Tag | Content |
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EnhancerAtlas ID | HS007-14762 |
Organism | Homo sapiens |
Tissue/cell | BE2C |
Coordinate | chr6:111870970-111874160 |
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: 2 | Chromosome | Start | End |
chr6 | 111871319 | 111871532 | chr6 | 111872301 | 111872524 |
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| Number: 2 | ID | Chromosome | Start | End |
GH06I111551 | chr6 | 111871404 | 111871603 | GH06I111550 | chr6 | 111871688 | 111877634 |
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Enhancer Sequence | TTGGTGTTAT ATCACCCCAG CTAGATTTTA AGTAATTAGA GAGCAAGAGC GTGTGTCACT 60 CATCTTTGTG CCAAGCATAT TACCTTGCAC ACAGTAGGCA TTTAATGAGT AGTTGGAGTC 120 TGGTTGCTAT GTGTTAGTTG CTGTGGGTGC TGCTGAACTC TCACCTTGCA GCCTTTCTGG 180 ATTAGCTTTT GAATGACAGT TTTATTAGGC ATGATGGAAC CAGACCTCCC ATGCTCACAC 240 TGTGGTGTCA GGGACTTCTG CCTCATGTGT CTTTTCAAAT AATAACATTA TGCTGGTACC 300 CAAAGTATAT GGTACCAGTT TAGAGTCTTG AATTTTAAAA ACCTGAATAT GGAAAGAACC 360 TGCTCAACCA CTTTGGAATG CCCCTGTTAA GCTCACCTTA CAGCATCAGA AGTGGACTCC 420 GCAGCCACCT ATTAGATCCA ATATGAAATG CCCTAAATAC TCCCCTTACT TGGTGCCTGG 480 AGGACCTCAG TCTTAAGCTT CTCCTTTGGA CTGAGGGCCT GACAAGGCCT GTGTAGGGCA 540 GGCTGAGCCA AGCCCTGGCT TGGATTAGGG GTATCATCCA GGAATGGAAT GAGCGAATGG 600 CTTCACCTTA AGGAAACCTT TTAAATGAGA TGAACAATGA CCTTCTTAAA CAAAATAGAG 660 AAAACATGAT GTAACCTTTT CCAGATGATT AAAGATATTG TTTTTAAAAC CAGTCACTTG 720 CTGTGAAAGC TGTGATGTTA TCAGTGACTT CTGAGGGGTG TTTATTGCTA TAGTACATGA 780 TCTGAACCAA TGAAGCTGGA CATTTTAATG TGGCTGTTTT GATTTGACCT GGGTGAAAAT 840 TAGAGGTAAG CTTGCTTTTA CAAACATTAC TTAGTGATTT TTTTAAAAGC TGAATATTTA 900 CTAGTGCTTT TCAGGGTGCT TCAAAATATT AATATTTTCA TGACAAAACC ACCTTGTCAA 960 AATGTCAGCT GTCATTTCCA TCAAGATGCT GGTCCTCTAA CCCTTCTTCC CTATTGTCCT 1020 GCTAAACTGG CAACTTCTAA CCTACCAAGC GTTAGAAAAA CAGAAAATTG CTCTTGTTAG 1080 AACCATGTAT ATAAAGTAAG AGTAAATGTG ATCTGGGTGA GGGTCTGATG GTTGTGTTAG 1140 GAATAAGAGT GGGGAGGTTT AGTGCCTAAG CCTTGGGATA CTGTTTTGGC TTGGAGGATT 1200 ATCCCATGAA ACCCTTTTCA CCACTGATGC CGTAGGTGGA ATTAGCTCTT CAGGCAGACA 1260 TTTTTTTCTT CTTAGGGTCA AAGGTAAGGT GACATGTGAA GGGGCAGCCA AGGCATCATC 1320 GGGAGGCTAG GGCTTGATGG AAGGGGTAAG GGGGGTGGTG CCGGGCATCT GGTTGGAGGG 