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EnhancerAtlas ID | HS176-39054 | Organism | Homo sapiens | Tissue/cell | SK-N-SH | Coordinate | chr8:155180-155760 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
DBP | MA0639.1 | chr8:155182-155194 | CATTACGTAACA | + | 6.37 | HLF | MA0043.2 | chr8:155182-155194 | CATTACGTAACA | + | 6.92 | RREB1 | MA0073.1 | chr8:155533-155553 | CCCAACCCCAACCCCAACCC | + | 6.16 | RREB1 | MA0073.1 | chr8:155681-155701 | CCCTACCCCAACCCCAACCC | + | 6.16 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TACATTACGT AACAGTGTAA TACAAATAAT AATTTATTAT TAGTAATAAT GTGAAATTAT 60 TTACAGTACC GTAACCCTAA CTCTCACCCC TAATCCTAAC CCTAACCCTA ACCCCTAACC 120 CTAATCCTAA CCCAAACCCT AACCCTAACC CAACCCTAAC CATAACCCAA CCCTAACCCT 180 AACCCTAGCC CCTAACCCAA CCCTAACCCA AACCTAACCC TAGCCCCTAA ACCTAAACCT 240 AACTCCTAAC CCCTAACTCC TAACCCTAAC CCTAACCCTA ACCCTAACCC CTAACCCTAA 300 CCCCTAACCC CTATCCCTAA CCCCTAACCC CTAACCCCAA CCCCAACCCT AAACCCAACC 360 CCAACCCCAA CCCGACCCTG ACCCCGACCC CTAACCCTAA ACCCTAACCC CTAACCCTAA 420 CCCTACCCCT AGCCCGAACC CGAACCCGAA CCCTAACCCT AACCCCTAAC CCTAACCCCT 480 AACCCTAACC CTTAACCCTA ACCCTACCCC AACCCCAACC CTAACCCCTA ACCCCTAACC 540 CTCACCCTAA CCCTAAACCA CATGAGCAAT GTGGGTATTA 580
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