Tag | Content |
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EnhancerAtlas ID | HS040-03346 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr1:223902460-223904790 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
TP53 | MA0106.3 | chr1:223903596-223903614 | TGCTTGCCAGGGCATGTT | + | 6.17 | TP53 | MA0106.3 | chr1:223903596-223903614 | TGCTTGCCAGGGCATGTT | - | 6.32 |
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| Number of super-enhancer constituents: 39 | ID | Coordinate | Tissue/cell |
SE_00224 | chr1:223891886-223912166 | Adipose_Nuclei | SE_01908 | chr1:223903739-223904850 | Aorta | SE_02306 | chr1:223899487-223903687 | Astrocytes | SE_04026 | chr1:223903291-223905474 | Brain_Anterior_Caudate | SE_05036 | chr1:223902343-223904766 | Brain_Cingulate_Gyrus | SE_05972 | chr1:223899184-223905867 | Brain_Hippocampus_Middle | SE_09681 | chr1:223899395-223907924 | CD14 | SE_19702 | chr1:223899422-223907008 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_23408 | chr1:223902389-223903605 | Colon_Crypt_1 | SE_23408 | chr1:223904046-223904670 | Colon_Crypt_1 | SE_24051 | chr1:223902436-223903004 | Colon_Crypt_2 | SE_24051 | chr1:223903089-223903543 | Colon_Crypt_2 | SE_24051 | chr1:223903970-223904550 | Colon_Crypt_2 | SE_25230 | chr1:223902434-223903064 | Colon_Crypt_3 | SE_26209 | chr1:223899230-223905388 | Duodenum_Smooth_Muscle | SE_26925 | chr1:223899336-223904834 | Esophagus | SE_31491 | chr1:223898405-223906097 | Gastric | SE_33950 | chr1:223900271-223904290 | HCC1954 | SE_34545 | chr1:223899419-223904575 | HCT-116 | SE_34979 | chr1:223899218-223904777 | HeLa | SE_36294 | chr1:223899426-223904613 | HMEC | SE_37129 | chr1:223899390-223911201 | HSMMtube | SE_38254 | chr1:223899363-223904539 | HUVEC | SE_38957 | chr1:223902403-223904692 | IMR90 | SE_42269 | chr1:223902366-223906841 | Lung | SE_44530 | chr1:223900206-223905349 | NHDF-Ad | SE_44904 | chr1:223902263-223903610 | NHLF | SE_44904 | chr1:223903924-223904809 | NHLF | SE_45872 | chr1:223899383-223910101 | Osteoblasts | SE_50365 | chr1:223899342-223907084 | Sigmoid_Colon | SE_51879 | chr1:223902338-223905051 | Skeletal_Muscle_Myoblast | SE_53249 | chr1:223902420-223905033 | Small_Intestine | SE_55958 | chr1:223898795-223906601 | u87 | SE_63671 | chr1:223902338-223906710 | HSMM | SE_64794 | chr1:223900231-223904926 | NHEK | SE_65644 | chr1:223902687-223903954 | Pancreatic_islets | SE_65644 | chr1:223904002-223904652 | Pancreatic_islets | SE_67677 | chr1:223898795-223906601 | u87 | SE_68376 | chr1:223892363-223922876 | TC32 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 5 | Chromosome | Start | End |
chr1 | 223904365 | 223904567 | chr1 | 223903033 | 223903347 | chr1 | 223902800 | 223903000 | chr1 | 223903000 | 223903425 | chr1 | 223903915 | 223904781 |
