Tag | Content |
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EnhancerAtlas ID | HS055-04455 |
Organism | Homo sapiens |
Tissue/cell | FT33 |
Coordinate | chr2:128164510-128165990 |
Target genes | |
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 | TACAGTGAAA AGTCCTCCCT CATCCCCAGT GCCCTCCCAC CCCAGGTAAT CACAGTTACC 60 AGGATTCAAT GCACATCCAA ACACAAACAA ACACAAACCA TGGTGTGTTT ATTGCCCATG 120 GAGGCTCTGT CTCAGGTCCC TGGGAATCAT TGGGAGTTGT GGATCCCAGC ACTTTGGGAG 180 GCTGAGGCAG GAGGATCGCT TGAGCCCAGG AGTTTTTTGA GACCAGCTTG AACAACATAG 240 TGAGACCCCA TCTCTACAAA AAATTAAAAA ATTAGCCAGG TGTGGCGGTC CATGCCGGTA 300 GTCCCAGCTA CTTGGGAGGC TGAGGCAGGA TGATCACTTG CACCTGGGAC GTTGAGGCGG 360 CAGTGAGCCG TGTTCGCGCC ACTGCACTCC AGCCTGGGTG ACACTGCAAG ACCCTGTCTC 420 AAAAAAAGTA GTCAAGGAGG CTGAGAGCCA GGAAGCCTCT GGCCAGCAGG TGAGCAGGCC 480 CTTTCCTGCT GCTGTGCATT GTATTTAAGA GAAAAGACAG ATACGTCTGA TACCTTCAAA 540 GGTGTTCTTC ATACAGCAGG TTGCAACCTA TTAATAGATC ATAAAATCAG TTTAGTGTTT 600 CATCATCATC ATCAAAAACC ACCACCAACA ACAAAAAGAC CCAGAACAGA TAGTGTAAAG 660 AGTGCATCCC TGCATTCCTG TATAGGGAGA AATATGGTTT TGTGGAACCT TGTTGCGATG 720 TAAAGTGTAC TTCTTAAGAT AAATACAGGG TTGAGGTTTT TGAAATAAAG TTTGAACAGG 780 ACCACCTTAA GCCACAGTGT AGACTTTCCA TAGGCCAAAA CCTGGATCAC CAAGACAGTG 840 TGCCCCAGGC TGCAGGCCAC ACTCCTGGGA GCCTCAGGCA ACCTTGTGCA GGCCTGACTT 900 CGAGACACTC TGAGCATGAG CTGGTTCCTG GGTAGCCTCC CCTCTACCTC TCCCCGCTTG 960 CCCTCCCTCC CTCCTTCTGC TCCTGTCTCT CCTCATCCCC TCCCCGAGTT GCTGCCTCCT 1020 CCTCCTCCTC CCCCACCACC TCTCCCCGTC TCCGAGTTGC CTGCCCCGCC CCCTCCTCTT 1080 CCCCCTGCCC CTCTCCGCGT CCTTCCCGCC TTCCCCCTCC TCGTCTCCCC CCTCCCCGCC 1140 CGCGCCGTCT GCGTCCCTCC CGGGCCCAGA CGCGGCGCGG TCAGGGGGCG CTGACTCACA 1200 GGCTGACTCA GCTGCAGGCG CGCTGCCAGG CGACGCAGCG GGCGGGTGGC CGGGCGCCGG 1260 CGGGCTCGCA GCCGGGCTGC TGGCAACGGT GCCGGCGGAG GTGGGGGCGT GGCGCGGGAT 1320 GGGCGGCGCG GGCCCTGCCG TGGTACCGCC TGGCAGCGTC CACCCCGCCG CTGGGGCGCC 1380 CTGGAGGCTC CTGGCCCTCC GTGGGGCCGT GACACCGGCG CTGCGGGGAG CGGTGGCCTC 1440 GCAGAGGCTG GGCATGGGAG GACGGCCGCC CCGGGTAAAG 1480
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