Variant report

Variant	rs10456943
Chromosome Location	chr6:121877965-121877966
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10457420	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs10457421	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12195446	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12209355	0.88[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs2031300	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs56887955	0.91[ASN][1000 genomes]
rs58972372	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs62427968	0.94[ASN][1000 genomes]
rs62429983	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs62429984	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs62429985	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs62429988	0.88[ASN][1000 genomes]
rs62429989	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs62429990	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs62429991	0.96[ASN][1000 genomes]
rs9398642	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv886594	chr6:121837314-122043117	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	esv1844166	chr6:121845356-121880939	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:121873800-121885400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr6:121877400-121878200	Enhancers	HUVEC	blood vessel
3	chr6:121877600-121883600	Weak transcription	Placenta	Placenta
4	chr6:121877800-121878600	Enhancers	Hela-S3	cervix

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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

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