Tag | Content |
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EnhancerAtlas ID | HS052-05170 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr10:88344670-88345720 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr10:88345380-88345399 | CAGTGCCACCCAGTGGCAG | - | 6.17 | KLF4 | MA0039.3 | chr10:88345438-88345449 | CCACACCCTGC | + | 6.62 |
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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 |
GH10I086585 | chr10 | 88344880 | 88345627 |
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Enhancer Sequence | AGCCCTGAGG GCTGCCGTAC CCAGGCCAAG GTCATGTGGA CTTGAGGCCA GAAGGCACAG 60 CAAGAGGACA GGAGGCCAGT TGTCTTTCTT TGGCACTGGA AGACTTCCCA GTGTTCTGGT 120 TGTCCTAACA CCAGTGTCTC TCCTCCATGT CCCTTAGCTA AGTGCTTTAA TGGAGACAGA 180 GCAACCCAGG ATAGCCACAC CAAAGGCCCT GGCCTCAGAG GCTCAGCCTG CTGCTGGCTG 240 GGGAAGGTGG CTGACAGAGG CTTCCAGCCC CCAGCTCCCT ACAGGTCGCT GTCCTATGGA 300 CTGGGCCAAA CCTCCCTGGG CACACCCCAC CCCTACCTCC CACCCAAACC AAGTGCGCAG 360 TGCCCTGAGA GCCTGCACTG TGAGAGACAG CCTGAACTAG AATGGCCTGC TGAGCACTCT 420 AACATCAAGA CTCAATTGCT GCCTCCTCCC CGGGCCCCTC AGCGGGAACC GGTTGTTCTT 480 GTGCTTCTAT TGGAGCAACT AATTACATCT ATTATTGGAA CAATTAATTT GTTGTCCATG 540 TGACTGTTCC ACTGTGGGCT CCTGGAAGGC AGGACCTATT TCATGTACCT CTTTGTAACC 600 CTAGATGGAA AGCAACTTGC CCAGCACAGG AGGGCCCAAG TGACGCTTTT CCCGTGCCAC 660 CCCTTCTCTG GGCAGTTTCC TTTAGGCGTG GTCCCCCTCC TGAGGCACCA CAGTGCCACC 720 CAGTGGCAGA ATTGCAGTAC TGAGCTCTCC GGGGAGGGCT CTTCTGCCCC ACACCCTGCT 780 GGGGGCTACT TACAGCAGGG GTTGAAGGCG AGTAAGGGGT CACCGTCCTG GCAGGGCCCT 840 CCTGCATGCC ACAACTAAGG TCCAAATGGG GTTGAAATGG CAGAGAAACA CAGCCAGTGC 900 CTTTGTGGGC TCCATGTATT GCGGTATCTG CTTGAGGCTC ATGCGGTTTC TCTCCCTGTC 960 CTTTTTTTTT GTAGAGACAG AGGTATCCCT ATGTTGCCCA GGCTGGTCTT GAACTCCTGG 1020 GCTCAAGCAA TCCTCTCACC TCGGACTCCC 1050
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