| Tag | Content |
|---|
EnhancerAtlas ID | HS056-08558 | Organism | Homo sapiens | Tissue/cell | GC_B_cell | Coordinate | chr2:39470660-39471770 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| REST | MA0138.2 | chr2:39471547-39471568 | CTTAGCACCCGGGCCAGCGGC | + | 6.38 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH02I039243 | chr2 | 39470743 | 39471341 |
| Enhancer Sequence | AAATCCACTT TATTTCCAGG CCTCTGGTCT TCAGCCTTCT TCATTTAATG ACAGTTCTCT 60
TTCTCGGCCA TAGGTAGGCC TCCGCCTTGC GCGCTCCTCG GCCCCCGCCG CCGCCCACTC 120
CCTGGGCAGC ACCATTTCCG CCCCGAGGGA CCCTCACCGG GTCAGTGCTG CCACCTCGAA 180
TCCGCCCCTT CCCTTCCAGG GGCCACCGAA GCGGAAGGCG GTCCCGCTTT TCTTTCGGGG 240
AACTTTTCTT GGTTCCTGCA ACTGGGATCC GCAGTCTAGA CCTCGCGGCT CACCCCATCA 300
ACCCCGCACG CTGCCCGCAG TTCCCCCGCC ACCGGCAGAA TCCGCACTTA CTGCACCCAC 360
AGGGCGACGG TGACGAAGCT TCGAGCAGCG CCGAACAGCC CCAGCCCCAG CTCCCGCGCG 420
TGTCGCTCGG AGGAGGCGCC GTGTACCCAG CGACTTCGGA GCCAGCGGAA CCGCCGCAGC 480
GTCTCCCGGG CAACCGGAAC GCTAGGGCGC GCGGGGCACT GCGGCTTCCG GAGCGGGTTC 540
CCCTGGCGCT GGCAGCCCCA GCCCTGATCC TTCTGAGAGG TGACAGCGTG CTGGCAGTCC 600
TCACAGCCCT CGCTCGGTCT CGACGCCTCC TATGCCTGGG CTCCCACTTT GGCGGCACTT 660
GAGGAGCCCT TCAGCCCACC GCTGCACTGT GGGAGCCCCT TTCTGGGCTG GCCAAGGCCG 720
GAGCCCACTC CCTCAGCTTG CAGGGAGCTG TGGAGGGAGA GGCGCGAGCG GGAACCGGGG 780
CTGCGCACGG CGCTTGCGGG CCAGCTGGAG TTCCGGGTGG GCGTGGGCTT GGCGGGCCCC 840
GCACTCTGAG CAGCCCGCCG GCTCTGCCGA CCCCGGGCAA TGAGGGACTT AGCACCCGGG 900
CCAGCGGCTG CAGAAGGTGT AATGGGTCCC CCAGCAGTGC CAGCCCACCG GCGCTGCGCT 960
CGATTTCTCA CTGGGCCTTA GCTGCCTTCC TGCGGGGCAG GGCTTGGGAC CTGCAGCCCG 1020
CCATACCTGA GCCTCCCACC CCCTCCATGG GTTCCTGTGC GGCCGGAACC TTCCCGACGA 1080
GTGCCACCCC CTGCTCCACG GCGCCCAGTC 1110
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