Tag | Content |
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EnhancerAtlas ID | HS003-41526 |
Organism | Homo sapiens |
Tissue/cell | A549 |
Coordinate | chr7:44773400-44775840 |
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) |
EWSR1-FLI1 | MA0149.1 | chr7:44773884-44773902 | CTTTCCTTTCCCCCTTCC | - | 6.39 | EWSR1-FLI1 | MA0149.1 | chr7:44773896-44773914 | CCTTCCTTTCTCCTTTCC | - | 6.85 | FOSL1 | MA0477.1 | chr7:44773527-44773538 | CATGAGTCACT | - | 6.14 | MEOX1 | MA0661.1 | chr7:44774070-44774080 | GCTAATTAAC | + | 6.02 | RORA(var.2) | MA0072.1 | chr7:44773542-44773556 | CTGACCTAGTTAAC | - | 6.26 | ZNF263 | MA0528.1 | chr7:44773891-44773912 | TTCCCCCTTCCTTTCTCCTTT | - | 6.01 | ZNF263 | MA0528.1 | chr7:44773884-44773905 | CTTTCCTTTCCCCCTTCCTTT | - | 6.06 | ZNF263 | MA0528.1 | chr7:44773753-44773774 | TCCCCTTCCTTCCACTCCCTC | - | 6.17 | ZNF263 | MA0528.1 | chr7:44773793-44773814 | TCCCCTCCCTTCCCATCCTTT | - | 6.17 | ZNF263 | MA0528.1 | chr7:44773845-44773866 | TCTCCTCCCTTCCCCTCCCTT | - | 6.19 | ZNF263 | MA0528.1 | chr7:44773787-44773808 | TTCCCCTCCCCTCCCTTCCCA | - | 6.1 | ZNF263 | MA0528.1 | chr7:44773733-44773754 | TTCCCTTCCCTCCCCTCCCTT | - | 6.28 | ZNF263 | MA0528.1 | chr7:44773763-44773784 | TCCACTCCCTCTCCCTCCCCT | - | 6.42 | ZNF263 | MA0528.1 | chr7:44773728-44773749 | TTCCCTTCCCTTCCCTCCCCT | - | 6.55 | ZNF263 | MA0528.1 | chr7:44773768-44773789 | TCCCTCTCCCTCCCCTCCCTT | - | 6.55 | ZNF263 | MA0528.1 | chr7:44773839-44773860 | CTCCCCTCTCCTCCCTTCCCC | - | 6.63 | ZNF263 | MA0528.1 | chr7:44773737-44773758 | CTTCCCTCCCCTCCCTTCCCC | - | 6.74 | ZNF263 | MA0528.1 | chr7:44773813-44773834 | TCCTCTTCCTTCCCCTTCCCC | - | 6.84 | ZNF263 | MA0528.1 | chr7:44773744-44773765 | CCCCTCCCTTCCCCTTCCTTC | - | 6.86 | ZNF263 | MA0528.1 | chr7:44773820-44773841 | CCTTCCCCTTCCCCCTCCACT | - | 6.99 | ZNF263 | MA0528.1 | chr7:44773778-44773799 | TCCCCTCCCTTCCCCTCCCCT | - | 6.9 | ZNF263 | MA0528.1 | chr7:44773772-44773793 | TCTCCCTCCCCTCCCTTCCCC | - | 7.32 | ZNF263 | MA0528.1 | chr7:44773832-44773853 | CCCTCCACTCCCCTCTCCTCC | - | 7.65 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr7 | 44775082 | 44775384 | chr7 | 44774433 | 44774663 |
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| Number: 1 | ID | Chromosome | Start | End |
GH07I044733 | chr7 | 44773001 | 44777145 |
