Tag | Content |
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EnhancerAtlas ID | HS092-22659 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr19:19595620-19598200 |
Target genes | Number: 18 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Ar | MA0007.3 | chr19:19598045-19598062 | GGGAACACCTTGTCCCT | - | 6.35 | CDX2 | MA0465.1 | chr19:19596477-19596488 | GAGCCATAAAA | + | 6.14 | INSM1 | MA0155.1 | chr19:19595920-19595932 | TGTCAGGGGGTG | + | 6.22 | NR3C1 | MA0113.3 | chr19:19598045-19598062 | GGGAACACCTTGTCCCT | - | 6.18 | NR3C2 | MA0727.1 | chr19:19598045-19598062 | GGGAACACCTTGTCCCT | - | 6.21 | NR3C2 | MA0727.1 | chr19:19598045-19598062 | GGGAACACCTTGTCCCT | + | 6 |
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| Number of super-enhancer constituents: 22 | ID | Coordinate | Tissue/cell |
SE_01191 | chr19:19597419-19601481 | Adrenal_Gland | SE_09215 | chr19:19595450-19601494 | CD14 | SE_11973 | chr19:19597794-19601624 | CD3 | SE_13867 | chr19:19595483-19596978 | CD34_Primary_RO01536 | SE_13867 | chr19:19597292-19601474 | CD34_Primary_RO01536 | SE_14578 | chr19:19595555-19601818 | CD4_Memory_Primary_7pool | SE_17284 | chr19:19597785-19601599 | CD4p_CD225int_CD127p_Tmem | SE_17695 | chr19:19595455-19601775 | CD4p_CD25-_CD45RAp_Naive | SE_18023 | chr19:19597051-19602095 | CD4p_CD25-_CD45ROp_Memory | SE_18475 | chr19:19595670-19601884 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19438 | chr19:19597486-19598710 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20088 | chr19:19595597-19596587 | CD56 | SE_20088 | chr19:19597646-19601744 | CD56 | SE_22348 | chr19:19595603-19601745 | CD8_primiary | SE_24291 | chr19:19597429-19601354 | Colon_Crypt_2 | SE_29832 | chr19:19595488-19596865 | Fetal_Muscle | SE_31176 | chr19:19597536-19598200 | Fetal_Thymus | SE_37262 | chr19:19595365-19597214 | HSMMtube | SE_41770 | chr19:19595872-19596602 | LNCaP | SE_41770 | chr19:19596688-19599943 | LNCaP | SE_53638 | chr19:19595818-19601579 | Spleen | SE_69075 | chr19:19596014-19597099 | H9 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr19 | 19597114 | 19597245 | chr19 | 19596921 | 19597089 |
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| Number: 1 | ID | Chromosome | Start | End |
GH19I019484 | chr19 | 19595616 | 19601954 |
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Enhancer Sequence | CGTGAGCCAC CGCGCCCAGC CTGTCATAGG ATTTTTCTAG GAGTGTTTCT TGAAGGCAGG 60 TAGAGAGACT GGATGAAGCA TGAGGAATTG CTTTCTGGCT TGACTCACTT CACTCCAGGT 120 GCTGCCTGAA GCTGGGGTGC CTCCCAGCCT GCAGACTGCC TCCTCCTTTT CCATGGGACC 180 CTCTTCAGCC CCTTTCATTG TTGGGCAGCT CTGGTCTCCC ACATGACCTT CCTAGAGCTG 240 TTCTCATCTT GAGTCTGCAC CTGTCTGGGG GGCCTCTGTG CAGGCTGCTG TTGGTCCCTC 300 TGTCAGGGGG