| Tag | Content |
|---|
EnhancerAtlas ID | HS105-16542 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr11:122512770-122514450 |
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 | GTAGATGGGA TTACAAGCAT GCACCATCAC GCCCGGCTAA TTTTTGTATT TTTAGTAGAG 60
ACAGGGTTTC ACCATGTTGG CCAGGCTGGT CTTGAACTCC TGACCTCAAG TGATCCGCCG 120
GCCTTGGCCT TCCAAAGTGC TGGGACTACA GGCGTAAGCC ACTGTGCCCA GCCGGTGACA 180
AGTTAACTTT AGTCTCTTTC CACTATCTCT TGTTCATAAC AATTTACTAG TCCATATATG 240
TACAGGTGTA AGCCACTGTG CCCAGCCAGT GACAAGTTAA CTTTAGTCTC TTTCCACTAT 300
CTCTTGTTCA TAACAATTTA CTAGTCCATA TATGAGATGT GATTATGAAA TAAAGAACAA 360
GATCGATATT TCATGTAACT ATACTGAAAT GAAAACATCT AAATCCCTGC CATCCCCAGC 420
ATAGCAGTAC ATCTTGGGAA GCTACCCACT TGGCCTAACT CCACTCACTG TGTTTGCTCA 480
AAACATTTTT GGAATGCTTC TCTCTGCCAG TCAGAGCCCC AAGCAGAAGA CATTCACAGG 540
AAATGAAATC AATGATTTAC TATTCATCCG CCATAGACTG TTACTCATCC TGAACAAGTG 600
AATGAGTGAT TATTTTCAAA ACAGACGAAC AGATAAGAGC AAGCCACAAC CCTCACACCA 660
CTTCACAGAG TGGCCATTCA GCACTCAGAC CAAGTATCCC TCAGCTTCCC AGAACTTTTT 720
CCAGATACGC TCAGAGAAGC ACTTGTTGGC AACTTCACCA GGAGCCACTT TCTAAATGGG 780
GAAGAGATTG GCTCTGAGGA ACAGCATGGA TTAGTCACAG GAGGCGAGGG ATGGTGACAT 840
TCCTGAAAAC AGAGGGGACC AGAAATAGAT TTACACATGT CTAGGGCACT CTTTTCTCTA 900
CAGAAAGGTT TAAAAACACT GGCTCTAATG AGGGGTGGGT GGTATGTAAC AAGGGTAATG 960
TGGGAGAGAG GCAAACCCAT TTCAGGGAAA AGCACTTCCC TGGAGATGTT CTCAAGAGCC 1020
TTTATTTACA GAAAAAGTTG CGTGACCGTG AGCATCCTGA AGAAGAACCA CCTTCCTCAG 1080
ATTTCAAAGG CCAATCATGT TGATGCTCTT AGCCAGTGAT TACTAGCTGG ATCTGTGGAT 1140
TTGTGAGACG CCTGTGTGGT GATGTGAAAA CGGAAAAGTC CAAGAACCGG AAGCCAAGCA 1200
GCTTAGACGG CTCTGGCACC TTGGGGCCAG TGCTAGGCAC TCAGAGTGAG AGCATCCCCT 1260
GCTCAGGTGA AGTAATCTTT CCTGCAAGGC TCTACAACCA CTGGAGAGAG ACCCAAGGTC 1320
CTCCGTCATT TGAAAGGCTT AACTGCAATT TCTTTTTTAT TTTACTTTAT GTCTAATTTT 1380
TAAAATAGAA ACAGGGTCTC TCAGGCCAGG CGCGGTGGCT CACGCCTATA ATCTCAGCAC 1440
TTTGGGAGGC CGAGGTGGGT GGATCATTTG ATGTCAAGAG TTCAAGACCA GCCTGACCAA 1500
CATGGTGAAA CCCCGTCTCT GCTGAAAATA CAGAATTAGC CAGAGATGGT AGTGCGTGCC 1560
TGTAATTCCA GCTACTCGGG AGGCTGAGGC AGGAGAATTG CTCGAATCTG GGACGCAGAG 1620
GTTGCAGTGA GCCGAGGTCA GGCCACTGCA CTCCAGCATG GGCAACAAGA GCTAAATGCT 1680
|
