Variant report

Variant	rs1431532
Chromosome Location	chr7:14476191-14476192
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 85 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:81)

rs_ID	r²[population]
rs10231750	0.84[CEU][hapmap]
rs10235540	1.00[CEU][hapmap]
rs10247453	0.96[CEU][hapmap];0.97[EUR][1000 genomes]
rs10260659	0.81[CEU][hapmap]
rs10263131	1.00[CEU][hapmap];0.97[EUR][1000 genomes]
rs1030578	0.88[CEU][hapmap];0.81[EUR][1000 genomes]
rs10499441	1.00[CEU][hapmap];0.82[AFR][1000 genomes];0.97[EUR][1000 genomes]
rs10499442	0.85[CEU][hapmap]
rs11762226	1.00[CEU][hapmap]
rs11767890	0.81[CEU][hapmap]
rs11767969	0.88[CEU][hapmap]
rs11771647	0.88[CEU][hapmap]
rs11771951	0.96[CEU][hapmap];0.88[EUR][1000 genomes]
rs11982590	0.90[CEU][hapmap]
rs12154477	0.83[CEU][hapmap]
rs12666867	0.82[CEU][hapmap]
rs12669548	0.81[CEU][hapmap]
rs12670458	0.92[CEU][hapmap]
rs12674261	0.84[CEU][hapmap]
rs12699617	1.00[CEU][hapmap]
rs12699618	1.00[CEU][hapmap]
rs12699619	1.00[CEU][hapmap];0.94[AFR][1000 genomes];0.97[EUR][1000 genomes]
rs12699621	0.96[CEU][hapmap];0.89[EUR][1000 genomes]
rs12699622	0.84[CEU][hapmap]
rs12699624	0.84[CEU][hapmap]
rs12699625	0.84[CEU][hapmap]
rs12699626	0.89[CEU][hapmap]
rs12699627	0.84[CEU][hapmap]
rs12699628	0.84[CEU][hapmap]
rs12699629	0.84[CEU][hapmap]
rs12699635	0.89[CEU][hapmap]
rs12699636	0.83[CEU][hapmap]
rs13223986	0.82[CEU][hapmap]
rs13236153	0.87[CEU][hapmap]
rs13238777	0.89[AFR][1000 genomes];0.97[EUR][1000 genomes]
rs13243691	1.00[CEU][hapmap]
rs13438642	0.80[CEU][hapmap]
rs1367780	0.92[CEU][hapmap];0.81[EUR][1000 genomes]
rs1367781	0.83[CEU][hapmap]
rs1431520	0.96[CEU][hapmap]
rs1431521	0.85[CEU][hapmap]
rs1431525	1.00[CEU][hapmap]
rs1431526	1.00[CEU][hapmap]
rs1431527	1.00[CEU][hapmap]
rs1431528	0.81[CEU][hapmap]
rs1431538	0.84[CEU][hapmap]
rs1541874	1.00[CEU][hapmap]
rs1897300	0.81[CEU][hapmap]
rs196751	0.81[CEU][hapmap]
rs1978671	0.95[CEU][hapmap];0.93[EUR][1000 genomes]
rs1991685	0.84[CEU][hapmap]
rs2116314	0.88[CEU][hapmap]
rs2116315	0.95[CEU][hapmap]
rs2116319	0.92[CEU][hapmap]
rs2884348	1.00[CEU][hapmap];0.92[EUR][1000 genomes]
rs3823843	0.84[CEU][hapmap]
rs4370419	0.85[CEU][hapmap]
rs4607508	0.90[EUR][1000 genomes]
rs4719405	0.97[EUR][1000 genomes]
rs4719406	1.00[CEU][hapmap];0.80[AFR][1000 genomes];0.98[EUR][1000 genomes]
rs4719407	0.84[CEU][hapmap];0.80[EUR][1000 genomes]
rs4719409	0.84[CEU][hapmap]
rs4721335	1.00[CEU][hapmap];0.82[AFR][1000 genomes];0.97[EUR][1000 genomes]
rs4721336	0.82[AFR][1000 genomes];0.97[EUR][1000 genomes]
rs4721337	0.82[AFR][1000 genomes];0.97[EUR][1000 genomes]
rs4721338	1.00[CEU][hapmap]
rs4721342	0.84[CEU][hapmap]
rs6461102	1.00[CEU][hapmap]
rs6461104	0.84[CEU][hapmap]
rs6943928	1.00[CEU][hapmap];0.92[AFR][1000 genomes];0.98[EUR][1000 genomes]
rs6959924	0.81[CEU][hapmap]
rs7777868	0.90[EUR][1000 genomes]
rs7782805	1.00[CEU][hapmap];0.91[EUR][1000 genomes]
rs7783911	0.92[EUR][1000 genomes]
rs7793372	0.84[CEU][hapmap]
rs7794554	0.92[EUR][1000 genomes]
rs7807072	0.85[CEU][hapmap]
rs9639203	0.81[CEU][hapmap]
rs9690425	1.00[CEU][hapmap];0.94[AFR][1000 genomes];0.98[EUR][1000 genomes]
rs987448	0.81[CEU][hapmap]
rs987449	0.84[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949033	chr7:14086106-14860323	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv915603	chr7:14443884-14624268	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	esv1848567	chr7:14464118-14579801	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv887707	chr7:14471682-14576163	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:14473200-14479800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr7:14476000-14476200	Enhancers	Psoas Muscle	Psoas

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links