Tag | Content |
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EnhancerAtlas ID | HS098-39288 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr3:100399980-100402150 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CREB1 | MA0018.3 | chr3:100401512-100401524 | AGTGACGTCACC | + | 6.22 | CREB1 | MA0018.3 | chr3:100401512-100401524 | AGTGACGTCACC | - | 6.22 | Gabpa | MA0062.2 | chr3:100401424-100401435 | CCGGAAGTGAC | + | 6.14 | Nr2f6(var.2) | MA0728.1 | chr3:100400373-100400388 | TGAACTCCTGACCTC | - | 6.22 | PAX5 | MA0014.3 | chr3:100401192-100401204 | GGGGTCACGCTT | - | 6.74 | ZNF263 | MA0528.1 | chr3:100400491-100400512 | TCCTCACTCTATGCCTCCTCC | - | 6.37 |
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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 |
GH03I100681 | chr3 | 100399852 | 100402743 |
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Enhancer Sequence | TCATTATAAA AGTACTAATG AAGATAAACC AAAATGGTGG ATAAAAATAA ATTTGTTTGA 60 CTTTGGAGAG GTTTTTTTTT TAACCTTTTT AGTTATTTAT TATGTGTGAG GAATATCAAG 120 ACTTTTAAAT AAAACAAAGA TGTGTTATTG AAAGACATCT TTTCTTTTCT TTTTTTTTTT 180 TTTCTTTTTT TTGAGACAGG GTCTCACTCT GTCACCCAGG CTGGAGTGAA GTGGCATGAT 240 CTCAGCTCAC TGCAACCTCC GCTTCCCGGG TTCAAGCAAT TCTCCTGCTT CAGTGTCCTG 300 AGTACCTGGG ATTACAGGCA TGTGCCACCA TGTCAGGCTA ATTTTTGTAT TTTCAGTAGA 360 GACAGGGTTT CACCATGTTG GCCAGGCTGG TCTTGAACTC CTGACCTCAA GTGATCCACC 420 CATCTCAGAC TCCCAAAGTG CTGGGATTAC AGTTGTGAGC CACCACACCA GACATTGAAA 480 GACATCTTGA AACCAGAATT TCTCTTTACA CTCCTCACTC TATGCCTCCT CCCATAGTGA 540 ACATTGCTCT TTACTCTGAT GAAAGAGCAA TGAAATTACT AAATGGACTT TACTCTCTGT 600 AGTATGGAAA CATGTCTTCT CTAAGCTGGC AGAATTCATT AAACTTCAGT AGAATGAAAA 660 TACTTCTCCC TTAAAGCACT CGCACCCTAC CAGGATCACC TGTATGAACA AACATCACCA 720 CTGAACTACC TGCACAGGGC AAGGAAAGGA GCCCCTTTTT GAAAGCTCAC TCCTGAAACT 780 CCAGACCATG AACCCTAAAA GCAAGGGAAT AATTCAAGGA ATCCACATGA TTGTTAGAAC 840 TTTTTGAGAA TTTTCAGTTT TGGTATTTAT TGAGATTACT TCCTAATGAT GCCAGCGGCA 900 GCCCATCTGA AGTGGCCGCT GCCATGGCTC CGGCTGCAGT GGGGTACAGG CGCAGGCTGT 960 GGGTCCTCAG ATGCAGATGC TGAGGCAGGC AGTCCCCAGA GCCTGCCCCA GGGAGCGCCC 1020 CCGGAGTCCA CCGCCCTGGG AACCCACCCC CGGGAGCTGC CCTGATGGGG CCGGACCCAG 1080 CCGCTCACCG GAGGGAGAGC AGTGCAGTCG GGCAAGGAAG AGCAAGCAGA GAGGGTCCCC 1140 AGGAGGAACT GGGTCTGGGG CGGTGCCACA CTTGCACATG GAACGTGGGA GCCAGGCCCG 1200 AGATGTAGAG CTGGGGTCAC GCTTCAGGGG ACCGGGGTGG GAAGTGGGAG CAGTGCCCGC 1260 TTCGAGGACC CAGCCAGCAA CGTGGCCACC GCGCCCAACC CGCCGACGGC GCCAAGTTCC 1320 TGCGCCTGGG GAACAGTCTC TGCTCCGAGT CACCTGAGGC TGCGTCCTCA GGATCTGCTC 1380 CACATCAAGG TGACCGCCGA GCCTGACGTT TCCAATGGCC AGGCCCAGGG CCCACGATCT 1440 GCTCCCGGAA GTGACCTCCA GTCAGGGCCA TGAGCCAGGC AAGGGGGAGC CCCAGGCTGC 1500 CCCTGAGTGC TGGGGCCACA AGAAGAACTT GCAGTGACGT CACCCCTGCT CCGGAGGCTG 1560 GCCCGGGCCC AGCGAGGACC TGAAGCTCCC ACTCCAGGCT GTGAGGAGGC ACGGCCAGGG 1620 CTACACACTC CACTGAGCCA GCGGGAACCG GGGGCAAGCG GGAGCCCCAC CTCTTCTCAG 1680 TTGGCCGGGT GGGAGCTCCC TGGGTGCAGT TGCAGTTGCC TTGTCGCAGC TGCTGACCGA 1740 GGCATCTTTG CACTCTCAGG GGTCCAGGAA GACCCCCCTG CCTGGGTGCC ATGAATAGAG 1800 GCAGGAGGCA GACAGGCTTT TGGGTGGAAG GGGGAGGGTC CGTGGTGAAG CCCCACCTTA 1860 AAGCCAGGGA GGGCCTGATG AGCAGCTCTA GTGAAGAGCT ACTGTCTCTC CTGAGAGCTG 1920 AGTGCTCATC GGAACACCCT GGCTAAGGAG AGGAGCTACC CACTGCGGCT GCAGGTGTCC 1980 TCTGAGCTGT TCTATCACTC AGTAAAGCTC CTTTTCGTCC TGCTCACCCT CCACTTGTCT 2040 GCATACCTCA TTCTGGATGC AGGACAAGAA CTAGGGACCC ACCAGAACGG CGGGGCTAAA 2100 AGAGCTGTAA CGCAAACAGG GCAGGGCTGA AACATGCCCT TTGTTCTCCA CATTGTGGGC 2160 AACAAGGAGA 2170
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