Tag | Content |
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EnhancerAtlas ID | HS134-05076 |
Organism | Homo sapiens |
Tissue/cell | Mesendoderm |
Coordinate | chr1:223902440-223903960 |
Target genes | |
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: 35 | 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_24051 | chr1:223902436-223903004 | Colon_Crypt_2 | SE_24051 | chr1:223903089-223903543 | 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_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_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: 3 | Chromosome | Start | End |
chr1 | 223903033 | 223903347 | chr1 | 223902800 | 223903000 | chr1 | 223903000 | 223903425 |
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Enhancer Sequence | CATTCAGTAA GCATTTCTCG AATACCTACT ATATGCTGGG CACAATGCAT ATGGTTTCTG 60 CTTCTGAAGA CTTACTTCTG AGGCTAGTGA GGGGACAGAG ACAGGTCCCC CAACAGTTGG 120 AAATGCCTGT GGGACTTCCA GATGAGGATG TAGAGGTCTA GAGATGATCT AGCGCCACTG 180 CTTAGGGCAG GCGGGCTGTG CACTGCACAA CTAAGGAAGA GTGTGACTTT TACGATCCCC 240 ATTTGCCAGT TGAAGAAATT GAGGCTTGGG AAGGTTAAAT ACTTGCTCAG AGTCAAGTGG 300 ATATAGGGCA TAGATCCAGG ACTGTGTGTA GTCTGTGCAT GTTGAGCCTA CCCCTTATGG 360 CTGCGCTCTC TGCCTCCTTC CTACCTTCTC AAATGCTGCT GAGGTCAGGC AAGGGGAGCA 420 CAGTTGTTTC CGCTGGATTT GAACACTAGC AAGTCATTGG TGAGTTTAGC AGAGCAATTT 480 CAATGGAAAG GTGAGAGTAG AAGCCAGATT GTTGTAGACT CCAGAGTAAA GGAACTGGAA 540 ATTAAGAACA TGATCAACTT ATTTAAGAAG GACCCCCGGG AAGAGAGGAG AACTGATAGG 600 TAGAGTAGGA CCTGGACTTT GAGAGCCTGT GTTTTTTTCA TATGAGAACA ACTTGAATGT 660 GTCATATGTT GAATCACCAG GAAGAAGGGA TTAAAGATAA AGGCAGGGAG GGGGCAGTGA 720 AACAGGATCC CTGAGGAAGT GAGAATACGG GTTGTGGGCA GGGGAGGGGA GCAGGTTAGC 780 CTTGCAGCAG GAGGAGCTGC TCTTCCTCGG AGAGAGGATT TCACAACACT GGCAAGAGTG 840 GCTCCAGTGC CTGGAGCGGG GATTAAAGCA GTAAGTCCAG TGGGGTCCAA GGGCCATGCA 900 GGGGTACAGT GAGGAGAAAG CAGGTGTGAT CCGGGTGGCA CATCAGATCC TTCCAGCAAC 960 CAGTCTGTTA GGAGCAAGGG CAGATGTTGT GAGCCCCTAT GTTTCCCCCA AGAAAATCAA 1020 ACCTCTGAGA GGTTTCTCAC TTGCTTATCT TCAGCTGGCC GAACTCAGCC TCAAACCCAT 1080 ATGTCCTGTC TCCAAGTTCA GTGACTGTTA TCATCAACTT CTTCAACAGT AATAATAATA 1140 GATCACATTT ATGGAGTGCT TGCCAGGGCA TGTTTACATC ATTATCTCAT TTAACACTCA 1200 GAACAATCCT CTGTGGTGGG TGTTTTCATC GTTCCCATTT TGCAGGTGAA AAAACTGAGA 1260 CTTCAAAAGG TTAAGTGACT TCCCAGGGTC CTACGACCTA CATAATAAGT GGCAGAGCCA 1320 GGATTCAAAC CTAGGTTATC AGAATAATGC AGCAAAGCCC AAACCCTCAG CCCCTTTTCA 1380 CTGACTGGTA AGACCCATAT TTAATTCGAT GCCCTACATG CCGTGCACAA GTTTCAGTTT 1440 TCTGAAGCAT CGCTTAGATG CTTAGGTGTT TAGCACCACT CTGAACTCTG ACTTTTCTAG 1500 AGAGGCTGCT AAAGGCATTA 1520
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