008others(61): Show | 69 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.667-10550A>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155270950 | ||||||
chr6:155270956
|
C | T | 1 | a0001c0001t0014g0229 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.667-10556G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155270956 | ||||||
chr6:155271052
|
G | A | 1 | a0001c0002t0005g0260 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.667-10652C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155271052 | ||||||
chr6:155271171
|
G | C | 7 | a0001c0001t0012g0024a0001c0001t0012g0262a0001c0001t0012g0264others(4): Show | 8 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.667-10771C>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155271171 | ||||||
chr6:155271376
|
T | C | 1 | a0001c0001t0001g0122 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.667-10976A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155271376 | ||||||
chr6:155271523
|
G | C | 1 | a0001c0002t0003g0214 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.667-11123C>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155271523 | ||||||
chr6:155271574
|
T | G | 1 | a0001c0001t0030g0050 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.667-11174A>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155271574 | ||||||
chr6:155271867
|
G | A | 13 | a0001c0001t0006g0005a0001c0001t0006g0222a0001c0001t0006g0223others(10): Show | 15 | HG00099.hp1 HG00738.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.667-11467C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155271867 | ||||||
chr6:155271927
|
G | T | 1 | a0001c0002t0011g0202 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.667-11527C>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155271927 | ||||||
chr6:155272265
|
G | A | 59 | a0001c0001t0001g0039a0001c0001t0002g0007a0001c0001t0002g0008others(56): Show | 64 | HG00558.hp2 HG00621.hp1 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.667-11865C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155272265 | ||||||
chr6:155272574
|
G | C | 2 | a0001c0001t0006g0178a0001c0001t0014g0179 | 2 | HG02109.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.667-12174C>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155272574 | ||||||
chr6:155272691
|
C | A | 1 | a0001c0001t0001g0074 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.667-12291G>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155272691 | ||||||
chr6:155272797
|
C | T | 1 | a0001c0001t0001g0158 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.666+12361G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155272797 | ||||||
chr6:155272895
|
A | G | 250 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(247): Show | 278 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(275): Show |
intron_variant | MODIFIER | c.666+12263T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155272895 | ||||||
chr6:155273124
|
A | C | 118 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(115): Show | 130 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(127): Show |
intron_variant | MODIFIER | c.666+12034T>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155273124 | ||||||
chr6:155273257
|
A | G | 3 | a0001c0001t0001g0039a0001c0001t0009g0231a0004c0007t0032g0051 | 3 | HG02257.hp1 HG02622.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.666+11901T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155273257 | ||||||
chr6:155273503
|
C | T | 251 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(248): Show | 279 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(276): Show |
intron_variant | MODIFIER | c.666+11655G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155273503 | ||||||
chr6:155273641
|
A | T | 251 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(248): Show | 279 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(276): Show |
intron_variant | MODIFIER | c.666+11517T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155273641 | ||||||
chr6:155273648
|
C | G | 2 | a0001c0001t0001g0039a0001c0001t0009g0231 | 2 | HG02257.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.666+11510G>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155273648 | ||||||
chr6:155273792
|
C | T | 13 | a0001c0001t0006g0005a0001c0001t0006g0222a0001c0001t0006g0223others(10): Show | 15 | HG00099.hp1 HG00738.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.666+11366G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155273792 | ||||||
chr6:155273810
|
T | C | 250 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(247): Show | 278 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(275): Show |
intron_variant | MODIFIER | c.666+11348A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155273810 | ||||||
chr6:155273985
|
T | G | 3 | a0001c0002t0003g0185a0001c0002t0003g0186a0001c0002t0003g0204 | 3 | HG01070.hp2 HG01071.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.666+11173A>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155273985 | ||||||
chr6:155274062
|
C | T | 2 | a0001c0002t0006g0219a0001c0002t0006g0220 | 2 | HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.666+11096G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155274062 | ||||||
chr6:155274074
|
A | G | 2 | a0001c0001t0013g0028a0001c0001t0013g0030 | 2 | HG02723.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.666+11084T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155274074 | ||||||
chr6:155274097
|
G | T | 1 | a0001c0001t0002g0274 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.666+11061C>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155274097 | ||||||
chr6:155274158
|
C | T | 2 | a0001c0002t0005g0245a0001c0002t0041g0250 | 2 | HG01074.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.666+11000G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155274158 | ||||||
chr6:155274348
|
G | C | 250 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(247): Show | 278 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(275): Show |
intron_variant | MODIFIER | c.666+10810C>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155274348 | ||||||
chr6:155274418
|
A | G | 13 | a0001c0001t0006g0005a0001c0001t0006g0222a0001c0001t0006g0223others(10): Show | 15 | HG00099.hp1 HG00738.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.666+10740T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155274418 | ||||||
chr6:155274559
|
G | A | 1 | a0001c0002t0007g0164 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.666+10599C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155274559 | ||||||
chr6:155274564
|
G | T | 41 | a0001c0002t0003g0002a0001c0002t0003g0004a0001c0002t0003g0018others(38): Show | 49 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.666+10594C>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155274564 | ||||||
chr6:155274688
|
G | A | 3 | a0001c0002t0006g0053a0001c0002t0014g0052a0001c0002t0029g0026 | 3 | HG02922.hp1 HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.666+10470C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155274688 | ||||||
chr6:155274691
|
T | C | 2 | a0001c0001t0026g0021a0001c0001t0042g0313 | 3 | HG02809.hp2 HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.666+10467A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155274691 | ||||||
chr6:155274748
|
C | T | 1 | a0001c0001t0040g0298 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.666+10410G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155274748 | ||||||
chr6:155274939
|
C | T | 6 | a0001c0001t0006g0222a0001c0001t0006g0223a0001c0001t0006g0227others(3): Show | 6 | HG00099.hp1 HG00738.hp1 HG01070.hp1 others(3): Show |
intron_variant | MODIFIER | c.666+10219G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155274939 | ||||||
chr6:155274993
|
C | T | 246 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(243): Show | 274 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(271): Show |
intron_variant | MODIFIER | c.666+10165G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155274993 | ||||||
chr6:155275062
|
CA | C | 57 | a0001c0001t0001g0039a0001c0001t0002g0007a0001c0001t0002g0008others(54): Show | 62 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.666+10095delT | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155275062 | ||||||
chr6:155275083
|
G | A | 1 | a0001c0001t0001g0039 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.666+10075C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155275083 | ||||||
chr6:155275098
|
C | T | 3 | a0001c0001t0006g0178a0001c0001t0014g0179a0001c0001t0014g0221 | 3 | HG02109.hp2 HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.666+10060G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155275098 | ||||||
chr6:155275151
|
A | G | 250 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(247): Show | 278 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(275): Show |
intron_variant | MODIFIER | c.666+10007T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155275151 | ||||||
chr6:155275212
|
T | C | 247 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(244): Show | 275 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.666+9946A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155275212 | ||||||
chr6:155275335
|
G | A | 1 | a0001c0001t0002g0280 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.666+9823C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155275335 | ||||||
chr6:155275346
|
C | T | 2 | a0001c0001t0001g0039a0001c0001t0009g0231 | 2 | HG02257.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.666+9812G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155275346 | ||||||
chr6:155275349
|
T | C | 2 | a0001c0001t0025g0310a0001c0001t0025g0311 | 2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.666+9809A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155275349 | ||||||
chr6:155275385
|
A | C | 3 | a0001c0001t0006g0178a0001c0001t0014g0179a0001c0001t0014g0221 | 3 | HG02109.hp2 HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.666+9773T>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155275385 | ||||||
chr6:155275482
|
C | T | 3 | a0001c0002t0006g0053a0001c0002t0014g0052a0001c0002t0029g0026 | 3 | HG02922.hp1 HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.666+9676G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155275482 | ||||||
chr6:155275566
|
T | C | 61 | a0001c0001t0001g0039a0001c0001t0002g0007a0001c0001t0002g0008others(58): Show | 66 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.666+9592A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155275566 | ||||||
chr6:155275721
|
T | A | 1 | a0001c0001t0015g0208 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.666+9437A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155275721 | ||||||
chr6:155275730
|
C | G | 2 | a0001c0001t0025g0310a0001c0001t0025g0311 | 2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.666+9428G>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155275730 | ||||||
chr6:155275767
|
T | C | 247 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(244): Show | 275 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.666+9391A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155275767 | ||||||
chr6:155275871
|
G | A | 1 | a0001c0001t0002g0281 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.666+9287C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155275871 | ||||||
chr6:155275980
|
G | A | 1 | a0001c0001t0001g0146 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.666+9178C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155275980 | ||||||
chr6:155275999
|
G | A | 1 | a0001c0001t0001g0039 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.666+9159C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155275999 | ||||||
chr6:155276013
|
C | T | 118 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(115): Show | 130 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(127): Show |
intron_variant | MODIFIER | c.666+9145G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155276013 | ||||||
chr6:155276071
|
T | A | 3 | a0001c0001t0006g0178a0001c0001t0014g0179a0001c0001t0014g0221 | 3 | HG02109.hp2 HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.666+9087A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155276071 | ||||||
chr6:155276265
|
C | T | 1 | a0001c0001t0002g0288 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.666+8893G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155276265 | ||||||
chr6:155276340
|
C | T | 1 | a0004c0007t0032g0051 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.666+8818G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155276340 | ||||||
chr6:155276510
|
A | G | 247 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(244): Show | 275 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.666+8648T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155276510 | ||||||
chr6:155276534
|
T | G | 3 | a0001c0001t0006g0178a0001c0001t0014g0179a0001c0001t0014g0221 | 3 | HG02109.hp2 HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.666+8624A>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155276534 | ||||||
chr6:155276552
|
C | G | 247 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(244): Show | 275 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.666+8606G>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155276552 | ||||||
chr6:155276620
|
G | A | 4 | a0001c0001t0008g0096a0001c0001t0008g0101a0001c0001t0008g0137others(1): Show | 4 | NA18941.hp2 NA18973.hp2 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.666+8538C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155276620 | ||||||
chr6:155276664
|
C | CTTTTTT | 247 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(244): Show | 275 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.666+8493_666+8494i others(8): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155276664 | ||||||
chr6:155277008
|
T | C | 48 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0025others(45): Show | 53 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.666+8150A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155277008 | ||||||
chr6:155277041
|
C | T | 1 | a0002c0005t0039g0312 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.666+8117G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155277041 | ||||||
chr6:155277091
|
T | C | 1 | a0001c0001t0001g0144 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.666+8067A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155277091 | ||||||
chr6:155277167
|
A | G | 1 | a0001c0002t0037g0049 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.666+7991T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155277167 | ||||||
chr6:155277543
|
A | C | 263 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(260): Show | 291 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(288): Show |
intron_variant | MODIFIER | c.666+7615T>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155277543 | ||||||
chr6:155277761
|
C | A | 3 | a0001c0001t0006g0178a0001c0001t0014g0179a0001c0001t0014g0221 | 3 | HG02109.hp2 HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.666+7397G>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155277761 | ||||||
chr6:155277855
|
C | T | 218 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(215): Show | 238 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(235): Show |
intron_variant | MODIFIER | c.666+7303G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155277855 | ||||||
chr6:155278074
|
C | T | 1 | a0001c0002t0003g0195 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.666+7084G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155278074 | ||||||
chr6:155278251
|
C | T | 118 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(115): Show | 130 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(127): Show |
intron_variant | MODIFIER | c.666+6907G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155278251 | ||||||
chr6:155278284
|
C | T | 2 | a0001c0001t0004g0175a0001c0001t0004g0177 | 2 | HG01243.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.666+6874G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155278284 | ||||||
chr6:155278403
|
C | T | 16 | a0001c0001t0004g0168a0001c0001t0004g0170a0001c0001t0004g0171others(13): Show | 16 | HG00733.hp2 HG01109.hp2 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.666+6755G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155278403 | ||||||
chr6:155278589
|
C | T | 1 | a0002c0005t0039g0312 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.666+6569G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155278589 | ||||||
chr6:155278692
|
T | C | 1 | a0001c0001t0001g0139 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.666+6466A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155278692 | ||||||
chr6:155278751
|
G | A | 12 | a0001c0001t0006g0005a0001c0001t0006g0222a0001c0001t0006g0223others(9): Show | 14 | HG00099.hp1 HG00738.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.666+6407C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155278751 | ||||||
chr6:155278770
|
G | A | 1 | a0002c0005t0039g0312 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.666+6388C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155278770 | ||||||
chr6:155278831
|
C | T | 2 | a0001c0001t0002g0274a0001c0001t0002g0275 | 2 | NA18944.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.666+6327G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155278831 | ||||||
chr6:155279073
|
T | C | 2 | a0001c0004t0020g0166a0001c0004t0020g0167 | 2 | HG02145.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.666+6085A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155279073 | ||||||
chr6:155279125
|
A | T | 13 | a0001c0001t0006g0005a0001c0001t0006g0222a0001c0001t0006g0223others(10): Show | 15 | HG00099.hp1 HG00738.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.666+6033T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155279125 | ||||||
chr6:155279213
|
C | CT | 248 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(245): Show | 275 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.666+5944dupA | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155279213 | ||||||
chr6:155279213
|
C | CTT | 8 | a0001c0001t0001g0059a0001c0001t0001g0068a0001c0001t0001g0086others(5): Show | 8 | NA18939.hp1 NA18944.hp2 NA18948.hp2 others(5): Show |
intron_variant | MODIFIER | c.666+5943_666+5944d others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155279213 | ||||||
chr6:155279245
|
A | T | 4 | a0001c0001t0002g0303a0001c0001t0002g0305a0001c0001t0002g0308others(1): Show | 4 | NA18949.hp1 NA18952.hp1 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.666+5913T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155279245 | ||||||
chr6:155279631
|
T | C | 1 | a0001c0001t0004g0174 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.666+5527A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155279631 | ||||||
chr6:155279683
|
T | A | 1 | a0001c0002t0004g0003 | 3 | HG02818.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.666+5475A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155279683 | ||||||
chr6:155279684
|
T | A | 14 | a0001c0001t0006g0005a0001c0001t0006g0222a0001c0001t0006g0223others(11): Show | 16 | HG00099.hp1 HG00738.hp1 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.666+5474A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155279684 | ||||||
chr6:155279708
|
T | C | 1 | a0001c0001t0001g0105 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.666+5450A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155279708 | ||||||
chr6:155279777
|
C | T | 5 | a0001c0001t0006g0222a0001c0001t0006g0223a0001c0001t0006g0227others(2): Show | 5 | HG00099.hp1 HG00738.hp1 HG01168.hp1 others(2): Show |
intron_variant | MODIFIER | c.666+5381G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155279777 | ||||||
chr6:155279779
|
C | A | 7 | a0001c0001t0013g0028a0001c0001t0013g0030a0001c0001t0013g0031others(4): Show | 7 | HG00639.hp1 HG01109.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.666+5379G>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155279779 | ||||||
chr6:155279991
|
A | C | 41 | a0001c0002t0003g0002a0001c0002t0003g0004a0001c0002t0003g0018others(38): Show | 49 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.666+5167T>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155279991 | ||||||
chr6:155280045
|
T | A | 2 | a0001c0004t0020g0166a0001c0004t0020g0167 | 2 | HG02145.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.666+5113A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155280045 | ||||||
chr6:155280056
|
G | T | 1 | a0001c0002t0005g0254 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.666+5102C>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155280056 | ||||||
chr6:155280060
|
A | C | 1 | a0001c0001t0030g0050 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.666+5098T>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155280060 | ||||||
chr6:155280350
|
A | G | 219 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(216): Show | 239 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(236): Show |
intron_variant | MODIFIER | c.666+4808T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155280350 | ||||||
chr6:155280351
|
C | T | 219 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(216): Show | 239 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(236): Show |
intron_variant | MODIFIER | c.666+4807G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155280351 | ||||||
chr6:155280384
|
C | T | 16 | a0001c0001t0004g0168a0001c0001t0004g0170a0001c0001t0004g0171others(13): Show | 16 | HG00733.hp2 HG01109.hp2 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.666+4774G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155280384 | ||||||
chr6:155280399
|
T | C | 1 | a0001c0001t0016g0271 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.666+4759A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155280399 | ||||||
chr6:155280427
|
G | A | 1 | a0001c0002t0019g0023 | 2 | HG01256.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.666+4731C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155280427 | ||||||
chr6:155280455
|
C | T | 118 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(115): Show | 130 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(127): Show |
