Tag | Content |
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EnhancerAtlas ID | HS038-22663 | Organism | Homo sapiens | Tissue/cell | ESC_neuron | Coordinate | chr9:120525170-120526630 | SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
JUN(var.2) | MA0489.1 | chr9:120525705-120525719 | TGGAAATGAGTCAT | + | 6.1 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GAGGCAGAGA TATGGATGGA GGATTGTTCA ATATTCTAAA AGAAGGGTGA TGGTAGTGTG 60 ATCCAGGAGC ATGCGAGTGG GCCTTTGGAG AGATGCCAAA GCAAAAGAAA GAAGGAAACT 120 TAGTGGCTGG CTAAGAGGGA TAAAGGTGGG GAAGAAATCT GAATGAACAC CTTGGTTTCT 180 GACTTGGGTG ACAGTTCATG GTGGCACCCC ACATTCAAAT AGAATTAAAA GAGTGCAGAA 240 GGAGGGACAG TCTCTTCTCC CTCTGGAGAT GGGATTTCTG CAGGGAGGAC ACTGGGTCCT 300 GTGACACTAG CTGTGCAGGT CACAGGCCTG CAGGAGCATT GAGCCAAGCA GGTCATTACA 360 GGCATATCCA CATCTGTTAT AAAAACTGAA CTCTAATCGT GCCAGACCCA CTCTGGCATA 420 ATAAGTGTGG TTTTTAACAT AATGCACTGC TGGAGCGAAG TTGTCAGAAA AGCAGGAGGC 480 GGAGGAGGTA ATCTGTGAGA CTTCAAAAAA GAAGATTGAA GCCATTTTAT GTGGCTGGAA 540 ATGAGTCATT TGTCAGCAAT GCCAATGTGC TGTCAGCTTT GGAGGAGAGA TGACGGGGCA 600 CCCTGGGGGG AGGGCTGGTG AAAGTGTCAA CCTTCAGTCA CCAGAGGCCA TGTGTGGGGT 660 AAAAAGTGTC AGTCACATCA CATCCCTGTC CTGACCTGGG TTAGAGGAAA ACCAGGGTCA 720 CAGCAGAGCA TTAGCCTTGT AACCAAGGAA CCTTGTAACC CTCCTCTCTC AGGAAGGAAC 780 TGATGTGCTC AGCGTTCTCA AAGACTGTTC AGAGCTTTAA TTCCTCGGGG CATGTGCACT 840 TTAAAAGAAG AGTGGGAGTG CAACACTTAG GAAGAAGAAA CTAAGGGGTA AGAGTGGATT 900 GGTGGCAGAA AGGAGGAGAG ATTTCGAGCA AGGACTTGCC TAAGGTCACT TACATAGGTG 960 AATACCCCTT CTCTCTACCT AGTTGCCAAG TCCAGGGTTA TCTCTGGGTC CTAATAGCTT 1020 GGAAGCCATT CCTGGGAGTG ACAACCCATT CTAAATGGAG TGATCCCTGC TTTGTATGTT 1080 ATTGCATTAC CTGACACTCC CCTACCCCCA TCATGCCAGT ATCGATCACT TGGATACTTA 1140 CTTGGGGTAC AGCAGCAGAT CATCCTAACT GGTTCAGCCT TCATTGCTCT GCTCTCATCC 1200 ATTTTTTTTT TTTTTTGAGG CCATAGTGAC CATCTTAACT TGAATTGAGT CTTCGCCTTT 1260 CCCTGTTCTT TGTGTCCTCC CAAGCTACCT GGCTTTGGTC TCTAACAACC TATACCATTT 1320 CAATCTCAAA CAAGAATAAC TTTTCCTTTG TTCTCTTCAC TCTACTCATG CTTGCCCTTT 1380 TTAGTTCCCT GAACACAGTG ACGTTTTGTC TTTCTCTAGA ACTTTGCTAA GGCTGGTCTC 1440 TCTTCTCAGG TAATGTCTAT 1460
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