| Tag | Content |
|---|
EnhancerAtlas ID | HS082-07287 |
Organism | Homo sapiens |
Tissue/cell | HCASMC |
Coordinate | chr11:122512310-122514480 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr11:122514239-122514254 | GATGTCAAGAGTTCA | + | 6.13 | | Nr2f6(var.2) | MA0728.1 | chr11:122512862-122512877 | TGAACTCCTGACCTC | - | 6.22 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I122641 | chr11 | 122512322 | 122514653 |
|
Enhancer Sequence | CCATTTCACC AAGATCACGT GCTAACTGGT CAGGAAAAGG AGATAGCCCA GATGTGTGTC 60
TGGGGATGAA AGGACTCTTG ACCATTACGT ATCGAGAAAA TAGTAGAGTT GACTACAAAT 120
TACTGGAGAT GGCAGACAAC AGTGGAAAAG TGTGGATTTC AGCTTCTGGT ACTTACTAAC 180
TGTGTTTGGG TAAATCTCAC CTGAGTCTTG CTTTTCTCAT CCGTAAAATG AGAAAAATAA 240
AACTTTAGTT ACAGGGATGT TATAAGGATT AAATGAAATA ATTCATATAA ACGACCTGAT 300
ATGCACTTGG TGATAAGTTA ACTTTATTTT TTTATTTTAT TATTATTTTT TAAGATGGAG 360
TCTTGCTCTG TCACCCAGGC TGGAGTGCAG CGGCACAATC TCAGCTCACT GCAACCTCCA 420
CCTCCCGAGT TCAAGCCATT CTCCTGCCTC AGCCTCCTGA GTAGATGGGA TTACAAGCAT 480
GCACCATCAC GCCCGGCTAA TTTTTGTATT TTTAGTAGAG ACAGGGTTTC ACCATGTTGG 540
CCAGGCTGGT CTTGAACTCC TGACCTCAAG TGATCCGCCG GCCTTGGCCT TCCAAAGTGC 600
TGGGACTACA GGCGTAAGCC ACTGTGCCCA GCCGGTGACA AGTTAACTTT AGTCTCTTTC 660
CACTATCTCT TGTTCATAAC AATTTACTAG TCCATATATG TACAGGTGTA AGCCACTGTG 720
CCCAGCCAGT GACAAGTTAA CTTTAGTCTC TTTCCACTAT CTCTTGTTCA TAACAATTTA 780
CTAGTCCATA TATGAGATGT GATTATGAAA TAAAGAACAA GATCGATATT TCATGTAACT 840
ATACTGAAAT GAAAACATCT AAATCCCTGC CATCCCCAGC ATAGCAGTAC ATCTTGGGAA 900
GCTACCCACT TGGCCTAACT CCACTCACTG TGTTTGCTCA AAACATTTTT GGAATGCTTC 960
TCTCTGCCAG TCAGAGCCCC AAGCAGAAGA CATTCACAGG AAATGAAATC AATGATTTAC 1020
TATTCATCCG CCATAGACTG TTACTCATCC TGAACAAGTG AATGAGTGAT TATTTTCAAA 1080
ACAGACGAAC AGATAAGAGC AAGCCACAAC CCTCACACCA CTTCACAGAG TGGCCATTCA 1140
GCACTCAGAC CAAGTATCCC TCAGCTTCCC AGAACTTTTT CCAGATACGC TCAGAGAAGC 1200
ACTTGTTGGC AACTTCACCA GGAGCCACTT TCTAAATGGG GAAGAGATTG GCTCTGAGGA 1260
ACAGCATGGA TTAGTCACAG GAGGCGAGGG ATGGTGACAT TCCTGAAAAC AGAGGGGACC 1320
AGAAATAGAT TTACACATGT CTAGGGCACT CTTTTCTCTA CAGAAAGGTT TAAAAACACT 1380
GGCTCTAATG AGGGGTGGGT GGTATGTAAC AAGGGTAATG TGGGAGAGAG GCAAACCCAT 1440
TTCAGGGAAA AGCACTTCCC TGGAGATGTT CTCAAGAGCC TTTATTTACA GAAAAAGTTG 1500
CGTGACCGTG AGCATCCTGA AGAAGAACCA CCTTCCTCAG ATTTCAAAGG CCAATCATGT 1560
TGATGCTCTT AGCCAGTGAT TACTAGCTGG ATCTGTGGAT TTGTGAGACG CCTGTGTGGT 1620
GATGTGAAAA CGGAAAAGTC CAAGAACCGG AAGCCAAGCA GCTTAGACGG CTCTGGCACC 1680
TTGGGGCCAG TGCTAGGCAC TCAGAGTGAG AGCATCCCCT GCTCAGGTGA AGTAATCTTT 1740
CCTGCAAGGC TCTACAACCA CTGGAGAGAG ACCCAAGGTC CTCCGTCATT TGAAAGGCTT 1800
AACTGCAATT TCTTTTTTAT TTTACTTTAT GTCTAATTTT TAAAATAGAA ACAGGGTCTC 1860
TCAGGCCAGG CGCGGTGGCT CACGCCTATA ATCTCAGCAC TTTGGGAGGC CGAGGTGGGT 1920
GGATCATTTG ATGTCAAGAG TTCAAGACCA GCCTGACCAA CATGGTGAAA CCCCGTCTCT 1980
GCTGAAAATA CAGAATTAGC CAGAGATGGT AGTGCGTGCC TGTAATTCCA GCTACTCGGG 2040
AGGCTGAGGC AGGAGAATTG CTCGAATCTG GGACGCAGAG GTTGCAGTGA GCCGAGGTCA 2100
GGCCACTGCA CTCCAGCATG GGCAACAAGA GCTAAATGCT CTTGTTGTTC TCAAAAAAAA 2160
AAAAAAAGAA 2170
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