Tag | Content |
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EnhancerAtlas ID | HS105-76803 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr8:21994310-21995440 |
Target genes | Number: 28 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr8:21995047-21995066 | TGCTGCCCTCTCGTGGCCA | - | 7.31 |
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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 |
GH08I022136 | chr8 | 21994481 | 21995511 |
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Enhancer Sequence | CACCCCCCAA AGATCGTTAT GAGAATTAAA TTAATATATG CCAGGGGCTT AGAGCAGCGT 60 CTGCGTGGGC AGCCACACTC TGGGCGCCAG CCGTTACTAC TGCCTGCATC CCTGCAGTGT 120 CTGGCAACAT GTCTGGTACC TGCTCGAGGC TCAATAAAGA TTCATTTTTG AATGAATTAA 180 TGAAGCGATA AGACAACCCC ACGATGCAAA GGCAGGCCAT GTTGGACGCC AGTGAGCCCC 240 TATACGTGAG AAGCTAAATC ACCGCAGCAG ATTAAGAGCC TCCCCCAAAT AAAACCTGGA 300 TAATCCCCAC ACCAAGAGTT AATCCACACT CTCTGGGGCC ACTCCAGGTT ACCACCCCAT 360 TTCCCCTCTT CTCATCCCAC ACTCTCACCC ACCTCTTTGC TTAATCAATC AAAAGCAGGG 420 AGGAGGAGCA GGTGCAGCAG TGGCAGAGGG GCGCACCCCG GGCATCATGG TGAGACCAGC 480 ACCGGGGCAG TAGAGGGCAG AGCTGGGTAC CCCGGTTGCC CCAGGGATCG GAGGAGTTGG 540 AGTGGAGCCA GCCAGGCAAA CAGCCTTGGT CTCAGGAGAG CAGAGACTCC TTGGATGGGG 600 CAGGCCAAGG ACCAGTGACC ACAAGCAGCA GGGAGGGCCA CTGAGTTCCG CCAGGCCCAG 660 CAGGGCGAGG CTCTGGCCAG TCTCCCAACC CCACCCTCCT TGACCTGGAA GCCGGGGGCA 720 GCCCAGATCC CAGACACTGC TGCCCTCTCG TGGCCACTCC TCAGAGGTGC AATGGTGCCC 780 CTGCGGGTAC CTGACTGTTT ACAGAACTTA ATGTCCCCAG AGCTGCCCCA GGGGGCTCCT 840 TCTTCCAGGC TCCTGGAGGA GATACTCCTC CCCAGGTCTC CTCTGCCTAG CTTCGACCTC 900 CCTATGGGAC TAACGTGCTG CCCCAAGCCC CTCCTGCCTG TGCTCCCACT GGTTTCTCTA 960 TAGCTGCACC TTCCTGCCAA GGCCTAACTG AAGTTTCGGG TTCTGACCAG TCCTCTGGAC 1020 TCGTCCCCAC TTTCCCATCA GTGCTCTCAA AACTCCCCAA AAGCTCCTTC GTGAAACCAT 1080 GTGCTGCATC ACAACTCTCT GTCAATGGTT CTGTCTCCCC CAGAGGACTG 1130
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