Tag | Content |
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EnhancerAtlas ID | HS195-03389 |
Organism | Homo sapiens |
Tissue/cell | VCaP |
Coordinate | chr19:39196910-39198750 |
Target genes | |
| Number of super-enhancer constituents: 41 | ID | Coordinate | Tissue/cell |
SE_00117 | chr19:39197743-39199485 | Adipose_Nuclei | SE_00865 | chr19:39197223-39205990 | Adrenal_Gland | SE_01543 | chr19:39194086-39205969 | Aorta | SE_03166 | chr19:39196433-39197174 | Brain_Angular_Gyrus | SE_03166 | chr19:39197894-39199452 | Brain_Angular_Gyrus | SE_03903 | chr19:39197211-39205540 | Brain_Anterior_Caudate | SE_04868 | chr19:39195321-39206058 | Brain_Cingulate_Gyrus | SE_05805 | chr19:39182078-39206004 | Brain_Hippocampus_Middle | SE_06803 | chr19:39195820-39205439 | Brain_Hippocampus_Middle_150 | SE_07777 | chr19:39194039-39206085 | Brain_Inferior_Temporal_Lobe | SE_08790 | chr19:39197897-39198156 | Brain_Mid_Frontal_Lobe | SE_08790 | chr19:39198408-39199265 | Brain_Mid_Frontal_Lobe | SE_09404 | chr19:39197597-39198685 | CD14 | SE_23062 | chr19:39197311-39199581 | Colon_Crypt_1 | SE_23732 | chr19:39197344-39197714 | Colon_Crypt_2 | SE_23732 | chr19:39198450-39198762 | Colon_Crypt_2 | SE_24739 | chr19:39197294-39197869 | Colon_Crypt_3 | SE_26525 | chr19:39194058-39205949 | Esophagus | SE_27614 | chr19:39180632-39201469 | Fetal_Intestine | SE_28533 | chr19:39164445-39201888 | Fetal_Intestine_Large | SE_29583 | chr19:39197343-39198677 | Fetal_Muscle | SE_31384 | chr19:39194037-39199678 | Gastric | SE_34299 | chr19:39197188-39198541 | HCT-116 | SE_38012 | chr19:39197217-39199928 | HUVEC | SE_40594 | chr19:39194015-39206697 | Left_Ventricle | SE_41601 | chr19:39197275-39199500 | LNCaP | SE_42097 | chr19:39194095-39205995 | Lung | SE_44161 | chr19:39197660-39199486 | NHDF-Ad | SE_45660 | chr19:39196090-39205729 | Osteoblasts | SE_47114 | chr19:39164477-39226374 | Panc1 | SE_47461 | chr19:39197437-39197841 | Pancreas | SE_48555 | chr19:39195085-39205958 | Right_Atrium | SE_49449 | chr19:39197429-39198476 | Right_Ventricle | SE_50056 | chr19:39194910-39205530 | Sigmoid_Colon | SE_51136 | chr19:39195385-39206359 | Skeletal_Muscle | SE_52339 | chr19:39194079-39204831 | Small_Intestine | SE_53291 | chr19:39194893-39205783 | Spleen | SE_54534 | chr19:39196075-39206175 | Stomach_Smooth_Muscle | SE_56725 | chr19:39197411-39199669 | VACO_400 | SE_65266 | chr19:39195019-39197876 | Pancreatic_islets | SE_65266 | chr19:39197900-39206193 | Pancreatic_islets |
