Tag | Content |
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EnhancerAtlas ID | HS110-05116 |
Organism | Homo sapiens |
Tissue/cell | KATO3 |
Coordinate | chr9:137257590-137259020 |
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 |
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| 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 |
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| 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 |
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Enhancer Sequence | GGTGGGGCCA GCTGTCGGTG GGTGAGGTGC CCCAGGGGAA GGGAGGGCCA GCCCAGAAGG 60 ACCCTCCCAT TACCCTCTGG TGGCTTGCCC ATGCCACCAT TCCTACTGCT AGGCTCAGGC 120 CTGTCTTGGG GAGGGTTCCT GGGCTGGGAT TGGCCGTCGG GGAGGTGCAC ACAGACGCTC 180 AGCACAGTTG TGGCTGCCTC CAGTCAGGCG TCCGCTGAGC GACCCCTAGG AGCCGCCTGT 240 CTTTGCAGGA GCCGCGGGGA TCATCTGGCG GCTGCCTCCA CCCCTGCCTC CACCCCTCCC 300 TTTTTGGGAG GTGGGGCTTG GCATCTTCAG CATCTCTCGT GCCTCAGTAA CAACCTGGGA 360 GCGGTGCTGT CCCTGGGTAC AGATGAGAAG CCAAGGCTCA GAGGCACCAG GGCCCCAGTG 420 GGAGGCGGCA GAGCCTCTGG TGGCTCCGTG TGGCATGTTC TGGGCTGTGT GTGGGGCCAG 480 GGAGGGTGTC TTCAGCACAG GTGCCCGCTG GGTGGTCTCC CATGTGTGCC CAGGAGGAGT 540 GCCACAGCCT CTCCCTCTGC CCACCCCCCC CATGCCTGCC CTGCCAGCAG GTCCAGCAGG 600 CCTTGGCACA GGCTCCAGAA TTGCACGTGA TCTCAGACGG TTCCCAGCTT CCTCTGCAGG 660 GCGGGGCTGC TCCAGTCTCT TACACCAGCG CATCTGCAAC TCATTACACA GCGGTGTCGG 720 TGGCAGAGTG GCCTGGCCAC GGCGAGCTCC TGGCGGGAGT CCCCCTCCCC AGCAGCCACC 780 CCGTGCCATG GGCCTCCAGG TCCCCCGGGT GCTGGCCTGG GGACAGCACC ACAGGGCCCA 840 GCCAGGGCTG GGGCAGGGAG GAAGGGCCCC TCCACTAGTG GGCTTTGGCC TCCTCGTGAG 900 GAGCTGGGTG GGGCTGGAGA AATCAGCTCC CGCCAGCCTG ATCTTCCTGC CTCAGAAGCT 960 GAACCCCGGG GACAGTGTTG GTCAGAAAAG CCATAGACTC TCCACGGAAA AGGAAGCCTG 1020 GCACCCCCCA TGTTTCACGT AGGCCACCCT AAGGTCCACA GATGCCTGGG GACAAGGATT 1080 AGTGTGAGCA AAGACACAGG AGTCGGGGAC ACATCCCAGT CGGAACGTGG TGGAAAGGCG 1140 CCAGGCAGGC TGAGTCGGAG ATGTCCCTCA GGCTCCTGCT GGGAGAAGGG GCTGGTGGTT 1200 CCCGGGCCTG CACATCCCCA CCCCTGCCCT GCGTGCCACT CTCAGCCTTT GCCCAGCACC 1260 AGGCTTATTA TCCGATTGGT TAATTGGTTG AGATACGGGT CACCTCCCGT AACAGTCATC 1320 TTTTTAAGGC GTGCAGTTCA GTGGGTTTTC ATCCACACAC TTGCACAGCC ACCACCACAG 1380 CCAGCTTTAG AATTTCGAAG CACTTCCACC AACCCCCCAA AAGAAGCCCC 1430
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