Tag | Content |
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EnhancerAtlas ID | HS182-22239 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr9:136370580-136372990 |
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) |
RREB1 | MA0073.1 | chr9:136371610-136371630 | AGTGGGGGGGTGGGTGGGGC | - | 6.51 | ZBTB18 | MA0698.1 | chr9:136371149-136371162 | CTTCCAGATGTGG | + | 6.11 |
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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: 2 | ID | Chromosome | Start | End |
GH09I133505 | chr9 | 136370572 | 136372600 | GH09I133507 | chr9 | 136372936 | 136373045 |
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Enhancer Sequence | GTGGCAGAAC AGGGCAGGAC AAAGGAGGCC GTGAGTGCAG TGTACAGCAC ACAGGACTCA 60 GAGACCCCAA ACTTGGGGCC GTGTCCTGGC TCTGTCAGTG TGAGGTCTCA CCCATGCAGA 120 CACTCCGTGG ATCCTTGGTT TTCCAGCTGG TGAGATGGGG AAGCCAAGAT GACTAAGATG 180 CATGGTGATG AGGAAGTGGT CCCAGGTGCG AGAGCCTGGT CCAGGCCTAA AGACCGTCAC 240 GGGAGTGATC TCGACAACTG GTAGGGCGAA GGCACCATGG GACCCAGCAT AGAAGAGCAG 300 GTGTCTGCAG GAGGGACAAG TGGAGCTCTG GGGCCTCTTA GGCTGCCTTC TGTGCTGACA 360 TCTTTGGTTC TGCCATTGTG GTTTCTGGAA TGGGCTGGCA GGCCAGGGGC CAGAGAACGC 420 CCCAGTTTCC TCTGCCCCTC CTCTCCTACC TCTGGAAGGC TCAGGCAGCC AGGGCCGGTG 480 GTCTGAGGCT GCAGCTTCCC GGAGCTCCAA GCCAGCAGCA GACGCTTATC AGCCTGCTGT 540 GGTGCGGGGG CCGAACTCTG CCCAAACGTC TTCCAGATGT GGCCGCAGCT ACTCGATAGC 600 CTGGCTCCAG CCGGGGCTCT AGGCCAGCAG GCTCCCGTTA GCCTAGCTGT TAGGAAAACA 660 AAACCCAATG AAGGCCCAAG GGACCCAGCT TCTCGGAAGG GAAGGGAGTG ATTGGGCAGA 720 AGCCCTGGCC AGGCCCGGCC ACTGGCCCTA AGCTTGGGGT GGTCATGGCC GTCTGCTGGC 780 TCCTCTGGGC TCCTCCTGGG GTGAGCCTGG GCCCCCTGGC TAAAGGGGTT CCCCTGTGTG 840 CAGGATGCAG CTTTTGTCTC TTTTGCTTCT CCACAGTGTG TGCGGGTGGG GGGCGTGGGG 900 TCATGTCCCT ATCACCGTAG ACAGGATGGC AGCTTGACAA CATGGTGCAG TTTGCCGATG 960 AGCCTGAGGG GCCGGTGCAC CTCTGCTGCC TTCCTGGCCC AGGGCGGGAC TGAACCCAGG 1020 CCAGGTTCTC AGTGGGGGGG TGGGTGGGGC TGGGTCCGAT GGCCCCGGCA GGATAAGCAG 1080 GTGTCACTGC TGGAAGTTTT GGGGACTGAA GGGCCTTACC CAAGGACACA CAGCCCCAGG 1140 GTGGGTACTC CAGAGCCAGT TCCTTTCTGG CTCATGGCCT GCTCCCGCCT GCGGCCGGTG 1200 TGCAGGTCAG CGGGGTCAAG GCTGTCTTCT GTGGTCACTG ACTAACTGTT TTTTGCATGT 1260 GGACTCGTCA GGGAGGCATA AACCTGCCCT TGCCAAGACA GATATGGAAA AATCCACTCA 1320 TCCATTCATT TGACAAATAT TTGTTAAGTG CCTGCCTACG GCCCGCCAGG CGGAGCGCGG 1380 GAACGCGATG CTGATTTAGA CACTCCCAGC CTGGGTCGAG CTTCCAGGCT TCATGGGACC 1440 ACATCCGCCC CTGGCCTGCT GGGCATGGTC TTGGCCTGTG TGATGCAGGC TGGGCCCTGA 1500 GCGACGGCTC TCCCGCCACC TCCGTCGTAC AAAGGCTGCA GGGGAACGAA TGACTAGGTA 1560 ACTGGGGGTG ACCTTGACTC TGTGTGGCTT TAAGACACAA GCCAGCTGTC CAAAAGCTTT 1620 GAGCTATGAT TGCTGGCAAC AATTTGCCTC AATACCCCTC CCAGACCAGG GCAGCTCCCC 1680 GCAGGCTGGG GGCCATGGCT GAGAACTGCT GGAGGGACAC ACGTCCCAGG CACCACCAGT 1740 CACCGATGAC TGGGCTTTGC ACCACTGGAA AACCAGCTGG GGGACTGGTG GGCCCCCAGT 1800 GAGCCCTGCT GATGCCACCT TCGCTCTCCC AGCGCCTCCC TCCTCCCCAC ACTCCTGCCT 1860 GGTGGACTTG GCTCCCTCCC GATGGGCAGC AGCCTTCCTG GTCTCTTTCT GCCACTGCCC 1920 ACCTCTTCAT GGAAGCCAGA CCCACTGTCA GGCTCCCCCA CCTAAAACCC TCACATCCTT 1980 AGAACCTGCC CACTGACGCC CACCTTGTGC AGTTCCCAGA CAAACCCTGT TAGATCTTTC 2040 TCCCTCTCCC TGGGCCACTG GCCCCTTCTC CTTCGGGTCT CCCAGCAGCG CCCGCACTGG 2100 GCAGCCTTTC TGACCCAGCG CCTCACTCCC CCAATCCCCC GCGATGGCTC AGTTCTGGGT 2160 CTGCCTCCCC CATCAGTCTG TGCACCATCG GAAGGCAGAG CCCAGGTCTG CTGGACTTGT 2220 GTGACTCCTT GGGGTTGGGA AAGCTGTGCG GCACATGGAG ACACTCAGGA AGGGGCGACG 2280 TTTAAACTGG GCCCTGGGAC CGAGCCCCCT GTTTCCTGCT GTTTCAGGTC AAGCGTTGGG 2340 GCGGCACAGC AAGACCAGGG CAGAGCTGGT GATATGACAC AGGGCACGAT TCACCCGAGA 2400 TGGTTGGAGG 2410
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