Tag | Content |
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EnhancerAtlas ID | HS102-00649 |
Organism | Homo sapiens |
Tissue/cell | HuCCT1 |
Coordinate | chr1:33190160-33191840 |
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 | TGGGGAGTGA AGTGACTTGC CCAATGTCAC ACTGCATGTT GTATAAAAAA CCAGCCTGGG 60 CCCCAAGAAG GCTGCTTTGC AGCCTGGGAA GAGGTGACAG GCCCTGGCAT GATCTGCCCT 120 GCCCTCTCAG GACCTGAATG CCCCTCTCCA CTCAGGACAA TGGGAACGCC TCCTGCCAAA 180 GCCACTGCTA TTCCTCTCAG TGGGGAGGAG GGAGAAGACA ATGAAAGAGG CTGGGGAATG 240 AGGGGTGTGG GGGACTCCAA ACAGAGCCAG CAACAAATGG GCAGGGCACA GAGTGGGGCA 300 GGAAGGATGG CCCTCTCTCC ACTGGGACTT TGAGAAGGGG CCATTTTGGC AGGAGGATGG 360 GCGCAGTCTG CCTACTGGTA TGCTTGAGCC CCTGGACAAC TTCATTCACT GTCTCTTTAC 420 ATCACTCCCT CCTGTGTGCC CAGAGCATAG GACGGGGACA CCAATGCACC AGCGCGCCAA 480 ATCTGCGTGA CCTCGTGCAA GCCACTTAGT CTCCTCACCT GTGAATTGGA GGTGATCGGC 540 CCTACTTCCC AGGGCTGTTC GGAGCATTAA AGGCAATCAC AGAAGTGAAG CACCCCAGCT 600 GGAGTGGGCG AGGCAGTCCA GCAAAGGCTA GTTGTTACAG TGGCAGAGGC GCTCCTCTCC 660 CAGACTGCCC CACACAGCTG GCAATGGTGG GGACTGGCCA GGAGAGCTTG TGGGGAGGAG 720 CCCTCTTCCT TCCTGCCCCT TCCAGCTGGG TATCAAGATC TGAGACCAGA TGTGTTGGTG 780 AGTGACTCAG CGCTTTCCTG CCTGGAAACT CCTCCCTGCC TGTCTCACCA GGCTGGGCCA 840 GGGAGGGTGA GACAGCAGAC TGGGGGTGGG AGTGGCTGGT TCCGAAAAAC CTCAGGGGAG 900 CCATGGGGGC AGGAAGGGAG AGGGAAGGAG GGATGAGAAT AGTGTGCCTT GGCCTGCAAG 960 ATGGGGATGG GATGAAGGAA GTGGGACACT TCCGAGACTG TCAAGGAAGA GCTAGGTTGA 1020 GGGTGTCCTT GTCTGTCTAG TCAACCTAAA ATGACCAGGT GGGAGGAGGA AAGCTCACCC 1080 CTTCCTCTTC CCACCTGCAT ACATCCTAGC CCCAGTATTT CCAGGCCAGC CCAAACCCAT 1140 TTGTCTTGCC CTCCTGGGCT GCATACCCAC ATGACGCTCC CTTCCTTCCC TTTCCTCTCC 1200 TCCTCTTCCC AGCCAACCAC CTCCACTTCC CCATCTCCCA CTCCACTGGA TCTGTTACTA 1260 ACTCCTTGGT GCCCACTCTC TCTGGAAGGT TGTCCTCTAT TGCCTAATCC CTCACCCTGA 1320 CAGCTTAAGC TGTCAGGGAC AGTAAGCATG GTTGACCTGG TCCTTCTGGA CCTTCATGGA 1380 GCTTTTGTTT TTGAGACGGA GGCTCTCTCT GTCGCCCAGG TTGGAGTGCA ATGGTGTGAT 1440 CTCGGCTCAC TGCAACCTCT GCCTCCCAGG TTCAAGCGAT TCTCCTGCTT CAGCCTCCCA 1500 AGTAGCTGGG ATCACAGGTG CGCACCACTT GGCTAATTTT TAAATTTTTA GTAGAGATGG 1560 GGTTTCACCA TGTTGTCCAG GCTGGTCTTG AACTCCTGAC CTCAGGTGAT CTGCCCACCT 1620 TGGCCTCCCA AAGTGCTGGG ATTACAGACC CGAGCCACCA TGCCCAGCAT CTTCTTGGAA 1680
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