geneid | 7942 |
---|---|
ensemblid | ENSG00000112561.19 |
hgncid | 11753 |
symbol | TFEB |
name | transcription factor EB |
refseq_nuc | NM_001271944.2 |
refseq_prot | NP_001258873.1 |
ensembl_nuc | ENST00000373033.6 |
ensembl_prot | ENSP00000362124.1 |
mane_status | MANE Select |
chr | chr6 |
start | 41683978 |
end | 41735608 |
strand | - |
ver | v1.2 |
region | chr6:41683978-41735608 |
region5000 | chr6:41678978-41740608 |
regionname0 | TFEB_chr6_41683978_41735608 |
regionname5000 | TFEB_chr6_41678978_41740608 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 476 | 397 | 91 | 81 | 163 | 14 | 46 | 118 | TFEB_chr6_41678978_41740608 | TFEB | copy fasta | chr6 | 41678978 | 41740608 |
a0002 | 0/0 | 476 | 6 | 0 | 0 | 6 | 0 | 0 | 5 | TFEB_chr6_41678978_41740608 | TFEB | copy fasta | chr6 | 41678978 | 41740608 |
a0003 | 0/0 | 476 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | copy fasta | chr6 | 41678978 | 41740608 |
a0004 | 0/0 | 476 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | copy fasta | chr6 | 41678978 | 41740608 |
a0005 | 0/0 | 476 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | copy fasta | chr6 | 41678978 | 41740608 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 1431 | 125 | 49 | 31 | 38 | 1 | 5 | TFEB_chr6_41678978_41740608 | TFEB | copy fasta | chr6 | 41678978 | 41740608 |
c0002 | 1/0 | 1431 | 96 | 7 | 16 | 58 | 4 | 10 | TFEB_chr6_41678978_41740608 | TFEB | copy fasta | chr6 | 41678978 | 41740608 |
c0003 | 0/0 | 1431 | 91 | 7 | 23 | 39 | 5 | 17 | TFEB_chr6_41678978_41740608 | TFEB | copy fasta | chr6 | 41678978 | 41740608 |
c0004 | 0/0 | 1431 | 46 | 5 | 8 | 25 | 2 | 6 | TFEB_chr6_41678978_41740608 | TFEB | copy fasta | chr6 | 41678978 | 41740608 |
c0005 | 0/0 | 1431 | 35 | 21 | 2 | 3 | 2 | 7 | TFEB_chr6_41678978_41740608 | TFEB | copy fasta | chr6 | 41678978 | 41740608 |
c0006 | 0/0 | 1431 | 6 | 0 | 0 | 6 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | copy fasta | chr6 | 41678978 | 41740608 |
c0007 | 0/0 | 1431 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | copy fasta | chr6 | 41678978 | 41740608 |
c0008 | 0/0 | 1431 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | copy fasta | chr6 | 41678978 | 41740608 |
c0009 | 0/0 | 1431 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | copy fasta | chr6 | 41678978 | 41740608 |
c0010 | 0/0 | 1431 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | copy fasta | chr6 | 41678978 | 41740608 |
c0011 | 0/0 | 1431 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | copy fasta | chr6 | 41678978 | 41740608 |
c0012 | 0/0 | 1431 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | copy fasta | chr6 | 41678978 | 41740608 |
c0013 | 0/0 | 1431 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | copy fasta | chr6 | 41678978 | 41740608 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 903 | 277 | 71 | 51 | 107 | 12 | 35 | TFEB_chr6_41678978_41740608 | TFEB | copy fasta | chr6 | 41678978 | 41740608 |
t0002 | 0/1 | 903 | 96 | 14 | 18 | 51 | 2 | 10 | TFEB_chr6_41678978_41740608 | TFEB | copy fasta | chr6 | 41678978 | 41740608 |
t0003 | 0/0 | 903 | 19 | 2 | 7 | 10 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | copy fasta | chr6 | 41678978 | 41740608 |
t0004 | 0/0 | 903 | 3 | 0 | 3 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | copy fasta | chr6 | 41678978 | 41740608 |
t0005 | 0/0 | 903 | 2 | 2 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | copy fasta | chr6 | 41678978 | 41740608 |
t0006 | 0/0 | 903 | 2 | 0 | 0 | 2 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | copy fasta | chr6 | 41678978 | 41740608 |
t0007 | 0/0 | 903 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | copy fasta | chr6 | 41678978 | 41740608 |
t0008 | 0/0 | 903 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | copy fasta | chr6 | 41678978 | 41740608 |
t0009 | 0/0 | 903 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | copy fasta | chr6 | 41678978 | 41740608 |
t0010 | 0/0 | 903 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | copy fasta | chr6 | 41678978 | 41740608 |
t0011 | 0/0 | 903 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | copy fasta | chr6 | 41678978 | 41740608 |
t0012 | 0/0 | 903 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | copy fasta | chr6 | 41678978 | 41740608 |
t0013 | 0/0 | 891 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | copy fasta | chr6 | 41678978 | 41740608 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 10 | 0 | 1 | 9 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0002 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0003 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0004 | 0/1 | 4 | 0 | 3 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0006 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0007 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0008 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0013 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0015 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0016 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0017 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0026 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0159 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0320 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0352 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 1431 | 125 | 49 | 31 | 38 | 1 | 5 | TFEB_chr6_41678978_41740608 | TFEB | copy fasta | chr6 | 41678978 | 41740608 |
a0001c0002 | 1/0 | 1431 | 96 | 7 | 16 | 58 | 4 | 10 | TFEB_chr6_41678978_41740608 | TFEB | copy fasta | chr6 | 41678978 | 41740608 |
a0001c0003 | 0/0 | 1431 | 91 | 7 | 23 | 39 | 5 | 17 | TFEB_chr6_41678978_41740608 | TFEB | copy fasta | chr6 | 41678978 | 41740608 |
a0001c0004 | 0/0 | 1431 | 46 | 5 | 8 | 25 | 2 | 6 | TFEB_chr6_41678978_41740608 | TFEB | copy fasta | chr6 | 41678978 | 41740608 |
a0001c0005 | 0/0 | 1431 | 35 | 21 | 2 | 3 | 2 | 7 | TFEB_chr6_41678978_41740608 | TFEB | copy fasta | chr6 | 41678978 | 41740608 |
a0001c0007 | 0/0 | 1431 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | copy fasta | chr6 | 41678978 | 41740608 |
a0001c0008 | 0/0 | 1431 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | copy fasta | chr6 | 41678978 | 41740608 |
a0001c0010 | 0/0 | 1431 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | copy fasta | chr6 | 41678978 | 41740608 |
a0001c0012 | 0/0 | 1431 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | copy fasta | chr6 | 41678978 | 41740608 |
a0002c0006 | 0/0 | 1431 | 6 | 0 | 0 | 6 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | copy fasta | chr6 | 41678978 | 41740608 |
a0003c0011 | 0/0 | 1431 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | copy fasta | chr6 | 41678978 | 41740608 |
a0004c0009 | 0/0 | 1431 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | copy fasta | chr6 | 41678978 | 41740608 |
a0005c0013 | 0/0 | 1431 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | copy fasta | chr6 | 41678978 | 41740608 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2333 | 53 | 36 | 14 | 1 | 1 | 1 | TFEB_chr6_41678978_41740608 | TFEB | copy fasta | chr6 | 41678978 | 41740608 |
a0001c0001t0002 | 0/1 | 2333 | 50 | 9 | 9 | 27 | 0 | 4 | TFEB_chr6_41678978_41740608 | TFEB | copy fasta | chr6 | 41678978 | 41740608 |
a0001c0001t0003 | 0/0 | 2333 | 19 | 2 | 7 | 10 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | copy fasta | chr6 | 41678978 | 41740608 |
a0001c0001t0008 | 0/0 | 2333 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | copy fasta | chr6 | 41678978 | 41740608 |
a0001c0001t0012 | 0/0 | 2333 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | copy fasta | chr6 | 41678978 | 41740608 |
a0001c0001t0013 | 0/0 | 2321 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | copy fasta | chr6 | 41678978 | 41740608 |
a0001c0002t0001 | 1/0 | 2333 | 94 | 7 | 14 | 58 | 4 | 10 | TFEB_chr6_41678978_41740608 | TFEB | copy fasta | chr6 | 41678978 | 41740608 |
a0001c0002t0007 | 0/0 | 2333 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | copy fasta | chr6 | 41678978 | 41740608 |
a0001c0002t0010 | 0/0 | 2333 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | copy fasta | chr6 | 41678978 | 41740608 |
a0001c0003t0001 | 0/0 | 2333 | 87 | 7 | 20 | 39 | 5 | 16 | TFEB_chr6_41678978_41740608 | TFEB | copy fasta | chr6 | 41678978 | 41740608 |
a0001c0003t0002 | 0/0 | 2333 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | copy fasta | chr6 | 41678978 | 41740608 |
a0001c0003t0004 | 0/0 | 2333 | 3 | 0 | 3 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | copy fasta | chr6 | 41678978 | 41740608 |
a0001c0004t0002 | 0/0 | 2333 | 43 | 5 | 8 | 23 | 2 | 5 | TFEB_chr6_41678978_41740608 | TFEB | copy fasta | chr6 | 41678978 | 41740608 |
a0001c0004t0006 | 0/0 | 2333 | 2 | 0 | 0 | 2 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | copy fasta | chr6 | 41678978 | 41740608 |
a0001c0004t0011 | 0/0 | 2333 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | copy fasta | chr6 | 41678978 | 41740608 |
a0001c0005t0001 | 0/0 | 2333 | 32 | 18 | 2 | 3 | 2 | 7 | TFEB_chr6_41678978_41740608 | TFEB | copy fasta | chr6 | 41678978 | 41740608 |
a0001c0005t0005 | 0/0 | 2333 | 2 | 2 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | copy fasta | chr6 | 41678978 | 41740608 |
a0001c0005t0009 | 0/0 | 2333 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | copy fasta | chr6 | 41678978 | 41740608 |
a0001c0007t0001 | 0/0 | 2333 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | copy fasta | chr6 | 41678978 | 41740608 |
a0001c0008t0002 | 0/0 | 2333 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | copy fasta | chr6 | 41678978 | 41740608 |
a0001c0010t0001 | 0/0 | 2333 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | copy fasta | chr6 | 41678978 | 41740608 |
a0001c0012t0001 | 0/0 | 2333 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | copy fasta | chr6 | 41678978 | 41740608 |
a0002c0006t0001 | 0/0 | 2333 | 6 | 0 | 0 | 6 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | copy fasta | chr6 | 41678978 | 41740608 |
a0003c0011t0001 | 0/0 | 2333 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | copy fasta | chr6 | 41678978 | 41740608 |
a0004c0009t0002 | 0/0 | 2333 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | copy fasta | chr6 | 41678978 | 41740608 |
a0005c0013t0001 | 0/0 | 2333 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | copy fasta | chr6 | 41678978 | 41740608 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0001g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0001g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0001g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0001g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0002g0004 | 0/1 | 4 | 0 | 3 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0002g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0002g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0002g0016 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0002g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0002g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0002g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0002g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0002g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0002g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0003g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0003g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0003g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0003g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0003g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0003g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0003g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0003g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0003g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0003g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0003g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0003g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0008g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0012g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0001t0013g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0002t0001g0001 | 0/0 | 10 | 0 | 1 | 9 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0002t0001g0002 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0002t0001g0017 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0002t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0002t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0002t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0002t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0002t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0002t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0002t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0002t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0002t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0002t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0002t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0002t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0002t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0002t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0002t0001g0159 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0002t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0002t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0002t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0002t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0002t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0002t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0002t0001g0320 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0002t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0002t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0002t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0002t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0002t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0002t0001g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0002t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0002t0007g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0002t0010g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0003t0001g0006 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0003t0001g0007 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0003t0001g0008 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0003t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0003t0001g0013 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0003t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0003t0001g0015 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0003t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0003t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0003t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0003t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0003t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0003t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0003t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0003t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0003t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0003t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0003t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0003t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0003t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0003t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0003t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0003t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0003t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0003t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0003t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0003t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0003t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0003t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0003t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0003t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0003t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0003t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0003t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0003t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0003t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0003t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0003t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0003t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0003t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0003t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0003t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0003t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0003t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0003t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0003t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0003t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0003t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0003t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0003t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0003t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0003t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0003t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0003t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0003t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0003t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0003t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0003t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0003t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0003t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0003t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0003t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0003t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0003t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0003t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0003t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0003t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0003t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0003t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0003t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0003t0001g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0003t0001g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0003t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0003t0001g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0003t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0003t0001g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0003t0002g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0003t0004g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0003t0004g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0004t0002g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0004t0002g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0004t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0004t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0004t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0004t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0004t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0004t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0004t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0004t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0004t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0004t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0004t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0004t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0004t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0004t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0004t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0004t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0004t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0004t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0004t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0004t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0004t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0004t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0004t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0004t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0004t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0004t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0004t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0004t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0004t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0004t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0004t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0004t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0004t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0004t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0004t0002g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0004t0002g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0004t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0004t0002g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0004t0002g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0004t0006g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0004t0011g0352 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0005t0001g0026 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0005t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0005t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0005t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0005t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0005t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0005t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0005t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0005t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0005t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0005t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0005t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0005t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0005t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0005t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0005t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0005t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0005t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0005t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0005t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0005t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0005t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0005t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0005t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0005t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0005t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0005t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0005t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0005t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0005t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0005t0001g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0005t0005g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0005t0009g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0007t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0008t0002g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0010t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0001c0012t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0002c0006t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0002c0006t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0002c0006t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0002c0006t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0002c0006t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0003c0011t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0004c0009t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
