Tag | Content |
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EnhancerAtlas ID | HS024-14098 |
Organism | Homo sapiens |
Tissue/cell | Cerebellum |
Coordinate | chr6:111872120-111874270 |
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) |
MEF2A | MA0052.3 | chr6:111873723-111873735 | ACTAAAAATAGA | + | 6.27 | MEF2B | MA0660.1 | chr6:111873723-111873735 | ACTAAAAATAGA | + | 6.32 | MEF2C | MA0497.1 | chr6:111873721-111873736 | GGACTAAAAATAGAA | + | 6.89 | RARA(var.2) | MA0730.1 | chr6:111873908-111873925 | AGGTCAGGCAAGGGACA | + | 6.21 | RFX5 | MA0510.2 | chr6:111873324-111873340 | AGTTGCCATGGCAAAC | - | 6.03 | RFX5 | MA0510.2 | chr6:111873324-111873340 | AGTTGCCATGGCAAAC | + | 6.34 | Rxra | MA0512.2 | chr6:111872243-111872257 | AGGGTCAAAGGTAA | + | 6.07 | ZNF263 | MA0528.1 | chr6:111873842-111873863 | TCCCTCTCCCCTCTCTCCCCA | - | 6.15 |
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| Number of super-enhancer constituents: 20 | ID | Coordinate | Tissue/cell |
SE_00043 | chr6:111872754-111874669 | Adipose_Nuclei | SE_01892 | chr6:111872775-111874783 | Aorta | SE_25836 | chr6:111872420-111874786 | Duodenum_Smooth_Muscle | SE_26930 | chr6:111872756-111874615 | Esophagus | SE_31696 | chr6:111871948-111874935 | Gastric | SE_33474 | chr6:111869902-111875281 | H2171 | SE_36956 | chr6:111871448-111878954 | HSMMtube | SE_41014 | chr6:111872539-111874578 | Left_Ventricle | SE_42404 | chr6:111872683-111874769 | Lung | SE_44157 | chr6:111871850-111874875 | NHDF-Ad | SE_44783 | chr6:111872522-111874865 | NHLF | SE_45702 | chr6:111872417-111874783 | Osteoblasts | SE_47224 | chr6:111870720-111877244 | Panc1 | SE_48418 | chr6:111872659-111874652 | Psoas_Muscle | SE_50264 | chr6:111871896-111874877 | Sigmoid_Colon | SE_51251 | chr6:111871765-111874852 | Skeletal_Muscle | SE_52559 | chr6:111872727-111874660 | Small_Intestine | SE_55947 | chr6:111872981-111874360 | u87 | SE_66964 | chr6:111869902-111875281 | H2171 | SE_67791 | chr6:111872981-111874360 | u87 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH06I111550 | chr6 | 111871688 | 111877634 |
