Tag | Content |
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EnhancerAtlas ID | HS184-02656 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr1:223350980-223351980 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr1:223351779-223351800 | AGGGGAGGCTGGGGAGGAGGG | + | 6.64 | ZNF263 | MA0528.1 | chr1:223351782-223351803 | GGAGGCTGGGGAGGAGGGAGA | + | 6.77 |
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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 |
GH01I223176 | chr1 | 223349824 | 223351742 |
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Enhancer Sequence | GGGTCCTGGT GGCCCCACAA CATTCTAAAT CTTTTATATG TGAAGGTCTT ACTCTGGCAT 60 TGGAAGCTTG CTTTCCAAAA TTATAATAAT GACAATCACT AACATTTAGG GAGCACCCCA 120 GATCCCCACT GAGGCTTTAT ACATGCATTG CCTCAACCCC TTGAGGCAGG TACTGTCATC 180 ATGCCCGCAG TGCAAGAGGT GAGAGAACTC ACCCAAGGTC ACAGTGAACA AACAGCCCAG 240 CTGGAACTTG AGCTTGGCTT GTCCCTAAAC CCGCCAGTGC TGTCAACCAC TGTATTCTGG 300 GAATTTGAGG AACAAGGAAT GAGGAAGTGG CAGACAGAAA ACGGTGCTCG AGTCTGGGGA 360 CATTCTGAAC ACTTTCAGGG AGGCCCAATA AGAAAAGAGA AATGCAGACA AATGAAATAA 420 AGCAGAGGCT GGGAAGCCAA CGCCCACAAC ACGACCAAGA CCCCAAGTTC CCAAAGAAAG 480 TGCTTTATTA TTTTCAAAAT AGCAATGTGT AAAAACGGCT TTTGCAGAAA AGAAGACAAA 540 AAGGCTAACC TTTACTGCAC CCCCAATAAT GCCAATTCCC CAGCCCTAGC CCAGCAGAAC 600 CGTGGGAAAG CAGCCTTTGC TGTATGTATG TAGGCTTTCA CTCAGGACAG GTAGATTTTT 660 CATAATGACT TTGCTTTTAA TCTAGGGAAG AGTGTAAAAT TGCACAGCAA GTCTTGGGGA 720 CTCTGACAGC CCAGTGGACC AGGAAGGAAT CTCCATCCAT CTCTGGGAGT CTCTGGGGTC 780 ACAGGGAGCC TGTAAGCCAA GGGGAGGCTG GGGAGGAGGG AGAGCGGCTG GAGAGATTTA 840 TACATAGTGC TGTCCTCCCC CTGCCTTGGA ATTACAGCAC CATGAGAAGC TGTGAGATTA 900 AATGAAGAGC AGGGCCCTGG AGAAGCTAAA GCATCAGTGG GAACAGGGGG TGCAGCAGGT 960 GATAAGCGGG AGATGCAGGT TAATTATGAT GCTGGCACAC 1000
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