Tag | Content |
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EnhancerAtlas ID | HS133-08923 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr13:114476610-114479240 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MYC | MA0147.3 | chr13:114478908-114478920 | GTGCACGTGGCC | - | 6.22 | RREB1 | MA0073.1 | chr13:114478154-114478174 | ACACAAACCACACACCACAC | + | 6.25 | RREB1 | MA0073.1 | chr13:114478019-114478039 | ACACAACACACCACACACCA | + | 6.43 | RREB1 | MA0073.1 | chr13:114477517-114477537 | CCACACACCACACACACACA | + | 6.68 |
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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 |
GH13I113774 | chr13 | 114477301 | 114477450 |
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Enhancer Sequence | CTTCTGGGCT GATGTTGTAT GGTGAACCCA TATTTCACAA TCTCACATTA ATTTAATACT 60 TGTGGTAGCT GGAACCTGGC TGTCCGTGAG TGCTGCGTGA TCGTAGGAAA CTTACTGAAG 120 CATTTCAGCC TCAGTTTCTT CATTTGCATG GTGGCTGGGA ACATTTGAGC CAATGCACAT 180 GAGAATGTCT TGTTCATGAC AGGTTTCGAG AAAGCGGTGG TCATTGTTAT ACACTGGTTT 240 TAAGTGCATA GATGTCAGAA CATTCAAGTT ATTTCAAAAG GCAGCAAGGC AGGCTGTCAA 300 CGTCAGCTAC AGAGAGAACG AGTGTATTTC CAGTGCTTCC AGATACACGT GAACACTTTT 360 TTCTCAATTT ATTTTTATTT TAAATTTTTA CCATAGAAAA CTTTAAGCAC ATACAAGGGT 420 GAAGAAAATC GCAATGAACC CTCCTTGCCC CCCACCCAAC TCCATCACTT GTCCTGTTCA 480 CCCCCCGCCT GCTTCTTCTC TTCCTATGTT GTTTAGAAGC AAATGCCAGA CGTGGCATCA 540 TTTCATTTAT AAAGATTTCA CTCTGTTCAC TTAAGGGATG AAATCTGATC ATTAGGAATG 600 GCTTCGCCAT TATCCCTACC CATTATCATG TTAGTCTCCG GTGACATCTG AAGAATGCCC 660 CAAATCACAT CAGCTTTAGG TATTTTTCCA CTGCTGAATG AGTTACTGTT TCCTCCTCAC 720 CCAAACAGAC ATATGAATCA TTTATTTCAG GAAGAGCTCT GTAACCTGGC ACAGTCCCAT 780 AGGTCCCACA GGGATGGGAA AGGGAAGGGC ATAAAACAGT GTTAACTGGC AATTCTCCTG 840 TGCCCCACGT ATGTGCACAT GCACAGACAC ACACGACACA CTCCACACAG TACAAAACAC 900 ATGCATGCCA CACACCACAC ACACACAACA CACATGACAC ACACACCACA CAACACACAA 960 ATGACACACA CCACACAATA CACACCACAT ATACCACACA CCACACACAC TATACACAAC 1020 ACACACCACA CATATGACAC ACACACCACA CATGACACAC ACACCACACA ATACACACCA 1080 CATACACTAC ACACACGACA CCACACACAC TACACACACC ACACACCACA CACAACACAC 1140 AATACACAAT ACACGCTCCA CACAATACAC TACACACACC ACCTACAACA CACACGACAC 1200 ACACAACACA CAATGCACAC CACATACACC ACACAACGCA CACCACACAC AAGACACAAT 1260 ATACAACACA CACTCCACAC AATACACTAC TCACACCACA CACACTGCAC ACAACACACG 1320 ACACACACCA CACAATGCAC ATCACACACA CCACACACCA CACACTCCAC ACAATACACA 1380 ACACACACCA CACATGACAC ACATTGCACA CACAACACAC CACACACCAC ACACTCCACA 1440 CACACCACAT ACACCACACA CAGCACACAA CACACACTCC ACACAATACA CTACACACAC 1500 CACATATATG ACACACACAC TACACAATGC ACACCACATA CACTACACAA ACCACACACC 1560 ACACATACTA CAACACCACA CACACCACAC ATACTATACA CACCACACAC AGAAGTCTTT 1620 GGTCTGGACT GAGCCCGTTT TCTCCATTCC TCTAAGTGCT GGAGGGTGAG GTCTCGGCCG 1680 CCTTCCTTGC GCCCTGCTTA GCTTCTGCTC AGGGCCTCGC TGTCGTGGGA GCCCCATCAG 1740 CCTTCCTGGG GCGTCGGGCC CCGCACCTTC TCCTGTGGAA GCTGTGAGGG TCTCCGCCCC 1800 TTTGGGTGGG GCTGGTGGAG AGTGGTTTCT GGGATCCCTG GATGGCAGTG TTGGGCGGCT 1860 CTGCGGGTCA CCGGTGAGGA CACTGTGAGC TGCCCAGGGC AAGAGCCCGT GCCAAGGCCC 1920 CACGGCCCCG AGTAGGTCCC ACAAGGGCCG GGTGTTCTGG AGGACAGGCG TTGAGTGGGC 1980 CCCATCCACT TGCCATCCAA CCCTGGATCC CACGACCTCA CCCACAGCGG GGGAATAACT 2040 GAGGGAGTGG AGCACAGGCG GAGCATGGGC ACAGGCGGCC ACACTCGCTG GGCACCCAGC 2100 TCGGGGTTGG TCCTGCCGGG CCCACAGCCT CACCACCGAG GCCTCTTTCC CTGAAGCTCC 2160 TGTGGCCCTG ATGAGGCCCC AGCTCTCCGT GCCTGTCAGG CACTGGGGGG TGTTTCTCAG 2220 GCCGGTGGCC CCACATCCCC GCCCAGGGAC CATGGGACCC CTGCGGCCCC ACAGGTGGCT 2280 TGAGTCAGAC TTTTCCAGGT GCACGTGGCC TGTGGCATCG GCAGGTCTCT GTGTGCAGCC 2340 ATGTGCGGCC TGTGAGCTGA AGCTGAGTCT TCCGGGCCGC CCCTCCTGGA CCGTGGTGGG 2400 ACCTGCCCAG GACACCAGTC CACACCTCCT CCATGCAAAC GCCTCAGGCC ACACCTGCAG 2460 GGGATGGGGT GAAGTTCAAA GAGGACCCTG TCCCGTCCCC CACTCTCTGC TCAAAGATGC 2520 TGCCACCTGA ACCCTCCAGA CTTGGGTTAA TTTTGGGAGA AGGGTGGGCA CTGGCACAAG 2580 GGTGGGTGAG TGGAGCGACT TGGGGGCCGC CCGCCCTGCC TTCTTTTCTG 2630
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