Tag | Content |
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EnhancerAtlas ID | HS037-03455 |
Organism | Homo sapiens |
Tissue/cell | ESC |
Coordinate | chr1:226314220-226317400 |
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: 7 | Chromosome | Start | End |
chr1 | 226314917 | 226315002 | chr1 | 226315055 | 226316024 | chr1 | 226316027 | 226316129 | chr1 | 226314646 | 226315237 | chr1 | 226315631 | 226315825 | chr1 | 226315308 | 226315548 | chr1 | 226316204 | 226316800 |
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| Number: 2 | ID | Chromosome | Start | End |
GH01I226126 | chr1 | 226314498 | 226317175 | GH01I226129 | chr1 | 226317384 | 226317970 |
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Enhancer Sequence | GGCTTATGCC TGTAATCCCA GGACTTTGGG AGGCCAAGGC GGGTGGGTCA CGAGGTCACG 60 AGATCGAGAC CATCCTGGCT AACACAGTGA AACCCCGTCT CTACTAAAAA TACAAAAAAT 120 TAGCTGGGCG TGGTGGCGGG CACCTGTAGT CCCAGCTGCT CGGGAGGCTG AGGCAGAAGA 180 ATGGCATGAA CCTGGGAGGT GGAGGTTGCA GTGAGCTGAG ATCGCGCCAC TGCACTCCAG 240 CCTGGGCGAC AGAGCAAGAA TCCGTCTAAA AAAAAAAGAG AGAGTCCCAG TGCTAAAACT 300 GAGAGTCCTG GGCAAACTGG AACAATTGAT CACACAATAA AGTGGGGGTT CTTGGGCTGG 360 GTATGGAGGC TCATGCTTAT AATCTCAGTG CTTTGGGAGG CCAAGGTGGA AGGATTGCTT 420 GAGCCCAGGG CTTCAAGACC AGCCTGGACA ACATAGCAAG ACCCTATCTC TACAAAAGAA 480 AAAACAAGCA CACACTTGTA GTCCCAGCTA CTTGGGAGGC TGAGGCAGGA GGACTGCTTA 540 AGGCCAGGAG GTGGAGGTTG CAATGGGCTA TGATGGCACC TCTGCACTCC AGCCTCAGTG 600 ACAGAGCAAA ACCTCATTTT GAAAACACAC ACATGAGGGG CGCTGGGAAT AGCCGCTCAT 660 GTCGGCTGAC GGAGCGGTGT GGGGCCGCAT GCGAAGCTGC CTCCGCGCCT TCCCCGAGCG 720 GCTGGCCGCC TGCGGGGCCG AGTAAGGACT TCTGCGCGCG GGAGTTCGAG GCCCTGCGGA 780 GCTGCTTCGC CGCCGCGGCC AAGAAGACGC TGGAGGGAGG CTGTTAGGAG GGACTCTGAG 840 CTTCACACCT GTCTGCTGCC GTGGTTGCAG AGCCCTAGTC CTGATGGCCC CCGGTGGCAT 900 ACATTGAATG CCTAGGGCAG AAAGGAAGTG GGAATGGCGA AGATGTGACG TGCCTCGGTG 960 TTAGATACTG TTTCTTCTTA ACAAGTTGAG GCGTGGGTAG AGCAGGAACT GGTTTTCCAG 1020 CATTGTGTCC GTAAACCTGA GTCAGAATAA GATGTAACAG AAGCCAGATA AAGACTCTGT 1080 CAAATCCTGC AAAAAAAAAA AAAAGAAAAA AAAGAAAACA CACACACACA CACATGCACA 1140 CAATGCATAA AGTGTTTCTG AAACTTTGGT GTGCATGAGA GACACCTGGG GACTTACAAA 1200 AACACAGATG GCTGGCCCCA CCCTAGAGTT TCTAATTTAG TAGGTCCAGG GTGGGGTCCG 1260 GTAATTTGCA TTTCTAACAA GTTTCCTGAT ACTGCTGCTG