| Tag | Content |
|---|
EnhancerAtlas ID | HS050-55454 | Organism | Homo sapiens | Tissue/cell | Fetal_stomach | Coordinate | chr5:132625260-132627490 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Arntl | MA0603.1 | chr5:132626735-132626745 | GGTCACGTGC | + | 6.02 | | FOXP2 | MA0593.1 | chr5:132627118-132627129 | TTTGTTTACAT | - | 6.14 | | KLF4 | MA0039.3 | chr5:132627465-132627476 | GGAGGGTGTGG | - | 6.32 | | KLF4 | MA0039.3 | chr5:132625815-132625826 | GCAGGGTGTGG | - | 6.62 | | Klf1 | MA0493.1 | chr5:132625817-132625828 | AGGGTGTGGCC | - | 6.32 | | Nr2f6(var.2) | MA0728.1 | chr5:132626917-132626932 | TGACCCTTGGACCTC | - | 6.29 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TTCCCCAGGA TCCATGCTGA AGGAAAAGGC CTCTAAGACA CAGGGCAGAG GGGCAGGTGT 60
CCTGCTGTGG TAGGCACCTG TCTTCCAGCT TGCCCAACTC TGGGACTAGT CCTGCAGCCT 120
GTCCTGGCAC AGATGTAGCC CAAAGCCTGA CATTCTGCCT CCAGAGCTGC CCAAAGACCA 180
GCACCAAGCC CTTAACTGGT AACACAACCT GATGGTACCA TGTCTCAGTG ATGGGTGGGG 240
GGACTTATTT CATCTGGCTC AGCCAGGCAC AGAGTTGTTT ATTTCAACTC TCTTTGGCTG 300
TCAGTTCACT TGACGAGAAA CAGAAATGAA GCAATGACTT CTGAAACAAA AAGAATCTTG 360
TCTCAATTGC ATTTGTATTC AAATGGGCAA AATAAATTCC AGGGCCTTTC TGAGAGTGTG 420
CCGGGAGTGA GGCCTGCGTG CAAAGTGGGT GCTGATGGCT CTCCATCCCC GAGAGAGTGG 480
CCAAGATCAA GAATTCAGCC TCAGAACAAA CCTTCGGCAG CCAATCTGTT AGGCAGCTGC 540
CCAGGTGCAG CACCAGCAGG GTGTGGCCCC TCGCAAAAGC AGCCTGATGA TTAATTACTG 600
TGTCTTGCCA TCCAGGACTG TGAGGAGGAG AGTGAATAAA CAACAGGGAA TTTTATGTAC 660
CCATGATGAG CAGGAGACAG GTGAGACTGT TTGCTGCTCT AAGTGAACAG AATGTTTGGA 720
GCTGCATCAG AGGGCACTCG CAATGCCTGC ACCTCTGCTG ATGCCCTCTG CCGCCAGCAC 780
TGGGCGAATG AGGAAAATGG AGCTGGGGGC AGAGCTCCTG TGAGGGCCAT CGGGGAGTCC 840
TTGAGCCTCT GTGGCATGGA GATAAGGCAA AGCTTCCAGC CTGGGTCTTC CCTCTTCATC 900
TGGCATCCCT GCTTCCCAGC AGGCCAGCAG CCTTGGGGAG GGGTCCCACA CGGGCGACTG 960
GGGCCCCAGG GAGTTGTACT TTCCACTGGG TCTGTGGATT ATGACATGGC TATCTGAAGC 1020
CCCTGAATTT TAGCTCTAGG CATTATGCCT AGGCTGTGTG GTCTCCTAGG ATGAGGTAAA 1080
GCAGGAACCA CAGCAGAGGG TGGCATGTGG CCTCCAACAC AGTCCCCGCC CCTGGAGCCC 1140
TCTTGGATGG CTCTAAGCAC TGCCCTCAGC TCAGTGACCT CAGCACACTT GGGGATGGAC 1200
AGGCCGGCAG ACAGGGGCCC ATGGCTCCAG GCCACCTGCC TTTGGCCCGC GGTCCCTCGC 1260
CTGCAATGTG GGCTGCTTCT TTTCAACATG ACCCCCTGTG GGACCCCACT GAAATGACAA 1320
TACAGCTGAA TGCTGGCCAG CCCGTCAGGG AGGAGATCGA GCCCAGTGAG TCCGCAGTGC 1380
TGGGCTTCCC ACTCTTGTGC CGCATCTCCC AGCCCCTCAG TCTCCCTAGA GCCTCCGTCT 1440
CCGACTCCCC ACCCATCTCC TGAGCCTGCG CTCAAGGTCA CGTGCAGCTC TCAAAGACTC 1500
AACCGCCCAC TTGGAAGCAC TTAACAATCC GATTACAAAA GAAGTACAAT GGGAAGGGGG 1560
AAAGTATGTT GGTGAGACAG GAGACACAGG AGGGGAGGGG AGTTTGGGGG AAGAGCGGGC 1620
CGTTGAGTCA CACTAAGTGT GTGGTGCCTC TAAGTAATGA CCCTTGGACC TCTTGGTCCC 1680
CTTGGACCTT AGGGACTTCT GAAGACCTGG TGCTGGAAAC CTCATGTCTG GAGGCGTGGG 1740
TGGGACAAGA CCCTCCCCAG GGCAGAGTAA ATTGAGGGGA GCAGCGCACC TGAGTGTCTC 1800
AGACAGGCCC TCCATCTGTT TTTGTAAATC AGGTTTTACT GGAACACAGA CACATTCATT 1860
TGTTTACATT TTATCTACAG CTGCCTCACG TTGCAATGTC AGAGTTCAGT GGCTGTGGTA 1920
GACACTGTAT GGCTTACAAG GCCTAAGATG CCTACATCCT GGCTCTCTAC CAAGAAAGTG 1980
TAAGGGGCTG GCAGGGGAAA GGAGCTCACT TTCAAATAAG ATGGAGAACA GGTGGCCAAA 2040
AAGGTGGAGA GCAAATGAGC GTCTCAAGGA GGGAGAGGTC CGGAGGGCCT GATCTGCAGA 2100
GAGGTCAGAC TGGATAAAGA TAGGAGTGTT CTCTGCCTAA GCCAACCGCA GGGCAAGAGT 2160
GACCTGTTGC AGGCCTCAGT TCCTGTACAG GTGTAGGGGA GGTGGGGAGG GTGTGGACGG 2220
AGCACAGAGG 2230
|
| |
|
|
|
