Tag | Content |
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EnhancerAtlas ID | HS109-00221 |
Organism | Homo sapiens |
Tissue/cell | Kasumi-1 |
Coordinate | chr1:17757940-17759320 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr1:17758006-17758027 | AAAAAAAAAAAGAAAGAAAGA | - | 6.25 | Nr2f6(var.2) | MA0728.1 | chr1:17757946-17757961 | GAGGTCAGGAGTTCA | + | 6.22 | SPI1 | MA0080.4 | chr1:17758296-17758310 | GAAAAGGGGAAGTG | + | 6.64 | SPIB | MA0081.2 | chr1:17758298-17758310 | AAAGGGGAAGTG | + | 6.07 | SREBF2 | MA0596.1 | chr1:17758078-17758088 | ATCACCCCAT | - | 6.02 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_68792 | chr1:17757864-17759558 | H9 |
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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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Enhancer Sequence | TCACCTGAGG TCAGGAGTTC AAGACCAACC ATGGTGACAA AGCCAGCCCT GTCTCAAAAA 60 AAAAAAAAAA AAAAAAAGAA AGAAAGAAAA AGAAAAAAGG GCAGCTCCAG GCCCAATCAT 120 TCTAACCTCT ACAGTGTGAT CACCCCATGG GTATGCTTTG GCAGTACGGC TCACGCATTT 180 CTAAGATTAC ACATCTTCAT GACGGATGAT TTCCACTTCA ATAGGAACCT TTACACGACC 240 CAAACCTGAT TAGGGCGTCC CCCAAGATAT AGGTTCCGTC ACGCTTGCCC ACTCCACCAC 300 ATTATGTAAC AGGAAAAAGA TGGTCAATCT ACAGGAATGC ATCCTGCAGT CCTCATGAAA 360 AGGGGAAGTG AGGCCAGCCG CGGTAGCTCA TGGCCCGTCA TCCCAGCACT TTGGGAGGCC 420 AAAGTGGGTG GATCACCTGC GGTCAGGAGT TTGAGACCAG CCTGGCCAAC ATGGTGAAAC 480 CCTGTCTCTA CTAAAAATAC AAAAAATTAG CCGGGTGTCT GTAATCCCAG CTACTTGGGA 540 AGCTGAGGCA AGAGAATCGC TTGAACCCAG GAGGCAGAGG TTGCAGCGAG CCGAGATCAC 600 ACCATTGCAC TCCAGCCTGG GCAACAAGAG CGAAACTCTG TCTCAAAAAG AGAAAAAAAA 660 AGTTGGGGGG AGGGAAGTGA AACAACACGG AAAGGGAGAA CAACTTTGGT TCATTTAAAT 720 TATTTAGAAA ATGACCTTAA TCAGAGGGTG GCCCAGCCCC TGCAGCACCC ACAACTCAGG 780 TTACTTGAAT TGGAGCCTAG CTTCCCCTGG TTATCTGCCC TTCTTTGTTT AACTGGCAGG 840 CCTGGCTGGA ATATGCTACA GGTCTATATT CAATGGCTTC TGTTGAAGTC CCTGTGGAAG 900 GAGAGGCCTC TGGGTCCTCT GCCCAAGCCT ACCAAGTTGG CATGGAGGGG GCAGTAGAGA 960 CCCAGGAAGG GTGCTAAGGC ACTGGAGACC AAGCTCCCAG GCCAGAGGGC AAGCCTAGAA 1020 AAGAGCCCTG GAATGCCAGC AACTGCAGAC CAGGCAGGCG GAGGTTCATG GGCACCTGTG 1080 CTCAGTATGA ACCATTGAAG TCAAACCACC CTACACTGAG ATGCAACCAC TGCAGCAAAA 1140 CTTCACAGTG CTGAGGCCAC ACCAGAAGCC TCAGCTCCAT CAGGCCAGAG GGCATGGTTC 1200 AGGGGCAAGT TCAGACAGCC AGAGCTTAAC CGCAGTGGCC TTGGCCTTGG GGAGGGAGTT 1260 TCCTGGGTGA CCTGGACATT TGGTCAAGGG CTCATGAAGA CTGATCCATC AAGCTAGCTA 1320 AGCATTTATA GGCAAACCCA ACCACGCCAA TAAAAATGTA TTTGTGGGCC GGGCATGGTG 1380
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