| Tag | Content |
|---|
EnhancerAtlas ID | HS195-06488 |
Organism | Homo sapiens |
Tissue/cell | VCaP |
Coordinate | chr7:149404150-149405540 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr7:149405034-149405055 | GTTTTGTTTCACTTTTTCTAC | + | 6.54 | | Mecom | MA0029.1 | chr7:149404362-149404376 | AAGAGAAGATAAGA | + | 6.13 | | ZIC1 | MA0696.1 | chr7:149404823-149404837 | TGCCCCCTGCTGTG | + | 6.83 | | ZIC3 | MA0697.1 | chr7:149404823-149404838 | TGCCCCCTGCTGTGT | + | 6.37 | | ZIC4 | MA0751.1 | chr7:149404823-149404838 | TGCCCCCTGCTGTGT | + | 6.41 |
|
| | 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 |
| GH07I149707 | chr7 | 149404492 | 149404692 |
|
Enhancer Sequence | AGGACTGGCT CCAGGGGTCC AGTTCATGCA CGAGTTCAAA TCTTGGAGTT CCCCATTAGC 60
TTTTCCTTGC AGAAAGTGCT TCCCATGTAG CACATTCCTG CTCTTCTAAG TCCATATTCT 120
AGCCCCCTCC ATGGTCTTGG ATGTATATAA ATCTATTCAT ATGGCTCTGT CTATAAAGTC 180
TTTACCATTT TGAGCCAATA GAAGACAAGG ACAAGAGAAG ATAAGAGAGT CTCTTTTAGT 240
AACAGGGTCC TGAACCCAAA GTCAGAAAGA GTAGACTGAA TCTGTCAATA AGGAGTGTGT 300
GTGCCTGGGA AGAACATTAA TGTTGAATCT CTGTTGTCAA ACGTGCACTA CGAAGGGCAC 360
AGATGAGTGA CTCTGAAGGC CCTTCCAGCT ATAAATGCCG GTGTCAGTCC TCTTCCTGAA 420
AGTACAAGGA AGCTGCTACA GGAAGAGGAA CTGTCACTTG TTTTGCATCA GGGAGATAAA 480
ATTGCAGTTA GGGAGGTTTG GCAGCTTTGA GGAGGCCCAG CTGGAATGAG CATCTGTGGT 540
AAAATTTTAT AGGAATGTTG GGCATGACTG CACAGTTAAA AGGTCTTGCT TAGGCTTACA 600
CTTCCATCAG GGGGTATAGC TCAGGGGTAG AGCATTTGAC TGCAGATCAA GAGGTCCCTG 660
GTTCAAATCC AGGTGCCCCC TGCTGTGTTC TTATTTTTAC CCTCTGGAGC TGGTGTTGAA 720
GATTCAGCAC CCTTCTCCAA TCCTAAATCT CAGGATACTG AGCCTCCCTA AATCTGTGAA 780
AAAGCCAGTA GCAACTTTAA ACCCTGTCAC TGTCTCAGAC TGATAAATTC CTTCAACTTG 840
GACTTTTTAT TTCACTTACC AAAGGCTTTG TTCTACCTTG CCTGGTTTTG TTTCACTTTT 900
TCTACACGTT TTCATGACCC CAAGTCAGTG AAGTGCAGGT AAATGTTTAA CGACCAGCTC 960
TGAAGGGGGT GATTTGTAGT GTTTTCCAGT TTCACAGAGT GAAAAATAAT CCCACCATGG 1020
CAAATTTCAA GCTACAAATA TGAGATGATG AACATGGAGT TGGGAAGGTG TGCTAACAAA 1080
TGGCTGTCTG CTGCAAGCTA GCTCAAGCAT AACACTGCCC CAATCCACCT TCCCGACAGA 1140
GGCCTGGGCT CTCTGGCCGT GCTCTATCTT CGCGATGCCT ACTGACATGA GGGCAGTGGT 1200
TCTCACTCAC CCATTCATCC ATGGAATCAT TCATTCATTC GTCATCTGAT TCCTTCTCAA 1260
TGCCAGACAC AGGAAAGACA GAGATAAGCA AGAACTGTCT GTGGTAAGCA AAATAGTCCG 1320
ATGAAGAAAT GATCCAAACA ACGACAAGGA CAGCTGAACA AAAAAAAGAA GGGGCGCTAT 1380
TTTTAAATGA 1390
|
