Tag | Content |
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EnhancerAtlas ID | HS093-15492 |
Organism | Homo sapiens |
Tissue/cell | HL-60 |
Coordinate | chr19:34306760-34308280 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr19:34307056-34307067 | AGTGACTCATG | + | 6.14 | Lhx3 | MA0135.1 | chr19:34307654-34307667 | AAATAATTAATTA | - | 6.71 | Nr2f6(var.2) | MA0728.1 | chr19:34307422-34307437 | GAGGTCATGAGTTCA | + | 6.26 | RARA | MA0729.1 | chr19:34307422-34307440 | GAGGTCATGAGTTCAAGA | + | 6.12 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_26999 | chr19:34306604-34307479 | Esophagus |
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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 |
GH19I033816 | chr19 | 34307474 | 34308105 |
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Enhancer Sequence | CTGGTGTGGC TACTGAGTAG GACCTTAACA TCCCAAGTCC CAAATCCCAA AGCTTCCTGA 60 TTTGAGGACT GACCAGAGAG CAGCAGCGTT GTCTCTAGGC GCTCAGTGCA CATGCTGTTG 120 GCAGATCTGG CGGGGAAAAT GGTGCAGGCA TGGCCTCCCT TTACCTCTCC AGACCCCCAA 180 GCCTGGACTC AAGTGTTCAG GCTGTGATGA GCATGTTGCA CTACGTTGGT GTTGCATACA 240 TGTATATCTG TGGACCAAAC CACTAACATT CAAAAGAAGG AAAGTGGGCG GGTCACAGTG 300 ACTCATGCCT GTAATCCCAA CACTTTGGGA GGCTGAGGCG GGTGGATTGC TCCAGCACAG 360 GAGTTCAAAA CGAGCCTGGG CAATTTGGTG AGACCCCATC TCTACAAAAG AATTTAAAAA 420 TAAGCCACTC ATGGTGGCAT GTGCCTATAG TCCCAGCTAC TCAGGAGGCT GAGGTGGGAG 480 GATCACTTGA GTTCAGGAGG TTGAGGCTGC AGTGAGCCAT GTTCACACCA CTGCACTCCA 540 GCCTAGACAA CAGAGCAAGC CCCGTCTCAA AATAAATAAA ATTAAAAAGA GAAAGCATGG 600 CTGGGTGTGG TGGCTCACAC CTGTAATGCC AGCACTTTGG GGCCAAGGTG GGTGGATCCC 660 CTGAGGTCAT GAGTTCAAGA CCAGCCTGGC CAACATGGCA AAACCCCGTC TCTACTAAAA 720 ATACAAAAAA AAAAGGATTA GCTGGGTGTG CTGGCATGTG CCTGTAGTCC CAGCTACTCG 780 GGAGGCTGGG GCACGAGAAT CGCTTGAACC CGGGAGGCAG AAGTCGCAGT GAGCCGAGAT 840 CGCACCACTG CACTCTAGCC TGGCGACAGA GCGAGGCTCC ATCTTAAAAT AAAAAAATAA 900 TTAATTAAAA AAAAAGGGAA GCACAGATGT GAGAAATGGG GAAACTATAT CCATTGAGCC 960 ACTGACCAAG ATAATATTTA ACTTGACTAA GCCTAGCAGA GCCTGCCCAC TTCCCCTCCC 1020 TAGAGGCCAA CCCATGTTCT CGAGGCAATG CTGTCTGCCA AGATGGCCCC ATCCCATCAA 1080 GCCCTGCCTT CCCTCCTGAT TCTCCAGAGA CAGGAAAATG GCTGCATTGG CCCTGGAAGA 1140 TACTCAATTT CTCCTAAGTA GATGACAAGG TGGAAAATAC AAAAATGGGA AACTGCCAGG 1200 GGATATTCAG TTGGAGGCAG GAAATCTGCC TCAGTTCAAA ACAATAGGGA GGTCTAGACA 1260 GAGCTAGAGG GACAACTGAT GGCCAGAGAA GGCAGCCGCT GGCCTGGATG GAGTCTGACA 1320 TCTGGGCTGA TGTAGCTGTT GTAGGAAGTA GGATGTCACA GGTTGATGGC CATCTCAAGG 1380 GGGGTAGGCA ATGTGTTTAG CCACAAGGCT CAAGTCAGCC AAGTAATATT GGTCTTGTCA 1440 CATGTGTGAT GAGAATGTGG GTGGCTCTCT TTGCTCACCC CAACCCCGCC CAAAGGAGGA 1500 GTTTCCTTGT AGAGAGAGGG 1520
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