Tag | Content |
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EnhancerAtlas ID | HS187-00437 | Organism | Homo sapiens | Tissue/cell | Th1 | Coordinate | chr1:26696480-26697920 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFYA | MA0060.3 | chr1:26696521-26696532 | AGCCAATCAGA | + | 6.32 | NFYB | MA0502.1 | chr1:26696516-26696531 | AGATTAGCCAATCAG | + | 6.31 | ZNF263 | MA0528.1 | chr1:26697061-26697082 | CCCTTCTCCTTTCCCTCTTTC | - | 6.23 | ZNF263 | MA0528.1 | chr1:26697072-26697093 | TCCCTCTTTCCTCACTCCTCC | - | 6.73 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 26696591 | 26696664 | chr1 | 26697689 | 26697730 |
| Enhancer Sequence | CTGTCTCAAT CAATCAATCA ATCAATCAAT CAATGGAGAT TAGCCAATCA GAAGTGAAGA 60 GCAGAGCTCT CCTGAGAGGA GAGGAAGGCC CTCACGGAGC TTACTTCCAA GTAAGTGCAG 120 AGATCTGAGG GAACATTCCA GATTCCTCAG GGCTACAAAG AAGCCACCCC CTTCTGTGCT 180 GAGAGGGGTC CCTGACTCTA CCAACCAGAG GCCCCCCACC AAGGGGAATC CTGCATCCTA 240 GCTCACCCAG ATAGCTCTTC TGGACAGCTG AGGACACCTC AGTGTCGTGT CACCCAGGCT 300 GCCCAGCTCA GCGCTCTCAC CAGGAATAAA GCCTGAATGA GTGGACCAAG CCCCCGGATG 360 CCCCTGACTG GCCTGACAGA GAGACGCGAG TGCCCAGCTG TCTGCTCATC CAGCACCAGG 420 CTTCTCTGCC ATCTTCCACC TGAGGCCACA CAGCACAGGG AACACTTCAG CCCAGCAAAT 480 GCCCCAAGAC CCCTTCCCCG TCACCTCAGG GACCACTCTT TGAATCCCAA ATGCCCCTCA 540 GACCCTAAGA CCCTCACTCC AGTGTCTCAG CCCTCTAAAA CCCCTTCTCC TTTCCCTCTT 600 TCCTCACTCC TCCCAACGCT GCTTCAGGTC TCAAAGCAAA TACCATGGAC CCCCGAAGGG 660 CTGCTGGCTG TGGGGCTCTC CACTCGGTGC TGCAGCAGTG CTCCTGGCTG GGAAGGAAGG 720 AGGTGGGCAG CCAGGCCACA GCTGCCTGTG GCTGAGGCCC CAGTGGGAGT GAGAGATGGC 780 AGGAAGGTGT TACATTTGAA GTTGCCACAG ATAGGAAGTG GGGGCAGGCA GGCTTGGGGG 840 CCCTGCAAGG TCTGACAAGG GGGCACTATC CACTCAGCTT TGCCTACCTG TGGCAACTCT 900 GGAGGACAAC CTGCTGATGT GGATTGCAGT GAACTGGGGC TACTGGAATT TCAGGATGTG 960 TGTGTGAGGG GGGCGGGCTG TTATTTCTGT TCTCAAAGTA CCCAGATGGC TGGACGGGAG 1020 GACAGAGTAG GGCTCAAAGG CTGAACAGGG GAGCCTTCTG TGGAGGGGAG CCAAGCTGAG 1080 ATGAAGATAG GCATTGATGA TGACAGGGAG ACAGTGATGG TGACAGGTAG GGACAGGAAC 1140 AGGCAGAGAC AAGAACAGGC AACATAGAAG GATATGGAAT GAGACAGAGG ACAGAGAAGG 1200 CAGCTGATCT CACAGAGATA CAGCAAACAC GTTTTCCTCC TCCAAGTCCC ATCTCAGATC 1260 TCCTGACCCT GGAAAGTTCT ATCCTCTAAT CTAGAGGCCC CAAGAGGCAA AAGATAATTC 1320 AAGCACATGG CCAGGTGAAG TGGCTCACAT CTGTAATCCC AGCACTTCAG GAGACCAAGG 1380 CAGACCCATC TCTTGAGCCC AGGAGTTTGA GATCAGCCTG GGCAACAAAG CAAGACCTCA 1440
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