Variant report

Variant	rs66967065
Chromosome Location	chr18:39916629-39916630
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs12958459	0.89[ASN][1000 genomes]
rs12958679	0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1841620	0.82[EUR][1000 genomes]
rs1841621	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1993752	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2085909	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2335780	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs34642158	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs346446	0.81[EUR][1000 genomes]
rs346450	0.80[EUR][1000 genomes]
rs369305	0.80[EUR][1000 genomes]
rs379604	0.80[EUR][1000 genomes]
rs391148	0.81[EUR][1000 genomes]
rs413718	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs414142	0.87[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs415805	0.80[AMR][1000 genomes];0.88[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs415810	0.81[EUR][1000 genomes]
rs421436	0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs428198	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs436343	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs449040	0.81[EUR][1000 genomes]
rs454565	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4621064	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs68001532	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7232300	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7232594	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7237280	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs922266	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs976071	0.87[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9947788	0.81[EUR][1000 genomes]
rs9947988	0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9948169	0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9959948	0.89[ASN][1000 genomes]
rs9960132	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9964453	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.99[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	nsv949609	chr18:39126941-40070286	Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
2	nsv1059409	chr18:39711099-40139446	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:39910400-39916800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr18:39915200-39917600	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
3	chr18:39916400-39917800	ZNF genes & repeats	Fetal Intestine Small	intestine
4	chr18:39916400-39921400	Enhancers	Liver	Liver
5	chr18:39916600-39916800	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr18:39916600-39918000	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
7	chr18:39916600-39918800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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