Tag | Content |
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EnhancerAtlas ID | HS158-04586 |
Organism | Homo sapiens |
Tissue/cell | Pancreas |
Coordinate | chr1:205253330-205254360 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Myog | MA0500.1 | chr1:205254178-205254189 | GACAGCTGCAG | + | 6.62 | Tcf12 | MA0521.1 | chr1:205254178-205254189 | GACAGCTGCAG | + | 6.14 |
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| Number of super-enhancer constituents: 31 | ID | Coordinate | Tissue/cell |
SE_02431 | chr1:205253201-205255000 | Astrocytes | SE_03194 | chr1:205253181-205253866 | Brain_Angular_Gyrus | SE_03194 | chr1:205253899-205254801 | Brain_Angular_Gyrus | SE_03963 | chr1:205252695-205257315 | Brain_Anterior_Caudate | SE_04837 | chr1:205252438-205255709 | Brain_Cingulate_Gyrus | SE_05801 | chr1:205252449-205257899 | Brain_Hippocampus_Middle | SE_06736 | chr1:205252450-205256085 | Brain_Hippocampus_Middle_150 | SE_07799 | chr1:205252396-205255918 | Brain_Inferior_Temporal_Lobe | SE_11085 | chr1:205251353-205259013 | CD20 | SE_26974 | chr1:205252457-205257684 | Esophagus | SE_29391 | chr1:205253543-205255044 | Fetal_Intestine_Large | SE_32765 | chr1:205252644-205254723 | H1 | SE_38936 | chr1:205252877-205255818 | IMR90 | SE_43852 | chr1:205252499-205258684 | MM1S | SE_46173 | chr1:205253006-205257823 | Osteoblasts | SE_50327 | chr1:205252697-205257801 | Sigmoid_Colon | SE_52983 | chr1:205252823-205257708 | Small_Intestine | SE_54130 | chr1:205252675-205258056 | Spleen | SE_55645 | chr1:205253025-205256564 | Thymus | SE_56704 | chr1:205252917-205256555 | u87 | SE_56879 | chr1:205252970-205254378 | VACO_400 | SE_58462 | chr1:205242169-205295027 | Ly1 | SE_58967 | chr1:205242236-205295022 | Ly3 | SE_60263 | chr1:205242326-205284722 | Ly4 | SE_60576 | chr1:205242267-205294889 | DHL6 | SE_61365 | chr1:205242037-205294994 | HBL1 | SE_61423 | chr1:205183427-205322469 | Toledo | SE_62465 | chr1:205242393-205294944 | Tonsil | SE_65493 | chr1:205252784-205254787 | Pancreatic_islets | SE_67308 | chr1:205252499-205258684 | MM1S | SE_68815 | chr1:205252846-205254572 | H9 |
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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 |
GH01I205283 | chr1 | 205252730 | 205258354 |
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Enhancer Sequence | CAACATACAA TAACCCTGAC AGTCTGTCAT TCTGTGCTTC TGTGACGTCA GCCTTAGGAG 60 TTATCAGGGA CCCAAACTTG GGCTTCACAG GGGGCAGGAT GGAGGCCCTG CCACTCGGAC 120 CAGACCAGGT TGTGGTGAGG GGCAAGGGTG GTGCCTCCAG GCACCAATCC AGAGTGACCT 180 CACTCTCTGC AGGCTCCCCT GGGGCCCTGA GGGAGGGTGG GGTGCTGGAC AGGCCTGCTA 240 GATGGGAGCA GGTTTGGAAG GAGGTTTAGG AAGGGTGCGG TGGGGAAGGT GTGCCGCTCA 300 GGTTCAGTGT GATCACTAGA GAGGGGCACG CCTGCCTGCA TCGTCTGCCA TGCCAGACAG 360 GGCAGGACAG CTTCTCCCCC AGCCTGGGCC TTTAGGATCC ACTGTGTGAC CATCCTGAGC 420 CCCTTAGCAA GGTGTGAGCG GGGTTGGACA CCCTCCCCTC AACATCCATC TAATGTCAGC 480 CACCAGCCCT GCCTTGCTGC ATGATGGGAA ATCAGGGTAA GGGAGCCAAA CCCCAGCTGC 540 TCTCAGAGCT GTGAGGACAA GAGTGGAAAA CCTGCCCTCA CAGGCCCAGC TGGCCAGAGG 600 GCTTGTCTCT TTCAGTCGCC CTCCCCCAGA GGGAGCAGGA GCAGACAATG GCCACCATGA 660 CTCACCAGTG AGCCATCTTC CCCTCCCCAC CCCTCCAGCC TGGCCCATGA CAGCTTAGCT 720 TGTCCTCCAA GGGAGCTGCA GCCCAGCCTC CCAGGGCCGC CAGCTTCCTC TCTCTTCACC 780 CAACCTGGCT CCCCCCCTGC TTGTGCAACA CCACATCAGA GGGTTGTGAA GTGGAGAGGG 840 AGGAGTTTGA CAGCTGCAGA CCCAGGCAGA CAGAGCAGAC TCCTTTGTGA AGGAGATAGA 900 GGCTGCAGGG GCCCAAGTCC AGCCTGTACT CCCCTGCCCT GACCCACAAG GCATCACCCA 960 GTCTCCCCAA ACCCTAGGGA AGTGGTCATT GTCATTTATT TGTTCCTTTC TTAGATAGAG 1020 CTTGGATCCT 1030
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