| Tag | Content |
|---|
EnhancerAtlas ID | HS184-05592 | Organism | Homo sapiens | Tissue/cell | T47D | Coordinate | chr11:60588960-60589920 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EBF1 | MA0154.3 | chr11:60589904-60589918 | TGTCCCTGGGGACT | - | 6.15 | | Nkx2-5(var.2) | MA0503.1 | chr11:60589370-60589381 | AGCCACTCAAG | + | 6.62 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GGAGGCTTAG GGAACATGGG CAGAGGCAGG CTCCGATCCC ACTCTGAGAC CCCAGCTTCG 60
TCCCTAGAAT GCCATGAGCA GGGTGCTGCT CCATTCATGG GTGTGGTGAG AGCTAAATGA 120
CTTGGTGCAC AGAGCAAGCT CGGTGCACTC AGGGCCAGCA CCTTGGAGGT AACCAATGTG 180
TTGGGCTTGA TGCCTGAGAT GGCCCTCACC CAAGCTTTCT AGGGTTCTGC AATCCTGCGG 240
TGCCCCTGGG ACGAAGAGGC CTGGTTCTGC GCCTGCCCTC ACTGGCTGGG GAAGTTGGCA 300
AGGTTCTTAT TCTCTCCAGG CCTCTGTTTT CTTGGCTGCC AAGGAAGGAG GTGGATGGGG 360
AGTTTGTCTA AGATCCTTTT CGGCAGAGAC ATGTGCACAG AGACCTGCCC AGCCACTCAA 420
GTCCTGGGAG ACACAGCCCC AACCCCGAAA GCCCAAGGCT TTAGCTCTGC GCCCTCCCCC 480
CTCCACCCCC AGGCCCTGCA GATCATTATC AGCTGCTGGC AACTGGTGGC TGGCAGGTTG 540
GGGGGCGGGC CGCATCCTGG CTGCCTCCTC GAGCTCCACC GAGTTCCCCA CCACTTACTT 600
GTACCCGCTG GCAGGAGGAG TGCTCCTGAG GACCCTGGAG ATCCCACTTG GTGGTGGCCC 660
AGAGACAGAG AGGACTGCAA AGACCAGGAC TGCAGATCCT CCCTGCACCC TTGGGAGGGA 720
GTTTGAGTCT GTGAAGTGGG AGTGAAGCTG CAGGGGGTGG AACTGTTCTG AGCTCGAGGG 780
GAAGTTCCAG GCCCACCCCA CATGGGATTG GATGGCCCAG GGGAGGCACT GGGCTGTTGA 840
GGCGGCCAGC TAAAGAGCTG AAGCTGGTTC ACAGCGTGTG GTGGGGGGAG TCGTGGCAAA 900
GGGCCTCTGC CCCAATATAT GCAGCCGAGG AAGGAGAAAG GTGGTGTCCC TGGGGACTTA 960
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