Tag | Content |
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EnhancerAtlas ID | HS053-03909 |
Organism | Homo sapiens |
Tissue/cell | Foreskin_keratinocyte |
Coordinate | chr1:226314470-226317190 |
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 | AGAGCAAGAA TCCGTCTAAA AAAAAAAGAG AGAGTCCCAG TGCTAAAACT GAGAGTCCTG 60 GGCAAACTGG AACAATTGAT CACACAATAA AGTGGGGGTT CTTGGGCTGG GTATGGAGGC 120 TCATGCTTAT AATCTCAGTG CTTTGGGAGG CCAAGGTGGA AGGATTGCTT GAGCCCAGGG 180 CTTCAAGACC AGCCTGGACA ACATAGCAAG ACCCTATCTC TACAAAAGAA AAAACAAGCA 240 CACACTTGTA GTCCCAGCTA CTTGGGAGGC TGAGGCAGGA GGACTGCTTA AGGCCAGGAG 300 GTGGAGGTTG CAATGGGCTA TGATGGCACC TCTGCACTCC AGCCTCAGTG ACAGAGCAAA 360 ACCTCATTTT GAAAACACAC ACATGAGGGG CGCTGGGAAT AGCCGCTCAT GTCGGCTGAC 420 GGAGCGGTGT GGGGCCGCAT GCGAAGCTGC CTCCGCGCCT TCCCCGAGCG GCTGGCCGCC 480 TGCGGGGCCG AGTAAGGACT TCTGCGCGCG GGAGTTCGAG GCCCTGCGGA GCTGCTTCGC 540 CGCCGCGGCC AAGAAGACGC TGGAGGGAGG CTGTTAGGAG GGACTCTGAG CTTCACACCT 600 GTCTGCTGCC GTGGTTGCAG AGCCCTAGTC CTGATGGCCC CCGGTGGCAT ACATTGAATG 660 CCTAGGGCAG AAAGGAAGTG GGAATGGCGA AGATGTGACG TGCCTCGGTG TTAGATACTG 720 TTTCTTCTTA ACAAGTTGAG GCGTGGGTAG AGCAGGAACT GGTTTTCCAG CATTGTGTCC 780 GTAAACCTGA GTCAGAATAA GATGTAACAG AAGCCAGATA AAGACTCTGT CAAATCCTGC 840 AAAAAAAAAA AAAAGAAAAA AAAGAAAACA CACACACACA CACATGCACA CAATGCATAA 900 AGTGTTTCTG AAACTTTGGT GTGCATGAGA GACACCTGGG GACTTACAAA AACACAGATG 960 GCTGGCCCCA CCCTAGAGTT TCTAATTTAG TAGGTCCAGG GTGGGGTCCG GTAATTTGCA 1020 TTTCTAACAA GTTTCCTGAT ACTGCTGCTG TTGCTCTTGG TTGGGGCCCA AACTTCCAGA 1080 ACAACTGGTC TGAATGAAGG GCTGGGTCCG GGACCTGCAA GTCCCACTGT GCTGCTTGCC 1140 CCGGTACCTC CTCCTAAGTC TGGCCCAGCA GGAAACGGAG CGCGGGTCAA AGTCCTCTCA 1200 CAGTCAACCA GGAGAAACCT GTGTCTTCCT GGCAGGGTGG CTGGGTGCTA TGGAAACAAG 1260 GCTCAGCCCA GAAGTGCCCA GCCTCCTTCC CAGAAGCAAC TTCAGCCTCT AGGGGAGGAG 1320 TGAAGTGAAC AAACAAACGG AAGGGCAGAG CTCAGTTCCT GGATGGAAGC GGCACCTGCA 1380 TGGAAGCGCC CTCAGCAACC TCAGGGCCCA GACTTCCGGG AAAGTCTCAC AGGGCCCCTG 1440 GCTTGAGTTT TGGAGCTGGA AGGGAACTTT GCAATCTTGG TTCAACTTTT TGTTTTATTT 1500 TCTGAGATGA ATCCTCGCTC TGTTGCCCAG GGTGGGGTGC AGTGGCGCAA TCTCGGCTCA 1560 CTGCAACCTC CGCCTCCCGG GTTCCAGCGA TGCTCCTGCC TCAGCCTCCT GAGTAGCTGG 1620 GATCACAGGT GCCTGCCACC ACGGTTGGCT AAATTTTGTA TTTTTAGTAG AGATGGGGGT 1680 TTCACCATGT TGGCCAGGCT GGTCTCGAAC TCCTTACCTC AGGTGATCCG CCCACCTCTG 1740 CCTTCCAAAG TGCTGGGATT ACAGGCATGA GCCACCGTGC CCGGCCCAGT ACATCTTTTA 1800 ACTGGGCTGT GAATGACACG ACTTGCTAAG ACCTGCCCAC TAAGAATGAG CTGCAGCCAG 1860 CACAATGTTG TCCGCTTCCA GCCACTTTCC TAGATACTCC TCCATTCCTC AGATTCCAGC 1920 CCCCACCCCA GCCTGGAACG CCCACAGTGC TTTTATCACA GCTCTTAACT CCACTTGGTT 1980 CCCCAAAGCT ATGAGCCCAC ATACCACCTC CCAGGGCTAC AACACTTTGG GTTTCTCAGA 2040 CACTGTCAAC ACTAAGCAGC ATGAACTGCA GGACACACAG GACAGCTGGA GAGGGGCAGT 2100 GAGTCACTGT GTCATAGTCC TGCCCAAATT CCAATGTTGA AATTGCAGAA GCCTGGGGCC 2160 CACCCTAGAG AATCTGATTC AGCAGGTTGG AGGGGGGGCC CAGGCACTGA TATTTTCAAG 2220 AGCCCTGGGT GATGTGGATG CCGATAGCAC TGGCTGCATG CTGAGAAACA CTGCCGATAG 2280 CATCATCTTC CACAGAAGGC CACCCAGGAA GAGATGATGA GGTGACAGAA CTTCATCACC 2340 CAACTCAAGA AGGCTTGGGA GGAAGGGGTA ATTTATTGGT TCTAAGCCCA GACCATGGAC 2400 AAAACAGAGT GCTATGGTTC AAATGTCCCC AGCAATGTTC ATGTTGAAAT GTAATTGCCG 2460 TTGTGATGGT GGCATTGGCA GGTGGGGCCT TTGCAAGGTA ATTAGGTTAT GAGGGCTCTG 2520 CCCTCAGGAA TGGATCCATG CCATCATCTC TGGAGTGGGT TCTTGATAAA AAGGATGATT 2580 CTGGACCACT TCCCTCTCAT GTCTCACATG CTTACCTCTG CCTTCCATCC TTCTGCCATG 2640 GTGGGGCCCT CACAAGATGC TGGTGCCATG CTCTTGGACT TTCCAGCCTC CAGGACTGTG 2700 GGAAATCAAT TTCTTTTCCA 2720
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