Tag | Content |
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EnhancerAtlas ID | HS061-14947 |
Organism | Homo sapiens |
Tissue/cell | GM12892 |
Coordinate | chr2:219150860-219152330 |
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: 36 | ID | Coordinate | Tissue/cell |
SE_00326 | chr2:219145665-219158265 | Adipose_Nuclei | SE_03432 | chr2:219149789-219152314 | Brain_Angular_Gyrus | SE_06270 | chr2:219145735-219164206 | Brain_Hippocampus_Middle | SE_08985 | chr2:219150395-219151017 | Brain_Mid_Frontal_Lobe | SE_08985 | chr2:219151033-219151582 | Brain_Mid_Frontal_Lobe | SE_08985 | chr2:219151601-219152174 | 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_58066 | chr2:219151254-219151909 | 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: 1 | Chromosome | Start | End |
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Enhancer Sequence | AAGGTCCCCA CTGGAAGCCT GAATTTTCCC AAAATACAGT AGGCATTCAC CTTCTGCTTG 60 TTTTTGTTTT TCTTTTTGTT TTGGTAGAAA CGGGGTTTCA CCATGTTGGC CAGGCTGGCA 120 AACTCCTGGC CTCAAGTGAT CCACCCACCG AGGCCTCCCA AAGTGCTGGG ATTACAGGCA 180 TGAGCCACTG TGTCTGGCCC ACCTTCTGCT TGAAGGAACT CCAGCAACAT GGAGCAAGCC 240 CCTTGTCTGC AGACAGCTCG ATTAGAACAT TCTTCCTTGC CTCACAATGC CTGTTATCAA 300 GGCATTCAGA CTGTGCCCTA TCCTTGCCCA TTATAGATCT AAGTTTGCTC CTCTCTCAGG 360 GCCCCAGTCC CCCATTAGGA AGGAACCAGA GCCCCTGCTT TCTACCACAG CAGCGGCACA 420 AGTGGGTGAG CTCAGACAGC AGGACTTGCT GGGTGTCAAG GTTTTCAGAT GCAGAGGCGG 480 AAGCACCTCC TCCCCTGGAG CCCTCTCAGT GTGGTAATCC TGCTGTCTGC CTACTGAGGC 540 CCCGGCTGGG GCTCTCCTGG GGGTATTTGA AGGGTTAAGG CTCCGGAATC TGCAGAGGAG 600 GCCTGAGCTA CTGGGGTTAC AGCAAGAGGA GAGTATGTGT ACTGGAGGGA GGGATGGAAA 660 GGAGCAGCTG ACTGGTCCAG GCAGCCTGCC CTCCTCCCTG CCAGAGACGG ATGCCCAGAG 720 TGGAAAAAAA TAGCTCAGAA TGCACATCTC AGGAAACCCC ACCCAGCAGG CGCAGGAGCA 780 CAGCCCAGAT CTGACGATTT GTTCCCCTCC CTTTTCCTTT ATCTGCCCCC ACAAGAAAAC 840 ACTTTATCCT CCTACCCCAG GGCACAGCTG ACCTCATAGC CACGAGAGCA AATGAGTAAA 900 AAGATACACC CAGGAGTGTC TGGGCAAGTC ACCAGGCCTG ATTCTGCACC AAGGGGGCCC 960 AGAATCAACT AAATATCCTT CCATCAGCCT GGACTTTGGG ACTAAGAGGA TGAAGCCACA 1020 GGGATCTAAA CACTAAAATA TCAGAGCTGG CTTAGACTTT GGATCTCACC TGGTCATTTG 1080 ACAGACAAGG AAACCCCAGA GCCAAGAAAG TTCCTGCTCC ACCCCAGAAC AGCCCTCTTC 1140 TTCGTCATGG GTTTGGAACT TCCCTTCCCA GCCCCGCCCA CTCTCTGAGT GATAGACACC 1200 AGCACACACC CTCTCCCAAG GAGGGGCCAG AACAAGCTAC CATTCTCTCA GTTCTCTAGT 1260 GACCTCTCAG CTCAGAAACA GTTAAGACCG GGCCGGGTGC AGTGGCTCAT GCCTGTAATC 1320 CCAGCACTTT GGGAGGCCGA GGCAGGTGGA TCACGAGGTC AGGAGATCAA GACCATCGTG 1380 GCCAACATGG TCAAACCCCA TGTCTACTAA AAAATACAAA AAATTAGCTG GGCGTGATAT 1440 CCCACACCTG AAGTCCCAGC TACTCGGGAG 1470
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