TTGCTCTTGG TTGGGGCCCA 1320 AACTTCCAGA ACAACTGGTC TGAATGAAGG GCTGGGTCCG GGACCTGCAA GTCCCACTGT 1380 GCTGCTTGCC CCGGTACCTC CTCCTAAGTC TGGCCCAGCA GGAAACGGAG CGCGGGTCAA 1440 AGTCCTCTCA CAGTCAACCA GGAGAAACCT GTGTCTTCCT GGCAGGGTGG CTGGGTGCTA 1500 TGGAAACAAG GCTCAGCCCA GAAGTGCCCA GCCTCCTTCC CAGAAGCAAC TTCAGCCTCT 1560 AGGGGAGGAG TGAAGTGAAC AAACAAACGG AAGGGCAGAG CTCAGTTCCT GGATGGAAGC 1620 GGCACCTGCA TGGAAGCGCC CTCAGCAACC TCAGGGCCCA GACTTCCGGG AAAGTCTCAC 1680 AGGGCCCCTG GCTTGAGTTT TGGAGCTGGA AGGGAACTTT GCAATCTTGG TTCAACTTTT 1740 TGTTTTATTT TCTGAGATGA ATCCTCGCTC TGTTGCCCAG GGTGGGGTGC AGTGGCGCAA 1800 TCTCGGCTCA CTGCAACCTC CGCCTCCCGG GTTCCAGCGA TGCTCCTGCC TCAGCCTCCT 1860 GAGTAGCTGG GATCACAGGT GCCTGCCACC ACGGTTGGCT AAATTTTGTA TTTTTAGTAG 1920 AGATGGGGGT TTCACCATGT TGGCCAGGCT GGTCTCGAAC TCCTTACCTC AGGTGATCCG 1980 CCCACCTCTG CCTTCCAAAG TGCTGGGATT ACAGGCATGA GCCACCGTGC CCGGCCCAGT 2040 ACATCTTTTA ACTGGGCTGT GAATGACACG ACTTGCTAAG ACCTGCCCAC TAAGAATGAG 2100 CTGCAGCCAG CACAATGTTG TCCGCTTCCA GCCACTTTCC TAGATACTCC TCCATTCCTC 2160 AGATTCCAGC CCCCACCCCA GCCTGGAACG CCCACAGTGC TTTTATCACA GCTCTTAACT 2220 CCACTTGGTT CCCCAAAGCT ATGAGCCCAC ATACCACCTC CCAGGGCTAC AACACTTTGG 2280 GTTTCTCAGA CACTGTCAAC ACTAAGCAGC ATGAACTGCA GGACACACAG GACAGCTGGA 2340 GAGGGGCAGT GAGTCACTGT GTCATAGTCC TGCCCAAATT CCAATGTTGA AATTGCAGAA 2400 GCCTGGGGCC CACCCTAGAG AATCTGATTC AGCAGGTTGG AGGGGGGGCC CAGGCACTGA 2460 TATTTTCAAG AGCCCTGGGT GATGTGGATG CCGATAGCAC TGGCTGCATG CTGAGAAACA 2520 CTGCCGATAG CATCATCTTC CACAGAAGGC CACCCAGGAA GAGATGATGA GGTGACAGAA 2580 CTTCATCACC CAACTCAAGA AGGCTTGGGA GGAAGGGGTA ATTTATTGGT TCTAAGCCCA 2640 GACCATGGAC AAAACAGAGT GCTATGGTTC AAATGTCCCC AGCAATGTTC ATGTTGAAAT 2700 GTAATTGCCG TTGTGATGGT GGCATTGGCA GGTGGGGCCT TTGCAAGGTA ATTAGGTTAT 2760 GAGGGCTCTG CCCTCAGGAA TGGATCCATG CCATCATCTC TGGAGTGGGT TCTTGATAAA 2820 AAGGATGATT CTGGACCACT TCCCTCTCAT GTCTCACATG CTTACCTCTG CCTTCCATCC 2880 TTCTGCCATG GTGGGGCCCT CACAAGATGC TGGTGCCATG CTCTTGGACT TTCCAGCCTC 2940 CAGGACTGTG GGAAATCAAT TTCTTTTCCA CCCAGTCTGT GGAATTCTTT TTAAAATTTT 3000 TTATACTATT ATTACTATTA TTATTTGAGA TGGAATCTTG CTCTGTCAGT CACCCAGACT 3060 GGAGTGCAGT GGTGCAATCT CCGCTCACTG CAACCTCCGC CTCCTGGGTT CAAGCAATTC 3120 TCCTGCCTCA GCCTCCCAAG TAGCTGGGAT CACAGGTGTG CGCCACCATG CTCTGCTAAT 3180
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