Tag | Content |
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EnhancerAtlas ID | HS053-02177 |
Organism | Homo sapiens |
Tissue/cell | Foreskin_keratinocyte |
Coordinate | chr1:109370100-109373180 |
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 | CAAGAAATTG CACCCCAGCA CAATTTGGCC TGATAAGAAA ATGTATACAA GACAGGCCAG 60 GCGCGGTGGC TCACGCCTGT AATCCCAGCA CTTTGGGAGG CTGAGGCGGG CGGATCACGA 120 GGTCAGGAGA TCGAGACCAT CCTGGCTAAC ACGGTGAAAC CCTGTCTCTA CTAAAAGTAC 180 AAAAAATTAG CTGGGCGCCG TAGTGGGTGC CTGTAGTCCC AGCTACTCGG GAGGCTGAGG 240 CAGGAGAATG GCGGGAACCC GGGAGGCGGA GCTTGCAGTG AGCCGAGATC GCGCCACTGC 300 ACTCCAGCCT GGGTGACAGA GCGAGACTCC TACTCAAAAA AAAAAAAAAG AAAATGTATA 360 CAAGACATGA AAAATAAATG TTTTGTTCTG CCGAGGTTAA TATCTAATCA TCACATACAC 420 ATTCACAAAA CACATTTGAA GTATGGAATT ATAAAATTTG GAGTTTTCCT CATGCATCAA 480 AATCCATTCC AGGCTGGGTA TGGTGGCTCA TGCCTGTAAT CCCAGCACTT TGGGAGGCCA 540 AGGAGGGTGG ATGGCTTGAG ACTAGGAGTT CAAGGTCAGC CAGGGCAACA TGGCAAAACC 600 TCATCTCAAA AACAAACAAA CAAACAAACA AACAAACAAA CAGTTCCTAC CAGGGGAAGA 660 AACTATGCTA TACGTCAGTA ATGGGTCACG TAGCTTTGGT CCTGGAAGTA CAAGCTGATT 720 ACATCCAACA ACTCCAGCAA AGTGGGCTTT GCCGGGTGTC TGTGGGACTA AAGGCTGAGG 780 GAGCACGTGA AGGTGATTTT AGTTGCACAT GGCCACCAGG TGGCGTCAGA AAGAAGCAAC 840 TGCAATGGAC ATTGTTCAGG AGCCTTCCTG TGGCCCACCT GCAGCTTCCT CCCTCCTCCT 900 CAGAAATCCC AACTCCTCCA AAGGAATTCG AATTAATAAC AGTTCTGAAC AAAGCTCTTG 960 CTAAGCTCCT GGGATACAGT CATAGCCCCC AGGGAAAGTT GTTCATTCTT AGTATGGAAG 1020 GCACTGTGCC CGAGATATCC TGGCATAAAT GAGGCAGATT GCCCAGGGCT AGGGTTTGAG 1080 CCCAAGGCAT TGCTGGGCAA ACACATGCTC GCCGCGCTGT GCCCTGGCCT GCTGTTGGCG 1140 GAGAAGGGAT GGGGCTGCGG GTTTGTGGGG CTGGGGCTGA GAAGCCAGGC TCTTTCCCTC 1200 CTCTTGGAAA AACATGCTGT CCTCTTGAGT CACATATTTT CTCACACCTC ATTTTCTGTC 1260 TCCACCCTTC TCCTCTGGGG CATTTGAACA TCTGCTCTCC AAAGTGGGAA ACTTGGATCT 1320 CACTCAAGTG CATGCAGTCC AACACAGGAC TTTTTCTGCT TTTAAACTCC TTTGTGTACT 1380 CAAATCTTCT GGCCAAACAT AATTCCTCTG GAGAAGACAG TTTTTCAACA AGACAAAGCA 1440 GCTAAAGTAC ACACTTAAAT