Tag | Content |
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EnhancerAtlas ID | HS133-10973 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr16:9165820-9168060 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CDX2 | MA0465.1 | chr16:9166550-9166561 | TTTTATGGCTT | - | 6.62 | RUNX1 | MA0002.2 | chr16:9166775-9166786 | GTCTGTGGTTT | + | 6.62 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_39989 | chr16:9166198-9167401 | K562 | SE_64976 | chr16:9166118-9168035 | NHEK |
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| Number: 1 | ID | Chromosome | Start | End |
GH16I009072 | chr16 | 9165982 | 9168053 |
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Enhancer Sequence | GCCTCCCAAG TAGCTGGGAC CCCAAGTGTG CGCCATCACG CCTGGCTAAT TTTTGTCCTT 60 TTTTTTTTTT CTGAGACAGA ATCTCACTCT GTCGCCCAGG CTGGAGTGCA ATGGCAAGAT 120 CTCGGCTCAC TGCAACCTCC ATCTCCTGGG TTCAAGCAAT TCTTCTGCCT CAGCCTCCCT 180 AGTAGCTAGG ATTACATGTG CATGCAACCA TGCCTGGCTA ATTTTTGTGT TTTTAGTAGA 240 GACAGGATTT TGCCATGTTG TCCAGGGTAG TCTCGAAGTC CTGACCTCAA GTGATCTGCC 300 TGCCTCGGCC TCCCAAAGTG CCAGGATTAC AGGCATGAGC CACCATGCCT AGCCAATTTT 360 TGTACTTTTT GTAGAGATGA AGTTTCACCA TGTTGGCCAG GCTGGTCTCC AGCTCTTGAC 420 TCAAGAGATC TACCCAGCTT GCCTTCCCAA AGTGCTAGGA TTATAGCCAT TAGCCACCGC 480 ACCTGGTCAG AAACCTGTCT ATTTTATGCT TAGGTTTGAT GAAGAGTGGA CAGCCATGGA 540 GAAGGATAAC TGGACACCGG GGCTATGACC TAATGGGAAT AAACTGGCTG GAAGTTGGCA 600 AGGCCTTTTT GTTTAGGCTT TTCCCTGTGT CTTCAGACAC AAGGATGTTT CTTTCCTCCA 660 GGTACAGGGT GTGTACCTCT GACAGGTCTT ACGATCTGTT CTAAAGGAAG ATCAGAGAAT 720 CCTTTTTGTG TTTTATGGCT TTTTTGCTTG AAGGGAGAAG GCAAAGGGAA GATGAGAGGG 780 ATCTTCCTGC TTCTGCTGTT TTTTTCAAAT GCCAAGGTAC CATATTTTGG GGTAGCATGA 840 GCCCCAACAA GGAAAACAGT TCATATTCTC AGCTGAATTC ATGATAGCAC ATTTCACAAG 900 ATGGCAACAA GCATGAGATA TAGCTATGAG CAGTACATTT TGGCTTAGCT TTGTAGTCTG 960 TGGTTTTCAG TTTCTGAAAA GACCCAAATG TTCTTTATTT AAAGAACCAA GGTTTACATG 1020 CCGTGGTGAA TCACAACGTG GTGGTTAGAG CCCAGTCAGA CGGTCCATTT GCTTTCTATT 1080 CTTAACTTTC TCGCTGGCCC CAGAGCCTCT TAGAACCTCC CTGGATAAAA ATAAGTGGTG 1140 TTTGGTAATC CTGAGCTGAA AGGTGGTACT TAAGTCAAAA GCACACCTGA ACACAGCTAA 1200 TTTGCACTAA TCATCTAGAT CTGCCATGAA TCAGCCAGAG GGGAAAACGT CATTATGATG 1260 CAACCACAAC CAGGTATTGC AGGACCTAAC CAACCTCAAA CATGATTTTC ATTTCTGAAA 1320 CCGACTTCTA AGCCCCCTCA TGTAGTGGTT ATCAAATGGG AGCCTGCATC AGAATCCCCT 1380 GGAGGATGTG TTACGAGATT GCCGGGTCCC AACCCTGGAG ATTCTGATTC CAGGTAACTG 1440 GAGAAGTCCT GAGTATTTTC TTGTTTTTTC TTTTTTCTTT TTTTTTTTTT TTTGAGACAG 1500 AGTCTTGGTC TGTCACCCAG GCTGGAGTGC AGTGGCGCGA TCTTGGCCCA CTGCAACCTC 1560 TGCCCTCGGG GTTCAAGTGA TTCTCCTGCC TCAGGCTCCG GAGTAGCTGG GATTACAGGC 1620 GCCCGCCACC ACGCCCTGCT AAATTTTGTA TTTTTAGTAG AGACGGTTTC ACCATGTTGG 1680 CGAGCCTGGT CTTAAACCCC TGACCTCAGA TGATCCGCGC GCCTTGGCTT CCCAAAGTAC 1740 TGGGATTACA GCCATGAGCC ACCATATCTG GCCCTGAGTA TTTTTATTTC TAACAAGATC 1800 TCAGATGGCG CTGAAGCTGC TGGTCCTGGG GCCACATTCT GAGACCCTCA TTTCCCATAC 1860 AAAACAAGGT TTCCTATCAG AACCTTATTT TTGCCAGTTT ATTTTTTATT TTTTCGAGAC 1920 AGAGTCTCGC TGTTGTCACC CAGGCTGGAG TGCAGTGGTG AGATCTTGGC TCACTGCAGC 1980 CTCTGCCTCC CGGGTTCCAG CAATTCTCCT GTCTCAGCCT CCTGGGTAGC TGGGATTACA 2040 GACACGCGCC ACCACGCCCT GCTAATTTTT GTATTTTTAG TAGAGATGGG GATTACAGGC 2100 CTGAGCCAAT GTGCCCAGCC CAGTTTATTT GTTTATTTTT TAAAGAGATG TGGTCTCACT 2160 CTATTGCCCA GGCTGGAGTG CATTGTCGCC ATCATAGCTC ACTGCAGCTA GAACTCCTGG 2220 ACTCAAGCGA CTCTCCTGCC 2240
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