geneid | 22797 |
---|---|
ensemblid | ENSG00000105967.16 |
hgncid | 11754 |
symbol | TFEC |
name | transcription factor EC |
refseq_nuc | NM_012252.4 |
refseq_prot | NP_036384.1 |
ensembl_nuc | ENST00000265440.12 |
ensembl_prot | ENSP00000265440.7 |
mane_status | MANE Select |
chr | chr7 |
start | 115935152 |
end | 116030763 |
strand | - |
ver | v1.2 |
region | chr7:115935152-116030763 |
region5000 | chr7:115930152-116035763 |
regionname0 | TFEC_chr7_115935152_116030763 |
regionname5000 | TFEC_chr7_115930152_116035763 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 347 | 383 | 90 | 70 | 166 | 14 | 41 | 126 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
a0002 | 0/0 | 347 | 4 | 0 | 1 | 0 | 0 | 3 | 0 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
a0003 | 0/0 | 347 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
a0004 | 0/0 | 347 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
a0005 | 0/0 | 347 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1044 | 366 | 77 | 68 | 164 | 14 | 41 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
c0002 | 0/0 | 1044 | 7 | 6 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
c0003 | 0/0 | 1044 | 4 | 0 | 1 | 0 | 0 | 3 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
c0004 | 0/0 | 1044 | 4 | 4 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
c0005 | 0/0 | 1044 | 3 | 3 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
c0006 | 0/0 | 1044 | 3 | 0 | 3 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
c0007 | 0/0 | 1044 | 2 | 0 | 0 | 0 | 0 | 2 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
c0008 | 0/0 | 1044 | 2 | 2 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
c0009 | 0/0 | 1044 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
c0010 | 0/0 | 1044 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
c0011 | 0/0 | 1044 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 5603 | 120 | 36 | 21 | 43 | 4 | 15 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
t0002 | 0/0 | 5603 | 103 | 8 | 22 | 56 | 4 | 13 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
t0003 | 1/0 | 5603 | 64 | 6 | 15 | 37 | 1 | 4 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
t0004 | 0/0 | 5603 | 19 | 3 | 10 | 0 | 4 | 2 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
t0005 | 0/0 | 5603 | 13 | 0 | 0 | 13 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
t0006 | 0/0 | 5603 | 8 | 8 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
t0007 | 0/0 | 5603 | 7 | 6 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
t0008 | 0/0 | 5602 | 6 | 0 | 0 | 6 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
t0009 | 0/0 | 5603 | 4 | 0 | 0 | 0 | 1 | 3 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
t0010 | 0/0 | 5603 | 4 | 4 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
t0011 | 0/0 | 5603 | 3 | 0 | 0 | 3 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
t0012 | 0/0 | 5600 | 3 | 0 | 0 | 3 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
t0013 | 0/0 | 5603 | 3 | 0 | 3 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
t0014 | 0/0 | 5603 | 3 | 3 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
t0015 | 0/0 | 5603 | 3 | 3 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
t0016 | 0/0 | 5603 | 3 | 3 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
t0017 | 0/0 | 5603 | 2 | 0 | 0 | 2 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
t0018 | 0/0 | 5603 | 2 | 1 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
t0019 | 0/0 | 5603 | 2 | 2 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
t0020 | 0/0 | 5603 | 2 | 0 | 0 | 2 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
t0021 | 0/0 | 5603 | 2 | 0 | 0 | 0 | 0 | 2 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
t0022 | 0/0 | 5603 | 2 | 0 | 0 | 0 | 0 | 2 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
t0023 | 0/0 | 5603 | 2 | 2 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
t0024 | 0/0 | 5603 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
t0025 | 0/0 | 5603 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
t0026 | 0/0 | 5603 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
t0027 | 0/0 | 5603 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
t0028 | 0/0 | 5603 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
t0029 | 0/0 | 5603 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
t0030 | 0/0 | 5603 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
t0031 | 0/0 | 5603 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
t0032 | 0/0 | 5603 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
t0033 | 0/0 | 5603 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
t0034 | 0/0 | 5603 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
t0035 | 0/0 | 5603 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
t0036 | 0/0 | 5603 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
t0037 | 0/0 | 5603 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0008 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0009 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0015 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0054 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0121 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0314 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0352 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0353 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0358 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1044 | 366 | 77 | 68 | 164 | 14 | 41 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
a0001c0002 | 0/0 | 1044 | 7 | 6 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
a0001c0004 | 0/0 | 1044 | 4 | 4 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
a0001c0005 | 0/0 | 1044 | 3 | 3 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
a0001c0009 | 0/0 | 1044 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
a0001c0010 | 0/0 | 1044 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
a0001c0011 | 0/0 | 1044 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
a0002c0003 | 0/0 | 1044 | 4 | 0 | 1 | 0 | 0 | 3 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
a0003c0006 | 0/0 | 1044 | 3 | 0 | 3 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
a0004c0007 | 0/0 | 1044 | 2 | 0 | 0 | 0 | 0 | 2 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
a0005c0008 | 0/0 | 1044 | 2 | 2 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 6646 | 102 | 27 | 16 | 43 | 4 | 11 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
a0001c0001t0002 | 0/0 | 6646 | 102 | 8 | 22 | 55 | 4 | 13 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
a0001c0001t0003 | 1/0 | 6646 | 63 | 6 | 15 | 36 | 1 | 4 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
a0001c0001t0004 | 0/0 | 6646 | 18 | 3 | 9 | 0 | 4 | 2 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
a0001c0001t0005 | 0/0 | 6646 | 13 | 0 | 0 | 13 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
a0001c0001t0006 | 0/0 | 6646 | 8 | 8 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
a0001c0001t0007 | 0/0 | 6646 | 7 | 6 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
a0001c0001t0008 | 0/0 | 6645 | 6 | 0 | 0 | 6 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
a0001c0001t0009 | 0/0 | 6646 | 4 | 0 | 0 | 0 | 1 | 3 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
a0001c0001t0010 | 0/0 | 6646 | 4 | 4 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
a0001c0001t0011 | 0/0 | 6646 | 3 | 0 | 0 | 3 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
a0001c0001t0012 | 0/0 | 6643 | 3 | 0 | 0 | 3 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
a0001c0001t0013 | 0/0 | 6646 | 3 | 0 | 3 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
a0001c0001t0014 | 0/0 | 6646 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
a0001c0001t0015 | 0/0 | 6646 | 3 | 3 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
a0001c0001t0016 | 0/0 | 6646 | 3 | 3 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
a0001c0001t0017 | 0/0 | 6646 | 2 | 0 | 0 | 2 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
a0001c0001t0018 | 0/0 | 6646 | 2 | 1 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
a0001c0001t0019 | 0/0 | 6646 | 2 | 2 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
a0001c0001t0020 | 0/0 | 6646 | 2 | 0 | 0 | 2 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
a0001c0001t0021 | 0/0 | 6646 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
a0001c0001t0022 | 0/0 | 6646 | 2 | 0 | 0 | 0 | 0 | 2 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
a0001c0001t0024 | 0/0 | 6646 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
a0001c0001t0025 | 0/0 | 6646 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
a0001c0001t0026 | 0/0 | 6646 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
a0001c0001t0027 | 0/0 | 6646 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
a0001c0001t0028 | 0/0 | 6646 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
a0001c0001t0030 | 0/0 | 6646 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
a0001c0001t0031 | 0/0 | 6646 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
a0001c0001t0033 | 0/0 | 6646 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
a0001c0001t0034 | 0/0 | 6646 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
a0001c0001t0035 | 0/0 | 6646 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
a0001c0001t0036 | 0/0 | 6646 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
a0001c0001t0037 | 0/0 | 6646 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
a0001c0002t0001 | 0/0 | 6646 | 7 | 6 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
a0001c0004t0001 | 0/0 | 6646 | 3 | 3 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
a0001c0004t0029 | 0/0 | 6646 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
a0001c0005t0014 | 0/0 | 6646 | 2 | 2 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
a0001c0005t0032 | 0/0 | 6646 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
a0001c0009t0003 | 0/0 | 6646 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
a0001c0010t0002 | 0/0 | 6646 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
a0001c0011t0004 | 0/0 | 6646 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
a0002c0003t0001 | 0/0 | 6646 | 3 | 0 | 1 | 0 | 0 | 2 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
a0002c0003t0021 | 0/0 | 6646 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
a0003c0006t0001 | 0/0 | 6646 | 3 | 0 | 3 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
a0004c0007t0001 | 0/0 | 6646 | 2 | 0 | 0 | 0 | 0 | 2 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
a0005c0008t0023 | 0/0 | 6646 | 2 | 2 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | copy fasta | chr7 | 115930152 | 116035763 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0121 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0352 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0358 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0001g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0002g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0002g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0002g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0002g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0002g0015 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0002g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0002g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0002g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0002g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0002g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0002g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0002g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0002g0353 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0003g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0003g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0003g0054 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0003g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0003g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0003g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0003g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0003g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0003g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0003g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0003g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0003g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0003g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0003g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0003g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0003g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0003g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0003g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0003g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0003g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0003g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0003g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0003g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0003g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0003g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0003g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0003g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0003g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0003g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0003g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0003g0314 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0003g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0003g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0003g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0003g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0003g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0003g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0003g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0003g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0003g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0003g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0003g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0003g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0003g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0003g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0003g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0003g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0003g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0003g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0003g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0003g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0003g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0003g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0003g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0003g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0003g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0003g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0003g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0003g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0003g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0003g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0004g0008 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0004g0009 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0004g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0004g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0004g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0004g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0004g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0004g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0004g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0004g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0004g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0004g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0004g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0004g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0004g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0004g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0005g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0005g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0005g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0005g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0005g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0005g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0005g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0005g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0005g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0005g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0006g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0006g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0006g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0006g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0006g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0006g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0007g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0007g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0007g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0007g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0007g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0007g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0008g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0008g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0008g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0008g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0009g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0009g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0009g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0009g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0010g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0010g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0010g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0010g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0011g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0011g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0011g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0012g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0012g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0012g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0013g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0013g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0014g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0015g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0015g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0015g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0016g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0016g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0016g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0017g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0017g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0018g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0018g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0019g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0019g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0020g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0020g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0021g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0022g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0022g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0024g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0025g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0026g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0027g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0028g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0030g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0031g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0033g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0034g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0035g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0036g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0001t0037g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0002t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0002t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0002t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0002t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0002t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0002t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0004t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0004t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0004t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0004t0029g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0005t0014g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0005t0014g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0005t0032g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0009t0003g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0010t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0001c0011t0004g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0002c0003t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0002c0003t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0002c0003t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0002c0003t0021g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0003c0006t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0003c0006t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0003c0006t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0004c0007t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0004c0007t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0005c0008t0023g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
a0005c0008t0023g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0002 | g0353 | EUR | GBR | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG00140 | hp2 | a0001 | c0001 | t0009 | g0137 | EUR | GBR | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG00280 | hp1 | a0001 | c0001 | t0003 | g0314 | EUR | FIN | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0122 | EUR | FIN | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG00323 | hp1 | a0001 | c0001 | t0004 | g0009 | EUR | FIN | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0091 | EUR | FIN | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG00408 | hp1 | a0001 | c0001 | t0003 | g0316 | EAS | CHS | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | CHS | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | CHS | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0368 | EAS | CHS | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0256 | EAS | CHS | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | CHS | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG00609 | hp1 | a0001 | c0001 | t0003 | g0119 | EAS | CHS | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG00609 | hp2 | a0001 | c0001 | t0005 | g0019 | EAS | CHS | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | CHS | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG00621 | hp2 | a0001 | c0001 | t0003 | g0308 | EAS | CHS | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0283 | AMR | PUR | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG00639 | hp2 | a0001 | c0001 | t0004 | g0042 | AMR | PUR | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0051 | AMR | PUR | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG00673 | hp1 | a0001 | c0001 | t0003 | g0343 | EAS | CHS | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | CHS | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG00733 | hp1 | a0001 | c0001 | t0003 | g0100 | AMR | PUR | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG00733 | hp2 | a0001 | c0001 | t0004 | g0295 | AMR | PUR | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0248 | AMR | PUR | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG00735 | hp2 | a0001 | c0001 | t0003 | g0133 | AMR | PUR | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0053 | AMR | PUR | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0153 | AMR | PUR | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG00741 | hp2 | a0001 | c0001 | t0004 | g0159 | AMR | PUR | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG01069 | hp1 | a0001 | c0001 | t0003 | g0030 | AMR | PUR | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG01069 | hp2 | a0001 | c0001 | t0013 | g0012 | AMR | PUR | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG01071 | hp1 | a0001 | c0001 | t0003 | g0045 | AMR | PUR | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG01071 | hp2 | a0001 | c0001 | t0013 | g0012 | AMR | PUR | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG01074 | hp1 | a0001 | c0001 | t0013 | g0190 | AMR | PUR | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0050 | AMR | PUR | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG01099 | hp2 | a0001 | c0001 | t0003 | g0328 | AMR | PUR | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG01106 | hp1 | a0001 | c0001 | t0004 | g0008 | AMR | PUR | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0052 | AMR | PUR | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG01109 | hp1 | a0001 | c0001 | t0004 | g0155 | AMR | PUR | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0224 | AMR | PUR | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0294 | AMR | PUR | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0231 | AMR | PUR | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG01175 | hp2 | a0001 | c0001 | t0003 | g0324 | AMR | PUR | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG01192 | hp1 | a0001 | c0001 | t0003 | g0310 | AMR | PUR | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0139 | AMR | PUR | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0366 | AMR | PUR | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | CLM | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG01256 | hp1 | a0001 | c0001 | t0004 | g0157 | AMR | CLM | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG01256 | hp2 | a0001 | c0001 | t0003 | g0312 | AMR | CLM | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG01257 | hp1 | a0003 | c0006 | t0001 | g0025 | AMR | CLM | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG01257 | hp2 | a0001 | c0001 | t0003 | g0325 | AMR | CLM | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG01258 | hp1 | a0003 | c0006 | t0001 | g0023 | AMR | CLM | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG01258 | hp2 | a0001 | c0001 | t0004 | g0156 | AMR | CLM | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | CLM | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0249 | AMR | CLM | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0225 | AMR | CLM | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG01346 | hp2 | a0001 | c0001 | t0028 | g0282 | AMR | CLM | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | CLM | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0226 | AMR | CLM | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0342 | AMR | CLM | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG01361 | hp2 | a0001 | c0001 | t0007 | g0300 | AMR | CLM | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG01433 | hp1 | a0001 | c0001 | t0003 | g0299 | AMR | CLM | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG01433 | hp2 | a0001 | c0001 | t0031 | g0154 | AMR | CLM | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG01496 | hp1 | a0001 | c0002 | t0001 | g0034 | AMR | CLM | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | CLM | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0232 | EUR | IBS | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0040 | EUR | IBS | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG01517 | hp1 | a0001 | c0001 | t0002 | g0230 | EUR | IBS | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG01517 | hp2 | a0001 | c0001 | t0004 | g0009 | EUR | IBS | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG01884 | hp1 | a0001 | c0001 | t0004 | g0164 | AFR | ACB | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0200 | AFR | ACB | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG01891 | hp1 | a0001 | c0001 | t0007 | g0044 | AFR | ACB | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG01891 | hp2 | a0001 | c0002 | t0001 | g0033 | AFR | ACB | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG01928 | hp1 | a0001 | c0001 | t0003 | g0123 | AMR | PEL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PEL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG01943 | hp1 | a0001 | c0001 | t0004 | g0160 | AMR | PEL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG01943 | hp2 | a0001 | c0001 | t0003 | g0129 | AMR | PEL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0245 | AMR | PEL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG01952 | hp2 | a0001 | c0001 | t0003 | g0311 | AMR | PEL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG01978 | hp1 | a0003 | c0006 | t0001 | g0024 | AMR | PEL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG01978 | hp2 | a0001 | c0001 | t0004 | g0166 | AMR | PEL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PEL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0199 | AMR | PEL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0246 | AMR | PEL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG01993 | hp2 | a0001 | c0011 | t0004 | g0152 | AMR | PEL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG02015 | hp2 | a0001 | c0001 | t0005 | g0317 | EAS | KHV | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG02027 | hp1 | a0001 | c0001 | t0005 | g0019 | EAS | KHV | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG02027 | hp2 | a0001 | c0001 | t0011 | g0147 | EAS | KHV | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | KHV | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0261 | EAS | KHV | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | ACB | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG02055 | hp2 | a0001 | c0004 | t0001 | g0275 | AFR | ACB | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG02071 | hp1 | a0001 | c0001 | t0003 | g0337 | EAS | KHV | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0204 | EAS | KHV | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | KHV | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG02074 | hp2 | a0001 | c0001 | t0003 | g0284 | EAS | KHV | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG02080 | hp1 | a0001 | c0001 | t0003 | g0322 | EAS | KHV | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0350 | EAS | KHV | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0258 | EAS | KHV | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG02129 | hp1 | a0001 | c0009 | t0003 | g0329 | EAS | KHV | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | KHV | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG02132 | hp1 | a0001 | c0001 | t0003 | g0305 | EAS | KHV | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | KHV | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | KHV | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | KHV | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | ACB | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG02148 | hp1 | a0001 | c0001 | t0003 | g0128 | AMR | PEL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG02148 | hp2 | a0002 | c0003 | t0001 | g0094 | AMR | PEL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG02155 | hp1 | a0001 | c0001 | t0003 | g0296 | EAS | CDX | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0236 | EAS | CDX | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0211 | EAS | CDX | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG02165 | hp2 | a0001 | c0001 | t0003 | g0318 | EAS | CDX | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG02257 | hp1 | a0005 | c0008 | t0023 | g0180 | AFR | ACB | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG02257 | hp2 | a0001 | c0001 | t0004 | g0008 | AFR | ACB | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0263 | AFR | ACB | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG02258 | hp2 | a0001 | c0001 | t0006 | g0272 | AFR | ACB | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0244 | AMR | PEL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PEL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG02300 | hp1 | a0001 | c0001 | t0003 | g0319 | AMR | PEL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0247 | AMR | PEL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG02451 | hp1 | a0001 | c0001 | t0033 | g0183 | AFR | ACB | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG02451 | hp2 | a0001 | c0001 | t0016 | g0361 | AFR | ACB | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG02572 | hp1 | a0001 | c0001 | t0002 | g0151 | AFR | GWD | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | GWD | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0048 | SAS | PJL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG02615 | hp1 | a0001 | c0001 | t0015 | g0038 | AFR | GWD | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG02622 | hp1 | a0001 | c0001 | t0035 | g0179 | AFR | GWD | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | GWD | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG02630 | hp1 | a0001 | c0001 | t0003 | g0355 | AFR | GWD | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG02630 | hp2 | a0001 | c0005 | t0014 | g0029 | AFR | GWD | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG02717 | hp1 | a0001 | c0001 | t0015 | g0359 | AFR | GWD | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG02717 | hp2 | a0001 | c0002 | t0001 | g0010 | AFR | GWD | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG02723 | hp1 | a0001 | c0001 | t0007 | g0297 | AFR | GWD | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG02723 | hp2 | a0001 | c0002 | t0001 | g0010 | AFR | GWD | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG02735 | hp1 | a0001 | c0001 | t0003 | g0302 | SAS | PJL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0182 | SAS | PJL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG02738 | hp1 | a0001 | c0001 | t0009 | g0140 | SAS | PJL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0208 | SAS | PJL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG02809 | hp1 | a0001 | c0001 | t0014 | g0264 | AFR | GWD | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG02818 | hp1 | a0001 | c0001 | t0034 | g0276 | AFR | GWD | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG02818 | hp2 | a0001 | c0001 | t0003 | g0356 | AFR | GWD | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG02886 | hp1 | a0001 | c0001 | t0002 | g0229 | AFR | GWD | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG02886 | hp2 | a0001 | c0001 | t0003 | g0334 | AFR | GWD | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG02895 | hp1 | a0001 | c0001 | t0006 | g0270 | AFR | GWD | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG02895 | hp2 | a0001 | c0001 | t0007 | g0020 | AFR | GWD | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | GWD | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG02896 | hp2 | a0001 | c0001 | t0007 | g0020 | AFR | GWD | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG02922 | hp1 | a0001 | c0002 | t0001 | g0037 | AFR | ESN | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG02922 | hp2 | a0001 | c0001 | t0030 | g0170 | AFR | ESN | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG02965 | hp1 | a0001 | c0001 | t0003 | g0332 | AFR | ESN | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0362 | AFR | ESN | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG02970 | hp1 | a0001 | c0001 | t0006 | g0271 | AFR | ESN | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | ESN | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0049 | SAS | PJL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG03017 | hp2 | a0004 | c0007 | t0001 | g0032 | SAS | PJL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | GWD | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG03041 | hp2 | a0001 | c0001 | t0007 | g0298 | AFR | GWD | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG03098 | hp1 | a0001 | c0005 | t0014 | g0112 | AFR | MSL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG03098 | hp2 | a0001 | c0001 | t0003 | g0333 | AFR | MSL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | ESN | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG03130 | hp2 | a0001 | c0005 | t0032 | g0111 | AFR | ESN | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | ESN | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG03139 | hp2 | a0001 | c0002 | t0001 | g0035 | AFR | ESN | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG03195 | hp1 | a0001 | c0001 | t0024 | g0175 | AFR | ESN | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG03195 | hp2 | a0001 | c0001 | t0006 | g0004 | AFR | ESN | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG03209 | hp2 | a0001 | c0004 | t0001 | g0273 | AFR | MSL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG03225 | hp1 | a0001 | c0002 | t0001 | g0036 | AFR | MSL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0364 | AFR | MSL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG03239 | hp1 | a0001 | c0001 | t0004 | g0163 | SAS | PJL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG03239 | hp2 | a0001 | c0001 | t0026 | g0043 | SAS | PJL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG03453 | hp1 | a0001 | c0001 | t0002 | g0134 | AFR | MSL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG03453 | hp2 | a0001 | c0001 | t0010 | g0171 | AFR | MSL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | MSL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG03486 | hp2 | a0001 | c0001 | t0019 | g0168 | AFR | MSL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG03490 | hp2 | a0002 | c0003 | t0021 | g0093 | SAS | PJL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0015 | SAS | PJL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG03492 | hp1 | a0001 | c0001 | t0021 | g0099 | SAS | PJL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0015 | SAS | PJL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG03516 | hp1 | a0005 | c0008 | t0023 | g0132 | AFR | ESN | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG03516 | hp2 | a0001 | c0001 | t0002 | g0267 | AFR | ESN | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG03540 | hp1 | a0001 | c0001 | t0006 | g0274 | AFR | GWD | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG03540 | hp2 | a0001 | c0001 | t0016 | g0360 | AFR | GWD | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG03579 | hp1 | a0001 | c0001 | t0010 | g0173 | AFR | MSL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | MSL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG03654 | hp1 | a0002 | c0003 | t0001 | g0092 | SAS | PJL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG03654 | hp2 | a0002 | c0003 | t0001 | g0114 | SAS | PJL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG03669 | hp1 | a0001 | c0001 | t0009 | g0141 | SAS | PJL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0351 | SAS | STU | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | STU | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG03704 | hp2 | a0001 | c0001 | t0003 | g0330 | SAS | PJL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | PJL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0046 | SAS | PJL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG03831 | hp1 | a0001 | c0001 | t0003 | g0303 | SAS | BEB | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0095 | SAS | BEB | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG03834 | hp1 | a0004 | c0007 | t0001 | g0031 | SAS | BEB | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG03834 | hp2 | a0001 | c0001 | t0018 | g0135 | SAS | BEB | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0212 | SAS | BEB | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG03927 | hp2 | a0001 | c0001 | t0027 | g0277 | SAS | BEB | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG03942 | hp1 | a0001 | c0001 | t0022 | g0251 | SAS | BEB | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0148 | SAS | BEB | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0352 | SAS | STU | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG04115 | hp2 | a0001 | c0001 | t0037 | g0118 | SAS | STU | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG04184 | hp1 | a0001 | c0001 | t0003 | g0326 | SAS | BEB | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG04184 | hp2 | a0001 | c0001 | t0025 | g0142 | SAS | BEB | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0209 | SAS | STU | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0358 | SAS | STU | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0186 | SAS | STU | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG04204 | hp2 | a0001 | c0001 | t0022 | g0081 | SAS | STU | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0047 | SAS | STU | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0210 | SAS | STU | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA18522 | hp1 | a0001 | c0001 | t0007 | g0116 | AFR | YRI | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | YRI | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0217 | EAS | CHB | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | CHB | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA18747 | hp1 | a0001 | c0001 | t0011 | g0144 | EAS | CHB | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | CHB | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA18906 | hp1 | a0001 | c0001 | t0002 | g0149 | AFR | YRI | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA18906 | hp2 | a0001 | c0001 | t0016 | g0357 | AFR | YRI | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA18942 | hp2 | a0001 | c0001 | t0012 | g0345 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA18945 | hp1 | a0001 | c0001 | t0008 | g0003 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA18949 | hp1 | a0001 | c0001 | t0017 | g0354 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA18949 | hp2 | a0001 | c0001 | t0005 | g0290 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA18951 | hp2 | a0001 | c0001 | t0003 | g0304 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA18952 | hp1 | a0001 | c0001 | t0003 | g0309 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA18953 | hp1 | a0001 | c0001 | t0003 | g0347 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA18954 | hp2 | a0001 | c0001 | t0003 | g0280 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA18956 | hp1 | a0001 | c0010 | t0002 | g0198 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA18957 | hp2 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA18959 | hp1 | a0001 | c0001 | t0003 | g0315 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA18959 | hp2 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA18960 | hp1 | a0001 | c0001 | t0003 | g0188 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA18962 | hp1 | a0001 | c0001 | t0003 | g0321 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA18965 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA18971 | hp2 | a0001 | c0001 | t0003 | g0348 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA18973 | hp1 | a0001 | c0001 | t0020 | g0073 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA18977 | hp1 | a0001 | c0001 | t0003 | g0279 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA18978 | hp1 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA18978 | hp2 | a0001 | c0001 | t0003 | g0349 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA18979 | hp1 | a0001 | c0001 | t0017 | g0223 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA18982 | hp1 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA18983 | hp1 | a0001 | c0001 | t0003 | g0285 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA18984 | hp2 | a0001 | c0001 | t0003 | g0341 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA18991 | hp1 | a0001 | c0001 | t0003 | g0339 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA18992 | hp1 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA18992 | hp2 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA18993 | hp1 | a0001 | c0001 | t0003 | g0307 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA18994 | hp1 | a0001 | c0001 | t0008 | g0003 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA18994 | hp2 | a0001 | c0001 | t0003 | g0301 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA18995 | hp1 | a0001 | c0001 | t0008 | g0262 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA19000 | hp2 | a0001 | c0001 | t0003 | g0286 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA19001 | hp1 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA19002 | hp2 | a0001 | c0001 | t0003 | g0313 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0255 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0367 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA19010 | hp2 | a0001 | c0001 | t0003 | g0306 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA19011 | hp1 | a0001 | c0001 | t0003 | g0320 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA19012 | hp1 | a0001 | c0001 | t0003 | g0323 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA19012 | hp2 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0363 | AFR | LWK | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA19030 | hp2 | a0001 | c0001 | t0015 | g0039 | AFR | LWK | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA19043 | hp1 | a0001 | c0001 | t0002 | g0197 | AFR | LWK | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA19043 | hp2 | a0001 | c0001 | t0006 | g0004 | AFR | LWK | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA19056 | hp2 | a0001 | c0001 | t0008 | g0003 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA19057 | hp2 | a0001 | c0001 | t0012 | g0344 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA19058 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA19062 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA19062 | hp2 | a0001 | c0001 | t0011 | g0146 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA19063 | hp1 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA19063 | hp2 | a0001 | c0001 | t0005 | g0287 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA19064 | hp2 | a0001 | c0001 | t0005 | g0292 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA19065 | hp2 | a0001 | c0001 | t0003 | g0340 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA19066 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA19066 | hp2 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA19067 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA19072 | hp2 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA19074 | hp1 | a0001 | c0001 | t0005 | g0289 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA19075 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA19075 | hp2 | a0001 | c0001 | t0012 | g0346 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA19077 | hp1 | a0001 | c0001 | t0008 | g0260 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA19077 | hp2 | a0001 | c0001 | t0036 | g0336 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA19081 | hp2 | a0001 | c0001 | t0003 | g0335 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA19082 | hp1 | a0001 | c0001 | t0008 | g0259 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA19086 | hp1 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA19086 | hp2 | a0001 | c0001 | t0003 | g0278 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA19087 | hp1 | a0001 | c0001 | t0003 | g0327 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA19087 | hp2 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA19088 | hp1 | a0001 | c0001 | t0020 | g0074 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA19088 | hp2 | a0001 | c0001 | t0003 | g0338 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA19090 | hp1 | a0001 | c0001 | t0005 | g0291 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA19091 | hp2 | a0001 | c0001 | t0005 | g0293 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | YRI | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA19240 | hp2 | a0001 | c0001 | t0010 | g0172 | AFR | YRI | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0145 | AFR | ASW | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA20129 | hp2 | a0001 | c0001 | t0010 | g0131 | AFR | ASW | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0242 | EUR | TSI | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA20752 | hp2 | a0001 | c0001 | t0004 | g0162 | EUR | TSI | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA20805 | hp1 | a0001 | c0001 | t0004 | g0165 | EUR | TSI | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0281 | EUR | TSI | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA20905 | hp1 | a0001 | c0001 | t0009 | g0138 | SAS | GIH | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA20905 | hp2 | a0001 | c0001 | t0004 | g0158 | SAS | GIH | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0243 | AMR | CLM | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | CLM | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG02109 | hp1 | a0001 | c0004 | t0029 | g0268 | AFR | ACB | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0365 | AFR | ACB | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | ACB | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG02486 | hp2 | a0001 | c0001 | t0019 | g0169 | AFR | ACB | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG02559 | hp1 | a0001 | c0001 | t0006 | g0004 | AFR | ACB | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG02559 | hp2 | a0001 | c0001 | t0018 | g0136 | AFR | ACB | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG03471 | hp1 | a0001 | c0001 | t0006 | g0176 | AFR | MSL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG03471 | hp2 | a0001 | c0001 | t0003 | g0265 | AFR | MSL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0269 | AFR | USA | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
HG06807 | hp2 | a0001 | c0001 | t0004 | g0161 | AFR | USA | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA18955 | hp1 | a0001 | c0001 | t0003 | g0331 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA18955 | hp2 | a0001 | c0001 | t0005 | g0288 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | USA | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | USA | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | LWK | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
NA21309 | hp2 | a0001 | c0004 | t0001 | g0177 | AFR | LWK | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0121 | REF | REF | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0003 | g0054 | REF | REF | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:115956763
|
C | T | 1 | a0005 | 2 | HG02257.hp1 HG03516.hp1 |
missense_variant | MODERATE | c.298G>A | p.Gly100Ser | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 4/8 | 501/6646 | 298/1044 | 100/347 | chr7 | 115956763 | ||
chr7:115984338
|
C | T | 1 | a0004 | 2 | HG03017.hp2 HG03834.hp1 |
missense_variant | MODERATE | c.104G>A | p.Ser35Asn | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/8 | 307/6646 | 104/1044 | 35/347 | chr7 | 115984338 | ||
chr7:115984342
|
C | T | 1 | a0003 | 3 | HG01257.hp1 HG01258.hp1 HG01978.hp1 |
missense_variant | MODERATE | c.100G>A | p.Asp34Asn | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/8 | 303/6646 | 100/1044 | 34/347 | chr7 | 115984342 | ||
chr7:115984424
|
C | G | 1 | a0002 | 4 | HG02148.hp2 HG03490.hp2 HG03654.hp1 others(1): Show |
missense_variant | MODERATE | c.18G>C | p.Gln6His | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/8 | 221/6646 | 18/1044 | 6/347 | chr7 | 115984424 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:115940623
|
G | A | 1 | a0001c0010 | 1 | NA18956.hp1 | synonymous_variant | LOW | c.972C>T | p.Ala324Ala | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 8/8 | 1175/6646 | 972/1044 | 324/347 | chr7 | 115940623 | ||
chr7:115940839
|
G | A | 1 | a0001c0011 | 1 | HG01993.hp2 | synonymous_variant | LOW | c.756C>T | p.Ser252Ser | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 8/8 | 959/6646 | 756/1044 | 252/347 | chr7 | 115940839 | ||
chr7:115956746
|
T | G | 1 | a0001c0004 | 4 | HG02055.hp2 HG02109.hp1 HG03209.hp2 others(1): Show |
synonymous_variant | LOW | c.315A>C | p.Ser105Ser | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 4/8 | 518/6646 | 315/1044 | 105/347 | chr7 | 115956746 | ||
chr7:115956767
|
A | G | 1 | a0001c0009 | 1 | HG02129.hp1 | synonymous_variant | LOW | c.294T>C | p.Tyr98Tyr | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 4/8 | 497/6646 | 294/1044 | 98/347 | chr7 | 115956767 | ||
chr7:115984271
|
T | C | 1 | a0001c0002 | 7 | HG01496.hp1 HG01891.hp2 HG02717.hp2 others(4): Show |
synonymous_variant | LOW | c.171A>G | p.Ala57Ala | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/8 | 374/6646 | 171/1044 | 57/347 | chr7 | 115984271 | ||
chr7:115984385
|
C | T | 1 | a0001c0005 | 3 | HG02630.hp2 HG03098.hp1 HG03130.hp2 |
synonymous_variant | LOW | c.57G>A | p.Val19Val | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/8 | 260/6646 | 57/1044 | 19/347 | chr7 | 115984385 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:115935201
|
C | T | 2 | a0001c0001t0010a0005c0008t0023 | 6 | HG02257.hp1 HG03453.hp2 HG03516.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5350G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 8/8 | 5350 | chr7 | 115935201 | |||||
chr7:115935503
|
G | T | 1 | a0001c0001t0028 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5048C>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 8/8 | 5048 | chr7 | 115935503 | |||||
chr7:115935515
|
G | A | 1 | a0001c0001t0024 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5036C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 8/8 | 5036 | chr7 | 115935515 | |||||
chr7:115935688
|
T | A | 3 | a0001c0001t0014a0001c0005t0014a0001c0005t0032 | 4 | HG02630.hp2 HG02809.hp1 HG03098.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4863A>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 8/8 | 4863 | chr7 | 115935688 | |||||
chr7:115935688
|
T | C | 1 | a0001c0001t0022 | 2 | HG03942.hp1 HG04204.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4863A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 8/8 | 4863 | chr7 | 115935688 | |||||
chr7:115935697
|
A | T | 1 | a0001c0001t0025 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4854T>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 8/8 | 4854 | chr7 | 115935697 | |||||
chr7:115935712
|
T | C | 2 | a0001c0001t0033a0001c0001t0034 | 2 | HG02451.hp1 HG02818.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4839A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 8/8 | 4839 | chr7 | 115935712 | |||||
chr7:115935852
|
C | T | 2 | a0001c0001t0021a0002c0003t0021 | 2 | HG03490.hp2 HG03492.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4699G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 8/8 | 4699 | chr7 | 115935852 | |||||
chr7:115935883
|
AC | A | 1 | a0001c0001t0008 | 6 | NA18945.hp1 NA18994.hp1 NA18995.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4667delG | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 8/8 | 4667 | chr7 | 115935883 | |||||
chr7:115935903
|
G | A | 1 | a0001c0001t0031 | 1 | HG01433.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4648C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 8/8 | 4648 | chr7 | 115935903 | |||||
chr7:115935907
|
A | G | 1 | a0001c0001t0020 | 2 | NA18973.hp1 NA19088.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4644T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 8/8 | 4644 | chr7 | 115935907 | |||||
chr7:115936080
|
A | C | 1 | a0001c0001t0013 | 3 | HG01069.hp2 HG01071.hp2 HG01074.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4471T>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 8/8 | 4471 | chr7 | 115936080 | |||||
chr7:115936165
|
AATG | A | 1 | a0001c0001t0012 | 3 | NA18942.hp2 NA19057.hp2 NA19075.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4383_*4385delCAT | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 8/8 | 4383 | chr7 | 115936165 | |||||
chr7:115936418
|
G | A | 2 | a0001c0001t0033a0001c0001t0034 | 2 | HG02451.hp1 HG02818.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4133C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 8/8 | 4133 | chr7 | 115936418 | |||||
chr7:115936746
|
T | G | 1 | a0001c0001t0026 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3805A>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 8/8 | 3805 | chr7 | 115936746 | |||||
chr7:115936827
|
A | C | 2 | a0001c0001t0033a0001c0001t0034 | 2 | HG02451.hp1 HG02818.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3724T>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 8/8 | 3724 | chr7 | 115936827 | |||||
chr7:115937134
|
A | T | 2 | a0001c0001t0009a0001c0001t0018 | 6 | HG00140.hp2 HG02559.hp2 HG02738.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3417T>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 8/8 | 3417 | chr7 | 115937134 | |||||
chr7:115937158
|
G | A | 1 | a0001c0004t0029 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3393C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 8/8 | 3393 | chr7 | 115937158 | |||||
chr7:115937165
|
G | A | 1 | a0001c0004t0029 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3386C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 8/8 | 3386 | chr7 | 115937165 | |||||
chr7:115937369
|
G | T | 1 | a0001c0001t0033 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3182C>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 8/8 | 3182 | chr7 | 115937369 | |||||
chr7:115937608
|
T | A | 4 | a0001c0001t0004a0001c0001t0030a0001c0001t0031others(1): Show | 21 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*2943A>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 8/8 | 2943 | chr7 | 115937608 | |||||
chr7:115937698
|
A | G | 1 | a0001c0001t0027 | 1 | HG03927.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2853T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 8/8 | 2853 | chr7 | 115937698 | |||||
chr7:115937760
|
C | T | 1 | a0001c0001t0011 | 3 | HG02027.hp2 NA18747.hp1 NA19062.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2791G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 8/8 | 2791 | chr7 | 115937760 | |||||
chr7:115938050
|
T | C | 3 | a0001c0001t0004a0001c0001t0031a0001c0011t0004 | 20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*2501A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 8/8 | 2501 | chr7 | 115938050 | |||||
chr7:115938070
|
G | T | 39 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(36): Show | 303 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(300): Show |
3_prime_UTR_variant | MODIFIER | c.*2481C>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 8/8 | 2481 | chr7 | 115938070 | |||||
chr7:115938081
|
T | C | 1 | a0001c0001t0030 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2470A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 8/8 | 2470 | chr7 | 115938081 | |||||
chr7:115938387
|
T | C | 3 | a0001c0001t0004a0001c0001t0031a0001c0011t0004 | 20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*2164A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 8/8 | 2164 | chr7 | 115938387 | |||||
chr7:115938571
|
C | A | 1 | a0001c0001t0024 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1980G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 8/8 | 1980 | chr7 | 115938571 | |||||
chr7:115938613
|
T | G | 26 | a0001c0001t0001a0001c0001t0004a0001c0001t0006others(23): Show | 173 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(170): Show |
3_prime_UTR_variant | MODIFIER | c.*1938A>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 8/8 | 1938 | chr7 | 115938613 | |||||
chr7:115938746
|
T | A | 3 | a0001c0001t0004a0001c0001t0031a0001c0011t0004 | 20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1805A>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 8/8 | 1805 | chr7 | 115938746 | |||||
chr7:115938761
|
A | G | 1 | a0001c0001t0005 | 13 | HG00609.hp2 HG02015.hp2 HG02027.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1790T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 8/8 | 1790 | chr7 | 115938761 | |||||
chr7:115938950
|
T | C | 1 | a0001c0005t0032 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1601A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 8/8 | 1601 | chr7 | 115938950 | |||||
chr7:115939038
|
G | A | 2 | a0001c0001t0033a0001c0001t0034 | 2 | HG02451.hp1 HG02818.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1513C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 8/8 | 1513 | chr7 | 115939038 | |||||
chr7:115939202
|
T | C | 1 | a0001c0001t0015 | 3 | HG02615.hp1 HG02717.hp1 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1349A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 8/8 | 1349 | chr7 | 115939202 | |||||
chr7:115939264
|
A | T | 1 | a0001c0001t0019 | 2 | HG02486.hp2 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1287T>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 8/8 | 1287 | chr7 | 115939264 | |||||
chr7:115939342
|
G | T | 1 | a0001c0001t0018 | 2 | HG02559.hp2 HG03834.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1209C>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 8/8 | 1209 | chr7 | 115939342 | |||||
chr7:115939419
|
T | C | 1 | a0001c0001t0006 | 8 | HG02258.hp2 HG02559.hp1 HG02895.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1132A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 8/8 | 1132 | chr7 | 115939419 | |||||
chr7:115939617
|
C | T | 1 | a0001c0001t0017 | 2 | NA18949.hp1 NA18979.hp1 |
3_prime_UTR_variant | MODIFIER | c.*934G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 8/8 | 934 | chr7 | 115939617 | |||||
chr7:115939778
|
G | A | 1 | a0001c0001t0035 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*773C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 8/8 | 773 | chr7 | 115939778 | |||||
chr7:115939818
|
C | G | 1 | a0001c0001t0007 | 7 | HG01361.hp2 HG01891.hp1 HG02723.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*733G>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 8/8 | 733 | chr7 | 115939818 | |||||
chr7:115939976
|
T | C | 1 | a0001c0001t0016 | 3 | HG02451.hp2 HG03540.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*575A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 8/8 | 575 | chr7 | 115939976 | |||||
chr7:115939995
|
T | C | 1 | a0001c0001t0024 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*556A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 8/8 | 556 | chr7 | 115939995 | |||||
chr7:115940059
|
G | A | 1 | a0001c0001t0036 | 1 | NA19077.hp2 | 3_prime_UTR_variant | MODIFIER | c.*492C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 8/8 | 492 | chr7 | 115940059 | |||||
chr7:115940317
|
T | C | 1 | a0005c0008t0023 | 2 | HG02257.hp1 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*234A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 8/8 | 234 | chr7 | 115940317 | |||||
chr7:115984497
|
T | C | 1 | a0001c0001t0037 | 1 | HG04115.hp2 | 5_prime_UTR_variant | MODIFIER | c.-56A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/8 | 56 | chr7 | 115984497 | |||||
chr7:115984509
|
G | T | 1 | a0001c0001t0024 | 1 | HG03195.hp1 | 5_prime_UTR_variant | MODIFIER | c.-68C>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/8 | 68 | chr7 | 115984509 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:115941089
|
C | T | 2 | a0005c0008t0023g0132a0005c0008t0023g0180 | 2 | HG02257.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.664-158G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 7/7 | chr7 | 115941089 | ||||||
chr7:115941413
|
C | T | 8 | a0001c0001t0001g0011a0001c0001t0001g0150a0001c0001t0001g0167others(5): Show | 9 | HG02572.hp2 HG02622.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.663+480G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 7/7 | chr7 | 115941413 | ||||||
chr7:115941516
|
G | A | 1 | a0001c0001t0024g0175 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.663+377C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 7/7 | chr7 | 115941516 | ||||||
chr7:115941764
|
G | A | 1 | a0001c0001t0003g0304 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.663+129C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 7/7 | chr7 | 115941764 | ||||||
chr7:115941805
|
G | A | 2 | a0001c0001t0003g0339a0001c0001t0003g0340 | 2 | NA18991.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.663+88C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 7/7 | chr7 | 115941805 | ||||||
chr7:115942277
|
G | A | 4 | a0001c0001t0002g0230a0001c0001t0002g0231a0001c0001t0002g0232others(1): Show | 4 | HG01175.hp1 HG01516.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.516-237C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115942277 | ||||||
chr7:115942303
|
T | C | 1 | a0001c0001t0003g0302 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.516-263A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115942303 | ||||||
chr7:115942542
|
T | G | 1 | a0001c0001t0001g0077 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.516-502A>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115942542 | ||||||
chr7:115942715
|
T | A | 1 | a0001c0001t0014g0264 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.516-675A>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115942715 | ||||||
chr7:115942732
|
G | A | 1 | a0001c0001t0002g0211 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.516-692C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115942732 | ||||||
chr7:115942776
|
G | A | 2 | a0001c0001t0010g0171a0001c0001t0010g0172 | 2 | HG03453.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.516-736C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115942776 | ||||||
chr7:115942902
|
A | G | 1 | a0001c0001t0002g0244 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.516-862T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115942902 | ||||||
chr7:115942953
|
C | T | 4 | a0001c0001t0001g0167a0001c0001t0002g0007a0001c0001t0002g0151others(1): Show | 5 | HG01074.hp2 HG01192.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.516-913G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115942953 | ||||||
chr7:115942959
|
G | A | 1 | a0001c0011t0004g0152 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.516-919C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115942959 | ||||||
chr7:115942964
|
T | C | 1 | a0001c0001t0002g0139 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.516-924A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115942964 | ||||||
chr7:115942985
|
G | T | 18 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0042others(15): Show | 20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.516-945C>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115942985 | ||||||
chr7:115942986
|
G | T | 1 | a0001c0001t0001g0351 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.516-946C>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115942986 | ||||||
chr7:115943051
|
T | C | 116 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0013others(113): Show | 128 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.516-1011A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115943051 | ||||||
chr7:115943145
|
TCAATGGA others(5): Show |
T | 1 | a0001c0001t0030g0170 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.516-1117_516-1106d others(14): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115943145 | ||||||
chr7:115943206
|
G | A | 1 | a0001c0001t0001g0021 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.516-1166C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115943206 | ||||||
chr7:115943403
|
G | A | 19 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0042others(16): Show | 21 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.516-1363C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115943403 | ||||||
chr7:115943510
|
ACACAATG others(4228): Show |
A | 5 | a0001c0001t0003g0304a0001c0001t0003g0318a0001c0001t0003g0323others(2): Show | 5 | HG01099.hp2 HG02165.hp2 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.515+3129_516-1471d others(2): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115943510 | ||||||
