Tag | Content |
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EnhancerAtlas ID | HS078-01828 |
Organism | Homo sapiens |
Tissue/cell | H2171 |
Coordinate | chr1:205253470-205254680 |
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 | GGCAAGGGTG GTGCCTCCAG GCACCAATCC AGAGTGACCT CACTCTCTGC AGGCTCCCCT 60 GGGGCCCTGA GGGAGGGTGG GGTGCTGGAC AGGCCTGCTA GATGGGAGCA GGTTTGGAAG 120 GAGGTTTAGG AAGGGTGCGG TGGGGAAGGT GTGCCGCTCA GGTTCAGTGT GATCACTAGA 180 GAGGGGCACG CCTGCCTGCA TCGTCTGCCA TGCCAGACAG GGCAGGACAG CTTCTCCCCC 240 AGCCTGGGCC TTTAGGATCC ACTGTGTGAC CATCCTGAGC CCCTTAGCAA GGTGTGAGCG 300 GGGTTGGACA CCCTCCCCTC AACATCCATC TAATGTCAGC CACCAGCCCT GCCTTGCTGC 360 ATGATGGGAA ATCAGGGTAA GGGAGCCAAA CCCCAGCTGC TCTCAGAGCT GTGAGGACAA 420 GAGTGGAAAA CCTGCCCTCA CAGGCCCAGC TGGCCAGAGG GCTTGTCTCT TTCAGTCGCC 480 CTCCCCCAGA GGGAGCAGGA GCAGACAATG GCCACCATGA CTCACCAGTG AGCCATCTTC 540 CCCTCCCCAC CCCTCCAGCC TGGCCCATGA CAGCTTAGCT TGTCCTCCAA GGGAGCTGCA 600 GCCCAGCCTC CCAGGGCCGC CAGCTTCCTC TCTCTTCACC CAACCTGGCT CCCCCCCTGC 660 TTGTGCAACA CCACATCAGA GGGTTGTGAA GTGGAGAGGG AGGAGTTTGA CAGCTGCAGA 720 CCCAGGCAGA CAGAGCAGAC TCCTTTGTGA AGGAGATAGA GGCTGCAGGG GCCCAAGTCC 780 AGCCTGTACT CCCCTGCCCT GACCCACAAG GCATCACCCA GTCTCCCCAA ACCCTAGGGA 840 AGTGGTCATT GTCATTTATT TGTTCCTTTC TTAGATAGAG CTTGGATCCT GTCTGCAATT 900 TATTCCTTCC TGCAAAACCA AGTATGTGAG GCAGAGGAAA GTCCTATTCC ATTCCAGGAG 960 GGACAGGGCT CCCTGTTGGA AAGTATTTCC TTTTGCTAAG TTTCTATCTG CCTCCCGGGT 1020 AGACTCCACT AGGCAGTATT TCAAGAAGTT AACGCACTTC CAATCCCCAT CTAACCTATA 1080 TTCTTTGCCG CAAGCCAAAT ACCCTTAGTT CTTTCAGTCA TTTCTCCTAA GACATGGATT 1140 TAAGACCTTT TGACAGCTTG GCCTGTATCC TCTGGAAACA TTTCCATTTA CCCAAGTTCT 1200 TCTTAAAACA 1210
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