Tag | Content |
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EnhancerAtlas ID | HS182-19990 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr7:74098410-74099630 |
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) |
NFYA | MA0060.3 | chr7:74099497-74099508 | AACCAATCAGA | + | 6.62 | NFYA | MA0060.3 | chr7:74099414-74099425 | TCTGATTGGTT | - | 6.62 | NFYB | MA0502.1 | chr7:74099492-74099507 | AAAGCAACCAATCAG | + | 6.7 | Pou2f3 | MA0627.1 | chr7:74099535-74099551 | TTGTATGCAAATGACG | + | 6.94 | STAT3 | MA0144.2 | chr7:74098842-74098853 | TTTCTGGGAAG | + | 6.02 | Znf423 | MA0116.1 | chr7:74098505-74098520 | CCCACCCAGGGTTGC | + | 6 |
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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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Enhancer Sequence | AAGACTCCAT GGGCCTGGCT CAGGTGGCTT CTGGAGCACC ACCTCCATCA AGGAGCTTTT 60 CCTGGGGTCC ATGTGTAGTC CATGTTGCCT GCTCTCCCAC CCAGGGTTGC TGTGCTTATT 120 ATACAAGATG GCCAATAAAG CATGACATAT ATTCAATAAA TGTTCATTTC TTTTTCCAAC 180 CCTTCTTATT TTAAGTTGAG GGTATTCATA AAAGGGATTG AGCATTTCCA TTTATGGACG 240 AGGCAACTGA GTACAGCCCC CAGGGGCACG CAGCGAGATG GCTGTCTGCT GAACCCATAC 300 ACCAGCTCTC TAGGCGTTTG GTCCTGTGGG GACCGGTGCA TCAGATGCTT CCTAAGCTGG 360 CGTCACCTGC CTGGCCCGAT GCCTCCTCTG GTGTTCATTG TTTAATTAAT GCCACCTCCT 420 GATGGCAGTT TCTTTCTGGG AAGAGGAGAA AAGAGAGCCG TCCCCAAGTG AAGGGTGCAG 480 GGAAGCCTCC ACGAATAGTT TCAACTAAGG ACTGTCCCAG GAAGGAAACT CTTGGGATGG 540 GCAAAGAACA GCGAACTTCC GGTGTGACCC GGATGCACCC ATTTCCAGAG AGCAGGAAGC 600 ACAGAGAAGG CCCGTGGGTC GCCCTTGGGG TGCTTTCCAT CCTGCAGGGC TCGCTGCCTG 660 CCCTGAAAGT TCTGATAAAG ACATAGGACC TTCATCACCA GGGGCGCCCC GTGGGCTGTT 720 GCTGTAGCGT CTGTCCCCCA TTTCTTACAC ACATTGAGTG TGATTGTTAC CAGTGGAGGG 780 TGTCCAATGG AAGAAGCACC AAAAGCCGAG ATTTATTGAA AGTGGAAGGT ACAGTCCACA 840 AAGAGGGGGC GGGCCGAGCC TGGGGGCTGA AGAGCCCCTT TACAGAATTT TCTGGGGTTT 900 AACTACCTTC TGGGGTTTAA CTTTCTGGGG TTTAATTTTC TAGAGGTTTC CCATTGGTTA 960 CCTGGTGTAC ATCCTTTGTA AATACAGTAG TGGCCTGCAA GCAGTCTGAT TGGTTGTGAA 1020 AAGCAACCAA TTAGAGGCTG ACTTGAAGTT ACAAAGGTTA CACCCTATGC AAGCATCTGT 1080 GGAAAGCAAC CAATCAGAGA CTAAAGTGAA GTTACAAAGT TACACTTGTA TGCAAATGAC 1140 GACTTGCCCT GCCGGGCTCC AGTAATCCCA GTACTTTGGG AGGCCAAGAT GGGTGGATTA 1200 CTTGAGGTCA CGAGTTCCAG 1220
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