Tag | Content |
---|
EnhancerAtlas ID | HS133-20657 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr21:44085070-44086890 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr21:44086468-44086486 | GGAAGGAGGGAGGGCAGC | + | 6.37 | JUN | MA0488.1 | chr21:44085101-44085114 | AAGATGAGGTCAT | + | 6.54 | JUND(var.2) | MA0492.1 | chr21:44085100-44085115 | CAAGATGAGGTCATA | + | 6.23 | KLF14 | MA0740.1 | chr21:44086275-44086289 | CAGTGGGCGTGGTC | - | 6.09 | KLF14 | MA0740.1 | chr21:44086213-44086227 | GTGGGGGCGTGGCC | - | 6.39 | KLF14 | MA0740.1 | chr21:44086234-44086248 | CAGTGGGCGTGGCC | - | 6.48 | KLF16 | MA0741.1 | chr21:44086215-44086226 | GGGGGCGTGGC | - | 6.62 | Klf12 | MA0742.1 | chr21:44086233-44086248 | GCAGTGGGCGTGGCC | - | 6.04 | Klf12 | MA0742.1 | chr21:44086274-44086289 | GCAGTGGGCGTGGTC | - | 6.05 | Klf12 | MA0742.1 | chr21:44086253-44086268 | CGAGAGGGCGTGGTC | - | 6.16 | Nr5a2 | MA0505.1 | chr21:44086351-44086366 | GCTGTCCTTGGACTT | - | 6.16 | RUNX1 | MA0002.2 | chr21:44085400-44085411 | CTCTGTGGTTT | + | 6.14 | SP1 | MA0079.4 | chr21:44086276-44086291 | AGTGGGCGTGGTCAT | - | 6.47 | SP1 | MA0079.4 | chr21:44086214-44086229 | TGGGGGCGTGGCCAC | - | 6.81 | SP1 | MA0079.4 | chr21:44086235-44086250 | AGTGGGCGTGGCCAC | - | 7.06 | SP3 | MA0746.2 | chr21:44086276-44086289 | AGTGGGCGTGGTC | - | 6.32 | SP3 | MA0746.2 | chr21:44086214-44086227 | TGGGGGCGTGGCC | - | 6.57 | SP3 | MA0746.2 | chr21:44086235-44086248 | AGTGGGCGTGGCC | - | 6.92 | SP4 | MA0685.1 | chr21:44086274-44086291 | GCAGTGGGCGTGGTCAT | - | 6.12 | SP4 | MA0685.1 | chr21:44086233-44086250 | GCAGTGGGCGTGGCCAC | - | 6.83 | SP4 | MA0685.1 | chr21:44086212-44086229 | GGTGGGGGCGTGGCCAC | - | 7.05 | SP8 | MA0747.1 | chr21:44086214-44086226 | TGGGGGCGTGGC | - | 6.11 | SP8 | MA0747.1 | chr21:44086276-44086288 | AGTGGGCGTGGT | - | 6.74 | SP8 | MA0747.1 | chr21:44086235-44086247 | AGTGGGCGTGGC | - | 7.22 |
|
| 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 |
GH21I042666 | chr21 | 44086201 | 44086470 |
|
