Tag | Content |
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EnhancerAtlas ID | HS098-40480 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr3:149540900-149543310 |
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) |
MEF2C | MA0497.1 | chr3:149541134-149541149 | AGCTATTTTTGTCAT | - | 6.07 | NR2C2 | MA0504.1 | chr3:149542579-149542594 | CTAGGTCAGAGGTCA | + | 6.84 | Nkx3-2 | MA0122.3 | chr3:149540929-149540942 | TAAAACACTTAAA | + | 6.33 | Nr2f6 | MA0677.1 | chr3:149542580-149542594 | TAGGTCAGAGGTCA | + | 6.55 | Rxra | MA0512.2 | chr3:149542580-149542594 | TAGGTCAGAGGTCA | + | 6.03 |
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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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Enhancer Sequence | AAGTATTACT GGGCAAGTAA CTGAACACTT AAAACACTTA AAAATAAGAG GAAATATTTA 60 TAAAGTGCTT GCTGTGTGTT AGGCACTGTT TTAAGCACTT TATGCTGTTG ATCTAAGTTT 120 TTATTCCTAT ATTTATGGAA AGACAGTGGA ACCTACTATA GAGTTGTGAG GATTAAAATA 180 AATAATGTAT ATTAAGGACT TAGCCAGATA TGTAGTAAGC ATTTGATAAA TATTAGCTAT 240 TTTTGTCATT TATAATTTCA CCTAACACCA ACAAAAGACC AAAAAAGGAG AATCGATACA 300 ATGAAATGCA CATTTATTTG GAAATATAAA TAGGAATGTT CTTTTCTGGA AAGCAATTGG 360 GCAATATGTA TGAAGTCTTA AAATGTTTCT TTGGTGTAGT GATTCCATGT CAAGGAATCT 420 ATCCCAAGAA GATAATCAGA AGTATGGAAA GATTTATATT CATTGGAAAA TTATTTGTAA 480 TAGTAAGAGT TCAATTCAAT GTTGTACAGC AAGAAAATAG ACAAAGTCAT GTGTCAGCCA 540 TATAAAGCAG TACAAAGTAG CTGTTAACAT AGTGGTTATG AAGAGTTTGA ACAACAAGGG 600 AAAATCTTTG TTATAATTTC AAGTAAAAAA GCATACAAAT CATAATACAA TATGATACAA 660 GTGATTACTT TGAACTTTGG AAGACATTAT ATTATTAAAA TAAAATAACA TGTTAAAATT 720 TTGAAGTAGC TACGGAGTTA AAGTTGTAAA AACAATACAA AGACCTTTAT GTTTTTTGTT 780 ATTTGAGAGA AAGTTGTTTC TCTGATGCTG TATATTCCTA TAAACAACAA TATTCTCTTT 840 AAAGAAATGG CTGATTTCAG GGCTGGGGCA GGAAAAGTAC AAGGCAGGAC TGGAAAATCT 900 TGTGCCAGAA AACAAGGAGG TGCTCAAGAA TGTTGGGAAC ATATCAAAAA GACACAAAAG 960 CTAGCTTGAA TAAGCCTCCA TTGGCCAAAC AATTGGACAT CAAAATGATA ATACAATAGC 1020 AGATTATAAC CCATTGAATA AAACAGTAAT CTGTGATTCC ACACTGATAT AAATAAGTAA 1080 ATGAATAAAT TAGAATGTTG CCAAGAAATG TGATAATTAC CGTGGTAGGC AGAATAATGA 1140 CTGCCCAAAG ATGTCCATAT CATAATACTT GGAATCTGTG AATATGTTAC CTTGTATGAG 1200 AAAAGGAACT TTGCAGATGT GATTAAGGAC CTCGGGTTGG GAAGATTATC TGTGTGGGCC 1260 CAGTGTAATC ACAAGTGTCC TTAAAAATGG AAGAGGGAGG CAGAAGAGGA GTTTGGAATA 1320 ATGTGCTATA AGAAGGAATT AATCTGCCAT TGCTGGCTTT GAAGATGGAA GAAGAGGCTA 1380 CAAGCCAAGG ATGTTGGCAG CCTCTAGAAG CTGATAAGTA TAACAATCAA ATTGTTGTAT 1440 AATGTAAAAC ATTTTCATTT AAAAACATAC ATGAATAATA TCCTAGACTA GAAAAAATAT 1500 ATGGTTTTTT TTTGTGAAAG GAAATGACCT CTGTCCTAGT TTTCCTTTGG GGCTTTTTTT 1560 TTTTAAAGAT ATACACACAA ATATAGTTAG GTAGATTGAT AAACACATAC AGGATTATAT 1620 GATTATGTCT AGTTAATGTC CATTTGTAAG TATGTCTGTA TCAAAAAGCT CCAAAAGAAC 1680 TAGGTCAGAG GTCATCCTCT TTTTTTTTTT TTTAATTTAA CTTATTTTAA GTTCAGGAGT 1740 ACATGTGCAG GTTTGTTATA TAGGTAAACT TGTGTCATGG GAGTTTGCTG ACTAGATTAT 1800 TTCATCACCC ACGTATTAAG CCTAGTACCT GTTAGTTATT TTTCCTGATT TTTTTTTTTT 1860 TTTTAAGATA CAAAGTCTTT CCGTGTTGCT CAGGCTGGAG TGCACTGGCG ATCATAGCTC 1920 ACTGCAGCCT CAAATCCTGG GCTCAAGCAA TCCTTCTGCC TTAGCCTTCT CAGTAGCTGG 1980 GACTATAGGT GCATGCCACC ACACCTGGCT AATTTTTGTA TTTTTTGTAG AGACAGAGTC 2040 TAGCTATGTT GCCCAGGCTC CAGCAACCCT TTTTTTTTTT TAAGGCTTAG TCTTGCTCTG 2100 TTGCCCAGGC TGGAGTGCAG TGGCACATTC TCTGCTCACT GTAACCTCTG CCTCCTGGGC 2160 TCAAGTGATT CAGCCTCCTA AGTAGCCGGG ATTACAGGCA CCACCACGCC TGGCTAATTT 2220 TTGTATTTTT AGTAGAGACA GGGTTTCACC ATGTTGTCCA GGCTGGTCTC AAACTCCTGA 2280 CCTCAGGTGA TCCGCCTGCC TCGGCCTCCC GGAGTGTTGG GATTACAGGT ATGAGCCACC 2340 ATGCCCCGCC TCCAGCAACC CTCTTGATGC AGATGTTGTA CATTCCAGGC CTGGTGCCTG 2400 CAGCTGTGCC 2410
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