Tag | Content |
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EnhancerAtlas ID | HS041-00895 |
Organism | Homo sapiens |
Tissue/cell | EWS502 |
Coordinate | chr1:33190140-33191850 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr1:33191748-33191763 | TGAACTCCTGACCTC | - | 6.22 | ZNF263 | MA0528.1 | chr1:33191065-33191086 | GGGGCAGGAAGGGAGAGGGAA | + | 6.43 | ZNF263 | MA0528.1 | chr1:33191348-33191369 | CCTTTCCTCTCCTCCTCTTCC | - | 6.64 | ZNF263 | MA0528.1 | chr1:33191342-33191363 | TCCTTCCCTTTCCTCTCCTCC | - | 6.98 | ZNF263 | MA0528.1 | chr1:33191345-33191366 | TTCCCTTTCCTCTCCTCCTCT | - | 7.24 |
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| Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
SE_00938 | chr1:33190447-33191596 | Adrenal_Gland | SE_23116 | chr1:33190582-33191538 | Colon_Crypt_1 | SE_26629 | chr1:33189838-33191609 | Esophagus | SE_41588 | chr1:33190432-33191573 | LNCaP | SE_65538 | chr1:33190156-33191692 | Pancreatic_islets |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr1 | 33190197 | 33191712 | chr1 | 33190298 | 33191276 | chr1 | 33191365 | 33191490 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I032724 | chr1 | 33190202 | 33191737 |
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Enhancer Sequence | ATGTGCAATA ACCCATCCTG TGGGGAGTGA AGTGACTTGC CCAATGTCAC ACTGCATGTT 60 GTATAAAAAA CCAGCCTGGG CCCCAAGAAG GCTGCTTTGC AGCCTGGGAA GAGGTGACAG 120 GCCCTGGCAT GATCTGCCCT GCCCTCTCAG GACCTGAATG CCCCTCTCCA CTCAGGACAA 180 TGGGAACGCC TCCTGCCAAA GCCACTGCTA TTCCTCTCAG TGGGGAGGAG GGAGAAGACA 240 ATGAAAGAGG CTGGGGAATG AGGGGTGTGG GGGACTCCAA ACAGAGCCAG CAACAAATGG 300 GCAGGGCACA GAGTGGGGCA GGAAGGATGG CCCTCTCTCC ACTGGGACTT TGAGAAGGGG 360 CCATTTTGGC AGGAGGATGG GCGCAGTCTG CCTACTGGTA TGCTTGAGCC CCTGGACAAC 420 TTCATTCACT GTCTCTTTAC ATCACTCCCT CCTGTGTGCC CAGAGCATAG GACGGGGACA 480 CCAATGCACC AGCGCGCCAA ATCTGCGTGA CCTCGTGCAA GCCACTTAGT CTCCTCACCT 540 GTGAATTGGA GGTGATCGGC CCTACTTCCC AGGGCTGTTC GGAGCATTAA AGGCAATCAC 600 AGAAGTGAAG CACCCCAGCT GGAGTGGGCG AGGCAGTCCA GCAAAGGCTA GTTGTTACAG 660 TGGCAGAGGC GCTCCTCTCC CAGACTGCCC CACACAGCTG GCAATGGTGG GGACTGGCCA 720 GGAGAGCTTG TGGGGAGGAG CCCTCTTCCT TCCTGCCCCT TCCAGCTGGG TATCAAGATC 780 TGAGACCAGA TGTGTTGGTG AGTGACTCAG CGCTTTCCTG CCTGGAAACT CCTCCCTGCC 840 TGTCTCACCA GGCTGGGCCA GGGAGGGTGA GACAGCAGAC TGGGGGTGGG AGTGGCTGGT 900 TCCGAAAAAC CTCAGGGGAG CCATGGGGGC AGGAAGGGAG AGGGAAGGAG GGATGAGAAT 960 AGTGTGCCTT GGCCTGCAAG ATGGGGATGG GATGAAGGAA GTGGGACACT TCCGAGACTG 1020 TCAAGGAAGA GCTAGGTTGA GGGTGTCCTT GTCTGTCTAG TCAACCTAAA ATGACCAGGT 1080 GGGAGGAGGA AAGCTCACCC CTTCCTCTTC CCACCTGCAT ACATCCTAGC CCCAGTATTT 1140 CCAGGCCAGC CCAAACCCAT TTGTCTTGCC CTCCTGGGCT GCATACCCAC ATGACGCTCC 1200 CTTCCTTCCC TTTCCTCTCC TCCTCTTCCC AGCCAACCAC CTCCACTTCC CCATCTCCCA 1260 CTCCACTGGA TCTGTTACTA ACTCCTTGGT GCCCACTCTC TCTGGAAGGT TGTCCTCTAT 1320 TGCCTAATCC CTCACCCTGA CAGCTTAAGC TGTCAGGGAC AGTAAGCATG GTTGACCTGG 1380 TCCTTCTGGA CCTTCATGGA GCTTTTGTTT TTGAGACGGA GGCTCTCTCT GTCGCCCAGG 1440 TTGGAGTGCA ATGGTGTGAT CTCGGCTCAC TGCAACCTCT GCCTCCCAGG TTCAAGCGAT 1500 TCTCCTGCTT CAGCCTCCCA AGTAGCTGGG ATCACAGGTG CGCACCACTT GGCTAATTTT 1560 TAAATTTTTA GTAGAGATGG GGTTTCACCA TGTTGTCCAG GCTGGTCTTG AACTCCTGAC 1620 CTCAGGTGAT CTGCCCACCT TGGCCTCCCA AAGTGCTGGG ATTACAGACC CGAGCCACCA 1680 TGCCCAGCAT CTTCTTGGAA CTCTTTTCTT 1710
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