| Tag | Content |
|---|
EnhancerAtlas ID | HS040-16881 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr18:21274550-21275650 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL2 | MA0478.1 | chr18:21275488-21275499 | ATGAGTCATCC | - | 6.62 | | JUN(var.2) | MA0489.1 | chr18:21275488-21275502 | ATGAGTCATCCTTA | - | 6.02 | | JUNB | MA0490.1 | chr18:21275488-21275499 | ATGAGTCATCC | - | 6.62 |
|
| | 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 |
| GH18I023694 | chr18 | 21274532 | 21276283 |
|
Enhancer Sequence | GATGTGTCCA AGATCACACA CTTAGTATGT GGTAAATCCA GATTTAAACC CAGGTACTCT 60
GGCTGCAGAA TTCACGCTCT TACCCGCTAT ACTACTGTCA CAGACATGCT AACTACTCCT 120
TCCTCTGAGT TCCAGCTAAA CTTTGCGTTG CCTTGCTAAT GCCACTTATC ACCTTGGAGC 180
CATCCATTAT CATGTCTGTC TCCTTATTAG GATCATGAGC TTCCTGAGGG TGGGGCCCTG 240
TCTTCCTGTT CATGTCTGGA CAGAGTATTG AGATGCCCCA TAGAGTAGAA TTCCTGTGCA 300
AAGTATGCTG CACTGTTTCC TTGTGGAAGC TTGTCTTAGA CACCCCATCA ATGCTTTTTG 360
AAGAAATATT CAAAAGGCAA CACCACCATA GAATTTACTT ATCAGAGCAA CACCCTGATG 420
GAATTGCTGT TTGATTTTAA AAGTACCTGA ATTTCAACAA TCTGTCTTCT GGAAGACAGG 480
TGTGGCCCTG CTGTGTCTGA TGCAGTGGCT GAACCCAATG CCCAGGACTG GACTCCCAGA 540
AGCTGGAAGA GGCAAGGAAG GATCCTTCCT CTACATATTT CAGAGGGAGG GCAGTCTTGC 600
TGACACCTTG ATTTTGGTCT TGTAGCCTCC AGCATGGTGA GAGAGAAATT TCAGTTGTTC 660
TAAGCCACCC ATTTTGTGCT ACTTTGTATG GCAGCCTTAG AAACTTAATG CAGTAACTTT 720
AGCTTCAACT CAGTTAACCA GCAGTTGTAT TGACCATTCA GTGTATGCGT GTTATCCCTG 780
TTTGGGAGAG CAGCAGAGAG GGGACCCTGC ATGAGGCTCT GTGTGTAGTT CTAGGGTCCT 840
GGTTTGTGAG ACTTTGCAAC CTGATAACTC AAAATGTGGC CCCTAAAAAG AATGAGAAGA 900
GCTCTAGGCT GAACAAATAT TTAGAGATCA CGCACATTAT GAGTCATCCT TAAGGCCAGG 960
AATGGTGGCT CATACTTATA ATCCTAGCAC TTTGGGAGGC TGAGGCGGGT GAATCACTTG 1020
AGGTCAGGAG TTTAAAACCA GCCTGGCCAA ATAAAAAATA AATTAGCTGG GCATGGTGGC 1080
GTGTGCCTGT AATCCCATCT 1100
|
