| Tag | Content |
|---|
EnhancerAtlas ID | HS041-02646 |
Organism | Homo sapiens |
Tissue/cell | EWS502 |
Coordinate | chr1:226313880-226316880 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Hnf4a | MA0114.3 | chr1:226315652-226315668 | CGGGTCAAAGTCCTCT | + | 6.49 | | STAT3 | MA0144.2 | chr1:226315755-226315766 | CTTCCCAGAAG | - | 6.14 |
|
| | Number of super-enhancer constituents: 28 | 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 | chr1:226313454-226314203 | Gastric | | 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 | chr1:226307893-226314281 | MM1S | | 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 | chr1:226307893-226314281 | MM1S | | SE_67238 | chr1:226314330-226317236 | MM1S |
|
| | 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 |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH01I226126 | chr1 | 226314498 | 226317175 | | GH01I226121 | chr1 | 226308702 | 226313903 |
|
Enhancer Sequence | CTGAATGAAT GGGTGAGAGC GGTGGCTTAT GCCTGTACTC CCAGCATTTT GGAAGATTGA 60
GGTGGGTGAA TTGCTTGAGC TCAGGAGTTC AAGACCAGCC TGGGCAACAT GGTGAAACCC 120
TGTCTTTACA AAAAAATACA AAAATTAGCT GGACATGGTG GCACACACCT GTAGTCCCAG 180
CTACCTGGGA GGCTGAGGTA GGAGGATTGC TTGAACCACG GGAGACAGAG GTCGCAGTGA 240
GCCAAGATTG TGCCACTTTA CTCCAGCCTG GATGACAGAG CGAGATTGTC TCAAAAAAAA 300
AAAAAAAAAG AAAAAAGAAA AAAAAAAAGC CGGGCACGGT GGCTTATGCC TGTAATCCCA 360
GGACTTTGGG AGGCCAAGGC GGGTGGGTCA CGAGGTCACG AGATCGAGAC CATCCTGGCT 420
AACACAGTGA AACCCCGTCT CTACTAAAAA TACAAAAAAT TAGCTGGGCG TGGTGGCGGG 480
CACCTGTAGT CCCAGCTGCT CGGGAGGCTG AGGCAGAAGA ATGGCATGAA CCTGGGAGGT 540
GGAGGTTGCA GTGAGCTGAG ATCGCGCCAC TGCACTCCAG CCTGGGCGAC AGAGCAAGAA 600
TCCGTCTAAA AAAAAAAGAG AGAGTCCCAG TGCTAAAACT GAGAGTCCTG GGCAAACTGG 660
AACAATTGAT CACACAATAA AGTGGGGGTT CTTGGGCTGG GTATGGAGGC TCATGCTTAT 720
AATCTCAGTG CTTTGGGAGG CCAAGGTGGA AGGATTGCTT GAGCCCAGGG CTTCAAGACC 780
AGCCTGGACA ACATAGCAAG ACCCTATCTC TACAAAAGAA AAAACAAGCA CACACTTGTA 840
GTCCCAGCTA CTTGGGAGGC TGAGGCAGGA GGACTGCTTA AGGCCAGGAG GTGGAGGTTG 900
CAATGGGCTA TGATGGCACC TCTGCACTCC AGCCTCAGTG ACAGAGCAAA ACCTCATTTT 960
GAAAACACAC ACATGAGGGG CGCTGGGAAT AGCCGCTCAT GTCGGCTGAC GGAGCGGTGT 1020
GGGGCCGCAT GCGAAGCTGC CTCCGCGCCT TCCCCGAGCG GCTGGCCGCC TGCGGGGCCG 1080
