Tag | Content |
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EnhancerAtlas ID | HS162-08469 |
Organism | Homo sapiens |
Tissue/cell | Plasma_cell_myeloma |
Coordinate | chr5:133435500-133436660 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFAT5 | MA0606.1 | chr5:133436081-133436091 | AATGGAAAAT | - | 6.02 | NFATC1 | MA0624.1 | chr5:133436081-133436091 | AATGGAAAAT | - | 6.02 | NFATC3 | MA0625.1 | chr5:133436081-133436091 | AATGGAAAAT | - | 6.02 | NFKB1 | MA0105.4 | chr5:133436370-133436383 | CGGGGAATCCCCT | + | 7.12 | NFKB1 | MA0105.4 | chr5:133436370-133436383 | CGGGGAATCCCCT | - | 7.22 | Pou2f3 | MA0627.1 | chr5:133436058-133436074 | TTTGATTTGCATACGA | - | 7.19 |
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| Number of super-enhancer constituents: 21 | ID | Coordinate | Tissue/cell |
SE_11859 | chr5:133434150-133437135 | CD3 | SE_14661 | chr5:133434420-133437118 | CD4_Memory_Primary_7pool | SE_15545 | chr5:133435504-133436989 | CD4_Memory_Primary_8pool | SE_15868 | chr5:133435555-133437149 | CD4_Naive_Primary_7pool | SE_16541 | chr5:133435396-133436995 | CD4_Naive_Primary_8pool | SE_16864 | chr5:133434714-133437989 | CD4p_CD225int_CD127p_Tmem | SE_17306 | chr5:133434013-133442187 | CD4p_CD25-_CD45RAp_Naive | SE_17779 | chr5:133433894-133442397 | CD4p_CD25-_CD45ROp_Memory | SE_18300 | chr5:133434019-133437989 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19131 | chr5:133434895-133438108 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20200 | chr5:133434504-133437215 | CD56 | SE_21652 | chr5:133435194-133437085 | CD8_Naive_7pool | SE_21973 | chr5:133435115-133437911 | CD8_Naive_8pool | SE_22418 | chr5:133434549-133438019 | CD8_primiary | SE_30897 | chr5:133434103-133437128 | Fetal_Thymus | SE_39383 | chr5:133435462-133437005 | Jurkat | SE_49860 | chr5:133435431-133437058 | RPMI-8402 | SE_50485 | chr5:133434455-133437093 | Sigmoid_Colon | SE_55097 | chr5:133434867-133436879 | Thymus | SE_62337 | chr5:133403949-133487040 | Tonsil | SE_66306 | chr5:133435462-133437005 | Jurkat |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr5 | 133435759 | 133436442 | chr5 | 133436200 | 133436400 | chr5 | 133436400 | 133436600 |
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| Number: 1 | ID | Chromosome | Start | End |
GH05I134098 | chr5 | 133433961 | 133438092 |
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Enhancer Sequence | TGGACTCAAG TAATCCTCCA GTCTCGGCCT CTCAAAGTGC TGGGATTGTG GGTGAGAGCC 60 ACCATGCCTG GCCCCAACTA CCTTCTTTAT CTCCCCAGAA CCTATCGTCC AGGCCCAGGG 120 TTGAGACAGA GTGGGAAGGG GTCCATCCCA CATTCCCCAG GCCTCGCTGG TACAGCCTGG 180 CCCCTTGGTT GGTATGGGGT CAATCCAAAC ACGCCCTGTG AGCCCAGCCT TATGTGGCTG 240 GCCCTGTGCA TAGGCACAGG CAGAGAAAAC AGAAGCAGCA GGATGCTTTT TATTTGTTAA 300 TCTAGCTTTG ATGCCCCACC TCCTTCTCAC AAGGAGTGGA GGCCCCTCAG GGAGTACTAA 360 GTGCCAGGAG TATAGACCCT AGCAGTGGCC TGGGCTGGTC TCCAGGAGGA GGAGGCAGTC 420 AGGGCTCTCC CTGAAAGCAA GCTGGGGTTA AATATTTTTA GGGCAGAGGA GGCACAAACC 480 AGCCAGAGCT ACCTTCCTTT CTAATCTTAC CCAGGCATTA AGCTTTGAGA GTATCCCCCT 540 CATTTACATA CATTCACATT TGATTTGCAT ACGATGCAAA GAATGGAAAA TTCCCCCAGT 600 GCTTAGCCCC AAGATTACAG TCTCTAATAC TTTATTCCCA CAACCGCGGC ACCCCGTGAC 660 AGACAGGGGG TCCTGCCTGT GATCTAGATC TGGGCTCCCT GCAGCCTGGG ACCCAGCCTG 720 CAGCCTCCTG CCTAGAGGTA GCAGCTCCTG TGAAGGGGGT GGCAGCAGCA GACGCAGGCC 780 TAGCAAAACA AGGTACTTTC ACATGTGACT CACACCAAGG ACCAGAAGCA GAATTACAGT 840 GTGAAAAACC AGAGCCGGCC GAGACTCCGT CGGGGAATCC CCTCCAGCTC CCTCTCTGTT 900 TCACTCCTTT AAAAAGCCCT GGCCATGGCC CAGCACTCTA GAACCCTCCA AGAAAGTGCT 960 GTGCCTCCCA TCCAGGATGG GCAGGGGCCA TGGCACTTCA GCCAGGCCCC TTGACTTTCT 1020 CTCTGGGTTC TTGGGCTCAG AAATTACATC TAAGCAGAGA AAGAGGCAGA AGTGGATTCA 1080 TCCCAGGGGC AGAGCTGGAA CTGGACCTGG GAGCAGTTGC TGCCTTGCAG GCCCCAGGGC 1140 TCCATGCTCA TATTTTTCTT 1160
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