Tag | Content |
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EnhancerAtlas ID | HS184-10388 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr14:77421850-77423470 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MAFF | MA0495.3 | chr14:77423113-77423128 | CTGCTGACTCAGCAC | + | 7.55 | MAFF | MA0495.3 | chr14:77423113-77423128 | CTGCTGACTCAGCAC | - | 7.61 | MAFG | MA0659.1 | chr14:77423110-77423131 | CCGCTGCTGACTCAGCACTTC | + | 6.16 | MAFG | MA0659.1 | chr14:77423110-77423131 | CCGCTGCTGACTCAGCACTTC | - | 6.47 | MAFK | MA0496.2 | chr14:77423111-77423130 | CGCTGCTGACTCAGCACTT | + | 6.78 | MAFK | MA0496.2 | chr14:77423111-77423130 | CGCTGCTGACTCAGCACTT | - | 7.17 | ZNF263 | MA0528.1 | chr14:77422786-77422807 | ACCCCCTCCTCTTGCTCCCCT | - | 6.14 |
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| Number of super-enhancer constituents: 28 | ID | Coordinate | Tissue/cell |
SE_01254 | chr14:77420883-77424353 | Adrenal_Gland | SE_08284 | chr14:77420765-77424468 | Brain_Inferior_Temporal_Lobe | SE_24529 | chr14:77421777-77422089 | Colon_Crypt_2 | SE_24529 | chr14:77422128-77423800 | Colon_Crypt_2 | SE_27091 | chr14:77419455-77426235 | Esophagus | SE_29618 | chr14:77420671-77424362 | Fetal_Muscle | SE_31928 | chr14:77421729-77426154 | Gastric | SE_32994 | chr14:77421752-77424066 | H1 | SE_33446 | chr14:77420480-77424488 | H2171 | SE_34422 | chr14:77418557-77429646 | HCT-116 | SE_34742 | chr14:77415823-77429622 | HeLa | SE_37233 | chr14:77415973-77429404 | HSMMtube | SE_38430 | chr14:77419198-77429214 | HUVEC | SE_41258 | chr14:77419224-77429300 | Left_Ventricle | SE_41987 | chr14:77421767-77424998 | LNCaP | SE_42676 | chr14:77420714-77426260 | Lung | SE_44184 | chr14:77419413-77424284 | NHDF-Ad | SE_46080 | chr14:77419415-77424550 | Osteoblasts | SE_46723 | chr14:77422105-77423789 | Ovary | SE_47949 | chr14:77422035-77423590 | Pancreas | SE_48706 | chr14:77421709-77426250 | Right_Atrium | SE_49653 | chr14:77421766-77424358 | Right_Ventricle | SE_50880 | chr14:77420706-77424364 | Sigmoid_Colon | SE_53991 | chr14:77419420-77424483 | Spleen | SE_55769 | chr14:77419401-77424613 | u87 | SE_65382 | chr14:77419164-77426315 | Pancreatic_islets | SE_67544 | chr14:77419401-77424613 | u87 | SE_68739 | chr14:77421020-77425262 | H9 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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Enhancer Sequence | TATCCATAGA TCCTGCACAG GAACACCCCC ACGCAGGCCC TGGCCCTCTC CTTGTTATGT 60 GTCCCTGAGG CTGTCCTCCC AGGACTTGGT TCACTTTCAG GTCTGCCACC CATTGGTGCA 120 TTCATTTCTG TATTTAATGT TACTGAGCAC CAACTATGTC CCACACACTC TTCCAGGTAC 180 TGGGGATACA GCAGAGCCAA ACAAAACCGA GAAAGTCTCT GCCCTCAAGC TTTTATTGAA 240 GGAGGGAAAT AGACAAAAGA GAAGCAAACA AACAAAAAAG GTAAAATCAG AGGGTGGTAA 300 AAGCTATGAA GGAAATAAAG CAGTATAACT GCTTAAGGAG CAGGGACCTC TGCAGGTGGA 360 TGGCAAGGGA AGGTCTCTCT GCAGAGACGA CATTGACATT CATGCTGAGA CCTGGGCCAG 420 CCATGCAAAG AAGGGGGGTG TAGGCAGAAG TGCCGCAGTG GGAACAGGCT AGAAGTTGGG 480 CCTGGTGCTG GGACAGTCCC AGTTCAGGCA TGTCCTCCTG GTGTCGTTTT TAATAGCTCA 540 TCCTTTCACA ATCAAGAGTG GCTCATGCCG GAGATGAGTT ACCCGCAATG AGGGGCTGGA 600 TTTATTCTAA GGGCAGAGGG AAGCCATCAC AGGAAATGAT GTGATTGATG TTTTGAAAAG 660 AACTCGCTGG CTGTTCCGTG AAGAATAAAT TAGAGGGGCA GGAGGGAAGA AGTCTGCCTG 720 GGGCGGCTGC AGCAACCCAG GCGTGCTGCG AGGTGCCCTT TGACTAGATT CCAGTGGGGG 780 CTTTCGGGCG AGCAGAAGAA CCCCAGGGAT CAGCTCTAGC CACGCTCAGC TCCCTGGGCC 840 GGCCCTGGGC ATTTCTGAGA CGGCCCTCGC GCTCAGGGAC CTCTCCTCGC AGTTCCATTG 900 TCTGTTCTTG CGGAGTCCTG CCACACTGGG AGGGCCACCC CCTCCTCTTG CTCCCCTCCC 960 CTCCCCGGGT CCAGCCCCTC CCCTGCCTGG CCCGGCTGCC GCCCAGCGCC AGCCAGAGCC 1020 CACCCCGCCT CCCTGCAGGA AGCCGGCTGG CGGCGCCTGC TGCGTGACCT TGGGCTGCAA 1080 AGTCGGGCGT TTGCAAAGTC AAAGCGAGTC ACTTCCTCCC CCAGGCCTCC CCCGAGCGGG 1140 CAGCCGGCCG CCGCTCCCTG CCCCCTCGCC CGCCGCGGGC CGGGGCTGGC GCTGGCACGA 1200 ACGCGCTCTG CATGCTAAGT GCTCGCGCCC GTTCCCGCCG CCCGGAGGCT CATTTGTCAC 1260 CCGCTGCTGA CTCAGCACTT CTGCAGAAGG CTTTTCCCTC CGCTTTGGAG GAGGAGGCCC 1320 GGAAATGAGG CAGAGGCTCT TCCTTCCCTT CCCTCCAGCA GGGGTGTGTG GCGTGGGTGT 1380 GTGCGGGTGT GGCAGGGTCT GTCTGTATGT CTGATGCCTG TCCATCACCG GTGTATATTT 1440 TCGCGGCTGT GTCTGTCTTT TGTGTATGGC TGAGTCTGTG TATGTGTCTT AGTGCATGTT 1500 GATCCCTGCG CCTGTCTGGT GGGTCTTTGT CCCTGTCTGT GGGCATCTGT GTTGGCCTGT 1560 GGGCCTGTCA TGTGTGTGTC ATACGTGTGT CTGGGTGAGT GTGTGTGTGT CCCCCCCACC 1620
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