| Tag | Content |
|---|
EnhancerAtlas ID | HS041-19123 | Organism | Homo sapiens | Tissue/cell | EWS502 | Coordinate | chr8:30513280-30514700 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HSF1 | MA0486.2 | chr8:30514596-30514609 | TTCGGGAACGTTC | + | 6.05 | | IRF1 | MA0050.2 | chr8:30513311-30513332 | TCTCAGTTTCAATTTTTTTTT | + | 6.34 | | IRF1 | MA0050.2 | chr8:30514329-30514350 | AAAAAAAAAAAAAAAGTAAAT | - | 6 | | Nr2f6(var.2) | MA0728.1 | chr8:30513549-30513564 | TGAACTCCTGACCTC | - | 6.22 | | Sox3 | MA0514.1 | chr8:30514574-30514584 | AAAACAAAGG | - | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TCACTGGACG GTGAATCAAA AACCTGCCTT CTCTCAGTTT CAATTTTTTT TTCTTTTTTT 60
TTGAGACAGA GTCTCGCTCT GCCGCCCAGG CTGGCAGAGT GCAGTGGTGC AATCTCGGCT 120
CAATGCAACC TCCGCCTCCT GGGCTCAAGC GATTCTCCTG GCTCAGCCTC CCGAGTAGCT 180
GGGACTACAG GCGCGCAGCA CCACGCCCCG CCAATGTCTG TATTTTTAGT AGAGACGGGG 240
TTCATTCACC ATGTTGGCCA AGCTGATCTT GAACTCCTGA CCTCAAGTGA TCCGCCCACC 300
TCAGCCTCCC AAAGTGCTTA GATTACAGGC GTGAGTCACC GCACCCGGCC TCAGTTTCAA 360
TTCCTAAAGC CACCTGGCTA GGCAACCCAC AAGGCCTCTA CATTCAATTT CATAAGTGAA 420
ATGAGGACGC TATGAAAGCT GTCCACATCC AGCCCAATTG TAAGAATGAG AAAATGTGTA 480
TGTTATTTTT TAAACAGTAA AGTCATAAAA ACGTGTTATT TCAGTATTAC TATTTTGAGT 540
TGGATCTGAA AGAAGGGAAT GATTTACCGG GCTGAGGAAA GTAGGAGACA GCCTTGGGAG 600
GAGGGAAAGC GTGGGGCCAA GAAGAAGAAA GGAGAATTGT CAAGTGAGAA GGTGGGAGCA 660
AAAAGTAAAT TTCTAGAACA GGAAACATTT GTGTCTTATT TCACGTTGCA AAGGCAGGAC 720
CTCAATCTGG ACTTTAAAAA AATTACTCTA AAAGATTTAA ATAGGCCGGG CGCAGCGGCT 780
CACGCCTGTA ATCCCAGCAC TTTGGGAGGC CGAGGAGGGC GGATCACGAG GTCAGGAGTT 840
CTAGACGAGT CTGGCCAACA TGGTGAAACT CCGTCTCCAT TAAAAATTTA AAAAATGTGC 900
AGGGTGTCGT TGCGGGTGCC TGTAATCCCA ACTACTTGGG AGGCTGAGGC AGGAGAATCG 960
CTTGAACCAG GGACGTGGAG CTTGCAGTAA GCCAAGATCG CGCCACTGCA CTCCAGCCCG 1020
GGCGACAGTG CGAGACTCCG TCTCAGAAAA AAAAAAAAAA AAAAGTAAAT AAAGCCGTAC 1080
AGTTTACAAC AAACTAAATG CTTACAGTAT TTGACCCTCG CAACTCTAGG AGCAAACAGG 1140
TATTAGTGTT ATTCCTATTT TAATACGTGA AATCTGAAGT GAAGCTGTCT GGTTAAGGTC 1200
GCACAGATGG AAGAGCCAGG GCCAGGAACC AAACCTCCTG ACTCCTAACT CAAGTGCTCC 1260
TTACACCAGA CCTGGAACGC TGGTAAAGGC CTTTAAAACA AAGGCCACCT GTGAGGTTCG 1320
GGAACGTTCA AAGGCATCTA GAGCAGAAAG CTTCGCAATG TCTGTCTTTC ACCATCACGT 1380
GCTCCGCCTA ACTTTTCCTC CTTTTTCAAA GACTACCCAA 1420
|
| |
|
|
|
