Tag | Content |
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EnhancerAtlas ID | HS047-27485 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr5:133846010-133848730 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr5:133846897-133846915 | CCTTCCTGGCTTCCTCCG | - | 6.15 | MYC | MA0147.3 | chr5:133846056-133846068 | GGCCACGTGCCC | + | 7.22 | POU4F2 | MA0683.1 | chr5:133846588-133846604 | ATGCATAAATAATGCA | + | 6.02 |
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| Number of super-enhancer constituents: 27 | ID | Coordinate | Tissue/cell |
SE_00886 | chr5:133846699-133848698 | Adrenal_Gland | SE_06180 | chr5:133846840-133848594 | Brain_Hippocampus_Middle | SE_18783 | chr5:133845942-133847750 | CD4p_CD25-_Il17-_PMAstim_Th | SE_23610 | chr5:133846319-133848715 | Colon_Crypt_1 | SE_24106 | chr5:133846675-133848587 | Colon_Crypt_2 | SE_27492 | chr5:133846655-133848468 | Esophagus | SE_28095 | chr5:133846136-133848767 | Fetal_Intestine | SE_29069 | chr5:133846123-133848878 | Fetal_Intestine_Large | SE_31692 | chr5:133846671-133848610 | Gastric | SE_32759 | chr5:133846492-133848541 | H1 | SE_34361 | chr5:133844075-133849005 | HCT-116 | SE_35006 | chr5:133846193-133848783 | HeLa | SE_35715 | chr5:133846424-133848631 | HepG2 | SE_40774 | chr5:133846897-133848529 | Left_Ventricle | SE_42303 | chr5:133846695-133848663 | Lung | SE_47397 | chr5:133836971-133849017 | Panc1 | SE_47625 | chr5:133846758-133848644 | Pancreas | SE_48716 | chr5:133846799-133848661 | Right_Atrium | SE_50526 | chr5:133846651-133848689 | Sigmoid_Colon | SE_52569 | chr5:133846320-133848665 | Small_Intestine | SE_53502 | chr5:133847238-133848376 | Spleen | SE_56789 | chr5:133846698-133848133 | VACO_400 | SE_57763 | chr5:133846313-133848601 | VACO_503 | SE_57976 | chr5:133846694-133848640 | VACO_9m | SE_62577 | chr5:133838672-133892328 | Tonsil | SE_65308 | chr5:133846505-133849018 | Pancreatic_islets | SE_68727 | chr5:133846491-133848773 | H9 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr5 | 133846500 | 133848623 | chr5 | 133846400 | 133848045 |
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| Number: 1 | ID | Chromosome | Start | End |
GH05I134508 | chr5 | 133844208 | 133848821 |
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Enhancer Sequence | TGAAAAGATC GATAGATATG AGTTCAGTAA ATATCCACTG AGTGCTGGCC ACGTGCCCAT 60 TGCTATGTCA TGTGTGGGTG AAATAAGGGG CTGACACTCC CAGTAGCCAT AGAGGGTCCT 120 TTTTCATTTT ATCATTATCC CCAACAATGC TGTGATCACC AATCCAGGCA CACTGTCCAA 180 TTTTGTCATC CACCTTGGAA TCTTTTTTTT TTTTTTTTGA GATAGGGCTC TTGCTCTGTC 240 ACACAGGCTG GAGGGCAGTG GTGTGATCAC AGCTCACTGC AGCCTCAATC TCCCAGGCTT 300 AAGCAATCCT CCCACCTCAG CCTCCAGAGT ATCTAGGACT ACAAGCAAGT GCCACCATGC 360 CCAGCTAATT TTTGTATTTT TTAAGAGACA AGGTCTCACT ATGTTGCCCA CGCTGGTCTC 