intron_variant | MODIFIER | c.666+4703G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155280455 | ||||||
chr6:155280677
|
A | C | 1 | a0001c0001t0001g0094 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.666+4481T>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155280677 | ||||||
chr6:155280741
|
A | T | 1 | a0001c0002t0007g0164 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.666+4417T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155280741 | ||||||
chr6:155280794
|
C | G | 41 | a0001c0002t0003g0002a0001c0002t0003g0004a0001c0002t0003g0018others(38): Show | 49 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.666+4364G>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155280794 | ||||||
chr6:155280868
|
C | T | 158 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(155): Show | 173 | HG00099.hp1 HG00558.hp1 HG00609.hp2 others(170): Show |
intron_variant | MODIFIER | c.666+4290G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155280868 | ||||||
chr6:155280932
|
A | G | 1 | a0002c0005t0039g0312 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.666+4226T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155280932 | ||||||
chr6:155281431
|
T | G | 2 | a0001c0001t0025g0310a0001c0001t0025g0311 | 2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.666+3727A>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155281431 | ||||||
chr6:155281448
|
G | T | 61 | a0001c0001t0001g0039a0001c0001t0002g0007a0001c0001t0002g0008others(58): Show | 66 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.666+3710C>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155281448 | ||||||
chr6:155281492
|
C | T | 1 | a0001c0002t0004g0093 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.666+3666G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155281492 | ||||||
chr6:155281520
|
G | A | 1 | a0001c0002t0011g0198 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.666+3638C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155281520 | ||||||
chr6:155281538
|
A | T | 1 | a0001c0001t0002g0284 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.666+3620T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155281538 | ||||||
chr6:155281599
|
G | C | 2 | a0001c0001t0002g0274a0001c0001t0002g0275 | 2 | NA18944.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.666+3559C>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155281599 | ||||||
chr6:155281615
|
G | A | 222 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(219): Show | 242 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(239): Show |
intron_variant | MODIFIER | c.666+3543C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155281615 | ||||||
chr6:155281655
|
G | C | 7 | a0001c0001t0013g0028a0001c0001t0013g0030a0001c0001t0013g0031others(4): Show | 7 | HG00639.hp1 HG01109.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.666+3503C>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155281655 | ||||||
chr6:155281721
|
C | CA | 16 | a0001c0001t0001g0130a0001c0001t0002g0286a0001c0001t0002g0287others(13): Show | 17 | HG00639.hp1 HG00642.hp2 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.666+3436dupT | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155281721 | ||||||
chr6:155281721
|
C | CAA | 131 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(128): Show | 148 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(145): Show |
intron_variant | MODIFIER | c.666+3435_666+3436d others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155281721 | ||||||
chr6:155281721
|
C | CAAA | 44 | a0001c0001t0001g0039a0001c0001t0001g0059a0001c0001t0001g0065others(41): Show | 45 | HG00609.hp1 HG00621.hp1 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.666+3434_666+3436d others(5): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155281721 | ||||||
chr6:155281721
|
CA | C | 39 | a0001c0001t0004g0170a0001c0001t0004g0172a0001c0001t0004g0173others(36): Show | 41 | HG00099.hp1 HG00733.hp2 HG01070.hp1 others(38): Show |
intron_variant | MODIFIER | c.666+3436delT | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155281721 | ||||||
chr6:155281821
|
T | TA | 93 | a0001c0002t0003g0002a0001c0002t0003g0004a0001c0002t0003g0018others(90): Show | 108 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.666+3336dupT | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155281821 | ||||||
chr6:155281821
|
TA | T | 119 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(116): Show | 131 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(128): Show |
intron_variant | MODIFIER | c.666+3336delT | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155281821 | ||||||
chr6:155281838
|
T | G | 1 | a0001c0001t0001g0124 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.666+3320A>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155281838 | ||||||
chr6:155281915
|
G | A | 3 | a0001c0002t0006g0053a0001c0002t0014g0052a0001c0002t0029g0026 | 3 | HG02922.hp1 HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.666+3243C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155281915 | ||||||
chr6:155282063
|
T | C | 217 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(214): Show | 237 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(234): Show |
intron_variant | MODIFIER | c.666+3095A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155282063 | ||||||
chr6:155282063
|
T | G | 2 | a0001c0004t0020g0166a0001c0004t0020g0167 | 2 | HG02145.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.666+3095A>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155282063 | ||||||
chr6:155282385
|
A | G | 2 | a0001c0002t0006g0219a0001c0002t0006g0220 | 2 | HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.666+2773T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155282385 | ||||||
chr6:155282395
|
C | T | 218 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(215): Show | 238 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(235): Show |
intron_variant | MODIFIER | c.666+2763G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155282395 | ||||||
chr6:155282537
|
A | G | 39 | a0001c0002t0003g0002a0001c0002t0003g0004a0001c0002t0003g0018others(36): Show | 47 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(44): Show |
intron_variant | MODIFIER | c.666+2621T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155282537 | ||||||
chr6:155282802
|
G | A | 1 | a0001c0001t0001g0146 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.666+2356C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155282802 | ||||||
chr6:155282886
|
C | A | 2 | a0001c0004t0020g0166a0001c0004t0020g0167 | 2 | HG02145.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.666+2272G>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155282886 | ||||||
chr6:155282917
|
C | T | 3 | a0001c0002t0006g0053a0001c0002t0014g0052a0001c0002t0029g0026 | 3 | HG02922.hp1 HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.666+2241G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155282917 | ||||||
chr6:155283012
|
T | C | 263 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(260): Show | 291 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(288): Show |
intron_variant | MODIFIER | c.666+2146A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155283012 | ||||||
chr6:155283133
|
C | T | 2 | a0001c0004t0020g0166a0001c0004t0020g0167 | 2 | HG02145.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.666+2025G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155283133 | ||||||
chr6:155283180
|
C | T | 218 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(215): Show | 238 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(235): Show |
intron_variant | MODIFIER | c.666+1978G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155283180 | ||||||
chr6:155283246
|
T | C | 1 | a0001c0001t0001g0039 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.666+1912A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155283246 | ||||||
chr6:155283422
|
C | T | 218 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(215): Show | 238 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(235): Show |
intron_variant | MODIFIER | c.666+1736G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155283422 | ||||||
chr6:155283661
|
T | C | 2 | a0001c0001t0004g0168a0001c0001t0004g0180 | 2 | HG02738.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.666+1497A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155283661 | ||||||
chr6:155283671
|
C | A | 1 | a0001c0002t0005g0240 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.666+1487G>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155283671 | ||||||
chr6:155283673
|
G | A | 3 | a0001c0001t0001g0112a0001c0001t0001g0115a0001c0001t0001g0116 | 3 | HG02129.hp2 HG02135.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.666+1485C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155283673 | ||||||
chr6:155283710
|
T | C | 41 | a0001c0002t0003g0002a0001c0002t0003g0004a0001c0002t0003g0018others(38): Show | 49 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.666+1448A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155283710 | ||||||
chr6:155283778
|
T | C | 1 | a0001c0001t0001g0073 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.666+1380A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155283778 | ||||||
chr6:155283866
|
T | C | 118 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(115): Show | 130 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(127): Show |
intron_variant | MODIFIER | c.666+1292A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155283866 | ||||||
chr6:155283958
|
T | C | 1 | a0001c0002t0003g0211 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.666+1200A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155283958 | ||||||
chr6:155283968
|
G | A | 219 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(216): Show | 239 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(236): Show |
intron_variant | MODIFIER | c.666+1190C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155283968 | ||||||
chr6:155284074
|
G | C | 3 | a0001c0002t0006g0053a0001c0002t0014g0052a0001c0002t0029g0026 | 3 | HG02922.hp1 HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.666+1084C>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155284074 | ||||||
chr6:155284092
|
G | A | 9 | a0001c0001t0004g0170a0001c0001t0004g0171a0001c0001t0004g0172others(6): Show | 9 | HG00733.hp2 HG01109.hp2 HG01167.hp2 others(6): Show |
intron_variant | MODIFIER | c.666+1066C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155284092 | ||||||
chr6:155284353
|
A | C | 157 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(154): Show | 172 | HG00099.hp1 HG00558.hp1 HG00609.hp2 others(169): Show |
intron_variant | MODIFIER | c.666+805T>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155284353 | ||||||
chr6:155284353
|
A | T | 1 | a0001c0001t0014g0221 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.666+805T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155284353 | ||||||
chr6:155284421
|
T | C | 1 | a0001c0001t0001g0144 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.666+737A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155284421 | ||||||
chr6:155284441
|
G | C | 1 | a0001c0001t0025g0310 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.666+717C>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155284441 | ||||||
chr6:155284793
|
G | A | 3 | a0001c0002t0006g0053a0001c0002t0014g0052a0001c0002t0029g0026 | 3 | HG02922.hp1 HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.666+365C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155284793 | ||||||
chr6:155285043
|
G | A | 1 | a0001c0001t0001g0039 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.666+115C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 5/6 | chr6 | 155285043 | ||||||
chr6:155285326
|
T | A | 41 | a0001c0002t0003g0002a0001c0002t0003g0004a0001c0002t0003g0018others(38): Show | 49 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.547-49A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155285326 | ||||||
chr6:155285397
|
A | G | 219 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(216): Show | 239 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(236): Show |
intron_variant | MODIFIER | c.547-120T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155285397 | ||||||
chr6:155285407
|
C | T | 1 | a0001c0001t0002g0304 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.547-130G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155285407 | ||||||
chr6:155285413
|
CAT | C | 6 | a0001c0002t0003g0018a0001c0002t0003g0194a0001c0002t0003g0214others(3): Show | 7 | HG00673.hp1 NA18972.hp2 NA18994.hp2 others(4): Show |
intron_variant | MODIFIER | c.547-138_547-137del others(2): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155285413 | ||||||
chr6:155285433
|
G | A | 1 | a0001c0001t0001g0069 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.547-156C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155285433 | ||||||
chr6:155285576
|
G | A | 2 | a0001c0001t0006g0005a0001c0001t0006g0232 | 4 | HG02280.hp1 HG02723.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.547-299C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155285576 | ||||||
chr6:155285831
|
G | A | 218 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(215): Show | 238 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(235): Show |
intron_variant | MODIFIER | c.547-554C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155285831 | ||||||
chr6:155285888
|
T | G | 6 | a0001c0001t0002g0025a0001c0001t0002g0276a0001c0001t0002g0289others(3): Show | 7 | NA18948.hp1 NA18960.hp2 NA18965.hp1 others(4): Show |
intron_variant | MODIFIER | c.547-611A>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155285888 | ||||||
chr6:155285901
|
A | G | 263 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(260): Show | 291 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(288): Show |
intron_variant | MODIFIER | c.547-624T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155285901 | ||||||
chr6:155285959
|
T | C | 1 | a0001c0001t0002g0292 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.547-682A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155285959 | ||||||
chr6:155286167
|
G | T | 1 | a0001c0001t0030g0050 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.547-890C>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155286167 | ||||||
chr6:155286339
|
C | T | 2 | a0001c0004t0020g0166a0001c0004t0020g0167 | 2 | HG02145.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.547-1062G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155286339 | ||||||
chr6:155286355
|
AAGAC | A | 42 | a0001c0001t0001g0060a0001c0002t0003g0002a0001c0002t0003g0004others(39): Show | 50 | HG00099.hp2 HG00280.hp2 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.547-1082_547-1079d others(6): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155286355 | ||||||
chr6:155286419
|
A | G | 2 | a0001c0001t0002g0236a0001c0001t0002g0273 | 2 | HG00735.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.547-1142T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155286419 | ||||||
chr6:155286479
|
A | G | 12 | a0001c0001t0006g0005a0001c0001t0006g0222a0001c0001t0006g0223others(9): Show | 14 | HG00099.hp1 HG00738.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.547-1202T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155286479 | ||||||
chr6:155286481
|
GTGTGTGT others(7): Show |
G | 256 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(253): Show | 284 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(281): Show |
intron_variant | MODIFIER | c.547-1218_547-1205d others(16): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155286481 | ||||||
chr6:155286481
|
GTGTGTGT others(21): Show |
G | 2 | a0001c0001t0006g0222a0001c0001t0006g0223 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.547-1232_547-1205d others(30): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155286481 | ||||||
chr6:155286489
|
ATATATAT others(45): Show |
A | 9 | a0001c0002t0004g0003a0001c0002t0004g0040a0001c0002t0004g0041others(6): Show | 11 | HG02451.hp2 HG02717.hp1 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.547-1264_547-1213d others(54): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155286489 | ||||||
chr6:155286497
|
GTGTGTAT others(33): Show |
G | 4 | a0001c0002t0003g0189a0001c0002t0011g0187a0001c0002t0011g0190others(1): Show | 4 | NA18948.hp2 NA18951.hp2 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.547-1260_547-1221d others(42): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155286497 | ||||||
chr6:155286503
|
A | ATATATAT others(17): Show |
1 | a0001c0001t0001g0110 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.547-1227_547-1226i others(26): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155286503 | ||||||
chr6:155286551
|
GTGTATAT others(3): Show |
G | 1 | a0001c0001t0004g0215 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.547-1284_547-1275d others(12): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155286551 | ||||||
chr6:155286585
|
GTATATGT others(5): Show |
G | 1 | a0001c0001t0001g0103 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.547-1320_547-1309d others(14): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155286585 | ||||||
chr6:155286603
|
G | A | 141 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(138): Show | 154 | HG00558.hp1 HG00621.hp2 HG00639.hp2 others(151): Show |
intron_variant | MODIFIER | c.547-1326C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155286603 | ||||||
chr6:155286603
|
GTGTGTAT others(5): Show |
G | 1 | a0002c0005t0039g0312 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.547-1338_547-1327d others(14): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155286603 | ||||||
chr6:155286615
|
A | G | 203 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(200): Show | 221 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(218): Show |
intron_variant | MODIFIER | c.547-1338T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155286615 | ||||||
chr6:155286620
|
T | C | 144 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(141): Show | 157 | HG00558.hp1 HG00621.hp2 HG00639.hp2 others(154): Show |
intron_variant | MODIFIER | c.547-1343A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155286620 | ||||||
chr6:155286626
|
T | C | 7 | a0001c0001t0013g0028a0001c0001t0013g0030a0001c0001t0013g0031others(4): Show | 7 | HG00639.hp1 HG01109.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.547-1349A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155286626 | ||||||
chr6:155286637
|
A | G | 1 | a0003c0006t0038g0235 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.547-1360T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155286637 | ||||||
chr6:155286637
|
ATG | A | 45 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0025others(42): Show | 50 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.547-1362_547-1361d others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155286637 | ||||||
chr6:155286649
|
GTA | G | 116 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(113): Show | 128 | HG00558.hp1 HG00621.hp2 HG00639.hp2 others(125): Show |
intron_variant | MODIFIER | c.547-1374_547-1373d others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155286649 | ||||||
chr6:155286659
|
A | G | 1 | a0001c0001t0001g0069 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.547-1382T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155286659 | ||||||
chr6:155286661
|
G | A | 1 | a0001c0001t0001g0069 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.547-1384C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155286661 | ||||||
chr6:155286668
|
T | C | 1 | a0001c0001t0001g0069 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.547-1391A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155286668 | ||||||
chr6:155286670
|
C | CAT | 6 | a0001c0001t0012g0024a0001c0001t0012g0262a0001c0001t0012g0264others(3): Show | 7 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.547-1395_547-1394d others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155286670 | ||||||
chr6:155286670
|
C | T | 1 | a0001c0001t0001g0069 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.547-1393G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155286670 | ||||||
chr6:155286681
|
A | T | 2 | a0001c0001t0001g0094a0001c0001t0001g0134 | 2 | HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.547-1404T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155286681 | ||||||
chr6:155286683
|
T | A | 3 | a0001c0002t0003g0019a0001c0002t0003g0199a0001c0002t0003g0200 | 4 | NA18983.hp1 NA19004.hp2 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.547-1406A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155286683 | ||||||
chr6:155286779
|
T | C | 218 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(215): Show | 238 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(235): Show |
intron_variant | MODIFIER | c.547-1502A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155286779 | ||||||
chr6:155286802
|
C | T | 13 | a0001c0001t0006g0005a0001c0001t0006g0222a0001c0001t0006g0223others(10): Show | 15 | HG00099.hp1 HG00738.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.547-1525G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155286802 | ||||||
chr6:155286819
|
A | G | 42 | a0001c0001t0001g0060a0001c0002t0003g0002a0001c0002t0003g0004others(39): Show | 50 | HG00099.hp2 HG00280.hp2 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.547-1542T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155286819 | ||||||
chr6:155286985
|
G | A | 48 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0025others(45): Show | 53 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.547-1708C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155286985 | ||||||
chr6:155286986
|
A | T | 218 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(215): Show | 238 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(235): Show |
intron_variant | MODIFIER | c.547-1709T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155286986 | ||||||
chr6:155287157
|
G | A | 16 | a0001c0001t0004g0168a0001c0001t0004g0170a0001c0001t0004g0171others(13): Show | 16 | HG00733.hp2 HG01109.hp2 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.547-1880C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155287157 | ||||||
