Variant report

Variant	rs7157092
Chromosome Location	chr14:39408356-39408357
allele	C/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]
rs10134656	0.88[ASN][1000 genomes]
rs10141079	0.88[ASN][1000 genomes]
rs10141081	0.87[ASN][1000 genomes]
rs10143720	0.87[AMR][1000 genomes];0.80[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10150756	0.86[ASN][1000 genomes]
rs10151960	0.90[ASN][1000 genomes]
rs1040680	0.85[ASN][1000 genomes]
rs10467711	0.85[ASN][1000 genomes]
rs11623907	0.87[ASN][1000 genomes]
rs11623945	0.87[ASN][1000 genomes]
rs11625689	0.88[ASN][1000 genomes]
rs11627264	0.84[ASN][1000 genomes]
rs11628480	0.95[ASN][1000 genomes]
rs11628564	0.87[ASN][1000 genomes]
rs11845793	0.87[ASN][1000 genomes]
rs11848067	0.87[ASN][1000 genomes]
rs12323565	0.85[ASN][1000 genomes]
rs12590373	0.85[ASN][1000 genomes]
rs17108576	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs17108596	0.88[ASN][1000 genomes]
rs17108664	0.88[ASN][1000 genomes]
rs17108696	0.87[ASN][1000 genomes]
rs1957065	0.83[ASN][1000 genomes]
rs2025061	0.94[ASN][1000 genomes]
rs2144528	0.88[ASN][1000 genomes]
rs28414518	0.87[ASN][1000 genomes]
rs28615884	0.87[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs55672305	0.88[ASN][1000 genomes]
rs55737943	0.84[ASN][1000 genomes]
rs56064304	0.88[ASN][1000 genomes]
rs7144625	0.88[ASN][1000 genomes]
rs7159520	0.88[ASN][1000 genomes]
rs72669386	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs743223	0.94[ASN][1000 genomes]
rs8019396	0.87[ASN][1000 genomes]
rs993675	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	nsv564416	chr14:39140536-39440106	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
2	nsv470631	chr14:39153764-39440106	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
3	esv3429206	chr14:39160730-39648836	Strong transcription Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers Enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
4	nsv932194	chr14:39173578-39411337	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
5	nsv901656	chr14:39370726-39423339	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	4 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	chr14:39406000-39412600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links