| Tag | Content |
|---|
EnhancerAtlas ID | HS190-13435 | Organism | Homo sapiens | Tissue/cell | Treg_cell | Coordinate | chrX:51138640-51139760 | 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 | GTTACACCAG TAAAGCTGTC ATTTTGAGAT AAAGGGAAGG GTCTCCCGGA CCCATTTTCA 60
ACAAGTGGCC AATCTTGGTA GTGCAGACTA AGAAGCAGCC CAGTAAGTTC TTAGAACCGG 120
AAACTCCCCT CCCCCCAAAC ACCCAACCGC GCAGCCCACG CTGCGGGGCC ACGACTTGGC 180
CGGATTTATG TTCATGGCTG AGGATGCCAT GGGCCGAGTA AGAAGGAGAA CCGCCACCCA 240
ACCACGCAGC CAAGAGCAAC CCAGGGATCC CTCCTCTGCT TGCTCCCCTC CCCCACCCCT 300
GCTGTACCTT CTGCGCAGCC ATCTCGGTAA CGGGCGTCAG GGGCGCTCGG CGGCCTGCTG 360
TCCAAGCTGG GGTCAGGAGC CTGGCGGTAG CAAAGAGCAT CACCGAAAGG AAGCTGGTAG 420
GCTAGCGAGG CCAGCCCCAA AGACCCACAG ATACACGCGC TGCTCCGAAC TCGCGGGCCC 480
GCGGCGTCCA CTAATGAGAT GAACCTGGGC GCGCAGCGGC TGGACCTCAG CTGCTAGGGC 540
GCCGCCAAGG CCCTGCTGGA CACCTTCTGG TACCTGGGCC TCGTGTATTA CACCTGTGGC 600
TGCCGCCGAG GCGCGGTTCA ATTTGAAGTC TGAGCCCCTA CAGGCCCGTG AATCCTGGAT 660
TACAACTGCA GTTTGTGCAA GAAGCAGCAG CACCTGCACT TCCACTTAGC AACCTCCGGC 720
TTCACGCTCC TCCAGGGCGC AGAGAGCATC AAAGCATTAT CACCGACCCA ACACACACCG 780
GCGCTGCGTA GTTTCTGCAG CAGGTGTGGG GTGAAGAGTT GCCACACAGC TGTCTGACAC 840
CGGGTGTACG GCGTCACCCC TCACTTCCTG GACAAGGCAA CATTTTCCTA AAGGTAAAGA 900
CCATGAACAT GTAGAGGCCC CCTTACTCTC ATGCTAGTCC GCATTCAGCC GGAAGCAATT 960
CAGCAAATTT GCCATTTAAG TGACGCCCTG GATCTGTCTT TCAGAGTAGT GGCTTACCCT 1020
GCAGCCTCAT TTCTCTGATA AGTATTTTTT TAAAGCCATT GATTCAGTTT GTTCATCTTT 1080
TTCTTGTTGG AAGAAGGGGG TGGGGTGACA ATTTCCAGCT 1120
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