Tag | Content |
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EnhancerAtlas ID | HS023-14829 |
Organism | Homo sapiens |
Tissue/cell | CD8+ |
Coordinate | chr2:128164780-128165990 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr2:128165606-128165624 | GCGTCCTTCCCGCCTTCC | - | 6.01 | KLF16 | MA0741.1 | chr2:128165572-128165583 | GCCCCGCCCCC | + | 6.02 | KLF16 | MA0741.1 | chr2:128165812-128165823 | GGGGGCGTGGC | - | 6.62 | KLF5 | MA0599.1 | chr2:128165572-128165582 | GCCCCGCCCC | + | 6.02 | SP3 | MA0746.2 | chr2:128165811-128165824 | TGGGGGCGTGGCG | - | 6.57 | SP8 | MA0747.1 | chr2:128165811-128165823 | TGGGGGCGTGGC | - | 6.11 | TFAP2A | MA0003.3 | chr2:128165379-128165390 | AGCCTCAGGCA | + | 6.32 | ZNF263 | MA0528.1 | chr2:128165526-128165547 | TCCTCCTCCTCCTCCCCCACC | - | 6.27 | ZNF263 | MA0528.1 | chr2:128165532-128165553 | TCCTCCTCCCCCACCACCTCT | - | 6.49 | ZNF263 | MA0528.1 | chr2:128165472-128165493 | CTCCCTCCCTCCTTCTGCTCC | - | 6.59 | ZNF263 | MA0528.1 | chr2:128165529-128165550 | TCCTCCTCCTCCCCCACCACC | - | 7.31 | ZNF263 | MA0528.1 | chr2:128165580-128165601 | CCCTCCTCTTCCCCCTGCCCC | - | 7.81 | ZNF263 | MA0528.1 | chr2:128165523-128165544 | GCCTCCTCCTCCTCCTCCCCC | - | 8.62 |
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| Number of super-enhancer constituents: 11 | ID | Coordinate | Tissue/cell |
SE_09644 | chr2:128164535-128166940 | CD14 | SE_23461 | chr2:128165153-128165765 | Colon_Crypt_1 | SE_23461 | chr2:128165766-128166677 | Colon_Crypt_1 | SE_24012 | chr2:128165266-128166623 | Colon_Crypt_2 | SE_24894 | chr2:128165065-128166599 | Colon_Crypt_3 | SE_28345 | chr2:128164776-128166852 | Fetal_Intestine | SE_29146 | chr2:128164682-128166773 | Fetal_Intestine_Large | SE_43376 | chr2:128165019-128166813 | Lung | SE_50833 | chr2:128165107-128166882 | Sigmoid_Colon | SE_52838 | chr2:128165093-128165615 | Small_Intestine | SE_52838 | chr2:128165639-128166869 | Small_Intestine |
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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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| Number: 1 | ID | Chromosome | Start | End |
GH02I127406 | chr2 | 128164514 | 128166975 |
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Enhancer Sequence | ATTAGCCAGG TGTGGCGGTC CATGCCGGTA GTCCCAGCTA CTTGGGAGGC TGAGGCAGGA 60 TGATCACTTG CACCTGGGAC GTTGAGGCGG CAGTGAGCCG TGTTCGCGCC ACTGCACTCC 120 AGCCTGGGTG ACACTGCAAG ACCCTGTCTC AAAAAAAGTA GTCAAGGAGG CTGAGAGCCA 180 GGAAGCCTCT GGCCAGCAGG TGAGCAGGCC CTTTCCTGCT GCTGTGCATT GTATTTAAGA 240 GAAAAGACAG ATACGTCTGA TACCTTCAAA GGTGTTCTTC ATACAGCAGG TTGCAACCTA 300 TTAATAGATC ATAAAATCAG TTTAGTGTTT CATCATCATC ATCAAAAACC ACCACCAACA 360 ACAAAAAGAC CCAGAACAGA TAGTGTAAAG AGTGCATCCC TGCATTCCTG TATAGGGAGA 420 AATATGGTTT TGTGGAACCT TGTTGCGATG TAAAGTGTAC TTCTTAAGAT AAATACAGGG 480 TTGAGGTTTT TGAAATAAAG TTTGAACAGG ACCACCTTAA GCCACAGTGT AGACTTTCCA 540 TAGGCCAAAA CCTGGATCAC CAAGACAGTG TGCCCCAGGC TGCAGGCCAC ACTCCTGGGA 600 GCCTCAGGCA ACCTTGTGCA GGCCTGACTT CGAGACACTC TGAGCATGAG CTGGTTCCTG 660 GGTAGCCTCC CCTCTACCTC TCCCCGCTTG CCCTCCCTCC CTCCTTCTGC TCCTGTCTCT 720 CCTCATCCCC TCCCCGAGTT GCTGCCTCCT CCTCCTCCTC CCCCACCACC TCTCCCCGTC 780 TCCGAGTTGC CTGCCCCGCC CCCTCCTCTT CCCCCTGCCC CTCTCCGCGT CCTTCCCGCC 840 TTCCCCCTCC TCGTCTCCCC CCTCCCCGCC CGCGCCGTCT GCGTCCCTCC CGGGCCCAGA 900 CGCGGCGCGG TCAGGGGGCG CTGACTCACA GGCTGACTCA GCTGCAGGCG CGCTGCCAGG 960 CGACGCAGCG GGCGGGTGGC CGGGCGCCGG CGGGCTCGCA GCCGGGCTGC TGGCAACGGT 1020 GCCGGCGGAG GTGGGGGCGT GGCGCGGGAT GGGCGGCGCG GGCCCTGCCG TGGTACCGCC 1080 TGGCAGCGTC CACCCCGCCG CTGGGGCGCC CTGGAGGCTC CTGGCCCTCC GTGGGGCCGT 1140 GACACCGGCG CTGCGGGGAG CGGTGGCCTC GCAGAGGCTG GGCATGGGAG GACGGCCGCC 1200 CCGGGTAAAG 1210
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