CCAAAGTTTT GCATCAGAAA TAACATAAAG GGATAAGCAT 1500 ATTTTACATT TTATACATAT GTAATTTATC CACTTATATA TAAACAATTT ACAAATATCC 1560 TGAAAACAGT ATGTACCTCA GCAAGCTTCA TAAAGGACAA GTCCCATCAG AGAGAGATTT 1620 AATCTTCTAA CAGAAAGAAT ATATAGTCCT CCCTTCAATC AATAATTCCT CAGGGATTAT 1680 GTAAGTTACA AGATTTTAAT TCATAAGTCA TGTGTATCTT CTCATCACTC CCCAGCAGTG 1740 GATTCACTGT GAGATTTGAT TTTACACTTG GTTGTGCTTG TCTTTCCAGC TTGTCTATCA 1800 TAAAAAAGTA TTATTTAGTC TGGAACATTG GTCCCTGTCT TGGTACTTAA TGTACTTCTG 1860 TAGGGTCTAG ACTAGGAATT TAGAAGAGAG AAATTTAGTA CCTTGAGTGC TTAATAAAAA 1920 TGGTTCTTTA ATGTCAAAAT ACTTTCATTA TACTTAGTAA AACCTTTAAA AATCCAAAAT 1980 TAGACTTTAA TTCAATAAAT AAAAATAGTA GGCCTGGGAT GACTCAGTGA GTAAGCTTCA 2040 TGAGTGCCCC TTGGATTAAA GGGCAGCTCA AAGCTGATGA CTGACATGGT GGTTTAATGA 2100 CCCACACACA ATGACACATG ACCATTTTTA GCACGAGCTT CATGCAGTTT CTTTTTTCAG 2160 GGGTGGACAC TCATTAGAAC TCTTAAGGCA GGTGCCCATT CCCACAATGG AATGCTTTCT 2220 AACAGGAAGC CTCAGTCTTT CAGACCCTGT CATCTGCTTC TATTAGAATC CATTACGTAC 2280 ATATAACAGT GGTTGCTAAA CACCTGCTGC CTCCCTGACT CTTGACCTTC CAAAGGTCAA 2340 TGAGCCGAGC TTTGGCCGGA GTCCACAGTG AGCTTAGAGG TAACATCTCT CGCTACCTGA 2400 AAGAAGCTTC AAATAAATGA TACTGAATCG ACACAGATTA ATAGTTGCAC CAATGGGTGT 2460 TTCAAAAACA AAGGATTTCT CCTGAGGATT TTACATGATT TACAGCTTGT TAGCTCTGGA 2520 AGATTTCGTC CTTAGGAATG GGAAGAAATC AGCCCTGAGA AGAGGGATGA GGCTTGTTCC 2580 TGGGACTGGG GGGCTCAGGT GAAACCCAAC AGAGAAGACT TTTGCTCATC ATAAGGAGAG 2640 AGTAGGGATG GTGGGAGCTG TTTGTTATAC AGGATAAGAA TCCCCCATGT GGGCAATGAT 2700 CAAAAGCCTA CAGGACCACC CTCCGTGGGC TGTAACCATG ATTCTTAACC AAGGGGGCTT 2760 ATCGGAATCA CCTGGGGAGA TTTAAAAGCA ATATTCCTAC CAGAGCCCCA CCGCTGGCGA 2820 TGCTGAGACA GTAGGTGGGA TGGAGGCATG TGCATGATTG TAAAATCTCC CATGGTGATT 2880 TTGATGGTCT CCCCAGTTGA GGACCACTGC TAGAGGATCT GTAGGGTGCG AGGGAGGCTG 2940 GGCTCTGTGC CCAGGCCTGA GATCTGTGAC TCTATAACTC AGCCAGTGGC CTCAGTTAGT 3000 TGCCGCCCAC TCTCACTGGA GTTACTATGC CAGGACTGAC TCCAATCCAC CCTGGGAATG 3060 TAGCCACAAG AAGCCCTCAC 3080
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