Tag | Content |
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EnhancerAtlas ID | HS038-21077 |
Organism | Homo sapiens |
Tissue/cell | ESC_neuron |
Coordinate | chr8:32637500-32638690 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
LMX1B | MA0703.2 | chr8:32637706-32637717 | AATTTAATTAA | + | 6.32 | Nr5a2 | MA0505.1 | chr8:32637977-32637992 | TCTGACCTTGAAATT | - | 6.47 | PHOX2A | MA0713.1 | chr8:32637705-32637716 | TAATTTAATTA | + | 6.62 | PROP1 | MA0715.1 | chr8:32637705-32637716 | TAATTTAATTA | - | 6.32 | PROP1 | MA0715.1 | chr8:32637705-32637716 | TAATTTAATTA | + | 6.62 | Phox2b | MA0681.1 | chr8:32637705-32637716 | TAATTTAATTA | + | 6.62 | TFAP4 | MA0691.1 | chr8:32637822-32637832 | ATCAGCTGTT | - | 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 |
GH08I032780 | chr8 | 32637519 | 32638041 |
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Enhancer Sequence | GCCCAGCACT TTGGCTCTAC TCCCTCCCTG CTTCTGTGAT TCAGCATCCA TGCACACACC 60 ATAAACAATC ACAATTTCCA TTTTAGGATT TGGTCTCCTG GTGCTGTGCT ACAGCCCCCG 120 TTTTTAGGAA ATTGGTGCTT GGCAAACGAT GAAAAGTTTC ACAGAATATG AAGGTTATGG 180 CACAGTTTTC TCCTGCCTCA TGGCTTAATT TAATTAAGTA TTCTGTAATA GCTCTGCAGC 240 AGACTTGTGC TGCGGAATGG GCTCCAATTT GCCCTATGGC AACTGCAGGA GCAGAGCAAC 300 TATAAGATAT GCAAGATGAC TCATCAGCTG TTGGAAAATG CAGTGAAACC TTTGCCTTTT 360 CAACAGGATC AGGCAAGGGG ACTGAGACAG CATCCCTGGG AATAGACACC TGGTAACTCA 420 GCATCTACAA GATCATTTTA AAACATGCTT ACAGTAGAGT AATCAGCAAA ACCACTGTCT 480 GACCTTGAAA TTATTCTATG GCTGCTGGAC CTTGAAGACA CTGATGGAAG CAGCTAAGTC 540 CAGCTGTCTG GGACTTTGAT CAACTATGTC TGCCCCCCTC AGTGTAGCCA AGACCTCCCT 600 TACAGCAGGT TCTCTAGGGC AGGAGGTGTA AGCAGAGAAG TCAGGAGACC AAGATGCTCT 660 TTCTTATTGT GGCAGATACC GAGTAACCTC ATGCCTTTGC AGGCTTTCGG CTGTGAGCAA 720 ATTCTGATAT TTATTATCCT TACTGGGGAC ACTCAGCTTC ACAGATTTTG TTTTTCAAAC 780 ATGAAAAAAG AAAAAATCGA GGCCCTGAAG TCACAGAATG TTTTGGCAGC TATGTTCAGG 840 CTTGATAGAA AGGCATCCCC ATGGGGACGT AGCTTTTGTC TGGTTCCGTT TAATTTGCTA 900 TCTTCAGAAG GGAAAGATGG AGAGATAACC GGTTGGGTGG GGCTATGTGA TGGAGATTTT 960 CTGTTAAGAT GGAAATGAGG GGAGCTTTAG GTAAGTGACA GATGACTTCC CAAGAAACTG 1020 CATGTAACTA GTCATGAACA ACGTTGCAAT CTAAGACACA AGTGACAGAG GTGGCCTAGG 1080 AGGCAATGCT CACATGTAGT CAGTTTGTAC AGCCATATTC CCTTGCAAGG TTGTAAAGGG 1140 GACCACTCTG TATTACTGCT CATAGCCATG GCTACGCTGT CTGCCTATTA 1190
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