a0005c0013t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0002 | t0001 | g0049 | EUR | GBR | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG00140 | hp2 | a0001 | c0005 | t0001 | g0026 | EUR | GBR | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG00280 | hp1 | a0001 | c0002 | t0001 | g0045 | EUR | FIN | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0104 | EUR | FIN | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG00323 | hp1 | a0001 | c0004 | t0002 | g0199 | EUR | FIN | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG00323 | hp2 | a0001 | c0003 | t0001 | g0065 | EUR | FIN | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG00408 | hp1 | a0001 | c0004 | t0002 | g0181 | EAS | CHS | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG00408 | hp2 | a0001 | c0003 | t0001 | g0298 | EAS | CHS | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0296 | EAS | CHS | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG00423 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG00438 | hp1 | a0001 | c0003 | t0001 | g0080 | EAS | CHS | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG00438 | hp2 | a0001 | c0002 | t0001 | g0347 | EAS | CHS | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG00544 | hp1 | a0002 | c0006 | t0001 | g0300 | EAS | CHS | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | CHS | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0330 | EAS | CHS | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG00558 | hp2 | a0001 | c0003 | t0001 | g0010 | EAS | CHS | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG00597 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | CHS | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG00597 | hp2 | a0001 | c0003 | t0001 | g0209 | EAS | CHS | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0313 | EAS | CHS | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG00609 | hp2 | a0001 | c0001 | t0003 | g0076 | EAS | CHS | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG00621 | hp1 | a0001 | c0004 | t0002 | g0182 | EAS | CHS | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0319 | EAS | CHS | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG00639 | hp1 | a0001 | c0002 | t0001 | g0346 | AMR | PUR | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0308 | AMR | PUR | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG00642 | hp1 | a0001 | c0003 | t0001 | g0102 | AMR | PUR | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0255 | AMR | PUR | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG00673 | hp1 | a0001 | c0003 | t0001 | g0010 | EAS | CHS | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | CHS | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0058 | AMR | PUR | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG00733 | hp2 | a0001 | c0003 | t0001 | g0160 | AMR | PUR | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG00735 | hp2 | a0005 | c0013 | t0001 | g0142 | AMR | PUR | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG00738 | hp1 | a0001 | c0003 | t0001 | g0015 | AMR | PUR | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG00738 | hp2 | a0001 | c0004 | t0002 | g0238 | AMR | PUR | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG00741 | hp2 | a0001 | c0001 | t0003 | g0250 | AMR | PUR | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG01069 | hp1 | a0001 | c0003 | t0004 | g0021 | AMR | PUR | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0307 | AMR | PUR | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG01070 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG01071 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG01074 | hp1 | a0001 | c0003 | t0001 | g0056 | AMR | PUR | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG01074 | hp2 | a0001 | c0004 | t0002 | g0237 | AMR | PUR | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0253 | AMR | PUR | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG01081 | hp2 | a0001 | c0002 | t0001 | g0143 | AMR | PUR | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG01099 | hp1 | a0001 | c0003 | t0001 | g0087 | AMR | PUR | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG01099 | hp2 | a0001 | c0003 | t0004 | g0021 | AMR | PUR | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG01106 | hp2 | a0001 | c0003 | t0001 | g0006 | AMR | PUR | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG01109 | hp1 | a0001 | c0003 | t0004 | g0043 | AMR | PUR | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG01109 | hp2 | a0001 | c0003 | t0001 | g0179 | AMR | PUR | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG01167 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG01168 | hp1 | a0001 | c0004 | t0002 | g0024 | AMR | PUR | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG01168 | hp2 | a0001 | c0005 | t0001 | g0118 | AMR | PUR | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG01169 | hp1 | a0001 | c0004 | t0002 | g0024 | AMR | PUR | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG01175 | hp1 | a0001 | c0003 | t0001 | g0064 | AMR | PUR | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG01175 | hp2 | a0001 | c0002 | t0001 | g0040 | AMR | PUR | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG01192 | hp1 | a0001 | c0002 | t0001 | g0044 | AMR | PUR | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG01192 | hp2 | a0001 | c0003 | t0001 | g0067 | AMR | PUR | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0016 | AMR | PUR | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG01243 | hp2 | a0001 | c0002 | t0001 | g0042 | AMR | PUR | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG01255 | hp1 | a0001 | c0002 | t0001 | g0322 | AMR | CLM | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG01255 | hp2 | a0001 | c0002 | t0001 | g0017 | AMR | CLM | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG01257 | hp2 | a0001 | c0003 | t0001 | g0052 | AMR | CLM | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | CLM | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | CLM | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0103 | AMR | CLM | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG01346 | hp1 | a0001 | c0003 | t0001 | g0006 | AMR | CLM | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG01346 | hp2 | a0001 | c0001 | t0003 | g0343 | AMR | CLM | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG01358 | hp1 | a0001 | c0004 | t0002 | g0003 | AMR | CLM | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG01358 | hp2 | a0001 | c0002 | t0001 | g0100 | AMR | CLM | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG01361 | hp1 | a0001 | c0005 | t0001 | g0269 | AMR | CLM | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG01361 | hp2 | a0001 | c0003 | t0001 | g0013 | AMR | CLM | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | CLM | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0099 | AMR | CLM | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG01515 | hp1 | a0001 | c0003 | t0001 | g0061 | EUR | IBS | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG01515 | hp2 | a0001 | c0004 | t0002 | g0055 | EUR | IBS | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG01516 | hp1 | a0001 | c0003 | t0001 | g0013 | EUR | IBS | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG01516 | hp2 | a0001 | c0003 | t0001 | g0041 | EUR | IBS | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | ACB | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | ACB | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0109 | AFR | ACB | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG01891 | hp2 | a0001 | c0001 | t0012 | g0353 | AFR | ACB | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG01928 | hp1 | a0001 | c0003 | t0001 | g0233 | AMR | PEL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG01934 | hp1 | a0001 | c0008 | t0002 | g0309 | AMR | PEL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG01934 | hp2 | a0001 | c0002 | t0001 | g0038 | AMR | PEL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG01943 | hp1 | a0001 | c0002 | t0007 | g0031 | AMR | PEL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG01943 | hp2 | a0001 | c0003 | t0001 | g0231 | AMR | PEL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG01952 | hp1 | a0001 | c0003 | t0001 | g0232 | AMR | PEL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG01952 | hp2 | a0001 | c0002 | t0001 | g0177 | AMR | PEL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG01975 | hp1 | a0001 | c0001 | t0003 | g0230 | AMR | PEL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG01975 | hp2 | a0001 | c0004 | t0002 | g0138 | AMR | PEL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG01981 | hp1 | a0001 | c0001 | t0008 | g0032 | AMR | PEL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG01981 | hp2 | a0001 | c0003 | t0001 | g0336 | AMR | PEL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG01993 | hp1 | a0001 | c0002 | t0001 | g0133 | AMR | PEL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG01993 | hp2 | a0001 | c0001 | t0003 | g0338 | AMR | PEL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG02004 | hp1 | a0001 | c0001 | t0003 | g0235 | AMR | PEL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG02004 | hp2 | a0001 | c0002 | t0010 | g0321 | AMR | PEL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG02015 | hp1 | a0001 | c0001 | t0003 | g0333 | EAS | KHV | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG02015 | hp2 | a0001 | c0001 | t0002 | g0288 | EAS | KHV | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG02027 | hp1 | a0001 | c0003 | t0001 | g0169 | EAS | KHV | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0151 | EAS | KHV | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | KHV | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG02040 | hp2 | a0001 | c0003 | t0001 | g0331 | EAS | KHV | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0283 | AFR | ACB | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG02055 | hp2 | a0001 | c0005 | t0001 | g0131 | AFR | ACB | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG02056 | hp1 | a0001 | c0003 | t0001 | g0335 | EAS | KHV | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0323 | EAS | KHV | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG02071 | hp1 | a0001 | c0003 | t0001 | g0310 | EAS | KHV | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG02071 | hp2 | a0001 | c0004 | t0002 | g0213 | EAS | KHV | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG02080 | hp1 | a0001 | c0003 | t0001 | g0074 | EAS | KHV | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG02080 | hp2 | a0001 | c0004 | t0002 | g0317 | EAS | KHV | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG02083 | hp1 | a0001 | c0002 | t0001 | g0312 | EAS | KHV | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0175 | EAS | KHV | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG02129 | hp1 | a0001 | c0001 | t0003 | g0079 | EAS | KHV | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | KHV | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG02132 | hp1 | a0001 | c0003 | t0001 | g0211 | EAS | KHV | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG02132 | hp2 | a0001 | c0003 | t0001 | g0010 | EAS | KHV | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG02135 | hp1 | a0001 | c0002 | t0001 | g0146 | EAS | KHV | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG02135 | hp2 | a0001 | c0002 | t0001 | g0279 | EAS | KHV | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG02145 | hp1 | a0001 | c0005 | t0001 | g0096 | AFR | ACB | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG02145 | hp2 | a0001 | c0005 | t0001 | g0345 | AFR | ACB | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG02148 | hp1 | a0001 | c0003 | t0001 | g0334 | AMR | PEL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG02148 | hp2 | a0001 | c0001 | t0003 | g0337 | AMR | PEL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0212 | EAS | CDX | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG02155 | hp2 | a0001 | c0002 | t0001 | g0200 | EAS | CDX | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | CDX | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG02165 | hp2 | a0001 | c0001 | t0003 | g0340 | EAS | CDX | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | ACB | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG02257 | hp2 | a0001 | c0005 | t0001 | g0240 | AFR | ACB | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG02273 | hp1 | a0001 | c0004 | t0002 | g0234 | AMR | PEL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG02273 | hp2 | a0001 | c0003 | t0001 | g0101 | AMR | PEL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0107 | AFR | ACB | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG02280 | hp2 | a0001 | c0005 | t0001 | g0270 | AFR | ACB | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0315 | AMR | PEL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0342 | AMR | PEL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG02300 | hp1 | a0001 | c0004 | t0002 | g0003 | AMR | PEL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG02300 | hp2 | a0001 | c0001 | t0003 | g0119 | AMR | PEL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG02451 | hp1 | a0001 | c0005 | t0001 | g0241 | AFR | ACB | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | ACB | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG02523 | hp1 | a0001 | c0004 | t0002 | g0215 | EAS | KHV | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG02523 | hp2 | a0001 | c0003 | t0001 | g0073 | EAS | KHV | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG02572 | hp1 | a0001 | c0003 | t0001 | g0291 | AFR | GWD | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | GWD | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG02602 | hp1 | a0001 | c0003 | t0001 | g0095 | SAS | PJL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG02602 | hp2 | a0001 | c0003 | t0001 | g0324 | SAS | PJL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG02615 | hp1 | a0001 | c0001 | t0013 | g0354 | AFR | GWD | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG02615 | hp2 | a0001 | c0003 | t0001 | g0060 | AFR | GWD | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG02622 | hp2 | a0001 | c0007 | t0001 | g0261 | AFR | GWD | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0273 | AFR | GWD | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG02647 | hp1 | a0001 | c0005 | t0005 | g0030 | AFR | GWD | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG02683 | hp1 | a0001 | c0003 | t0001 | g0325 | SAS | PJL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG02683 | hp2 | a0001 | c0002 | t0001 | g0054 | SAS | PJL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG02698 | hp1 | a0001 | c0003 | t0001 | g0090 | SAS | PJL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG02698 | hp2 | a0001 | c0002 | t0001 | g0145 | SAS | PJL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG02717 | hp1 | a0001 | c0001 | t0002 | g0091 | AFR | GWD | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG02717 | hp2 | a0001 | c0005 | t0001 | g0127 | AFR | GWD | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG02723 | hp1 | a0001 | c0003 | t0001 | g0272 | AFR | GWD | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | GWD | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0083 | SAS | PJL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG02735 | hp2 | a0001 | c0003 | t0001 | g0062 | SAS | PJL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG02738 | hp1 | a0001 | c0002 | t0001 | g0050 | SAS | PJL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG02809 | hp1 | a0001 | c0004 | t0002 | g0348 | AFR | GWD | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0223 | AFR | GWD | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG02818 | hp1 | a0001 | c0005 | t0001 | g0225 | AFR | GWD | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | GWD | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | GWD | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG02886 | hp2 | a0001 | c0002 | t0001 | g0251 | AFR | GWD | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | GWD | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | GWD | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG02896 | hp2 | a0001 | c0005 | t0001 | g0267 | AFR | GWD | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG02897 | hp1 | a0001 | c0005 | t0001 | g0268 | AFR | GWD | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0260 | AFR | ESN | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0108 | AFR | ESN | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | ESN | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG02965 | hp2 | a0001 | c0001 | t0003 | g0164 | AFR | ESN | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | ESN | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG02976 | hp1 | a0001 | c0005 | t0005 | g0030 | AFR | ESN | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | ESN | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG03017 | hp1 | a0001 | c0005 | t0001 | g0097 | SAS | PJL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG03017 | hp2 | a0001 | c0004 | t0011 | g0352 | SAS | PJL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG03041 | hp1 | a0001 | c0004 | t0002 | g0124 | AFR | GWD | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG03041 | hp2 | a0001 | c0003 | t0001 | g0292 | AFR | GWD | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG03098 | hp1 | a0001 | c0001 | t0002 | g0094 | AFR | MSL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG03098 | hp2 | a0001 | c0005 | t0001 | g0257 | AFR | MSL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | ESN | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG03130 | hp2 | a0001 | c0002 | t0001 | g0258 | AFR | ESN | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | ESN | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | ESN | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ESN | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0254 | AFR | ESN | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG03209 | hp1 | a0001 | c0004 | t0002 | g0226 | AFR | MSL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG03209 | hp2 | a0001 | c0010 | t0001 | g0265 | AFR | MSL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG03225 | hp1 | a0001 | c0001 | t0002 | g0222 | AFR | MSL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | MSL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG03239 | hp1 | a0001 | c0002 | t0001 | g0123 | SAS | PJL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG03239 | hp2 | a0001 | c0002 | t0001 | g0051 | SAS | PJL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG03453 | hp1 | a0001 | c0003 | t0001 | g0290 | AFR | MSL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | MSL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG03486 | hp1 | a0001 | c0005 | t0001 | g0242 | AFR | MSL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG03486 | hp2 | a0001 | c0005 | t0001 | g0276 | AFR | MSL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0022 | SAS | PJL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG03490 | hp2 | a0001 | c0004 | t0002 | g0280 | SAS | PJL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0022 | SAS | PJL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG03492 | hp2 | a0001 | c0004 | t0002 | g0243 | SAS | PJL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG03516 | hp2 | a0001 | c0005 | t0009 | g0259 | AFR | ESN | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG03540 | hp1 | a0001 | c0005 | t0001 | g0221 | AFR | GWD | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG03540 | hp2 | a0001 | c0005 | t0001 | g0239 | AFR | GWD | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG03579 | hp1 | a0001 | c0002 | t0001 | g0136 | AFR | MSL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG03579 | hp2 | a0001 | c0002 | t0001 | g0017 | AFR | MSL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG03654 | hp1 | a0001 | c0002 | t0001 | g0162 | SAS | PJL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG03654 | hp2 | a0001 | c0003 | t0001 | g0008 | SAS | PJL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG03669 | hp1 | a0001 | c0004 | t0002 | g0188 | SAS | PJL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG03669 | hp2 | a0001 | c0005 | t0001 | g0287 | SAS | PJL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG03688 | hp1 | a0001 | c0002 | t0001 | g0163 | SAS | STU | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG03688 | hp2 | a0001 | c0003 | t0001 | g0035 | SAS | STU | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0289 | SAS | PJL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG03704 | hp2 | a0001 | c0003 | t0001 | g0089 | SAS | PJL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG03710 | hp1 | a0001 | c0012 | t0001 | g0121 | SAS | PJL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG03710 | hp2 | a0001 | c0004 | t0002 | g0171 | SAS | PJL | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG03831 | hp1 | a0001 | c0002 | t0001 | g0149 | SAS | BEB | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG03831 | hp2 | a0001 | c0003 | t0001 | g0008 | SAS | BEB | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG03927 | hp1 | a0001 | c0003 | t0001 | g0277 | SAS | BEB | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG03927 | hp2 | a0001 | c0005 | t0001 | g0161 | SAS | BEB | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG03942 | hp1 | a0001 | c0003 | t0001 | g0154 | SAS | BEB | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG03942 | hp2 | a0001 | c0003 | t0001 | g0007 | SAS | BEB | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG04115 | hp1 | a0001 | c0002 | t0001 | g0046 | SAS | STU | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG04115 | hp2 | a0001 | c0003 | t0001 | g0088 | SAS | STU | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG04184 | hp1 | a0001 | c0005 | t0001 | g0153 | SAS | BEB | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG04184 | hp2 | a0001 | c0005 | t0001 | g0106 | SAS | BEB | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG04199 | hp1 | a0001 | c0003 | t0002 | g0278 | SAS | STU | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG04199 | hp2 | a0001 | c0002 | t0001 | g0053 | SAS | STU | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG04204 | hp1 | a0001 | c0003 | t0001 | g0015 | SAS | STU | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG04204 | hp2 | a0001 | c0005 | t0001 | g0284 | SAS | STU | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG04228 | hp1 | a0001 | c0003 | t0001 | g0047 | SAS | STU | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG04228 | hp2 | a0001 | c0005 | t0001 | g0066 | SAS | STU | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA18522 | hp1 | a0001 | c0003 | t0001 | g0059 | AFR | YRI | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0252 | AFR | YRI | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA18747 | hp1 | a0001 | c0002 | t0001 | g0173 | EAS | CHB | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA18747 | hp2 | a0001 | c0003 | t0001 | g0075 | EAS | CHB | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA18906 | hp1 | a0001 | c0002 | t0001 | g0156 | AFR | YRI | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA18906 | hp2 | a0001 | c0002 | t0001 | g0120 | AFR | YRI | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA18939 | hp1 | a0001 | c0002 | t0001 | g0327 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA18939 | hp2 | a0001 | c0004 | t0002 | g0206 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA18940 | hp1 | a0002 | c0006 | t0001 | g0027 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA18940 | hp2 | a0001 | c0004 | t0002 | g0203 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA18941 | hp1 | a0001 | c0002 | t0001 | g0304 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA18941 | hp2 | a0001 | c0002 | t0001 | g0155 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA18944 | hp1 | a0001 | c0004 | t0006 | g0003 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA18944 | hp2 | a0001 | c0002 | t0001 | g0176 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA18945 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0302 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA18946 | hp1 | a0001 | c0003 | t0001 | g0299 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA18946 | hp2 | a0001 | c0002 | t0001 | g0332 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA18950 | hp1 | a0001 | c0005 | t0001 | g0039 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA18950 | hp2 | a0002 | c0006 | t0001 | g0293 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA18952 | hp1 | a0001 | c0004 | t0002 | g0339 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA18952 | hp2 | a0001 | c0003 | t0001 | g0078 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA18954 | hp1 | a0001 | c0003 | t0001 | g0068 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA18954 | hp2 | a0001 | c0002 | t0001 | g0141 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA18960 | hp1 | a0004 | c0009 | t0002 | g0183 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA18960 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA18963 | hp1 | a0001 | c0003 | t0001 | g0297 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA18963 | hp2 | a0001 | c0004 | t0002 | g0205 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA18966 | hp1 | a0001 | c0003 | t0001 | g0189 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA18966 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA18967 | hp1 | a0001 | c0003 | t0001 | g0081 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA18967 | hp2 | a0001 | c0002 | t0001 | g0147 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0328 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA18969 | hp2 | a0001 | c0002 | t0001 | g0193 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA18970 | hp1 | a0001 | c0002 | t0001 | g0341 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA18970 | hp2 | a0001 | c0003 | t0001 | g0204 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA18971 | hp1 | a0001 | c0002 | t0001 | g0207 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA18971 | hp2 | a0001 | c0003 | t0001 | g0282 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA18973 | hp1 | a0002 | c0006 | t0001 | g0027 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA18973 | hp2 | a0001 | c0002 | t0001 | g0150 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA18974 | hp1 | a0001 | c0003 | t0001 | g0014 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA18974 | hp2 | a0001 | c0002 | t0001 | g0168 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0318 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA18979 | hp2 | a0001 | c0002 | t0001 | g0148 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA18980 | hp1 | a0001 | c0001 | t0002 | g0303 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA18980 | hp2 | a0001 | c0003 | t0001 | g0178 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA18981 | hp1 | a0001 | c0003 | t0001 | g0082 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA18981 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA18982 | hp1 | a0002 | c0006 | t0001 | g0295 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA18982 | hp2 | a0001 | c0004 | t0002 | g0186 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA18983 | hp1 | a0001 | c0003 | t0001 | g0077 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA18983 | hp2 | a0001 | c0004 | t0002 | g0191 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA18984 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA18984 | hp2 | a0001 | c0004 | t0002 | g0190 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA18985 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA18985 | hp2 | a0001 | c0002 | t0001 | g0152 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA18988 | hp1 | a0001 | c0004 | t0002 | g0218 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA18988 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA18990 | hp1 | a0001 | c0002 | t0001 | g0286 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA18990 | hp2 | a0001 | c0002 | t0001 | g0157 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA18991 | hp1 | a0001 | c0004 | t0002 | g0117 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA18991 | hp2 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA18993 | hp1 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA18993 | hp2 | a0001 | c0004 | t0002 | g0208 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0311 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA18995 | hp2 | a0001 | c0004 | t0002 | g0192 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA18999 | hp1 | a0002 | c0006 | t0001 | g0294 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA18999 | hp2 | a0001 | c0002 | t0001 | g0020 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA19000 | hp1 | a0001 | c0004 | t0002 | g0185 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA19000 | hp2 | a0001 | c0004 | t0002 | g0219 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA19001 | hp1 | a0001 | c0002 | t0001 | g0135 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA19001 | hp2 | a0001 | c0004 | t0002 | g0184 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA19004 | hp1 | a0001 | c0003 | t0001 | g0007 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA19004 | hp2 | a0001 | c0001 | t0003 | g0201 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA19007 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA19007 | hp2 | a0001 | c0002 | t0001 | g0217 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA19009 | hp1 | a0001 | c0002 | t0001 | g0020 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA19009 | hp2 | a0001 | c0003 | t0001 | g0144 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA19010 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA19010 | hp2 | a0001 | c0005 | t0001 | g0275 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA19011 | hp1 | a0001 | c0004 | t0006 | g0003 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0329 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA19012 | hp1 | a0001 | c0003 | t0001 | g0071 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA19012 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA19030 | hp1 | a0001 | c0003 | t0001 | g0036 | AFR | LWK | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0350 | AFR | LWK | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA19054 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA19054 | hp2 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA19056 | hp2 | a0001 | c0003 | t0001 | g0037 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA19059 | hp1 | a0001 | c0003 | t0001 | g0014 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA19059 | hp2 | a0001 | c0002 | t0001 | g0167 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA19060 | hp1 | a0001 | c0004 | t0002 | g0202 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA19060 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA19062 | hp1 | a0001 | c0002 | t0001 | g0195 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA19062 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA19063 | hp1 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA19063 | hp2 | a0001 | c0003 | t0001 | g0092 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA19064 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA19064 | hp2 | a0001 | c0003 | t0001 | g0084 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA19065 | hp1 | a0001 | c0001 | t0003 | g0166 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA19065 | hp2 | a0001 | c0002 | t0001 | g0316 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA19066 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA19066 | hp2 | a0001 | c0003 | t0001 | g0033 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA19067 | hp1 | a0001 | c0004 | t0002 | g0210 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA19067 | hp2 | a0001 | c0002 | t0001 | g0271 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA19068 | hp2 | a0001 | c0003 | t0001 | g0007 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA19070 | hp2 | a0001 | c0003 | t0001 | g0158 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA19072 | hp1 | a0001 | c0002 | t0001 | g0140 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA19072 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA19074 | hp1 | a0001 | c0003 | t0001 | g0070 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA19074 | hp2 | a0001 | c0002 | t0001 | g0128 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA19077 | hp1 | a0001 | c0002 | t0001 | g0306 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA19077 | hp2 | a0001 | c0002 | t0001 | g0174 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA19080 | hp1 | a0001 | c0002 | t0001 | g0285 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA19080 | hp2 | a0001 | c0004 | t0002 | g0198 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA19082 | hp1 | a0001 | c0002 | t0001 | g0134 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA19082 | hp2 | a0001 | c0001 | t0002 | g0314 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA19083 | hp1 | a0001 | c0002 | t0001 | g0244 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA19083 | hp2 | a0001 | c0002 | t0001 | g0305 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA19087 | hp1 | a0001 | c0004 | t0002 | g0180 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA19087 | hp2 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA19088 | hp1 | a0001 | c0003 | t0001 | g0085 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA19088 | hp2 | a0001 | c0002 | t0001 | g0086 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA19089 | hp1 | a0001 | c0002 | t0001 | g0214 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA19089 | hp2 | a0001 | c0002 | t0001 | g0326 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA19090 | hp1 | a0001 | c0002 | t0001 | g0172 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA19090 | hp2 | a0001 | c0003 | t0001 | g0069 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0351 | AFR | YRI | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA19240 | hp2 | a0001 | c0004 | t0002 | g0126 | AFR | YRI | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | ASW | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA20129 | hp2 | a0003 | c0011 | t0001 | g0229 | AFR | ASW | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA20752 | hp1 | a0001 | c0005 | t0001 | g0026 | EUR | TSI | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA20752 | hp2 | a0001 | c0002 | t0001 | g0320 | EUR | TSI | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA20805 | hp1 | a0001 | c0002 | t0001 | g0098 | EUR | TSI | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA20805 | hp2 | a0001 | c0003 | t0001 | g0057 | EUR | TSI | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA20905 | hp1 | a0001 | c0004 | t0002 | g0034 | SAS | GIH | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA20905 | hp2 | a0001 | c0003 | t0001 | g0008 | SAS | GIH | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG01123 | hp1 | a0001 | c0003 | t0001 | g0072 | AMR | CLM | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG01123 | hp2 | a0001 | c0003 | t0001 | g0006 | AMR | CLM | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG02486 | hp1 | a0001 | c0001 | t0003 | g0165 | AFR | ACB | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG02486 | hp2 | a0001 | c0004 | t0002 | g0125 | AFR | ACB | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | ACB | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0349 | AFR | USA | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
HG06807 | hp2 | a0001 | c0005 | t0001 | g0274 | AFR | USA | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA18955 | hp1 | a0001 | c0005 | t0001 | g0063 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA18955 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA20300 | hp1 | a0001 | c0002 | t0001 | g0137 | AFR | USA | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA20300 | hp2 | a0001 | c0005 | t0001 | g0281 | AFR | USA | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA21309 | hp1 | a0001 | c0005 | t0001 | g0344 | AFR | LWK | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | LWK | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0004 | REF | REF | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
homoSapiens_grch38 | hp1 | a0001 | c0002 | t0001 | g0159 | REF | REF | TFEB_chr6_41678978_41740608 | TFEB | chr6 | 41678978 | 41740608 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:41684885
|
G | C | 1 | a0005 | 1 | HG00735.hp2 | missense_variant | MODERATE | c.1145C>G | p.Pro382Arg | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 9/9 | 1426/2333 | 1145/1431 | 382/476 | chr6 | 41684885 | ||
chr6:41685059
|
C | T | 1 | a0004 | 1 | NA18960.hp1 | missense_variant | MODERATE | c.971G>A | p.Arg324Gln | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 9/9 | 1252/2333 | 971/1431 | 324/476 | chr6 | 41685059 | ||
chr6:41690743
|
C | T | 1 | a0002 | 6 | HG00544.hp1 NA18940.hp1 NA18950.hp2 others(3): Show |
missense_variant | MODERATE | c.388G>A | p.Val130Met | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 3/9 | 669/2333 | 388/1431 | 130/476 | chr6 | 41690743 | ||
chr6:41691062
|
G | A | 1 | a0003 | 1 | NA20129.hp2 | missense_variant | MODERATE | c.152C>T | p.Pro51Leu | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 2/9 | 433/2333 | 152/1431 | 51/476 | chr6 | 41691062 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:41684776
|
C | T | 2 | a0001c0003a0002c0006 | 97 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(94): Show |
synonymous_variant | LOW | c.1254G>A | p.Ala418Ala | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 9/9 | 1535/2333 | 1254/1431 | 418/476 | chr6 | 41684776 | ||
chr6:41684866
|
T | C | 9 | a0001c0001a0001c0003a0001c0004others(6): Show | 307 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(304): Show |
synonymous_variant | LOW | c.1164A>G | p.Pro388Pro | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 9/9 | 1445/2333 | 1164/1431 | 388/476 | chr6 | 41684866 | ||
chr6:41690786
|
C | T | 1 | a0001c0012 | 1 | HG03710.hp1 | synonymous_variant | LOW | c.345G>A | p.Pro115Pro | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 3/9 | 626/2333 | 345/1431 | 115/476 | chr6 | 41690786 | ||
chr6:41690828
|
C | T | 2 | a0001c0004a0004c0009 | 47 | HG00323.hp1 HG00408.hp1 HG00621.hp1 others(44): Show |
synonymous_variant | LOW | c.303G>A | p.Gly101Gly | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 3/9 | 584/2333 | 303/1431 | 101/476 | chr6 | 41690828 | ||
chr6:41691046
|
G | A | 1 | a0001c0007 | 1 | HG02622.hp2 | synonymous_variant | LOW | c.168C>T | p.Pro56Pro | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 2/9 | 449/2333 | 168/1431 | 56/476 | chr6 | 41691046 | ||
chr6:41691061
|
C | T | 1 | a0001c0008 | 1 | HG01934.hp1 | synonymous_variant | LOW | c.153G>A | p.Pro51Pro | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 2/9 | 434/2333 | 153/1431 | 51/476 | chr6 | 41691061 | ||
chr6:41691151
|
C | T | 7 | a0001c0001a0001c0004a0001c0007others(4): Show | 176 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(173): Show |
synonymous_variant | LOW | c.63G>A | p.Gln21Gln | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 2/9 | 344/2333 | 63/1431 | 21/476 | chr6 | 41691151 | ||
chr6:41691166
|
C | T | 1 | a0001c0007 | 1 | HG02622.hp2 | synonymous_variant | LOW | c.48G>A | p.Ala16Ala | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 2/9 | 329/2333 | 48/1431 | 16/476 | chr6 | 41691166 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:41684156
|
G | C | 1 | a0001c0005t0009 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*443C>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 9/9 | 443 | chr6 | 41684156 | |||||
chr6:41684366
|
G | A | 2 | a0001c0001t0003a0001c0001t0008 | 20 | HG00597.hp1 HG00609.hp2 HG00741.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*233C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 9/9 | 233 | chr6 | 41684366 | |||||
chr6:41684398
|
G | A | 7 | a0001c0001t0002a0001c0003t0002a0001c0004t0002others(4): Show | 99 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*201C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 9/9 | 201 | chr6 | 41684398 | |||||
chr6:41684430
|
C | A | 1 | a0001c0002t0010 | 1 | HG02004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*169G>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 9/9 | 169 | chr6 | 41684430 | |||||
chr6:41684484
|
G | A | 1 | a0001c0003t0004 | 3 | HG01069.hp1 HG01099.hp2 HG01109.hp1 |
3_prime_UTR_variant | MODIFIER | c.*115C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 9/9 | 115 | chr6 | 41684484 | |||||
chr6:41735397
|
G | A | 1 | a0001c0004t0011 | 1 | HG03017.hp2 | 5_prime_UTR_variant | MODIFIER | c.-70C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/9 | 44184 | chr6 | 41735397 | |||||
chr6:41735504
|
CCGCCGCC others(5): Show |
C | 1 | a0001c0001t0013 | 1 | HG02615.hp1 | 5_prime_UTR_variant | MODIFIER | c.-189_-178delCCGACG others(6): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/9 | 44292 | chr6 | 41735504 | |||||
chr6:41735507
|
C | A | 1 | a0001c0001t0012 | 1 | HG01891.hp2 | 5_prime_UTR_variant | MODIFIER | c.-180G>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/9 | 44294 | chr6 | 41735507 | |||||
chr6:41735571
|
C | A | 1 | a0001c0005t0005 | 2 | HG02647.hp1 HG02976.hp1 |
5_prime_UTR_variant | MODIFIER | c.-244G>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/9 | 44358 | chr6 | 41735571 | |||||
chr6:41735583
|
C | T | 1 | a0001c0001t0008 | 1 | HG01981.hp1 | 5_prime_UTR_variant | MODIFIER | c.-256G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/9 | 44370 | chr6 | 41735583 | |||||
chr6:41735601
|
C | T | 1 | a0001c0002t0007 | 1 | HG01943.hp1 | 5_prime_UTR_variant | MODIFIER | c.-274G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/9 | 44388 | chr6 | 41735601 | |||||
chr6:41735608
|
C | A | 1 | a0001c0004t0006 | 2 | NA18944.hp1 NA19011.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-281G>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/9 | chr6 | 41735608 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:41685133
|
G | A | 1 | a0001c0002t0001g0140 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.952-55C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 8/8 | chr6 | 41685133 | ||||||
chr6:41685180
|
G | C | 1 | a0001c0003t0001g0036 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.952-102C>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 8/8 | chr6 | 41685180 | ||||||
chr6:41685214
|
A | G | 1 | a0001c0010t0001g0265 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.952-136T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 8/8 | chr6 | 41685214 | ||||||
chr6:41685255
|
A | G | 54 | a0001c0001t0001g0110a0001c0001t0002g0083a0001c0001t0002g0094others(51): Show | 57 | HG00323.hp1 HG00408.hp1 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.952-177T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 8/8 | chr6 | 41685255 | ||||||
chr6:41685265
|
G | A | 9 | a0001c0005t0001g0096a0001c0005t0001g0118a0001c0005t0001g0131others(6): Show | 9 | HG01168.hp2 HG02055.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.952-187C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 8/8 | chr6 | 41685265 | ||||||
chr6:41685300
|
A | C | 1 | a0001c0005t0001g0240 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.952-222T>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 8/8 | chr6 | 41685300 | ||||||
chr6:41685319
|
T | A | 15 | a0001c0001t0001g0009a0001c0001t0001g0111a0001c0001t0001g0122others(12): Show | 17 | HG00642.hp2 HG01081.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.952-241A>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 8/8 | chr6 | 41685319 | ||||||
chr6:41685358
|
A | G | 8 | a0001c0005t0001g0127a0001c0005t0001g0239a0001c0005t0001g0240others(5): Show | 9 | HG02257.hp2 HG02451.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.952-280T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 8/8 | chr6 | 41685358 | ||||||
chr6:41685378
|
T | C | 55 | a0001c0001t0001g0025a0001c0001t0001g0093a0001c0001t0001g0112others(52): Show | 60 | HG00597.hp1 HG00609.hp2 HG00741.hp2 others(57): Show |
intron_variant | MODIFIER | c.952-300A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 8/8 | chr6 | 41685378 | ||||||
chr6:41685573
|
A | ACTAGAAC others(3): Show |
1 | a0001c0002t0001g0140 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.952-505_952-496dup others(10): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 8/8 | chr6 | 41685573 | ||||||
chr6:41685664
|
C | T | 15 | a0001c0001t0001g0023a0001c0001t0001g0048a0001c0001t0001g0104others(12): Show | 16 | HG00280.hp2 HG00741.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.951+426G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 8/8 | chr6 | 41685664 | ||||||
chr6:41685669
|
G | A | 1 | a0001c0007t0001g0261 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.951+421C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 8/8 | chr6 | 41685669 | ||||||
chr6:41685748
|
G | C | 13 | a0001c0001t0001g0025a0001c0001t0001g0112a0001c0001t0001g0113others(10): Show | 14 | HG01891.hp2 HG02559.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.951+342C>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 8/8 | chr6 | 41685748 | ||||||
chr6:41685859
|
G | A | 9 | a0001c0005t0001g0096a0001c0005t0001g0118a0001c0005t0001g0131others(6): Show | 9 | HG01168.hp2 HG02055.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.951+231C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 8/8 | chr6 | 41685859 | ||||||
chr6:41685984
|
C | T | 5 | a0001c0001t0001g0093a0001c0001t0001g0115a0001c0001t0001g0116others(2): Show | 5 | HG02451.hp2 HG02622.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.951+106G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 8/8 | chr6 | 41685984 | ||||||
chr6:41686299
|
A | G | 1 | a0001c0003t0001g0069 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.804-62T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 7/8 | chr6 | 41686299 | ||||||
chr6:41686372
|
G | A | 88 | a0001c0001t0001g0110a0001c0001t0001g0236a0001c0001t0002g0004others(85): Show | 100 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.804-135C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 7/8 | chr6 | 41686372 | ||||||
chr6:41686475
|
C | CA | 276 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0025others(273): Show | 310 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(307): Show |
intron_variant | MODIFIER | c.804-239dupT | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 7/8 | chr6 | 41686475 | ||||||
chr6:41686495
|
C | G | 1 | a0001c0002t0001g0137 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.804-258G>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 7/8 | chr6 | 41686495 | ||||||
chr6:41686503
|
CCTTT | C | 9 | a0001c0001t0001g0112a0001c0001t0001g0248a0001c0001t0001g0249others(6): Show | 9 | HG01891.hp2 HG02559.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.804-270_804-267del others(4): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 7/8 | chr6 | 41686503 | ||||||
chr6:41686508
|
C | CT | 28 | a0001c0001t0001g0093a0001c0001t0001g0115a0001c0001t0001g0116others(25): Show | 29 | HG00140.hp2 HG00408.hp2 HG01515.hp1 others(26): Show |
intron_variant | MODIFIER | c.804-272dupA | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 7/8 | chr6 | 41686508 | ||||||
chr6:41686508
|
C | CTT | 78 | a0001c0002t0001g0137a0001c0003t0001g0006a0001c0003t0001g0007others(75): Show | 91 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.804-273_804-272dup others(2): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 7/8 | chr6 | 41686508 | ||||||
chr6:41686508
|
CT | C | 114 | a0001c0001t0001g0110a0001c0001t0001g0114a0001c0001t0001g0197others(111): Show | 134 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.804-272delA | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 7/8 | chr6 | 41686508 | ||||||
chr6:41686508
|
CTT | C | 10 | a0001c0001t0002g0012a0001c0001t0002g0058a0001c0001t0002g0083others(7): Show | 11 | HG00558.hp1 HG00733.hp1 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.804-273_804-272del others(2): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 7/8 | chr6 | 41686508 | ||||||
chr6:41686585
|
G | A | 2 | a0001c0004t0002g0124a0001c0004t0002g0126 | 2 | HG03041.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.804-348C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 7/8 | chr6 | 41686585 | ||||||
chr6:41686604
|
C | T | 13 | a0001c0001t0001g0023a0001c0001t0001g0048a0001c0001t0001g0104others(10): Show | 14 | HG00280.hp2 HG00741.hp1 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.804-367G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 7/8 | chr6 | 41686604 | ||||||
chr6:41686683
|
G | T | 276 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0025others(273): Show | 310 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(307): Show |
intron_variant | MODIFIER | c.803+411C>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 7/8 | chr6 | 41686683 | ||||||
chr6:41686794
|
G | A | 1 | a0001c0003t0001g0144 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.803+300C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 7/8 | chr6 | 41686794 | ||||||
chr6:41686990
|
A | G | 2 | a0001c0005t0001g0269a0001c0005t0001g0270 | 2 | HG01361.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.803+104T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 7/8 | chr6 | 41686990 | ||||||
chr6:41687194
|
A | G | 15 | a0001c0001t0001g0009a0001c0001t0001g0111a0001c0001t0001g0122others(12): Show | 17 | HG00642.hp2 HG01081.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.728-25T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 6/8 | chr6 | 41687194 | ||||||
chr6:41687267
|
G | A | 261 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0048others(258): Show | 294 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(291): Show |
intron_variant | MODIFIER | c.728-98C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 6/8 | chr6 | 41687267 | ||||||
chr6:41687447
|
A | G | 6 | a0001c0004t0002g0180a0001c0004t0002g0182a0001c0004t0002g0184others(3): Show | 6 | HG00621.hp1 NA18940.hp2 NA18960.hp1 others(3): Show |
intron_variant | MODIFIER | c.728-278T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 6/8 | chr6 | 41687447 | ||||||
chr6:41687602
|
C | T | 87 | a0001c0001t0001g0236a0001c0001t0002g0004a0001c0001t0002g0011others(84): Show | 99 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.727+151G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 6/8 | chr6 | 41687602 | ||||||
chr6:41687724
|
G | A | 2 | a0001c0005t0001g0127a0001c0005t0005g0030 | 3 | HG02647.hp1 HG02717.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.727+29C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 6/8 | chr6 | 41687724 | ||||||
chr6:41687739
|
G | A | 2 | a0001c0001t0001g0122a0001c0001t0001g0132 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.727+14C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 6/8 | chr6 | 41687739 | ||||||
chr6:41688076
|
G | A | 34 | a0001c0001t0001g0236a0001c0001t0002g0004a0001c0001t0002g0011others(31): Show | 43 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.550-48C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 4/8 | chr6 | 41688076 | ||||||
chr6:41688095
|
C | T | 1 | a0001c0003t0002g0278 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.550-67G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 4/8 | chr6 | 41688095 | ||||||
chr6:41688154
|
C | G | 15 | a0001c0001t0001g0009a0001c0001t0001g0111a0001c0001t0001g0122others(12): Show | 17 | HG00642.hp2 HG01081.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.550-126G>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 4/8 | chr6 | 41688154 | ||||||
chr6:41688160
|
C | T | 1 | a0001c0002t0001g0140 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.550-132G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 4/8 | chr6 | 41688160 | ||||||
chr6:41688204
|
A | G | 85 | a0001c0002t0001g0137a0001c0003t0001g0006a0001c0003t0001g0007others(82): Show | 98 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.550-176T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 4/8 | chr6 | 41688204 | ||||||
chr6:41688237
|
G | C | 20 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116others(17): Show | 23 | HG00597.hp1 HG00609.hp2 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.550-209C>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 4/8 | chr6 | 41688237 | ||||||
chr6:41688345
|
G | T | 1 | a0001c0005t0001g0106 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.550-317C>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 4/8 | chr6 | 41688345 | ||||||
chr6:41688604
|
G | GGA | 150 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0048others(147): Show | 168 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.550-578_550-577dup others(2): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 4/8 | chr6 | 41688604 | ||||||
chr6:41688753
|
G | A | 1 | a0001c0004t0002g0190 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.550-725C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 4/8 | chr6 | 41688753 | ||||||
chr6:41688773
|
T | C | 15 | a0001c0001t0001g0023a0001c0001t0001g0048a0001c0001t0001g0104others(12): Show | 16 | HG00280.hp2 HG00741.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.550-745A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 4/8 | chr6 | 41688773 | ||||||
chr6:41688859
|
C | T | 1 | a0001c0001t0002g0099 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.550-831G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 4/8 | chr6 | 41688859 | ||||||
chr6:41688902
|
G | A | 2 | a0001c0002t0001g0123a0001c0002t0001g0163 | 2 | HG03239.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.549+829C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 4/8 | chr6 | 41688902 | ||||||
chr6:41688990
|
C | T | 275 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0025others(272): Show | 309 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(306): Show |
intron_variant | MODIFIER | c.549+741G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 4/8 | chr6 | 41688990 | ||||||
chr6:41688994
|
C | T | 1 | a0001c0004t0002g0215 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.549+737G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 4/8 | chr6 | 41688994 | ||||||
chr6:41689149
|
A | G | 5 | a0001c0001t0001g0093a0001c0001t0001g0115a0001c0001t0001g0116others(2): Show | 5 | HG02451.hp2 HG02622.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.549+582T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 4/8 | chr6 | 41689149 | ||||||
chr6:41689197
|
C | A | 1 | a0001c0001t0001g0315 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.549+534G>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 4/8 | chr6 | 41689197 | ||||||
chr6:41689358
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.549+373G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 4/8 | chr6 | 41689358 | ||||||
chr6:41689590
|
A | G | 274 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0025others(271): Show | 308 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(305): Show |
intron_variant | MODIFIER | c.549+141T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 4/8 | chr6 | 41689590 | ||||||
chr6:41689621
|
C | T | 17 | a0001c0001t0001g0025a0001c0001t0001g0112a0001c0001t0001g0113others(14): Show | 18 | HG01891.hp2 HG02559.hp1 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.549+110G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 4/8 | chr6 | 41689621 | ||||||
chr6:41689935
|
G | A | 15 | a0001c0001t0001g0023a0001c0001t0001g0048a0001c0001t0001g0104others(12): Show | 16 | HG00280.hp2 HG00741.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.469-124C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 3/8 | chr6 | 41689935 | ||||||
chr6:41689964
|
T | A | 17 | a0001c0001t0003g0005a0001c0001t0003g0076a0001c0001t0003g0079others(14): Show | 20 | HG00597.hp1 HG00609.hp2 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.469-153A>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 3/8 | chr6 | 41689964 | ||||||
chr6:41690072
|
G | A | 14 | a0001c0001t0003g0005a0001c0001t0003g0076a0001c0001t0003g0079others(11): Show | 17 | HG00597.hp1 HG00609.hp2 HG01346.hp2 others(14): Show |
intron_variant | MODIFIER | c.469-261C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 3/8 | chr6 | 41690072 | ||||||
chr6:41690135
|
C | T | 1 | a0001c0001t0002g0301 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.469-324G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 3/8 | chr6 | 41690135 | ||||||
chr6:41690135
|
CT | C | 34 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0048others(31): Show | 37 | HG00280.hp2 HG00642.hp2 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.469-325delA | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 3/8 | chr6 | 41690135 | ||||||