chr7:115943606
|
T | C | 7 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0083others(4): Show | 7 | HG02015.hp1 NA18747.hp2 NA18945.hp2 others(4): Show |
intron_variant | MODIFIER | c.516-1566A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115943606 | ||||||
chr7:115943647
|
T | C | 3 | a0001c0001t0001g0101a0002c0003t0001g0092a0002c0003t0001g0094 | 3 | HG02148.hp2 HG03490.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.516-1607A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115943647 | ||||||
chr7:115943659
|
A | T | 1 | a0001c0001t0002g0001 | 4 | NA18943.hp1 NA18954.hp1 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.516-1619T>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115943659 | ||||||
chr7:115943758
|
G | A | 1 | a0001c0001t0002g0234 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.516-1718C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115943758 | ||||||
chr7:115943868
|
T | G | 1 | a0001c0001t0030g0170 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.516-1828A>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115943868 | ||||||
chr7:115943906
|
GTACAATC | G | 7 | a0001c0001t0010g0131a0001c0001t0010g0171a0001c0001t0010g0172others(4): Show | 7 | HG02257.hp1 HG02622.hp1 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.516-1873_516-1867d others(9): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115943906 | ||||||
chr7:115943915
|
G | T | 7 | a0001c0001t0010g0131a0001c0001t0010g0171a0001c0001t0010g0172others(4): Show | 7 | HG02257.hp1 HG02622.hp1 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.516-1875C>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115943915 | ||||||
chr7:115943965
|
T | A | 106 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0028others(103): Show | 111 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.516-1925A>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115943965 | ||||||
chr7:115943996
|
T | A | 1 | a0001c0001t0003g0334 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.516-1956A>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115943996 | ||||||
chr7:115944013
|
A | AT | 24 | a0001c0001t0001g0011a0001c0001t0001g0167a0001c0001t0001g0184others(21): Show | 26 | HG01175.hp2 HG01361.hp2 HG01952.hp2 others(23): Show |
intron_variant | MODIFIER | c.516-1974dupA | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115944013 | ||||||
chr7:115944013
|
A | ATT | 6 | a0001c0001t0001g0181a0001c0001t0003g0128a0001c0001t0003g0343others(3): Show | 8 | HG00673.hp1 HG02148.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.516-1975_516-1974d others(4): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115944013 | ||||||
chr7:115944013
|
A | ATTTTT | 9 | a0001c0001t0001g0063a0001c0001t0001g0071a0001c0001t0001g0076others(6): Show | 9 | HG00741.hp2 HG01257.hp1 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.516-1978_516-1974d others(7): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115944013 | ||||||
chr7:115944013
|
A | ATTTTTTT others(3): Show |
2 | a0001c0001t0001g0109a0001c0001t0002g0203 | 2 | HG02145.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.516-1983_516-1974d others(12): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115944013 | ||||||
chr7:115944013
|
A | ATTTTTTT others(5): Show |
1 | a0001c0001t0002g0153 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.516-1985_516-1974d others(14): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115944013 | ||||||
chr7:115944013
|
A | ATTTTTTT others(6): Show |
4 | a0001c0001t0001g0022a0001c0004t0001g0177a0001c0004t0001g0273others(1): Show | 4 | HG02055.hp2 HG03209.hp2 NA21309.hp1 others(1): Show |
intron_variant | MODIFIER | c.516-1986_516-1974d others(15): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115944013 | ||||||
chr7:115944013
|
A | ATTTTTTT others(7): Show |
4 | a0001c0001t0004g0166a0001c0001t0024g0175a0001c0001t0028g0282others(1): Show | 4 | HG01346.hp2 HG01978.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.516-1987_516-1974d others(16): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115944013 | ||||||
chr7:115944013
|
A | ATTTTTTT others(8): Show |
8 | a0001c0001t0001g0061a0001c0001t0001g0110a0001c0001t0004g0009others(5): Show | 9 | HG00323.hp1 HG00639.hp2 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.516-1988_516-1974d others(17): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115944013 | ||||||
chr7:115944013
|
A | ATTTTTTT others(9): Show |
22 | a0001c0001t0001g0060a0001c0001t0001g0064a0001c0001t0001g0069others(19): Show | 24 | HG00733.hp2 HG01069.hp2 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.516-1989_516-1974d others(18): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115944013 | ||||||
chr7:115944013
|
A | ATTTTTTT others(10): Show |
24 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0057others(21): Show | 24 | HG00280.hp2 HG00621.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.516-1990_516-1974d others(19): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115944013 | ||||||
chr7:115944013
|
A | ATTTTTTT others(11): Show |
13 | a0001c0001t0001g0028a0001c0001t0001g0120a0001c0001t0001g0126others(10): Show | 14 | HG00741.hp1 HG01109.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.516-1991_516-1974d others(20): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115944013 | ||||||
chr7:115944013
|
A | ATTTTTTT others(12): Show |
23 | a0001c0001t0001g0125a0001c0001t0002g0007a0001c0001t0002g0051others(20): Show | 26 | HG00558.hp1 HG00642.hp1 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.516-1992_516-1974d others(21): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115944013 | ||||||
chr7:115944013
|
A | ATTTTTTT others(13): Show |
27 | a0001c0001t0002g0018a0001c0001t0002g0047a0001c0001t0002g0048others(24): Show | 28 | HG00735.hp1 HG01099.hp1 HG01123.hp1 others(25): Show |
intron_variant | MODIFIER | c.516-1993_516-1974d others(22): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115944013 | ||||||
chr7:115944013
|
A | ATTTTTTT others(14): Show |
17 | a0001c0001t0001g0362a0001c0001t0001g0365a0001c0001t0002g0046others(14): Show | 17 | HG00423.hp1 HG00738.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.516-1994_516-1974d others(23): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115944013 | ||||||
chr7:115944013
|
A | ATTTTTTT others(15): Show |
15 | a0001c0001t0001g0078a0001c0001t0001g0263a0001c0001t0001g0364others(12): Show | 16 | HG00140.hp2 HG00673.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.516-1995_516-1974d others(24): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115944013 | ||||||
chr7:115944013
|
A | ATTTTTTT others(16): Show |
14 | a0001c0001t0001g0363a0001c0001t0002g0013a0001c0001t0002g0052others(11): Show | 15 | HG00408.hp2 HG01106.hp2 HG01516.hp1 others(12): Show |
intron_variant | MODIFIER | c.516-1996_516-1974d others(25): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115944013 | ||||||
chr7:115944013
|
A | ATTTTTTT others(17): Show |
10 | a0001c0001t0002g0149a0001c0001t0002g0202a0001c0001t0002g0205others(7): Show | 10 | HG02630.hp2 HG03130.hp2 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.516-1997_516-1974d others(26): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115944013 | ||||||
chr7:115944013
|
A | ATTTTTTT others(18): Show |
6 | a0001c0001t0001g0059a0001c0001t0001g0366a0001c0001t0002g0194others(3): Show | 6 | HG01175.hp1 HG01243.hp2 NA18978.hp1 others(3): Show |
intron_variant | MODIFIER | c.516-1998_516-1974d others(27): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115944013 | ||||||
chr7:115944013
|
A | ATTTTTTT others(19): Show |
4 | a0001c0001t0001g0058a0001c0001t0002g0049a0001c0001t0002g0219others(1): Show | 4 | HG02027.hp2 HG03017.hp1 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.516-1999_516-1974d others(28): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115944013 | ||||||
chr7:115944013
|
A | ATTTTTTT others(20): Show |
1 | a0001c0001t0002g0283 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.516-2000_516-1974d others(29): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115944013 | ||||||
chr7:115944013
|
A | ATTTTTTT others(21): Show |
2 | a0001c0001t0002g0353a0001c0001t0009g0140 | 2 | HG00140.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.516-1974_516-1973i others(30): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115944013 | ||||||
chr7:115944013
|
A | ATTTTTTT others(23): Show |
1 | a0001c0005t0014g0112 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.516-1974_516-1973i others(32): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115944013 | ||||||
chr7:115944013
|
AT | A | 7 | a0001c0001t0002g0213a0001c0001t0003g0280a0001c0001t0003g0301others(4): Show | 7 | HG02257.hp1 HG02818.hp2 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.516-1974delA | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115944013 | ||||||
chr7:115944013
|
ATTTTTT | A | 31 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0055others(28): Show | 34 | HG00323.hp2 HG00423.hp2 HG01255.hp1 others(31): Show |
intron_variant | MODIFIER | c.516-1979_516-1974d others(8): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115944013 | ||||||
chr7:115944013
|
ATTTTTTT others(5): Show |
A | 1 | a0001c0001t0010g0131 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.516-1985_516-1974d others(14): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115944013 | ||||||
chr7:115944047
|
A | G | 3 | a0001c0001t0004g0155a0001c0001t0004g0156a0001c0001t0004g0157 | 3 | HG01109.hp1 HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.516-2007T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115944047 | ||||||
chr7:115944132
|
T | C | 1 | a0001c0001t0001g0040 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.516-2092A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115944132 | ||||||
chr7:115944145
|
A | G | 1 | a0001c0001t0030g0170 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.516-2105T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115944145 | ||||||
chr7:115944192
|
T | C | 1 | a0001c0001t0001g0068 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.516-2152A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115944192 | ||||||
chr7:115944321
|
A | C | 1 | a0001c0001t0030g0170 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.516-2281T>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115944321 | ||||||
chr7:115944381
|
G | C | 1 | a0001c0001t0002g0267 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.516-2341C>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115944381 | ||||||
chr7:115944392
|
G | T | 1 | a0001c0001t0003g0332 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.516-2352C>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115944392 | ||||||
chr7:115944405
|
C | T | 1 | a0001c0001t0001g0071 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.516-2365G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115944405 | ||||||
chr7:115944514
|
T | G | 106 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0028others(103): Show | 111 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.516-2474A>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115944514 | ||||||
chr7:115944791
|
A | G | 9 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0161others(6): Show | 11 | HG00323.hp1 HG00733.hp2 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.516-2751T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115944791 | ||||||
chr7:115944973
|
G | A | 4 | a0001c0001t0001g0011a0001c0001t0001g0150a0001c0001t0001g0181others(1): Show | 5 | HG02572.hp2 HG02809.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.516-2933C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115944973 | ||||||
chr7:115945061
|
A | G | 1 | a0001c0001t0003g0301 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.516-3021T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115945061 | ||||||
chr7:115945063
|
T | A | 11 | a0001c0001t0003g0119a0001c0001t0003g0123a0001c0001t0003g0307others(8): Show | 11 | HG00609.hp1 HG00621.hp2 HG00673.hp1 others(8): Show |
intron_variant | MODIFIER | c.516-3023A>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115945063 | ||||||
chr7:115945122
|
AC | A | 118 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0013others(115): Show | 130 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.516-3083delG | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115945122 | ||||||
chr7:115945140
|
CT | C | 146 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0021others(143): Show | 155 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.516-3101delA | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115945140 | ||||||
chr7:115945198
|
G | A | 1 | a0001c0001t0001g0189 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.516-3158C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115945198 | ||||||
chr7:115945383
|
A | G | 2 | a0001c0001t0033g0183a0001c0001t0034g0276 | 2 | HG02451.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.516-3343T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115945383 | ||||||
chr7:115945503
|
G | C | 7 | a0001c0001t0001g0060a0001c0001t0001g0263a0001c0001t0001g0362others(4): Show | 7 | HG01243.hp2 HG02055.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.516-3463C>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115945503 | ||||||
chr7:115945601
|
C | T | 281 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0011others(278): Show | 303 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(300): Show |
intron_variant | MODIFIER | c.516-3561G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115945601 | ||||||
chr7:115945613
|
T | C | 1 | a0001c0001t0030g0170 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.516-3573A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115945613 | ||||||
chr7:115945634
|
T | A | 81 | a0001c0001t0002g0001a0001c0001t0002g0013a0001c0001t0002g0014others(78): Show | 92 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.516-3594A>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115945634 | ||||||
chr7:115945704
|
C | A | 1 | a0001c0001t0003g0321 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.516-3664G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115945704 | ||||||
chr7:115945718
|
T | C | 18 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0042others(15): Show | 20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.516-3678A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115945718 | ||||||
chr7:115945785
|
T | C | 115 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0026others(112): Show | 120 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.516-3745A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115945785 | ||||||
chr7:115945817
|
C | T | 281 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0011others(278): Show | 303 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(300): Show |
intron_variant | MODIFIER | c.516-3777G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115945817 | ||||||
chr7:115945890
|
C | T | 1 | a0001c0001t0003g0279 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.516-3850G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115945890 | ||||||
chr7:115945944
|
G | A | 1 | a0001c0001t0014g0264 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.516-3904C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115945944 | ||||||
chr7:115945983
|
C | A | 1 | a0001c0001t0001g0028 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.516-3943G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115945983 | ||||||
chr7:115946012
|
A | G | 1 | a0001c0001t0002g0050 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.516-3972T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115946012 | ||||||
chr7:115946069
|
T | C | 1 | a0001c0001t0001g0021 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.516-4029A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115946069 | ||||||
chr7:115946089
|
T | A | 11 | a0001c0001t0001g0178a0001c0001t0006g0004a0001c0001t0006g0176others(8): Show | 13 | HG02055.hp2 HG02109.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.516-4049A>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115946089 | ||||||
chr7:115946095
|
C | A | 1 | a0001c0001t0001g0178 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.516-4055G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115946095 | ||||||
chr7:115946261
|
C | T | 1 | a0001c0001t0016g0357 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.516-4221G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115946261 | ||||||
chr7:115946275
|
A | G | 11 | a0001c0001t0001g0178a0001c0001t0006g0004a0001c0001t0006g0176others(8): Show | 13 | HG02055.hp2 HG02109.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.516-4235T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115946275 | ||||||
chr7:115946333
|
T | A | 2 | a0005c0008t0023g0132a0005c0008t0023g0180 | 2 | HG02257.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.516-4293A>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115946333 | ||||||
chr7:115946380
|
A | T | 106 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0028others(103): Show | 111 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.516-4340T>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115946380 | ||||||
chr7:115946396
|
C | CGT | 23 | a0001c0001t0001g0187a0001c0001t0002g0014a0001c0001t0002g0143others(20): Show | 24 | HG02027.hp2 HG02071.hp2 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.516-4358_516-4357d others(4): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115946396 | ||||||
chr7:115946396
|
C | CGTGT | 47 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0017others(44): Show | 52 | HG00558.hp1 HG00673.hp2 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.516-4360_516-4357d others(6): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115946396 | ||||||
chr7:115946396
|
C | CGTGTGT | 43 | a0001c0001t0002g0013a0001c0001t0002g0015a0001c0001t0002g0016others(40): Show | 47 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(44): Show |
intron_variant | MODIFIER | c.516-4362_516-4357d others(8): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115946396 | ||||||
chr7:115946396
|
C | CGTGTGTG others(1): Show |
5 | a0001c0001t0002g0048a0001c0001t0002g0186a0001c0001t0002g0199others(2): Show | 5 | HG01981.hp2 HG02602.hp1 HG04204.hp1 others(2): Show |
intron_variant | MODIFIER | c.516-4364_516-4357d others(10): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115946396 | ||||||
chr7:115946396
|
C | CGTGTGTG others(3): Show |
12 | a0001c0001t0002g0046a0001c0001t0002g0200a0001c0001t0002g0205others(9): Show | 14 | HG01261.hp2 HG01884.hp2 HG01952.hp1 others(11): Show |
intron_variant | MODIFIER | c.516-4366_516-4357d others(12): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115946396 | ||||||
chr7:115946396
|
C | CGTGTGTG others(5): Show |
1 | a0001c0001t0008g0259 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.516-4368_516-4357d others(14): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115946396 | ||||||
chr7:115946396
|
C | CGTGTGTG others(7): Show |
1 | a0001c0001t0009g0140 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.516-4370_516-4357d others(16): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115946396 | ||||||
chr7:115946396
|
CGT | C | 71 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0022others(68): Show | 79 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.516-4358_516-4357d others(4): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115946396 | ||||||
chr7:115946396
|
CGTGT | C | 10 | a0001c0001t0001g0178a0001c0001t0003g0326a0001c0001t0006g0004others(7): Show | 12 | HG02258.hp2 HG02451.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.516-4360_516-4357d others(6): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115946396 | ||||||
chr7:115946396
|
CGTGTGT | C | 6 | a0001c0001t0001g0269a0001c0001t0004g0155a0001c0001t0004g0156others(3): Show | 6 | HG00741.hp2 HG01109.hp1 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.516-4362_516-4357d others(8): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115946396 | ||||||
chr7:115946419
|
G | GTGTT | 5 | a0001c0001t0001g0026a0001c0001t0001g0027a0003c0006t0001g0023others(2): Show | 5 | HG01255.hp2 HG01257.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.516-4380_516-4379i others(6): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115946419 | ||||||
chr7:115946419
|
G | GTT | 73 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0057others(70): Show | 75 | HG00280.hp2 HG00558.hp2 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.516-4380_516-4379i others(4): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115946419 | ||||||
chr7:115946419
|
G | T | 32 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0055others(29): Show | 35 | HG00323.hp2 HG00423.hp2 HG01255.hp1 others(32): Show |
intron_variant | MODIFIER | c.516-4379C>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115946419 | ||||||
chr7:115946478
|
C | T | 1 | a0001c0002t0001g0036 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.515+4396G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115946478 | ||||||
chr7:115946510
|
G | T | 2 | a0001c0001t0018g0135a0001c0001t0018g0136 | 2 | HG02559.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.515+4364C>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115946510 | ||||||
chr7:115946622
|
TTCTC | T | 128 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0021others(125): Show | 135 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.515+4248_515+4251d others(6): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115946622 | ||||||
chr7:115946641
|
TTTTC | T | 15 | a0001c0001t0001g0011a0001c0001t0001g0150a0001c0001t0001g0167others(12): Show | 16 | HG02257.hp1 HG02572.hp2 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.515+4229_515+4232d others(6): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115946641 | ||||||
chr7:115946650
|
T | A | 1 | a0001c0001t0014g0264 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.515+4224A>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115946650 | ||||||
chr7:115946734
|
G | A | 1 | a0001c0001t0001g0068 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.515+4140C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115946734 | ||||||
chr7:115946789
|
T | C | 111 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0026others(108): Show | 116 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.515+4085A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115946789 | ||||||
chr7:115947027
|
G | A | 1 | a0001c0001t0001g0358 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.515+3847C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115947027 | ||||||
chr7:115947155
|
G | A | 18 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0042others(15): Show | 20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.515+3719C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115947155 | ||||||
chr7:115947210
|
G | T | 1 | a0001c0001t0001g0187 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.515+3664C>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115947210 | ||||||
chr7:115947367
|
C | T | 13 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0178others(10): Show | 15 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.515+3507G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115947367 | ||||||
chr7:115947368
|
T | C | 13 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0178others(10): Show | 15 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.515+3506A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115947368 | ||||||
chr7:115947482
|
A | G | 18 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0042others(15): Show | 20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.515+3392T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115947482 | ||||||
chr7:115947489
|
C | T | 18 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0042others(15): Show | 20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.515+3385G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115947489 | ||||||
chr7:115947743
|
G | A | 4 | a0001c0001t0009g0137a0001c0001t0009g0138a0001c0001t0009g0140others(1): Show | 4 | HG00140.hp2 HG02738.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.515+3131C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115947743 | ||||||
chr7:115947771
|
G | GT | 283 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0011others(280): Show | 305 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(302): Show |
intron_variant | MODIFIER | c.515+3102dupA | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115947771 | ||||||
chr7:115947913
|
GT | G | 4 | a0001c0001t0014g0264a0001c0005t0014g0029a0001c0005t0014g0112others(1): Show | 4 | HG02630.hp2 HG02809.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.515+2960delA | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115947913 | ||||||
chr7:115948122
|
T | C | 19 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0042others(16): Show | 21 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.515+2752A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115948122 | ||||||
chr7:115948210
|
C | T | 2 | a0001c0001t0033g0183a0001c0001t0034g0276 | 2 | HG02451.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.515+2664G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115948210 | ||||||
chr7:115948364
|
C | G | 7 | a0001c0001t0010g0131a0001c0001t0010g0171a0001c0001t0010g0172others(4): Show | 7 | HG02257.hp1 HG02622.hp1 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.515+2510G>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115948364 | ||||||
chr7:115948473
|
A | C | 1 | a0001c0001t0002g0149 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.515+2401T>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115948473 | ||||||
chr7:115948474
|
G | A | 1 | a0001c0001t0002g0149 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.515+2400C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115948474 | ||||||
chr7:115948561
|
T | C | 1 | a0001c0001t0002g0148 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.515+2313A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115948561 | ||||||
chr7:115948581
|
G | A | 1 | a0001c0001t0002g0145 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.515+2293C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115948581 | ||||||
chr7:115948692
|
C | T | 1 | a0001c0001t0030g0170 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.515+2182G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115948692 | ||||||
chr7:115948855
|
T | C | 3 | a0001c0001t0003g0265a0001c0001t0003g0355a0001c0001t0003g0356 | 3 | HG02630.hp1 HG02818.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.515+2019A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115948855 | ||||||
chr7:115949064
|
C | T | 2 | a0001c0001t0024g0175a0001c0001t0030g0170 | 2 | HG02922.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.515+1810G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115949064 | ||||||
chr7:115949083
|
T | C | 7 | a0001c0001t0001g0060a0001c0001t0001g0263a0001c0001t0001g0362others(4): Show | 7 | HG01243.hp2 HG02055.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.515+1791A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115949083 | ||||||
chr7:115949093
|
T | C | 95 | a0001c0001t0002g0001a0001c0001t0002g0013a0001c0001t0002g0014others(92): Show | 106 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.515+1781A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115949093 | ||||||
chr7:115949114
|
A | T | 1 | a0001c0001t0016g0361 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.515+1760T>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115949114 | ||||||
chr7:115949178
|
A | C | 116 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0013others(113): Show | 128 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.515+1696T>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115949178 | ||||||
chr7:115949188
|
G | T | 1 | a0001c0001t0002g0204 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.515+1686C>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115949188 | ||||||
chr7:115949245
|
A | G | 8 | a0001c0001t0002g0013a0001c0001t0002g0194a0001c0001t0002g0195others(5): Show | 9 | HG00408.hp2 NA18942.hp1 NA18956.hp1 others(6): Show |
intron_variant | MODIFIER | c.515+1629T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115949245 | ||||||
chr7:115949265
|
C | A | 1 | a0001c0001t0033g0183 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.515+1609G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115949265 | ||||||
chr7:115949388
|
C | T | 3 | a0001c0001t0003g0304a0001c0001t0003g0318a0001c0001t0003g0323 | 3 | HG02165.hp2 NA18951.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.515+1486G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115949388 | ||||||
chr7:115949438
|
T | G | 1 | a0001c0001t0037g0118 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.515+1436A>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115949438 | ||||||
chr7:115949547
|
A | G | 1 | a0001c0001t0001g0096 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.515+1327T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115949547 | ||||||
chr7:115949547
|
A | T | 1 | a0001c0001t0003g0306 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.515+1327T>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115949547 | ||||||
chr7:115949650
|
G | T | 18 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0042others(15): Show | 20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.515+1224C>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115949650 | ||||||
chr7:115949669
|
C | A | 1 | a0001c0001t0001g0269 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.515+1205G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115949669 | ||||||
chr7:115949938
|
C | T | 1 | a0001c0001t0024g0175 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.515+936G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115949938 | ||||||
chr7:115950015
|
C | CTT | 264 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0021others(261): Show | 285 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(282): Show |
intron_variant | MODIFIER | c.515+857_515+858dup others(2): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115950015 | ||||||
chr7:115950015
|
C | CTTT | 10 | a0001c0001t0001g0011a0001c0001t0001g0167a0001c0001t0001g0178others(7): Show | 11 | HG02055.hp2 HG02622.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.515+856_515+858dup others(3): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115950015 | ||||||
chr7:115950077
|
T | C | 6 | a0001c0002t0001g0010a0001c0002t0001g0033a0001c0002t0001g0034others(3): Show | 7 | HG01496.hp1 HG01891.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.515+797A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115950077 | ||||||
chr7:115950105
|
A | G | 18 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0042others(15): Show | 20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.515+769T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115950105 | ||||||
chr7:115950164
|
A | C | 1 | a0001c0001t0006g0270 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.515+710T>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115950164 | ||||||
chr7:115950202
|
G | C | 1 | a0001c0001t0001g0021 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.515+672C>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115950202 | ||||||
chr7:115950231
|
T | C | 1 | a0001c0001t0024g0175 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.515+643A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115950231 | ||||||
chr7:115950297
|
C | T | 1 | a0002c0003t0001g0114 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.515+577G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115950297 | ||||||
chr7:115950416
|
T | C | 5 | a0001c0001t0003g0265a0001c0001t0003g0299a0001c0001t0003g0302others(2): Show | 5 | HG01433.hp1 HG02630.hp1 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.515+458A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115950416 | ||||||
chr7:115950950
|
C | T | 1 | a0001c0001t0002g0051 | 1 | HG00642.hp1 | splice_acceptor_variant&intron_variant | HIGH | c.440-1G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 5/7 | chr7 | 115950950 | ||||||
chr7:115951104
|
C | T | 19 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0042others(16): Show | 21 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.440-155G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 5/7 | chr7 | 115951104 | ||||||
chr7:115951246
|
C | T | 19 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0042others(16): Show | 21 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.440-297G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 5/7 | chr7 | 115951246 | ||||||
chr7:115951363
|
C | T | 3 | a0001c0001t0001g0167a0001c0001t0001g0184a0001c0001t0001g0187 | 3 | HG02622.hp2 HG02970.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.440-414G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 5/7 | chr7 | 115951363 | ||||||
chr7:115951826
|
G | A | 1 | a0001c0002t0001g0036 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.440-877C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 5/7 | chr7 | 115951826 | ||||||
chr7:115951945
|
C | G | 5 | a0001c0001t0004g0155a0001c0001t0004g0156a0001c0001t0004g0157others(2): Show | 5 | HG00741.hp2 HG01109.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.440-996G>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 5/7 | chr7 | 115951945 | ||||||
chr7:115952264
|
T | A | 18 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0042others(15): Show | 20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.440-1315A>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 5/7 | chr7 | 115952264 | ||||||
chr7:115952387
|
T | C | 18 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0042others(15): Show | 20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.440-1438A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 5/7 | chr7 | 115952387 | ||||||
chr7:115952486
|
