Tag | Content |
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EnhancerAtlas ID | HS197-11966 |
Organism | Homo sapiens |
Tissue/cell | ZR75-30 |
Coordinate | chr2:128164060-128165990 |
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 | IRF1 | MA0050.2 | chr2:128164100-128164121 | AAAAAAAAAAAGAAAGAAAAG | - | 6.41 | KLF16 | MA0741.1 | chr2:128165572-128165583 | GCCCCGCCCCC | + | 6.02 | KLF16 | MA0741.1 | chr2:128165812-128165823 | GGGGGCGTGGC | - | 6.62 | KLF4 | MA0039.3 | chr2:128164372-128164383 | GCAGGGTGTGG | - | 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: 2 | Chromosome | Start | End |
chr2 | 128164124 | 128164411 | chr2 | 128164878 | 128165800 |
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| Number: 2 | ID | Chromosome | Start | End |
GH02I127407 | chr2 | 128164177 | 128164376 | GH02I127406 | chr2 | 128164514 | 128166975 |
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Enhancer Sequence | GCACATACAC CGTGAACCTA AAACAAAAGT TTACCAAAAA AAAAAAAAAA AGAAAGAAAA 60 GAAAAGAAAA AGAAAAAAAA TTTCAAGACC TAGATCAGAA ATCAGCTCCT TGGCCAGGCA 120 TACTGGCTCA TGCTTGAGCA AGGCAGGAGG ATTGCTTGAG CCCAGGAATT TGAGACCAGC 180 CTGGGCAATA CTGTGTGACT TCATCTCAAA AAAAAAAAAA AAGGAAAAAA AATTATATAT 240 AAAATAAAGC ATTCTGAGGC TTCATCCACT CCTCACTCCT CAGAGAAGTA CTGAAGCTAG 300 CTAGAGATTT CTGCAGGGTG TGGAATGGGG AGAAAGGCAG CGTGACTGTG TGTCACATTT 360 GTTTCTGACA CCTTTTTGTA GGTCTGAAAT GCTTTTAAAT AAACATTTTT AAGTAATATA 420 TACGTGACAA AAATTCAAAC AGCAGCAAAG TACAGTGAAA AGTCCTCCCT CATCCCCAGT 480 GCCCTCCCAC CCCAGGTAAT CACAGTTACC AGGATTCAAT GCACATCCAA ACACAAACAA 540 ACACAAACCA TGGTGTGTTT ATTGCCCATG GAGGCTCTGT CTCAGGTCCC TGGGAATCAT 600 TGGGAGTTGT GGATCCCAGC ACTTTGGGAG GCTGAGGCAG GAGGATCGCT TGAGCCCAGG 660 AGTTTTTTGA GACCAGCTTG AACAACATAG TGAGACCCCA TCTCTACAAA AAATTAAAAA 720 ATTAGCCAGG TGTGGCGGTC CATGCCGGTA GTCCCAGCTA CTTGGGAGGC TGAGGCAGGA 780 TGATCACTTG CACCTGGGAC GTTGAGGCGG CAGTGAGCCG TGTTCGCGCC ACTGCACTCC 840 AGCCTGGGTG ACACTGCAAG ACCCTGTCTC AAAAAAAGTA GTCAAGGAGG CTGAGAGCCA 900 GGAAGCCTCT GGCCAGCAGG TGAGCAGGCC CTTTCCTGCT GCTGTGCATT GTATTTAAGA 960 GAAAAGACAG ATACGTCTGA TACCTTCAAA GGTGTTCTTC ATACAGCAGG TTGCAACCTA 1020 TTAATAGATC ATAAAATCAG TTTAGTGTTT CATCATCATC ATCAAAAACC ACCACCAACA 1080 ACAAAAAGAC CCAGAACAGA TAGTGTAAAG AGTGCATCCC TGCATTCCTG TATAGGGAGA 1140 AATATGGTTT TGTGGAACCT TGTTGCGATG TAAAGTGTAC TTCTTAAGAT AAATACAGGG 1200 TTGAGGTTTT TGAAATAAAG TTTGAACAGG ACCACCTTAA GCCACAGTGT AGACTTTCCA 1260 TAGGCCAAAA CCTGGATCAC CAAGACAGTG TGCCCCAGGC TGCAGGCCAC ACTCCTGGGA 1320 GCCTCAGGCA ACCTTGTGCA GGCCTGACTT CGAGACACTC TGAGCATGAG CTGGTTCCTG 1380 GGTAGCCTCC CCTCTACCTC TCCCCGCTTG CCCTCCCTCC CTCCTTCTGC TCCTGTCTCT 1440 CCTCATCCCC TCCCCGAGTT GCTGCCTCCT CCTCCTCCTC CCCCACCACC TCTCCCCGTC 1500 TCCGAGTTGC CTGCCCCGCC CCCTCCTCTT CCCCCTGCCC CTCTCCGCGT CCTTCCCGCC 1560 TTCCCCCTCC TCGTCTCCCC CCTCCCCGCC CGCGCCGTCT GCGTCCCTCC CGGGCCCAGA 1620 CGCGGCGCGG TCAGGGGGCG CTGACTCACA GGCTGACTCA GCTGCAGGCG CGCTGCCAGG 1680 CGACGCAGCG GGCGGGTGGC CGGGCGCCGG CGGGCTCGCA GCCGGGCTGC TGGCAACGGT 1740 GCCGGCGGAG GTGGGGGCGT GGCGCGGGAT GGGCGGCGCG GGCCCTGCCG TGGTACCGCC 1800 TGGCAGCGTC CACCCCGCCG CTGGGGCGCC CTGGAGGCTC CTGGCCCTCC GTGGGGCCGT 1860 GACACCGGCG CTGCGGGGAG CGGTGGCCTC GCAGAGGCTG GGCATGGGAG GACGGCCGCC 1920 CCGGGTAAAG 1930
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