1380 AAGTAGGAAC ACAGGCAGAA GCAGAGAAGG GCCCTTAGTG CTGCCGAGCA CAGGCTGCTG 1440 CTTGACGCGC AGCCCTCAGC TGGCTGGCCC TGGCTGGAGA ATTTCTCCGC AGGTCATTGG 1500 TTTTACCACA GTCTTGTTTG GAAACCATCT GTGTTCTAGG AGCCCATGGA GAACGGGCAT 1560 CTTATTTTGA AAATCAGTTT GAAGCTAAAG TGGACTTTTT AATTACAAAT GAGAGCAATG 1620 AAAATATAGC TATTGAACTT TATTGTTATT TTGGCCTCGT AAAAATTAAA AGTAAACTTT 1680 TTTAACTCAA GAGGATTTTA TAAAATCTCC CCATTTGTGT ACATTTCAGA CATGAGACTC 1740 TACCACCCCA GAACCCATCT GAGAGGAATT TAAATCTCAG GAAAGTAGCA GCTTTCTTCA 1800 AGTTTCTGAG TAACTGAACC TTGTAGATAA CAACAGATTG GAAGATAGAA TCAGTTAATC 1860 CCTGAACTCA AGGAACCCTT GGCCCATAGC CCAGACAATA CAGCATGCTG AAAATTGGTC 1920 TGGTCCCAGC CTCACGTAAA CCTGTTTCTC CTCTCCTGAG AAGAATGCAG CTTTTGACCA 1980 CTGCCCAGTG TGAGAGCCCG GCCTCACTGT TAACACCTCA GTGAAGGCAA GAACAAGTGG 2040 TTTGCAGTGG AGGGCATCGC CTGGAAGGTG GCAAAGGCCA GGCAGGTACC TGCGGCCCAG 2100 CTGCTGCTCG ACGATGAGGC TGGCAGCCAA GTCTAGCGCC AGCCTTTTCA AAAGCAGCCC 2160 TTTTGATAAC ACTGATTACA TTTCCCTCAC CGGAGCCTTG GGTTAATTGA GCAACAGCCA 2220 ACTTCTCTGG GTAACAAAGA GGAGGGGAAA GTAATCCAAA CACAGGTTTT ATTATAAAAA 2280 CCAGGGAGTG AGAGAAGTGT GTTTATTCTG TAAGATAACA CACCTGCTCG GTGCCGGGGA 2340 GGCTCATTTC CATCAGTTGC CATGGCAAAC TCGTTATACT TCAAGGCCAT GTGGCTTTGT 2400 TTCCTTTTGG GATCTGGTCC TTGTCCTACC TTTTCTAACA ACTCCAACAC AATGACATGG 2460 AAGCCTGCGA CAGCATAATT GATTTCTCCT TCCCTCTATC AACGGTTCAC ATTTGTTCAG 2520 CACAGGACTG AGTCTGCCTT CTCCTTTGAA CTCCTTGCTA AGCATGAAGG CATGCTTCAG 2580 AGAGCCACCC TCATTAACAT TCCAGGTCCC TCTTCCCTGT CAGCAATAAA CAAGCCCTGC 2640 ATCAATGGCC TCCTGCCTTC CACTTTTACA AATGAGTGGC TCAGTTCCAT GTTTTGCTGC 2700 TGATCCAGGT GCCCAGGCGC ATACAACGCG AGCCTAAGAA GCACGCGGGA GGGACTAAAA 2760 ATAGAACAGC AGTTTTGGAT GCATACCAGA GCAGCTACTT CATCTCAACT TGCTTTGCAC 2820 GCTAAGCCTA ATGGGATCCA TCAGGCATGA GTTCTCTCGC GCGCTAGCTC CCTCCCTCTC 2880 CCCTCTCTCC CCAGCTGCCG ATTTCCATCA GCCCCTTCCT GGTGAAGGGA GCAAAGGGAG 2940 GTCAGGCAAG GGACAAGAAA TGTGTGCCCT TATGGTTTTC GTTTACAAGC CCTGGGAGAT 3000 CTGGGGGCTG CAGTTACTCC TTCCATAAGA GAGTTTCTAG AAAAAAAGCA GGCAGGCCCA 3060 GAACATGGTC ACCTCTGCCC AGGTACACTT TGGTCCAAGA CTTTCATTGT TTAGCAAAGC 3120 CTCAAATATC ACTTCCTAAT CACCCAATAC CTATAACCTG GACCCATGCT CCTATATTCC 3180 TTGAAAAGTT 3190
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