| Tag | Content |
|---|
EnhancerAtlas ID | HS092-39058 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr9:137257120-137259450 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESX1 | MA0644.1 | chr9:137258868-137258878 | GTTAATTGGT | - | 6.02 | | ZNF740 | MA0753.2 | chr9:137258150-137258163 | CCACCCCCCCCAT | + | 6.46 |
|
| | Number of super-enhancer constituents: 30 | ID | Coordinate | Tissue/cell |
| SE_00174 | chr9:137256755-137259829 | Adipose_Nuclei | | SE_00860 | chr9:137255901-137260558 | Adrenal_Gland | | SE_02933 | chr9:137257000-137258918 | Bladder | | SE_05812 | chr9:137248771-137260982 | Brain_Hippocampus_Middle | | SE_09174 | chr9:137254160-137271835 | CD14 | | SE_23121 | chr9:137257215-137258962 | Colon_Crypt_1 | | SE_23757 | chr9:137257477-137258890 | Colon_Crypt_2 | | SE_24707 | chr9:137255976-137259679 | Colon_Crypt_3 | | SE_26524 | chr9:137256603-137261031 | Esophagus | | SE_28276 | chr9:137255240-137260623 | Fetal_Intestine | | SE_29238 | chr9:137255536-137260979 | Fetal_Intestine_Large | | SE_31436 | chr9:137257235-137259271 | Gastric | | SE_33498 | chr9:137255830-137262370 | H2171 | | SE_34123 | chr9:137257219-137258975 | HCC1954 | | SE_34906 | chr9:137257194-137259877 | HeLa | | SE_40986 | chr9:137256096-137259621 | Left_Ventricle | | SE_41556 | chr9:137243649-137273607 | LNCaP | | SE_42130 | chr9:137254678-137260854 | Lung | | SE_43440 | chr9:137245134-137261072 | MCF-7 | | SE_47617 | chr9:137257494-137258929 | Pancreas | | SE_48050 | chr9:137252285-137278501 | Psoas_Muscle | | SE_49423 | chr9:137256346-137259249 | Right_Atrium | | SE_50152 | chr9:137256575-137259121 | Sigmoid_Colon | | SE_51460 | chr9:137256881-137259251 | Skeletal_Muscle | | SE_52424 | chr9:137256233-137259619 | Small_Intestine | | SE_53315 | chr9:137256820-137259081 | Spleen | | SE_54834 | chr9:137256437-137259599 | Stomach_Smooth_Muscle | | SE_65247 | chr9:137243550-137260818 | Pancreatic_islets | | SE_68695 | chr9:137256582-137258009 | H9 | | SE_68695 | chr9:137258952-137260384 | H9 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr9 | 137257428 | 137257617 | | chr9 | 137257724 | 137257990 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH09I134363 | chr9 | 137255386 | 137260783 |
|
Enhancer Sequence | GCAGGCGCTC GAGCTGAAAG CCCTCGCCCC TCGTGGTGGG GCAGCGCGTC CCTGGGTGAG 60
TGACCAGGCG GCCTTGGGTC TCTGGTGAGC TCAGGGAGCG GGGTCCACGT TGCCTGGCCC 120
AGGTGGGATT TGGCGGGTAA CGCTCGTGGT GTGTCCTGGT GTGAGACCCG GTGTTCTTGG 180
CTGATGTGTG GGTTTGCTCA TGGGGTGGAC CAGGCCGCTG CCCCTGCCTC CTGTCTCTGG 240
