| Tag | Content |
|---|
EnhancerAtlas ID | HS041-22559 | Organism | Homo sapiens | Tissue/cell | EWS502 | Coordinate | chrX:18892970-18893920 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF4 | MA0039.3 | chrX:18893442-18893453 | CCACACCCTGC | + | 6.62 | | USF2 | MA0526.2 | chrX:18893849-18893865 | GGAGGTCACGTGGGCC | + | 6.5 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TACAACCTGA TTTCAGATGC CCCTCTGCCA TCAAGGGTAT GGGAAACTCT GGACAAATGA 60
CATGGGCATT CGGAGCCTCC ATTTATCGTA ACCACAACCA CATCCCGGGA CCATAGCAAA 120
GATGAGAGCG AATGTACGTG AAGCACGTAG CACAGGAAGC GGTATCTCGT TGTAGTGGAA 180
GCTGTTGGCC CCGCTGCATC CCCTTTATTG GCCGGTGCAC TCATCCTCCA GCTTCTAGGA 240
ATGTTGGGTG CCAGCAACGC ACAGCGACCC CCTTTCCTGG TGCATTGCCC TGGACTGATG 300
GGAGGTGCTT GCCTAAGAGC TTGTGTCCCA TCCGCGTCCC CCCCAACTGC CCCCATTGCC 360
ACCCGCGGGC AGCCAGCAGT CACTGGCTAA CTGATGGCAG AGGCTGCTTT TATCTTGCAG 420
TGCTCACTCC AGAGCCCCCT GTGGCGTCGG GCTGGCTGGG TTCCACCTGA TGCCACACCC 480
TGCTCAGCTC CTTCCCCTGT CACTCTTGCT TCCTTCCAGG CTGCTCCCTG GAGCACACTC 540
TTGGCATTTC ACTTGTACAA CATGCCTGGC CCTGGCACGC TGCTGGTGCT GGTGTGCACA 600
CTGATCACAT AAGCTTGTGA GCATTCAGCG CTGAAGGCCA AGGATGCCTT GTGCTCTGAG 660
AATGGGATCT GCTTGGGGGC AGGAGAGACT TGGGGTCGGG GTGCGTTGCT GGGGAACAGA 720
CAAGGGATCT GTCGCCTCCT GGGAAGCTGG GAAATGGTGT GGGGTGGGGC GACTGGGAGA 780
GGACGGCCAG GGACAGCTTC AGGCCTGGTG TCCTGCAAAA CCTGACACCT AGCAGATGGG 840
AAGATGCGGC TCAGCTACCT CCTCCCGGAG CCAGGCTGAG GAGGTCACGT GGGCCCAGGA 900
GGTTCAGCCT CAGTTGGGCT GTGCTTGGGG AAATAAATCA TCAGGACTCA 950
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