Tag | Content |
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EnhancerAtlas ID | HS047-20841 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr20:5045760-5047180 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nfe2l2 | MA0150.2 | chr20:5046738-5046753 | TGCTAAGTCATGGTC | - | 6.25 | Nr5a2 | MA0505.1 | chr20:5046853-5046868 | CCTGGCCTTGGGCTT | - | 6.16 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr20 | 5046140 | 5046913 | chr20 | 5045902 | 5047064 |
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| Number: 1 | ID | Chromosome | Start | End |
GH20I005064 | chr20 | 5045439 | 5047732 |
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Enhancer Sequence | CATTATAAAG ACTAACTTCC TCAGCCAGGT GTGGTGGCTC TCACCTGTGA TCCCAGCACT 60 TTGGGAGGCC GAGGTGGGAA AGATCACCTG AGCTCGAGTT TGAGAACAGC CTAGGCAACA 120 TGGCAAGACC CCATCTCTCA AAAAAAAAAA GATTAACTTC CCAATGCATT GAAATAACCC 180 ATGAGTATCA TGAACTCTGT CACAAGGAAG GGACACCAGA GGCTCAGATG TTGGCTGAGA 240 GGTGACCAAT TGTCAGGAGC AGGGGCACTG GTGATCTTAG GGGATGGGAA CAGAGAAATC 300 TCTGTTTCTG TGATTTCCAT GATCCATTTC CCTGAGCTGC TTGTTTTCAC CAATGGTCCT 360 TGTTGTTATG GGCAGCAAAG TCCCTCTAAT GATCTCTTTG AGGCTAGCCA GCAGGGGAGA 420 AGTGGCTGTG AGTGGGGCCT ATTTTCCTGG CTTGCAGGAA GCCAGGGGGC CAGAGCAGAG 480 GCCCCCTACT GCCCTTCACT CCTCACTACC ACCAGCTTCC CAGGTGTCCT GGACGCATGT 540 GGGATGCCTC TGAGATAACC GGGTTAAGGC CAGGGCCTGT CTAACGCCTG GGCTCTGGAG 600 CAGGACCCGG GTTCTGTGGG AGCTCATATG AAGGACAGGA AGTGACCAGT CCACAGACTG 660 GACCAAAGGT CTGTGACTCA CTGGTTGTAT GTAGTAGGGA TCACGCCCCT GCCATGCCAA 720 ACACCAAAAC TGTAGGTCAG ATTGGAGTTG TACTGGAGTA ATACCATGAC GAGGAGTGGG 780 CTGCACTGGA GACCCCCGTC CCTGGAATGA CCGGGGAAGC AGGGGCTGAT GTGAGGAAGG 840 GTGGAGAGGG GCTGCGGTGA TGGCGAAGGA GGCCACAAGT TCCCGGTTTT GGCATGCTGC 900 TCAGGCCTTC GCCTCCCCAT GCTGGCTGTA TTCTACCCGC ACACCCATAT TGGCCCAGAC 960 TGGGAAACCT CACAGCTTTG CTAAGTCATG GTCAGGTTAG TCAAGGCCAG TAAACCACGT 1020 GGGTGATGCA TCATTGCCAC CCTGGCACGC CTCCTTCCAG ACCAGGCTGG GACTGGCTCT 1080 CCACATCCCA GGGCCTGGCC TTGGGCTTCT CTGCCAGCTG GTCAGGGTGA GTCACTCTTC 1140 TTTGGAGGAT GCTGCCTTCC TCTAATGTTG GACATGAAGG GCTTTTTTGT CCTCCTAGAG 1200 TTCTGGAGCA TCCCAGAAAA GGCAAAACTA GGGAGCAGAG GAAAGAGAAC ATTTTTTAAA 1260 AAACAAAAAT GTTGCCTGGG CGCGGTGGCT CACGCCTGTA ATCCCAGCAC TTTGGGAGGC 1320 TGAGGTGTGA GGATCATCTG AAGTCAGGAG TTTGAGACCA GCCTGGCCAA CATGGTGAAA 1380 CCCCGTTTCT ACTAAAAGTA CAAAAAAATT AGCTGGGTGT 1420
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