Tag | Content |
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EnhancerAtlas ID | HS127-18696 |
Organism | Homo sapiens |
Tissue/cell | Macrophage |
Coordinate | chr2:238622910-238625780 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Gata4 | MA0482.1 | chr2:238625143-238625154 | AAGAGATAAGA | - | 6.02 |
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| Number of super-enhancer constituents: 35 | ID | Coordinate | Tissue/cell |
SE_00318 | chr2:238623753-238625059 | Adipose_Nuclei | SE_01566 | chr2:238623660-238624709 | Aorta | SE_02327 | chr2:238623064-238624942 | Astrocytes | SE_03013 | chr2:238623802-238624499 | Bladder | SE_09199 | chr2:238623410-238624864 | CD14 | SE_11030 | chr2:238621497-238625470 | CD20 | SE_14422 | chr2:238622453-238623564 | CD4_Memory_Primary_7pool | SE_18373 | chr2:238621902-238623651 | CD4p_CD25-_Il17-_PMAstim_Th | SE_23331 | chr2:238623587-238624553 | Colon_Crypt_1 | SE_23963 | chr2:238623661-238624539 | Colon_Crypt_2 | SE_24998 | chr2:238623717-238624966 | Colon_Crypt_3 | SE_25815 | chr2:238622344-238625761 | Duodenum_Smooth_Muscle | SE_26722 | chr2:238623632-238624748 | Esophagus | SE_28399 | chr2:238623224-238625284 | Fetal_Intestine | SE_29463 | chr2:238622880-238625334 | Fetal_Intestine_Large | SE_29646 | chr2:238622538-238625705 | Fetal_Muscle | SE_31908 | chr2:238623623-238624722 | Gastric | SE_36919 | chr2:238622146-238636987 | HSMMtube | SE_38133 | chr2:238622779-238625696 | HUVEC | SE_40633 | chr2:238623277-238624849 | Left_Ventricle | SE_42111 | chr2:238623595-238624904 | Lung | SE_44921 | chr2:238622785-238624912 | NHLF | SE_45786 | chr2:238623014-238623975 | Osteoblasts | SE_48071 | chr2:238623276-238624924 | Psoas_Muscle | SE_48757 | chr2:238623611-238624753 | Right_Atrium | SE_50280 | chr2:238623478-238624856 | Sigmoid_Colon | SE_51094 | chr2:238620130-238627568 | Skeletal_Muscle | SE_51777 | chr2:238622629-238624968 | Skeletal_Muscle_Myoblast | SE_52590 | chr2:238623608-238624681 | Small_Intestine | SE_53427 | chr2:238623708-238624817 | Spleen | SE_54582 | chr2:238622548-238626021 | Stomach_Smooth_Muscle | SE_59868 | chr2:238570692-238624050 | Ly4 | SE_63565 | chr2:238622556-238624982 | HSMM | SE_64519 | chr2:238622746-238624872 | NHEK | SE_65656 | chr2:238623775-238624768 | Pancreatic_islets |
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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: 2 | ID | Chromosome | Start | End |
GH02I237714 | chr2 | 238622691 | 238625616 | GH02I237716 | chr2 | 238625618 | 238628219 |
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Enhancer Sequence | GTCCAAAAGG TAGGCTCTTC TTTCTTTATT TTCTAACTTG CATGTACTGT TTTTTCCTTG 60 CCAAGGGCCT GGTCACCTTT CAGAAATAAC ACCTTGCACT GAAGATACAT AGAAGTTCTT 120 ACTGTTTATT TTACTACTTT GTGTATGAAT TTGTTTGAAC AAGAATGCCT AGATCCTCAT 180 CTTGCCCCAC TCAAAGCAAC AGTCAGACAC ATTTCTGTGT ACTGAATGCT TTTGTCATCT 240 GCATTTTCCT CAAGAAATGT AAAAATTGTT TCTTTGAGAA GAAAAGTAAT TCTAAGGCAA 300 AATTATATTT CAGAATGTGG ATAGCCTTCT GAAATTATGT ATGGAAAGAA AAAGATGATT 