Tag | Content |
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EnhancerAtlas ID | HS010-02017 |
Organism | Homo sapiens |
Tissue/cell | B_cell_blood |
Coordinate | chr18:11947140-11948260 |
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 | AAAGGTGACC CAAGTAAAAG TGTACACCCC TTAAGGGAAA AAAAAATTAT TTTCATTTAA 60 AATCGTTTTC TTTATCTTTA AAGTGAAAGT GCCATATCTG GCTTCCTAAG GAGGAACCAC 120 AAACCGCGTA GACTCAGGCC AGCCGCTGGG CCTGGGCCTG TGTGTCCCTC AGGCGGCGAC 180 CTTTGGCCCA CTTCAGGCCG GCCGTATTTA CCAGCTTAGA GGCGCCGCGG CGTTGGCGAG 240 TCCTTTTTCA CCCACCCCTT CCCTCCGTTC TCAGGCTTGA ACTTGAACAG GCACTCATGA 300 CTCAGCAAAC GGTACTTGAT AGGGTTCTTT ACACGTCAGT CAGGCTATTT TTTAAAATCA 360 CTCTTCCTGG AGATCTTCAA ACCAGAAGCA CCGCGGGCCC TCCCCAACGG GCTTCTGCTT 420 ACCTCCACTA CGTGATGCAG TATGGCCCCC GGGAGGCCGC CCCCAGATTC TAGAGGGGCT 480 TACCCCAGAC ACACCCGAAG GACCACCTCG TGACCTCAGA GGAACAGCCC TAGACCCAGG 540 AGAGACTGCC AGACACCCCC GTGGCAGCCC GCCAGGGCCC AGCTCTACTT GTCGCCTGGA 600 GGTGCTGCCT CCCTTCCACG CCGCCCCAGG GAATGGCCGC CCCTCTGGGG CTCCTCCCAA 660 TCCCCCTTCC CAGGACTGAC AATGGCCCGG CGCCCTGCTT TGGGCCAGGA TCGGCCTCGA 720 GCCTTCCTCA CTAGCGGCCA AGAGCCGGAA ACCTTGCGTC TCAGATTCCC CGGGTCTGTG 780 CACCCCCACC CCAACCGGTC TTCCCACCCA GGCCCCCCCT GATGCCAGCT GCGGGCCTGG 840 ACCTAGCCCG GGGCCCTGCC CCTCCGCCCC TCTCGCTGGA CAGCCCAGGC CGGCGCCCGA 900 GGGATAGGCT CGGGAGCGCG GGGAAGACGC TGCAGCCGGA GCTGGAGCCA GGGCCCACCT 960 GTCCAGCGCC GTCCTGAGCT CACACAAAGA CCCTTCCAGC CTCACCGAGG CCGCGAGCCC 1020 AAGCCAAGAT CTTACAGATG TCAGGAAGTC TGGTTTAAAA CCCATTGGTT AAGAAACTAA 1080 TGACAATTTT TTTTTCTTAA TAGGAAATCT GGGTGACTAG 1120
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