| Tag | Content |
|---|
EnhancerAtlas ID | HS038-22446 |
Organism | Homo sapiens |
Tissue/cell | ESC_neuron |
Coordinate | chr9:92057570-92059710 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| JUN(var.2) | MA0489.1 | chr9:92058018-92058032 | AGGAGGTGACTCAC | + | 6.17 |
|
| | Number of super-enhancer constituents: 33 | ID | Coordinate | Tissue/cell |
| SE_03177 | chr9:92058488-92064708 | Brain_Angular_Gyrus | | SE_03905 | chr9:92054548-92064883 | Brain_Anterior_Caudate | | SE_04779 | chr9:92053976-92080229 | Brain_Cingulate_Gyrus | | SE_05782 | chr9:92054240-92082406 | Brain_Hippocampus_Middle | | SE_06723 | chr9:92053932-92078733 | Brain_Hippocampus_Middle_150 | | SE_07735 | chr9:92054317-92080642 | Brain_Inferior_Temporal_Lobe | | SE_09037 | chr9:92059037-92059265 | Brain_Mid_Frontal_Lobe | | SE_09170 | chr9:92054083-92061427 | CD14 | | SE_11477 | chr9:92055725-92059917 | CD20 | | SE_11886 | chr9:92058448-92060669 | CD3 | | SE_14475 | chr9:92054408-92060484 | CD4_Memory_Primary_7pool | | SE_15473 | chr9:92058558-92060406 | CD4_Memory_Primary_8pool | | SE_15940 | chr9:92058193-92060155 | CD4_Naive_Primary_7pool | | SE_16354 | chr9:92057286-92060391 | CD4_Naive_Primary_8pool | | SE_16924 | chr9:92057908-92060489 | CD4p_CD225int_CD127p_Tmem | | SE_17355 | chr9:92053993-92065524 | CD4p_CD25-_CD45RAp_Naive | | SE_17792 | chr9:92054086-92062874 | CD4p_CD25-_CD45ROp_Memory | | SE_18250 | chr9:92053940-92065020 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_19118 | chr9:92054561-92061664 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_20089 | chr9:92058324-92061549 | CD56 | | SE_21155 | chr9:92058310-92059883 | CD8_Memory_7pool | | SE_21665 | chr9:92058225-92060796 | CD8_Naive_7pool | | SE_21969 | chr9:92057987-92060891 | CD8_Naive_8pool | | SE_22409 | chr9:92057540-92062777 | CD8_primiary | | SE_26933 | chr9:92054283-92059600 | Esophagus | | SE_32149 | chr9:92054630-92059435 | Gastric | | SE_41833 | chr9:92054598-92058769 | LNCaP | | SE_50088 | chr9:92054675-92059690 | Sigmoid_Colon | | SE_52548 | chr9:92057492-92059510 | Small_Intestine | | SE_53415 | chr9:92056477-92058276 | Spleen | | SE_60002 | chr9:92014899-92064443 | Ly4 | | SE_62222 | chr9:92014516-92154755 | Tonsil | | SE_68703 | chr9:92054492-92059072 | H9 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH09I089439 | chr9 | 92054613 | 92061272 |
|
Enhancer Sequence | TAGCAAAGAA TCAGACCCAC TCACCCTGAG CTGTCAGGAT ACATGCAAGG GGAGGGGAGG 60
