Tag | Content |
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EnhancerAtlas ID | HS091-01479 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr1:43749040-43751110 |
Target genes | Number: 13 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Klf12 | MA0742.1 | chr1:43750480-43750495 | GGCCACGCCCTCCTC | + | 6.74 | SP4 | MA0685.1 | chr1:43750478-43750495 | CTGGCCACGCCCTCCTC | + | 6.06 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_29457 | chr1:43748843-43752786 | Fetal_Intestine_Large | SE_31961 | chr1:43749328-43752683 | Gastric |
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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 |
GH01I043281 | chr1 | 43747379 | 43749176 |
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Enhancer Sequence | TAGAAAATAA CATAGGTATG GGTGTCAGGG ATGGTCACAG GGTGCACTTT CCAGGTCACA 60 CTCACAGCCA TGGTAGCCCT GCACAAACTC TGGGGACTGG ACAACTGACC ACACCAGCTC 120 TCCACAGAAG AGAAACAAGC TGAGCCTACA GAAACTGGCT ATTTGTAAGG GACCATCACA 180 GGGTTTGGCT CTGGAAGCTG CTAAAAAAAA AATAAATTGT AGAACTTACT GAGCATTCCT 240 TATAATTCAA GCACCAGGCA TCATGCTCAC AAAACCCAGT AAGGTAAGTA TAAACATTAT 300 CCCCACTTTA TAGATGAGGG CTCTGAGGCT GAAAAAGGTG AACTGACTCA ACTAAAGTCT 360 TCAGATTCGA ACCCAGAGCC CAGTCTGTTG CACTGCTTGG TAAGCTGAGG ATGGGAGACA 420 GGGGCAGAGG TGGGTCCTGG CTCCCGAAGG TCAGAAAACA GCAATTGCTT GGAGCTACCC 480 AGCCAAAGCG GAGACCACAT ATGGGGAGGG TGATGCAAGT TGCTACTGAG GACAGGGGCC 540 CTGGACACAG CCAGAGCAGC CCTGGCCCTT CTAAGTTGAA AGCCGCTGCT GCCCACCTCT 600 ACCCTCAGCC CTTCAAGCAA ACCCCTGTCC TTTCACCTCT ACTCAAAGGA GGCCCACACT 660 CTGCCCCCAC AGGGAGGCTC AAGCCAGGGA GTATCCAAAT GAGGATCACC TGAATCAGGA 720 AATTATCACC CAGGGCTGGG GACACCTAGA GGAGGAACAC TTCAATTAGG GGAGTAGCTG 780 GAGGAAGATC ATCCAGGCAT GGAAACACCT GTAGGAGGAG CACCTGGATC AAAGGAGTGT 840 CTGGAGGAGG CGCACCTGAA TCTGGGGAGT ATCTAGAGGA GGAGCATGAA AGTTAGAAGT 900 ACCTGGCAGA CGAACAGCTA GGGCAGGAGC ATATCTGCCA GTGGAGCACC TGAACCAGGG 960 GAGTCCTTGG GGGCAGAGTA GCCGGGCTAG GGAAGTACTT AGGAGAGAAG TTGAGGGGAG 1020 TACCCCAGTA TATTCTTTGA TACAAGTGCC TTCAAACCCC CCCCAACCTC CTCACATCCA 1080 ACCTGGTATC AATCCCCATC ATGTCTTCCA CTAAACATCT CTGGAATGAC AATACCCTCT 1140 TCTCCACCCC ACTGCCACAG CTGAGTCCAA GCCACCTTCC TCTTGTACTC TAGCCATAAT 1200 CTCCTAACTG GGCTCCCCAC CTCTGGTCTC TTCCACAGAG TGATGGGCCT ACAACCCAAA 1260 TCTGACCCCA TCACTAGCCT GGTTAAAATC CCTTCAAAAG CTCCCCATGC CCCACAGTGC 1320 CTTGCAATCC AGCACACGGC CCTCAAGCCA AACTCTTCTT CCTCTTCTCC ACAGTTCCCT 1380 CCCCAGCACT TCAGACAGAC ACACATGCCC TCCTCCCACT CACCCACCCT CCTGCTCCCT 1440 GGCCACGCCC TCCTCAGTTT TTGGGGCGCC AGTCTGTCAA GGCCAAATCA GACCATACCT 1500 GCCTGTGAGG TTGTCCCTGG ACCTACCCTG GATGACCTGT CACCATCCTG CCCAGTCAAC 1560 CACCAGTCAG AACCAGTCAT TGCTAGGCGG GCAGCTCCCC GTGGGCAACG GCTGGCTGAA 1620 GGATCTGTAC CCTGGCGCTG CAGGGAGCTG GGCGTTCAGC CCCTCAGTGT GGTGCTTGTG 1680 AAATTAACGA GGGGAGCGTG AGAGTGAATA TACAGGTGGG AGCGGGAGAG ACGTCCTGGG 1740 AAGGAGAGGT CAGCTGCTCA TTCATTCCTC AGCCTGCTGT GGGCCTCATC CTAGTACTAG 1800 GTCCGCAAAA CATGAGAATG TGTTACACTG GAATGAACTG AATTCAATTT GACGTTTCTA 1860 AGGTTGTATT CCTATTCCTT TCCTCCCTGC CCTGTGAATT CTTCCCAAGA AGACACACAC 1920 ACACTAACCT TCCAAGGGTG CATATACACT CCCCAACAGG CCTCTGAACT CACAGCCCAC 1980 ACTGATCTGC CCATCCCCCA TACGCACAGC CCCTCCCCCC AGGTCACACT TTCCTCCACC 2040 AACAAACACC CCTCTGACAT GCACAGACAC 2070
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