Tag | Content |
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EnhancerAtlas ID | HS076-46782 | Organism | Homo sapiens | Tissue/cell | H1 | Coordinate | chr5:172730620-172732130 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFE2L1 | MA0089.2 | chr5:172731096-172731111 | CCATGACTCAGCTCT | + | 6.16 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| | Number: 2 | ID | Chromosome | Start | End |
GH05I173301 | chr5 | 172728368 | 172731669 | GH05I173304 | chr5 | 172731721 | 172731870 |
| Enhancer Sequence | CATCTGGGGA ACACCTTAAA AAAAAAACTT TTTAAAATAG AAGATTTAAA TTGGGTCAGA 60 GATAAAACTC ATGCATTGGG AAGGTTCGTT CAAGCTGGAG GAGTCTGGGA AGGGGTCAAG 120 GAGGAGCGGG GATTAGTTCT AGGGGCTGTA GGAGGGTGAC AGTCCTGGAC TGAAGGTCAC 180 CTGCTTGGCT CTGATGATTT GGAGAAAGAT TTCCCTCAGT AAGAAAACAG GGGGAGGGGC 240 AAAGCGGTTG CTGCTGAGCA AATTGCCTCC GTGGTGCCCG GTCAGTCTTC ATAGTCCCCT 300 AACATTTGAA GCTGCCTCAA CTGCAGACTC TGGCATCAGT TCTGTGACCA GCCAGGAGTG 360 TGAGTGTGAA CATTTCCTCT AATGTCTCTC TGGCTGAGTC AACACTACGG TTGTCACCTC 420 ACTGTGACCT ACAGCCCCAG CAGGCCCCTC TCCTGTCTTG TTTCTCAGTG ACCCTGCCAT 480 GACTCAGCTC TACCCGGATT CTTCACTTGA AACCTGATTC CATCTGGGGG TGGGGGGTCC 540 TGCCGTGATC CGAGTCTTTG CAGGTGCTGA GCGCTGTCCA GGAACCTCCA GCTAGGTCCC 600 TGTTGCCAGG CCGTGCACAT TTCTGCTCTG CCCTTCACCT ATTTCTGTCT GCCTGGCTCT 660 CCCTAATCTG CCTGCCCCTT TTGGTTGGAC CATCTGAGCT CCGGGCTTTG GCTGGTCCTC 720 ATGCATTCAT TGCATCCAGA CAGGCATGGC TAGGATGGGT TCTGGGGACA GTAAACTCCT 780 TCTGCCCTCT GCCAATTTGC CTCCTTCTCT CCAAGAACCA CAGTGTCTCT CCAGCACCTT 840 CCATGACACG TGGGGTGCGG CGAGAGGCAA TGACCGTCCC AAGGTCACTT GGAGGTTCTG 900 CAGTTTTATT CAGAAATGTT AGTGTAGCAT TCTGAGGTTC TCAGATGGTA CTCAGGGGGC 960 AAATATTGTT AGAGCAGTGC AGAACGACTT TCCCTTCTGG TTTTGGAGGA ATCGGAAGGG 1020 AAAAACTTGG AATTCTATAT GCTCCAGCTC GTGGCCTCGT CTTGACAAAA GCCCTTTGAG 1080 GATTGAAATA ACTGCACCTC CCGGCTAGCA CCAGCAGCAC TTTCTCTTTG TCTGGAAACT 1140 GCTGTGCTGG TGTTTGCAGA AGGGGATCCT CCCTGCTAAC TGTGTACTCT TTCAGCCCTG 1200 CAGAAGGCCG ACTTCCTAGG AAACAGGACT GCTCATTCCA CCGGGCCTCC CTGTTGTGTA 1260 TCTTGTCTTC AAATGAATCA TTGCTTCTCG TGACTTATTG ACAGGCCTGA TTTGGCCCTG 1320 CAGAGAACCC AAAAGCTGCG GGTGGCAGAC CCCTCGGAGG ACAGGAACCT GGACTTAGTC 1380 TTTGGATTCC TGAGGTTAAG CCTAAGACCC TCCAGTTACA ACCTGGGGGA AGTTGCTTTA 1440 CCTCTGAGAG TCTGTTTCTT GATCTGTAAA GTAGGAATAA CCATTTCCAC CTTACTGGGG 1500 GGCATCGTGA 1510
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