Tag | Content |
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EnhancerAtlas ID | HS034-02526 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr1:205252740-205254560 |
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 |
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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: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I205283 | chr1 | 205252730 | 205258354 |
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Enhancer Sequence | CTCCTCATCT CTGGTGACAA AAACGTTTCT TTCCCCCCGG GGACAGGGAG AAAAGGGAGG 60 AGGTCAGAGT TTGTCTTTTG TATCAGCTGT TTTTCAAGTG AGAGTAACCC TTATGCTGAA 120 ATGGCATATT TTGGTGTGGC ATATTCTGTC CCTCTTCAAA GATACATGAG ACGACATATG 180 CAAAGCATTT TGCATTGTAA GATGCTTATT ACTGTCACTT CACAGATGGG AAATGAGATC 240 TAGGCAACTC TCAGGGTCCA GCCACCAGAA GGTTGAGGAA TGCGGGCTCT AACCTACATC 300 TGTCGACTCC AAAGCCACAC AGCCGCCCAC ACAAGGTAGC TCTTTTCCTC ACCTCACCCC 360 CTGAGCTCTG GAACACCTTT GTTCTGCCCA AACGAGAATG AAGCAGCAAC GGAGGCAGCG 420 GCAGGGGAAC TGTAAGGTGG CCCCAAACTC AGACTGTCCC CAAGTTGGAG GCCTGCTAGG 480 GCCTGGGAGC ACAGCAGTCC CCCACCAGGG AGTCTTCCCT TCCCCACCTG CCCACTGCAG 540 ACTGGGCACC CCTGCTGCAT GTGTCTGACC TCTGTGAACC TCAGTTTCCC CAACATACAA 600 TAACCCTGAC AGTCTGTCAT TCTGTGCTTC TGTGACGTCA GCCTTAGGAG TTATCAGGGA 660 CCCAAACTTG GGCTTCACAG GGGGCAGGAT GGAGGCCCTG CCACTCGGAC CAGACCAGGT 720 TGTGGTGAGG GGCAAGGGTG GTGCCTCCAG GCACCAATCC AGAGTGACCT CACTCTCTGC 780 AGGCTCCCCT GGGGCCCTGA GGGAGGGTGG GGTGCTGGAC AGGCCTGCTA GATGGGAGCA 840 GGTTTGGAAG GAGGTTTAGG AAGGGTGCGG TGGGGAAGGT GTGCCGCTCA GGTTCAGTGT 900 GATCACTAGA GAGGGGCACG CCTGCCTGCA TCGTCTGCCA TGCCAGACAG GGCAGGACAG 960 CTTCTCCCCC AGCCTGGGCC TTTAGGATCC ACTGTGTGAC CATCCTGAGC CCCTTAGCAA 1020 GGTGTGAGCG GGGTTGGACA CCCTCCCCTC AACATCCATC TAATGTCAGC CACCAGCCCT 1080 GCCTTGCTGC ATGATGGGAA ATCAGGGTAA GGGAGCCAAA CCCCAGCTGC TCTCAGAGCT 1140 GTGAGGACAA GAGTGGAAAA CCTGCCCTCA CAGGCCCAGC TGGCCAGAGG GCTTGTCTCT 1200 TTCAGTCGCC CTCCCCCAGA GGGAGCAGGA GCAGACAATG GCCACCATGA CTCACCAGTG 1260 AGCCATCTTC CCCTCCCCAC CCCTCCAGCC TGGCCCATGA CAGCTTAGCT TGTCCTCCAA 1320 GGGAGCTGCA GCCCAGCCTC CCAGGGCCGC CAGCTTCCTC TCTCTTCACC CAACCTGGCT 1380 CCCCCCCTGC TTGTGCAACA CCACATCAGA GGGTTGTGAA GTGGAGAGGG AGGAGTTTGA 1440 CAGCTGCAGA CCCAGGCAGA CAGAGCAGAC TCCTTTGTGA AGGAGATAGA GGCTGCAGGG 1500 GCCCAAGTCC AGCCTGTACT CCCCTGCCCT GACCCACAAG GCATCACCCA GTCTCCCCAA 1560 ACCCTAGGGA AGTGGTCATT GTCATTTATT TGTTCCTTTC TTAGATAGAG CTTGGATCCT 1620 GTCTGCAATT TATTCCTTCC TGCAAAACCA AGTATGTGAG GCAGAGGAAA GTCCTATTCC 1680 ATTCCAGGAG GGACAGGGCT CCCTGTTGGA AAGTATTTCC TTTTGCTAAG TTTCTATCTG 1740 CCTCCCGGGT AGACTCCACT AGGCAGTATT TCAAGAAGTT AACGCACTTC CAATCCCCAT 1800 CTAACCTATA TTCTTTGCCG 1820
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