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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 |
GH19I038673 | chr19 | 39164536 | 39206516 |
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Enhancer Sequence | CAAGCCCATG GGAAGGTCAC CTGGTCCTCT CTGAGGAAGA GGAGGCAGTT TCCCAGCCAT 60 CCTGGCTGAA GGCAGTAAGG TCAGCCCTCT CGCCGGCCTA ATAGAACGTT CTTCGTCCCC 120 AGGCAAGGTG ACTCTCAGAA GCAACAATAA AGCTTTTCAT TTTTGAGACA GGGTCTTGTG 180 CTGTCACCCA GACTGGAGGG CAGTGGTGTG ATCACTCATC CCTGCTGCCT TGGCCTAGGC 240 TCAAGTGATC CTCCTGTCTC AGCCTCCCAA GTAGCTGGGA CTGCAGGTGC ATGCAGCCAC 300 ACCTGGCTAA TTTTTAATTT TTATTTTTAG TAGGAACAGG GTCTCCCTAT GTTGCCCAGG 360 CTGGACTTGA ACTCCTGAGC TCAAGCAGTC CTCCTACCCC GGCCTCCCAA AGTGCTGGGA 420 CTACAGATGT GAGCCACTGC CTGCCTCTGG CCTCTTCCTT TATTTTGACA GCTCAGGAGT 480 GAATTGTTTT TAGAATTGCT AGTAAATTTA GTGTTGGGGA AAAATGTACT CTGTGGCTGC 540 TAAGATGAAC AAGCCTCAGC TCCACCATGA ACCTGCTTCC CTCAGGGTGA GCGGGAGATG 600 AGACATGTCC ACCATCCCCG TAGCTGAGGC GAGCATGGGC ACTGCCGCAT GAGGTCCAGG 660 GGGCGGCAAG AGGCAGGCCT GCCTGGTGGT TGGGAGCACT GGCTCTGGGG GCGGTCCTGA 720 GGTCAGATCC GGTTTGCCTT GTGGCTCCAC CCTCTGAGTC TCCTGGATGG CCCGCACAGG 780 AATGAAGAGC AGGGCCTCAT GGGGTTTGCA GCGGCCTCAG GCTCTCTGGG ACCCTTGCTG 840 GGTACAGAGG GCTTTTCCCA TCGTGCTCAC CCTGATAGCA TGTGGTCCCT CCCTTGGTCA 900 CTCTTCTCTG TGTGTCTTCT TTTTTTTCCT GCCACTAACT GACTGAATCT TTCTATAGTT 960 TCCATTCATT TTCTTCAACT AGTAAGTATC TAGCATGCCC GCTGCATGCC GTTAGTGGAG 1020 ATACAGTGGC ACCCAAACAA AGTTCCCATT TGTGGGAAGT TTACACCACA GCGCGGGGAC 1080 CAGCTGTTAG CACAGCGGCC AGTAATCCTG CAGCATAACT TCAGTGAGAA GTGCTGCACA 1140 AAGACAGGGA AGTCAGATGA AGAAAGTTCC CTGGGTGGCC TTTCTGAGGA GGTGACATCG 1200 AGCTTGACCT CAGAGGGAAC CAACCCTTAG AGGGTCTCAG GGAGGAGAAT GTGACCCATA 1260 TAGCTTGTAA CTGACCAACT TGTGGCCTTG GGGAAGGTCT CTTTCCTCCA GAGACCAGCA 1320 TGCCAAGTGA AATCCTGGCA TTTAGCCAGC CCACGGACTG GCCTTCCTGT AAGTCAGGTC 1380 CGCCAGGGTG TGGAGGCCAC ACAGCACAAA CACCAGCATC CTGCAGTGGC CACCTCCCCC 1440 GAAGCGGCCT GTCTGGTTCA GGGCGGCCTC CCATGGAAGG TGCTAGCAGT TATAAAGCAG 1500 TTGTCAGGAG TCAGGCACTG ATCCAAGCAT TTACTCATTT AATCCGCACA ACAGCCCTAT 1560 GTAGCAGGTA TGTCACTATC CCCATCATAC AGATGTGGAA ACCGAGATAG CCTGGCTTAC 1620 CCGAGGTCAC ACTGTCAGTA GGCAGAAGAG TCAGGATTTG ATCACAGACT GCCTGGCCCC 1680 AGAGGTCATG CTTGCAGCCT CTCTGCCACA CTGTCTCCAT GCAGTGCCTG GCACAGGCCA 1740 GACTGCAGTG AATGGGAATT AGTCACTGCT GTGGGTGCAC AGGGCCATAC GGCACTCTCA 1800 TGACAGTGAG CGGGCCCTCC TATAACCTTT GCCTTTCCTT 1840
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