Tag | Content |
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EnhancerAtlas ID | HS049-01164 |
Organism | Homo sapiens |
Tissue/cell | Fetal_spinal_cord |
Coordinate | chr10:125726100-125727570 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr10:125727364-125727383 | GCCTGCCCCCTGCTGGCTG | - | 6.55 | RREB1 | MA0073.1 | chr10:125726254-125726274 | CCCCACCCCATCCCCCCACT | + | 6.13 |
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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 |
GH10I123967 | chr10 | 125727241 | 125727470 |
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Enhancer Sequence | GAGGTGGGGG CCTGCACAGA ACCTGGGGGA GCAAACCCTG GCCTCAGACA TGAAGTCTGA 60 CAAAAGAGCC TTGTGTGGTG TAGGGCTCAG AGTCCAGTTT CTTGTGCTGA GAACCAAGTG 120 GAGGATCGCG TGTCTGCCTA CCCGCCCCAT GTCCCCCCAC CCCATCCCCC CACTGAGCGC 180 CCACTGCTTG CATCGGGGCC ATCAGGAATA GCAGTGAGGG GGGCTCTGTG GCTCCCTGGA 240 GCTCTCAGCC GCCTTGCATA TCTCCAGGGG CTTCTGGAAT GGTCTGGATC TGTATACAGT 300 TTCAGGGTTT CCTTGCTTTT CCAGTCTGAG ACTGAAACTC ATCCTCTAAG CATTTGAAAG 360 AAACAACAGG AAAACTCAAT CCTCTTTCCT TCCACAGCAC ATTTAGGGTG AGAGCTTCAC 420 AGCTGAAAAT CTCCTTTAAA GAAAACGCGG CCCAAATATG CTGGGAGGAG AAGCCAGTGG 480 ATCTAGGAGG GGCCGGCGTT GCCGGCTCTG TCTCTGGGCT GACAACCTGG TTTCAGTATT 540 GGTAAGTGGG TCAACCCCAG CTCCAGCGGC TCCTCCTCAC CTCTGCCGAT TGAGGGCCAC 600 TGCAAATTTC AAGCAGAATA AAAGAGTATT CTGAGGGCCA CTGCAAATTT CAAGTAGAAT 660 AAGAGTATTC CACAGTTAAA GAAAATTTTA TATATCTATA TCCATCTCGC ACAGATTACG 720 TACTAGGCCT TCGTCTAAGC ACTTCTTAAT TATTAACTCA TTCAGTCCCA TTTTACAGAT 780 GACAAAACTA CCAAGTGGAG AACCAAGGTC ACGTTGCTAC TAAATGGCAG AGCCAAGAGT 840 TGAGGCCAGG CTATCTAGGT AGGACCAGGA CCCAGAGTGG AGGGTGGGCC CAGGGCTGCC 900 AGGTGGGCTC AGCGGGCCTG GAGCTGGTTT GAAACACAGG CGCTGCGGTG ACCAAGTGAG 960 CTGGCCCTGA AGGGCAGCGT GAGGGAAGAA GCCAGACCCC CCAGCCAGAG CCCCAGCCCT 1020 CAAGGGACAA CTTGGCCAGG ACAAGCTACT GGAACAGGCC AGGGCCCTTT TGGCGGGGAA 1080 GGGAGAACTG GACCACCCGG CCGAGAATTC CAGAGACTTT TCTCACTGAT GGGAAGAAAA 1140 CTGGGTCCCG GTAGGGGCCA GTGGGGAACG GGGCTTTGAA GGAACTCAGG ACTCAGGCGT 1200 CCTTGGGATC ATCTCGGCAA ACTGCAGGTC TCCGGGGAGC CGCTCCGGTG CATTCCCAGG 1260 TCCAGCCTGC CCCCTGCTGG CTGTGTCGGG GAACCAAACA CAGGCGTCAG CCTCATCGTG 1320 CAAAGGTGGA CTTCTGAGTT CTCAGATACC CCCGTGAAGC CCACGCTAAT AAACTGGGAA 1380 TGACACGTCA CAAAATCAGT TATAGAGTGC TGCTGATACA GTCATCATTC ATTCTAACCA 1440 CGTATTTAAA CCGAGAAGAT TGCATGTATG 1470
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