| Tag | Content |
|---|
EnhancerAtlas ID | HS120-00242 |
Organism | Homo sapiens |
Tissue/cell | LNCaP-abl |
Coordinate | chr1:48024130-48025760 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr1:48025232-48025244 | GTTTGTTTGTTT | + | 6.32 | | Gata1 | MA0035.3 | chr1:48025627-48025638 | ACAGATAAGGA | - | 6.14 | | USF1 | MA0093.2 | chr1:48024732-48024743 | GCCACGTGACC | + | 6.62 | | USF2 | MA0526.2 | chr1:48024730-48024746 | TTGCCACGTGACCAGC | - | 6.52 |
|
| | 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 |
| GH01I047558 | chr1 | 48023941 | 48026628 |
|
Enhancer Sequence | GAAGCCTGAA TTTCAGTAAC GCACAATCTC AGCTTACAGT CCACCCTGGT GCTAAGCCCT 60
CTTGCCCAGG AATGCCAAAT GGGCATTACT CATTACCCCA GAGGCCAGTG GGTCCTGGGG 120
TACCCTGGAC CTATAGGCAA CCTTCAGGGC TGGCTTACTG GACAGGGGGC AGGTGACTTC 180
CTGAGATCTG CTCAATCCTT GCCACTGAAA TCCCTCTTGG CACCTGTACC TGGGCAGCAG 240
ATCTGAACCC ATTATTGACC ACAATTGACA CCCTCCCTTC ATTCAAGGGA AGAAAGTCAT 300
GTTGACTCAC CTCCTTACGT TAGGCACAGA CCATTTTATT GAACGTTAAC GCAAATCACA 360
CGGGCAGGAA ATGTCGTAAA GAGAAAAGTA ATCTTCTGAC GGAAAAATAA ATTATCAGCC 420
GTGTTCCGAA GGAAAAGAAA CATTCTTAAA TAATTTCTCT TGCTGTTGGT ATTGGCTGGC 480
AGTGTGGGCC AGCCAAGCAA ATGGTAATTT CCAAATTAGA TTATACATTA TGTCATATTA 540
GTTTTATATT AGAAAAACAA ACGGGATCAG AGGAGAAGTG CCAAGGTTGG CGAGCTGTGC 600
TTGCCACGTG ACCAGCCGTG TTTCCACTGC AGAATGTTTA ATGATTCCGG GAGAGGTGGA 660
AGAGCAAACA TTCAGACCGA CGCGGGGGAG AGTTGAGGTT GGTTGCACAG AGGTAGGCTC 720
TTCCAGGAGG GAAAGGACAG CTCCCAGGCT GGGCCCCTCT GAGTATGGGT ACGCAACCAG 780
GCTGGGGAGG CAGGGAGCAC CCCCACAACA GTCTCGTTTT CTTTTCTCCA GGTATTTGGA 840
CCTTCCCTTG GAAAAGCTGG TCTGGGGCAT GGGCTTTGGA GTCAGGGCAC CATGGCCAGT 900
CCATGTTCAC AGGAGCAGCA GGTGGAGGTG CCCCATGTCA GTCCCAGAAG TCTGAGTGGG 960
GCTATGTTGG TGGCCTACTT CCCTAGAGAG CTGCCCTTGG GCAGTGGGGG CAGATATCTG 1020
TCTCCCTAGT GTGCAGGGCC AGGGGAATGA TAAGGAGGAG ACTTTAAATG AGACTCATAT 1080
TGCTAGCTCA TGGTTTTTTT TTGTTTGTTT GTTTTTTGTT TTTTTTTTTT TTTTTTTTTT 1140
TTTGAGACAG AGTCTTGTTC TGTTGCCCAG GCTAGAGTGC AGTGGCATGA TCTTGGCTCA 1200
TTGCAGCCTC CACCTCCCAG GTTCAGGTGA TTCGTGTGCC TCAGCTAGGA TTACAGGTAT 1260
GCGCTACCAC ACCAGCTAAT TGTTGTATTT TTAGTACAGA TGGGGTTTCA CCATGTTGGC 1320
CAGGCTGGTT TTGAACTCCT GGCCTCAAGT GACTTGCCTA CCTGGTTCTC CCAAAGTGCT 1380
GGGATTACAG GCGTGAGCCA CCACACCCAT CCAGCCAGCT CATCTTTGGT GAAGACTACT 1440
CCATGCCAGG CGATTTACCT GTACTTACTC CTCACGGCAA TTCCACCAGA CCATGTTACA 1500
GATAAGGAAA TGGAGAGACA GAGAGGGCAA ATAACTTGTC TGAGATCACA TTATTGAGAA 1560
CTGGCAGAGC CTGTGCATAA ACCAAAGCTC CAAGGCTGAA ATCTGCACCA CCACAGCAAA 1620
TGCCTGTGAG 1630
|
