| Tag | Content |
|---|
EnhancerAtlas ID | HS108-02526 | Organism | Homo sapiens | Tissue/cell | K562 | Coordinate | chr1:111323190-111323990 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr1:111323672-111323691 | CGCTGCCCTCTGGTGGTAA | - | 7.59 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 111323200 | 111323289 | | chr1 | 111323326 | 111323526 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH01I110780 | chr1 | 111323423 | 111323930 |
| Enhancer Sequence | CCAGCGAATG AAGGACTGTC CCAAATTCTA CAACGAAATC CTCCGTGAAG CGGGCCCTCA 60
GCTTGAGCGC AGGCTTTGAG GAGGTCTAAA ACGTGAAGCT CTAGCGCTGC AGAGAGGAGC 120
AGCCCCTCAC CTTGGGTCGC TTTCCTTCCC CGTCCTTTGT ATCAAATGCT CACGCCCAAT 180
TCGCAGGGGC GACGGGAGTG AATCCAGCCT GGGTCCTGCC CGGCCGATGG CGCTGTTCCT 240
CCGCCCCCTT CCCTCAGCCC ATTTTCTCCT CATCAGGCAA CAGAAATGTC TGAACACCTG 300
CGGGGGCACA GACTGGGGTG AGAGGCCTAA GCAGGCAGAA TGTCTGTAAT TATAAAGTGC 360
TGTCCAAGAT CCTAGGCCAA ACCTCGGGGA AACGGAATAG GAAGAACTGC GTCCAGGCCT 420
TGGGGAGGAT TCTCCACGCA CACGGTGAGG TGTTTGGCGG CTCAAGGGTC TCTGTGGTGA 480
AGCGCTGCCC TCTGGTGGTA AGAGGTAGAA ATGACCACGT CTTCTTGGCC TGGTTCCAAG 540
AGCATCAGAG ACGTAAGCAT CAGAGACATA AGCCCCAAAT CTGAGCTGGG CTCTTGAAAT 600
CCTCTAGGAA AGGGTCTTGT TCCCACTGAC TTTCTGCAAA GAGGAAAAAG AGAAGTGTGC 660
AGGGAGGTGG TGGGGAGAAA ACGCTGGACT GGTCACCTGG ACGCTCAGCT TGCGGTTGTG 720
TAAACAACTG CCAGCTTTCC CTAAAGAAAT GGTTCCATCT AGCTCCTGAG GTCCCACGGG 780
GCTGGAAAGA GCTGAATGTT 800
|
| |
|
|
|