T | G | 1 | a0001c0001t0003g0279 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.440-1537A>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 5/7 | chr7 | 115952486 | ||||||
chr7:115952503
|
T | C | 2 | a0001c0002t0001g0033a0001c0002t0001g0037 | 2 | HG01891.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.440-1554A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 5/7 | chr7 | 115952503 | ||||||
chr7:115952840
|
G | T | 7 | a0001c0001t0010g0131a0001c0001t0010g0171a0001c0001t0010g0172others(4): Show | 7 | HG02257.hp1 HG02622.hp1 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.439+1746C>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 5/7 | chr7 | 115952840 | ||||||
chr7:115952940
|
A | C | 1 | a0001c0001t0003g0321 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.439+1646T>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 5/7 | chr7 | 115952940 | ||||||
chr7:115952981
|
G | A | 1 | a0001c0001t0001g0350 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.439+1605C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 5/7 | chr7 | 115952981 | ||||||
chr7:115953162
|
G | GTGCAGAA others(15): Show |
11 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0042others(8): Show | 13 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.439+1402_439+1423d others(24): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 5/7 | chr7 | 115953162 | ||||||
chr7:115953226
|
C | G | 1 | a0001c0005t0014g0029 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.439+1360G>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 5/7 | chr7 | 115953226 | ||||||
chr7:115953277
|
CTTTATGA others(6): Show |
C | 1 | a0001c0001t0001g0250 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.439+1296_439+1308d others(15): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 5/7 | chr7 | 115953277 | ||||||
chr7:115953363
|
T | C | 1 | a0001c0001t0010g0173 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.439+1223A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 5/7 | chr7 | 115953363 | ||||||
chr7:115953470
|
G | C | 1 | a0001c0001t0001g0167 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.439+1116C>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 5/7 | chr7 | 115953470 | ||||||
chr7:115953481
|
T | G | 1 | a0001c0005t0014g0112 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.439+1105A>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 5/7 | chr7 | 115953481 | ||||||
chr7:115953505
|
T | A | 3 | a0001c0001t0002g0046a0001c0001t0002g0048a0001c0001t0002g0049 | 3 | HG02602.hp1 HG03017.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.439+1081A>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 5/7 | chr7 | 115953505 | ||||||
chr7:115953565
|
C | T | 1 | a0001c0001t0003g0349 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.439+1021G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 5/7 | chr7 | 115953565 | ||||||
chr7:115953634
|
G | A | 1 | a0001c0001t0001g0127 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.439+952C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 5/7 | chr7 | 115953634 | ||||||
chr7:115953708
|
A | G | 281 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0011others(278): Show | 303 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(300): Show |
intron_variant | MODIFIER | c.439+878T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 5/7 | chr7 | 115953708 | ||||||
chr7:115953732
|
A | G | 1 | a0001c0001t0002g0244 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.439+854T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 5/7 | chr7 | 115953732 | ||||||
chr7:115953906
|
C | T | 18 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0042others(15): Show | 20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.439+680G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 5/7 | chr7 | 115953906 | ||||||
chr7:115954051
|
C | T | 1 | a0001c0001t0034g0276 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.439+535G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 5/7 | chr7 | 115954051 | ||||||
chr7:115954159
|
G | A | 1 | a0001c0001t0009g0140 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.439+427C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 5/7 | chr7 | 115954159 | ||||||
chr7:115954384
|
C | T | 5 | a0001c0001t0002g0143a0001c0001t0011g0144a0001c0001t0011g0146others(2): Show | 5 | HG02027.hp2 HG04184.hp2 NA18747.hp1 others(2): Show |
intron_variant | MODIFIER | c.439+202G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 5/7 | chr7 | 115954384 | ||||||
chr7:115954468
|
G | A | 2 | a0001c0001t0017g0223a0001c0001t0017g0354 | 2 | NA18949.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.439+118C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 5/7 | chr7 | 115954468 | ||||||
chr7:115954673
|
C | T | 1 | a0001c0001t0002g0047 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.383-31G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 4/7 | chr7 | 115954673 | ||||||
chr7:115954719
|
C | T | 86 | a0001c0001t0001g0011a0001c0001t0001g0150a0001c0001t0001g0167others(83): Show | 98 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.383-77G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 4/7 | chr7 | 115954719 | ||||||
chr7:115954840
|
G | A | 1 | a0001c0001t0001g0342 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.383-198C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 4/7 | chr7 | 115954840 | ||||||
chr7:115954994
|
A | G | 18 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0042others(15): Show | 20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.383-352T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 4/7 | chr7 | 115954994 | ||||||
chr7:115955015
|
A | G | 4 | a0001c0001t0014g0264a0001c0005t0014g0029a0001c0005t0014g0112others(1): Show | 4 | HG02630.hp2 HG02809.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.383-373T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 4/7 | chr7 | 115955015 | ||||||
chr7:115955088
|
C | A | 1 | a0001c0001t0006g0004 | 3 | HG02559.hp1 HG03195.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.383-446G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 4/7 | chr7 | 115955088 | ||||||
chr7:115955111
|
A | G | 2 | a0001c0001t0009g0140a0001c0001t0009g0141 | 2 | HG02738.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.383-469T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 4/7 | chr7 | 115955111 | ||||||
chr7:115955144
|
C | T | 1 | a0001c0001t0014g0264 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.383-502G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 4/7 | chr7 | 115955144 | ||||||
chr7:115955431
|
A | T | 1 | a0001c0001t0003g0324 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.383-789T>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 4/7 | chr7 | 115955431 | ||||||
chr7:115955493
|
T | C | 5 | a0001c0001t0002g0139a0001c0001t0009g0137a0001c0001t0009g0138others(2): Show | 5 | HG00140.hp2 HG01243.hp1 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.383-851A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 4/7 | chr7 | 115955493 | ||||||
chr7:115955509
|
G | A | 1 | a0001c0001t0003g0305 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.383-867C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 4/7 | chr7 | 115955509 | ||||||
chr7:115955676
|
T | A | 1 | a0001c0001t0001g0021 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.382+1003A>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 4/7 | chr7 | 115955676 | ||||||
chr7:115955936
|
A | T | 1 | a0001c0001t0003g0338 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.382+743T>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 4/7 | chr7 | 115955936 | ||||||
chr7:115956012
|
G | T | 281 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0011others(278): Show | 303 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(300): Show |
intron_variant | MODIFIER | c.382+667C>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 4/7 | chr7 | 115956012 | ||||||
chr7:115956191
|
T | G | 35 | a0001c0001t0002g0007a0001c0001t0002g0046a0001c0001t0002g0047others(32): Show | 36 | HG00140.hp2 HG00642.hp1 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.382+488A>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 4/7 | chr7 | 115956191 | ||||||
chr7:115956296
|
T | A | 1 | a0001c0001t0006g0004 | 3 | HG02559.hp1 HG03195.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.382+383A>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 4/7 | chr7 | 115956296 | ||||||
chr7:115956411
|
A | G | 2 | a0001c0001t0003g0128a0001c0001t0003g0129 | 2 | HG01943.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.382+268T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 4/7 | chr7 | 115956411 | ||||||
chr7:115956474
|
A | C | 18 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0042others(15): Show | 20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.382+205T>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 4/7 | chr7 | 115956474 | ||||||
chr7:115956565
|
T | C | 3 | a0001c0001t0005g0005a0001c0001t0005g0287a0001c0001t0005g0288 | 5 | NA18955.hp2 NA18992.hp2 NA19001.hp1 others(2): Show |
intron_variant | MODIFIER | c.382+114A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 4/7 | chr7 | 115956565 | ||||||
chr7:115956834
|
T | C | 1 | a0001c0001t0030g0170 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.268-41A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115956834 | ||||||
chr7:115956996
|
C | T | 5 | a0001c0001t0001g0026a0001c0001t0001g0027a0003c0006t0001g0023others(2): Show | 5 | HG01255.hp2 HG01257.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.268-203G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115956996 | ||||||
chr7:115957387
|
T | A | 1 | a0001c0001t0001g0057 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.268-594A>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115957387 | ||||||
chr7:115957708
|
T | C | 2 | a0001c0005t0014g0112a0001c0005t0032g0111 | 2 | HG03098.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.268-915A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115957708 | ||||||
chr7:115957804
|
C | A | 1 | a0001c0001t0001g0080 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.268-1011G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115957804 | ||||||
chr7:115957881
|
T | C | 1 | a0001c0001t0003g0320 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.268-1088A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115957881 | ||||||
chr7:115957985
|
G | A | 1 | a0001c0001t0003g0323 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.268-1192C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115957985 | ||||||
chr7:115958118
|
T | G | 1 | a0001c0001t0002g0191 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.268-1325A>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115958118 | ||||||
chr7:115958161
|
A | G | 18 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0042others(15): Show | 20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.268-1368T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115958161 | ||||||
chr7:115958169
|
C | T | 18 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0042others(15): Show | 20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.268-1376G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115958169 | ||||||
chr7:115958474
|
C | A | 1 | a0001c0001t0003g0322 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.268-1681G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115958474 | ||||||
chr7:115958477
|
G | A | 1 | a0001c0001t0001g0269 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.268-1684C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115958477 | ||||||
chr7:115958687
|
A | G | 1 | a0001c0001t0022g0251 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.268-1894T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115958687 | ||||||
chr7:115958710
|
G | A | 2 | a0001c0001t0019g0168a0001c0001t0019g0169 | 2 | HG02486.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.268-1917C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115958710 | ||||||
chr7:115958710
|
G | T | 282 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0011others(279): Show | 304 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(301): Show |
intron_variant | MODIFIER | c.268-1917C>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115958710 | ||||||
chr7:115958748
|
G | A | 1 | a0001c0001t0003g0312 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.268-1955C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115958748 | ||||||
chr7:115958765
|
T | C | 1 | a0001c0001t0002g0201 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.268-1972A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115958765 | ||||||
chr7:115958876
|
T | C | 1 | a0001c0001t0004g0163 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.268-2083A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115958876 | ||||||
chr7:115958987
|
T | C | 1 | a0001c0001t0001g0064 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.268-2194A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115958987 | ||||||
chr7:115959060
|
T | C | 1 | a0001c0001t0001g0089 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.268-2267A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115959060 | ||||||
chr7:115959168
|
A | G | 1 | a0001c0001t0014g0264 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.268-2375T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115959168 | ||||||
chr7:115959309
|
C | G | 1 | a0001c0001t0024g0175 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.268-2516G>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115959309 | ||||||
chr7:115959321
|
A | T | 1 | a0001c0001t0001g0167 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.268-2528T>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115959321 | ||||||
chr7:115959389
|
G | C | 1 | a0001c0001t0001g0021 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.268-2596C>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115959389 | ||||||
chr7:115959422
|
C | T | 2 | a0001c0001t0001g0127a0001c0001t0014g0264 | 2 | HG00642.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.268-2629G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115959422 | ||||||
chr7:115959755
|
C | T | 1 | a0001c0001t0003g0324 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.268-2962G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115959755 | ||||||
chr7:115959867
|
T | C | 4 | a0001c0001t0008g0003a0001c0001t0008g0259a0001c0001t0008g0260others(1): Show | 6 | NA18945.hp1 NA18994.hp1 NA18995.hp1 others(3): Show |
intron_variant | MODIFIER | c.268-3074A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115959867 | ||||||
chr7:115959973
|
G | A | 282 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0011others(279): Show | 304 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(301): Show |
intron_variant | MODIFIER | c.268-3180C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115959973 | ||||||
chr7:115959986
|
G | A | 1 | a0001c0001t0024g0175 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.268-3193C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115959986 | ||||||
chr7:115960052
|
G | T | 1 | a0001c0001t0001g0192 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.268-3259C>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115960052 | ||||||
chr7:115960119
|
C | A | 2 | a0001c0001t0002g0052a0001c0001t0002g0053 | 2 | HG00738.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.268-3326G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115960119 | ||||||
chr7:115960203
|
A | T | 35 | a0001c0001t0002g0007a0001c0001t0002g0046a0001c0001t0002g0047others(32): Show | 36 | HG00140.hp2 HG00642.hp1 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.268-3410T>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115960203 | ||||||
chr7:115960267
|
C | T | 1 | a0001c0001t0027g0277 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.268-3474G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115960267 | ||||||
chr7:115960373
|
C | T | 2 | a0001c0001t0004g0165a0001c0001t0004g0295 | 2 | HG00733.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.268-3580G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115960373 | ||||||
chr7:115960436
|
A | G | 10 | a0001c0001t0005g0005a0001c0001t0005g0019a0001c0001t0005g0287others(7): Show | 13 | HG00609.hp2 HG02015.hp2 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.268-3643T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115960436 | ||||||
chr7:115960503
|
T | C | 4 | a0001c0001t0010g0131a0001c0001t0010g0171a0001c0001t0010g0172others(1): Show | 4 | HG03453.hp2 HG03579.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.268-3710A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115960503 | ||||||
chr7:115960549
|
C | T | 367 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0011others(364): Show | 393 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(390): Show |
intron_variant | MODIFIER | c.268-3756G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115960549 | ||||||
chr7:115960645
|
A | C | 1 | a0001c0001t0015g0039 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.268-3852T>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115960645 | ||||||
chr7:115960902
|
C | T | 176 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0021others(173): Show | 184 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.268-4109G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115960902 | ||||||
chr7:115961105
|
A | G | 1 | a0001c0001t0027g0277 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.268-4312T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115961105 | ||||||
chr7:115961116
|
C | T | 1 | a0001c0001t0030g0170 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.268-4323G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115961116 | ||||||
chr7:115961290
|
A | G | 1 | a0001c0001t0002g0245 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.268-4497T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115961290 | ||||||
chr7:115961336
|
T | C | 1 | a0001c0001t0003g0323 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.268-4543A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115961336 | ||||||
chr7:115961362
|
C | A | 32 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0055others(29): Show | 35 | HG00323.hp2 HG00423.hp2 HG01255.hp1 others(32): Show |
intron_variant | MODIFIER | c.268-4569G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115961362 | ||||||
chr7:115961399
|
T | C | 10 | a0001c0001t0002g0001a0001c0001t0002g0014a0001c0001t0002g0193others(7): Show | 14 | HG00639.hp1 HG01346.hp1 HG01358.hp2 others(11): Show |
intron_variant | MODIFIER | c.268-4606A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115961399 | ||||||
chr7:115961446
|
G | A | 1 | a0001c0001t0034g0276 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.268-4653C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115961446 | ||||||
chr7:115961471
|
T | C | 1 | a0001c0001t0034g0276 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.268-4678A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115961471 | ||||||
chr7:115961473
|
T | C | 14 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0178others(11): Show | 16 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.268-4680A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115961473 | ||||||
chr7:115961755
|
A | G | 4 | a0001c0001t0014g0264a0001c0005t0014g0029a0001c0005t0014g0112others(1): Show | 4 | HG02630.hp2 HG02809.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.268-4962T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115961755 | ||||||
chr7:115961849
|
A | G | 1 | a0001c0001t0003g0299 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.268-5056T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115961849 | ||||||
chr7:115961955
|
A | C | 125 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0021others(122): Show | 132 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.268-5162T>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115961955 | ||||||
chr7:115962068
|
G | A | 1 | a0001c0001t0001g0011 | 2 | HG02809.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.268-5275C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115962068 | ||||||
chr7:115962070
|
A | C | 6 | a0001c0002t0001g0010a0001c0002t0001g0033a0001c0002t0001g0034others(3): Show | 7 | HG01496.hp1 HG01891.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.268-5277T>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115962070 | ||||||
chr7:115962087
|
C | T | 18 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0042others(15): Show | 20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.268-5294G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115962087 | ||||||
chr7:115962162
|
A | G | 2 | a0001c0001t0002g0186a0001c0001t0002g0208 | 2 | HG02738.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.268-5369T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115962162 | ||||||
chr7:115962167
|
A | T | 18 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0042others(15): Show | 20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.268-5374T>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115962167 | ||||||
chr7:115962725
|
T | A | 1 | a0004c0007t0001g0032 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.268-5932A>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115962725 | ||||||
chr7:115962760
|
G | A | 281 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0011others(278): Show | 303 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(300): Show |
intron_variant | MODIFIER | c.268-5967C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115962760 | ||||||
chr7:115962763
|
C | A | 18 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0042others(15): Show | 20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.268-5970G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115962763 | ||||||
chr7:115962828
|
C | G | 1 | a0001c0001t0005g0290 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.268-6035G>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115962828 | ||||||
chr7:115962844
|
C | T | 3 | a0001c0001t0003g0265a0001c0001t0003g0355a0001c0001t0003g0356 | 3 | HG02630.hp1 HG02818.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.268-6051G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115962844 | ||||||
chr7:115962894
|
G | C | 1 | a0001c0001t0035g0179 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.268-6101C>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115962894 | ||||||
chr7:115962959
|
G | C | 1 | a0001c0001t0001g0366 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.268-6166C>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115962959 | ||||||
chr7:115963243
|
C | T | 18 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0042others(15): Show | 20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.268-6450G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115963243 | ||||||
chr7:115963284
|
C | T | 1 | a0001c0001t0007g0297 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.268-6491G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115963284 | ||||||
chr7:115963298
|
G | C | 14 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0178others(11): Show | 16 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.268-6505C>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115963298 | ||||||
chr7:115963321
|
A | G | 1 | a0001c0001t0002g0143 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.268-6528T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115963321 | ||||||
chr7:115963343
|
G | A | 1 | a0001c0001t0030g0170 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.268-6550C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115963343 | ||||||
chr7:115963392
|
G | GT | 4 | a0001c0001t0014g0264a0001c0005t0014g0029a0001c0005t0014g0112others(1): Show | 4 | HG02630.hp2 HG02809.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.268-6600dupA | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115963392 | ||||||
chr7:115963439
|
G | A | 1 | a0001c0001t0024g0175 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.268-6646C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115963439 | ||||||
chr7:115963610
|
C | T | 2 | a0001c0001t0001g0070a0001c0001t0001g0095 | 2 | HG03669.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.268-6817G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115963610 | ||||||
chr7:115963948
|
A | G | 1 | a0001c0001t0024g0175 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.268-7155T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115963948 | ||||||
chr7:115964107
|
G | A | 281 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0011others(278): Show | 303 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(300): Show |
intron_variant | MODIFIER | c.268-7314C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115964107 | ||||||
chr7:115964155
|
A | C | 1 | a0001c0001t0024g0175 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.268-7362T>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115964155 | ||||||
chr7:115964229
|
T | G | 18 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0042others(15): Show | 20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.268-7436A>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115964229 | ||||||
chr7:115964279
|
A | C | 4 | a0001c0001t0010g0131a0001c0001t0010g0171a0001c0001t0010g0172others(1): Show | 4 | HG03453.hp2 HG03579.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.268-7486T>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115964279 | ||||||
chr7:115965101
|
C | A | 281 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0011others(278): Show | 303 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(300): Show |
intron_variant | MODIFIER | c.268-8308G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115965101 | ||||||
chr7:115965191
|
T | C | 20 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0042others(17): Show | 22 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.268-8398A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115965191 | ||||||
chr7:115965279
|
T | C | 1 | a0001c0001t0001g0351 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.268-8486A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115965279 | ||||||
chr7:115965346
|
A | G | 1 | a0001c0001t0001g0026 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.268-8553T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115965346 | ||||||
chr7:115965478
|
G | A | 1 | a0001c0001t0034g0276 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.268-8685C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115965478 | ||||||
chr7:115965509
|
G | C | 1 | a0001c0001t0002g0216 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.267+8661C>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115965509 | ||||||
chr7:115965527
|
C | T | 18 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0042others(15): Show | 20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.267+8643G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115965527 | ||||||
chr7:115965884
|
C | G | 35 | a0001c0001t0002g0007a0001c0001t0002g0046a0001c0001t0002g0047others(32): Show | 36 | HG00140.hp2 HG00642.hp1 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.267+8286G>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115965884 | ||||||
chr7:115965922
|
T | C | 1 | a0001c0001t0003g0280 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.267+8248A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115965922 | ||||||
chr7:115966745
|
T | C | 1 | a0001c0001t0002g0148 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.267+7425A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115966745 | ||||||
chr7:115966827
|
C | T | 7 | a0001c0001t0002g0205a0001c0001t0002g0206a0001c0001t0002g0207others(4): Show | 7 | NA18612.hp1 NA18947.hp1 NA18949.hp1 others(4): Show |
intron_variant | MODIFIER | c.267+7343G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115966827 | ||||||
chr7:115966866
|
C | A | 1 | a0001c0001t0024g0175 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.267+7304G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115966866 | ||||||
chr7:115966946
|
T | C | 3 | a0001c0004t0001g0177a0001c0004t0001g0273a0001c0004t0001g0275 | 3 | HG02055.hp2 HG03209.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.267+7224A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115966946 | ||||||
chr7:115966963
|
G | T | 1 | a0001c0001t0002g0204 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.267+7207C>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115966963 | ||||||
chr7:115967373
|
A | G | 1 | a0001c0001t0010g0131 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.267+6797T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115967373 | ||||||
chr7:115967400
|
T | A | 34 | a0001c0001t0002g0007a0001c0001t0002g0046a0001c0001t0002g0047others(31): Show | 35 | HG00140.hp2 HG00642.hp1 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.267+6770A>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115967400 | ||||||
chr7:115967433
|
A | G | 1 | a0001c0001t0001g0086 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.267+6737T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115967433 | ||||||
chr7:115967441
|
T | C | 18 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0042others(15): Show | 20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.267+6729A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115967441 | ||||||
chr7:115967818
|
T | G | 1 | a0001c0001t0024g0175 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.267+6352A>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115967818 | ||||||
chr7:115967851
|
C | G | 4 | a0001c0001t0014g0264a0001c0005t0014g0029a0001c0005t0014g0112others(1): Show | 4 | HG02630.hp2 HG02809.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.267+6319G>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115967851 | ||||||
chr7:115968104
|
T | C | 4 | a0001c0001t0003g0045a0001c0001t0003g0128a0001c0001t0003g0129others(1): Show | 4 | HG01071.hp1 HG01943.hp2 HG02148.hp1 others(1): Show |
intron_variant | MODIFIER | c.267+6066A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115968104 | ||||||
chr7:115968301
|
T | G | 35 | a0001c0001t0002g0007a0001c0001t0002g0046a0001c0001t0002g0047others(32): Show | 36 | HG00140.hp2 HG00642.hp1 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.267+5869A>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115968301 | ||||||
chr7:115968540
|
T | A | 2 | a0001c0001t0006g0176a0001c0001t0006g0272 | 2 | HG02258.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.267+5630A>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115968540 | ||||||
chr7:115968718
|
G | T | 1 | a0001c0001t0003g0315 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.267+5452C>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115968718 | ||||||
chr7:115968859
|
T | G | 1 | a0001c0001t0002g0217 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.267+5311A>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115968859 | ||||||
chr7:115968872
|
C | G | 1 | a0001c0001t0001g0110 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.267+5298G>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115968872 | ||||||
chr7:115969029
|
G | T | 1 | a0001c0001t0003g0280 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.267+5141C>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115969029 | ||||||
chr7:115969124
|
G | A | 1 | a0001c0001t0001g0187 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.267+5046C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115969124 | ||||||
chr7:115969635
|
T | C | 14 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0178others(11): Show | 16 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.267+4535A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115969635 | ||||||
chr7:115969741
|
T | C | 3 | a0001c0001t0003g0327a0001c0001t0003g0347a0001c0001t0003g0348 | 3 | NA18953.hp1 NA18971.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.267+4429A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115969741 | ||||||
chr7:115969771
|
G | T | 86 | a0001c0001t0001g0011a0001c0001t0001g0150a0001c0001t0001g0167others(83): Show | 98 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.267+4399C>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115969771 | ||||||
chr7:115969794
|
T | C | 281 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0011others(278): Show | 303 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(300): Show |
intron_variant | MODIFIER | c.267+4376A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115969794 | ||||||
chr7:115969857
|
A | C | 1 | a0001c0001t0003g0304 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.267+4313T>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115969857 | ||||||
chr7:115969928
|
C | T | 1 | a0001c0001t0003g0308 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.267+4242G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115969928 | ||||||
chr7:115969976
|
C | T | 2 | a0001c0001t0019g0168a0001c0001t0019g0169 | 2 | HG02486.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.267+4194G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115969976 | ||||||
chr7:115970206
|
G | A | 5 | a0001c0001t0003g0265a0001c0001t0003g0299a0001c0001t0003g0302others(2): Show | 5 | HG01433.hp1 HG02630.hp1 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.267+3964C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115970206 | ||||||
chr7:115970797
|
C | T | 3 | a0001c0001t0003g0338a0001c0001t0003g0339a0001c0001t0003g0340 | 3 | NA18991.hp1 NA19065.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.267+3373G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115970797 | ||||||
chr7:115971241
|
T | C | 18 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0042others(15): Show | 20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.267+2929A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115971241 | ||||||
chr7:115971255
|
G | A | 60 | a0001c0001t0001g0028a0001c0001t0001g0040a0001c0001t0001g0041others(57): Show | 61 | HG00280.hp2 HG00558.hp2 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.267+2915C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115971255 | ||||||
