Tag | Content |
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EnhancerAtlas ID | HS182-05457 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr12:117485780-117486820 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr5a2 | MA0505.1 | chr12:117486500-117486515 | AGGTTCAAGGTCACA | + | 6.2 | ZNF263 | MA0528.1 | chr12:117486378-117486399 | CATGGAGGAGGGAGAGGAGGA | + | 6.35 | ZNF263 | MA0528.1 | chr12:117486381-117486402 | GGAGGAGGGAGAGGAGGAAAC | + | 8.1 |
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| Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
SE_40918 | chr12:117481903-117492805 | Left_Ventricle | SE_43268 | chr12:117485523-117487557 | Lung | SE_49648 | chr12:117485738-117487315 | Right_Ventricle | SE_59898 | chr12:117480744-117519396 | Ly4 | SE_65704 | chr12:117485653-117487031 | Pancreatic_islets | SE_69204 | chr12:117485565-117487387 | H9 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr12 | 117485940 | 117486292 | chr12 | 117486360 | 117486669 |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I117047 | chr12 | 117485512 | 117486986 |
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Enhancer Sequence | TCAAGTTATC CTCCCCACTC AGCCTCCTAA AGTGCTGGGA TTACAGGAGT GCACCACTGA 60 GCCCAGCTGG CATTTACTGA ACACTGACCA GATGCCCAGG TGTGCAAAGC GCTTCACAAA 120 CCTCTGTCTC CCTCTCACCC AACCCCAAGA GGCCAGGGAT GCCTGAGCCC TGCCTCCCAG 180 ACAGACTGTC AAAGCTCACG GAAGTTAAGG CGTTTGCCCA CGGCCACACC ACTAAGGGAC 240 AGGAAACCAG GGATTTGGAC CTGAGTCCGT CCTGTTCCAC GCCCCTTGGA GCAGACAGGA 300 AGCCAGGCTC ACACCAGGGA TCCACCCCCG CCACCCGGGC TGTTCCCACC AGCCCCGCAT 360 ACACATTCCA GTGCTAAATA TAGCGAAGTC CCATGTTTAC ATTTTCTTGA TGAGGAGGCT 420 GACCTGGGGC GGGACACAGA GGGATGTCAG GAGTCATGGG AAAGGCCACA GGAAAAGGAG 480 ATGTGACTCG GGGCACTGCC TGGGACCTGT GCGGCTGGCC AGCTGGGACC ACAACTGAAC 540 CCACTCGGGA GCCAGAACAT AGTGGGGCTG GTCTCAGGAA CCCAGCAATA GCACAGCCCA 600 TGGAGGAGGG AGAGGAGGAA ACTGACTTTA GGGAGCGCTT CCTGTGTGCC AAAGGCTGAC 660 TGTGTGATCT TACCCAGCCC TCAGAACCAC GCATGATCGG CATACCCACG TTCTGGGTCA 720 AGGTTCAAGG TCACATGGCT GGTGAGACGG GCCACACTGG AACCCAGGTC TTTGCATCAA 780 GGGCCTTGTT TCACATCCAC CGCACAACCC CCTTCTAGTC CCAGGAAGCC ACAAGCTGCT 840 GAGGAATGTT TAGGATGAAG GTGCCGGGAA CGGGAGACAG CAATGCCAGC CTCACAGGGA 900 CGAGGGCTGG TGGCCCCAAG CCCTCCAAGC CCCCAAGCCA ATGCACACCC AGCCTCCTGC 960 TGCAGAGGCG CCTTGCGTTC TGAGGTCTTA GGGGAGGCTG CACCCCAGGC CAGGTGTGAG 1020 CAAGGGGACT CAGTGGCACG 1040
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