| Tag | Content |
|---|
EnhancerAtlas ID | HS007-17910 | Organism | Homo sapiens | Tissue/cell | BE2C | Coordinate | chrX:18892830-18893880 | 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 | TCGAACCCCT AACCTTAAGT GATCCACCCC CACCTCGGCC TCCCAAAGTG CTGGGATTAC 60
AGGCCTGAGC CACCGTGCCC GGCCGGCGTT TTGTATTTTT AGTTGTCAAC TCTGGCAACC 120
CTACATGGAC TTTGAAGTCA TACAACCTGA TTTCAGATGC CCCTCTGCCA TCAAGGGTAT 180
GGGAAACTCT GGACAAATGA CATGGGCATT CGGAGCCTCC ATTTATCGTA ACCACAACCA 240
CATCCCGGGA CCATAGCAAA GATGAGAGCG AATGTACGTG AAGCACGTAG CACAGGAAGC 300
GGTATCTCGT TGTAGTGGAA GCTGTTGGCC CCGCTGCATC CCCTTTATTG GCCGGTGCAC 360
TCATCCTCCA GCTTCTAGGA ATGTTGGGTG CCAGCAACGC ACAGCGACCC CCTTTCCTGG 420
TGCATTGCCC TGGACTGATG GGAGGTGCTT GCCTAAGAGC TTGTGTCCCA TCCGCGTCCC 480
CCCCAACTGC CCCCATTGCC ACCCGCGGGC AGCCAGCAGT CACTGGCTAA CTGATGGCAG 540
AGGCTGCTTT TATCTTGCAG TGCTCACTCC AGAGCCCCCT GTGGCGTCGG GCTGGCTGGG 600
TTCCACCTGA TGCCACACCC TGCTCAGCTC CTTCCCCTGT CACTCTTGCT TCCTTCCAGG 660
CTGCTCCCTG GAGCACACTC TTGGCATTTC ACTTGTACAA CATGCCTGGC CCTGGCACGC 720
TGCTGGTGCT GGTGTGCACA CTGATCACAT AAGCTTGTGA GCATTCAGCG CTGAAGGCCA 780
AGGATGCCTT GTGCTCTGAG AATGGGATCT GCTTGGGGGC AGGAGAGACT TGGGGTCGGG 840
GTGCGTTGCT GGGGAACAGA CAAGGGATCT GTCGCCTCCT GGGAAGCTGG GAAATGGTGT 900
GGGGTGGGGC GACTGGGAGA GGACGGCCAG GGACAGCTTC AGGCCTGGTG TCCTGCAAAA 960
CCTGACACCT AGCAGATGGG AAGATGCGGC TCAGCTACCT CCTCCCGGAG CCAGGCTGAG 1020
GAGGTCACGT GGGCCCAGGA GGTTCAGCCT 1050
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