| Tag | Content |
|---|
EnhancerAtlas ID | HS040-03540 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr1:231913570-231914970 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HOXA13 | MA0650.2 | chr1:231914510-231914521 | CCCAATAAAAC | + | 6.62 | | KLF5 | MA0599.1 | chr1:231914002-231914012 | GCCCCGCCCC | + | 6.02 | | MEF2A | MA0052.3 | chr1:231913891-231913903 | TCTAAAAATAGA | + | 7.22 | | MEF2C | MA0497.1 | chr1:231913889-231913904 | TATCTAAAAATAGAC | + | 6.68 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I231775 | chr1 | 231911245 | 231915153 |
|
Enhancer Sequence | GGTTTGTTGG GCAATATATT GTTTTTATGC CCATTTTGCA GATGAGGCTG CTGAGGGTCC 60
AAGTTCACAC AGCCGTAAAA GCAGTGCCCT CACGTCTTTG GCGAATTTTT AATGCAGAGG 120
GAATCCAGAG ATGGTTCACA CTGATGGCCT GGGAGAGACC AGGCCTTGGA CAGAGTGCTT 180
AGTCCAGCAA TGGAAAGAAG TCCAGCCCAG CAGAGCCGTG GGTCTGTGGG CCCAAGGAAA 240
AGAGAATGGA TGTCCCTCCA GGCCAGGGAT GGTTGTCTCT GTGTGCCTAG TGTTGCCTGA 300
TTGGATTGGA GCCAAGGTGT ATCTAAAAAT AGACAGCCTG GGAAGACCAA ACAGGCAACT 360
GTCTCAAGTC AGAGAGGTCT GTCAGACGTT CCAAAGAAAG AAATGTGAGA GGAAGAGAAA 420
CTGGAAAGCA AGGCCCCGCC CCAGGGCTAG AGGAACTGGT ATTACTTGTC TGTGAAAAGA 480
GGGTTTGAAC TGGGTGGCGT GGAAGGTCTT TTCTGGTTCT ACAATACTTT GCACTTTAGT 540
ATTTTATGAA ATAAGTTAAA ATAAGCTGCC TAAAAACCCC TCATAATTCT ATTCCTAGGA 600
GCTCTATGTT AAGTTCCTCC TTAAAGTTCC CTGGGCAGGC TGTGACCATC CACAGGCCAC 660
GGTGCTCCAG CTGGCACTTT CCTTAGGGCT GGTCCCTAGA GCATGGACCT GAGCAAAGCC 720
TGCTTTCCAA GCACTGCTGC TGCAGCTCAG AGCTTAGACC TCGCCTCACC ATTGTATATC 780
CTCCCGTTTT CTTCTGGAAA GTCGTCATTA CAGGCAACGT GGAAAAGTTT ACCAGACTAT 840
AATCTGGTAA AGGAGGAAGA GGATTGGAAA AGAAGGAAGA GATTTGAAAA TCCCCCTTAT 900
CTGGCTGGGT ACAGATGCTG CTCACCAGGA AATGTAGGTT CCCAATAAAA CAGGACCCCC 960
ATTTCCAGTT TTCATTGCGT TGTAAATTAA AAATAAAATC TTAAGCCCCC AACCACTGAA 1020
CGGATTCCCT CTTGGCCAAG GAGACCCCAG AGACTCCATA CAAACTGAGT TCCCAGCCCC 1080
AGTGGGCCGG GAGGTCGGAT TTGCCTTGTT ATAATCCCTC CCTTTTGTAG CTTAGACATA 1140
ACAACAGAGC AGCATCAATG CTAAAACGAG ATCATAAGAA CTGATGGAAC AGACTCTCGG 1200
TGGCAATAAG ATACCAAATT ATAAACAAGA CCTAAGGCCA TGCCAGGCAG GGATAAGTCT 1260
CACACCCCTG CACCTAAAGA GTAAACTACC TTCTGACTGC CACCTGGGTT TTCTTTTTCT 1320
CTAGCGGCTA AACGAGCACT GTCCTAGAGA TGAGCTATCT TAAAACCATG GCAGTCCTTG 1380
CACCGCCAGA TGCTGACTGA 1400
|
