| Tag | Content |
|---|
EnhancerAtlas ID | HS182-03357 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr11:2117240-2119620 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RREB1 | MA0073.1 | chr11:2117427-2117447 | CCCCAAACCACGGCCCCCCA | + | 6.56 | | SOX10 | MA0442.2 | chr11:2117304-2117315 | TCCTTTGTTTT | - | 6.32 | | Sox3 | MA0514.1 | chr11:2117305-2117315 | CCTTTGTTTT | + | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I002095 | chr11 | 2116249 | 2119847 |
|
Enhancer Sequence | CCCACAGGTC CGGTTACTGG GGGAAGTGGC AGCACCGATT TTGAAATCCT TTTGAAAATG 60
TTTTTCCTTT GTTTTGTTTT ATTTAGAAAT TTCCCAAATT TTTACCAAGT TAAAGAGACA 120
ACCACAAGAA TGTGTAGCCA GGGTGAACAA TTGGCATAAA CAACCCCTCC CCCACTGCCC 180
AGCCTCCCCC CAAACCACGG CCCCCCAACT CAGCAGCAAA AAATGCCAGA CATGTATAAG 240
AAAATAGAAG CCGTGAGGAT AGAGCTGGGT GAGGAGCACA GGCCCCATGC CTGGGCTGCA 300
GCGTGCACAC AGGGACCACG CACGTGCACC CATGTACACA CGCACCTGCA CACATGCACA 360
TACATGCTTG CACATACGTA CGCACGCCAG CATGCACATC ACACACAGGG CCTCAGGGTA 420
ACCTTTTCCC CAGTCCCGGC TGTGATATTG CGAAAGGAGC TCAGGGTGGG GGGCGGGCTG 480
CTGGGTCCAG GCCCCCACCG TCCTGCCTAG CAGTCATTTG GTTTCTCTTT GCCTCAGTTT 540
CCCTTTCTCT GCCCCTCACA CCTCCCAAAG TCCTTTGGAG AATCCGTGAG ATGGGGGGGT 600
GACAGGCCCT GTATGTCAGC ACACACAGCC ACGTGATGTG GGACCCCAGC CCGTGTCCCG 660
CAGAGGCCCT TGCAGCTGGG GACCCAGGGC CTGCTCCAGG GCACAGTGGG TCCCCTTTGG 720
CCATAGCAAC CCTGCCCTGG CCTGCCTTAG ACCTACCCCT GCAACCCCAA GGCTACAACC 780
CCAAGGCTGC ACCCCCAAAG TTGTGCCACC CAAGGCTGTA CCAGAGGCTG AACCCCCAAG 840
GCAGCATGCC CCTCAAGTCT GTGCCCCCAG GCTGTCTGCC CCACAGCATC CCCAGCTCCT 900
CCCTAGACCC CTTCCATACC CCTCCGTGAA CTGCCCACTC CACAGGAAGC TGCCCTGCTC 960
ACGGGCACTG ACAGTCTTCA CTGCCTGGGG TTCTCCCCTG GAGAGGCAGA TTCCTTGGCC 1020
CAGAATACGC AGCTTTAAGA AACCAAGTTG GGATCCGAAT GCAGGGACTT CCTGCTCCAA 1080
CTGCTGGCCC GAGGGCCCGC TCTGAGGCTC TGAGGCTCCC AGTCTGGGGC ACCCGCACAC 1140
CACGGCCCTC CCGCCCACGG TGAACGCCCC ACCCGGCCCC AAGAGGCATC GGGAGGCGCT 1200
GCTTGGCCCA GAGGAGAACA GCACTGATGC GGAGGCCCAG AGAGCTGGGG AGGCCTTGGG 1260
GGCGCCAATG GGAGGGTCTA AGAGCCCCCC GATCTCCCCT CGGGAAGATG AGCTCTGGCA 1320
CTCCACGAAG GACAAGCTGG TCTTGGGGAA TTTCGCTGGC ACAGAGACAG GAAGGAGAGG 1380
ATCTTGGCCT TCTAAAATGT TTACTACATC AGGAAACGAA CGCACTACGC GCGGGCTCAG 1440
TGATGAAGAA TAAACACACA CACTCACTCA GGACACATTG AGTGCAGGCC CAGCCCCGGG 1500
CTTCCCGCTG CGGGGGAGGC TGGGAGGGTT CAGGCATGCC GCAGCCACAG ACCATGAGCT 1560
TGGGGGTCAG GCGGGCGGGG GCCAAGGGCA GGGCCACGTC CCAGCCCTCC CCACCCAGGT 1620
CCGGGCGCCT GCCCGCCCGC CCTGGCTGCT CTGATCTGGC TGTCACGGTT ACACAAGGCC 1680
AGCCTCCATT TCTTCATTAA TGCCTCACCA AGGGGGGCCG CTAACCCGCA GCCTCAGGAA 1740
TGTGCCTTTA CAGAGCAGAG GATGCAGCCG CTGAAGGGCC GGGCAAGCTG CACCGGCCGG 1800
GGCTGGAGGT CCTGGCCTGG ACTGCTCCCC CGGCCCTCCC CACTCTGGCC CGTGCTGGTC 1860
CAGGCCAGGG CAGAAGGAGG TCAACTTGTG CAATGCCTCT CTGGGTGAGC TCTGCACCGG 1920
GAGCTGGTGA TGGGGACAGA GGAGGCCCTG GAAGAGGGGA CGTGAGTTGA GAGAGCAGCA 1980
CAAACCCAGG ACATGCCTCC AGCATCTCTG CCTCCCTTCG TCCACAGAGA CTGCTGCGGG 2040
GTCAGGCAGC ACAGCTTCTT GCCTGAGCTC TGTGGCCTCG GGCAAGGAAG GTCCAGGAGT 2100
CAGGTGCTGG TCTGCAACAT GGGATCATCT CGCTCTCCAG AAAGGCTGCC AGGGGATCTT 2160
AGGGGAGGCC CTCACTCTCG TCTCTCCCCT GTAGTCCTGA CACCTGCCGA CCTCACACAT 2220
GGGCCCTCTG GGCGCCTGCC CTCCCCCCTC GTCCTTGCAT GCATGCTGTT CCAGCCTTCG 2280
GAAATGCTGT TCCCTGGTGA CCACTCCTAC TCCAGCCCCC TGTGCCAGTG TCTTCCAAAA 2340
TTTTCCTTCA TTTCTGAAAC CAAAGGAGTG TCTAGTCCAG 2380
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