Tag | Content |
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EnhancerAtlas ID | HS091-13275 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr14:55310860-55312480 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Myog | MA0500.1 | chr14:55310898-55310909 | GACAGCTGCTG | + | 6.14 | Tcf12 | MA0521.1 | chr14:55310898-55310909 | GACAGCTGCTG | + | 6.02 |
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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 |
GH14I054843 | chr14 | 55310086 | 55312994 |
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Enhancer Sequence | TCTACAAAAT AAGGCAACAC AGGTTGTTTA AAGGAGTAGA CAGCTGCTGG TTTGGTTTTT 60 AAAAGCAGGC CTAAAGATTA AATCTCAGCT CACAGTTACC AAGTATATCG AAATATCCCT 120 TCTTACACAA ATGTTATCTA TTAGGTTCAT GCAAAAGTAA CTGCGGTTCT TGCTATTGAA 180 CATAATGGCA AAAACTGCAA TTATCTTTGC AGCAACCTAA ACTTTTTGTT CTTGAAGTTG 240 TCTTGCAACT TTTATTTTTA TCAGTAGTTG ATCCTTAAAG CATCCAAAAA GGGGAAAAAT 300 GGAATTTTCT TCTGGGGTGA AAGTAATATA AAAGGTCTAC AGAGTTACTT AACTTCTAGA 360 TCAAAAGAAA GTCAGAATTC TCACTTGCTC TGCCTTCAGG ACCAAGACAG CACTATGCTA 420 GCCTAGGTGT TCAGATAAAT GCTCAAGTAT ACTGATGTCA CCAGGCAGAA TTCAGATAAT 480 GGTGACCAGA GATCCTGTCT GAGCAACCTG GTGACATTAG ATACCAGACA TAGAACAGAG 540 TTCACACCAC GTCACAGAAC ACATATGAAC TTTGTCCACA CAACAGCTGC AATTCTCTTA 600 ACTCATCCTA ACTTAAAGAA ATGTACCAAT TCTTGGCTTT ATTTTTTAAA TGTGTGACAA 660 AATATTAGAA AAACTCGGCT TGGAGCAACA GAGAGCTAAA GAAGAAATCA AGAGAAGACA 720 TAAAATCAAG AGAAGACATA AAAATGGCTA TTGGCGTGGT GGCTCACGCC AGTAATCTCA 780 GTATTTTGGG AGGCTGAGGT GGGCAGATCA CTTGAGGTCA GGAGTTTGAG ATCCCCAGCC 840 TGGCCAACAT GGTGAAATCC CATCTCTACT AAATACGAAA ATTAGCTGGG TGTGGTGGCG 900 GGCACCTGTA ATCCCAGCTA TTTGGGAGGC TGAGGCAGGA GAATCGCTTG AACCTGGGAG 960 GCAGAGGTTG CAGTGAGCCA AGATCACACC ATTGCACTCC AGCCTGGGTG AGAGAGCAAG 1020 ACCCTGTCTT GAGCATTTTT AAAAAATGGC GATTGAGCTG GGCGCAGGGG CTCACGCCTG 1080 TAATCCTAGC ACTTTGGGAG GCCGTGACGG GTGGATCATG AGGTCAGGAG TTCGAGACCA 1140 GCCTGGCCGA CATGATGAAA CCCCATCTCT ATTAAATATA CAAAAATTAG CCGGGCATGG 1200 TGACACACAC CTGTGGTCCC AGCTACTCGG GAGGCTGAGG CAGGAGAATC GCTTGAACCC 1260 GGGAGGTGGA GGTTGCAGTG AGCCGAGATT GCACCACTGC ACTCCAGCCT GGGCGACAGA 1320 GTGAGGCTCC ATCTCAAAAA AAAAAAAGGC TATTGATTAT GCAAATCTCT ACACCTGTGC 1380 TTTTAACTCC CTATGCCTCC ACAAGCCCCA TCCTACCCTC AAAAAATACT TCTCCCATAT 1440 TCTGTTCCTA TATCAGTAAC AGTAAATGAA AGTGGTAAAA GAGCTTTAGG CTCAGGGATG 1500 GAAATCTACA GTTATCATAT CAGTTGTGTG GCATCACCTG GTGCTACAAA ATATGAGAAG 1560 CACTAAATAG CAAGATCACT TCTAGTGCAC CATTATGACG TTACTAAAGG CAGATGCAGA 1620
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