Tag | Content |
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EnhancerAtlas ID | HS107-01412 | Organism | Homo sapiens | Tissue/cell | Jurkat | Coordinate | chr1:162891520-162893000 | SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXP2 | MA0593.1 | chr1:162892577-162892588 | TTTGTTTACTT | - | 6.62 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CTGGGATTAT CTGAGAGGGC CCTGGTCACC AAGGATCGTG GATGGAGAAG GAGGGTTGAT 60 GCAGCAGGGA CCTGCACTAA ACCAAAGACT GGTTAGGCAC AAAACCAACA AACATGTACC 120 TGTTCAGGTG GGTAACAGCC CTCTTTGCCT CCCCTAGGCC CCACTGACCT TGTCCCTGAA 180 CCCATTGTTT AGCTTTGCAT AATCTGTCCT CTGAAATCAG GAAAACCCTG AGGAAGTTGG 240 GGGATGGGGC TGATAACCAA ATTGATTAAG TTTCTGCCTC TCAGCAGATT AAAGATGTAC 300 AAGTAGATTT TGAATTGAGT TATAGAAAAA TAAGTTTGCA TTTAAATACT TTTCAGTTTG 360 CCGGTTAAAA TTCTTATCTG CTATAGTTAA TACCTTTAAC TAAATTATTT AGAATCTTCC 420 CAAAGATCCT GCTGGATTTC TTTCATCCCC ACATCACAGA TGAGAAATTG TGACCAAGAA 480 ATTATGTAAC TTACCCAAAG GCACATAACT GGCAAATGGA AGGAGGGGAA TTTGTTGTTT 540 TGCCGATAAA GTCTCTGCTC TTTCTAGAAA CCACACAGCT TTGAAGGATA TGGCTGCCAT 600 GGAAAGGTGG GGTAGGCAGA AAACGAAAGC AACCAATTAA AGGGAGCCAA TCCAGAATTT 660 GCCAGTTGCC AAAATCTCTT TGAAATAACT GTGATTCACT CACAAGGAGG AAGGAAGTGG 720 CTTTAAAAGA ATCAAAATGT GTCTTGTGAC AAGAGGCAAT TAAATTCTGT TCCCCTTGAG 780 TTAAATCCCC TTTATGGCTC TTTGGTGGAC ACACAATGAC TAAAATTTTG TCTAAAGAAA 840 AGGCTGTTTA CTCTTGGCTG TATATTGATG GGTTAAACAC AGGGCACACT CTTAGCACAT 900 TTGTAAATAT GGTCCTTAGG GTTGGCTCCG TATAGAAGGC TTCTTTGTAT GTCTACGATT 960 AGCAGAAACA ACGCCCAGGA GGACCAAAAG CAAGGGTCCC TATTCCCGGT ACAATTAAGG 1020 ACAAACTTAC TGCCAAAGCT GATAGAATTA TTTGGGGTTT GTTTACTTGT GGTAGCTATT 1080 GAAGAGCTTA TGGAAGGTGG AGAGGTGGCT GTTGGCTCTT AGTTCACTTC ACAGACTCCA 1140 GGACAGGGGA TGGATATAGC CCCCTTTACT TCAAAAAGCA CTGTTAATGG GCATTTAAGT 1200 TGCCTTGAAT AGGCCAAGCT ATCTCAACAA GTGAATGGGA GGAATAAAGA AAAGAAACAC 1260 GTATAATTTA GTAGCACCTG CTTCAAGGAC TGTTTCACTA AATTGGATTG TTGCTGTATG 1320 GGCATTTACA AAGCAATTAA AAAAATAAAA CTACATAAAA AACTTTGCCT TCGTTTATGG 1380 TTCAAAAATA CATGAATGTT TTTATTTAGA CCTCACAAAT AAGTAAGACT TCAGGGTTTA 1440 ATATATGGTT TTATTTGGTT CCAATCATTG CCTTTAGTAA 1480
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