Tag | Content |
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EnhancerAtlas ID | HS143-03086 |
Organism | Homo sapiens |
Tissue/cell | NGP |
Coordinate | chr8:11812540-11814090 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CEBPA | MA0102.3 | chr8:11813928-11813939 | TATTGTGCAAT | - | 6.62 | KLF5 | MA0599.1 | chr8:11813513-11813523 | GGGGCGGGGC | - | 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 |
GH08I011954 | chr8 | 11812470 | 11814195 |
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Enhancer Sequence | ACATGGCTGT GGGAAACCCA AGCCCAACTC CAGTGTGTGC CCTCTTAGGG GTGCTCCATT 60 CCGTCCAGGG CAGCCACCAG TACTTGTAAA GCATTGGACC AGGTGGAAAA AGACCAACAG 120 TAAAGCCACC AGTGCAGTGA CATGCCGAGG TGGGATGTAG CGGTTTCCCT GGGGCCACTA 180 CCTGCCTGAG CAACTCTCCC CACACTCCCT GCGGGCCCCT CCATAGTCAC ATATGGTGCC 240 GTCAAGGAAG GGGGCTGAGG AGCAGGAGAG TGGACACCCG GATCTAGACA GTGATCGAGG 300 CTTTAATTCC TGCTCTGGAT TAAAAACGAC TGGACTGCAC TGAGACTTTC AACGTGGACC 360 AAATGAATGG ACTGTGGTCA GCAGCCTGGG GGCTCAGGAC GGGGAGCAAG GACTCAGAAA 420 GGGAGGCTCC TCTGTCATCT GTTCCTAACT CAGCTGCTGT GCACCCCAGC GCAGTGTGGA 480 GGAGGGAGGA GGTCAGGCTG GGAGAGGCGG CCACGTGCAG GGGCAGTGCT GGCCCCGGGT 540 GGCAGGGACC CTGGAGCAAG GCTGTGGCTC CTCTGATTTG AAGGCTGTGG CTGACACTCC 600 ACAGAGCCCC GTCCTGTGCC AAAGTAACCA GAGCAGAGGC CAGCCTTGGT GCTCCCTTCC 660 GCTCCCGTTC CGGAGGGCTG GCTGGCTGAT AGCTGAATCC CTCAGATGAA GTCATCTGTT 720 TTGGTGCCAG GGAAGGGAAG GGCTGGGGGA GCCGGCGGAG GGGCCATCAG GGCCCGTGCT 780 CTGTCTGCTT TTCCCAGGCT GGCGCCGCAG GGAGGAAAGC CTGGGTCTTG TCTGGGAGTG 840 CCCATCGCTC GGGAGGCAGT GGGTGGGTGG CTCGAGGGCA GGGCCTGTGC ATTGTTAGAA 900 AATCAGGAAG GGAGAACAGG AGCTCGGTTG AAATGTCAGC GGGGCGGTGG GGGGTTGGCG 960 GGGCGAGGGG GGTGGGGCGG GGCGGTCTGT AGGCTTCTTG CTAATGTTCT CTAGCTAATG 1020 TTTTGAATGA TTTCCTCCGT GATCGGATGT GAGCACGCAT CTTGGAAGAC ACACTGTCCT 1080 ACAGTCTATG GAAGATGAAA AGGACTGAAA GGGCATTCAG CACTGTAAAC ACTTGGCCCT 1140 GCTGTCTGGC GCTTCTGTGA TTTGTTGCTC TTTGAGGGAA GCCCTACGCA GTTTGCAAAT 1200 TTTCTATCTA GACCTCAGCA AAGCTTGGAT TTTTCATAAA TTCTATCTTG TCAAATGGAA 1260 TCTGGGTGTA GGTCTGACAT GTGCTATCAA TTCTTATCAT CAATGAATAG AATCAGATGC 1320 ACTCAACATC TACTGAACTC ACATGAGGTA CTAGATATTG GGCTAACTAC ATTAACTTCC 1380 TCATGCTGTA TTGTGCAATT ATTATTTTTC TGTTTACCAG TGAGTAACTG AAGTTCAGAA 1440 AGTTCAATAC CTTTCCTAAT GTCATGTAGC TAGTAAGTGA CACACTGAGC AGAGCCCAGG 1500 CTGACTGCAT CCAAGTCTCT AACATCTTTC AGTGCTGTTC TCTTGGTACT 1550
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