Tag | Content |
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EnhancerAtlas ID | HS052-02102 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr1:109370470-109373180 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr1:109370909-109370928 | TGGCCACCAGGTGGCGTCA | + | 7.66 | FOSL2 | MA0478.1 | chr1:109372116-109372127 | GGATGACTCAG | + | 6.32 | Foxd3 | MA0041.1 | chr1:109370709-109370721 | AAACAAACAAAC | - | 6.32 | Foxd3 | MA0041.1 | chr1:109370713-109370725 | AAACAAACAAAC | - | 6.32 | Foxd3 | MA0041.1 | chr1:109370717-109370729 | AAACAAACAAAC | - | 6.32 | Foxd3 | MA0041.1 | chr1:109370721-109370733 | AAACAAACAAAC | - | 6.32 | Foxd3 | MA0041.1 | chr1:109370725-109370737 | AAACAAACAAAC | - | 6.32 | Foxd3 | MA0041.1 | chr1:109370729-109370741 | AAACAAACAAAC | - | 6.32 | JUNB | MA0490.1 | chr1:109372116-109372127 | GGATGACTCAG | + | 6.14 | Nkx2-5(var.2) | MA0503.1 | chr1:109372001-109372012 | CTTGAGTGCTT | - | 6.02 | Nr5a2 | MA0505.1 | chr1:109370665-109370680 | GAGTTCAAGGTCAGC | + | 8.73 | SOX10 | MA0442.2 | chr1:109372564-109372575 | AAAACAAAGGA | + | 6.32 | Sox3 | MA0514.1 | chr1:109372564-109372574 | AAAACAAAGG | - | 6.02 | TCF3 | MA0522.2 | chr1:109372398-109372408 | AACACCTGCT | + | 6.02 | ZNF143 | MA0088.2 | chr1:109372298-109372314 | TTCCCACAATGGAATG | + | 6.01 |
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| Number of super-enhancer constituents: 9 | ID | Coordinate | Tissue/cell |
SE_30391 | chr1:109370337-109374495 | Fetal_Muscle | SE_36681 | chr1:109370360-109373490 | HMEC | SE_37339 | chr1:109370071-109375258 | HSMMtube | SE_44724 | chr1:109370379-109375021 | NHDF-Ad | SE_44981 | chr1:109370319-109374859 | NHLF | SE_46396 | chr1:109370357-109374983 | Osteoblasts | SE_52099 | chr1:109370333-109374370 | Skeletal_Muscle_Myoblast | SE_63886 | chr1:109370319-109374573 | HSMM | SE_65077 | chr1:109370440-109375164 | NHEK |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 109371058 | 109371477 | chr1 | 109370643 | 109372061 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I108827 | chr1 | 109370415 | 109375263 |
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Enhancer Sequence | AAAATAAATG TTTTGTTCTG CCGAGGTTAA TATCTAATCA TCACATACAC ATTCACAAAA 60 CACATTTGAA GTATGGAATT ATAAAATTTG GAGTTTTCCT CATGCATCAA AATCCATTCC 120 AGGCTGGGTA TGGTGGCTCA TGCCTGTAAT CCCAGCACTT TGGGAGGCCA AGGAGGGTGG 180 ATGGCTTGAG ACTAGGAGTT CAAGGTCAGC CAGGGCAACA TGGCAAAACC TCATCTCAAA 240 AACAAACAAA CAAACAAACA AACAAACAAA CAGTTCCTAC CAGGGGAAGA AACTATGCTA 300 TACGTCAGTA ATGGGTCACG TAGCTTTGGT CCTGGAAGTA CAAGCTGATT ACATCCAACA 360 ACTCCAGCAA AGTGGGCTTT GCCGGGTGTC TGTGGGACTA AAGGCTGAGG GAGCACGTGA 420 AGGTGATTTT AGTTGCACAT GGCCACCAGG TGGCGTCAGA AAGAAGCAAC