| Tag | Content |
|---|
EnhancerAtlas ID | HS120-04593 |
Organism | Homo sapiens |
Tissue/cell | LNCaP-abl |
Coordinate | chr3:58105560-58106880 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myod1 | MA0499.1 | chr3:58106838-58106851 | AGCAGCTGTTGCT | + | 6.59 | | Tcf12 | MA0521.1 | chr3:58106837-58106848 | CAGCAGCTGTT | - | 6.32 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_41578 | chr3:58105465-58106508 | LNCaP | | SE_41578 | chr3:58106664-58107602 | LNCaP |
|
| | 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 |
| GH03I058119 | chr3 | 58105663 | 58106970 |
|
Enhancer Sequence | CCTGTGGAAC ACATTTGGCT GTATTTATTT TGCATTAAAG TTGCCCTGCT GTATAAACCT 60
ACTTCTTCGG CCTGCCTTCC AACAGTGCAT CTCGGGAATC ATTCACTCCT ACATCTTTTC 120
CGTCTGTGTT TACTGCTGAG TGGCTCCAGA CTGGATGTAC CTCAGGGCTC ACATTCACCT 180
GGTTTCAGGC TTACTGAGGC AGGGCTGAGT GCATACCCCC AGGACGGGGC CTCCTGTATT 240
CACCTGTGAG GGTTTCTCCA GAGTACCACT AGCAGTGCCA TTAGTGAGCA TCTTCCTTCA 300
CTCGTGACCC AAGTGCACAA GTTGCAAGCA AGGCCAGCTC CCAGTTGCAG AGATCCAAAG 360
TGAGAGCTCA CTGTTGGCTT TTGTGGCTGG AGCAGCCAGC TCTGAGTGTG TAAACGTCCA 420
CTGCCCAACC CTGTCATGTG TCCCCTTGTC ACTCCTTTCC CCAAGACACT GAGAGCTTTG 480
ACTCCAGAAC AGGAAAAGCA GGGTGCCAAT TAGGAAAGCC TCTTTTCCGG TGGGAAGTAG 540
CGATCCGGGA CCTCCTTGCC TGTGGTTCGG CAGTGTCCAT CTTGCCAGGC CCTATGTTCC 600
TTCAGAGTCA AGGTTCTCTG GGTTGTGGCA GGGGCCCTGT GTTCCCAGTG CTTTTGTTTT 660
GGGTAAAGTC CTTTCCCTGT TCTTGTCTAA TCTAACACTT GGGCTTCCTG CAGCCCTGCT 720
TTGCAGAGAC CTTTTGGAAA CCATCACGGT ACAGTCAGTT CTCAGCACTT GCTTCAATCG 780
GCTCGCATTT GGCAGCTCTG TGACTTCTGC TTTCTTGAGG GGGAGGGGTG CCTATAAGAT 840
GGAGTTGGCT GCCAAGAATT AGTAAATAAA ACATTGACTT ATGAGGGTGT TTGGATATCA 900
AGTTAACACC AAAAGTAAGT AAATAAGAGA CGACAGTGTC AGATTACAAC TTTCTGGTCA 960
GCAAAGATTG TGGGGTCAGG TAAATTTCAC TTTGAGTCCC AGCTTGGCAG GCTGCTGCAT 1020
ATGTCACCCT GGACAAGTTA CTTAACCTCT CTGAGCATCA GTTTCCCCAT CTGTGAAAGC 1080
CATTGGTTAA TAATAAATAC CCCATAGGAT TGTGGTGAAA ATTAAGACAA TAACCTATTT 1140
GTGCTTGGCA TATAAAATGC ATTCAGTAAA TGATAGCCGT TATTGCTGTC ATCACTAATT 1200
GATTATTGTG CCGACACTTG TTGTTACTGA GGCTGAGATG CTGATGATAC TTACTCAGCT 1260
TTGCTGCTTG TCCTCTGCAG CAGCTGTTGC TTACAGTGGA GGCTGAGATA AGTCCCCGTG 1320
|
