Tag | Content |
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EnhancerAtlas ID | HS051-10782 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr16:75234670-75235760 |
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) |
SPI1 | MA0080.4 | chr16:75235306-75235320 | AAAAACAGGAAGTG | + | 6.36 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr16 | 75235137 | 75235495 | chr16 | 75235063 | 75235504 |
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| Number: 2 | ID | Chromosome | Start | End |
GH16I075200 | chr16 | 75234705 | 75234830 | GH16I075201 | chr16 | 75235215 | 75235522 |
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Enhancer Sequence | TTAATTTCTC TTCATGTCCT TATAATTAAA TTCCATCTAT AACCTTAATT CCAACCTATT 60 AGACGCATCA TCAGAACGGC TGACAGTGCA CGGGCAGAGA AAGGTATTAG GAAAGCCAGT 120 GAAGTAGAAA ATGCAGGAGG GAGCCCATTC CATTCCTGCC AAGATGCCGG GTTAGTGTGG 180 AATGTTGGCT GCCCCCCAGG ACCAGCCATG ATAGATTTTT TTTAGATGGA GTCTCACTCT 240 GTCACCAGGC TGGAGTGCAG TGGCAAGATC TCGCCTCACT GCAACCTCTG CCTCCTGGGT 300 TCAAGCGATT CTCCTGCCTC AGCCTCCTGA GTAGCTGGGA CTACAGACAC CCACTACCAC 360 ACCTGGCTAA TTTTTGTATT TTAATAGCAA TGGGGTTTCA CCATGTTGGC CAGGATGGTC 420 TCAATTTCCT GACCTCATGA TCTGCCCTCC TCGGCCCCCA AAAGTGCTAG GATTACAGGC 480 GTAAGCCACC ATTCCCAGCC CATGATGGAT CTTTAGAGGG AAACATCAAG AGACAGGAAG 540 ACCTGGGAGA AGAAGCAAAG ATCGGAACCT GTGGTTACGT GGGGAGGCTA GAGCTGTGGC 600 CCAAGGCAGA AGGCTGTGAA CTCGGCTGTG CAAGGAAAAA ACAGGAAGTG AGCACCAGGG 660 TTCTGCTCTG CTTCCGACCC AGCTCCAGGG CTTTGGGGCA ATGGGTGCCT GCCCCTGGCC 720 TGCAGGTGCC CTCAGGATAA AGTGGGTCAT GCCGAGGCAC TGTACAGGGG AGGAAATGAA 780 AAAGACTTAG AACTATAAAG TGTGTATCAA ATTGCAATAA AAAAGGCCAG GTGTGGTGGC 840 TCACACCTGT AATCTCAGCA CTTTAGGAAG CCGAGGTAGG TGGATCAGTT GAGGTCAGGA 900 GTTTGAGACC AGCCTGGCCA ACATGGTGAA ACCCTGTTCT TACTAAAAAT ACAAAAATTA 960 GCCAGGCATG GTGGTGGACA CCTGTAATCC CAGCTATTTG GGAGGCTGAG GAGGGAGAAT 1020 CACTTGAACT CAGGAGAGGT TGCAGTGAGC AGAAATCATG CCACTGCATT CTAGTCTGAG 1080 CATAAGAGCA 1090
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