Tag | Content |
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EnhancerAtlas ID | HS136-11140 |
Organism | Homo sapiens |
Tissue/cell | Monocyte |
Coordinate | chr2:152778370-152780780 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL2 | MA0478.1 | chr2:152778566-152778577 | CTGAGTCATCC | - | 6.32 | JUNB | MA0490.1 | chr2:152778566-152778577 | CTGAGTCATCC | - | 6.14 | SCRT1 | MA0743.1 | chr2:152779589-152779604 | AGGCAACAGGTGGAA | + | 6.09 | ZNF263 | MA0528.1 | chr2:152778598-152778619 | TCTCTCTCTTCTGCCTCCCTC | - | 6.2 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I151922 | chr2 | 152779338 | 152780439 |
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Enhancer Sequence | AAGATGTGCC TGCCTCCCCT TCCCCTTCGC CTTCCGCCAT GATTCTAAGT TTCCTGAGGC 60 CTCCCAGCCA TGCTTCCTGT ACAGCCTTCA GAACTGTGAG TCAAACCTCT TTTCTTCATA 120 AACTACCCAG TCTCAGGTAG TTCTTTATAG CAGTGTGAGA ATGGACTAAT ACAATATTCA 180 AAAAAGTAAT GTCAGACTGA GTCATCCTCA CAATGCCATC TCTCTTGTTC TCTCTCTTCT 240 GCCTCCCTCT TCCACTCACA AGAACCCAAG TGATTACATA AGACTCACTG GGATAATCCT 300 GTACAATCTC CCCATCTCAA GGTCAACTGA TAAGTAAATT TACCTTTTTA TTTATTTTAT 360 TTTTGAGATG GGGGTCTCCC TCTATTGCCT AGGTTAGAGT CAATGACATG ATCATAGCTC 420 ATTGCAGCCT CATCCTCCTG GGCTCAAGGG ATCTTCTCAC CTCTGCATCC TAAGTAACTG 480 GGACTATAGG CGTGTGCTGC CTTGGCTGGC TAATTTTATA ATTTTTTGTA GGGATGGAGT 540 CTTGCTGTGT TGCCCAGGCT GGTCTTGAAC TCCTGGCCTC AAGCAATCCT GCTGGCTCCA 600 CCTCCCAAAG TGCTGGGATT AAAAGCGTGA ACTATGATAC CCAGTTAATA AGCAACTTTA 660 ACTCCCATTT CTCATGAAAC CCAACATATT CACAGATTCC AGGGATTAGT ATGTGGACAT 720 CTTTGGGCAG CCATTGTTCT GCCCAGCATG AGGAGTTTAG ATGAAATTTG CCCTGTGTGA 780 GGCAGGGGCT TATATGATTC ATGACATTTC CAGTATCAGA TCTTTGGCAT GTATAGTCTG 840 AAGTTTTCTG ACAATCAGAA CTTTCCAAAA GATATTTACC AAGACAGTTG CAGTTTGTGG 900 ACTCCAGCAG CTGGTAAAAC TCACAAATCC TGTTTTCATT CTAATATTTT TTAGACCTTT 960 TGAATTTTGC AAGTCAGTTT CATAAAACAT TGAGTTGATT CCTAAAAGAT CAAATGTAGT 1020 CAATACTGAG CGTTTGTTGA TTTTGCCTAC TGCAAAAGAA CCTCAAGTTG GAATCTCTCT 1080 ACATTCATAT TTGTGAGTCT ATGAGGATTG CCAGCTTGTC TTAAGGAACT GTGCTCACTC 1140 CCTGCCCAGT TGTGCAATAC CCAGAACTCT GAAGAAACAG CAAGGCTGGG CTCATTGCGG 1200 ACTTGTCTGA ATGGGTGTGA GGCAACAGGT GGAACCATGG TGAAATGGAG AGCACATGAA 1260 AGTATTTCAG GTAAGCATTA TTTTAAGAAA TAATAACAAC TATGCTCAAC CAAACAAAAG 1320 CAACTGCAAG TCAGAGTTAG CCTCCAGACT ATGTGGTGGC TCCTCCTCCT AGCTATTGCT 1380 TCTATTCTGA AACTGGGTCC AACACCTAAA CTCCAGAGGA CTCCACTACT TTGCTTTTAG 1440 ACCTCACCTC ATTTGCCCTC TCAGTTGCAT AGGGCAGGGT GTCCTTAAAG ACTCTGCCAT 1500 CCCATCTTGG TCTTTATTTA TGTGCTGGAT CTCTCACCTG CTAGCTTGGC TTTCAACACA 1560 TTGCTGTCTA GACTTGAACT TCCATGCTTT GCTCCCCAGT CTTGGCAGCA GGCCCATGAC 1620 CCCGTGTAGC CCCTTGCTGA GCACATGACT TGCTGTTATA GAAACTAGGT GCAGGGAGCT 1680 GGAGGAAGCC TGGGTGGAGG CCCGGATGGC ATCTAGCTGA CATTCCATTC TTCAAGTACA 1740 AAATATCAGT CTTGGCCAGA TAATTTCAGA CTGGCCTACA GAATTCTAAT GGGAAACGTT 1800 TTTGCTAAGC ATCAGCCAAT AAAAGCTCAT TTACAAAATG CAAGAAGAAC CATAAGACTA 1860 AGGAAACTTG GATTCTATTC CTAACCCTCT TGCAGATTGG CTGGGTAACC CTAGGAAAGT 1920 TCCTCACCTC TAAAAATTGA TCTGTTTCCT CACGACTAAA ATGTGGAAGA CTGGGAAATT 1980 GTTTCCTGAT TTCATGGACC CAACACTAAG TAAAGTAAAA TTAAAGCAAG GTAATACTTT 2040 CACATACTCA GGCAGTATAA TTCGGTAATT TCTAGTAATT CTCCATGAGT TTCCATCTCA 2100 TCTCCATTCA GAGGGACTGG TTTTTTAATG TGACTCTATG ATACATTATA TACCTACATA 2160 GATACATGCA TTTATACATG CATACATACA TACGTGCGTG TAATCTATTC TGAAATCTTT 2220 TTTTTTTTTT TTTTTTTTTT GAGACAGAGT CTCGCTCTGT CGCCCAGGCT GGAGTGCAGT 2280 GGCGCAATCT CGGCTCACTG CTAGCTCCAC CTCCCGGGTT CATGCCATTC TCCTGCCTCA 2340 ACCTCCCGAG TAGCTGGGAC TACAGGCGCC CACTACCACT CCCGGCTAAT TATTTGTATT 2400 TTTAGTAGAG 2410
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