Tag | Content |
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EnhancerAtlas ID | HS050-61512 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr7:5738800-5741920 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
JUN(var.2) | MA0489.1 | chr7:5740932-5740946 | ATGAGTCATCTTCT | - | 7.73 | LMX1B | MA0703.2 | chr7:5740264-5740275 | ATTTTAATTAA | + | 6.62 | NFE2L1 | MA0089.2 | chr7:5740928-5740943 | AGTGATGAGTCATCT | - | 6 | Nr5a2 | MA0505.1 | chr7:5739585-5739600 | TCTGACCTTGAATTC | - | 6.57 |
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| Number of super-enhancer constituents: 27 | ID | Coordinate | Tissue/cell |
SE_01866 | chr7:5738985-5739978 | Aorta | SE_01866 | chr7:5740111-5741266 | Aorta | SE_02438 | chr7:5738824-5739923 | Astrocytes | SE_03391 | chr7:5738792-5740122 | Brain_Angular_Gyrus | SE_03391 | chr7:5740146-5742094 | Brain_Angular_Gyrus | SE_04030 | chr7:5729828-5745249 | Brain_Anterior_Caudate | SE_05212 | chr7:5729900-5745475 | Brain_Cingulate_Gyrus | SE_06175 | chr7:5729425-5745460 | Brain_Hippocampus_Middle | SE_07209 | chr7:5729922-5744744 | Brain_Hippocampus_Middle_150 | SE_07974 | chr7:5729957-5745101 | Brain_Inferior_Temporal_Lobe | SE_08973 | chr7:5738978-5739826 | Brain_Mid_Frontal_Lobe | SE_09320 | chr7:5738676-5744761 | CD14 | SE_25870 | chr7:5725806-5740594 | Duodenum_Smooth_Muscle | SE_27317 | chr7:5738910-5740078 | Esophagus | SE_27317 | chr7:5740257-5741011 | Esophagus | SE_27317 | chr7:5741146-5742017 | Esophagus | SE_32636 | chr7:5730678-5742668 | GM12878 | SE_39019 | chr7:5738945-5740246 | IMR90 | SE_41176 | chr7:5738881-5744272 | Left_Ventricle | SE_42638 | chr7:5738999-5740042 | Lung | SE_42638 | chr7:5740055-5741839 | Lung | SE_46002 | chr7:5738657-5740286 | Osteoblasts | SE_49031 | chr7:5738860-5742008 | Right_Atrium | SE_54013 | chr7:5739009-5740000 | Spleen | SE_54524 | chr7:5722787-5744777 | Stomach_Smooth_Muscle | SE_58698 | chr7:5717211-5744366 | Ly1 | SE_62726 | chr7:5717154-5742191 | Tonsil |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr7 | 5739659 | 5740040 | chr7 | 5740810 | 5741077 |
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| Number: 1 | ID | Chromosome | Start | End |
GH07I005687 | chr7 | 5726833 | 5741881 |
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Enhancer Sequence | CTACCTGTTC ACTCATCCCT CCTCCTTCAG TATAATTTTG AAGCAAATCC CAGATTACAA 60 ATCTTTTCAT TTATAAATAT TTCAGTTTGT ATCTGCAAAA GATAAAGACT CTTGAAACTA 120 ATGCAGCATA TCAAAATTAC ACCTAAAAAC ACAAATAACA ATGAGAAACC CTGGATTTGA 180 CTCCTGATGC TGTCACTTAC TAGCTGTGTG ACTTTGAGCA GATAAGGAGT AAAAAGCCCC 240 TAAAACCCAG GAAGAGTTTT ATTAGCAAAT ACCTAGACCT CAGCCTGTTT TAACTATGAT 300 GCCAAACTCC CTGCTCAAGC TATTCTTCCC ATACTGGCCC TGATGATCTG ACAGAATTGA 360 ACACTAGCTT TTTGTTGTGT TCTTCACCCA CTACCTCAGC AGATTGGATT TCGTTTCTCA 420 TCACGGCTCT GCATTACCAA GGATATTCAC AGTCCATCTT CCCAGGGGAA TTGTACAGAA 480 ACAGAGCACG AACTGTTATT TAGTTTCAGA AGAGATGGCA GGGACTGCTG CCTTAGCCTG 540 TTACACTGGA CATGAAGGGC AGCAGGCTTT CTGGGGCTGG GTGGTTGATT CCACTTGCAG 600 TGATGTACTG