| Tag | Content |
|---|
EnhancerAtlas ID | HS052-18448 | Organism | Homo sapiens | Tissue/cell | Fibroblast_foreskin | Coordinate | chr19:12550540-12551720 | 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 | AAGCAATACC TCTGCCTTAG CCTCCCAAGG TGCTGGAATT ACAGGAATGA CCCACCGTGT 60
TCAGGAACCC AAAACAATTC TTTCAAGAAA AAGCCATACA TTGCTAGCTG AAAACAAGAT 120
GACAAACTAG TGAAATATCG CCTGGGGCCA AACAGTTCAT ACTGTTGCTG TGAATTAAGG 180
ACAGAAGGTT AGCCTGGGGA AGTCTCTGGA AACCAAGAGA TTTGCTGCCA GCCCTAGGAA 240
GAGTCAGGAT GAGAGAACAC AGTGGTGGAT TTGAGACCCT GCTGCCCACG TCTTTGGAAG 300
ACTCAGAGGG GAAACGGTCG CCCTTGGAAA GGAAGAAAGG ACTGAGGACC ACGGAAACCA 360
CAGCTCCTCC CACACACAAA CCCCACACAC GAGTCTGGAT TCCACCTGGT GACTCGTCGT 420
CACCGTGCAG CCTCCTCACC GGGTTCACAG GAACTGCGAG CCAGGCTGGA GGCGAGATTG 480
CAGTTAGATA TTAAACAGGT GCCCTCAGCC CCGCTGCCTC AAGGGGCCGC CTCCCTGAGA 540
GTCAGGTCAC AGCAGACGCT GACCGCCGGC TTCCCCATTG TGCCTGGGGA TAAGATCTCC 600
GAGTGCTGCT CAAGAGTCGC CGGAGTTCTC AGATCCTGAA TCCCAGCAGA AAGGCTGGCG 660
CCAACCAGGT TGAAGACCCC ACGAGGGAGC CCTCTCAGCA GAATGCGGTT TCTTCACCTC 720
CTGTCCCAGG ATTCACCCCT CACTTCCCCA CCAACCAAGG ACGCTACACC CAGCCGCCCC 780
CGTCCAGACC CCAAATCCCT CAGGGAGGCG GATCTGGGGT GTCCTCCCCT CTCCTCCTGT 840
TAAACCGTTT CTGCTGCAGC CCTCGGCGTC TCGGTGCAGT GAGTCGGGCC GCGAACCTGT 900
GTTGGTTACA GCCGCACAAT CTGGGGAGAC CCGGGGCTGC GGGCTCGGAG CTGCCCAGAG 960
AGGGCGCCGG GGCCGCAGTC GCCGCGCAGG AACGGGACAG GACGCCCGGG GTCCCGGCTG 1020
CATGCCCAGC CCCACCCTGC GGCCGAGGGC CGACCTACGC CAGGGGGACC CGGGTCCGTA 1080
GATCCCGAAG TCGCCCTTGG GGAGGCCCGG GTCCAGCCAC AGCCGATTAC GGCCGGTTCC 1140
ACCTAACCCC TCCCCCGCCT CGGGACGCCG GCCCAGCACA 1180
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