chr7:115971372
|
GA | G | 5 | a0001c0001t0001g0026a0001c0001t0001g0027a0003c0006t0001g0023others(2): Show | 5 | HG01255.hp2 HG01257.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.267+2797delT | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115971372 | ||||||
chr7:115971471
|
T | A | 1 | a0001c0001t0001g0057 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.267+2699A>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115971471 | ||||||
chr7:115971637
|
C | G | 3 | a0001c0001t0001g0192a0001c0001t0001g0239a0001c0001t0001g0240 | 3 | NA18941.hp1 NA18968.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.267+2533G>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115971637 | ||||||
chr7:115972060
|
C | T | 1 | a0001c0001t0001g0358 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.267+2110G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115972060 | ||||||
chr7:115972215
|
T | C | 1 | a0001c0009t0003g0329 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.267+1955A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115972215 | ||||||
chr7:115972271
|
T | C | 1 | a0001c0001t0001g0027 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.267+1899A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115972271 | ||||||
chr7:115972396
|
A | T | 1 | a0001c0001t0003g0310 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.267+1774T>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115972396 | ||||||
chr7:115972585
|
A | G | 3 | a0001c0001t0001g0067a0001c0001t0001g0072a0001c0001t0003g0347 | 3 | NA18946.hp1 NA18953.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.267+1585T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115972585 | ||||||
chr7:115972686
|
T | C | 18 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0042others(15): Show | 20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.267+1484A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115972686 | ||||||
chr7:115972701
|
A | G | 18 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0042others(15): Show | 20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.267+1469T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115972701 | ||||||
chr7:115972791
|
C | A | 10 | a0001c0001t0001g0067a0001c0001t0001g0069a0001c0001t0001g0072others(7): Show | 10 | HG00621.hp1 HG02080.hp2 HG02135.hp2 others(7): Show |
intron_variant | MODIFIER | c.267+1379G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115972791 | ||||||
chr7:115972849
|
C | T | 1 | a0001c0001t0001g0368 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.267+1321G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115972849 | ||||||
chr7:115973088
|
A | C | 1 | a0001c0001t0033g0183 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.267+1082T>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115973088 | ||||||
chr7:115973091
|
A | G | 2 | a0001c0001t0019g0168a0001c0001t0019g0169 | 2 | HG02486.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.267+1079T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115973091 | ||||||
chr7:115973097
|
GA | G | 89 | a0001c0001t0001g0011a0001c0001t0001g0150a0001c0001t0001g0167others(86): Show | 101 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.267+1072delT | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115973097 | ||||||
chr7:115973513
|
T | G | 1 | a0001c0001t0001g0098 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.267+657A>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115973513 | ||||||
chr7:115973730
|
T | C | 1 | a0001c0001t0035g0179 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.267+440A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115973730 | ||||||
chr7:115973833
|
T | C | 2 | a0001c0001t0001g0184a0001c0001t0033g0183 | 2 | HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.267+337A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115973833 | ||||||
chr7:115973859
|
T | C | 2 | a0001c0001t0003g0030a0001c0001t0003g0100 | 2 | HG00733.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.267+311A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115973859 | ||||||
chr7:115973898
|
T | C | 1 | a0001c0001t0001g0021 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.267+272A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115973898 | ||||||
chr7:115974087
|
C | T | 1 | a0001c0001t0007g0116 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.267+83G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115974087 | ||||||
chr7:115974381
|
T | A | 1 | a0001c0001t0016g0360 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.181-125A>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115974381 | ||||||
chr7:115974405
|
A | AATATATA others(3): Show |
1 | a0001c0001t0003g0328 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.181-150_181-149ins others(10): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115974405 | ||||||
chr7:115974406
|
T | A | 1 | a0001c0001t0003g0328 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.181-150A>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115974406 | ||||||
chr7:115974406
|
T | TTA | 24 | a0001c0001t0001g0068a0001c0001t0001g0096a0001c0001t0001g0106others(21): Show | 24 | HG00408.hp1 HG00733.hp1 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.181-152_181-151dup others(2): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115974406 | ||||||
chr7:115974406
|
T | TTATA | 38 | a0001c0001t0001g0065a0001c0001t0001g0069a0001c0001t0001g0083others(35): Show | 39 | HG01069.hp2 HG01071.hp1 HG01071.hp2 others(36): Show |
intron_variant | MODIFIER | c.181-154_181-151dup others(4): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115974406 | ||||||
chr7:115974406
|
T | TTATATA | 25 | a0001c0001t0001g0021a0001c0001t0001g0041a0001c0001t0001g0066others(22): Show | 25 | HG00140.hp2 HG00738.hp1 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.181-156_181-151dup others(6): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115974406 | ||||||
chr7:115974406
|
T | TTATATAT others(1): Show |
24 | a0001c0001t0001g0084a0001c0001t0001g0095a0001c0001t0001g0107others(21): Show | 24 | HG00280.hp1 HG00280.hp2 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.181-158_181-151dup others(8): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115974406 | ||||||
chr7:115974406
|
T | TTATATAT others(3): Show |
28 | a0001c0001t0001g0006a0001c0001t0001g0026a0001c0001t0001g0027others(25): Show | 29 | HG01109.hp2 HG01255.hp2 HG01346.hp2 others(26): Show |
intron_variant | MODIFIER | c.181-160_181-151dup others(10): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115974406 | ||||||
chr7:115974406
|
T | TTATATAT others(5): Show |
15 | a0001c0001t0001g0002a0001c0001t0001g0055a0001c0001t0001g0075others(12): Show | 17 | HG00323.hp2 HG00642.hp2 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.181-162_181-151dup others(12): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115974406 | ||||||
chr7:115974406
|
T | TTATATAT others(7): Show |
15 | a0001c0001t0001g0040a0001c0001t0001g0076a0001c0001t0001g0089others(12): Show | 15 | HG00423.hp2 HG00642.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.181-164_181-151dup others(14): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115974406 | ||||||
chr7:115974406
|
T | TTATATAT others(9): Show |
6 | a0001c0001t0001g0062a0001c0001t0001g0077a0001c0001t0001g0126others(3): Show | 6 | HG00558.hp2 HG00621.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.181-166_181-151dup others(16): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115974406 | ||||||
chr7:115974406
|
T | TTATATAT others(11): Show |
1 | a0001c0001t0003g0327 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.181-168_181-151dup others(18): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115974406 | ||||||
chr7:115974406
|
T | TTATATAT others(13): Show |
1 | a0001c0001t0001g0078 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.181-170_181-151dup others(20): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115974406 | ||||||
chr7:115974406
|
TTA | T | 9 | a0001c0001t0003g0265a0001c0001t0003g0309a0001c0001t0003g0320others(6): Show | 9 | HG03471.hp2 NA18942.hp2 NA18952.hp1 others(6): Show |
intron_variant | MODIFIER | c.181-152_181-151del others(2): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115974406 | ||||||
chr7:115974406
|
TTATA | T | 3 | a0001c0001t0003g0119a0001c0001t0003g0296a0001c0001t0003g0313 | 3 | HG00609.hp1 HG02155.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.181-154_181-151del others(4): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115974406 | ||||||
chr7:115974406
|
TTATATAT others(1): Show |
T | 4 | a0001c0001t0007g0044a0001c0001t0007g0300a0001c0001t0019g0168others(1): Show | 4 | HG01361.hp2 HG01891.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.181-158_181-151del others(8): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115974406 | ||||||
chr7:115974406
|
TTATATAT others(3): Show |
T | 1 | a0001c0001t0007g0020 | 2 | HG02895.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.181-160_181-151del others(10): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115974406 | ||||||
chr7:115974406
|
TTATATAT others(5): Show |
T | 1 | a0001c0001t0003g0308 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.181-162_181-151del others(12): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115974406 | ||||||
chr7:115974406
|
TTATATAT others(13): Show |
T | 1 | a0001c0001t0003g0133 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.181-170_181-151del others(20): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115974406 | ||||||
chr7:115974421
|
TATATATA others(23): Show |
T | 89 | a0001c0001t0001g0011a0001c0001t0001g0150a0001c0001t0001g0167others(86): Show | 101 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.181-195_181-166del others(30): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115974421 | ||||||
chr7:115974423
|
TATATATA others(21): Show |
T | 1 | a0001c0001t0002g0218 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.181-195_181-168del others(28): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115974423 | ||||||
chr7:115974427
|
TATATATA others(17): Show |
T | 1 | a0001c0001t0001g0064 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.181-195_181-172del others(24): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115974427 | ||||||
chr7:115974433
|
TATATATA others(11): Show |
T | 3 | a0001c0005t0014g0029a0001c0005t0014g0112a0003c0006t0001g0024 | 3 | HG01978.hp1 HG02630.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.181-195_181-178del others(18): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115974433 | ||||||
chr7:115974435
|
TATATATA others(9): Show |
T | 2 | a0001c0001t0004g0042a0001c0005t0032g0111 | 2 | HG00639.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.181-195_181-180del others(16): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115974435 | ||||||
chr7:115974437
|
TATATATA others(7): Show |
T | 16 | a0001c0001t0004g0008a0001c0001t0004g0155a0001c0001t0004g0156others(13): Show | 17 | HG00741.hp2 HG01106.hp1 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.181-195_181-182del others(14): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115974437 | ||||||
chr7:115974439
|
TATATATA others(5): Show |
T | 4 | a0001c0001t0001g0097a0001c0001t0004g0009a0001c0001t0004g0295others(1): Show | 5 | HG00323.hp1 HG00733.hp2 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.181-195_181-184del others(12): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115974439 | ||||||
chr7:115974441
|
TATATATA others(3): Show |
T | 2 | a0001c0001t0002g0149a0001c0001t0031g0154 | 2 | HG01433.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.181-195_181-186del others(10): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115974441 | ||||||
chr7:115974447
|
T | TATATATA others(3): Show |
1 | a0001c0001t0016g0360 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.181-192_181-191ins others(10): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115974447 | ||||||
chr7:115974447
|
TATAA | T | 7 | a0001c0001t0001g0022a0001c0001t0001g0109a0001c0001t0001g0110others(4): Show | 7 | HG02055.hp2 HG02145.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.181-195_181-192del others(4): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115974447 | ||||||
chr7:115974449
|
TAA | T | 14 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0060others(11): Show | 16 | HG01074.hp2 HG01192.hp2 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.181-195_181-194del others(2): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115974449 | ||||||
chr7:115974450
|
A | ATATATAT others(6): Show |
1 | a0001c0001t0007g0297 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.181-195_181-194ins others(13): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115974450 | ||||||
chr7:115974450
|
A | ATATATAT others(16): Show |
1 | a0001c0001t0003g0284 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.181-195_181-194ins others(23): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115974450 | ||||||
chr7:115974451
|
A | T | 141 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0021others(138): Show | 147 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.181-195T>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115974451 | ||||||
chr7:115974452
|
A | T | 3 | a0001c0001t0003g0284a0002c0003t0021g0093a0003c0006t0001g0023 | 3 | HG01258.hp1 HG02074.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.181-196T>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115974452 | ||||||
chr7:115974453
|
A | T | 3 | a0001c0001t0001g0101a0002c0003t0001g0092a0002c0003t0001g0114 | 3 | HG03490.hp1 HG03654.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.181-197T>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115974453 | ||||||
chr7:115974457
|
C | G | 11 | a0001c0001t0002g0001a0001c0001t0002g0014a0001c0001t0002g0193others(8): Show | 15 | HG00639.hp1 HG01346.hp1 HG01358.hp2 others(12): Show |
intron_variant | MODIFIER | c.181-201G>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115974457 | ||||||
chr7:115974510
|
C | A | 1 | a0001c0001t0030g0170 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.181-254G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115974510 | ||||||
chr7:115974587
|
GTATC | G | 89 | a0001c0001t0001g0011a0001c0001t0001g0150a0001c0001t0001g0167others(86): Show | 101 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.181-335_181-332del others(4): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115974587 | ||||||
chr7:115974874
|
A | C | 2 | a0001c0001t0001g0065a0001c0001t0001g0066 | 2 | NA18965.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.181-618T>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115974874 | ||||||
chr7:115975057
|
T | C | 1 | a0001c0001t0003g0334 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.181-801A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115975057 | ||||||
chr7:115975203
|
T | TA | 18 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0042others(15): Show | 20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.181-948dupT | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115975203 | ||||||
chr7:115975508
|
T | C | 2 | a0001c0001t0003g0119a0001c0001t0003g0313 | 2 | HG00609.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.181-1252A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115975508 | ||||||
chr7:115975704
|
C | T | 1 | a0001c0001t0001g0021 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.181-1448G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115975704 | ||||||
chr7:115975705
|
G | A | 89 | a0001c0001t0001g0011a0001c0001t0001g0150a0001c0001t0001g0167others(86): Show | 101 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.181-1449C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115975705 | ||||||
chr7:115975819
|
C | A | 18 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0042others(15): Show | 20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.181-1563G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115975819 | ||||||
chr7:115975902
|
G | A | 226 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0011others(223): Show | 245 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(242): Show |
intron_variant | MODIFIER | c.181-1646C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115975902 | ||||||
chr7:115976068
|
C | T | 1 | a0001c0001t0001g0120 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.181-1812G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115976068 | ||||||
chr7:115976069
|
G | A | 18 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0042others(15): Show | 20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.181-1813C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115976069 | ||||||
chr7:115977005
|
C | T | 1 | a0001c0001t0030g0170 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.181-2749G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115977005 | ||||||
chr7:115977169
|
A | T | 281 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0011others(278): Show | 303 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(300): Show |
intron_variant | MODIFIER | c.181-2913T>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115977169 | ||||||
chr7:115977548
|
TA | T | 5 | a0001c0001t0001g0026a0001c0001t0001g0027a0003c0006t0001g0023others(2): Show | 5 | HG01255.hp2 HG01257.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.181-3293delT | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115977548 | ||||||
chr7:115977673
|
G | A | 2 | a0001c0001t0005g0292a0001c0001t0005g0293 | 2 | NA19064.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.181-3417C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115977673 | ||||||
chr7:115977812
|
G | C | 1 | a0001c0001t0003g0315 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.181-3556C>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115977812 | ||||||
chr7:115977910
|
AC | A | 262 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0011others(259): Show | 282 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.181-3655delG | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115977910 | ||||||
chr7:115977952
|
A | G | 1 | a0001c0001t0003g0304 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.181-3696T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115977952 | ||||||
chr7:115978034
|
T | C | 1 | a0001c0001t0002g0294 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.181-3778A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115978034 | ||||||
chr7:115978109
|
C | T | 18 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0042others(15): Show | 20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.181-3853G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115978109 | ||||||
chr7:115978149
|
A | C | 2 | a0001c0001t0019g0168a0001c0001t0019g0169 | 2 | HG02486.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.181-3893T>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115978149 | ||||||
chr7:115978353
|
G | T | 34 | a0001c0001t0002g0007a0001c0001t0002g0046a0001c0001t0002g0047others(31): Show | 35 | HG00140.hp2 HG00642.hp1 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.181-4097C>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115978353 | ||||||
chr7:115978497
|
C | T | 113 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0026others(110): Show | 118 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.181-4241G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115978497 | ||||||
chr7:115978795
|
T | A | 1 | a0001c0001t0001g0082 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.181-4539A>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115978795 | ||||||
chr7:115978951
|
A | G | 4 | a0001c0001t0002g0230a0001c0001t0002g0231a0001c0001t0002g0232others(1): Show | 4 | HG01175.hp1 HG01516.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.181-4695T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115978951 | ||||||
chr7:115978970
|
G | A | 7 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0083others(4): Show | 7 | HG02015.hp1 NA18747.hp2 NA18945.hp2 others(4): Show |
intron_variant | MODIFIER | c.181-4714C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115978970 | ||||||
chr7:115979241
|
A | G | 1 | a0001c0004t0001g0275 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.181-4985T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115979241 | ||||||
chr7:115979244
|
C | T | 60 | a0001c0001t0001g0028a0001c0001t0001g0040a0001c0001t0001g0041others(57): Show | 61 | HG00280.hp2 HG00558.hp2 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.181-4988G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115979244 | ||||||
chr7:115979576
|
G | A | 87 | a0001c0001t0001g0011a0001c0001t0001g0167a0001c0001t0001g0181others(84): Show | 99 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.180+4686C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115979576 | ||||||
chr7:115979674
|
C | T | 1 | a0001c0001t0001g0187 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.180+4588G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115979674 | ||||||
chr7:115979730
|
G | A | 1 | a0001c0001t0030g0170 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.180+4532C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115979730 | ||||||
chr7:115979800
|
C | T | 18 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0042others(15): Show | 20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.180+4462G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115979800 | ||||||
chr7:115980486
|
A | G | 1 | a0001c0001t0001g0185 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.180+3776T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115980486 | ||||||
chr7:115980641
|
C | G | 18 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0042others(15): Show | 20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.180+3621G>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115980641 | ||||||
chr7:115980680
|
G | A | 18 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0042others(15): Show | 20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.180+3582C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115980680 | ||||||
chr7:115980747
|
G | T | 284 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0011others(281): Show | 306 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(303): Show |
intron_variant | MODIFIER | c.180+3515C>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115980747 | ||||||
chr7:115980769
|
C | CA | 109 | a0001c0001t0001g0011a0001c0001t0001g0150a0001c0001t0001g0167others(106): Show | 122 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.180+3492dupT | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115980769 | ||||||
chr7:115980774
|
A | C | 1 | a0001c0001t0003g0318 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.180+3488T>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115980774 | ||||||
chr7:115980778
|
C | A | 1 | a0001c0001t0002g0219 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.180+3484G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115980778 | ||||||
chr7:115980778
|
C | CA | 6 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0030g0170others(3): Show | 6 | HG01255.hp2 HG01257.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.180+3483dupT | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115980778 | ||||||
chr7:115980951
|
A | T | 1 | a0001c0001t0001g0067 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.180+3311T>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115980951 | ||||||
chr7:115981056
|
A | G | 89 | a0001c0001t0001g0011a0001c0001t0001g0167a0001c0001t0001g0181others(86): Show | 101 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.180+3206T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115981056 | ||||||
chr7:115981306
|
A | G | 1 | a0005c0008t0023g0180 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.180+2956T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115981306 | ||||||
chr7:115981341
|
A | G | 18 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0042others(15): Show | 20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.180+2921T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115981341 | ||||||
chr7:115981345
|
A | T | 1 | a0001c0001t0035g0179 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.180+2917T>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115981345 | ||||||
chr7:115981408
|
C | T | 282 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0011others(279): Show | 304 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(301): Show |
intron_variant | MODIFIER | c.180+2854G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115981408 | ||||||
chr7:115981425
|
C | A | 7 | a0001c0001t0001g0060a0001c0001t0001g0263a0001c0001t0001g0362others(4): Show | 7 | HG01243.hp2 HG02055.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.180+2837G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115981425 | ||||||
chr7:115981459
|
G | C | 1 | a0001c0001t0003g0030 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.180+2803C>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115981459 | ||||||
chr7:115981725
|
C | T | 1 | a0001c0001t0001g0358 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.180+2537G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115981725 | ||||||
chr7:115981805
|
C | A | 1 | a0001c0001t0035g0179 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.180+2457G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115981805 | ||||||
chr7:115981833
|
G | GT | 89 | a0001c0001t0001g0011a0001c0001t0001g0167a0001c0001t0001g0181others(86): Show | 101 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.180+2428dupA | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115981833 | ||||||
chr7:115981966
|
G | A | 1 | a0001c0001t0002g0220 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.180+2296C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115981966 | ||||||
chr7:115982086
|
C | A | 2 | a0001c0001t0003g0314a0001c0001t0003g0315 | 2 | HG00280.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.180+2176G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115982086 | ||||||
chr7:115982138
|
T | C | 3 | a0001c0001t0007g0116a0001c0001t0007g0297a0001c0001t0007g0298 | 3 | HG02723.hp1 HG03041.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.180+2124A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115982138 | ||||||
chr7:115982257
|
G | A | 282 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0011others(279): Show | 304 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(301): Show |
intron_variant | MODIFIER | c.180+2005C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115982257 | ||||||
chr7:115982262
|
C | A | 1 | a0001c0001t0001g0061 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.180+2000G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115982262 | ||||||
chr7:115982507
|
T | C | 128 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0021others(125): Show | 135 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.180+1755A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115982507 | ||||||
chr7:115982701
|
G | A | 39 | a0001c0001t0001g0150a0001c0001t0002g0007a0001c0001t0002g0046others(36): Show | 40 | HG00140.hp2 HG00642.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.180+1561C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115982701 | ||||||
chr7:115982722
|
T | C | 1 | a0001c0001t0002g0222 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.180+1540A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115982722 | ||||||
chr7:115982793
|
C | A | 1 | a0001c0001t0004g0163 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.180+1469G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115982793 | ||||||
chr7:115982900
|
AT | A | 18 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0042others(15): Show | 20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.180+1361delA | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115982900 | ||||||
chr7:115983135
|
A | G | 4 | a0001c0001t0014g0264a0001c0005t0014g0029a0001c0005t0014g0112others(1): Show | 4 | HG02630.hp2 HG02809.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.180+1127T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115983135 | ||||||
chr7:115983236
|
G | A | 4 | a0001c0001t0010g0131a0001c0001t0010g0171a0001c0001t0010g0172others(1): Show | 4 | HG03453.hp2 HG03579.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.180+1026C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115983236 | ||||||
chr7:115983292
|
G | A | 282 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0011others(279): Show | 304 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(301): Show |
intron_variant | MODIFIER | c.180+970C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115983292 | ||||||
chr7:115983313
|
C | A | 263 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0011others(260): Show | 283 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(280): Show |
intron_variant | MODIFIER | c.180+949G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115983313 | ||||||
chr7:115983453
|
A | G | 26 | a0001c0001t0003g0119a0001c0001t0003g0123a0001c0001t0003g0188others(23): Show | 29 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.180+809T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115983453 | ||||||
chr7:115983458
|
C | G | 2 | a0001c0001t0003g0301a0001c0001t0003g0349 | 2 | NA18978.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.180+804G>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115983458 | ||||||
chr7:115983569
|
T | A | 107 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0028others(104): Show | 112 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.180+693A>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115983569 | ||||||
chr7:115983774
|
T | C | 3 | a0001c0001t0015g0038a0001c0001t0015g0039a0001c0001t0015g0359 | 3 | HG02615.hp1 HG02717.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.180+488A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115983774 | ||||||
chr7:115983809
|
G | T | 1 | a0001c0001t0003g0316 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.180+453C>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115983809 | ||||||
chr7:115983913
|
T | C | 1 | a0001c0001t0001g0189 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.180+349A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115983913 | ||||||
chr7:115984098
|
T | G | 1 | a0001c0001t0002g0261 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.180+164A>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115984098 | ||||||
chr7:115984113
|
TAATA | T | 3 | a0001c0005t0014g0029a0001c0005t0014g0112a0001c0005t0032g0111 | 3 | HG02630.hp2 HG03098.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.180+145_180+148del others(4): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115984113 | ||||||
chr7:115984157
|
C | T | 4 | a0001c0001t0014g0264a0001c0005t0014g0029a0001c0005t0014g0112others(1): Show | 4 | HG02630.hp2 HG02809.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.180+105G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115984157 | ||||||
chr7:115984234
|
T | C | 18 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0042others(15): Show | 20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.180+28A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115984234 | ||||||
chr7:115985014
|
G | A | 4 | a0001c0001t0014g0264a0001c0005t0014g0029a0001c0005t0014g0112others(1): Show | 4 | HG02630.hp2 HG02809.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-72-501C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115985014 | ||||||
chr7:115985021
|
G | GA | 89 | a0001c0001t0001g0011a0001c0001t0001g0167a0001c0001t0001g0181others(86): Show | 101 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.-72-509dupT | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115985021 | ||||||
chr7:115985034
|
A | T | 1 | a0001c0001t0003g0331 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-72-521T>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115985034 | ||||||
chr7:115985085
|
AT | A | 89 | a0001c0001t0001g0011a0001c0001t0001g0167a0001c0001t0001g0181others(86): Show | 101 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.-72-573delA | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115985085 | ||||||
chr7:115985118
|
T | A | 4 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0104others(1): Show | 4 | HG01168.hp2 HG01169.hp2 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.-72-605A>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115985118 | ||||||
chr7:115985414
|
G | A | 2 | a0001c0001t0001g0021a0001c0001t0001g0266 | 2 | HG02145.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.-72-901C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115985414 | ||||||
chr7:115985488
|
T | C | 4 | a0001c0001t0014g0264a0001c0005t0014g0029a0001c0005t0014g0112others(1): Show | 4 | HG02630.hp2 HG02809.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-72-975A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115985488 | ||||||
chr7:115985491
|
A | T | 1 | a0001c0001t0030g0170 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-72-978T>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115985491 | ||||||
chr7:115985560
|
T | C | 106 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0028others(103): Show | 111 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.-72-1047A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115985560 | ||||||
chr7:115985660
|
T | C | 1 | a0001c0001t0001g0184 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-72-1147A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115985660 | ||||||
chr7:115985672
|
T | C | 1 | a0001c0001t0002g0267 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-72-1159A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115985672 | ||||||
chr7:115985785
|
T | C | 106 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0028others(103): Show | 111 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.-72-1272A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115985785 | ||||||
