Tag | Content |
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EnhancerAtlas ID | HS136-02931 |
Organism | Homo sapiens |
Tissue/cell | Monocyte |
Coordinate | chr10:112184830-112187440 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr10:112187417-112187435 | TCTTTTTTCCTTCCTTCC | - | 6.79 | EWSR1-FLI1 | MA0149.1 | chr10:112187345-112187363 | CCTTCCTTTCTTTCTTTC | - | 7.02 | EWSR1-FLI1 | MA0149.1 | chr10:112187421-112187439 | TTTTCCTTCCTTCCTTTC | - | 7.66 | EWSR1-FLI1 | MA0149.1 | chr10:112187333-112187351 | TTCTCCTTCCTTCCTTCC | - | 7.67 | EWSR1-FLI1 | MA0149.1 | chr10:112187341-112187359 | CCTTCCTTCCTTTCTTTC | - | 8.57 | EWSR1-FLI1 | MA0149.1 | chr10:112187337-112187355 | CCTTCCTTCCTTCCTTTC | - | 9.6 | Foxa2 | MA0047.2 | chr10:112186112-112186124 | TGTTTACATAGT | + | 6.22 | HSF1 | MA0486.2 | chr10:112185565-112185578 | TTCTGGAATATTC | + | 6.48 | NEUROD2 | MA0668.1 | chr10:112186088-112186098 | ACCATATGGC | - | 6.02 | Nfe2l2 | MA0150.2 | chr10:112185808-112185823 | CACTCTGACTCAGCA | + | 6.15 | RREB1 | MA0073.1 | chr10:112185951-112185971 | GTGAAGGGGTTGGTTTGGTG | - | 6.17 | Sox3 | MA0514.1 | chr10:112186793-112186803 | AAAACAAAGG | - | 6.02 | TEAD1 | MA0090.2 | chr10:112186900-112186910 | CACATTCCAT | + | 6.02 | ZNF263 | MA0528.1 | chr10:112187333-112187354 | TTCTCCTTCCTTCCTTCCTTT | - | 6.07 |
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| Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
SE_34624 | chr10:112166474-112192739 | HeLa | SE_43727 | chr10:112179907-112185396 | MM1S | SE_45114 | chr10:112184850-112187468 | NHLF | SE_46227 | chr10:112184707-112187511 | Osteoblasts | SE_56435 | chr10:112185126-112187495 | u87 | SE_65942 | chr10:112186095-112187812 | Pancreatic_islets | SE_67385 | chr10:112179907-112185396 | MM1S | SE_67956 | chr10:112185126-112187495 | u87 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr10 | 112185759 | 112186089 | chr10 | 112186754 | 112186909 |
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| Number: 1 | ID | Chromosome | Start | End |
GH10I110424 | chr10 | 112184569 | 112187494 |
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Enhancer Sequence | ATCTCTTAAA ATTAGCACAT ACTATATATG ATGAACACCC CCTCCCAAAT AAATATGAAA 60 GGGGCTGGAA GGGGTCAGGT GGTCAACTCT CTCCAAGGTG CAACCAGAGG TAGCTGAGAC 120 TAACATGACA TAGGTCCCTG TTGGAGGACG ATGTCCCCAG TAAACCCAAA TTAATTGAGT 180 GACACCATAA AAAAACAGAA TAGGGAGGAG TGGGGAAGAC CAGTCCCTTT CCTTGTGTCC 240 AGGGATCCCA CCCATCTACA CCTCCATCCT CCAGTGCCTG GCTAAGGCCC TCCTTAGTGC 300 CCGGGCACAG ACTGTGCTCT TCGGAGATGG CTCAAGTGGG CTGTGTGCTT AGGGAGATGG 360 GGCACATGAC TGTTAACTAC TTTAAAAGTC CTCAATGGGT TTTTTGTTGT TTCTGTTTTT 420 