Tag | Content |
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EnhancerAtlas ID | HS133-10992 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr16:11405620-11407650 |
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) |
Foxq1 | MA0040.1 | chr16:11407297-11407308 | TATTGTTTATT | + | 6.62 | IRF1 | MA0050.2 | chr16:11406673-11406694 | TTTCACTTTCAGTTTCTTGGA | + | 6.04 | IRF1 | MA0050.2 | chr16:11406667-11406688 | CTCTGGTTTCACTTTCAGTTT | + | 8.97 | IRF2 | MA0051.1 | chr16:11406666-11406684 | TCTCTGGTTTCACTTTCA | - | 6.24 | Nr5a2 | MA0505.1 | chr16:11405898-11405913 | CATGGCCTTGGACTC | - | 6.17 | TFAP2A | MA0003.3 | chr16:11407184-11407195 | TGCCTCAGGCA | + | 6.02 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_33035 | chr16:11406212-11407358 | H1 | SE_62053 | chr16:11386770-11424077 | Toledo | SE_68718 | chr16:11405593-11411409 | H9 |
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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 |
GH16I011306 | chr16 | 11400381 | 11411109 |
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Enhancer Sequence | GCTACTCTGG AGGCTGAGGT GGGAGGATGG ATTGAGCCCA GGAGTTCAAG GCTGCAGTGA 60 GTCATGATTG CGCCACTGCC CTCCAGCCTG GGCAACAGAG CAAGACAGTG TGTCAAAACA 120 AAAACAAAAA CCAAAAACCA GACTCTGTGG CTCACCTCCC ACTCACAGGG TCAGGAACTC 180 AAGAGGGGCC CAGCACGAGG TATTTTCACA GACCTGCCTG TGAGAGCCTC TGCCCAGAGC 240 TCAGTGGTGA GGACAAGCGC TCTGCCTTTC CATAGCTCCA TGGCCTTGGA CTCAGTGCTT 300 ACCCTGTCTG GCCTCAGTTT TCTCGTTTGT AAAATGAGCA TAATAACAGG ACCCACTTCA 360 TAGGATGTTT TGGGGATTAA AGGGACTCAT GTTTGTACTA TGCTTGAAAC AGTCCTTGGC 420 ACCTAGCTAG CACTCAATAA ATGGCCGTAA AATTTAAAGT TAAGGCCCTG GCCAGGCACG 480 GTGGCTCACG CCTGTAATCC CAGCACTTTG GGAGGCCGTG GTGGGTGGAT CACCTGAGTT 540 CAGGAGTTTG AGACCAGCTT GTCCAACATG GCAAAACCCT GTCTCTACTA AAAATACAAA 600 AATTAGCCAG CTGTGGTGGT GCATGCCTGT AATCCCAGCT ACTTGAGAGG CTGAGGCAAG 660 AGAATCACTT GAACCCAGGA GGCGGAGGTT ACACGAGCTG AGATTGCACC ATTGCACTCC 720 AGCCTGTGCA ACAGGAGCAA AACTCCATCT CAAAAAAATA AATAAATAAA GTTTAGGCCC 780 TGTCTCGCCC AAGGGAGGTT GGCACTAGCA TGACTTGACA AATCAGTGCC ATATAACTGT 840 TGTTCCAGTT GGGACACAGG AAACTTGCCA CCTGCAAGCC CTGGCCCAGT GTAAAGCTCA 900 AGTCCAGAGG GCTGGGGTTT GTGGGAGACA GAACTGTCAC CCCAGGACTA TCAGAGAGAG 960 AGGGGCTCCT GGCTCTTATT TCTGCAGAAG CAGCTAGATG GACAGGTCCC TCACTCCAAG 1020 GAGCCTCCAC CACGTGCCCA CACCTTTCTC TGGTTTCACT TTCAGTTTCT TGGAAAGGCT 1080 GTCCTTCCCT ACTCCAAGCC CCTCCCCTCA CTCCCCACCC AGGATCTGGG CACTGGAGGC 1140 GCCAGACATC TTATGCCCTG TCCAAGGCTA GCAGGTAAGA AACGCCCCTT GTATCTGCCA 1200 AGGTCAAAAT CATACACACC CAGGTGGGGC AGTCCCACCT CTGGGAGGTG TCTTGCAGAA 1260 GCACTCCTAG GAGTGTGAGG TGATTTGGCT CCACAGTGCT TGTGGTCAGA AACAACTGGA 1320 AAGAAGTTGT GTGCTCAGCA GCATGGTGGG GTGAGGGGGT TGCAGGGCAT CCCACGCCAT 1380 AACCCACGAG GTAGCCTCTA TGGGCTGATG GGGGATCAGT GCAGGGTGGT AAGGGCCAGG 1440 GCCAGGTCTG AAGGGAGAGT GGGCTCCCAT TCATGTGAGT GGGAAAAGCA ATGTATGTGT 1500 CCAGGTGCGC CAGGTCGTGC AGAGCATATC TTGAAAAGGC ACACAAGGGA TTGATCAGAG 1560 AGGTTGCCTC AGGCAGGATA ACTGAGATCT GGAAATGGTG TGGGAGGGGA ACCAGTTTTT 1620 TTTCTGTGAA GTCCTTGGAT GCTTTGAATT TTTGTTTAAG TCATGCGCAT GCATGATTAT 1680 TGTTTATTCC CTGCCCCCAC CCCACCTCAA GTACAGAAGA AAAGAAAGAC AGTTTCTTTC 1740 TTAAACTAGT TTGCTGGAGG GCTGGACATC CTTTGTTGCT CATTTTCTGG GAGATGTAGG 1800 TTAAAATTAA CCTACATCTT TGGAGGGCTT TGGAGTCAGA CTGTCTGTGT TCAAGTCCTG 1860 GCTGCCCCAC TTTGTAGCTT CTCGAGCAAG TCGCTTAACT TCTCTGAGCT TTTATTTTCT 1920 CTCCTGTAAA ATGGCACAAT ATTATTGATA TAATGTTGAC ATTATTATGG ATACATTGAT 1980 TTTTTTTTTT TTGAGACAGG GCCTCCATCT CTCACCCAGG TTGGAGTGCA 2030
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