Tag | Content |
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EnhancerAtlas ID | HS182-13617 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr20:11175520-11177780 |
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) |
NFIA | MA0670.1 | chr20:11176535-11176545 | ACTTGGCACC | - | 6.02 | TBXT | MA0009.2 | chr20:11176485-11176501 | TCACACACATGTGCGA | + | 6.74 | TBXT | MA0009.2 | chr20:11176485-11176501 | TCACACACATGTGCGA | - | 6.82 | ZNF263 | MA0528.1 | chr20:11176359-11176380 | TCCTCTCTCTTCCCCTCCTCT | - | 7.42 | ZNF740 | MA0753.2 | chr20:11176815-11176828 | CCGCCCCCCCCCC | + | 6.64 |
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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 |
GH20I011195 | chr20 | 11175658 | 11177760 |
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Enhancer Sequence | CAAGCCAAAT CACTCAGCCT GCTGAGATCT CAGTTGTTTT TTTTCATCCT GGACAATGGG 60 CATGATGCTG ACTGTCCCTC TGGGTGGTTC TGAGGATCTT GGGAGGATGG ATATAAGTGC 120 AACTTAAACT CTGGAGCCCT TTACAACTGC AAGGCAGCAT TATTCACTCA AACATAAAAA 180 TAGGTCATTA AGCATCATCA AAGGGAAAAG TAAATGTTCA GGGATCATCT CTGCTGCACT 240 GTTGCTGGGG AAAGAGGCTC TTTGTCCCTT TAAGAGCTTT CAGACACATC TCTAGTCACA 300 TCCTAAAAGC CTTCCTAGTT GTGTAGCTTA GGTGCATCCG GTAGCACAGC CGTGTTCTGA 360 TCTTCCTGGC AGATGTCATA ATTTACTGTC ACCCCCATGC AGGAATGCAG GGCGAGGGGC 420 CCCCATGCCG GCTCTGTGAT CCATTGCCTG ACAAGTCCTG AGTGTCAACC TCAGGCAGGC 480 CCAGCGGAGG TGGAACACCA TTTACCTGAT AGTGCCTGTG ATAAAGTGGG CAATTAGACG 540 CACTTGGAAA AGCCTGGCTG GAAACTGGCT GGCATTTACA CAACATTACA GCCAAGTCAG 600 GCTTCATAAA AGTTAATGGA GAAAAATGAA GTCCTTCAAG ATCTACCTTG CTCTCTGAGG 660 AAGTCAGGAA CACAGGACTC TGTAGCTTTA TTTCTTTTTG TGTCTCTCCC ACCTTTTCAC 720 TCTATTTCCC CCAGACAGGG TAATATATTC TCATTGGAGA TGGGAGTAAA GGAAAGCGAA 780 TTGAGAGTTG AGGTCTTAAG TGTTTGATCT CAGAGGCATG TTATTTCTTT AGTCTTCAAT 840 CCTCTCTCTT CCCCTCCTCT CTGTCTCTCT CTCACACACA CACATGCACA CACACACACA 900 CACTCTATAC TTCTATAGAG TATACACACT CTATATTTCT CTGTCTTTCT GTCTCTGTCT 960 CTCTCTCACA CACATGTGCG AGCACACACA CACACAATCA CAGTGCTAGG ATTTAACTTG 1020 GCACCTTGGC TTACAATTTG CCTCTCACTG GAGTTTCTGG AGTTTGGTGC CAGTTCAAGA 1080 GCATGATCTG TTTGACATGA ATTCTACAGC CCTCTCTTCA TTTCCTCCTA ACTGGATAGC 1140 TTCAGTTTGC CGATGATTAA TGAGTCTGGA AGGTGAGCGA CAGTTATCTT AAGGGCTCTC 1200 AAAAGTTTAT TTCAGAGACT AGCCAAACTC TCCTGCTACA TTAACTGCAG CGAAGTTTCC 1260 TGTTTAACAG CCCATGGAAA ATAACTGCCT GACCCCCGCC CCCCCCCCAA ACCAAGCTGC 1320 CATGAGCGCA GCTCTGTTTA TTGGCCAACA GTGTGCATGT TCTCTCTATC GCTTCCTTTC 1380 AGGCAGACGA ACATTTTACC TATGAGAAGT AGGAAGTCCA TTGTGAGGCT GGTCCAATAC 1440 TGGACCTCAT TTGGATGTGG AGGATTTCTG AAATTGGAAA GTCAGGACTG ATCTGGAAAA 1500 TGTGCTTACA GATAGTGGAA CAGGAAAATG ATTCGCTCCC CAAGGCCAGT TCCTCCTCCT 1560 CTGCTGGGTG GAAAAGGTGG GAGGAAGGGA CAGGGTGTTC TGCCTGTGAT TGGAATTCCC 1620 CTGTAGAGTC ATAGAGGATG AGCAAGCCTT TGGTTTTCCT TTTTCATATT TTATTTTGCA 1680 CCTACAATAA TAAGCATGCA GAGAGGAGAC AGAGAGGCCT AAATGAGTTT TTTTCCTTTC 1740 TAAATAATGA CCAGCTCTGT ATCAATCTGA AGGCTACTGA GGGATGCTGG TGGCTGGATG 1800 GCGGGGCCTA TTTAGGGTTT TGGCCTGATT AAAAGTTAGT CCCAGGGACA TGCAGGCCTA 1860 CCAGGTGCAC ACTGGTGCCA GCCACTTCAG TGGGGTGGGG GAAATTACTG GGCCTGCTGT 1920 CTCAAGTTTG AGAGGACATC TGAGATTCGG GTCCGATAGG GTCACAATGT CTTCAACACG 1980 AATAAATAGG CAGTTGTAGG TTGGGGAAGG GAAAGCTAAA GTGGAAAATA AATAACTTAA 2040 GACACCAGAC AAGTTCTGGA GACTGAGGTA GAGAGATGAT GGAGTGCTCT TCACCCATGT 2100 ACACTTCAGC CTCTCATGTC ATCGTGGTGA TGCTGCCAAA ATAGACCCAA GTTACATTTT 2160 CCTTATGATC TCATTTTACT GGGCTTGAAG CCTACCTCAC TCAACATCTT TGGAGGGTAC 2220 ATTGAAACGA GCTGTTTGTA AGACAGTATT AAAGGAAGTG 2260
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