Enhancer Sequence | GAAATAGGGT ATTTGCAGAC ATAATCACAT CAAGATGAGG TCATACTGCA TTGGGATGGG 60 CCTCAAGCCC ATATGCCCGC CATCCTTCTA AGGAGAGGGA AAGGCAGACA CACATTTGTC 120 CATGGAAATG AGAACGGAAG ACGTAGAGAC AGAATCAGGC CATGTAAAGA CAGACTCAGA 180 GACCAGAGTG ATGCATGTAC AAGCCAGGCT CTGCGGGCAG CCCCTAGAAG CTGGAAGAGG 240 CAAGCCTCCT CCCTGGAGTC CTGGGAAGGA GCCAGCCCCG CCCATGCCTC GAGCTCAGGC 300 TTCAGGCCTC CGGAGCCAAG AGAGATAAAC CTCTGTGGTT TCATGTCACC CAGTTTGTGG 360 TCTTTGTTAT AGCAGCCCCA GGACACTCAG GGGGTTGCCT TGTCCACCCC CATCCTGGCC 420 CTCTGAGGGA CTGGTTGGCT CTTAGAAGAC CGTTCAACCT GCCCTCTGGT CCTCCTCCCC 480 CACCCAGAGA CCCCTGGCTA CACCCTGCCC AAGGGAGCTC ACCAAAGCCC ACAGGGTCCC 540 TGTGATCTTG TCACCTGGGC TCCCACAGGC CAGCAGTGTT GGAACCTGGA CATCTGGCTC 600 CAGCCTTGGT GGCCACCCCC GACCTTGCTC TGCTCCTACA GCTCCCGGCC TTCCCTGCCC 660 TGGCCGGCCC TTGCTGAATG TCCCCGCTCC TAGGAAGCCG GATGTGTCGC GTGCAGGTGC 720 CTCTCTGCAC TGTAATAACT CCTCACCAGG CACCCTTGGA GCCCAGGATC AAGTCACTCA 780 CCTTCCAACC CTGCCCCTGC CCAGAGACTG GCACGAGAAC CAGTAACAGT TGTTGAATAA 840 TGAACAATGG ATGCATGCAG CTCACCCGTG AGAGGGCGTT GCTCGGCTGG GCCAGGGATG 900 AAGCTTCTCC CGCGTGGCTC CACCGTCTAT CCCTCAAGCT CCTGATGCTC CCCTGGGCAC 960 CTCTGCGCCA TGAGGCCCCG TTGAAGTCAG TTGGGGAGGC AGTGTGGACC GTGAGAAGGG 1020 AGTCCTAAGC ACAGGAAACG CTGCCTTCCT GGGGCCCTAA AGAACAGGCT CACCTTCCCC 1080 AAGGGCCTTC AGGCCCTGAC ATCTAAAAAG ATGTTCTTTA TCAAAGGGGA AAGCAGCCCT 1140 GGGGTGGGGG CGTGGCCACC AGTGCAGTGG GCGTGGCCAC AACCGAGAGG GCGTGGTCAT 1200 TCGTGCAGTG GGCGTGGTCA TCAAGAAAGG GCGTGGCTGC AGCCGGAAGG GCGTGGCTAT 1260 CAGCTCCAGA AGGCCCTTCT TGCTGTCCTT GGACTTGGGT TCTCCTTGTC GACGAGGATC 1320 TCAGCTGGAG CTGCCAGGGG CAGGGCTGGC ACCAAAGCAC TTCTGAAGTC TCCCCGCCTC 1380 CCAAGTGTGA GGCTGTGGGG AAGGAGGGAG GGCAGCTGGC TTGTTTCTGG ATGAGCCCAT 1440 CTGACTCAGC AGCTGGGACC CAGCAGGAGC GCAGAGCAGG TCCTGAAGGT GCCGAGGCCC 1500 CACCCGCAGC TCCGTCTCAG CTTTGTGAGG GCTGCACTCC CCCGTGTGCA TCCGGCGTCA 1560 CAAAGGACCA CAGGCCCGGC GGCCTCCACA GCAGACACCA AGGCCCTCGC GGTCTGAAGG 1620 CCGAATTCCC AGGTCAGGCT GCAGCAGGGC TGGTTCCTGA GGCCTCTCCT GGGCTGGCAC 1680 CTCCTCCCCG TGTCCATGCA GGGCCGAGCC TCTGCATGTC TGTGTCCTCG GCGCCTCGTT 1740 TTACAAGGAC ATCTCATTTT AAAGGCCCGG TCTCCAAATA AGGTCATATC GTGAAGTGCT 1800 GGGGTCAGAA CTACAGCATG 1820
|