chr6:155287225
|
T | G | 2 | a0001c0001t0001g0077a0001c0001t0001g0142 | 2 | HG02602.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.547-1948A>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155287225 | ||||||
chr6:155287321
|
C | T | 144 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(141): Show | 157 | HG00558.hp1 HG00621.hp2 HG00639.hp2 others(154): Show |
intron_variant | MODIFIER | c.547-2044G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155287321 | ||||||
chr6:155287398
|
T | A | 1 | a0001c0001t0001g0152 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.547-2121A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155287398 | ||||||
chr6:155287532
|
ACTC | A | 53 | a0001c0001t0001g0039a0001c0001t0002g0007a0001c0001t0002g0008others(50): Show | 58 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.547-2258_547-2256d others(5): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155287532 | ||||||
chr6:155287535
|
C | G | 1 | a0001c0001t0002g0280 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.547-2258G>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155287535 | ||||||
chr6:155287551
|
A | AGTGT | 41 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0086others(38): Show | 49 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.547-2278_547-2275d others(6): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155287551 | ||||||
chr6:155287551
|
A | AGTGTGT | 36 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(33): Show | 39 | HG00609.hp2 HG00673.hp2 HG01192.hp2 others(36): Show |
intron_variant | MODIFIER | c.547-2280_547-2275d others(8): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155287551 | ||||||
chr6:155287551
|
A | AGTGTGTG others(1): Show |
72 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0014others(69): Show | 81 | HG00639.hp2 HG00642.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.547-2282_547-2275d others(10): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155287551 | ||||||
chr6:155287551
|
A | AGTGTGTG others(3): Show |
12 | a0001c0001t0001g0074a0001c0001t0001g0087a0001c0001t0001g0089others(9): Show | 12 | HG00621.hp2 HG02109.hp2 HG02135.hp1 others(9): Show |
intron_variant | MODIFIER | c.547-2284_547-2275d others(12): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155287551 | ||||||
chr6:155287551
|
A | AGTGTGTG others(5): Show |
33 | a0001c0001t0001g0110a0001c0001t0001g0136a0001c0001t0004g0168others(30): Show | 36 | HG00733.hp2 HG01109.hp1 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.547-2286_547-2275d others(14): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155287551 | ||||||
chr6:155287551
|
A | AGTGTGTG others(7): Show |
19 | a0001c0001t0001g0039a0001c0001t0002g0280a0001c0001t0002g0281others(16): Show | 19 | HG00099.hp1 HG00639.hp1 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.547-2288_547-2275d others(16): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155287551 | ||||||
chr6:155287551
|
A | AGTGTGTG others(9): Show |
43 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0025others(40): Show | 48 | HG00558.hp2 HG00621.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.547-2290_547-2275d others(18): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155287551 | ||||||
chr6:155287551
|
A | AGTGTGTG others(11): Show |
3 | a0001c0001t0002g0278a0001c0001t0006g0232a0001c0001t0009g0231 | 3 | HG00609.hp1 HG02723.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.547-2292_547-2275d others(20): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155287551 | ||||||
chr6:155287551
|
A | AGTGTGTG others(13): Show |
1 | a0001c0001t0030g0050 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.547-2294_547-2275d others(22): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155287551 | ||||||
chr6:155287551
|
A | AGTGTGTG others(15): Show |
1 | a0002c0005t0039g0312 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.547-2296_547-2275d others(24): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155287551 | ||||||
chr6:155287551
|
A | AGTGTGTG others(17): Show |
1 | a0001c0001t0016g0271 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.547-2298_547-2275d others(26): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155287551 | ||||||
chr6:155287856
|
T | C | 1 | a0001c0002t0004g0093 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.547-2579A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155287856 | ||||||
chr6:155287896
|
C | T | 126 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(123): Show | 139 | HG00558.hp1 HG00621.hp2 HG00639.hp2 others(136): Show |
intron_variant | MODIFIER | c.547-2619G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155287896 | ||||||
chr6:155287900
|
T | C | 1 | a0001c0001t0001g0071 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.547-2623A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155287900 | ||||||
chr6:155287959
|
T | G | 1 | a0001c0001t0002g0295 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.547-2682A>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155287959 | ||||||
chr6:155288269
|
G | T | 1 | a0001c0001t0030g0050 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.547-2992C>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155288269 | ||||||
chr6:155288382
|
T | C | 2 | a0001c0004t0020g0166a0001c0004t0020g0167 | 2 | HG02145.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.547-3105A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155288382 | ||||||
chr6:155288568
|
T | A | 13 | a0001c0001t0006g0005a0001c0001t0006g0222a0001c0001t0006g0223others(10): Show | 15 | HG00099.hp1 HG00738.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.547-3291A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155288568 | ||||||
chr6:155288588
|
A | G | 11 | a0001c0001t0001g0011a0001c0001t0001g0075a0001c0001t0001g0081others(8): Show | 12 | HG00558.hp1 HG00673.hp2 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.547-3311T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155288588 | ||||||
chr6:155288616
|
G | A | 218 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(215): Show | 238 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(235): Show |
intron_variant | MODIFIER | c.547-3339C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155288616 | ||||||
chr6:155288948
|
G | C | 1 | a0002c0005t0039g0312 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.547-3671C>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155288948 | ||||||
chr6:155289064
|
G | GT | 108 | a0001c0001t0001g0060a0001c0001t0001g0086a0001c0001t0002g0007others(105): Show | 123 | HG00099.hp2 HG00280.hp2 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.547-3788dupA | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155289064 | ||||||
chr6:155289115
|
T | G | 2 | a0001c0004t0020g0166a0001c0004t0020g0167 | 2 | HG02145.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.547-3838A>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155289115 | ||||||
chr6:155289125
|
C | T | 1 | a0001c0002t0003g0213 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.547-3848G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155289125 | ||||||
chr6:155289166
|
T | C | 1 | a0001c0001t0001g0218 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.547-3889A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155289166 | ||||||
chr6:155289252
|
GAA | G | 28 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0071others(25): Show | 33 | HG01069.hp1 HG01071.hp1 HG01099.hp1 others(30): Show |
intron_variant | MODIFIER | c.547-3977_547-3976d others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155289252 | ||||||
chr6:155289258
|
G | C | 1 | a0001c0001t0012g0264 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.547-3981C>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155289258 | ||||||
chr6:155289290
|
A | C | 3 | a0001c0001t0006g0227a0001c0001t0006g0228a0001c0001t0018g0241 | 3 | HG00099.hp1 HG00738.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.547-4013T>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155289290 | ||||||
chr6:155289368
|
C | G | 1 | a0002c0005t0039g0312 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.547-4091G>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155289368 | ||||||
chr6:155289685
|
T | C | 2 | a0001c0002t0005g0256a0001c0002t0005g0261 | 2 | HG01069.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.547-4408A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155289685 | ||||||
chr6:155289742
|
G | A | 6 | a0001c0001t0008g0001a0001c0001t0008g0096a0001c0001t0008g0097others(3): Show | 9 | NA18941.hp2 NA18949.hp2 NA18972.hp1 others(6): Show |
intron_variant | MODIFIER | c.547-4465C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155289742 | ||||||
chr6:155289756
|
G | T | 1 | a0001c0002t0023g0037 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.547-4479C>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155289756 | ||||||
chr6:155289766
|
C | T | 1 | a0004c0007t0032g0051 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.547-4489G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155289766 | ||||||
chr6:155289833
|
T | C | 1 | a0001c0001t0001g0124 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.547-4556A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155289833 | ||||||
chr6:155289888
|
G | A | 218 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(215): Show | 238 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(235): Show |
intron_variant | MODIFIER | c.547-4611C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155289888 | ||||||
chr6:155289995
|
T | C | 1 | a0001c0001t0001g0080 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.547-4718A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155289995 | ||||||
chr6:155290023
|
G | C | 1 | a0001c0001t0033g0100 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.547-4746C>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155290023 | ||||||
chr6:155290057
|
A | C | 1 | a0001c0001t0014g0221 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.547-4780T>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155290057 | ||||||
chr6:155290252
|
G | A | 1 | a0001c0001t0001g0153 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.547-4975C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155290252 | ||||||
chr6:155290335
|
G | A | 7 | a0001c0001t0013g0028a0001c0001t0013g0030a0001c0001t0013g0031others(4): Show | 7 | HG00639.hp1 HG01109.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.547-5058C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155290335 | ||||||
chr6:155290373
|
G | A | 2 | a0001c0001t0001g0071a0001c0002t0003g0211 | 2 | HG02683.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.547-5096C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155290373 | ||||||
chr6:155290388
|
C | CAAAA | 36 | a0001c0001t0001g0060a0001c0002t0003g0002a0001c0002t0003g0004others(33): Show | 44 | HG00099.hp2 HG00280.hp2 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.547-5115_547-5112d others(6): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155290388 | ||||||
chr6:155290406
|
A | AAAG | 6 | a0001c0001t0001g0111a0001c0001t0001g0125a0001c0001t0001g0169others(3): Show | 6 | HG02109.hp2 HG02717.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.547-5130_547-5129i others(5): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155290406 | ||||||
chr6:155290406
|
A | AAG | 188 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(185): Show | 208 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(205): Show |
intron_variant | MODIFIER | c.547-5130_547-5129i others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155290406 | ||||||
chr6:155290406
|
A | AG | 16 | a0001c0001t0001g0039a0001c0001t0001g0095a0001c0001t0001g0112others(13): Show | 16 | HG00621.hp1 HG01099.hp1 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.547-5130_547-5129i others(3): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155290406 | ||||||
chr6:155290406
|
A | G | 1 | a0001c0001t0001g0139 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.547-5129T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155290406 | ||||||
chr6:155290602
|
T | C | 1 | a0001c0002t0003g0200 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.547-5325A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155290602 | ||||||
chr6:155290769
|
G | C | 1 | a0001c0002t0010g0054 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.547-5492C>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155290769 | ||||||
chr6:155290913
|
C | G | 2 | a0001c0002t0006g0053a0001c0002t0014g0052 | 2 | HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.547-5636G>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155290913 | ||||||
chr6:155291029
|
CCTGAGTT others(3): Show |
C | 2 | a0001c0004t0020g0166a0001c0004t0020g0167 | 2 | HG02145.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.547-5762_547-5753d others(12): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155291029 | ||||||
chr6:155291079
|
A | G | 1 | a0001c0001t0016g0271 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.547-5802T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155291079 | ||||||
chr6:155291083
|
A | G | 1 | a0001c0001t0030g0050 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.547-5806T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155291083 | ||||||
chr6:155291161
|
G | A | 1 | a0001c0002t0003g0203 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.546+5792C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155291161 | ||||||
chr6:155291225
|
A | G | 263 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(260): Show | 291 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(288): Show |
intron_variant | MODIFIER | c.546+5728T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155291225 | ||||||
chr6:155291758
|
T | C | 1 | a0002c0005t0039g0312 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.546+5195A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155291758 | ||||||
chr6:155291765
|
A | T | 1 | a0001c0001t0016g0271 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.546+5188T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155291765 | ||||||
chr6:155291844
|
G | C | 1 | a0001c0002t0005g0254 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.546+5109C>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155291844 | ||||||
chr6:155291878
|
A | C | 32 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(29): Show | 35 | HG00558.hp1 HG00609.hp2 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.546+5075T>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155291878 | ||||||
chr6:155291957
|
G | A | 2 | a0001c0001t0001g0039a0001c0001t0009g0231 | 2 | HG02257.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.546+4996C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155291957 | ||||||
chr6:155292013
|
A | G | 2 | a0001c0001t0001g0039a0001c0001t0009g0231 | 2 | HG02257.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.546+4940T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155292013 | ||||||
chr6:155292297
|
A | T | 1 | a0001c0001t0030g0050 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.546+4656T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155292297 | ||||||
chr6:155292345
|
T | C | 1 | a0001c0001t0001g0136 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.546+4608A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155292345 | ||||||
chr6:155292429
|
C | T | 2 | a0001c0001t0026g0021a0001c0001t0042g0313 | 3 | HG02809.hp2 HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.546+4524G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155292429 | ||||||
chr6:155292539
|
G | A | 4 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0001t0001g0128others(1): Show | 4 | HG02559.hp1 HG02572.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.546+4414C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155292539 | ||||||
chr6:155292580
|
A | G | 3 | a0001c0002t0006g0053a0001c0002t0014g0052a0001c0002t0029g0026 | 3 | HG02922.hp1 HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.546+4373T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155292580 | ||||||
chr6:155292597
|
T | C | 1 | a0001c0001t0012g0265 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.546+4356A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155292597 | ||||||
chr6:155292598
|
T | C | 263 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(260): Show | 291 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(288): Show |
intron_variant | MODIFIER | c.546+4355A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155292598 | ||||||
chr6:155292634
|
A | G | 2 | a0001c0001t0001g0039a0001c0001t0009g0231 | 2 | HG02257.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.546+4319T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155292634 | ||||||
chr6:155292772
|
A | G | 39 | a0001c0002t0003g0002a0001c0002t0003g0004a0001c0002t0003g0018others(36): Show | 47 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(44): Show |
intron_variant | MODIFIER | c.546+4181T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155292772 | ||||||
chr6:155292885
|
A | T | 1 | a0001c0001t0002g0281 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.546+4068T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155292885 | ||||||
chr6:155292983
|
C | T | 250 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(247): Show | 276 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(273): Show |
intron_variant | MODIFIER | c.546+3970G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155292983 | ||||||
chr6:155293012
|
TG | T | 3 | a0001c0001t0001g0074a0001c0001t0001g0089a0001c0001t0001g0090 | 3 | HG00621.hp2 HG02135.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.546+3940delC | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155293012 | ||||||
chr6:155293058
|
C | T | 39 | a0001c0002t0003g0002a0001c0002t0003g0004a0001c0002t0003g0018others(36): Show | 47 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(44): Show |
intron_variant | MODIFIER | c.546+3895G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155293058 | ||||||
chr6:155293157
|
T | TCATA | 105 | a0001c0001t0001g0039a0001c0001t0002g0007a0001c0001t0002g0008others(102): Show | 118 | HG00099.hp2 HG00280.hp2 HG00558.hp2 others(115): Show |
intron_variant | MODIFIER | c.546+3792_546+3795d others(6): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155293157 | ||||||
chr6:155293157
|
T | TCATACAT others(1): Show |
40 | a0001c0001t0004g0168a0001c0001t0004g0170a0001c0001t0004g0171others(37): Show | 43 | HG00099.hp1 HG00733.hp2 HG00738.hp1 others(40): Show |
intron_variant | MODIFIER | c.546+3788_546+3795d others(10): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155293157 | ||||||
chr6:155293157
|
T | TCATACAT others(5): Show |
115 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(112): Show | 127 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(124): Show |
intron_variant | MODIFIER | c.546+3784_546+3795d others(14): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155293157 | ||||||
chr6:155293157
|
T | TCATACAT others(9): Show |
3 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0008g0096 | 3 | NA18973.hp1 NA18977.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.546+3780_546+3795d others(18): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155293157 | ||||||
chr6:155293238
|
A | G | 2 | a0001c0002t0003g0185a0001c0002t0003g0186 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.546+3715T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155293238 | ||||||
chr6:155293249
|
G | A | 2 | a0001c0004t0020g0166a0001c0004t0020g0167 | 2 | HG02145.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.546+3704C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155293249 | ||||||
chr6:155293619
|
T | C | 1 | a0003c0006t0038g0235 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.546+3334A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155293619 | ||||||
chr6:155293747
|
C | T | 61 | a0001c0001t0001g0039a0001c0001t0002g0007a0001c0001t0002g0008others(58): Show | 66 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.546+3206G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155293747 | ||||||
chr6:155293748
|
T | G | 1 | a0001c0001t0018g0263 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.546+3205A>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155293748 | ||||||
chr6:155293938
|
A | G | 1 | a0001c0001t0002g0299 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.546+3015T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155293938 | ||||||
chr6:155293991
|
C | T | 1 | a0001c0001t0013g0035 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.546+2962G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155293991 | ||||||
chr6:155294105
|
G | A | 44 | a0001c0002t0003g0002a0001c0002t0003g0004a0001c0002t0003g0018others(41): Show | 52 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.546+2848C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155294105 | ||||||
chr6:155294114
|
C | T | 3 | a0001c0001t0006g0005a0001c0001t0006g0230a0001c0001t0006g0232 | 5 | HG02280.hp1 HG02723.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.546+2839G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155294114 | ||||||
chr6:155294176
|
T | C | 2 | a0001c0001t0004g0168a0001c0001t0004g0180 | 2 | HG02738.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.546+2777A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155294176 | ||||||
chr6:155294214
|
T | C | 13 | a0001c0001t0006g0005a0001c0001t0006g0222a0001c0001t0006g0223others(10): Show | 15 | HG00099.hp1 HG00738.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.546+2739A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155294214 | ||||||
chr6:155294238
|
A | G | 118 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(115): Show | 130 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(127): Show |
intron_variant | MODIFIER | c.546+2715T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155294238 | ||||||
chr6:155294480
|
A | G | 13 | a0001c0001t0006g0005a0001c0001t0006g0222a0001c0001t0006g0223others(10): Show | 15 | HG00099.hp1 HG00738.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.546+2473T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155294480 | ||||||
