Tag | Content |
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EnhancerAtlas ID | HS133-25404 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr5:112394460-112395800 |
Target genes | |
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) |
RREB1 | MA0073.1 | chr5:112394576-112394596 | CCCCACAACACCTAACACCA | + | 6.08 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_37425 | chr5:112394316-112396290 | HSMMtube | SE_56238 | chr5:112394265-112395870 | u87 | SE_67710 | chr5:112394265-112395870 | u87 |
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| Number: 1 | ID | Chromosome | Start | End |
GH05I113058 | chr5 | 112394185 | 112395950 |
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Enhancer Sequence | TAAGTTGTGG AAAGGATACG GCAGGCCCTG AAGCAGGCAG CTGGTGCTGC CACACAGCAC 60 CTGTCCTGTG GGAGTAAGAG AGAAGGTGGC CACTTTCCTG ATGGCTTTGC CAACAGCCCC 120 ACAACACCTA ACACCAGACT CAGAGATGCC CTGAGCTATT GGCCACCAGC AGGTCATCCA 180 GAATCCCTCC ATCCCAGGGA GAACGAAAGC TGCCAGTGGT TGAATGGACT TGAGAAATCA 240 CCTAGCCCTA ACACGAACGC AGGCAGGCAG AGACTGACAG GCGCTGCCAC CCTTAGGGCC 300 CGGAGCCTCA TCCATGGCAG GCAGGGAAGG CTTTTGTTTC ACCCACCTTG CTATGAGTAT 360 AGTTTTCAAA GAGGAAGGAA ATAAAAAAAA AAAATAACAA AAGATCTCAG TCCACAGATC 420 TTACCCTGTT GGAAGCACAG AGCTTTAAAA TGCTTTTAGT GGAGAAAGTT TAATTTCAAG 480 ATAAACCTCA CAGCCCCTCC GGCTTCCCTT CTCCTGCTTC CAGGACAGCA GCGGGGAACA 540 GATCAGGCGA GGTTAATTAC AATTCTGCTT TGAGCTCTTA ACGTTTCACT GCGGAATATG 600 ATTATGACAA TGGTAGGGGA GGGGAAGCCA CTGGCCTTTT CTCTGGCCTC ACAGACAAAG 660 GCGCTGGCGG TCTCCCAAGG GCCTGCTGCT GGCTGCTGGG CAAGGGTTAA GTCATCCATT 720 AATTCTCCCA GCTTGGAATG CTGGATGATC TCAGTTGTCA AGGGGGAATC AATCACTTTC 780 TGTGGCTGCA TTATTCCTCC TCTCCAGAAC AGGAGCCTGT CTGTGTTCTC TGAGAGCGAC 840 TGTGGGGGAA GGCTAATGAC AAAAACCCTC GCCACACATG TGTGTCTTGC TCTGGCTTCT 900 TGAGGAGCTA GTCTAGGATG TGTGGGTTTC TCCTTTCCGT GATGCTCTGC TGGAGCTCCC 960 GTCACGCTGG CTTTCCTCTG CATCTGTTCA TTGCCAGCAG CTCTTCCAGC ACAAAGCATA 1020 CACAGCAGGC CTGTAGCCTG GTGGGAATGC GGGGCTGGCT GGTTCGGGAC GGTTCGGGCC 1080 GACCCACTCT CCACCTACCC TGTCCACTAT AGGAGAAGCT GTTCAAACCA GCTATCGACG 1140 TCAAATATCC TCTCTTCTAT CCCTCTCCAC CATGCCCCAC CTCTGTCCTC AAGACAGTCC 1200 CCCAGCCTGC TCATTAGAAG AAAAATTCAT TTTTCATAGC CTCCTCAGCT TGCCTTGGTG 1260 GAAGGCTAGA AGGACATTTC ATTTCTTTTG CCTTGAAAAT CCGTGATGAC ATTTTCCTGA 1320 AGTTTTCATC AACATCTTAC 1340
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