| Tag | Content |
|---|
EnhancerAtlas ID | HS121-09881 |
Organism | Homo sapiens |
Tissue/cell | LNCaP |
Coordinate | chr12:133354390-133357380 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Zfx | MA0146.2 | chr12:133354920-133354934 | GAGGCCGAGGCGGG | - | 6.01 |
|
Enhancer Sequence | CCTAGGAGGA AGGAAGCCAC GTTGTCCATG CCCTGCGTGA CACCCACAGC TTTATGACGT 60
GCCGGGCGCA GGGGGTGAAT GCACTCCCGG CCCCGTGCAT GTCCTGGCTG CCGGCGTGTG 120
CTTCTCCACA GGCCTGTCAA GTTCCTTGTA AAGATGAAAC CACCTGACCC GGAGCTCGGC 180
ACGCAGCAAG TGCACACTTA TGTGGCTGCT GCTATCTGTT GAATGAACAC ATTTATTCGA 240
GATTTCTCGG TCTAAATAGT TTTTATAGTC TTCTTCCAGT GTATTCACAG CCTGGACAAC 300
ATAGCAAGAC CCTGTCTCCA CAAAAAATAA AAAAATTAGC AGGGCATGGT GGTCCCAGGT 360
ACTCAGGAGG CTGAGGTGGA AGGATCACTT GAGCTCAGGA GTTCCAGGCT GCAGGGGAGC 420
TGTGATCGCG CCACTGCACT CCAGCTGGGG TGACAGAGTG AGACCCGGTC CCAAAAATGA 480
AATAAATAGG CCAGGCGTGG CGGCTCACGC CTGTAATCCC AGCACTGTGG GAGGCCGAGG 540
CGGGTGGATC ACGAGGTCAG ATCGAGACTA TCCTGGCTAA CACGGGGAAA CCCCGTCTCT 600
ACTAAAAATA CAAAAAATTA GCCAGGCGTG GTGGCGGGCA CCTGTAGTCC CAGCTACTCA 660
GGAGGCTGAG GCAGGAGAAT GGCGTGAACC CGGGAGGTGG AGCTTGCAGT GAGCCGAGAT 720
CGCGCCACTG CACTCCGGCC TGGGCGACAG AGCGAGACTC CATCTCAAAA TCTCAAAAAA 780
ATAAACAAAT AAATAAATAA AAATAATAAA ATAAAATAAA TACATTTAAA AAATAAAAAT 840
AAAATTAATT GGAAGGCCAA GGCGGGCAGG TCATCAGGTC AGGAGATTGA GACCATCCTG 900
GCTAATATGG TGAAACCCCA TCTCTACTAA AATACAAAAA ATTAGCCAGG CATGGTGGTG 960
CACGCCTGTA GTTCCAGCTA CTGGGGAGGC TGAGGCAGGA GAATCACTTG AACCCGGGAG 1020
GCAGAGGTTA CAGTGAACCA AGATTAAGCC ACTGCACTCC AGCCTGGTGA CAAAGTGAGA 1080
CTCCGTCTGA AAAAAAAAAA ACCGAAAAAA ATTCAGTGAA CCCTAAGCAC GGAGCGAAAG 1140
CTGGAGAGCT GGGGCACCGT GTGAGCCAGC CTGAACCACG GCCCAGCAGC AGGCCCCAGG 1200
CCAGGGTTAA ACGGCCGGGC GGATGAGGCC TGTGGGGCCA AGAGAAAGCT GTTAACTGCT 1260
CCTGTTAAAA TATTCCAGCC ACATTTTTTT TTTGAGACGG AGTTTCCCAC TTGTTGCCCA 1320
GGCTGGAGTG CAATGGTGTG ATCTTGGCTC ACCACAACCT CCGCCTCCTG GTTCAAGCGA 1380
TTCTCCTGCC TCAGCCTCCC GAGTAGCTGG GACTACAGGC ATGTGCCACC ACGCCAGGCT 1440
AATTTTGTAT TCATAGTAGA GACAGGGTTT CTCCATGTTG GTCAGCCTGG TCTTGAACTC 1500
CCGACCTCAG GTGATCTGCC TGCCTCAGCC TCCCAAAGTG CTGGGATTAC AGGCATGAGC 1560
CACCGCGCCC AGCCACCTGC CACATCTTAA AATTAATTCT ATTTATAAAG AAACTTTGTT 1620
GTTTCACCCC TTAAAAAAAA TCAAGAACCT TTTTCTTTTC ATCTCAATTA CATTATCATA 1680
GAAAAGTTCT TAAAGGTTGT GGCAAAGCCA GGTCATAGGA ACGAAAGCAG CTTCACTGTT 1740
AGGCCGAAAA GTTTGAATTG TGAAGCAATT ACTTTTTTAC AAGTTCAATT CAAACGGGAT 1800
TTAAAGGAAA AGTGATGTGT TCTTTCCTGC CTTTCTCTAG AGACAACCAG TTATTTCTTG 1860
TGTTCCTCCT AGAAATTTTC TACATATACA TCAGCATCAA ATGCATGCAC ACACACCACA 1920
GCCCAGGCAC ACACGTGCGC ACACACACCA CAGCCCTTGC ATGGACACCC CCCCCGTGCA 1980
CATACACACA CCCCAGGCAC ACACGTGTGT GCACACACAC CACAGCCCTT GCACGGACAC 2040
CCCCCCGCGC ACATACACAC ACCTCAGGCA CACACGTGTG TACAGACATC ACAACTCTTG 2100
CACGCACAGC CCCCCGCATG CACACAACCC AGGCACACAC GCGTATACAG ACATCACAAC 2160
CCTTCCACGC ACAGCCCGCG TGCACACACA CCCCAGGCAC ACACGTGCGC ACACACACCA 2220
CAGCCCTTGC ACGGACACCC CCCCGCGCAC ATACACACAC ACACCCCAGG CACACGTGTG 2280
TGCAGACATC ACACTTGCAC GCACAGCCCC CCGCGTGCAC ACACCCCAGG CACACGTGTG 2340
TACAGACATC ACAACACTTG CATGCACAGC CCCCCGCGTG CACACACACC ACACCCCAGG 2400
CACACGTGCA CGCACACCCC CCATGTGCAC ACACACGGCA AGCGTACTAG GAGTAGCTGC 2460
TCTGTGCCAG GTATGGCGGA GGTAGCCAGC AAGCAGCAGC GTTCTAACAG AGGAGCAGGG 2520
CCCAGACAGG GCACCTGGGG GTCAGGATGG GCCTCTGCTG GCGACGTGAC CAACGTGTCA 2580
GTGAACACCT GAAGCAGGGC AGGGGCCAGC CACGAAAAGA CAGCTCTCTA CACAGAGAAG 2640
GGTCCACAGA ACCACCCCTC TTATCTGCCG AACACAAATG GGATCATATG CTATTCTCAA 2700
GTTTGCTTTT GCAATGCAAC ACGACATACA GGACACCACT CCCAGCACAA TATAAATACA 2760
CATGCACGCG GAGCTCATTG GCCCCAGGCC CTCACAGCTG CACTGCCATT TAATCTAACG 2820
CCACCTTCTA CGGACCAGAG CAGGTGCTCT GCGGCCTCCG TCACCAACAA CTGCAACACA 2880
CCTTTGCTCT GTGTAACTGC TGGAAGGAGG CTGGTGTGTG AAGGACCCTG CATAGATTTC 2940
TAGGCACTGG AGCGTCCTCT GGAACGCCCT GTGAGACGGA AGGTGGCACG 2990
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