Tag | Content |
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EnhancerAtlas ID | HS133-01701 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr1:61368820-61370690 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Esrra | MA0592.2 | chr1:61369174-61369185 | ATGACCTTGAG | - | 6.02 | Esrrg | MA0643.1 | chr1:61369174-61369184 | ATGACCTTGA | - | 6.02 | FOXP1 | MA0481.2 | chr1:61369109-61369121 | AAGTAAACAGAG | + | 6.37 | FOXP2 | MA0593.1 | chr1:61369109-61369120 | AAGTAAACAGA | + | 6.32 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_33423 | chr1:61367101-61374520 | H2171 | SE_66886 | chr1:61367101-61374520 | H2171 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I060903 | chr1 | 61368717 | 61371173 |
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Enhancer Sequence | CCTCGGAAGT AAGGCTGCAT TTTAATAGCA GCCAAAAATG GGTGCAATTC CTGGGTAAGT 60 GAATTTCATC CAGCAGTAAG CAGGTAGAGA CGGATTGGGG AGAGTTTTGG ATCTTTCCCA 120 AAGCCTCTTG AAAACGTAAC ATGTCAGTGG CTGCTTTCAA CGTTTATAAT TGGAAGACTG 180 CGAATCATAG TCAACTGAAA TGTATTAAGC AAGGTGCATT CGCTTAAATT ATTTTATCTA 240 ACCCTCGCAT CAAGCCCATG AGGTATATAC TTTACCCCAT TTCACAGATA AGTAAACAGA 300 GGCTGAAGGA ATCTCAATGA CTTGTTCCCC AGCACACTGA CAGCACACTG TTGCATGACC 360 TTGAGTCAGT CCCTTCTTTC TCAGAACCAG GTCTCTGTCA AAGGAGGCCC TCGGCCCTGG 420 GAATGCCTTC CCAGCTGCCT CTAGCCCTCC CAGGCCTCAG AATGCTTGTT TTGGGCCCTC 480 CTCTTCCAGG CTGTGAGGTC CAGATCCTGG GCAGATGTCT CTCACCATAT GCTGAGGGTG 540 ATTTAACAAG GCCAAATGGG CAGCCCCGTG GTTAGAGGCG CTCTCGTTAC ATATACGCCG 600 GTTGCTGCGG CCTGGCCAGC TGTCCCAGCC CTCGCCCGCT CCTTCTTGGA GACAGCAGCC 660 TGCAATTGCA GATGCCAAGC AGCGGAAGAT ATTTTTAAAG CTACAGCATC TGTCTCCTTG 720 GCAGCCTCCA CCCACTGGTG GGCCGGGTGT TTTGGAGTTG CCTTTGGGCA CTTCACATGG 780 TTTGGCATCT GATCCATTGT CTAGGCTGCC TTTTAGAGCT CAGCTTTTTT TGTGGGGTGG 840 AGGGGGGGGT CCCCTAAAAC CAACTTTTGA TGATGACCTG GGTCTCCCCT CTCAGTGACA 900 TCAGTGTGTC TCTGGATCTT TTGTAATATT TTTTTTTAAC TTTCCTTTAA AAAAAAAAAA 960 GAAAAAACAA GTGATGAAAG AATGAAAGAA AGAGCATTTC CCCTCTGCCA GAGTGGGTTT 1020 GAATAGAAAA CTGCCCAGTA GCTGTGCAGC TGCCCAAATC TCGCCCACCA TGTCCACATT 1080 CTGACTAGTG CAGAACACGG CTTTCTTGGC ATCCAAACTT CCCTCAGGCT TGACTATTCC 1140 TCAAATGTCT CCCTGGGGAG GTGAGGGATT TCTTTTTTCA TTTTTCCCCG CTGCTTTTGC 1200 AAAAGACTGT GAAGCTTCCT GTCTACATGC AAATAGCCAT TCAAAAAAAC AGACACTGAC 1260 ACTTAATTCC CCCTGGCAAG CTGTATTAAG TTTTTTCCTT CTCTTAGAAA GGTGCATTTT 1320 AGGGAAGACC AGCTCCCAGC CTGCAAACTC AGGCCTGGGG ACTTGGCCCT GTTTCAGAAC 1380 ACCAGTTTGA AGATGACTTC TAGTGAGGAT TTCAGGCCTA GTGACAAGAA AATTATCTCA 1440 GTTGGGGCAA CAGGCTCCTG TGTCATGGGG CTGGGCAAGG CACCAGCCTG CCTCTCACTC 1500 ATGACTTGGC AAGAGTGCCG AATGTGGTCT TTTCTCCAGC CAACAGGCAC AGGCAGTGGC 1560 TACCAGAGGA TGCCAGTGGG CAGGAGTAAT CACCAGGGCC CAGCCAGGCT GGCTAGAGGG 1620 TGGTGTTTTT AAGTAACCAG CATCACTGGG CACTCCTTGT CCCATTAAGC CACACTGATA 1680 TAAGACCCAA AGAATCACTA ACCCTCACCC CCACCCACAG AGCAGGAGTC TGGAGCTGAC 1740 ATAGGTAACT GGGGTGCATT TCTTCCACTT AAGGTCAATG AAAGATAGCA GTATTCCCGC 1800 CATATGATAA GGGAAATTTC TAACACTTCC TCTATACTGT TCTAAGTGCA TTATACGTAT 1860 TTCCCCAGCT 1870
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