Tag | Content |
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EnhancerAtlas ID | HS193-23211 |
Organism | Homo sapiens |
Tissue/cell | U87 |
Coordinate | chr3:46036060-46037210 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RREB1 | MA0073.1 | chr3:46036134-46036154 | CCCCACCCCTCCCCCACACC | + | 6.35 | RREB1 | MA0073.1 | chr3:46036145-46036165 | CCCCACACCAGCCCCCAACA | + | 7.17 |
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| Number of super-enhancer constituents: 10 | ID | Coordinate | Tissue/cell |
SE_12170 | chr3:46034153-46038021 | CD3 | SE_16689 | chr3:46034183-46037920 | CD4_Naive_Primary_8pool | SE_19761 | chr3:46034035-46038083 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_22687 | chr3:46033593-46038285 | CD8_primiary | SE_25625 | chr3:46032531-46038516 | DND41 | SE_26485 | chr3:46033084-46038068 | Duodenum_Smooth_Muscle | SE_51129 | chr3:46022721-46038176 | Skeletal_Muscle | SE_59148 | chr3:46001905-46039214 | Ly3 | SE_62841 | chr3:45980257-46038045 | Tonsil | SE_66753 | chr3:46035767-46038166 | Jurkat |
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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 | CTCACTCAAC AGGGGTCCAC TTCAGAAGGT GGGAACTACT GAAAGCAGAA AACCTTGGCA 60 TGATAGCTCC AGCTCCCCAC CCCTCCCCCA CACCAGCCCC CAACACCCTC CAGCCGCATT 120 AGGCAGATGG CAGGGGAATT AAGCTTGCAG CCTGAGACCA CAAGGCCTGC ACGGGCAGGA 180 GAACCAGTGA GCAGATTAAG CCCTGGATCC TCTGCCCCGC AAAAGCCCCT GACCCATTTC 240 TCTGTCGGGA AAGGAAACTG CTGTGGTAAG ACAAGCAGAG GGGCTGAGAG GCTCTGGCCA 300 ACACAGGCAG TTTCAACAAG TGTTCTATTT TTTTTTCTGG AGAGGACACC CAATGGGAAC 360 AGTGAAGAGT GACAGGGACA TCAGAGAATA CATGTGCTTT AACAGGGGGC CACGCGGTTA 420 ACGTGTCAAC CACATGTGCT TTTCTTACAA AAAATAAAAT CCCGCCATCC TCCCCCCTCC 480 CCGCCCCACC CCCGCCAGGT TTCAACAGCA CGGACTCCAG TCCAGTGCAG TGCCGCCACA 540 CCAGAGACAA CAGGTGTTTC GGGAAAAGAC CCCTGGGGGC TAGCTCGAGA CCCTGCGCAT 600 GGGCACAAGG GGCAGTGGAT AGTGAATAGG TCTTGGCCAA AGGATGGGCC AGGAAGAAAG 660 AAGCTTCTTC CCCTCCTGGG AAGAGGGCAG AGATCCGAGC ACCAGCGGAG TCTTGCAAAG 720 TGAAGGTCTG GGCTGTCCCG GCCCAACTGG GCCAGAGACT AAACTTCCTA AAGACCACGC 780 AGGCAGGAAC TCCGGGGCCT GCCCCATCCT GCGCTAAGAC ATTCAGGCTT GTTCTGAGAC 840 GCCGCATGGT GGGCTCCTTT CCTTTGCGGG CCCTCCGCCC TCCGGGGTCT TGGAACTGGT 900 GTTTGGGGTC TGTCTTTCTA ACCGACCAAC AGAGGCAGGC TGGGTGCCTG GGCCGGCTTC 960 CACCTGCCCG AGGTGCTTCC CGGCCCGCTG GGCAAGGACG GGGGCGCTCG GGCAGGGTCT 1020 GAGGGAGACC TGGGATGGGC GGGGACTGTA AGGGCAACAG GTGACAAGCC GCGCCCCGAG 1080 CGAAGCTCTC GCCTCAGGGA TCGTGAGCGA CCCAGGTGCC CCCAGAGTCC AGCCGGTCTT 1140 CCGCGGCACT 1150
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