| Tag | Content |
|---|
EnhancerAtlas ID | HS062-08929 |
Organism | Homo sapiens |
Tissue/cell | GM18486 |
Coordinate | chr2:44271210-44272060 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF4 | MA0039.3 | chr2:44271796-44271807 | CCACACCCTCC | + | 6.32 | | Klf1 | MA0493.1 | chr2:44271794-44271805 | AGCCACACCCT | + | 6.02 | | Zfx | MA0146.2 | chr2:44271983-44271997 | GAGGCCGAGGCGGG | - | 6.01 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I044044 | chr2 | 44271242 | 44271939 |
|
Enhancer Sequence | TATATATATA TATATATATA TATAAATACT TGAAAATAGT CACCTGCCTT TAGACAGTTG 60
TAAGCCACAG GGGAAACTCT TTGAATTCCC ACCAATAACC ATTTGGCTTA GAACGACTTT 120
CAGCTGTTTC TAAAAATCAA ATTCACCCTG AAACGAGGGT GGTTTGCTCT CACCTCACGA 180
TGGTGGGGAG AAGGTGGGCA GCAGTTAAAT ATGCCGTGGG GCTGAATGTG ACCAACACGA 240
CAGTGCAGGG AAAGCTCCTT TGTCCCTGCG CGGCCCAGAC TGGGACGCTA GATGGCAGGC 300
TCACCTTCTA GATGGAAGCT TCCGGCTCCT TCTAGAGGGA AGCAGCCAGC CCTGGCAGCC 360
CGGCCTCTGC TGGCAGTAGC CACACACTCC TGAGCAGTTC CCAGGGGCCT CCAGTGGGCT 420
CCCCAGGGAG GGTGTGACCG ATCCTCAGTG GAAGGCCCCA GAAGTGTCTG ATGTGAGAAC 480
AGGGAACGCC TGCCTGTCTC CTGCAGCTGC AGTGGGATCA GGGTTAGGGC CCACTTGATC 540
CCAAACCTCA TGGTTTGTGG CTATGGTGAC TCCACTGGGC TGCCAGCCAC ACCCTCCTCC 600
CACCTGCCTG TCCCCGTATG GGGGTGAGAA ATGTCTCCAG CTTTCTTGGG CTGGCCCAAG 660
GTTCGAGGTC TTTCAGGATG TCTGAAACTT GAGGTTACGC TTTATGCAAC CTATTATCAA 720
ATAGAGGGTC TGGTGGGGTG TGGTGGCTCA TGCCTGTAAT CCCAGCACTC TGGGAGGCCG 780
AGGCGGGCAG ATCACCTGAG GTCAGGAGTT CTAGACCAGC CTGGCCAACA TGGCGTAACC 840
CTGTCTCTAG 850
|
