Tag | Content |
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EnhancerAtlas ID | HS104-27311 |
Organism | Homo sapiens |
Tissue/cell | HUVEC |
Coordinate | chr18:11946700-11948340 |
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 | TTACATTACA CGTGCTGGTT TTATCTTCCC AACTAGAAGA TAAACCATAG AATCAGAAAA 60 ACAATTTTAT CATTTTATTT CCAAAATTAC ATAGCCCAGG ATTGAACTGT CCATAAACAT 120 CTATCGGATG GTCAGCTTCA AAACTAACTG CAATGCTGAT GAGTTAAAAT AGCTCCTTTT 180 GTTGGCACCA GATAATAGAT AAACATGAGA AGCCAGTGCA GTGGCTCATG CTTGTAACCT 240 CAGCACTTCG GGAGGTCTAG GAGGGAGGAT GGCTTGAGCC CAGGAGCCCA TAGTGAGCTA 300 TGATTGAGCC ACTGCACTCT AGTGTGAGCA ACAGAGCAAG ACCTCGTCTC TATACAAAAT 360 AAAATTATAC ATTTTTTTTA CATAAGAAAA CTTGAGAGAG ATCATACTTT TGGGTTTCTT 420 TATTAAAAGA AAGAAGACCA AAAGGTGACC CAAGTAAAAG TGTACACCCC TTAAGGGAAA 480 AAAAAATTAT TTTCATTTAA AATCGTTTTC TTTATCTTTA AAGTGAAAGT GCCATATCTG 540 GCTTCCTAAG GAGGAACCAC AAACCGCGTA GACTCAGGCC AGCCGCTGGG CCTGGGCCTG 600 TGTGTCCCTC AGGCGGCGAC CTTTGGCCCA CTTCAGGCCG GCCGTATTTA CCAGCTTAGA 660 GGCGCCGCGG CGTTGGCGAG TCCTTTTTCA CCCACCCCTT CCCTCCGTTC TCAGGCTTGA 720 ACTTGAACAG GCACTCATGA CTCAGCAAAC GGTACTTGAT AGGGTTCTTT ACACGTCAGT 780 CAGGCTATTT TTTAAAATCA CTCTTCCTGG AGATCTTCAA ACCAGAAGCA CCGCGGGCCC 840 TCCCCAACGG GCTTCTGCTT ACCTCCACTA CGTGATGCAG TATGGCCCCC GGGAGGCCGC 900 CCCCAGATTC TAGAGGGGCT TACCCCAGAC ACACCCGAAG GACCACCTCG TGACCTCAGA 960 GGAACAGCCC TAGACCCAGG AGAGACTGCC AGACACCCCC GTGGCAGCCC GCCAGGGCCC 1020 AGCTCTACTT GTCGCCTGGA GGTGCTGCCT CCCTTCCACG CCGCCCCAGG GAATGGCCGC 1080 CCCTCTGGGG CTCCTCCCAA TCCCCCTTCC CAGGACTGAC AATGGCCCGG CGCCCTGCTT 1140 TGGGCCAGGA TCGGCCTCGA GCCTTCCTCA CTAGCGGCCA AGAGCCGGAA ACCTTGCGTC 1200 TCAGATTCCC CGGGTCTGTG CACCCCCACC CCAACCGGTC TTCCCACCCA GGCCCCCCCT 1260 GATGCCAGCT GCGGGCCTGG ACCTAGCCCG GGGCCCTGCC CCTCCGCCCC TCTCGCTGGA 1320 CAGCCCAGGC CGGCGCCCGA GGGATAGGCT CGGGAGCGCG GGGAAGACGC TGCAGCCGGA 1380 GCTGGAGCCA GGGCCCACCT GTCCAGCGCC GTCCTGAGCT CACACAAAGA CCCTTCCAGC 1440 CTCACCGAGG CCGCGAGCCC AAGCCAAGAT CTTACAGATG TCAGGAAGTC TGGTTTAAAA 1500 CCCATTGGTT AAGAAACTAA TGACAATTTT TTTTTCTTAA TAGGAAATCT GGGTGACTAG 1560 AAAATAGAGG GAAGGGAGAC ATTTTCATAA CACCCTGTCA CCTTTGCATT TCATGCACAT 1620 GCAGAGTTGC ATTCATATTA 1640
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