Tag | Content |
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EnhancerAtlas ID | HS048-03174 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr1:205253420-205254420 |
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 | GGGGCAGGAT GGAGGCCCTG CCACTCGGAC CAGACCAGGT TGTGGTGAGG GGCAAGGGTG 60 GTGCCTCCAG GCACCAATCC AGAGTGACCT CACTCTCTGC AGGCTCCCCT GGGGCCCTGA 120 GGGAGGGTGG GGTGCTGGAC AGGCCTGCTA GATGGGAGCA GGTTTGGAAG GAGGTTTAGG 180 AAGGGTGCGG TGGGGAAGGT GTGCCGCTCA GGTTCAGTGT GATCACTAGA GAGGGGCACG 240 CCTGCCTGCA TCGTCTGCCA TGCCAGACAG GGCAGGACAG CTTCTCCCCC AGCCTGGGCC 300 TTTAGGATCC ACTGTGTGAC CATCCTGAGC CCCTTAGCAA GGTGTGAGCG GGGTTGGACA 360 CCCTCCCCTC AACATCCATC TAATGTCAGC CACCAGCCCT GCCTTGCTGC ATGATGGGAA 420 ATCAGGGTAA GGGAGCCAAA CCCCAGCTGC TCTCAGAGCT GTGAGGACAA GAGTGGAAAA 480 CCTGCCCTCA CAGGCCCAGC TGGCCAGAGG GCTTGTCTCT TTCAGTCGCC CTCCCCCAGA 540 GGGAGCAGGA GCAGACAATG GCCACCATGA CTCACCAGTG AGCCATCTTC CCCTCCCCAC 600 CCCTCCAGCC TGGCCCATGA CAGCTTAGCT TGTCCTCCAA GGGAGCTGCA GCCCAGCCTC 660 CCAGGGCCGC CAGCTTCCTC TCTCTTCACC CAACCTGGCT CCCCCCCTGC TTGTGCAACA 720 CCACATCAGA GGGTTGTGAA GTGGAGAGGG AGGAGTTTGA CAGCTGCAGA CCCAGGCAGA 780 CAGAGCAGAC TCCTTTGTGA AGGAGATAGA GGCTGCAGGG GCCCAAGTCC AGCCTGTACT 840 CCCCTGCCCT GACCCACAAG GCATCACCCA GTCTCCCCAA ACCCTAGGGA AGTGGTCATT 900 GTCATTTATT TGTTCCTTTC TTAGATAGAG CTTGGATCCT GTCTGCAATT TATTCCTTCC 960 TGCAAAACCA AGTATGTGAG GCAGAGGAAA GTCCTATTCC 1000
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