Tag | Content |
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EnhancerAtlas ID | HS041-00484 |
Organism | Homo sapiens |
Tissue/cell | EWS502 |
Coordinate | chr1:17518360-17521130 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
STAT3 | MA0144.2 | chr1:17520331-17520342 | CTTCCCAGAAA | - | 6.02 | TFAP2A | MA0003.3 | chr1:17519408-17519419 | AGCCTCAGGCA | + | 6.32 | ZNF263 | MA0528.1 | chr1:17518380-17518401 | TCTTCTTCTTCTTCTTCTTCC | - | 6.05 | ZNF263 | MA0528.1 | chr1:17518446-17518467 | TCCTCTTCCTCCTCTTCTTCT | - | 6.08 | ZNF263 | MA0528.1 | chr1:17518449-17518470 | TCTTCCTCCTCTTCTTCTTCT | - | 6.12 | ZNF263 | MA0528.1 | chr1:17518386-17518407 | TCTTCTTCTTCTTCCTCTTCT | - | 6.25 | ZNF263 | MA0528.1 | chr1:17518464-17518485 | TCTTCTTGTCCCTCTTCCTTC | - | 6.62 | ZNF263 | MA0528.1 | chr1:17518443-17518464 | TCTTCCTCTTCCTCCTCTTCT | - | 6.89 | ZNF263 | MA0528.1 | chr1:17518383-17518404 | TCTTCTTCTTCTTCTTCCTCT | - | 6.98 | ZNF263 | MA0528.1 | chr1:17518413-17518434 | TCTTCTTCTTCTTCCTCTTCC | - | 7.05 | ZNF263 | MA0528.1 | chr1:17518416-17518437 | TCTTCTTCTTCCTCTTCCTCT | - | 7.16 | ZNF263 | MA0528.1 | chr1:17518419-17518440 | TCTTCTTCCTCTTCCTCTTCC | - | 7.48 | ZNF263 | MA0528.1 | chr1:17518428-17518449 | TCTTCCTCTTCCTCCTCTTCC | - | 7.79 | ZNF263 | MA0528.1 | chr1:17518431-17518452 | TCCTCTTCCTCCTCTTCCTCT | - | 7.94 | ZNF263 | MA0528.1 | chr1:17518434-17518455 | TCTTCCTCCTCTTCCTCTTCC | - | 8.07 | ZNF263 | MA0528.1 | chr1:17518422-17518443 | TCTTCCTCTTCCTCTTCCTCC | - | 8.76 | ZNF263 | MA0528.1 | chr1:17518425-17518446 | TCCTCTTCCTCTTCCTCCTCT | - | 9.12 | ZNF263 | MA0528.1 | chr1:17518440-17518461 | TCCTCTTCCTCTTCCTCCTCT | - | 9.12 | ZNF263 | MA0528.1 | chr1:17518437-17518458 | TCCTCCTCTTCCTCTTCCTCC | - | 9.18 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_33802 | chr1:17515316-17521239 | HCC1954 | SE_35060 | chr1:17515559-17520800 | HeLa | SE_47238 | chr1:17518623-17522813 | Panc1 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 17518941 | 17519138 | chr1 | 17518400 | 17520600 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I017188 | chr1 | 17515247 | 17520418 |
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Enhancer Sequence | CTTCTTCTTC TTCTTCTTCT TCTTCTTCTT CTTCTTCTTC CTCTTCTTCT TGTTCTTCTT 60 CTTCTTCCTC TTCCTCTTCC TCCTCTTCCT CTTCCTCCTC TTCTTCTTCT TGTCCCTCTT 120 CCTTCTCCTT TTTCTTCTTC TTCTTCTTTT TGAGACAGAG TCTCACTCTG CTGCCCAGGG 180 CTGCTGTGCA GTGGCGTGAA CATGGCTCAC TGCATCCTCG ACCTTCCAGG CTCATGTGAT 240 ACTTCCACCT CAGCCTCCCG AGTAGCTGGG ATTAGGCATG CACCACCATG CCTGGCTAAT 300 TTTTTTTATC TCTTGTAGAG ACAGGGTTTC ACCATGTTAT TCAGTCTGGT CTCGAACTCC 360 TGGGCTCAAG CAATCCACCT GCCTTGGCCT CCCAAAGTGC TGGGATTACA GGCATGAGCC 420 ACTGCGCCTG GCCTCAAACA TTCTCTTCTG ATACGCAACT GCAGACCTTA AGCCATTTCA 480 GCAGCTTATA