Tag | Content |
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EnhancerAtlas ID | HS182-17630 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr5:73678400-73680600 |
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) |
EWSR1-FLI1 | MA0149.1 | chr5:73680071-73680089 | GGAAGGAAGACTGGAAAG | + | 6.27 | RAX | MA0718.1 | chr5:73678716-73678726 | GCCAATTAAC | + | 6.02 | ZNF263 | MA0528.1 | chr5:73679806-73679827 | TGAGGAGGAGAAGGAGGGTGC | + | 6.08 | ZNF263 | MA0528.1 | chr5:73679800-73679821 | GGTGGATGAGGAGGAGAAGGA | + | 7.36 | ZNF263 | MA0528.1 | chr5:73679803-73679824 | GGATGAGGAGGAGAAGGAGGG | + | 8.5 |
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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 |
GH05I074381 | chr5 | 73677747 | 73680010 |
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Enhancer Sequence | CCAGGACATT TTAAGCCAGA AAGCAGATGG AATAAGAGCA ATATAAATTA CTGTAACTGT 60 ATTTTGCCAA TTGCAAAGTG ACTCTAATGC CAAACAGAAC TTCTTCTCCC CAACTTGTTG 120 ACTGCATACG TATTTGTTTT TAATTTACAC TTGGTAGAGT TTGGTGAGAT GTTTGGAGTT 180 CGAATGATAG AATCTACAGG TCTAGGGAAC ACCAAATCTA GCCAAACCAC CCACAGAGTA 240 TCCAATTAAG GAAACAAGCA CATAATGTAC AAAAAGGTAT TTTCAGTGAA AAATAATATT 300 CATGCATGTT ATATAAGCCA ATTAACAAAA ACTGTGCCTG TAGCAATTTT TAAGGAATGT 360 CTTACAAATA GGAAGTACGT TAAATACTGA ACAGAAGGAC AAAACTTCAT CAGCAGTCCT 420 TCCTGGCCTT GGTGCTCTCA ACATGATCTC CAGCCTGTCT CTTAGATGTC TTGGCAGCTT 480 CCCAAAGGAA GAGTCTTGGC CTCTGGTCGT CAGACTCAGA GAATCCTGAC TTTAATCCTG 540 ACTCAATTCA CTCTAGACCA TCAATTCAGG GCTCAGTAAG ATTTGTCCAA ATTACCCTGA 600 CTGGAGTCAA ATAACGCAGT CCTGTGAGAA TCTAACCAGC TAATTTTTGA AAGAGGAGGG 660 AGAGGTTGAC ACAGATTTTT CACTGCAGTG CAAATTGTAG TAAAGGGACA ATCTGATGAC 720 TTCTTGGTGA ATCTGTCTCT GCTTCATATT CCAGTAAGGT GCTCGGGCCT TGAGCCATTT 780 CCTTGGGCTA GGTTTGAGCT AGGATGTGAT TTCATCAACA GGCTATTTTT AACCAAGGCA 840 GCCTAGAAAC CAGCCTCAGG GGACTCGTGC TGAGATAAAT TCACACAAAT CACTCCCCAG 900 CCCACTGACC AGCAAGACTC CTGCTTGGAC AAGAAATCTT GCTCCATAGC CTAAATTATG 960 ACAGCCTTGA ATTTTCAAAG CCCAAATTTT CAATGACAAG CCACTTTAGA GTCTGAATGA 1020 TAAGAATGGA ATGAAGATTT CCCCTGCATC TGCAGTCTCT CCTCCCAACC ACATAAATAC 1080 AGGGTAGCAC AGAACTGCAT ATTCATGATA AAACAAACAG GCACTACAAG GTGTTTGCTG 1140 CATTCTTACA TTTTTTTTAA TAGGCAAGAC CTCTTTACTC TTTTACCTCT GCCCCAAACA 1200 CATCTTCATA CCCCCTTGCC CAGTTTCAAA TCTCATGCAC TGCCACTATC GGGTAGAAAG 1260 ACTCAGGAAT CAGCATCTGG AAATACATTA ATTTTGCATG AAAATGGAGG ATGATAGCAG 1320 AAATTACAAA GAGACTACAC ACTAGAAGCA TCTGTTCATT ACAGCATTTT AACGTGCAAT 1380 TATGGAACAG CATGAAGCAG GGTGGATGAG GAGGAGAAGG AGGGTGCCCA GGGAAGGCGC 1440 CCTCCACCCC AGGTGTGAAG AGGGCAGGCA ACTTTGGAGG GAGCTGGAAG AGACAAACCA 1500 GGGAAATGAA ACTGGCTTAA CTCACTCAGA TGTGGAAGAG CATATGCCCT GATAATGCAG 1560 GTGAGGTGAG AGGAATTAGA ACTCCCCGTC CCTAGGAAGC GCAGCGTCGG CCTTCATTCA 1620 GATCTCTACA GCAGTGAGAA AGGATGCAAG GACTATTCTT CTGGAATCCC AGGAAGGAAG 1680 ACTGGAAAGA CAACACATCT GACCCAGTAC CCATGTGCAA GCACTCGGTC TGTGCCAAGC 1740 AAATGCAAAG ATGCAGACTT TCATACAATC ATACACTGTG ATCATTTATC AATCTCCTTG 1800 AGGATTCATA GTCAACACAA TGGCATAGTT TACCACAGGC CTCTGCCCTT CAGAACTCAA 1860 CCAGTCTCTT GGCAGCTGCT TCTAGAATGG GGGTTGGGGG TGCAGTCCAC CACGAGAGCT 1920 TTGAGGCAAC TGGGCAGCTT CAGGCACCTC ACGGCTTCTC CTTCTGAGAT AATTCCCACC 1980 ACAACAAACC TGTATGCCTA CAGGAGTGGC GAAGGTAGCC ACCATCCCAG AAATAAATGG 2040 TGCATACCAT CGGGGTTAAA CCCAGTGCTG AAGATTTGTA AATTCCATTT CCTGCAAAGT 2100 TTCTGGGGGA GAAAAGTGGG TGGGGCTGTA GAGTGCAAAC ATAACAACAT TCACGTACCT 2160 CAGAGGACGG TGGAAAGAAA TGGCTAATAA AAATTATTAC 2200
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