Tag | Content |
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EnhancerAtlas ID | HS103-04113 |
Organism | Homo sapiens |
Tissue/cell | HUES64 |
Coordinate | chr11:44488400-44489880 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFYA | MA0060.3 | chr11:44489627-44489638 | GGCCAATCAGA | + | 6.02 | ZNF263 | MA0528.1 | chr11:44488703-44488724 | GGGGCAGGGAGGGGAGGGATA | + | 6.22 | ZNF263 | MA0528.1 | chr11:44488712-44488733 | AGGGGAGGGATAGGGAGGGGA | + | 6.39 | ZNF263 | MA0528.1 | chr11:44488856-44488877 | TGAGGAGGAAGAGCTGGGGAA | + | 6.55 |
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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: 2 | ID | Chromosome | Start | End |
GH11I044467 | chr11 | 44489081 | 44489250 | GH11I044468 | chr11 | 44489581 | 44489750 |
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Enhancer Sequence | GGGACGTCCT TCATGCCAGA AAGAAAGAAC GAATGTGTTT TCTCTGCCTG TTGAAAATGA 60 TTCCGAGCGA AGGGCTGTGC TTCCTGGCTG GCGCGAGCCT GACTCTGCTG TGTCAGAAGA 120 TGATCTTTCA CAGATGCTGA AAAGTTAGGA AGTGTAATTA TGGGGAAATT GCGCTCAGGC 180 AAACGAGTAC AAGCCAAGGG CTGCCAGGCC CCATTCCTCA CCTGAACGCC CTGATTGTGG 240 CCGACAGCCC CACATCTGTA TGTGCTTTGC AGCCAGAAGA GGAAAGAGAG GGGAAGCAGG 300 AATGGGGCAG GGAGGGGAGG GATAGGGAGG GGACCTGGAG CCACCCCTGC CAACGGCTCC 360 CCAGCTTCCT CGGGGAGGAG CTGAGGGAAG GCTGAGGCCT GGGGCACATT CCTGAGTTCC 420 GAGGGCCTTC TGGGGCGCCC TCATTCTTGG GGGCGATGAG GAGGAAGAGC TGGGGAAGAC 480 CAGCAGAGCT GAGGCCACTT CTATTCTATC CTTTTCACGT TACTGGTGAG GAAACTGAGG 540 CTGCAGATGG CCAAGGGGCA CACAGTGAGT TAACAGTGCA GGCAGGATAA GATCCTCCAC 600 CTTCTGACCA GCAGGGGCTC TTGCCAGAAC CCCTGAGGGG CAGGGTGGGA GGGACAAATA 660 AGGGGCAGAC CTGGTGAGCA GCAGGATGCC CCTGCCTCCC AGCCAGCATC TGGTACCAGC 720 CTTTGGGGTA ACTCTGACCA CTGGGCAGCC TTGGCATTCC TTAAATTCCT GGCTTTCATC 780 CTCCCACCAG GGCTCCTGCC CCATGGCCCC TCTCTGCTGG GACAACTGGG ACTCCTCTCA 840 GCAGAGGGAC CTGCAGCTCC TCCTTTGCTC TGTTTTTTTC CCACTGGGCC CCTTCCCTCG 900 CCTCTCCTTT CAGCTCCTGG GATAGCCCAG AGCCTGGAGC TGCCCCCTCT TGTTTAAACC 960 CTCCTGGGCC AACTCAAGGG CACCCTGATG CCCTCTGCTC CCCGCAGGAT GGGCACTCCC 1020 TCCCTCCCAC TCCTTGGCCC TCTCCTGGTC TATGGAAACA ATTCTTCCCA TTGGGCACTA 1080 AGTTTGCTCC CCACCTCCAT GCTTCTGGAA ACAAGCCGCC CTGCCCCCGA GCCTCAGAGG 1140 AGGTACAGGC AGGCCCAGGC TGGATAATTA TCCCAACGTC CTCCTGGCCC CAGAAATTGA 1200 GTCAGGGAAG GATGTGTGAC TCCACAGGGC CAATCAGAAT TCTTCCCTGA GAAGGACACT 1260 GGGAGCAGGA AGCTGGCTTC AGTCCCTCTG CAGCTGATAG ATTGGGAAGC TGGAGGTTTG 1320 GAAATCCAGC CTTTTCTTTA TCCTGTAAAG TAGCCCACCT GCAGGAGGTA AGAGTGACGC 1380 ACACAGAGAG TTAGAGGTGG GAGCGGGGCA TGAAGAAATG ACTGATTGTT AGCATTTTTG 1440 AACTCTGGAT TTAGTCCTGT CTTCATCCCC ATACTTCCCA 1480
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