Tag | Content |
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EnhancerAtlas ID | HS133-10099 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr15:58766880-58768330 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
BCL6B | MA0731.1 | chr15:58768121-58768138 | TTAATTAATGGAAAGCA | - | 6.08 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_35670 | chr15:58766975-58770066 | HepG2 | SE_36980 | chr15:58760344-58769972 | HSMMtube | SE_39421 | chr15:58764704-58770574 | Jurkat | SE_66825 | chr15:58764704-58770574 | Jurkat |
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| Number: 2 | ID | Chromosome | Start | End |
GH15I058465 | chr15 | 58757745 | 58766936 | GH15I058474 | chr15 | 58767000 | 58769834 |
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Enhancer Sequence | GGTACGCAGG ATCCCTGAGG GTGACAACCT TCGAGGTCGT TCCCTGGCCT CTCTGCCCAG 60 GGTGAGCATC CTCAGAGACC TCAGCTCTCC TCTCAGCATG CAATTCTCCT CCACTCATGG 120 CCCTCCCAGC TGCCCCTGGC TTCTCAAAGC TACTCCTGCA TGGAGGCAAG TACAACTAGC 180 CAATGAGCCT CCTGACCTGC CCCATCCCAG AGAGCAACTG CTGCTAGGTC CTCGTGGATT 240 CTGGGCCTCT GTCCAGTGAC CAAAGGAGAG GACACATCTC CAGCTACCAT CCCTCCACCT 300 ATTTTCTAAG GAAACCAATG AGTTCTCAAA TGCCACCTGT GGTGGCCCCT TCTCAGCCCT 360 CACCCTGAGA GGCCTTCCCC AAGTCAGAAT TTCCCACAGG GGAAGTTACT GTGGGCTTCT 420 CTCTCCTTCC CCCACCTCAT GTGGTCAGGA AGTCCAGCTG GCTTTTTCTC CTGTCTGTCT 480 CTCAAATGTG TCCCCTGGCT CCCCTCCATT GCCACTGCCC TCTTCAGTGT CTGGCCTGTG 540 CTCCCACAAC AACAGGCTTG AAGCTGGCTG CCCTCTCCCC TCCATCTTCC ACACCATAAT 600 CCAGGTGATC CTTCTAAGAG GCAAAGGTAA TCATGTTTCT TCCCTGCTCA AGATCTGTCA 660 AAAGATTCTG TGGCCTCCAT AGAAAAGGCA GACAGCCCGG CCACCCAGGC CCTTCACCAT 720 CTGCCTCTTG ACCATCTCCA GTGTCCTGCA GTGTCCTGAA TATACCTTTT CCCTGCCTCT 780 GCCCAACACA CTCCCGTTCT TTCAACACCC AACTCAACTA TTACCTTCTC TCCATCAGAT 840 CTTCCCTGAA CCACCCCCCA GAAACAAAGG TGACTGTCCC CTCTGGTTCC CCACAGCCAC 900 CCCACCACTT ACCCCTGTGC TCAGGCACTC CTGGAGCACT GCATTGCAAC CATTGGCTCA 960 CACATCTGTC TCTACCAGCA AACCACTAAA CCGTGAATAA GTGGCTTCCT GAGCCAGGCC 1020 TTGTGCAATG AATGGATTTG CAACAAAGGG AGCCACTGAG AGATTACATG AGCCAAGTCA 1080 TGGCAATTAG TCCCCATGGA AGCAGCAGCT CAGGGCAGGG TCCAGACTTG GGCAGACTTA 1140 ACTATGCAGG ACATTCCATT AACAATAAGC ACCACTCTGA GCATTTCCTA TGTGCCAGGA 1200 ACTACGTGAA GCTCTAGATT CTGTCATTAG AAAGGACTGA GTTAATTAAT GGAAAGCAGG 1260 TAGCACAGTG CCTGACACAG TATAAGCACT GAACACACGT TAGCAAGAAA AGTGACAGAT 1320 CATTTACGGG ATGGTTCTTA CACCAGGCAG CGTGCCAAGC ACAGTCCATA CATTGTCTCA 1380 CTCTTCATGA CAACCTTAGG AAGAGAGCAG TCCTGTTTGT CCCCATTTTA CAGAAAAAGA 1440 TACTGAGTCT 1450
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