| Tag | Content |
|---|
EnhancerAtlas ID | HS122-01198 |
Organism | Homo sapiens |
Tissue/cell | LoVo |
Coordinate | chr1:205253010-205255010 |
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 | GGTTGAGGAA TGCGGGCTCT AACCTACATC TGTCGACTCC AAAGCCACAC AGCCGCCCAC 60
ACAAGGTAGC TCTTTTCCTC ACCTCACCCC CTGAGCTCTG GAACACCTTT GTTCTGCCCA 120
AACGAGAATG AAGCAGCAAC GGAGGCAGCG GCAGGGGAAC TGTAAGGTGG CCCCAAACTC 180
AGACTGTCCC CAAGTTGGAG GCCTGCTAGG GCCTGGGAGC ACAGCAGTCC CCCACCAGGG 240
AGTCTTCCCT TCCCCACCTG CCCACTGCAG ACTGGGCACC CCTGCTGCAT GTGTCTGACC 300
TCTGTGAACC TCAGTTTCCC CAACATACAA TAACCCTGAC AGTCTGTCAT TCTGTGCTTC 360
TGTGACGTCA GCCTTAGGAG TTATCAGGGA CCCAAACTTG GGCTTCACAG GGGGCAGGAT 420
GGAGGCCCTG CCACTCGGAC CAGACCAGGT TGTGGTGAGG GGCAAGGGTG GTGCCTCCAG 480
GCACCAATCC AGAGTGACCT CACTCTCTGC AGGCTCCCCT GGGGCCCTGA GGGAGGGTGG 540
GGTGCTGGAC AGGCCTGCTA GATGGGAGCA GGTTTGGAAG GAGGTTTAGG AAGGGTGCGG 600
TGGGGAAGGT GTGCCGCTCA GGTTCAGTGT GATCACTAGA GAGGGGCACG CCTGCCTGCA 660
TCGTCTGCCA TGCCAGACAG GGCAGGACAG CTTCTCCCCC AGCCTGGGCC TTTAGGATCC 720
ACTGTGTGAC CATCCTGAGC CCCTTAGCAA GGTGTGAGCG GGGTTGGACA CCCTCCCCTC 780
AACATCCATC TAATGTCAGC CACCAGCCCT GCCTTGCTGC ATGATGGGAA ATCAGGGTAA 840
GGGAGCCAAA CCCCAGCTGC TCTCAGAGCT GTGAGGACAA GAGTGGAAAA CCTGCCCTCA 900
CAGGCCCAGC TGGCCAGAGG GCTTGTCTCT TTCAGTCGCC CTCCCCCAGA GGGAGCAGGA 960
GCAGACAATG GCCACCATGA CTCACCAGTG AGCCATCTTC CCCTCCCCAC CCCTCCAGCC 1020
TGGCCCATGA CAGCTTAGCT TGTCCTCCAA GGGAGCTGCA GCCCAGCCTC CCAGGGCCGC 1080
CAGCTTCCTC TCTCTTCACC CAACCTGGCT CCCCCCCTGC TTGTGCAACA CCACATCAGA 1140
GGGTTGTGAA GTGGAGAGGG AGGAGTTTGA CAGCTGCAGA CCCAGGCAGA CAGAGCAGAC 1200
TCCTTTGTGA AGGAGATAGA GGCTGCAGGG GCCCAAGTCC AGCCTGTACT CCCCTGCCCT 1260
GACCCACAAG GCATCACCCA GTCTCCCCAA ACCCTAGGGA AGTGGTCATT GTCATTTATT 1320
TGTTCCTTTC TTAGATAGAG CTTGGATCCT GTCTGCAATT TATTCCTTCC TGCAAAACCA 1380
AGTATGTGAG GCAGAGGAAA GTCCTATTCC ATTCCAGGAG GGACAGGGCT CCCTGTTGGA 1440
AAGTATTTCC TTTTGCTAAG TTTCTATCTG CCTCCCGGGT AGACTCCACT AGGCAGTATT 1500
TCAAGAAGTT AACGCACTTC CAATCCCCAT CTAACCTATA TTCTTTGCCG CAAGCCAAAT 1560
ACCCTTAGTT CTTTCAGTCA TTTCTCCTAA GACATGGATT TAAGACCTTT TGACAGCTTG 1620
GCCTGTATCC TCTGGAAACA TTTCCATTTA CCCAAGTTCT TCTTAAAACA TTATGTCTTT 1680
GTCCAGGTGC AGTGGCTCAC GCCTGTAATC TCAAAGTGGA GGCTGAGGGA GGAGCATCAG 1740
TTGGGTCCAG GAGTTTGAGA TCAGCCTGGG CAAGATGACA AGACCCCATC TCTAGTTAAA 1800
AAAAAAAAAA AAAATTACTG ATTCTCACCA AAAAAAAAAA AAAAGCCAGG CGTGAAGACA 1860
TGGGCCACCT ACTTGGGAGG CTGAGGTGGG AAGATCGCTT GAGCCTGGGA GATCAAGGCT 1920
CTTGAGCCTG GGAGATCAAG GCTGCAGTGA GCTGTGATCA CGCCACTGTA CTCTAGCCTA 1980
CGCGACAGAG TGAGACTCCA 2000
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