Tag | Content |
---|
EnhancerAtlas ID | HS108-41757 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr9:134582530-134584310 |
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 |
|
| 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 |
|
| 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 |
|
Enhancer Sequence | TCTCCTGGCT GGCTGGAGAC ACCAGCCCAC ACGGTGCTGA ATTCAGAAGA GTACCGCATC 60 TTGGTCTGCT TCAGTAAATA CCGGTGTCTG CTAAGGCCCA TTCTGAAGAC ACTGTACTAT 120 GTATGACACA GTCAGAACTG GTTCTTTATT TTAATGTGTA AAAATACATG AAAGAAAGTA 180 TAACAAACCT CATATATCGA TGACCTGGAC TCTAACACTT GTTAAACTTA TCCCATTTTG 240 CTTATCTTAG GTCCCCATTT ATTTATACAG TATATTTTGC TGAACCTGTT TTTTTATTTT 300 GATTTTTTCT TTTTTGAAAC AGAGGCTCTC TCTGTTGCCC AGGCTGGAGT GCAGTGGCAT 360 GACCTCAGCT CACTACAACC TCCGCCTCCT GGGCTCAAGC AGTTCTTGTG CCTCAGCCTC 420 CCGAGTAGCT GGGATTACAG ATGTGCACCA GCACGCCTGG CTAATTTTTG TATTTTTAGT 480 AGAGATGGGG TTTTATCATG TTGGCCAGGC TGGTCTTGAA CTCCTGGCCT CATGTGATCT 540 GCCTGCCTCG GCCTTCCAAA GTGCTGGGAT TACAGTATTG TTTTTAATTG GAGAAAAGGC 600 ATACAAATTT ATTAACGTGT ATACAGGGAA AATCACAGAG TGATTATGAT TTTAGAGAGT 660 AAATTATAGA TAGCATAACT CTTCACCCTT AAATACTTCA GCATGACTAT TCAAAAAAGC 720 ACACACTCCT ACATGACTCA GCACCGTTTC ACACATAATC ACATGAGCAA CAGTTCCTCA 780 TTATAATCCA CCATGGAGTT CATATTCAAA TTTCCCGAAC TGTCCCCCAA TGTCTTTAAT 840 AGCCGTTTTG TTCAAACTTG GATCCAATCA AGGATTGCTA AGGAGTACCC TTTCCAAAGT 900 AACATGTTAG ACAAAAGAAT GACTCACAGA AAGTCAGAAG GGCTGGAACC TGACAGTAAA 960 TTAGCATCCC ACCTACTTTC TTTTTAAGAG AAAATGATCT ATGATTTGAC AAACAGCAAC 1020 TGCTCTTAAT ATTTCCATGC ATTTTCTTCC AGTTATTTGT TTTCTTTTCA TAAACACACC 1080 CATATATGCA GTTGTGAAAA AACTGTCTTG CTACTGATCA AATGCTACCG CAACTTCTTC 1140 TGGCAAGAGG AGGCAAAGAC CTGGTGAAGT CTCGCATATG TCATCTCTGG CATGCCTGCC 1200 AGCCGGCCGG TCTCCTGGGT CAATAACTGT GATAAAAGGC CGCTGAGTGC GTCAACAGAC 1260 TGTCCTGCAC TGAGACACTA TTAAAGGTCC TTGAGCTCCA AATGTACCAC TGCACTGCTC 1320 TGTGGCCCTG CCAACTTCCT CCTCCTCAAG CTGACATGAC CCCAAGCCCT AGAGAGACAG 1380 AGTAGGTGTT AAGAGAGGCT GTTGTCCCAC TTCCTGGGTG TCCAGGATGG ATAAATGAAA 1440 GATTTTACAG AAAGTACCTT GAAAGTACTT TGGAACTTTT GGAAGTGCTA TATATTTAAA 1500 AGCTGTTAAT AACATTATCT AAATCAAAAA ATATCACAAA AGCCTCAAAC TCCTAGATAT 1560 CAAAGCTTTG ACCTGGGATA TTTCTTTTTC TTTCTTTCTT TTTTTTTTGA GACAGTTTCA 1620 CTCTGTCACC CAGGCTGGAG TGCAGTGGCG CAATCTCGGC TACTGTAACC TCCACATTCT 1680 GGGTTTAAGC GATTCTCCTG TCTCAGCCTT ATGCCTGTAG CTGGAAATAC AGGTGCCCAC 1740 CACCAGGCCT GGCTAATTTT TGTATTATTA GTAGAGACGG 1780
|