Tag | Content |
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EnhancerAtlas ID | HS092-24669 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr2:128163960-128165990 |
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: 3 | ID | Chromosome | Start | End |
GH02I127404 | chr2 | 128161977 | 128163977 | GH02I127407 | chr2 | 128164177 | 128164376 | GH02I127406 | chr2 | 128164514 | 128166975 |
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Enhancer Sequence | AAGAAAAGAA TTTGAATTGG GTACTAGGCA TAGTACCTGG GTGATGAAAT AATCTGTACC 60 ACAAACCCCC ATGATACAAG TTTACCTATA TAACAAACCT GCACATACAC CGTGAACCTA 120 AAACAAAAGT TTACCAAAAA AAAAAAAAAA AGAAAGAAAA GAAAAGAAAA AGAAAAAAAA 180 TTTCAAGACC TAGATCAGAA ATCAGCTCCT TGGCCAGGCA TACTGGCTCA TGCTTGAGCA 240 AGGCAGGAGG ATTGCTTGAG CCCAGGAATT TGAGACCAGC CTGGGCAATA CTGTGTGACT 300 TCATCTCAAA AAAAAAAAAA AAGGAAAAAA AATTATATAT AAAATAAAGC ATTCTGAGGC 360 TTCATCCACT CCTCACTCCT CAGAGAAGTA CTGAAGCTAG CTAGAGATTT CTGCAGGGTG 420 TGGAATGGGG AGAAAGGCAG CGTGACTGTG TGTCACATTT GTTTCTGACA CCTTTTTGTA 480 GGTCTGAAAT GCTTTTAAAT AAACATTTTT AAGTAATATA TACGTGACAA AAATTCAAAC 540 AGCAGCAAAG TACAGTGAAA AGTCCTCCCT CATCCCCAGT GCCCTCCCAC CCCAGGTAAT 600 CACAGTTACC AGGATTCAAT GCACATCCAA ACACAAACAA ACACAAACCA TGGTGTGTTT 660 ATTGCCCATG GAGGCTCTGT CTCAGGTCCC TGGGAATCAT TGGGAGTTGT GGATCCCAGC 720 ACTTTGGGAG GCTGAGGCAG GAGGATCGCT TGAGCCCAGG AGTTTTTTGA GACCAGCTTG 780 AACAACATAG TGAGACCCCA TCTCTACAAA AAATTAAAAA ATTAGCCAGG TGTGGCGGTC 840 CATGCCGGTA GTCCCAGCTA CTTGGGAGGC TGAGGCAGGA TGATCACTTG CACCTGGGAC 900 GTTGAGGCGG CAGTGAGCCG TGTTCGCGCC ACTGCACTCC AGCCTGGGTG ACACTGCAAG 960 ACCCTGTCTC AAAAAAAGTA GTCAAGGAGG CTGAGAGCCA GGAAGCCTCT GGCCAGCAGG 1020 TGAGCAGGCC CTTTCCTGCT GCTGTGCATT GTATTTAAGA GAAAAGACAG ATACGTCTGA 1080 TACCTTCAAA GGTGTTCTTC ATACAGCAGG TTGCAACCTA TTAATAGATC ATAAAATCAG 1140 TTTAGTGTTT CATCATCATC ATCAAAAACC ACCACCAACA ACAAAAAGAC CCAGAACAGA 1200 TAGTGTAAAG AGTGCATCCC TGCATTCCTG TATAGGGAGA AATATGGTTT TGTGGAACCT 1260 TGTTGCGATG TAAAGTGTAC TTCTTAAGAT AAATACAGGG TTGAGGTTTT TGAAATAAAG 1320 TTTGAACAGG ACCACCTTAA GCCACAGTGT AGACTTTCCA TAGGCCAAAA CCTGGATCAC 1380 CAAGACAGTG TGCCCCAGGC TGCAGGCCAC ACTCCTGGGA GCCTCAGGCA ACCTTGTGCA 1440 GGCCTGACTT CGAGACACTC TGAGCATGAG CTGGTTCCTG GGTAGCCTCC CCTCTACCTC 1500 TCCCCGCTTG CCCTCCCTCC CTCCTTCTGC TCCTGTCTCT CCTCATCCCC TCCCCGAGTT 1560 GCTGCCTCCT CCTCCTCCTC CCCCACCACC TCTCCCCGTC TCCGAGTTGC CTGCCCCGCC 1620 CCCTCCTCTT CCCCCTGCCC CTCTCCGCGT CCTTCCCGCC TTCCCCCTCC TCGTCTCCCC 1680 CCTCCCCGCC CGCGCCGTCT GCGTCCCTCC CGGGCCCAGA CGCGGCGCGG TCAGGGGGCG 1740 CTGACTCACA GGCTGACTCA GCTGCAGGCG CGCTGCCAGG CGACGCAGCG GGCGGGTGGC 1800 CGGGCGCCGG CGGGCTCGCA GCCGGGCTGC TGGCAACGGT GCCGGCGGAG GTGGGGGCGT 1860 GGCGCGGGAT GGGCGGCGCG GGCCCTGCCG TGGTACCGCC TGGCAGCGTC CACCCCGCCG 1920 CTGGGGCGCC CTGGAGGCTC CTGGCCCTCC GTGGGGCCGT GACACCGGCG CTGCGGGGAG 1980 CGGTGGCCTC GCAGAGGCTG GGCATGGGAG GACGGCCGCC CCGGGTAAAG 2030
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