Tag | Content |
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EnhancerAtlas ID | HS038-04862 |
Organism | Homo sapiens |
Tissue/cell | ESC_neuron |
Coordinate | chr12:67813180-67814090 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nfe2l2 | MA0150.2 | chr12:67813823-67813838 | CACCATTACTCAGCA | + | 6.05 | RFX2 | MA0600.2 | chr12:67813714-67813730 | GGTTTCCATGGGAACG | - | 6.3 | RFX2 | MA0600.2 | chr12:67813714-67813730 | GGTTTCCATGGGAACG | + | 6.41 | RFX5 | MA0510.2 | chr12:67813714-67813730 | GGTTTCCATGGGAACG | + | 6.21 | RFX5 | MA0510.2 | chr12:67813714-67813730 | GGTTTCCATGGGAACG | - | 6.42 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr12 | 67813214 | 67813319 | chr12 | 67813345 | 67813954 |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I067419 | chr12 | 67813641 | 67813890 |
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Enhancer Sequence | AAAGGGTTTG GGGCTTTCAA GAGCAGTCCA CTACGGGAAG GTAAATGCAT GGGGAACTCT 60 TGTGGAAGCC AGGGGCTATC TTGGCAAGGT GTGTGTGTTC AGGTCCATCT CAGTGGTGAC 120 TTTCTGTCTT CTTCATGGCC TTAAAAATTC CCTTGGAGAG GCAATTTATG GCAGTCCTCA 180 TTTCCCAGGA ATTTCTGATT TGAGTCAGAT TTTTTAAGAA AGAGAAGCTC TTGGAAGACT 240 TCTTTCTGCA TCTGTCGGAT CTCAAAATAG TCCTATCCCA AAGTGGCATA TTTTGGGGTG 300 GCGTATTTAC CAATCCCCTT CAGGTTTCAT TCATCCCTTC ACCAAAAGTT TACCCACTGC 360 TTATCAACCA AAATTCATTG AGATACAAAG TTGACTGACA CGTGGCTTCT GCTCTCAAGG 420 AACTTACAGC TTGATCGACA AGGCACATGC ATTTCTGAAA GTAATGCAAC TCTCAGGCTG 480 TTATAACTAA ATGCTGTAAT AGGATAGTAT GTATCTTACA CATTAGAATA ATTAGGTTTC 540 CATGGGAACG CTGTCATAGC CCCTGGCCAA CCTGCTGTGC TCAGTTCCTC CTAGCTCCTG 600 TGACAATAGA GGTAAAGGTG ACGCAGCATA TCCATAGAGT GATCACCATT ACTCAGCAGC 660 AACATGACCA GCATGTGTTA CGGACCTGTG GGGAAGGTAC CGAGATATCG CAAGAACCAG 720 GATGTTACAT ACAGGAGGCA TGGTTTTTCA CAGGCTGTTT TTCAAATGAT ACAAATTAGT 780 TATGCTGGAT TTTCAGGGTG ATACGGTTGG CATTAGATAA GGCTGGGTAG GGCCCCACTC 840 AGAACTTGTT ACTGGGAAGG GGTCCTGATC CAGACCCCAA GAGAGGGTTC TTGGATCTTG 900 TGCAAGAAAG 910
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