Tag | Content |
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EnhancerAtlas ID | HS121-22286 |
Organism | Homo sapiens |
Tissue/cell | LNCaP |
Coordinate | chr2:131878550-131881140 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Zfx | MA0146.2 | chr2:131879711-131879725 | CCCGCCTCGGCCTC | + | 6.01 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_29399 | chr2:131877908-131878815 | Fetal_Intestine_Large |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I131120 | chr2 | 131877909 | 131878815 |
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Enhancer Sequence | AGTGAGTACA GGATGTGCGG TCTGCGATCG GCATTGCCGA AGGGCAGTCT CTATTTCTGT 60 TTGCTTAAAG TTGATCATAT TTAAAAGCAA ATAACAAAGT TTTATGAGTG CTATGGCCTT 120 GAGTTTCCCC TTGGACATTC CTAGATCTCT GTGAACTGTC TTGCACACCA CGGAGCTCCT 180 CCTTGGTTGC TGAGTTGACA GGAACCAGGA AATGATGGCA GTCCCTGCTG CTTTCGCTCT 240 CCTCACTAGC ATGCTTTACT TTTTAATTTT AATTTATTTT ATTTATTTAT TTTTTGAGGC 300 AGAGTTTCAC TCTTGTTGTG GAGTGCAGTG GCGCGATCTC GGCTCACCGC AGCCTCCGCT 360 TCCTGGGTTC AAGTGATTCT CCTGCCTCAG CCTCCCGAGT AGCTGGGATC ACAGGCACAC 420 ACCACCATGC CCGGCTAATT TTGTATTTTT AGTAGAGAAG GGGTTTCTCC CTGTTGGCCA 480 GGCTGGTCTC AAACTCCCGA CCTCAGGTGA TCTGCCCACC TGGGTTCCCA AAGTGTTGGG 540 ATTACAAGCG TGAGCCACCG TGCCCAGCTG CGTGCTTTAT TATTAATGAT GGATCTGGGA 600 CTGCCTGGAT CTAACTGAGC CCAGCTGAGA TACTGGAACA GAGGTGCTGG TCTCTCTGCC 660 TGTCTTATCT GGGGATTGAG CAGTGACTCA GATTCTCAAA TATTGGAGTC TTTGTAATTA 720 TGTGGCTGAA GAGTTGATCT GAGGCAATGA GTTCATCTAA AACCAAAACT TTTGTGTCTC 780 CAAAAGGACT AGAGAAGAGA CTCAGTTCTT TTTTTATGGG ATTGAGATCC ACTTTCCTAG 840 GCTTATCTCT GCAAACCTGT CTTTCATACA CTGTCTGCTT ATCTCTGAGG CTGTCACTCC 900 AGGTGGGATT CATACTGTGT TTTATTTTTA TTTATTTATT TATTTATTTT TTGAGATGGA 960 ATTTTGCTCT TGTTGCCCAG GCGCGATCTT GGCTCACTGC AACCTCCGCC TCCCAGGTTC 1020 AAGTAATTCT CCTGCCTCAG CCTCCCGAGT AGCTGGGATT ACAGGCGCAC GCCACCATGC 1080 CTGGCTAATT TTGTATTTTT AGTAGAGACG GAGTTTCTCC ATGTTGAGCC TGGTCTCGAA 1140 CTCCTGACCT CAGGTGGTCT GCCCGCCTCG GCCTCCCAAA GTGCTGGGAT TACAGGCAAA 1200 GTGCTGGGAT TACAGGCGTG AGCCACCGCG CCCGGCCTCA TACTGTGTTT TAAAGTGGGA 1260 AGAACCAGTC TTATTTATTA AAAAATGCAA GCAGAATATT CTGCTATACT AGAAAGAGTG 1320 AAGTTAAGGG AAAAGTGACT ACCATGTCAT TTATGATTCT AGTCAAAAAC TGAGCTGTAT 1380 CACATACCAT TGATTGTTCA GAGACTTGAG TTTATCTATG AGGGTTACTT TCAGAAATTT 1440 AGCTAAAGTC AAGTCTACCA GTAAGAATTG ATGGCATACC TGAGATGGTT TATCAAAACT 1500 ATTGTTTACG AATTGTTTGT GTTCCTGTTA AATAGATTTT ATGTATATAT TCTTAATTCT 1560 CACAACAGCT GTATGAGAGG TAAGTGGTAT TATTTCCAGT TGAAGAAATT GAGATTCAGT 1620 GAGGTTAGGT ACTTGTCTAA GTGTGAACTG TGGGTGACAA ACCTACATTC AAAGTCAGGA 1680 CTGTGTGATT TCAACACTGA CATTATATGC ACCCAGAGAC CGGTCTTCAG CCTGTGTGTC 1740 TGTGACTAGT TCCATGTTCC CAACCTGGAG CTGAACTGTA TGTCCCCTTG TCTGTTAGTC 1800 CTGTAGTCTT AGAATAGACA AAGGTGTCGT AATGTTAGCT TCACAAAGAA AGTCCTGGCT 1860 TGTTGAAGTC TAGCCCAAGT TTCCTAGTCT TGGGTTTTGC GGTCTCAACG TCCCCATGGT 1920 CAGGGGACAT GGGGACCCTT GCTCAGACCT TGAGGGTGTG CCCTCCTTTG GCCCTTTGGA 1980 TGTCCTTTGC CACACCCTTG TTTGAGGGCA AGCTTTCCCT TTTCCACCAC AACTTGAAGT 2040 AAGTGCTCTG TCAACATAGT GATCAGTGAC TCTTTTGACA ATTTTGTCCT CCCCATCACG 2100 CCTAGCATGG TGATGTACAC AAAATAGATG TACTTTAAAT AAGTCACATA GACTTTTCCA 2160 GTGTTCTGGT CCATGGGTGT TTCAGAAGTG TGTATTCAGA CGATTTACTC TGTATATAAC 2220 CCCATCCCCA TATGTATGGG TTAATTTTCC TTCTTTCCTG AAAGTAGAAG TATCAATGCC 2280 AGTAAAACGA GGTGAGATAC ATTATATTCA CGGGGTTGTA GAGCAGCAGA GATACACATG 2340 TGATGTGGTC ACAGGTAGGC AAAGCCAGCC TTGGGACTTA TTTTCCTGCC ATTGCCACAT 2400 GTACTGTTGG GACCCAGTCC TGGCCTCTGG AGGACAGCCT GACTTGGGAG TCTGCAGCCA 2460 GGGCTTTGAT GGCAGGTGAG ATACTTGGGC AGAACTCCCT GACCCAGTGG TTCCACCTGT 2520 CTCTGTGTTT CTGTGGCTCT ATTTAGTAGG GCTTTTTGTT TGTTTGAGAC AGAGTCTTGC 2580 TTTGTCGCCC 2590
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