GTTCCTGGGG TTCATAACTG CATCCGTCCC AGAGAGGGAT CAGCACCAGA CAGTGTCTGG 120
CATGGCTGCA GCCCTCCCCA TCCTTCTCAC CATTTCCCAG CGAGGAAACA CCAGACCCGG 180
GCAGATGTGA GTCAATGCTG GGGACCCTGG TTCACGCATG TGCCGGTGTC GTCTGCAAAC 240
CTGGGCCCCG GGCCTGGGCT GGGACAAGCC TGTCATCACA CAGCCTGTGA GACTTTTAAG 300
GGCCTTCACT GGGGCTAGAG CAACCTCGGA TGCCCACCAG GACCGTGCTC AGCAGCAGGA 360
GGGCCCCCTG CACCCCTACA GCATGCCTGC ACAGCCTCTG CCTGACCTGG GACTGAAGCC 420
TCCCAGGAGG AAGGCGGCTC TTCTCCCCAG GAGGTGACTC ACAGTCCAGA GCCCAGCCCC 480
ATCAGGTCCC CTAGGGACTT CTCCACAGCT TCAAGAGTGA GACTTCCCTG TCAGTGGCGG 540
GATTATGACC ACCCACACTA CCCCCCTGGA CAGAGGCCGG GTCGCGAGGT GCTCTGGAGA 600
AGAACGGATG CCAGTGCTCA ACTGGACACA CACTCCAGCC ACAAGCCATA TGTGGGCTGA 660
ACAAGGAGCT TAAACAGGGC CACCAGGATG CCCATGGGCC CAGTCTCCAG CCACCTTCCC 720
ACGGGGCCTG GCTGCCCTGT CCACCTTCTC ACTGACCTCG AAGCGGGTGT ACCACGGTCC 780
TGTTGTCCCT GCAGAGTGGA GCCTTCAGCT GTCTGACAGA AAATGAGCCC TCCCAGTAAA 840
GCACAGCGTG GACTCCACCC GCCCATAATA GCCACCCGGG AAGCAGGTCC GGCCAGCAGC 900
AGCCGCCAGA GGAGGATCTG CCTGGGGTAG GCGGGTGGCG GACGGCCCTG GCCCTGCAGC 960
GCTCAGCTGC ACCCCACCCC ATGCCTGCCT CCGAGCTGGT GGCCAGGACC TGGCTGCCTC 1020
CTGTCCTGGC TGTGAGTCCT GTATGGGCTG GCACCTGAAA CTCTCTACCC TCCCTCCACA 1080
GCATGGGTGG GGCTGGGGTC ACCAGTGGGT AACTGCAGGC CCTGACCTCC TGGGCTCCCT 1140
GCATAGGTGT GGCCTGCCCT GCTAAAGCAG TGCCACAGAA GATGGGGCAC AGAGAGCATT 1200
TGGAGACTGC GAGGTGCCAG CTGCCAGAGG TGCCTGGGCA TGGGCATCCT CAGGGGCCCA 1260
GAGTCAGGCA GCCCTGGGCC AGGCACAGGC ACCTAAGCTG CAGTGACACG GTCACCCCAC 1320
TGCATGCCCA TGCATCCTCC CACCACGGGC AGAGTCAGGG CACTCATGCC CAAAGGAAAT 1380
CCAAGCAGTG GGTGGGTCCC TGACACGAAG GGTTCTCTTT TCACTGCTCC CCCCATAATA 1440
AACCTGCTTT ACATTTATTG TCCTAGACAC CTTGCCTTTT AGAAATTATA CCTACCTACC 1500
ATAGACATAA TTCTGCGTCC ACCTGGTGGT CTCTGTTTTC CTGCTTCACC TTGGCCTCCC 1560
TCCCCACCTC CATGGCCTCC TCCCTGGCTG CCCCTCTAGC ACAGCTACAG TGTACCCACC 1620
CTTATCATGC TCTGCCCAGG AGTCATAAGG AGAAACACAG GCAAACACAT ACAGGCATAC 1680
ACAGGAGCAC TCCTGCCATC ACGGCTCACA AAGCACGTCA TCACACACAC AGCACATGAG 1740
GGGACTCCTC CCAGCTATCA GCACTTGCTC TGCAGCCGCT ACTGACGGGA TGTGGGCACG 1800
TGAAGAGACA AGCAGGCCAG CGAGTGGGAT GGAGGATCCC CAGACGGAAC CCAGTTTACA 1860
TGAGACCCTA ACAGACCACA GAGCTGTCAT TCAATTCATT GGTCAAAGGA CGGATTATTG 1920
ACTAATTAGT GCTGGCACAC TGGAAGGAAA CAAAATTGCC CTCCCCCACC CCAAGCATAT 1980
TATTTCATGT TAAAAGCATT CTAGACACGT TCAAGAGTTT AATTCAAACA CACAAAACAA 2040
GAAAACTCCT GCCAGAAAAT CCTCAGACAA CCCATGTAAT CTTCTTAACA AACGCTGGTA 2100
CCCACGAGCC CTAAGAGAAA AGAGACATAT TCGACCATAA 2140
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