Tag | Content |
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EnhancerAtlas ID | HS182-01896 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr1:212840220-212842320 |
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 | HNF1A | MA0046.2 | chr1:212842243-212842258 | TGTTAATTATTAGTT | - | 6.27 | 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: 2 | Chromosome | Start | End |
chr1 | 212841280 | 212841455 | chr1 | 212840606 | 212841015 |
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Enhancer Sequence | CAGTGCGCAA TCATTCCATG TGTGTTGACG GACTGCAGGG CACATTGGCT CTGAAGGCTT 60 TACCAAGCTG GCTCTCAGTC ATATATATAT TTTTTTAATT TTTGAGACAG GGTCTCACTC 120 TGTTGCCCAG GCTGGAGTGC AGTGGCACAA TCATGGCTCA TAGCAGGCTC GAACTCTGGG 180 GTTCAAGCGA TCCTCCCACC TCAGTCTTCT GAGTAGTTGG GACTACAGGT GCCTGCCACC 240 ACACCTGGCT AATTTTTATT TTATATTTTA GAGATGGGGA TCTCATCATG TTGCCTGGAG 300 CTGATCTCAA ACTCCTGTGC TCAATCAATC CTCCCTCCTA GGCCTCCCAA AGCGCTGGGA 360 TTGCAGGAGT GAGCCAACAA ACCTGGCCTC AATCAGGTCT TTAACCGTCC AATTTATTCA 420 ATTCTGCCAG AGGGCCCCCT GCTGAAGCTG TTCACAGATT GCTCTGATAT CATTAAAAAG 480 CTAACCACAT ATGCAAATGA AGTGTTGGAG GTGTGAGGGT GGCTTGGGGT AGACAGTGCT 540 TCTGGTTCAT CTAGGAAGGC TTCCTGGTGG GGGAAGGGGA GGGGCTGAAG TTGTCATTGA 600 AAAGGATGGA GTTTGATACA ATGAGGGGGG TGGTGTGGTT TTAGGCCATA ACCCTCCCTT 660 TCCTGGGGCA GGTCCTCACA TGAGTCATTC CAGAGTTCCC TTGCTGGTCA GTGGGAACAT 720 TCTAGTGTGT GACATCTCCC TGGCAACAAG CTGAGTTCCT GGAAAACAAC AATCACAGAG 780 AGACAGTCCA CCACCTCTAC CCTCTTAACT CTTCCTTAGA AATCCTACTG TCTGCAGCTG 840 GGAATGAATG GAATGAAGGT CAAGGATGAA GTAATAACCA AATATTGGGT TTTGGGTGCC 900 CTGGTAACTG TCCGGTTTCC AGTTAGGGTT CCTGGGTGAC ATCTTCCTTC TGGGGGAAGA 960 CAGAGTCAAA TGAGAAACGT GAGTTGAGCC CAGGGGAAAG GATCATCCGG GAGATGCCTG 1020 AGGGGCTCCA GGGCATCGTA ATCTCTTGCT CAGCTGGCAG AGTGGGGCTG ACACGGCCAG 1080 CTGCTCTCTG GAGTCCTCGG CCTTCCTGTT TCCCCCTGAG GACTTTGAGT GGGGAATCTA 1140 AACCATATGT CTCTGATTCA TTTACTGTGA ACTCATCAAG TTGCTGTTTG GCAAGAGTCC 1200 TTGGATGTCT CGGAAGAGCT TTTGGTTTGG TTTCATTTGT TCTTTCTAGT GCTTTTCCTT 1260 TGAAATAGGA AGTTTATGTT TGCCAAAAAT AAGTTGAAAA GCTAGATTTG ATATTGGATC 1320 AGAGCATAAA AAGAAATCAA GAAGATATTA TCCTTTGTGT TTCCCTATTT TTAACTTCGC 1380 AATGCAGGCA AGTCATAGCT GACATTTAAT TCTGCGAATT GGGTGCTATC ATTATCCCCA 1440 TTTTACAAAT GAGAAAACTA AAGCCTAGAG TGGTTAAGTA AATTGCCCAA GTCCACATAG 1500 CTAGTAAAGT GGCAGCTTTA TATACGTGCA CAGTAGCATC ACCAAGGGCC TATCTTGCTT 1560 TTAGGGGCCT ATGTAAATAT TTTAATTTCT TTTAAAATCA GAAAAAATGA ACTTGATGTT 1620 GAAAGAGAAT TTAATGTATT TGTCTTTCTA CCAACACAGT CATATAAAGT TTAACCCTTT 1680 CAGAAGCAGC ACCATCTTGA GTACCAGGGA GAATGAGAGA GAGAATGGAA GGAGCAGTGG 1740 TTGGGTGTCC ACTGTGCTCG GCGGGGCTGA CCACTGTGTG AAAGTGGCCC AGATGCCACG 1800 TCAGCCCCCT CACTGAGGGG ACTAAGCCCA CACCCTAAGA TAGAGAAGAC TGTATTTAAT 1860 AAAGTGCCAC TGGGCTTTGA CTAGGTAGAT CACACGAGGC TTCACGAAGG AGCTGGGATT 1920 TGAGAAGAGG GTTAAACATG AAAGGATGGG AAAGTAGAGA CAATTTGAGG AATGGAGAAT 1980 TCCCTGTATG GGGGGAGACT GGGGGTAGCT GATGTAGAGG TTGTGTTAAT TATTAGTTAA 2040 AACTCGGTTT CTAAACTACT TTTGAATTGT ATTTTGTTTG TATTTCACTT TGAAGATCTG 2100
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