Tag | Content |
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EnhancerAtlas ID | HS185-00766 |
Organism | Homo sapiens |
Tissue/cell | T98G |
Coordinate | chr1:205253640-205254620 |
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 | GATCACTAGA GAGGGGCACG CCTGCCTGCA TCGTCTGCCA TGCCAGACAG GGCAGGACAG 60 CTTCTCCCCC AGCCTGGGCC TTTAGGATCC ACTGTGTGAC CATCCTGAGC CCCTTAGCAA 120 GGTGTGAGCG GGGTTGGACA CCCTCCCCTC AACATCCATC TAATGTCAGC CACCAGCCCT 180 GCCTTGCTGC ATGATGGGAA ATCAGGGTAA GGGAGCCAAA CCCCAGCTGC TCTCAGAGCT 240 GTGAGGACAA GAGTGGAAAA CCTGCCCTCA CAGGCCCAGC TGGCCAGAGG GCTTGTCTCT 300 TTCAGTCGCC CTCCCCCAGA GGGAGCAGGA GCAGACAATG GCCACCATGA CTCACCAGTG 360 AGCCATCTTC CCCTCCCCAC CCCTCCAGCC TGGCCCATGA CAGCTTAGCT TGTCCTCCAA 420 GGGAGCTGCA GCCCAGCCTC CCAGGGCCGC CAGCTTCCTC TCTCTTCACC CAACCTGGCT 480 CCCCCCCTGC TTGTGCAACA CCACATCAGA GGGTTGTGAA GTGGAGAGGG AGGAGTTTGA 540 CAGCTGCAGA CCCAGGCAGA CAGAGCAGAC TCCTTTGTGA AGGAGATAGA GGCTGCAGGG 600 GCCCAAGTCC AGCCTGTACT CCCCTGCCCT GACCCACAAG GCATCACCCA GTCTCCCCAA 660 ACCCTAGGGA AGTGGTCATT GTCATTTATT TGTTCCTTTC TTAGATAGAG CTTGGATCCT 720 GTCTGCAATT TATTCCTTCC TGCAAAACCA AGTATGTGAG GCAGAGGAAA GTCCTATTCC 780 ATTCCAGGAG GGACAGGGCT CCCTGTTGGA AAGTATTTCC TTTTGCTAAG TTTCTATCTG 840 CCTCCCGGGT AGACTCCACT AGGCAGTATT TCAAGAAGTT AACGCACTTC CAATCCCCAT 900 CTAACCTATA TTCTTTGCCG CAAGCCAAAT ACCCTTAGTT CTTTCAGTCA TTTCTCCTAA 960 GACATGGATT TAAGACCTTT 980
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