Tag | Content |
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EnhancerAtlas ID | HS049-03150 |
Organism | Homo sapiens |
Tissue/cell | Fetal_spinal_cord |
Coordinate | chr17:5000210-5001310 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Ar | MA0007.3 | chr17:5000807-5000824 | AAGAACACCATGTACTC | + | 6.81 | Ar | MA0007.3 | chr17:5000807-5000824 | AAGAACACCATGTACTC | - | 7.2 | NR3C1 | MA0113.3 | chr17:5000807-5000824 | AAGAACACCATGTACTC | + | 6.8 | NR3C1 | MA0113.3 | chr17:5000807-5000824 | AAGAACACCATGTACTC | - | 6.94 | NR3C2 | MA0727.1 | chr17:5000807-5000824 | AAGAACACCATGTACTC | + | 6.39 | NR3C2 | MA0727.1 | chr17:5000807-5000824 | AAGAACACCATGTACTC | - | 6.49 |
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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 |
GH17I005096 | chr17 | 5000210 | 5001530 |
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Enhancer Sequence | AACTTAAAAA AAAAAAAAAG ACCGAGTCAC TTCCCCAATA ATTTCCTCTT CACCGCACCC 60 CTCAGCTTTT GGAATGAAGC TATGTCAAAA AGACCTGCCT GGGTGAACCC CTGCAAATGG 120 AGGTCAGCTG GACCTCAGTA AAAGCCCAGT GGGAAGGAGC GGGGACGATT CTGGCGATCA 180 CATGAGGAAG GGAGCAGCCT CAGCAGCGCA GGTGGACACA GTCGTCAACC ACTCGCTGGC 240 CGCCTGCGAC GTGAAGCACC TGCGCTGGGC GCGGCGGGTA AGCGCCGACA CTAGCGGGCG 300 CCTGAACAGT CCAGCGGCGT CAGCGCTGCG GAGCAGGAAA GGGTCCCAAA CGCAGGGCGG 360 CCATGCAGCG TGGCGCCCAC CTGTCCCTCT CCTCGAAGCG CTGAGCCAGC ACGATGCACA 420 TAAGGGAAGG AGGAAGGTGG CTTGAGGGCA GTGACCGAGC GGACAGCGGA AGCCCATTTC 480 AGGAGCCCCG GTACCCGAGC TCGGGCCCCT TTCCAATCCC CCAGGCGTCC TTCCCATGTC 540 CTTGTCTCCT AGTCCTGGGA ATCCACGGCC ACTCCACTCT CCTGCAGTAC CGCGGACAAG 600 AACACCATGT ACTCTTCACA GGCAGGTGTC TTCTGGTGGA CCCAACTCTG TTGGTACTTG 660 TCGTCTCCAA AAAGTCCCCA AATGCGCTAG AGGCCAGCCA GCCCGGTATC CGAGAGGTAA 720 GAGCCCCGGC GGCGCAGGCG GAAGCGTGTC TGTCGCGAGG CCTCTCTAGG ACTCCGGGAG 780 GACCCCTCGT TAGCGCAGGA CCTCGGCAGC CGGGGGTTGG GCTCGAGGGC TGAGGGCGGC 840 GCGCCATGCG CGGATTAGCT GCCATCCGGC GGGTCTTTCT GCCGGGGACC AGTGGGGTCG 900 GACGCTGAGG GCCGAGGAAC CCCGCCCCCC CACCGCACCG GGCGGGCTCT GGGGCGTCCG 960 CGGAGGCTCC CGCGTGCGTG TGCGGGGTGG GGTCGGGGTG GCAGTTGGGG GCAAATCAAT 1020 GGGCCTGTAC TTTTGTCTCT CCGCCTGCTG GGATTTGCAG TTTGTGAGGA CGTTTCACAT 1080 CTCACGGATA TTTACGGAGT 1100
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