| Tag | Content |
|---|
EnhancerAtlas ID | HS056-10560 | Organism | Homo sapiens | Tissue/cell | GC_B_cell | Coordinate | chr22:41984590-41985720 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SPDEF | MA0686.1 | chr22:41985107-41985118 | CACATCCGGGT | - | 6.32 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TCAGGTGATC TGCCCACCAT GGCCTCCCAA AGTGCTGGGA TTACAGGCGT GACCCACAAG 60
CAAATGGCCC ACCTTTGCTC CAGTCCTGCT ATCTTCCTCC CGGATCCACC CCTGCAGGAA 120
GGCCTCCAGG GCCCAAGCCA GGGCAACTTC ACCACAGAGG ATGGGGAGGG GCATTCGGGA 180
CCTAAGAGAG GAGGCTAAGA CCTGGGTTCC CATCAGCCAC TGCCCAGTAA AGCCCATCCC 240
ACTGCTCCCC CACGCTAGGA GACCTGTTGG TTGGTCCTTG AGGCCCCCAG ACTGGAGGGT 300
GGGTTACCCA CAGGGAGGGC ATGAATGAAG CCTGCTTACT GATGCATCCA GCTGGTGAGG 360
GGGCTTTTGG GGACTCACTC ACAATGAGAC CCAATGGGAG AAAAACTGAG CAGAGGTAAG 420
AGGCTCAACA CAGCGAGAGT CTTTAGAAGA AAACTAGACT CTTACCCTCA CTATTCCTCA 480
GTGTCCTCAC AGCAAACAGG CTAGGCCTGG AGCCTCTCAC ATCCGGGTGG GTAGAGCTCA 540
TAAACGAATT TGAAAAGAAG CCCTCTCTGC TCCACGACTG GGGGTGGAAG GTAAAGTGGG 600
TGATGGGGCT TCAGAAACTA GACCCAGTCC CAGGCCTGCA AAGGTCGGGG TGGGAAGACT 660
CCGAGACGCC CTGTCTCCCA CCAGATGATG ACTGACGCTT GGCTGTGTGC TTGTGTGCCT 720
GGAACCCCGG TTCAGAAGCC AGCTCCGACC ACTGGTGTGT CGTAGGGCTG AACTAGGGTG 780
GGATCCCCAG CTCAGGAGGC GGGGGCGTCC GTGAGCCAGG CCTTAGCGGC GTGTGACAGC 840
CTCCGGGGAG GGAGGGAGCT AGGCCCCTGC TCGCAGCCTC CTCCCTCCAG TACTGGATCC 900
AACCCCAGCA CTCCCAAGCA GAACACAGGC AAGGACGCTG CGGGGTCAGT GACGTGAGGG 960
CCAGGTCCCC TCACTCCCGG TGGGTGGCCC CGGATGTCAG GGGGCCGGGT ACCGCCGCAT 1020
CCCACACTCG GTCCCCGGGT GTCCACGGTC ACGCTGCTGC AGACCCCACA CTCAGCCTCG 1080
GGGGTGTCCG CGTGACACTC CCGGTGGGAG CTTCCAATCT TCAGGGTCCT 1130
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