Tag | Content |
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EnhancerAtlas ID | HS184-15250 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr19:13171660-13172610 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
USF2 | MA0526.2 | chr19:13171876-13171892 | GGGAGTCACGTGGCCT | + | 6.38 |
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| Number of super-enhancer constituents: 32 | ID | Coordinate | Tissue/cell |
SE_00024 | chr19:13160708-13176960 | Adipose_Nuclei | SE_01540 | chr19:13160665-13178618 | Aorta | SE_02418 | chr19:13171180-13172515 | Astrocytes | SE_03137 | chr19:13170783-13178623 | Brain_Angular_Gyrus | SE_03859 | chr19:13170623-13178764 | Brain_Anterior_Caudate | SE_04986 | chr19:13170672-13191599 | Brain_Cingulate_Gyrus | SE_05848 | chr19:13160560-13191529 | Brain_Hippocampus_Middle | SE_06678 | chr19:13160758-13191322 | Brain_Hippocampus_Middle_150 | SE_07717 | chr19:13170719-13191634 | Brain_Inferior_Temporal_Lobe | SE_08780 | chr19:13172020-13172142 | Brain_Mid_Frontal_Lobe | SE_08780 | chr19:13172144-13172306 | Brain_Mid_Frontal_Lobe | SE_08780 | chr19:13172464-13173193 | Brain_Mid_Frontal_Lobe | SE_26520 | chr19:13170726-13172925 | Esophagus | SE_29770 | chr19:13170653-13173122 | Fetal_Muscle | SE_31390 | chr19:13170808-13172511 | Gastric | SE_33451 | chr19:13170810-13173012 | H2171 | SE_35947 | chr19:13170773-13172690 | HMEC | SE_40665 | chr19:13170765-13182230 | Left_Ventricle | SE_41557 | chr19:13171785-13172566 | LNCaP | SE_42481 | chr19:13160839-13178550 | Lung | SE_44148 | chr19:13169444-13174963 | NHDF-Ad | SE_44758 | chr19:13170742-13172615 | NHLF | SE_45899 | chr19:13170746-13173452 | Osteoblasts | SE_46667 | chr19:13171802-13172399 | Ovary | SE_47172 | chr19:13160769-13173616 | Panc1 | SE_47634 | chr19:13170755-13172452 | Pancreas | SE_48143 | chr19:13169567-13183512 | Psoas_Muscle | SE_48559 | chr19:13170693-13178599 | Right_Atrium | SE_51076 | chr19:13169565-13183749 | Skeletal_Muscle | SE_54519 | chr19:13170666-13172644 | Stomach_Smooth_Muscle | SE_57153 | chr19:13171180-13172733 | VACO_400 | SE_67980 | chr19:13100968-13183275 | TC32 |
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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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| Number: 1 | ID | Chromosome | Start | End |
GH19I013050 | chr19 | 13161049 | 13173134 |
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Enhancer Sequence | GGCTGCTGCC GCCACTGCAG AGGGCGCTGA TTTTTTTTTT CTTCCTGACT TTTCTCCATT 60 TCTGTCTCTG GTTCCTGATC TCTGACTTTT ATTCTCCATT TTTTCACTTT TTATGGGGAT 120 GGGGTAGAGA TCTTCCTTTT CAAGTGTTTA CCAATTGCAG AGACAAGTCT GCACTGCCAA 180 AAGGTGAGGG CATCCTGGGT GCGTTAGGAA TACTCCGGGA GTCACGTGGC CTTAGACCCC 240 CCCCTCCCCC CCAAATCGAG GGCAGCTCCG TTCTGAAAGA AGCAGGCAGG ATTCAGAGCG 300 GCAGCCACAC AGGGTGGGAC CGGGCTCACT GGATAACCCC CAGTCAAGCT ATGCACCTGG 360 CAGGTCCCCC GCCTTCTATT CGCCCACCCA TTTCGCAGTC CCCTTTCCAT CCGGCCCATG 420 CACCGCAAGC TGTTCCTAAT CAATGCGAAC GGGAAACTCG GCCCTCATAT CACGGGATGT 480 GTTTGGCAGC GACAGCAACA GGAGCCGCTG CCACGGGCAG CTCCTTCCTT GGTGCATAAA 540 CCAGGGTCCC AGTGGCCTGG GCCTGAGTGG GTTCTTCTCC TTCCTCTTGG GACCCCCTGG 600 GTATGCAGAG GGAACCACAT CCCCTGGAGC TCTGGGCCGG TCGCTGGCCG CGCCCCGCCG 660 CAGCCCTCGG AGGGCAGCTA GTGTTAACTC GCTGCGCCAC CTAGCTATGG CGTCCAGGAG 720 TGCAGCGCTT CGCTCCCTGA ACCGCGTCGC TTCCTGAGCC GCGCCGCTCC CTGAGCCGTG 780 CTGCTCGGCA GCCTGGGGAA AACCTCTTTT TGGTCCTTCA GGGAGCTATG AATGAGGAAT 840 TTGGCAGCTG TCAGTCGGAG GATCAGTGTC ACTTTGTTCC TTCAGCAGCC TTTGCTGTCC 900 TTATGCAAGC TTGGTACTTT ATAGTATATA AAACTCAAAG TTAAAATATG 950
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