| Tag | Content |
|---|
EnhancerAtlas ID | HS121-26924 | Organism | Homo sapiens | Tissue/cell | LNCaP | Coordinate | chr3:48717660-48718710 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFE2L1 | MA0089.2 | chr3:48717680-48717695 | GCATGACTCAGCACA | + | 7.05 | | Nfe2l2 | MA0150.2 | chr3:48717678-48717693 | AGGCATGACTCAGCA | + | 7.3 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TCCTAGAGGG AGAGGGCAAG GCATGACTCA GCACACTCCC TGCCCTCACC ATCTCCAGGG 60
AGCCTCCAAG GCCTGGAGAG TCCATCTGTG GACTTTTACT CCATGAACTC AAGTCCCTCC 120
TGGCCCACAC TGGACAGGAG GCTCAACTCC AGTCTTGATG ACCTCCCAGG ACAGGAGTCA 180
ACGGGAGACT CATCTGTAGG GGGTTTTCAA CAGCTCGCCT CTCATCCCAG ACCTGGATAA 240
ACACCCCCAA CTAGGAGGGC CATGAACTCT GTCACTGCCA GAATGTGACT CTGAGACCTC 300
ACTCTCCCAT TCCACACAAA ATGGCACAGG CCTGTCATCT ACCAACTTGC CACATTTTCC 360
TTGAACCCTG CTGACCAGGC ACTAGCTGTT GTGCCCAGCA CAGCCAAGCC CATTGGCCCA 420
CTCCCCAACA CCCAAACCAG AAGTGTAACA GGAACCATGG AGCACTAAAG AGGGACCTTT 480
GGTCTGTCTG ACCCCCATCA TGTATGCTGG GCTCACTGCC CCCATCCTGC TCATGAGTGC 540
CAAGGATCCC ACCCATCCCA TGATGCCCAC ACACCTCACT CCCTCTCATC CATGTCAGCA 600
CCTAGGACTC CATCCCAGCT CTCCCAGCAC CCATGTCTCT TACTGCCAAG GTCAGCAAGG 660
CACTACCCTC ACCCACGCCG TGTCCATTCC TTCCCTGCAG CCAGACAGAA CTCTTGGCCA 720
CCCGCATGTC GTCTTATCTG TCACCTGCCC CAGGTCTCAC CTCCTCCTAC AGCACCCACT 780
CCCTCACTCC CTGTGTTCCA GTCCTGCAGG CCTTGTTCCA CTTCCTCCCA CAAGCCAGGC 840
TCAGTCCTGC CTTGTGGCCC TTGTCCAGGC TGCGCATCTG CCTGGAATGC TTGTCCTTCC 900
TTTCTGCTTC AGAAATCAGC TCAACGTCCC CAGTGCCCAG CACAGTAAGA GCTCAGAGCC 960
AGAGCTTGAG AAATACCTGT AATGTACAGG CTGGACAAGT GTGTGACGGT GGGAACAGGG 1020
TGGGTAGCAG GGTGGCCCTG CTGTGCCGCC 1050
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