Tag | Content |
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EnhancerAtlas ID | HS041-11379 |
Organism | Homo sapiens |
Tissue/cell | EWS502 |
Coordinate | chr2:85134280-85135620 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr2:85135303-85135318 | TGAACTCCTGACCTC | - | 6.22 | ZNF263 | MA0528.1 | chr2:85134297-85134318 | GGGGGAGGGGAGGGGGGAAGA | + | 8.29 |
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| Number of super-enhancer constituents: 35 | ID | Coordinate | Tissue/cell |
SE_10467 | chr2:85131590-85135088 | CD19_Primary | SE_10467 | chr2:85135227-85136890 | CD19_Primary | SE_14858 | chr2:85131289-85135119 | CD4_Memory_Primary_7pool | SE_14858 | chr2:85135188-85136997 | CD4_Memory_Primary_7pool | SE_15828 | chr2:85131869-85135075 | CD4_Naive_Primary_7pool | SE_17329 | chr2:85130947-85136942 | CD4p_CD25-_CD45RAp_Naive | SE_18307 | chr2:85131266-85137084 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19290 | chr2:85131445-85135057 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_22056 | chr2:85131291-85135204 | CD8_Naive_8pool | SE_22056 | chr2:85135206-85137140 | CD8_Naive_8pool | SE_22465 | chr2:85132044-85135190 | CD8_primiary | SE_22465 | chr2:85135210-85137011 | CD8_primiary | SE_24195 | chr2:85131825-85134945 | Colon_Crypt_2 | SE_27502 | chr2:85131737-85135107 | Esophagus | SE_27502 | chr2:85135275-85135928 | Esophagus | SE_32545 | chr2:85132233-85134677 | GM12878 | SE_32545 | chr2:85135283-85135964 | GM12878 | SE_34685 | chr2:85131225-85136053 | HeLa | SE_35873 | chr2:85131527-85136323 | HMEC | SE_37561 | chr2:85131822-85135186 | HSMMtube | SE_39196 | chr2:85132734-85135003 | IMR90 | SE_43289 | chr2:85131260-85135094 | Lung | SE_45342 | chr2:85132064-85135010 | NHLF | SE_47378 | chr2:85131796-85135146 | Panc1 | SE_50337 | chr2:85131601-85137121 | Sigmoid_Colon | SE_52528 | chr2:85131648-85135077 | Small_Intestine | SE_52528 | chr2:85135266-85136775 | Small_Intestine | SE_54030 | chr2:85131547-85135890 | Spleen | SE_55507 | chr2:85131722-85134977 | Thymus | SE_55909 | chr2:85131352-85134985 | u87 | SE_57573 | chr2:85132704-85134887 | VACO_503 | SE_58212 | chr2:85132726-85134724 | VACO_9m | SE_65145 | chr2:85131959-85135039 | NHEK | SE_65145 | chr2:85135282-85135965 | NHEK | SE_67823 | chr2:85131352-85134985 | u87 |
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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 | GAACCAACAC TAGAACTGGG GGAGGGGAGG GGGGAAGAGC TTTTGTCTTT TAACCCTAGT 60 TCAGAACCTC CCACAAAAAC ATTAGCCATT AGAGGAAGTG CTAGACTGAT CTGCTACCAC 120 CCAGTGCTCA GCAGGAAGGG TGGGGATGTG GTGGGAGGGA GGAAGGGTGG GCTGGCGCTG 180 GCGCTGGCGG CCAAGCTCCA AGGGATGACA CCTCAAACCC ACAGGGAAGG AATAGGACCA 240 GCCCAAGGGG GCCTGACAGT TGGGAACCTG GGGCTGCAGG CCATTCAGAA GCAGAAGAAA 300 CAGGCTTATA AAGACAGGGG TGGAGTTTTC TTTAAGGAAG GTGGATAGGA CACTGCTTAG 360 AGATTCGTCC CACATTTTTG CCCGGCCCCA AGAGGCTGGG CACTGGGTGA AGACAGTTAA 420 TTCGAATAAG ATACGGTCCC TGTCCACGAG GAATTTAAAA TCTGGTGAGT GAGATAGCCA 480 CAGCAGACCA GAGTCAGGAC ACCTAGGCTT GGCAGGGAGA CTCATGCCCA AAGGCATTCT 540 CTCTGAACTC CTATCTGCAC CTCCCTCCTG GTACCTGGAC ACATACATCA CCTCCCCCAT 600 TAGAGTAAAT AGAGAGACTT TTTTTTTTTT TTTTTTTTTG AGACGGAGTT TCGCTCTTGT 660 CTCCCAGACT GGACTGCAAT GGTGCGATCT CGGCTCACTG CCTCCGCCTC CCGGGTACAA 720 GCGATTTTCC TGCCTCAGCC TCCCCAGTAG CTGGGATTAC AGGCATGAGC CACCACGCCT 780 GGCTAACTTT TTGGTTGTTG TTTTTTTTTT TTTTTTTTTT TTTGAAATGG AGTTTCGCTC 840 TTGTTGCCCA GGCTGGAGTG CAATGGTGCA ATCTCAGCTC ACCACAACTT CCACACCTCC 900 GCCTCCCGAG TTCTCCTGCC TCAGCCTCCT GAGTAGCTGG GATTACAGGC ATGCACCACC 960 ACGCCCGGCT AATTTTGTAT TTTTAGTAGA GACGGGGTTT CGCCATGTTA GCCAGGCTGG 1020 TCTTGAACTC CTGACCTCTG GTGATCCACC CGTCTCAGCC TCTCAAAGTG CTGGGATTAC 1080 AGGCGTGAGC CACCATGCCC GGCTGAAAGA TTCTTATTAA TTGATATTGG TGACTCTCAC 1140 AGTAGTCAGC ACTTAGTAGA CACTCATAAG TGCTCACTGA ATTGTAACTG AAGTATCATA 1200 TGGCCTCGCC TGCTCCAACT TGGCTATGCT AAAGCCAAGC TGCTACCAGC CCTCCTCCCC 1260 CACTGTCTTG TTGGTTCTAT TCTATTCTAT GTACACATTG ACAGGGCCCA AGCATGGTGA 1320 ACTTGTGGAA GTTCAGGGAA 1340
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