chr6:155294594
|
A | G | 263 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(260): Show | 291 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(288): Show |
intron_variant | MODIFIER | c.546+2359T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155294594 | ||||||
chr6:155294657
|
G | A | 39 | a0001c0002t0003g0002a0001c0002t0003g0004a0001c0002t0003g0018others(36): Show | 47 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(44): Show |
intron_variant | MODIFIER | c.546+2296C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155294657 | ||||||
chr6:155294706
|
G | A | 1 | a0001c0002t0003g0201 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.546+2247C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155294706 | ||||||
chr6:155294728
|
T | C | 1 | a0001c0001t0001g0068 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.546+2225A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155294728 | ||||||
chr6:155294814
|
C | T | 41 | a0001c0002t0003g0002a0001c0002t0003g0004a0001c0002t0003g0018others(38): Show | 49 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.546+2139G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155294814 | ||||||
chr6:155294851
|
A | G | 263 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(260): Show | 291 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(288): Show |
intron_variant | MODIFIER | c.546+2102T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155294851 | ||||||
chr6:155295095
|
A | G | 1 | a0001c0001t0014g0221 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.546+1858T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155295095 | ||||||
chr6:155295137
|
C | A | 1 | a0001c0001t0001g0039 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.546+1816G>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155295137 | ||||||
chr6:155295142
|
G | C | 1 | a0002c0005t0039g0312 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.546+1811C>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155295142 | ||||||
chr6:155295222
|
C | T | 2 | a0001c0001t0001g0039a0001c0001t0009g0231 | 2 | HG02257.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.546+1731G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155295222 | ||||||
chr6:155295283
|
G | A | 44 | a0001c0002t0003g0002a0001c0002t0003g0004a0001c0002t0003g0018others(41): Show | 52 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.546+1670C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155295283 | ||||||
chr6:155295479
|
T | C | 1 | a0001c0002t0004g0033 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.546+1474A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155295479 | ||||||
chr6:155295580
|
C | G | 143 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(140): Show | 156 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(153): Show |
intron_variant | MODIFIER | c.546+1373G>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155295580 | ||||||
chr6:155295653
|
C | T | 2 | a0001c0002t0005g0006a0001c0002t0005g0268 | 4 | HG00280.hp1 HG01515.hp2 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.546+1300G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155295653 | ||||||
chr6:155295680
|
T | C | 1 | a0001c0001t0001g0078 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.546+1273A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155295680 | ||||||
chr6:155295763
|
T | C | 48 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0025others(45): Show | 53 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.546+1190A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155295763 | ||||||
chr6:155295815
|
C | A | 2 | a0001c0004t0020g0166a0001c0004t0020g0167 | 2 | HG02145.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.546+1138G>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155295815 | ||||||
chr6:155295970
|
C | T | 1 | a0001c0001t0016g0271 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.546+983G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155295970 | ||||||
chr6:155296059
|
G | C | 263 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(260): Show | 291 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(288): Show |
intron_variant | MODIFIER | c.546+894C>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155296059 | ||||||
chr6:155296096
|
T | C | 7 | a0001c0001t0013g0028a0001c0001t0013g0030a0001c0001t0013g0031others(4): Show | 7 | HG00639.hp1 HG01109.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.546+857A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155296096 | ||||||
chr6:155296107
|
G | T | 7 | a0001c0001t0013g0028a0001c0001t0013g0030a0001c0001t0013g0031others(4): Show | 7 | HG00639.hp1 HG01109.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.546+846C>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155296107 | ||||||
chr6:155296147
|
G | A | 13 | a0001c0001t0006g0005a0001c0001t0006g0222a0001c0001t0006g0223others(10): Show | 15 | HG00099.hp1 HG00738.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.546+806C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155296147 | ||||||
chr6:155296246
|
T | C | 1 | a0001c0001t0001g0128 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.546+707A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155296246 | ||||||
chr6:155296265
|
C | T | 3 | a0001c0002t0006g0053a0001c0002t0014g0052a0001c0002t0029g0026 | 3 | HG02922.hp1 HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.546+688G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155296265 | ||||||
chr6:155296407
|
C | A | 41 | a0001c0002t0003g0002a0001c0002t0003g0004a0001c0002t0003g0018others(38): Show | 49 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.546+546G>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155296407 | ||||||
chr6:155296426
|
A | AT | 68 | a0001c0001t0001g0039a0001c0001t0001g0104a0001c0001t0001g0105others(65): Show | 73 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.546+526dupA | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155296426 | ||||||
chr6:155296426
|
A | ATT | 9 | a0001c0001t0002g0285a0001c0001t0002g0292a0001c0001t0002g0300others(6): Show | 9 | HG02055.hp2 HG02145.hp1 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.546+525_546+526dup others(2): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155296426 | ||||||
chr6:155296426
|
AT | A | 97 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(94): Show | 109 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(106): Show |
intron_variant | MODIFIER | c.546+526delA | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155296426 | ||||||
chr6:155296426
|
ATTTTTTT | A | 38 | a0001c0002t0003g0002a0001c0002t0003g0004a0001c0002t0003g0018others(35): Show | 45 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.546+520_546+526del others(7): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155296426 | ||||||
chr6:155296426
|
ATTTTTTT others(1): Show |
A | 8 | a0001c0002t0003g0019a0001c0002t0003g0196a0001c0002t0003g0197others(5): Show | 9 | NA18939.hp2 NA18981.hp2 NA18982.hp2 others(6): Show |
intron_variant | MODIFIER | c.546+519_546+526del others(8): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155296426 | ||||||
chr6:155296530
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.546+423C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155296530 | ||||||
chr6:155296687
|
A | AGTGGCAT others(19): Show |
59 | a0001c0001t0001g0039a0001c0001t0002g0007a0001c0001t0002g0008others(56): Show | 64 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.546+240_546+265dup others(26): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155296687 | ||||||
chr6:155296688
|
G | GTGGCATC others(19): Show |
1 | a0001c0001t0002g0236 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.546+264_546+265ins others(26): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 4/6 | chr6 | 155296688 | ||||||
chr6:155297212
|
T | C | 7 | a0001c0001t0013g0028a0001c0001t0013g0030a0001c0001t0013g0031others(4): Show | 7 | HG00639.hp1 HG01109.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.395-108A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 3/6 | chr6 | 155297212 | ||||||
chr6:155297232
|
A | C | 1 | a0001c0001t0004g0168 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.395-128T>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 3/6 | chr6 | 155297232 | ||||||
chr6:155297318
|
G | A | 1 | a0004c0007t0032g0051 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.395-214C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 3/6 | chr6 | 155297318 | ||||||
chr6:155297536
|
T | C | 1 | a0001c0001t0015g0102 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.395-432A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 3/6 | chr6 | 155297536 | ||||||
chr6:155297703
|
G | T | 2 | a0001c0001t0013g0031a0001c0001t0013g0032 | 2 | HG01109.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.395-599C>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 3/6 | chr6 | 155297703 | ||||||
chr6:155297883
|
G | A | 1 | a0001c0001t0008g0096 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.394+594C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 3/6 | chr6 | 155297883 | ||||||
chr6:155297889
|
A | T | 261 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(258): Show | 289 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(286): Show |
intron_variant | MODIFIER | c.394+588T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 3/6 | chr6 | 155297889 | ||||||
chr6:155298107
|
A | G | 14 | a0001c0001t0006g0005a0001c0001t0006g0222a0001c0001t0006g0223others(11): Show | 16 | HG00099.hp1 HG00738.hp1 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.394+370T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 3/6 | chr6 | 155298107 | ||||||
chr6:155298299
|
G | A | 53 | a0001c0001t0001g0039a0001c0001t0002g0007a0001c0001t0002g0008others(50): Show | 58 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.394+178C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 3/6 | chr6 | 155298299 | ||||||
chr6:155298727
|
C | T | 1 | a0001c0001t0002g0297 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.286-142G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155298727 | ||||||
chr6:155298841
|
T | A | 53 | a0001c0001t0001g0039a0001c0001t0002g0007a0001c0001t0002g0008others(50): Show | 58 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.286-256A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155298841 | ||||||
chr6:155299092
|
G | C | 44 | a0001c0002t0003g0002a0001c0002t0003g0004a0001c0002t0003g0018others(41): Show | 52 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.286-507C>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155299092 | ||||||
chr6:155299104
|
C | T | 2 | a0001c0001t0001g0145a0001c0001t0001g0148 | 2 | NA18981.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.286-519G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155299104 | ||||||
chr6:155299659
|
T | C | 1 | a0001c0001t0004g0215 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.286-1074A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155299659 | ||||||
chr6:155299762
|
T | C | 48 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0025others(45): Show | 53 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.286-1177A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155299762 | ||||||
chr6:155299885
|
G | A | 143 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(140): Show | 156 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(153): Show |
intron_variant | MODIFIER | c.286-1300C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155299885 | ||||||
chr6:155299918
|
T | C | 45 | a0001c0001t0001g0060a0001c0002t0003g0002a0001c0002t0003g0004others(42): Show | 53 | HG00099.hp2 HG00280.hp2 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.286-1333A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155299918 | ||||||
chr6:155300057
|
C | A | 1 | a0001c0001t0014g0221 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.286-1472G>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155300057 | ||||||
chr6:155300106
|
T | C | 1 | a0004c0007t0032g0051 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.286-1521A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155300106 | ||||||
chr6:155300277
|
T | G | 1 | a0001c0001t0009g0231 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.286-1692A>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155300277 | ||||||
chr6:155300295
|
T | C | 2 | a0001c0002t0006g0219a0001c0002t0006g0220 | 2 | HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.286-1710A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155300295 | ||||||
chr6:155300378
|
T | G | 1 | a0001c0002t0011g0202 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.286-1793A>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155300378 | ||||||
chr6:155300423
|
A | G | 4 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0103others(1): Show | 6 | HG01069.hp1 HG01071.hp1 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.286-1838T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155300423 | ||||||
chr6:155300478
|
CCA | C | 3 | a0001c0002t0006g0053a0001c0002t0014g0052a0001c0002t0029g0026 | 3 | HG02922.hp1 HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.286-1895_286-1894d others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155300478 | ||||||
chr6:155300493
|
C | G | 2 | a0001c0001t0001g0039a0001c0001t0009g0231 | 2 | HG02257.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.286-1908G>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155300493 | ||||||
chr6:155300524
|
T | C | 1 | a0001c0001t0014g0221 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.286-1939A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155300524 | ||||||
chr6:155300551
|
T | A | 3 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131 | 3 | HG03490.hp1 HG03492.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.286-1966A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155300551 | ||||||
chr6:155300688
|
G | A | 142 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(139): Show | 155 | HG00558.hp1 HG00621.hp2 HG00639.hp2 others(152): Show |
intron_variant | MODIFIER | c.286-2103C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155300688 | ||||||
chr6:155300804
|
T | C | 1 | a0001c0001t0001g0143 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.286-2219A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155300804 | ||||||
chr6:155300867
|
C | T | 4 | a0001c0001t0002g0008a0001c0001t0002g0297a0001c0001t0002g0300others(1): Show | 6 | HG00738.hp2 HG01433.hp1 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.286-2282G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155300867 | ||||||
chr6:155300931
|
A | G | 1 | a0001c0001t0001g0078 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.286-2346T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155300931 | ||||||
chr6:155300936
|
C | G | 7 | a0001c0001t0013g0028a0001c0001t0013g0030a0001c0001t0013g0031others(4): Show | 7 | HG00639.hp1 HG01109.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.286-2351G>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155300936 | ||||||
chr6:155300954
|
A | G | 261 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(258): Show | 289 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(286): Show |
intron_variant | MODIFIER | c.286-2369T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155300954 | ||||||
chr6:155301124
|
T | C | 2 | a0001c0001t0001g0133a0001c0001t0009g0132 | 2 | NA18960.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.286-2539A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155301124 | ||||||
chr6:155301347
|
T | C | 115 | a0001c0001t0001g0039a0001c0001t0001g0060a0001c0001t0002g0007others(112): Show | 131 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.286-2762A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155301347 | ||||||
chr6:155301507
|
A | G | 1 | a0001c0001t0001g0086 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.286-2922T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155301507 | ||||||
chr6:155301514
|
C | A | 3 | a0001c0001t0001g0134a0001c0001t0009g0231a0001c0002t0037g0049 | 3 | HG02970.hp1 HG03209.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.286-2929G>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155301514 | ||||||
chr6:155301764
|
C | T | 4 | a0001c0001t0028g0027a0001c0002t0006g0053a0001c0002t0014g0052others(1): Show | 4 | HG02622.hp2 HG02922.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.286-3179G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155301764 | ||||||
chr6:155301828
|
A | G | 4 | a0001c0001t0028g0027a0001c0002t0006g0053a0001c0002t0014g0052others(1): Show | 4 | HG02622.hp2 HG02922.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.286-3243T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155301828 | ||||||
chr6:155302145
|
T | A | 1 | a0001c0001t0008g0096 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.286-3560A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155302145 | ||||||
chr6:155302146
|
C | G | 1 | a0001c0001t0008g0096 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.286-3561G>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155302146 | ||||||
chr6:155302156
|
A | G | 1 | a0001c0001t0008g0096 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.286-3571T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155302156 | ||||||
chr6:155302178
|
C | G | 279 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(276): Show | 308 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(305): Show |
intron_variant | MODIFIER | c.286-3593G>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155302178 | ||||||
chr6:155302196
|
T | C | 2 | a0001c0001t0028g0027a0001c0002t0029g0026 | 2 | HG02622.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.286-3611A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155302196 | ||||||
chr6:155302490
|
G | A | 45 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0025others(42): Show | 50 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.286-3905C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155302490 | ||||||
chr6:155302575
|
G | A | 258 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(255): Show | 285 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(282): Show |
intron_variant | MODIFIER | c.286-3990C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155302575 | ||||||
chr6:155302715
|
T | C | 1 | a0001c0001t0009g0141 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.286-4130A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155302715 | ||||||
chr6:155302768
|
T | C | 1 | a0001c0001t0025g0311 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.286-4183A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155302768 | ||||||
chr6:155302829
|
A | C | 1 | a0001c0001t0016g0271 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.286-4244T>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155302829 | ||||||
chr6:155302836
|
A | C | 1 | a0001c0001t0001g0143 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.286-4251T>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155302836 | ||||||
chr6:155302907
|
A | G | 1 | a0001c0001t0002g0284 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.286-4322T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155302907 | ||||||
chr6:155302945
|
A | G | 280 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(277): Show | 309 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(306): Show |
intron_variant | MODIFIER | c.286-4360T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155302945 | ||||||
chr6:155302948
|
C | T | 4 | a0001c0002t0010g0054a0001c0002t0010g0055a0001c0002t0010g0057others(1): Show | 4 | HG03490.hp2 NA18965.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.286-4363G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155302948 | ||||||
chr6:155303022
|
A | G | 1 | a0001c0001t0001g0075 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.286-4437T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155303022 | ||||||
chr6:155303140
|
CTAATTT | C | 17 | a0001c0001t0001g0169a0001c0001t0004g0168a0001c0001t0004g0170others(14): Show | 17 | HG00733.hp2 HG01109.hp2 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.286-4561_286-4556d others(8): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155303140 | ||||||
chr6:155303169
|
C | A | 3 | a0001c0001t0006g0178a0001c0001t0014g0179a0001c0001t0014g0221 | 3 | HG02109.hp2 HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.286-4584G>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155303169 | ||||||
chr6:155303184
|
A | G | 1 | a0001c0001t0001g0094 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.286-4599T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155303184 | ||||||
chr6:155303191
|
A | C | 1 | a0001c0001t0001g0169 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.286-4606T>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155303191 | ||||||
chr6:155303218
|
G | C | 186 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(183): Show | 207 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.286-4633C>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155303218 | ||||||
chr6:155303231
|
C | T | 9 | a0001c0001t0013g0028a0001c0001t0013g0030a0001c0001t0013g0031others(6): Show | 9 | HG00639.hp1 HG01109.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.286-4646G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155303231 | ||||||
chr6:155303400
|
T | C | 1 | a0001c0001t0001g0039 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.286-4815A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155303400 | ||||||
chr6:155303464
|
C | T | 257 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(254): Show | 284 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(281): Show |
intron_variant | MODIFIER | c.286-4879G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155303464 | ||||||
chr6:155303558
|
G | A | 1 | a0001c0001t0016g0271 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.286-4973C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155303558 | ||||||
chr6:155303582
|
T | C | 2 | a0001c0002t0004g0045a0001c0002t0023g0046 | 2 | HG02970.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.286-4997A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155303582 | ||||||
