Tag | Content |
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EnhancerAtlas ID | HS092-39022 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr9:134582820-134583980 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
JUN(var.2) | MA0489.1 | chr9:134583443-134583457 | AAAGAATGACTCAC | + | 6.1 | NFE2L1 | MA0089.2 | chr9:134583260-134583275 | ACATGACTCAGCACC | + | 6.38 | Nfe2l2 | MA0150.2 | chr9:134583258-134583273 | CTACATGACTCAGCA | + | 6.83 |
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| Number of super-enhancer constituents: 32 | ID | Coordinate | Tissue/cell |
SE_00686 | chr9:134578827-134586282 | Adipose_Nuclei | SE_04525 | chr9:134581763-134583038 | Brain_Anterior_Caudate | SE_04525 | chr9:134583196-134584452 | Brain_Anterior_Caudate | SE_09150 | chr9:134579551-134586375 | CD14 | SE_10884 | chr9:134578645-134586673 | CD20 | SE_14804 | chr9:134582888-134584251 | CD4_Memory_Primary_7pool | SE_17952 | chr9:134582822-134589309 | CD4p_CD25-_CD45ROp_Memory | SE_18769 | chr9:134582861-134586789 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19472 | chr9:134583310-134584259 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20363 | chr9:134583141-134584353 | CD56 | SE_22914 | chr9:134582931-134584438 | CD8_primiary | SE_27117 | chr9:134583170-134584009 | Esophagus | SE_30786 | chr9:134583043-134584279 | Fetal_Muscle | SE_31710 | chr9:134583451-134584107 | Gastric | SE_32578 | chr9:134579764-134584637 | GM12878 | SE_33628 | chr9:134577230-134584040 | H2171 | SE_36750 | chr9:134582064-134584444 | HMEC | SE_36915 | chr9:134578813-134586435 | HSMMtube | SE_38234 | chr9:134581951-134586634 | HUVEC | SE_40722 | chr9:134578196-134586143 | Left_Ventricle | SE_42566 | chr9:134578769-134584551 | Lung | SE_49262 | chr9:134583381-134584566 | Right_Atrium | SE_50405 | chr9:134583359-134584213 | Sigmoid_Colon | SE_52037 | chr9:134581971-134584280 | Skeletal_Muscle_Myoblast | SE_52732 | chr9:134583012-134584184 | Small_Intestine | SE_54202 | chr9:134583118-134584240 | Spleen | SE_58352 | chr9:134520171-134620333 | Ly1 | SE_58881 | chr9:134579557-134620273 | Ly3 | SE_60991 | chr9:134494570-134620113 | HBL1 | SE_62218 | chr9:134495530-134621458 | Tonsil | SE_63796 | chr9:134581971-134584262 | HSMM | SE_64992 | chr9:134582081-134584259 | NHEK |
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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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Enhancer Sequence | TTTTTATTTT GATTTTTTCT TTTTTGAAAC AGAGGCTCTC TCTGTTGCCC AGGCTGGAGT 60 GCAGTGGCAT GACCTCAGCT CACTACAACC TCCGCCTCCT GGGCTCAAGC AGTTCTTGTG 120 CCTCAGCCTC CCGAGTAGCT GGGATTACAG ATGTGCACCA GCACGCCTGG CTAATTTTTG 180 TATTTTTAGT AGAGATGGGG TTTTATCATG TTGGCCAGGC TGGTCTTGAA CTCCTGGCCT 240 CATGTGATCT GCCTGCCTCG GCCTTCCAAA GTGCTGGGAT TACAGTATTG TTTTTAATTG 300 GAGAAAAGGC ATACAAATTT ATTAACGTGT ATACAGGGAA AATCACAGAG TGATTATGAT 360 TTTAGAGAGT AAATTATAGA TAGCATAACT CTTCACCCTT AAATACTTCA GCATGACTAT 420 TCAAAAAAGC ACACACTCCT ACATGACTCA GCACCGTTTC ACACATAATC ACATGAGCAA 480 CAGTTCCTCA TTATAATCCA CCATGGAGTT CATATTCAAA TTTCCCGAAC TGTCCCCCAA 540 TGTCTTTAAT AGCCGTTTTG TTCAAACTTG GATCCAATCA AGGATTGCTA AGGAGTACCC 600 TTTCCAAAGT AACATGTTAG ACAAAAGAAT GACTCACAGA AAGTCAGAAG GGCTGGAACC 660 TGACAGTAAA TTAGCATCCC ACCTACTTTC TTTTTAAGAG AAAATGATCT ATGATTTGAC 720 AAACAGCAAC TGCTCTTAAT ATTTCCATGC ATTTTCTTCC AGTTATTTGT TTTCTTTTCA 780 TAAACACACC CATATATGCA GTTGTGAAAA AACTGTCTTG CTACTGATCA AATGCTACCG 840 CAACTTCTTC TGGCAAGAGG AGGCAAAGAC CTGGTGAAGT CTCGCATATG TCATCTCTGG 900 CATGCCTGCC AGCCGGCCGG TCTCCTGGGT CAATAACTGT GATAAAAGGC CGCTGAGTGC 960 GTCAACAGAC TGTCCTGCAC TGAGACACTA TTAAAGGTCC TTGAGCTCCA AATGTACCAC 1020 TGCACTGCTC TGTGGCCCTG CCAACTTCCT CCTCCTCAAG CTGACATGAC CCCAAGCCCT 1080 AGAGAGACAG AGTAGGTGTT AAGAGAGGCT GTTGTCCCAC TTCCTGGGTG TCCAGGATGG 1140 ATAAATGAAA GATTTTACAG 1160
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