Tag | Content |
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EnhancerAtlas ID | HS105-81615 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr9:92035060-92037990 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOS | MA0476.1 | chr9:92037185-92037196 | TCTGACTCATT | + | 6.32 | KLF4 | MA0039.3 | chr9:92037214-92037225 | GGAGGGTGTGG | - | 6.32 | mix-a | MA0621.1 | chr9:92035357-92035368 | AATTAATTAGG | + | 6.32 |
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| Number of super-enhancer constituents: 29 | ID | Coordinate | Tissue/cell |
SE_03905 | chr9:92034665-92036401 | Brain_Anterior_Caudate | SE_04779 | chr9:92034853-92037750 | Brain_Cingulate_Gyrus | SE_06723 | chr9:92034636-92036533 | Brain_Hippocampus_Middle_150 | SE_09170 | chr9:92034692-92042561 | CD14 | SE_11886 | chr9:92032792-92036607 | CD3 | SE_11886 | chr9:92036792-92037730 | CD3 | SE_14475 | chr9:92031657-92036637 | CD4_Memory_Primary_7pool | SE_14475 | chr9:92036736-92037843 | CD4_Memory_Primary_7pool | SE_16354 | chr9:92031722-92035951 | CD4_Naive_Primary_8pool | SE_16924 | chr9:92032952-92036844 | CD4p_CD225int_CD127p_Tmem | SE_16924 | chr9:92036872-92038023 | CD4p_CD225int_CD127p_Tmem | SE_17355 | chr9:92032066-92053749 | CD4p_CD25-_CD45RAp_Naive | SE_17792 | chr9:92030302-92045427 | CD4p_CD25-_CD45ROp_Memory | SE_18250 | chr9:92030354-92045641 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19118 | chr9:92031054-92045779 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20089 | chr9:92032836-92035554 | CD56 | SE_21155 | chr9:92032684-92035660 | CD8_Memory_7pool | SE_21155 | chr9:92036818-92038114 | CD8_Memory_7pool | SE_21665 | chr9:92033117-92035716 | CD8_Naive_7pool | SE_21969 | chr9:92033002-92035727 | CD8_Naive_8pool | SE_22409 | chr9:92032176-92038225 | CD8_primiary | SE_26933 | chr9:92035261-92036180 | Esophagus | SE_32149 | chr9:92037151-92037778 | Gastric | SE_50088 | chr9:92034870-92036565 | Sigmoid_Colon | SE_52548 | chr9:92034761-92036519 | Small_Intestine | SE_52548 | chr9:92036910-92038053 | Small_Intestine | SE_53415 | chr9:92036950-92037671 | Spleen | SE_60002 | chr9:92014899-92064443 | Ly4 | SE_62222 | chr9:92014516-92154755 | Tonsil |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr9 | 92035617 | 92036104 | chr9 | 92036953 | 92037404 |
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| Number: 1 | ID | Chromosome | Start | End |
GH09I089417 | chr9 | 92032405 | 92045324 |
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Enhancer Sequence | GGGGGTTCAT ATCTAGCCTC CAAAAACAGC TGCCAGCCCC AAGGTTCCTG AGTGGGAACA 60 CACTTCCTTT CTTAGTGAAT TGCCCAGGCC CCAACCCCGC GTTGCCTTCA CCCTACACAT 120 ACACGGTTTG TTTCTTCTTT CTCAGCGTGC AACCCCACAG TTATGAGTTA CCTGGCTTAA 180 AAATGCAAAC CCACACTTCT CATGTAATTA CTCATCATGC TGTTTTAACT CATATCTCCC 240 AACTCCTGAC AGCACAGGTA AAAAGAATCC AATGGCCTGT TCATCAAAAA GCAATGAAAT 300 TAATTAGGAG AGAGAAGCAT TTCCCTCTCA TGGCCTTCAC ATCCTCTCCT GGTGCACCCC 360 CTCTAGTGCA GGAGAGTGTG GGGCTCCAAC GCCCAGGCCT TGCGAACAGG TATTTAGTGG 420 TCGCTGATGG