GCCACAGATA CAGACGCACA TTTTCTAACT GTGGTCTGTG GGAAGGCCAT 660 GTGGCCTCTG GGAACTGGAG ATGTGACAGA GACCCTCTGT ATTCTTTATC TTTGTCTCAA 720 AGTCAGGGAA GACACTGAGG AATAAAAGGC CTTTTACGTT CTCAGCTACC ACATTGCAAC 780 TGGAATCTGA CCTTGAATTC AAGGATAAAC ACAAGAAATT CCACCCAACA GCAGCTTCAG 840 CTTAGGCTTT GCTCTCATCT TGCTCGATGC CCTAAACACT CCTCTTTGCT ACTGTTCCCC 900 TTCTCCACAT TCCCCGCCCT GACACAGACA CCCACGGGGA CAGGGGGTGT TTTCATGCTT 960 GCGGTATTAC CATAGCAACA ATTTCTCTTC TACCTGGAAG GCTGGAAACC CTGCAGTGCT 1020 CTGTGCTGAG AATGCAAAGA GGGAACACTA TCACTTTCCA CCTCAGCACA CACCACAAGC 1080 CGCACACGTG CACTCACACA CAGCCCCTTC TCAAGGACAT CACAATGAGA TCATGACAAC 1140 AAATCAGGAT GCTGACACCT AACAACACAA AATCAGTGCA ATGACAAAAA GGAGGTAAAA 1200 CATTTCTTAT AAAAAGGTAT TTTGTAGGTA TCAATTCTTG AGGGATTTTT ATTGTGAAAT 1260 TTCTAACATG CATCTCTCCC TTGATGAGGC CACAGACACA GAAAAATGTC ATTAAATTAT 1320 TTTAGTAAAA TATACAAAGG AACTTAATAG GTGGTGTGTG GTTTCTAGAA AGAGGGCCAC 1380 TCCAAGCTTC TGATCCCCAC AGGCTGTGAC AAGCCTGAGA AGCAATAGCT AACTAGTACA 1440 CAAAACCACA AAAAGAGCCA CTAAATTTTA ATTAAGTACC CATAGAAACT CGTTAAAAAT 1500 CCACAGAGAA TCTTTTTCTG TGAGTACTAC AGACAGTGTG TTTTAGTAGA GACCAAAAAT 1560 AACAACAACA AAGAGACAAG TAGGTGTGTC CTTCCACAAG GACAGTCCAA GGTGAGCAGC 1620 CCTGGCATCC AAGCCTGCCC GCTGCCATGG GTGGGCAGGA TGACCAGTGC CCTCCCAGTA 1680 GGACAAAAAC TCATGCCCAA TGCACCAAGA AGACAAACCC TGGATTTCCA TCTCTCCACT 1740 GCAACTAATT TGGAGTTCTC TAGTATAGCG TATCGCCGTC TTTGTTTCTA GGCCCCTCCT 1800 GTACTCATTT CTTCTGAATG TCATCCCTGA GATTCTAAAC CTTCTGAGTA GGAGTAAGAA 1860 ATCAACATGA AACCTGAGAG AAGGAGCACA GCAGTGCTGT GGACAGAGAG TGCAGACCCT 1920 GAGAGTGGGA GCACACACAC GACAGCCTCC CCCAGCACGT GGCTCTCCCC AGGTTGCACA 1980 GGGCCCTTCT CTGAACTTGA ATAACGTGGA CTAAAGGAGA GCTGTCATTT CTTATAGAAT 2040 GTATCAGTTA GCAAAAAAAT CAGGTTGAAA AATCTACCCC TTTACATGGC AGAACACTGG 2100 GGAGCTGGTA GAAATGAGTT GAGTGGTGAG TGATGAGTCA TCTTCTGTTC CCTGATGGGA 2160 TTTTCCACCT GCCCACTTTA GGGGAACTCC ATGCTCTTGT GGCAGCAGGT TCACAAAACT 2220 GGAGGCAGTT CCCCCTTTCT AGGATCTCCG TTCATCTCCT GAGGCCGCAC ATCTGCACAC 2280 ACCATCCTCA CTGGGCAGCT ATTACTTCGT GACACAAAGT GCCAGGCACT GCACTTGACA 2340 CTTTACCCAC GCTGTTTCCA TTGGTTTTGC ACAAAAGCTC TACGAGGTAG GTGCAACCGT 2400 TCTTATTGTA CACGGAAAGG AAATGTGGCT TAGGGAGATC AAGTATTCAC CCTATGTCAC 2460 AAAGCTAGTG AGTGGAGGAG CTAGAATTAA AGCATAAGTG GGTTTAATAT CAAAATCCCT 2520 TGTCTTAACC ACTGAGCTAT ACCGTTTCCC TCACTGTGAT GCAGCAACAG CCACGCATTT 2580 CACTGCCATT CATGGCCTCA CAGCACCCAG TGCTGTGCAG AGCTGCACAT CAATCAACAC 2640 TTCTCACGTA AGGGCTTCAA AAGAACTGTT GAAACAGACA ACTTACTATG AAAGCCCAGC 2700 AAAAGACGTG TCCCAAACAA TGCCTCTTCA TGTGAATGGA ACAGGAGGTT CGTGACTGGT 2760 CTCCTGAGAA GGTGGAAACA CTAACCCAGG AAGGCAGCTC AGGACCAGAA GGGAGCACCA 2820 GGATGTTGTC TGGGACAAGG AAGAGCCAGG CCCATTTCCT AGGGATCAGG GAGGTCGGCG 2880 ACATCTGAGG CCCCAGGTCG CTGCCGGGTT CTCGGAGCCC ACGCTGACTC TAGACTTCCT 2940 TGGCTCTGAA ATGCAGGTGG GTGTGGGCTC TGCCACCTGC CGGGGGGTCA GCAGTTGCCT 3000 CTGCGAGTTT CGAGGGGAGA AACCTGAGGG GCTGCAGCAG CCCTGCAGAG GGAGTGGGAG 3060 TGGCAGCATA GTCCATGTTC ACTCACAGCT CCCAGCCTCC TCCAAGGCGG GCCAAGGGGA 3120
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