| Tag | Content |
|---|
EnhancerAtlas ID | HS037-03100 |
Organism | Homo sapiens |
Tissue/cell | ESC |
Coordinate | chr1:205253040-205255070 |
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: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I205283 | chr1 | 205252730 | 205258354 |
|
Enhancer Sequence | TGTCGACTCC AAAGCCACAC AGCCGCCCAC ACAAGGTAGC TCTTTTCCTC ACCTCACCCC 60
CTGAGCTCTG GAACACCTTT GTTCTGCCCA AACGAGAATG AAGCAGCAAC GGAGGCAGCG 120
GCAGGGGAAC TGTAAGGTGG CCCCAAACTC AGACTGTCCC CAAGTTGGAG GCCTGCTAGG 180
GCCTGGGAGC ACAGCAGTCC CCCACCAGGG AGTCTTCCCT TCCCCACCTG CCCACTGCAG 240
ACTGGGCACC CCTGCTGCAT GTGTCTGACC TCTGTGAACC TCAGTTTCCC CAACATACAA 300
TAACCCTGAC AGTCTGTCAT TCTGTGCTTC TGTGACGTCA GCCTTAGGAG TTATCAGGGA 360
CCCAAACTTG GGCTTCACAG GGGGCAGGAT GGAGGCCCTG CCACTCGGAC CAGACCAGGT 420
TGTGGTGAGG GGCAAGGGTG GTGCCTCCAG GCACCAATCC AGAGTGACCT CACTCTCTGC 480
AGGCTCCCCT GGGGCCCTGA GGGAGGGTGG GGTGCTGGAC AGGCCTGCTA GATGGGAGCA 540
GGTTTGGAAG GAGGTTTAGG AAGGGTGCGG TGGGGAAGGT GTGCCGCTCA GGTTCAGTGT 600
GATCACTAGA GAGGGGCACG CCTGCCTGCA TCGTCTGCCA TGCCAGACAG GGCAGGACAG 660
CTTCTCCCCC AGCCTGGGCC TTTAGGATCC ACTGTGTGAC CATCCTGAGC CCCTTAGCAA 720
GGTGTGAGCG GGGTTGGACA CCCTCCCCTC AACATCCATC TAATGTCAGC CACCAGCCCT 780
GCCTTGCTGC ATGATGGGAA ATCAGGGTAA GGGAGCCAAA CCCCAGCTGC TCTCAGAGCT 840
GTGAGGACAA GAGTGGAAAA CCTGCCCTCA CAGGCCCAGC TGGCCAGAGG GCTTGTCTCT 900
TTCAGTCGCC CTCCCCCAGA GGGAGCAGGA GCAGACAATG GCCACCATGA CTCACCAGTG 960
AGCCATCTTC CCCTCCCCAC CCCTCCAGCC TGGCCCATGA CAGCTTAGCT TGTCCTCCAA 1020
GGGAGCTGCA GCCCAGCCTC CCAGGGCCGC CAGCTTCCTC TCTCTTCACC CAACCTGGCT 1080
CCCCCCCTGC TTGTGCAACA CCACATCAGA GGGTTGTGAA GTGGAGAGGG AGGAGTTTGA 1140
CAGCTGCAGA CCCAGGCAGA CAGAGCAGAC TCCTTTGTGA AGGAGATAGA GGCTGCAGGG 1200
GCCCAAGTCC AGCCTGTACT CCCCTGCCCT GACCCACAAG GCATCACCCA GTCTCCCCAA 1260
ACCCTAGGGA AGTGGTCATT GTCATTTATT TGTTCCTTTC TTAGATAGAG CTTGGATCCT 1320
GTCTGCAATT TATTCCTTCC TGCAAAACCA AGTATGTGAG GCAGAGGAAA GTCCTATTCC 1380
ATTCCAGGAG GGACAGGGCT CCCTGTTGGA AAGTATTTCC TTTTGCTAAG TTTCTATCTG 1440
CCTCCCGGGT AGACTCCACT AGGCAGTATT TCAAGAAGTT AACGCACTTC CAATCCCCAT 1500
CTAACCTATA TTCTTTGCCG CAAGCCAAAT ACCCTTAGTT CTTTCAGTCA TTTCTCCTAA 1560
GACATGGATT TAAGACCTTT TGACAGCTTG GCCTGTATCC TCTGGAAACA TTTCCATTTA 1620
CCCAAGTTCT TCTTAAAACA TTATGTCTTT GTCCAGGTGC AGTGGCTCAC GCCTGTAATC 1680
TCAAAGTGGA GGCTGAGGGA GGAGCATCAG TTGGGTCCAG GAGTTTGAGA TCAGCCTGGG 1740
CAAGATGACA AGACCCCATC TCTAGTTAAA AAAAAAAAAA AAAATTACTG ATTCTCACCA 1800
AAAAAAAAAA AAAAGCCAGG CGTGAAGACA TGGGCCACCT ACTTGGGAGG CTGAGGTGGG 1860
AAGATCGCTT GAGCCTGGGA GATCAAGGCT CTTGAGCCTG GGAGATCAAG GCTGCAGTGA 1920
GCTGTGATCA CGCCACTGTA CTCTAGCCTA CGCGACAGAG TGAGACTCCA TCTCTAAAAA 1980
AACGAAACTA ACCAACCAAA AAAAAAAAAA AACCACAAAA AGCATGTTGT 2030
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