GAGATGGAGT TTTGCTCTTG TTGCCCAGGC TGGAGTGCAA TGGCGTGACC TCAGCAACCT 480 GCAACGTCCG CCTCCCAGAT TCAAGGGATT CTCCTACCTC AGCCTCCCAA GTAGCTGGGA 540 TTACAGGTGT CTGCCACCAC ACCCAGCTAA TTTTTTGTAT TTTTAGTAGA GATGGGGTTT 600 CACCATGTTG GTCAGGCTGG TCTCGAACTT CTGACCTCAG GTGATCCACC CTCCTCGGCC 660 TCCCAAAGTG TTGAAATTAC AGGCGTGAGC CACCGTGCCC GACCCTGAAT GTTTCTGAAG 720 CATGCTGTTT CTTCATTCTG GAATATTCAC TAAAAGAGCC CCTACGAATA ATTAACCCAG 780 TAGTAATAAT AATGCCCACC ATTTGTCATT CTTTCTATGT GCTCTGTACA TTACACGTGC 840 ATCTCAGTTT ATCCCAATCA GTAGGCGGTT CCATCCTTCA ATTTCATTTT ACAAATGAAG 900 AAACCAAAGC TCACAGGGGA CATGTAACTT GCCGAAGTTC ACATAGCCAC AGAGGGCAGA 960 AGCTGAATTC AAACCACTCA CTCTGACTCA GCATCCACCT CAGAGCAGCC ATTCAGTGGC 1020 CTCTTGTGAC ACATAAAGCA AGAAGATACC AGTGAGTTTT TGGACCATGT CTTCTTGGTA 1080 AAGTTACCAT TAGTCTGACC ACAGATGTTT CTCAAGAAGC AGTGAAGGGG TTGGTTTGGT 1140 GATGTCAGTG GCCGGGGTCA GATGAACCAA ACCATTGCTA GGCTGTGATG TCTGAGGCTG 1200 CCCACGAACT GGTTATTGCC CAGATTTAAA AGAAAGGTGG AAAAAATTAT CCTAGTCTAC 1260 CATATGGCTC AGCCAGCCAT AGTGTTTACA TAGTCAGAAA AGGTCAACAC AGAATAGCGA 1320 TATAATCAAA ATTACCCTCT ACGGTGTGGC TGTATTGGGA AGAGAGAGGC GGGGGTGGGT 1380 GTGAGGCAAC AGGAGCTAAA AGAACTCCTG GTCTCCCAGG GCAGGAAATC AAGAAAAAAC 1440 TCCTAAAACT ACACAGATCA AGAAGAAACT ATGTGAGATG TTATTTAGAG ACATGAAAGT 1500 GAACATTCCA AAGAATCCGT TTCAAGAGTC GAAAGTGGCC ACCCTGGAGA TGGGTCAGGG 1560 CTGCAGTTGT TCATGACTAA CTTTGTACAT TTCTGAGAAA TCTATGCTTA TGTGTAACTT 1620 CTCTTAAAAT AAAAAATTTA ATAAAATCCA AAGCAAAAAC AAACAGAGCA ATTCTGGCCC 1680 CATTTGGGGA GGGAGTGGGC TGTGATTACG AGAATGAGGG CCCAGCGGGT GGGGATTCCT 1740 CTGTCAGGCA TGCAACGGGA AGCTGGTGGG GTCTTGGCAA GGCTTTGGTG GAGAGACGTC 1800 ATTGGAATGG TGACCTCATT TGGAACCGGT GAGGGCAGGA GAAGGTAGAA GGGTTAAAAA 1860 GAAGAAGAAC CACCAAAGGA GAAGAAAAGG AAGCCTGGTC ATTCTACAGC CAAGGTCATA 1920 CTCCCAGGAG ACCTACGGCC TTTTGTCGGG GTTACACAAA TGTAAAACAA AGGTGTGGTC 1980 TCTCCACTAA ATGGGGAAGT TTCCACCAGG AGGCCAGTGT GTCATTGAGT AATGTGAATA 2040 GTGGAACCCA TCCCCAGCTA GTCAGGCCCA CACATTCCAT ACCAGGACCC ACGGGCCTCG 2100 GGGGTAGAGG CAGGAAGGTA GCATTTGTCT ATTGTGAGAA CAAGCAGCTT ATGTAGACAT 2160 CAAAGGTCTC AGGATAGCGT ATATTCTTCC AGATCTGTGA GGCCCAAACA CACACACATG 2220 GAGGAGGATC CCAGGGTCTC AGCCCCTCCC CAGATTCTCA AGACTCAGGC CTTGTCCCCT 2280 CTCCCATGGG GGTCCTATTG AAAGGAATCC AGAGACCCTG GGAGAATCTG AGTAGGAAGA 2340 GGGAACTGGA CTTACTGCCA TAGGCCCAGG CCTGGGTCAG GACTGTGTCT CTCTGGAAAA 2400 GCCACTCTCT TGGGAACTGA GAAAGCCCAG AGCTTGGGCC CAGAGCAGCC CAGGCCTTGA 2460 CTGGCCTGCC TGTTCCGTCC TCCTGTCTTC TCCAGGAAGC ATTTTCTCCT TCCTTCCTTC 2520 CTTTCTTTCT TTCTTTCTTT CTTTCTTTCT TTCTTTCTTT CTTTCTTTCT TTCTTTCTTT 2580 CTTTCTTTCT TTTTTCCTTC CTTCCTTTCT 2610
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