Variant report

Variant	rs9327989
Chromosome Location	chr5:106425470-106425471
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs10055139	1.00[AMR][1000 genomes]
rs10061217	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10065551	1.00[AMR][1000 genomes]
rs10067562	1.00[AMR][1000 genomes]
rs10071074	1.00[AMR][1000 genomes]
rs12332507	1.00[AMR][1000 genomes]
rs13355116	1.00[AMR][1000 genomes]
rs13356561	1.00[AMR][1000 genomes]
rs13357132	1.00[AMR][1000 genomes]
rs13358415	1.00[AMR][1000 genomes]
rs13360429	1.00[AMR][1000 genomes]
rs28463192	1.00[AMR][1000 genomes]
rs28522914	1.00[AMR][1000 genomes]
rs28572078	1.00[AMR][1000 genomes]
rs28647772	1.00[AMR][1000 genomes]
rs28711024	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1030118	chr5:106006097-106847949	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent Enhancer Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
2	nsv823170	chr5:106326293-106673695	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv599332	chr5:106403516-106502006	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	esv2752056	chr5:106422649-106563101	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:106423800-106430000	Weak transcription	Aorta	Aorta
2	chr5:106424400-106426400	Enhancers	HSMMtube	muscle
3	chr5:106425000-106426200	Weak transcription	Muscle Satellite Cultured Cells	--
4	chr5:106425200-106426200	Weak transcription	HSMM	muscle
5	chr5:106425200-106426400	Weak transcription	Skeletal Muscle Female	skeletal muscle

Quick Search:

Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

what's new

Quick links