Tag | Content |
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EnhancerAtlas ID | HS133-22416 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr3:58982990-58985430 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CREB3 | MA0638.1 | chr3:58984458-58984472 | TGATGACGTGTCCC | - | 6.27 | Esrra | MA0592.2 | chr3:58983862-58983873 | TTCAAGGTCAT | + | 6.62 | Esrrg | MA0643.1 | chr3:58983863-58983873 | TCAAGGTCAT | + | 6.02 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_36209 | chr3:58982522-58987015 | HMEC | SE_64622 | chr3:58982724-58986663 | NHEK |
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| Number: 1 | ID | Chromosome | Start | End |
GH03I058996 | chr3 | 58982542 | 58986598 |
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Enhancer Sequence | ATAAGTACTA TTAATATTAT TATCTCTACC CTATAGATGA GAAAAATGGA AGCACAAATG 60 TTAAACATAG TAAGTAATGA GCTGGGATCT GGCTCTAGAA CATGCTCTTA CCACTTCACT 120 ATACTGCCTC CTTTGAAATC TGAATCCTCA TGACAATTCA GTGAGGAAAA CAATGTCGCC 180 ATTTAAGAGT TGAGAGACAG CACTCCTAGA TTGTTAGCTT CCCAAAGACA AAGGCTGTAC 240 TAATTGATTC TGCATATTCT CTCTAGAAGC CTCTAATGAT GGCCTCAAGC TCATAGGCAT 300 TGTAGAGAAA TGCAGAAGTG TCATGAAACA TGGCCTTCTA CTCTCATGAA GCTCACAACC 360 TCATGGAAGA GATACTACCA AGTACAAAGT GGAAGGGCTG CTCTGCCCTG GGCTTGGAAG 420 AATGAATGTG AGGATCAAAA AATTATTTTA AGGACCTCTA AGCCTTGAAA GTAAACAGGT 480 CTAGTCTTGT AAGACTGTAA ATGCCCACAT GTCTTATTCT ACCATTTGTA CACTAATGAG 540 ATACAGGAAG AGGGACAAAT AAGTAACTCT CGATAGCAAT GTACAGACTG TAGGGTCTGT 600 CTTCTGCCTT GGGGAGTGGG TATAGGGGGG TCCAGCAAAG AATTAGACAA ATAAGATCCC 660 ATAGAAGGCA AGGTCAAGAC AGTACGTAAA TTTATCCTAC TCTCCAAAAG TGGGATTGAG 720 AGCTTCAGAG TCCACAGTCA GTCTTCCACA GAGTTGGCCT CTGTGATTTG AATAAAGTGA 780 TCAAAAGCAC TAGCCCAAGC TTGAAGGTTA CTGTAACCAA AGTCTTTGGA CTTTGGTAGC 840 TGTGGGGTAG ACAGCTGTCT ACGGGCAAGT CCTTCAAGGT CATGGCAGAT TCTGCAGAAG 900 TGGTACAGAC TGCAGTAGCA GCAGTGAAAT AAGCTCATTA AGTTTAGGAG GGACCCTCTC 960 AATACATGTC TTCTGAAGTA GTAAAAGATT AGGAGCAAAG ATTCTGAAGT CTCATAGGTC 1020 TGTTTTAAAT GCCCATTTTG TTCCTTGCAA ACTGTATATG ACTGTGGAGA ATTTAGCTAT 1080 CCTCTGTAAG CCTAAGTTTA CTCGTTTGTA AATGGGTGAT AACAATATCA AACTCATGGG 1140 ATTAAACTAT ATGACACCCA CCCATACAGT ACTTAGCATA GAACATGCCA CAGACTTAAC 1200 AAAACAACTG ATGCTTTACT GCGTCCTTAC CATGTGCCAG GAACCCTTTT AAGCTCTCAT 1260 GCCTATTAAC TAATTTATAC TTCACAATAA TCCTATGAGG CAGCATGGTT GACTACATTA 1320 TTAATCACAA ACAGCCCCTG CTCCTATCTT TGTGGAGGAG GATATAGCCC CACCCTGTGA 1380 CTCTAGGGTA AGCCATGTGA TAGACATTAG TCAGTGGAAC TGAGCAGACA TGACTCAACA 1440 GAAACTCTCA TCACGATACT GGCCCTGATG ATGACGTGTC CCAGAAACAG GAGCTACTCT 1500 TCACTCTGCA CCGTAGAATG AAAAAGAACA AAGATGCAGT CTACCTATTG CCCACATGTC 1560 ATGAGCAAGA AATAAATGCT AGCCATTAAA AATTATGGAG ACTTGTGGAT TATTTGGTAT 1620 TATTACTAAC TTCATTTTCT GTGGAAGAAA TTAAGGCACA CAGAGGTTAA GTCCTTTGTC 1680 CAAACTCACA CAGCTGGTGG ACAGTTAAAC TCCAAACTCC TGCACATTAA CCTCTGTTAC 1740 CATCATCTTC ACTGATGAGG ACTGAGACAC CTAGGGAAAG TTTATTAGCA GACAGACATG 1800 AGAGGGAGAT CCAGTGATGC TAGAGGAAGA GAAGAAAGCA GATCAGCAGT CCTGGTATTT 1860 AAATGTGATA GAGCTGCAGA TCTGTAAGTA TGGTAAGAGT GGATGTTATT GTGAACACAC 1920 AGATTATGGG AGACTTGAAC AAGGTCAGTG GAACATATGC TTTATGTGGT GGAAAATTAG 1980 AAGCCAGTGA TGTCTGGGAG GCCAGGCAAG AAGCCATAAG ACAAACAGGC AGCCAAATGG 2040 CCTTGAAAAA TGCCGACTAG AGATAGCAGC AAGGAGGCTG CTCCAGGCTT CAGACAAGGA 2100 GCTAAGATAG GGTGGGGACA GTGGCAGTGT CAACAGAGGC CCACTGAGTA ACAGGAGACC 2160 TTCACTGACT ATCTGAATGT AACAAGAGTC ACATATCCAG CCATGCTTGT TAAACGAAAG 2220 GAGTGAGGGA TAGACAAAGG GGCCTAAAGA CTCAAGCCTG GGACAACTAA TACCATAATG 2280 ATGGTATCCA GGCCTGGAGT TATAGATCTT GCACAATTAA ATGGACTCTT GGCCCTCTCC 2340 TTGGACTGTT ACAGTGAATC ACTAGAGCTG ACTCAAAAAG GGTCTTAATA GATCTTAACA 2400 GGACTTCAGG GATTGTACCT GGTGGTAGTT GGCAATTGAC 2440
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