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Enhancer Sequence | ATAGTGCCCG GCTAATTTTT GTATTTTTAG TAGTGACGGA GTTTTGCCAT TTTAGCCAGG 60 CTGGTCTCAA ACTCCTGGCC TCAAGTGATT CACCCGCTTT GGCCTCCCAA AGTTCTGGGA 120 TTACAGGCAT GAGTCACTGC TCCTGACCTA GTTAACTTGA TTTAATCATT CCACAGTGTA 180 TACATATAAT AATACCTTTT ACCCTATAAT GATATACAAT TATTATTTGT CAATTAGACA 240 TAAAGTTATA AAAAAATTCA AGTGACCCAG AATAGCCAAA ACAACCTTGA AAAAAAGACA 300 GCAAAGTTGG AAAACTCACA CTTCCCAATT CCCTTCCCTT CCCTCCCCTC CCTTCCCCTT 360 CCTTCCACTC CCTCTCCCTC CCCTCCCTTC CCCTCCCCTC CCTTCCCATC CTTTCCTCTT 420 CCTTCCCCTT CCCCCTCCAC TCCCCTCTCC TCCCTTCCCC TCCCTTACTC TTCCCTCCCC 480 TCACCTTTCC TTTCCCCCTT CCTTTCTCCT TTCCTTGTTT GTTTTGTTTT TACAGACAGG 540 ATCTCTCTCC CAAGCTGGAG TGCAGTGGTG CAATTATAGC TCACTGCACC CTCAAACTCC 600 TGAGCTAAAG CAATCCTCCC ATTTCAGCCT CCTGAATAGC TAGGGCTACA GGTGCATGCC 660 ACCAAGCCCA GCTAATTAAC AAAATATATT TTTTGGCTAG GTGTAGTGGC TCACACCTGT 720 AATCCCAGCA CTTTGGGAGG CCGAGGATGG CAGATCACCT GAGTTCAGGA GTTCCAGGCC 780 AGCCTGGCCA ACGTGGCGAA AGCCTGTCTC TACTAAAAAT ACAAAAATTA GCCAGGCATG 840 GGGGCGGGAG CCTATAATTC AGCTACTCAG GAGGCTGAGG AGGGAGAATT GCTTGAACCC 900 AGGAGGCAGT GGTTGCAGTG AGCCAAGATC ATACCACTGC AATCCAGCCT GGGCAACAAG 960 AGCAAAACTC CATCTCAAAA AAAAAAAAAA TTCTTTTGTA TAGACAGGAT CTTGATGAGT 1020 TGCCCATGCT GGTCTTGAAC TCTTGGCCTC AAGGGATCCT CAATCCTCAG TCTCCTACAG 1080 CACTGGGATT ATATGTATGA GCCATGGAAC CTGGGCCCCA ATTTTAACTT ACTACAAAGC 1140 TACAGTAATC AGATCAGTGA GGTACCGGCA TAAGGAGAGA TACATAAATC AATGGAATAG 1200 AATTGAAAGT CCAGACATAG GCTGGACGCA GTGGCTCACG CCTGTAATCC TAGCACATTG 1260 GGAGGCTGAG GTGGGCAGAT CACGAGGTCA GGAGTTCGAG ACCAGCCTGA CCAACATGGT 1320 GAAACCCCGT CTCTACTAAA AATACAAAAA TTAGCCAGGC GTGGTGGCGG GCGCCTGTAA 1380 TTCATGCCAC TGCACTCCAG CCTGGGCAAC AGAGCAAGAC TCCATCTCAA AAAAAAAAAA 1440 AAAAAGGAAA AAAAAATAAG TGAAAGGACA ATCCACAGAA TAGGAGAAAA TGTTTACAAA 1500 TTATATCTGA TAAGGGACTT GTGTCCAGAA TATACAAAGA ATTCCAAGTT GGGAGCAGTG 1560 GCGTGTGCCT CTAGTCCCAG CTACTCAGGA GGCTGAGGCA AGAGGATCAC TTGAGCCCAG 1620 GTGTTAGACA CCAGCCTGGG CAACACAGGG AGACCCTCAT CCTCTTGAAA AGAAATCCAA 1680 TTTAAGAACG GGTAAAGGAT CTGAATAGTC ATTTCTCCAA GGAAGATATA CAAATGGCAG 1740 TAAGTATGTG AAAAGATTCT CAACATCATG AATCATTAGG GAAATGCCAA CGAAAACCAC 1800 AATGAGATGC CACGTCACAC CTACTAGAAT GACTAATAAA AAGACACAGG ATGTAGAGAA 1860 GCTGGAACCC TCATACACTG CTGGTGGGAA TGTCAAATAG TACAGCTGCT TTGGAGAACA 1920 GGAAGATCAT CTGGTAGTTT CTCCAAGTTT AAACATAGAG TTACCATTAA ACCCATTAAT 1980 TCCACTTACA AGTATGTACC CAGAGAAGTG AAAGCATGTC CACACAGAGA CTTATACATG 2040 AATGTTCATA GCTGCATTAT TCATAGTAGC CAAAAAGCTG AAATAACCAA AATGTCCATC 2100 AACTCATGAA CAGATAAACA GAATGTGGTG TATCCCTATG ATGGAATATT ATTCAGCAAT 2160 GAAAAGGAAT AAAGTGCTGA TACATGCTAC AACATGAATA AACCATGAAA GCATTATGCT 2220 CAGTGAAAGA AGCCAGATAC AAAAGATCAC ATATTTTATT ATTCCGTATA TATTAAATGT 2280 CCAGAATAGG CAAACCATAG GAACAAAAAG TAGATTATTG GTTGCCAGGG GCTGGGGAGG 2340 AGGTAATGCG GAATGACATC TAATGGATAT AGGATCTCTT CTGACAGTGA TAAAAATGCT 2400 CTAAAATTGA TTATGTTCAT ATACATAACA CTGTTGAATT 2440
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