chr6:155303593
|
G | A | 4 | a0001c0002t0004g0003a0001c0002t0004g0045a0001c0002t0023g0046others(1): Show | 6 | HG02622.hp1 HG02818.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.286-5008C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155303593 | ||||||
chr6:155303642
|
T | C | 1 | a0001c0001t0001g0086 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.286-5057A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155303642 | ||||||
chr6:155303869
|
A | G | 3 | a0001c0001t0024g0233a0001c0001t0024g0234a0003c0006t0038g0235 | 3 | HG02895.hp1 HG02897.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.286-5284T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155303869 | ||||||
chr6:155303970
|
A | G | 187 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(184): Show | 208 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.286-5385T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155303970 | ||||||
chr6:155303990
|
A | G | 4 | a0001c0002t0004g0003a0001c0002t0004g0045a0001c0002t0023g0046others(1): Show | 6 | HG02622.hp1 HG02818.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.286-5405T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155303990 | ||||||
chr6:155304078
|
C | T | 1 | a0001c0001t0001g0149 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.286-5493G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155304078 | ||||||
chr6:155304155
|
G | A | 53 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0025others(50): Show | 59 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.286-5570C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155304155 | ||||||
chr6:155304222
|
C | A | 4 | a0001c0002t0004g0040a0001c0002t0004g0041a0001c0002t0004g0042others(1): Show | 4 | HG02451.hp2 HG02717.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.286-5637G>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155304222 | ||||||
chr6:155304276
|
C | G | 2 | a0001c0001t0004g0168a0001c0001t0004g0180 | 2 | HG02738.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.286-5691G>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155304276 | ||||||
chr6:155304288
|
A | G | 1 | a0001c0002t0010g0047 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.286-5703T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155304288 | ||||||
chr6:155304411
|
G | A | 4 | a0001c0001t0028g0027a0001c0002t0006g0053a0001c0002t0014g0052others(1): Show | 4 | HG02622.hp2 HG02922.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.286-5826C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155304411 | ||||||
chr6:155304424
|
T | A | 4 | a0001c0001t0028g0027a0001c0002t0006g0053a0001c0002t0014g0052others(1): Show | 4 | HG02622.hp2 HG02922.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.286-5839A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155304424 | ||||||
chr6:155304599
|
G | A | 3 | a0001c0001t0006g0224a0001c0001t0006g0225a0001c0002t0003g0002 | 6 | HG00733.hp1 HG01106.hp1 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.286-6014C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155304599 | ||||||
chr6:155304679
|
G | A | 4 | a0001c0001t0028g0027a0001c0002t0006g0053a0001c0002t0014g0052others(1): Show | 4 | HG02622.hp2 HG02922.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.286-6094C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155304679 | ||||||
chr6:155304737
|
C | T | 1 | a0001c0001t0001g0153 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.286-6152G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155304737 | ||||||
chr6:155304862
|
C | A | 1 | a0001c0001t0008g0101 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.286-6277G>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155304862 | ||||||
chr6:155304891
|
T | C | 2 | a0001c0001t0004g0175a0001c0001t0004g0177 | 2 | HG01243.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.285+6297A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155304891 | ||||||
chr6:155305117
|
T | A | 1 | a0001c0001t0001g0069 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.285+6071A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305117 | ||||||
chr6:155305122
|
ATATACAT others(141): Show |
A | 1 | a0001c0001t0028g0027 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.285+5918_285+6065d others(2): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305122 | ||||||
chr6:155305123
|
TATAC | T | 67 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0025others(64): Show | 73 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.285+6061_285+6064d others(6): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305123 | ||||||
chr6:155305127
|
C | A | 3 | a0001c0002t0006g0053a0001c0002t0014g0052a0001c0002t0029g0026 | 3 | HG02922.hp1 HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.285+6061G>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305127 | ||||||
chr6:155305131
|
A | T | 3 | a0001c0002t0006g0053a0001c0002t0014g0052a0001c0002t0029g0026 | 3 | HG02922.hp1 HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.285+6057T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305131 | ||||||
chr6:155305132
|
T | A | 3 | a0001c0002t0006g0053a0001c0002t0014g0052a0001c0002t0029g0026 | 3 | HG02922.hp1 HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.285+6056A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305132 | ||||||
chr6:155305136
|
A | T | 3 | a0001c0002t0006g0053a0001c0002t0014g0052a0001c0002t0029g0026 | 3 | HG02922.hp1 HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.285+6052T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305136 | ||||||
chr6:155305137
|
T | A | 3 | a0001c0002t0006g0053a0001c0002t0014g0052a0001c0002t0029g0026 | 3 | HG02922.hp1 HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.285+6051A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305137 | ||||||
chr6:155305139
|
T | A | 3 | a0001c0002t0006g0053a0001c0002t0014g0052a0001c0002t0029g0026 | 3 | HG02922.hp1 HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.285+6049A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305139 | ||||||
chr6:155305140
|
TTA | T | 66 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0025others(63): Show | 72 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.285+6046_285+6047d others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305140 | ||||||
chr6:155305146
|
ATATAAAT others(43): Show |
A | 1 | a0001c0001t0016g0271 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.285+5992_285+6041d others(52): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305146 | ||||||
chr6:155305148
|
A | T | 3 | a0001c0002t0006g0053a0001c0002t0014g0052a0001c0002t0029g0026 | 3 | HG02922.hp1 HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.285+6040T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305148 | ||||||
chr6:155305151
|
A | C | 3 | a0001c0002t0006g0053a0001c0002t0014g0052a0001c0002t0029g0026 | 3 | HG02922.hp1 HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.285+6037T>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305151 | ||||||
chr6:155305156
|
A | G | 3 | a0001c0001t0024g0233a0001c0001t0024g0234a0003c0006t0038g0235 | 3 | HG02895.hp1 HG02897.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.285+6032T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305156 | ||||||
chr6:155305172
|
TTA | T | 4 | a0001c0002t0010g0054a0001c0002t0010g0055a0001c0002t0010g0057others(1): Show | 4 | HG03490.hp2 NA18965.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.285+6014_285+6015d others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305172 | ||||||
chr6:155305173
|
T | TAC | 10 | a0001c0001t0012g0024a0001c0001t0012g0262a0001c0001t0012g0264others(7): Show | 11 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.285+6014_285+6015i others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305173 | ||||||
chr6:155305174
|
ATATATAT others(15): Show |
A | 44 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0025others(41): Show | 49 | HG00558.hp2 HG00609.hp1 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.285+5992_285+6013d others(24): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305174 | ||||||
chr6:155305175
|
T | C | 12 | a0001c0001t0002g0296a0001c0001t0013g0028a0001c0001t0013g0030others(9): Show | 12 | HG00621.hp1 HG00639.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.285+6013A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305175 | ||||||
chr6:155305177
|
TATATATT others(125): Show |
T | 1 | a0001c0001t0006g0178 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.285+5879_285+6010d others(2): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305177 | ||||||
chr6:155305178
|
ATATATTA others(85): Show |
A | 1 | a0001c0002t0007g0164 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.285+5918_285+6009d others(94): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305178 | ||||||
chr6:155305179
|
T | TATAA | 3 | a0001c0002t0006g0053a0001c0002t0014g0052a0001c0002t0029g0026 | 3 | HG02922.hp1 HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.285+6008_285+6009i others(6): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305179 | ||||||
chr6:155305180
|
ATATTAAA others(9): Show |
A | 1 | a0001c0002t0003g0204 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.285+5992_285+6007d others(18): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305180 | ||||||
chr6:155305190
|
ATATATTT others(157): Show |
A | 1 | a0001c0001t0014g0179 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.285+5834_285+5997d others(2): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305190 | ||||||
chr6:155305196
|
TTATATAT others(69): Show |
T | 38 | a0001c0001t0001g0016a0001c0001t0001g0077a0001c0001t0001g0078others(35): Show | 42 | HG00280.hp2 HG00673.hp1 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.285+5916_285+5991d others(78): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305196 | ||||||
chr6:155305196
|
TTATATAT others(71): Show |
T | 1 | a0001c0001t0001g0146 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.285+5914_285+5991d others(80): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305196 | ||||||
chr6:155305197
|
T | C | 44 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0025others(41): Show | 49 | HG00558.hp2 HG00609.hp1 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.285+5991A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305197 | ||||||
chr6:155305197
|
T | TAC | 16 | a0001c0001t0002g0296a0001c0001t0012g0024a0001c0001t0012g0264others(13): Show | 17 | HG00621.hp1 HG00639.hp1 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.285+5990_285+5991i others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305197 | ||||||
chr6:155305198
|
ATATATAT others(65): Show |
A | 3 | a0001c0001t0024g0233a0001c0001t0024g0234a0003c0006t0038g0235 | 3 | HG02895.hp1 HG02897.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.285+5918_285+5989d others(74): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305198 | ||||||
chr6:155305199
|
T | A | 2 | a0001c0001t0016g0271a0001c0002t0003g0204 | 2 | HG02280.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.285+5989A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305199 | ||||||
chr6:155305199
|
T | C | 2 | a0001c0002t0006g0219a0001c0002t0006g0220 | 2 | HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.285+5989A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305199 | ||||||
chr6:155305200
|
ATATATAT others(13): Show |
A | 1 | a0001c0002t0004g0093 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.285+5968_285+5987d others(22): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305200 | ||||||
chr6:155305201
|
TATATATT others(101): Show |
T | 1 | a0001c0002t0003g0181 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.285+5879_285+5986d others(2): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305201 | ||||||
chr6:155305202
|
ATATATTA others(11): Show |
A | 2 | a0001c0001t0001g0094a0001c0001t0001g0134 | 2 | HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.285+5968_285+5985d others(20): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305202 | ||||||
chr6:155305212
|
T | A | 1 | a0001c0002t0029g0026 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.285+5976A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305212 | ||||||
chr6:155305214
|
ATATATTT others(133): Show |
A | 5 | a0001c0001t0004g0176a0001c0001t0004g0215a0001c0001t0014g0221others(2): Show | 5 | HG02273.hp2 HG02965.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.285+5834_285+5973d others(2): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305214 | ||||||
chr6:155305214
|
ATATATTT others(165): Show |
A | 13 | a0001c0001t0001g0169a0001c0001t0004g0168a0001c0001t0004g0170others(10): Show | 13 | HG00733.hp2 HG01109.hp2 HG01167.hp2 others(10): Show |
intron_variant | MODIFIER | c.285+5802_285+5973d others(2): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305214 | ||||||
chr6:155305217
|
T | A | 1 | a0001c0001t0013g0030 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.285+5971A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305217 | ||||||
chr6:155305220
|
T | TTA | 5 | a0001c0001t0030g0050a0001c0002t0005g0020a0001c0002t0005g0239others(2): Show | 6 | HG01496.hp2 HG02258.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.285+5966_285+5967d others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305220 | ||||||
chr6:155305220
|
TTA | T | 19 | a0001c0001t0001g0070a0001c0001t0001g0098a0001c0001t0008g0001others(16): Show | 22 | HG02280.hp2 HG02451.hp2 HG02717.hp1 others(19): Show |
intron_variant | MODIFIER | c.285+5966_285+5967d others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305220 | ||||||
chr6:155305220
|
TTATATAT others(45): Show |
T | 1 | a0001c0001t0008g0137 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.285+5916_285+5967d others(54): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305220 | ||||||
chr6:155305221
|
T | A | 1 | a0001c0002t0029g0026 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.285+5967A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305221 | ||||||
chr6:155305221
|
T | TAC | 9 | a0001c0001t0013g0028a0001c0001t0013g0030a0001c0001t0013g0031others(6): Show | 9 | HG00639.hp1 HG01109.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.285+5966_285+5967i others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305221 | ||||||
chr6:155305222
|
A | C | 1 | a0002c0005t0039g0312 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.285+5966T>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305222 | ||||||
chr6:155305222
|
ATATATAT others(41): Show |
A | 5 | a0001c0001t0012g0024a0001c0001t0012g0264a0001c0001t0012g0265others(2): Show | 6 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.285+5918_285+5965d others(50): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305222 | ||||||
chr6:155305223
|
T | A | 1 | a0001c0002t0029g0026 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.285+5965A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305223 | ||||||
chr6:155305223
|
T | C | 45 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0025others(42): Show | 50 | HG00558.hp2 HG00609.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.285+5965A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305223 | ||||||
chr6:155305224
|
A | T | 1 | a0001c0002t0029g0026 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.285+5964T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305224 | ||||||
chr6:155305225
|
T | A | 3 | a0001c0001t0001g0094a0001c0001t0001g0134a0001c0002t0004g0093 | 3 | HG02965.hp1 HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.285+5963A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305225 | ||||||
chr6:155305225
|
T | TATATAA | 16 | a0001c0001t0001g0069a0001c0001t0001g0082a0001c0001t0001g0091others(13): Show | 18 | HG00735.hp2 HG01074.hp1 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.285+5962_285+5963i others(8): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305225 | ||||||
chr6:155305225
|
TATATATA others(77): Show |
T | 1 | a0001c0002t0010g0183 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.285+5879_285+5962d others(86): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305225 | ||||||
chr6:155305226
|
ATATATAT others(37): Show |
A | 79 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(76): Show | 86 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(83): Show |
intron_variant | MODIFIER | c.285+5918_285+5961d others(46): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305226 | ||||||
chr6:155305229
|
T | A | 10 | a0001c0001t0013g0028a0001c0001t0013g0030a0001c0001t0013g0031others(7): Show | 10 | HG00639.hp1 HG01109.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.285+5959A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305229 | ||||||
chr6:155305229
|
T | TAA | 3 | a0001c0001t0002g0296a0001c0002t0006g0219a0001c0002t0006g0220 | 3 | HG00621.hp1 HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.285+5958_285+5959i others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305229 | ||||||
chr6:155305229
|
TATATTA | T | 14 | a0001c0001t0001g0061a0001c0001t0001g0155a0001c0001t0006g0222others(11): Show | 19 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.285+5953_285+5958d others(8): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305229 | ||||||
chr6:155305238
|
T | A | 14 | a0001c0001t0001g0061a0001c0001t0001g0155a0001c0001t0006g0222others(11): Show | 19 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.285+5950A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305238 | ||||||
chr6:155305246
|
T | A | 1 | a0001c0002t0029g0026 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.285+5942A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305246 | ||||||
chr6:155305246
|
T | TTA | 3 | a0001c0002t0019g0023a0001c0004t0020g0166a0001c0004t0020g0167 | 4 | HG01256.hp1 HG01496.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.285+5940_285+5941d others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305246 | ||||||
chr6:155305246
|
TTA | T | 5 | a0001c0002t0005g0237a0001c0002t0010g0054a0001c0002t0010g0055others(2): Show | 5 | HG01358.hp1 HG03490.hp2 NA18965.hp2 others(2): Show |
intron_variant | MODIFIER | c.285+5940_285+5941d others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305246 | ||||||
chr6:155305247
|
T | A | 14 | a0001c0001t0001g0061a0001c0001t0001g0155a0001c0001t0006g0222others(11): Show | 19 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.285+5941A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305247 | ||||||
chr6:155305248
|
ATATATAT others(15): Show |
A | 38 | a0001c0001t0002g0007a0001c0001t0002g0025a0001c0001t0002g0236others(35): Show | 41 | HG00609.hp1 HG00735.hp1 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.285+5918_285+5939d others(24): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305248 | ||||||
chr6:155305249
|
T | A | 15 | a0001c0001t0001g0061a0001c0001t0001g0155a0001c0001t0006g0222others(12): Show | 20 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.285+5939A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305249 | ||||||
chr6:155305249
|
T | C | 1 | a0001c0001t0016g0271 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.285+5939A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305249 | ||||||
chr6:155305249
|
T | TATATATA others(1): Show |
23 | a0001c0001t0001g0069a0001c0001t0001g0091a0001c0001t0001g0092others(20): Show | 25 | HG00639.hp1 HG00735.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.285+5938_285+5939i others(10): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305249 | ||||||
chr6:155305249
|
T | TATATATA others(33): Show |
1 | a0001c0001t0021g0034 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.285+5938_285+5939i others(42): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305249 | ||||||
chr6:155305249
|
T | TATATATA others(65): Show |
1 | a0001c0001t0001g0082 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.285+5938_285+5939i others(74): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305249 | ||||||
chr6:155305250
|
A | T | 14 | a0001c0001t0001g0061a0001c0001t0001g0155a0001c0001t0006g0222others(11): Show | 19 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.285+5938T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305250 | ||||||
chr6:155305252
|
ATATATTA others(11): Show |
A | 13 | a0001c0001t0001g0070a0001c0001t0001g0094a0001c0001t0001g0098others(10): Show | 16 | HG02965.hp1 HG02970.hp1 HG03041.hp2 others(13): Show |
intron_variant | MODIFIER | c.285+5918_285+5935d others(20): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305252 | ||||||
chr6:155305253
|
T | TATAA | 8 | a0001c0001t0002g0008a0001c0001t0002g0280a0001c0001t0002g0281others(5): Show | 10 | HG00558.hp2 HG01433.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.285+5934_285+5935i others(6): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305253 | ||||||
chr6:155305253
|
T | TATAAATA others(53): Show |
1 | a0001c0002t0006g0219 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.285+5934_285+5935i others(62): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305253 | ||||||
chr6:155305256
|
ATTAAATT others(144): Show |
A | 1 | a0001c0001t0002g0296 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.285+5781_285+5931d others(2): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305256 | ||||||
chr6:155305258
|
TAAATTA | T | 14 | a0001c0001t0001g0061a0001c0001t0001g0155a0001c0001t0006g0222others(11): Show | 19 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.285+5924_285+5929d others(8): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305258 | ||||||
chr6:155305270
|
T | A | 14 | a0001c0001t0001g0061a0001c0001t0001g0155a0001c0001t0006g0222others(11): Show | 19 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.285+5918A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305270 | ||||||
chr6:155305271
|
T | C | 3 | a0001c0001t0024g0233a0001c0001t0024g0234a0003c0006t0038g0235 | 3 | HG02895.hp1 HG02897.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.285+5917A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305271 | ||||||
chr6:155305272
|
A | T | 1 | a0001c0002t0007g0164 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.285+5916T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305272 | ||||||
chr6:155305273
|
