| Tag | Content |
|---|
EnhancerAtlas ID | HS195-05419 | Organism | Homo sapiens | Tissue/cell | VCaP | Coordinate | chr5:1227220-1228670 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| POU2F2 | MA0507.1 | chr5:1227700-1227713 | AACATTTGCATAT | + | 6.21 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr5 | 1227409 | 1227924 | | chr5 | 1228000 | 1228400 |
| Enhancer Sequence | TTGCCCGCCG ACGCCTTGCC CGTCGATGCC TTGCCCGCCG ATGACTTGCC CGCCGATGCC 60
TTGCCCGCCG ATGCCTTGCC CACCGAAACC CAGTTACCAT TGCTAAGCGC CTGCAGTGTA 120
CTGGAAGTGT CTGGCACTAG CCTCCCTTAA ACTCAGCTGC TCCACGCTGG GGCAAAGCTG 180
GGGAGGCCCC CACCTGGGGT GCTGCTGAGG AGGGAGAACA GCCCTGCCCG CCAGCTGCGC 240
GGGGACTTCA GGGCTGCTCC ACTCATGAAC GACTCTACCA TCAATCTCCT GATGCAAGCC 300
ACCGGGTTGC ATGTCATGAA ACATCCAAGT TTATTTAACT CACACACTTC CTAAGGGCCG 360
TGCCATCAGC ATTCTCACCC TGTGTGTGAA CATGCCCTTC ACTTTGTCTC GCTGTGAGGA 420
TCACTCATTG ATGATTTTGA AAACAAGATA TAATTAAGAA GCAGGTACTG TGTAGCTTTT 480
AACATTTGCA TATACTCATG ACTACCAAAG GCGAATATTA TTTGCTCTCC CATTCATAAG 540
TATTCAACTA CATAAATGTT CTCTTCAAAG CTAAGACTTG TAAAGCAACA TTGTAACAGA 600
ATGTAGCAAA ACGTTGCGGT AAAGATTTAC AGTGATTTTC TCACACCTAT GACATTTCAT 660
GGCAGCTGCT TTATTACACA TTCAGCGTCT TTAAATCAAA GGAACGTAGA CTCGTAAATG 720
CCAAGCGATG GGTTCAGGCC AGCTGCCCGG GACACTCTAA CACTTGCTGT GGTTTAAGGT 780
TTCAACCCAG GAAGCTTTTA TGACTAAGCT GGTGGCCCTG GGCTGGCTGT GTCCACACAC 840
GTGAGGTCAC TCATCAAGCG CGCCCCCTCC CCGCTACTTC CTGCCTCCGG TGTTCAACCG 900
ACTTCTGTAT CTGGTAGGTG CTGTTGAGAT CTGTGGATTC TTGCACCAAA AACGACACTG 960
TATTAATTAC TATGGCTTCT TCGTTAGTCT CGACGCCTAG TAGTAGAGCA AGGCCTTTTT 1020
TTTTTATTCT TTGAACTTTT GCCAGCTGCT ACTTTTCCTC TGAGCTTTAC ACCAGGTTGT 1080
CAATTTCCAG AAGAGATTCT TCGGCGCTCC CTTGGCCCTG TGCTGCTTTC TACACTGCCC 1140
GGGGGGAGTT TCCACCTTGA CGGCCTTCAC GCCTTGGAGG CAGTGCCCAG GCAGTGGGGG 1200
CTGGCACTGG AGCACCATCT GCCGTCTGCA CCCTCGCGGC TCCCGGCTCG GTCTCCTTTC 1260
TGCCTTCCTG CGGGTCTCTC CATCATGACC CTGGGCGTGT CTCTGGTTGA TTCTCAGCAA 1320
TCCCTGGCTT TTGCCGCTGC TCTGAGCAGA GCCTGCTTCT CCTCTGCATT TGCTCAGTGG 1380
CTGCACTGCG GCCTCTGCAT CTCTCAGCCT CGTGTGGTGG GGTGCAGGTT TCTCTCGATC 1440
CTGCGTGGAT 1450
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