Tag | Content |
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EnhancerAtlas ID | HS051-12868 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr18:11947250-11948190 |
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 |
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| 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 |
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| Number: 1 | ID | Chromosome | Start | End |
GH18I011945 | chr18 | 11945770 | 11949587 |
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Enhancer Sequence | GAGGAACCAC AAACCGCGTA GACTCAGGCC AGCCGCTGGG CCTGGGCCTG TGTGTCCCTC 60 AGGCGGCGAC CTTTGGCCCA CTTCAGGCCG GCCGTATTTA CCAGCTTAGA GGCGCCGCGG 120 CGTTGGCGAG TCCTTTTTCA CCCACCCCTT CCCTCCGTTC TCAGGCTTGA ACTTGAACAG 180 GCACTCATGA CTCAGCAAAC GGTACTTGAT AGGGTTCTTT ACACGTCAGT CAGGCTATTT 240 TTTAAAATCA CTCTTCCTGG AGATCTTCAA ACCAGAAGCA CCGCGGGCCC TCCCCAACGG 300 GCTTCTGCTT ACCTCCACTA CGTGATGCAG TATGGCCCCC GGGAGGCCGC CCCCAGATTC 360 TAGAGGGGCT TACCCCAGAC ACACCCGAAG GACCACCTCG TGACCTCAGA GGAACAGCCC 420 TAGACCCAGG AGAGACTGCC AGACACCCCC GTGGCAGCCC GCCAGGGCCC AGCTCTACTT 480 GTCGCCTGGA GGTGCTGCCT CCCTTCCACG CCGCCCCAGG GAATGGCCGC CCCTCTGGGG 540 CTCCTCCCAA TCCCCCTTCC CAGGACTGAC AATGGCCCGG CGCCCTGCTT TGGGCCAGGA 600 TCGGCCTCGA GCCTTCCTCA CTAGCGGCCA AGAGCCGGAA ACCTTGCGTC TCAGATTCCC 660 CGGGTCTGTG CACCCCCACC CCAACCGGTC TTCCCACCCA GGCCCCCCCT GATGCCAGCT 720 GCGGGCCTGG ACCTAGCCCG GGGCCCTGCC CCTCCGCCCC TCTCGCTGGA CAGCCCAGGC 780 CGGCGCCCGA GGGATAGGCT CGGGAGCGCG GGGAAGACGC TGCAGCCGGA GCTGGAGCCA 840 GGGCCCACCT GTCCAGCGCC GTCCTGAGCT CACACAAAGA CCCTTCCAGC CTCACCGAGG 900 CCGCGAGCCC AAGCCAAGAT CTTACAGATG TCAGGAAGTC 940
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