T | C | 1 | a0001c0001t0012g0262 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.285+5915A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305273 | ||||||
chr6:155305275
|
T | A | 107 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(104): Show | 122 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(119): Show |
intron_variant | MODIFIER | c.285+5913A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305275 | ||||||
chr6:155305275
|
T | TATAA | 3 | a0001c0001t0001g0082a0001c0001t0001g0152a0001c0001t0021g0034 | 3 | HG01074.hp1 HG04184.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.285+5912_285+5913i others(6): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305275 | ||||||
chr6:155305275
|
T | TATATAA | 26 | a0001c0001t0001g0069a0001c0001t0001g0091a0001c0001t0001g0092others(23): Show | 28 | HG00639.hp1 HG00735.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.285+5912_285+5913i others(8): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305275 | ||||||
chr6:155305277
|
T | TATAAAC | 3 | a0001c0001t0001g0039a0001c0004t0020g0166a0001c0004t0020g0167 | 3 | HG02145.hp1 HG02257.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.285+5910_285+5911i others(8): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305277 | ||||||
chr6:155305277
|
T | TATATATT others(25): Show |
1 | a0001c0001t0018g0255 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.285+5879_285+5910d others(34): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305277 | ||||||
chr6:155305279
|
T | A | 43 | a0001c0001t0002g0007a0001c0001t0002g0025a0001c0001t0002g0236others(40): Show | 47 | HG00609.hp1 HG00735.hp1 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.285+5909A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305279 | ||||||
chr6:155305279
|
T | TAA | 8 | a0001c0001t0002g0008a0001c0001t0002g0280a0001c0001t0002g0281others(5): Show | 10 | HG00558.hp2 HG01433.hp1 HG02056.hp2 others(7): Show |
intron_variant | MODIFIER | c.285+5908_285+5909i others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305279 | ||||||
chr6:155305296
|
TTA | T | 18 | a0001c0001t0001g0069a0001c0001t0001g0091a0001c0001t0001g0092others(15): Show | 18 | HG00639.hp1 HG00735.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.285+5890_285+5891d others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305296 | ||||||
chr6:155305299
|
T | C | 1 | a0001c0001t0028g0027 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.285+5889A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305299 | ||||||
chr6:155305305
|
T | A | 2 | a0001c0001t0001g0082a0001c0001t0001g0152 | 2 | HG01074.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.285+5883A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305305 | ||||||
chr6:155305307
|
AACAT | A | 44 | a0001c0001t0002g0007a0001c0001t0002g0025a0001c0001t0002g0236others(41): Show | 47 | HG00609.hp1 HG00735.hp1 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.285+5877_285+5880d others(6): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305307 | ||||||
chr6:155305308
|
A | T | 2 | a0001c0002t0006g0053a0001c0002t0014g0052 | 2 | HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.285+5880T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305308 | ||||||
chr6:155305309
|
C | T | 186 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(183): Show | 210 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.285+5879G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305309 | ||||||
chr6:155305322
|
A | ATATATTT others(25): Show |
1 | a0001c0001t0030g0050 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.285+5865_285+5866i others(34): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305322 | ||||||
chr6:155305322
|
ATATATTT others(25): Show |
A | 1 | a0001c0002t0005g0268 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.285+5834_285+5865d others(34): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305322 | ||||||
chr6:155305328
|
TTA | T | 29 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(26): Show | 32 | HG00609.hp2 HG00639.hp1 HG01099.hp1 others(29): Show |
intron_variant | MODIFIER | c.285+5858_285+5859d others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305328 | ||||||
chr6:155305331
|
TATATATA others(1): Show |
T | 4 | a0001c0001t0024g0233a0001c0001t0024g0234a0001c0002t0029g0026others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.285+5849_285+5856d others(10): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305331 | ||||||
chr6:155305334
|
ATATAAAT others(172): Show |
A | 3 | a0001c0001t0002g0281a0001c0001t0002g0282a0001c0001t0002g0283 | 3 | HG00558.hp2 NA19054.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.285+5675_285+5853d others(2): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305334 | ||||||
chr6:155305337
|
T | A | 8 | a0001c0001t0001g0069a0001c0001t0001g0082a0001c0001t0001g0091others(5): Show | 8 | HG00735.hp2 HG01074.hp1 HG01975.hp2 others(5): Show |
intron_variant | MODIFIER | c.285+5851A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305337 | ||||||
chr6:155305344
|
A | AT | 3 | a0001c0001t0001g0084a0001c0001t0001g0086a0001c0001t0009g0085 | 3 | HG03831.hp2 NA18944.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.285+5843dupA | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305344 | ||||||
chr6:155305352
|
TTGTA | T | 4 | a0001c0001t0002g0007a0001c0001t0002g0279a0001c0001t0002g0292others(1): Show | 6 | NA18967.hp1 NA18974.hp1 NA18977.hp2 others(3): Show |
intron_variant | MODIFIER | c.285+5832_285+5835d others(6): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305352 | ||||||
chr6:155305354
|
G | A | 231 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(228): Show | 256 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(253): Show |
intron_variant | MODIFIER | c.285+5834C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305354 | ||||||
chr6:155305360
|
T | A | 5 | a0001c0001t0002g0007a0001c0001t0002g0279a0001c0001t0002g0292others(2): Show | 7 | NA18967.hp1 NA18969.hp2 NA18974.hp1 others(4): Show |
intron_variant | MODIFIER | c.285+5828A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305360 | ||||||
chr6:155305360
|
TTA | T | 146 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(143): Show | 158 | HG00099.hp1 HG00558.hp1 HG00609.hp1 others(155): Show |
intron_variant | MODIFIER | c.285+5826_285+5827d others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305360 | ||||||
chr6:155305368
|
ATAAATAT others(4): Show |
A | 1 | a0001c0002t0029g0026 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.285+5809_285+5819d others(13): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305368 | ||||||
chr6:155305369
|
T | A | 11 | a0001c0001t0001g0062a0001c0001t0001g0095a0001c0001t0001g0134others(8): Show | 13 | HG01099.hp1 HG01433.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.285+5819A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305369 | ||||||
chr6:155305371
|
A | T | 1 | a0001c0001t0001g0139 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.285+5817T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305371 | ||||||
chr6:155305376
|
A | AT | 4 | a0001c0002t0004g0003a0001c0002t0004g0045a0001c0002t0023g0046others(1): Show | 6 | HG02622.hp1 HG02818.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.285+5811dupA | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305376 | ||||||
chr6:155305381
|
A | G | 1 | a0001c0001t0002g0272 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.285+5807T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305381 | ||||||
chr6:155305383
|
A | G | 2 | a0001c0001t0002g0008a0001c0001t0002g0300 | 4 | HG01433.hp1 HG02738.hp2 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.285+5805T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305383 | ||||||
chr6:155305384
|
TTGTATA | T | 3 | a0001c0001t0024g0233a0001c0001t0024g0234a0003c0006t0038g0235 | 3 | HG02895.hp1 HG02897.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.285+5798_285+5803d others(8): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305384 | ||||||
chr6:155305386
|
G | A | 243 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(240): Show | 272 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(269): Show |
intron_variant | MODIFIER | c.285+5802C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305386 | ||||||
chr6:155305392
|
T | A | 3 | a0001c0001t0024g0233a0001c0001t0024g0234a0003c0006t0038g0235 | 3 | HG02895.hp1 HG02897.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.285+5796A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305392 | ||||||
chr6:155305392
|
TTA | T | 105 | a0001c0001t0001g0016a0001c0001t0001g0078a0001c0001t0001g0079others(102): Show | 117 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.285+5794_285+5795d others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305392 | ||||||
chr6:155305394
|
A | ATATATAA others(21): Show |
5 | a0001c0001t0006g0005a0001c0001t0006g0230a0001c0001t0006g0232others(2): Show | 7 | HG01891.hp1 HG02280.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.285+5793_285+5794i others(30): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305394 | ||||||
chr6:155305395
|
TATATATA others(34): Show |
T | 2 | a0001c0001t0001g0140a0001c0001t0009g0141 | 2 | HG02056.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.285+5752_285+5792d others(43): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305395 | ||||||
chr6:155305398
|
ATATAAAT others(108): Show |
A | 2 | a0001c0001t0002g0008a0001c0001t0002g0300 | 4 | HG01433.hp1 HG02738.hp2 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.285+5675_285+5789d others(2): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305398 | ||||||
chr6:155305400
|
ATAAATAT others(2): Show |
A | 5 | a0001c0001t0001g0069a0001c0001t0001g0082a0001c0001t0001g0147others(2): Show | 5 | HG01074.hp1 HG01975.hp2 HG02155.hp1 others(2): Show |
intron_variant | MODIFIER | c.285+5779_285+5787d others(11): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305400 | ||||||
chr6:155305401
|
T | A | 94 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(91): Show | 105 | HG00558.hp1 HG00609.hp2 HG00639.hp2 others(102): Show |
intron_variant | MODIFIER | c.285+5787A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305401 | ||||||
chr6:155305402
|
A | ATTAAATT others(7): Show |
2 | a0001c0002t0006g0053a0001c0002t0014g0052 | 2 | HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.285+5785_285+5786i others(16): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305402 | ||||||
chr6:155305403
|
A | T | 2 | a0001c0002t0006g0053a0001c0002t0014g0052 | 2 | HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.285+5785T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305403 | ||||||
chr6:155305408
|
AT | A | 253 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(250): Show | 280 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(277): Show |
intron_variant | MODIFIER | c.285+5779delA | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305408 | ||||||
chr6:155305409
|
T | A | 1 | a0001c0001t0002g0296 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.285+5779A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305409 | ||||||
chr6:155305409
|
T | TATTAAAT others(24): Show |
1 | a0001c0001t0030g0050 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.285+5778_285+5779i others(33): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305409 | ||||||
chr6:155305416
|
A | G | 1 | a0001c0001t0002g0280 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.285+5772T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305416 | ||||||
chr6:155305419
|
A | G | 1 | a0001c0002t0005g0268 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.285+5769T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305419 | ||||||
chr6:155305424
|
TTTATATA others(49): Show |
T | 1 | a0001c0001t0001g0069 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.285+5708_285+5763d others(58): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305424 | ||||||
chr6:155305425
|
TTA | T | 19 | a0001c0001t0001g0059a0001c0001t0001g0077a0001c0001t0001g0149others(16): Show | 20 | HG00639.hp1 HG01109.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.285+5761_285+5762d others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305425 | ||||||
chr6:155305428
|
TATATATA others(1): Show |
T | 31 | a0001c0001t0001g0062a0001c0001t0001g0091a0001c0001t0001g0092others(28): Show | 31 | HG00733.hp2 HG00735.hp2 HG01099.hp1 others(28): Show |
intron_variant | MODIFIER | c.285+5752_285+5759d others(10): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305428 | ||||||
chr6:155305431
|
A | ATAAATAT others(9): Show |
1 | a0001c0001t0021g0034 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.285+5756_285+5757i others(18): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305431 | ||||||
chr6:155305433
|
A | ATATTAAA others(9): Show |
2 | a0001c0002t0006g0053a0001c0002t0014g0052 | 2 | HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.285+5754_285+5755i others(18): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305433 | ||||||
chr6:155305434
|
T | A | 102 | a0001c0001t0001g0016a0001c0001t0001g0078a0001c0001t0001g0079others(99): Show | 116 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.285+5754A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305434 | ||||||
chr6:155305436
|
A | AATATATA others(17): Show |
1 | a0001c0004t0020g0167 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.285+5728_285+5751d others(26): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305436 | ||||||
chr6:155305436
|
A | T | 3 | a0001c0001t0021g0034a0001c0002t0006g0053a0001c0002t0014g0052 | 3 | HG02922.hp1 HG03471.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.285+5752T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305436 | ||||||
chr6:155305448
|
A | G | 39 | a0001c0001t0002g0007a0001c0001t0002g0025a0001c0001t0002g0236others(36): Show | 42 | HG00609.hp1 HG00735.hp1 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.285+5740T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305448 | ||||||
chr6:155305456
|
T | TATAAATA others(9): Show |
4 | a0001c0002t0004g0003a0001c0002t0004g0045a0001c0002t0023g0046others(1): Show | 6 | HG02622.hp1 HG02818.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.285+5731_285+5732i others(18): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305456 | ||||||
chr6:155305457
|
TTA | T | 19 | a0001c0001t0002g0296a0001c0001t0012g0024a0001c0001t0012g0262others(16): Show | 20 | HG00621.hp1 HG01109.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.285+5729_285+5730d others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305457 | ||||||
chr6:155305457
|
TTATATAT others(75): Show |
T | 10 | a0001c0001t0002g0272a0001c0001t0002g0278a0001c0001t0002g0295others(7): Show | 10 | HG00609.hp1 HG00738.hp2 HG02683.hp1 others(7): Show |
intron_variant | MODIFIER | c.285+5649_285+5730d others(84): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305457 | ||||||
chr6:155305460
|
TATATATA others(1): Show |
T | 4 | a0001c0001t0001g0082a0001c0001t0001g0153a0001c0001t0006g0178others(1): Show | 4 | HG01074.hp1 HG02155.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.285+5720_285+5727d others(10): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305460 | ||||||
chr6:155305463
|
A | ATAAATAT others(9): Show |
3 | a0001c0001t0013g0035a0001c0001t0021g0036a0001c0002t0004g0033 | 3 | HG00639.hp1 HG02647.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.285+5724_285+5725i others(18): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305463 | ||||||
chr6:155305463
|
ATATAAAT others(43): Show |
A | 5 | a0001c0001t0002g0007a0001c0001t0002g0279a0001c0001t0002g0292others(2): Show | 7 | NA18967.hp1 NA18969.hp2 NA18974.hp1 others(4): Show |
intron_variant | MODIFIER | c.285+5675_285+5724d others(52): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305463 | ||||||
chr6:155305463
|
ATATAAAT others(99): Show |
A | 23 | a0001c0001t0002g0025a0001c0001t0002g0236a0001c0001t0002g0269others(20): Show | 24 | HG00735.hp1 HG03704.hp1 NA18941.hp1 others(21): Show |
intron_variant | MODIFIER | c.285+5619_285+5724d others(2): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305463 | ||||||
chr6:155305465
|
A | T | 4 | a0001c0002t0004g0003a0001c0002t0004g0045a0001c0002t0023g0046others(1): Show | 6 | HG02622.hp1 HG02818.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.285+5723T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305465 | ||||||
chr6:155305466
|
T | A | 55 | a0001c0001t0001g0077a0001c0001t0006g0005a0001c0001t0006g0222others(52): Show | 65 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.285+5722A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305466 | ||||||
chr6:155305467
|
A | ATT | 90 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(87): Show | 100 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(97): Show |
intron_variant | MODIFIER | c.285+5720_285+5721i others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305467 | ||||||
chr6:155305467
|
A | T | 1 | a0001c0001t0001g0152 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.285+5721T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305467 | ||||||
chr6:155305468
|
A | T | 7 | a0001c0001t0013g0035a0001c0001t0021g0036a0001c0002t0004g0003others(4): Show | 9 | HG00639.hp1 HG02622.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.285+5720T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305468 | ||||||
chr6:155305468
|
AATATATA others(97): Show |
A | 1 | a0001c0001t0002g0280 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.285+5616_285+5719d others(2): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305468 | ||||||
chr6:155305470
|
T | A | 91 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(88): Show | 101 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(98): Show |
intron_variant | MODIFIER | c.285+5718A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305470 | ||||||
chr6:155305471
|
A | T | 92 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(89): Show | 102 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(99): Show |
intron_variant | MODIFIER | c.285+5717T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305471 | ||||||
chr6:155305473
|
A | AT | 5 | a0001c0002t0004g0038a0001c0002t0004g0048a0001c0002t0010g0047others(2): Show | 5 | HG02647.hp1 HG02809.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.285+5714dupA | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305473 | ||||||
chr6:155305474
|
T | A | 1 | a0001c0001t0001g0087 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.285+5714A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305474 | ||||||
chr6:155305476
|
TTA | T | 91 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(88): Show | 101 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(98): Show |
intron_variant | MODIFIER | c.285+5710_285+5711d others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305476 | ||||||
chr6:155305479
|
A | T | 1 | a0001c0001t0001g0087 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.285+5709T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305479 | ||||||
chr6:155305480
|
A | ATTATATA others(1): Show |
25 | a0001c0001t0001g0077a0001c0001t0001g0145a0001c0001t0001g0148others(22): Show | 32 | HG00099.hp1 HG00639.hp1 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.285+5700_285+5707d others(10): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305480 | ||||||
chr6:155305480
|
A | ATTATATA others(49): Show |
3 | a0001c0002t0004g0043a0001c0002t0004g0044a0001c0002t0005g0256 | 3 | HG02486.hp1 HG02717.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.285+5652_285+5707d others(58): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305480 | ||||||
chr6:155305480
|
A | T | 91 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(88): Show | 101 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(98): Show |
intron_variant | MODIFIER | c.285+5708T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305480 | ||||||
chr6:155305483
|
A | ATATATT | 8 | a0001c0001t0012g0024a0001c0001t0012g0262a0001c0001t0012g0264others(5): Show | 9 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.285+5704_285+5705i others(8): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305483 | ||||||
chr6:155305483
|
A | T | 2 | a0001c0001t0001g0087a0001c0002t0006g0220 | 2 | HG02486.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.285+5705T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305483 | ||||||
chr6:155305486
|
T | C | 10 | a0001c0001t0015g0208a0001c0002t0007g0017a0001c0002t0007g0058others(7): Show | 11 | HG02040.hp1 HG02071.hp1 HG02129.hp1 others(8): Show |
intron_variant | MODIFIER | c.285+5702A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305486 | ||||||
chr6:155305487
|
A | ATT | 3 | a0001c0001t0024g0233a0001c0001t0024g0234a0003c0006t0038g0235 | 3 | HG02895.hp1 HG02897.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.285+5700_285+5701i others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305487 | ||||||
chr6:155305487
|
A | G | 1 | a0001c0002t0022g0207 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.285+5701T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305487 | ||||||
chr6:155305488
|
TATAAATA others(9): Show |
T | 2 | a0001c0001t0002g0296a0001c0001t0016g0271 | 2 | HG00621.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.285+5684_285+5699d others(18): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305488 | ||||||
chr6:155305489
|
A | T | 85 | a0001c0001t0001g0016a0001c0001t0001g0062a0001c0001t0001g0078others(82): Show | 91 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(88): Show |
intron_variant | MODIFIER | c.285+5699T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305489 | ||||||
chr6:155305490
|
TAA | T | 3 | a0001c0001t0001g0082a0001c0001t0001g0153a0001c0001t0006g0178 | 3 | HG01074.hp1 HG02155.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.285+5696_285+5697d others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305490 | ||||||
chr6:155305492
|
A | AATATATA others(41): Show |
4 | a0001c0002t0005g0020a0001c0002t0005g0238a0001c0002t0005g0239others(1): Show | 5 | HG01496.hp2 HG02258.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.285+5648_285+5695d others(50): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305492 | ||||||
chr6:155305492
|
