Tag | Content |
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EnhancerAtlas ID | HS118-04892 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr12:113362310-113363800 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF4 | MA0039.3 | chr12:113363085-113363096 | CCACACCCTCC | + | 6.32 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr12 | 113362617 | 113363241 | chr12 | 113362415 | 113362485 |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I112924 | chr12 | 113362515 | 113364839 |
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Enhancer Sequence | TGAACTTGGA GTTTCTTTTC ATTAATTTTT GTCCTCTTTA GTGACAGTGA CAATGTTTTA 60 TCATTTTCCC TGCAGAGGTC TTTCATGGTT TTTGTCATAT GTATTCCCAA GTATTTGTTT 120 CAGTACTATC GTACTTGGCA TGCTTTCTTT AATTTCATTT TGCAATGGTT GCTTCATGGG 180 AGACTTAAAC ATTTTCAGTG GTGATATTTG GCTATAGCAT TATAGGTGAT CTTTATACTT 240 TTCTAAATTT TCTGTGGCCA CGGGAAATAA TAAAGACACT TTTCTTGCAC AGAAAAAAAA 300 AACTTTTGGG AAGTATTTCT CACAGCTAAG ATCTGATAGT TTACGCAAAG TTGGCAGGCA 360 CAGGCTACAG AAAGCTCTGG GGTGCTGTTG TTTGGAGCTG CTGGTTCAAG GACAAATTCA 420 CAAGATTTGG AAACAGAGGA CCAAGTGTGT AAGGACGAGG GAAACTATGG TATAACATTG 480 AAGCACCTGA GCTGGAAATT TCTGAGCCCT CAGAGATAAA TTTCCTCAGC TCCTCCCTGC 540 CGAGAAAACA AAACTAAAAA GAGTTAATGT TTAGCCAACA GAAATGAGAG TGAAGTTCAC 600 AGAAGAAATT AGGGCACAGC TGGAAGTGTT CAAAATGAGG AAACGTTCAA TGTCAAGTTT 660 GAGATCCAGG GTTGATGGGT GAACTCTGCA CGCTCAGCTT CATGTTAGGT CTCCCAGCTC 720 AACGAGGGGG TGAATTTTGG TGTACTGCTG TCTTTGAGGC CCTGCGTGAA CTCTCCCACA 780 CCCTCCCCCT TTTCCTCATA CAAATCCCCT CCTTGCACAC CCCTCACGCC TGTCTGTGAG 840 GTGCCAGGGC CCCTCTCCCA GCCAACCGCA GGCCAGTATT GCCCCTCCCC AAACTTCCCT 900 TCAGGCAGAT CAAACCCAGG GCTCTGGAGT CACACTGCCT GGGCTCAAAT CCTGCTTCTG 960 AATCTTATGA GACATCAAGT CACTTACCTA ACTCCTTGGT GAAACAGGCT CTCCTCTGTC 1020 AAATAGGTGT GCATGCTTTG GGAGGCCAAG GCAGGAGGAT TGCTTGAGCC CAGGAGTTCA 1080 AGACCAGCCT GGGTAACATA GTGAGACCCT GTCTCTATAA AAATAAAAAA ATTAGCCAGG 1140 TGTGGTGGCT CATGCCTGTA GTCCCAGCTA CTCAGGAGGC TGAGGAGGAA GAATTCCTTG 1200 AGCCCACGAA GTCAAGGCTG CAGTGAGCCA TGATCAAGCC GCTGCACTCC AGCCTGGGCA 1260 ACAGAATGCG ACCCTGTCTC AGAAATAAGT AAATAAATAA ATACATAAAT AAATTTGGGT 1320 GCAATTGTGG CTCTTAGTGT TACAGAGAGG ACTGAAGGAG CTAATGGATG ATGGATTTAT 1380 GGCAGTACCT CACATATAGC TTATCCTAAA GGAAGTTAGA GCTTATTATG ATGATTATTC 1440 AAAAATATTT ATCAAAGGTC TGCCCTGGGC CATGTTCTGA GCTAAGTGCT 1490
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