| Tag | Content |
|---|
EnhancerAtlas ID | HS040-02048 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr1:95045100-95046150 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL2 | MA0478.1 | chr1:95045547-95045558 | CTGAGTCATCC | - | 6.32 | | JUNB | MA0490.1 | chr1:95045547-95045558 | CTGAGTCATCC | - | 6.14 | | NFE2L1 | MA0089.2 | chr1:95045543-95045558 | ATGGCTGAGTCATCC | - | 6.36 |
|
| | 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 |
| GH01I094579 | chr1 | 95044561 | 95046719 |
|
Enhancer Sequence | AGCCTGAATG TGCCTGTAGG AAGTGGCTAG AGATCCCGGT CTTTCAGTCA GGAGGAATGG 60
GATCAGAGAT CTGCTTAAAG AAGCAGTTTG GCTGCTTTTT TGTAGAGCAG CTGTGCTGTG 120
TTGGGGATCC CTTCAGCCCC CAGTTGGTTT AGGTTCTGCA ATATCCTCAG GCTGGACCAG 180
CTGAGATGCC CAAACAGCCA AGGTGTTGGC CTGCCCCACC ACCCCAGGCT CCCCATCCCA 240
GGGAGAAATT AGAACTCTGT CGGCCATAGA ACATGGGCAG GGAAGGCCAA GTCCTCTGCT 300
GGGGGGACCA ACACCTTAGG AGAAGTGGAT CAGGGTTCTG CTTGAAGAAG CAGTCTGACC 360
ATGCCTCAAC AAAACAGCCA TGTTGTGCTG GGAAGCTGCC TCTGCTTCTG TAGACTTGGA 420
CTCTCCAAAG CCTGCAGGCT AGAATGGCTG AGTCATCCAA ACAACCAAGG TAGTGGCCCA 480
CCCTTCCTCC TCAGGCATTC CATCCCGGGA GAGATCAGAT TCCTGCTTAA AGAAGCATTC 540
TGGCCAGGCT CTGGCAAAGC AGCTGTGCTG TGCTAGGGAG ACACCTCCTC ATCTGGACTG 600
TCTGACTCTC CAAAGCCCAC AGTCTGGAAT GGCCAAGTAG ATCAAACAGC AGAGATGGCA 660
CCCGCCCCTC CCCCTAGGGG TTCAGTCTTG TATCAGGCAG GCTCCACCCT GTTGCTGGTG 720
GCTTGCTGGA ATTCCAAGCC AGTGGGTTTT ATCTTGTGAG GTGCCGTGAA AGTGGGGCCC 780
ACAGACTGAT GCTGCTCAGC CTCCTGGATT CAGCCCACTT CTTTGGGGTA TGCACGGACC 840
TCCTGATTTG CCTCGTTGCA TACACCTTTA TTAGAGATCC TGAGGCCAGA GTATGTAAAG 900
CTCCTGGGTC TCTGTGTGTG CCTGAGCAGG CACTCTGCCA AGACTCCATA CAGCTCCGTG 960
TGTTGAACCT AAGGCCCTGA TGGTGTGGGC TCACAAAGGG ATTCCCTGAT CTGCGGGTTG 1020
CAAAGATCTG TGGGAAAAGC ATGGTTTCCC 1050
|