A | T | 90 | a0001c0001t0001g0016a0001c0001t0001g0062a0001c0001t0001g0078others(87): Show | 96 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(93): Show |
intron_variant | MODIFIER | c.285+5696T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305492 | ||||||
chr6:155305494
|
TA | T | 5 | a0001c0001t0013g0028a0001c0001t0013g0030a0001c0001t0013g0031others(2): Show | 5 | HG01109.hp1 HG02723.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.285+5693delT | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305494 | ||||||
chr6:155305498
|
T | A | 5 | a0001c0001t0013g0028a0001c0001t0013g0030a0001c0001t0013g0031others(2): Show | 5 | HG01109.hp1 HG02723.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.285+5690A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305498 | ||||||
chr6:155305502
|
A | ATAT | 5 | a0001c0001t0013g0028a0001c0001t0013g0030a0001c0001t0013g0031others(2): Show | 5 | HG01109.hp1 HG02723.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.285+5685_285+5686i others(5): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305502 | ||||||
chr6:155305504
|
A | T | 5 | a0001c0001t0013g0028a0001c0001t0013g0030a0001c0001t0013g0031others(2): Show | 5 | HG01109.hp1 HG02723.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.285+5684T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305504 | ||||||
chr6:155305513
|
T | A | 5 | a0001c0001t0013g0028a0001c0001t0013g0030a0001c0001t0013g0031others(2): Show | 5 | HG01109.hp1 HG02723.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.285+5675A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305513 | ||||||
chr6:155305513
|
TTA | T | 33 | a0001c0001t0001g0016a0001c0001t0001g0062a0001c0001t0001g0091others(30): Show | 34 | HG00733.hp2 HG00735.hp2 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.285+5673_285+5674d others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305513 | ||||||
chr6:155305516
|
T | A | 17 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0279others(14): Show | 21 | HG00558.hp2 HG00621.hp1 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.285+5672A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305516 | ||||||
chr6:155305516
|
T | TATATAA | 9 | a0001c0001t0012g0024a0001c0001t0012g0262a0001c0001t0012g0264others(6): Show | 10 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.285+5671_285+5672i others(8): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305516 | ||||||
chr6:155305516
|
T | TATATATA others(1): Show |
8 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0006g0178others(5): Show | 8 | HG00639.hp1 HG02155.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.285+5671_285+5672i others(10): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305516 | ||||||
chr6:155305519
|
A | G | 41 | a0001c0001t0015g0208a0001c0002t0003g0004a0001c0002t0003g0018others(38): Show | 46 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.285+5669T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305519 | ||||||
chr6:155305523
|
ATT | A | 47 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(44): Show | 52 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.285+5663_285+5664d others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305523 | ||||||
chr6:155305528
|
A | T | 47 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(44): Show | 52 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.285+5660T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305528 | ||||||
chr6:155305529
|
T | A | 47 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(44): Show | 52 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.285+5659A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305529 | ||||||
chr6:155305532
|
T | A | 2 | a0001c0001t0024g0233a0001c0001t0024g0234 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.285+5656A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305532 | ||||||
chr6:155305534
|
T | TTA | 47 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(44): Show | 52 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.285+5653_285+5654i others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305534 | ||||||
chr6:155305536
|
T | A | 47 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(44): Show | 52 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.285+5652A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305536 | ||||||
chr6:155305537
|
T | A | 2 | a0001c0001t0024g0233a0001c0001t0024g0234 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.285+5651A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305537 | ||||||
chr6:155305537
|
TTA | T | 7 | a0001c0001t0002g0281a0001c0001t0002g0282a0001c0001t0002g0283others(4): Show | 7 | HG00558.hp2 HG02145.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.285+5649_285+5650d others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305537 | ||||||
chr6:155305537
|
TTATATAT others(27): Show |
T | 1 | a0001c0002t0022g0207 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.285+5617_285+5650d others(36): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305537 | ||||||
chr6:155305538
|
TATATATA others(3): Show |
T | 2 | a0001c0001t0001g0069a0001c0001t0001g0082 | 2 | HG01074.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.285+5640_285+5649d others(12): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305538 | ||||||
chr6:155305539
|
A | T | 5 | a0001c0001t0012g0024a0001c0001t0012g0262a0001c0001t0012g0264others(2): Show | 6 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.285+5649T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305539 | ||||||
chr6:155305539
|
ATATATAT others(23): Show |
A | 1 | a0001c0001t0031g0083 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.285+5619_285+5648d others(32): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305539 | ||||||
chr6:155305545
|
A | T | 47 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(44): Show | 52 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.285+5643T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305545 | ||||||
chr6:155305546
|
T | A | 1 | a0001c0001t0002g0296 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.285+5642A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305546 | ||||||
chr6:155305547
|
A | T | 89 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(86): Show | 99 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(96): Show |
intron_variant | MODIFIER | c.285+5641T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305547 | ||||||
chr6:155305548
|
A | AATATATA others(41): Show |
3 | a0001c0002t0004g0040a0001c0002t0004g0041a0001c0002t0004g0042 | 3 | HG02451.hp2 HG03041.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.285+5592_285+5639d others(50): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305548 | ||||||
chr6:155305548
|
A | T | 47 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(44): Show | 52 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.285+5640T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305548 | ||||||
chr6:155305548
|
AATATATA others(51): Show |
A | 1 | a0001c0001t0028g0027 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.285+5582_285+5639d others(60): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305548 | ||||||
chr6:155305549
|
ATATATAT others(13): Show |
A | 3 | a0001c0002t0010g0054a0001c0002t0010g0055a0001c0002t0022g0056 | 3 | HG03490.hp2 NA19005.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.285+5619_285+5638d others(22): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305549 | ||||||
chr6:155305550
|
T | A | 89 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(86): Show | 99 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(96): Show |
intron_variant | MODIFIER | c.285+5638A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305550 | ||||||
chr6:155305551
|
A | T | 89 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(86): Show | 99 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(96): Show |
intron_variant | MODIFIER | c.285+5637T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305551 | ||||||
chr6:155305556
|
TTA | T | 86 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(83): Show | 96 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(93): Show |
intron_variant | MODIFIER | c.285+5630_285+5631d others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305556 | ||||||
chr6:155305556
|
TTAA | T | 3 | a0001c0001t0001g0084a0001c0001t0001g0086a0001c0001t0009g0085 | 3 | HG03831.hp2 NA18944.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.285+5629_285+5631d others(5): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305556 | ||||||
chr6:155305560
|
A | G | 1 | a0001c0001t0002g0296 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.285+5628T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305560 | ||||||
chr6:155305560
|
A | T | 86 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(83): Show | 96 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(93): Show |
intron_variant | MODIFIER | c.285+5628T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305560 | ||||||
chr6:155305562
|
TA | T | 3 | a0001c0001t0001g0084a0001c0001t0001g0086a0001c0001t0009g0085 | 3 | HG03831.hp2 NA18944.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.285+5625delT | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305562 | ||||||
chr6:155305569
|
T | A | 89 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(86): Show | 99 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(96): Show |
intron_variant | MODIFIER | c.285+5619A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305569 | ||||||
chr6:155305569
|
T | TTA | 12 | a0001c0001t0002g0007a0001c0001t0002g0279a0001c0001t0002g0292others(9): Show | 15 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.285+5617_285+5618d others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305569 | ||||||
chr6:155305569
|
T | TTATATAT others(27): Show |
1 | a0001c0002t0037g0049 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.285+5618_285+5619i others(36): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305569 | ||||||
chr6:155305569
|
TTA | T | 46 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0080others(43): Show | 51 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(48): Show |
intron_variant | MODIFIER | c.285+5617_285+5618d others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305569 | ||||||
chr6:155305569
|
TTATATAT others(53): Show |
T | 15 | a0001c0001t0001g0169a0001c0001t0004g0168a0001c0001t0004g0170others(12): Show | 15 | HG00733.hp2 HG01109.hp2 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.285+5559_285+5618d others(62): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305569 | ||||||
chr6:155305570
|
TATATATA others(25): Show |
T | 1 | a0001c0001t0016g0271 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.285+5586_285+5617d others(34): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305570 | ||||||
chr6:155305571
|
A | T | 1 | a0001c0001t0001g0081 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.285+5617T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305571 | ||||||
chr6:155305572
|
T | A | 111 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(108): Show | 122 | HG00609.hp2 HG00621.hp2 HG00639.hp2 others(119): Show |
intron_variant | MODIFIER | c.285+5616A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305572 | ||||||
chr6:155305572
|
T | TATATAA | 4 | a0001c0001t0002g0296a0001c0001t0006g0178a0001c0002t0003g0211others(1): Show | 4 | HG00621.hp1 HG02486.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.285+5615_285+5616i others(8): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305572 | ||||||
chr6:155305572
|
T | TATATAAA others(1): Show |
3 | a0001c0001t0002g0281a0001c0001t0002g0282a0001c0001t0002g0283 | 3 | HG00558.hp2 NA19054.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.285+5615_285+5616i others(10): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305572 | ||||||
chr6:155305572
|
T | TATATATA others(1): Show |
21 | a0001c0001t0001g0016a0001c0001t0001g0069a0001c0001t0001g0139others(18): Show | 22 | HG00639.hp1 HG01069.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.285+5615_285+5616i others(10): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305572 | ||||||
chr6:155305576
|
TATATTAA others(19): Show |
T | 16 | a0001c0001t0001g0062a0001c0001t0001g0091a0001c0001t0001g0092others(13): Show | 16 | HG00735.hp2 HG00738.hp2 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.285+5586_285+5611d others(28): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305576 | ||||||
chr6:155305579
|
ATT | A | 5 | a0001c0001t0002g0272a0001c0001t0002g0278a0001c0001t0002g0295others(2): Show | 5 | HG00609.hp1 HG03209.hp1 NA18949.hp1 others(2): Show |
intron_variant | MODIFIER | c.285+5607_285+5608d others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305579 | ||||||
chr6:155305584
|
A | G | 3 | a0001c0001t0002g0281a0001c0001t0002g0282a0001c0001t0002g0283 | 3 | HG00558.hp2 NA19054.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.285+5604T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305584 | ||||||
chr6:155305584
|
A | T | 5 | a0001c0001t0002g0272a0001c0001t0002g0278a0001c0001t0002g0295others(2): Show | 5 | HG00609.hp1 HG03209.hp1 NA18949.hp1 others(2): Show |
intron_variant | MODIFIER | c.285+5604T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305584 | ||||||
chr6:155305585
|
T | A | 5 | a0001c0001t0002g0272a0001c0001t0002g0278a0001c0001t0002g0295others(2): Show | 5 | HG00609.hp1 HG03209.hp1 NA18949.hp1 others(2): Show |
intron_variant | MODIFIER | c.285+5603A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305585 | ||||||
chr6:155305590
|
T | TTA | 5 | a0001c0001t0002g0272a0001c0001t0002g0278a0001c0001t0002g0295others(2): Show | 5 | HG00609.hp1 HG03209.hp1 NA18949.hp1 others(2): Show |
intron_variant | MODIFIER | c.285+5597_285+5598i others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305590 | ||||||
chr6:155305592
|
T | A | 5 | a0001c0001t0002g0272a0001c0001t0002g0278a0001c0001t0002g0295others(2): Show | 5 | HG00609.hp1 HG03209.hp1 NA18949.hp1 others(2): Show |
intron_variant | MODIFIER | c.285+5596A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305592 | ||||||
chr6:155305593
|
T | TTA | 3 | a0001c0001t0001g0039a0001c0001t0030g0050a0001c0004t0020g0166 | 3 | HG02257.hp1 HG03579.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.285+5593_285+5594d others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305593 | ||||||
chr6:155305593
|
TTATATAT others(3): Show |
T | 1 | a0001c0002t0029g0026 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.285+5585_285+5594d others(12): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305593 | ||||||
chr6:155305593
|
TTATATAT others(5): Show |
T | 12 | a0001c0001t0001g0077a0001c0001t0006g0005a0001c0001t0006g0222others(9): Show | 17 | HG00099.hp1 HG00733.hp1 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.285+5583_285+5594d others(14): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305593 | ||||||
chr6:155305597
|
A | ATATATTA others(3): Show |
1 | a0001c0001t0006g0227 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.285+5590_285+5591i others(12): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305597 | ||||||
chr6:155305600
|
TAA | T | 148 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(145): Show | 160 | HG00558.hp1 HG00609.hp2 HG00621.hp1 others(157): Show |
intron_variant | MODIFIER | c.285+5586_285+5587d others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305600 | ||||||
chr6:155305601
|
A | T | 5 | a0001c0001t0002g0272a0001c0001t0002g0278a0001c0001t0002g0295others(2): Show | 5 | HG00609.hp1 HG03209.hp1 NA18949.hp1 others(2): Show |
intron_variant | MODIFIER | c.285+5587T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305601 | ||||||
chr6:155305602
|
A | T | 7 | a0001c0001t0002g0272a0001c0001t0002g0278a0001c0001t0002g0295others(4): Show | 7 | HG00609.hp1 HG00738.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.285+5586T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305602 | ||||||
chr6:155305602
|
AATAT | A | 59 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0279others(56): Show | 69 | HG00099.hp2 HG00280.hp2 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.285+5582_285+5585d others(6): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305602 | ||||||
chr6:155305603
|
A | ATATATAT others(13): Show |
1 | a0001c0002t0006g0220 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.285+5584_285+5585i others(22): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305603 | ||||||
chr6:155305605
|
A | T | 1 | a0001c0001t0006g0227 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.285+5583T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305605 | ||||||
chr6:155305606
|
T | A | 164 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(161): Show | 176 | HG00558.hp1 HG00609.hp2 HG00621.hp1 others(173): Show |
intron_variant | MODIFIER | c.285+5582A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305606 | ||||||
chr6:155305606
|
T | TATATTAA others(53): Show |
2 | a0001c0001t0001g0039a0001c0004t0020g0166 | 2 | HG02257.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.285+5581_285+5582i others(62): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305606 | ||||||
chr6:155305627
|
TTA | T | 65 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0272others(62): Show | 75 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(72): Show |
intron_variant | MODIFIER | c.285+5559_285+5560d others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305627 | ||||||
chr6:155305630
|
TATATATA others(1): Show |
T | 7 | a0001c0001t0002g0297a0001c0001t0002g0299a0001c0001t0025g0310others(4): Show | 7 | HG00738.hp2 HG02683.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.285+5550_285+5557d others(10): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305630 | ||||||
chr6:155305632
|
TATATAA | T | 24 | a0001c0001t0002g0025a0001c0001t0002g0236a0001c0001t0002g0269others(21): Show | 25 | HG00621.hp1 HG00735.hp1 HG03704.hp1 others(22): Show |
intron_variant | MODIFIER | c.285+5550_285+5555d others(8): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305632 | ||||||
chr6:155305656
|
T | C | 1 | a0001c0001t0001g0142 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.285+5532A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305656 | ||||||
chr6:155305659
|
TTA | T | 84 | a0001c0001t0002g0025a0001c0001t0002g0236a0001c0001t0002g0269others(81): Show | 90 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(87): Show |
intron_variant | MODIFIER | c.285+5527_285+5528d others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305659 | ||||||
chr6:155305662
|
TATATATA others(1): Show |
T | 3 | a0001c0001t0028g0027a0001c0002t0006g0053a0001c0002t0014g0052 | 3 | HG02622.hp2 HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.285+5518_285+5525d others(10): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305662 | ||||||
chr6:155305664
|
TATATAA | T | 3 | a0001c0001t0002g0281a0001c0001t0002g0282a0001c0001t0002g0283 | 3 | HG00558.hp2 NA19054.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.285+5518_285+5523d others(8): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305664 | ||||||
chr6:155305665
|
ATATAAAT others(49): Show |
A | 7 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0279others(4): Show | 11 | HG01433.hp1 HG02738.hp2 HG03491.hp1 others(8): Show |
intron_variant | MODIFIER | c.285+5467_285+5522d others(58): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305665 | ||||||
chr6:155305670
|
AATATATA others(47): Show |
A | 1 | a0001c0001t0006g0178 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.285+5464_285+5517d others(56): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305670 | ||||||
chr6:155305683
|
T | TA | 6 | a0001c0001t0012g0024a0001c0001t0012g0262a0001c0001t0012g0264others(3): Show | 7 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.285+5504_285+5505i others(3): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305683 | ||||||
chr6:155305689
|
A | T | 6 | a0001c0001t0012g0024a0001c0001t0012g0262a0001c0001t0012g0264others(3): Show | 7 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.285+5499T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305689 | ||||||
chr6:155305691
|
T | A | 7 | a0001c0001t0012g0024a0001c0001t0012g0262a0001c0001t0012g0264others(4): Show | 8 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.285+5497A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305691 | ||||||
chr6:155305691
|
T | TTA | 188 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(185): Show | 209 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.285+5495_285+5496d others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305691 | ||||||
chr6:155305694
|
TATATAA | T | 10 | a0001c0001t0013g0031a0001c0001t0013g0032a0001c0001t0013g0035others(7): Show | 10 | HG00639.hp1 HG01109.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.285+5488_285+5493d others(8): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305694 | ||||||
chr6:155305697
|
A | ATATATTA others(11): Show |
3 | a0001c0001t0013g0028a0001c0001t0013g0030a0001c0002t0010g0029 | 3 | HG02723.hp2 HG03453.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.285+5490_285+5491i others(20): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305697 | ||||||
chr6:155305697
|
A | ATATATTA others(35): Show |
1 | a0001c0002t0029g0026 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.285+5490_285+5491i others(44): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305697 | ||||||
chr6:155305699
|
AAATATAT others(15): Show |
A | 1 | a0001c0001t0014g0179 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.285+5467_285+5488d others(24): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305699 | ||||||
chr6:155305700
|
A | T | 4 | a0001c0001t0013g0028a0001c0001t0013g0030a0001c0002t0010g0029others(1): Show | 4 | HG02723.hp2 HG03453.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.285+5488T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305700 | ||||||
chr6:155305712
|
AT | A | 10 | a0001c0001t0012g0024a0001c0001t0012g0262a0001c0001t0012g0264others(7): Show | 11 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.285+5475delA | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305712 | ||||||
chr6:155305721
|
