Tag | Content |
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EnhancerAtlas ID | HS034-02727 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr1:226314750-226317140 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr1:226317086-226317104 | TCTGCCTTCCATCCTTCT | - | 6.01 | Hnf4a | MA0114.3 | chr1:226315652-226315668 | CGGGTCAAAGTCCTCT | + | 6.49 | STAT3 | MA0144.2 | chr1:226315755-226315766 | CTTCCCAGAAG | - | 6.14 |
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| Number of super-enhancer constituents: 25 | ID | Coordinate | Tissue/cell |
SE_10465 | chr1:226314329-226317263 | CD19_Primary | SE_11118 | chr1:226314228-226323738 | CD20 | SE_23364 | chr1:226314431-226316913 | Colon_Crypt_1 | SE_23849 | chr1:226314482-226315331 | Colon_Crypt_2 | SE_23849 | chr1:226315334-226316161 | Colon_Crypt_2 | SE_23849 | chr1:226316204-226316855 | Colon_Crypt_2 | SE_24831 | chr1:226314416-226316628 | Colon_Crypt_3 | SE_26794 | chr1:226314386-226317368 | Esophagus | SE_31597 | chr1:226314394-226317203 | Gastric | SE_41844 | chr1:226314696-226315324 | LNCaP | SE_41844 | chr1:226315457-226316066 | LNCaP | SE_41844 | chr1:226316166-226316615 | LNCaP | SE_43265 | chr1:226314581-226317218 | Lung | SE_43763 | chr1:226314330-226317236 | MM1S | SE_47729 | chr1:226314790-226315311 | Pancreas | SE_47729 | chr1:226315339-226316040 | Pancreas | SE_47729 | chr1:226316205-226316603 | Pancreas | SE_50502 | chr1:226314371-226317219 | Sigmoid_Colon | SE_52861 | chr1:226314391-226316889 | Small_Intestine | SE_56941 | chr1:226314700-226316129 | VACO_400 | SE_56941 | chr1:226316193-226316621 | VACO_400 | SE_62016 | chr1:226296810-226321627 | Toledo | SE_63137 | chr1:226295246-226322063 | Tonsil | SE_65669 | chr1:226312586-226317084 | Pancreatic_islets | SE_67238 | chr1:226314330-226317236 | MM1S |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 6 | Chromosome | Start | End |
chr1 | 226314917 | 226315002 | chr1 | 226315055 | 226316024 | chr1 | 226316027 | 226316129 | chr1 | 226315631 | 226315825 | chr1 | 226315308 | 226315548 | chr1 | 226316204 | 226316800 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I226126 | chr1 | 226314498 | 226317175 |
