| Tag | Content |
|---|
EnhancerAtlas ID | HS184-24162 | Organism | Homo sapiens | Tissue/cell | T47D | Coordinate | chr5:71178700-71179560 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| JUND(var.2) | MA0492.1 | chr5:71179251-71179266 | AGAAATGAGGTCATA | + | 6.55 | | PHOX2A | MA0713.1 | chr5:71178788-71178799 | TAATTGAATTA | - | 6.14 | | Phox2b | MA0681.1 | chr5:71178788-71178799 | TAATTGAATTA | - | 6.14 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GGCGAACCAT CACTCATTTA TAAAAATGAA GGATTCGTGA GCAACTCCTC TGGCTGCCAG 60
CAGAGTTTAT GCAGGTTCTG ATCCACTTTA ATTGAATTAA GCTGTGTTTA TTTAATCAGC 120
CCAGAGATAT GTATCCTCAG GCAGGAATTT GATGACGGCT TCTAAATCGT GTTTTTGTCT 180
GTGGGAGGAG AAGGGCTGTG ATCTACTTGG TATTTTTGAA GGATTGGGGG CCCAAGGGAC 240
AGGCTGGCAT CAAGGCTCAG ACTGGACCCT GCAGGGACAC TGCATTCAGC AGCTGTGCAT 300
GTGATTGTGT GTGCCTGTGT GAGTGTGAGT GTGTGTGTGT GCATGTGTGA ATGTGTGTGC 360
CTGTGTGAAT GTGGACATAT ATGTGTGCAG GTGCAAGTAT GTGTGTGTGC ACATGTCCAG 420
ACACCCTGTG GTGAGTATGC ATGGGCAGAG CTCTTTTTGC TCAGTGCCCC AGGACCTTGG 480
GGCAGGACTG TCAGAGAAGC CAGACCTGCC AGTAGTCTGT GTTCTCAGCC ACCACAGAAG 540
AAAAGCATTA GAGAAATGAG GTCATACTGA GGCTTGAGGA CAGTATTGTT CAAATTGTGC 600
TCCATAAATC TCCATGGGTG CTGGTTAAGC ACACTGATGC CCAGGCCCCA CACCAAGGCT 660
TGCTGAATCA CACTATAAAT AACCTCAGGA GTGTTTGCAT TTTAAGGTTG GAGGCGGGGC 720
AGGCAGAGGA CAGTGACTGA GACTTACTTA GTGGGAATCA TGATGCTGGT AGTGGGCATG 780
GGTGTCTAAG CCTCACACCC GGGTCTGGGC AGTGCTCAGC GTGAGCTGCG CAGCCGAGTC 840
ATTTACGGGT GGGGCTGAGC 860
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