| Tag | Content |
|---|
EnhancerAtlas ID | HS040-02774 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr1:178971610-178972400 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXH1 | MA0479.1 | chr1:178971625-178971636 | TGTGGATTGGG | - | 6.14 | | PAX6 | MA0069.1 | chr1:178971973-178971987 | AACTCAAGCATGAA | - | 6.55 |
|
| | 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 |
| GH01I179002 | chr1 | 178971429 | 178973891 |
|
Enhancer Sequence | GCAGGAATAG TCTGCTGTGG ATTGGGACCC CTGAATGTTC CAGAGGGATT TAAGTGTGCG 60
GAATTCAGAC GTCTTCCCTG TTGTGGCTGG CCTTCCCGCC TCCCCAGCCG TCTGCCCGAA 120
TGAGTGCTTA CTAATGAGCC AGAGAGCTCT GAGCCGGCCT GTGTAGGGCA TCCATGCAGG 180
GCTCCAGGGG CCCCTCTCAG TGAAACAACA TGACTGTGAA AACAATCTGC TGCTCTTCTT 240
CTTCACCCTG ACCTTGGGTC ATTCTGGCGT AAAAGATTAC TTTGCTCCCA GCCTCGGGGA 300
AGTTTTTGTA CAATTAGCTA CAACTCGGCA GAAAGACCCT GCAGAGAGAG CCCTGGGGTC 360
ACCAACTCAA GCATGAAAGG ACACTGACCC CGTGTGGTCA TGTTTGGAGG TGCAGCACGG 420
GGAGAGAGGA AAGGCCCCGG CACGGTCCTT TGGCCAAACG ACCCCTGCAG GCCCTCCCTG 480
ACCGACCTTG CTCTGTCCCT GCTCACTTCA CAAGACCCTG GGGAGAGGAC CTGGCCCTAT 540
CAGGGCCTGC TGACTCGTTC TCCCCTGGCG AAATGTCCCC ACCAGGTGCT CTCAACTCTG 600
GGGTATGACT TCACAGGCCA TTTGAGTTCA GATGGGTAAG GCGTGTAGGA AATGAGCTCA 660
AAGGGTAGGA TGGATTTTGA TGGGGTAAGA AGAGAGTGTT TCTCACTCAC CCAAAGCACT 720
GAGCACAGTG TCCCAAACAT AATGTGGAGT AAACACGCGC ATGCACACGT GCACTTCAGG 780
TGCAGGAGAC 790
|
