| Tag | Content |
|---|
EnhancerAtlas ID | HS182-15493 | Organism | Homo sapiens | Tissue/cell | Spleen | Coordinate | chr3:13301940-13302870 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NKX2-5 | MA0063.2 | chr3:13302719-13302729 | ACCACTTGAG | + | 6.02 | | REST | MA0138.2 | chr3:13302216-13302237 | GAAGCTGACCTTGGTGCCGGC | - | 6.12 | | SNAI2 | MA0745.2 | chr3:13302010-13302020 | AACAGGTGCA | + | 6.02 | | ZNF263 | MA0528.1 | chr3:13302336-13302357 | GAAGGAAGAGGAGAGTGGAGG | + | 6.55 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CAATACTCTC ATTTCTGTCC AGTAGGGGCA TGATTTTCTC ATCTTTCACT GAGTGACAAT 60
TTTTGATCAA AACAGGTGCA TCTGGCAAAG ACAGCCAAAG CCCACGTTCC TAAGGGAATC 120
TGCAAAAGTC CTGGTGTCCC AGGCTGCCTG AGAAGCAGCA CCCCTCACCG ATGCCTGAGT 180
CTACCATCAA GGCCTGACCC GCCGCTGCCT CTTCCAACTC CAGCTCTGTG CCAGACACTA 240
TGCAGGGACT GAGGACACAG AGACCACGAT GGCCAAGAAG CTGACCTTGG TGCCGGCTCC 300
ACAGTCCTCC TGGCAGGGTG CACGGGGCGT GGAAGGAGAA AGCCACATTG TCCTGGGGCC 360
CGGGAGACAG GCCCAGCCAA GGAGGCTGAA AGCTTTGAAG GAAGAGGAGA GTGGAGGGGG 420
TCCTCTGTGC TGAGCAGGAC ACATGGTGCA TATGAGGAGT CCCCAGTGCT GGGCAGTGCA 480
GAGGCCACCC AGCCCCCACA GCAGAGACTG GTGGAAATGA AGGGTTGAGA GGTGTGGGGA 540
CTGGGGATGG CCAAGGTCTT CCCTGACCGA CGGCCTCAAG CTGCCATCAC TCTCTCCCTA 600
CCTCCCAAGA GTGAGGGACA GATTTTTCAG AGGCGAGGAC ATGGCACTTG ATTTGTATAT 660
AGAAAGATCA GCCTGACCAG CTATAGCGGA CACTGGGGAG GCCGCCCAGG CGCCCTCCAG 720
GACCTGTTCC CTGTCCCCGC CTGCCAGGAG TGCTGGCTGC TGAGGGCTCC CAGCTGAGTA 780
CCACTTGAGG ACTGTCCTTG GCCAAGGTCA CGCCTCCCTC CCCCAGGGGC CACACACAAT 840
GTCCGGTCGA TGTGGAGGGA CAAAGGGCAG TGCCCTGGCC TTGATTAGGG ACACCCCTTC 900
AGAGCCTTCC CAGCTCCAGA GCTCTGGTGG 930
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