Tag | Content |
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EnhancerAtlas ID | HS098-27239 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr19:13142890-13143900 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr19:13142943-13142964 | GGGGGAGGGGGGCAGGAGAGA | + | 6.06 |
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| Number of super-enhancer constituents: 30 | ID | Coordinate | Tissue/cell |
SE_00024 | chr19:13106663-13152679 | Adipose_Nuclei | SE_01540 | chr19:13140196-13146524 | Aorta | SE_02418 | chr19:13142237-13143956 | Astrocytes | SE_03137 | chr19:13134766-13146400 | Brain_Angular_Gyrus | SE_03859 | chr19:13122647-13152397 | Brain_Anterior_Caudate | SE_04900 | chr19:13122231-13152649 | Brain_Cingulate_Gyrus | SE_05829 | chr19:13106701-13152645 | Brain_Hippocampus_Middle | SE_06678 | chr19:13122257-13152530 | Brain_Hippocampus_Middle_150 | SE_07717 | chr19:13121683-13152553 | Brain_Inferior_Temporal_Lobe | SE_08780 | chr19:13142973-13144514 | Brain_Mid_Frontal_Lobe | SE_24497 | chr19:13142992-13145426 | Colon_Crypt_2 | SE_26006 | chr19:13142028-13145849 | Duodenum_Smooth_Muscle | SE_26520 | chr19:13115825-13152105 | Esophagus | SE_29659 | chr19:13142187-13143908 | Fetal_Muscle | SE_31390 | chr19:13141688-13146220 | Gastric | SE_35947 | chr19:13141902-13144015 | HMEC | SE_40665 | chr19:13140190-13152144 | Left_Ventricle | SE_41557 | chr19:13140222-13146413 | LNCaP | SE_44148 | chr19:13123027-13144064 | NHDF-Ad | SE_44758 | chr19:13141881-13143957 | NHLF | SE_45899 | chr19:13141968-13150175 | Osteoblasts | SE_47172 | chr19:13141819-13143830 | Panc1 | SE_47634 | chr19:13141985-13143067 | Pancreas | SE_48559 | chr19:13141566-13146405 | Right_Atrium | SE_50434 | chr19:13141876-13146412 | Sigmoid_Colon | SE_51076 | chr19:13106668-13152566 | Skeletal_Muscle | SE_53207 | chr19:13142270-13146403 | Small_Intestine | SE_54519 | chr19:13141589-13143929 | Stomach_Smooth_Muscle | SE_64579 | chr19:13142213-13148771 | NHEK | 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 |
GH19I013030 | chr19 | 13141136 | 13149343 |
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Enhancer Sequence | TGCTCGCACA AAAGGCCTCT TTGATTTCTT GTTTGTTTTC ATTTGCCAGT GGAGGGGGAG 60 GGGGGCAGGA GAGAAAGAGC TTCTGGGTTT TAAAATTTTT ATTTGGGTTG CTTCATTCTC 120 AGAGGAGTTG GCTCCCTGGA ACTCCTTTCT GAGTTGGGGG CTCAGAGTTG AACGGCAGCC 180 TTCTGAAGAG AGGGCTAGTG TAGGAGTGGA GGGTTGGGTG GAGCTCCCAG GGTGACAGGA 240 GGAGGTGTAG GGGTTTAAAT ATAGTTATTG ATTCATCCTA CAAACACTTT GGGCAGATCT 300 TATGTGCTAG GCCTAAGGGC AGCCCTGCCT GTTGGGTAGA GGAAAGGTCT GAGGTGTCTG 360 GCACATGACA TTCCCCTGTG TGTTGCATCG TTCGAGGACT CCTCACAGCT GTGGATTTGC 420 ACAGTTGTGA ACTTTGACTT TGTTATTTTT CCTTTTTTGT CCCAGATTCC GCCTTTGAAG 480 GGATTCTACT AGCATACACA CTTCTTGGAG ACTCAGTACT TCAGAATACA GGTTGGGGCT 540 TCCCACCCTA AATCAGAGAA TGAGGGAGAG GGAGTGAGAG GTTTATAGAG CAGCTAGGTG 600 TCTTCCTGGG AATGGTGTGC AGAGGACCTG GGCCCACAGC TTGTTTTGGA CTTTGAGGGC 660 AGGTCAGTGC TGCTGAGACC TTGGTGAGTA GGGAGTTGAG GCCAAAAAGA AATGGAAGGC 720 CATGTTTGTC CAAGGTTTCG AACAAGAGAC ACCCAAACCA GTGCCTGTTG GGGTGCGTAC 780 CTTAACACAT GTGGGCACGT CCCTATATCC CAGTAAGAAG AGGTGCAGCC TGCTGGTTTA 840 CATGCCTGTA TGGAGGCCTA ATTGTCAGGG CTTGGGAAGA GAGTGCCACA GACCGAGACT 900 CAGGCAGGTG GTCACGGGCA TCAGCAACAG GGAAGTGTGC CCATTGGGTG AGGGGGGGCT 960 CACAGGGCCT GGTTGGCAGA CGGGAGGAGG AGGCTGGGGG GCTGAGAGAT 1010
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