GAGTCTGCAA ACAAGCTGTC TTTGTGTCCT GCACCTTTTG CTATAAAGAA 540 CGAAATTCCA CCTCATTTTA GTACTAGAAC CCTAGCCCAA AGTGAAAGTG GGGTCTGCTT 600 TACACTACGT GTGTGAAAGT GGGGCGTGCA TTACACTACG TGTGCCTGTG TGCATACACT 660 CCCCTCCCTT CATAAATATG GATAGCCTTT CCCGCAAACC TGCTGAATAT GTATGACTCT 720 ATTGCGTCAT ATGGGCTCCA TGAGGCACAA AACCCAACCT GCCCTTTTCC TCTCCCAAGA 780 GAGAGCACGT CCAGAACACG CCAGAGACTG TCTCTTCCTG GTTTGCAAAC TCATACCACT 840 AGTAAAGCTC CTTTCTGCTA TTTAGCTATC CTGGTGGTCT TTTGGGCAAC ATGCTTATCT 900 GGGAAGAGCT GTCTTGTAAT CTCTGTGTCT GCATCAGACT CTGCCAGCCC TAGATTGGGA 960 GCTCTGAGAT GACATAGGCT GCGTCCCACC CCAGCAGCAG CATGCAAGGT TGGGGACACA 1020 TGTGAGGGTG TGTGGTGCAG CCCTGAACAG CCTCAGGCAG ACTCCCTGTA TTCTTGTTCC 1080 CAACCTCCTC CCTCCCTAGG TCAAAAGGCT GTGGCAGGAG GCCAGGCAGA TCACAGCGTC 1140 CATGCCTAGA TGCTCCCTGA CCCCCAGGAA CCAGAAGTGC TGTCTCCTGA AGGCTCTGGA 1200 AACCCGGAAT CAGCCTACGA GGCACCAGGG CCACCTTGGA GGGTGGAAAT GAGGACCTCA 1260 GGCCCCAGAG GGCATGCAGG CGAGGTGAAG TTCAGGAGAG GTAAGCCTAA GGACCCTCAG 1320 AGCTATCACA CTATGCCCTC CACCCAAATG ATGCAGACAG GAAAACTGTG GCCTAGACCG 1380 GACCACCACG GCCAAAAAGG ATCTTTGTCT TGTCTTGTCC CACAGCCAGG AAGTGTCCCC 1440 CTCTTCCCGG CCTGCTGTAT CCCAGGACAC AGGGCGTAAG TGTGGAGGAG GAAGGGCTGC 1500 AGGGTGAGGC AGCCCACACT TTGGCTCAGG ACAGGGATGG GACCGGGACA TATGGGAAAA 1560 TAGTCTGGGG GTCCTGGGTA ATGGCAGGAG CATGAGCTCA GGGTCGGGTG GCTGTCCTGG 1620 ATGACCTGTG GGACTCTCTT CCTCTCCAAG CCACGCTTTC CTCAACTGTC CCTTCCTTGT 1680 GGGATGCAAG AGGCCACGGC GAGCGAAGGC ATGTGCCAAG AGCTGCCACT CAATGTGAGT 1740 CAGCGTGCTG GTCCTCCCTC CTTTTCTCCA GGGGGCCTAG GACTTTTGGG GGGAGCCTGA 1800 GGACATGCTT CGCTGATGTC ACTGTGTGGA GTGTACAAAT GGCCACCCTG CTGCTCGTTG 1860 GTTCTATATG GGCATCCAGG CTGGAGAGCA GGGGGTGGGG AGATGGAGAT GCCACCAGCA 1920 GGGGACTGGT TCCTAGAAGA GAGGGCGAGT TTGGGTGGTC CCAGAGGTGT TCTTCCCAGA 1980 AAAGAGAGCA GGAGGCAGGA GGTGGGCATG GAGAATGTGG AGGGGGGCAT TGACAGTGTT 2040 CTCCACCACC CATCAGATAA GACCTGGAGC CTCATTACCA AAGACTTAAT GAGATTCGCT 2100 TTGTTTTCTT ATGAGCCAGG CAAGGTGCCA GGGGAAGCGG CTTCCAGCCC CAGGCTCTGC 2160 AGCTGGCTGC TGTGTGACCC AGAGCCAGGC ACCACACCTC TCTGGGCCTT AGACTCCTTA 2220 TCCATGAGCT TCCTGCCTGC ACCCTAACAT TCAGTGTCAT TGGCCGAGTT ACCCAATGGC 2280 TCCCAGCCTC AGTTTCTTCA TCTGCACATT AGGGATAAGT ACAGCCATCC ACCTGGGAGG 2340 TGTCAAGGGG GTGTGGCCGC AGCACCCAGC CCATGCACAA GTTCAGTGAT CATTACCTGT 2400 CTCCCCCAGC CCTGCCTGAG TGCCAGGATC AGCAGGCTTG GGAAGGGGGA GCCCCCAGGG 2460 ATGTGGAAAG TGGAGAGGGA GCACATGGGC TCTGGGGCCT CGGGGCTCCT GGGCTCTGTT 2520 CTGCCTGTCT GGGAGCTGTC TCCTGCTCTC CCTTGCAGTG TCTCTGTCTC TCTTCGTTCT 2580 GTTCCTCCCT CTGTCCTTCA GTTTTTCCCT CTCCATCTCA GTCTCTGGTT GTCTCAGTCT 2640 CTCTTTGCAC CTCACTGTCT CTGCCTTTCT CTGCATCTCT CTTCCTTTCC TGGGCTCTCT 2700 CTCTCTCTTT CATCCCTGTT TTGGGCTTTC TCTGTCTGTG TCTCTCTGTT TTTCAGTCTG 2760 CTTCTTTCTG 2770
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