| Tag | Content |
|---|
EnhancerAtlas ID | HS147-19884 |
Organism | Homo sapiens |
Tissue/cell | NHEK |
Coordinate | chr18:77443070-77445360 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MEF2A | MA0052.3 | chr18:77444442-77444454 | TCTATAAATAGC | + | 6.37 | | MEF2B | MA0660.1 | chr18:77444442-77444454 | TCTATAAATAGC | + | 6.27 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 3 | ID | Chromosome | Start | End |
| GH18I079682 | chr18 | 77442917 | 77443176 | | GH18I079686 | chr18 | 77444188 | 77444596 | | GH18I079684 | chr18 | 77444782 | 77445326 |
|
Enhancer Sequence | CCACTTGGAG GCTGGAAGGT GAAGACATCA GGGAAGAGGA ACTGCCTTCA ACCGTCATTG 60
ACTCTGCTCA CCAGCCCAGG TGTTTGATTT TTACTAAGCA AGTTCCCAGA ATTGCACGTG 120
GGCTGTTTTA TAATTGACTT ATCTTGACCA CCTCTAAAAG TTCTCTTGAA GTTACAGATT 180
CCTGAGATCT TTATCTGGGA GAGCAAGCAT TTGGTTGAAG TTTGCTTTAA ATGTTTATAG 240
ACTGATTATC GTGTATTGAT CCTTAGAGTA CCCCTTTCAG ATTATGCAAA TAACACGCAC 300
TTGTATAGAC AAGCATGGGC AGAATCCACA ACTGCTTTTG TGGAGGCTCC AACCCTGGCT 360
TCAGCTCATC TGCGTGTGAG GGCAGGGGAG GTGCAGAATC TGCTCCTGGG CTTGTGCTGA 420
AAGGAGGTCC CTTTTAACAG GGACCTCCCA GCACCAATGG AACCCCGTGG CTCTTGGTGA 480
GAGAGAGCAG GTCCTGCCCA GCTGATGGAT CAGAAACTCA GGTGTCAGAA ACGGGGTTTC 540
AGGGCGGCTG CCTGAGGAAT GCGCAGGCGA TCTGACGTTG GAATTCTGGC TTGGGCGAAG 600
CCCTTGATGT GGCCACACAG TTTTGGTCCC TCAAGGGCTT ACTGGTTGCC TGCGTGCCCT 660
GGTGGCTCCT TGGTGAGGGG CCTTTGGAGA AAGTCTTGGG AAATCAGATT TCCCGAGGGT 720
GTTGTTGAGG ACATTGCTGA CGAGGTGTGG GATTTACGGG GAGGACAGCC TGTCTCTTGA 780
GGCTTGGTCG CTGTGTTCAC CCTGCAGGTG TTATGAATTA GCTTCTGGCC CAGGACGGTT 840
TTGGGACCGG GGGGTGCCTA CCCACTGTTG TTCCTTTATC TTGATCCTTT CACAGGGCTT 900
ATAAAAATAC TTATTTTTCA GGAATAACGG GAAGTATCTT TGAAAACATA GCATTAAATC 960
TGCTGAACTG GAGCTTGCAG AGAGCAGACA GCGGCAGCAG CCTGAGTGTG CTAAGCTCAA 1020
GCGTCGCTTG TGTGCCATCA CCTTAGTGAA GGTGGCTCTT GACCCCACTG GCCGCCGGCT 1080
GCTTGACAGT AACTTGTTTA GCTGAGACTG TGTTTGAGAA ACTGAGAGGT GTGGATGTTG 1140
CTTGTACATG TGCAGCCAGC ATGCTCACAG TGCCGAGGAG CAGACTACGC GCTGCTCCAG 1200
AGCGTAGATT AGAACGTCAG TCTAAACAGT TCTTTATAGC ATGGAATTTT AACAAAGAAA 1260
GAAGAATCCC ACGTGGGTAT GTGTGAGTGA GCCTTGTGTA GCTTAGTGTC GGTTACTGAG 1320
GCGGAGCACT GCGGAGAGAG GTAATGGAAC CTGTGGCCCT GTGAAACCTC CCTCTATAAA 1380
TAGCAGGTGT GAGTGAACCT GTGAAAAGCA CCAGCACCAG CCAGGCAGGG TGGGTCCGTG 1440
CCCTCGTTGC CTGCATTGTT GTCACCAGGC AAGGTGGGTC CCTGCTCTTG TTACCTTCAT 1500
TGTTGTCACC AGGCAAGGTG GGTCCGTGCC CTCGTTGCCT GCGTTGTTGT CACCAGGCAA 1560
GGTGGGTCCG TGCCCTCGTT GCCTGCATTG TTGTTACCAG CAACATTTAT CCTAACCACA 1620
TCAGTGGTTA TTTTTAGACA AAGAACCATT CTGGGAACTT AAAAACACTG CATTTGGGTG 1680
AAGTTACAAT AGTCACTAGA TTGTCGTTTT GATCTTTAAT AAGATTGTAT GTTTTTGTCG 1740
GGCTTCATCC TATCTGGCAG AAGTAAGAAC CTCCTCACTC CATTGGAAAG AAACTGAGGT 1800
TCCAAGAAGT TTGGACCTGC CCTGCCCCTT ACAGGGTGTG AGGTCCTGGT GAGGAGGACG 1860
GTGCAGGGAC CTCGTGGTCT CTACTCCCGG TTTCTCTGCG GTGCTCCTTA CGGGGTGTGA 1920
GGTCCTGGTG AGGAGGACGG TGCAGGGACC TCGTGGTCTC TACTCCCAGT TTCTCTGCGG 1980
TGCTCCTTAC GGGGTGTGAG GTCCTGGTGA GGAGGACGGT GCAGATGCCT CGTGGTGTGC 2040
TCAGGCCCTT GAGAGAGCCT CTGTCCTTGG TTCTCTGCGT GCTGCTCTCT GTAGACCAGG 2100
TTTCAGCCCT GGAGATTCCT AGTGTGGGGG GAGTAGCTAG AACAATAGTG TTTGTCTGCT 2160
TTTATAATAT TTATGTGGAG TACAATTATT TTAATAGAAA ATATTCTGAC AGGTCACCAT 2220
CTTTCAGAAA CTAAGTCTTT TTTTTCCTGC AGATTTCTTT GCTTTGGCTT TTTCCCAGTC 2280
ACTCACAGGG 2290
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