chr6:41690136
|
T | C | 1 | a0001c0001t0002g0301 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.469-325A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 3/8 | chr6 | 41690136 | ||||||
chr6:41690169
|
C | T | 101 | a0001c0002t0001g0137a0001c0003t0001g0006a0001c0003t0001g0007others(98): Show | 115 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.469-358G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 3/8 | chr6 | 41690169 | ||||||
chr6:41690240
|
C | G | 2 | a0001c0005t0001g0127a0001c0005t0005g0030 | 3 | HG02647.hp1 HG02717.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.468+423G>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 3/8 | chr6 | 41690240 | ||||||
chr6:41690287
|
C | T | 1 | a0001c0001t0001g0139 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.468+376G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 3/8 | chr6 | 41690287 | ||||||
chr6:41690344
|
G | C | 1 | a0001c0001t0001g0220 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.468+319C>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 3/8 | chr6 | 41690344 | ||||||
chr6:41690374
|
G | C | 144 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0048others(141): Show | 162 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.468+289C>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 3/8 | chr6 | 41690374 | ||||||
chr6:41690516
|
G | T | 2 | a0001c0001t0001g0252a0001c0001t0013g0354 | 2 | HG02615.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.468+147C>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 3/8 | chr6 | 41690516 | ||||||
chr6:41690655
|
T | A | 6 | a0001c0004t0002g0180a0001c0004t0002g0182a0001c0004t0002g0184others(3): Show | 6 | HG00621.hp1 NA18940.hp2 NA18960.hp1 others(3): Show |
splice_region_variant&intron_variant | LOW | c.468+8A>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 3/8 | chr6 | 41690655 | ||||||
chr6:41691325
|
C | T | 1 | a0001c0002t0001g0251 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-22-90G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41691325 | ||||||
chr6:41691566
|
C | T | 140 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0025others(137): Show | 156 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.-22-331G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41691566 | ||||||
chr6:41691589
|
G | A | 55 | a0001c0001t0001g0110a0001c0001t0001g0112a0001c0001t0002g0083others(52): Show | 58 | HG00323.hp1 HG00408.hp1 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.-22-354C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41691589 | ||||||
chr6:41691622
|
C | T | 1 | a0001c0001t0001g0139 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-22-387G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41691622 | ||||||
chr6:41691759
|
C | T | 1 | a0001c0001t0001g0114 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-22-524G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41691759 | ||||||
chr6:41691895
|
C | T | 1 | a0001c0001t0002g0330 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-22-660G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41691895 | ||||||
chr6:41691994
|
C | A | 16 | a0001c0001t0003g0005a0001c0001t0003g0076a0001c0001t0003g0079others(13): Show | 19 | HG00597.hp1 HG00609.hp2 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.-22-759G>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41691994 | ||||||
chr6:41692016
|
C | T | 15 | a0001c0001t0001g0023a0001c0001t0001g0048a0001c0001t0001g0104others(12): Show | 16 | HG00280.hp2 HG00741.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.-22-781G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41692016 | ||||||
chr6:41692128
|
A | T | 1 | a0001c0004t0002g0184 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-22-893T>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41692128 | ||||||
chr6:41692129
|
T | A | 1 | a0001c0004t0002g0184 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-22-894A>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41692129 | ||||||
chr6:41692359
|
C | T | 15 | a0001c0001t0001g0023a0001c0001t0001g0048a0001c0001t0001g0104others(12): Show | 16 | HG00280.hp2 HG00741.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.-22-1124G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41692359 | ||||||
chr6:41692363
|
T | TGCAGTTC others(4): Show |
1 | a0001c0001t0002g0301 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-22-1139_-22-1129d others(13): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41692363 | ||||||
chr6:41692446
|
C | T | 1 | a0002c0006t0001g0294 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-22-1211G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41692446 | ||||||
chr6:41692459
|
C | G | 2 | a0001c0001t0001g0122a0001c0001t0001g0132 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-22-1224G>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41692459 | ||||||
chr6:41692791
|
T | G | 4 | a0001c0002t0001g0133a0001c0002t0001g0143a0001c0002t0007g0031others(1): Show | 4 | HG00735.hp2 HG01081.hp2 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.-22-1556A>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41692791 | ||||||
chr6:41692852
|
T | C | 15 | a0001c0001t0001g0009a0001c0001t0001g0111a0001c0001t0001g0122others(12): Show | 17 | HG00642.hp2 HG01081.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.-22-1617A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41692852 | ||||||
chr6:41693017
|
T | G | 15 | a0001c0001t0001g0009a0001c0001t0001g0111a0001c0001t0001g0122others(12): Show | 17 | HG00642.hp2 HG01081.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.-22-1782A>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41693017 | ||||||
chr6:41693280
|
A | G | 2 | a0001c0001t0002g0222a0001c0001t0002g0223 | 2 | HG02809.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-22-2045T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41693280 | ||||||
chr6:41693487
|
C | G | 1 | a0001c0001t0002g0301 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-22-2252G>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41693487 | ||||||
chr6:41693517
|
A | T | 1 | a0001c0001t0003g0333 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-22-2282T>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41693517 | ||||||
chr6:41693604
|
C | T | 2 | a0001c0001t0001g0252a0001c0001t0013g0354 | 2 | HG02615.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-22-2369G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41693604 | ||||||
chr6:41693785
|
C | T | 1 | a0001c0001t0002g0301 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-22-2550G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41693785 | ||||||
chr6:41693841
|
C | T | 1 | a0001c0005t0001g0345 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-22-2606G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41693841 | ||||||
chr6:41693922
|
C | T | 1 | a0001c0001t0002g0288 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-22-2687G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41693922 | ||||||
chr6:41694057
|
C | A | 6 | a0001c0005t0001g0239a0001c0005t0001g0240a0001c0005t0001g0241others(3): Show | 6 | HG02257.hp2 HG02451.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-22-2822G>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41694057 | ||||||
chr6:41694281
|
A | G | 38 | a0001c0001t0001g0025a0001c0001t0001g0093a0001c0001t0001g0113others(35): Show | 42 | HG00597.hp1 HG00609.hp2 HG00741.hp2 others(39): Show |
intron_variant | MODIFIER | c.-22-3046T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41694281 | ||||||
chr6:41694395
|
A | C | 2 | a0001c0005t0001g0127a0001c0005t0005g0030 | 3 | HG02647.hp1 HG02717.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-22-3160T>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41694395 | ||||||
chr6:41694485
|
G | A | 2 | a0001c0005t0001g0127a0001c0005t0005g0030 | 3 | HG02647.hp1 HG02717.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-22-3250C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41694485 | ||||||
chr6:41694515
|
T | C | 1 | a0001c0005t0001g0281 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-22-3280A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41694515 | ||||||
chr6:41694545
|
G | A | 2 | a0001c0001t0001g0122a0001c0001t0001g0132 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-22-3310C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41694545 | ||||||
chr6:41694561
|
G | A | 89 | a0001c0001t0001g0110a0001c0001t0001g0112a0001c0001t0001g0236others(86): Show | 101 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.-22-3326C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41694561 | ||||||
chr6:41694739
|
C | G | 16 | a0001c0001t0003g0005a0001c0001t0003g0076a0001c0001t0003g0079others(13): Show | 19 | HG00597.hp1 HG00609.hp2 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.-22-3504G>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41694739 | ||||||
chr6:41694750
|
C | T | 1 | a0001c0001t0002g0314 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-22-3515G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41694750 | ||||||
chr6:41694838
|
C | T | 273 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0025others(270): Show | 307 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(304): Show |
intron_variant | MODIFIER | c.-22-3603G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41694838 | ||||||
chr6:41694839
|
T | C | 3 | a0001c0001t0002g0083a0001c0001t0002g0288a0001c0001t0002g0289 | 3 | HG02015.hp2 HG02735.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.-22-3604A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41694839 | ||||||
chr6:41694852
|
C | T | 1 | a0001c0004t0002g0191 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-22-3617G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41694852 | ||||||
chr6:41694860
|
C | T | 1 | a0001c0001t0001g0114 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-22-3625G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41694860 | ||||||
chr6:41694903
|
G | T | 1 | a0003c0011t0001g0229 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-22-3668C>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41694903 | ||||||
chr6:41694910
|
C | T | 23 | a0001c0001t0001g0009a0001c0001t0001g0111a0001c0001t0001g0122others(20): Show | 26 | HG00642.hp2 HG01081.hp1 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.-22-3675G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41694910 | ||||||
chr6:41694958
|
C | A | 18 | a0001c0001t0001g0025a0001c0001t0001g0093a0001c0001t0001g0113others(15): Show | 19 | HG01891.hp2 HG02451.hp2 HG02559.hp2 others(16): Show |
intron_variant | MODIFIER | c.-22-3723G>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41694958 | ||||||
chr6:41694964
|
G | T | 1 | a0001c0001t0002g0301 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-22-3729C>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41694964 | ||||||
chr6:41695019
|
C | T | 1 | a0001c0001t0002g0308 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-22-3784G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41695019 | ||||||
chr6:41695045
|
T | C | 23 | a0001c0001t0001g0009a0001c0001t0001g0111a0001c0001t0001g0122others(20): Show | 26 | HG00642.hp2 HG01081.hp1 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.-22-3810A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41695045 | ||||||
chr6:41695105
|
G | C | 173 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0025others(170): Show | 193 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(190): Show |
intron_variant | MODIFIER | c.-22-3870C>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41695105 | ||||||
chr6:41695151
|
T | G | 9 | a0001c0005t0001g0096a0001c0005t0001g0118a0001c0005t0001g0131others(6): Show | 9 | HG01168.hp2 HG02055.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.-22-3916A>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41695151 | ||||||
chr6:41695152
|
C | G | 177 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0025others(174): Show | 197 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.-22-3917G>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41695152 | ||||||
chr6:41695198
|
T | C | 3 | a0001c0001t0001g0273a0001c0003t0001g0331a0001c0010t0001g0265 | 3 | HG02040.hp2 HG02630.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-22-3963A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41695198 | ||||||
chr6:41695554
|
C | G | 3 | a0001c0001t0002g0296a0001c0001t0002g0303a0001c0001t0002g0313 | 3 | HG00423.hp1 HG00609.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.-22-4319G>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41695554 | ||||||
chr6:41695673
|
T | G | 2 | a0001c0003t0001g0068a0001c0003t0001g0071 | 2 | NA18954.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.-22-4438A>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41695673 | ||||||
chr6:41695712
|
G | A | 1 | a0001c0001t0001g0114 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-22-4477C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41695712 | ||||||
chr6:41696003
|
G | A | 4 | a0001c0002t0001g0017a0001c0002t0001g0120a0001c0002t0001g0258others(1): Show | 5 | HG01255.hp2 HG03130.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.-22-4768C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41696003 | ||||||
chr6:41696258
|
C | A | 14 | a0001c0001t0001g0023a0001c0001t0001g0048a0001c0001t0001g0104others(11): Show | 15 | HG00280.hp2 HG00741.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.-22-5023G>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41696258 | ||||||
chr6:41696294
|
C | A | 160 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0048others(157): Show | 179 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.-22-5059G>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41696294 | ||||||
chr6:41696343
|
C | T | 18 | a0001c0002t0001g0045a0001c0005t0001g0096a0001c0005t0001g0118others(15): Show | 19 | HG00280.hp1 HG01168.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.-22-5108G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41696343 | ||||||
chr6:41696383
|
C | T | 272 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0025others(269): Show | 306 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(303): Show |
intron_variant | MODIFIER | c.-22-5148G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41696383 | ||||||
chr6:41696385
|
A | T | 1 | a0001c0001t0002g0301 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-22-5150T>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41696385 | ||||||
chr6:41696490
|
C | T | 134 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0048others(131): Show | 150 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.-22-5255G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41696490 | ||||||
chr6:41696619
|
G | A | 2 | a0001c0004t0002g0180a0001c0004t0002g0185 | 2 | NA19000.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.-22-5384C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41696619 | ||||||
chr6:41696763
|
G | T | 89 | a0001c0001t0001g0110a0001c0001t0001g0112a0001c0001t0001g0236others(86): Show | 101 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.-22-5528C>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41696763 | ||||||
chr6:41696823
|
G | A | 3 | a0001c0003t0001g0013a0001c0003t0001g0067a0001c0003t0001g0072 | 4 | HG01123.hp1 HG01192.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.-22-5588C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41696823 | ||||||
chr6:41696950
|
C | A | 1 | a0001c0002t0001g0322 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-22-5715G>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41696950 | ||||||
chr6:41696989
|
T | C | 267 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0048others(264): Show | 300 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(297): Show |
intron_variant | MODIFIER | c.-22-5754A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41696989 | ||||||
chr6:41696999
|
T | C | 1 | a0001c0001t0001g0245 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-22-5764A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41696999 | ||||||
chr6:41697045
|
C | A | 2 | a0001c0002t0001g0147a0001c0002t0001g0152 | 2 | NA18967.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.-22-5810G>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41697045 | ||||||
chr6:41697135
|
T | C | 266 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0048others(263): Show | 299 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(296): Show |
intron_variant | MODIFIER | c.-22-5900A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41697135 | ||||||
chr6:41697213
|
G | A | 1 | a0001c0001t0001g0194 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-22-5978C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41697213 | ||||||
chr6:41697318
|
G | C | 8 | a0001c0005t0001g0127a0001c0005t0001g0239a0001c0005t0001g0240others(5): Show | 9 | HG02257.hp2 HG02451.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.-22-6083C>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41697318 | ||||||
chr6:41697354
|
A | G | 268 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0048others(265): Show | 301 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(298): Show |
intron_variant | MODIFIER | c.-22-6119T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41697354 | ||||||
chr6:41697408
|
C | CAA | 5 | a0002c0006t0001g0027a0002c0006t0001g0293a0002c0006t0001g0294others(2): Show | 6 | HG00544.hp1 NA18940.hp1 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.-22-6175_-22-6174d others(4): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41697408 | ||||||
chr6:41697408
|
C | CAAAAA | 9 | a0001c0001t0003g0005a0001c0001t0003g0164a0001c0001t0003g0166others(6): Show | 12 | HG00597.hp1 HG01346.hp2 HG01981.hp1 others(9): Show |
intron_variant | MODIFIER | c.-22-6178_-22-6174d others(7): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41697408 | ||||||
chr6:41697408
|
C | CAAAAAAA others(2): Show |
11 | a0001c0001t0001g0009a0001c0001t0001g0111a0001c0001t0001g0130others(8): Show | 13 | HG02257.hp1 HG02895.hp2 HG02896.hp1 others(10): Show |
intron_variant | MODIFIER | c.-22-6182_-22-6174d others(11): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41697408 | ||||||
chr6:41697408
|
C | CAAAAAAA others(3): Show |
15 | a0001c0001t0001g0023a0001c0001t0001g0025a0001c0001t0001g0104others(12): Show | 17 | HG00280.hp2 HG00642.hp2 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.-22-6183_-22-6174d others(12): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41697408 | ||||||
chr6:41697408
|
C | CAAAAAAA others(4): Show |
38 | a0001c0001t0001g0105a0001c0001t0001g0196a0001c0001t0001g0197others(35): Show | 41 | HG00323.hp1 HG00408.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.-22-6184_-22-6174d others(13): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41697408 | ||||||
chr6:41697408
|
C | CAAAAAAA others(5): Show |
26 | a0001c0001t0002g0223a0001c0002t0001g0285a0001c0002t0001g0286others(23): Show | 27 | HG00140.hp2 HG00323.hp2 HG01943.hp2 others(24): Show |
intron_variant | MODIFIER | c.-22-6185_-22-6174d others(14): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41697408 | ||||||
chr6:41697408
|
C | CAAAAAAA others(6): Show |
55 | a0001c0001t0003g0076a0001c0001t0003g0079a0001c0002t0001g0137others(52): Show | 62 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.-22-6186_-22-6174d others(15): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41697408 | ||||||
chr6:41697408
|
C | CAAAAAAA others(7): Show |
23 | a0001c0003t0001g0007a0001c0003t0001g0008a0001c0003t0001g0014others(20): Show | 29 | HG00438.hp1 HG00642.hp1 HG01192.hp2 others(26): Show |
intron_variant | MODIFIER | c.-22-6187_-22-6174d others(16): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41697408 | ||||||
chr6:41697408
|
C | CAAAAAAA others(8): Show |
13 | a0001c0001t0001g0113a0001c0003t0001g0060a0001c0003t0001g0069others(10): Show | 13 | HG02071.hp1 HG02257.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.-22-6188_-22-6174d others(17): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41697408 | ||||||
chr6:41697408
|
C | CAAAAAAA others(10): Show |
4 | a0001c0001t0001g0093a0001c0001t0001g0115a0001c0001t0001g0129others(1): Show | 4 | HG02451.hp2 HG02622.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-22-6190_-22-6174d others(19): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41697408 | ||||||
chr6:41697408
|
C | CAAAAAAA others(11): Show |
5 | a0001c0005t0001g0118a0001c0005t0001g0225a0001c0005t0001g0257others(2): Show | 5 | HG01168.hp2 HG02818.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-22-6191_-22-6174d others(20): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41697408 | ||||||
chr6:41697408
|
C | CAAAAAAA others(12): Show |
3 | a0001c0001t0001g0116a0001c0002t0001g0258a0001c0005t0001g0344 | 3 | HG02647.hp2 HG03130.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-22-6192_-22-6174d others(21): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41697408 | ||||||
chr6:41697408
|
C | CAAAAAAA others(13): Show |
3 | a0001c0001t0001g0114a0001c0005t0001g0131a0001c0005t0001g0345 | 3 | HG02055.hp2 HG02145.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-22-6174_-22-6173i others(22): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41697408 | ||||||
chr6:41697408
|
C | CAAAAAAA others(14): Show |
5 | a0001c0001t0001g0248a0001c0001t0001g0262a0001c0001t0001g0264others(2): Show | 5 | HG02145.hp1 HG02622.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.-22-6174_-22-6173i others(23): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41697408 | ||||||
chr6:41697408
|
C | CAAAAAAA others(15): Show |
3 | a0001c0001t0001g0249a0001c0001t0001g0252a0001c0001t0013g0354 | 3 | HG02615.hp1 HG02886.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-22-6174_-22-6173i others(24): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41697408 | ||||||
chr6:41697408
|
C | CAAAAAAA others(17): Show |
1 | a0001c0001t0012g0353 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-22-6174_-22-6173i others(26): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41697408 | ||||||
chr6:41697408
|
CAAAAAAA | C | 59 | a0001c0001t0001g0048a0001c0001t0001g0110a0001c0001t0001g0273others(56): Show | 68 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.-22-6180_-22-6174d others(9): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41697408 | ||||||
chr6:41697427
|
A | AAAAAAAA others(9): Show |
1 | a0001c0002t0001g0251 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-22-6193_-22-6192i others(18): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41697427 | ||||||
chr6:41697487
|
A | G | 3 | a0001c0001t0001g0245a0001c0001t0001g0252a0001c0001t0013g0354 | 3 | HG02615.hp1 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-22-6252T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41697487 | ||||||
chr6:41697503
|
A | AC | 232 | a0001c0001t0001g0009a0001c0001t0001g0025a0001c0001t0001g0048others(229): Show | 264 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(261): Show |
intron_variant | MODIFIER | c.-22-6269dupG | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41697503 | ||||||
chr6:41697503
|
A | C | 1 | a0001c0001t0001g0249 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-22-6268T>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41697503 | ||||||
chr6:41697503
|
AC | A | 15 | a0001c0001t0001g0023a0001c0001t0001g0104a0001c0001t0001g0105others(12): Show | 16 | HG00280.hp2 HG00323.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.-22-6269delG | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41697503 | ||||||
chr6:41697511
|
C | G | 1 | a0001c0002t0001g0195 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-22-6276G>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41697511 | ||||||
chr6:41697524
|
T | A | 4 | a0001c0001t0001g0110a0001c0001t0002g0107a0001c0001t0002g0108others(1): Show | 4 | HG01891.hp1 HG02280.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-22-6289A>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41697524 | ||||||
chr6:41697619
|
A | G | 6 | a0001c0005t0001g0239a0001c0005t0001g0240a0001c0005t0001g0241others(3): Show | 6 | HG02257.hp2 HG02451.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-22-6384T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41697619 | ||||||
chr6:41697624
|
T | A | 1 | a0001c0001t0002g0323 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-22-6389A>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41697624 | ||||||
chr6:41697649
|
C | T | 2 | a0001c0001t0002g0016a0001c0001t0002g0091 | 3 | HG01243.hp1 HG02717.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.-22-6414G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41697649 | ||||||
chr6:41697688
|
G | C | 1 | a0001c0001t0002g0029 | 2 | HG00544.hp2 HG00673.hp2 |
intron_variant | MODIFIER | c.-22-6453C>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41697688 | ||||||
chr6:41697745
|
C | T | 54 | a0001c0001t0001g0187a0001c0001t0001g0194a0001c0001t0001g0196others(51): Show | 57 | HG00323.hp1 HG00408.hp1 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.-22-6510G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41697745 | ||||||
chr6:41697768
|
T | G | 55 | a0001c0001t0001g0187a0001c0001t0001g0194a0001c0001t0001g0196others(52): Show | 58 | HG00323.hp1 HG00408.hp1 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.-22-6533A>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41697768 | ||||||
chr6:41697912
|
G | C | 19 | a0001c0001t0001g0315a0001c0001t0002g0011a0001c0001t0002g0028others(16): Show | 22 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(19): Show |
intron_variant | MODIFIER | c.-22-6677C>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41697912 | ||||||
chr6:41697947
|
G | C | 1 | a0001c0001t0013g0354 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-22-6712C>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41697947 | ||||||
chr6:41698038
|
G | GA | 36 | a0001c0001t0001g0093a0001c0001t0001g0115a0001c0001t0001g0116others(33): Show | 39 | HG00597.hp1 HG00741.hp2 HG01168.hp2 others(36): Show |
intron_variant | MODIFIER | c.-22-6804dupT | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41698038 | ||||||
chr6:41698153
|
G | A | 1 | a0001c0001t0001g0048 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.-22-6918C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41698153 | ||||||
chr6:41698169
|
C | T | 67 | a0001c0001t0001g0187a0001c0001t0001g0194a0001c0001t0001g0196others(64): Show | 70 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.-22-6934G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41698169 | ||||||
chr6:41698327
|
G | A | 19 | a0001c0001t0001g0023a0001c0001t0001g0104a0001c0001t0001g0220others(16): Show | 23 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.-22-7092C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41698327 | ||||||
chr6:41698554
|
