Tag | Content |
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EnhancerAtlas ID | HS109-01811 |
Organism | Homo sapiens |
Tissue/cell | Kasumi-1 |
Coordinate | chr1:205253540-205254640 |
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 | GGGAGGGTGG GGTGCTGGAC AGGCCTGCTA GATGGGAGCA GGTTTGGAAG GAGGTTTAGG 60 AAGGGTGCGG TGGGGAAGGT GTGCCGCTCA GGTTCAGTGT GATCACTAGA GAGGGGCACG 120 CCTGCCTGCA TCGTCTGCCA TGCCAGACAG GGCAGGACAG CTTCTCCCCC AGCCTGGGCC 180 TTTAGGATCC ACTGTGTGAC CATCCTGAGC CCCTTAGCAA GGTGTGAGCG GGGTTGGACA 240 CCCTCCCCTC AACATCCATC TAATGTCAGC CACCAGCCCT GCCTTGCTGC ATGATGGGAA 300 ATCAGGGTAA GGGAGCCAAA CCCCAGCTGC TCTCAGAGCT GTGAGGACAA GAGTGGAAAA 360 CCTGCCCTCA CAGGCCCAGC TGGCCAGAGG GCTTGTCTCT TTCAGTCGCC CTCCCCCAGA 420 GGGAGCAGGA GCAGACAATG GCCACCATGA CTCACCAGTG AGCCATCTTC CCCTCCCCAC 480 CCCTCCAGCC TGGCCCATGA CAGCTTAGCT TGTCCTCCAA GGGAGCTGCA GCCCAGCCTC 540 CCAGGGCCGC CAGCTTCCTC TCTCTTCACC CAACCTGGCT CCCCCCCTGC TTGTGCAACA 600 CCACATCAGA GGGTTGTGAA GTGGAGAGGG AGGAGTTTGA CAGCTGCAGA CCCAGGCAGA 660 CAGAGCAGAC TCCTTTGTGA AGGAGATAGA GGCTGCAGGG GCCCAAGTCC AGCCTGTACT 720 CCCCTGCCCT GACCCACAAG GCATCACCCA GTCTCCCCAA ACCCTAGGGA AGTGGTCATT 780 GTCATTTATT TGTTCCTTTC TTAGATAGAG CTTGGATCCT GTCTGCAATT TATTCCTTCC 840 TGCAAAACCA AGTATGTGAG GCAGAGGAAA GTCCTATTCC ATTCCAGGAG GGACAGGGCT 900 CCCTGTTGGA AAGTATTTCC TTTTGCTAAG TTTCTATCTG CCTCCCGGGT AGACTCCACT 960 AGGCAGTATT TCAAGAAGTT AACGCACTTC CAATCCCCAT CTAACCTATA TTCTTTGCCG 1020 CAAGCCAAAT ACCCTTAGTT CTTTCAGTCA TTTCTCCTAA GACATGGATT TAAGACCTTT 1080 TGACAGCTTG GCCTGTATCC 1100
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