Tag | Content |
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EnhancerAtlas ID | HS150-02646 |
Organism | Homo sapiens |
Tissue/cell | NT2-D1 |
Coordinate | chr12:6372960-6374370 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxd3 | MA0041.1 | chr12:6374112-6374124 | AAACAAACATAC | - | 6.37 | HSF1 | MA0486.2 | chr12:6373811-6373824 | TTCCAGAACTTTC | + | 6.29 |
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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 |
GH12I006263 | chr12 | 6372803 | 6374370 |
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Enhancer Sequence | AGCAGATTGT CCTCTATGAT GTGGATGGGC CTCATCCAAC TCGTCAAAGG CGTGAAGAGA 60 ACGAGAGACT GACCCCCCCA CAGCAGGAGA GAATTCTGTG GTGAACTGCA AGAGGGGGTC 120 TTCCCTGGGT CTCCCACCTG ACAGCCTACC CTGCAGACTG GGACCTCACC AAGACTCCAT 180 AACCCACGAG CCAATTCCTT AAAGTAAATC TCTGAATATA TACATATATA TGTCTACACA 240 CATGCACACG CGTATCTTAT TGGCTGTTCC CTGGAGAACC CTGACTAACA CAGCCCCTCA 300 CTGTGGCCAG CATGGGCCGG TGGTTAGTCA AGGTCACTGT CTCCAGGGCT GTTGTGAAGC 360 TGAATGGAGA TCAGTTTTGC ACAGAAACAT GTGAGGTCTT ATCAGCACTC CCAGCCTCCC 420 TGCTAGCAGG AGGGAAGCAC TGTAATCTGA TTCCCAAGCA GCTTTAGAAA GGTACCTCTG 480 TGGTACAGGC CACTCCATCT TCATAAGCAG CTTCTCTGAT TGCTGTTCTG CTGACCAGGG 540 GCAGGCTTTC TTGTGGGTGC AGGATTGCTG GCTGAAACAT CACCCTCTGC TTCCTCCAGG 600 AGAGAAATTC CCAGCTATAT CCAAATGTTC CAGAGTATAA AACCTGAGAC GCTTCCATCA 660 AGCTAAAGTG GCTTAAACAG GGAAGTGGCC TTAGAAATGC CCTGGCCAAG GCTCCTGTTT 720 TGCAGATGGG AACAGAAGTG CACAAGGCGG AGGCCATTTG CATAAGGACA TTGGCAGCAG 780 CAGCAGAAGC AGGGCCCACT GGCGTCGTGC CAGCCCTTTC AGGTAACTTA GGTCAATGAG 840 AAACAAACAG GTTCCAGAAC TTTCTCTAGA TCATACTGCA GCAGGTGCTG AAGTGGGGAT 900 TTGAACCAGG TTCACCACAC TTTGAAACCC ATGCTCTCTT TACCACCGCT TGAGACACCC 960 AAACACACAC ATGTATCGGC ACGGCTACGT CTCCCGGTCT GTTTCCAGTT TCACGTTCCT 1020 CCCTCCTGGG CCAAACCACC ACTGGGGACT CTTTTCTTCC TACAGCTCCA GGCAGCGCTG 1080 CATCATGGAA AGGTCACTCA GCTCACATTC ATGACATGCT TTCTGTATGC AAGGCAGATC 1140 AGATCTAAGG GCAAACAAAC ATACCCAAAC CCAGGGGACT ACTGAGCACA GACAAATAAA 1200 TAAGCAATTA CAGTACAAAA CAAGAAGTGA TCAAGAGATA CATAAGAGGA CCCAAGAGCC 1260 CTCAGAAGGC CACTTACACT GCAGGAGGGG CCTTAGGAAA TACTTCCCTG AGAAAGTGAC 1320 ATTTAAGCTG AGACCAAGGT ATTAATACTA CAAAGGAGTT ACCTAAGGAA GGAAGACAGG 1380 GGGTGAGGGA GGGCCATCCA CACAGGCTCT 1410
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