chr7:115985848
|
C | A | 3 | a0001c0001t0007g0116a0001c0001t0007g0297a0001c0001t0007g0298 | 3 | HG02723.hp1 HG03041.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-72-1335G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115985848 | ||||||
chr7:115985890
|
T | A | 5 | a0001c0001t0001g0263a0001c0001t0001g0362a0001c0001t0001g0363others(2): Show | 5 | HG02109.hp2 HG02258.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-72-1377A>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115985890 | ||||||
chr7:115985986
|
T | C | 36 | a0001c0001t0001g0150a0001c0001t0002g0007a0001c0001t0002g0046others(33): Show | 37 | HG00140.hp2 HG00642.hp1 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.-72-1473A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115985986 | ||||||
chr7:115986235
|
T | C | 31 | a0001c0001t0001g0178a0001c0001t0001g0187a0001c0001t0001g0269others(28): Show | 35 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.-72-1722A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115986235 | ||||||
chr7:115986245
|
T | G | 3 | a0001c0001t0007g0116a0001c0001t0007g0297a0001c0001t0007g0298 | 3 | HG02723.hp1 HG03041.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-72-1732A>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115986245 | ||||||
chr7:115986275
|
C | T | 282 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0011others(279): Show | 304 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(301): Show |
intron_variant | MODIFIER | c.-72-1762G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115986275 | ||||||
chr7:115986629
|
T | C | 107 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0028others(104): Show | 112 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.-72-2116A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115986629 | ||||||
chr7:115986744
|
C | T | 2 | a0001c0001t0001g0189a0001c0001t0030g0170 | 2 | HG02922.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.-72-2231G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115986744 | ||||||
chr7:115986746
|
C | A | 1 | a0001c0001t0030g0170 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-72-2233G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115986746 | ||||||
chr7:115986918
|
T | TA | 283 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0011others(280): Show | 305 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(302): Show |
intron_variant | MODIFIER | c.-72-2406dupT | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115986918 | ||||||
chr7:115986939
|
T | A | 1 | a0001c0001t0030g0170 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-72-2426A>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115986939 | ||||||
chr7:115987115
|
C | T | 1 | a0001c0001t0002g0267 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-72-2602G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115987115 | ||||||
chr7:115987116
|
G | A | 2 | a0001c0001t0001g0021a0001c0001t0001g0266 | 2 | HG02145.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.-72-2603C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115987116 | ||||||
chr7:115987164
|
G | C | 1 | a0001c0001t0003g0296 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-72-2651C>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115987164 | ||||||
chr7:115987357
|
T | C | 2 | a0001c0001t0034g0276a0001c0001t0035g0179 | 2 | HG02622.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-72-2844A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115987357 | ||||||
chr7:115987430
|
T | C | 8 | a0001c0001t0002g0013a0001c0001t0002g0194a0001c0001t0002g0195others(5): Show | 9 | HG00408.hp2 NA18942.hp1 NA18956.hp1 others(6): Show |
intron_variant | MODIFIER | c.-72-2917A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115987430 | ||||||
chr7:115987462
|
G | A | 7 | a0001c0001t0001g0060a0001c0001t0001g0263a0001c0001t0001g0362others(4): Show | 7 | HG01243.hp2 HG02055.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.-72-2949C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115987462 | ||||||
chr7:115987485
|
T | C | 4 | a0001c0001t0010g0131a0001c0001t0010g0171a0001c0001t0010g0172others(1): Show | 4 | HG03453.hp2 HG03579.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.-72-2972A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115987485 | ||||||
chr7:115987495
|
G | A | 8 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(5): Show | 8 | HG00280.hp2 HG00642.hp2 HG00741.hp1 others(5): Show |
intron_variant | MODIFIER | c.-72-2982C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115987495 | ||||||
chr7:115987511
|
C | A | 18 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0042others(15): Show | 20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.-72-2998G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115987511 | ||||||
chr7:115987776
|
G | A | 1 | a0001c0001t0003g0302 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-72-3263C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115987776 | ||||||
chr7:115987781
|
T | A | 5 | a0001c0001t0001g0351a0001c0001t0001g0352a0001c0001t0002g0018others(2): Show | 6 | HG00423.hp1 HG02135.hp1 HG03688.hp1 others(3): Show |
intron_variant | MODIFIER | c.-72-3268A>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115987781 | ||||||
chr7:115988018
|
A | G | 1 | a0001c0001t0007g0020 | 2 | HG02895.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.-72-3505T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115988018 | ||||||
chr7:115988050
|
T | C | 36 | a0001c0001t0001g0150a0001c0001t0002g0007a0001c0001t0002g0046others(33): Show | 37 | HG00140.hp2 HG00642.hp1 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.-72-3537A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115988050 | ||||||
chr7:115988084
|
T | C | 127 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0021others(124): Show | 134 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.-72-3571A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115988084 | ||||||
chr7:115988208
|
T | G | 1 | a0001c0002t0001g0010 | 2 | HG02717.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.-72-3695A>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115988208 | ||||||
chr7:115988272
|
A | G | 1 | a0001c0001t0035g0179 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-72-3759T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115988272 | ||||||
chr7:115988298
|
G | C | 2 | a0005c0008t0023g0132a0005c0008t0023g0180 | 2 | HG02257.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-72-3785C>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115988298 | ||||||
chr7:115988353
|
A | G | 1 | a0001c0001t0004g0166 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-72-3840T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115988353 | ||||||
chr7:115988394
|
T | C | 1 | a0001c0001t0001g0178 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-72-3881A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115988394 | ||||||
chr7:115988502
|
A | G | 18 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0042others(15): Show | 20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.-72-3989T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115988502 | ||||||
chr7:115988535
|
G | A | 1 | a0001c0004t0001g0273 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-72-4022C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115988535 | ||||||
chr7:115988735
|
C | T | 1 | a0001c0001t0002g0267 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-72-4222G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115988735 | ||||||
chr7:115988892
|
G | A | 106 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0028others(103): Show | 111 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.-72-4379C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115988892 | ||||||
chr7:115988894
|
T | C | 2 | a0001c0001t0002g0194a0001c0001t0002g0195 | 2 | NA18957.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.-72-4381A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115988894 | ||||||
chr7:115989238
|
T | G | 107 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0028others(104): Show | 112 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.-72-4725A>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115989238 | ||||||
chr7:115989411
|
G | A | 2 | a0001c0001t0001g0021a0001c0001t0001g0266 | 2 | HG02145.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.-72-4898C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115989411 | ||||||
chr7:115989450
|
G | A | 6 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0017g0223others(3): Show | 6 | HG01255.hp2 HG01257.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.-72-4937C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115989450 | ||||||
chr7:115989475
|
C | T | 2 | a0001c0001t0034g0276a0001c0001t0035g0179 | 2 | HG02622.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-72-4962G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115989475 | ||||||
chr7:115989484
|
C | G | 13 | a0001c0001t0001g0178a0001c0001t0001g0187a0001c0001t0001g0269others(10): Show | 15 | HG02055.hp2 HG02109.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.-72-4971G>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115989484 | ||||||
chr7:115989564
|
G | A | 282 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0011others(279): Show | 304 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(301): Show |
intron_variant | MODIFIER | c.-72-5051C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115989564 | ||||||
chr7:115989576
|
T | A | 1 | a0001c0001t0002g0224 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-72-5063A>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115989576 | ||||||
chr7:115989609
|
G | A | 1 | a0001c0005t0014g0029 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-72-5096C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115989609 | ||||||
chr7:115989657
|
C | T | 1 | a0001c0001t0003g0356 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-72-5144G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115989657 | ||||||
chr7:115989847
|
C | A | 87 | a0001c0001t0001g0011a0001c0001t0001g0167a0001c0001t0001g0181others(84): Show | 99 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.-72-5334G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115989847 | ||||||
chr7:115990094
|
T | A | 35 | a0001c0001t0001g0150a0001c0001t0002g0007a0001c0001t0002g0046others(32): Show | 36 | HG00140.hp2 HG00642.hp1 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.-72-5581A>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115990094 | ||||||
chr7:115990136
|
A | T | 6 | a0001c0001t0006g0004a0001c0001t0006g0176a0001c0001t0006g0270others(3): Show | 8 | HG02258.hp2 HG02559.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.-72-5623T>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115990136 | ||||||
chr7:115990170
|
T | C | 18 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0042others(15): Show | 20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.-72-5657A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115990170 | ||||||
chr7:115990249
|
G | T | 1 | a0001c0001t0002g0196 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-72-5736C>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115990249 | ||||||
chr7:115990335
|
G | A | 263 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0011others(260): Show | 283 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(280): Show |
intron_variant | MODIFIER | c.-72-5822C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115990335 | ||||||
chr7:115990574
|
T | G | 1 | a0001c0001t0001g0358 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-72-6061A>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115990574 | ||||||
chr7:115990634
|
T | C | 1 | a0001c0001t0001g0041 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-72-6121A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115990634 | ||||||
chr7:115990849
|
G | A | 1 | a0001c0001t0002g0197 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-72-6336C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115990849 | ||||||
chr7:115990874
|
C | T | 1 | a0001c0001t0002g0134 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-72-6361G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115990874 | ||||||
chr7:115990875
|
A | G | 2 | a0001c0001t0001g0021a0001c0001t0001g0266 | 2 | HG02145.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.-72-6362T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115990875 | ||||||
chr7:115990946
|
G | T | 1 | a0001c0001t0001g0266 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-72-6433C>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115990946 | ||||||
chr7:115991032
|
C | A | 1 | a0001c0001t0030g0170 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-72-6519G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115991032 | ||||||
chr7:115991065
|
G | A | 18 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0042others(15): Show | 20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.-72-6552C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115991065 | ||||||
chr7:115991105
|
C | T | 2 | a0001c0001t0001g0065a0001c0001t0001g0066 | 2 | NA18965.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.-72-6592G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115991105 | ||||||
chr7:115991107
|
A | C | 1 | a0001c0001t0001g0011 | 2 | HG02809.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-72-6594T>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115991107 | ||||||
chr7:115991152
|
A | T | 1 | a0001c0001t0002g0015 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-72-6639T>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115991152 | ||||||
chr7:115991161
|
C | T | 18 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0042others(15): Show | 20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.-72-6648G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115991161 | ||||||
chr7:115991321
|
C | T | 18 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0042others(15): Show | 20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.-72-6808G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115991321 | ||||||
chr7:115991391
|
T | G | 1 | a0001c0001t0002g0015 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-72-6878A>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115991391 | ||||||
chr7:115991442
|
A | C | 18 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0042others(15): Show | 20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.-72-6929T>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115991442 | ||||||
chr7:115991472
|
A | G | 7 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(4): Show | 7 | HG00280.hp2 HG00642.hp2 HG00741.hp1 others(4): Show |
intron_variant | MODIFIER | c.-72-6959T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115991472 | ||||||
chr7:115991644
|
G | A | 1 | a0001c0001t0002g0153 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-72-7131C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115991644 | ||||||
chr7:115991695
|
C | A | 1 | a0001c0001t0001g0096 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-72-7182G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115991695 | ||||||
chr7:115991764
|
T | C | 4 | a0001c0001t0010g0131a0001c0001t0010g0171a0001c0001t0010g0172others(1): Show | 4 | HG03453.hp2 HG03579.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.-72-7251A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115991764 | ||||||
chr7:115991972
|
C | A | 1 | a0001c0001t0003g0303 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-72-7459G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115991972 | ||||||
chr7:115992066
|
A | T | 4 | a0001c0001t0003g0338a0001c0001t0003g0339a0001c0001t0003g0340others(1): Show | 4 | NA18984.hp2 NA18991.hp1 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.-72-7553T>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115992066 | ||||||
chr7:115992120
|
G | A | 1 | a0001c0001t0034g0276 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-72-7607C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115992120 | ||||||
chr7:115992175
|
C | A | 1 | a0001c0001t0001g0040 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-72-7662G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115992175 | ||||||
chr7:115992321
|
T | C | 2 | a0001c0001t0002g0249a0001c0009t0003g0329 | 2 | HG01261.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.-72-7808A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115992321 | ||||||
chr7:115992356
|
C | A | 11 | a0001c0001t0001g0178a0001c0001t0006g0004a0001c0001t0006g0176others(8): Show | 13 | HG02055.hp2 HG02109.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.-72-7843G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115992356 | ||||||
chr7:115992474
|
A | T | 6 | a0001c0001t0010g0131a0001c0001t0010g0171a0001c0001t0010g0172others(3): Show | 6 | HG02257.hp1 HG03453.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.-72-7961T>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115992474 | ||||||
chr7:115992491
|
T | A | 3 | a0001c0001t0012g0344a0001c0001t0012g0345a0001c0001t0012g0346 | 3 | NA18942.hp2 NA19057.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.-72-7978A>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115992491 | ||||||
chr7:115992580
|
A | G | 1 | a0001c0001t0003g0188 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-72-8067T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115992580 | ||||||
chr7:115992634
|
A | C | 282 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0011others(279): Show | 304 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(301): Show |
intron_variant | MODIFIER | c.-72-8121T>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115992634 | ||||||
chr7:115992674
|
T | C | 1 | a0001c0001t0024g0175 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-72-8161A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115992674 | ||||||
chr7:115992863
|
C | A | 2 | a0001c0001t0013g0012a0001c0001t0013g0190 | 3 | HG01069.hp2 HG01071.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.-72-8350G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115992863 | ||||||
chr7:115992973
|
G | A | 2 | a0001c0001t0001g0021a0001c0001t0001g0266 | 2 | HG02145.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.-72-8460C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115992973 | ||||||
chr7:115993054
|
G | A | 19 | a0001c0001t0001g0108a0001c0001t0004g0008a0001c0001t0004g0009others(16): Show | 21 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.-72-8541C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115993054 | ||||||
chr7:115993122
|
C | T | 18 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0042others(15): Show | 20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.-72-8609G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115993122 | ||||||
chr7:115993284
|
T | C | 1 | a0001c0001t0035g0179 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-72-8771A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115993284 | ||||||
chr7:115993380
|
T | G | 5 | a0001c0001t0001g0178a0001c0004t0001g0177a0001c0004t0001g0273others(2): Show | 5 | HG02055.hp2 HG02109.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-72-8867A>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115993380 | ||||||
chr7:115993420
|
C | A | 4 | a0001c0001t0003g0265a0001c0001t0003g0299a0001c0001t0003g0355others(1): Show | 4 | HG01433.hp1 HG02630.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.-72-8907G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115993420 | ||||||
chr7:115993474
|
A | G | 4 | a0001c0001t0014g0264a0001c0005t0014g0029a0001c0005t0014g0112others(1): Show | 4 | HG02630.hp2 HG02809.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-72-8961T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115993474 | ||||||
chr7:115993578
|
G | T | 131 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0021others(128): Show | 138 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.-72-9065C>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115993578 | ||||||
chr7:115993694
|
C | A | 1 | a0001c0001t0001g0086 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-72-9181G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115993694 | ||||||
chr7:115993756
|
A | G | 1 | a0001c0001t0001g0028 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-72-9243T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115993756 | ||||||
chr7:115993760
|
C | T | 1 | a0001c0001t0003g0307 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.-72-9247G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115993760 | ||||||
chr7:115993761
|
G | A | 3 | a0001c0001t0001g0087a0001c0001t0013g0012a0001c0001t0013g0190 | 4 | HG01069.hp2 HG01071.hp2 HG01074.hp1 others(1): Show |
intron_variant | MODIFIER | c.-72-9248C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115993761 | ||||||
chr7:115993816
|
A | AG | 18 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0042others(15): Show | 20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.-72-9304dupC | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115993816 | ||||||
chr7:115993877
|
G | A | 18 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0042others(15): Show | 20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.-72-9364C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115993877 | ||||||
chr7:115993892
|
T | C | 1 | a0001c0005t0014g0029 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-72-9379A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115993892 | ||||||
chr7:115994026
|
G | A | 2 | a0001c0001t0002g0007a0001c0001t0002g0151 | 3 | HG01074.hp2 HG01192.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.-72-9513C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115994026 | ||||||
chr7:115994143
|
G | A | 2 | a0001c0001t0034g0276a0001c0001t0035g0179 | 2 | HG02622.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-72-9630C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115994143 | ||||||
chr7:115994156
|
T | G | 2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | HG00280.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-72-9643A>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115994156 | ||||||
chr7:115994331
|
GCAACAAA others(3): Show |
G | 2 | a0001c0001t0018g0135a0001c0001t0018g0136 | 2 | HG02559.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.-72-9828_-72-9819d others(12): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115994331 | ||||||
chr7:115994346
|
A | T | 2 | a0001c0001t0018g0135a0001c0001t0018g0136 | 2 | HG02559.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.-72-9833T>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115994346 | ||||||
chr7:115994382
|
C | T | 2 | a0001c0001t0003g0306a0001c0001t0003g0331 | 2 | NA18955.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.-72-9869G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115994382 | ||||||
chr7:115994383
|
G | A | 5 | a0001c0001t0003g0280a0001c0001t0010g0131a0001c0001t0010g0171others(2): Show | 5 | HG03453.hp2 HG03579.hp1 NA18954.hp2 others(2): Show |
intron_variant | MODIFIER | c.-72-9870C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115994383 | ||||||
chr7:115994469
|
C | A | 4 | a0001c0001t0014g0264a0001c0005t0014g0029a0001c0005t0014g0112others(1): Show | 4 | HG02630.hp2 HG02809.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-72-9956G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115994469 | ||||||
chr7:115994566
|
C | T | 18 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0042others(15): Show | 20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.-72-10053G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115994566 | ||||||
chr7:115994600
|
C | A | 5 | a0001c0001t0001g0026a0001c0001t0001g0027a0003c0006t0001g0023others(2): Show | 5 | HG01255.hp2 HG01257.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.-72-10087G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115994600 | ||||||
chr7:115994701
|
G | A | 282 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0011others(279): Show | 304 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(301): Show |
intron_variant | MODIFIER | c.-72-10188C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115994701 | ||||||
chr7:115994842
|
G | A | 129 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0021others(126): Show | 136 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.-72-10329C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115994842 | ||||||
chr7:115994907
|
T | C | 7 | a0001c0001t0002g0139a0001c0001t0009g0137a0001c0001t0009g0138others(4): Show | 7 | HG00140.hp2 HG01243.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.-72-10394A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115994907 | ||||||
chr7:115994969
|
T | C | 2 | a0001c0001t0003g0119a0001c0001t0003g0313 | 2 | HG00609.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.-72-10456A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115994969 | ||||||
chr7:115994989
|
C | T | 1 | a0001c0001t0001g0358 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-72-10476G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115994989 | ||||||
chr7:115995007
|
T | C | 282 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0011others(279): Show | 304 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(301): Show |
intron_variant | MODIFIER | c.-72-10494A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115995007 | ||||||
chr7:115995045
|
T | C | 1 | a0001c0001t0003g0330 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-72-10532A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115995045 | ||||||
chr7:115995135
|
G | A | 2 | a0001c0001t0004g0165a0001c0001t0004g0295 | 2 | HG00733.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-72-10622C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115995135 | ||||||
chr7:115995175
|
C | G | 1 | a0001c0001t0002g0256 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-72-10662G>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115995175 | ||||||
chr7:115995266
|
G | A | 35 | a0001c0001t0001g0150a0001c0001t0002g0007a0001c0001t0002g0046others(32): Show | 36 | HG00140.hp2 HG00642.hp1 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.-72-10753C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115995266 | ||||||
chr7:115995338
|
G | T | 18 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0042others(15): Show | 20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.-72-10825C>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115995338 | ||||||
chr7:115995418
|
T | C | 1 | a0001c0001t0003g0133 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-72-10905A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115995418 | ||||||
chr7:115995421
|
G | T | 5 | a0001c0001t0001g0263a0001c0001t0001g0362a0001c0001t0001g0363others(2): Show | 5 | HG02109.hp2 HG02258.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-72-10908C>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115995421 | ||||||
chr7:115995451
|
C | T | 1 | a0001c0001t0030g0170 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-72-10938G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115995451 | ||||||
chr7:115995750
|
G | A | 1 | a0001c0001t0030g0170 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-72-11237C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115995750 | ||||||
chr7:115995789
|
C | T | 5 | a0001c0001t0001g0026a0001c0001t0001g0027a0003c0006t0001g0023others(2): Show | 5 | HG01255.hp2 HG01257.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.-72-11276G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115995789 | ||||||
chr7:115996324
|
T | A | 1 | a0001c0001t0024g0175 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-72-11811A>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115996324 | ||||||
chr7:115996405
|
G | A | 3 | a0001c0001t0001g0108a0001c0001t0001g0113a0001c0001t0001g0174 | 3 | HG02615.hp2 HG03041.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-72-11892C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115996405 | ||||||
chr7:115996448
|
G | A | 3 | a0001c0001t0003g0265a0001c0001t0003g0355a0001c0001t0003g0356 | 3 | HG02630.hp1 HG02818.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-72-11935C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115996448 | ||||||
chr7:115996700
|
A | T | 1 | a0001c0001t0007g0116 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-72-12187T>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115996700 | ||||||
chr7:115996701
|
C | G | 1 | a0001c0010t0002g0198 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-72-12188G>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115996701 | ||||||
chr7:115996796
|
G | C | 1 | a0001c0001t0002g0225 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-72-12283C>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115996796 | ||||||
chr7:115996844
|
G | A | 18 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0042others(15): Show | 20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.-72-12331C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115996844 | ||||||
chr7:115997000
|
G | A | 1 | a0001c0001t0034g0276 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-72-12487C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115997000 | ||||||
chr7:115997065
|
G | A | 2 | a0001c0001t0001g0021a0001c0001t0001g0266 | 2 | HG02145.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.-72-12552C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115997065 | ||||||
chr7:115997175
|
T | C | 1 | a0001c0001t0001g0088 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-72-12662A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115997175 | ||||||
chr7:115997308
|
A | G | 3 | a0001c0001t0015g0038a0001c0001t0015g0039a0001c0001t0015g0359 | 3 | HG02615.hp1 HG02717.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-72-12795T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115997308 | ||||||
chr7:115997414
|
G | A | 2 | a0001c0001t0003g0306a0001c0001t0003g0331 | 2 | NA18955.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.-72-12901C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115997414 | ||||||
chr7:115997516
|
T | C | 132 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0021others(129): Show | 139 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(136): Show |
intron_variant | MODIFIER | c.-72-13003A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115997516 | ||||||
chr7:115997527
|
C | T | 35 | a0001c0001t0001g0150a0001c0001t0002g0007a0001c0001t0002g0046others(32): Show | 36 | HG00140.hp2 HG00642.hp1 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.-72-13014G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115997527 | ||||||
chr7:115997645
|
T | C | 1 | a0001c0001t0002g0145 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-72-13132A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115997645 | ||||||
chr7:115997677
|
T | C | 1 | a0001c0001t0002g0049 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-72-13164A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115997677 | ||||||
chr7:115997714
|
G | A | 3 | a0001c0001t0004g0164a0001c0001t0004g0165a0001c0001t0004g0295 | 3 | HG00733.hp2 HG01884.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-72-13201C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115997714 | ||||||
chr7:115997972
|
A | G | 263 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0011others(260): Show | 283 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(280): Show |
intron_variant | MODIFIER | c.-72-13459T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115997972 | ||||||
chr7:115998145
|
C | A | 2 | a0001c0001t0003g0306a0001c0001t0003g0331 | 2 | NA18955.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.-72-13632G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115998145 | ||||||
chr7:115998146
|
C | T | 1 | a0001c0001t0001g0064 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-72-13633G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115998146 | ||||||
chr7:115998193
|
G | A | 18 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0042others(15): Show | 20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.-72-13680C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115998193 | ||||||
chr7:115998558
|
C | A | 2 | a0001c0001t0002g0052a0001c0001t0002g0053 | 2 | HG00738.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.-72-14045G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115998558 | ||||||
chr7:115998561
|
A | G | 18 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0042others(15): Show | 20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.-72-14048T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115998561 | ||||||
chr7:115998610
|
A | G | 1 | a0001c0001t0002g0234 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-72-14097T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115998610 | ||||||
chr7:115998849
|
T | C | 1 | a0001c0001t0002g0199 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-72-14336A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115998849 | ||||||
chr7:115998851
|
AAGAG | A | 106 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0028others(103): Show | 111 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.-72-14342_-72-1433 others(8): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115998851 | ||||||
chr7:115998852
|
A | G | 18 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0042others(15): Show | 20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.-72-14339T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115998852 | ||||||
chr7:115998951
|
A | G | 1 | a0001c0001t0025g0142 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-72-14438T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115998951 | ||||||
chr7:115999191
|
T | C | 89 | a0001c0001t0001g0011a0001c0001t0001g0167a0001c0001t0001g0181others(86): Show | 101 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.-72-14678A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115999191 | ||||||
chr7:115999291
|
