| Tag | Content |
|---|
EnhancerAtlas ID | HS195-00238 |
Organism | Homo sapiens |
Tissue/cell | VCaP |
Coordinate | chr1:46504790-46505810 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Zfx | MA0146.2 | chr1:46504933-46504947 | CCCGCCTCGGCCTC | + | 6.01 |
|
| | 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 |
| GH01I046039 | chr1 | 46504935 | 46505626 |
|
Enhancer Sequence | GCAATTCTCA TGCCTCAGCC TCCCGAGTAG CTGGGATTAC AGGTGCATGC TACCACGCCC 60
AGCTAATTTT TGTACTTTTA GTAGAGACGG GGTTTCACCA CGTTGGCCAG GCTGTTCTCG 120
AACTCCTGAC CTCAGGTGAT CCACCCGCCT CGGCCTCCCA AAGTGCTGGG ATTACAGGCA 180
TGAGCCACCA CGCCCAGCCC CAAGTAAACA AGTTTGAAGT GTCGGTGAGA TACCCAGGAG 240
CCCAGTGGAA ACATCCAGCC AGCGGGTAGA GTTCAGAAGA AAGAACTGGG AAGGAGCTAG 300
GAATTTGAGC ATCCTAAACA CAGAAGTGCG AACAACTCTG GGATTAGGAG AAATCCATAG 360
TTCCTGGCAG TGGTCTTGGG ATGCTGTGTA GCTAAAGTGT AGTGGGGAGA AAAGACATAG 420
GCAAGGTCAC TTAGAACAAC AGGCTGTTCC CTGCCCAATC TGACTTATTT ATAATTGAGT 480
ACACATGGGT GGGGCCTGAG ACATGGATGA GCGCTGCAAT ATCCTATGCA ACAAGAGGTT 540
ATCGCATGTT GGCTCATTAC GTTCCCAGAA TACAGGAAGC TCAACAGTGT GCCTTGGCAG 600
GAGATGACAA GGGCCTGGGG CAATAAGAGG ATAGATTATA AAGCTGGGCC CATTTCCCCC 660
TCCCCCAGAG TAGAATGTGG AAACACTTCA TTCTGGGCAG AAATATGAGA ACCAATAAAC 720
AGCTTATTAG GAGTGGGCAG TGAGGTGTGG AGGAAATGGC ATTCAGTTTT AATTTTCTCA 780
GAGTCAGTAT CTAAGACTTC TGTGTCTGTG TTCGGTGGAC AGGACTCTGG CATCATGCCT 840
AGTTGGAGTC AATGTCCTCC CCTAGGAAGA AAAGAGCCTC TGGCTGCCCC AGTACTAGTC 900
TTTTGGTGCT TACTGGAGAG AAGGTTTGGA AGTTTCAAGG GCTGTTCAAC ACCTGAGTAC 960
TCTTCTCTCT TGACCCCCAC TCTGCCCCCA GCCCACCCCT TCATAGCATG AAGACAAAAA 1020
|
