| Tag | Content |
|---|
EnhancerAtlas ID | HS012-15062 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr18:11947060-11948100 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFE2L1 | MA0089.2 | chr18:11947434-11947449 | TCATGACTCAGCAAA | + | 7.25 | | Nfe2l2 | MA0150.2 | chr18:11947432-11947447 | ACTCATGACTCAGCA | + | 6.24 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr18 | 11947272 | 11947721 | | chr18 | 11947516 | 11947742 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH18I011945 | chr18 | 11945770 | 11949587 |
|
Enhancer Sequence | AAAATTATAC ATTTTTTTTA CATAAGAAAA CTTGAGAGAG ATCATACTTT TGGGTTTCTT 60
TATTAAAAGA AAGAAGACCA AAAGGTGACC CAAGTAAAAG TGTACACCCC TTAAGGGAAA 120
AAAAAATTAT TTTCATTTAA AATCGTTTTC TTTATCTTTA AAGTGAAAGT GCCATATCTG 180
GCTTCCTAAG GAGGAACCAC AAACCGCGTA GACTCAGGCC AGCCGCTGGG CCTGGGCCTG 240
TGTGTCCCTC AGGCGGCGAC CTTTGGCCCA CTTCAGGCCG GCCGTATTTA CCAGCTTAGA 300
GGCGCCGCGG CGTTGGCGAG TCCTTTTTCA CCCACCCCTT CCCTCCGTTC TCAGGCTTGA 360
ACTTGAACAG GCACTCATGA CTCAGCAAAC GGTACTTGAT AGGGTTCTTT ACACGTCAGT 420
CAGGCTATTT TTTAAAATCA CTCTTCCTGG AGATCTTCAA ACCAGAAGCA CCGCGGGCCC 480
TCCCCAACGG GCTTCTGCTT ACCTCCACTA CGTGATGCAG TATGGCCCCC GGGAGGCCGC 540
CCCCAGATTC TAGAGGGGCT TACCCCAGAC ACACCCGAAG GACCACCTCG TGACCTCAGA 600
GGAACAGCCC TAGACCCAGG AGAGACTGCC AGACACCCCC GTGGCAGCCC GCCAGGGCCC 660
AGCTCTACTT GTCGCCTGGA GGTGCTGCCT CCCTTCCACG CCGCCCCAGG GAATGGCCGC 720
CCCTCTGGGG CTCCTCCCAA TCCCCCTTCC CAGGACTGAC AATGGCCCGG CGCCCTGCTT 780
TGGGCCAGGA TCGGCCTCGA GCCTTCCTCA CTAGCGGCCA AGAGCCGGAA ACCTTGCGTC 840
TCAGATTCCC CGGGTCTGTG CACCCCCACC CCAACCGGTC TTCCCACCCA GGCCCCCCCT 900
GATGCCAGCT GCGGGCCTGG ACCTAGCCCG GGGCCCTGCC CCTCCGCCCC TCTCGCTGGA 960
CAGCCCAGGC CGGCGCCCGA GGGATAGGCT CGGGAGCGCG GGGAAGACGC TGCAGCCGGA 1020
GCTGGAGCCA GGGCCCACCT 1040
|