A | G | 2 | a0001c0001t0001g0021a0001c0001t0001g0266 | 2 | HG02145.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.-72-14778T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115999291 | ||||||
chr7:115999396
|
A | T | 1 | a0001c0001t0001g0263 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-72-14883T>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115999396 | ||||||
chr7:115999447
|
G | T | 1 | a0001c0001t0002g0201 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-72-14934C>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115999447 | ||||||
chr7:115999513
|
T | C | 1 | a0001c0001t0010g0131 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-72-15000A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115999513 | ||||||
chr7:115999653
|
G | A | 1 | a0001c0001t0012g0344 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-72-15140C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115999653 | ||||||
chr7:115999844
|
C | CA | 176 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0021others(173): Show | 186 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.-72-15332dupT | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115999844 | ||||||
chr7:115999844
|
C | CAA | 100 | a0001c0001t0001g0011a0001c0001t0001g0026a0001c0001t0001g0027others(97): Show | 112 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.-72-15333_-72-1533 others(6): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115999844 | ||||||
chr7:116000022
|
A | C | 1 | a0001c0001t0009g0137 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-72-15509T>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116000022 | ||||||
chr7:116000096
|
C | A | 1 | a0001c0001t0003g0356 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-72-15583G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116000096 | ||||||
chr7:116000180
|
T | C | 1 | a0001c0001t0004g0158 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-72-15667A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116000180 | ||||||
chr7:116000205
|
C | T | 1 | a0004c0007t0001g0031 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-72-15692G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116000205 | ||||||
chr7:116000261
|
C | A | 2 | a0001c0001t0010g0171a0001c0001t0010g0172 | 2 | HG03453.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-72-15748G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116000261 | ||||||
chr7:116000261
|
C | T | 1 | a0001c0001t0003g0335 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-72-15748G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116000261 | ||||||
chr7:116000518
|
T | C | 4 | a0001c0001t0010g0131a0001c0001t0010g0171a0001c0001t0010g0172others(1): Show | 4 | HG03453.hp2 HG03579.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.-72-16005A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116000518 | ||||||
chr7:116000662
|
G | T | 2 | a0001c0001t0010g0171a0001c0001t0010g0172 | 2 | HG03453.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-72-16149C>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116000662 | ||||||
chr7:116000716
|
T | G | 1 | a0001c0001t0003g0305 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-72-16203A>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116000716 | ||||||
chr7:116000803
|
A | G | 1 | a0001c0001t0030g0170 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-72-16290T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116000803 | ||||||
chr7:116000882
|
A | T | 1 | a0001c0001t0002g0007 | 2 | HG01074.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.-72-16369T>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116000882 | ||||||
chr7:116000940
|
GA | G | 19 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0042others(16): Show | 21 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.-72-16428delT | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116000940 | ||||||
chr7:116000959
|
A | C | 1 | a0001c0001t0001g0022 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-72-16446T>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116000959 | ||||||
chr7:116001108
|
C | G | 4 | a0002c0003t0001g0092a0002c0003t0001g0094a0002c0003t0001g0114others(1): Show | 4 | HG02148.hp2 HG03490.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.-72-16595G>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116001108 | ||||||
chr7:116001111
|
A | G | 1 | a0001c0001t0012g0345 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-72-16598T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116001111 | ||||||
chr7:116001444
|
G | A | 3 | a0001c0001t0002g0046a0001c0001t0002g0048a0001c0001t0002g0049 | 3 | HG02602.hp1 HG03017.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.-72-16931C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116001444 | ||||||
chr7:116001486
|
C | T | 1 | a0001c0001t0003g0305 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-72-16973G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116001486 | ||||||
chr7:116001527
|
A | C | 1 | a0001c0001t0031g0154 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-72-17014T>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116001527 | ||||||
chr7:116001578
|
T | C | 1 | a0001c0001t0001g0187 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-72-17065A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116001578 | ||||||
chr7:116001795
|
T | C | 1 | a0001c0001t0011g0146 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-72-17282A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116001795 | ||||||
chr7:116001952
|
G | A | 35 | a0001c0001t0001g0150a0001c0001t0002g0007a0001c0001t0002g0046others(32): Show | 36 | HG00140.hp2 HG00642.hp1 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.-72-17439C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116001952 | ||||||
chr7:116001960
|
A | C | 282 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0011others(279): Show | 304 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(301): Show |
intron_variant | MODIFIER | c.-72-17447T>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116001960 | ||||||
chr7:116002035
|
G | A | 1 | a0001c0001t0037g0118 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-72-17522C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116002035 | ||||||
chr7:116002073
|
C | T | 1 | a0001c0001t0002g0243 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-72-17560G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116002073 | ||||||
chr7:116002585
|
A | G | 1 | a0001c0010t0002g0198 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-72-18072T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116002585 | ||||||
chr7:116002888
|
A | G | 1 | a0001c0001t0001g0061 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-72-18375T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116002888 | ||||||
chr7:116002916
|
G | T | 1 | a0001c0001t0002g0199 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-72-18403C>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116002916 | ||||||
chr7:116003119
|
C | T | 1 | a0001c0001t0001g0062 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-72-18606G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116003119 | ||||||
chr7:116003251
|
TA | T | 261 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0011others(258): Show | 281 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.-72-18739delT | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116003251 | ||||||
chr7:116003257
|
A | G | 11 | a0001c0001t0003g0119a0001c0001t0003g0123a0001c0001t0003g0307others(8): Show | 11 | HG00609.hp1 HG00621.hp2 HG00673.hp1 others(8): Show |
intron_variant | MODIFIER | c.-72-18744T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116003257 | ||||||
chr7:116003281
|
G | A | 18 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0042others(15): Show | 20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.-72-18768C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116003281 | ||||||
chr7:116003320
|
A | G | 364 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0011others(361): Show | 390 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(387): Show |
intron_variant | MODIFIER | c.-72-18807T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116003320 | ||||||
chr7:116003570
|
G | T | 2 | a0004c0007t0001g0031a0004c0007t0001g0032 | 2 | HG03017.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.-72-19057C>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116003570 | ||||||
chr7:116003615
|
C | G | 1 | a0001c0001t0001g0061 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-72-19102G>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116003615 | ||||||
chr7:116003681
|
T | C | 1 | a0001c0001t0001g0358 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-72-19168A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116003681 | ||||||
chr7:116003721
|
T | C | 1 | a0001c0001t0010g0131 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-72-19208A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116003721 | ||||||
chr7:116003754
|
C | T | 1 | a0001c0010t0002g0198 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-72-19241G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116003754 | ||||||
chr7:116004254
|
A | C | 1 | a0001c0001t0002g0243 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-72-19741T>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116004254 | ||||||
chr7:116004271
|
T | C | 18 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0042others(15): Show | 20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.-72-19758A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116004271 | ||||||
chr7:116004330
|
A | G | 2 | a0001c0001t0019g0168a0001c0001t0019g0169 | 2 | HG02486.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-72-19817T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116004330 | ||||||
chr7:116004482
|
G | A | 4 | a0001c0001t0010g0131a0001c0001t0010g0171a0001c0001t0010g0172others(1): Show | 4 | HG03453.hp2 HG03579.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.-72-19969C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116004482 | ||||||
chr7:116004795
|
A | G | 1 | a0001c0001t0002g0353 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-72-20282T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116004795 | ||||||
chr7:116004880
|
C | T | 18 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0042others(15): Show | 20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.-72-20367G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116004880 | ||||||
chr7:116005063
|
G | T | 5 | a0001c0001t0001g0263a0001c0001t0001g0362a0001c0001t0001g0363others(2): Show | 5 | HG02109.hp2 HG02258.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-72-20550C>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116005063 | ||||||
chr7:116005113
|
T | C | 1 | a0001c0001t0002g0226 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-72-20600A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116005113 | ||||||
chr7:116005150
|
G | T | 4 | a0001c0001t0014g0264a0001c0005t0014g0029a0001c0005t0014g0112others(1): Show | 4 | HG02630.hp2 HG02809.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-72-20637C>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116005150 | ||||||
chr7:116005156
|
A | T | 18 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0042others(15): Show | 20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.-72-20643T>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116005156 | ||||||
chr7:116005214
|
C | T | 87 | a0001c0001t0001g0011a0001c0001t0001g0167a0001c0001t0001g0181others(84): Show | 99 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.-72-20701G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116005214 | ||||||
chr7:116005253
|
T | C | 5 | a0001c0001t0001g0026a0001c0001t0001g0027a0003c0006t0001g0023others(2): Show | 5 | HG01255.hp2 HG01257.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.-72-20740A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116005253 | ||||||
chr7:116005302
|
A | T | 1 | a0001c0001t0001g0185 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-72-20789T>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116005302 | ||||||
chr7:116005348
|
C | T | 1 | a0001c0001t0003g0133 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-72-20835G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116005348 | ||||||
chr7:116005479
|
T | C | 282 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0011others(279): Show | 304 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(301): Show |
intron_variant | MODIFIER | c.-72-20966A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116005479 | ||||||
chr7:116005716
|
G | A | 39 | a0001c0001t0001g0150a0001c0001t0002g0007a0001c0001t0002g0046others(36): Show | 40 | HG00140.hp2 HG00642.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.-72-21203C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116005716 | ||||||
chr7:116005968
|
C | A | 1 | a0001c0001t0002g0182 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-72-21455G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116005968 | ||||||
chr7:116005999
|
C | T | 1 | a0001c0001t0003g0306 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-72-21486G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116005999 | ||||||
chr7:116006000
|
G | A | 2 | a0001c0001t0034g0276a0001c0001t0035g0179 | 2 | HG02622.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-72-21487C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116006000 | ||||||
chr7:116006005
|
T | A | 282 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0011others(279): Show | 304 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(301): Show |
intron_variant | MODIFIER | c.-72-21492A>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116006005 | ||||||
chr7:116006006
|
C | G | 262 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0011others(259): Show | 282 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.-72-21493G>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116006006 | ||||||
chr7:116006007
|
A | T | 4 | a0001c0001t0005g0005a0001c0001t0005g0019a0001c0001t0005g0287others(1): Show | 7 | HG00609.hp2 HG02027.hp1 NA18955.hp2 others(4): Show |
intron_variant | MODIFIER | c.-72-21494T>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116006007 | ||||||
chr7:116006103
|
G | A | 2 | a0001c0001t0034g0276a0001c0001t0035g0179 | 2 | HG02622.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-72-21590C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116006103 | ||||||
chr7:116006164
|
G | A | 4 | a0001c0001t0001g0109a0001c0004t0001g0177a0001c0004t0001g0273others(1): Show | 4 | HG02055.hp2 HG02145.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-72-21651C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116006164 | ||||||
chr7:116006180
|
G | A | 87 | a0001c0001t0001g0011a0001c0001t0001g0167a0001c0001t0001g0181others(84): Show | 99 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.-72-21667C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116006180 | ||||||
chr7:116006326
|
A | G | 1 | a0001c0001t0001g0022 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-72-21813T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116006326 | ||||||
chr7:116006428
|
T | C | 1 | a0001c0001t0008g0262 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-72-21915A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116006428 | ||||||
chr7:116006515
|
G | A | 4 | a0001c0001t0014g0264a0001c0005t0014g0029a0001c0005t0014g0112others(1): Show | 4 | HG02630.hp2 HG02809.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-72-22002C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116006515 | ||||||
chr7:116006653
|
T | C | 1 | a0001c0001t0002g0227 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-72-22140A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116006653 | ||||||
chr7:116006834
|
T | C | 1 | a0001c0001t0003g0335 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-72-22321A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116006834 | ||||||
chr7:116006837
|
G | A | 1 | a0001c0001t0003g0045 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.-72-22324C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116006837 | ||||||
chr7:116007117
|
C | T | 2 | a0004c0007t0001g0031a0004c0007t0001g0032 | 2 | HG03017.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.-72-22604G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116007117 | ||||||
chr7:116007158
|
G | A | 106 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0028others(103): Show | 111 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.-72-22645C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116007158 | ||||||
chr7:116007223
|
G | A | 2 | a0001c0001t0003g0343a0001c0001t0036g0336 | 2 | HG00673.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.-72-22710C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116007223 | ||||||
chr7:116007329
|
A | G | 7 | a0001c0001t0001g0060a0001c0001t0001g0263a0001c0001t0001g0362others(4): Show | 7 | HG01243.hp2 HG02055.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.-72-22816T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116007329 | ||||||
chr7:116007410
|
C | T | 1 | a0001c0001t0001g0167 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-72-22897G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116007410 | ||||||
chr7:116007447
|
G | A | 18 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0042others(15): Show | 20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.-72-22934C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116007447 | ||||||
chr7:116007449
|
A | C | 18 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0042others(15): Show | 20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.-72-22936T>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116007449 | ||||||
chr7:116007514
|
C | T | 5 | a0001c0001t0002g0139a0001c0001t0009g0137a0001c0001t0009g0138others(2): Show | 5 | HG00140.hp2 HG01243.hp1 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.-72-23001G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116007514 | ||||||
chr7:116007515
|
G | A | 1 | a0001c0001t0003g0133 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-72-23002C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116007515 | ||||||
chr7:116007571
|
T | C | 1 | a0001c0001t0002g0191 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-72-23058A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116007571 | ||||||
chr7:116007772
|
C | G | 10 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(7): Show | 10 | HG00642.hp1 HG00738.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.-73+22861G>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116007772 | ||||||
chr7:116007830
|
T | G | 1 | a0001c0001t0002g0228 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-73+22803A>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116007830 | ||||||
chr7:116007846
|
A | G | 1 | a0001c0001t0002g0148 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-73+22787T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116007846 | ||||||
chr7:116007992
|
GA | G | 4 | a0001c0001t0010g0131a0001c0001t0010g0171a0001c0001t0010g0172others(1): Show | 4 | HG03453.hp2 HG03579.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.-73+22640delT | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116007992 | ||||||
chr7:116008166
|
T | C | 112 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0026others(109): Show | 117 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.-73+22467A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116008166 | ||||||
chr7:116008251
|
G | A | 18 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0042others(15): Show | 20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.-73+22382C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116008251 | ||||||
chr7:116008525
|
T | A | 4 | a0001c0001t0010g0131a0001c0001t0010g0171a0001c0001t0010g0172others(1): Show | 4 | HG03453.hp2 HG03579.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.-73+22108A>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116008525 | ||||||
chr7:116008578
|
G | A | 1 | a0001c0001t0003g0279 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-73+22055C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116008578 | ||||||
chr7:116008693
|
A | G | 1 | a0001c0001t0001g0238 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-73+21940T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116008693 | ||||||
chr7:116008755
|
G | A | 14 | a0001c0001t0001g0022a0001c0001t0001g0178a0001c0001t0001g0187others(11): Show | 16 | HG02055.hp2 HG02109.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.-73+21878C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116008755 | ||||||
chr7:116008797
|
C | T | 1 | a0001c0001t0004g0158 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-73+21836G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116008797 | ||||||
chr7:116008853
|
C | T | 18 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0042others(15): Show | 20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.-73+21780G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116008853 | ||||||
chr7:116008860
|
T | C | 89 | a0001c0001t0001g0011a0001c0001t0001g0167a0001c0001t0001g0181others(86): Show | 101 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.-73+21773A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116008860 | ||||||
chr7:116008920
|
G | T | 1 | a0001c0001t0001g0367 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-73+21713C>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116008920 | ||||||
chr7:116008977
|
A | T | 1 | a0001c0001t0001g0189 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-73+21656T>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116008977 | ||||||
chr7:116009102
|
T | G | 3 | a0001c0001t0030g0170a0001c0001t0034g0276a0001c0001t0035g0179 | 3 | HG02622.hp1 HG02818.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-73+21531A>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116009102 | ||||||
chr7:116009169
|
C | T | 1 | a0001c0001t0033g0183 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-73+21464G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116009169 | ||||||
chr7:116009215
|
T | C | 1 | a0001c0001t0002g0229 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-73+21418A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116009215 | ||||||
chr7:116009297
|
C | G | 1 | a0001c0001t0002g0197 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-73+21336G>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116009297 | ||||||
chr7:116009311
|
C | G | 1 | a0001c0001t0001g0040 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-73+21322G>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116009311 | ||||||
chr7:116009400
|
G | A | 1 | a0001c0001t0003g0337 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-73+21233C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116009400 | ||||||
chr7:116009431
|
C | T | 1 | a0001c0001t0003g0305 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-73+21202G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116009431 | ||||||
chr7:116009572
|
A | G | 2 | a0001c0002t0001g0033a0001c0002t0001g0037 | 2 | HG01891.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-73+21061T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116009572 | ||||||
chr7:116009573
|
T | C | 1 | a0001c0001t0001g0089 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-73+21060A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116009573 | ||||||
chr7:116009590
|
A | G | 1 | a0001c0001t0002g0196 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-73+21043T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116009590 | ||||||
chr7:116009761
|
T | C | 5 | a0001c0001t0001g0026a0001c0001t0001g0027a0003c0006t0001g0023others(2): Show | 5 | HG01255.hp2 HG01257.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.-73+20872A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116009761 | ||||||
chr7:116009969
|
C | T | 36 | a0001c0001t0001g0150a0001c0001t0002g0007a0001c0001t0002g0046others(33): Show | 37 | HG00140.hp2 HG00642.hp1 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.-73+20664G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116009969 | ||||||
chr7:116010119
|
G | A | 4 | a0001c0001t0002g0230a0001c0001t0002g0231a0001c0001t0002g0232others(1): Show | 4 | HG01175.hp1 HG01516.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.-73+20514C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116010119 | ||||||
chr7:116010216
|
G | A | 1 | a0001c0001t0002g0233 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-73+20417C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116010216 | ||||||
chr7:116010480
|
G | A | 1 | a0005c0008t0023g0132 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-73+20153C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116010480 | ||||||
chr7:116010544
|
A | G | 2 | a0001c0002t0001g0033a0001c0002t0001g0037 | 2 | HG01891.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-73+20089T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116010544 | ||||||
chr7:116010805
|
T | A | 1 | a0001c0001t0001g0090 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-73+19828A>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116010805 | ||||||
chr7:116011286
|
T | C | 1 | a0001c0001t0001g0040 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-73+19347A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116011286 | ||||||
chr7:116011292
|
A | G | 1 | a0001c0001t0003g0304 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-73+19341T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116011292 | ||||||
chr7:116011344
|
T | C | 38 | a0001c0001t0001g0021a0001c0001t0001g0150a0001c0001t0001g0266others(35): Show | 39 | HG00140.hp2 HG00642.hp1 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.-73+19289A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116011344 | ||||||
chr7:116011446
|
T | A | 1 | a0001c0001t0024g0175 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-73+19187A>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116011446 | ||||||
chr7:116011509
|
T | C | 1 | a0001c0001t0002g0182 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-73+19124A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116011509 | ||||||
chr7:116011514
|
T | C | 2 | a0001c0001t0001g0367a0001c0001t0001g0368 | 2 | HG00423.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.-73+19119A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116011514 | ||||||
chr7:116011562
|
A | T | 1 | a0001c0001t0024g0175 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-73+19071T>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116011562 | ||||||
chr7:116011781
|
C | T | 282 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0011others(279): Show | 304 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(301): Show |
intron_variant | MODIFIER | c.-73+18852G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116011781 | ||||||
chr7:116011824
|
A | G | 1 | a0001c0001t0003g0303 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-73+18809T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116011824 | ||||||
chr7:116011853
|
C | A | 1 | a0001c0001t0015g0038 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-73+18780G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116011853 | ||||||
chr7:116011913
|
G | A | 14 | a0001c0001t0001g0022a0001c0001t0001g0178a0001c0001t0001g0187others(11): Show | 16 | HG02055.hp2 HG02109.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.-73+18720C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116011913 | ||||||
chr7:116011935
|
C | T | 2 | a0001c0001t0024g0175a0001c0001t0030g0170 | 2 | HG02922.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-73+18698G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116011935 | ||||||
chr7:116012211
|
T | G | 20 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0042others(17): Show | 22 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.-73+18422A>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116012211 | ||||||
chr7:116012302
|
C | T | 2 | a0001c0001t0034g0276a0001c0001t0035g0179 | 2 | HG02622.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-73+18331G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116012302 | ||||||
chr7:116012329
|
C | T | 2 | a0001c0001t0001g0058a0001c0001t0001g0059 | 2 | NA19003.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.-73+18304G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116012329 | ||||||
chr7:116012451
|
C | G | 3 | a0001c0001t0010g0171a0001c0001t0010g0172a0001c0001t0010g0173 | 3 | HG03453.hp2 HG03579.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-73+18182G>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116012451 | ||||||
chr7:116012648
|
A | C | 14 | a0001c0001t0001g0022a0001c0001t0001g0178a0001c0001t0001g0187others(11): Show | 16 | HG02055.hp2 HG02109.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.-73+17985T>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116012648 | ||||||
chr7:116012783
|
T | C | 1 | a0001c0001t0001g0185 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-73+17850A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116012783 | ||||||
chr7:116012816
|
T | A | 1 | a0001c0001t0001g0091 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-73+17817A>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116012816 | ||||||
chr7:116012826
|
GA | G | 216 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0011others(213): Show | 236 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(233): Show |
intron_variant | MODIFIER | c.-73+17806delT | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116012826 | ||||||
chr7:116012826
|
GAA | G | 52 | a0001c0001t0001g0021a0001c0001t0001g0057a0001c0001t0001g0150others(49): Show | 53 | HG00140.hp2 HG00642.hp1 HG00733.hp1 others(50): Show |
intron_variant | MODIFIER | c.-73+17805_-73+1780 others(6): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116012826 | ||||||
chr7:116012826
|
GAAA | G | 14 | a0001c0001t0001g0022a0001c0001t0001g0187a0001c0001t0001g0269others(11): Show | 16 | HG02109.hp1 HG02258.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.-73+17804_-73+1780 others(7): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116012826 | ||||||
chr7:116012961
|
T | C | 4 | a0001c0004t0001g0177a0001c0004t0001g0273a0001c0004t0001g0275others(1): Show | 4 | HG02055.hp2 HG02109.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-73+17672A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116012961 | ||||||
chr7:116013000
|
T | C | 1 | a0001c0001t0002g0148 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-73+17633A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116013000 | ||||||
chr7:116013124
|
T | C | 112 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0026others(109): Show | 117 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.-73+17509A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116013124 | ||||||
chr7:116013216
|
T | C | 1 | a0001c0001t0001g0178 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-73+17417A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116013216 | ||||||
chr7:116013233
|
T | G | 107 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0028others(104): Show | 112 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.-73+17400A>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116013233 | ||||||
chr7:116013280
|
T | G | 2 | a0001c0001t0002g0234a0001c0001t0002g0235 | 2 | NA19084.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.-73+17353A>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116013280 | ||||||
chr7:116013288
|
T | A | 101 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0167others(98): Show | 115 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.-73+17345A>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116013288 | ||||||
chr7:116013381
|
A | C | 1 | a0001c0001t0003g0133 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-73+17252T>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116013381 | ||||||
chr7:116013523
|
G | C | 1 | a0001c0001t0001g0187 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-73+17110C>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116013523 | ||||||
chr7:116013753
|
A | G | 1 | a0001c0001t0030g0170 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-73+16880T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116013753 | ||||||
chr7:116013861
|
T | C | 1 | a0001c0001t0022g0251 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-73+16772A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116013861 | ||||||
chr7:116013944
|
A | G | 87 | a0001c0001t0001g0011a0001c0001t0001g0167a0001c0001t0001g0181others(84): Show | 99 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.-73+16689T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116013944 | ||||||
chr7:116013945
|
T | C | 1 | a0001c0001t0002g0236 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-73+16688A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116013945 | ||||||
chr7:116014021
|
C | T | 171 | a0001c0001t0001g0011a0001c0001t0001g0021a0001c0001t0001g0022others(168): Show | 188 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.-73+16612G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116014021 | ||||||
chr7:116014066
|
C | T | 1 | a0001c0001t0010g0131 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-73+16567G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116014066 | ||||||
chr7:116014092
|
G | C | 1 | a0001c0001t0034g0276 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-73+16541C>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116014092 | ||||||
chr7:116014164
|
T | C | 2 | a0005c0008t0023g0132a0005c0008t0023g0180 | 2 | HG02257.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-73+16469A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116014164 | ||||||
chr7:116014270
|
A | G | 3 | a0001c0001t0002g0046a0001c0001t0002g0048a0001c0001t0002g0049 | 3 | HG02602.hp1 HG03017.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.-73+16363T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116014270 | ||||||
chr7:116014304
|
