| Tag | Content |
|---|
EnhancerAtlas ID | HS148-08517 | Organism | Homo sapiens | Tissue/cell | NHLF | Coordinate | chr19:12550480-12551720 | 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 | ATTTACACTA GAGACAAAGT CTTGCCATGT TGCCCAGGCT GGTCTGGAAC TACTGGGATC 60
AAGCAATACC TCTGCCTTAG CCTCCCAAGG TGCTGGAATT ACAGGAATGA CCCACCGTGT 120
TCAGGAACCC AAAACAATTC TTTCAAGAAA AAGCCATACA TTGCTAGCTG AAAACAAGAT 180
GACAAACTAG TGAAATATCG CCTGGGGCCA AACAGTTCAT ACTGTTGCTG TGAATTAAGG 240
ACAGAAGGTT AGCCTGGGGA AGTCTCTGGA AACCAAGAGA TTTGCTGCCA GCCCTAGGAA 300
GAGTCAGGAT GAGAGAACAC AGTGGTGGAT TTGAGACCCT GCTGCCCACG TCTTTGGAAG 360
ACTCAGAGGG GAAACGGTCG CCCTTGGAAA GGAAGAAAGG ACTGAGGACC ACGGAAACCA 420
CAGCTCCTCC CACACACAAA CCCCACACAC GAGTCTGGAT TCCACCTGGT GACTCGTCGT 480
CACCGTGCAG CCTCCTCACC GGGTTCACAG GAACTGCGAG CCAGGCTGGA GGCGAGATTG 540
CAGTTAGATA TTAAACAGGT GCCCTCAGCC CCGCTGCCTC AAGGGGCCGC CTCCCTGAGA 600
GTCAGGTCAC AGCAGACGCT GACCGCCGGC TTCCCCATTG TGCCTGGGGA TAAGATCTCC 660
GAGTGCTGCT CAAGAGTCGC CGGAGTTCTC AGATCCTGAA TCCCAGCAGA AAGGCTGGCG 720
CCAACCAGGT TGAAGACCCC ACGAGGGAGC CCTCTCAGCA GAATGCGGTT TCTTCACCTC 780
CTGTCCCAGG ATTCACCCCT CACTTCCCCA CCAACCAAGG ACGCTACACC CAGCCGCCCC 840
CGTCCAGACC CCAAATCCCT CAGGGAGGCG GATCTGGGGT GTCCTCCCCT CTCCTCCTGT 900
TAAACCGTTT CTGCTGCAGC CCTCGGCGTC TCGGTGCAGT GAGTCGGGCC GCGAACCTGT 960
GTTGGTTACA GCCGCACAAT CTGGGGAGAC CCGGGGCTGC GGGCTCGGAG CTGCCCAGAG 1020
AGGGCGCCGG GGCCGCAGTC GCCGCGCAGG AACGGGACAG GACGCCCGGG GTCCCGGCTG 1080
CATGCCCAGC CCCACCCTGC GGCCGAGGGC CGACCTACGC CAGGGGGACC CGGGTCCGTA 1140
GATCCCGAAG TCGCCCTTGG GGAGGCCCGG GTCCAGCCAC AGCCGATTAC GGCCGGTTCC 1200
ACCTAACCCC TCCCCCGCCT CGGGACGCCG GCCCAGCACA 1240
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