Tag | Content |
---|
EnhancerAtlas ID | HS101-03722 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr1:205252800-205255350 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Myog | MA0500.1 | chr1:205254178-205254189 | GACAGCTGCAG | + | 6.62 | TFAP4 | MA0691.1 | chr1:205252821-205252831 | ATCAGCTGTT | - | 6.02 | 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: 3 | Chromosome | Start | End |
chr1 | 205254805 | 205255191 | chr1 | 205253892 | 205254222 | chr1 | 205252845 | 205255229 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH01I205283 | chr1 | 205252730 | 205258354 |
|
Enhancer Sequence | AGGTCAGAGT TTGTCTTTTG TATCAGCTGT TTTTCAAGTG AGAGTAACCC TTATGCTGAA 60 ATGGCATATT TTGGTGTGGC ATATTCTGTC CCTCTTCAAA GATACATGAG ACGACATATG 120 CAAAGCATTT TGCATTGTAA GATGCTTATT ACTGTCACTT CACAGATGGG AAATGAGATC 180 TAGGCAACTC TCAGGGTCCA GCCACCAGAA GGTTGAGGAA TGCGGGCTCT AACCTACATC 240 TGTCGACTCC AAAGCCACAC AGCCGCCCAC ACAAGGTAGC TCTTTTCCTC ACCTCACCCC 300 CTGAGCTCTG GAACACCTTT GTTCTGCCCA AACGAGAATG AAGCAGCAAC GGAGGCAGCG 360 GCAGGGGAAC TGTAAGGTGG CCCCAAACTC AGACTGTCCC CAAGTTGGAG GCCTGCTAGG 420 GCCTGGGAGC ACAGCAGTCC CCCACCAGGG AGTCTTCCCT TCCCCACCTG CCCACTGCAG 480 ACTGGGCACC CCTGCTGCAT GTGTCTGACC TCTGTGAACC TCAGTTTCCC CAACATACAA 540 TAACCCTGAC AGTCTGTCAT TCTGTGCTTC TGTGACGTCA GCCTTAGGAG TTATCAGGGA 600 CCCAAACTTG GGCTTCACAG GGGGCAGGAT GGAGGCCCTG CCACTCGGAC CAGACCAGGT 660 TGTGGTGAGG GGCAAGGGTG GTGCCTCCAG GCACCAATCC AGAGTGACCT CACTCTCTGC 720 AGGCTCCCCT GGGGCCCTGA GGGAGGGTGG GGTGCTGGAC AGGCCTGCTA GATGGGAGCA 780 GGTTTGGAAG GAGGTTTAGG AAGGGTGCGG TGGGGAAGGT GTGCCGCTCA GGTTCAGTGT 840 GATCACTAGA GAGGGGCACG CCTGCCTGCA TCGTCTGCCA TGCCAGACAG GGCAGGACAG 900 CTTCTCCCCC AGCCTGGGCC TTTAGGATCC ACTGTGTGAC CATCCTGAGC CCCTTAGCAA 960 GGTGTGAGCG GGGTTGGACA CCCTCCCCTC AACATCCATC TAATGTCAGC CACCAGCCCT 1020 GCCTTGCTGC ATGATGGGAA ATCAGGGTAA GGGAGCCAAA CCCCAGCTGC TCTCAGAGCT 1080 GTGAGGACAA GAGTGGAAAA CCTGCCCTCA CAGGCCCAGC TGGCCAGAGG GCTTGTCTCT 1140 TTCAGTCGCC CTCCCCCAGA GGGAGCAGGA GCAGACAATG GCCACCATGA CTCACCAGTG 1200 AGCCATCTTC CCCTCCCCAC CCCTCCAGCC TGGCCCATGA CAGCTTAGCT TGTCCTCCAA 1260 GGGAGCTGCA GCCCAGCCTC CCAGGGCCGC CAGCTTCCTC TCTCTTCACC CAACCTGGCT 1320 CCCCCCCTGC TTGTGCAACA CCACATCAGA GGGTTGTGAA GTGGAGAGGG AGGAGTTTGA 1380 CAGCTGCAGA CCCAGGCAGA CAGAGCAGAC TCCTTTGTGA AGGAGATAGA GGCTGCAGGG 1440 GCCCAAGTCC AGCCTGTACT CCCCTGCCCT GACCCACAAG GCATCACCCA GTCTCCCCAA 1500 ACCCTAGGGA AGTGGTCATT GTCATTTATT TGTTCCTTTC TTAGATAGAG CTTGGATCCT 1560 GTCTGCAATT TATTCCTTCC TGCAAAACCA AGTATGTGAG GCAGAGGAAA GTCCTATTCC 1620 ATTCCAGGAG GGACAGGGCT CCCTGTTGGA AAGTATTTCC TTTTGCTAAG TTTCTATCTG 1680 CCTCCCGGGT AGACTCCACT AGGCAGTATT TCAAGAAGTT AACGCACTTC CAATCCCCAT 1740 CTAACCTATA TTCTTTGCCG CAAGCCAAAT ACCCTTAGTT CTTTCAGTCA TTTCTCCTAA 1800 GACATGGATT TAAGACCTTT TGACAGCTTG GCCTGTATCC TCTGGAAACA TTTCCATTTA 1860 CCCAAGTTCT TCTTAAAACA TTATGTCTTT GTCCAGGTGC AGTGGCTCAC GCCTGTAATC 1920 TCAAAGTGGA GGCTGAGGGA GGAGCATCAG TTGGGTCCAG GAGTTTGAGA TCAGCCTGGG 1980 CAAGATGACA AGACCCCATC TCTAGTTAAA AAAAAAAAAA AAAATTACTG ATTCTCACCA 2040 AAAAAAAAAA AAAAGCCAGG CGTGAAGACA TGGGCCACCT ACTTGGGAGG CTGAGGTGGG 2100 AAGATCGCTT GAGCCTGGGA GATCAAGGCT CTTGAGCCTG GGAGATCAAG GCTGCAGTGA 2160 GCTGTGATCA CGCCACTGTA CTCTAGCCTA CGCGACAGAG TGAGACTCCA TCTCTAAAAA 2220 AACGAAACTA ACCAACCAAA AAAAAAAAAA AACCACAAAA AGCATGTTGT TTTGAACAGA 2280 GCGCAGTGCT CCAGCTAAGG TCAGGCCAGC ACAGAGGGTG CTAATGAAAT TCACCTCGCA 2340 GGCTCTGGCA CTGTGGTTCT CATGAGCTCT GTTAGCTTGC CGGTATTTTC AGACCCACAT 2400 AGGCATGTCC TTGTTGAGCA GGTCACTTCG GTTCATGAAT ACGGCCACCA AGGATTTGAG 2460 GCCCCTCTGC CTGCCCCCCA TGGAGGGAGC CCTAGGGCTC AGATGGTGGC TCTTAACAGA 2520 CCTCAATGGT CTGATGAAAA CTCTGCATCC 2550
|