| Tag | Content |
|---|
EnhancerAtlas ID | HS184-05795 | Organism | Homo sapiens | Tissue/cell | T47D | Coordinate | chr11:66753080-66754130 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NRF1 | MA0506.1 | chr11:66753856-66753867 | GCGCCTGCGCA | + | 6.62 |
| | | 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 |
| GH11I066986 | chr11 | 66753761 | 66753891 |
| Enhancer Sequence | CTCCTCACCA CCTTCTTCAT CATGTTAGAG AGTAAAAGCT CTGTGGCCAA ACTGCCCGGG 60
TTTGAATCCT GGCTCTGCCA CTTGCTAGCT GGGTGACATC AGGCAAGCCA CTTAACCTCT 120
CTGTCCCTCG AATTGGCTGT CCCTCCTTAC AAGATTGTTG AGTTAGTACA TGTAAAACAT 180
GTGGAGCAGT TGGTCCTTGG TTCTTAGGAG CCAGTTCCAG GATGTTCTCC CTGTGCAACC 240
CAGGGCAGGT CTCATCTCTG AGCCTCAGCA GCCTCCTCTG AAAAATGGGG ATGTTAATAA 300
TAGCACCTGG CTGGAGGCGA CCTGGAGGAT GGAGCAGGGC CAAGGCACAC ACTGTGCTGA 360
GCCCAGGGCC AGCCCACAGA AGCGCCGGCT CAATGAGTGC CTCGGAAGCC TGGCATTTGG 420
AGCCCAGTGT GTCCTCAGCT CACCTTGGCT GGTCTTGGCC TTGGCAGGCC CATGGGCAGC 480
AGGGAAGGGC CATCAGGATC TGGGAAAGTG GGTCCAGCCC CAGACCAGAT GGCCACCCTG 540
GGGCCTCCCA GGAGGTGGGC TGTCCTTTAA TGACCTGCAT GGTCGTGGGT TTGGGAGGAA 600
GGAGCTTTCT CCCGGCCCCC TACTCCCACT GTGGCTGCCA AAGAACCCTC CCTGTCCCAC 660
CCCAGCCAGG CCATGTCTCC CTTCTCTGAG CTTCAGGTAC AAGCAGTCAG TTAGTCAATA 720
GTTGGCAAGG CTCACTCAGG GCCCTGCTAG GGCGAGGACT TCAGCAAAGA TGAGTCGCGC 780
CTGCGCACTG AAGTCCAGCC AGGTAGAGCC CACATCCCAG CACAAAGGTG CCCTGAGAAA 840
GGCAAGGTTA GCTCTTGGAG GGTGGGCACC AGAGACAGCC TCCTGAGGAG GGGCCGGCAG 900
AGCTGAGTGT GGGCTACCCC AGTGGAAGAG TTGGAAAGGC ACATGAGGCA GAGGGAACGG 960
CAGGTGCAAA GGCATGCAGA TATGGAACAG CTGGAATATT GGGAGAACAA GGCAAACTCA 1020
GTTTCCTGGG GAAAAGGTGG AACTGGGGGA 1050
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