Tag | Content |
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EnhancerAtlas ID | HS047-11833 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr15:76067650-76068810 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr15:76067947-76067965 | CCTGCCTTCCTCCCCACC | - | 6.03 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr15 | 76067670 | 76067975 | chr15 | 76068444 | 76068760 |
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| Number: 2 | ID | Chromosome | Start | End |
GH15I075776 | chr15 | 76067741 | 76067890 | GH15I075775 | chr15 | 76068331 | 76068987 |
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Enhancer Sequence | AAGCAAAAGC CGGCCCCTCC CCTCTCCCAG AGTAGGCAGG CCCCACCCCT CTCCCCAAGT 60 GGGTGGGGAC AGCATTTGCA TAGGCAGCTT TCCCTGTGAT GCCACAGGTT CCTCGGGACA 120 AACTGCTGCC TGGCCATGCC TCCTTTCCCT TTCATCTTTC TCATTGACCA ATGGGCTTGG 180 AGCATTAAGG CCACACCCCT ATTCTGTGTT CTAGTGGGGC CCTGGTTACG CCTCCTCTGG 240 CTCAGTCACA CAGGTGCCTG ATACGTGACT GGAGGTGTTC GCTGATGTGG CCCCAACCCT 300 GCCTTCCTCC CCACCCCACG ATGTTAGAAG AAACTCAACA GAGTAAATTG GCAGCAGCCA 360 AGAAAAAGGT AAAACACACG AGTTCATGGC CCCCCAACCC AGCCAGAGAT CCCTCCAATG 420 ACAAGACCAC TGCTAGAGTC CATACCACTC CTGAGGCATA CCGGGCTGGG CCCCCCCAAT 480 TTGGGGCCTC TGGACTCCCC CCACCAAAGT CTTGTCAGTC AGCCCTGCCC CTTCAAGCAA 540 GCAGCCCAGC CCCTGCCCTC ACCAACCACC CCAGGGTGAC TTTGGGTGGG TGACTCCTAG 600 TGCTCCCTGC TCCACACTCT GCCCTCATGT CCTGCCACCC CAAGCCTGAC CTCCCTGGGT 660 TCTTTGGGCT CATCTCTCCA AGGACCTGGG TCCCCAGCCC CAGCCCCTCC CGTCACCAGT 720 CATCCCTGGG TGACTTTGGG CTGGTGATTC CTGGGGTTCC CTGCTGCAGA CTCTGCTCTC 780 CCCTCCTGCT GACCCAAGCC CAACATCCCT GGGCTATTTG GACTGGAGTC TCCAAGGACC 840 TGGGTCCCAG CCCTAAGTCC CCCTCCCCCA TCGTGGATCG GTGACTCAGC CATCACACTG 900 ATGAGGTTTC CCCCACCCCC AGGAGGAGTG GAATGTAGTG ATGTCACAGT CCCCCTAGGA 960 ACTGTCATTA CTGCTGCAAG ACCAGCCTTT GATCTTATGA CCCAATCCCC TAAGCATTCT 1020 CCCCCCATTT CTGGTTCCTC TGGTTGCAGC ACAAATTTCC AGCTGGAAGG GGAATGGGGA 1080 CTATGGGACC TAAGAGCAAG AGGTTTCAGG CTGCTTTATT CCCTTCACAT AGACGTTGAC 1140 AGTGTGAAAA GCCTACACTT 1160
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