Tag | Content |
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EnhancerAtlas ID | HS187-12125 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr19:18617180-18619080 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HSF1 | MA0486.2 | chr19:18618282-18618295 | GAAAGTTCTGGAA | - | 6.29 | RARA(var.2) | MA0730.1 | chr19:18618822-18618839 | AGGTCACATACAGGTCA | + | 7.01 |
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| Number of super-enhancer constituents: 28 | 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_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: 2 | Chromosome | Start | End |
chr19 | 18617449 | 18618539 | chr19 | 18618400 | 18618511 |
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| Number: 1 | ID | Chromosome | Start | End |
GH19I018498 | chr19 | 18609234 | 18621009 |
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Enhancer Sequence | CCCTCTCCCC CAGGGGGAAA GGGATCCAAA GCTCCTGTGC CTCTGGGGTG CAGCATCAGC 60 CCAGACTTCT GCTCGGCTGG GTGCCATGGC TCACGCCTGT AAGCCCAGCA CATTGGGAGG 120 CCAAGGCAGG AAGTTCGTTT GAGGTCAGGG GTTTGAGACC AGGCTGAGCA ACACAGGGAG 180 ACTCTGTCTC CATATAAATA AAAAATTAGC CAGGTGTGGT GCCACGCACT TGTAGTCCCA 240 GCTATTTGGG AGGCTGAGGT AGGAGGATCA CTTGAGCCCG GGAGCCAAGG CTGCAGTGAG 300 CTATGATCAC ACCACTGCAC CCCAGCCTGG ATGACAGAGC AAGACCTCGT CTGAAAAAAC 360 AAAAGCAGAC TTCCGTTCAA CAGCATGTGA ACCTCACCTT GCACACCTAG GAGTTCGTTA 420 CCCTCCTCAG CTCAGAGATT AGAGGGAACT CTCCCCACAG AGATGCTATG ATCAGAGGGC 480 CAGGGACCCT GTCTCATTGA TCCTACGCTC TACGCCAGAC ATCGCCTCAG AATCCTTCTC 540 AACACGGCTC CACTTCCTAT CTACAAGGAG CTGGCCTACA AGATGGAAGC GATTCCTACA 600 TTATGGGGTC ATGTGGCTCC AGGCACATGG CCCTCGACCA GTGGGAGCCT GTGCACAGGT 660 AAGAGAGCCA GGGCAGCCTG GAGATGAGCT GGACACAGGC TGCCAGCACT GGCTGTCCCC 720 TCCCACTTGC CAAATCCAGT GTGAGCTGAG CACATTTCAC TGGAACAAGC AGGCGTCTGA 780 GAGCATCCAA CTCCAAAAAT AGTGCCACCA GGAGAGGAAG GAACACGCTC TTCTAGCTGC 840 ACCCGCTCCC TGCCCTCAGA TACCTCCCTG CACAGTCTGT GCCTGGCCTG TGGCAGTTCA 900 AGGGTCACAC CCAACTCTGA AAAGGGAGAG ATAACATCCC CAGATAAGAA GAGTGAAAAC 960 AGGCCAAGTC TGCTGCCAGA GCCTGGCCAC AGACCCACAG CCCCTTGGCA GAGAACTGCT 1020 CAGGAAGTCC TCCTCTGAGT CTTTCAAGCC ACTGGTATCT AACAAAGAAT CTAATCTGCA 1080 CACGGCACTT GCCCCGAGCT AAGAAAGTTC TGGAAGGGTC TCCTAGGTCT CCCCAGCCCA 1140 AGGTGAGCTT GCTTCTGTGG AGGGAGATGC CTGCCTGCCC ATGTCCACCA CCACTGCACA 1200 CCAAGCCAGT CTGAAGCCAC CATGATCTGG CTGTTGCTGG TTTATGGTGC ACCTCCCCGC 1260 TGCGAAGAAG TGGGCCATGT GAGCGCAGGG GCTTCATCCC TCCTGCTTCT TACTGGAGAA 1320 ACACTCCTGG AGGCAGCCGA ACCCTCACTG GGTGCAATCC CTCTGTGTAG GAGATTGCAC 1380 TGTGTAGGTT GTGCCCCGCC GAACAACCAC GCAGCTGAGG CTCAGCTCAG AGACTGCATT 1440 CAGAGCCCAA CTAGAATCAG ACACAGGTTC TGCGGGCCCC ACTACCCATC TGGAGGCAGA 1500 CGCCTGACCC CCAGCTCCAT CCCCAGAGAT GAGGATGCAG CAGGCTGAGG CTGACTCCAT 1560 GCGGCAGCTG CTCCCAACTC CACAAGGGAC ACACAAGCCA GCCCTTCCCA TCCAGGCTGC 1620 ACATGACTGT GTTTTGTTTC AAAGGTCACA TACAGGTCAC AAATAAAGAG GCCGGTTCCC 1680 ACTGGAGGCT ATGTCAGGAT TGATGCAGTC CCTGAGAAAA ACTCCCGGAA AACCCAGGGA 1740 CTCCCATGCG GGCTGAGAAA CATTTTGAGT TTGCATGAGA TCAAAATAGG AGTCACAGCT 1800 GAGTGTGGTG GCTCACGCCT ATAGCACTTT GGGAGGCCAA GGCGGGAGGA TCACTTGAGG 1860 CCAGGAGTTA ACAGACTGCA GTGAGCTATG ATCACACCAC 1900
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