Tag | Content |
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EnhancerAtlas ID | HS095-28477 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr7:107851200-107852960 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFE2L1 | MA0089.2 | chr7:107852078-107852093 | GCATGACTCAGCAGA | + | 7.23 | NFE2L1 | MA0089.2 | chr7:107852103-107852118 | GCATGACTCAGCAGA | + | 7.23 | Nfe2l2 | MA0150.2 | chr7:107852101-107852116 | TTGCATGACTCAGCA | + | 6.68 | Nfe2l2 | MA0150.2 | chr7:107852076-107852091 | CTGCATGACTCAGCA | + | 7.41 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH07I108210 | chr7 | 107851208 | 107853006 |
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Enhancer Sequence | TTCAACACAA AAATTTCCTA AGTACTGAAC TATACACCAA GCACTGAGCT GTGTGTTGGG 60 AAGATGATGA AGAAAATATG GTCCAGGCCC TCAGGAAGAT AACAATATTT GTCAATAGAA 120 ATGCAAGTGA CTCTGAATAA GAACAGCTCA GCCCAGAAGG GATCATCATG GCAGATGGGA 180 GGCAGAACTA CATTGCAGCT CTGATGCGGA TGGACAGAGC AGCATGTGGA GGCTTGCATC 240 GTGAATTTTA GCTCCAGAAT AACTGCAAGA ACAAACCTGC TGAAAGGACT CACAGACTCT 300 CTGAAGGAAT TGGACTGCTC CTGCAGGACC CGGGAGATAT CCCAAATACT GTGAGTGCCC 360 AAACTGCAGA AGTGAAAAAC TGGTTTGTGG GAGAAGTTTC TGACTTTACC TGGAGCTGAG 420 TCAATTTAGA GAGCTGAGTG AAATACAGGG GTAGAGGAAG CAGCAGGAAA GGCCTTGGGA 480 GCTCGCTGGG TCCCCAAGCA GGCCATTCCT GCCTGGCACC ACAGAGATCC TTCAGGAGGG 540 CAGCCAGAGG TGTGGGGAAA ATGCCACAGG GAGAAGGAAG TCTCCAGCTG AACTTTATAA 600 CAATTTGAAC CAGACGAGAA ACCTCCTGGC CAGAACTCGG GAAAGGGCAT GAATCCAGCA 660 TGCAGACTCC ATAGGCTGGG GAAGAACTAA GCCCTTTTCT TTTGCCGCTG GGAGGTGGAT 720 AGTCTGGGGC AAGTTCTCAA GCCCCGCTCA CCCACTGCCT GGAAACAGAC TTGGGGCTGT 780 TAGGGTAGGC ACTGTGGGAG TGAGACTGGC CTTTTGGTTT GCGTGGGAGC TGGGTGAGGC 840 CTGTGACTGC TGGATTTCCC TCGCTTCCCC AACAACCTGC ATGACTCAGC AGAGGGACAA 900 CTTGCATGAC TCAGCAGAGG CAGCCTTAAT CCTCCTAGGT ACACAACTCC ATTGATCTGG 960 GAACCTCACC CCCTCCCCCA CAGCAGCCAC AGCAAGACCC AAAGAGAGTC TGAGCTCAGA 1020 CACACCTAGC CCTACCCCCA CCTGAGGGGC CTTCTCTACC AACTCTGGTA GCTGAAGACA 1080 AAGGGCATAT AATCTTGGGA GTTCTAGTGC TCCACTCACC ACCAGTTCCT CTCCATACTA 1140 CCAGAACTGA TACTCTCTGG AAAGCACCTG GCAGGAGGCC AACCAGCACA AAAATAGAAC 1200 ATTAAACCAC CAAACCTAAG AACCCTCACA GAGTCCATTT CAACCCCCTG CCACCTCCAC 1260 CAGAACAGGT GCTGGTATCT ATGGTGGAGA GGCCGATGGT TCACATCACA GGACTCTGTG 1320 CAAACAAACT CCAATAGCAG CCTGGAGATG GGTAGACTTG CCAGGTGGCT AGACCCAGAA 1380 GAGAGATAAC AATCACTGCA GCTTGGCTCA TAGGAAGCCA CATCCATAGG AAAACGGGGA 1440 GAGTACTACA TCAAGGGAAA ACCCCATGGG ACAAAAGAAT CTGAACAACA GACTTCAGCC 1500 CTAGACCTTC CCTCTGACAG AATCTACCCA AATGAGAAGG AACCAGAAAA CCAACTCTGG 1560 TAATATGACT AAACAAGGAT TTTTAACACC CACCAAAGAA TCACACTAGC TCACCAGCAA 1620 TGGATCCAAA CCAAGAAGAA ATCCCTGATT TACCTGAAAA AGAATTCAGA AGGTTAGTTA 1680 TTAAGCTTAT CAGAGAGGCA CCAGAGAAAG GCAAAGCCCA ATGTAAGGAA ATCCAAAAAA 1740 CAATACAAGA AGCAAAGGGA 1760
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