Tag | Content |
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EnhancerAtlas ID | HS133-03987 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr1:243893190-243895010 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFYB | MA0502.1 | chr1:243893487-243893502 | CCAGGGACCAATCAG | + | 6.02 | ONECUT3 | MA0757.1 | chr1:243894853-243894867 | TAAAAATCAATAGA | + | 6 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_09870 | chr1:243886511-243899071 | CD14 | SE_61577 | chr1:243872466-243894121 | Toledo |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I243729 | chr1 | 243893168 | 243896472 |
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Enhancer Sequence | GCCTGTATTT TCCAAGTCTC TCTACTGACA CCTTCCTAAC AGCTTTAAAT ATTTGTGTAT 60 TTCAGAAATA AAATTGTGAT AGTGGCAGGA GGCAGACAAA TTCCTAGGCA GATTGGGACA 120 GGTCCCCAGT GAAACCCAAC CTTCAGGGCA CACACAGCAT GAAGCCTGAA AACCTGGCTG 180 CTCCTTCTAG CTGGAATCCA CAACCTGGAG GGAGAATTTC CTTTACGCCT TTCAGCCAAT 240 GAAATGGTGT TTTTTCCAGG TCCACCCATG GACCACTCAG CACGCACTTC CTCCTGCCCA 300 GGGACCAATC AGCACACACT TCCTCCATTT TGAGCCCATA AAAACCCCAG CTTCAGCTGG 360 ACTCAAGGTA AGTAAGGACT ACCCTTAGGA GCTGCCCGCT TTGGGTCTCC TCTCTGCTGA 420 GCTGTTCTGC TACTCAGTAA AACTTCTCCA CCTTGCTCAC CTTCCAGTTG TCCACGTAAC 480 CTCATTCTTC CTGGACAAAG GACCAGAATT CGGGACCCAC CCAACAGTGG GCATGAAAAG 540 GGCTGCAACA CTTTCCTGGC CAACTCACCA AACTGTGGTG GTGACATGCT CCCATTTGCT 600 GGACTGCAGG AGTGAAAAGC AGTGACACTT CTGGGGGCCG AGACATCAGG ATTTCCCAAG 660 CCAGGGCTGT AACACTATAG CCTTCCTGCC TTCTGCCTGC ATTGGGCAGC TGCCCCATGT 720 GACAGGAAGT GGCAGTGGAG CTGGGCCAGC CTGGGAGCCG CCGGCTGGGG TGAGGTGGTG 780 GGACTGAACA AGCTGAAACC TGCTCCCCCT GCTCGCCGAG CCGCGGGTGG AGAGAATGAG 840 AGAGCACGCC TGACCCACTC CTTGAGGCTC TGCAGTTGCT GGCGTCCCCA AGTTTTTAGG 900 TGCCACCGCA TCCCCCTTTT CCAGACACCA GCACCTGCAC CAGAAACTAC GTGTGGTACG 960 CCTGCTCCAG CTGCAGCCTG GCAAGGAGCC GGCACCTCTG CCAGCACCCA GAGCTGCCTG 1020 CCCCACCACA GCTGGCCGGA CCCTGTGTTA GCTCTCTCAC ACACCCTTCA GTGCTCTGAG 1080 CCTGGTTTGC CCTCATCAGG CGTGGGATCC GGGTTGGGCG AACTGAGTGC AGCCTGCCGG 1140 GCTGAGTGGG TGGAACGAGC ACAGTGGGAG TGAGTGAAAC TCAAGCAGGG GCGCCACAGG 1200 CCACAATGGT TCCCGGCTGG CAGAGTGACA CCTGAAGGAT CCCGTGACAT TTCGATTATT 1260 TCTGCTCATA GCATAAACTC TTATATGTAA GTATCTACCA CATGCCAAAA TGAAAGCAAA 1320 AAATATATAT AATAGCCTGC TGTAGATATA TATTATGTTG TTGTAGCAGC TCATGTTTTC 1380 TACCATCCAT ACGTTTAAGA TAAATGGCAT GCAATATCAC CAATAATAAG GCAATAGAGA 1440 ACAAAGAGTC TGCAAGAATT TAGAAAACAC TTGCTTTGAT ATACAGCAAG AACTAAGGGG 1500 CAAGAAGAGG TAATGGGCAA GCTCTGAGTC ACTCTTACTG GATGGTCTCA GTACAGCAAC 1560 AGTAACTAGG ATAAGCCAAG GCGTCCTCTA CACACATAGT GAGGCCAGCT TGAAACAAGG 1620 AAGTACATAG TTGCAGACTT GGAAGCTAGC CACCGCAGCT ATTTAAAAAT CAATAGAGAG 1680 ATTATTTTTT AAACCCTCTT TATCCAAAAA GAGTGTTCTG TGAAGAGAAA TAGAAGGCAC 1740 TAGAAGTGAC GCACTGAAAG ATCTCAGTTC ATGGAATGAT CACATTTGTA AACTAATAGT 1800 TTGTGCCTCT TTTTAGAGTC 1820
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