Tag | Content |
---|
EnhancerAtlas ID | HS187-25777 | Organism | Homo sapiens | Tissue/cell | Th1 | Coordinate | chrX:51138430-51139890 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RREB1 | MA0073.1 | chrX:51138771-51138791 | CCCCCAAACACCCAACCGCG | + | 6.49 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TTTTTTAAAA TATGAGATTA CTGGGAACCA GAGAACTTCG GAGTCATTTC CATGGTTACA 60 GGGCAGGTAT GTAACAGCAT GAGCACGGAA ACCCTGGTAT GTAATGCCAA CGCACACAAG 120 GACGGCAGCA TAGGCAATCT CCATACCTAT GTGTGGACAA TGTAAAAATA CCTCTTGGGA 180 GAAGGGGCTG CAAATACAGT TTACCAACAT GTTACACCAG TAAAGCTGTC ATTTTGAGAT 240 AAAGGGAAGG GTCTCCCGGA CCCATTTTCA ACAAGTGGCC AATCTTGGTA GTGCAGACTA 300 AGAAGCAGCC CAGTAAGTTC TTAGAACCGG AAACTCCCCT CCCCCCAAAC ACCCAACCGC 360 GCAGCCCACG CTGCGGGGCC ACGACTTGGC CGGATTTATG TTCATGGCTG AGGATGCCAT 420 GGGCCGAGTA AGAAGGAGAA CCGCCACCCA ACCACGCAGC CAAGAGCAAC CCAGGGATCC 480 CTCCTCTGCT TGCTCCCCTC CCCCACCCCT GCTGTACCTT CTGCGCAGCC ATCTCGGTAA 540 CGGGCGTCAG GGGCGCTCGG CGGCCTGCTG TCCAAGCTGG GGTCAGGAGC CTGGCGGTAG 600 CAAAGAGCAT CACCGAAAGG AAGCTGGTAG GCTAGCGAGG CCAGCCCCAA AGACCCACAG 660 ATACACGCGC TGCTCCGAAC TCGCGGGCCC GCGGCGTCCA CTAATGAGAT GAACCTGGGC 720 GCGCAGCGGC TGGACCTCAG CTGCTAGGGC GCCGCCAAGG CCCTGCTGGA CACCTTCTGG 780 TACCTGGGCC TCGTGTATTA CACCTGTGGC TGCCGCCGAG GCGCGGTTCA ATTTGAAGTC 840 TGAGCCCCTA CAGGCCCGTG AATCCTGGAT TACAACTGCA GTTTGTGCAA GAAGCAGCAG 900 CACCTGCACT TCCACTTAGC AACCTCCGGC TTCACGCTCC TCCAGGGCGC AGAGAGCATC 960 AAAGCATTAT CACCGACCCA ACACACACCG GCGCTGCGTA GTTTCTGCAG CAGGTGTGGG 1020 GTGAAGAGTT GCCACACAGC TGTCTGACAC CGGGTGTACG GCGTCACCCC TCACTTCCTG 1080 GACAAGGCAA CATTTTCCTA AAGGTAAAGA CCATGAACAT GTAGAGGCCC CCTTACTCTC 1140 ATGCTAGTCC GCATTCAGCC GGAAGCAATT CAGCAAATTT GCCATTTAAG TGACGCCCTG 1200 GATCTGTCTT TCAGAGTAGT GGCTTACCCT GCAGCCTCAT TTCTCTGATA AGTATTTTTT 1260 TAAAGCCATT GATTCAGTTT GTTCATCTTT TTCTTGTTGG AAGAAGGGGG TGGGGTGACA 1320 ATTTCCAGCT TCTTTACATG AAAGAGCTGA AACCAGAAGT CTCGCTTGTG ACCATTTTTG 1380 CAATATACTA CAATCACTAT AAGCCTATGA TTTAGAAATA TCATGGTAAA TGCCTGAGAA 1440 GCAGAAAAAA TAGTTGAAAG 1460
|
| |
|
|
|