A | C | 21 | a0001c0001t0001g0023a0001c0001t0001g0104a0001c0001t0001g0105others(18): Show | 25 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.-22-7319T>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41698554 | ||||||
chr6:41698620
|
G | A | 3 | a0001c0001t0001g0105a0001c0003t0001g0035a0001c0005t0001g0106 | 3 | HG02738.hp2 HG03688.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.-22-7385C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41698620 | ||||||
chr6:41698628
|
T | G | 1 | a0001c0001t0001g0263 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-22-7393A>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41698628 | ||||||
chr6:41698840
|
C | T | 2 | a0001c0001t0001g0115a0001c0001t0001g0116 | 2 | HG02647.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.-22-7605G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41698840 | ||||||
chr6:41698901
|
T | A | 1 | a0001c0005t0001g0344 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-22-7666A>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41698901 | ||||||
chr6:41699295
|
A | C | 20 | a0001c0001t0001g0114a0001c0001t0001g0245a0001c0001t0001g0273others(17): Show | 23 | HG00597.hp1 HG00741.hp2 HG01346.hp2 others(20): Show |
intron_variant | MODIFIER | c.-22-8060T>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41699295 | ||||||
chr6:41699299
|
C | T | 54 | a0001c0001t0001g0048a0001c0001t0001g0110a0001c0001t0001g0315others(51): Show | 60 | HG00140.hp1 HG00423.hp1 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.-22-8064G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41699299 | ||||||
chr6:41699354
|
C | T | 1 | a0001c0001t0002g0307 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-22-8119G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41699354 | ||||||
chr6:41699377
|
T | C | 1 | a0001c0005t0001g0274 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-22-8142A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41699377 | ||||||
chr6:41699454
|
G | A | 1 | a0001c0001t0002g0288 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-22-8219C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41699454 | ||||||
chr6:41699460
|
G | A | 1 | a0001c0002t0001g0326 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-22-8225C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41699460 | ||||||
chr6:41699560
|
A | C | 1 | a0001c0002t0001g0172 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-22-8325T>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41699560 | ||||||
chr6:41699575
|
G | A | 1 | a0001c0004t0002g0243 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.-22-8340C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41699575 | ||||||
chr6:41699640
|
C | T | 2 | a0001c0001t0001g0122a0001c0001t0001g0132 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-22-8405G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41699640 | ||||||
chr6:41699768
|
A | C | 38 | a0001c0001t0001g0023a0001c0001t0001g0104a0001c0001t0001g0105others(35): Show | 45 | HG00280.hp1 HG00280.hp2 HG00597.hp1 others(42): Show |
intron_variant | MODIFIER | c.-22-8533T>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41699768 | ||||||
chr6:41699802
|
G | A | 1 | a0001c0002t0001g0176 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-22-8567C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41699802 | ||||||
chr6:41699840
|
G | C | 1 | a0001c0005t0001g0274 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-22-8605C>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41699840 | ||||||
chr6:41699896
|
A | T | 2 | a0001c0001t0001g0048a0001c0001t0002g0058 | 2 | HG00733.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.-22-8661T>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41699896 | ||||||
chr6:41700025
|
C | T | 2 | a0001c0001t0002g0288a0001c0001t0002g0289 | 2 | HG02015.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.-22-8790G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41700025 | ||||||
chr6:41700188
|
T | C | 69 | a0001c0001t0001g0110a0001c0001t0001g0187a0001c0001t0001g0196others(66): Show | 73 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.-22-8953A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41700188 | ||||||
chr6:41700205
|
G | A | 1 | a0001c0008t0002g0309 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-22-8970C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41700205 | ||||||
chr6:41700213
|
TC | T | 18 | a0001c0001t0001g0025a0001c0001t0001g0224a0001c0001t0001g0246others(15): Show | 19 | HG00741.hp2 HG01884.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.-22-8979delG | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41700213 | ||||||
chr6:41700232
|
T | C | 1 | a0001c0008t0002g0309 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-22-8997A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41700232 | ||||||
chr6:41700238
|
G | A | 1 | a0001c0001t0002g0094 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-22-9003C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41700238 | ||||||
chr6:41700334
|
C | T | 1 | a0001c0002t0001g0136 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-22-9099G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41700334 | ||||||
chr6:41700383
|
G | A | 1 | a0001c0003t0001g0035 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-22-9148C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41700383 | ||||||
chr6:41700390
|
C | T | 1 | a0002c0006t0001g0300 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-22-9155G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41700390 | ||||||
chr6:41700402
|
C | G | 1 | a0002c0006t0001g0300 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-22-9167G>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41700402 | ||||||
chr6:41700407
|
A | G | 1 | a0002c0006t0001g0300 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-22-9172T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41700407 | ||||||
chr6:41700458
|
T | A | 118 | a0001c0001t0001g0023a0001c0001t0001g0104a0001c0001t0001g0105others(115): Show | 129 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.-22-9223A>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41700458 | ||||||
chr6:41700465
|
C | CA | 13 | a0001c0001t0001g0113a0001c0002t0001g0148a0001c0002t0001g0271others(10): Show | 13 | HG00438.hp1 HG01981.hp2 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.-22-9231dupT | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41700465 | ||||||
chr6:41700465
|
CA | C | 92 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0132others(89): Show | 99 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.-22-9231delT | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41700465 | ||||||
chr6:41700465
|
CAA | C | 56 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0025others(53): Show | 63 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.-22-9232_-22-9231d others(4): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41700465 | ||||||
chr6:41700550
|
C | T | 2 | a0001c0005t0001g0345a0001c0005t0009g0259 | 2 | HG02145.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-22-9315G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41700550 | ||||||
chr6:41700797
|
G | C | 1 | a0001c0003t0001g0078 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-22-9562C>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41700797 | ||||||
chr6:41700842
|
C | A | 15 | a0001c0001t0003g0005a0001c0001t0003g0119a0001c0001t0003g0164others(12): Show | 18 | HG00597.hp1 HG00741.hp2 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.-22-9607G>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41700842 | ||||||
chr6:41700880
|
G | C | 2 | a0001c0005t0001g0269a0001c0005t0001g0270 | 2 | HG01361.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.-22-9645C>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41700880 | ||||||
chr6:41700916
|
G | T | 1 | a0001c0004t0002g0181 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-22-9681C>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41700916 | ||||||
chr6:41700926
|
C | T | 2 | a0001c0001t0002g0222a0001c0001t0002g0223 | 2 | HG02809.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-22-9691G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41700926 | ||||||
chr6:41701155
|
A | C | 12 | a0001c0001t0003g0005a0001c0001t0003g0119a0001c0001t0003g0166others(9): Show | 15 | HG00597.hp1 HG01346.hp2 HG01975.hp1 others(12): Show |
intron_variant | MODIFIER | c.-22-9920T>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41701155 | ||||||
chr6:41701182
|
C | T | 1 | a0001c0001t0002g0022 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-22-9947G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41701182 | ||||||
chr6:41701272
|
C | A | 1 | a0001c0001t0002g0301 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-22-10037G>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41701272 | ||||||
chr6:41701273
|
A | C | 1 | a0001c0001t0002g0301 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-22-10038T>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41701273 | ||||||
chr6:41701274
|
C | A | 1 | a0001c0001t0002g0301 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-22-10039G>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41701274 | ||||||
chr6:41701498
|
G | T | 1 | a0001c0001t0001g0350 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-22-10263C>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41701498 | ||||||
chr6:41701638
|
A | C | 3 | a0001c0002t0001g0086a0001c0002t0001g0134a0001c0003t0001g0204 | 3 | NA18970.hp2 NA19082.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.-22-10403T>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41701638 | ||||||
chr6:41701722
|
A | T | 1 | a0001c0002t0001g0200 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-22-10487T>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41701722 | ||||||
chr6:41701829
|
C | G | 4 | a0001c0002t0001g0320a0001c0002t0001g0322a0001c0002t0010g0321others(1): Show | 4 | HG01255.hp1 HG02004.hp2 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.-22-10594G>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41701829 | ||||||
chr6:41701939
|
C | T | 7 | a0001c0002t0001g0258a0001c0005t0001g0096a0001c0005t0001g0118others(4): Show | 7 | HG01168.hp2 HG02145.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.-22-10704G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41701939 | ||||||
chr6:41701940
|
G | A | 4 | a0001c0005t0001g0239a0001c0005t0001g0240a0001c0005t0001g0241others(1): Show | 4 | HG02257.hp2 HG02451.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-22-10705C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41701940 | ||||||
chr6:41701944
|
C | CAAA | 39 | a0001c0001t0001g0009a0001c0001t0001g0025a0001c0001t0001g0113others(36): Show | 42 | HG00642.hp2 HG01070.hp1 HG01167.hp1 others(39): Show |
intron_variant | MODIFIER | c.-22-10712_-22-1071 others(7): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41701944 | ||||||
chr6:41701944
|
C | CAAAA | 76 | a0001c0001t0001g0023a0001c0001t0001g0104a0001c0001t0001g0105others(73): Show | 83 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.-22-10713_-22-1071 others(8): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41701944 | ||||||
chr6:41701944
|
C | CAAAAA | 12 | a0001c0001t0003g0201a0001c0002t0001g0167a0001c0002t0001g0168others(9): Show | 12 | HG00438.hp2 HG01952.hp2 HG02155.hp2 others(9): Show |
intron_variant | MODIFIER | c.-22-10714_-22-1071 others(9): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41701944 | ||||||
chr6:41701944
|
CA | C | 6 | a0001c0001t0001g0093a0001c0001t0001g0122a0001c0001t0002g0083others(3): Show | 6 | HG00639.hp1 HG01993.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-22-10710delT | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41701944 | ||||||
chr6:41701991
|
C | T | 4 | a0001c0002t0001g0167a0001c0004t0002g0117a0001c0004t0002g0218others(1): Show | 4 | NA18988.hp1 NA18991.hp1 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.-22-10756G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41701991 | ||||||
chr6:41702320
|
T | C | 138 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0025others(135): Show | 149 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.-22-11085A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41702320 | ||||||
chr6:41702445
|
G | T | 1 | a0001c0003t0001g0189 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-22-11210C>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41702445 | ||||||
chr6:41702474
|
A | G | 1 | a0001c0005t0001g0345 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-22-11239T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41702474 | ||||||
chr6:41702615
|
TCAGCCTA others(7): Show |
T | 22 | a0001c0002t0001g0279a0001c0002t0001g0285a0001c0003t0001g0010others(19): Show | 26 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.-22-11394_-22-1138 others(18): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41702615 | ||||||
chr6:41702865
|
C | G | 3 | a0001c0001t0001g0273a0001c0005t0001g0257a0001c0010t0001g0265 | 3 | HG02630.hp1 HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-22-11630G>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41702865 | ||||||
chr6:41702870
|
C | T | 60 | a0001c0001t0003g0076a0001c0001t0003g0079a0001c0003t0001g0007others(57): Show | 68 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.-22-11635G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41702870 | ||||||
chr6:41702895
|
C | T | 68 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0187others(65): Show | 71 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.-22-11660G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41702895 | ||||||
chr6:41702988
|
C | T | 22 | a0001c0001t0001g0023a0001c0001t0001g0104a0001c0001t0001g0105others(19): Show | 26 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.-22-11753G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41702988 | ||||||
chr6:41702993
|
G | A | 2 | a0001c0001t0002g0016a0001c0001t0002g0091 | 3 | HG01243.hp1 HG02717.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.-22-11758C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41702993 | ||||||
chr6:41703031
|
C | T | 123 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0025others(120): Show | 133 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.-22-11796G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41703031 | ||||||
chr6:41703170
|
G | T | 2 | a0001c0002t0001g0020a0001c0002t0001g0176 | 3 | NA18944.hp2 NA18999.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.-22-11935C>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41703170 | ||||||
chr6:41703349
|
C | A | 1 | a0001c0002t0001g0306 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-22-12114G>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41703349 | ||||||
chr6:41703480
|
T | TCAGCCTC others(2): Show |
126 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0025others(123): Show | 136 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.-22-12254_-22-1224 others(13): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41703480 | ||||||
chr6:41703611
|
A | G | 8 | a0001c0001t0001g0122a0001c0001t0001g0132a0001c0001t0001g0349others(5): Show | 9 | HG02647.hp1 HG02717.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.-22-12376T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41703611 | ||||||
chr6:41703639
|
T | C | 1 | a0001c0001t0001g0113 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-22-12404A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41703639 | ||||||
chr6:41703644
|
G | A | 1 | a0001c0001t0001g0113 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-22-12409C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41703644 | ||||||
chr6:41703837
|
A | T | 8 | a0001c0001t0001g0122a0001c0001t0001g0132a0001c0001t0001g0349others(5): Show | 9 | HG02647.hp1 HG02717.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.-22-12602T>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41703837 | ||||||
chr6:41703840
|
C | A | 21 | a0001c0001t0001g0023a0001c0001t0001g0104a0001c0001t0001g0105others(18): Show | 25 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.-22-12605G>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41703840 | ||||||
chr6:41703924
|
T | C | 1 | a0001c0003t0001g0336 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-22-12689A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41703924 | ||||||
chr6:41703939
|
A | G | 171 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0025others(168): Show | 189 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.-22-12704T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41703939 | ||||||
chr6:41704140
|
T | C | 1 | a0001c0002t0001g0162 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-22-12905A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41704140 | ||||||
chr6:41704214
|
G | A | 68 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0187others(65): Show | 71 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.-22-12979C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41704214 | ||||||
chr6:41704272
|
G | A | 3 | a0001c0001t0001g0105a0001c0003t0001g0035a0001c0005t0001g0106 | 3 | HG02738.hp2 HG03688.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.-22-13037C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41704272 | ||||||
chr6:41704273
|
C | A | 3 | a0001c0001t0001g0105a0001c0003t0001g0035a0001c0005t0001g0106 | 3 | HG02738.hp2 HG03688.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.-22-13038G>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41704273 | ||||||
chr6:41704303
|
C | G | 91 | a0001c0001t0001g0023a0001c0001t0001g0104a0001c0001t0001g0105others(88): Show | 98 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.-22-13068G>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41704303 | ||||||
chr6:41704581
|
G | A | 35 | a0001c0001t0003g0005a0001c0001t0003g0119a0001c0001t0003g0164others(32): Show | 42 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(39): Show |
intron_variant | MODIFIER | c.-22-13346C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41704581 | ||||||
chr6:41704731
|
C | T | 2 | a0001c0001t0001g0048a0001c0001t0002g0058 | 2 | HG00733.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.-22-13496G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41704731 | ||||||
chr6:41704750
|
GGGAAGCA others(12): Show |
G | 2 | a0001c0003t0001g0047a0001c0003t0001g0052 | 2 | HG01257.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.-22-13534_-22-1351 others(23): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41704750 | ||||||
chr6:41704901
|
A | G | 134 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0025others(131): Show | 144 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.-22-13666T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41704901 | ||||||
chr6:41705031
|
T | C | 79 | a0001c0001t0001g0110a0001c0001t0001g0315a0001c0001t0002g0012others(76): Show | 89 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.-22-13796A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41705031 | ||||||
chr6:41705118
|
C | T | 4 | a0001c0001t0001g0023a0001c0001t0001g0227a0001c0001t0001g0228others(1): Show | 5 | HG01257.hp1 HG01258.hp1 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.-22-13883G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41705118 | ||||||
chr6:41705320
|
C | T | 1 | a0001c0002t0001g0320 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-22-14085G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41705320 | ||||||
chr6:41705329
|
T | C | 21 | a0001c0001t0001g0023a0001c0001t0001g0104a0001c0001t0001g0105others(18): Show | 25 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.-22-14094A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41705329 | ||||||
chr6:41705560
|
C | T | 2 | a0001c0001t0001g0105a0001c0005t0001g0106 | 2 | HG02738.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.-22-14325G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41705560 | ||||||
chr6:41705842
|
G | A | 70 | a0001c0001t0001g0187a0001c0001t0001g0194a0001c0001t0001g0196others(67): Show | 74 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.-22-14607C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41705842 | ||||||
chr6:41705908
|
G | A | 46 | a0001c0001t0002g0012a0001c0001t0002g0058a0001c0001t0002g0296others(43): Show | 53 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(50): Show |
intron_variant | MODIFIER | c.-22-14673C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41705908 | ||||||
chr6:41705989
|
G | A | 2 | a0001c0001t0001g0115a0001c0001t0001g0116 | 2 | HG02647.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.-22-14754C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41705989 | ||||||
chr6:41706073
|
T | C | 1 | a0001c0005t0001g0131 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-22-14838A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41706073 | ||||||
chr6:41706362
|
G | T | 18 | a0001c0001t0002g0296a0001c0003t0001g0010a0001c0003t0001g0160others(15): Show | 22 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(19): Show |
intron_variant | MODIFIER | c.-22-15127C>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41706362 | ||||||
chr6:41706366
|
T | C | 1 | a0001c0004t0002g0339 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-22-15131A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41706366 | ||||||
chr6:41706491
|
C | A | 1 | a0001c0004t0002g0055 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-22-15256G>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41706491 | ||||||
chr6:41706508
|
C | T | 114 | a0001c0001t0001g0187a0001c0001t0001g0194a0001c0001t0001g0196others(111): Show | 126 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.-22-15273G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41706508 | ||||||
chr6:41706566
|
A | G | 1 | a0001c0001t0001g0254 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-22-15331T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41706566 | ||||||
chr6:41706567
|
C | T | 1 | a0001c0003t0001g0088 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-22-15332G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41706567 | ||||||
chr6:41706606
|
G | C | 9 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0224others(6): Show | 9 | HG01168.hp2 HG02145.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.-22-15371C>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41706606 | ||||||
chr6:41706667
|
T | C | 4 | a0001c0005t0001g0239a0001c0005t0001g0240a0001c0005t0001g0241others(1): Show | 4 | HG02257.hp2 HG02451.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-22-15432A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41706667 | ||||||
chr6:41706686
|
G | A | 23 | a0001c0001t0001g0023a0001c0001t0001g0104a0001c0001t0001g0105others(20): Show | 27 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.-22-15451C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41706686 | ||||||
chr6:41706739
|
A | G | 1 | a0001c0002t0001g0120 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-22-15504T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41706739 | ||||||
chr6:41706772
|
A | G | 1 | a0001c0004t0002g0171 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-22-15537T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41706772 | ||||||
chr6:41706777
|
C | G | 22 | a0001c0001t0001g0350a0001c0001t0002g0289a0001c0001t0002g0296others(19): Show | 26 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(23): Show |
intron_variant | MODIFIER | c.-22-15542G>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41706777 | ||||||
chr6:41706818
|
T | C | 2 | a0001c0003t0001g0072a0001c0004t0002g0024 | 3 | HG01123.hp1 HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-22-15583A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41706818 | ||||||
chr6:41706824
|
C | G | 2 | a0001c0001t0001g0115a0001c0001t0001g0116 | 2 | HG02647.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.-22-15589G>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41706824 | ||||||
chr6:41706905
|
A | T | 1 | a0001c0003t0001g0064 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-22-15670T>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41706905 | ||||||
chr6:41706937
|
C | T | 3 | a0001c0001t0003g0164a0001c0001t0003g0165a0001c0001t0003g0250 | 3 | HG00741.hp2 HG02486.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-22-15702G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41706937 | ||||||
chr6:41707367
|
C | T | 1 | a0001c0004t0002g0213 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-22-16132G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41707367 | ||||||
chr6:41707487
|
G | A | 1 | a0001c0001t0002g0103 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-22-16252C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41707487 | ||||||
chr6:41707582
|
G | A | 1 | a0001c0002t0001g0214 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-22-16347C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41707582 | ||||||
chr6:41707629
|
G | A | 2 | a0001c0001t0002g0222a0001c0001t0002g0223 | 2 | HG02809.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-22-16394C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41707629 | ||||||
chr6:41707653
|
G | A | 1 | a0001c0002t0001g0149 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-22-16418C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41707653 | ||||||
chr6:41707930
|
A | C | 1 | a0001c0003t0001g0047 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-22-16695T>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41707930 | ||||||
chr6:41707975
|
G | A | 1 | a0001c0001t0001g0104 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-22-16740C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41707975 | ||||||
chr6:41707982
|
G | A | 70 | a0001c0001t0001g0093a0001c0001t0001g0187a0001c0001t0001g0194others(67): Show | 75 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.-22-16747C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41707982 | ||||||
chr6:41708002
|
T | C | 286 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0025others(283): Show | 330 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(327): Show |
intron_variant | MODIFIER | c.-22-16767A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41708002 | ||||||
chr6:41708009
|
G | A | 1 | a0001c0001t0001g0245 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-22-16774C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41708009 | ||||||
chr6:41708029
|
G | C | 4 | a0001c0005t0001g0267a0001c0005t0001g0268a0001c0005t0001g0269others(1): Show | 4 | HG01361.hp1 HG02280.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-22-16794C>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41708029 | ||||||
chr6:41708083
|
G | A | 1 | a0001c0005t0001g0274 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-22-16848C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41708083 | ||||||
chr6:41708108
|
