Tag | Content |
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EnhancerAtlas ID | HS120-04836 |
Organism | Homo sapiens |
Tissue/cell | LNCaP-abl |
Coordinate | chr4:10007640-10009060 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ELF3 | MA0640.1 | chr4:10007989-10008002 | TACACGGAAGTAA | + | 6.28 | MAFF | MA0495.3 | chr4:10008691-10008706 | TTGCTGACTTAGCAT | - | 6.48 | MAFF | MA0495.3 | chr4:10008691-10008706 | TTGCTGACTTAGCAT | + | 6.5 | MAFK | MA0496.2 | chr4:10008689-10008708 | CTTTGCTGACTTAGCATTG | - | 6.3 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_10112 | chr4:10005592-10009723 | CD14 | SE_34108 | chr4:10004440-10012184 | HCC1954 | SE_36611 | chr4:10004166-10010815 | HMEC | SE_53020 | chr4:10006896-10010249 | Small_Intestine |
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| Number: 1 | ID | Chromosome | Start | End |
GH04I010005 | chr4 | 10006629 | 10011225 |
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Enhancer Sequence | TAAAAACCGG AAATTGGGGT GGTTGGTGGT AGTGTTGTTG ATATTTTTAC TGCTATATTT 60 GTAAAATAAG GGGCCTAGGC TCATTTATTT GTCAGATTCA AGAATCCATG AATCACTTAC 120 CATTATCTCC CAGGCCAGGA ACCTGGGGAC CAAGCCTCTG GACATAAAAT TGAACTCTGC 180 AATTCCCAGC CAAGACTGGC TTAGAGCATC TCCAAATAAT AAAAGAAATT GCCAGACAAT 240 GGGAGGCAAA TTACCTCGTA GCCCGTTTAA CAATATTAAT GTGCCTTACT GATTCACACA 300 GAGCCTCCCG TGAACTCACT TGGAACGATT CTCAGGAGTC CTGTAAAAAT ACACGGAAGT 360 AACACTTGGT AGCTGGGCCA GAGTACACAC ACCATTGCAT AAGAGAGGAA GTCATGCCAC 420 AATGCCTTAG GGCTTTATAA AGACAGTCTG CACCACTGAA CACACTGGCA CAGGGAAGAA 480 CGCAGTCCAG AAGTCCTTAA AAAAGTACCC ATTGTTGAAC CAGGCCCTCT GAAGTTAGGG 540 CCCCACAAGA ACAAAATTCC ACAATCCCAG CAGTGCTACC TAATGTCGCC TGGCTCCCCG 600 AGGTAAGGCC TCCTGTGTAG AAAAGAGCTC TCACAGCACG CCTGAGACTT CTCTTCCTAG 660 AAAAGCCTGC TGCAGGGTAA GTCCCGGGCT TGCATCTGGG AACTTGGATG TTGGAAGGGT 720 TGCCACCGTT CCCAGATCTG GTAAGAGTGA CTCAGTGTAC CTAAACTGTG CAAACAGTGT 780 GGTTTATGCT GTCTCAGTGT GGTTTATATC TGCTTTCTTT CTGGGAATCT GGAATTTTCT 840 GCTTGCCAAG CAGAGAGTGC CTATGTGACC ACCCCCCGAG AAAAACCCTG GACTCCAAGT 900 CTCTAATGAG TTTCCTTGTT AGACAAATTT CACAAGAGTT GTCACAACTC GTTGCTGTGG 960 GGATGAAGCG CGTCCCGTGA GGCTCTGCTA GAAGAGTTCT TTGGAGCTTG CCCCTGGTTT 1020 CCTCTGGACT TCACCCCTGC ACCTTTTTCC TTTGCTGACT TAGCATTGTG TTCCACCACT 1080 GTGATCAGTC ATAGCTGTGA GTACTACCGC ATTCCTGTGC CAACGCCTGT GACTCATGCC 1140 AGTGAATTAT CCTACCTGAA GGTGGTGTTG GGTGACCCCA GTACACCTCC CTTGTCCTAA 1200 GGAAAAAACT CAGCTCCCAT TTTGGCTTGA CTTGAGCATT AGGTTTGCAG GTTTGTGGTG 1260 TTTTTTCCTC CTCCCCAAGT GATTCTCCCA GAGGAGCCTG GCTGACTCAC TGGGAAAGAG 1320 GCTCCTGTGC CTCCAGACAC CTGAGACTAT TTTGTTCCCA CAGTTAGCTT TCAGAATGAA 1380 ATGAAACATG ATGAAAGAGG AAACATCAAT TACAAGCAAC 1420
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