| Tag | Content |
|---|
EnhancerAtlas ID | HS047-16869 | Organism | Homo sapiens | Tissue/cell | Fetal_placenta | Coordinate | chr19:12550520-12551720 | 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 | GGTCTGGAAC TACTGGGATC AAGCAATACC TCTGCCTTAG CCTCCCAAGG TGCTGGAATT 60
ACAGGAATGA CCCACCGTGT TCAGGAACCC AAAACAATTC TTTCAAGAAA AAGCCATACA 120
TTGCTAGCTG AAAACAAGAT GACAAACTAG TGAAATATCG CCTGGGGCCA AACAGTTCAT 180
ACTGTTGCTG TGAATTAAGG ACAGAAGGTT AGCCTGGGGA AGTCTCTGGA AACCAAGAGA 240
TTTGCTGCCA GCCCTAGGAA GAGTCAGGAT GAGAGAACAC AGTGGTGGAT TTGAGACCCT 300
GCTGCCCACG TCTTTGGAAG ACTCAGAGGG GAAACGGTCG CCCTTGGAAA GGAAGAAAGG 360
ACTGAGGACC ACGGAAACCA CAGCTCCTCC CACACACAAA CCCCACACAC GAGTCTGGAT 420
TCCACCTGGT GACTCGTCGT CACCGTGCAG CCTCCTCACC GGGTTCACAG GAACTGCGAG 480
CCAGGCTGGA GGCGAGATTG CAGTTAGATA TTAAACAGGT GCCCTCAGCC CCGCTGCCTC 540
AAGGGGCCGC CTCCCTGAGA GTCAGGTCAC AGCAGACGCT GACCGCCGGC TTCCCCATTG 600
TGCCTGGGGA TAAGATCTCC GAGTGCTGCT CAAGAGTCGC CGGAGTTCTC AGATCCTGAA 660
TCCCAGCAGA AAGGCTGGCG CCAACCAGGT TGAAGACCCC ACGAGGGAGC CCTCTCAGCA 720
GAATGCGGTT TCTTCACCTC CTGTCCCAGG ATTCACCCCT CACTTCCCCA CCAACCAAGG 780
ACGCTACACC CAGCCGCCCC CGTCCAGACC CCAAATCCCT CAGGGAGGCG GATCTGGGGT 840
GTCCTCCCCT CTCCTCCTGT TAAACCGTTT CTGCTGCAGC CCTCGGCGTC TCGGTGCAGT 900
GAGTCGGGCC GCGAACCTGT GTTGGTTACA GCCGCACAAT CTGGGGAGAC CCGGGGCTGC 960
GGGCTCGGAG CTGCCCAGAG AGGGCGCCGG GGCCGCAGTC GCCGCGCAGG AACGGGACAG 1020
GACGCCCGGG GTCCCGGCTG CATGCCCAGC CCCACCCTGC GGCCGAGGGC CGACCTACGC 1080
CAGGGGGACC CGGGTCCGTA GATCCCGAAG TCGCCCTTGG GGAGGCCCGG GTCCAGCCAC 1140
AGCCGATTAC GGCCGGTTCC ACCTAACCCC TCCCCCGCCT CGGGACGCCG GCCCAGCACA 1200
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