Tag | Content |
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EnhancerAtlas ID | HS175-00164 |
Organism | Homo sapiens |
Tissue/cell | SK-N-MC |
Coordinate | chr1:11025160-11026410 |
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 | CTCTGCCCCT CCCAGGCTGC CCTCATTCAG CCACATAAGA AGAACCCAAG TCTAAGCTTT 60 GCGGTGGGGC CTGAGAAGGG TGACGGGGCT GTCAGAGAAG GGCGACCACA GAGAGGAAGA 120 GAAAGAGGAG GAGCAGGGTA GTTCCCAAAA TTCCTTCCCC CACTCCAGAC CACAGCCCCA 180 CTCAGGAAAA ACTCTGGACT GGGTCAAGGA AGGGAGCACA AAGAAATGGA AAGGGGAAGT 240 GGAGGTGAGG AAAAGACAAG AAAAAAAAAA CTGTGAGCCA AACTGTGCGG CTGGTTGTCC 300 CCTTGCAGGA CCCCTGGAGT GAAATTTAAG TAACAAGAAT GCTGGCACAG TGGCTCATTC 360 CTATCATCTC AACACATTGG GACACCGAGG CGGGAGGATG GCTTGAGCCT GGGAATTCCA 420 GACCAGCCTG GGCAACATGG TGAAACCCCA TCTTCTACAA AAAGTACAAA AATTACCTGG 480 GTGTAGTGGT GCATGCCTGT AGTCCCAGCT ACTCTGGGGG CCGAGGTGGG TGGATCACTT 540 GAGGTCAGAA GCTCAAGACC AGCCTGGCCA ACAAGGTGAA ACCCCGCCTT TACCAAGTAG 600 TCTCAGCTAC TTCAGAGGCT GAGGCAGGGG AATCGCTTGA ACCTGGGAGG CGGAAGTTGC 660 AGTGAGCCGA GATTGCGTCA CTGCACTCCA GCCTGGGTGC CAGAGCGAGC CTCCGTCAAA 720 AAAAAAAAAA AAAGGAAAAA GAATACAAAA ATATCTTGCT TCTGTAAATT TTAGAGTCAC 780 ATGGTCTCGT GAGCCCATAA TGGGCCTGTG CAAGTGAGGG CTGTCAGTCA GTCTTTGCAA 840 CTCCTCAGCA CCATTTATTC ACTTCATTCA GCACTTACTG AGTACCTACT GTGTGCCAGG 900 CCCTGAGGCA AGCCTGTGGG TGTGACTGCC TCACCCCAGA GACTCCAGGT CCAGCAGGAT 960 ATGGTGTGTG AGTGGGCACA TTATGAGTCA GTGTTGGCAA TGATAGAAGC AGGTCTACTG 1020 CACAGAGAAG GGGGGATTCT CAGGAGGACT GCCTGGAGGA GGCAGCATCT GAGCTGGGCG 1080 GCCTTTTAAT ATCTATGCCC ATAAACTCCA TGAGGGCAGA GACTTCTGGT CTCCCTCAGC 1140 TCAGTTTCTG CAGAGGAATA ATGGTGCAGT GTCTCCTTAC TTGATATCTG AGCTCAGGCT 1200 TAGCTCCTTA AATCTCCCTT TAAAAAAAAA AAAAGAAAAG TTTCCCAAAC 1250
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