Tag | Content |
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EnhancerAtlas ID | HS052-24123 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr21:30486700-30487800 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6 | MA0677.1 | chr21:30487273-30487287 | TGACCTTTGACACA | - | 6.23 | TCF7L2 | MA0523.1 | chr21:30487421-30487435 | TTCCTTTGATGTGT | - | 6.91 |
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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 |
GH21I029114 | chr21 | 30486483 | 30488253 |
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Enhancer Sequence | TTATATTTAT TTATTTTTTA TTTATTTTTG AGACAGGGCC TTGCTCTGCC ACCCAGGCTG 60 GAGGACAGTG GTGCAATCAC GGCTCACTGC AACCTCGACC TCTCGAGCTC AATTGATCCT 120 CCCACCTCAG CCTCTCAAGT AGCTGAGTCT ACAGGTGTGA GCCACTACAC CTGGCTAAGC 180 TTTGTATTTT TTGTAGAGAC AGGTTCTTGC TATGTTGCCC AGGCTGGTCT CAAACTCCTG 240 GGCTCAAAAG ATCCACCTGC CTTGGCTTCC CAAAGTGCTG GGATTACAGG CATGAGCCAC 300 TGCACCTGGC TATGATTTTT AAAATTCAAA AGCAGAGTAT AGATGGAAAC CTAAATGACG 360 GCAAATAATA ATAATAATAA ACTCTCAGAG ACTGTAGGGT GTAGACCAGG CCCTGGATTA 420 ATGGGAATGT CTACATTCCA TCCCCTTGAG CTCAAATATT CTAGTCAAAG TGAGTCACCC 480 AAGGTTACTT TCGATAGAAG GTGGGTGTGG AAAGACTTGG ACAAGAAAAT CTAGGAGCCA 540 CAGGAGGCCA GATGCTTCTC TCTACAGGAG ACTTGACCTT TGACACAGAG CCCTGAGGAA 600 ATCTTGACTG TTTTCTTTAG TATTTGATCC TCAGCTGATG CAAACCATTT ATTTATGTTT 660 GCCCATTGGA CAGCAGGGGG TTTGGGCTGT TTTCACGTCT ATATAAGGCA GTGCAGAGTG 720 CTTCCTTTGA TGTGTCCCGC CTCTGCTGTG GCCTCATCAT GCCGGGCTAA CTTGGTCTTC 780 CCCATGTAGG GCTCTAGATC CCACTCCTAA AAACTCTAAT TTGAGGATCA GAGTCTGAAA 840 TAGCCCAAAA GGTATCCTGT TTAGCTTGTC ATTTAAATAG CTAAGCCCCT GCTACGACCA 900 TTTAAAACCA TCTCACCTTT CATTTAGCTA AGCAGTTCTT TTTTCAGATT TGGCTTGTTT 960 GTGTTTTTCT CTATTCACTG CAATTCTGCA TCTATAAAAA GCATTGATGG AAGGAGGAAA 1020 GAGTGAAATC AACATTCTTT TTAGTAGAGG GCCTTAGTTG GAATTGCAGA AATATCAGGG 1080 AACTTAGCTA TAAAGGCCTC 1100
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