Tag | Content |
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EnhancerAtlas ID | HS119-00350 |
Organism | Homo sapiens |
Tissue/cell | LNCaP-1F5 |
Coordinate | chr19:18617490-18618630 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HSF1 | MA0486.2 | chr19:18618282-18618295 | GAAAGTTCTGGAA | - | 6.29 |
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| Number of super-enhancer constituents: 29 | ID | Coordinate | Tissue/cell |
SE_01013 | chr19:18616790-18618942 | Adrenal_Gland | SE_04099 | chr19:18612612-18621162 | Brain_Anterior_Caudate | SE_06012 | chr19:18609083-18619184 | Brain_Hippocampus_Middle | SE_08139 | chr19:18611825-18620707 | Brain_Inferior_Temporal_Lobe | SE_08861 | chr19:18618070-18618386 | Brain_Mid_Frontal_Lobe | SE_08861 | chr19:18618502-18618688 | Brain_Mid_Frontal_Lobe | SE_12155 | chr19:18614992-18619095 | CD3 | SE_15037 | chr19:18615264-18618963 | CD4_Memory_Primary_7pool | SE_17983 | chr19:18613350-18619260 | CD4p_CD25-_CD45ROp_Memory | SE_19379 | chr19:18612797-18619131 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20439 | chr19:18615273-18618899 | CD56 | SE_21047 | chr19:18616059-18618949 | CD8_Memory_7pool | SE_22689 | chr19:18615399-18619616 | CD8_primiary | SE_23216 | chr19:18612701-18620963 | Colon_Crypt_1 | SE_23893 | chr19:18617508-18618912 | Colon_Crypt_2 | SE_26932 | chr19:18616253-18618743 | Esophagus | SE_30600 | chr19:18617865-18619920 | Fetal_Muscle | SE_31681 | chr19:18616275-18619182 | Gastric | SE_41123 | chr19:18609803-18620443 | Left_Ventricle | SE_41560 | chr19:18615472-18620976 | LNCaP | SE_42344 | chr19:18610919-18620435 | Lung | SE_46271 | chr19:18617926-18619177 | Osteoblasts | SE_47511 | chr19:18617763-18618281 | Pancreas | SE_48120 | chr19:18610995-18621599 | Psoas_Muscle | SE_48694 | chr19:18610987-18621062 | Right_Atrium | SE_50125 | chr19:18610975-18620517 | Sigmoid_Colon | SE_51145 | chr19:18609758-18621004 | Skeletal_Muscle | SE_52434 | chr19:18610979-18621003 | Small_Intestine | SE_53541 | chr19:18617401-18619093 | Spleen |
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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 |
GH19I018498 | chr19 | 18609234 | 18621009 |
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Enhancer Sequence | ACCACTGCAC CCCAGCCTGG ATGACAGAGC AAGACCTCGT CTGAAAAAAC AAAAGCAGAC 60 TTCCGTTCAA CAGCATGTGA ACCTCACCTT GCACACCTAG GAGTTCGTTA CCCTCCTCAG 120 CTCAGAGATT AGAGGGAACT CTCCCCACAG AGATGCTATG ATCAGAGGGC CAGGGACCCT 180 GTCTCATTGA TCCTACGCTC TACGCCAGAC ATCGCCTCAG AATCCTTCTC AACACGGCTC 240 CACTTCCTAT CTACAAGGAG CTGGCCTACA AGATGGAAGC GATTCCTACA TTATGGGGTC 300 ATGTGGCTCC AGGCACATGG CCCTCGACCA GTGGGAGCCT GTGCACAGGT AAGAGAGCCA 360 GGGCAGCCTG GAGATGAGCT GGACACAGGC TGCCAGCACT GGCTGTCCCC TCCCACTTGC 420 CAAATCCAGT GTGAGCTGAG CACATTTCAC TGGAACAAGC AGGCGTCTGA GAGCATCCAA 480 CTCCAAAAAT AGTGCCACCA GGAGAGGAAG GAACACGCTC TTCTAGCTGC ACCCGCTCCC 540 TGCCCTCAGA TACCTCCCTG CACAGTCTGT GCCTGGCCTG TGGCAGTTCA AGGGTCACAC 600 CCAACTCTGA AAAGGGAGAG ATAACATCCC CAGATAAGAA GAGTGAAAAC AGGCCAAGTC 660 TGCTGCCAGA GCCTGGCCAC AGACCCACAG CCCCTTGGCA GAGAACTGCT CAGGAAGTCC 720 TCCTCTGAGT CTTTCAAGCC ACTGGTATCT AACAAAGAAT CTAATCTGCA CACGGCACTT 780 GCCCCGAGCT AAGAAAGTTC TGGAAGGGTC TCCTAGGTCT CCCCAGCCCA AGGTGAGCTT 840 GCTTCTGTGG AGGGAGATGC CTGCCTGCCC ATGTCCACCA CCACTGCACA CCAAGCCAGT 900 CTGAAGCCAC CATGATCTGG CTGTTGCTGG TTTATGGTGC ACCTCCCCGC TGCGAAGAAG 960 TGGGCCATGT GAGCGCAGGG GCTTCATCCC TCCTGCTTCT TACTGGAGAA ACACTCCTGG 1020 AGGCAGCCGA ACCCTCACTG GGTGCAATCC CTCTGTGTAG GAGATTGCAC TGTGTAGGTT 1080 GTGCCCCGCC GAACAACCAC GCAGCTGAGG CTCAGCTCAG AGACTGCATT CAGAGCCCAA 1140
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