Tag | Content |
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EnhancerAtlas ID | HS050-05508 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr1:205253350-205255390 |
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: 2 | Chromosome | Start | End |
chr1 | 205254805 | 205255191 | chr1 | 205253892 | 205254222 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I205283 | chr1 | 205252730 | 205258354 |
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Enhancer Sequence | AGTCTGTCAT TCTGTGCTTC TGTGACGTCA GCCTTAGGAG TTATCAGGGA CCCAAACTTG 60 GGCTTCACAG GGGGCAGGAT GGAGGCCCTG CCACTCGGAC CAGACCAGGT TGTGGTGAGG 120 GGCAAGGGTG GTGCCTCCAG GCACCAATCC AGAGTGACCT CACTCTCTGC AGGCTCCCCT 180 GGGGCCCTGA GGGAGGGTGG GGTGCTGGAC AGGCCTGCTA GATGGGAGCA GGTTTGGAAG 240 GAGGTTTAGG AAGGGTGCGG TGGGGAAGGT GTGCCGCTCA GGTTCAGTGT GATCACTAGA 300 GAGGGGCACG CCTGCCTGCA TCGTCTGCCA TGCCAGACAG GGCAGGACAG CTTCTCCCCC 360 AGCCTGGGCC TTTAGGATCC ACTGTGTGAC CATCCTGAGC CCCTTAGCAA GGTGTGAGCG 420 GGGTTGGACA CCCTCCCCTC AACATCCATC TAATGTCAGC CACCAGCCCT GCCTTGCTGC 480 ATGATGGGAA ATCAGGGTAA GGGAGCCAAA CCCCAGCTGC TCTCAGAGCT GTGAGGACAA 540 GAGTGGAAAA CCTGCCCTCA CAGGCCCAGC TGGCCAGAGG GCTTGTCTCT TTCAGTCGCC 600 CTCCCCCAGA GGGAGCAGGA GCAGACAATG GCCACCATGA CTCACCAGTG AGCCATCTTC 660 CCCTCCCCAC CCCTCCAGCC TGGCCCATGA CAGCTTAGCT TGTCCTCCAA GGGAGCTGCA 720 GCCCAGCCTC CCAGGGCCGC CAGCTTCCTC TCTCTTCACC CAACCTGGCT CCCCCCCTGC 780 TTGTGCAACA CCACATCAGA GGGTTGTGAA GTGGAGAGGG AGGAGTTTGA CAGCTGCAGA 840 CCCAGGCAGA CAGAGCAGAC TCCTTTGTGA AGGAGATAGA GGCTGCAGGG GCCCAAGTCC 900 AGCCTGTACT CCCCTGCCCT GACCCACAAG GCATCACCCA GTCTCCCCAA ACCCTAGGGA 960 AGTGGTCATT GTCATTTATT TGTTCCTTTC TTAGATAGAG CTTGGATCCT GTCTGCAATT 1020 TATTCCTTCC TGCAAAACCA AGTATGTGAG GCAGAGGAAA GTCCTATTCC ATTCCAGGAG 1080 GGACAGGGCT CCCTGTTGGA AAGTATTTCC TTTTGCTAAG TTTCTATCTG CCTCCCGGGT 1140 AGACTCCACT AGGCAGTATT TCAAGAAGTT AACGCACTTC CAATCCCCAT CTAACCTATA 1200 TTCTTTGCCG CAAGCCAAAT ACCCTTAGTT CTTTCAGTCA TTTCTCCTAA GACATGGATT 1260 TAAGACCTTT TGACAGCTTG GCCTGTATCC TCTGGAAACA TTTCCATTTA CCCAAGTTCT 1320 TCTTAAAACA TTATGTCTTT GTCCAGGTGC AGTGGCTCAC GCCTGTAATC TCAAAGTGGA 1380 GGCTGAGGGA GGAGCATCAG TTGGGTCCAG GAGTTTGAGA TCAGCCTGGG CAAGATGACA 1440 AGACCCCATC TCTAGTTAAA AAAAAAAAAA AAAATTACTG ATTCTCACCA AAAAAAAAAA 1500 AAAAGCCAGG CGTGAAGACA TGGGCCACCT ACTTGGGAGG CTGAGGTGGG AAGATCGCTT 1560 GAGCCTGGGA GATCAAGGCT CTTGAGCCTG GGAGATCAAG GCTGCAGTGA GCTGTGATCA 1620 CGCCACTGTA CTCTAGCCTA CGCGACAGAG TGAGACTCCA TCTCTAAAAA AACGAAACTA 1680 ACCAACCAAA AAAAAAAAAA AACCACAAAA AGCATGTTGT TTTGAACAGA GCGCAGTGCT 1740 CCAGCTAAGG TCAGGCCAGC ACAGAGGGTG CTAATGAAAT TCACCTCGCA GGCTCTGGCA 1800 CTGTGGTTCT CATGAGCTCT GTTAGCTTGC CGGTATTTTC AGACCCACAT AGGCATGTCC 1860 TTGTTGAGCA GGTCACTTCG GTTCATGAAT ACGGCCACCA AGGATTTGAG GCCCCTCTGC 1920 CTGCCCCCCA TGGAGGGAGC CCTAGGGCTC AGATGGTGGC TCTTAACAGA CCTCAATGGT 1980 CTGATGAAAA CTCTGCATCC TCTTCCAAGA AAAACGCATC TACTCAAAAA TTCTCTATAT 2040
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