Tag | Content |
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EnhancerAtlas ID | HS133-16477 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr2:20695850-20697560 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nfe2l2 | MA0150.2 | chr2:20696337-20696352 | TGCTGACTCATGGCA | - | 6.1 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_34707 | chr2:20695049-20698159 | HeLa |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I020491 | chr2 | 20691321 | 20698247 |
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Enhancer Sequence | AGTTTATACT CATAAACATT TACTATATTA ACAGAGAGGC TCTGAGATTC CAATGCCCTC 60 ATTATACATT CCCTGTTTCT AGAGAAGAGC CCAAGAATCC CCAAGGGGCA TTTTGGCATT 120 CACTGGAGCA AGAACAACTG GTCATCCCTG ATTCCTACTC TTCTGTTGTT GAGGAGCTAG 180 TCGTTGCCTG GTGACTCACT GTGCTGGGAG GGACAGACTA GCCTTTACTG TCCAGCTAAT 240 GTCCCTGGTG GCATGCCACC ACCCTCCAGG TGTGGGGGTG GCTGAGCTCC AGGATGAGTG 300 AGTCCACTCT GGGTTTGGGG TGGGGCAGTG GTGTGGGGGC AGAGACGTTC AGGGGACAGA 360 CTACACGGAG CCCCTCTCCC ACTTTCTACC TCATTAGGAT GAAAAGACAA AAGCAATTCC 420 AAGCAAATGT AGCAGAAGTT GTCCCCCTAG TTCTGCTCAT GTCCTGGCAA AGAGTGCGGA 480 CTGAGCCTGC TGACTCATGG CACTCTAGTT CAGGTCTCCC ACTAGAAGAC AAAGCAGGGT 540 CAGGGCACAC AGTGTTGCCC TCAGGACACC ATGAAGCTCA AGGAAGCCTG GAGCGGTGGC 600 TGGCTGAGGA GCAGGCCGCT GCTAGGCAGC TTTGTGCGTT TCGTGACTTT GCTGGAAATG 660 CATCAAACGC TTGGCAAAAA CACTTCCTCC TCCAGTGACA GGCACTCACG TTTCAGAAGG 720 CATCAAATTG CTCTGAAAGG TGACAATAGC ACCTGTCAAC TTCTGCACAT AGAACACTGT 780 TTTCTACTGC AAGAATGTTT TTCTTGATCT TCTGGAACTG TATAGACTGC AGACCAAGCA 840 TCATCCATGT CCTGAAGCCC AGCTGGGTGG CGGATGGGAC ATGGGAGGGC AGGACAATGT 900 CTGCAGAGGT GGTGGAGAGC ACGGGGGAGC GGTGCCTTCT CAGCACTCCA TTTGCCGGGT 960 GGGGTAGGAG GGGAGGGTGA GGGTTCTGGG ACATTCTTGA GCCCCAGGCA CAGCTGCGAA 1020 GGGCAGTAGC TGCAGAGCCC CCGCATGGGG CTGAGCGTGG CCTCTCCTTC CTTGGGCTGA 1080 GTGGACAACC TCCTGCTCCC TCAGCTATAT TGCTGGCTGG GGTTGGCAGA GGCCAGGCAC 1140 TCAGTCCTCA TCCACAGCGA GGTGTGAGTA AGTGGAGAGG GGGAAGCTGG CTTCCAAGGT 1200 GAAGAACAAC GGGGACAGAA GTGCAGAGGC GGCGTGGTGC CTGGTGCTTT CGGGGGACTG 1260 AAAAGAGGAC ACGTTTATTA TTTTGATGCA TTTGTGACTT AAGCTGAACT CCTTCCTATG 1320 GGCAATGCTG CTGAAATAGG GGATGTGTGT AGGGCAGCTG TGGCAAAAGT GAATGCTGAG 1380 GAAGTCGGGA AGGGCTTTGA GCTAGGTTGG GACAGGAGCA GGAGGTGAGT CCACCTGCAG 1440 GGTGGAGGAA AGCTGGATGG GCGTGCACAC TGGGGGCTGA CCAGTGGCCC GGGGAGGCCG 1500 TTATGGGCTG AACAAGGAAC AGAGTGGAGA GAGTGGAGGG AATGGAAAGG GGGACGCAGC 1560 AGGAGCCCCA GTGAATCTGA GAATCTAGGG TGTGCTGCTC CCCTCAGCCT GAGCTCAACA 1620 AAATGCTCCA GGCTTTCCCC TCCCCTGTTA GGAGCTTGGT GGACCCCCAC GTCTGGCTTA 1680 TGCTCTATTG CAGTGACAAG AGGCCTAGTG 1710
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