Tag | Content |
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EnhancerAtlas ID | HS074-00093 |
Organism | Homo sapiens |
Tissue/cell | GM19239 |
Coordinate | chr1:11025000-11026410 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr1:11025700-11025715 | GAGGTCAGAAGCTCA | + | 6.15 | RARA | MA0729.1 | chr1:11025700-11025718 | GAGGTCAGAAGCTCAAGA | + | 6.01 | SPIB | MA0081.2 | chr1:11025389-11025401 | AAAGGGGAAGTG | + | 6.07 | ZNF263 | MA0528.1 | chr1:11025271-11025292 | AGAGGAAGAGAAAGAGGAGGA | + | 7.36 |
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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 |
GH01I010964 | chr1 | 11024590 | 11026962 |
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Enhancer Sequence | TGAGACATAA AATTCCCATT TTACAGATGA GGCAGTTGAG GCTTAGAGAA GGTAAATGAC 60 TAAGCCAAAG GCATGTGGCC ATTTCTGAGA CTAGATGTGA GAGCTGGTCT AGCTCATTCC 120 GGTACAAGGC GGACTTCAAA GATGTCAAAC CAATGGGTCC CTCTGCCCCT CCCAGGCTGC 180 CCTCATTCAG CCACATAAGA AGAACCCAAG TCTAAGCTTT GCGGTGGGGC CTGAGAAGGG 240 TGACGGGGCT GTCAGAGAAG GGCGACCACA GAGAGGAAGA GAAAGAGGAG GAGCAGGGTA 300 GTTCCCAAAA TTCCTTCCCC CACTCCAGAC CACAGCCCCA CTCAGGAAAA ACTCTGGACT 360 GGGTCAAGGA AGGGAGCACA AAGAAATGGA AAGGGGAAGT GGAGGTGAGG AAAAGACAAG 420 AAAAAAAAAA CTGTGAGCCA AACTGTGCGG CTGGTTGTCC CCTTGCAGGA CCCCTGGAGT 480 GAAATTTAAG TAACAAGAAT GCTGGCACAG TGGCTCATTC CTATCATCTC AACACATTGG 540 GACACCGAGG CGGGAGGATG GCTTGAGCCT GGGAATTCCA GACCAGCCTG GGCAACATGG 600 TGAAACCCCA TCTTCTACAA AAAGTACAAA AATTACCTGG GTGTAGTGGT GCATGCCTGT 660 AGTCCCAGCT ACTCTGGGGG CCGAGGTGGG TGGATCACTT GAGGTCAGAA GCTCAAGACC 720 AGCCTGGCCA ACAAGGTGAA ACCCCGCCTT TACCAAGTAG TCTCAGCTAC TTCAGAGGCT 780 GAGGCAGGGG AATCGCTTGA ACCTGGGAGG CGGAAGTTGC AGTGAGCCGA GATTGCGTCA 840 CTGCACTCCA GCCTGGGTGC CAGAGCGAGC CTCCGTCAAA AAAAAAAAAA AAAGGAAAAA 900 GAATACAAAA ATATCTTGCT TCTGTAAATT TTAGAGTCAC ATGGTCTCGT GAGCCCATAA 960 TGGGCCTGTG CAAGTGAGGG CTGTCAGTCA GTCTTTGCAA CTCCTCAGCA CCATTTATTC 1020 ACTTCATTCA GCACTTACTG AGTACCTACT GTGTGCCAGG CCCTGAGGCA AGCCTGTGGG 1080 TGTGACTGCC TCACCCCAGA GACTCCAGGT CCAGCAGGAT ATGGTGTGTG AGTGGGCACA 1140 TTATGAGTCA GTGTTGGCAA TGATAGAAGC AGGTCTACTG CACAGAGAAG GGGGGATTCT 1200 CAGGAGGACT GCCTGGAGGA GGCAGCATCT GAGCTGGGCG GCCTTTTAAT ATCTATGCCC 1260 ATAAACTCCA TGAGGGCAGA GACTTCTGGT CTCCCTCAGC TCAGTTTCTG CAGAGGAATA 1320 ATGGTGCAGT GTCTCCTTAC TTGATATCTG AGCTCAGGCT TAGCTCCTTA AATCTCCCTT 1380 TAAAAAAAAA AAAAGAAAAG TTTCCCAAAC 1410
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