| Tag | Content |
|---|
EnhancerAtlas ID | HS145-27130 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr9:137257650-137258570 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF740 | MA0753.2 | chr9:137258150-137258163 | CCACCCCCCCCAT | + | 6.46 |
|
| | Number of super-enhancer constituents: 29 | 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 |
|
| | 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 |
| GH09I134363 | chr9 | 137255386 | 137260783 |
|
Enhancer Sequence | ACCCTCCCAT TACCCTCTGG TGGCTTGCCC ATGCCACCAT TCCTACTGCT AGGCTCAGGC 60
CTGTCTTGGG GAGGGTTCCT GGGCTGGGAT TGGCCGTCGG GGAGGTGCAC ACAGACGCTC 120
AGCACAGTTG TGGCTGCCTC CAGTCAGGCG TCCGCTGAGC GACCCCTAGG AGCCGCCTGT 180
CTTTGCAGGA GCCGCGGGGA TCATCTGGCG GCTGCCTCCA CCCCTGCCTC CACCCCTCCC 240
TTTTTGGGAG GTGGGGCTTG GCATCTTCAG CATCTCTCGT GCCTCAGTAA CAACCTGGGA 300
GCGGTGCTGT CCCTGGGTAC AGATGAGAAG CCAAGGCTCA GAGGCACCAG GGCCCCAGTG 360
GGAGGCGGCA GAGCCTCTGG TGGCTCCGTG TGGCATGTTC TGGGCTGTGT GTGGGGCCAG 420
GGAGGGTGTC TTCAGCACAG GTGCCCGCTG GGTGGTCTCC CATGTGTGCC CAGGAGGAGT 480
GCCACAGCCT CTCCCTCTGC CCACCCCCCC CATGCCTGCC CTGCCAGCAG GTCCAGCAGG 540
CCTTGGCACA GGCTCCAGAA TTGCACGTGA TCTCAGACGG TTCCCAGCTT CCTCTGCAGG 600
GCGGGGCTGC TCCAGTCTCT TACACCAGCG CATCTGCAAC TCATTACACA GCGGTGTCGG 660
TGGCAGAGTG GCCTGGCCAC GGCGAGCTCC TGGCGGGAGT CCCCCTCCCC AGCAGCCACC 720
CCGTGCCATG GGCCTCCAGG TCCCCCGGGT GCTGGCCTGG GGACAGCACC ACAGGGCCCA 780
GCCAGGGCTG GGGCAGGGAG GAAGGGCCCC TCCACTAGTG GGCTTTGGCC TCCTCGTGAG 840
GAGCTGGGTG GGGCTGGAGA AATCAGCTCC CGCCAGCCTG ATCTTCCTGC CTCAGAAGCT 900
GAACCCCGGG GACAGTGTTG 920
|