CAGAAGGACA GAGCCACTGG CAGCGCCTTC ATCTGGCCTC CATCCTGCAG 480 ACATGACCTC GCCTTCTGGG CGTACTCCCT AAGCAGGGAC CTGGTGTTCT TCAGCACACA 540 GAGAAGACAA GTGGGATGAA GCAAGAGCAA GGGGCTCTGC AATCAGAGGA ACCTGGGTTC 600 CAGTCCTGGC TTCTCCAAGT TGTGTGTTCC TGAGGGAAGT TACTGAGCCT CTCTGGGCCT 660 CTGTTTCCTT ATCCAAAAAG TGGGCATACT AATACTGCCT GTCTCATTTG GTTATGAGGA 720 TCCATGACTA ATCAGTTAAT GCTTCCTAGT GCTTTCCTAG GTGCCCGATG CTGTTTAAGC 780 ACTGGGAGGC ATTAACTATC ATTCTTACCA CTTGTGAAAT GAAGCCAGTT ATATCTGCCT 840 AGCTAAGAAG ACTCAGAGAG ATATAACAAG CAGGGTGCAG CTATTAGCAC ATCTAACAAC 900 CCCTACTGCC AGGGACTGTG GGCTCCACCA GCCTCCTCCT GCACACACGG GGGATCGGGG 960 CTTCCCCAGG TCCACATAGA CTCCTGGAAG CAGGGCTTAG GAACACTGTG ACAGGCAGCA 1020 CTGCTGTGGC TGTGGACGGG GAGAGGGCCG TGAGCCCCTT CTGCTCAATC TCCTCATCCT 1080 GGCCCAGAAG CAGGTAAGGA AGTTCCGGAG GCAGAGAGCA ATGGGGGACC TTCTGCTGAA 1140 ATTGGCACTG CAGCACACAC CTCGATGGGG TAGGCATGCA TATTACAACA CAATACCATT 1200 ACACTCTGCT GAGCAGGGCA CCCATGAGAA AGGCTGGCTA CAAAGTACAC AGACAGGGCC 1260 CGGAGGACAT GTTTCCGCAC CCTGCTGGGC AACACCTGCC AAGAAGCTAC ATCCAGAATC 1320 TCTGATCCAA CAGTCCTCTA CCAAGAATTC AGTATGGATA TACCCCATGT GTGCAATATG 1380 ACTGGAACGA GGCTATTCAA TAGGTAAACT CCAAAGACAC CCAGAAGTCC ACCAGTGTGT 1440 GTGCGTCTAT GTGCATGGGT ACACACAGAT ACAGCATAGA ACGTTTTCTA TACAAATTAT 1500 TGCACATTCC AGAGGATGGA ATACTATGCA ACTGTTAAAA AGAATAAAGC TGCAATTGTA 1560 TGAAAGGGCG CTGTTCAGTA AAAAGTAAGG TTCCCAAAAA TGTGAGTAGT ATGTTTCCGT 1620 CTGTGCAGGC ACATGGTGTG TGACCGTGTG TGTGCGTGTG TGTGTGTGTG TGGGTGTGCA 1680 CACAGGCTCA TCAGAAGGAT GATTCAAGAG ATCACAATTT AATCAAGAAC CTGCTGGCAG 1740 CAATGCCTAT AGAGAGAATT TGATCTGCAA AAGGAGTGTG CTTCATTTTT CATGATTTTG 1800 ATTCTTTAGA ACTATTCGAA TTCCTTCCTT AATCATGTGG TTTTCTAACT AAAATATTTT 1860 AAATCTGATA TCAAAAGTAA AATACAGTAA TTGTAGAAAA TTTGAAAAAT TCAAGAAAGG 1920 CAAGAGAACA CATTGCTGAC GATCTCTAAA AAGGTTACAC AGGTTATAAC GCTGGTTAAA 1980 GTAAGATCCC AGCTCGGGTG TCTCCTGTAC TAACTTTACT AAGAGGAAGA TTTCATCAAA 2040 ATGGAAATTT TTAAGAACAG CAGACAGACA TGACATACAG TTCTGGTCTT TCTGGCATTT 2100 TGGTGAATTC CTCATTCTAA GAAACTCTGA CTCATTCACT CAACAGTCAC TACTGGAGGG 2160 TGTGGGGTGA AGGTGAGAGT CAGATATAGA CTGTAGACCC CCAGCCCCTG CTTTCTGGCT 2220 TGGGGAGGGC AGGCCACAGC AACCGCACAG GACGGTTGGG GGGCCCTGCT GGCTCTGTAA 2280 CATGGGAAGT GGGACAGGCA GGCTGGGAGC CATGCAAGAG GAGACCTGAA GTCCAAGAGA 2340 GAGGCTGGAG CCTACAGGCT GGTAGAGGAA GAGGGCCCGC GTGGGTCACG TCCAGGTCCT 2400 GTGTGTCCCT GCCCCGAGCA CCATGCGTGC GCATCCCCGT GCCGTTTATT ACGTGGTGCC 2460 CTCAGCAGCC TGTCACGGCT GTGCAATATT CCATAATTAA ATATCATAAT GTGGGACATT 2520 CCGATCCTTT CCAACTCTCC ACTTACAATT CATTTTTCTT TAACCACCAG CAGTACCCGG 2580 CCAAGAATCT TTTCTGTCTG GAATGTTCAC AGTGATGTTA CAGAGGTCTA GGCACCACAC 2640 AGAGGGCACT GGGAGATGGG CACGGGGGAG ATTCCATGGT TCCATCATGT CTGTCTGCTG 2700 TTCTTGAAAA TCTCCATTTT GATGAAATCT CTTAATAAAG TTAGTACAGA AGACACAAGT 2760 GCTGGGATCT TTAGTAGTCG TTACAACCTG TATAACCATT TTAGAGACTG TCAGCAATGT 2820 GTCAGCAATG TGTTCTTCTC TTGCCTTTCT TAAACAGAGG CTCAGGGCTT CTACTGATCA 2880 GGCTGACAGG TTTGCTTCCT TTAACTGGGA AATAATCACA CATAACTTCC 2930
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