Tag | Content |
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EnhancerAtlas ID | HS187-13598 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr2:96980920-96982510 |
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) |
Nfe2l2 | MA0150.2 | chr2:96981424-96981439 | TGCTGAGTCACTGGG | - | 6.54 | ZNF263 | MA0528.1 | chr2:96981951-96981972 | CCCTCCACCCCCTCCTCATCC | - | 7.95 |
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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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| Number: 1 | ID | Chromosome | Start | End |
GH02I096314 | chr2 | 96980654 | 96982696 |
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Enhancer Sequence | CAGAGCATGC CTGCATGTTC TTGCTGGGTG TGCCAGGAAT GCAAGGCCCT GGCCACACTT 60 TCCTAGGCCC TTTCCCAGAG CTGTATGTGT AGTGGGCAAC CTTGAGGGAT AAGGTAATGT 120 CTTCCATCAG GACAAAGAGA AGAATGGCCA TGAAATAGGT AGTTTCCCTG AAATCAGAAT 180 TCCTTGTCTG CAATGCAAAC CGTACCATGC ATAGCATCCA CCTGGGCCTC TCCATGTTGC 240 CCCTGTGGGA CTTGAGAGAG CAAGGAGAAT TGACACAAAC AGGATGCTAG TGCTGATTGT 300 TGTGCCATGA GTCATAAATT ATTCTGTCTC TGACCCAGGA GTCTTGTGTC TTCTGCCAGC 360 ATCCATGAAA CAGCAACAGT AACTATCTTT TAAGTAGGGT AAAATTCCAG ACTTTTGACA 420 GTTTGGATGG AAAGGATTTA ATGTTGTCAT AACTATGGGG CAGCAAGCCT TGCAGCCACA 480 GCCAAAAGGC AACATGATTG TGGGTGCTGA GTCACTGGGT CCCTAAAACT GAGACAAATG 540 GCATCAGCAA TGAGGATATA GAGCTTCCAG TGGACCGAAA GCACTGGAGC GTGCAAAATC 600 TTGTTTATTG GAACAGAGCT GCTCTCTCCC TTTGTGCGAC TGATTCTTTG GACCCCTCCC 660 CAACCTCAGC TATGTTAAGG AAAAAGCTGA GTATGTTGGG GAACTTCACG GAAGGGGCTT 720 TGTTACAGGA ACCCAAGTCA CCATCCTCCC CGGTCCTGTG GCAGGAAGCG GTGCTAGGCG 780 CAGCTGGAGT GGTTTTAGAG CAGCCTGAAA TAAAAGACAC TCAGTCCCTC AGGGCCAGAA 840 TCAGAGGAGG CTGTGGCCAG AAAAATCCCA GCTACTGGAT GAGCCTGAGG ACAAAGCCTA 900 GGCAGGCAAA CACAGCCAGA AACTAAAGGG CATCACAAAC AGGAAATCTG ACGCTGGCAA 960 CATAAAGGGG TCACCACCTC AGTAGAAGCA GGGACCAGAG CCCTTCAAGA GTGAATAGAT 1020 GGACACACAG ACCCTCCACC CCCTCCTCAT CCACATGGAG GGAACTCCAC TCCCTCTACA 1080 ACTCAGGGCC CCAAATTCTA CATGGTTTCT GTGGAAGCAA GTCCTCATGG ATCTAGTTTT 1140 AGTCCCTGGA GAGCTGGTCT CTTGGCCCCT GGATAAGGTG AAAACCTGGT AGGCACTAGA 1200 AAAGACTGCC CTTCCCTTGT TCCCCGCTAT TTGTCCTTCC CATTCCCACT TAGTTCCTTT 1260 GTCTTTTCTC CATTCTACAT GCTCTGTCTC AACGTGGGAC TAAAATATAT ATTGTTATTA 1320 GTTACAGGGT TATTGATTAA GTTTTGGTTT CTAAACTTGC TCTTAAAATG CAGTTGCATT 1380 GAACATTTGA TTTGCCTTTC TTTATTATTA TTATTAAGAC AAAGTCTCAC TCTAACCCCA 1440 GCTGGAGTGC AGTGATGCGA TCATAGCTCA TTGCAACCTC CAACTTCAAC TCCCGGGCTC 1500 AGGTGAGCCT CCTGCCTCAG CCTCCCAAGT GGCTAGGACC ACAGGCACTC GCCACCATGT 1560 CCAGTTAATT TTTTAATTTT TATTTTTGTA 1590
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