Tag | Content |
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EnhancerAtlas ID | HS048-36677 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr8:145993760-145994590 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr8:145993963-145993984 | CTTTCCCCTTCTTTCTCCCTC | - | 6.29 | ZNF263 | MA0528.1 | chr8:145993960-145993981 | TCCCTTTCCCCTTCTTTCTCC | - | 6.32 |
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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 |
GH08I144766 | chr8 | 145992150 | 145994409 |
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Enhancer Sequence | CCAGCCAGAG TCTGAACCTT ACAGGCATGA GCACTGCACC CAGCCAGAGT CTGAACCTTA 60 TAGGCATAAG CCCCTACTCC CAGCAAGAGT CTGAACCTTA CAGGCATAAG CCCCTACTCC 120 CAGCCAGAGC CTGAACCTTA CAGGCATGAG CACTGCACCC AGCCAGAGTC TGAACCTCTT 180 AATCACCTTG CACTCTTTTC TCCCTTTCCC CTTCTTTCTC CCTCAGCCAT GACTCACCCT 240 CATCCCTCCC CACCCCGGAC ATAGTTTTAT CTTTAGAGCC CCTACCTATT CCACCATCCT 300 GGGCCTTCCT ACCTGGTCCA GCTGAATCTC TCTGCCTGCT CTCTGCAGAC CGTAGGCTTT 360 GGTTCTCAGC AGAAATGCAC GTGTTGTGTT TCCATCTCTG CCAGCAGAAT TTTCAGGCCT 420 CAAACCTGAC CTGATCTTCT AGCTGGAGAG AGAGGAAGAG CCATGGCTGC CAGATGTTCC 480 AGGGACTGAA AATACAGACA CACAGAGATG CTCCTTCCCA GGTGAGAAGA GGGAAGCAGT 540 TCTGGAGGAG GCAGTAGTGG GATACATTAG GAGACATAAC CTGAAAAAAC AGAGCCAGGC 600 GGCTGCGCGC GGTGGCTCAC GCCTGTAATC CCAGCACTTT GGGAGGCAGA GGCAGGCGGA 660 TCACAAAGTC AGGAGACCAT TCCAGCTAAC ACGGTGAAAC CTCGTCTCTA CTAAAAATAC 720 AAAAAATTAG CTGGGCGTGG TGGCAGGCGC CTGTAGTCCC AGCTACTCGG GAGGCTGAGG 780 CAGAAGAATG GCATGAACCC AGGAGGCAGA GCTTGCAGTG AGCCGAGATC 830
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