| Tag | Content |
|---|
EnhancerAtlas ID | HS062-08933 | Organism | Homo sapiens | Tissue/cell | GM18486 | Coordinate | chr2:45182020-45183800 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr2:45182465-45182486 | GGAGCAGGACAGGGAGGGAAG | + | 6.74 |
| | | 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 |
| GH02I044954 | chr2 | 45181323 | 45183647 |
| Enhancer Sequence | TCAGTGCGCG CAGCCTCCTG CACACCGTTT TCGCGCGACC TCCTTGCCTC GGTCTCCAGG 60
GGTCAAGCCA ACCCAGCGCG GGAATGTTCC ATTTGCCCTT TTGGGACATT CAGAGAGGCT 120
TTTCCGGGCT GCCGCGGCGC TTCCACGCAG AGGAGGCGTC GGCTTCCAGG CAGCTTGGCG 180
ATCTTGTTAT TGGACACGCG AGAGTTTAGA GACCCAGAGA AATGGAGTGA GTCAAAGTCA 240
AACTCAAGTT TCTCGGCCCC TAGTCCTGCG ATTCTTCCAT TGCACATTGC ACCCCTGGGC 300
CTTTCACATC TGCTCCTAGC GAGCTTGGAG TGTAGGTGCG ACCAGGGCGC ATCTGTGCCA 360
GTGCGTGTCT GCGTGCGTGG CCTTTGGGTG ACTCCACGCC CGCAACTGTC TCCGACTGTG 420
TGGGCGCGTG TGTGGCAGGT ACCCAGGAGC AGGACAGGGA GGGAAGCCTC AGCTTCCAGA 480
CCCGCTCTCG CGTGCTGGCG GGAGCGGTGG GTAGGAGCAG GAGGTATGTG GTGAAGGATG 540
TAGGCGGACT AGGGCTCTGT CCCCGCAGAA GAGTCCAGGA CGCAACCCCT CACGCCGGGC 600
CAGCGGGGAG GCAGGAGTAT GGTGGACCCG TTCCCCCAGG GATGGGAGAG CTGAGGAAGG 660
CTGCAGGTCG GATAGCTAGA TTCCATGATG CCCCCAAGAA GTTGCCAGAC TCCAGTCTGG 720
GAGCTCTCAA GAGCCAGAGA CCCAGGGAAG TCCCCTCTTT GGCCTCCGAG GACCCCGAAG 780
CCTGGCAGCA GTGCTCAGCC TTGGACCCCG CGGTTCCGCG GCCGGACGCC CCTCGCGCTG 840
GCTGTGCGCA CCCTGGCGCA AAGCACTGCA GGTTGGAGGC GGAAAGCAGC GCGCTCTGGG 900
GCCACTGGCG GGTTTTTGCT GCCACCTCGC GGCGATGGTG CATAGCATGC GAACCCTCCG 960
CACCGCGGGC CTTGGTAGTG CACGTGGGTG GTGTGGGGGG CCTTGCCCTG CCGCGCTGTC 1020
CTTTTCTGCT CGAGTTTTCG CAACACCTCT TCCACCGGGA TAGCCTGCTT CTCCTCTTGA 1080
GGGACTGCGC GCTGTCTTAT ACCAAAGTCC ACCATTTTGC GTGGGTAGGA CCCTCCACCC 1140
TGGCCTGTGG GATTTGGAGT CACCTTTCTA GCTCCTTTCT CTTGCTTTAC TACTTGATCC 1200
CGTGGCTGCC CACCTGGACT TGCAATAGGT CTCATGCTAA TATTTCCCTT CTTCGGCACT 1260
ATTAACTTCT TGTCTTGCAG ATAGATGCCT CTAGGTCTCC TACAGCGGGA GTGTGGGGCT 1320
GTCTTCCATG GTGATAGGCT GTCTGGTGGG AAGCCATGCG GAGCTAGTAC CCTCTCCTCT 1380
CCACAAGGGC TTGCTGAAGG CCTTCCATAT GCCTGACGCT GCCACACCTT GGAGACAGCC 1440
AATGGCAGCC TAGACCCTGG CCCTGCGATT ATAGTTTAGT GCAAGCAGAG AAACACAATA 1500
CACAAATTAT CATTGAAGCT GCCATATGGA GGTATGGACA AAGTGGGAGC CCGAGGAGGG 1560
CCTTTGAAAC AAATCTTGAT GGATAAGCAT GAGTTTTCCA GGCCAGTGAG GAGGGAAGGA 1620
CAGTCAAGGG ACTGGGAAGT GTGTGTCCAA AGACACCTGG GTACAAAAGA GCATTGGGTG 1680
CTGAGAGGGA CAGCTGTTTC CTGGGGTGCT CCACAGTCTG ATGGTGAAGA CATTGCTTTG 1740
CTCTGGACAG CATAGCCAGC CAGCTTGGGC GAATGTATTG 1780
|
| |
|
|
|
