Tag | Content |
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EnhancerAtlas ID | HS146-01468 |
Organism | Homo sapiens |
Tissue/cell | NHDF |
Coordinate | chr1:249167000-249168770 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MEF2A | MA0052.3 | chr1:249167156-249167168 | TCTAAAAATAGA | + | 7.22 | MEF2C | MA0497.1 | chr1:249167154-249167169 | AGTCTAAAAATAGAA | + | 7.58 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_12804 | chr1:249167545-249167799 | CD34_fetal | SE_21287 | chr1:249165758-249169105 | CD8_Memory_7pool | SE_42088 | chr1:249167099-249168183 | LNCaP | SE_43352 | chr1:249166222-249168985 | Lung |
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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 |
GH01I248871 | chr1 | 249165877 | 249169108 |
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Enhancer Sequence | TCTCGAACTC CCGACCTCAG GTGATCCGCC CACCTCCCAA CGTGGTGGCG GGATTACAGG 60 CATGAGCCAC CGCGCCCGGC TGCATGACAT ATATTTTAGT TTTTGAAAAA TATTTTAGCA 120 AAAGTCACTT TAGTGAGGCC TTACTTAACT GCACAGTCTA AAAATAGAAC TTCTCCACCA 180 CTTCATTGCT TTTGGTTTTT CCTCACACTC TGTACATGTG ATTGTGCTGG TCATCTCCTT 240 CACTAGCAAA TCAGCTCACC AAGTTGGGGC TTTGTCTATT TACCGTTGTG TTCCCAGTGG 300 ACACTCGATG TTAAGATTCA ACGAATGAAT GCCTGGACGA GTGGTATCTG GGCTCACAGG 360 TAACCTCACA GCCCACCGGG AGGACACTGC CAGAGCTGCT CTGCACTGCG AGTCCCGGGC 420 CTTCCCATTG GACGCTAAGG CACTCGTTAA CTGCTGTGTA AACGCAGCCT GACTTCCCTC 480 ACCTCAGGCG AGGCCCGCAT CAGGCCCCTC TGACCTAGGA CCTCCCGATC CGGCCGTTAT 540 CGCCAACCGT ATCTGTGTGG TTTCGTGGAG GAAGCGCGGT GGACCTTGAG GGGAGGGTAC 600 GCGCAGGCAC AATAAAGCAG AAAGCCGCTA TAATAATGAT GATAATGAAG AAAAACAAAA 660 GCATCCATTC GTCACTTAGT GGCAAGCGTT TTTCCAACTA CTTTCCGAGT AGTAACTGCT 720 TGCCAGAGTT TCCCCAGCTT GGGCCGGAAG GTGAGGCGGT AGCTCGAGCT TTGCCTTTCT 780 CAGGCATTGT CCTGCGTTTG CGGGGCCAGG CGCTGGCACA CGGTCACTAA CCCCTGGTCG 840 TTAGCTTCGA TTCCCGGCCT GGGAGAGCGC TATCGGCCAC TCCTGGCTGC ATTGCAGTCG 900 CGGCTTTCTC CAGAGCTCCG CCGGGAACGG GAAGCGCTGA AACGTCGCGA CCAGTCAGTA 960 GGGTTCCCAC GGCCGCAACT CGGGTGTGAC GCGGCAGGCT GGCACCAGCG GACACAAGTA 1020 TGAGGCTAAG TGAGAAGCGC TCTGCTTCCG AGTGTCAGGA TGGCCGAGTG GTCTAAGGCG 1080 CCAGACTCAA GGTAAGCACC TTGCCTGCGG GCTTTCTGGT CTCCGGATGG AGGCGTGGGT 1140 TCGAATCCCA CTTCTGACAC ATTCGTTTTA TTAGCATTTT ATTCCCCGGA AGAAACCCCA 1200 GAATTTTCCC GGAGTCCGTT GGTATTTTAT TGTCTTCTCC AGGAAGAAGG TTACAACTAG 1260 ACTACTCATC TTTGCTGCCC GGTTTTCCCT GTCTGCCGCA GCAAGGGGGC TACCTACCAA 1320 GGGGAGGGAA GCAGTCTGCA TATTCCCAAA TGTTGCGAGA AAACCGCATC CAATCATGTT 1380 TCTATAGGAG ATACGTCACA GGATATTTAT TTAGTATAGC ATATTGCTAA ATGACGCATC 1440 ATGTCTTCCC TGGTGGTCTA GTGGTTAGGA TTCGGCGCTC TCACCGCCGC GGCCCGGGTT 1500 CGATTCCCGG TCAGGAAAGT AAGCCGTTTT AAAAACTGTT GCCGCAGGGC TAACCATAGG 1560 TGATGTTCCC AGAGTCAGCT ATGACTTGAC TTCTAAACAA AGGGCAAAAC GCACCTGGTG 1620 TCCTCATTTT GCAGAGTAGT TACCTGAAAT GGACTCTACT GCAGTTTATG CGCGCCGTAT 1680 ATGTAGTCAG TGTCTTTACT CATGATATCT TAAGAACGGA GAAAAAATGC CAGCAGCACA 1740 AAATGATCCA AAAAGATAGC TCTGGGTATG 1770
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