Tag | Content |
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EnhancerAtlas ID | HS091-29320 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr2:234255700-234258150 |
Target genes | |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
E2F3 | MA0469.3 | chr2:234257891-234257907 | ATTTTGGTGCCAAAAT | + | 6.31 | E2F3 | MA0469.3 | chr2:234257891-234257907 | ATTTTGGTGCCAAAAT | - | 6.32 | EWSR1-FLI1 | MA0149.1 | chr2:234255962-234255980 | CCTTCCTTCCTTCCTTCC | - | 10.83 | EWSR1-FLI1 | MA0149.1 | chr2:234255954-234255972 | CCGTCTGTCCTTCCTTCC | - | 6.47 | EWSR1-FLI1 | MA0149.1 | chr2:234255974-234255992 | CCTTCCTTTATTCCTCCC | - | 6.73 | EWSR1-FLI1 | MA0149.1 | chr2:234255986-234256004 | CCTCCCTCCCTCCCTTCC | - | 7.08 | EWSR1-FLI1 | MA0149.1 | chr2:234255994-234256012 | CCTCCCTTCCTTCCTTCG | - | 7.79 | EWSR1-FLI1 | MA0149.1 | chr2:234255966-234255984 | CCTTCCTTCCTTCCTTTA | - | 7.95 | EWSR1-FLI1 | MA0149.1 | chr2:234255998-234256016 | CCTTCCTTCCTTCGTTTC | - | 7.97 | EWSR1-FLI1 | MA0149.1 | chr2:234255970-234255988 | CCTTCCTTCCTTTATTCC | - | 8.01 | EWSR1-FLI1 | MA0149.1 | chr2:234255990-234256008 | CCTCCCTCCCTTCCTTCC | - | 8.13 | EWSR1-FLI1 | MA0149.1 | chr2:234255958-234255976 | CTGTCCTTCCTTCCTTCC | - | 8.52 | Stat6 | MA0520.1 | chr2:234255923-234255938 | GTTTCTCTGGAAACA | - | 6.08 | ZNF263 | MA0528.1 | chr2:234255962-234255983 | CCTTCCTTCCTTCCTTCCTTT | - | 6.16 | ZNF263 | MA0528.1 | chr2:234255973-234255994 | TCCTTCCTTTATTCCTCCCTC | - | 6.16 | ZNF263 | MA0528.1 | chr2:234255970-234255991 | CCTTCCTTCCTTTATTCCTCC | - | 6.22 | ZNF263 | MA0528.1 | chr2:234255990-234256011 | CCTCCCTCCCTTCCTTCCTTC | - | 7.19 | ZNF263 | MA0528.1 | chr2:234255986-234256007 | CCTCCCTCCCTCCCTTCCTTC | - | 7.38 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_10279 | chr2:234257168-234260579 | CD19_Primary | SE_10983 | chr2:234256162-234279279 | CD20 | SE_61725 | chr2:234221157-234273267 | Toledo | SE_63118 | chr2:234256820-234273687 | Tonsil |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr2 | 234256501 | 234256551 | chr2 | 234256628 | 234257377 |
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Enhancer Sequence | GGTCATGAGT TGGTTGATTT GTTGGGGAGG CTGAGTTGAT GACATGACAC AAGCTGCCAC 60 CATTAGGGTC CCTGGAGTGG GAGGGTTGGG GAGAGGGAGG CCAGCCTCCC ACGGAAGGGC 120 TCACCACTCC CATGAGGGAG AGAAGGCGTC TGGAAATCAA TGTGCTCACC AGGTGGGGCC 180 CTCGGTGTGT CCAGGGGCTT TCCTAGGAGT CCCAGTCTGA GCTGTTTCTC TGGAAACAGT 240 GCCTTCCCGT CTGTCCGTCT GTCCTTCCTT CCTTCCTTCC TTTATTCCTC CCTCCCTCCC 300 TTCCTTCCTT CGTTTCGCTC TTGTTGCCCA GGCTGGAGTG