C | A | 1 | a0001c0001t0012g0353 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-22-16873G>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41708108 | ||||||
chr6:41708240
|
G | A | 2 | a0001c0001t0001g0253a0001c0004t0002g0208 | 2 | HG01081.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.-22-17005C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41708240 | ||||||
chr6:41708254
|
C | G | 4 | a0001c0005t0001g0267a0001c0005t0001g0268a0001c0005t0001g0269others(1): Show | 4 | HG01361.hp1 HG02280.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-22-17019G>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41708254 | ||||||
chr6:41708264
|
A | C | 18 | a0001c0001t0001g0025a0001c0001t0001g0246a0001c0001t0001g0247others(15): Show | 19 | HG01168.hp2 HG01884.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.-22-17029T>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41708264 | ||||||
chr6:41708351
|
G | C | 1 | a0001c0001t0001g0113 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-22-17116C>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41708351 | ||||||
chr6:41708383
|
T | C | 2 | a0001c0002t0001g0173a0001c0002t0001g0244 | 2 | NA18747.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.-22-17148A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41708383 | ||||||
chr6:41708531
|
G | A | 23 | a0001c0001t0001g0023a0001c0001t0001g0104a0001c0001t0001g0220others(20): Show | 27 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.-22-17296C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41708531 | ||||||
chr6:41708569
|
C | T | 4 | a0001c0005t0001g0267a0001c0005t0001g0268a0001c0005t0001g0269others(1): Show | 4 | HG01361.hp1 HG02280.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-22-17334G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41708569 | ||||||
chr6:41708644
|
C | T | 2 | a0001c0001t0002g0016a0001c0001t0002g0091 | 3 | HG01243.hp1 HG02717.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.-22-17409G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41708644 | ||||||
chr6:41708696
|
A | G | 2 | a0001c0001t0001g0115a0001c0001t0001g0116 | 2 | HG02647.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.-22-17461T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41708696 | ||||||
chr6:41708714
|
G | A | 26 | a0001c0001t0001g0023a0001c0001t0001g0104a0001c0001t0001g0105others(23): Show | 30 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.-22-17479C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41708714 | ||||||
chr6:41708761
|
G | A | 23 | a0001c0001t0001g0023a0001c0001t0001g0104a0001c0001t0001g0220others(20): Show | 27 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.-22-17526C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41708761 | ||||||
chr6:41708772
|
G | A | 1 | a0001c0004t0002g0202 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-22-17537C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41708772 | ||||||
chr6:41708789
|
C | G | 1 | a0001c0003t0001g0324 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-22-17554G>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41708789 | ||||||
chr6:41709144
|
T | A | 3 | a0001c0001t0001g0273a0001c0001t0012g0353a0001c0010t0001g0265 | 3 | HG01891.hp2 HG02630.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-22-17909A>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41709144 | ||||||
chr6:41709144
|
T | C | 238 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0025others(235): Show | 274 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(271): Show |
intron_variant | MODIFIER | c.-22-17909A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41709144 | ||||||
chr6:41709293
|
TTCA | T | 25 | a0001c0001t0001g0023a0001c0001t0001g0104a0001c0001t0001g0220others(22): Show | 29 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.-22-18061_-22-1805 others(7): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41709293 | ||||||
chr6:41709411
|
C | A | 69 | a0001c0001t0001g0093a0001c0001t0001g0187a0001c0001t0001g0194others(66): Show | 74 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.-22-18176G>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41709411 | ||||||
chr6:41709461
|
T | C | 1 | a0001c0001t0002g0022 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-22-18226A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41709461 | ||||||
chr6:41709529
|
G | GTGGA | 8 | a0001c0001t0001g0187a0001c0001t0002g0029a0001c0001t0002g0302others(5): Show | 9 | HG00544.hp2 HG00673.hp2 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.-22-18298_-22-1829 others(8): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41709529 | ||||||
chr6:41709529
|
G | GTGGATGG others(1): Show |
85 | a0001c0001t0001g0093a0001c0001t0001g0194a0001c0001t0001g0196others(82): Show | 94 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.-22-18302_-22-1829 others(12): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41709529 | ||||||
chr6:41709529
|
G | GTGGATGG others(5): Show |
19 | a0001c0001t0002g0289a0001c0001t0003g0005a0001c0001t0003g0119others(16): Show | 22 | HG00597.hp1 HG00741.hp2 HG01346.hp2 others(19): Show |
intron_variant | MODIFIER | c.-22-18306_-22-1829 others(16): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41709529 | ||||||
chr6:41709529
|
G | GTGGATGG others(9): Show |
2 | a0001c0001t0003g0333a0001c0001t0003g0340 | 2 | HG02015.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.-22-18310_-22-1829 others(20): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41709529 | ||||||
chr6:41709529
|
GTGGA | G | 11 | a0001c0001t0001g0009a0001c0001t0001g0245a0001c0001t0001g0252others(8): Show | 13 | HG00642.hp2 HG01081.hp1 HG01928.hp1 others(10): Show |
intron_variant | MODIFIER | c.-22-18298_-22-1829 others(8): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41709529 | ||||||
chr6:41709529
|
GTGGATGG others(1): Show |
G | 81 | a0001c0001t0001g0023a0001c0001t0001g0104a0001c0001t0001g0105others(78): Show | 101 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.-22-18302_-22-1829 others(12): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41709529 | ||||||
chr6:41709529
|
GTGGATGG others(5): Show |
G | 23 | a0001c0001t0001g0025a0001c0001t0001g0113a0001c0001t0001g0114others(20): Show | 24 | HG01168.hp2 HG01884.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.-22-18306_-22-1829 others(16): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41709529 | ||||||
chr6:41709595
|
C | T | 4 | a0001c0005t0001g0267a0001c0005t0001g0268a0001c0005t0001g0269others(1): Show | 4 | HG01361.hp1 HG02280.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-22-18360G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41709595 | ||||||
chr6:41709768
|
T | C | 1 | a0001c0002t0001g0054 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-22-18533A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41709768 | ||||||
chr6:41709918
|
T | C | 4 | a0001c0005t0001g0267a0001c0005t0001g0268a0001c0005t0001g0269others(1): Show | 4 | HG01361.hp1 HG02280.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-22-18683A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41709918 | ||||||
chr6:41709987
|
T | C | 72 | a0001c0001t0001g0093a0001c0001t0001g0187a0001c0001t0001g0194others(69): Show | 77 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.-22-18752A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41709987 | ||||||
chr6:41710026
|
C | T | 5 | a0001c0005t0001g0239a0001c0005t0001g0240a0001c0005t0001g0241others(2): Show | 5 | HG02257.hp2 HG02451.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-22-18791G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41710026 | ||||||
chr6:41710080
|
C | T | 2 | a0001c0003t0001g0290a0001c0003t0001g0291 | 2 | HG02572.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-22-18845G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41710080 | ||||||
chr6:41710283
|
A | T | 79 | a0001c0001t0001g0093a0001c0001t0001g0105a0001c0001t0001g0187others(76): Show | 84 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.-22-19048T>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41710283 | ||||||
chr6:41710321
|
A | G | 1 | a0001c0001t0001g0112 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-22-19086T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41710321 | ||||||
chr6:41710410
|
C | A | 73 | a0001c0001t0001g0093a0001c0001t0001g0105a0001c0001t0001g0187others(70): Show | 78 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.-22-19175G>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41710410 | ||||||
chr6:41710440
|
C | G | 1 | a0001c0005t0001g0269 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-22-19205G>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41710440 | ||||||
chr6:41710989
|
T | C | 197 | a0001c0001t0001g0009a0001c0001t0001g0025a0001c0001t0001g0093others(194): Show | 229 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.-22-19754A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41710989 | ||||||
chr6:41711117
|
T | G | 1 | a0001c0001t0001g0262 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-22-19882A>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41711117 | ||||||
chr6:41711207
|
C | T | 1 | a0001c0001t0002g0212 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-22-19972G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41711207 | ||||||
chr6:41711490
|
G | A | 1 | a0001c0005t0009g0259 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-22-20255C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41711490 | ||||||
chr6:41711953
|
C | T | 23 | a0001c0001t0001g0023a0001c0001t0001g0104a0001c0001t0001g0220others(20): Show | 27 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.-22-20718G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41711953 | ||||||
chr6:41712125
|
G | A | 4 | a0001c0005t0001g0267a0001c0005t0001g0268a0001c0005t0001g0269others(1): Show | 4 | HG01361.hp1 HG02280.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-22-20890C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41712125 | ||||||
chr6:41712237
|
A | G | 1 | a0001c0002t0001g0020 | 2 | NA18999.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.-22-21002T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41712237 | ||||||
chr6:41712376
|
T | C | 1 | a0001c0001t0002g0323 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-22-21141A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41712376 | ||||||
chr6:41712509
|
A | G | 187 | a0001c0001t0001g0009a0001c0001t0001g0025a0001c0001t0001g0093others(184): Show | 216 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.-22-21274T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41712509 | ||||||
chr6:41712772
|
G | A | 49 | a0001c0001t0001g0112a0001c0001t0001g0122a0001c0001t0001g0129others(46): Show | 65 | HG00423.hp2 HG00735.hp2 HG01070.hp2 others(62): Show |
intron_variant | MODIFIER | c.-22-21537C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41712772 | ||||||
chr6:41712928
|
T | C | 226 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0025others(223): Show | 259 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(256): Show |
intron_variant | MODIFIER | c.-22-21693A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41712928 | ||||||
chr6:41712976
|
C | G | 1 | a0001c0005t0001g0063 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-22-21741G>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41712976 | ||||||
chr6:41713086
|
G | A | 2 | a0001c0001t0001g0130a0001c0001t0001g0224 | 2 | HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-22-21851C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41713086 | ||||||
chr6:41713273
|
C | T | 6 | a0001c0001t0001g0009a0001c0001t0001g0252a0001c0001t0001g0253others(3): Show | 8 | HG00642.hp2 HG01081.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.-22-22038G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41713273 | ||||||
chr6:41713298
|
G | A | 27 | a0001c0001t0001g0023a0001c0001t0001g0104a0001c0001t0001g0220others(24): Show | 31 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.-23+22052C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41713298 | ||||||
chr6:41713303
|
G | A | 1 | a0001c0004t0002g0243 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.-23+22047C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41713303 | ||||||
chr6:41713306
|
G | A | 9 | a0001c0001t0002g0329a0001c0002t0001g0304a0001c0002t0001g0305others(6): Show | 9 | HG02602.hp2 HG02683.hp1 HG04199.hp1 others(6): Show |
intron_variant | MODIFIER | c.-23+22044C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41713306 | ||||||
chr6:41713445
|
G | A | 28 | a0001c0001t0001g0023a0001c0001t0001g0104a0001c0001t0001g0220others(25): Show | 32 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.-23+21905C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41713445 | ||||||
chr6:41713488
|
C | T | 2 | a0001c0002t0001g0017a0001c0002t0001g0120 | 3 | HG01255.hp2 HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-23+21862G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41713488 | ||||||
chr6:41713490
|
C | T | 3 | a0001c0001t0001g0105a0001c0003t0001g0035a0001c0005t0001g0106 | 3 | HG02738.hp2 HG03688.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.-23+21860G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41713490 | ||||||
chr6:41713494
|
C | G | 1 | a0001c0001t0001g0105 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-23+21856G>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41713494 | ||||||
chr6:41713498
|
T | A | 1 | a0001c0003t0001g0061 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-23+21852A>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41713498 | ||||||
chr6:41713592
|
G | A | 184 | a0001c0001t0001g0009a0001c0001t0001g0025a0001c0001t0001g0093others(181): Show | 213 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(210): Show |
intron_variant | MODIFIER | c.-23+21758C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41713592 | ||||||
chr6:41713602
|
G | A | 184 | a0001c0001t0001g0009a0001c0001t0001g0025a0001c0001t0001g0093others(181): Show | 213 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(210): Show |
intron_variant | MODIFIER | c.-23+21748C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41713602 | ||||||
chr6:41713835
|
G | A | 2 | a0001c0003t0001g0059a0001c0003t0001g0060 | 2 | HG02615.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-23+21515C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41713835 | ||||||
chr6:41713884
|
T | A | 225 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0025others(222): Show | 258 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(255): Show |
intron_variant | MODIFIER | c.-23+21466A>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41713884 | ||||||
chr6:41713946
|
C | T | 1 | a0001c0002t0001g0155 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-23+21404G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41713946 | ||||||
chr6:41713953
|
G | A | 2 | a0001c0005t0001g0267a0001c0005t0001g0268 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-23+21397C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41713953 | ||||||
chr6:41713954
|
C | T | 3 | a0001c0002t0001g0046a0001c0004t0002g0034a0001c0004t0002g0186 | 3 | HG04115.hp1 NA18982.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.-23+21396G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41713954 | ||||||
chr6:41714016
|
C | T | 1 | a0001c0001t0013g0354 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-23+21334G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41714016 | ||||||
chr6:41714025
|
C | T | 9 | a0001c0002t0001g0251a0001c0002t0001g0258a0001c0003t0001g0272others(6): Show | 9 | HG01168.hp2 HG02145.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.-23+21325G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41714025 | ||||||
chr6:41714049
|
G | A | 186 | a0001c0001t0001g0009a0001c0001t0001g0025a0001c0001t0001g0093others(183): Show | 215 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(212): Show |
intron_variant | MODIFIER | c.-23+21301C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41714049 | ||||||
chr6:41714097
|
G | A | 25 | a0001c0001t0001g0023a0001c0001t0001g0104a0001c0001t0001g0220others(22): Show | 26 | HG00280.hp1 HG00280.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.-23+21253C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41714097 | ||||||
chr6:41714110
|
C | CGT | 28 | a0001c0001t0001g0023a0001c0001t0001g0104a0001c0001t0001g0220others(25): Show | 32 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(29): Show |
intron_variant | MODIFIER | c.-23+21238_-23+2123 others(6): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41714110 | ||||||
chr6:41714110
|
C | T | 1 | a0001c0004t0002g0180 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-23+21240G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41714110 | ||||||
chr6:41714111
|
G | A | 87 | a0001c0001t0001g0105a0001c0001t0001g0122a0001c0001t0001g0129others(84): Show | 108 | HG00140.hp2 HG00423.hp2 HG00597.hp1 others(105): Show |
intron_variant | MODIFIER | c.-23+21239C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41714111 | ||||||
chr6:41714133
|
A | G | 6 | a0001c0004t0002g0180a0001c0004t0002g0181a0001c0004t0002g0182others(3): Show | 6 | HG00408.hp1 HG00621.hp1 NA18960.hp1 others(3): Show |
intron_variant | MODIFIER | c.-23+21217T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41714133 | ||||||
chr6:41714140
|
C | T | 24 | a0001c0001t0001g0023a0001c0001t0001g0104a0001c0001t0001g0220others(21): Show | 28 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.-23+21210G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41714140 | ||||||
chr6:41714140
|
CGT | C | 169 | a0001c0001t0001g0025a0001c0001t0001g0093a0001c0001t0001g0105others(166): Show | 196 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.-23+21208_-23+2120 others(6): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41714140 | ||||||
chr6:41714142
|
T | TGTGTGCA others(9): Show |
15 | a0001c0001t0001g0009a0001c0001t0001g0252a0001c0001t0001g0253others(12): Show | 17 | HG00642.hp2 HG01081.hp1 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.-23+21207_-23+2120 others(20): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41714142 | ||||||
chr6:41714142
|
T | TGTGTGCA others(17): Show |
2 | a0001c0001t0001g0263a0001c0001t0001g0264 | 2 | HG02572.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-23+21207_-23+2120 others(28): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41714142 | ||||||
chr6:41714167
|
ATG | A | 49 | a0001c0001t0001g0112a0001c0001t0001g0122a0001c0001t0001g0129others(46): Show | 65 | HG00423.hp2 HG00735.hp2 HG01070.hp2 others(62): Show |
intron_variant | MODIFIER | c.-23+21181_-23+2118 others(6): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41714167 | ||||||
chr6:41714174
|
CGT | C | 92 | a0001c0001t0001g0009a0001c0001t0001g0025a0001c0001t0001g0093others(89): Show | 100 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.-23+21174_-23+2117 others(6): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41714174 | ||||||
chr6:41714179
|
G | A | 1 | a0001c0005t0001g0284 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-23+21171C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41714179 | ||||||
chr6:41714200
|
C | T | 91 | a0001c0001t0001g0009a0001c0001t0001g0025a0001c0001t0001g0093others(88): Show | 99 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.-23+21150G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41714200 | ||||||
chr6:41714230
|
C | T | 24 | a0001c0001t0001g0023a0001c0001t0001g0104a0001c0001t0001g0220others(21): Show | 28 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.-23+21120G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41714230 | ||||||
chr6:41714309
|
C | G | 2 | a0001c0001t0002g0222a0001c0001t0002g0223 | 2 | HG02809.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-23+21041G>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41714309 | ||||||
chr6:41714316
|
C | G | 1 | a0001c0001t0002g0330 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-23+21034G>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41714316 | ||||||
chr6:41714484
|
C | T | 3 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0224 | 3 | HG02622.hp1 HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-23+20866G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41714484 | ||||||
chr6:41714685
|
C | A | 88 | a0001c0001t0001g0112a0001c0001t0001g0115a0001c0001t0001g0116others(85): Show | 109 | HG00140.hp2 HG00423.hp2 HG00597.hp1 others(106): Show |
intron_variant | MODIFIER | c.-23+20665G>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41714685 | ||||||
chr6:41714718
|
C | A | 1 | a0001c0002t0001g0285 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-23+20632G>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41714718 | ||||||
chr6:41714719
|
G | A | 2 | a0001c0001t0003g0164a0001c0001t0003g0250 | 2 | HG00741.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-23+20631C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41714719 | ||||||
chr6:41714743
|
C | T | 1 | a0001c0003t0001g0037 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.-23+20607G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41714743 | ||||||
chr6:41714748
|
C | T | 33 | a0001c0001t0001g0023a0001c0001t0001g0025a0001c0001t0001g0220others(30): Show | 35 | HG00280.hp1 HG00642.hp1 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.-23+20602G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41714748 | ||||||
chr6:41714856
|
T | C | 1 | a0001c0001t0001g0249 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-23+20494A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41714856 | ||||||
chr6:41714876
|
C | T | 1 | a0001c0002t0001g0162 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-23+20474G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41714876 | ||||||
chr6:41715024
|
C | T | 1 | a0001c0002t0001g0044 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-23+20326G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41715024 | ||||||
chr6:41715121
|
C | T | 2 | a0001c0003t0001g0160a0001c0005t0001g0161 | 2 | HG00733.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.-23+20229G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41715121 | ||||||
chr6:41715161
|
C | T | 1 | a0001c0001t0003g0164 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-23+20189G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41715161 | ||||||
chr6:41715223
|
A | G | 1 | a0001c0001t0003g0333 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-23+20127T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41715223 | ||||||
chr6:41715331
|
C | T | 1 | a0001c0008t0002g0309 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-23+20019G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41715331 | ||||||
chr6:41715539
|
G | A | 2 | a0001c0001t0002g0222a0001c0001t0002g0223 | 2 | HG02809.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-23+19811C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41715539 | ||||||
chr6:41715585
|
G | A | 4 | a0001c0003t0001g0231a0001c0003t0001g0232a0001c0003t0001g0233others(1): Show | 4 | HG01928.hp1 HG01943.hp2 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.-23+19765C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41715585 | ||||||
chr6:41715626
|
C | T | 1 | a0001c0003t0001g0084 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-23+19724G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41715626 | ||||||
chr6:41715657
|
G | A | 23 | a0001c0001t0001g0023a0001c0001t0001g0104a0001c0001t0001g0105others(20): Show | 24 | HG00280.hp2 HG00642.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.-23+19693C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41715657 | ||||||
chr6:41715676
|
GA | G | 37 | a0001c0001t0001g0023a0001c0001t0001g0025a0001c0001t0001g0104others(34): Show | 42 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.-23+19673delT | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41715676 | ||||||
chr6:41715682
|
A | G | 9 | a0001c0001t0001g0246a0001c0001t0001g0247a0001c0001t0001g0248others(6): Show | 9 | HG01884.hp1 HG02486.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.-23+19668T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41715682 | ||||||
chr6:41715714
|
C | T | 5 | a0001c0001t0001g0246a0001c0001t0001g0247a0001c0001t0001g0248others(2): Show | 5 | HG01884.hp1 HG02886.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-23+19636G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41715714 | ||||||
chr6:41715803
|
C | T | 1 | a0001c0001t0013g0354 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-23+19547G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41715803 | ||||||
chr6:41715804
|
G | A | 1 | a0001c0003t0001g0169 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-23+19546C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41715804 | ||||||
chr6:41715949
|
C | T | 12 | a0001c0001t0002g0175a0001c0002t0001g0020a0001c0002t0001g0172others(9): Show | 14 | HG00438.hp2 HG01069.hp1 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.-23+19401G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41715949 | ||||||
chr6:41715967
|
C | T | 4 | a0001c0005t0001g0239a0001c0005t0001g0240a0001c0005t0001g0241others(1): Show | 4 | HG02257.hp2 HG02451.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-23+19383G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41715967 | ||||||
chr6:41715974
|
C | T | 13 | a0001c0001t0001g0025a0001c0001t0001g0114a0001c0001t0001g0260others(10): Show | 14 | HG01361.hp1 HG02280.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.-23+19376G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41715974 | ||||||
chr6:41716063
|
G | A | 1 | a0001c0001t0002g0151 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-23+19287C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41716063 | ||||||
chr6:41716066
|
A | G | 3 | a0001c0002t0001g0304a0001c0002t0001g0305a0001c0002t0001g0306 | 3 | NA18941.hp1 NA19077.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.-23+19284T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41716066 | ||||||
chr6:41716268
|
C | G | 4 | a0001c0001t0001g0246a0001c0001t0001g0247a0001c0001t0001g0248others(1): Show | 4 | HG01884.hp1 HG02886.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-23+19082G>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41716268 | ||||||
chr6:41716282
|
C | G | 7 | a0001c0001t0001g0246a0001c0001t0001g0247a0001c0001t0001g0248others(4): Show | 7 | HG01884.hp1 HG02145.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-23+19068G>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41716282 | ||||||
chr6:41716419
|
A | AG | 19 | a0001c0001t0001g0025a0001c0001t0001g0246a0001c0001t0001g0247others(16): Show | 20 | HG01361.hp1 HG01884.hp1 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.-23+18930_-23+1893 others(5): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41716419 | ||||||
chr6:41716448
|
C | A | 1 | a0001c0002t0001g0286 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-23+18902G>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41716448 | ||||||
