| Tag | Content |
|---|
EnhancerAtlas ID | HS050-71786 | Organism | Homo sapiens | Tissue/cell | Fetal_stomach | Coordinate | chrX:51138450-51139680 | 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 | CTGGGAACCA GAGAACTTCG GAGTCATTTC CATGGTTACA GGGCAGGTAT GTAACAGCAT 60
GAGCACGGAA ACCCTGGTAT GTAATGCCAA CGCACACAAG GACGGCAGCA TAGGCAATCT 120
CCATACCTAT GTGTGGACAA TGTAAAAATA CCTCTTGGGA GAAGGGGCTG CAAATACAGT 180
TTACCAACAT GTTACACCAG TAAAGCTGTC ATTTTGAGAT AAAGGGAAGG GTCTCCCGGA 240
CCCATTTTCA ACAAGTGGCC AATCTTGGTA GTGCAGACTA AGAAGCAGCC CAGTAAGTTC 300
TTAGAACCGG AAACTCCCCT CCCCCCAAAC ACCCAACCGC GCAGCCCACG CTGCGGGGCC 360
ACGACTTGGC CGGATTTATG TTCATGGCTG AGGATGCCAT GGGCCGAGTA AGAAGGAGAA 420
CCGCCACCCA ACCACGCAGC CAAGAGCAAC CCAGGGATCC CTCCTCTGCT TGCTCCCCTC 480
CCCCACCCCT GCTGTACCTT CTGCGCAGCC ATCTCGGTAA CGGGCGTCAG GGGCGCTCGG 540
CGGCCTGCTG TCCAAGCTGG GGTCAGGAGC CTGGCGGTAG CAAAGAGCAT CACCGAAAGG 600
AAGCTGGTAG GCTAGCGAGG CCAGCCCCAA AGACCCACAG ATACACGCGC TGCTCCGAAC 660
TCGCGGGCCC GCGGCGTCCA CTAATGAGAT GAACCTGGGC GCGCAGCGGC TGGACCTCAG 720
CTGCTAGGGC GCCGCCAAGG CCCTGCTGGA CACCTTCTGG TACCTGGGCC TCGTGTATTA 780
CACCTGTGGC TGCCGCCGAG GCGCGGTTCA ATTTGAAGTC TGAGCCCCTA CAGGCCCGTG 840
AATCCTGGAT TACAACTGCA GTTTGTGCAA GAAGCAGCAG CACCTGCACT TCCACTTAGC 900
AACCTCCGGC TTCACGCTCC TCCAGGGCGC AGAGAGCATC AAAGCATTAT CACCGACCCA 960
ACACACACCG GCGCTGCGTA GTTTCTGCAG CAGGTGTGGG GTGAAGAGTT GCCACACAGC 1020
TGTCTGACAC CGGGTGTACG GCGTCACCCC TCACTTCCTG GACAAGGCAA CATTTTCCTA 1080
AAGGTAAAGA CCATGAACAT GTAGAGGCCC CCTTACTCTC ATGCTAGTCC GCATTCAGCC 1140
GGAAGCAATT CAGCAAATTT GCCATTTAAG TGACGCCCTG GATCTGTCTT TCAGAGTAGT 1200
GGCTTACCCT GCAGCCTCAT TTCTCTGATA 1230
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