Tag | Content |
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EnhancerAtlas ID | HS180-04486 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr1:212840380-212842220 |
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: 2 | Chromosome | Start | End |
chr1 | 212841280 | 212841455 | chr1 | 212840606 | 212841015 |
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Enhancer Sequence | TAGCAGGCTC GAACTCTGGG GTTCAAGCGA TCCTCCCACC TCAGTCTTCT GAGTAGTTGG 60 GACTACAGGT GCCTGCCACC ACACCTGGCT AATTTTTATT TTATATTTTA GAGATGGGGA 120 TCTCATCATG TTGCCTGGAG CTGATCTCAA ACTCCTGTGC TCAATCAATC CTCCCTCCTA 180 GGCCTCCCAA AGCGCTGGGA TTGCAGGAGT GAGCCAACAA ACCTGGCCTC AATCAGGTCT 240 TTAACCGTCC AATTTATTCA ATTCTGCCAG AGGGCCCCCT GCTGAAGCTG TTCACAGATT 300 GCTCTGATAT CATTAAAAAG CTAACCACAT ATGCAAATGA AGTGTTGGAG GTGTGAGGGT 360 GGCTTGGGGT AGACAGTGCT TCTGGTTCAT CTAGGAAGGC TTCCTGGTGG GGGAAGGGGA 420 GGGGCTGAAG TTGTCATTGA AAAGGATGGA GTTTGATACA ATGAGGGGGG TGGTGTGGTT 480 TTAGGCCATA ACCCTCCCTT TCCTGGGGCA GGTCCTCACA TGAGTCATTC CAGAGTTCCC 540 TTGCTGGTCA GTGGGAACAT TCTAGTGTGT GACATCTCCC TGGCAACAAG CTGAGTTCCT 600 GGAAAACAAC AATCACAGAG AGACAGTCCA CCACCTCTAC CCTCTTAACT CTTCCTTAGA 660 AATCCTACTG TCTGCAGCTG GGAATGAATG GAATGAAGGT CAAGGATGAA GTAATAACCA 720 AATATTGGGT TTTGGGTGCC CTGGTAACTG TCCGGTTTCC AGTTAGGGTT CCTGGGTGAC 780 ATCTTCCTTC TGGGGGAAGA CAGAGTCAAA TGAGAAACGT GAGTTGAGCC CAGGGGAAAG 840 GATCATCCGG GAGATGCCTG AGGGGCTCCA GGGCATCGTA ATCTCTTGCT CAGCTGGCAG 900 AGTGGGGCTG ACACGGCCAG CTGCTCTCTG GAGTCCTCGG CCTTCCTGTT TCCCCCTGAG 960 GACTTTGAGT GGGGAATCTA AACCATATGT CTCTGATTCA TTTACTGTGA ACTCATCAAG 1020 TTGCTGTTTG GCAAGAGTCC TTGGATGTCT CGGAAGAGCT TTTGGTTTGG TTTCATTTGT 1080 TCTTTCTAGT GCTTTTCCTT TGAAATAGGA AGTTTATGTT TGCCAAAAAT AAGTTGAAAA 1140 GCTAGATTTG ATATTGGATC AGAGCATAAA AAGAAATCAA GAAGATATTA TCCTTTGTGT 1200 TTCCCTATTT TTAACTTCGC AATGCAGGCA AGTCATAGCT GACATTTAAT TCTGCGAATT 1260 GGGTGCTATC ATTATCCCCA TTTTACAAAT GAGAAAACTA AAGCCTAGAG TGGTTAAGTA 1320 AATTGCCCAA GTCCACATAG CTAGTAAAGT GGCAGCTTTA TATACGTGCA CAGTAGCATC 1380 ACCAAGGGCC TATCTTGCTT TTAGGGGCCT ATGTAAATAT TTTAATTTCT TTTAAAATCA 1440 GAAAAAATGA ACTTGATGTT GAAAGAGAAT TTAATGTATT TGTCTTTCTA CCAACACAGT 1500 CATATAAAGT TTAACCCTTT CAGAAGCAGC ACCATCTTGA GTACCAGGGA GAATGAGAGA 1560 GAGAATGGAA GGAGCAGTGG TTGGGTGTCC ACTGTGCTCG GCGGGGCTGA CCACTGTGTG 1620 AAAGTGGCCC AGATGCCACG TCAGCCCCCT CACTGAGGGG ACTAAGCCCA CACCCTAAGA 1680 TAGAGAAGAC TGTATTTAAT AAAGTGCCAC TGGGCTTTGA CTAGGTAGAT CACACGAGGC 1740 TTCACGAAGG AGCTGGGATT TGAGAAGAGG GTTAAACATG AAAGGATGGG AAAGTAGAGA 1800 CAATTTGAGG AATGGAGAAT TCCCTGTATG GGGGGAGACT 1840
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