Tag | Content |
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EnhancerAtlas ID | HS012-16963 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr2:219151070-219152960 |
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) |
EWSR1-FLI1 | MA0149.1 | chr2:219151503-219151521 | GGAGGGAGGGATGGAAAG | + | 6.31 | SP2 | MA0516.2 | chr2:219152026-219152043 | CCCAGCCCCGCCCACTC | + | 7.11 | SP4 | MA0685.1 | chr2:219152027-219152044 | CCAGCCCCGCCCACTCT | + | 6.41 |
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| Number of super-enhancer constituents: 39 | ID | Coordinate | Tissue/cell |
SE_00326 | chr2:219145665-219158265 | Adipose_Nuclei | SE_03432 | chr2:219149789-219152314 | Brain_Angular_Gyrus | SE_03432 | chr2:219152339-219152890 | Brain_Angular_Gyrus | SE_06270 | chr2:219145735-219164206 | Brain_Hippocampus_Middle | SE_08985 | chr2:219151033-219151582 | Brain_Mid_Frontal_Lobe | SE_08985 | chr2:219151601-219152174 | Brain_Mid_Frontal_Lobe | SE_08985 | chr2:219152421-219152794 | Brain_Mid_Frontal_Lobe | SE_10092 | chr2:219146718-219159598 | CD14 | SE_11206 | chr2:219145902-219159097 | CD20 | SE_12180 | chr2:219148529-219157314 | CD3 | SE_14014 | chr2:219148910-219157816 | CD34_Primary_RO01536 | SE_15197 | chr2:219146865-219158111 | CD4_Memory_Primary_7pool | SE_16725 | chr2:219148483-219152907 | CD4_Naive_Primary_8pool | SE_17020 | chr2:219147008-219153025 | CD4p_CD225int_CD127p_Tmem | SE_17694 | chr2:219145927-219158488 | CD4p_CD25-_CD45RAp_Naive | SE_17933 | chr2:219145740-219158304 | CD4p_CD25-_CD45ROp_Memory | SE_18906 | chr2:219145938-219158335 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19423 | chr2:219148822-219157978 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20197 | chr2:219147855-219154246 | CD56 | SE_21204 | chr2:219148412-219158157 | CD8_Memory_7pool | SE_22529 | chr2:219146601-219158435 | CD8_primiary | SE_26022 | chr2:219146503-219160474 | Duodenum_Smooth_Muscle | SE_26969 | chr2:219146053-219152975 | Esophagus | SE_27658 | chr2:219148708-219161413 | Fetal_Intestine | SE_28578 | chr2:219146925-219161400 | Fetal_Intestine_Large | SE_30125 | chr2:219148759-219153194 | Fetal_Muscle | SE_32144 | chr2:219145915-219152965 | Gastric | SE_36018 | chr2:219146032-219158345 | HMEC | SE_41500 | chr2:219145847-219154222 | Left_Ventricle | SE_45286 | chr2:219149757-219152886 | NHLF | SE_47526 | chr2:219149905-219152925 | Pancreas | SE_50394 | chr2:219149842-219160653 | Sigmoid_Colon | SE_51585 | chr2:219145632-219158203 | Skeletal_Muscle | SE_52542 | chr2:219149722-219160735 | Small_Intestine | SE_57570 | chr2:219149965-219152053 | VACO_503 | SE_57570 | chr2:219152277-219152769 | VACO_503 | SE_58066 | chr2:219151254-219151909 | VACO_9m | SE_58066 | chr2:219152411-219152693 | VACO_9m | SE_64537 | chr2:219148646-219152988 | NHEK |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr2 | 219152622 | 219152760 | chr2 | 219151208 | 219151930 |
