| Tag | Content |
|---|
EnhancerAtlas ID | HS121-09294 |
Organism | Homo sapiens |
Tissue/cell | LNCaP |
Coordinate | chr12:105456800-105459040 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HOXA13 | MA0650.2 | chr12:105458832-105458843 | CCCCATAAAAC | + | 6.02 | | IRF1 | MA0050.2 | chr12:105457257-105457278 | AAAAAAAAAAAGAAAGAAAGA | - | 6.25 | | RREB1 | MA0073.1 | chr12:105457446-105457466 | GGTGGGGAGGTGTTGGGGGT | - | 6.14 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr12 | 105458435 | 105458696 | | chr12 | 105458779 | 105458819 |
|
Enhancer Sequence | CTAGTAAAGA GATCAAACAC AGATTGTAAA ATCAGGAGAA AAGCTGTTCA TAGCGGTATG 60
TATAAGCATC ATTCTCTGCA AAAACGCTGA AGTTCATATT ATCATCTGTA ATAAAATTGA 120
GACACCACAA TGGGAGAAAC TGTCTCAAAC ATCCATAGAA ATGACACAAG GTGGCCGGGC 180
ACAGTGGCTC ACGCCTGTAA TCCCAGCACT TTGGGAGGCA GAGGCAGGCA GATCACGAGG 240
TCAGGAGATC GAGACCATCT TGGCTAACAC GGTGAAACCC CGTCTCTACT AAAAATACAA 300
AAAATTAGCT GGGCATAGTG GCGGGCACCT GTAGTCCCAG CTACTCGGGA GGCTGAGGCA 360
GGAGAATGGC GTGAACCCGG GAGGCGGAGC TTGCAGTGAG CCGAGATTGT GCCATTGCAC 420
TCCAGCCTGG GCGACAGAGC CAGACTCTGT CTCAAAGAAA AAAAAAAAGA AAGAAAGAAA 480
GAAATGACAC AAGGCAAGAA ATAGTCTGTG AATATGTCAC TGGAGAGTCC AAAATGCCCC 540
ACATCCAGGT GACATGAGTA TGCATTTATC ACATATTTGC ATTGATACAA AGGTGAATGA 600
GATAAAAAGC TCTCAGCCTT TATAGCCTGA AGGTAGGGTT TGGGTGGGTG GGGAGGTGTT 660
GGGGGTGGGC GTCAATGATG GGCAATGCAC AGTGGTCACC AGACTATTAC AGTGCAGGGT 720
GGTAAGTGAT GAGAAGCACA GGGTGCTTTG TGAGTCAGTT CATGGAAAAA GGATTGGATC 780
CAGAGAGTAA CCAAGAGACA CTGACGCTGA CTGCATTATT ATTGCACTTC TAGGATGATC 840
AGCTATCATT TATGGAGCAC TATTATGATT ATGCTATAAT GGTTTGTTGA ATACTTACTC 900
TAGGCCCAGG GCTAAGTACT TAAATGAGTT AACATGTATT AATTCTTTTT TTTTTTTTTT 960
TGAGACAGAG TCTTGCTCTG TCACCCAGGC TGGTGCAATC TCGCTGCAAC CTCTGCCTCC 1020
CGGGTTCAAA TGATTCTCCT GCCTTAGCCT CCCAAGTAGC TGGGATTACA GGCACATGCC 1080
ACCACACCGA GCTTTTTTTT TTTTTTTTTT TTTTTTTTTT TTTTTTTTTT TTGTATTTTT 1140
AGTAGAGACA GGGTTTTGCC ATGTTGGCCA GGCTGATCTC GAACTCCTGA CCTGGGTAAT 1200
CCTCCCACCT CGGCCTCCCA AAGTGCTGGG ATTACAGGTG TGAGCCACCA TGGCTGGCCA 1260
ACTCATTTAA TCTTCACAAT TACCCATAAC CTAAGGGAGG CAGTATTATT AGTCCCATTT 1320
TACATTGAGG AAACCAAGGC ACCCAGTGGT TAAGAAACCT GCCCGAGGTT ACACAGTAAA 1380
TTTTCATAGA AGCATTCTGG CTTCAGATCC TGCACTCTTA ACCATTACAC TAAACTCCCT 1440
CCCTTGGTCA CCCATCGAGC CCATGGATTT TTATTGGCAC TTAGTATGTA CCCAGACTCC 1500
TGCTTAACTG CTGAGATTAT CAAGACAATC ACATGAAGCC CTTGCCCCTA AGGAGTTCAC 1560
AGTCTAGTGT TGGGGGGAAT AAAGAGACCC TCACAATATA TGATGTGCGA TGCCAGAGGT 1620
AGGCAGAGTG TTGCTGGAAC CCAGAGATGG GCCATCAGAC CCTGCCAGTC TGGGCATGTG 1680
AGATCAGGAA ACCTCCCCGA AGAGGTGAAA CCTGAGAGCC TGGGCTGAGT CAATTACCCA 1740
TGGATAGAAG ACCCTTCAGG CCCTGCCCGC CTCTCCCGCC TCAGCTCTCC CCATGCCTGT 1800
CCTCACAGTT CAGACCCTGG CTTCACTGAA CTCCTTTTGC AAGTCCTTGA CCAGGTGCTG 1860
GAGTCTCTTA TCTCTGGGGC TTCACCTACT TGTCTTGCTC TCAACCTGGT TAACTCTTCT 1920
CGAGCAAAGC AGTGAGCTTT TCTAGGAAGC CTTTCCTAAC ATGCCTGAGT CTCAGCCTCC 1980
ATGATAGCGT TTATCTTACT GCACTGAGAA TGTTTATTCA CTTCTCTGCA CTCCCCATAA 2040
AACTGCAGGC TCCTTAGATC AGGCGCTGGA TTTAGTGTCT GCTGCACAAT AAATGCTTAA 2100
TACATGCTGA GTAAAGGGGA GAGTGAATCA CAGACCTGCC TCATGACCAA GGAAGAACCA 2160
TGGGAAGCCC AGATTTATCT GTAATATCTC TTACAAAGGT AATAATCGGG GAGGGGGGTG 2220
GGGGGAGTGG TCCCTAAAAC 2240
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