| Tag | Content |
|---|
EnhancerAtlas ID | HS116-15864 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr18:11947340-11948300 |
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: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH18I011945 | chr18 | 11945770 | 11949587 |
|
Enhancer Sequence | GCCGTATTTA CCAGCTTAGA GGCGCCGCGG CGTTGGCGAG TCCTTTTTCA CCCACCCCTT 60
CCCTCCGTTC TCAGGCTTGA ACTTGAACAG GCACTCATGA CTCAGCAAAC GGTACTTGAT 120
AGGGTTCTTT ACACGTCAGT CAGGCTATTT TTTAAAATCA CTCTTCCTGG AGATCTTCAA 180
ACCAGAAGCA CCGCGGGCCC TCCCCAACGG GCTTCTGCTT ACCTCCACTA CGTGATGCAG 240
TATGGCCCCC GGGAGGCCGC CCCCAGATTC TAGAGGGGCT TACCCCAGAC ACACCCGAAG 300
GACCACCTCG TGACCTCAGA GGAACAGCCC TAGACCCAGG AGAGACTGCC AGACACCCCC 360
GTGGCAGCCC GCCAGGGCCC AGCTCTACTT GTCGCCTGGA GGTGCTGCCT CCCTTCCACG 420
CCGCCCCAGG GAATGGCCGC CCCTCTGGGG CTCCTCCCAA TCCCCCTTCC CAGGACTGAC 480
AATGGCCCGG CGCCCTGCTT TGGGCCAGGA TCGGCCTCGA GCCTTCCTCA CTAGCGGCCA 540
AGAGCCGGAA ACCTTGCGTC TCAGATTCCC CGGGTCTGTG CACCCCCACC CCAACCGGTC 600
TTCCCACCCA GGCCCCCCCT GATGCCAGCT GCGGGCCTGG ACCTAGCCCG GGGCCCTGCC 660
CCTCCGCCCC TCTCGCTGGA CAGCCCAGGC CGGCGCCCGA GGGATAGGCT CGGGAGCGCG 720
GGGAAGACGC TGCAGCCGGA GCTGGAGCCA GGGCCCACCT GTCCAGCGCC GTCCTGAGCT 780
CACACAAAGA CCCTTCCAGC CTCACCGAGG CCGCGAGCCC AAGCCAAGAT CTTACAGATG 840
TCAGGAAGTC TGGTTTAAAA CCCATTGGTT AAGAAACTAA TGACAATTTT TTTTTCTTAA 900
TAGGAAATCT GGGTGACTAG AAAATAGAGG GAAGGGAGAC ATTTTCATAA CACCCTGTCA 960
|
