| Tag | Content |
|---|
EnhancerAtlas ID | HS040-13426 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr16:50335130-50336400 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF5 | MA0599.1 | chr16:50336003-50336013 | GCCCCGCCCC | + | 6.02 | | SP1 | MA0079.4 | chr16:50336000-50336015 | CTGGCCCCGCCCCTC | + | 6.11 | | SP4 | MA0685.1 | chr16:50336000-50336017 | CTGGCCCCGCCCCTCCA | + | 6.11 | | ZNF263 | MA0528.1 | chr16:50335216-50335237 | TGTGGAGGGAGAGGTGGGGAA | + | 6.15 |
|
| | 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 |
| GH16I050300 | chr16 | 50334891 | 50336294 |
|
Enhancer Sequence | AGGGCTCAGA GGCCGCAGCT GGGGGGGACC CGGAGGGACT GGAGGGGCCC TGGAGAGCCT 60
GGCCCGCACC TTGGAGGAAA CCCCCATGTG GAGGGAGAGG TGGGGAAGGG CCCTGCCTGG 120
GCAGGAGTGA GCTCCCTGTT CCCAGGCACA TTCTAGGCAC CGAGTAGCCA CTCCCTGGGC 180
CTCCATTCTT TTCTATGTGA TGGGAAAACA GCGCCTGCCT CACCAGAAGG AGCTAATCCG 240
AGCGAGGCCT TCACAGTGCG CCTGGCACGT CACAGCATTC TATGTATTCT CGTCACTCTT 300
GGTTTATTTT CCATGAGGTG GTTATTAATC TCCCAGATTT CCGAGAGACA CACTTTCAAA 360
ACAAGCTTTG GATGAAACTC AGGAAAGCAG GGAGTGGCCT GGGAGCCACT GGGCAGGAGC 420
CTCTGAGTGT CCTGGGTGCT GACTGCAGGT CCCCTGGTGG CTCCAGGACC CCACGGTGGA 480
GGAGGCAGTT CCACTGCCCT GGCCAGGTGG GGCCCGCCTT GGCCTGTCTG CTGCCCGACC 540
CTGGCCTGCT TCAGGGAGTC CGGCACGTCT GGCCACTTCT CTGTGAATCA TCCATGAGGC 600
TTGCTCAAGA ATGTCGGCCC AGCCAGCGAG TGGCTCCTTT CACTCTGGTC CTCGCTATGC 660
CTTGGGGCTG GCCCGACTGC CAGACCCTGG GGGACCAAGG GCTGGCCTGT GAGCCTCCCT 720
ACACATCTGC TGGCCTCACT CTGCCCCCAG CACCCCCAGT GCTGCACCAT CCATACTGAG 780
CCAGCATCTG GGAAAACCCC TGCCGGTACC TGTGTCCCAT TCCACCACCC TCCTAGAATA 840
GGGCCCTGAT CCTCGCCCTG TACCCCGGCC CTGGCCCCGC CCCTCCAAGC CCCTTCCCCT 900
GCTCTCCTGT CCCCCTCACC CCACCTGGTC TCCTCCTGCC CTTCCACTAC CAGGGTGGTG 960
GCACCCGCAG GTCCCTGCAC TCAAAACACT CCTCCCTCCG TCCCTAATGC CCTTGCTTGT 1020
TTATCCATTT TCCTTGTCTG TTGTCAGCAT GAGTGCCATG CCGGGGGGCT CCTCCTCTCC 1080
AGGCTGCAGC CCCCCACCCC GTGCTGAGAT GGATGCCCGG CTCGAAGCTA GTGCTCAGAT 1140
AGCCCTTGAA TGAGTGAAGC AGAGCTCCTC ACCCAGGAGG CTCCAAAATC CACCCCCGCA 1200
GGCTGCCAGG TTGAGCAGGG AAAACTGCAG GCTGCCTGGG CCGACTTGAA TTTCAGATAA 1260
CTGTAAATCA 1270
|