AGTAAGGACT TCTGCGCGCG GGAGTTCGAG GCCCTGCGGA GCTGCTTCGC CGCCGCGGCC 1140
AAGAAGACGC TGGAGGGAGG CTGTTAGGAG GGACTCTGAG CTTCACACCT GTCTGCTGCC 1200
GTGGTTGCAG AGCCCTAGTC CTGATGGCCC CCGGTGGCAT ACATTGAATG CCTAGGGCAG 1260
AAAGGAAGTG GGAATGGCGA AGATGTGACG TGCCTCGGTG TTAGATACTG TTTCTTCTTA 1320
ACAAGTTGAG GCGTGGGTAG AGCAGGAACT GGTTTTCCAG CATTGTGTCC GTAAACCTGA 1380
GTCAGAATAA GATGTAACAG AAGCCAGATA AAGACTCTGT CAAATCCTGC AAAAAAAAAA 1440
AAAAGAAAAA AAAGAAAACA CACACACACA CACATGCACA CAATGCATAA AGTGTTTCTG 1500
AAACTTTGGT GTGCATGAGA GACACCTGGG GACTTACAAA AACACAGATG GCTGGCCCCA 1560
CCCTAGAGTT TCTAATTTAG TAGGTCCAGG GTGGGGTCCG GTAATTTGCA TTTCTAACAA 1620
GTTTCCTGAT ACTGCTGCTG TTGCTCTTGG TTGGGGCCCA AACTTCCAGA ACAACTGGTC 1680
TGAATGAAGG GCTGGGTCCG GGACCTGCAA GTCCCACTGT GCTGCTTGCC CCGGTACCTC 1740
CTCCTAAGTC TGGCCCAGCA GGAAACGGAG CGCGGGTCAA AGTCCTCTCA CAGTCAACCA 1800
GGAGAAACCT GTGTCTTCCT GGCAGGGTGG CTGGGTGCTA TGGAAACAAG GCTCAGCCCA 1860
GAAGTGCCCA GCCTCCTTCC CAGAAGCAAC TTCAGCCTCT AGGGGAGGAG TGAAGTGAAC 1920
AAACAAACGG AAGGGCAGAG CTCAGTTCCT GGATGGAAGC GGCACCTGCA TGGAAGCGCC 1980
CTCAGCAACC TCAGGGCCCA GACTTCCGGG AAAGTCTCAC AGGGCCCCTG GCTTGAGTTT 2040
TGGAGCTGGA AGGGAACTTT GCAATCTTGG TTCAACTTTT TGTTTTATTT TCTGAGATGA 2100
ATCCTCGCTC TGTTGCCCAG GGTGGGGTGC AGTGGCGCAA TCTCGGCTCA CTGCAACCTC 2160
CGCCTCCCGG GTTCCAGCGA TGCTCCTGCC TCAGCCTCCT GAGTAGCTGG GATCACAGGT 2220
GCCTGCCACC ACGGTTGGCT AAATTTTGTA TTTTTAGTAG AGATGGGGGT TTCACCATGT 2280
TGGCCAGGCT GGTCTCGAAC TCCTTACCTC AGGTGATCCG CCCACCTCTG CCTTCCAAAG 2340
TGCTGGGATT ACAGGCATGA GCCACCGTGC CCGGCCCAGT ACATCTTTTA ACTGGGCTGT 2400
GAATGACACG ACTTGCTAAG ACCTGCCCAC TAAGAATGAG CTGCAGCCAG CACAATGTTG 2460
TCCGCTTCCA GCCACTTTCC TAGATACTCC TCCATTCCTC AGATTCCAGC CCCCACCCCA 2520
GCCTGGAACG CCCACAGTGC TTTTATCACA GCTCTTAACT CCACTTGGTT CCCCAAAGCT 2580
ATGAGCCCAC ATACCACCTC CCAGGGCTAC AACACTTTGG GTTTCTCAGA CACTGTCAAC 2640
ACTAAGCAGC ATGAACTGCA GGACACACAG GACAGCTGGA GAGGGGCAGT GAGTCACTGT 2700
GTCATAGTCC TGCCCAAATT CCAATGTTGA AATTGCAGAA GCCTGGGGCC CACCCTAGAG 2760
AATCTGATTC AGCAGGTTGG AGGGGGGGCC CAGGCACTGA TATTTTCAAG AGCCCTGGGT 2820
GATGTGGATG CCGATAGCAC TGGCTGCATG CTGAGAAACA CTGCCGATAG CATCATCTTC 2880
CACAGAAGGC CACCCAGGAA GAGATGATGA GGTGACAGAA CTTCATCACC CAACTCAAGA 2940
AGGCTTGGGA GGAAGGGGTA ATTTATTGGT TCTAAGCCCA GACCATGGAC AAAACAGAGT 3000
|
