Tag | Content |
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EnhancerAtlas ID | HS182-01012 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr1:62802260-62804840 |
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 | chr1:62803502-62803520 | GAAAGGGAGGGAGGGAGG | + | 6.13 | NFYA | MA0060.3 | chr1:62803790-62803801 | TCTGATTGGCC | - | 6.02 | NFYB | MA0502.1 | chr1:62803791-62803806 | CTGATTGGCCCGGCT | - | 6.16 | SOX10 | MA0442.2 | chr1:62803136-62803147 | AAAACAAAGAC | + | 6.14 | ZNF263 | MA0528.1 | chr1:62803504-62803525 | AAGGGAGGGAGGGAGGGAGAG | + | 6.58 |
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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 |
GH01I062336 | chr1 | 62802093 | 62804728 |
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Enhancer Sequence | TGTGTGTTCT CATGATTTAG TTCCTGCTTA GAAGTAAGAA CATGCGATCT TTGGTTTTCT 60 GTTCTGCAGG GTCTCTCTTA AGATATTCAG AACAGAGGAA AAAGCAGGAG TTAGATGGGT 120 CTTGAGTGAC TCTTTCTAGG CCAGCGTCCT TGTTTCCCAA GTCCAGTTCT CTTCCCCCAG 180 GCTCCTCCCC TGGGAGCCTG GAGGCCCCTA CACCTGGAGG AGCCGGGCCA AGGTTGGATG 240 GCTGCCTGCC TGCCGAGGGC ACTGTAGAGC GGGTGGTGGG TAGTGGATGA GGGTGGCACT 300 TGACGCTGAG ACCCCGCCGA CAGCCTGGGC ATCCTTGACT CGGGAAGTTA CACAGAGTGA 360 TGGACCTTCC TGTTAGGACT GTTTTACTAT AAATGAAACA GGAAAATATG AGAGAGTTCT 420 TGAACTCTCC TGGGAGGAAG ACAGTAACAA GCCATCTGAC CACCCAACTG CAGCTCACTT 480 TAAATAACTT TCTATGGCTA TTTTAAGACA GAAATGGACA TTCTCCTATT AATAAGCCTG 540 GCTAAGTAAG GCTGATCTGC AGCCAGGGTG AATCTGAAAG CCTCCTTCCC CACAGAGTCC 600 CCAAGGGCAA CAGACAGAGG GGCGTGCTCT TGTCGATGGA CAGGCCCACA CTGGTCATTT 660 CGGGCAGGAA ATTCTGTAGG GGAAGAGATT CCTCAACCTC TTATGCCTGC TCTTGCCCTT 720 CTTGGAGGAG CTCAAAAGCA GAATTTCTGT GGCTGAAAGG AGGATTTCCC CAGGGCCAGG 780 CGTTGCCTCT CCCAGGCTCC GCACTGACAC TCCTGGACAC TCCCACAGCC TAAGGAAGGA 840 GGGTCTATTC TTATTCCCTC CTTCCTTATA GATGTGAAAA CAAAGACAGG GGAGAGTTCA 900 TTCTTCTCCA AGTTCTCACA GTTAGAAAGG GAAGCTGGGA ATTGAGAGGG TTGCAAGTCA 960 CCACTCCCCA CCGTGCCTGC CCTCCTGAGG CACGGTTTAG ATGCTGCCCA GGCCTTCGAA 1020 GCCAACTTCT TGCTTTGCCT GGGCAGTGGT GGGAGGCGGC TGCTCATCAC CGCTGGGCTC 1080 TCCCTTTCTT GCTCACTTGG CTCTTTGGTG TCCTTGTCAT AACTGAAAAA GCCATCATGG 1140 GCTGACGACC AGGTCCCCTT CACCCCAGAA CCATTTTGTG GGAGTGGTCA CTGCCCGGCT 1200 CCCCTCCCCT CCTGTGTCAT CAGACACTCA GTCACCCAAA GAGAAAGGGA GGGAGGGAGG 1260 GAGAGCCTGG GGCAGGGGCA GAGGCGCCTC AGCCTGACAT CATGGCTTCT GTCTGTGTCA 1320 CTGCCTTTCT CCTGCCTTTC CCAGTCTGAC TTCTCACTGT AAGGCTTCTA CTAGCCAGTT 1380 CTCTGCTTCC CCCATCTCTC TCTTCCTCAT AGGCCCCCCA GCTCTAGCTC CACCATCTGG 1440 AATCTTCCGA GGAGTTCCTG TGGCCTCCAG TCCCGCAGCG GACAGACTGC ATGTCTCAGC 1500 ATTTCTTGGT TCAAATTCCT GAGGCAGGAA TCTGATTGGC CCGGCTCCCT TTTCGTGCTG 1560 GGCCACAGGT CATAGGTTGC TGGCCAGCCT CAGTTGGCTG TCCACGGACA GCCAGAGTTG 1620 AGTGGGACAA AACACAGCTG AGGAATGTCC CCTCCTTTCA GCCGAGGCTG TTTGTTGAAT 1680 TGTTCCTTTT AGAAGGGACA ATGGCCAACA TTTGTACTGT GCTTCTAAAG CCTCTGCTGG 1740 CCTGAGGCAG GAACACAGTC TTTTGGGTCC TTTATAAATA ACTGTTTTAA CTGCTAGAAC 1800 AACTTACAAT ACGAAGGCTC TCACTCCAGC TTTCACTACG GCGTACCCCA TCTCTTTCAG 1860 ACTCCTCTCC TTGCCCCAAA TCTGTCCCTG GGAGCCCCCA GTGGTGACTC AGGGGTGAGT 1920 CCAGTCTGCA GCCGACTGCC TCCCACCGCA AATACTGCTG GCCCCACGAC CTTTGACACT 1980 TGGATTTTAG CAGCGGTCAC TCTATCTCCC GGCCCCAGAG TCGCCTCTGC CGACGGCCTC 2040 AGCATACCCA AGCCCTGCCA TGATTCAAGG AATAGCCACA GGGAGAGCTC TTCTCCCTGT 2100 TTGTGGGCCT CACCCCCTAT TAAATAGGAT TTTAATACTC GGGCCCCGAT GGCTTAGGGG 2160 CCGGAATGCC TAGTTTTTGC TCGAAGGCCA CTACGCCCAG GATCCAGCAC AAATGCCTGT 2220 GAGGCCAGGA CTGGGGATGC AGGGGCAAAG TTAAGGGGGG GACAGCAGGA CTTCCCTTGC 2280 CTGGGCCTGG GGGTGACCGC ACTTGACTTG ATTCCCCTGG GAGAAGTTAT TTCCCCACAG 2340 ACTCCTTGGT CTCTTGGGCC GTAGACTTGG GTGGGCCTCC CCAGAAAGTC TGGCTCTCAG 2400 GGGTGAAGGT ACTTAACATG GGGCGCCCAC CCACCCAGTC TCCCCCACCT GGTGGTGGAA 2460 ATAGGACCAG CTTTTTGCTC TACATACAAC CTAGTGTGAG AGGGAGAGAC CAAACAACAT 2520 GGCAGTACGG CCAGTGGCCC GGGGGCAGAC AAGCCTGTCC TCTCATGCCA GGGACCCCTC 2580
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