Tag | Content |
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EnhancerAtlas ID | HS193-03034 |
Organism | Homo sapiens |
Tissue/cell | U87 |
Coordinate | chr1:212840620-212842190 |
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) |
BCL6B | MA0731.1 | chr1:212840971-212840988 | TGAGTTCCTGGAAAACA | - | 6.28 | FOXC1 | MA0032.2 | chr1:212841789-212841800 | TATGTAAATAT | + | 6.62 | POU2F2 | MA0507.1 | chr1:212840708-212840721 | ATATGCAAATGAA | - | 7.82 | RREB1 | MA0073.1 | chr1:212840729-212840749 | GGTGTGAGGGTGGCTTGGGG | - | 6.51 |
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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 | TTAACCGTCC AATTTATTCA ATTCTGCCAG AGGGCCCCCT GCTGAAGCTG TTCACAGATT 60 GCTCTGATAT CATTAAAAAG CTAACCACAT ATGCAAATGA AGTGTTGGAG GTGTGAGGGT 120 GGCTTGGGGT AGACAGTGCT TCTGGTTCAT CTAGGAAGGC TTCCTGGTGG GGGAAGGGGA 180 GGGGCTGAAG TTGTCATTGA AAAGGATGGA GTTTGATACA ATGAGGGGGG TGGTGTGGTT 240 TTAGGCCATA ACCCTCCCTT TCCTGGGGCA GGTCCTCACA TGAGTCATTC CAGAGTTCCC 300 TTGCTGGTCA GTGGGAACAT TCTAGTGTGT GACATCTCCC TGGCAACAAG CTGAGTTCCT 360 GGAAAACAAC AATCACAGAG AGACAGTCCA CCACCTCTAC CCTCTTAACT CTTCCTTAGA 420 AATCCTACTG TCTGCAGCTG GGAATGAATG GAATGAAGGT CAAGGATGAA GTAATAACCA 480 AATATTGGGT TTTGGGTGCC CTGGTAACTG TCCGGTTTCC AGTTAGGGTT CCTGGGTGAC 540 ATCTTCCTTC TGGGGGAAGA CAGAGTCAAA TGAGAAACGT GAGTTGAGCC CAGGGGAAAG 600 GATCATCCGG GAGATGCCTG AGGGGCTCCA GGGCATCGTA ATCTCTTGCT CAGCTGGCAG 660 AGTGGGGCTG ACACGGCCAG CTGCTCTCTG GAGTCCTCGG CCTTCCTGTT TCCCCCTGAG 720 GACTTTGAGT GGGGAATCTA AACCATATGT CTCTGATTCA TTTACTGTGA ACTCATCAAG 780 TTGCTGTTTG GCAAGAGTCC TTGGATGTCT CGGAAGAGCT TTTGGTTTGG TTTCATTTGT 840 TCTTTCTAGT GCTTTTCCTT TGAAATAGGA AGTTTATGTT TGCCAAAAAT AAGTTGAAAA 900 GCTAGATTTG ATATTGGATC AGAGCATAAA AAGAAATCAA GAAGATATTA TCCTTTGTGT 960 TTCCCTATTT TTAACTTCGC AATGCAGGCA AGTCATAGCT GACATTTAAT TCTGCGAATT 1020 GGGTGCTATC ATTATCCCCA TTTTACAAAT GAGAAAACTA AAGCCTAGAG TGGTTAAGTA 1080 AATTGCCCAA GTCCACATAG CTAGTAAAGT GGCAGCTTTA TATACGTGCA CAGTAGCATC 1140 ACCAAGGGCC TATCTTGCTT TTAGGGGCCT ATGTAAATAT TTTAATTTCT TTTAAAATCA 1200 GAAAAAATGA ACTTGATGTT GAAAGAGAAT TTAATGTATT TGTCTTTCTA CCAACACAGT 1260 CATATAAAGT TTAACCCTTT CAGAAGCAGC ACCATCTTGA GTACCAGGGA GAATGAGAGA 1320 GAGAATGGAA GGAGCAGTGG TTGGGTGTCC ACTGTGCTCG GCGGGGCTGA CCACTGTGTG 1380 AAAGTGGCCC AGATGCCACG TCAGCCCCCT CACTGAGGGG ACTAAGCCCA CACCCTAAGA 1440 TAGAGAAGAC TGTATTTAAT AAAGTGCCAC TGGGCTTTGA CTAGGTAGAT CACACGAGGC 1500 TTCACGAAGG AGCTGGGATT TGAGAAGAGG GTTAAACATG AAAGGATGGG AAAGTAGAGA 1560 CAATTTGAGG 1570
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