| Tag | Content |
|---|
EnhancerAtlas ID | HS184-15230 | Organism | Homo sapiens | Tissue/cell | T47D | Coordinate | chr19:12550640-12551720 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RREB1 | MA0073.1 | chr19:12550909-12550929 | CCACACACAAACCCCACACA | + | 6.06 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TTGCTAGCTG AAAACAAGAT GACAAACTAG TGAAATATCG CCTGGGGCCA AACAGTTCAT 60
ACTGTTGCTG TGAATTAAGG ACAGAAGGTT AGCCTGGGGA AGTCTCTGGA AACCAAGAGA 120
TTTGCTGCCA GCCCTAGGAA GAGTCAGGAT GAGAGAACAC AGTGGTGGAT TTGAGACCCT 180
GCTGCCCACG TCTTTGGAAG ACTCAGAGGG GAAACGGTCG CCCTTGGAAA GGAAGAAAGG 240
ACTGAGGACC ACGGAAACCA CAGCTCCTCC CACACACAAA CCCCACACAC GAGTCTGGAT 300
TCCACCTGGT GACTCGTCGT CACCGTGCAG CCTCCTCACC GGGTTCACAG GAACTGCGAG 360
CCAGGCTGGA GGCGAGATTG CAGTTAGATA TTAAACAGGT GCCCTCAGCC CCGCTGCCTC 420
AAGGGGCCGC CTCCCTGAGA GTCAGGTCAC AGCAGACGCT GACCGCCGGC TTCCCCATTG 480
TGCCTGGGGA TAAGATCTCC GAGTGCTGCT CAAGAGTCGC CGGAGTTCTC AGATCCTGAA 540
TCCCAGCAGA AAGGCTGGCG CCAACCAGGT TGAAGACCCC ACGAGGGAGC CCTCTCAGCA 600
GAATGCGGTT TCTTCACCTC CTGTCCCAGG ATTCACCCCT CACTTCCCCA CCAACCAAGG 660
ACGCTACACC CAGCCGCCCC CGTCCAGACC CCAAATCCCT CAGGGAGGCG GATCTGGGGT 720
GTCCTCCCCT CTCCTCCTGT TAAACCGTTT CTGCTGCAGC CCTCGGCGTC TCGGTGCAGT 780
GAGTCGGGCC GCGAACCTGT GTTGGTTACA GCCGCACAAT CTGGGGAGAC CCGGGGCTGC 840
GGGCTCGGAG CTGCCCAGAG AGGGCGCCGG GGCCGCAGTC GCCGCGCAGG AACGGGACAG 900
GACGCCCGGG GTCCCGGCTG CATGCCCAGC CCCACCCTGC GGCCGAGGGC CGACCTACGC 960
CAGGGGGACC CGGGTCCGTA GATCCCGAAG TCGCCCTTGG GGAGGCCCGG GTCCAGCCAC 1020
AGCCGATTAC GGCCGGTTCC ACCTAACCCC TCCCCCGCCT CGGGACGCCG GCCCAGCACA 1080
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