| Tag | Content |
|---|
EnhancerAtlas ID | HS176-20898 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr2:71169620-71170780 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RREB1 | MA0073.1 | chr2:71170455-71170475 | AGGGAGTGGGTGAGGTGGGG | - | 6.26 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | CTGGGAAGGG GAGGGACTTT TGGTTTTTCT TTGGCATGGG GTGGCTCGGG GCCAGGCTTG 60
CCCAAAGCAA GAGGGTAAGT GAACCGAGAA CCAGTGTGGT CCAGCAAGAA GCACAGGGTG 120
GGTTCCCAGC CCCAGCTCTG CTACAGATGT GCTGTGTGGC CCTGGGCAAG GCTTCTCACA 180
CTTCTGGGCC CCATTTTCCT TGCCTGTGAA AGAGGGGTTG GGCCACTCCC CTCTGCATCC 240
TGCCAGCCTG TGGCTGACCC AGAGGCCTCA CAGACCCCCT GCCCACCTTG CCAAATGCCT 300
TCATCTCAGG TGTCTCATCT CATTGGTGCA TCACAAGAAC CTCAGAGAAG GGCACTGGTC 360
AGGACTATGG GCAAGGGACT GTCCCAGGTC TCTCAGCCAG CCTCTAGCAG AACCAAAACT 420
AGGCTTGCCT CCCGCAAGTC CACAGCTTCT TCTATGGGAG TTAGGAAGTA TTTTTTGGCA 480
TCTAACCCAA TTCCCTATGC AAGCTGAGCT CATTTGCCAT GTGTGGGTCT CTGCAGCTGC 540
CACATCTGCA GGCATTTCCC TCCTTCCCTT GCCTTTTCAC TCCCTCCCCT CCCATGCTGA 600
GCACCCAGTG AGCCTGGGGA GTCCAGGAAC CTTGTGATGA GAGCAGAGGC CCCGTCTGGT 660
TTTTCTCACT GACGTCTGCA CCCCCTACAC ACCACATACA CACACACACA CACACACTGC 720
TCAATCAGTG TGGGGTGAAT GGAGGGAAAT GCAGTCCTGG TGAGGGCAGA GGAGGGCACT 780
TTTCGGCCAC AGCCGGGGGC CAGGAGCTTT TGGAAAATGC TTGGAGTGAG AGAGGAGGGA 840
GTGGGTGAGG TGGGGGTTGA AGCCAGAGGG GAAGCAGCCT CAGGGATGAG AGGCCTCTGT 900
GTGGTGGGGG CGGACTCTGA GGAGGCCTCT GCCCTCTGCC TGGCCCTCCC CCAGCCTCCT 960
GCAGGTGTCC GAGCAGCAGG GGCCCTGCGG GCAGGGGCAT GACCCTTACA GCAATGGTGG 1020
CTGGCCCTGT CACAGCTAAT GACCCTGACG GCCCAGGCTG GGAAGGAGGT GGGGTGTGGA 1080
GAGAGGAAGG GAAGGCAGAG GATGCCTCTG TGTGTGTGAG CAGGGTGTTT GGGGTGAGAC 1140
CCCTACTCAC CCCCGCCCCT 1160
|
