Tag | Content |
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EnhancerAtlas ID | HS049-05101 |
Organism | Homo sapiens |
Tissue/cell | Fetal_spinal_cord |
Coordinate | chr20:62405720-62407030 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr20:62406662-62406681 | GGGCCGGCAGGGGGCGCCC | + | 6.26 | Sox3 | MA0514.1 | chr20:62406355-62406365 | CCTTTGTTTT | + | 6.02 |
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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 |
GH20I063774 | chr20 | 62406224 | 62407667 |
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Enhancer Sequence | CGTAAAGAAA CAGAGAAACA GATATACTTC CCAAATCCCA GCATCAAGGA CAGCTGGCAC 60 GTTTCCTTCC TTCACTTCCC TCAATACTCA GCAAACAATG TGTCCACACC ACTCAGCACG 120 CCTGGACCCC AGCCGCGGAG GTGGGGGCAT CTCATGCCGG ACTCGCTCCC TCCTCCCCTG 180 GAGAGAAACG GGAGGCGCCT CACTCACTCT CAGCCGCATG CTGAGTGCCA GCTATGTGCT 240 AGGTGCCAGC ACCAGGCCTT GCCCGGGGGC CCACATGAGC GCGAGACCAG AAGGCAGCTG 300 GCTGGGGGCT GGCTGCGGTG GGTTTTTTTT GTTTTTTTTT TTGTTTTTTT TTTTGAGACA 360 GAGTCTCCCT CTGTCGCCCC GGCTGGAGTG CAGTGGCGCG ATCTCGGCTC ACTGCAAGCT 420 CTGCCTGCCG GGTTCACGCC ATTCTCCTGC CTCAGTCTCC CGAGTAGCTG GGACTACAGG 480 CGCCCGCCAC CACGCCCGGC TAATTTTTTG TATTTTTAGT AGAGACGGGG TTTCACCGTG 540 TTGGCCAAGA TGGTCTCGAT CTCCTGACCT CGTGGTCTGC CCGCCTCAGC CTCCCAAAGT 600 GCTGGGATTG CAGGCGTGAG CCACCGCGCC CGGCCCCTTT GTTTTTTTAA ACTCCGAAAG 660 CTGAATGCCC CCGTCTTGTC AGGAAGTCAG TCAGTCTGGG GTGAGCCCGA CACGCAGCAG 720 TGGCTGAACT TTTGGCCACA TCTCGGCAGG CGCGTCGTCG TTTGGATTCA GCTGGGGACA 780 TTTACGTTTT AAAGACAACC TCCGACGCAT CTTTAAAAGT CACACGCCAC CAGCATCATC 840 CAGCGAAGGC AACGCAAGGC GAGGCCCCCA AGTGCAATCG GCTCGCAGCG GCCGCCCCCA 900 TCTCCCTTGC GCGAAACGAG CCTCAGCACG AAGGCGACAG AGGGGCCGGC AGGGGGCGCC 960 CGAGCCCGTC TCTGGAGCAC AAAGACCCCC GGCCCCTGCG CGACCCGGAC GAGCTCGCAT 1020 TCAGCCAACG ACTCCTGTGA GAAACATTCC AGCAAGCACT CGGCTGCTCC CCTGCCCGCC 1080 GCGCTCACAA CCGCGTCCAT TCCCTCCTCA CTCTAAAGCC AGCCCCCCGT GCACCTGAGA 1140 GGCCAGTCCA GGCTGTGACG CCGCATCCTC ACCTCCCGCA ACAGGGAGGT CAGCAGGCGG 1200 CCGAGCAGCA GGGACAGACC CTCAGCCTCA TCTCATCTTG GCCCGGGACC TGCAACCCTC 1260 AGCCTTCAAA ACCACACCAA AGCCAAGCGG CCCCCAGGGC CTGCACTTAC 1310
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