chr6:41716536
|
G | C | 1 | a0001c0004t0002g0171 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-23+18814C>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41716536 | ||||||
chr6:41716564
|
A | T | 1 | a0001c0001t0002g0083 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-23+18786T>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41716564 | ||||||
chr6:41716652
|
A | G | 44 | a0001c0001t0002g0012a0001c0001t0003g0076a0001c0001t0003g0079others(41): Show | 52 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.-23+18698T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41716652 | ||||||
chr6:41716653
|
A | G | 1 | a0001c0003t0001g0061 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-23+18697T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41716653 | ||||||
chr6:41716907
|
A | C | 42 | a0001c0001t0001g0023a0001c0001t0001g0025a0001c0001t0001g0104others(39): Show | 44 | HG00280.hp2 HG00642.hp1 HG01106.hp1 others(41): Show |
intron_variant | MODIFIER | c.-23+18443T>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41716907 | ||||||
chr6:41716946
|
G | C | 1 | a0001c0001t0001g0112 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-23+18404C>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41716946 | ||||||
chr6:41717278
|
C | T | 2 | a0001c0003t0001g0014a0001c0003t0001g0080 | 3 | HG00438.hp1 NA18974.hp1 NA19059.hp1 |
intron_variant | MODIFIER | c.-23+18072G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41717278 | ||||||
chr6:41717416
|
A | G | 1 | a0001c0005t0001g0274 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-23+17934T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41717416 | ||||||
chr6:41717640
|
C | G | 1 | a0001c0001t0002g0328 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-23+17710G>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41717640 | ||||||
chr6:41717658
|
C | A | 1 | a0001c0004t0002g0213 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-23+17692G>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41717658 | ||||||
chr6:41717676
|
A | C | 19 | a0001c0001t0001g0025a0001c0001t0001g0246a0001c0001t0001g0247others(16): Show | 20 | HG01361.hp1 HG01884.hp1 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.-23+17674T>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41717676 | ||||||
chr6:41717701
|
A | C | 3 | a0001c0002t0001g0173a0001c0002t0001g0174a0001c0002t0001g0244 | 3 | NA18747.hp1 NA19077.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.-23+17649T>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41717701 | ||||||
chr6:41717788
|
G | A | 6 | a0001c0002t0001g0207a0001c0003t0001g0169a0001c0003t0001g0209others(3): Show | 6 | HG00597.hp2 HG02027.hp1 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.-23+17562C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41717788 | ||||||
chr6:41717807
|
G | C | 1 | a0001c0001t0003g0079 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-23+17543C>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41717807 | ||||||
chr6:41717911
|
G | C | 12 | a0001c0001t0001g0025a0001c0001t0001g0260a0001c0001t0001g0262others(9): Show | 13 | HG01361.hp1 HG02280.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.-23+17439C>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41717911 | ||||||
chr6:41718054
|
T | C | 2 | a0001c0001t0001g0113a0001c0001t0001g0114 | 2 | HG02630.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-23+17296A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41718054 | ||||||
chr6:41718071
|
G | T | 1 | a0001c0005t0001g0276 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-23+17279C>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41718071 | ||||||
chr6:41718161
|
T | C | 23 | a0001c0001t0001g0023a0001c0001t0001g0104a0001c0001t0001g0105others(20): Show | 24 | HG00280.hp2 HG00642.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.-23+17189A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41718161 | ||||||
chr6:41718185
|
G | GT | 72 | a0001c0001t0001g0009a0001c0001t0001g0187a0001c0001t0001g0194others(69): Show | 79 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.-23+17164dupA | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41718185 | ||||||
chr6:41718185
|
GT | G | 7 | a0001c0001t0001g0246a0001c0001t0001g0247a0001c0001t0001g0248others(4): Show | 7 | HG01884.hp1 HG02145.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-23+17164delA | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41718185 | ||||||
chr6:41718188
|
T | C | 2 | a0001c0005t0001g0240a0001c0005t0001g0241 | 2 | HG02257.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.-23+17162A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41718188 | ||||||
chr6:41718280
|
C | T | 1 | a0001c0003t0001g0297 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-23+17070G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41718280 | ||||||
chr6:41718285
|
T | C | 1 | a0001c0002t0001g0019 | 2 | NA18993.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.-23+17065A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41718285 | ||||||
chr6:41718346
|
C | G | 1 | a0001c0001t0012g0353 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-23+17004G>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41718346 | ||||||
chr6:41718383
|
A | AT | 7 | a0001c0002t0001g0042a0001c0003t0001g0006a0001c0003t0001g0041others(4): Show | 9 | HG01074.hp1 HG01099.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.-23+16966dupA | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41718383 | ||||||
chr6:41718391
|
G | A | 2 | a0001c0001t0001g0115a0001c0001t0001g0116 | 2 | HG02647.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.-23+16959C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41718391 | ||||||
chr6:41718401
|
A | G | 5 | a0001c0003t0001g0014a0001c0003t0001g0033a0001c0003t0001g0080others(2): Show | 6 | HG00438.hp1 NA18967.hp1 NA18974.hp1 others(3): Show |
intron_variant | MODIFIER | c.-23+16949T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41718401 | ||||||
chr6:41718675
|
C | CT | 22 | a0001c0001t0001g0025a0001c0001t0001g0105a0001c0001t0001g0246others(19): Show | 23 | HG01361.hp1 HG01884.hp1 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.-23+16674dupA | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41718675 | ||||||
chr6:41718724
|
T | C | 1 | a0001c0003t0001g0272 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-23+16626A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41718724 | ||||||
chr6:41718768
|
T | G | 1 | a0001c0003t0001g0211 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-23+16582A>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41718768 | ||||||
chr6:41718811
|
A | C | 4 | a0001c0005t0001g0239a0001c0005t0001g0240a0001c0005t0001g0241others(1): Show | 4 | HG02257.hp2 HG02451.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-23+16539T>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41718811 | ||||||
chr6:41718842
|
C | T | 1 | a0001c0003t0001g0272 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-23+16508G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41718842 | ||||||
chr6:41718855
|
G | A | 63 | a0001c0001t0001g0187a0001c0001t0001g0194a0001c0001t0001g0196others(60): Show | 68 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.-23+16495C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41718855 | ||||||
chr6:41718895
|
G | A | 1 | a0001c0001t0012g0353 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-23+16455C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41718895 | ||||||
chr6:41718953
|
C | T | 63 | a0001c0001t0001g0187a0001c0001t0001g0194a0001c0001t0001g0196others(60): Show | 68 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.-23+16397G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41718953 | ||||||
chr6:41719108
|
T | C | 18 | a0001c0001t0001g0025a0001c0001t0001g0246a0001c0001t0001g0247others(15): Show | 19 | HG01361.hp1 HG01884.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.-23+16242A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41719108 | ||||||
chr6:41719142
|
G | A | 12 | a0001c0001t0001g0025a0001c0001t0001g0260a0001c0001t0001g0262others(9): Show | 13 | HG01361.hp1 HG02280.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.-23+16208C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41719142 | ||||||
chr6:41719213
|
C | T | 6 | a0001c0001t0001g0246a0001c0001t0001g0247a0001c0001t0001g0248others(3): Show | 6 | HG01884.hp1 HG02145.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-23+16137G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41719213 | ||||||
chr6:41719225
|
C | T | 12 | a0001c0001t0001g0025a0001c0001t0001g0260a0001c0001t0001g0262others(9): Show | 13 | HG01361.hp1 HG02280.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.-23+16125G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41719225 | ||||||
chr6:41719226
|
G | A | 2 | a0001c0001t0002g0016a0001c0001t0002g0091 | 3 | HG01243.hp1 HG02717.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.-23+16124C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41719226 | ||||||
chr6:41719250
|
A | G | 6 | a0001c0001t0002g0296a0002c0006t0001g0027a0002c0006t0001g0293others(3): Show | 7 | HG00423.hp1 HG00544.hp1 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.-23+16100T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41719250 | ||||||
chr6:41719253
|
G | A | 5 | a0001c0003t0001g0014a0001c0003t0001g0033a0001c0003t0001g0080others(2): Show | 6 | HG00438.hp1 NA18967.hp1 NA18974.hp1 others(3): Show |
intron_variant | MODIFIER | c.-23+16097C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41719253 | ||||||
chr6:41719305
|
T | C | 2 | a0001c0001t0001g0252a0001c0001t0001g0253 | 2 | HG01081.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-23+16045A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41719305 | ||||||
chr6:41719514
|
G | C | 41 | a0001c0001t0001g0023a0001c0001t0001g0025a0001c0001t0001g0104others(38): Show | 43 | HG00280.hp2 HG00642.hp1 HG01106.hp1 others(40): Show |
intron_variant | MODIFIER | c.-23+15836C>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41719514 | ||||||
chr6:41719519
|
G | A | 2 | a0001c0001t0002g0328a0001c0001t0002g0330 | 2 | HG00558.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.-23+15831C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41719519 | ||||||
chr6:41719603
|
G | A | 1 | a0001c0001t0001g0350 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-23+15747C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41719603 | ||||||
chr6:41719628
|
T | C | 178 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0025others(175): Show | 195 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.-23+15722A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41719628 | ||||||
chr6:41719699
|
C | T | 1 | a0001c0004t0002g0034 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-23+15651G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41719699 | ||||||
chr6:41719904
|
TCCTGAGG others(14): Show |
T | 6 | a0001c0001t0001g0246a0001c0001t0001g0247a0001c0001t0001g0248others(3): Show | 6 | HG01884.hp1 HG02145.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-23+15425_-23+1544 others(25): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41719904 | ||||||
chr6:41719960
|
G | A | 1 | a0001c0001t0001g0114 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-23+15390C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41719960 | ||||||
chr6:41720001
|
A | G | 1 | a0001c0001t0001g0245 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-23+15349T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41720001 | ||||||
chr6:41720045
|
A | G | 1 | a0001c0004t0002g0171 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-23+15305T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41720045 | ||||||
chr6:41720177
|
C | CA | 65 | a0001c0001t0001g0187a0001c0001t0001g0194a0001c0001t0001g0196others(62): Show | 70 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.-23+15172dupT | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41720177 | ||||||
chr6:41720182
|
C | T | 18 | a0001c0001t0001g0025a0001c0001t0001g0246a0001c0001t0001g0247others(15): Show | 19 | HG01361.hp1 HG01884.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.-23+15168G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41720182 | ||||||
chr6:41720362
|
C | A | 49 | a0001c0001t0001g0112a0001c0001t0001g0122a0001c0001t0001g0129others(46): Show | 65 | HG00423.hp2 HG00735.hp2 HG01070.hp2 others(62): Show |
intron_variant | MODIFIER | c.-23+14988G>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41720362 | ||||||
chr6:41720450
|
G | A | 1 | a0001c0001t0001g0266 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-23+14900C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41720450 | ||||||
chr6:41720479
|
T | C | 5 | a0001c0001t0002g0212a0001c0004t0002g0117a0001c0004t0002g0213others(2): Show | 5 | HG02071.hp2 HG02155.hp1 NA18988.hp1 others(2): Show |
intron_variant | MODIFIER | c.-23+14871A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41720479 | ||||||
chr6:41720493
|
G | A | 18 | a0001c0001t0001g0025a0001c0001t0001g0246a0001c0001t0001g0247others(15): Show | 19 | HG01361.hp1 HG01884.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.-23+14857C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41720493 | ||||||
chr6:41720664
|
A | T | 47 | a0001c0001t0001g0112a0001c0001t0001g0122a0001c0001t0001g0129others(44): Show | 63 | HG00423.hp2 HG00735.hp2 HG01070.hp2 others(60): Show |
intron_variant | MODIFIER | c.-23+14686T>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41720664 | ||||||
chr6:41720706
|
C | T | 1 | a0001c0001t0012g0353 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-23+14644G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41720706 | ||||||
chr6:41720928
|
C | T | 4 | a0001c0005t0001g0239a0001c0005t0001g0240a0001c0005t0001g0241others(1): Show | 4 | HG02257.hp2 HG02451.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-23+14422G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41720928 | ||||||
chr6:41720954
|
G | A | 1 | a0001c0001t0003g0235 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-23+14396C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41720954 | ||||||
chr6:41721022
|
C | T | 2 | a0001c0001t0001g0115a0001c0001t0001g0116 | 2 | HG02647.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.-23+14328G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41721022 | ||||||
chr6:41721025
|
G | C | 1 | a0001c0004t0002g0055 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-23+14325C>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41721025 | ||||||
chr6:41721252
|
T | C | 53 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0273others(50): Show | 61 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.-23+14098A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41721252 | ||||||
chr6:41721261
|
T | C | 29 | a0001c0001t0001g0025a0001c0001t0001g0224a0001c0001t0001g0246others(26): Show | 31 | HG01168.hp2 HG01361.hp1 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.-23+14089A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41721261 | ||||||
chr6:41721313
|
A | G | 18 | a0001c0001t0001g0025a0001c0001t0001g0246a0001c0001t0001g0247others(15): Show | 19 | HG01361.hp1 HG01884.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.-23+14037T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41721313 | ||||||
chr6:41721368
|
C | T | 2 | a0001c0005t0001g0267a0001c0005t0001g0268 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-23+13982G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41721368 | ||||||
chr6:41721372
|
T | TAC | 45 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0104others(42): Show | 48 | HG00280.hp2 HG00558.hp1 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.-23+13976_-23+1397 others(6): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41721372 | ||||||
chr6:41721372
|
T | TACAC | 42 | a0001c0001t0001g0342a0001c0001t0002g0283a0001c0001t0002g0289others(39): Show | 50 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(47): Show |
intron_variant | MODIFIER | c.-23+13974_-23+1397 others(8): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41721372 | ||||||
chr6:41721372
|
T | TACACAC | 9 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0349others(6): Show | 9 | HG00544.hp1 HG01346.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.-23+13972_-23+1397 others(10): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41721372 | ||||||
chr6:41721372
|
TAC | T | 8 | a0001c0001t0002g0016a0001c0001t0002g0091a0001c0002t0001g0120others(5): Show | 9 | HG01243.hp1 HG02717.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.-23+13976_-23+1397 others(6): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41721372 | ||||||
chr6:41721372
|
TACAC | T | 50 | a0001c0001t0001g0112a0001c0001t0001g0122a0001c0001t0001g0129others(47): Show | 65 | HG00423.hp2 HG00735.hp2 HG01070.hp2 others(62): Show |
intron_variant | MODIFIER | c.-23+13974_-23+1397 others(8): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41721372 | ||||||
chr6:41721372
|
TACACACA others(1): Show |
T | 15 | a0001c0001t0001g0025a0001c0001t0001g0246a0001c0001t0001g0247others(12): Show | 16 | HG01884.hp1 HG02145.hp2 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.-23+13970_-23+1397 others(12): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41721372 | ||||||
chr6:41721372
|
TACACACA others(7): Show |
T | 1 | a0001c0004t0002g0171 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-23+13964_-23+1397 others(18): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41721372 | ||||||
chr6:41721376
|
C | T | 2 | a0001c0005t0001g0269a0001c0005t0001g0270 | 2 | HG01361.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.-23+13974G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41721376 | ||||||
chr6:41721568
|
C | T | 1 | a0001c0001t0002g0170 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-23+13782G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41721568 | ||||||
chr6:41721616
|
C | T | 2 | a0001c0001t0001g0113a0001c0001t0001g0114 | 2 | HG02630.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-23+13734G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41721616 | ||||||
chr6:41721643
|
G | T | 2 | a0001c0001t0002g0222a0001c0001t0002g0223 | 2 | HG02809.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-23+13707C>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41721643 | ||||||
chr6:41721850
|
A | G | 2 | a0001c0001t0001g0115a0001c0001t0001g0116 | 2 | HG02647.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.-23+13500T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41721850 | ||||||
chr6:41721977
|
A | ATAT | 5 | a0001c0002t0001g0123a0001c0005t0001g0239a0001c0005t0001g0240others(2): Show | 5 | HG02257.hp2 HG02451.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.-23+13370_-23+1337 others(7): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41721977 | ||||||
chr6:41722015
|
G | A | 2 | a0001c0001t0001g0093a0001c0001t0002g0094 | 2 | HG02451.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-23+13335C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41722015 | ||||||
chr6:41722092
|
G | C | 1 | a0001c0004t0002g0215 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-23+13258C>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41722092 | ||||||
chr6:41722231
|
C | G | 2 | a0001c0003t0001g0059a0001c0003t0001g0060 | 2 | HG02615.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-23+13119G>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41722231 | ||||||
chr6:41722286
|
G | C | 18 | a0001c0001t0001g0025a0001c0001t0001g0246a0001c0001t0001g0247others(15): Show | 19 | HG01361.hp1 HG01884.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.-23+13064C>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41722286 | ||||||
chr6:41722314
|
T | C | 2 | a0001c0003t0001g0056a0001c0003t0001g0057 | 2 | HG01074.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.-23+13036A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41722314 | ||||||
chr6:41722353
|
A | T | 1 | a0001c0005t0001g0275 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-23+12997T>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41722353 | ||||||
chr6:41722564
|
C | T | 18 | a0001c0001t0001g0025a0001c0001t0001g0246a0001c0001t0001g0247others(15): Show | 19 | HG01361.hp1 HG01884.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.-23+12786G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41722564 | ||||||
chr6:41722592
|
A | G | 4 | a0001c0001t0001g0349a0001c0001t0001g0350a0001c0001t0001g0351others(1): Show | 4 | HG02809.hp1 HG06807.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.-23+12758T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41722592 | ||||||
chr6:41722634
|
G | T | 18 | a0001c0001t0001g0025a0001c0001t0001g0246a0001c0001t0001g0247others(15): Show | 19 | HG01361.hp1 HG01884.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.-23+12716C>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41722634 | ||||||
chr6:41722756
|
G | A | 18 | a0001c0001t0001g0025a0001c0001t0001g0246a0001c0001t0001g0247others(15): Show | 19 | HG01361.hp1 HG01884.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.-23+12594C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41722756 | ||||||
chr6:41722904
|
G | A | 1 | a0001c0003t0001g0272 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-23+12446C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41722904 | ||||||
chr6:41722986
|
C | T | 3 | a0001c0001t0001g0105a0001c0003t0001g0035a0001c0005t0001g0106 | 3 | HG02738.hp2 HG03688.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.-23+12364G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41722986 | ||||||
chr6:41723042
|
G | A | 1 | a0001c0001t0002g0058 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-23+12308C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41723042 | ||||||
chr6:41723085
|
C | A | 217 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0025others(214): Show | 247 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(244): Show |
intron_variant | MODIFIER | c.-23+12265G>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41723085 | ||||||
chr6:41723285
|
C | T | 18 | a0001c0001t0001g0025a0001c0001t0001g0246a0001c0001t0001g0247others(15): Show | 19 | HG01361.hp1 HG01884.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.-23+12065G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41723285 | ||||||
chr6:41723314
|
C | A | 14 | a0001c0001t0001g0342a0001c0001t0003g0005a0001c0001t0003g0166others(11): Show | 17 | HG00597.hp1 HG01346.hp2 HG01981.hp1 others(14): Show |
intron_variant | MODIFIER | c.-23+12036G>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41723314 | ||||||
chr6:41723388
|
C | A | 18 | a0001c0001t0001g0025a0001c0001t0001g0246a0001c0001t0001g0247others(15): Show | 19 | HG01361.hp1 HG01884.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.-23+11962G>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41723388 | ||||||
chr6:41723400
|
TTCACACA others(5): Show |
T | 2 | a0001c0001t0001g0113a0001c0001t0001g0114 | 2 | HG02630.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-23+11938_-23+1194 others(16): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41723400 | ||||||
chr6:41723429
|
ACT | A | 5 | a0001c0001t0001g0224a0001c0001t0002g0222a0001c0001t0002g0223others(2): Show | 5 | HG01168.hp2 HG02809.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.-23+11919_-23+1192 others(6): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41723429 | ||||||
chr6:41723444
|
CGCGTGT | C | 10 | a0001c0001t0001g0009a0001c0001t0001g0252a0001c0001t0001g0253others(7): Show | 12 | HG00642.hp2 HG01081.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.-23+11900_-23+1190 others(10): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41723444 | ||||||
chr6:41723558
|
A | G | 53 | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0273others(50): Show | 61 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.-23+11792T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41723558 | ||||||
chr6:41723563
|
C | CCTCATTT others(9): Show |
1 | a0001c0001t0001g0122 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.-23+11771_-23+1178 others(20): Show |
TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41723563 | ||||||
chr6:41723614
|
T | C | 18 | a0001c0001t0001g0025a0001c0001t0001g0246a0001c0001t0001g0247others(15): Show | 19 | HG01361.hp1 HG01884.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.-23+11736A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41723614 | ||||||
chr6:41723638
|
T | C | 1 | a0001c0001t0001g0249 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-23+11712A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41723638 | ||||||
chr6:41723750
|
C | A | 18 | a0001c0001t0001g0025a0001c0001t0001g0246a0001c0001t0001g0247others(15): Show | 19 | HG01361.hp1 HG01884.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.-23+11600G>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41723750 | ||||||
chr6:41723756
|
C | T | 18 | a0001c0001t0001g0025a0001c0001t0001g0246a0001c0001t0001g0247others(15): Show | 19 | HG01361.hp1 HG01884.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.-23+11594G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41723756 | ||||||
chr6:41723762
|
G | A | 10 | a0001c0001t0001g0009a0001c0001t0001g0252a0001c0001t0001g0253others(7): Show | 12 | HG00642.hp2 HG01081.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.-23+11588C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41723762 | ||||||
chr6:41723770
|
C | T | 3 | a0001c0003t0001g0334a0001c0003t0001g0335a0001c0003t0001g0336 | 3 | HG01981.hp2 HG02056.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.-23+11580G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41723770 | ||||||
chr6:41723861
|
C | A | 17 | a0001c0001t0001g0342a0001c0001t0003g0005a0001c0001t0003g0164others(14): Show | 20 | HG00597.hp1 HG00741.hp2 HG01346.hp2 others(17): Show |
intron_variant | MODIFIER | c.-23+11489G>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41723861 | ||||||
chr6:41723928
|
C | G | 18 | a0001c0001t0001g0025a0001c0001t0001g0246a0001c0001t0001g0247others(15): Show | 19 | HG01361.hp1 HG01884.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.-23+11422G>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41723928 | ||||||
chr6:41723965
|
C | A | 6 | a0001c0001t0001g0246a0001c0001t0001g0247a0001c0001t0001g0248others(3): Show | 6 | HG01884.hp1 HG02145.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-23+11385G>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41723965 | ||||||
chr6:41724018
|
C | A | 1 | a0001c0004t0002g0226 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-23+11332G>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41724018 | ||||||
chr6:41724044
|
G | A | 18 | a0001c0001t0001g0025a0001c0001t0001g0246a0001c0001t0001g0247others(15): Show | 19 | HG01361.hp1 HG01884.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.-23+11306C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41724044 | ||||||
