| Tag | Content |
|---|
EnhancerAtlas ID | HS121-05768 |
Organism | Homo sapiens |
Tissue/cell | LNCaP |
Coordinate | chr11:295690-298100 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr11:295894-295912 | GGAAGGAGGCAAGGACGC | + | 6.31 | | EWSR1-FLI1 | MA0149.1 | chr11:295886-295904 | GGAGGGAGGGAAGGAGGC | + | 6.4 | | EWSR1-FLI1 | MA0149.1 | chr11:295890-295908 | GGAGGGAAGGAGGCAAGG | + | 6.84 | | RUNX1 | MA0002.2 | chr11:297948-297959 | AAACCACAGAG | - | 6.14 | | TCF7L2 | MA0523.1 | chr11:297963-297977 | AGAGATCAAAGGCC | + | 6.18 |
|
| | 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 |
| GH11I000296 | chr11 | 296981 | 298398 |
|
Enhancer Sequence | AGCCGCTGTG CTTCCTTCTG AAGTGAGGGC CGTGCCCCGG GTCCCATTTC TCCTTTCACT 60
TGAGTCGGGA AGCACAGCAA CTTTAAGGCT CGCGCCCAGC AACATGGCTC CCCTCGCATC 120
TGCATCTCCC TCCTGCTCTG GTGTTGCCGC TGCACCCTGT CCTCGGAGGA CAGCAGAGGT 180
TTGGACGGAG ACTCAGGGAG GGAGGGAAGG AGGCAAGGAC GCCTGTGGAA ACATCTTTCA 240
GGCAGCTCTA GGGTCTGGGG GCCAGGATGC CTGGGTCTCC CAAGGCCTGT CTGCTGTCTC 300
TGCCACCCTC AGCGGCTGCC AGAAGCAGCG TGTGGGGGAG GCATGTGCTG CAGCACACCT 360
GCGGCCGAGA CCAGCACTCA GAGGTCGGCT CCCCTGACAG GAACCGTGTA GGGTGCAGAA 420
GGCTGAGACC TGTGGACACT GCGTGTTTTA TGGCAGCTTG CTTGCTGGGG CTCATGGCCA 480
CAGTGGAGAG GGGCCGTGGG TCAGGGCAGC CCAGTGTGCA GTCCAGTGCC GGGCAGGAGT 540
CTTGCAGGGG CTCATGACCA CAGTGGAGAG GGGCTGTGGG TCAGGGGCAG CCTGGCGTGC 600
AGTCCAGTGC CGGGCAGGAG TCTCACAGGG GCTCGTGGCC ACAGTGGAGA GGGGCTGTGG 660
GTCAGGGGGC AGCCCGGCAT GCAGTCCAGT GCCGGGCAGG AGTCTCGCAG AATGCAGCCT 720
GACGCCTCCA CGTGGCTCCC CCGGCCCCTA CAGGCTCCCT CAGCTGCAGA GCTGGGTCCC 780
ATCCGACGCT GTCGCTGGGC AGCGAGAGGC AGAGGCAGGT TCCCCGAGGG AAGCATGGGC 840
CCCTTCTCCC GGCCACGGTT GCCCCAGCAG GAGTTCATCT TTGCAGCCCC AGAGCCAGGG 900
TGATGTGGGC ACAGGTGTCA AGTCAGGGTG GTCGGTAGCC TTGCGCCCGC AGGAGAGATA 960
TGGCCTGAAG CCTGCTGCAC GTGCGTGCCA CACGCGTGTG GGGCCACCTC TGCACATCCT 1020
GAGGTGACCC TTTTGGGGGG GTCGTGATGG TCAGTGCACG TGTGCCGGCA GGGCTGGTCA 1080
GGGTTCATCG CCTGCCCAGG AGCCTGAGCC TGAGGCAGGG AGGTGCTGGT GACCGTTCCC 1140
CCAAGGTGGC TCACCCACAG CACCGGGAAT GGACCAGGTC GTCCCTGCCC CTCAGTAAGC 1200
CTGGGGACTG GCAGACCGTC TCTTTTCTGG GGACACGTAT CCAGCCACAC ATGGGCTGAC 1260
CCCCTCCCAG TCTCTGCACC CGACACAGTT TGATCCCTTC TCAGGCCAAT CCTGAGGCTC 1320
AGGGCTGGCA CACTGTCTCT ATCCCAAGGC AAGCACAGGT GGGCACACTG CCCTTGTCCT 1380
TGGTCCACTG TGGGACTGGT CCTGTCTGTC TCCAGCGCCC AGCATGGCCT CCACACACCT 1440
CTGCCTCCAG GGCTGGCTGG GCCTGCCCTC AGAGTCCCTG CCACGCCAGC CGTTGGCTGC 1500
AGGCATATCA CAGATAGGGG ATGCTGCCCA GGGCTCCGAG TAGACCAAAA GATTCCTGCC 1560
CACAGCCCAG GAAGAGCAGG CAGGCAACGG CGATTCCCCG GGAAGGGAAG GGCCCCGGAG 1620
TGGGGTGCTC AGAACCCTGG GCCACTGTGC TGTTAACCAC CACCTCCCGG CAATGGCTGG 1680
CCTCAGCGAG GCCCCAGGGC CTCCCCGCAG CCTCGCAGTG TGCATGTCCC TGGCCCTCTC 1740
CCATCACCAG GCTGTGGTGG GTGTGTGGGG AGGCTGTGGT ACACAACGCA GGTAAAATAA 1800
TATGAGAACA TGCACCCAGC ACCAGGGGAC TCAGAGAATG TTGCACACAT GCCCATTTTC 1860
TGCCTTTCTG GATATAGTTT GGTTGGGGTG TGTGTGTGTG TGTGTGTGTG AGAGAGAAAG 1920
GGAAGCTGCT ATCCTTCCCA CATGTGTTTG TGTGTGTGTC CAGCCCCACC CATGGGATCG 1980
TCCCCGCCCT GCCTTTCTAG CCACCCTCAC TGGCCCAGGA GGGAGGGAAA CCACCGTGGG 2040
GACTGGGATT TCTCAGAATT AAGGGGGCAC GCAGGGTCAT GGGGACAGAC AGAATGACCC 2100
AGAAAGGAAG GAGGTGTACA CCAGACCGCA GATGGAGCCC ACCCACAGGC ACGGACTCTC 2160
ACGCAGACTT CGAGCACGCA CACACATGCG CACAGAGAGA TGGGGTGGAC ACACGTGGGG 2220
TTGGGACGCA CCCATGATGT TCTGGAGCAC AGGCCGCTAA ACCACAGAGC AGCAGAGATC 2280
AAAGGCCTGG GCTCTCAAAC TTAGTCTAAA ATACTCTGGG CCTCCGCCCC GTAAGCCACA 2340
GGCCGCCCAG TGGCTGAGAG AAGGGGACAG TTGGGGCCAA GCAGGGCTGC TGAGCTGCGG 2400
GGGGCGCTCC 2410
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