| Tag | Content |
|---|
EnhancerAtlas ID | HS193-02882 |
Organism | Homo sapiens |
Tissue/cell | U87 |
Coordinate | chr1:205253110-205255440 |
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 | | ZEB1 | MA0103.3 | chr1:205253262-205253273 | CCCACCTGCCC | + | 6.14 |
|
| | 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 |
|
| | 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 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I205283 | chr1 | 205252730 | 205258354 |
|
Enhancer Sequence | GAACACCTTT GTTCTGCCCA AACGAGAATG AAGCAGCAAC GGAGGCAGCG GCAGGGGAAC 60
TGTAAGGTGG CCCCAAACTC AGACTGTCCC CAAGTTGGAG GCCTGCTAGG GCCTGGGAGC 120
ACAGCAGTCC CCCACCAGGG AGTCTTCCCT TCCCCACCTG CCCACTGCAG ACTGGGCACC 180
CCTGCTGCAT GTGTCTGACC TCTGTGAACC TCAGTTTCCC CAACATACAA TAACCCTGAC 240
AGTCTGTCAT TCTGTGCTTC TGTGACGTCA GCCTTAGGAG TTATCAGGGA CCCAAACTTG 300
GGCTTCACAG GGGGCAGGAT GGAGGCCCTG CCACTCGGAC CAGACCAGGT TGTGGTGAGG 360
GGCAAGGGTG GTGCCTCCAG GCACCAATCC AGAGTGACCT CACTCTCTGC AGGCTCCCCT 420
GGGGCCCTGA GGGAGGGTGG GGTGCTGGAC AGGCCTGCTA GATGGGAGCA GGTTTGGAAG 480
GAGGTTTAGG AAGGGTGCGG TGGGGAAGGT GTGCCGCTCA GGTTCAGTGT GATCACTAGA 540
GAGGGGCACG CCTGCCTGCA TCGTCTGCCA TGCCAGACAG GGCAGGACAG CTTCTCCCCC 600
AGCCTGGGCC TTTAGGATCC ACTGTGTGAC CATCCTGAGC CCCTTAGCAA GGTGTGAGCG 660
GGGTTGGACA CCCTCCCCTC AACATCCATC TAATGTCAGC CACCAGCCCT GCCTTGCTGC 720
ATGATGGGAA ATCAGGGTAA GGGAGCCAAA CCCCAGCTGC TCTCAGAGCT GTGAGGACAA 780
GAGTGGAAAA CCTGCCCTCA CAGGCCCAGC TGGCCAGAGG GCTTGTCTCT TTCAGTCGCC 840
CTCCCCCAGA GGGAGCAGGA GCAGACAATG GCCACCATGA CTCACCAGTG AGCCATCTTC 900
CCCTCCCCAC CCCTCCAGCC TGGCCCATGA CAGCTTAGCT TGTCCTCCAA GGGAGCTGCA 960
GCCCAGCCTC CCAGGGCCGC CAGCTTCCTC TCTCTTCACC CAACCTGGCT CCCCCCCTGC 1020
TTGTGCAACA CCACATCAGA GGGTTGTGAA GTGGAGAGGG AGGAGTTTGA CAGCTGCAGA 1080
CCCAGGCAGA CAGAGCAGAC TCCTTTGTGA AGGAGATAGA GGCTGCAGGG GCCCAAGTCC 1140
AGCCTGTACT CCCCTGCCCT GACCCACAAG GCATCACCCA GTCTCCCCAA ACCCTAGGGA 1200
AGTGGTCATT GTCATTTATT TGTTCCTTTC TTAGATAGAG CTTGGATCCT GTCTGCAATT 1260
TATTCCTTCC TGCAAAACCA AGTATGTGAG GCAGAGGAAA GTCCTATTCC ATTCCAGGAG 1320
GGACAGGGCT CCCTGTTGGA AAGTATTTCC TTTTGCTAAG TTTCTATCTG CCTCCCGGGT 1380
AGACTCCACT AGGCAGTATT TCAAGAAGTT AACGCACTTC CAATCCCCAT CTAACCTATA 1440
TTCTTTGCCG CAAGCCAAAT ACCCTTAGTT CTTTCAGTCA TTTCTCCTAA GACATGGATT 1500
TAAGACCTTT TGACAGCTTG GCCTGTATCC TCTGGAAACA TTTCCATTTA CCCAAGTTCT 1560
TCTTAAAACA TTATGTCTTT GTCCAGGTGC AGTGGCTCAC GCCTGTAATC TCAAAGTGGA 1620
GGCTGAGGGA GGAGCATCAG TTGGGTCCAG GAGTTTGAGA TCAGCCTGGG CAAGATGACA 1680
AGACCCCATC TCTAGTTAAA AAAAAAAAAA AAAATTACTG ATTCTCACCA AAAAAAAAAA 1740
AAAAGCCAGG CGTGAAGACA TGGGCCACCT ACTTGGGAGG CTGAGGTGGG AAGATCGCTT 1800
GAGCCTGGGA GATCAAGGCT CTTGAGCCTG GGAGATCAAG GCTGCAGTGA GCTGTGATCA 1860
CGCCACTGTA CTCTAGCCTA CGCGACAGAG TGAGACTCCA TCTCTAAAAA AACGAAACTA 1920
ACCAACCAAA AAAAAAAAAA AACCACAAAA AGCATGTTGT TTTGAACAGA GCGCAGTGCT 1980
CCAGCTAAGG TCAGGCCAGC ACAGAGGGTG CTAATGAAAT TCACCTCGCA GGCTCTGGCA 2040
CTGTGGTTCT CATGAGCTCT GTTAGCTTGC CGGTATTTTC AGACCCACAT AGGCATGTCC 2100
TTGTTGAGCA GGTCACTTCG GTTCATGAAT ACGGCCACCA AGGATTTGAG GCCCCTCTGC 2160
CTGCCCCCCA TGGAGGGAGC CCTAGGGCTC AGATGGTGGC TCTTAACAGA CCTCAATGGT 2220
CTGATGAAAA CTCTGCATCC TCTTCCAAGA AAAACGCATC TACTCAAAAA TTCTCTATAT 2280
GACACCAGGA CTCCCTGCAG ACCATCCTCA GACCCCAGGT TAGGAATTTC 2330
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