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Enhancer Sequence | TGAAGGAACT CCAGCAACAT GGAGCAAGCC CCTTGTCTGC AGACAGCTCG ATTAGAACAT 60 TCTTCCTTGC CTCACAATGC CTGTTATCAA GGCATTCAGA CTGTGCCCTA TCCTTGCCCA 120 TTATAGATCT AAGTTTGCTC CTCTCTCAGG GCCCCAGTCC CCCATTAGGA AGGAACCAGA 180 GCCCCTGCTT TCTACCACAG CAGCGGCACA AGTGGGTGAG CTCAGACAGC AGGACTTGCT 240 GGGTGTCAAG GTTTTCAGAT GCAGAGGCGG AAGCACCTCC TCCCCTGGAG CCCTCTCAGT 300 GTGGTAATCC TGCTGTCTGC CTACTGAGGC CCCGGCTGGG GCTCTCCTGG GGGTATTTGA 360 AGGGTTAAGG CTCCGGAATC TGCAGAGGAG GCCTGAGCTA CTGGGGTTAC AGCAAGAGGA 420 GAGTATGTGT ACTGGAGGGA GGGATGGAAA GGAGCAGCTG ACTGGTCCAG GCAGCCTGCC 480 CTCCTCCCTG CCAGAGACGG ATGCCCAGAG TGGAAAAAAA TAGCTCAGAA TGCACATCTC 540 AGGAAACCCC ACCCAGCAGG CGCAGGAGCA CAGCCCAGAT CTGACGATTT GTTCCCCTCC 600 CTTTTCCTTT ATCTGCCCCC ACAAGAAAAC ACTTTATCCT CCTACCCCAG GGCACAGCTG 660 ACCTCATAGC CACGAGAGCA AATGAGTAAA AAGATACACC CAGGAGTGTC TGGGCAAGTC 720 ACCAGGCCTG ATTCTGCACC AAGGGGGCCC AGAATCAACT AAATATCCTT CCATCAGCCT 780 GGACTTTGGG ACTAAGAGGA TGAAGCCACA GGGATCTAAA CACTAAAATA TCAGAGCTGG 840 CTTAGACTTT GGATCTCACC TGGTCATTTG ACAGACAAGG AAACCCCAGA GCCAAGAAAG 900 TTCCTGCTCC ACCCCAGAAC AGCCCTCTTC TTCGTCATGG GTTTGGAACT TCCCTTCCCA 960 GCCCCGCCCA CTCTCTGAGT GATAGACACC AGCACACACC CTCTCCCAAG GAGGGGCCAG 1020 AACAAGCTAC CATTCTCTCA GTTCTCTAGT GACCTCTCAG CTCAGAAACA GTTAAGACCG 1080 GGCCGGGTGC AGTGGCTCAT GCCTGTAATC CCAGCACTTT GGGAGGCCGA GGCAGGTGGA 1140 TCACGAGGTC AGGAGATCAA GACCATCGTG GCCAACATGG TCAAACCCCA TGTCTACTAA 1200 AAAATACAAA AAATTAGCTG GGCGTGATAT CCCACACCTG AAGTCCCAGC TACTCGGGAG 1260 GCTGAGGCAG GGGGATCGCT CGAACCCGAG AGGCAGAGGT TGCAGTGAGC CAAGAACATG 1320 CCATTGCACT CCAGCCTGGG CAACAAGAGT GAAACCCCAT CTCAAAAAAA AAGACAGCCA 1380 GCCCTCGACT TCTGGCCCCC AACTCGAGGC CACCCCTCCC AGCCCCCTCT CTAGCCAGGG 1440 TGGCCTCTCT CTGGACCCAT GGAGACCGAG GGGTGGCTCC AAGCTCCCAG GAGGGAGAGG 1500 CTGTCCTGGG GATCACGAGA GGACCCAGGC ACCGCAGCTC CGCCACCCTT GTCTGGAGCA 1560 GAATCCTGTG ATCAGAATGG TAATCTCGGG TTACCCCACC CAAGTCAGGA TGGCCTGGGA 1620 GTACAGATAA GGGAAGAGGA AGCCATTAGC AGGCTGATGC TATAATACTT CTGAGCACAG 1680 TCCCTGTTCA CTTCCTTCTT TGTTTCATCT CCTGTCTTTT CATTGAACTT CAAGATTAGG 1740 AGGGGAAAGA GACAGACAAA GGAGACTGAT AACTAACCCC AAAAAAGAAC TAGGGAAGGG 1800 GCCAGGCATG GCGGCTCACG CCTGTAATCC CAGCACTTTG GGAGGCCAAG GCGGGCGGAT 1860 CACGAGGTCA GGAGATCGAG ACCATCCTGG 1890
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