Tag | Content |
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EnhancerAtlas ID | HS053-20804 |
Organism | Homo sapiens |
Tissue/cell | Foreskin_keratinocyte |
Coordinate | chr2:43404760-43407090 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXF2 | MA0030.1 | chr2:43406393-43406407 | TCAAGGTAAACAAA | + | 6.7 | ZNF263 | MA0528.1 | chr2:43406196-43406217 | CACCCCTGCTCCCCTTCCTCC | - | 6.38 | ZNF263 | MA0528.1 | chr2:43405533-43405554 | GGAGGAGGCAGGGCCAGAGGA | + | 6.4 |
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| Number of super-enhancer constituents: 42 | ID | Coordinate | Tissue/cell |
SE_03102 | chr2:43405034-43407173 | Bladder | SE_09287 | chr2:43404602-43407281 | CD14 | SE_11722 | chr2:43405238-43406788 | CD20 | SE_11879 | chr2:43404845-43406867 | CD3 | SE_12501 | chr2:43405034-43405407 | CD34_adult | SE_12501 | chr2:43405453-43406127 | CD34_adult | SE_12758 | chr2:43405497-43405782 | CD34_fetal | SE_13409 | chr2:43404300-43407894 | CD34_Primary_RO01536 | SE_14384 | chr2:43400219-43408412 | CD4_Memory_Primary_7pool | SE_16107 | chr2:43405323-43406823 | CD4_Naive_Primary_7pool | SE_16950 | chr2:43405189-43406902 | CD4p_CD225int_CD127p_Tmem | SE_17323 | chr2:43404653-43407139 | CD4p_CD25-_CD45RAp_Naive | SE_17875 | chr2:43395625-43407220 | CD4p_CD25-_CD45ROp_Memory | SE_18565 | chr2:43400105-43406913 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19552 | chr2:43404989-43406913 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20901 | chr2:43404381-43408464 | CD8_Memory_7pool | SE_22349 | chr2:43404562-43406734 | CD8_primiary | SE_23059 | chr2:43404855-43406796 | Colon_Crypt_1 | SE_23724 | chr2:43404942-43406674 | Colon_Crypt_2 | SE_24685 | chr2:43404928-43406747 | Colon_Crypt_3 | SE_26374 | chr2:43404952-43407135 | Duodenum_Smooth_Muscle | SE_26557 | chr2:43404629-43407112 | Esophagus | SE_27617 | chr2:43404753-43406882 | Fetal_Intestine | SE_28536 | chr2:43404713-43407125 | Fetal_Intestine_Large | SE_30898 | chr2:43405428-43406709 | Fetal_Thymus | SE_31392 | chr2:43403915-43408015 | Gastric | SE_33376 | chr2:43404839-43406830 | H1 | SE_34919 | chr2:43404423-43409363 | HeLa | SE_38828 | chr2:43404837-43407124 | HUVEC | SE_40066 | chr2:43404740-43407810 | K562 | SE_43203 | chr2:43404724-43406909 | Lung | SE_47826 | chr2:43405061-43406747 | Pancreas | SE_49954 | chr2:43404447-43406783 | RPMI-8402 | SE_50052 | chr2:43404769-43406907 | Sigmoid_Colon | SE_52337 | chr2:43404682-43406959 | Small_Intestine | SE_53288 | chr2:43405163-43406850 | Spleen | SE_55101 | chr2:43405389-43406674 | Thymus | SE_58412 | chr2:43352450-43425007 | Ly1 | SE_61450 | chr2:43354337-43468354 | Toledo | SE_62203 | chr2:43354169-43468733 | Tonsil | SE_65350 | chr2:43405021-43407124 | Pancreatic_islets | SE_68698 | chr2:43404861-43409084 | H9 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I043167 | chr2 | 43394741 | 43409195 |