CTGTGGCCAT GGCTGTGTGG ACCAGGCTGG GGCTGCACTG GGGCCTGGGT GGTAGGGGGT 300
GATCTGCTTG TCCAGTGGTT TCTGTGGCTT TTCTGGGGTC CTGGGCTGTC CCTCAGCAGG 360
CCTGGGACTG GGCGGGGACA GTGGGGATGA GTTTCAGGTC TGTTCTTGGT GGCTGTTAAC 420
TCTAGGCCAG ATGTAGCCCT GAGGGGCCCG GCAGAGTCTC GGTGGGTCTC GGTGGGGCCA 480
GCTGTCGGTG GGTGAGGTGC CCCAGGGGAA GGGAGGGCCA GCCCAGAAGG ACCCTCCCAT 540
TACCCTCTGG TGGCTTGCCC ATGCCACCAT TCCTACTGCT AGGCTCAGGC CTGTCTTGGG 600
GAGGGTTCCT GGGCTGGGAT TGGCCGTCGG GGAGGTGCAC ACAGACGCTC AGCACAGTTG 660
TGGCTGCCTC CAGTCAGGCG TCCGCTGAGC GACCCCTAGG AGCCGCCTGT CTTTGCAGGA 720
GCCGCGGGGA TCATCTGGCG GCTGCCTCCA CCCCTGCCTC CACCCCTCCC TTTTTGGGAG 780
GTGGGGCTTG GCATCTTCAG CATCTCTCGT GCCTCAGTAA CAACCTGGGA GCGGTGCTGT 840
CCCTGGGTAC AGATGAGAAG CCAAGGCTCA GAGGCACCAG GGCCCCAGTG GGAGGCGGCA 900
GAGCCTCTGG TGGCTCCGTG TGGCATGTTC TGGGCTGTGT GTGGGGCCAG GGAGGGTGTC 960
TTCAGCACAG GTGCCCGCTG GGTGGTCTCC CATGTGTGCC CAGGAGGAGT GCCACAGCCT 1020
CTCCCTCTGC CCACCCCCCC CATGCCTGCC CTGCCAGCAG GTCCAGCAGG CCTTGGCACA 1080
GGCTCCAGAA TTGCACGTGA TCTCAGACGG TTCCCAGCTT CCTCTGCAGG GCGGGGCTGC 1140
TCCAGTCTCT TACACCAGCG CATCTGCAAC TCATTACACA GCGGTGTCGG TGGCAGAGTG 1200
GCCTGGCCAC GGCGAGCTCC TGGCGGGAGT CCCCCTCCCC AGCAGCCACC CCGTGCCATG 1260
GGCCTCCAGG TCCCCCGGGT GCTGGCCTGG GGACAGCACC ACAGGGCCCA GCCAGGGCTG 1320
GGGCAGGGAG GAAGGGCCCC TCCACTAGTG GGCTTTGGCC TCCTCGTGAG GAGCTGGGTG 1380
GGGCTGGAGA AATCAGCTCC CGCCAGCCTG ATCTTCCTGC CTCAGAAGCT GAACCCCGGG 1440
GACAGTGTTG GTCAGAAAAG CCATAGACTC TCCACGGAAA AGGAAGCCTG GCACCCCCCA 1500
TGTTTCACGT AGGCCACCCT AAGGTCCACA GATGCCTGGG GACAAGGATT AGTGTGAGCA 1560
AAGACACAGG AGTCGGGGAC ACATCCCAGT CGGAACGTGG TGGAAAGGCG CCAGGCAGGC 1620
TGAGTCGGAG ATGTCCCTCA GGCTCCTGCT GGGAGAAGGG GCTGGTGGTT CCCGGGCCTG 1680
CACATCCCCA CCCCTGCCCT GCGTGCCACT CTCAGCCTTT GCCCAGCACC AGGCTTATTA 1740
TCCGATTGGT TAATTGGTTG AGATACGGGT CACCTCCCGT AACAGTCATC TTTTTAAGGC 1800
GTGCAGTTCA GTGGGTTTTC ATCCACACAC TTGCACAGCC ACCACCACAG CCAGCTTTAG 1860
AATTTCGAAG CACTTCCACC AACCCCCCAA AAGAAGCCCC GTGCCCGCTG GAGCTGCTGC 1920
AGTGCCCCGC CTGACCCCAC CAGCCACTCC CCTGCCTGCC TTCTTTGTGG ATCTGCCTGG 1980
TCTGGCGTTT GTGATCTCCC TCCATCTTCA CAGCAGTCTA GGTGCTGCGC TGGGCAGGGA 2040
CTGAGTCTGC GGTGGGGGGG AGGGTGGTGA CCCTGTCCGG GGAGACCCAG CCTTGCTCCC 2100
CGGAGCCCAC CCTTCCACTC TCTGTGGGAA GAGAAGGACA CTGAGTCTGC CTTGGGTTTC 2160
TCTTGCGTCC CCACATGCAG GGACGACGTG CCAGGGCCCG CTGTGTGCCC TTACCGTGGA 2220
GATCCCACTT TACAGATGGG AAACTGAGGT TCAGTGGTCG AGGAGCCAGC ACTTGGAGAC 2280
AGGATGTGAA ACCCCCGGCT CCTGGCCCCT CGGCCAAGCT GTCGGTGCAG 2330
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