Variant report

Variant	rs12095328
Chromosome Location	chr1:76656245-76656246
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	chr1:76655272..76656892-chr1:76697191..76699562,2	K562	blood:

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs10518526	1.00[ASN][1000 genomes]
rs11162089	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11162098	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11162099	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1146657	1.00[ASN][1000 genomes]
rs1146659	1.00[ASN][1000 genomes]
rs11577339	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11583963	1.00[ASN][1000 genomes]
rs11584597	1.00[ASN][1000 genomes]
rs11587725	1.00[ASN][1000 genomes]
rs11590555	1.00[ASN][1000 genomes]
rs12091356	1.00[ASN][1000 genomes]
rs12122853	1.00[ASN][1000 genomes]
rs1251466	1.00[ASN][1000 genomes]
rs1251468	1.00[ASN][1000 genomes]
rs1251469	1.00[ASN][1000 genomes]
rs1684948	1.00[ASN][1000 genomes]
rs17609927	1.00[ASN][1000 genomes]
rs17610084	1.00[ASN][1000 genomes]
rs17610851	1.00[ASN][1000 genomes]
rs17626151	1.00[ASN][1000 genomes]
rs17660872	1.00[ASN][1000 genomes]
rs17662194	1.00[ASN][1000 genomes]
rs36050099	1.00[ASN][1000 genomes]
rs434302	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs481510	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs518915	1.00[ASN][1000 genomes]
rs522414	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs538977	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs541675	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs549014	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61771334	1.00[ASN][1000 genomes]
rs61771335	1.00[ASN][1000 genomes]
rs61771336	1.00[ASN][1000 genomes]
rs61771337	1.00[ASN][1000 genomes]
rs61773761	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61773762	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61773763	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61773764	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61773765	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6667200	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72690235	1.00[ASN][1000 genomes]
rs923246	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv870621	chr1:76620313-76997071	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 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	chr1:76646600-76658000	Weak transcription	Fetal Stomach	stomach
2	chr1:76647000-76665600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links