| Tag | Content |
|---|
EnhancerAtlas ID | HS105-83919 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr9:137229720-137232500 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RREB1 | MA0073.1 | chr9:137232192-137232212 | GTGGGGATGGTGGTTTGGGG | - | 6.91 | | Stat6 | MA0520.1 | chr9:137232246-137232261 | AGTTCCCAGGAAGTG | - | 6.52 | | TCFL5 | MA0632.2 | chr9:137231217-137231227 | GTGCGCGTGA | - | 6.02 |
|
| | Number of super-enhancer constituents: 27 | ID | Coordinate | Tissue/cell |
| SE_00174 | chr9:137230168-137233916 | Adipose_Nuclei | | SE_00860 | chr9:137229675-137234105 | Adrenal_Gland | | SE_05812 | chr9:137229665-137243441 | Brain_Hippocampus_Middle | | SE_09174 | chr9:137229871-137239297 | CD14 | | SE_23121 | chr9:137230021-137234886 | Colon_Crypt_1 | | SE_23757 | chr9:137229957-137234856 | Colon_Crypt_2 | | SE_24707 | chr9:137229660-137231531 | Colon_Crypt_3 | | SE_24707 | chr9:137231621-137235205 | Colon_Crypt_3 | | SE_26524 | chr9:137230554-137231608 | Esophagus | | SE_26524 | chr9:137231813-137237016 | Esophagus | | SE_31436 | chr9:137230364-137231461 | Gastric | | SE_31436 | chr9:137231704-137235635 | Gastric | | SE_41371 | chr9:137229502-137237311 | Left_Ventricle | | SE_41556 | chr9:137228624-137236303 | LNCaP | | SE_42130 | chr9:137229578-137237558 | Lung | | SE_47841 | chr9:137228792-137231739 | Pancreas | | SE_48050 | chr9:137218344-137231679 | Psoas_Muscle | | SE_48050 | chr9:137231710-137234311 | Psoas_Muscle | | SE_50152 | chr9:137229753-137237108 | Sigmoid_Colon | | SE_51460 | chr9:137229222-137231524 | Skeletal_Muscle | | SE_51460 | chr9:137232018-137234369 | Skeletal_Muscle | | SE_52424 | chr9:137229666-137234603 | Small_Intestine | | SE_53315 | chr9:137230677-137231513 | Spleen | | SE_53315 | chr9:137231679-137234514 | Spleen | | SE_65247 | chr9:137218874-137243530 | Pancreatic_islets | | SE_68695 | chr9:137230756-137232073 | H9 | | SE_68695 | chr9:137232214-137234459 | H9 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 5 | Chromosome | Start | End |
| chr9 | 137229945 | 137230162 | | chr9 | 137230182 | 137231531 | | chr9 | 137231518 | 137231916 | | chr9 | 137231588 | 137231771 | | chr9 | 137231889 | 137232148 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH09I134338 | chr9 | 137230026 | 137237246 |
|
Enhancer Sequence | AAGAAACGAG ACAGGCGGGT TTCGTTCAGT TCAGGTGGCC GCGTGCCAGC CCTGAGAGGT 60
GGCGGGGGAG AGATGGGTGA CTGCGCCCCC AGTGCTCACG GAGGGCCCCT CTGTCCAGAG 120
CCGCTCTGAG GATGCGACAG GCAGGTCCTT GCCCTCGTGG GCTGCCAGGC CAGCGGGGGA 180
GATGGGCGGT CAGCGGCAGC CACAGACGAC GTAGGGCTCA GGAAGGGCAT GGAGGGAAAC 240
GCTGGGCAGT GACCACAGGG AGGGACAGAG GTGTCAGGAG CCCTGACAGA AGACAAGCAT 300
GTGGTTCTGC TGCACTGTCC CGGGGCCTCC CTGGGCCTCC CTCTGGCTGG TAGCACGGGC 360
AGGTGTGTGG GGCACGGCCA TCGCCAGGCA TTCGACCCCT GCTGGCTCAT TCTTGGCTCC 420
