Tag | Content |
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EnhancerAtlas ID | HS129-20461 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr2:128164850-128165990 |
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 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH02I127406 | chr2 | 128164514 | 128166975 |
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Enhancer Sequence | CACCTGGGAC GTTGAGGCGG CAGTGAGCCG TGTTCGCGCC ACTGCACTCC AGCCTGGGTG 60 ACACTGCAAG ACCCTGTCTC AAAAAAAGTA GTCAAGGAGG CTGAGAGCCA GGAAGCCTCT 120 GGCCAGCAGG TGAGCAGGCC CTTTCCTGCT GCTGTGCATT GTATTTAAGA GAAAAGACAG 180 ATACGTCTGA TACCTTCAAA GGTGTTCTTC ATACAGCAGG TTGCAACCTA TTAATAGATC 240 ATAAAATCAG TTTAGTGTTT CATCATCATC ATCAAAAACC ACCACCAACA ACAAAAAGAC 300 CCAGAACAGA TAGTGTAAAG AGTGCATCCC TGCATTCCTG TATAGGGAGA AATATGGTTT 360 TGTGGAACCT TGTTGCGATG TAAAGTGTAC TTCTTAAGAT AAATACAGGG TTGAGGTTTT 420 TGAAATAAAG TTTGAACAGG ACCACCTTAA GCCACAGTGT AGACTTTCCA TAGGCCAAAA 480 CCTGGATCAC CAAGACAGTG TGCCCCAGGC TGCAGGCCAC ACTCCTGGGA GCCTCAGGCA 540 ACCTTGTGCA GGCCTGACTT CGAGACACTC TGAGCATGAG CTGGTTCCTG GGTAGCCTCC 600 CCTCTACCTC TCCCCGCTTG CCCTCCCTCC CTCCTTCTGC TCCTGTCTCT CCTCATCCCC 660 TCCCCGAGTT GCTGCCTCCT CCTCCTCCTC CCCCACCACC TCTCCCCGTC TCCGAGTTGC 720 CTGCCCCGCC CCCTCCTCTT CCCCCTGCCC CTCTCCGCGT CCTTCCCGCC TTCCCCCTCC 780 TCGTCTCCCC CCTCCCCGCC CGCGCCGTCT GCGTCCCTCC CGGGCCCAGA CGCGGCGCGG 840 TCAGGGGGCG CTGACTCACA GGCTGACTCA GCTGCAGGCG CGCTGCCAGG CGACGCAGCG 900 GGCGGGTGGC CGGGCGCCGG CGGGCTCGCA GCCGGGCTGC TGGCAACGGT GCCGGCGGAG 960 GTGGGGGCGT GGCGCGGGAT GGGCGGCGCG GGCCCTGCCG TGGTACCGCC TGGCAGCGTC 1020 CACCCCGCCG CTGGGGCGCC CTGGAGGCTC CTGGCCCTCC GTGGGGCCGT GACACCGGCG 1080 CTGCGGGGAG CGGTGGCCTC GCAGAGGCTG GGCATGGGAG GACGGCCGCC CCGGGTAAAG 1140
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