| Tag | Content |
|---|
EnhancerAtlas ID | HS161-04121 |
Organism | Homo sapiens |
Tissue/cell | PC3 |
Coordinate | chr12:122203480-122204610 |
Target genes | | Number: 13 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr12:122203598-122203616 | GGGAGGGAGCAAGGCAGG | + | 6.33 | | FOS | MA0476.1 | chr12:122203642-122203653 | TGTGACTCATC | + | 6.14 | | JUND | MA0491.1 | chr12:122203642-122203653 | TGTGACTCATC | + | 6.14 | | NFYA | MA0060.3 | chr12:122204468-122204479 | TCTGATTGGCC | - | 6.02 | | NFYB | MA0502.1 | chr12:122204542-122204557 | CTGATTGGTTGGCTG | - | 6.02 | | RELA | MA0107.1 | chr12:122204290-122204300 | GGGAATTTCC | + | 6.02 | | ZNF263 | MA0528.1 | chr12:122203682-122203703 | CCCTCCTCCAGCTCCTCCTCA | - | 7.05 |
|
| | 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 |
| GH12I121765 | chr12 | 122203081 | 122206677 |
|
Enhancer Sequence | CTGGGCCCAA ATAGATGCAT TATCTTCTAT TTAGGTTAGT CTAAAAGTAT TTGTGTTTTG 60
CAGTCATTTT TTGCACCAAC CTAATAGAAG GACTACAGGA GCTGGGGCCA GCTTGTCGGG 120
GAGGGAGCAA GGCAGGTGGG CTAAATCCGA GTGACTCATA CTTGTGACTC ATCTTCCACA 180
TCTGTTGGAG ATTTAGCCTC CGCCCTCCTC CAGCTCCTCC TCAGGGCTGA TTGATCCTGG 240
GGGCAGGCAA GGGAGATGCC TTGGAGGCCT CCCCTCCTGC TTGGTTCTTT ACCAGGGAGT 300
AGCTCAGAAG CCCTTGCAGG AGAGCCTGTG TGGAGGCGGT GGGAGGTGAG ACTGGGATGA 360
ACTCTAGTTT CTCATCCCTG AAGCATCCAC TCACTCGGGG CTGGTGCGCG CCGTCAACAC 420
CCCACAGTCT TTGCCGAAGT GACCCAAACC CAAGTTCTGC GTGAGGAAGG GTCCTGGGGC 480
CATCACGGCA TTCTAGAGAC GGCGTCGCTG AACCCTACGG GCCTCCTGGG GGCCTGCTGC 540
CCTGTTTTGT CTGATGGAGG CGCTTTTGTC CAGTTCTGGC TGCACCTGAG ATTTGAATTG 600
GGACAGGAGG TGTGGTCAGG GGAGCAGGTA GGGGTGGGGA CTTCCTCATC GAGATATGAA 660
GCCACCCTCG GTTTGTGTCT GGTGCCTGCC AAGTGAGATG CCACTCATCA GCTCAGCATA 720
ATAAGCAAGT CAGCTCTTGT AAACTTGAAA ATGATGGAAA ACCATCCCAT AGGGACTAAA 780
CCTGAAGGGG TCTTATGGGC CCATGTAACT GGGAATTTCC ATTCAAGGAG GTCAGGAGGG 840
CTCAGGAGGT GTTCATGGCC CGGCTCCAGC TCCCTGTTCT GTTTTCCCCT GCGATGGCCC 900
CCAGCGGCCC CCAGGCAGGC CTCCCACCAG CAGTAACCCC TGGGCTGACA GACCTCCCTC 960
CACCCCAGTT GGAATCTTGA CACAGACTTC TGATTGGCCA GGCTTGGGTG ACCTACTGAT 1020
CTCTGAGAGC CAGTCACTGT TGCCAGAGGA CTGCAGAGGG TCCTGATTGG TTGGCTGGGG 1080
GTCATGTGCT TGGGTATAAG ACTGTGGTCT ATCCCAGCCA CCCAGACTGA 1130
|
