Tag | Content |
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EnhancerAtlas ID | HS133-19305 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr20:48469340-48471100 |
Target genes | Number: 14 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ELK4 | MA0076.2 | chr20:48469833-48469844 | CCACTTCCGGC | + | 6.62 | EWSR1-FLI1 | MA0149.1 | chr20:48470160-48470178 | CTTCCCTTTCTTCCTTCC | - | 7.02 | ZBTB7A | MA0750.2 | chr20:48469832-48469845 | ACCACTTCCGGCT | - | 6.01 | ZNF263 | MA0528.1 | chr20:48470168-48470189 | TCTTCCTTCCCTTTCTTCTTC | - | 6.49 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_01994 | chr20:48467267-48471751 | Aorta |
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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 |
GH20I049853 | chr20 | 48469648 | 48471150 |
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Enhancer Sequence | TGTAACATGA TTTATACAAA GCATTTCCCC CAGCCTTTTG TTTGTTTTGT TTTTTTCAGT 60 TAATTTAGAA AGTTTATTTT GCCAAGGTTG AGCATGCGCA CCCGTGACAG CCTCAGGAGG 120 TCCTGACGAC ATGTACCCAA GATGATCAGA GCACAGTTTG GTTTTATACA TTTTAGGGAC 180 ACATGAGACA TCAGTCAACT TATGTAAGAT GGACGTTGCC CCAACCTTTT ATTATGAAAA 240 ATTTTAAACA TACAGAAAAG GTGAAGCATT GTGAAGTGAA TACCCATAAA CAAATTTTTA 300 AAATATAAAA GGTGTATCCT GCAGGGGTAG GAGAGGCACA GGACAGGGAA CTTGGGAGCC 360 TGTGGTGGGC CTGCGCTTCA CTGAGGCTGG AGTATAGTGG CATGATCACA GCTCGCTGTA 420 GCCTCAAACT CCTGAGCTCA AGCTGTCCTC CTGCCTCAGC CTCCTGAGTA GCTCGGACTA 480 CAGGTATGCG GCACCACTTC CGGCTAATTT TTGTGTGTGT AGAGATAGGG TTCTCTCTAT 540 ATTGCCCAGG CTGGTCCTGA ACTCCTGAGC TCAAGCCATC CTCCCACCTC AGCCTCCTAA 600 AGTGTTGGGA TTACAGGCGT GAGCCACTGT GCCCGGCCCA GGATACACTT TTTAGACATC 660 ATCCTCCTTC CTTCACGGCC TCTGGTGATG GGGCTGTGGT TGATGAGAGT GAAAATAAAA 720 GAGCGACCAG AAGCTCTGTC TGGGTTGTGG TGCAAGGGCC TGGGGACCAG CCACCAATAA 780 AATAGGATCT CCCAGATGGG CAGTTGTTTA GTGGAGTTAC CTTCCCTTTC TTCCTTCCCT 840 TTCTTCTTCC CACCTGCCTG CCTGCTTGCC TTCTGCAAGT GTCTCTGGGC CATGCCCAGT 900 ACAGACCCTG GGAATTCACC CATGACGAAA ATTCAGCATC CACTCCCTTG GAGCTCACAG 960 GCCTGTGATG ACCTCTGTGA GGACAGGCGA AGTCTGGGAA CTGAATCCTC AGCCTGGGAT 1020 CCGGAGGCAC TCTGGGTTAA TGCGCATGAG TCACATTCAC AGGCAGCTAC CATGGAAACC 1080 AGAGGCCAGA TGATTGACTT CTGAAGAGAA CTGTACCTGG CAAGGCAGCC AGGCATTTCC 1140 TCAGTCAGCT CTCCTCTCCC TGACCCTGCA GCCAAAAGAT CACCCATTGA AGGCTGCTCA 1200 GCCGAGCATC CTTTTCCCCC TAGACCCAGG CTTGGTGAGG GTGGGAAGCT CAGGGCAGTC 1260 GTCTCTGGCT GATGACTGAC ACAGGCTGGC CATTGGGTCT CCATGTTTTG GCTGGTGTTG 1320 TGGAAGGGGG CAGACCCACC ATTCTGCTGC CCTGGAAAGA AAGTTGCAAC AGGCATGGCA 1380 CAGAGGCTTG TGGGAAAATC ACCAAAGGGC AGGGAGAGTG AATTGTCCAG GCTCATGTGG 1440 CACATGAGGC CCCTTGAGGG AGCTGGTCCT GCCTCCCTCG CCAGCCTCTT ATGGCTCCTG 1500 CCACTCACCC CACCCCCACC ACCACATGCA CCTTCCTTCT GTTCCTCAGG CAGCAGGCTT 1560 GCTCCCACCG CAGGAGTCGC TTGCTGTCAC CTCAGCCTGC AGCTCTTGGC CTGGCCAGCT 1620 GCTTCTTAAC ATGTAGGTTC TTGCTTACAT GTGTCATCCC TTCACAGAGG CCTCTCCAGA 1680 CCGCCCCATC TAAGTGGCTC CCACACCCAC ACCCCCACCC CACCTTCCCA CGTCACCTCA 1740 ATTGATTTCC TGGGTCACAT 1760
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