| Tag | Content |
|---|
EnhancerAtlas ID | HS034-31252 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr9:137257580-137258570 |
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 | GGTGGGTCTC GGTGGGGCCA GCTGTCGGTG GGTGAGGTGC CCCAGGGGAA GGGAGGGCCA 60
GCCCAGAAGG ACCCTCCCAT TACCCTCTGG TGGCTTGCCC ATGCCACCAT TCCTACTGCT 120
AGGCTCAGGC CTGTCTTGGG GAGGGTTCCT GGGCTGGGAT TGGCCGTCGG GGAGGTGCAC 180
ACAGACGCTC AGCACAGTTG TGGCTGCCTC CAGTCAGGCG TCCGCTGAGC GACCCCTAGG 240
AGCCGCCTGT CTTTGCAGGA GCCGCGGGGA TCATCTGGCG GCTGCCTCCA CCCCTGCCTC 300
CACCCCTCCC TTTTTGGGAG GTGGGGCTTG GCATCTTCAG CATCTCTCGT GCCTCAGTAA 360
CAACCTGGGA GCGGTGCTGT CCCTGGGTAC AGATGAGAAG CCAAGGCTCA GAGGCACCAG 420
GGCCCCAGTG GGAGGCGGCA GAGCCTCTGG TGGCTCCGTG TGGCATGTTC TGGGCTGTGT 480
GTGGGGCCAG GGAGGGTGTC TTCAGCACAG GTGCCCGCTG GGTGGTCTCC CATGTGTGCC 540
CAGGAGGAGT GCCACAGCCT CTCCCTCTGC CCACCCCCCC CATGCCTGCC CTGCCAGCAG 600
GTCCAGCAGG CCTTGGCACA GGCTCCAGAA TTGCACGTGA TCTCAGACGG TTCCCAGCTT 660
CCTCTGCAGG GCGGGGCTGC TCCAGTCTCT TACACCAGCG CATCTGCAAC TCATTACACA 720
GCGGTGTCGG TGGCAGAGTG GCCTGGCCAC GGCGAGCTCC TGGCGGGAGT CCCCCTCCCC 780
AGCAGCCACC CCGTGCCATG GGCCTCCAGG TCCCCCGGGT GCTGGCCTGG GGACAGCACC 840
ACAGGGCCCA GCCAGGGCTG GGGCAGGGAG GAAGGGCCCC TCCACTAGTG GGCTTTGGCC 900
TCCTCGTGAG GAGCTGGGTG GGGCTGGAGA AATCAGCTCC CGCCAGCCTG ATCTTCCTGC 960
CTCAGAAGCT GAACCCCGGG GACAGTGTTG 990
|
