Tag | Content |
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EnhancerAtlas ID | HS053-39873 |
Organism | Homo sapiens |
Tissue/cell | Foreskin_keratinocyte |
Coordinate | chr9:2361130-2363040 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFE2L1 | MA0089.2 | chr9:2362607-2362622 | GGATGACACAGCAAT | + | 6.47 | SP2 | MA0516.2 | chr9:2361451-2361468 | TGAAGCCCCACCCACTT | + | 6.3 | TP53 | MA0106.3 | chr9:2362372-2362390 | AACATGTCTGGGCATAAA | - | 6.03 | ZNF263 | MA0528.1 | chr9:2361381-2361402 | TAAGGAGGAGGGAGGAGAAGG | + | 7.16 | ZNF263 | MA0528.1 | chr9:2361384-2361405 | GGAGGAGGGAGGAGAAGGGCA | + | 7.34 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr9 | 2361289 | 2361386 | chr9 | 2362114 | 2362729 |
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| Number: 1 | ID | Chromosome | Start | End |
GH09I002361 | chr9 | 2361578 | 2362997 |
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Enhancer Sequence | AAGGTGCCAA CTAACAGAAG ACTGAAAATA GCAAGAGCCA GTACAATTAC AGGTTTATTT 60 TTCTGTCTAG TAATCAGTGT CTGGAAGTAG CAAGTCCAGG GCTGATACGG CAAATCCTAT 120 CACAGGAATC AGATTCCCTC TTACCTTTCT GCACTGCTAT CCTTGCTTAG TGCCTACCTG 180 CAAACCTTAA GTTTACGTCA AGGTACAAAG CACTTTTAGA ACCTTGGCCA TTTGTATCCA 240 ATTCCAGGAC CTAAGGAGGA GGGAGGAGAA GGGCAAACAT GTGCCTGAGC TTGGGTCTCT 300 TTCTACTTTA AGGAGAGTTC CTGAAGCCCC ACCCACTTCT ACTTCCATCT CATTGGCTGG 360 ACCTTAGTTG TATGGTCACC CCTATCTACA AGAGAGATTA GGACACACAA TTTTTAAGCA 420 GAATACATTG TCACTCTGAA TAAAATTAAA TTTTCTTTTT CAAAAAGAAG AGGAGAGTAG 480 ATATCGATGG GTAGTCTGCA GGGGATACCA AAGACCTCAG TTGGGCTTAA CCCAAGATGT 540 GGATACAACA GTCATAGAGG AAGACAAGTG AACCTTAATC CTTACTGCCT ACTTGACTAC 600 TTCACCCTCT TGTTATCATG GGAGCCAAGG AGCCTCCTGG GAATACTTCA TACCAGCCTG 660 AAACTGAACT TCAGACATAC ACCACCTGGC ATGTCACATG GCCTGGGCAG AGTTAGGTAA 720 ACAGGTCCTC AAAAGTCTGT TAGAAAAAGT CAGGGTTGGG CCAGGCACGG TGGCTCGTGC 780 CTGTAATCCT AGCACTTTGG GAGGTCAAGG CGGGTGGATC ATCTGAGGTC AGGAGTTTGA 840 GACCAGCCTG GCCAACATGG TGAAACCCCG TCTCTACTAA AAATACAAAA AATTAGTTGG 900 GCATCGTGGT AGTCACCTGT AATCCCAGCT ACTCGGGAGG CCAAGGCAGA AGAATCGCTT 960 GAAGCCAGGA GGTGGAGGTT GCAATGAGCT GAGATCACGC CATTGCACTT CAACCTGGGC 1020 AACAAGAGTG AAACTTTGTC TCAAGAAAAA AAACAAAAAA AGTCAGGGTC CTTGAGAGAG 1080 AATTCACCAT GAGGAAGAAA AAATTTGCAC GTCTGAGTGT GAGGTAAGCA TGACTCTGGG 1140 TAAATCTTGG CAGCTGGTAC TAAGATCCAC CCTGACTCAC CTACCTGTGT GTTAGTCCAC 1200 ACTTTGCATA GAAACTCAAG TGGCTATATT ATTAAACTCA GTAACATGTC TGGGCATAAA 1260 CAATCTTGCC GTGGCACTCC CTCTAACTGA GTGTGACAGA GGGAATAAGG CATTCTTATT 1320 ATTGTGATTT CATCTGCTGA ATTAGTGAGG TGACTTGAGG ATTAAGCATA TGACAGCCAG 1380 GCCTGGTGTG TTGGCTCATA GCAGTAATGC CAACACTTTT GGAGGCCAAG GAAAGAGGAT 1440 CACTTGAGGC CAGGAGTTCA AGGTTGCAGT ATAGCTTGGA TGACACAGCA ATACCCTGTC 1500 TCTTAAGAAA AAAAAATGGC AGTTAAGGAT ATCCACAGGA TGTCTACCTC ATTGCAGCTG 1560 ACAAGAAAGG CAGCATGGTA AAGATAAAAG GGACAGAGAA CAATGTTGAG TGATGTATGT 1620 AGGATAATCC TGGATACTCT TCCAAGTTAC TGGTACGGGG TTCTTTTCAT GAGGTTGGAA 1680 ATTCTGTATG TCGTGGTCCA GATACTAGAG TTTGTAACGT TCAGATTTAA CTGTAATATG 1740 ATGTTATTTG TTCATAAACA TATTGAGACC TGGGGTTATT TGGGTTACTT TAAGTTCACA 1800 TAGGTTTCAG CTGAGTTCTA TGGGTAGCTC AAACACCAAT CCCTGAGCCC GGAAAACACA 1860 ACTTGAAACT AACTTAACCT CCTCCCTTAC CCTCTCCTAA ATCCCCCTGC 1910
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