| Tag | Content |
|---|
EnhancerAtlas ID | HS040-34609 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr9:92040060-92042310 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MEF2A | MA0052.3 | chr9:92041796-92041808 | GCTAAAAATAGA | + | 6.92 | | MEF2B | MA0660.1 | chr9:92041796-92041808 | GCTAAAAATAGA | + | 6.44 | | MEF2C | MA0497.1 | chr9:92041794-92041809 | GTGCTAAAAATAGAC | + | 6.99 | | MYC | MA0147.3 | chr9:92040392-92040404 | CAGCACGTGGCC | - | 6.37 |
|
| | Number of super-enhancer constituents: 30 | ID | Coordinate | Tissue/cell |
| SE_03177 | chr9:92039603-92042070 | Brain_Angular_Gyrus | | SE_03905 | chr9:92039342-92045792 | Brain_Anterior_Caudate | | SE_04779 | chr9:92038176-92053883 | Brain_Cingulate_Gyrus | | SE_05782 | chr9:92038008-92053861 | Brain_Hippocampus_Middle | | SE_06723 | chr9:92038472-92046613 | Brain_Hippocampus_Middle_150 | | SE_07735 | chr9:92038409-92046165 | Brain_Inferior_Temporal_Lobe | | SE_09170 | chr9:92034692-92042561 | CD14 | | SE_11886 | chr9:92039521-92043400 | CD3 | | SE_14475 | chr9:92038405-92044542 | CD4_Memory_Primary_7pool | | SE_16354 | chr9:92040048-92042346 | CD4_Naive_Primary_8pool | | SE_16924 | chr9:92039904-92040421 | CD4p_CD225int_CD127p_Tmem | | SE_16924 | chr9:92040863-92042506 | 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 | chr9:92039519-92043345 | CD56 | | SE_21155 | chr9:92041162-92042446 | CD8_Memory_7pool | | SE_21665 | chr9:92040282-92042768 | CD8_Naive_7pool | | SE_21969 | chr9:92040362-92042770 | CD8_Naive_8pool | | SE_22409 | chr9:92038260-92044154 | CD8_primiary | | SE_32149 | chr9:92040147-92041098 | Gastric | | SE_50088 | chr9:92039365-92045727 | Sigmoid_Colon | | SE_52548 | chr9:92039358-92045623 | Small_Intestine | | SE_53415 | chr9:92040986-92041853 | Spleen | | SE_60002 | chr9:92014899-92064443 | Ly4 | | SE_62222 | chr9:92014516-92154755 | Tonsil | | SE_66275 | chr9:92041258-92041967 | Jurkat | | SE_68703 | chr9:92039787-92041031 | H9 | | SE_68703 | chr9:92041323-92041912 | 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 |
| GH09I089417 | chr9 | 92032405 | 92045324 |
|
Enhancer Sequence | GCCAGGACCG AGAACTGGCC TGCATCCACC AGATTTCCTG CCTTGCCCAG TGTTACCCAG 60
GCCTTGCCAC CTCCCCTAGG TATGTCCTGA GTCCATCCTT GACACCCACC CACTGAAATC 120
CTGGCTGTCC ACTGTGGCTC AGCTCGAAGG CCAGGGCAAC CTCAGACCTG CCCTCTGGGA 180
ACAGATGCCT CCCCTCAGCT GGTCTTCATT CACGGGGTCT CCTGGGGGAA AATGTAAGCA 240
