Variant report

Variant	rs1424967
Chromosome Location	chr2:53326891-53326892
allele	A/G
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:15)

rs_ID	r²[population]
rs11899579	0.96[ASN][1000 genomes]
rs12471667	0.85[ASN][1000 genomes]
rs12475926	0.85[ASN][1000 genomes]
rs12478233	0.88[CHB][hapmap]
rs17044122	0.90[EUR][1000 genomes]
rs17044123	0.90[EUR][1000 genomes]
rs17267748	0.96[EUR][1000 genomes]
rs3861569	0.96[ASN][1000 genomes]
rs55694730	0.90[EUR][1000 genomes]
rs56276721	0.98[EUR][1000 genomes]
rs56329869	0.87[EUR][1000 genomes]
rs66492582	0.92[EUR][1000 genomes]
rs66795271	0.99[EUR][1000 genomes]
rs66801688	0.85[ASN][1000 genomes]
rs6752368	0.93[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv520722	chr2:53039770-53421015	Flanking Active TSS Weak transcription ZNF genes & repeats Enhancers Active TSS Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv1012463	chr2:53187151-53377118	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
3	nsv874141	chr2:53263644-53352630	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:53325000-53327000	Enhancers	Fetal Intestine Small	intestine
2	chr2:53326200-53330200	Weak transcription	A549	lung
3	chr2:53326200-53331000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr2:53326800-53327000	Enhancers	Fetal Brain Male	brain
5	chr2:53326800-53327200	Enhancers	Fetal Intestine Large	intestine
6	chr2:53326800-53330200	Weak transcription	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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