Tag | Content |
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EnhancerAtlas ID | HS105-51745 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr21:38965030-38966500 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MEF2A | MA0052.3 | chr21:38965301-38965313 | TTTATTTTTAGA | - | 6.07 | REST | MA0138.2 | chr21:38965136-38965157 | TCCAGCACCCAGGGCAGCCCT | + | 6 |
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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 |
GH21I037590 | chr21 | 38963231 | 38967192 |
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Enhancer Sequence | CTGGTGAGCC CTGCTCCCGC CCCAGATGAC CCCTCATGAC CCCTAATCTT TGGGGACAAG 60 CCTGCTGACA CTGACCAGGC TGGAGGACAT TTGTTTGCTC CCCTCCTCCA GCACCCAGGG 120 CAGCCCTGGA GTTTTTTCTA GCTTTCCCCG ATTCTTTTTT CAGCCCTATT TTATTTTCTG 180 CATCTTTTTT TCCTATATCT CAAGTAGCCT GCAATCAAAC CAAAGCCACG GTCTGAATGT 240 TGTGGTTATT GAGAGGGTAA AGTTTTTTAT TTTTATTTTT AGAGATGGCA TCTCTCACTG 300 TTACCCAGGC TGGAGTGCAG TGGTGTGATC CTTTGGACTC AGTTGATCCT CCCGCTTCAG 360 CCTCTTGAGT AGCTGAGTCT ACAGGCATGC ACCACTGTGG AGTCCAAATT AGTAAGCAAC 420 AATGAGAAAG GGGCCCCCTG TGGGGACAGC CATTGTTCTG AGAGACCGGT AATCACAGAC 480 AACCCACTAG CACAACATCC TGTTCCCAAA TACCTCGCGC CACACAGCGC CAGCAGCACA 540 ACCTCATTCT GCACATAGCC CCCTCCAGTG TGAACCTATA AAACTTCCCT CCAGCCCCTG 600 CCTCTCTGCA CACAGCCCTT TCTCTGCTGT GCTGTCCATT AAACCCTTGC AACATTTCTC 660 TGTACCTTAC CTAATAAATT GGCCTTTCTT TACTTACAAC TGTCTTGGTA AAATCTTCTA 720 CCACCTGTGA TGCTGGCCCC AGCCAGTCGC ACCCACGACA GCCACCATGT CCGGCTTTTT 780 AAAAAAATTT TTGTAGAGAT GGGGTCTTGC CATGTTGCCC AGGCTGGTCT TGAACTCCTG 840 GCTTCAAATG ATCCTCCTGC CTCAGCCATC TAATATGCTG GGATTACAAG CGCAAGCCAC 900 CGTGCCTAGG CTGCAAACGT TTTTCTAAAC GTTAAAGCAA TCATTTGTTT AAAACTATTT 960 TTAATTTGAA AAGAGAGAGA AAGTACAATA GGTAAATGCG TGAAATTGGT GGTGGGCTGC 1020 AAAAATGCTC ATACTGAGTT CTTTCTGTCT GTCCCCTCTC GACTTGGTTA TCAATTCCTG 1080 CACCCCCTTG GGCTCTGTCA GGATTGCATC CTGCCTGCTT TGTACACATG GAACAGACTT 1140 CTGGGTTCTT GGCAGCCCTA AGGGATCAGG CTCTAGTGAG TGATCACAGC CAGCGCTGCC 1200 TTCCTTTCAG GCCCTGGTGC TTCTCTGTTT ATGTGCCTTA CGGCTTCTGC AGCGCTGCGA 1260 TGCCTGGAGG AAGAATTTCC CACTTAGAGG CTTACTGCTC TGTGCACAGA CACGCGAGTT 1320 GCAGAATGAG TGTCTAATTT GGCGTGGCCC ATGAAGGGTG AAGGCTCAGC CCCACGTCTT 1380 GGTTTACCTT CAGCTGCTGG CAATGGAGGT GAGGGGGAGG GTGGGGCCGT GGGTTTCCAC 1440 TTAATTTGTT TCTCCTGGAT CTTTGGCCCT 1470
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