| Tag | Content |
|---|
EnhancerAtlas ID | HS040-32860 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr8:21994380-21995520 |
Target genes | | Number: 21 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr8:21995047-21995066 | TGCTGCCCTCTCGTGGCCA | - | 7.31 |
|
| | 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 |
| GH08I022136 | chr8 | 21994481 | 21995511 |
|
Enhancer Sequence | AGCCACACTC TGGGCGCCAG CCGTTACTAC TGCCTGCATC CCTGCAGTGT CTGGCAACAT 60
GTCTGGTACC TGCTCGAGGC TCAATAAAGA TTCATTTTTG AATGAATTAA TGAAGCGATA 120
AGACAACCCC ACGATGCAAA GGCAGGCCAT GTTGGACGCC AGTGAGCCCC TATACGTGAG 180
AAGCTAAATC ACCGCAGCAG ATTAAGAGCC TCCCCCAAAT AAAACCTGGA TAATCCCCAC 240
ACCAAGAGTT AATCCACACT CTCTGGGGCC ACTCCAGGTT ACCACCCCAT TTCCCCTCTT 300
CTCATCCCAC ACTCTCACCC ACCTCTTTGC TTAATCAATC AAAAGCAGGG AGGAGGAGCA 360
GGTGCAGCAG TGGCAGAGGG GCGCACCCCG GGCATCATGG TGAGACCAGC ACCGGGGCAG 420
TAGAGGGCAG AGCTGGGTAC CCCGGTTGCC CCAGGGATCG GAGGAGTTGG AGTGGAGCCA 480
GCCAGGCAAA CAGCCTTGGT CTCAGGAGAG CAGAGACTCC TTGGATGGGG CAGGCCAAGG 540
ACCAGTGACC ACAAGCAGCA GGGAGGGCCA CTGAGTTCCG CCAGGCCCAG CAGGGCGAGG 600
CTCTGGCCAG TCTCCCAACC CCACCCTCCT TGACCTGGAA GCCGGGGGCA GCCCAGATCC 660
CAGACACTGC TGCCCTCTCG TGGCCACTCC TCAGAGGTGC AATGGTGCCC CTGCGGGTAC 720
CTGACTGTTT ACAGAACTTA ATGTCCCCAG AGCTGCCCCA GGGGGCTCCT TCTTCCAGGC 780
TCCTGGAGGA GATACTCCTC CCCAGGTCTC CTCTGCCTAG CTTCGACCTC CCTATGGGAC 840
TAACGTGCTG CCCCAAGCCC CTCCTGCCTG TGCTCCCACT GGTTTCTCTA TAGCTGCACC 900
TTCCTGCCAA GGCCTAACTG AAGTTTCGGG TTCTGACCAG TCCTCTGGAC TCGTCCCCAC 960
TTTCCCATCA GTGCTCTCAA AACTCCCCAA AAGCTCCTTC GTGAAACCAT GTGCTGCATC 1020
ACAACTCTCT GTCAATGGTT CTGTCTCCCC CAGAGGACTG GGCTCCTTCA GCCTTAGACC 1080
TAGGCTAGGA CTGGGCTGTC CCATTTCAAG GGTGTGAGGC GAGCAACGGG AGTAAGAATC 1140
|
