| Tag | Content |
|---|
EnhancerAtlas ID | HS121-27182 |
Organism | Homo sapiens |
Tissue/cell | LNCaP |
Coordinate | chr3:52861210-52863130 |
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 | chr3:52862932-52862950 | GGATGGAGGGAAGGACGG | + | 6.77 | | Gfi1b | MA0483.1 | chr3:52862512-52862523 | AAATCACAGCT | + | 6.14 | | POU4F2 | MA0683.1 | chr3:52861346-52861362 | GCCATTTATTATGCAC | - | 6.27 | | STAT3 | MA0144.2 | chr3:52862484-52862495 | TTTCTGGGAAG | + | 6.02 | | ZEB1 | MA0103.3 | chr3:52861551-52861562 | CCCACCTGCCC | + | 6.14 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr3 | 52861523 | 52861815 | | chr3 | 52861600 | 52861905 | | chr3 | 52861903 | 52862098 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH03I052827 | chr3 | 52861961 | 52862090 |
|
Enhancer Sequence | ATCCTGGGGG CAGAAGGGTG GGAGTTGTTG AGAGCCTGGT GGCAGGGGCC CATTCCACTC 60
CTGCCTCCTC CAGAGAGCCT TTCTGGACTC GGTGTGCCTC TTGACACAGT GACTCCCATC 120
TTTGCCTGAG CCCAGTGCCA TTTATTATGC ACCTACCGCA TACAGGACCC TGTGCAGGGC 180
ACTCTGCAAA GTGCTCCAGG CCTCTAGCTC CCGGAGGTGT GTACAGTAAC AGTAAGCATT 240
CATTTTATAG AAGGGACGAA GGGGAGGCTG CAGAGGGGCA GGGCCGGGCT AAATCCTGCC 300
TTCTCTCCAC CTGTCCAGTC TGGCCGAAGC TGGCCCACAT TCCCACCTGC CCCTTCCATT 360
TCACGGACTG TTCCAGGGGA ACTAGTTCAT CACCAGCAAG AGCTCTCTGA GTCACACTTG 420
TTCCCAGCCC TGCGTGCAGC CGTGTGGGGC CAGGACTGAG GAGGAAGCAG ACGTAGGGCT 480
GGAGGCTCTG AGCACTTTCC CCCTACAGCA GTCTCCCCGC TCCCTCCCAC AAGAGGCAGG 540
CACCCTATAG GGAGGCTGGC ATATCTGGAA GGAGGTTTTG GACAACTGGT GGACGGGACT 600
CCTGGGTGTG TGGACACACT CCTAGCAGCC ATCCTTTGGG GGCTGAGAAA GAATGGCCCA 660
GGCCATTTCT CAGGGAGGAA AACGACTTTT TCAGAGCCTC CTTGTGGGGT GTGTAGGGAT 720
GTGCCTGGTC AACTTCATGT GGTAGTGTGT GGCAGTGGGC AGGAGGGGGA GCAGCCAGGA 780
TGTCAGGACT ACGCGTCCCT CCTGCCTGAC CTTCCTGGTT ATAATTTAAC TCTAGCCCGG 840
GATGGGGCTG GTGAGTGGGC AGTGGCACTC CTCCCCCTGG GTAGGCAGTG CTTCATCTCT 900
CCAGATGGCC AGCTGGGGCT CCTGGCCAGG TCAGGGAGCA GGGAACCTGC TCTCTGCTCC 960
CCTAACTCAT GCAGCAACAG GTTCTGGGTC TAGAGAAGGC AAGTGACAGT CTTGGGCTCT 1020
CAGCAGATGC CACGGGCCTG GACCTGGCAA CTGCTGACCC TGGCACCCAT GTCGAAGGCT 1080
GACACAGCCC GTGGGGCTTG CACTGCAAGC TGGGCAGCAT AGGCCCGGGC TCTGGGTTAG 1140
GAAAAGTAGA GGCTGCGGTG GAGTGGGGGA TGCTTGGCGC CTGAGGGAGG AGACTAGCCC 1200
CCACTGCAGT TTTCCAGAGG CCACAGTGTG GGACCCCACA TGAGACACTC CCTCTCTGCC 1260
CCACCATCGC CCTGTTTCTG GGAAGAGTCT TGCCCTTGTC CTAAATCACA GCTTTTCCTG 1320
GCAGCAAGGG ACAGGCGGCA TCCTGGTGCA TTTAGTAAAC ATTGGAAACT GAGTTGGGAA 1380
GGGTAGGGGA GGGTGGCAGA GGACAAAGTG AGGACCATCC TTGGCTCATA GAATTCAGAG 1440
AAACCTCAGG CATCTCTCAC GCAGCCTGAG CAAAAATGTC CTCTGCAGGA TCCCAGCTGG 1500
GGCAGACCTA GGAGAATCCT CCTCAAGCCA CTCTCCACTG TGAGGAAGCC AAGGGTCTAG 1560
AAGGTTTTCT GTACTTTGAG CTGGAATGTG CATTTTGGTG ACTCCCTCTT GCCTGGTCTG 1620
GCCTCAGGAG GCCTCAAGTC TGTGCTCCTC AAAGGCAAAG TCACAAAGAT TCTGTGGTTC 1680
TCTGCCTAAC ACCTGGACAG CACTTAGGGA TGATGAATGG CTGGATGGAG GGAAGGACGG 1740
GGGCATCTTT GAGAATAAGT CCTTTGGCAA GCCCCTGTTC CTGTGTGGCC CCAGGTGCAG 1800
GGTGTACTCC TGAAGATGTA CACCCTGGCA TGCCTTACTT CAAGAAGAGG GTTTGCTGGC 1860
ACAGAGCGAT GGAGTCATAG CACTGGGGGG TGTGGAGAGG GGAGGAGGGT GGGAAGGCAC 1920
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