C | T | 1 | a0001c0001t0001g0127 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-73+16329G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116014304 | ||||||
chr7:116014330
|
C | T | 1 | a0001c0001t0001g0056 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.-73+16303G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116014330 | ||||||
chr7:116014460
|
C | A | 4 | a0001c0001t0010g0131a0001c0001t0010g0171a0001c0001t0010g0172others(1): Show | 4 | HG03453.hp2 HG03579.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.-73+16173G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116014460 | ||||||
chr7:116014510
|
T | C | 4 | a0001c0001t0010g0131a0001c0001t0010g0171a0001c0001t0010g0172others(1): Show | 4 | HG03453.hp2 HG03579.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.-73+16123A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116014510 | ||||||
chr7:116014943
|
A | G | 8 | a0001c0001t0010g0131a0001c0001t0010g0171a0001c0001t0010g0172others(5): Show | 8 | HG02257.hp1 HG02922.hp2 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.-73+15690T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116014943 | ||||||
chr7:116015068
|
T | G | 4 | a0001c0001t0003g0338a0001c0001t0003g0339a0001c0001t0003g0340others(1): Show | 4 | NA18984.hp2 NA18991.hp1 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.-73+15565A>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116015068 | ||||||
chr7:116015107
|
A | G | 2 | a0001c0005t0014g0112a0001c0005t0032g0111 | 2 | HG03098.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-73+15526T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116015107 | ||||||
chr7:116015332
|
A | G | 157 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0021others(154): Show | 163 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(160): Show |
intron_variant | MODIFIER | c.-73+15301T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116015332 | ||||||
chr7:116015341
|
G | C | 2 | a0001c0001t0034g0276a0001c0001t0035g0179 | 2 | HG02622.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-73+15292C>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116015341 | ||||||
chr7:116015344
|
A | G | 1 | a0001c0001t0003g0296 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-73+15289T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116015344 | ||||||
chr7:116015572
|
A | T | 1 | a0001c0001t0003g0279 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-73+15061T>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116015572 | ||||||
chr7:116015632
|
C | T | 177 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0021others(174): Show | 185 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.-73+15001G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116015632 | ||||||
chr7:116015728
|
G | T | 2 | a0001c0001t0001g0184a0001c0001t0033g0183 | 2 | HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.-73+14905C>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116015728 | ||||||
chr7:116015924
|
G | T | 278 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0011others(275): Show | 300 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(297): Show |
intron_variant | MODIFIER | c.-73+14709C>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116015924 | ||||||
chr7:116015926
|
G | A | 6 | a0001c0001t0010g0131a0001c0001t0010g0171a0001c0001t0010g0172others(3): Show | 6 | HG02257.hp1 HG03453.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.-73+14707C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116015926 | ||||||
chr7:116015987
|
T | C | 112 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0026others(109): Show | 117 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.-73+14646A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116015987 | ||||||
chr7:116016038
|
C | A | 2 | a0001c0001t0034g0276a0001c0001t0035g0179 | 2 | HG02622.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-73+14595G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116016038 | ||||||
chr7:116016054
|
A | G | 3 | a0001c0001t0002g0013a0001c0001t0002g0194a0001c0001t0002g0195 | 4 | HG00408.hp2 NA18957.hp2 NA19064.hp1 others(1): Show |
intron_variant | MODIFIER | c.-73+14579T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116016054 | ||||||
chr7:116016265
|
C | T | 3 | a0001c0001t0014g0264a0001c0001t0034g0276a0001c0001t0035g0179 | 3 | HG02622.hp1 HG02809.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-73+14368G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116016265 | ||||||
chr7:116016266
|
A | G | 284 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0011others(281): Show | 306 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(303): Show |
intron_variant | MODIFIER | c.-73+14367T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116016266 | ||||||
chr7:116016432
|
A | C | 1 | a0001c0001t0001g0181 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-73+14201T>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116016432 | ||||||
chr7:116016536
|
C | T | 1 | a0001c0001t0012g0344 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-73+14097G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116016536 | ||||||
chr7:116016614
|
T | C | 1 | a0001c0001t0030g0170 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-73+14019A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116016614 | ||||||
chr7:116016629
|
T | A | 1 | a0001c0001t0002g0237 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.-73+14004A>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116016629 | ||||||
chr7:116016676
|
C | T | 1 | a0001c0001t0001g0351 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-73+13957G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116016676 | ||||||
chr7:116016703
|
G | A | 1 | a0001c0001t0003g0265 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-73+13930C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116016703 | ||||||
chr7:116016845
|
T | C | 1 | a0001c0001t0001g0350 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-73+13788A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116016845 | ||||||
chr7:116016927
|
T | G | 1 | a0001c0002t0001g0037 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-73+13706A>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116016927 | ||||||
chr7:116017096
|
T | C | 120 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0026others(117): Show | 125 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.-73+13537A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116017096 | ||||||
chr7:116017134
|
T | A | 1 | a0001c0001t0006g0274 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-73+13499A>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116017134 | ||||||
chr7:116017179
|
A | T | 8 | a0001c0001t0010g0131a0001c0001t0010g0171a0001c0001t0010g0172others(5): Show | 8 | HG02257.hp1 HG02922.hp2 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.-73+13454T>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116017179 | ||||||
chr7:116017231
|
T | C | 112 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0026others(109): Show | 117 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.-73+13402A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116017231 | ||||||
chr7:116017254
|
C | T | 1 | a0001c0001t0002g0047 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-73+13379G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116017254 | ||||||
chr7:116017405
|
G | T | 8 | a0001c0001t0002g0016a0001c0001t0002g0017a0001c0001t0002g0018others(5): Show | 11 | HG00423.hp1 HG00673.hp2 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.-73+13228C>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116017405 | ||||||
chr7:116017411
|
A | G | 1 | a0001c0001t0002g0046 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-73+13222T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116017411 | ||||||
chr7:116017432
|
C | T | 1 | a0001c0001t0030g0170 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-73+13201G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116017432 | ||||||
chr7:116017454
|
C | T | 87 | a0001c0001t0001g0011a0001c0001t0001g0167a0001c0001t0001g0181others(84): Show | 99 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.-73+13179G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116017454 | ||||||
chr7:116017699
|
A | G | 1 | a0001c0001t0004g0155 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-73+12934T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116017699 | ||||||
chr7:116017981
|
G | GTGCACAG others(5): Show |
155 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0021others(152): Show | 161 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(158): Show |
intron_variant | MODIFIER | c.-73+12651_-73+1265 others(16): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116017981 | ||||||
chr7:116018199
|
A | G | 2 | a0001c0001t0001g0150a0001c0001t0002g0134 | 2 | HG03453.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-73+12434T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116018199 | ||||||
chr7:116018282
|
A | G | 2 | a0001c0001t0034g0276a0001c0001t0035g0179 | 2 | HG02622.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-73+12351T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116018282 | ||||||
chr7:116018358
|
C | T | 1 | a0001c0001t0030g0170 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-73+12275G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116018358 | ||||||
chr7:116018389
|
A | G | 1 | a0001c0001t0001g0055 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-73+12244T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116018389 | ||||||
chr7:116018610
|
C | G | 150 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0021others(147): Show | 156 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.-73+12023G>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116018610 | ||||||
chr7:116018615
|
G | A | 7 | a0001c0001t0002g0243a0001c0001t0002g0244a0001c0001t0002g0245others(4): Show | 7 | HG00735.hp1 HG01123.hp1 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.-73+12018C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116018615 | ||||||
chr7:116018991
|
A | C | 1 | a0001c0004t0029g0268 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-73+11642T>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116018991 | ||||||
chr7:116019073
|
A | G | 2 | a0001c0001t0018g0135a0001c0001t0018g0136 | 2 | HG02559.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.-73+11560T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116019073 | ||||||
chr7:116019192
|
C | T | 1 | a0001c0001t0002g0252 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-73+11441G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116019192 | ||||||
chr7:116019247
|
C | A | 1 | a0001c0001t0024g0175 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-73+11386G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116019247 | ||||||
chr7:116019315
|
C | T | 2 | a0001c0001t0001g0124a0001c0001t0001g0125 | 2 | HG01928.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.-73+11318G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116019315 | ||||||
chr7:116019753
|
C | A | 2 | a0001c0001t0001g0097a0001c0001t0001g0098 | 2 | HG01255.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.-73+10880G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116019753 | ||||||
chr7:116020203
|
T | C | 1 | a0001c0001t0002g0353 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-73+10430A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116020203 | ||||||
chr7:116020279
|
T | G | 2 | a0001c0001t0001g0021a0001c0001t0001g0266 | 2 | HG02145.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.-73+10354A>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116020279 | ||||||
chr7:116020281
|
G | A | 1 | a0001c0001t0030g0170 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-73+10352C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116020281 | ||||||
chr7:116020471
|
C | T | 1 | a0001c0001t0002g0193 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-73+10162G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116020471 | ||||||
chr7:116020483
|
C | T | 7 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(4): Show | 7 | HG00280.hp2 HG00642.hp2 HG00741.hp1 others(4): Show |
intron_variant | MODIFIER | c.-73+10150G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116020483 | ||||||
chr7:116020555
|
A | G | 5 | a0001c0001t0001g0026a0001c0001t0001g0027a0003c0006t0001g0023others(2): Show | 5 | HG01255.hp2 HG01257.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.-73+10078T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116020555 | ||||||
chr7:116020660
|
A | C | 1 | a0001c0001t0024g0175 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-73+9973T>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116020660 | ||||||
chr7:116020759
|
C | T | 1 | a0001c0001t0030g0170 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-73+9874G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116020759 | ||||||
chr7:116020785
|
T | C | 3 | a0001c0001t0015g0038a0001c0001t0015g0039a0001c0001t0015g0359 | 3 | HG02615.hp1 HG02717.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-73+9848A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116020785 | ||||||
chr7:116020795
|
A | G | 1 | a0001c0001t0002g0182 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-73+9838T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116020795 | ||||||
chr7:116020875
|
A | G | 1 | a0001c0001t0016g0360 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-73+9758T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116020875 | ||||||
chr7:116020912
|
T | C | 1 | a0001c0001t0001g0150 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-73+9721A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116020912 | ||||||
chr7:116020971
|
T | G | 1 | a0001c0001t0001g0187 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-73+9662A>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116020971 | ||||||
chr7:116021193
|
C | A | 105 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0028others(102): Show | 110 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.-73+9440G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116021193 | ||||||
chr7:116021273
|
C | T | 9 | a0001c0001t0005g0005a0001c0001t0005g0019a0001c0001t0005g0287others(6): Show | 12 | HG00609.hp2 HG02027.hp1 NA18949.hp2 others(9): Show |
intron_variant | MODIFIER | c.-73+9360G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116021273 | ||||||
chr7:116021340
|
T | A | 1 | a0001c0001t0014g0264 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-73+9293A>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116021340 | ||||||
chr7:116021563
|
T | C | 11 | a0001c0001t0001g0028a0001c0001t0001g0101a0001c0001t0001g0102others(8): Show | 11 | HG00733.hp1 HG01109.hp2 HG01168.hp2 others(8): Show |
intron_variant | MODIFIER | c.-73+9070A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116021563 | ||||||
chr7:116021635
|
T | C | 1 | a0001c0001t0001g0106 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-73+8998A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116021635 | ||||||
chr7:116021899
|
T | C | 1 | a0001c0001t0001g0107 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-73+8734A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116021899 | ||||||
chr7:116021953
|
G | A | 1 | a0001c0001t0002g0242 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-73+8680C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116021953 | ||||||
chr7:116021960
|
C | G | 1 | a0001c0001t0003g0286 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.-73+8673G>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116021960 | ||||||
chr7:116021991
|
A | T | 90 | a0001c0001t0001g0011a0001c0001t0001g0130a0001c0001t0001g0167others(87): Show | 102 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.-73+8642T>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116021991 | ||||||
chr7:116022075
|
C | T | 6 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(3): Show | 6 | HG01109.hp2 HG01255.hp2 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.-73+8558G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116022075 | ||||||
chr7:116022078
|
G | A | 3 | a0001c0001t0001g0021a0001c0001t0001g0266a0001c0001t0003g0265 | 3 | HG02145.hp1 HG02896.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-73+8555C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116022078 | ||||||
chr7:116022189
|
T | C | 1 | a0001c0001t0003g0343 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-73+8444A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116022189 | ||||||
chr7:116022222
|
C | A | 1 | a0001c0001t0001g0187 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-73+8411G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116022222 | ||||||
chr7:116022306
|
A | G | 1 | a0001c0005t0014g0029 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-73+8327T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116022306 | ||||||
chr7:116022346
|
G | A | 2 | a0001c0001t0002g0007a0001c0001t0002g0151 | 3 | HG01074.hp2 HG01192.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.-73+8287C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116022346 | ||||||
chr7:116022375
|
T | C | 3 | a0001c0001t0012g0344a0001c0001t0012g0345a0001c0001t0012g0346 | 3 | NA18942.hp2 NA19057.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.-73+8258A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116022375 | ||||||
chr7:116022498
|
G | A | 15 | a0001c0001t0001g0110a0001c0001t0001g0178a0001c0001t0001g0187others(12): Show | 17 | HG02055.hp2 HG02109.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.-73+8135C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116022498 | ||||||
chr7:116022551
|
G | A | 2 | a0001c0001t0034g0276a0001c0001t0035g0179 | 2 | HG02622.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-73+8082C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116022551 | ||||||
chr7:116022568
|
G | T | 1 | a0001c0001t0028g0282 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-73+8065C>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116022568 | ||||||
chr7:116022584
|
A | G | 1 | a0001c0001t0001g0181 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-73+8049T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116022584 | ||||||
chr7:116022899
|
G | T | 1 | a0001c0001t0001g0040 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-73+7734C>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116022899 | ||||||
chr7:116022905
|
G | C | 15 | a0001c0001t0001g0110a0001c0001t0001g0178a0001c0001t0001g0187others(12): Show | 17 | HG02055.hp2 HG02109.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.-73+7728C>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116022905 | ||||||
chr7:116023038
|
A | G | 3 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0003g0123 | 3 | HG01928.hp1 HG01928.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.-73+7595T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116023038 | ||||||
chr7:116023083
|
C | CA | 25 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0150others(22): Show | 26 | HG00140.hp2 HG01074.hp2 HG01192.hp2 others(23): Show |
intron_variant | MODIFIER | c.-73+7549dupT | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116023083 | ||||||
chr7:116023083
|
CA | C | 19 | a0001c0001t0001g0192a0001c0001t0001g0281a0001c0001t0004g0008others(16): Show | 21 | HG00323.hp1 HG00639.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.-73+7549delT | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116023083 | ||||||
chr7:116023206
|
T | C | 2 | a0001c0001t0003g0347a0001c0001t0003g0348 | 2 | NA18953.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.-73+7427A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116023206 | ||||||
chr7:116023491
|
G | A | 1 | a0001c0001t0035g0179 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-73+7142C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116023491 | ||||||
chr7:116023492
|
A | G | 1 | a0001c0001t0030g0170 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-73+7141T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116023492 | ||||||
chr7:116023827
|
A | C | 1 | a0001c0005t0032g0111 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-73+6806T>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116023827 | ||||||
chr7:116024077
|
G | T | 1 | a0001c0001t0002g0191 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-73+6556C>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116024077 | ||||||
chr7:116024129
|
C | T | 1 | a0001c0001t0031g0154 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-73+6504G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116024129 | ||||||
chr7:116024345
|
A | C | 3 | a0001c0001t0016g0357a0001c0001t0016g0360a0001c0001t0016g0361 | 3 | HG02451.hp2 HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-73+6288T>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116024345 | ||||||
chr7:116024403
|
G | A | 2 | a0001c0001t0001g0351a0001c0001t0001g0352 | 2 | HG03688.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.-73+6230C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116024403 | ||||||
chr7:116024547
|
T | A | 2 | a0001c0001t0034g0276a0001c0001t0035g0179 | 2 | HG02622.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-73+6086A>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116024547 | ||||||
chr7:116024638
|
A | G | 1 | a0001c0005t0014g0029 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-73+5995T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116024638 | ||||||
chr7:116024777
|
A | G | 29 | a0001c0001t0001g0150a0001c0001t0002g0007a0001c0001t0002g0134others(26): Show | 30 | HG00140.hp2 HG01074.hp2 HG01192.hp2 others(27): Show |
intron_variant | MODIFIER | c.-73+5856T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116024777 | ||||||
chr7:116024784
|
ATTTCCAT others(69): Show |
A | 3 | a0001c0001t0001g0021a0001c0001t0001g0266a0001c0001t0003g0265 | 3 | HG02145.hp1 HG02896.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-73+5773_-73+5848d others(78): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116024784 | ||||||
chr7:116024802
|
A | G | 2 | a0001c0001t0003g0279a0001c0001t0003g0280 | 2 | NA18954.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.-73+5831T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116024802 | ||||||
chr7:116024900
|
T | G | 17 | a0001c0001t0002g0016a0001c0001t0002g0017a0001c0001t0002g0018others(14): Show | 22 | HG00423.hp1 HG00558.hp1 HG00673.hp2 others(19): Show |
intron_variant | MODIFIER | c.-73+5733A>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116024900 | ||||||
chr7:116025370
|
G | A | 1 | a0001c0001t0001g0127 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-73+5263C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116025370 | ||||||
chr7:116025489
|
G | C | 1 | a0001c0001t0003g0349 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-73+5144C>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116025489 | ||||||
chr7:116025634
|
G | A | 29 | a0001c0001t0001g0021a0001c0001t0001g0026a0001c0001t0001g0027others(26): Show | 31 | HG00323.hp1 HG00639.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.-73+4999C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116025634 | ||||||
chr7:116025858
|
T | C | 1 | a0001c0001t0001g0110 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-73+4775A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116025858 | ||||||
chr7:116025879
|
C | A | 99 | a0001c0001t0001g0011a0001c0001t0001g0113a0001c0001t0001g0130others(96): Show | 111 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.-73+4754G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116025879 | ||||||
chr7:116026280
|
C | T | 2 | a0001c0001t0001g0130a0001c0001t0003g0278 | 2 | HG00621.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.-73+4353G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116026280 | ||||||
chr7:116026325
|
C | T | 89 | a0001c0001t0001g0281a0001c0001t0001g0342a0001c0001t0002g0283others(86): Show | 93 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(90): Show |
intron_variant | MODIFIER | c.-73+4308G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116026325 | ||||||
chr7:116026455
|
T | C | 1 | a0004c0007t0001g0032 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-73+4178A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116026455 | ||||||
chr7:116026566
|
C | T | 1 | a0001c0001t0026g0043 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-73+4067G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116026566 | ||||||
chr7:116026613
|
C | T | 1 | a0001c0001t0001g0167 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-73+4020G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116026613 | ||||||
chr7:116026614
|
T | G | 1 | a0001c0001t0001g0185 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-73+4019A>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116026614 | ||||||
chr7:116026645
|
T | C | 1 | a0001c0001t0002g0267 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-73+3988A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116026645 | ||||||
chr7:116026867
|
C | T | 3 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122 | 3 | HG00280.hp2 HG00741.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-73+3766G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116026867 | ||||||
chr7:116026891
|
A | G | 17 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0042others(14): Show | 19 | HG00323.hp1 HG00639.hp2 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.-73+3742T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116026891 | ||||||
chr7:116026937
|
T | C | 1 | a0002c0003t0001g0114 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-73+3696A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116026937 | ||||||
chr7:116027019
|
G | A | 111 | a0001c0001t0001g0130a0001c0001t0001g0150a0001c0001t0001g0189others(108): Show | 124 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.-73+3614C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116027019 | ||||||
chr7:116027100
|
G | C | 1 | a0001c0001t0001g0187 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-73+3533C>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116027100 | ||||||
chr7:116027173
|
T | C | 205 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0027others(202): Show | 222 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.-73+3460A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116027173 | ||||||
chr7:116027248
|
A | G | 3 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0002g0153 | 3 | HG00738.hp2 HG01358.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.-73+3385T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116027248 | ||||||
chr7:116027337
|
G | A | 2 | a0001c0001t0001g0263a0005c0008t0023g0132 | 2 | HG02258.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-73+3296C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116027337 | ||||||
chr7:116027495
|
G | A | 5 | a0001c0001t0001g0021a0001c0001t0001g0266a0001c0001t0003g0265others(2): Show | 5 | HG02145.hp1 HG02809.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-73+3138C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116027495 | ||||||
chr7:116027503
|
G | A | 1 | a0001c0001t0037g0118 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-73+3130C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116027503 | ||||||
chr7:116027539
|
G | T | 1 | a0001c0011t0004g0152 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-73+3094C>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116027539 | ||||||
chr7:116027603
|
A | T | 28 | a0001c0001t0001g0150a0001c0001t0002g0007a0001c0001t0002g0134others(25): Show | 29 | HG00140.hp2 HG00735.hp2 HG01074.hp2 others(26): Show |
intron_variant | MODIFIER | c.-73+3030T>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116027603 | ||||||
chr7:116027664
|
C | A | 5 | a0001c0001t0001g0021a0001c0001t0001g0266a0001c0001t0003g0265others(2): Show | 5 | HG02145.hp1 HG02809.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-73+2969G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116027664 | ||||||
chr7:116027677
|
T | C | 1 | a0001c0001t0034g0276 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-73+2956A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116027677 | ||||||
chr7:116027967
|
T | G | 3 | a0001c0001t0003g0355a0001c0001t0003g0356a0001c0001t0016g0357 | 3 | HG02630.hp1 HG02818.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-73+2666A>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116027967 | ||||||
chr7:116027968
|
C | T | 84 | a0001c0001t0001g0281a0001c0001t0001g0342a0001c0001t0001g0350others(81): Show | 88 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.-73+2665G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116027968 | ||||||
chr7:116028032
|
G | A | 84 | a0001c0001t0001g0281a0001c0001t0001g0342a0001c0001t0001g0350others(81): Show | 88 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.-73+2601C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116028032 | ||||||
chr7:116028129
|
T | C | 1 | a0001c0001t0001g0358 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-73+2504A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116028129 | ||||||
chr7:116028151
|
C | T | 1 | a0005c0008t0023g0132 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-73+2482G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116028151 | ||||||
chr7:116028245
|
C | A | 1 | a0001c0001t0003g0119 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-73+2388G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116028245 | ||||||
chr7:116028273
|
G | A | 1 | a0001c0001t0010g0131 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-73+2360C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116028273 | ||||||
chr7:116028274
|
C | G | 1 | a0001c0001t0010g0131 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-73+2359G>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116028274 | ||||||
chr7:116028426
|
T | C | 1 | a0001c0005t0014g0029 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-73+2207A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116028426 | ||||||
chr7:116028932
|
TAA | T | 85 | a0001c0001t0001g0281a0001c0001t0001g0342a0001c0001t0001g0350others(82): Show | 89 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.-73+1699_-73+1700d others(4): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116028932 | ||||||
chr7:116028943
|
T | C | 1 | a0001c0001t0002g0267 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-73+1690A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116028943 | ||||||
chr7:116029110
|
G | A | 8 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0027others(5): Show | 8 | HG01109.hp2 HG01255.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.-73+1523C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116029110 | ||||||
chr7:116029224
|
T | C | 1 | a0001c0004t0001g0275 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-73+1409A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116029224 | ||||||
chr7:116029315
|
C | G | 2 | a0004c0007t0001g0031a0004c0007t0001g0032 | 2 | HG03017.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.-73+1318G>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116029315 | ||||||
chr7:116029378
|
A | G | 85 | a0001c0001t0001g0281a0001c0001t0001g0342a0001c0001t0001g0350others(82): Show | 89 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.-73+1255T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116029378 | ||||||
chr7:116029414
|
G | A | 9 | a0001c0001t0001g0269a0001c0001t0006g0004a0001c0001t0006g0270others(6): Show | 11 | HG02055.hp2 HG02109.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.-73+1219C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116029414 | ||||||
chr7:116029643
|
A | G | 8 | a0001c0001t0001g0362a0001c0001t0001g0363a0001c0001t0001g0364others(5): Show | 8 | HG01243.hp2 HG02109.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-73+990T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116029643 | ||||||
chr7:116029763
|
C | T | 1 | a0001c0001t0001g0130 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-73+870G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116029763 | ||||||
chr7:116029771
|
C | A | 10 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(7): Show | 10 | HG00280.hp2 HG00642.hp2 HG00741.hp1 others(7): Show |
intron_variant | MODIFIER | c.-73+862G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116029771 | ||||||
chr7:116029771
|
C | T | 1 | a0001c0001t0003g0030 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-73+862G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116029771 | ||||||
chr7:116029904
|
C | CA | 256 | a0001c0001t0001g0011a0001c0001t0001g0021a0001c0001t0001g0022others(253): Show | 279 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.-73+728dupT | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116029904 | ||||||
chr7:116029958
|
T | C | 1 | a0001c0001t0034g0276 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-73+675A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116029958 | ||||||
chr7:116030002
|
G | A | 85 | a0001c0001t0001g0281a0001c0001t0001g0342a0001c0001t0001g0350others(82): Show | 89 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.-73+631C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116030002 | ||||||
chr7:116030013
|
C | A | 8 | a0001c0001t0001g0362a0001c0001t0001g0363a0001c0001t0001g0364others(5): Show | 8 | HG01243.hp2 HG02109.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-73+620G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116030013 | ||||||
chr7:116030105
|
C | A | 2 | a0001c0001t0001g0367a0001c0001t0001g0368 | 2 | HG00423.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.-73+528G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116030105 | ||||||
chr7:116030319
|
A | C | 8 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0027others(5): Show | 8 | HG01109.hp2 HG01255.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.-73+314T>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116030319 | ||||||
chr7:116030383
|
A | G | 1 | a0001c0001t0001g0021 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-73+250T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116030383 |