Tag | Content |
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EnhancerAtlas ID | HS091-10051 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr12:56394280-56395990 |
Target genes | Number: 32 | Name | Ensembl ID |
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SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HEY2 | MA0649.1 | chr12:56395050-56395060 | GGCACGTGTC | - | 6.02 | MEF2A | MA0052.3 | chr12:56394741-56394753 | TCTATTTTTAGT | - | 6.27 | MEF2B | MA0660.1 | chr12:56394741-56394753 | TCTATTTTTAGT | - | 6.32 | MEF2C | MA0497.1 | chr12:56394740-56394755 | TTCTATTTTTAGTAG | - | 6.57 | Npas2 | MA0626.1 | chr12:56395050-56395060 | GGCACGTGTC | + | 6.02 | SOX10 | MA0442.2 | chr12:56394562-56394573 | TTCTTTGTTTT | - | 6.62 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_28263 | chr12:56394730-56396550 | Fetal_Intestine | SE_28988 | chr12:56394361-56396611 | Fetal_Intestine_Large |
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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 |
GH12I056000 | chr12 | 56394566 | 56396278 |
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Enhancer Sequence | CTCAGCCCCG GTTCCCGCTC GCACCTCTCC CTCCACACCT CCCTGCAAGC TGAGGGAGCC 60 GACTCTGGCC TTGGCCAGCC CAGAAAGGGG CTCCCACAGT GCAGCGGCGA GCTGAAGGGC 120 TCCTCAAGTG CCGCCAAAGT GGGAGCCCAG GCAGAGGAGG CACCGAGAGT GAGCAAGGGC 180 TGTGAGGACT GCCAGCACAA TGTCACTTCT CACTAGGATT ATAAGGGTGA GCCACCACAC 240 CCAGCTCTTT TATTACAGTA TAATGTTATA ATTTTTTTCT TTTTCTTTGT TTTTTTTTTG 300 AGACGTTTGA GACGGAGTCT CACTCTGTCG CCCAGGCTGG AGTGCAGTGG CGCGATCTCG 360 GCTCACTGCA ACCTCCGCCT CCTGGGTTCA CGCCATTCTC CTGTCTCCGG AGTAGCAGGG 420 ACTACAGGCG CCCGCCGCCA AGCCCGGCTA ATTTTTTTTT TTCTATTTTT AGTAGAGATG 480 AGGTTTCGCC GCGTTAGCCA GGATGGTTTC GATCTCCTGA CATCGTGATC TGCCCGTCTC 540 AGCCTCCCAA AGTGCTGGGA TTACAGGCGT AAGCCACTGC GCCGGGCTAA TTTTTCTATT 600 TTGTTATTGT TGTTAATCTC TCTTTTTTTT TTTTTTTTTT TTTTTTGAGA TGGAGTCTCT 660 CTCTGTTGCC CAGACTGGAG AGCAGTGGCG TGATCTCAGC TCACTGCAAC CTCCACCTCC 720 CAGGTTCAGG TGATTCTCCT GCCTCAGCCT CCCGAGTAGC TGGGGTTACA GGCACGTGTC 780 ACCATGCCTG GCTTATTTTT GAATTTTTGT AGAGACAGGT TTTCCCCATT TTGGCCAGGC 840 TGGTCTCAAA CTCCTGACCT CAGGTGATTT GCCCGCCTCA GCCTCCCAAA GTGCTGGGAT 900 TACAGACGTG AGCCACTGCG CCGGGCATTG TTGTTAATCT CTTACTGTGG GTAATTTAGT 960 AATTAAACTA TAAGAGGTAT GTATGTATGG GGGAAAAAAC AGTAATATAG GGTTTGGTGC 1020 AATCTGTGGT TTCAAACATC TACTGGGGGT CGTAGAACAT ATCCCCAGTG GATAAGGGGG 1080 TACTACTGTA CTTGTTGGCT CTTCATGTTA GCTCTGCTAG GCAGATGTCA TTTCAGAGAT 1140 GAGGAAGCAA GTTCAGAACG GCTTGGAATC TTGCTCAGGA AATCGGGCTG GTTAATGAAT 1200 AACAAGAGAT CCAGTTTCAC AAACCCAAGG CATTTTGCCC CCAGAATCTG GGCTTCTTCA 1260 CCCATTTAGG CTGTCACTAC TTTTTTTTCA CTTTTTTATC CCTGTTTAAG TCAGTCTGAC 1320 CCACAGTTGT CCTCTGCTGA CTTCAGAAAT AATAATCTGG CCAGTAGACA TTTGGTTTCG 1380 GTCCTTTAGG CCCTTCGCCC CAGGCATCGT TCTCTATGGT GGACAAAGTT CAGAATGGAA 1440 GATGGGAGAA AGGTGATTCT GATTCTAGAA GCACCCATCC CTCCTACCCC ATTCCCCACC 1500 CGCATTACCT GCCATCCTGT CAGCACAGTC TGTCTCTGAA GTGCTCCAAG TTTTCTCTAA 1560 GGGCCCATTT GGACTCCCAC TCTCAAGACT CCTCACTTGC CCAGAAAGCT CCTTGCTGAC 1620 CTTCTCTGTG TCTTCCTCTC ACCCATTCCC TTAGGCCTCC CTAATATCCC CTCCCAGGGT 1680 CTCCCTATCT TGATCCCAGA ATCTTCCTTC 1710
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