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Enhancer Sequence | GGGGAGGTTT AGTGCCTAAG CCTTGGGATA CTGTTTTGGC TTGGAGGATT ATCCCATGAA 60 ACCCTTTTCA CCACTGATGC CGTAGGTGGA ATTAGCTCTT CAGGCAGACA TTTTTTTCTT 120 CTTAGGGTCA AAGGTAAGGT GACATGTGAA GGGGCAGCCA AGGCATCATC GGGAGGCTAG 180 GGCTTGATGG AAGGGGTAAG GGGGGTGGTG CCGGGCATCT GGTTGGAGGG AAGTAGGAAC 240 ACAGGCAGAA GCAGAGAAGG GCCCTTAGTG CTGCCGAGCA CAGGCTGCTG CTTGACGCGC 300 AGCCCTCAGC TGGCTGGCCC TGGCTGGAGA ATTTCTCCGC AGGTCATTGG TTTTACCACA 360 GTCTTGTTTG GAAACCATCT GTGTTCTAGG AGCCCATGGA GAACGGGCAT CTTATTTTGA 420 AAATCAGTTT GAAGCTAAAG TGGACTTTTT AATTACAAAT GAGAGCAATG AAAATATAGC 480 TATTGAACTT TATTGTTATT TTGGCCTCGT AAAAATTAAA AGTAAACTTT TTTAACTCAA 540 GAGGATTTTA TAAAATCTCC CCATTTGTGT ACATTTCAGA CATGAGACTC TACCACCCCA 600 GAACCCATCT GAGAGGAATT TAAATCTCAG GAAAGTAGCA GCTTTCTTCA AGTTTCTGAG 660 TAACTGAACC TTGTAGATAA CAACAGATTG GAAGATAGAA TCAGTTAATC CCTGAACTCA 720 AGGAACCCTT GGCCCATAGC CCAGACAATA CAGCATGCTG AAAATTGGTC TGGTCCCAGC 780 CTCACGTAAA CCTGTTTCTC CTCTCCTGAG AAGAATGCAG CTTTTGACCA CTGCCCAGTG 840 TGAGAGCCCG GCCTCACTGT TAACACCTCA GTGAAGGCAA GAACAAGTGG TTTGCAGTGG 900 AGGGCATCGC CTGGAAGGTG GCAAAGGCCA GGCAGGTACC TGCGGCCCAG CTGCTGCTCG 960 ACGATGAGGC TGGCAGCCAA GTCTAGCGCC AGCCTTTTCA AAAGCAGCCC TTTTGATAAC 1020 ACTGATTACA TTTCCCTCAC CGGAGCCTTG GGTTAATTGA GCAACAGCCA ACTTCTCTGG 1080 GTAACAAAGA GGAGGGGAAA GTAATCCAAA CACAGGTTTT ATTATAAAAA CCAGGGAGTG 1140 AGAGAAGTGT GTTTATTCTG TAAGATAACA CACCTGCTCG GTGCCGGGGA GGCTCATTTC 1200 CATCAGTTGC CATGGCAAAC TCGTTATACT TCAAGGCCAT GTGGCTTTGT TTCCTTTTGG 1260 GATCTGGTCC TTGTCCTACC TTTTCTAACA ACTCCAACAC AATGACATGG AAGCCTGCGA 1320 CAGCATAATT GATTTCTCCT TCCCTCTATC AACGGTTCAC ATTTGTTCAG CACAGGACTG 1380 AGTCTGCCTT CTCCTTTGAA CTCCTTGCTA AGCATGAAGG CATGCTTCAG AGAGCCACCC 1440 TCATTAACAT TCCAGGTCCC TCTTCCCTGT CAGCAATAAA CAAGCCCTGC ATCAATGGCC 1500 TCCTGCCTTC CACTTTTACA AATGAGTGGC TCAGTTCCAT GTTTTGCTGC TGATCCAGGT 1560 GCCCAGGCGC ATACAACGCG AGCCTAAGAA GCACGCGGGA GGGACTAAAA ATAGAACAGC 1620 AGTTTTGGAT GCATACCAGA GCAGCTACTT CATCTCAACT TGCTTTGCAC GCTAAGCCTA 1680 ATGGGATCCA TCAGGCATGA GTTCTCTCGC GCGCTAGCTC CCTCCCTCTC CCCTCTCTCC 1740 CCAGCTGCCG ATTTCCATCA GCCCCTTCCT GGTGAAGGGA GCAAAGGGAG GTCAGGCAAG 1800 GGACAAGAAA TGTGTGCCCT TATGGTTTTC GTTTACAAGC CCTGGGAGAT CTGGGGGCTG 1860 CAGTTACTCC TTCCATAAGA GAGTTTCTAG AAAAAAAGCA GGCAGGCCCA GAACATGGTC 1920 ACCTCTGCCC AGGTACACTT TGGTCCAAGA CTTTCATTGT TTAGCAAAGC CTCAAATATC 1980 ACTTCCTAAT CACCCAATAC CTATAACCTG GACCCATGCT CCTATATTCC TTGAAAAGTT 2040 AAGTAGAAAA CTAAAGTACA CTGAGTGTTC CTCTTACAGA TCCCACCTGC TTGCTTGAGG 2100 CTAAGAATTT GGGAGCAAAT GCACAGTGAG TTGGCAACAT GTGACTGCCA 2150
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