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Enhancer Sequence | GGACTGCTTA AGGCCAGGAG GTGGAGGTTG CAATGGGCTA TGATGGCACC TCTGCACTCC 60 AGCCTCAGTG ACAGAGCAAA ACCTCATTTT GAAAACACAC ACATGAGGGG CGCTGGGAAT 120 AGCCGCTCAT GTCGGCTGAC GGAGCGGTGT GGGGCCGCAT GCGAAGCTGC CTCCGCGCCT 180 TCCCCGAGCG GCTGGCCGCC TGCGGGGCCG AGTAAGGACT TCTGCGCGCG GGAGTTCGAG 240 GCCCTGCGGA GCTGCTTCGC CGCCGCGGCC AAGAAGACGC TGGAGGGAGG CTGTTAGGAG 300 GGACTCTGAG CTTCACACCT GTCTGCTGCC GTGGTTGCAG AGCCCTAGTC CTGATGGCCC 360 CCGGTGGCAT ACATTGAATG CCTAGGGCAG AAAGGAAGTG GGAATGGCGA AGATGTGACG 420 TGCCTCGGTG TTAGATACTG TTTCTTCTTA ACAAGTTGAG GCGTGGGTAG AGCAGGAACT 480 GGTTTTCCAG CATTGTGTCC GTAAACCTGA GTCAGAATAA GATGTAACAG AAGCCAGATA 540 AAGACTCTGT CAAATCCTGC AAAAAAAAAA AAAAGAAAAA AAAGAAAACA CACACACACA 600 CACATGCACA CAATGCATAA AGTGTTTCTG AAACTTTGGT GTGCATGAGA GACACCTGGG 660 GACTTACAAA AACACAGATG GCTGGCCCCA CCCTAGAGTT TCTAATTTAG TAGGTCCAGG 720 GTGGGGTCCG GTAATTTGCA TTTCTAACAA GTTTCCTGAT ACTGCTGCTG TTGCTCTTGG 780 TTGGGGCCCA AACTTCCAGA ACAACTGGTC TGAATGAAGG GCTGGGTCCG GGACCTGCAA 840 GTCCCACTGT GCTGCTTGCC CCGGTACCTC CTCCTAAGTC TGGCCCAGCA GGAAACGGAG 900 CGCGGGTCAA AGTCCTCTCA CAGTCAACCA GGAGAAACCT GTGTCTTCCT GGCAGGGTGG 960 CTGGGTGCTA TGGAAACAAG GCTCAGCCCA GAAGTGCCCA GCCTCCTTCC CAGAAGCAAC 1020 TTCAGCCTCT AGGGGAGGAG TGAAGTGAAC AAACAAACGG AAGGGCAGAG CTCAGTTCCT 1080 GGATGGAAGC GGCACCTGCA TGGAAGCGCC CTCAGCAACC TCAGGGCCCA GACTTCCGGG 1140 AAAGTCTCAC AGGGCCCCTG GCTTGAGTTT TGGAGCTGGA AGGGAACTTT GCAATCTTGG 1200 TTCAACTTTT TGTTTTATTT TCTGAGATGA ATCCTCGCTC TGTTGCCCAG GGTGGGGTGC 1260 AGTGGCGCAA TCTCGGCTCA CTGCAACCTC CGCCTCCCGG GTTCCAGCGA TGCTCCTGCC 1320 TCAGCCTCCT GAGTAGCTGG GATCACAGGT GCCTGCCACC ACGGTTGGCT AAATTTTGTA 1380 TTTTTAGTAG AGATGGGGGT TTCACCATGT TGGCCAGGCT GGTCTCGAAC TCCTTACCTC 1440 AGGTGATCCG CCCACCTCTG CCTTCCAAAG TGCTGGGATT ACAGGCATGA GCCACCGTGC 1500 CCGGCCCAGT ACATCTTTTA ACTGGGCTGT GAATGACACG ACTTGCTAAG ACCTGCCCAC 1560 TAAGAATGAG CTGCAGCCAG CACAATGTTG TCCGCTTCCA GCCACTTTCC TAGATACTCC 1620 TCCATTCCTC AGATTCCAGC CCCCACCCCA GCCTGGAACG CCCACAGTGC TTTTATCACA 1680 GCTCTTAACT CCACTTGGTT CCCCAAAGCT ATGAGCCCAC ATACCACCTC CCAGGGCTAC 1740 AACACTTTGG GTTTCTCAGA CACTGTCAAC ACTAAGCAGC ATGAACTGCA GGACACACAG 1800 GACAGCTGGA GAGGGGCAGT GAGTCACTGT GTCATAGTCC TGCCCAAATT CCAATGTTGA 1860 AATTGCAGAA GCCTGGGGCC CACCCTAGAG AATCTGATTC AGCAGGTTGG AGGGGGGGCC 1920 CAGGCACTGA TATTTTCAAG AGCCCTGGGT GATGTGGATG CCGATAGCAC TGGCTGCATG 1980 CTGAGAAACA CTGCCGATAG CATCATCTTC CACAGAAGGC CACCCAGGAA GAGATGATGA 2040 GGTGACAGAA CTTCATCACC CAACTCAAGA AGGCTTGGGA GGAAGGGGTA ATTTATTGGT 2100 TCTAAGCCCA GACCATGGAC AAAACAGAGT GCTATGGTTC AAATGTCCCC AGCAATGTTC 2160 ATGTTGAAAT GTAATTGCCG TTGTGATGGT GGCATTGGCA GGTGGGGCCT TTGCAAGGTA 2220 ATTAGGTTAT GAGGGCTCTG CCCTCAGGAA TGGATCCATG CCATCATCTC TGGAGTGGGT 2280 TCTTGATAAA AAGGATGATT CTGGACCACT TCCCTCTCAT GTCTCACATG CTTACCTCTG 2340 CCTTCCATCC TTCTGCCATG GTGGGGCCCT CACAAGATGC TGGTGCCATG 2390
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