Tag | Content |
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EnhancerAtlas ID | HS155-14618 |
Organism | Homo sapiens |
Tissue/cell | Ovary |
Coordinate | chr9:137257030-137258970 |
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: 2 | Chromosome | Start | End |
chr9 | 137257428 | 137257617 | chr9 | 137257724 | 137257990 |
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| Number: 1 | ID | Chromosome | Start | End |
GH09I134363 | chr9 | 137255386 | 137260783 |
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Enhancer Sequence | AAGCCCCTCG TGGGCCATCT CCCGGAGTTC TCTTGAGGGC CCCTGTCTTA CGGATGAGGA 60 GATAGAGGTT GAGGATCACA GCCCCAGCCT GCAGGCGCTC GAGCTGAAAG CCCTCGCCCC 120 TCGTGGTGGG GCAGCGCGTC CCTGGGTGAG TGACCAGGCG GCCTTGGGTC TCTGGTGAGC 180 TCAGGGAGCG GGGTCCACGT TGCCTGGCCC AGGTGGGATT TGGCGGGTAA CGCTCGTGGT 240 GTGTCCTGGT GTGAGACCCG GTGTTCTTGG CTGATGTGTG GGTTTGCTCA TGGGGTGGAC 300 CAGGCCGCTG CCCCTGCCTC CTGTCTCTGG CTGTGGCCAT GGCTGTGTGG ACCAGGCTGG 360 GGCTGCACTG GGGCCTGGGT GGTAGGGGGT GATCTGCTTG TCCAGTGGTT TCTGTGGCTT 420 TTCTGGGGTC CTGGGCTGTC CCTCAGCAGG CCTGGGACTG GGCGGGGACA GTGGGGATGA 480 GTTTCAGGTC TGTTCTTGGT GGCTGTTAAC TCTAGGCCAG ATGTAGCCCT GAGGGGCCCG 540 GCAGAGTCTC GGTGGGTCTC GGTGGGGCCA GCTGTCGGTG GGTGAGGTGC CCCAGGGGAA 600 GGGAGGGCCA GCCCAGAAGG ACCCTCCCAT TACCCTCTGG TGGCTTGCCC ATGCCACCAT 660 TCCTACTGCT AGGCTCAGGC CTGTCTTGGG GAGGGTTCCT GGGCTGGGAT TGGCCGTCGG 720 GGAGGTGCAC ACAGACGCTC AGCACAGTTG TGGCTGCCTC CAGTCAGGCG TCCGCTGAGC 780 GACCCCTAGG AGCCGCCTGT CTTTGCAGGA GCCGCGGGGA TCATCTGGCG GCTGCCTCCA 840 CCCCTGCCTC CACCCCTCCC TTTTTGGGAG GTGGGGCTTG GCATCTTCAG CATCTCTCGT 900 GCCTCAGTAA CAACCTGGGA GCGGTGCTGT CCCTGGGTAC AGATGAGAAG CCAAGGCTCA 960 GAGGCACCAG GGCCCCAGTG GGAGGCGGCA GAGCCTCTGG TGGCTCCGTG TGGCATGTTC 1020 TGGGCTGTGT GTGGGGCCAG GGAGGGTGTC TTCAGCACAG GTGCCCGCTG GGTGGTCTCC 1080 CATGTGTGCC CAGGAGGAGT GCCACAGCCT CTCCCTCTGC CCACCCCCCC CATGCCTGCC 1140 CTGCCAGCAG GTCCAGCAGG CCTTGGCACA GGCTCCAGAA TTGCACGTGA TCTCAGACGG 1200 TTCCCAGCTT CCTCTGCAGG GCGGGGCTGC TCCAGTCTCT TACACCAGCG CATCTGCAAC 1260 TCATTACACA GCGGTGTCGG TGGCAGAGTG GCCTGGCCAC GGCGAGCTCC TGGCGGGAGT 1320 CCCCCTCCCC AGCAGCCACC CCGTGCCATG GGCCTCCAGG TCCCCCGGGT GCTGGCCTGG 1380 GGACAGCACC ACAGGGCCCA GCCAGGGCTG GGGCAGGGAG GAAGGGCCCC TCCACTAGTG 1440 GGCTTTGGCC TCCTCGTGAG GAGCTGGGTG GGGCTGGAGA AATCAGCTCC CGCCAGCCTG 1500 ATCTTCCTGC CTCAGAAGCT GAACCCCGGG GACAGTGTTG GTCAGAAAAG CCATAGACTC 1560 TCCACGGAAA AGGAAGCCTG GCACCCCCCA TGTTTCACGT AGGCCACCCT AAGGTCCACA 1620 GATGCCTGGG GACAAGGATT AGTGTGAGCA AAGACACAGG AGTCGGGGAC ACATCCCAGT 1680 CGGAACGTGG TGGAAAGGCG CCAGGCAGGC TGAGTCGGAG ATGTCCCTCA GGCTCCTGCT 1740 GGGAGAAGGG GCTGGTGGTT CCCGGGCCTG CACATCCCCA CCCCTGCCCT GCGTGCCACT 1800 CTCAGCCTTT GCCCAGCACC AGGCTTATTA TCCGATTGGT TAATTGGTTG AGATACGGGT 1860 CACCTCCCGT AACAGTCATC TTTTTAAGGC GTGCAGTTCA GTGGGTTTTC ATCCACACAC 1920 TTGCACAGCC ACCACCACAG 1940
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