CTGTGGCGTG ATCTCAGCTC 360 ACTGCAAGCT CCGCCTCCCG GGTTCACGCC ATTCTCCTGC CTCGGCCTCC TGAGTAGCTG 420 GGATTACAGG CGTGTGCCAC CATGCCCGCC TAATTTTTTG TATTTTTATT AGAGACAGGG 480 TTTCACCATG TTAGCCAGGC TGGTCTCAAA CTGCTGACCT CAGGTGATCC ACCCACCTTA 540 GCCTCCCAAA GTGCTGGGAT TACAGGCGTG AGCCACTGCG CCTGGCCACC AGTGTATGTT 600 TCTAATTACC TGACCAGTCC CAACTTCCAG GCCCCTAAAG AGCCTCCTAA GTTAAATAGG 660 GCAGAGAACA TCTGTGGACA AAAATACTCT TGGTTAATGA TTCAACTTTT GGGTCCAGGT 720 GTCTGTTTGA GCTTTGGGTT GTTGGTAAAG TTCTATTCAA TGCAAGAAGC AAAATCAGAT 780 TTGGTTAAAT TAAGGTGGGG AGAAGGAATG TAGTGGGAGG ACCCCGGTGT GATCAGAGAA 840 CTGAAGGACA AACCTGAGCT GCCACACCTG GGGTAAGCAG GAATCAGAGA AGCTTCAGGG 900 GTCAGGGACC CACTCTCCAG GGCGGCTCTT CATGCAGCTC AGCACCATAC GTTCCCAGCT 960 CTGCGTCTCT TGGTCCCAGT GGGCAGTTAT TGGGAAGGAG AATCCAACTG GCTCAGCTTT 1020 GGCTGGGAGG ATCAACACCC CGTGGTCAGC GATGGCAGAG CCCAGCCCTG GAGATGGAGA 1080 GTCCCAGAAA AGGGGGTTGA TTGTGAGTCA CATGGGCTTA CTTAGAGCGT GCTTCACTGA 1140 GACTGGGCGT GAGAGGCATA GGGGAGAGCA CTCTGAGTGT CAGGGAGGAA GGTGAACTGC 1200 AGGTGGAGGA GGGATAATAG AGGTGATACC AGGGCCTTTC CTTTGTGGGG TCCCTTCCTG 1260 CCCTGAGGTA CCCACCGGGC CTGCTGCTGA TGGCACAGAT ACTGAACAGG CTCATGGCGG 1320 CCAAGGAGAG GATGGAGATG CATAGGCTCT GGTCCATCTC TGGTCCATGC TTTAAGGGAG 1380 CAGGGTAAAG GGGGGTTGGA GATTCCTCCA CAGTTCAACC CACTCACAGA AGGCAGAGGG 1440 TGAGTGGGAG GGGTTCTAGA TGGGGAGTAC ACGTGGATCA GGCTTCTGGG ATGGAACATG 1500 GCGACAGAGG GCTGGCCAGG GTATGGGTTC CATACACATG AAGGTTCCCA GCATCTGGGG 1560 TTGTTCAGAA GGATTCCAGC TGTTCGGGTC CTGGAGATTG GGATTTAGAT GAGGAGGCTC 1620 CACTTGGGAA GCTTGGATGG GATCCCAGAC AAAGCGAGGT GTGGACCCGT GTGCTGGCTC 1680 ACGCATCCTG GCATTGGGAG GAGGATTTAT AATACACTAG ACTACAGGTG GAAGATTGGT 1740 CCTTCAGGCT GCGAGTTAGC AGGATCAGAC ACAGTCCCTC GTTCTTTTTC TCTCTATGCT 1800 AAGGTAATGG TGCACGACCA TTTCAACCCA TGCTCCCCTC AGGGCACGCA GACAAGGGAT 1860 GGCCAGGGTG GCACACTCCT CTGAGGATTC CCAAAGCTGT TCCCCATTGC ACTGAGCCCT 1920 TCCCCTGTCC TCTGCCACAG CACACAGGCT GCTGTGTTTA GCTCCTGCTA GAGCTCTTGG 1980 GCTAGCCCAG GGCCTGGGAT TCTGCCCTGT GGTGCCTGGT GAGAGGACCA GCCCGTTGGT 2040 TCCTGCATTG CTTGACCCCA GGACATCCTA AGTCAGGGTG GACGTTAATA AGCCCGACCT 2100 TTGGAACTAC GTGGGTGAGA GAGCTGGAGG GAAGGGCTGG AAGACCAATC CCTGGAGAGC 2160 AGAGGTCAGC ACAGCCCTTA CCCTCCTAGT TATTTTGGTG CCAAAATGTC TCGATACGCC 2220 CTCCAGGTGC TGGCTTGTTT ATGGCCTGCA GCTGGCCACG CTGGGGAGGG AGTTGGGGGA 2280 GGAAGCGAGC AGCCAGCTGC CCTGAGCAGA AAGTGGAAGC TTGGCTCAGC TCAGCCTGCA 2340 CATGTGTGGG GCTGTCTACT GGCATGTAGT GTCCCTTGGT ATCAGGAGGC AGGAAGTCTA 2400 CGTGCAGGTT GAATGTGTGG CCCAGAGTTT TTGGGACAGA TGCAGTGCAA 2450
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