Tag | Content |
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EnhancerAtlas ID | HS095-06404 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr11:129185380-129186860 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr11:129186473-129186494 | CCACCCTTCACCTCCTCCCTC | - | 6.26 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr11 | 129185429 | 129186371 | chr11 | 129185478 | 129186400 |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I129314 | chr11 | 129184794 | 129188129 |
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Enhancer Sequence | AGTGGAAGAG AGTGGGTGTG ACTGAAGCCA GCCCCGATGT CTGGAGAGAG GCTCTGCAGT 60 ATCTGGTCAG GTCTTGTTCT TTTAAACTGG ACCATCCAAG ATGACACCAG GAAGTTAGCC 120 TTTGGTAAGA ACGAATGTTG CCCAGCCTTG TTCCAGCCTT CCTCCTGGGT CTTCACTCCC 180 TTGAGACTTC CTTTCCATCT CCTCGCTCAT TCCTGGTCCC ACAAGCTCCT GCCCTCTGTC 240 TTCACATCCT GTGATGACCT CAGGTTCCTG CAGGACTGAT CTCAGCTTGC CTAGCTTAGC 300 CCACGACTGG CCCTTCAAAC ACGGTCAGCT CAGCAGGCCC AGGCTGGCAG AGAAAAGCCT 360 GTGGCAGACA ATAGTGTTTA TTCTAGGCAG TTGTCCCAGA TGGGTCACTC CCAGCTTACT 420 CCACACCTGC TGCTGCTTGC TGTTTTTCCC AGGATCTGAA TTCCTCCTCC CCAAGCACTG 480 GCTAGGGGGC TCCCTCTCGC AGCCCTGCCC AGAGTCACTC AAGGGGCTGG ACCATCCTCA 540 GTCCTTTAGC TGAGAGAGGA GAATGTCATC AGCAGGCCAG ACATGATTTA CAGCTGTCCT 600 CTCATTCGCT TCTGCTGCCC CAGGTAACAG AGGCTCCGGA TCAGGGCCGT CGCTGGGCTC 660 CACCCCAGCA CTAACCGGCT CGGCCAGGTT TACCTCACCC CCTTCAAAAA GGATGGTGTG 720 AGGAATGCAT GTCCTGCCCC AGGAAGACGG ATCTGTTCAG GAAGAAGAGG ACAAAGGGCA 780 GGACTTCAAA GCAATTTGGG CCACAACACT GGGCTTCTGG CTCCTGTGTT GAGGGGAAGA 840 GAGTGGGGAG AGGTCGGACC AGCATTCAAC TCACAGGCTC TTCCCAGCTT CCATCCCCTT 900 TGCCCTGGAG CTGCAGAATT TCCTGACCCT GGAGAAGGCA CCTGCCAGTG CAAATCCCCA 960 GCACAGGTTC TGGAAGCCAT GCTGCTGTTT GCCCTGCACA GCCTGAGCCA TGGCCCCTCT 1020 GCCTAGGGTG GGCTTCCGGG GGAATGAGGC CTCTGAGCTC CCCCCTGGGG CCTCCACCTC 1080 CCCACTTACT CAGCCACCCT TCACCTCCTC CCTCTCTTGT CTCATTGAGA CCCCTTTCTT 1140 TCCTTTCCAG GGATGATTAT TTTTCAATCA CGTAGACTTG GAGATAAAGG AAGAGTAAGG 1200 GCAGAGAAAG GCTGGGGCAT GAGCAGCTGA GGGCAGGGGT TAAGAAGGTG GCAGTAACAG 1260 AATAAAACCT GAGTCTGTCT TTAAACCTCC AGGCCTGAGG CCACGTTTGG AGGGTGGGGG 1320 TCTCACTTCA GTTTTTCTGT AAGTTTTTCT GAAAGTCTGA TTATTCTGTT CCACCCACAG 1380 CAAGACGGGG AGCTTCAATC CCAGACGCTT GTGGCGATGG GAGTGGGGAG GAAGGATAGG 1440 ACTTAGGAAC TTCTTGCTGG GCATTTGCAT CTGTCTATAA 1480
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