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Enhancer Sequence | ATAAAGTATG CAAGAAGTTA GGTGTGGGTT ATTTGTAAAT ACTATGCCAT TTTATATCAC 60 GGACTTGAGC TTCTGTGGAT TTCAATATCC ATGGGAGTCT TGGAACCAAT CCCCCCGCCA 120 CAATACCCCT AGGATACAGA GGGAGGGACA ACTGTTCACA GAGGAGCTCC CAACACTTGT 180 TGGGTTTCCT CAACATTGCA AGGATGATAG TTTTGTCTTC TCCAATGGCC CAGGAAGCTT 240 TTTGAGGGCA GGTACCATGT GATACTTGCC TTGTGTCCAC ACCCACACCA CCCCCATTGT 300 GGACCACTGG ACCATTGTGG GAGCTCAGTT CTATGGACTG AGTGGTTCTG TAGACCCAAC 360 AGTGGATAGG GCCAAGACAG GGGGCCTGGG AGATTGTGGA TATCATCACC CCCTGGCCCT 420 GGTGCACTCA TACTCAGTTC TTAAGACCCA GCTCTTTCTG ACTCCTCCAG AAAGACTTCT 480 CTGTCCCTCA GGCTGGGTCA GGCCCCTCAG CGTCCCACTG CACACATGGC AGATAAGTCT 540 TGATCGATGT GCTGTGATAA AGCAGTTATC TGTGTGTACA GCTGGCTCCC CAAGAGACCG 600 TGCCCTCCCT TCTCACTATT CTCTGGAGTC AGGCTCTGTA GCAGCCCAAC ATGGTTTTGA 660 TGAATGAATT AATAAATTTG CTCTGTGATC ATGAGCAAAT TCCCTCTGTC CTGTTCTCAA 720 CAACGGGAAG GCACTATCTT TACTAGATAA GTGAGAGGAA GGGGCCCGGA GGTGGAGGAG 780 GCAGGGCCAG AGGAGGAATG GAGTGGCTCG TGACACCCAC TGTGGGCAGA TGGGATCTGT 840 TAGGAGTGGC TTTGGCTCAC TGGGGCAGGC CAGGGTGGAG AACTGTCACA TACCCTGGTG 900 TACCTCTGGC AAGGAGCTCT GGTGCCATGT GGGAATAGAA GTGCATGGTC CCTTGGCAAG 960 GCTAACGTTT TGTTTTTAAA GAAGTCTGTG TTTCCAGCCT CTTCCTATCT AGTGACCTGG 1020 TCCCTGAGAC CTGCCCACCC TCCCGGGCCA TAGCACCAGC CATGCGACCT TGAACCGGTC 1080 ACCACTCATC CCTGAACCTC CAAGTTCTCA GCTCTACTGA CAGGGCTGCA GTGCCTTCAT 1140 GGGCTGGTGC CTGCCTGGGA GGGAGCCCAG GGATAGAAGC CTGGTTCGCT GGCCACCTCC 1200 CGCTGGGGCG TTGGCCCAGG CTGCCAGGTT TCACGTTTCA GCTTTCAGAG TGTTTTCTTG 1260 TCTAGGGCAC TTTCTATTTT TCAATACTTT TCCTATCACA GCCAAACAAC AAAAAAGGAA 1320 ATTGGTTGAG CCTTCTGAAG ACCAAGGTCT GGGAGGGTGG GGGTGGGCAG AACCCACCAT 1380 GGGAAAAGCT GGAGTCAGGG CTGAGGGAGG AGAGGCCTCT CCACCCGATT CCCCAGCACC 1440 CCTGCTCCCC TTCCTCCGGG GCTGACTCAT TGTTTTGCAA CAAACAGCCG GCAGCCAGGT 1500 CCCAGCAGTT TCTCAAGCCT GGCCCCCAGG CTGGCTGGGC TCAATCCTGG CCCTCCCAAC 1560 TGCCTGGCCA GGCCCTGAAC GATTGAGTTA TCTCCACTCG CATCCCCTTT GTTTGGGGCG 1620 GCTACTTGCC CACTCAAGGT AAACAAATTC TGGGCCTGTG TGAAAAGAAA GGAACGGTTA 1680 TCTCTGAGGC CCTCAGCGGC CTGGCTGGGG AGCAAGACTT TCAGAGGCTT CTGTCTCCAA 1740 AGAGAGGAGG GATTTCGGAG CATAGCGTCC AGAGGCCAGC TGCCTGGGTT CAAGCTCCAC 1800 CTCGGCCACT GACTGCTGAT GACCTTGGGC AAGTCCCTGA CCTTCTGCTT CAACTTTTTT 1860 ACCTGTAAAA TTTGGGCACA ATAATATCTA TATCATAAAG TTGTTCTGAG GATTGATGAG 1920 TTCATATTTA TAAAATGCTA CATAAAGGAT GTGAGGTTTT TTGGGGTTTT TTTGTTTTAT 1980 TTTGTTTTTT GAGACCGAGT CTCGTTCTGT TGCCCAGGCT GGAGCGCAGT GGGGCAATCT 2040 TGGCTTACTG CAACCTCTGC CTCCCGGGCT CAAGCGATTC TTCTGCCTCA GACTCCTGAG 2100 TAGCTGGGAC TACAGTCACA CACCTCACAC ACCACCACGC CCAGCTAATT TTTATATTTT 2160 TAGTAGAGAC AGGGTTTCTC CTTGTTGGCC AGGGTCGTCT CGAACTCCTG ACCCCAGGTG 2220 ATCCACCCGC CTCAGCCTCC CAAAGTGCTG GGATTAGAGG TGTAAGCCAC CGCACCCGGC 2280 CTGATGTGAG TTTTTTAAAA AGCTACGTAC AAGAGATGTT AAATGGGGGA 2330
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