Tag | Content |
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EnhancerAtlas ID | HS051-00458 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr1:26689650-26690730 |
Target genes | Number: 24 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr1:26690485-26690504 | GGGCGCCCCCTGCTGGGCG | - | 7.06 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I026363 | chr1 | 26690341 | 26690550 |
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Enhancer Sequence | TCAGATGCGG GATAAATGCT GCCAACTGCC CAGCACCCCT AGCAGGGCCT GAGGTCCTCT 60 CCAAATCTCT GCCCACTTCT CTCTCCCTCC CCGTCATCTC CCTCAGGGCC CATCATCCCC 120 AGGATACTCT ACTCTTTCTG CTGCCCTGTA GGGGAGATGG CAGTGGTCAG AAGGCCAGGG 180 GTAAGAGGTA CCCCAGGTAT ATTGTGGAAC ACTGCTATTC AAAATGTGGT TCACAGACCA 240 GCAGTGCTGG TATCACACTT TGGGAGCATG TTAGAAATGC AGGTTCTCAA GTCCGGCCCC 300 AGACCTGCTG AATCAAAAAC TCTGGGAGGG CTGGGCACAC TCTCGTGGCT GTAATCCCAG 360 CATTTTGGGA GGCCGAGGAG GGAGGATCAA TGGAGCCCAG GAGTTCAATA CCAGCCTGAG 420 AAACACATTG GGACCCCGTA TGCACAAAAA ATTTGAAAGT TAACGAGGAG TGGTGGTGTT 480 TACCCTTCGT CCCAGCTACC GGGGAGGATG AAGTGGGAGA ATCCCTTAAG CCCAGGAGTT 540 TGAGACCAGC GTGGGCGACA GAATGAGACT CCATATGGAA AAAAAAAAAA AAAAAAAAGA 600 TAACTCTGGG GCTGGGAGCT ACTCTGGAGG CTGAGGTGGG AGGATCACAA AAACTCTAGG 660 AATCTGCATG TTTACTAGCT CTCCAGGTGG TCTGAGGCTC ATGAAAGTTT AAGAACTCCT 720 GCCCTGCAGG ATCCAGCAGG GCTTCTCCCC ATAACCACAA TGTGCCTTCA ACTTCAGAAC 780 TAGCCAGAGA GCGCACAGTT TCCGCCCTTT GCTAACGCAC TGAGATGCGC TCCCTGGGCG 840 CCCCCTGCTG GGCGATGCGG ATGGTGAGGC CAATCGCATC GGCGGTCGCG CAGATTTGTG 900 GGATCCCACT TGAAAAAGGT TGGTCATCGG ACTGTGGTCT AGACTCACCA AAATCTACCC 960 ATTCCCTCAT CTGACTGCCC AAAAAAATAA ATAAGAAGCT TAACTTGGAG TCCAGAAAGG 1020 ATGGTTGTCC AGGTAAGGGC TTTCTTTGCC CAGAGCAAAT GTTGAGAGAC TAAACCTAAC 1080
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