Tag | Content |
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EnhancerAtlas ID | HS176-36958 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr7:44773110-44775860 |
SNPs | Number: 2 | 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 | Nr2f6(var.2) | MA0728.1 | chr7:44773332-44773347 | TGAACTCCTGACCTC | - | 6.22 | Nr5a2 | MA0505.1 | chr7:44773324-44773339 | ACTGGCCTTGAACTC | - | 7.4 | RARA | MA0729.1 | chr7:44773329-44773347 | CCTTGAACTCCTGACCTC | - | 6.73 | 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: 3 | Chromosome | Start | End |
chr7 | 44775082 | 44775384 | chr7 | 44773349 | 44774056 | chr7 | 44774433 | 44774663 |
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| Number: 1 | ID | Chromosome | Start | End |
GH07I044733 | chr7 | 44773001 | 44777145 |
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Enhancer Sequence | AGTAGCTGGG ACTGCCCACC ACCATGCCCA GCTAATTTTT GCATTTTTAG TAGAGACAGG 60 ATTTCACCAT ATTGGTCAGG TTGGTCTCAA ACTCCTGACC TCAGGTGATC CACCCACCTT 120 GGCCTCCCAA AGTGCTGGGA TTACAGGTGT GAGCCACCAC GTCTGGCCAA TTTTTGTATT 180 TTTAGTACAG ATGGGGTTTC GCCATGTTGG CCAGACTGGC CTTGAACTCC TGACCTCAGG 240 TGATCCACCC GCCTCTGCCT CTCAAAGTGC TAGGATTACA GGTGTGAGCC ATAGTGCCCG 300 GCTAATTTTT GTATTTTTAG TAGTGACGGA GTTTTGCCAT TTTAGCCAGG CTGGTCTCAA 360 ACTCCTGGCC TCAAGTGATT CACCCGCTTT GGCCTCCCAA AGTTCTGGGA TTACAGGCAT 420 GAGTCACTGC TCCTGACCTA GTTAACTTGA TTTAATCATT CCACAGTGTA TACATATAAT 480 AATACCTTTT ACCCTATAAT GATATACAAT TATTATTTGT CAATTAGACA TAAAGTTATA 540 AAAAAATTCA AGTGACCCAG AATAGCCAAA ACAACCTTGA AAAAAAGACA GCAAAGTTGG 600 AAAACTCACA CTTCCCAATT CCCTTCCCTT CCCTCCCCTC CCTTCCCCTT CCTTCCACTC 660 CCTCTCCCTC CCCTCCCTTC CCCTCCCCTC CCTTCCCATC CTTTCCTCTT CCTTCCCCTT 720 CCCCCTCCAC TCCCCTCTCC TCCCTTCCCC TCCCTTACTC TTCCCTCCCC TCACCTTTCC 780 TTTCCCCCTT CCTTTCTCCT TTCCTTGTTT GTTTTGTTTT TACAGACAGG ATCTCTCTCC 840 CAAGCTGGAG TGCAGTGGTG CAATTATAGC TCACTGCACC CTCAAACTCC TGAGCTAAAG 900 CAATCCTCCC ATTTCAGCCT CCTGAATAGC TAGGGCTACA GGTGCATGCC ACCAAGCCCA 960 GCTAATTAAC AAAATATATT TTTTGGCTAG GTGTAGTGGC TCACACCTGT AATCCCAGCA 1020 CTTTGGGAGG CCGAGGATGG CAGATCACCT GAGTTCAGGA GTTCCAGGCC AGCCTGGCCA 1080 ACGTGGCGAA AGCCTGTCTC TACTAAAAAT ACAAAAATTA GCCAGGCATG GGGGCGGGAG 1140 CCTATAATTC AGCTACTCAG GAGGCTGAGG AGGGAGAATT GCTTGAACCC AGGAGGCAGT 1200 GGTTGCAGTG AGCCAAGATC ATACCACTGC AATCCAGCCT GGGCAACAAG AGCAAAACTC 1260 CATCTCAAAA AAAAAAAAAA TTCTTTTGTA TAGACAGGAT CTTGATGAGT TGCCCATGCT 1320 GGTCTTGAAC TCTTGGCCTC AAGGGATCCT CAATCCTCAG TCTCCTACAG CACTGGGATT 1380 ATATGTATGA GCCATGGAAC CTGGGCCCCA ATTTTAACTT ACTACAAAGC TACAGTAATC 1440 AGATCAGTGA GGTACCGGCA TAAGGAGAGA TACATAAATC AATGGAATAG AATTGAAAGT 1500 CCAGACATAG GCTGGACGCA GTGGCTCACG CCTGTAATCC TAGCACATTG GGAGGCTGAG 1560 GTGGGCAGAT CACGAGGTCA GGAGTTCGAG ACCAGCCTGA CCAACATGGT GAAACCCCGT 1620 CTCTACTAAA AATACAAAAA TTAGCCAGGC GTGGTGGCGG GCGCCTGTAA TTCATGCCAC 1680 TGCACTCCAG CCTGGGCAAC AGAGCAAGAC TCCATCTCAA AAAAAAAAAA AAAAAGGAAA 1740 AAAAAATAAG TGAAAGGACA ATCCACAGAA TAGGAGAAAA TGTTTACAAA TTATATCTGA 1800 TAAGGGACTT GTGTCCAGAA TATACAAAGA ATTCCAAGTT GGGAGCAGTG GCGTGTGCCT 1860 CTAGTCCCAG CTACTCAGGA GGCTGAGGCA AGAGGATCAC TTGAGCCCAG GTGTTAGACA 1920 CCAGCCTGGG CAACACAGGG AGACCCTCAT CCTCTTGAAA AGAAATCCAA TTTAAGAACG 1980 GGTAAAGGAT CTGAATAGTC ATTTCTCCAA GGAAGATATA CAAATGGCAG TAAGTATGTG 2040 AAAAGATTCT CAACATCATG AATCATTAGG GAAATGCCAA CGAAAACCAC AATGAGATGC 2100 CACGTCACAC CTACTAGAAT GACTAATAAA AAGACACAGG ATGTAGAGAA GCTGGAACCC 2160 TCATACACTG CTGGTGGGAA TGTCAAATAG TACAGCTGCT TTGGAGAACA GGAAGATCAT 2220 CTGGTAGTTT CTCCAAGTTT AAACATAGAG TTACCATTAA ACCCATTAAT TCCACTTACA 2280 AGTATGTACC CAGAGAAGTG AAAGCATGTC CACACAGAGA CTTATACATG AATGTTCATA 2340 GCTGCATTAT TCATAGTAGC CAAAAAGCTG AAATAACCAA AATGTCCATC AACTCATGAA 2400 CAGATAAACA GAATGTGGTG TATCCCTATG ATGGAATATT ATTCAGCAAT GAAAAGGAAT 2460 AAAGTGCTGA TACATGCTAC AACATGAATA AACCATGAAA GCATTATGCT CAGTGAAAGA 2520 AGCCAGATAC AAAAGATCAC ATATTTTATT ATTCCGTATA TATTAAATGT CCAGAATAGG 2580 CAAACCATAG GAACAAAAAG TAGATTATTG GTTGCCAGGG GCTGGGGAGG AGGTAATGCG 2640 GAATGACATC TAATGGATAT AGGATCTCTT CTGACAGTGA TAAAAATGCT CTAAAATTGA 2700 TTATGTTCAT ATACATAACA CTGTTGAATT GTATACTTTA TATAGGTGAA 2750
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