GGAAGAATAA CTAACACCCG CCATAAGGCA AGGGTGAGGA AGTGACTGTT CTACTGGGTT 300
CTGCGAGGGT CAGGCTGTGA GTCACCTGGA AGCAGCACGT GGCCCTGACA TCTGGGAAGG 360
GGCTGCTCAC ACCTCCCATG TTCATAGCTC CCTGGCAGGC TCCTCACTAA CCCTCGTATC 420
TGACATCTGA CTGAATCCCA GTGTTCAAGA GGCCTGGGCA AGGACAGCCT ACAAGCCCGC 480
TGCTTTGACA TCAGGGGCAG GAGTCCTGAA AGCCTGACCC TGTGGCCCCA CTGGCTGTAC 540
ATCCACCCCC TCCCCCAGTG TGCCCCACTG GAGACAGGTT TTACAGCACT GCTGGGAAGA 600
GGAAAAACAG GCTCAGAAAA ATGCAACAAC CGTCTAGAGC CACTGGGAGA GGTGAGATGC 660
CCTCCCGGGT CCTGCAGTGA CCCCAGGACC ATGACTGGCA CAGTGCTCTC CAGCTGTGCT 720
GAGGCTCCAC CTGCCCTGAG CCAACAGCTT CCTCCTCCAG GGACACCAGG GCAGAGACAG 780
GCCCTTCAGA AACAATGGCT CCTTCTCTTT GCCAACTGCC AGCAGTGAAG GCATCACAGA 840
ATCTGCCAGA ACCATCCAGA ACCCTGAACT GGTTCAGGAC TACAGGCAGC CTGGGGAGAT 900
GCCCTGCACT CAGAGGCATC CCTAGTCCCC ACCAAGTGTC CGCAGGGGGA GCGCATGCAG 960
TTTCTCCAGG GGACTGGACC TCCTCCAGGC CGGGATCCTC CTCCCCTGCT GCCCTCAGAC 1020
TCAGCCCAGC TGCAAAGGCG CCAGAGGCCT GCTCGTTCTG CCACGGTGCA GGCACGGCAT 1080
GAGGGGATAG GCCCAGGAGC CTCAGGACAG GCCCCAGTCC AAGTGGGAAT TTCTTTTTTA 1140
AGTCTCAAAA CCACAAAATG CCACTTTCCT TGCTTTCATC TTTAGTGATT CTTTAAATAT 1200
ATACACTACA ATTACAAAGT TAGACCACCA TGACCACAGC TCGTAACCAG AATAGAGTCA 1260
ACAGGGAACC TAGTCAACAG GAGGCTCTCC CTCACTATCC GGGCCTCCTC CCCAGGACAT 1320
GGCTTTTGCC AGCCTTAGCA ACAGCGTGGC AAACCCACCA GAGAACCACA AGCTCCAGCC 1380
AGAGCTCTGC GAAGGCCCCA GCTTTGCCTC ACTCCAGGCG GGAAACAAAA GGATGTTCGC 1440
CATTTCATCA TCTGGGGCTG TCAGTTCCCG TCTCAGTACT GACCTTAAAT GCTGTCTTAC 1500
CGTCGTGCGC AGACACCAGG TGCACGCAGC CTCGACCTGA TCTACCAGCC CCCAAAGCCC 1560
CTCAGAGGCC ACAAGAACCT CCCTCAACCT CAGTATCAGA GGAAGCAACT TCAACTAAGC 1620
TCATAATTAT TTTAAGACTC TCCTACATCT TAACCATATT CAAACCAAAC CAACTCACTT 1680
CCCATCAACA GTAGACCAAG TGGTCACTGT GGGCAGGTGA CAAGCATCAC AGAAGTGCTA 1740
AAAATAGACA ATGTGACAAC CACAACACCC GGCTACGATG GTAAGGAGCA AACACTGCAG 1800
GCCACACCTG TGCCCTAGGT CTGTCCCCAG CGAGTTCCCC CTTTGCCACT AAGACAATTA 1860
CTGCCCATAT GGATGGCCAG AATTTCAATC AATTTCTATT TCCAAATCAC CAAATGACCC 1920
TCTAGCTGAA TGTCACAAGC CCAGTATTGG GTCAGAGGTA GATACACTCT ACTCTAATGA 1980
ATTATAGTCA ATCCCCACGT TCAACTCACT AAATCCATCC TCCCTTGCAG TGCAAGGGAA 2040
ATGATATTTC TTCTCCTCTC TTCCAGATGC TTCCAGCCCA AGTAAGGCAG TCCCTCAATT 2100
CCCTTCCTGG GGAGTCAGAA GAGGGGGGCA GCCTAAAATG ATACAGTCAG TCACTCAGGT 2160
CCATCCAACC CCAAATAGCC GTAGATGCCA GAAGAGGGTC AAGTGCATAT GGACTAAGGA 2220
GGCGGTGTGA CCCTGGTGAG ATGCCTGTAT 2250
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