Tag | Content |
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EnhancerAtlas ID | HS003-03916 |
Organism | Homo sapiens |
Tissue/cell | A549 |
Coordinate | chr1:226314550-226317120 |
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: 1 | ID | Chromosome | Start | End |
GH01I226126 | chr1 | 226314498 | 226317175 |
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Enhancer Sequence | CACACAATAA AGTGGGGGTT CTTGGGCTGG GTATGGAGGC TCATGCTTAT AATCTCAGTG 60 CTTTGGGAGG CCAAGGTGGA AGGATTGCTT GAGCCCAGGG CTTCAAGACC AGCCTGGACA 120 ACATAGCAAG ACCCTATCTC TACAAAAGAA AAAACAAGCA CACACTTGTA GTCCCAGCTA 180 CTTGGGAGGC TGAGGCAGGA GGACTGCTTA AGGCCAGGAG GTGGAGGTTG CAATGGGCTA 240 TGATGGCACC TCTGCACTCC AGCCTCAGTG ACAGAGCAAA ACCTCATTTT GAAAACACAC 300 ACATGAGGGG CGCTGGGAAT AGCCGCTCAT GTCGGCTGAC GGAGCGGTGT GGGGCCGCAT 360 GCGAAGCTGC CTCCGCGCCT TCCCCGAGCG GCTGGCCGCC TGCGGGGCCG AGTAAGGACT 420 TCTGCGCGCG GGAGTTCGAG GCCCTGCGGA GCTGCTTCGC CGCCGCGGCC AAGAAGACGC 480 TGGAGGGAGG CTGTTAGGAG GGACTCTGAG CTTCACACCT GTCTGCTGCC GTGGTTGCAG 540 AGCCCTAGTC CTGATGGCCC CCGGTGGCAT ACATTGAATG CCTAGGGCAG AAAGGAAGTG 600 GGAATGGCGA AGATGTGACG TGCCTCGGTG TTAGATACTG TTTCTTCTTA ACAAGTTGAG 660 GCGTGGGTAG AGCAGGAACT GGTTTTCCAG CATTGTGTCC GTAAACCTGA GTCAGAATAA 720 GATGTAACAG AAGCCAGATA AAGACTCTGT CAAATCCTGC AAAAAAAAAA AAAAGAAAAA 780 AAAGAAAACA CACACACACA CACATGCACA CAATGCATAA AGTGTTTCTG AAACTTTGGT 840 GTGCATGAGA GACACCTGGG GACTTACAAA AACACAGATG GCTGGCCCCA CCCTAGAGTT 900 TCTAATTTAG TAGGTCCAGG GTGGGGTCCG GTAATTTGCA TTTCTAACAA GTTTCCTGAT 960 ACTGCTGCTG TTGCTCTTGG TTGGGGCCCA AACTTCCAGA ACAACTGGTC TGAATGAAGG 1020 GCTGGGTCCG GGACCTGCAA GTCCCACTGT GCTGCTTGCC CCGGTACCTC CTCCTAAGTC 1080 TGGCCCAGCA GGAAACGGAG CGCGGGTCAA AGTCCTCTCA CAGTCAACCA GGAGAAACCT 1140 GTGTCTTCCT GGCAGGGTGG CTGGGTGCTA TGGAAACAAG GCTCAGCCCA GAAGTGCCCA 1200 GCCTCCTTCC CAGAAGCAAC TTCAGCCTCT AGGGGAGGAG TGAAGTGAAC AAACAAACGG 1260 AAGGGCAGAG CTCAGTTCCT GGATGGAAGC GGCACCTGCA TGGAAGCGCC CTCAGCAACC 1320 TCAGGGCCCA GACTTCCGGG AAAGTCTCAC AGGGCCCCTG GCTTGAGTTT TGGAGCTGGA 1380 AGGGAACTTT GCAATCTTGG TTCAACTTTT TGTTTTATTT TCTGAGATGA ATCCTCGCTC 1440 TGTTGCCCAG GGTGGGGTGC AGTGGCGCAA TCTCGGCTCA CTGCAACCTC CGCCTCCCGG 1500 GTTCCAGCGA TGCTCCTGCC TCAGCCTCCT GAGTAGCTGG GATCACAGGT GCCTGCCACC 1560 ACGGTTGGCT AAATTTTGTA TTTTTAGTAG AGATGGGGGT TTCACCATGT TGGCCAGGCT 1620 GGTCTCGAAC TCCTTACCTC AGGTGATCCG CCCACCTCTG CCTTCCAAAG TGCTGGGATT 1680 ACAGGCATGA GCCACCGTGC CCGGCCCAGT ACATCTTTTA ACTGGGCTGT GAATGACACG 1740 ACTTGCTAAG ACCTGCCCAC TAAGAATGAG CTGCAGCCAG CACAATGTTG TCCGCTTCCA 1800 GCCACTTTCC TAGATACTCC TCCATTCCTC AGATTCCAGC CCCCACCCCA GCCTGGAACG 1860 CCCACAGTGC TTTTATCACA GCTCTTAACT CCACTTGGTT CCCCAAAGCT ATGAGCCCAC 1920 ATACCACCTC CCAGGGCTAC AACACTTTGG GTTTCTCAGA CACTGTCAAC ACTAAGCAGC 1980 ATGAACTGCA GGACACACAG GACAGCTGGA GAGGGGCAGT GAGTCACTGT GTCATAGTCC 2040 TGCCCAAATT CCAATGTTGA AATTGCAGAA GCCTGGGGCC CACCCTAGAG AATCTGATTC 2100 AGCAGGTTGG AGGGGGGGCC CAGGCACTGA TATTTTCAAG AGCCCTGGGT GATGTGGATG 2160 CCGATAGCAC TGGCTGCATG CTGAGAAACA CTGCCGATAG CATCATCTTC CACAGAAGGC 2220 CACCCAGGAA GAGATGATGA GGTGACAGAA CTTCATCACC CAACTCAAGA AGGCTTGGGA 2280 GGAAGGGGTA ATTTATTGGT TCTAAGCCCA GACCATGGAC AAAACAGAGT GCTATGGTTC 2340 AAATGTCCCC AGCAATGTTC ATGTTGAAAT GTAATTGCCG TTGTGATGGT GGCATTGGCA 2400 GGTGGGGCCT TTGCAAGGTA ATTAGGTTAT GAGGGCTCTG CCCTCAGGAA TGGATCCATG 2460 CCATCATCTC TGGAGTGGGT TCTTGATAAA AAGGATGATT CTGGACCACT TCCCTCTCAT 2520 GTCTCACATG CTTACCTCTG CCTTCCATCC TTCTGCCATG GTGGGGCCCT 2570
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