360 TTATTAGAAA ACTTAAAAAA TTCCATACAA ATTACCACAC ATTGAGAGAT TATTAGATAT 420 TGAGTTAAAA ATCTGAGTAA AAGGACAGTG ATGATATAAA ATGAACCTGC CATTCATCCC 480 TAATGCTCAG AGATCATAAA ATGACGTGCC TCTCTGTTTC CTAGTATTTT GTAGAAGCAG 540 CTGAGGTTTA GAAGTAAATA CACTGGGCAG GCCAGATACA GAAAATAAAG ACAAGCAAGT 600 CAGTGATTCA AGATCTAGCA AAAATGAAGT CAGAAGTGAG CGAGTTCCTT GAGAATTTAT 660 AGAATTTGTA TACACGGGAG TCTTTCCCAT AAATGAATTT AGTTTGATAC TTAAAACATC 720 TGTGATAGTT TCCTTTTATA AATTTAGTTT CTAGACAACA ACTGTATTTT TCTCTTAGAG 780 CAGATGAGAA AATCAGAATA AGATCACTTA ATTTCGGAGG TTAGAGCACA CAGGCCTCGG 840 AATGCACGGG CAGTAAATTT AAGAGCCTGT TGTGTTGGAT TCCTGTGCTG GCCATGATGA 900 CGAATCGCCT TCCCTGCTGG AGCCCTGCAC TCTGCATAGC TGCTGTCCCG AAGAGTGCAA 960 AGAAATTTGT TAAGTAGATG CCAGAATCTC TTGTGCTTGA CTAGTGTTTC CAGGGCCCAA 1020 GTGTAGAAAT GGATATTGCA GCTGGAGTTC CTGGTCGTCC TCAGAGAGCC TCGGGAAGAA 1080 CTGGACAGGT GCAAGGCCAG GCGGGGAGCC CTCCCTGTAA CTGACAGCAG GACGCTCTCA 1140 TCCAAAACCT GGAAGAGGGG CTCTATCTGG TCGTTTCCAC TTGCATTCAT GCCTTTCTTG 1200 TGCTAGGTCA CATTATTTTC TTTTTACTAA CGTGCCAGGG ATACATTGTG AGAACTTTGT 1260 CAGAATGTGA ATTTGTGTAG AATGTGAAGC TAGAAGGAGC CCCGGAAACC TGCAGTGGAG 1320 GAGCAGAGGC ACAGTTTTGT AGTAAAGGTG TGCCCAGGGA AGGGAAGGCT TTCCTCATTG 1380 CTGAGATGTC TGGGGAGGAG AGGAGGCGGC GATTGCGCCT CCGGCCCAGC CAGCTGCTTT 1440 GCGGAACAGT TTCTCTGGAA TCAAAGCTAT TTCTGAAAGT AGCGCGGCTC CTGCTTCCCT 1500 CCGCATGGCT TCCGGATCAT GGTAGTGATT GACGTTTGAA ATGTTTGCCC TTCCTGGACT 1560 TTGCTGTGCT AGTGCTGCTG GCTAACCCAG GAACTACTAG TTAATTGCAC TTGCTGTTAC 1620 TAGGGGCGTT CTCTCCCCAG GAATGACATG GAAATGCAGT TACAGTAGCC ACTTATAAGA 1680 CCACCCATGA ACGAGGTGAA AGATTTTCAG AACTGGTCCT TTGTCATGAA AAGAGCAAGT 1740 TAGAGTGTGC AGATATAATG GGCAAAAAGA AATCTATGAA AACAGAAAAA CTGACAGTAC 1800 AGATTCTTTT GGAATTTAAA TAATTTTATT GTGAATTTAT ATAGCCCCCA TCCTTCTAAA 1860 AACATATTTT GCTTCCCTCT TTCTAGTTAA GCCAAAAAAT AAGGGAGGAG TGATGGCATC 1920 ATATTTTACT TGTGAAAAAT CTGGAACTTG GCAGGTGCTA ACATTAATTG AATGCAAAAT 1980 AGCTTTAAGC TGATGCATTT CCCTGACATT GAAGTTAAAA CATGACTTTG GGATGTTTGT 2040 TTTTATTTCC TTTCTGAATT TATATTCCAA GGGAATAACC TACAGAAAAA GATATGGCTC 2100 ATGTCCTTTT TGTCTTTTTT GTCCTTTTTG TACTCATGTC CTTTTTGTAT TATTGAATTT 2160 TTAAAAGTAT TGTTAAATTC TCCCTCCTAA TTTCTGCTCT TCCAATTTTC TACTTACTGT 2220 CACCTCTAAG AGAAAGAGAT AAGACCGTCT GAAAACTGCT TATTTTTAAA TCTGGCCGCC 2280 CTTCGAAATG AAACAAAACC AAACATAGCA ACAGCATGTT TTTGGTTATT GTAAAACAAT 2340 TTCAAAAATG GTCTTGTATT TCTAGCACCT GATTTTTTCT CTTGATTATA AGATTTTAAT 2400 GTATGAAGAG AAAACTCACA TCTGTGTTAT AATGATACGG AAGTTTGCTT AGTTGTTTCT 2460 TGATTTTCTT ACTGGAAATT AAATAAAAAG GAGAGAAGCA AAACCCCATT ATTTGGGCCC 2520 ATGACCTGGC TTCCCACCTA CCTTTGGGAT TCCCTGATTG AGTGGCAGCA GTAGCCGTTC 2580 TGAATCTGCT TTTCTCATTT TAACTTGGAC CACTGAACAG GATAAAAACA TGGAAGTATA 2640 AGCTAAAGCA AGCTTGTCCA ACCTGCGGGC CACATGCAGC CCAGAATGGC TATGAATGCA 2700 GCTGAACACA AATCGTAAAC TCTTTTAAAA CATTATGAAA TTTTTTTTGC AATTTTTTTT 2760 TTTTAGCTTA TCAGCTATCG TTAGTGTAGT TTATGTGTGG CCCAAGACAC TTCTTCCAGT 2820 GTGGTCCAAG GAAGCCAAAA GATTGGACAC CCCTGAGCTA ATGTCACCTC 2870
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