| Tag | Content |
|---|
EnhancerAtlas ID | HS108-19638 | Organism | Homo sapiens | Tissue/cell | K562 | Coordinate | chr19:12550530-12551720 | 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 | TACTGGGATC AAGCAATACC TCTGCCTTAG CCTCCCAAGG TGCTGGAATT ACAGGAATGA 60
CCCACCGTGT TCAGGAACCC AAAACAATTC TTTCAAGAAA AAGCCATACA TTGCTAGCTG 120
AAAACAAGAT GACAAACTAG TGAAATATCG CCTGGGGCCA AACAGTTCAT ACTGTTGCTG 180
TGAATTAAGG ACAGAAGGTT AGCCTGGGGA AGTCTCTGGA AACCAAGAGA TTTGCTGCCA 240
GCCCTAGGAA GAGTCAGGAT GAGAGAACAC AGTGGTGGAT TTGAGACCCT GCTGCCCACG 300
TCTTTGGAAG ACTCAGAGGG GAAACGGTCG CCCTTGGAAA GGAAGAAAGG ACTGAGGACC 360
ACGGAAACCA CAGCTCCTCC CACACACAAA CCCCACACAC GAGTCTGGAT TCCACCTGGT 420
GACTCGTCGT CACCGTGCAG CCTCCTCACC GGGTTCACAG GAACTGCGAG CCAGGCTGGA 480
GGCGAGATTG CAGTTAGATA TTAAACAGGT GCCCTCAGCC CCGCTGCCTC AAGGGGCCGC 540
CTCCCTGAGA GTCAGGTCAC AGCAGACGCT GACCGCCGGC TTCCCCATTG TGCCTGGGGA 600
TAAGATCTCC GAGTGCTGCT CAAGAGTCGC CGGAGTTCTC AGATCCTGAA TCCCAGCAGA 660
AAGGCTGGCG CCAACCAGGT TGAAGACCCC ACGAGGGAGC CCTCTCAGCA GAATGCGGTT 720
TCTTCACCTC CTGTCCCAGG ATTCACCCCT CACTTCCCCA CCAACCAAGG ACGCTACACC 780
CAGCCGCCCC CGTCCAGACC CCAAATCCCT CAGGGAGGCG GATCTGGGGT GTCCTCCCCT 840
CTCCTCCTGT TAAACCGTTT CTGCTGCAGC CCTCGGCGTC TCGGTGCAGT GAGTCGGGCC 900
GCGAACCTGT GTTGGTTACA GCCGCACAAT CTGGGGAGAC CCGGGGCTGC GGGCTCGGAG 960
CTGCCCAGAG AGGGCGCCGG GGCCGCAGTC GCCGCGCAGG AACGGGACAG GACGCCCGGG 1020
GTCCCGGCTG CATGCCCAGC CCCACCCTGC GGCCGAGGGC CGACCTACGC CAGGGGGACC 1080
CGGGTCCGTA GATCCCGAAG TCGCCCTTGG GGAGGCCCGG GTCCAGCCAC AGCCGATTAC 1140
GGCCGGTTCC ACCTAACCCC TCCCCCGCCT CGGGACGCCG GCCCAGCACA 1190
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