Tag | Content |
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EnhancerAtlas ID | HS146-15508 |
Organism | Homo sapiens |
Tissue/cell | NHDF |
Coordinate | chr9:134582440-134584210 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXC1 | MA0032.2 | chr9:134582464-134582475 | TAAGTAAACAT | + | 6.02 | 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: 2 | Chromosome | Start | End |
chr9 | 134583114 | 134584077 | chr9 | 134583176 | 134583545 |
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Enhancer Sequence | GGAGAACCAG AGACAATCCA AACGTAAGTA AACATATTAA ATTTCTATTC TAAAAGTGGT 60 GCTTTTAAGT AGTTGGATCA ATGCTGATTT TCTCCTGGCT GGCTGGAGAC ACCAGCCCAC 120 ACGGTGCTGA ATTCAGAAGA GTACCGCATC TTGGTCTGCT TCAGTAAATA CCGGTGTCTG 180 CTAAGGCCCA TTCTGAAGAC ACTGTACTAT GTATGACACA GTCAGAACTG GTTCTTTATT 240 TTAATGTGTA AAAATACATG AAAGAAAGTA TAACAAACCT CATATATCGA TGACCTGGAC 300 TCTAACACTT GTTAAACTTA TCCCATTTTG CTTATCTTAG GTCCCCATTT ATTTATACAG 360 TATATTTTGC TGAACCTGTT TTTTTATTTT GATTTTTTCT TTTTTGAAAC AGAGGCTCTC 420 TCTGTTGCCC AGGCTGGAGT GCAGTGGCAT GACCTCAGCT CACTACAACC TCCGCCTCCT 480 GGGCTCAAGC AGTTCTTGTG CCTCAGCCTC CCGAGTAGCT GGGATTACAG ATGTGCACCA 540 GCACGCCTGG CTAATTTTTG TATTTTTAGT AGAGATGGGG TTTTATCATG TTGGCCAGGC 600 TGGTCTTGAA CTCCTGGCCT CATGTGATCT GCCTGCCTCG GCCTTCCAAA GTGCTGGGAT 660 TACAGTATTG TTTTTAATTG GAGAAAAGGC ATACAAATTT ATTAACGTGT ATACAGGGAA 720 AATCACAGAG TGATTATGAT TTTAGAGAGT AAATTATAGA TAGCATAACT CTTCACCCTT 780 AAATACTTCA GCATGACTAT TCAAAAAAGC ACACACTCCT ACATGACTCA GCACCGTTTC 840 ACACATAATC ACATGAGCAA CAGTTCCTCA TTATAATCCA CCATGGAGTT CATATTCAAA 900 TTTCCCGAAC TGTCCCCCAA TGTCTTTAAT AGCCGTTTTG TTCAAACTTG GATCCAATCA 960 AGGATTGCTA AGGAGTACCC TTTCCAAAGT AACATGTTAG ACAAAAGAAT GACTCACAGA 1020 AAGTCAGAAG GGCTGGAACC TGACAGTAAA TTAGCATCCC ACCTACTTTC TTTTTAAGAG 1080 AAAATGATCT ATGATTTGAC AAACAGCAAC TGCTCTTAAT ATTTCCATGC ATTTTCTTCC 1140 AGTTATTTGT TTTCTTTTCA TAAACACACC CATATATGCA GTTGTGAAAA AACTGTCTTG 1200 CTACTGATCA AATGCTACCG CAACTTCTTC TGGCAAGAGG AGGCAAAGAC CTGGTGAAGT 1260 CTCGCATATG TCATCTCTGG CATGCCTGCC AGCCGGCCGG TCTCCTGGGT CAATAACTGT 1320 GATAAAAGGC CGCTGAGTGC GTCAACAGAC TGTCCTGCAC TGAGACACTA TTAAAGGTCC 1380 TTGAGCTCCA AATGTACCAC TGCACTGCTC TGTGGCCCTG CCAACTTCCT CCTCCTCAAG 1440 CTGACATGAC CCCAAGCCCT AGAGAGACAG AGTAGGTGTT AAGAGAGGCT GTTGTCCCAC 1500 TTCCTGGGTG TCCAGGATGG ATAAATGAAA GATTTTACAG AAAGTACCTT GAAAGTACTT 1560 TGGAACTTTT GGAAGTGCTA TATATTTAAA AGCTGTTAAT AACATTATCT AAATCAAAAA 1620 ATATCACAAA AGCCTCAAAC TCCTAGATAT CAAAGCTTTG ACCTGGGATA TTTCTTTTTC 1680 TTTCTTTCTT TTTTTTTTGA GACAGTTTCA CTCTGTCACC CAGGCTGGAG TGCAGTGGCG 1740 CAATCTCGGC TACTGTAACC TCCACATTCT 1770
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