| Tag | Content |
|---|
EnhancerAtlas ID | HS042-30970 | Organism | Homo sapiens | Tissue/cell | Fetal_brain | Coordinate | chr22:50877190-50878120 | SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GGTGGTGCTG GGCGCCAGGG GCTGGGAGTG TGGGTATCGG GGACAGGACA TGGTACCCCG 60
GCCTGGGTGT TGTGGAGGCT TCATTTGGAG CTGAGGCATT TGGGGCTCAC TGTGGCCCGG 120
AGCCTGAATC CCCAGCTATT TCCCAGCCGT CCTGAGTAGG GGTCTGTGCT GCGCTGTGCC 180
CAGCGCAAGG TGGCCTCCTG CCCCTGCCTT GCAGTTGTGG TCACTCAGCC ACGTTGCCAA 240
GGCTGGTGGG TGGTGTCCAC CTAGTCTCCA TCGTCCGTCC AGCCCCCACA CAGTCAGGCA 300
CAGGCCTGAC GCCCTCCCCA GCACAGCAGC ACAGGCCGGC CGCCACCTTC ATGGCCGACA 360
TCTATGGCAG GAGCCAGTCC ACCTCACAGG CCGCATGGCT GATGAGACCC CTCTCCTTAC 420
CCTGCCCTGG GGGCAGCACT GAGGCACTCA GGACTTTGGT GGCGGGGGCA GAGATCTCTG 480
TTAGGAGGGG CTGAGCTCTT CGCTGACAGA GCAAGGGTGA CACCCTGGGG AAGCAGGAAC 540
ATCCCAGATA GGAGGAAGAC ACCCCATCCT CGAGGCCAGG AAGGGGCCAG TGGTGCTCGG 600
TGAGCTGCCG GCTCTGTGGG TTGCGGTCCT GGGTAGGACA GGGCAGTGGC ATCACCTCCA 660
CACTGTCAGT GTCAGTCCTG CTGGAGGCCT GGGGGCCCTC AGGCACCTGA CTGAGCCCCA 720
GGTCACACGC CCCATGGGTG TCGGCAGCTT GTCAGGACCC TCGAGCTGTC CCCTGTTGCT 780
CCTTGAGGGG CTGACGGGCA CTGCCTGGGC CTCCCTCCTG GAGCAGCCCC ATCTTCCTGT 840
CAACCTCTGA GGGGCTCCCG GGGCAGGGGC GCTGCCTCCC CTTTGCCTGC AGCACCCCAG 900
GCCTGCCCAC GCCTGACCAC TGTGTCTCTC 930
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