Tag | Content |
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EnhancerAtlas ID | HS091-01187 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr1:33189950-33191920 |
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 | GCTCTCGGGA GGCTGAGGCA GAGAATTGCT TGAACCCAGG AGGCGGAGGT TGTAGTGAGC 60 CAAGATCACG CCACTGCACT CCAGCCTGGG TGACAGAGTG AGACTCCGTC TCAAAAAAAA 120 AAAAAAATTA CTATTGGGGC TAGTCTGGCC TAGAGAAGAA CAGTGATTTG CACGCTCTCC 180 TGTATGATGT ATGTGCAATA ACCCATCCTG TGGGGAGTGA AGTGACTTGC CCAATGTCAC 240 ACTGCATGTT GTATAAAAAA CCAGCCTGGG CCCCAAGAAG GCTGCTTTGC AGCCTGGGAA 300 GAGGTGACAG GCCCTGGCAT GATCTGCCCT GCCCTCTCAG GACCTGAATG CCCCTCTCCA 360 CTCAGGACAA TGGGAACGCC TCCTGCCAAA GCCACTGCTA TTCCTCTCAG TGGGGAGGAG 420 GGAGAAGACA ATGAAAGAGG CTGGGGAATG AGGGGTGTGG GGGACTCCAA ACAGAGCCAG 480 CAACAAATGG GCAGGGCACA GAGTGGGGCA GGAAGGATGG CCCTCTCTCC ACTGGGACTT 540 TGAGAAGGGG CCATTTTGGC AGGAGGATGG GCGCAGTCTG CCTACTGGTA TGCTTGAGCC 600 CCTGGACAAC TTCATTCACT GTCTCTTTAC ATCACTCCCT CCTGTGTGCC CAGAGCATAG 660 GACGGGGACA CCAATGCACC AGCGCGCCAA ATCTGCGTGA CCTCGTGCAA GCCACTTAGT 720 CTCCTCACCT GTGAATTGGA GGTGATCGGC CCTACTTCCC AGGGCTGTTC GGAGCATTAA 780 AGGCAATCAC AGAAGTGAAG CACCCCAGCT GGAGTGGGCG AGGCAGTCCA GCAAAGGCTA 840 GTTGTTACAG TGGCAGAGGC GCTCCTCTCC CAGACTGCCC CACACAGCTG GCAATGGTGG 900 GGACTGGCCA GGAGAGCTTG TGGGGAGGAG CCCTCTTCCT TCCTGCCCCT TCCAGCTGGG 960 TATCAAGATC TGAGACCAGA TGTGTTGGTG AGTGACTCAG CGCTTTCCTG CCTGGAAACT 1020 CCTCCCTGCC TGTCTCACCA GGCTGGGCCA GGGAGGGTGA GACAGCAGAC TGGGGGTGGG 1080 AGTGGCTGGT TCCGAAAAAC CTCAGGGGAG CCATGGGGGC AGGAAGGGAG AGGGAAGGAG 1140 GGATGAGAAT AGTGTGCCTT GGCCTGCAAG ATGGGGATGG GATGAAGGAA GTGGGACACT 1200 TCCGAGACTG TCAAGGAAGA GCTAGGTTGA GGGTGTCCTT GTCTGTCTAG TCAACCTAAA 1260 ATGACCAGGT GGGAGGAGGA AAGCTCACCC CTTCCTCTTC CCACCTGCAT ACATCCTAGC 1320 CCCAGTATTT CCAGGCCAGC CCAAACCCAT TTGTCTTGCC CTCCTGGGCT GCATACCCAC 1380 ATGACGCTCC CTTCCTTCCC TTTCCTCTCC TCCTCTTCCC AGCCAACCAC CTCCACTTCC 1440 CCATCTCCCA CTCCACTGGA TCTGTTACTA ACTCCTTGGT GCCCACTCTC TCTGGAAGGT 1500 TGTCCTCTAT TGCCTAATCC CTCACCCTGA CAGCTTAAGC TGTCAGGGAC AGTAAGCATG 1560 GTTGACCTGG TCCTTCTGGA CCTTCATGGA GCTTTTGTTT TTGAGACGGA GGCTCTCTCT 1620 GTCGCCCAGG TTGGAGTGCA ATGGTGTGAT CTCGGCTCAC TGCAACCTCT GCCTCCCAGG 1680 TTCAAGCGAT TCTCCTGCTT CAGCCTCCCA AGTAGCTGGG ATCACAGGTG CGCACCACTT 1740 GGCTAATTTT TAAATTTTTA GTAGAGATGG GGTTTCACCA TGTTGTCCAG GCTGGTCTTG 1800 AACTCCTGAC CTCAGGTGAT CTGCCCACCT TGGCCTCCCA AAGTGCTGGG ATTACAGACC 1860 CGAGCCACCA TGCCCAGCAT CTTCTTGGAA CTCTTTTCTT CATCTCAAAT ATCACCCTGC 1920 TGGTTTCCCT TCTATCTTTT GGACAATTCC TTCTCTAATC TCTTCTTCCC 1970
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