| Tag | Content |
|---|
EnhancerAtlas ID | HS040-07342 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr11:111998920-112000090 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Tcf12 | MA0521.1 | chr11:111999705-111999716 | CAGCAGCTGTT | - | 6.32 |
|
| | 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 |
| GH11I112128 | chr11 | 111998729 | 112000881 |
|
Enhancer Sequence | GGGTTTGGTG GCATGTGCCT GTAGTCCCAG CTACCCCAGA GGCTGAGGCA GGAGAATCGC 60
TTGAACCCCA GAGGTGGAGG TTGCAGTGAG CCCAGACTGT ACCACTGCAC TCTAACCTGG 120
GCCACACCAC GAGACACTCG GTCTAAAAAA AAAAAAAGAA AAAAAAATTA GTTTGTCTTC 180
TTCTACCTAA GGGTGAAAAT AACATGTGAG CTTCAAGATT CAATGCATGG CTTCCAACCC 240
TGATGGGCTA GCTGGAGAGT GGTGGAGTGA GAAGACAAGG TGGCAGACCC AAGGTGGATT 300
GTCAGATGGC AGAGATGGGA AGACACCAGG AAACCAGGCT CATATTTTCA TGGAACCACT 360
GGCTGCTGAA GCCTGTGACT TTGGCAGGCA GCCCAGGGTG AATCACTACT TAGATGAATG 420
AGGAGATTCT GCTTTGTCCC TGACACTTCA AATTGTTATT CCTTCCTTAA GCAATTTATG 480
GGCACTCCCA TAGACTCTCT AGCCTTTGGA GCCTTTGCAT TAGGAGCTTG ATTTATGGAT 540
ATCTGTATAG TTACAGGAAA TAATGTCGTA TAAAAGGCAT TTAATATGGA GGGGCTTTAT 600
GACCCCTTGC TTGGGTGTAA CCATCCCTGT CAGGGTGCCA GGAGAGAAGG GTGGAGCCTT 660
TTTGGATGCT GGGAAGTGAG GGTGTGAGGT GTTATCCAGG TGGGAAAGGC ATGCTGAGAG 720
GGAGGGCCCC TGTGTGGTTC TGAACACTGT GCTCCATCCA CACAGCCCTC CTCGGGGGCT 780
GGGTGCAGCA GCTGTTGGAG TTCTTTCTTC ACAGTAAATA TTTAACCACG TAAGATGCCC 840
AGGCTACCAG CCACTGCTAA GTGACAGGCA AAATCCTAAG CCACAGATGT TGCCCTCTGG 900
CTCTCAGCTC AGAGAGCTGA GGCTGTTGAC TGGAGTCCTC AGAACTTCAG AGAGCTTGGA 960
AGTTTGTGCA TTTCATCAAC TGACTTGCTT TGTCTGCCAG AAAGCATTAA GCCTCAGAAT 1020
TTATACCTTC CCTTCTTCAT TCATTTGTGT ATATTCATAC ATTGAGCACC TGCTCTGGTC 1080
CGGGTTCTGC GCTTAGGTGA TTGGGATACA TCAGTGAATA AAACAGACAA AGGTCTCTGC 1140
CTCTGGGACC CAACGTTCTA CCAAGGAAGA 1170
|