TGCTTTAAGG CTCAGTGGGT AGTTACTTGG GTAAACCCTT TCTTTCCCCC 360 TTCTCTTTCC CTGCTTTGTC CCAGGGTAGC ATCTGAGGGA GGAAGTGGAG TTACAGTGAT 420 ATGGGTTAGC TCCCCAGGGG CCAGCCTGGG CCATTGGCTC CATTAGCTTA GTGGTTTAAA 480 GCAGCGAGGT ATTGACGTTT TTCAGTCTGT CAGTTCTGCT GGTTGGCTGG TCCCGCCCAG 540 CTGGGCACTG TTGCTGGGGC CCTCTGGTCT TTGCAGTTGC ATGTCAGCTG GGCTGGGTGT 600 CCCCAGTGGT TTCATCACTC ACATGTGATG GCCAAAACAG CTGGGACTGG CTGGACCAGT 660 CTCTGTGCCT GTCTCCATCT CCCCCACTAT AGCGGGGGCT AGTGTGGGCC TCTGATCCCG 720 TGGTGGTTTG GGGCAGTCAG ACCTCAGCTC TCCTAGAGCA AGCATTCCGA GGGCTCAGGC 780 AGAAGCTGCA AGGCTTCTGT GACCTCACCT GAAAAGGCTG CCACGTCACT TCCTCTGCAT 840 TCTGTAGTTT GGGAATTGAG CCATAAAACC AGCCCAGGTC AAGTACTACG GGGGCTATGA 900 GTAGATGCAG CCAGAGCCTC CGGCCTCCTC AGGACTGCAG AGATGGGCCG GGGGCCTTGC 960 AGAGTTTGGT CTGGTGTACA GGGTTTGTCA GCCATGAGTA TTAGGGCTCC TTCTTCATAT 1020 CCACAAAAGC GCTTGGACTC AAAAAATAGG AATTTGGCTT CCAGGGTCTG TTGCTTTACA 1080 AAGACGCACG ATGACACACA ATTCAGAAAT CCTTGTGAGT GAGTTTCCCT TTCCTCCAGC 1140 AGCACAACAT CTATGTGCAC GAGGGAAGCA GCTGCCCACC GTGCAAGGGG GTCCATCAGT 1200 CCGTGGCGCT GGTTCCTCCT GAACTCACAG CCCCAACCCT GGAACCTCCA TCAAGGCAAG 1260 AGGAGGAAGT GGGCGCTCCC CAGCCTTGCC AGGCCCCCAG CAGACCCAGT CTGCCCTTGG 1320 GGGGTTTGTG AATGTTCAGG TGTCACATTT CAGGACCTGT TTACTGAGAT TGTCTGCTCT 1380 GTAATGGGCT CCCACTCTTT CCTCAGAAAG CTGTCAGGTC AGGCAGATGT TTCAGGTTTG 1440 CCATTGCTTC CATCTGGGAG CTGCAAGGCG AAGGCACGGG CGGCCTGTTT GCTGCCCTTA 1500 TCTTCCCAGT GTTGGGGACC CCAGGAAGTA CTGTCTTCTA AGGCCCGACA ATCCAAAAGA 1560 AAATCACTCC TGCATGCTCC TATCCCCTTC AAGGTTGCAT CCTGTCAGAG CATCCATCTT 1620 GCCTCTGGAG GCCGTGGTGC TGCTGCCATC TGGGTTTTGG GGGCTGCTGG ATGTGGGCGG 1680 CTGGCTCTGA AGAGGCAGCA TGTGATCTGA CAGCAGGATG CTCCCGCCCC ACCAAATGAC 1740 AGCCTTGGGG CAGCTCCCGG CAAACAACTC CATTTCCTTC TCCGAGGTGG GAATGGGACC 1800 TGGTGCAGGG GACGCAGGCT GTCGGGGCAA ACCTCTCTCT CCATTCTAGG GGCATGCAGG 1860 GTGGCTATGA GTGCTCTCAG GAAGGTCACT GTTCCCGAGG CCTGAGCTGA GCACTTTCAG 1920 ATCAGCAGGG CTGCCTGATC CCCCTGCAGC CAGCCGGCTG TCTAAGGTGC CCGAGCCTCC 1980 TCAGCACTGA AGTCTCACCT CACCAGGCAG CCCTGAGAGG CTGCGGGACA GGGATTCCTC 2040 TGCCCTGCCA TGCAGGAGCC ATGGAGAGGG AAGTGTCACT TGCAAGAGGC AGAATCAAGT 2100 GAGACCCAGG TGTCTTCTAG CTCACTGGGT GAGGGCTCTC TCCACAGCCT GACTTGCCGG 2160 CAGTCGTTTG AAGTCCAAGG CTGGGCAAGG GTGGCCAGTG AGCTCCAGGC CTCAGCTTGC 2220 TAAAGGAGCT ACTCCACAGG AGCATGCGGG CTCAGGGCTC AGCACCCTCA CATGACAGGC 2280 TCAGCCAGCC TCTCCCCCAT CCCCAGCCAT CATAGACTTA GGAGGAGATT CCTGGCTCTG 2340 AGGACATGGG GGCTTGCCCC CTTCTCTGGG GCTGTGGTAT CACCCCAGGG CTGGATACCC 2400 CCTTGCCCTT TGTTCATCTG GTCCTGGGAA CACCTTGTCC CTTGTTGGGA GCTGAGGCTG 2460 TGCCACAGAG TGGGGCCATA GGTCCCTGGG TGCTGTGCCG GTGCCACACC CACCTGAAGG 2520 AGGTCGTGAT GGCCCCCAGC TCAGGGTGCA GGAACCTGCT TGTCAGACAG GTGCTGACAT 2580
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