| Tag | Content |
|---|
EnhancerAtlas ID | HS121-28544 |
Organism | Homo sapiens |
Tissue/cell | LNCaP |
Coordinate | chr4:992230-994390 |
Target genes | | Number: 27 | Name | Ensembl ID |
|
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| PLAG1 | MA0163.1 | chr4:992672-992686 | CCCCCATGGCCCCC | - | 6.02 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH04I000995 | chr4 | 989044 | 992431 |
|
Enhancer Sequence | GATGCGGCAC AAAGCCAGCT GCCACAGGAG GTGCACTGCC CCACGGGCAG CTGTGCTCAC 60
CTGCGTGGCG TCCGCAGGAA GCCCTCAGAC CCTGGCCAGC CTGGTCTCTG CTTCTCACTC 120
CAGGCTCAAG GCTGGCTGCT ATTCCATTCA CCCCATTCCC TTTCCCTCAG GCCAGAAGCA 180
TCACTCACAA CTCCAGACCC TTGCACACCA ATCTCCTCAC TCAGTTCACC CTCAGATGTC 240
CAACTCCACA TGGCCAAAAC CGAGACCAGT CTCACTCCAA GCTCATCCAC CCGCCTAGCT 300
GCCCAAGCTG AAATCCACAG TTGCCCTGTA CGACCCCCCG ACCCCCCACC TCACCCCCCA 360
GCTCACCTCA AACCTCATCA GTCCCTCTGC TCACAGCCTG CACAGCCACC ACCCAGTCTG 420
GGCACCATAC CTCTCTGGGC AACCCCCATG GCCCCCAGCC AGTCTTCCAG CTCCCACCCT 480
GACTCCAGTG AGCTGCCAGA GGGATCCTTG AAAAATGCTC TGGAAGCCAA GGTGGGCGGA 540
TCACGAGGTC AGGAAATGGA AACCATCCTG GCTAACATGG TGAAACTCCG TCTCTACTAA 600
AAATACAAAA AAATTAGCCG GGCGTGGTGG CGGGCGCCTG TAGTCCCAGC TACTCAGGAG 660
GCTGAGGCAG GAGAATGGTG TGAACCCGGG AGGGGGAGCT TGCAGTGAGC CGAGATCGCG 720
CCACTGCACC CCAGGCTGGG CAACAGAGTG AGACTCTGTC TCAAAAAAAA AAAAAAGAAA 780
AAAGAAAAAT GCCCTGGCAC TGCTCAGCTC AGAACCTTGA AAGGGATCCT TGTTTCGCTC 840
TGGGTCAGGG TCCCATCCTC AAAGCAGTCA CTTCCAGAGC CCCATGGAGC CTCATATCCC 900
ATGATATCCA CCCTTATTCT GTCTCAGGCC CACCAGCTGC CTCCCTGCTG CCTGATTGTC 960
ATGTGTGCAT TCCTGTTCCA GAGCCTTTGC ACTGGCGATG CCATCTGCTG CCTGGATGTC 1020
TTCCTGCTGG CTGGTCCCGT TGCATGGTAG CCTTAGGTGT CTCCTCAGAG AGGTCCCTCG 1080
CTGACCATCA GGCTCCTCAC TCCCTGTCGT ATCCCCTTCA CCAAAGATTC CCATTCCCTG 1140
ACGACGCCTG TCCCCTCGGA ATGCAGGCCT CGTGGGAATT CAGCCCATCC GCAAGTGCAG 1200
TGGCAGGGCG GCCCCCTTCC CCCTTGACGA CGCCTGTCCC CTTGGAATGC AGGCCTCGTG 1260
GGAATTCAGC CCATCTGCAA GTGCAGTGGC AGGGCGGCCC CCTTCTCCCT TGAGGACGCC 1320
TGTCCCCTCG TAATGCAGGC CTCGTGGGAA TTCAGCCCAT CTGCAAGTGC AGTGGCAGGG 1380
CGGCCCCCTT CTCCCTTGAG GACGCCTGTC CCCTCGTAAT GCAGGCCTCG TGGGAATTCA 1440
GCCCATCTGC AAGTGCAGTG GCAGGGCGGC CCCCTTCTCC CTTGAGGACG CCTGTCCCCT 1500
CGGAATGCAG GCCTCGTGGG AATTCAGCCC CATCTGCAAG TGCAGTGGCA GGGCGGCCCC 1560
CTTCTCCCTT GACGACGCCT GTCCCCTCGG AATGCAGGCC TCGTGGGAAT TCAGCCCCAT 1620
CGGCAAGTGC AGTGGCAGGG CGGCCCCCTT CACCCTTGAC GACGCCTGTC CCCTCGGAAT 1680
GCAGGCCTCA TGGGAATTCA GCCCATCTGC AAGTGCAGTG GCAGGGTGGC CCCCTTCTCC 1740
CTTTCCTGTG CACTCATGTT GCCTCTTGGG GTGTGGGAGG GGAAATGGGG CACTCCTGGG 1800
CCTCCAGGAG GTGCAGAGAA CCAGGGTGAG GTGTCCACCA GGTCCTGCCT GGCTCCTGAC 1860
CCCTGGCCCC TGCTGCTCGC GACTGGCCTG CCTCGTGCCA CTGAGCCTCA GAGCCATTCC 1920
GAACCCCCAC CCCAAGTTTT CCATCTCTTG ATGGTGTAGG GTTGGGGGGT CTCCATGTAC 1980
AGATACTCTA GTTCATACCA GGCCTTCATA GGGTTATTTT CCAAGGGGAA GGGCCCCTCG 2040
GGAAGCCGGG ATCGGAGTCC TGTGTGGCAC CTTGCAGGCT CCCACATGCT CCGTTGTGGC 2100
CACGGTTCCA GCCTGGAGCA TGGAGCTGTG TGGGCACCCT GCTTCCTGAC GCTGACCGTC 2160
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