| Tag | Content |
|---|
EnhancerAtlas ID | HS121-07876 |
Organism | Homo sapiens |
Tissue/cell | LNCaP |
Coordinate | chr11:120198350-120200680 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MEF2C | MA0497.1 | chr11:120198636-120198651 | AAGACAAAAATAGAA | + | 6.49 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_45242 | chr11:120195463-120198651 | NHLF | | SE_47436 | chr11:120195033-120198913 | Panc1 | | SE_47436 | chr11:120199202-120205424 | Panc1 |
|
Enhancer Sequence | TAGGTAGGGG ATTTTCCCTT AGGGATTTAT GATTTGGGGG TAGTCTTAGA AGTATGGGAC 60
TTTTAAACAG AATTTGTACA ATACTGAAGA CTAATTCCCA TTATAATTTT GTATTGGAAT 120
CCTTATTCTT CTTCATTGTT AACTCTGATA TTGTTTATGT CACCTGTTGT TTCTGCTTTT 180
CATAACTCTC TACTTTTAAA ACAGATTTTA AATTGCTTGT TACAATTTAA TTGGAAATAC 240
AAAAACTATA AAGCCAGTAT CAACATCTTC CACTACCACC CCCGAAAAGA CAAAAATAGA 300
ACTGTATCAT ACATATTTTT GGCAACTTGC AACTTTTACT TGACTGTCTA TTCAAAAGAC 360
AGCATCTTTC CATGTCTATG TTAAGAGGAT GAGATGTTCC TTATCCTTTT TGTTACTAGA 420
TGTACAAGTG TTACTTTCAG AAGTATGCAA TTTTTTTTTT TTTGAGATGG AGTCTTGCTC 480
TGTTGCCCAG GCTGGGGTGC AGTGGCTCAA TCTCAGCAAG CTCCGCCTCC CAGGATCACG 540
CCATTCTCCT GCCTCAGCCT CCCGAGTAGC TGGGACTACA GGTGCCCGCC ACCATGCCCA 600
GCTAATTTTT TTTGTATTTT TAGTAGAGAT GGGGTTTCAC TGTGTTAGTC AGGATGGTCT 660
CGATCTCCTG ACCTCGTGAT CCACCCGCCT TGGCCTCCCA AAGTGCTGGG ATTACAGGTG 720
TGAGCCACCG CACCCGGCCA AGTATGCAAA AATTTTACCC CCTTGTATTA ATTGGTTGGG 780
GCTGCCATAA CACAGTACCA CAGAGTGGGT GGCTTAACCA GATGTTCATT TTCTTAAAAT 840
TCTAGAGGCT AGAAGTCGGA GTTCAAGTTG TTAGCAGGTT TGGTTTCTTC TGAGGCCTCT 900
GTCCTTGGCT TGCACATGGC CGCTCTCCCA CTGTGTCCTT CCATGGTCTC CCCTCTGTGT 960
GTGTGTGTGT GTATGTGTGT GTGTTTGTAT ATGTATGCAT ATCTGTGTCC TAATCCCTTC 1020
TAAGGATAAC AGTCATAGTG TGTGTGTGTG TGTGTGTGTG TGTGTGTATG TTTATGTATG 1080
CATACCTGTG TCCTAATCCC TTCTAAGGAT AACAGTCATA TTGTGTGTGT GTGTGTGCGC 1140
GTGTATGTTT GTATATGTAT GCATATCTGT GTCCTAATCC CTTCTAAGGA TAACAGTCAT 1200
AGTGTGTGTG TGTGTGTGTG TGTATGTATA TGTATGCATA TCTGTGTCCT AATCCCTTCT 1260
AAGGATAACA GTCATAGTGT GTGTGTGTGT GTGTGTGTGT GTGTTTGTGT ATGTTTATGT 1320
ATGCATATCT GTGTCCTAAT CCCTTCTAAG GATAACAGTC ATAGTGTGTG TGTGTGTGTA 1380
TGTGTTTGTA TATGTATGCG TATCTGTGTC CTTATCCCTT CTAAGGATAA CAGTCATATT 1440
GTGTGTGTGT GTGTGTGTGT GTGTGTGTGT ATGTATGCAT ATCTGTGTCC TAATCCCTTT 1500
TAAGTATAAC AGTCATATTG GATTACTCTA ATTACCCCAT TTTAACTTGA TTACCTCTTT 1560
AAAGACCTTA TTTTCAAATA CACTCACATT CTGAGGTACT ACCAGTTAAG GGCTTTAACG 1620
TGAATTTGGG GAGGGAGGAC ACAATGCAGC CCTTAACTCC CCTGGAATAT AATTTTTAAA 1680
ATATTTCTTT AGCTTTTCTT ACTGAATTTC TGAGTTTCCC CCCAAACTGT CAAACTAATG 1740
AAACCAACTG TTACGCTTTG TGTTTTATGT GAAGATTCTA AATGGTTTCA AATATGTCAG 1800
GTCCTTAAAA CCTATGTTCC TGGACATGAG CACACACTAA CTTTTGGGGC CCTCTCCAGA 1860
ATCTACTTTC AGGATGGGTT AAGACCACTG AGTGTTCAAT AACGTAACCC ATTAAGCTGA 1920
GAAAAAAATC TGACATTCAG GAAACAATGA TTCAAGAGTC TGGAAATAAA CCTTTAGCAG 1980
AGTAAAAAAA AAAAATAAAG TTTAGGATTT TAATTGAAGG AACAAAATAA TGGGATTTTA 2040
TGCTGTTCCG CGGAGAGGAT ACTGAGATTA TTGCCTGTGT TCATTGAAGG ATGCAAACTC 2100
ATTGAAGTCT GATTCATCAG AACAGCATTT CCTGGGGTCT GAACATCGTT TAGTTTGATA 2160
AAGACCTAGA TTTTATATTT TAGTCTTTCT TTGGTCCTCA TTAAAAAGCA TGTGCCTGCT 2220
ATTGTTTTTG TTTCTTTAGT GTCTAGTAAG GTTTGAAAGA CAACAACATA GGATCCCTGT 2280
GCAAGGTAAC ACAATTCCCA GTCACTCAAT TTGCTTCTGT CTTGGTTTGT 2330
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