T | A | 2 | a0001c0004t0020g0166a0001c0004t0020g0167 | 2 | HG02145.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.285+5467A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305721 | ||||||
chr6:155305721
|
TTA | T | 182 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(179): Show | 203 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.285+5465_285+5466d others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305721 | ||||||
chr6:155305724
|
T | A | 10 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0279others(7): Show | 14 | HG01433.hp1 HG02109.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.285+5464A>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305724 | ||||||
chr6:155305724
|
T | TATATAA | 37 | a0001c0001t0002g0025a0001c0001t0002g0236a0001c0001t0002g0269others(34): Show | 38 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.285+5463_285+5464i others(8): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305724 | ||||||
chr6:155305747
|
A | C | 1 | a0001c0001t0001g0039 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.285+5441T>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305747 | ||||||
chr6:155305820
|
A | G | 1 | a0001c0001t0001g0076 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.285+5368T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305820 | ||||||
chr6:155305875
|
T | C | 1 | a0001c0001t0001g0144 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.285+5313A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305875 | ||||||
chr6:155305908
|
T | C | 1 | a0001c0001t0002g0296 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.285+5280A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305908 | ||||||
chr6:155305947
|
C | T | 9 | a0001c0001t0013g0028a0001c0001t0013g0030a0001c0001t0013g0031others(6): Show | 9 | HG00639.hp1 HG01109.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.285+5241G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155305947 | ||||||
chr6:155306029
|
A | G | 1 | a0001c0001t0001g0149 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.285+5159T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155306029 | ||||||
chr6:155306096
|
G | A | 260 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(257): Show | 287 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(284): Show |
intron_variant | MODIFIER | c.285+5092C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155306096 | ||||||
chr6:155306198
|
A | G | 71 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0025others(68): Show | 77 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.285+4990T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155306198 | ||||||
chr6:155306226
|
T | C | 71 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0025others(68): Show | 77 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.285+4962A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155306226 | ||||||
chr6:155306296
|
C | T | 1 | a0001c0001t0002g0279 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.285+4892G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155306296 | ||||||
chr6:155306303
|
A | T | 1 | a0001c0001t0001g0075 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.285+4885T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155306303 | ||||||
chr6:155306394
|
G | C | 2 | a0001c0001t0001g0145a0001c0001t0001g0148 | 2 | NA18981.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.285+4794C>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155306394 | ||||||
chr6:155306501
|
C | T | 1 | a0001c0001t0001g0010 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.285+4687G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155306501 | ||||||
chr6:155306696
|
G | A | 1 | a0001c0001t0002g0272 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.285+4492C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155306696 | ||||||
chr6:155306843
|
G | T | 1 | a0001c0001t0001g0074 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.285+4345C>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155306843 | ||||||
chr6:155307136
|
T | TAC | 9 | a0001c0001t0002g0269a0001c0001t0017g0257a0001c0002t0005g0006others(6): Show | 11 | HG00280.hp1 HG00642.hp2 HG01069.hp2 others(8): Show |
intron_variant | MODIFIER | c.285+4050_285+4051d others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155307136 | ||||||
chr6:155307136
|
T | TACAC | 5 | a0001c0001t0002g0272a0001c0001t0016g0271a0001c0002t0006g0053others(2): Show | 5 | HG02572.hp1 HG02922.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.285+4048_285+4051d others(6): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155307136 | ||||||
chr6:155307136
|
T | TACACAC | 10 | a0001c0001t0002g0236a0001c0001t0002g0273a0001c0001t0002g0274others(7): Show | 10 | HG00609.hp1 HG00735.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.285+4046_285+4051d others(8): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155307136 | ||||||
chr6:155307136
|
T | TACACACA others(1): Show |
21 | a0001c0001t0002g0007a0001c0001t0002g0025a0001c0001t0002g0279others(18): Show | 24 | HG00558.hp2 HG00621.hp1 HG02056.hp2 others(21): Show |
intron_variant | MODIFIER | c.285+4044_285+4051d others(10): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155307136 | ||||||
chr6:155307136
|
T | TACACACA others(3): Show |
15 | a0001c0001t0002g0008a0001c0001t0002g0297a0001c0001t0002g0299others(12): Show | 17 | HG00738.hp2 HG01433.hp1 HG02683.hp1 others(14): Show |
intron_variant | MODIFIER | c.285+4042_285+4051d others(12): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155307136 | ||||||
chr6:155307136
|
T | TACATACA others(7): Show |
2 | a0001c0001t0024g0233a0001c0001t0024g0234 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.285+4051_285+4052i others(16): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155307136 | ||||||
chr6:155307136
|
TAC | T | 9 | a0001c0001t0001g0039a0001c0001t0001g0146a0001c0001t0001g0147others(6): Show | 9 | HG00099.hp1 HG00738.hp1 HG01975.hp2 others(6): Show |
intron_variant | MODIFIER | c.285+4050_285+4051d others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155307136 | ||||||
chr6:155307136
|
TACAC | T | 172 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(169): Show | 193 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(190): Show |
intron_variant | MODIFIER | c.285+4048_285+4051d others(6): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155307136 | ||||||
chr6:155307138
|
C | CACACACA others(1): Show |
9 | a0001c0001t0013g0028a0001c0001t0013g0030a0001c0001t0013g0031others(6): Show | 9 | HG00639.hp1 HG01109.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.285+4049_285+4050i others(10): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155307138 | ||||||
chr6:155307166
|
CAT | C | 6 | a0001c0001t0012g0024a0001c0001t0012g0262a0001c0001t0012g0264others(3): Show | 7 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.285+4020_285+4021d others(4): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155307166 | ||||||
chr6:155307168
|
T | C | 61 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0025others(58): Show | 66 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.285+4020A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155307168 | ||||||
chr6:155307273
|
G | A | 2 | a0001c0002t0004g0003a0004c0007t0032g0051 | 4 | HG02622.hp1 HG02818.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.285+3915C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155307273 | ||||||
chr6:155307323
|
A | C | 9 | a0001c0001t0013g0028a0001c0001t0013g0030a0001c0001t0013g0031others(6): Show | 9 | HG00639.hp1 HG01109.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.285+3865T>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155307323 | ||||||
chr6:155307409
|
G | A | 4 | a0001c0001t0028g0027a0001c0002t0006g0053a0001c0002t0014g0052others(1): Show | 4 | HG02622.hp2 HG02922.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.285+3779C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155307409 | ||||||
chr6:155307574
|
C | T | 67 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0025others(64): Show | 73 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.285+3614G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155307574 | ||||||
chr6:155307667
|
T | G | 4 | a0001c0001t0028g0027a0001c0002t0006g0053a0001c0002t0014g0052others(1): Show | 4 | HG02622.hp2 HG02922.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.285+3521A>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155307667 | ||||||
chr6:155307688
|
C | T | 1 | a0003c0006t0038g0235 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.285+3500G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155307688 | ||||||
chr6:155307713
|
C | T | 1 | a0001c0002t0035g0182 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.285+3475G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155307713 | ||||||
chr6:155307863
|
G | A | 1 | a0001c0001t0001g0152 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.285+3325C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155307863 | ||||||
chr6:155307909
|
GA | G | 60 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0025others(57): Show | 66 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.285+3278delT | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155307909 | ||||||
chr6:155307965
|
A | C | 6 | a0001c0001t0012g0024a0001c0001t0012g0262a0001c0001t0012g0264others(3): Show | 7 | HG01884.hp2 HG01891.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.285+3223T>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155307965 | ||||||
chr6:155308014
|
T | C | 1 | a0001c0001t0001g0153 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.285+3174A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155308014 | ||||||
chr6:155308244
|
A | G | 9 | a0001c0001t0013g0028a0001c0001t0013g0030a0001c0001t0013g0031others(6): Show | 9 | HG00639.hp1 HG01109.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.285+2944T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155308244 | ||||||
chr6:155308323
|
C | T | 2 | a0001c0001t0025g0310a0001c0001t0025g0311 | 2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.285+2865G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155308323 | ||||||
chr6:155308345
|
C | A | 9 | a0001c0001t0013g0028a0001c0001t0013g0030a0001c0001t0013g0031others(6): Show | 9 | HG00639.hp1 HG01109.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.285+2843G>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155308345 | ||||||
chr6:155308474
|
C | T | 1 | a0001c0002t0014g0052 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.285+2714G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155308474 | ||||||
chr6:155308544
|
T | C | 113 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(110): Show | 124 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(121): Show |
intron_variant | MODIFIER | c.285+2644A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155308544 | ||||||
chr6:155308851
|
C | T | 259 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(256): Show | 286 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(283): Show |
intron_variant | MODIFIER | c.285+2337G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155308851 | ||||||
chr6:155309106
|
G | GA | 4 | a0001c0001t0001g0218a0001c0002t0010g0055a0001c0002t0010g0057others(1): Show | 4 | NA18956.hp1 NA18965.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.285+2081dupT | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155309106 | ||||||
chr6:155309188
|
G | A | 1 | a0001c0001t0034g0154 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.285+2000C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155309188 | ||||||
chr6:155309265
|
A | G | 1 | a0001c0002t0003g0181 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.285+1923T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155309265 | ||||||
chr6:155309288
|
T | C | 2 | a0001c0001t0002g0308a0001c0001t0016g0309 | 2 | NA18949.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.285+1900A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155309288 | ||||||
chr6:155309519
|
G | A | 42 | a0001c0001t0015g0208a0001c0002t0003g0004a0001c0002t0003g0018others(39): Show | 47 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(44): Show |
intron_variant | MODIFIER | c.285+1669C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155309519 | ||||||
chr6:155309608
|
G | A | 1 | a0001c0001t0001g0155 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.285+1580C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155309608 | ||||||
chr6:155309678
|
A | G | 4 | a0001c0002t0004g0040a0001c0002t0004g0041a0001c0002t0004g0042others(1): Show | 4 | HG02451.hp2 HG02717.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.285+1510T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155309678 | ||||||
chr6:155309686
|
G | A | 4 | a0001c0001t0028g0027a0001c0002t0006g0053a0001c0002t0014g0052others(1): Show | 4 | HG02622.hp2 HG02922.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.285+1502C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155309686 | ||||||
chr6:155309908
|
C | G | 1 | a0001c0001t0001g0073 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.285+1280G>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155309908 | ||||||
chr6:155310208
|
A | G | 2 | a0001c0001t0028g0027a0001c0002t0029g0026 | 2 | HG02622.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.285+980T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155310208 | ||||||
chr6:155310655
|
C | T | 2 | a0001c0002t0006g0219a0001c0002t0006g0220 | 2 | HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.285+533G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155310655 | ||||||
chr6:155310686
|
C | G | 2 | a0001c0004t0020g0166a0001c0004t0020g0167 | 2 | HG02145.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.285+502G>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155310686 | ||||||
chr6:155310842
|
C | T | 2 | a0001c0001t0006g0222a0001c0001t0006g0223 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.285+346G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155310842 | ||||||
chr6:155310906
|
T | TA | 43 | a0001c0001t0004g0180a0001c0001t0015g0208a0001c0002t0003g0004others(40): Show | 48 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.285+281dupT | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155310906 | ||||||
chr6:155310956
|
A | C | 4 | a0001c0001t0028g0027a0001c0002t0006g0053a0001c0002t0014g0052others(1): Show | 4 | HG02622.hp2 HG02922.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.285+232T>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155310956 | ||||||
chr6:155310999
|
T | C | 7 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0159others(4): Show | 7 | HG01168.hp2 HG01175.hp2 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.285+189A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155310999 | ||||||
chr6:155311125
|
A | G | 4 | a0001c0001t0028g0027a0001c0002t0006g0053a0001c0002t0014g0052others(1): Show | 4 | HG02622.hp2 HG02922.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.285+63T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 2/6 | chr6 | 155311125 | ||||||
chr6:155311363
|
A | T | 1 | a0001c0001t0009g0072 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.134-24T>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 1/6 | chr6 | 155311363 | ||||||
chr6:155311427
|
C | A | 1 | a0001c0002t0003g0214 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.134-88G>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 1/6 | chr6 | 155311427 | ||||||
chr6:155311628
|
T | C | 67 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0025others(64): Show | 73 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.134-289A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 1/6 | chr6 | 155311628 | ||||||
chr6:155311710
|
T | C | 59 | a0001c0001t0001g0169a0001c0001t0004g0168a0001c0001t0004g0170others(56): Show | 64 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(61): Show |
intron_variant | MODIFIER | c.134-371A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 1/6 | chr6 | 155311710 | ||||||
chr6:155311804
|
T | C | 257 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(254): Show | 284 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(281): Show |
intron_variant | MODIFIER | c.134-465A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 1/6 | chr6 | 155311804 | ||||||
chr6:155311816
|
G | C | 1 | a0001c0001t0004g0215 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.134-477C>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 1/6 | chr6 | 155311816 | ||||||
chr6:155311851
|
A | G | 1 | a0001c0001t0021g0034 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.134-512T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 1/6 | chr6 | 155311851 | ||||||
chr6:155311853
|
A | G | 1 | a0001c0001t0001g0039 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.134-514T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 1/6 | chr6 | 155311853 | ||||||
chr6:155311871
|
A | G | 4 | a0001c0002t0007g0017a0001c0002t0007g0058a0001c0002t0007g0164others(1): Show | 5 | HG02129.hp1 HG02523.hp2 NA19002.hp1 others(2): Show |
intron_variant | MODIFIER | c.134-532T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 1/6 | chr6 | 155311871 | ||||||
chr6:155311988
|
T | C | 4 | a0001c0001t0006g0005a0001c0001t0006g0230a0001c0001t0006g0232others(1): Show | 6 | HG02280.hp1 HG02723.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.134-649A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 1/6 | chr6 | 155311988 | ||||||
chr6:155312105
|
T | C | 2 | a0001c0001t0004g0216a0001c0001t0004g0217 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.134-766A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 1/6 | chr6 | 155312105 | ||||||
chr6:155312200
|
C | T | 2 | a0001c0002t0004g0038a0001c0002t0023g0037 | 2 | HG03225.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.134-861G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 1/6 | chr6 | 155312200 | ||||||
chr6:155312223
|
G | A | 2 | a0001c0001t0025g0310a0001c0001t0025g0311 | 2 | HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.134-884C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 1/6 | chr6 | 155312223 | ||||||
chr6:155312334
|
C | T | 9 | a0001c0001t0013g0028a0001c0001t0013g0030a0001c0001t0013g0031others(6): Show | 9 | HG00639.hp1 HG01109.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.134-995G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 1/6 | chr6 | 155312334 | ||||||
chr6:155312774
|
A | G | 1 | a0001c0001t0001g0071 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.134-1435T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 1/6 | chr6 | 155312774 | ||||||
chr6:155312818
|
T | C | 1 | a0001c0002t0005g0267 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.133+1478A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 1/6 | chr6 | 155312818 | ||||||
chr6:155312835
|
G | A | 2 | a0001c0002t0005g0006a0001c0002t0005g0268 | 4 | HG00280.hp1 HG01515.hp2 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.133+1461C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 1/6 | chr6 | 155312835 | ||||||
chr6:155312858
|
A | G | 13 | a0001c0001t0001g0009a0001c0001t0001g0059a0001c0001t0001g0060others(10): Show | 14 | HG00609.hp2 HG02071.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.133+1438T>C | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 1/6 | chr6 | 155312858 | ||||||
chr6:155313018
|
C | T | 1 | a0001c0002t0003g0002 | 4 | HG00733.hp1 HG01192.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.133+1278G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 1/6 | chr6 | 155313018 | ||||||
chr6:155313234
|
T | C | 5 | a0001c0001t0001g0218a0001c0002t0010g0054a0001c0002t0010g0055others(2): Show | 5 | HG03490.hp2 NA18956.hp1 NA18965.hp2 others(2): Show |
intron_variant | MODIFIER | c.133+1062A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 1/6 | chr6 | 155313234 | ||||||
chr6:155313255
|
GA | G | 11 | a0001c0001t0002g0269a0001c0001t0013g0028a0001c0001t0013g0030others(8): Show | 11 | HG01109.hp1 HG02647.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.133+1040delT | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 1/6 | chr6 | 155313255 | ||||||
chr6:155313480
|
C | T | 125 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(122): Show | 136 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(133): Show |
intron_variant | MODIFIER | c.133+816G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 1/6 | chr6 | 155313480 | ||||||
chr6:155313533
|
T | C | 47 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0025others(44): Show | 52 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.133+763A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 1/6 | chr6 | 155313533 | ||||||
chr6:155313746
|
C | T | 1 | a0001c0002t0007g0058 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.133+550G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 1/6 | chr6 | 155313746 | ||||||
chr6:155313832
|
G | A | 2 | a0001c0002t0006g0219a0001c0002t0006g0220 | 2 | HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.133+464C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 1/6 | chr6 | 155313832 | ||||||
chr6:155314028
|
C | A | 1 | a0001c0001t0014g0221 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.133+268G>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 1/6 | chr6 | 155314028 | ||||||
chr6:155314047
|
T | C | 13 | a0001c0001t0006g0005a0001c0001t0006g0222a0001c0001t0006g0223others(10): Show | 18 | HG00099.hp1 HG00733.hp1 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.133+249A>G | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 1/6 | chr6 | 155314047 | ||||||
chr6:155314147
|
G | GTTC | 193 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(190): Show | 214 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.133+146_133+148dup others(3): Show |
TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 1/6 | chr6 | 155314147 | ||||||
chr6:155314172
|
C | T | 1 | a0001c0001t0002g0236 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.133+124G>A | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 1/6 | chr6 | 155314172 | ||||||
chr6:155314261
|
G | A | 1 | a0002c0005t0039g0312 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.133+35C>T | TFB1M | ENSG00000029639.11 | transcript | ENST00000367166.5 | protein_coding | 1/6 | chr6 | 155314261 |