Tag | Content |
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EnhancerAtlas ID | HS182-22044 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr9:129294210-129296520 |
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) |
SREBF2 | MA0596.1 | chr9:129295535-129295545 | ATCACCCCAT | - | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr9 | 129294211 | 129295157 | chr9 | 129295182 | 129295387 |
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| Number: 1 | ID | Chromosome | Start | End |
GH09I126530 | chr9 | 129293168 | 129297039 |
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Enhancer Sequence | TTCTTACAGC TCCTCAGAGG ATGGTTCTCT TACTATCTCA GTCCAAACCC CTCCTTCAGC 60 CAGTTCTTTT TCCTATCCTC CTTAACTCCC TCCTGCTGTA GGAGAAATCT TTTTGTTCCT 120 GCTGAGCCTC CAGGGAGACA GGGAACAGCT GGTCAGCATC TGGTGCTCTC CATTAGCCAG 180 GACTCCTGCC CCCTGGGCCT TCCGCTCCCC GGGCAGAATA ACTCTGCTTC CTCTAACCTT 240 TCGGCTGGGT CCCGTGCTCC AGGGCTTTCA TCATGTCCTT CATACCTCTG AAGCCACTCC 300 AGGCTCCCTG GCCCTCCTGT GGCTTCTGTT GGGCCCTGCC AGGCGGGCCA GCCAGGGCAG 360 GGGCAGAGGG CGAATGACCC TCTCCCCTCC CAGCCCAGAG AAGCGGGGGG TGCGGGCAGC 420 CATGTCTGGG GAAGGAGGCA GATGTCACAG CTGTGCCAGG TTCCTCCTAC TGCAGGGTGA 480 GCCTGAGCTT GTCTTCTGGA AAATGCGGAC TGATGCCCTT TCTGCAAGGT TTGGTAAGAG 540 GATGCCATGT GGTGGTACGG GTAGAGCCCC CTGCCTCTGT TCCAGGCCAC CCTGAACTTC 600 TCTTTCCCCA TTGGATGACC TTGGATAAAT GACCTCACTT CTCAAACCTC AGCTTTTTCA 660 TCTGTAAAGG GGTAGTTAGG AAGATTCTAG AGATAAGGTC CTAATGAGCC TGGCCCTGAC 720 CCACAGCGAG AGCTGTGCGG GGCCCATATT TTCAGCGACA TTATCTCTGT TTTATTGTTA 780 GTCATCTCAG GCCAGGAATG TGCACACCCA GGGGCTCAGC TGTCTGGCTT TGCTCGACCC 840 TAGAGTCCTG GATTCTGAGC CTGTTGGATT CTGCTGCAGC CTGCTCCTAC CTAGGAAAGG 900 AGGGGTCTGT AAACACGGCC GAGTTAGCTC TTCCTCCGCA ACACTTCCAA AATCCATTTG 960 GGGATCTCCT CTTTCCAGAA GCTTCCGAGG CCCCAGTGAG ATGTCTCTGC CAGCCACAGG 1020 GGCACAGGAG GGCTAAATCC AGTGGCCCTC TCCCTTCTCT CCCTAGCTTG GGTTCCTTTG 1080 TGCCACCCCG CGAGCGGGGT GTGTGTGCCC CAAGCCGACA TGGGCACCTA CAGATGAGGC 1140 CTGGTGGGCT GAACCGTCCA CACTCAGCAT TTACAGACTT GAATGAAAAC CGAGCTCACA 1200 GAAGCTCCAG CCACCATCCT GGCCTCAGGT CACGTCCCTT AGAGACCCAC CGCTGTGAAG 1260 GTGTCCCAGA AATGCCAGTT GTCTTTTGTC CAAAGATAGC ATAAGCTGTC TTTGATTTAG 1320 GAGGGATCAC CCCATCCCAA CACCCGGCTC TCAGAGGCAC CTCATTCTGG AAAGAGCTGG 1380 AGAGGCCATC TTGTTGGTCT CCTGCTACTG ACCTGGGCCG TCTCCCATCC TCCTCCCCGC 1440 AGGCCTCTGT GAACCCCCCA GACCCCAAGT CTTGCTCTGC AGCTCACGGG GCTAGGAATG 1500 GGCCCTTGGT GGCATCCACA ACTCCCCCCT GCCACAAAGC ACATCTGCAC AGACACCCAG 1560 CACGCACCTG ACGATTCACT TGGTGATAAA AATTGGAAAG AATCCCAGAG AGAGATTTTT 1620 ATTAAATGCA AACTTCTAAT TATTCCTTTA GTCGTCTTTT TTCTAGTGAC TGAGCTACGA 1680 CGTATTTTCC TAGCAATTAT TTTTAACATC TCGAAAACTG CCCTTAAGAT ATGCAAAACA 1740 CACTCACTTA AGAGAGGCAA GTTCCCTTTT CCCTCTATCT CAGTTATTAA GAAAATAGGA 1800 AGTTAAATTT GTTCATAATC ACATTTCCGC AGCAGACCAT AACAGGGGTC ACGCCTCCAA 1860 AATGAACAAG GAAAGAAAAC CAAGAAATAA AAAACCAGAA CGCCTTGGCG TGTTTGCGAT 1920 TCCTGCCAGG GTGTGTAGGT TTGACGGTGG GATTTTCCTG GCATCAAACA GCAGTGAGCC 1980 CCAGGCTCCC CCAGGATCCT TCAGGGTCCG TAAGTGGGTC AAGGAGTTCA GAGTTGGACC 2040 TTACCTGCGG GCGTCCCGAG GGGCAGGCTG GGCTCAGGAG CTGACCGTGC CAGGGCTGGG 2100 CCACAGAAGG TGAAGGCGCG GTGCGTGGAG GCCCTTTGTG GACAGGTGCA TGGGCCCATC 2160 TCTCTCCGAG GCGCTACCTG CGGTTTACTG GACGTTTATT AGAAGCTCAC ACAATATCAT 2220 GAAGCACCTG CAGGCAATAA AATCCCTTAC ATGTGTGAGG CCTTGAGGAA ATTAACGGCT 2280 CCTCCCTGGG GATGCATATT TTGTGAAGAT 2310
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