| Tag | Content |
|---|
EnhancerAtlas ID | HS001-05134 | Organism | Homo sapiens | Tissue/cell | 786-O | Coordinate | chr2:239009360-239010580 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr2:239010448-239010469 | GAAGGAGGAAGGAGCTGGAAG | + | 6.17 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GGGGATGGGG CAGCCTGGCT CCACGAAGCT GGCTGGGGTG GAACCAGGGA GGTGTGAGCC 60
ACGGAGGATC AGAGTACTGG CCACCCCGGG CTCCATGGCC CTGGGCCCTT TGTTTCTCTT 120
GGGGACTCAG TCAGTGGTTA CCGTCTCTGC CCCACGCCTC TCAGAGCACA AAGGCTTGAG 180
AGCCAAGAAC ACCTCCTAAA TTTTCTTATC ACCTTCCCTG CCAGGAAGCT GGGCGTTGCC 240
AGTGGGGGTC TTGCCAGATA TCAGGACCCC TGTCTCTGAT CAGGCCTGGT CCACAGGGCC 300
TGCCTCCCAA AGGGTCTAGA AAGGGATCCT TACAGAAGCA CTGTGGGAAC TTGGGCTTGA 360
GAGCTGGGAG CCTAGCCCTG GGGGACGGGA GTTAGGGCTG CTGATGGTGA TCGTCTTGTC 420
CGGATCGTTT CTACTGGGCC CCCCTCCCCT ATCCTGCCTG CCCAGTCCCC TTTGTGCAGG 480
CGAGGCCCTT AGAGCTGTCG CTCAGCCCTG TGGAGCTTTC AGGGCTGAGG GTGAGCAGGA 540
CTGACCGGCC TTAGAACGCC GCCGCCCAGA GGTCAGAGTT GAGGTGGGGG CCGGTGGGGC 600
CTGCTTAGAC TGCGGAGCGG GAAGGTTCCC CAGCACCTGG CTCGCCAGAG CACCTGAGAG 660
TCCCGGCCCA GCATCCTGTT CCTGTCGGCC CTTCCGCCAA ACCCAAGGGC AGCAGGCGGG 720
AGCTGTGCCT GCCTGGGGAT CCATTCTGAC AGGGCCCTTG GAGAAGGCCC AGGTCTGCTG 780
GACCCCTGAC ACCTGTGGTA GGAACGCTCC CTGGCCCCGG GACCCTGTGG CCAGCGGGAG 840
GGCACTGGGG CAGGGGACCA GCCAGAGGTA GGTGTCCTGG GAAGCCTTTC TGACCATGAG 900
CAGAGTGGGC AGGTGTCTGC GGGCACCCGA CTGCGTGGGA AAGGGCCTTC TCCACACTGG 960
GGACGGGCCC AGGAGAGGGC AGGGTTGCCA GAGGTGGCCT CCCAAGACCT GGACCTGAGT 1020
CCTGGCCCTC CTCTCACCTC AGTCCCAGCA GGGAGCACCT CCCTCCATGT TGCAGGCAGA 1080
AACGGAGGGA AGGAGGAAGG AGCTGGAAGC CCCTTCACTG GGTTGCAGGC AGTGTGAGCC 1140
CTCGCCCAGG GCCCACCTCC GGCAGCTGGC TCTGACCTCA CGGCCTACCC CCCACTCACT 1200
GACCTACCCG GGGCTTGGTA 1220
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