Variant report

Variant	rs6658643
Chromosome Location	chr1:86518530-86518531
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:86516859..86518628-chr1:86521588..86524119,2	K562	blood:

Extended variants
information (count: 97 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:92)

rs_ID	r²[population]
rs10518360	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs10518362	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11161727	0.88[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12057842	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12077017	0.88[AFR][1000 genomes];0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12353970	0.88[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12354099	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12354100	0.92[ASN][1000 genomes]
rs12729890	0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12730639	0.88[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs12743320	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12744993	0.98[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12748730	0.98[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12750946	0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1359419	0.88[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1698742	1.00[ASN][1000 genomes]
rs1698743	1.00[ASN][1000 genomes]
rs1698744	1.00[ASN][1000 genomes]
rs17405880	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17405900	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17406104	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17406138	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17406173	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17406644	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs17414498	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17414519	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17414568	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17414617	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17414884	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs34848727	0.88[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs471070	1.00[ASN][1000 genomes]
rs477562	0.90[ASN][1000 genomes]
rs489267	1.00[ASN][1000 genomes]
rs4912442	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4912443	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4912455	0.88[EUR][1000 genomes]
rs4912459	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs500756	1.00[ASN][1000 genomes]
rs511363	0.95[ASN][1000 genomes]
rs511732	1.00[ASN][1000 genomes]
rs516799	1.00[ASN][1000 genomes]
rs518538	1.00[ASN][1000 genomes]
rs519361	1.00[ASN][1000 genomes]
rs521253	1.00[ASN][1000 genomes]
rs532684	1.00[ASN][1000 genomes]
rs538256	0.95[ASN][1000 genomes]
rs547023	1.00[ASN][1000 genomes]
rs551670	1.00[ASN][1000 genomes]
rs55766419	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56040491	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56229462	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56353901	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs56392000	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs567565	1.00[ASN][1000 genomes]
rs567617	0.95[ASN][1000 genomes]
rs569409	1.00[ASN][1000 genomes]
rs570172	1.00[ASN][1000 genomes]
rs574780	1.00[ASN][1000 genomes]
rs580540	1.00[ASN][1000 genomes]
rs582517	0.95[ASN][1000 genomes]
rs584895	0.95[ASN][1000 genomes]
rs586240	0.95[ASN][1000 genomes]
rs586629	0.97[ASN][1000 genomes]
rs599761	1.00[ASN][1000 genomes]
rs612256	1.00[ASN][1000 genomes]
rs615805	1.00[ASN][1000 genomes]
rs616281	1.00[ASN][1000 genomes]
rs617652	0.90[ASN][1000 genomes]
rs631512	1.00[ASN][1000 genomes]
rs632295	1.00[ASN][1000 genomes]
rs632697	1.00[ASN][1000 genomes]
rs634946	1.00[ASN][1000 genomes]
rs635391	1.00[ASN][1000 genomes]
rs635397	1.00[ASN][1000 genomes]
rs635713	1.00[ASN][1000 genomes]
rs636210	1.00[ASN][1000 genomes]
rs647380	1.00[ASN][1000 genomes]
rs650216	1.00[ASN][1000 genomes]
rs663463	0.95[ASN][1000 genomes]
rs663901	0.95[ASN][1000 genomes]
rs664099	1.00[ASN][1000 genomes]
rs664412	0.95[ASN][1000 genomes]
rs6682503	1.00[ASN][1000 genomes]
rs6703328	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs679256	1.00[ASN][1000 genomes]
rs680179	0.95[ASN][1000 genomes]
rs72716130	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72958291	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72958294	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs72960324	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs72960354	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7411998	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[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	nsv817212	chr1:86127851-86658426	Enhancers Weak transcription Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv546722	chr1:86278315-86891073	Enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	9 gene(s)	inside rSNPs	diseases
3	nsv1010312	chr1:86469730-86686426	Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Strong transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv525678	chr1:86487914-86549498	Enhancers Weak transcription Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv1012467	chr1:86494935-86686426	Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Bivalent Enhancer Active TSS Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:86507800-86520400	Weak transcription	Fetal Lung	lung
2	chr1:86517400-86519200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr1:86518200-86519800	Enhancers	GM12878-XiMat	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links