Tag | Content |
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EnhancerAtlas ID | HS017-02276 |
Organism | Homo sapiens |
Tissue/cell | CD14+_monocyte |
Coordinate | chr1:161699480-161700750 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr1:161699848-161699863 | TGAACTCCTGACCTC | - | 6.22 | TBX21 | MA0690.1 | chr1:161700095-161700105 | TTCACACCTT | - | 6.02 | TBX2 | MA0688.1 | chr1:161700094-161700105 | ATTCACACCTT | - | 6.02 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_56629 | chr1:161698532-161702049 | u87 | SE_58760 | chr1:161674084-161711741 | Ly1 | SE_59497 | chr1:161674276-161714796 | Ly3 | SE_61570 | chr1:161674449-161712145 | Toledo |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I161729 | chr1 | 161699268 | 161701012 |
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Enhancer Sequence | CTTTGTGGCT CTGATTTCCA GCTTTCTGAT GCAGGCTCAT CTCACTTCTC AGAACTCTCT 60 TCCAAGGCCA CCTTTCCTAG CTAACTGCAC TCTATTTCAG TGCCCAGGCT CTTTTCCCCT 120 TCTGATTTTG TTTCCCTGAG ATTTCTGCTT TTTTTTTTTT TTTTTTTTTT TGAGACGGAG 180 TCTCACATCT CACTCTGTCA CCCAGGCTGG AGCAATCTCA GCTCATTGCA ACCTCCGCCT 240 CCCAGGTTCA AGTGATTCTT CCACCTCAGC CTCCCCAGTA GCTGGGATTA CAGGCACCTG 300 CCATCATGCC AGGCTAATTT TTGTATTTTT GTAGAGACGG GGTTTCACCG TGTTGGCCAG 360 GCTGGTCTTG AACTCCTGAC CTCAGGTGAT CCACCTGCCT CAGCCTCCCA AAGTGCAGGG 420 ATTACAGGCT TGGGCCACCG CGCCCGGCCG GTTTCTGCCA TCTTGATATA GACAGGAAGT 480 GACTAACATT AGTGGCAAGA GGCTTAGTAA TCAAAGAATC TCAGGTCATT TAAAAAATCA 540 GTTGATCATT TTTTAAGAGT ACAAAAAAGA GAAATAGTTA CTCAAAGGAG AGCTAGGGCA 600 GCAGTATCTC TTTCATTCAC ACCTTTTTGG CAACATCAAC ATCCTTGTTC TTGTTTTGCC 660 ATCTACTTCC ATTTAGAACT AGGATGCGGG GGGATGGGGA AGAACAAGGA CTTTTTGGTG 720 AGAGTGAAAA TCATTCATGA CTCAACTTTC TGGTGTAGGG GAGAGGAATT GACTCATATG 780 GCCTGTAGAC TCCACTGTCT TCTTCGTGTA CCCCAGCTTT TAAGAGGAGG GCAGGATCAA 840 GATGATCTTC TAAGATATCT GTTATTGATC TCCCAGGAAG ACCTGCATTA AGGAAATATC 900 AGCTTCATCT TCATCCCTTT TGTTTGAGGT TCCTACATGC ATTTAGGGAA ACCAGAAGGC 960 TAGCTAGCCC AGGTTGTCCA AGGGGACTCT CAGAGCTCAT TCCCAAACAG CAGGGATGGC 1020 AGAAAAATGC TGGAGAAACC TAGGGAGGAA TCTGCTTCTC TCTGATACTC TGATCAGTTT 1080 GGTGTCTCAG ACTTAGGCTG CAAACCCTAA TCCTGCGGCT GTCCATAGCA GATGCCAGAC 1140 AAGGAACCCC AATGTCCGCT ATCAGAGAGC AGAAAAAATT CTGTCGCATT CCCTTTGGAT 1200 TTCAGCCTTA CTCTTTAAAC TGTTCTCCTT GAGTCTCAGT TTTTACTTGA CCTTACACTA 1260 TGAAAGGGGG 1270
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