| Tag | Content |
|---|
EnhancerAtlas ID | HS056-02572 | Organism | Homo sapiens | Tissue/cell | GC_B_cell | Coordinate | chr11:64682960-64684430 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr11:64683973-64683988 | GGGGTCAAGAGGTCA | + | 8.07 | | Nr2f6 | MA0677.1 | chr11:64683329-64683343 | AAGGTTAGAGGTCA | + | 6.06 | | RARA | MA0729.1 | chr11:64683973-64683991 | GGGGTCAAGAGGTCAGGG | + | 6.56 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CCACTTCAGA GGCCCCAGAT ACTCAGTTTC TTTGGGGGCC TTCAAGGCGG GGCCTGCAGG 60
CTGAGCTGGG AGGGAGGAGG GGCTGGTTAT CAAGAAAGCG CCTGCATTCC ACCAGGGCCC 120
TAGAGAAGCC AATTCAATCC CCAACAAGAG GGCAGGGAAC AGGAGTAGGG GCGTTTTCTG 180
GAGCTGAAAG TAAAAAGGGG AAGCCTAGGG CTGGGTATGG TGGTTCATGC CTATAATCTC 240
AGCACTTTGG GAGGCTGAGG TGGGAGGATC CCTTCAGGGG TTCAAGGCTA GCCTGGGCAA 300
CATAGCGAAA TCCTGTCTCT ATAAAAATAA AAAAGGGGCA GCCTAGAGAC GGCCTTAGAG 360
GCTGAGGCTA AGGTTAGAGG TCAGAGAGGG CTTCCTACAC CAGAATTCAC AGACAGCAGG 420
CCACTGGGGG GTGCCCCCAG TTCAGGGCCC ACGATTATCC TACCCCACAT TTGCTCACCA 480
GGGCCTGGCC TACCCCCAAA GCCTAGCTCT TCTGCCCAGA TTAGCAGCCC CCTGAGTCCA 540
GCCACAAAAC TGAGAAGTCC CTGCCTCCAT GCCCACCCCT GCTGCTCTGG ACCTGGTGGA 600
TCGACCAGGA CGCGCCTCTA ATTGGTGGCT CCTTCAAAGC TCCCCAGGTC AGCTGAGCTG 660
TGAGTCAGGG CTCCTCACCG TTCCCAGCCT CAAGCCTCTG ACCTTACACC TCTTGGCCTC 720
CCTAGCATCT CCCTTGGCCT CCTCCCGGCT TGAAGCCAGA TCTCCCCACC TTTCCTCCAG 780
GGCCTCCCTC CAGGCAGGGA CACTGAGCCG GGGGGGTCGG TGGGAGATGT AGGTGGGGGC 840
CATCCAGTCC CTCCCTAGAC ACCCACTTGG CCCATCCCAC TCTCCCAAAA GCAGGAAGTA 900
GGCAGCGACC CAGGCACACG AGGTGTTGAT CAACACTGGT ACTGACGTAC TGACGCGGTT 960
GTTGACATAC ACATCCGGTG GTTTGTTGAT CCCACCTACG GGCTCAGGAC CGTGGGGTCA 1020
AGAGGTCAGG GCACATGATC CACAGGTGTC CTCGCCAGGG CTCCGGACCC CTACCAGCTT 1080
CCCCCACCAG CTGCGCAGGC CCAAGTCTGT CACTGCCCTG GCCCAGCTCA GTTCCTACGC 1140
TCCCTCCCCA GCCCCTCCTC AGCCCGAGAG CCAACCTCCT TAACTCAGCC CCCAAACTCG 1200
ACGAGTTTGT CTTGCATTCT CCAGACAGGT GATCTTGCCC TCTCCAGCCT CAGTTTCTCC 1260
TCCCGTGGAG ACAGAAACCC CTTCCCGCTC AGTTTCTGGC TCTGGTAAGG AACTGAAGAG 1320
GCCAGCCGGG GTGCCTCTGA CGCCTGGAGA GGGCAAGATT CCCCTGGCCT CTCTACGCCC 1380
GGTGCCTGAT CCCCCAGCCC GATCCTGCCG CAGGGAGCCT CAGGTCGCTG CGCTCCCACC 1440
CTCCGCACCT TCCTGGACTC GGGCCTGGCT 1470
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