Variant report

Variant	rs4113248
Chromosome Location	chr18:14832211-14832212
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs10468701	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs10468702	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10775421	0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10775422	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12326166	0.80[ASN][1000 genomes]
rs12457328	0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12606627	0.85[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs12607816	0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12966403	0.87[EUR][1000 genomes]
rs12970537	0.87[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1622544	0.86[ASN][1000 genomes]
rs1713886	0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1713892	0.80[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1713895	0.80[EUR][1000 genomes]
rs1770756	0.80[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1970446	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs28454867	0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs3126404	0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs3878726	0.80[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4890750	0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs55721158	0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs55774912	0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs55929438	0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9283029	0.80[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs9284405	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9303862	0.80[AMR][1000 genomes];0.88[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs9303863	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs9303864	0.85[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs9303869	0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9675365	0.82[AMR][1000 genomes]
rs9675641	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9676173	0.87[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs9709715	0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9748546	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9797358	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9989501	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv428006	chr18:14087067-14874733	Weak transcription Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	36 gene(s)	inside rSNPs	diseases
2	nsv916419	chr18:14418522-15165372	Enhancers Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	27 gene(s)	inside rSNPs	diseases
3	esv2751771	chr18:14704694-15106727	Flanking Bivalent TSS/Enh Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	18 gene(s)	inside rSNPs	diseases
4	esv2756821	chr18:14741611-14865985	Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island lncRNA miRNA	8 gene(s)	inside rSNPs	diseases
5	nsv2216	chr18:14776359-14841989	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	TF binding region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:14828200-14838800	Weak transcription	Osteobl	bone

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links