CTGTGGCTGC CGTGGGACAT GGTTTCTAAA GAACAAATGC CAGCTGTGGC GCTGAAAGGG 480
CCTCCTCATG TCAGGGTGCC CCTGGCTGCA GGACACAGGC CACTTCTGGT CCCAGATTGA 540
CGGGCCTCCA GCCCAAGTGG CACCTGGGTC CCTCTGACCT GGGCTGGCAT CCCCCAGGCC 600
ATGGGGTCAC AGGGGAGGTC ACTGCCACTC TTGCTGGCTG GGAGAGGCGT GTCCCCACGT 660
GCGTCTGGCC GCAGTCAGTG GCCAGGACCT GCCTGCGTGT GGACAGTTAG GCCTCCTGCC 720
TAGGAAGCAG TGATGCTTGC CGGCTGCTGG TGGGGGCAGG GGAGGGGCTG GCTGCCGGAT 780
CCCACGCAGC CTGGACGTGG CTGATAAGCT GTGAACTCAT TATCGGAGGG GGCAGCTGGT 840
GCCCCTCTCC CTGCAGCCGG CACCCCAGCC TTGCCCTGGG GCCAGACCCC TGCACTGTGC 900
CCAGCCTTGC GGGTGAGACT GGGGGAGCGA GCAGGCCTCT GTTGGGACTT GGGAGTCTCC 960
AGGGTCCCCC AGAGCCCAGA GATCCTCCCT CCAGGACTCT GGAGACAGCC GCCGTTCTGC 1020
CCTCCCTGCT GACCCCTCTG CCCTCCCTCA GGTCTGCCTG GCCGCCTTTC TGAGAACAAG 1080
GAGCCGATTG TTGTCACCAC TGCTGTCTGC CTCCTGCTGT GGATGCCTTG CTTGGCGCTG 1140
GCAGTGCCCA CACCGGCAGG GACCTGGGGA CTTGGAGCCG GACCTAGGTC GCCGGCCGTG 1200
TGCCTGGTGT CGGGGCAGGG CTGGTGGTCA CCCCCCCTGG GGTTGGCCCC GTGGGCTCAG 1260
GGCCCTGCCT CCCTGTGCCC TGTCCGTAGG GACCCTCTCA TGCCCTCTGG CCAGCCTGGA 1320
GAGCTCTTGG CAGAAAGGCC AGGACTGAGG TGGCTGGCAT GGCGCCTCCC GCGCTGTTCC 1380
TCCCTCCCTG CCTGGCCTTC AGGGGCGCGT CGTCCTCCCC AGACCCTCCT CTGTCTGCGT 1440
GTGAGCCCGT GAGCCTGTGT GGGCTTATGT GTGTGGCTGG GATTCCAGCC AGGGTTTGTG 1500
CGCGTGAGCC TCTGTCTGCG TGTGAGCCCG TGAGCCTGTG TGTGAGAGTG TGTGGGTGCC 1560
ATGCCTGTGT GAGTGTGTGC CTGTGTGTGA GCCTGTGTGT GGGTGTGCAT GCCCACGCCC 1620
TTGTGTGAGT GTGTGTGAGT CTGTGTGTGT GTGTGTGTGA GCCCGTGTGT GTGTGAGTCT 1680
CTGCATACCC ATGGCCTTTT GTGAGCCTGT GTGTGTGAGC CTGTGCGTGT GTTTCTGTGT 1740
GAGTCTCTGT GTGTGTGAGC CTGTGCGTGT GTCTGTGTGT GTGCCTGTGT GTGTGTGAGC 1800
CTGTGTGTGT GTGTGTCTCT GTGTGTGTGC CTGTGTGTGT TTGAGCCTGT GTGTGTGTGT 1860
CTATGTGTGA GATCCCGTGT GTGTCTGTGC ACACCCATGC CCTTGTGTGA GCCTGTGTGT 1920
ATGAGTCTGT GTGTAAGCCT CTGTGTGTGT GTGTGTGTGA GTCTGTGTGT GTGTGAGCCC 1980
ATGTGTGTGT GTCTGTGAAC ATCCATGCCC TTGTGTGAGC CTGTGTGTGT CTGTGTGTGA 2040
ACCTGTGTGT ATGTGAGTGT GCACGCCTGT GCTCTTGTGT GAGCCTGTCT GTGTGCACCC 2100
GTGCATGTGT GTTCCTCTGT GCACATCTGT GTCCATGTCT GAGCCTGTAT CTGTGTGCAC 2160
CCATGTCTGT GTCCCTCTGT CCCTGTCCCT GTGTGAGTGT GTATCCGTGT GCACTTGTGT 2220
CCTCGTGTCT CCCTGTGCCC GTGCTGTGTC GGCATGTGTG CCTGTGTGTG CTTCTGTGTG 2280
TCTTGTGCCC CACACCTTCT GATGGCTTGT GCCTGCGGGT CCAGGTTTGA GACTGGCCAC 2340
TGCCCGTGCT GTCCGGCTCC CTCCTTAGCT AAGGGTCCTG AGGGCTCGGG GTCCAGGACA 2400
GGAGAATGAG AAGCTGTAGG GGGCTGTGGA GGGCTGCAGG CAGATATATG TTCTAGAAAG 2460
ACTTTGGCCA TCGTGGGGAT GGTGGTTTGG GGCAGACCAG TGATGCCACC CACTGACCTT 2520
TCAGCCAGTT CCCAGGAAGT GTCACAGGGG TGATAATTGT CCAGCCAGGA GTGAGGGCCG 2580
AGGGGCTTTA GGAAGTGCCA GGGAGCACTC TGAAGCAGTA TGTTTTGGTC TAAGTGGGGC 2640
TCACGTGGCA CCGGCTCACT GCCTGCCCTC TGGCCTACAG CGTGGCAGGT ATCACCGACC 2700
ACCCGAAGCA CTCAGATCCC TTTCTGCAGG CACCCAGGCA GACGGTCTCG GTGCATGAGC 2760
CTCGATGCAC GCCTCGGCCC 2780
|