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Enhancer Sequence | AATACCTACT ATATGCTGGG CACAATGCAT ATGGTTTCTG CTTCTGAAGA CTTACTTCTG 60 AGGCTAGTGA GGGGACAGAG ACAGGTCCCC CAACAGTTGG AAATGCCTGT GGGACTTCCA 120 GATGAGGATG TAGAGGTCTA GAGATGATCT AGCGCCACTG CTTAGGGCAG GCGGGCTGTG 180 CACTGCACAA CTAAGGAAGA GTGTGACTTT TACGATCCCC ATTTGCCAGT TGAAGAAATT 240 GAGGCTTGGG AAGGTTAAAT ACTTGCTCAG AGTCAAGTGG ATATAGGGCA TAGATCCAGG 300 ACTGTGTGTA GTCTGTGCAT GTTGAGCCTA CCCCTTATGG CTGCGCTCTC TGCCTCCTTC 360 CTACCTTCTC AAATGCTGCT GAGGTCAGGC AAGGGGAGCA CAGTTGTTTC CGCTGGATTT 420 GAACACTAGC AAGTCATTGG TGAGTTTAGC AGAGCAATTT CAATGGAAAG GTGAGAGTAG 480 AAGCCAGATT GTTGTAGACT CCAGAGTAAA GGAACTGGAA ATTAAGAACA TGATCAACTT 540 ATTTAAGAAG GACCCCCGGG AAGAGAGGAG AACTGATAGG TAGAGTAGGA CCTGGACTTT 600 GAGAGCCTGT GTTTTTTTCA TATGAGAACA ACTTGAATGT GTCATATGTT GAATCACCAG 660 GAAGAAGGGA TTAAAGATAA AGGCAGGGAG GGGGCAGTGA AACAGGATCC CTGAGGAAGT 720 GAGAATACGG GTTGTGGGCA GGGGAGGGGA GCAGGTTAGC CTTGCAGCAG GAGGAGCTGC 780 TCTTCCTCGG AGAGAGGATT TCACAACACT GGCAAGAGTG GCTCCAGTGC CTGGAGCGGG 840 GATTAAAGCA GTAAGTCCAG TGGGGTCCAA GGGCCATGCA GGGGTACAGT GAGGAGAAAG 900 CAGGTGTGAT CCGGGTGGCA CATCAGATCC TTCCAGCAAC CAGTCTGTTA GGAGCAAGGG 960 CAGATGTTGT GAGCCCCTAT GTTTCCCCCA AGAAAATCAA ACCTCTGAGA GGTTTCTCAC 1020 TTGCTTATCT TCAGCTGGCC GAACTCAGCC TCAAACCCAT ATGTCCTGTC TCCAAGTTCA 1080 GTGACTGTTA TCATCAACTT CTTCAACAGT AATAATAATA GATCACATTT ATGGAGTGCT 1140 TGCCAGGGCA TGTTTACATC ATTATCTCAT TTAACACTCA GAACAATCCT CTGTGGTGGG 1200 TGTTTTCATC GTTCCCATTT TGCAGGTGAA AAAACTGAGA CTTCAAAAGG TTAAGTGACT 1260 TCCCAGGGTC CTACGACCTA CATAATAAGT GGCAGAGCCA GGATTCAAAC CTAGGTTATC 1320 AGAATAATGC AGCAAAGCCC AAACCCTCAG CCCCTTTTCA CTGACTGGTA AGACCCATAT 1380 TTAATTCGAT GCCCTACATG CCGTGCACAA GTTTCAGTTT TCTGAAGCAT CGCTTAGATG 1440 CTTAGGTGTT TAGCACCACT CTGAACTCTG ACTTTTCTAG AGAGGCTGCT AAAGGCATTA 1500 GAAAGTTTCT GAAGTATAAT GGAAAAACCC TGCTGGAGTA AGTGCCTGGC ACACTCAGGA 1560 TTATCAGTGT GATTCTTTAT AATAAACAGG CTCCCAGCAC CAAGCCCAAT CTATTCCATC 1620 AGCTGGATAA GAGCTCTCTG GCAGGCCTTG GGCCAAGCTG GCTTCCTTTG CCTCAGCAGA 1680 AGAGCATTCT GATTCTCTCT GCCATCCCCA AAACTGACAG GAGCAGAGAG AAACAAGGCA 1740 GAGGCATGAA GGGAATGTCC TCTGCGGCAG ATGGTGCTTC CGGAAGAGCT CCCACAATCT 1800 GAGCTAGAAT GAACAGGGGC TAGATCCAAG TCTCATATAG GCATACTTCT GCTTGACAGA 1860 GTGGGCATGC CGAGGGCCGT TGGGTGGAGG CAGGCGTGTG CAACCCAAGC AGACATGAGA 1920 CGCAGCTCCT TCAAGGCAAG GTTGCCTGAG CCCAGAGAGG CTCAAATTTG TGCCCCAACT 1980 TCCTCTGTGG CTTTTGGGTG GGGCTCTTCA GAATCGAAAC ACACTCAGAG GGCTGCTGAA 2040 AGGGCTAAGA AGTGTTCAAG GTTGGCTTCC ATCAGGCTGC TCATGACAAT GGCCCCTGAG 2100 GTTTTAACAC CCTTGAACGC TTGGTACTAA ATCAATTAGA GGCAGGGCAG GAGCAGAAAG 2160 AGTTGGCGCA TTTGATCAGT AAGTTCCAAT GCCAGTGCTG TCTATTATCT GTGAACTGTG 2220 TTAACTTTGG ACACGTCACT TCACCTTTTT GAGCTGTTTC CTCGTCTGTA AAAGGGGGAT 2280 AATACCCATT CCATGAGGTA AAGCTTTGAG CACAGTCTCT GATGTAAGCA 2330
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