| Tag | Content |
|---|
EnhancerAtlas ID | HS121-10652 |
Organism | Homo sapiens |
Tissue/cell | LNCaP |
Coordinate | chr14:24521400-24522910 |
Target genes | | Number: 30 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF5 | MA0599.1 | chr14:24521833-24521843 | GCCCCGCCCC | + | 6.02 | | REST | MA0138.2 | chr14:24521780-24521801 | GGAGCTGCCCCTGGTCCTGAC | - | 7.7 | | RREB1 | MA0073.1 | chr14:24522531-24522551 | ACACCCCACACCCCCACACA | + | 6.44 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH14I024053 | chr14 | 24522541 | 24522630 |
|
Enhancer Sequence | AGGTACGAGG CTGCCTCGGT CTCTGGGACG CCCCGTCCGG GAGCATCCCA GACCCAGCGC 60
GTTCCTCCCC GTGGTGCATC CCAGCCCGGT GTCTCACACC CCTCACCCCA TGCATCCTGG 120
CTCCAAGGCA GCCCCTGCAT TCCAGTCCGG GCATCGCTGT CCCCGGAGCA TCCTCCGCTG 180
CCTGCCTCGC CTCACCCGGT CGGGACCTTC CTGTCCCGGA GCCGCCCGTC CCGCCCTTCG 240
GTGACAGGTG CAGTTCCCTG GCGCTCCCTG GGGCTGACTC TCGGCGTTCC TAGCCCACCC 300
TCGGCGAAGC GTCCAGTCTC CCATCCGGAG AGTCCCCGCT TCCCCGCCGG GCGGGGCCAA 360
GCCCGCCCCT CCCTGCGATG GGAGCTGCCC CTGGTCCTGA CCGCTGCGTG GCTTAACACC 420
CTCCCTCCTC CCGGCCCCGC CCCGGAACTG GCCCTGAAGA GCCCCTTAGG AGCTGGGCAG 480
CGCCCAGGCC AGTGGGGCAA AGAAAGGAGT CAGGGAAGAG GCCCTGGATT GGAGCTAAAA 540
CCAAGAGCAG GAGGGTCTCT GAGGCTCGCC TCCCACAGCC CCGTCCCAGC CTGCTTCCTT 600
CTCGCTACCC ACCACCCACA CATCAAGGCT TCTCCCGTTT GCATGGTTCT CAGACCTAGC 660
CCAAACCCAG GCCCGGCCAC CCAGCACTGC CACAACCCTG ACCCCCAGAG ACGGGAGCAC 720
AGGCTAGCCC ACGCAAAGCG CAGGATGCTC GTGGATACTC AGAGGCATGC TGCGCCGTGG 780
CAATCTCCCA CACCTGCACA CACACACAGC ACAATCATTA GACGTGTGTA AACACATCTT 840
CACAGAGATG GCACCCCAGC ACACGCGCGT GCACACACAC ACACACACAC TATATCTGGG 900
TGGTTCTGCC AGCAGATGGG TATGGGGCTC ATTTAAACAT TAATTCTTCT CCCCGCCCAA 960
CACACACAGA GGAAGTGTCT GGCTCTGTGC CCCTTCCACA GCATACTCAT TCACACTTAC 1020
CTGTCCCCAC CAATGCCACA CTCAGGCTCC CTGACATCTC CAGGAGGCAT GCACACTCTC 1080
ATAGTAAAGG CAGACACTCA CACCCGGACC ACCTAGAATA TAGTCAAAGG GACACCCCAC 1140
ACCCCCACAC AGTGACTCAC TTTGTATGTG TCAATGGCTG TTGTAGTGCA TGGGTTGGAA 1200
AAATTCTTCA CACCCTCAGA AGTGTGAGAC ACACCCTCCC ACAGACAGTC AGCAACCGTC 1260
CCCTGACTCA GGGACATCAG GAGCCGGAGT TTTCTCCACA CCCTACTCCC TCTCTAATAG 1320
GAAGAGAAAA GTCAAAAAAG AGACAGTGTG AAAAGTCACC CAAGAAGGAA TGCCCTCTGT 1380
CCCTGTCCTC CCTTCTTTGT CTCTCTGTTT CTCTCTTATC CCATTTGACC CTGACCCTGC 1440
CTCTATCTGG AGAGCTCTGG GAGGTGGGGG TGGCCAGGGT AAGGTGAAGC TCTGAGCAGG 1500
CTCCCACCCC 1510
|