TGCAATGGAC 480 ATTGTTCAGG AGCCTTCCTG TGGCCCACCT GCAGCTTCCT CCCTCCTCCT CAGAAATCCC 540 AACTCCTCCA AAGGAATTCG AATTAATAAC AGTTCTGAAC AAAGCTCTTG CTAAGCTCCT 600 GGGATACAGT CATAGCCCCC AGGGAAAGTT GTTCATTCTT AGTATGGAAG GCACTGTGCC 660 CGAGATATCC TGGCATAAAT GAGGCAGATT GCCCAGGGCT AGGGTTTGAG CCCAAGGCAT 720 TGCTGGGCAA ACACATGCTC GCCGCGCTGT GCCCTGGCCT GCTGTTGGCG GAGAAGGGAT 780 GGGGCTGCGG GTTTGTGGGG CTGGGGCTGA GAAGCCAGGC TCTTTCCCTC CTCTTGGAAA 840 AACATGCTGT CCTCTTGAGT CACATATTTT CTCACACCTC ATTTTCTGTC TCCACCCTTC 900 TCCTCTGGGG CATTTGAACA TCTGCTCTCC AAAGTGGGAA ACTTGGATCT CACTCAAGTG 960 CATGCAGTCC AACACAGGAC TTTTTCTGCT TTTAAACTCC TTTGTGTACT CAAATCTTCT 1020 GGCCAAACAT AATTCCTCTG GAGAAGACAG TTTTTCAACA AGACAAAGCA GCTAAAGTAC 1080 ACACTTAAAT CCAAAGTTTT GCATCAGAAA TAACATAAAG GGATAAGCAT ATTTTACATT 1140 TTATACATAT GTAATTTATC CACTTATATA TAAACAATTT ACAAATATCC TGAAAACAGT 1200 ATGTACCTCA GCAAGCTTCA TAAAGGACAA GTCCCATCAG AGAGAGATTT AATCTTCTAA 1260 CAGAAAGAAT ATATAGTCCT CCCTTCAATC AATAATTCCT CAGGGATTAT GTAAGTTACA 1320 AGATTTTAAT TCATAAGTCA TGTGTATCTT CTCATCACTC CCCAGCAGTG GATTCACTGT 1380 GAGATTTGAT TTTACACTTG GTTGTGCTTG TCTTTCCAGC TTGTCTATCA TAAAAAAGTA 1440 TTATTTAGTC TGGAACATTG GTCCCTGTCT TGGTACTTAA TGTACTTCTG TAGGGTCTAG 1500 ACTAGGAATT TAGAAGAGAG AAATTTAGTA CCTTGAGTGC TTAATAAAAA TGGTTCTTTA 1560 ATGTCAAAAT ACTTTCATTA TACTTAGTAA AACCTTTAAA AATCCAAAAT TAGACTTTAA 1620 TTCAATAAAT AAAAATAGTA GGCCTGGGAT GACTCAGTGA GTAAGCTTCA TGAGTGCCCC 1680 TTGGATTAAA GGGCAGCTCA AAGCTGATGA CTGACATGGT GGTTTAATGA CCCACACACA 1740 ATGACACATG ACCATTTTTA GCACGAGCTT CATGCAGTTT CTTTTTTCAG GGGTGGACAC 1800 TCATTAGAAC TCTTAAGGCA GGTGCCCATT CCCACAATGG AATGCTTTCT AACAGGAAGC 1860 CTCAGTCTTT CAGACCCTGT CATCTGCTTC TATTAGAATC CATTACGTAC ATATAACAGT 1920 GGTTGCTAAA CACCTGCTGC CTCCCTGACT CTTGACCTTC CAAAGGTCAA TGAGCCGAGC 1980 TTTGGCCGGA GTCCACAGTG AGCTTAGAGG TAACATCTCT CGCTACCTGA AAGAAGCTTC 2040 AAATAAATGA TACTGAATCG ACACAGATTA ATAGTTGCAC CAATGGGTGT TTCAAAAACA 2100 AAGGATTTCT CCTGAGGATT TTACATGATT TACAGCTTGT TAGCTCTGGA AGATTTCGTC 2160 CTTAGGAATG GGAAGAAATC AGCCCTGAGA AGAGGGATGA GGCTTGTTCC TGGGACTGGG 2220 GGGCTCAGGT GAAACCCAAC AGAGAAGACT TTTGCTCATC ATAAGGAGAG AGTAGGGATG 2280 GTGGGAGCTG TTTGTTATAC AGGATAAGAA TCCCCCATGT GGGCAATGAT CAAAAGCCTA 2340 CAGGACCACC CTCCGTGGGC TGTAACCATG ATTCTTAACC AAGGGGGCTT ATCGGAATCA 2400 CCTGGGGAGA TTTAAAAGCA ATATTCCTAC CAGAGCCCCA CCGCTGGCGA TGCTGAGACA 2460 GTAGGTGGGA TGGAGGCATG TGCATGATTG TAAAATCTCC CATGGTGATT TTGATGGTCT 2520 CCCCAGTTGA GGACCACTGC TAGAGGATCT GTAGGGTGCG AGGGAGGCTG GGCTCTGTGC 2580 CCAGGCCTGA GATCTGTGAC TCTATAACTC AGCCAGTGGC CTCAGTTAGT TGCCGCCCAC 2640 TCTCACTGGA GTTACTATGC CAGGACTGAC TCCAATCCAC CCTGGGAATG TAGCCACAAG 2700 AAGCCCTCAC 2710
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