Tag | Content |
---|
EnhancerAtlas ID | HS105-48978 | Organism | Homo sapiens | Tissue/cell | IMR90 | Coordinate | chr20:3173100-3174600 | SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Zfx | MA0146.2 | chr20:3174260-3174274 | CCCGCCTCGGCCTC | + | 6.01 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GGCCCACTCC TGCCTTGCCT TCGCTGGCCG CCCCACTGGC CTGGTCCCCC ACAACCTGAC 60 ACACCCACAC TTTTTATCCA TCCTCTTTAT ACCATCTGAG GCACTGAGCC CACCCTTGAA 120 ATCACTGTCA CTAATACCGC TGAGTGCTTT CCAGCACAGC CACGTTCTGT GCTCCAAGTG 180 CTTCTTCATA CCCTCAGTAG AAACCTGAGT TCCCAAGGGC GCAGCGAAGG GTCCACCGCT 240 GTGTCCACAC AGGCACCTGC CCCCACTACC CCAACACACA GCACAGGACT TGAGAAAAGG 300 CAGTTCTTTT GCATTTCTGT GAATCCTCCA CCGCAAATGA GCTGGGGGAG GACTGACATG 360 GTGACACCTC CCTGACTGCA GATAGCATGT GACTTGTTTG AAATGCCAAA GCCGTATGTA 420 CAAGCAAGAA GGCAAGCGAG AGGCAGCTGG GTCAGGATGG GCAAGGACAA AGTGACGTGG 480 TCAGCTGGTC TCTACCTACA AAACAGGGAT CAGGCAGCGG GCTCTCAGTG ACAGTGTGGT 540 GCGAGAACAT GAAGTCACCC CAGGTGCTCC CTGATGACCT GGCCTGAGGT GCTGCTGGGG 600 CCAAAACACG TTTGATAAAA CAAGCTAGGT GTGGTGGCAC CCACCTGCAA TCTCAGCTAC 660 TCAGGAGGCA GAGGCAGGAA GATCGCCTGA GCCCAGCCAT GGTCAGACAG GAGAATGGAA 720 CAAGATCGAG TGAACCCTAC ACCTCTCATA AACGATGCTG GGTGCAGGCA TGTTCCTCCA 780 GTTCTGAAAT CTTAAGGCAA AAAAGGTCTA TCCCCTTGGA GCAAGGAGGA AAGCAGACAG 840 ACTGAATTTC AGAAGTCCTC CTTTTCCTTG CAAGACAGCA GCTCTAGAAG AATTAGCCAG 900 CACAGGCTGG AAAAACTTTT TTTCTTTTTT TTTTGAGACA GAGTCTCACT CTGTCGCCCA 960 GGCTGGAGTG CAGTGGCACC ATCTTGCCTC ACTGCAACCT CCACCTCCTG GGTTCAAGTG 1020 ATTCTCCTGC CTCAGCCTCC TGAGTAGCTG GGACTACAGG TGTGCACCAC CATGCCTGGC 1080 TAATTTTTGT ATTTTTAGCA GAGATGGGGT TTCAGCATGT TGCCCAGGCT AGTCTCAAAC 1140 TCCTGACCTC AAGTGATCTG CCCGCCTCGG CCTCTCAAAG TGCTGGGATT GCAGGCGTGA 1200 GCCACCATGC CCGGACAAGC TGGAAAAACT TCTAAGCTCC AAAAGAGTTT GGAGAACTCC 1260 CAGAGAATAG TTACCTCCAG GGAGCCACCA AAAGTGAGGG CTAGAACTGG GGACCTTTCT 1320 TCTGGTTTCT GCAGAGTAAA GGGGGATGTT GAAGCTGACC CCCTCCTCTA ATTCCACCTG 1380 GGAAGGCTTC CTGGGGAGGG GCTTCAGGAC CATCTTACTG CCTACTGGGT AGGTGGGGAC 1440 AAGTTCCAAA CAGCAGCAGG CAAGTGTGAG AAATAACCTG CCCGGCCACA GCCCCTAATC 1500
|
| |
|
|
|