chr6:41724194
|
C | T | 1 | a0001c0001t0001g0227 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-23+11156G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41724194 | ||||||
chr6:41724277
|
C | T | 1 | a0001c0002t0001g0040 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-23+11073G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41724277 | ||||||
chr6:41724355
|
T | C | 18 | a0001c0001t0001g0025a0001c0001t0001g0246a0001c0001t0001g0247others(15): Show | 19 | HG01361.hp1 HG01884.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.-23+10995A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41724355 | ||||||
chr6:41724391
|
C | T | 6 | a0001c0001t0001g0009a0001c0001t0001g0252a0001c0001t0001g0253others(3): Show | 8 | HG00642.hp2 HG01081.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.-23+10959G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41724391 | ||||||
chr6:41724486
|
G | C | 1 | a0001c0001t0001g0245 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-23+10864C>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41724486 | ||||||
chr6:41724586
|
T | C | 1 | a0001c0001t0001g0245 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-23+10764A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41724586 | ||||||
chr6:41724634
|
G | A | 18 | a0001c0001t0001g0025a0001c0001t0001g0246a0001c0001t0001g0247others(15): Show | 19 | HG01361.hp1 HG01884.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.-23+10716C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41724634 | ||||||
chr6:41724664
|
C | T | 64 | a0001c0001t0001g0187a0001c0001t0001g0194a0001c0001t0001g0196others(61): Show | 69 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.-23+10686G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41724664 | ||||||
chr6:41724749
|
C | T | 9 | a0001c0001t0001g0224a0001c0001t0002g0022a0001c0001t0002g0222others(6): Show | 10 | HG01168.hp2 HG02615.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.-23+10601G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41724749 | ||||||
chr6:41724758
|
C | T | 18 | a0001c0001t0001g0025a0001c0001t0001g0246a0001c0001t0001g0247others(15): Show | 19 | HG01361.hp1 HG01884.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.-23+10592G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41724758 | ||||||
chr6:41724815
|
G | A | 15 | a0001c0001t0001g0342a0001c0001t0002g0289a0001c0001t0003g0005others(12): Show | 18 | HG00597.hp1 HG01346.hp2 HG01981.hp1 others(15): Show |
intron_variant | MODIFIER | c.-23+10535C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41724815 | ||||||
chr6:41724815
|
G | T | 64 | a0001c0001t0001g0187a0001c0001t0001g0194a0001c0001t0001g0196others(61): Show | 69 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.-23+10535C>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41724815 | ||||||
chr6:41724819
|
G | A | 1 | a0001c0012t0001g0121 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-23+10531C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41724819 | ||||||
chr6:41724957
|
G | A | 54 | a0001c0001t0001g0112a0001c0001t0001g0122a0001c0001t0001g0129others(51): Show | 70 | HG00423.hp2 HG00735.hp2 HG01070.hp2 others(67): Show |
intron_variant | MODIFIER | c.-23+10393C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41724957 | ||||||
chr6:41724994
|
C | G | 2 | a0001c0001t0001g0115a0001c0001t0001g0116 | 2 | HG02647.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.-23+10356G>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41724994 | ||||||
chr6:41725063
|
G | A | 1 | a0001c0003t0001g0158 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-23+10287C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41725063 | ||||||
chr6:41725074
|
G | A | 291 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0025others(288): Show | 334 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(331): Show |
intron_variant | MODIFIER | c.-23+10276C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41725074 | ||||||
chr6:41725404
|
G | T | 1 | a0001c0005t0001g0039 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-23+9946C>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41725404 | ||||||
chr6:41725570
|
A | G | 1 | a0001c0001t0002g0303 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-23+9780T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41725570 | ||||||
chr6:41725630
|
G | A | 1 | a0001c0003t0001g0272 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-23+9720C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41725630 | ||||||
chr6:41725739
|
T | G | 21 | a0001c0001t0001g0025a0001c0001t0001g0105a0001c0001t0001g0246others(18): Show | 22 | HG01361.hp1 HG01884.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.-23+9611A>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41725739 | ||||||
chr6:41725775
|
T | A | 1 | a0001c0001t0002g0022 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-23+9575A>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41725775 | ||||||
chr6:41725852
|
C | G | 64 | a0001c0001t0001g0187a0001c0001t0001g0194a0001c0001t0001g0196others(61): Show | 69 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.-23+9498G>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41725852 | ||||||
chr6:41725878
|
C | T | 1 | a0002c0006t0001g0293 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-23+9472G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41725878 | ||||||
chr6:41726357
|
C | T | 3 | a0001c0003t0001g0290a0001c0003t0001g0291a0001c0003t0001g0292 | 3 | HG02572.hp1 HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-23+8993G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41726357 | ||||||
chr6:41726413
|
T | C | 10 | a0001c0001t0001g0009a0001c0001t0001g0252a0001c0001t0001g0253others(7): Show | 12 | HG00642.hp2 HG01081.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.-23+8937A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41726413 | ||||||
chr6:41726472
|
C | T | 10 | a0001c0001t0001g0009a0001c0001t0001g0252a0001c0001t0001g0253others(7): Show | 12 | HG00642.hp2 HG01081.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.-23+8878G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41726472 | ||||||
chr6:41726482
|
C | T | 1 | a0001c0003t0001g0169 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-23+8868G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41726482 | ||||||
chr6:41726483
|
A | G | 82 | a0001c0001t0001g0025a0001c0001t0001g0187a0001c0001t0001g0194others(79): Show | 88 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.-23+8867T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41726483 | ||||||
chr6:41726507
|
G | A | 1 | a0001c0001t0001g0245 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-23+8843C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41726507 | ||||||
chr6:41726604
|
A | C | 18 | a0001c0001t0001g0025a0001c0001t0001g0246a0001c0001t0001g0247others(15): Show | 19 | HG01361.hp1 HG01884.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.-23+8746T>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41726604 | ||||||
chr6:41726629
|
T | C | 18 | a0001c0001t0001g0025a0001c0001t0001g0246a0001c0001t0001g0247others(15): Show | 19 | HG01361.hp1 HG01884.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.-23+8721A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41726629 | ||||||
chr6:41726698
|
C | T | 1 | a0001c0002t0001g0251 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-23+8652G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41726698 | ||||||
chr6:41726885
|
C | T | 82 | a0001c0001t0001g0025a0001c0001t0001g0187a0001c0001t0001g0194others(79): Show | 88 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.-23+8465G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41726885 | ||||||
chr6:41726906
|
C | T | 2 | a0001c0002t0001g0167a0001c0002t0001g0168 | 2 | NA18974.hp2 NA19059.hp2 |
intron_variant | MODIFIER | c.-23+8444G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41726906 | ||||||
chr6:41727034
|
C | T | 53 | a0001c0001t0001g0112a0001c0001t0001g0122a0001c0001t0001g0129others(50): Show | 69 | HG00423.hp2 HG00735.hp2 HG01070.hp2 others(66): Show |
intron_variant | MODIFIER | c.-23+8316G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41727034 | ||||||
chr6:41727035
|
G | A | 23 | a0001c0001t0001g0023a0001c0001t0001g0104a0001c0001t0001g0105others(20): Show | 24 | HG00280.hp2 HG00642.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.-23+8315C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41727035 | ||||||
chr6:41727058
|
G | A | 1 | a0001c0001t0001g0245 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-23+8292C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41727058 | ||||||
chr6:41727198
|
G | T | 1 | a0001c0003t0001g0037 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.-23+8152C>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41727198 | ||||||
chr6:41727332
|
T | C | 1 | a0001c0003t0001g0087 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-23+8018A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41727332 | ||||||
chr6:41727375
|
G | C | 1 | a0001c0005t0001g0345 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-23+7975C>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41727375 | ||||||
chr6:41727464
|
C | G | 40 | a0001c0001t0001g0273a0001c0001t0001g0342a0001c0001t0001g0349others(37): Show | 45 | HG00140.hp2 HG00597.hp1 HG00741.hp2 others(42): Show |
intron_variant | MODIFIER | c.-23+7886G>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41727464 | ||||||
chr6:41727787
|
C | A | 3 | a0001c0004t0002g0117a0001c0004t0002g0218a0001c0004t0002g0219 | 3 | NA18988.hp1 NA18991.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.-23+7563G>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41727787 | ||||||
chr6:41727816
|
C | A | 2 | a0001c0001t0001g0350a0001c0001t0001g0351 | 2 | NA19030.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-23+7534G>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41727816 | ||||||
chr6:41727935
|
G | A | 1 | a0001c0001t0001g0245 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-23+7415C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41727935 | ||||||
chr6:41728296
|
T | G | 1 | a0001c0002t0001g0332 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-23+7054A>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41728296 | ||||||
chr6:41728369
|
C | T | 1 | a0001c0001t0003g0333 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-23+6981G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41728369 | ||||||
chr6:41728561
|
C | T | 79 | a0001c0001t0001g0187a0001c0001t0001g0194a0001c0001t0001g0196others(76): Show | 85 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.-23+6789G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41728561 | ||||||
chr6:41728676
|
T | C | 2 | a0001c0001t0001g0093a0001c0001t0002g0094 | 2 | HG02451.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-23+6674A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41728676 | ||||||
chr6:41728723
|
G | A | 1 | a0001c0001t0012g0353 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-23+6627C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41728723 | ||||||
chr6:41729074
|
C | A | 1 | a0001c0003t0001g0272 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-23+6276G>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41729074 | ||||||
chr6:41729093
|
G | A | 1 | a0001c0001t0001g0351 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-23+6257C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41729093 | ||||||
chr6:41729104
|
G | A | 4 | a0001c0003t0001g0008a0001c0003t0001g0015a0001c0003t0001g0088others(1): Show | 7 | HG00738.hp1 HG03654.hp2 HG03704.hp2 others(4): Show |
intron_variant | MODIFIER | c.-23+6246C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41729104 | ||||||
chr6:41729151
|
C | T | 18 | a0001c0001t0001g0273a0001c0001t0001g0342a0001c0001t0003g0005others(15): Show | 21 | HG00597.hp1 HG00741.hp2 HG01346.hp2 others(18): Show |
intron_variant | MODIFIER | c.-23+6199G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41729151 | ||||||
chr6:41729581
|
C | T | 1 | a0001c0003t0001g0036 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-23+5769G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41729581 | ||||||
chr6:41729775
|
A | G | 9 | a0001c0001t0001g0224a0001c0001t0002g0022a0001c0001t0002g0222others(6): Show | 10 | HG01168.hp2 HG02615.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.-23+5575T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41729775 | ||||||
chr6:41729821
|
G | C | 1 | a0001c0003t0001g0035 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-23+5529C>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41729821 | ||||||
chr6:41729910
|
G | A | 1 | a0001c0002t0001g0162 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-23+5440C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41729910 | ||||||
chr6:41729915
|
C | T | 1 | a0001c0005t0001g0097 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-23+5435G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41729915 | ||||||
chr6:41730017
|
G | A | 1 | a0001c0003t0001g0272 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-23+5333C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41730017 | ||||||
chr6:41730122
|
G | GA | 60 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0273others(57): Show | 68 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.-23+5227dupT | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41730122 | ||||||
chr6:41730122
|
GA | G | 112 | a0001c0001t0001g0048a0001c0001t0001g0093a0001c0001t0001g0115others(109): Show | 129 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.-23+5227delT | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41730122 | ||||||
chr6:41730174
|
A | C | 1 | a0001c0001t0012g0353 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-23+5176T>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41730174 | ||||||
chr6:41730254
|
C | G | 1 | a0001c0002t0001g0018 | 2 | NA18991.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.-23+5096G>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41730254 | ||||||
chr6:41730393
|
C | A | 2 | a0001c0001t0002g0016a0001c0001t0002g0091 | 3 | HG01243.hp1 HG02717.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.-23+4957G>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41730393 | ||||||
chr6:41730396
|
A | G | 66 | a0001c0001t0001g0187a0001c0001t0001g0194a0001c0001t0001g0196others(63): Show | 71 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.-23+4954T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41730396 | ||||||
chr6:41730439
|
G | A | 1 | a0001c0001t0001g0245 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-23+4911C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41730439 | ||||||
chr6:41730715
|
A | G | 1 | a0001c0001t0012g0353 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-23+4635T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41730715 | ||||||
chr6:41730764
|
G | C | 14 | a0001c0001t0001g0025a0001c0001t0001g0245a0001c0001t0001g0260others(11): Show | 15 | HG01361.hp1 HG01891.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.-23+4586C>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41730764 | ||||||
chr6:41730804
|
G | A | 1 | a0001c0002t0001g0163 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-23+4546C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41730804 | ||||||
chr6:41730895
|
C | A | 2 | a0001c0001t0001g0105a0001c0005t0001g0106 | 2 | HG02738.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.-23+4455G>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41730895 | ||||||
chr6:41731049
|
A | G | 3 | a0001c0001t0003g0164a0001c0001t0003g0165a0001c0001t0003g0250 | 3 | HG00741.hp2 HG02486.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-23+4301T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41731049 | ||||||
chr6:41731241
|
A | G | 1 | a0001c0012t0001g0121 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-23+4109T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41731241 | ||||||
chr6:41731312
|
G | A | 4 | a0001c0001t0001g0246a0001c0001t0001g0247a0001c0001t0001g0248others(1): Show | 4 | HG01884.hp1 HG02886.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-23+4038C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41731312 | ||||||
chr6:41731357
|
T | C | 1 | a0001c0002t0001g0346 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-23+3993A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41731357 | ||||||
chr6:41731498
|
T | A | 4 | a0001c0001t0001g0236a0001c0004t0002g0024a0001c0004t0002g0237others(1): Show | 5 | HG00735.hp1 HG00738.hp2 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.-23+3852A>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41731498 | ||||||
chr6:41731514
|
C | G | 1 | a0001c0004t0011g0352 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-23+3836G>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41731514 | ||||||
chr6:41731515
|
C | T | 1 | a0001c0003t0001g0035 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-23+3835G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41731515 | ||||||
chr6:41731555
|
G | A | 5 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0002g0107others(2): Show | 5 | HG01891.hp1 HG02280.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.-23+3795C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41731555 | ||||||
chr6:41731644
|
C | A | 3 | a0001c0001t0001g0349a0001c0001t0001g0350a0001c0001t0001g0351 | 3 | HG06807.hp1 NA19030.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-23+3706G>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41731644 | ||||||
chr6:41731774
|
C | T | 1 | a0001c0002t0001g0020 | 2 | NA18999.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.-23+3576G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41731774 | ||||||
chr6:41731813
|
C | G | 3 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0003t0001g0272 | 3 | HG02630.hp2 HG02723.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-23+3537G>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41731813 | ||||||
chr6:41731821
|
C | T | 12 | a0001c0001t0001g0025a0001c0001t0001g0260a0001c0001t0001g0262others(9): Show | 13 | HG01361.hp1 HG02280.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.-23+3529G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41731821 | ||||||
chr6:41731842
|
C | G | 2 | a0001c0002t0001g0017a0001c0002t0001g0120 | 3 | HG01255.hp2 HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-23+3508G>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41731842 | ||||||
chr6:41731983
|
C | T | 8 | a0001c0001t0001g0025a0001c0001t0001g0260a0001c0001t0001g0262others(5): Show | 9 | HG02559.hp2 HG02572.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.-23+3367G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41731983 | ||||||
chr6:41732083
|
G | A | 1 | a0001c0003t0001g0092 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-23+3267C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41732083 | ||||||
chr6:41732105
|
C | T | 2 | a0001c0001t0002g0301a0001c0001t0002g0302 | 2 | NA18945.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.-23+3245G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41732105 | ||||||
chr6:41732123
|
T | C | 299 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0025others(296): Show | 334 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(331): Show |
intron_variant | MODIFIER | c.-23+3227A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41732123 | ||||||
chr6:41732247
|
G | A | 1 | a0001c0001t0001g0245 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-23+3103C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41732247 | ||||||
chr6:41732406
|
C | T | 1 | a0001c0004t0002g0034 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-23+2944G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41732406 | ||||||
chr6:41732451
|
T | A | 1 | a0001c0001t0012g0353 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-23+2899A>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41732451 | ||||||
chr6:41732698
|
T | G | 4 | a0001c0005t0001g0239a0001c0005t0001g0240a0001c0005t0001g0241others(1): Show | 4 | HG02257.hp2 HG02451.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-23+2652A>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41732698 | ||||||
chr6:41732856
|
C | A | 5 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0002g0107others(2): Show | 5 | HG01891.hp1 HG02280.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.-23+2494G>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41732856 | ||||||
chr6:41733118
|
G | A | 1 | a0001c0004t0002g0243 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.-23+2232C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41733118 | ||||||
chr6:41733120
|
T | C | 10 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0002g0099others(7): Show | 10 | HG00280.hp2 HG00642.hp1 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.-23+2230A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41733120 | ||||||
chr6:41733291
|
A | G | 1 | a0001c0001t0003g0119 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-23+2059T>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41733291 | ||||||
chr6:41733292
|
T | C | 1 | a0001c0002t0001g0244 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-23+2058A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41733292 | ||||||
chr6:41733312
|
T | G | 1 | a0001c0001t0001g0245 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-23+2038A>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41733312 | ||||||
chr6:41733469
|
T | C | 2 | a0001c0001t0001g0093a0001c0001t0002g0094 | 2 | HG02451.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-23+1881A>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41733469 | ||||||
chr6:41733574
|
C | A | 4 | a0001c0001t0001g0246a0001c0001t0001g0247a0001c0001t0001g0248others(1): Show | 4 | HG01884.hp1 HG02886.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-23+1776G>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41733574 | ||||||
chr6:41733586
|
G | A | 1 | a0001c0001t0003g0250 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-23+1764C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41733586 | ||||||
chr6:41733699
|
AC | A | 10 | a0001c0001t0001g0009a0001c0001t0001g0252a0001c0001t0001g0253others(7): Show | 12 | HG00642.hp2 HG01081.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.-23+1650delG | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41733699 | ||||||
chr6:41733903
|
G | A | 12 | a0001c0001t0001g0025a0001c0001t0001g0260a0001c0001t0001g0262others(9): Show | 13 | HG01361.hp1 HG02280.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.-23+1447C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41733903 | ||||||
chr6:41733991
|
C | G | 1 | a0001c0005t0001g0118 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-23+1359G>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41733991 | ||||||
chr6:41734314
|
C | G | 1 | a0001c0004t0002g0117 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-23+1036G>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41734314 | ||||||
chr6:41734318
|
G | C | 1 | a0001c0002t0001g0271 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-23+1032C>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41734318 | ||||||
chr6:41734489
|
G | C | 10 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0002g0099others(7): Show | 10 | HG00280.hp2 HG00642.hp1 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.-23+861C>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41734489 | ||||||
chr6:41734494
|
G | A | 1 | a0001c0003t0001g0095 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-23+856C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41734494 | ||||||
chr6:41734619
|
A | T | 30 | a0001c0001t0002g0283a0001c0001t0002g0288a0001c0001t0002g0289others(27): Show | 35 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(32): Show |
intron_variant | MODIFIER | c.-23+731T>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41734619 | ||||||
chr6:41734824
|
G | C | 1 | a0001c0005t0001g0096 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-23+526C>G | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41734824 | ||||||
chr6:41734844
|
C | T | 165 | a0001c0001t0001g0048a0001c0001t0001g0093a0001c0001t0001g0113others(162): Show | 190 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.-23+506G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41734844 | ||||||
chr6:41734881
|
C | A | 10 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0002g0099others(7): Show | 10 | HG00280.hp2 HG00642.hp1 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.-23+469G>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41734881 | ||||||
chr6:41734925
|
G | A | 1 | a0001c0003t0001g0272 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-23+425C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41734925 | ||||||
chr6:41734951
|
G | T | 2 | a0001c0001t0001g0273a0001c0005t0001g0274 | 2 | HG02630.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-23+399C>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41734951 | ||||||
chr6:41734960
|
C | T | 1 | a0001c0001t0001g0112 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-23+390G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41734960 | ||||||
chr6:41734970
|
G | A | 4 | a0001c0001t0001g0349a0001c0001t0001g0350a0001c0001t0001g0351others(1): Show | 4 | HG02809.hp1 HG06807.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.-23+380C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41734970 | ||||||
chr6:41734989
|
C | G | 5 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0002g0107others(2): Show | 5 | HG01891.hp1 HG02280.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.-23+361G>C | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41734989 | ||||||
chr6:41735031
|
C | T | 1 | a0001c0003t0001g0033 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-23+319G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41735031 | ||||||
chr6:41735142
|
C | T | 10 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0002g0099others(7): Show | 10 | HG00280.hp2 HG00642.hp1 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.-23+208G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41735142 | ||||||
chr6:41735241
|
C | T | 73 | a0001c0001t0001g0048a0001c0001t0001g0093a0001c0001t0002g0011others(70): Show | 85 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.-23+109G>A | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41735241 | ||||||
chr6:41735293
|
G | A | 1 | a0001c0001t0012g0353 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-23+57C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41735293 | ||||||
chr6:41735303
|
G | A | 89 | a0001c0001t0001g0273a0001c0001t0001g0315a0001c0001t0001g0342others(86): Show | 102 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.-23+47C>T | TFEB | ENSG00000112561.19 | transcript | ENST00000373033.6 | protein_coding | 1/8 | chr6 | 41735303 |