Tag | Content |
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EnhancerAtlas ID | HS120-02962 |
Organism | Homo sapiens |
Tissue/cell | LNCaP-abl |
Coordinate | chr17:79694110-79695310 |
Target genes | Number: 32 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
BHLHE40 | MA0464.2 | chr17:79694216-79694226 | GTCACGTGAT | - | 6.02 | FOSL1 | MA0477.1 | chr17:79695136-79695147 | CATGAGTCACC | - | 6.62 | Foxd3 | MA0041.1 | chr17:79695167-79695179 | GTTTGTTTGTTT | + | 6.32 | JUND | MA0491.1 | chr17:79695136-79695147 | CATGAGTCACC | - | 6.02 | Nr2f6(var.2) | MA0728.1 | chr17:79695075-79695090 | TGAACTCTTAACCTC | - | 6.53 | TFEB | MA0692.1 | chr17:79694216-79694226 | GTCACGTGAT | - | 6.02 | YY1 | MA0095.2 | chr17:79694583-79694595 | GCAGCCATCTTG | - | 6.74 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_24622 | chr17:79694215-79694862 | Colon_Crypt_2 | SE_24986 | chr17:79694274-79694842 | Colon_Crypt_3 | SE_27510 | chr17:79694061-79695025 | Esophagus | SE_41699 | chr17:79694211-79694856 | LNCaP |
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| Number: 1 | ID | Chromosome | Start | End |
GH17I081727 | chr17 | 79694338 | 79695210 |
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Enhancer Sequence | AGGCAGAGAT TGCAGTGAGC CAAGATTGCA CCACTGCACT CCAGCCTGGG CTACAGAGCT 60 AAACTGTCTC AAAAATAAAT AAAGTAATAA AATAATAAAA TAAATAGTCA CGTGATGCTT 120 CAGGTCATCT GACATCCTGC CCCCCACCCC TTAGTAAAAT GCCTGCTGTT TTATTCAAGC 180 AGCTACCACC CCACCCCAGT CCTTGGGCCT CAAGGGCACC AGGGCCTGAC CCCAGCTCCC 240 AGCATGAATA GGGTTGGTTT AAACCAGTCG GCATGGCCCA CAGTGACTGG TTTAGGCATG 300 GGCCTGTCAC CCACACTGGG CCAATGATAT GTAAGATGTT TATTGTAGCT TCCGGGATGG 360 AAACTTCTCT GCCAGCTTGT GGGTTGGGCA AGGACGACAC TCCGGGCCCT ACCGGCGGAA 420 GCTCTGCTCC TGTCGTGCGT GGACCACGCA GCAAATGGCC TTGGAGGCTG CTGGCAGCCA 480 TCTTGTGACC ATGAGGCAAG TCAGCGCAGG CCGAAGCTGA CGACGCGAAG ACAATGAGGA 540 GAGGGAGAAA GAGCCGATCT TTGGTGTGTA TTGGCTGTGA CGTGCTGCCG CCTCTCTGGA 600 GACCGGGTTC ATTATACTTT TCCTGGTATC TTCTCATGTT TGCTCTGCTG GCTTTGGGCC 660 CGAGTTTTAC CTCCTGGGTG TATTGTGTGT GCCTGTTTTG TGGTGTTGGT TTTGCTCCTG 720 GGTTTGTTGA CCCTTGGGTG TCTGCTCTTT TTTTTTTTTT TTTTTTTTTT TGGGACAGAG 780 TCTCACGCTG TCACCCAGGC TGGAGTGCAG TGACCTGATC TTGGCTCACT GCAGCCTCTA 840 CCTCCTGGGT ACAAGCGATT CTTCTGCCTC GGCCTCCTGA ATAGCTGGGA TTACAGGTGC 900 CTGCCACGGC TAATTTTTTT ACTTTTAGTA GAGATGGGGT TTTGCCATGT TGGCTAGGCT 960 GGTCTTGAAC TCTTAACCTC AGGTGATCTG CCCACCTCCG CCTCCCAAAG TGCTAGGATT 1020 TATAGGCATG AGTCACCGTA TCCAGCATTT TTTGCTTGTT TGTTTGTTTT GAGACGGAGT 1080 CTCGCTGTGT CACCCAGGCT GGAGTGCAGC GGTGTGATCT CGGCTCACTG CAAGCTCCGC 1140 CTCCCAGGTT CACACCATCC TCCTGCCTCA GCCTCCTGAG TTGAGTATCT GGGACTGCAG 1200
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