420 AAACACCTAG ACTCAAGCAA TCCTCCTCCC TTAGCCTCCC GAAGTGTTAG GATTATAGGC 480 ATGAGCCACT GGCCCTGTCC AGGGACCATT TTTATATAAA CTTTCCAGTG AAATCCAGGC 540 TGCTCTAGTC TGCCTTTTGC CTACTAGCCT CCTTGTATAT GCATAAATAA TGCAGACTCA 600 TTTTAACTTG ATGTTGATCT TACATAAAGT GTGGGTGGAA AAGTATATCT GCTGGGCAAG 660 CATCTAGTGC ATCAAATAAC GAATCCTAAA GTTAAATGGA AATTATTTTT AGGTTGTCTG 720 GGCAAATAGC ACAGAAGGTG GGGGGAATCC AGAGATATGA CCTCAGATGT GACACATGCA 780 GACACACGAC ACACCACACA TACACACACA CACACACACA CACACACACG CATATGGGTA 840 CACACAAATG CACCTTCTCT CTTCCTTCTG CCCCCACACT AGCAGCTCCT TCCTGGCTTC 900 CTCCGCCCCT CACTCACACA AAGGGCCAAA GCAAATACTT CAGCACTGAG TCATGTCCTA 960 CCTCATCTTG TTTCCAGCCT AGGAATCTCA CCTCCCCACC TGGGCTGTGA GGTCTTCTGG 1020 GGCAAAGATG GTGTCTGCTT CTCCTTAGGT GTGCCCTCCT AGTCTGATCA GCCAGAGGAC 1080 TGGACACCTA GGAGCTGCTT GCCTTTCCTT GAGCTCCGAG GGCAGTTGAG GATCAGGGAG 1140 GCAAGGGAGC TAGATGTCCA GTGGTAGACG CTCTCTAGGG CAGCCTCTTT GCCCCCCCAG 1200 GAATCTGCCT CTCCTGCCCA ACCCGGATGC CAGATAACAT AGGTTTCTTT TTTCTGTAGC 1260 ACTCTCCTAG AGGAGCTGTG TTAGGTAGAT AATCTGCCTA GAGCTGGCCT AGCTGGGGAT 1320 CAACTCAACA AGAATTTCTT GTTTCCAAGC GTCTCCTTCA CATGGGCATC CAGTGCCAAT 1380 TTGTGTCCAA GTCTCTTCCC TAGCACACGG GATGGAGGTC CAGCATATTT GGAGACAGCT 1440 CACTGTGTGC CAGAGCCACA GGTCCTAGAA TATCCAGCAA TCACAGTACC CAGGGCCACC 1500 CCAGCCTCAC AAGTCACTGT GCCCAAGGCC CTGAGGGAAG AACAGCTTGC TCACTAGTGC 1560 CTGAAGGAGG CTCCCAAGGC AGCCACCTTG TACACTGGAG ACACTCCCAG CAGTGGGAGG 1620 CAGATCAAGG CCAGGACACC GTTAATGAAG CTTTGACTAG GGTGAGGCAT CTCAGGGCCA 1680 GCTGGCCTTG CTGCTTCTCA CCCCACTCTA AGCCTTGATC TGTCCACATA CTTGACCCTG 1740 TTAGAATCTG GTGTCTGCCC CTCCCCCATC CTGATGTAAC ACATCTCTGT AGCCTGAAGC 1800 CGGCCCAGTT CTTGGCTCAG AGCTACTGCG TCTGCAGCAC AGATCTGTCC CTGAGCACAG 1860 CTCGCACCAG CTTCCCTGCA GGCCTAGAGC CCAAGCCCTG GCCTCAGGCA ATCTCCGCTT 1920 CCCTTGAGGC CAGCCCAGAG CCCCAACTCA GTGAGTTCTC ATGAACTGTT TAGACTCCAC 1980 CAGGTAATGA ATTGTCCCCA CTCTGCTGTC TCAGGAGCCA GGCTGGGCCA GGTATTCTCA 2040 GATTGAATTT GTTGGGAAGA AAGGGCACTC CACCTGCTGG AGGAGGGAGC ACCTCCTGGA 2100 GGCCATGCCG CTCAGAAACT TTCTTCCCAC ACAGCTTCCA GCCCCAGGCT GCCCACCCAA 2160 GTCTCAGCAG GCCAAAGGCC TAGTGAGGCT TTTCTGTGCC CCTGCTGGAG CCCAACGTCC 2220 ATGAGAAGGC TCTAGAATGC ATTTAGGATC TGAGACTGGT CCAGCTGAAA CAGCCCAGAG 2280 AGACCCTAAT CCTGGGGCCC AGAGAGAGCC AAACAGGCCC CAGGCCACAC AGAGGGCAGC 2340 CCTGAGGCTA GCCTAGAGGG CAGGTTTCTT GCCCCTTCCT ACCAGGAGAA GCGTGTCCTT 2400 GCCACACCAA TGATGTTTCT GTCCCTGGGT GGATTCCAAG CACCTGCGGG GCAACCAGCA 2460 CTGCCCAAAT GCAGAGGGCT TCTTGGGTTC CCCCAGTAAC CCCAAGGTCG ACTCCTCCCC 2520 TCCATCTCCA CAGCTCCTGC CCCTGCCCTT CCCCCCTTCC CAGTCTTGCT CCCTACATAC 2580 TCCAGTACAA GCAAATTCAT GAATTCGGTA CATACATTTC CAGACCTTTT TTTCCCGTAC 2640 AAAAATGCAC ATGTTTGTGT CTCTGTGTGT GTTCAGAGAA AAATGTAAAC TTTCATTTTG 2700 TAGGGTTTTT TTTTTGTTTG 2720
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