Variant report

Variant	rs11600328
Chromosome Location	chr11:74771376-74771377
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr11:74720213..74722321-chr11:74770764..74773550,2	K562	blood:
2	chr11:74770127..74772846-chr11:74773872..74776209,2	K562	blood:
3	chr11:74762519..74764058-chr11:74769921..74771618,2	K562	blood:
4	chr11:74770400..74772058-chr11:74780541..74783446,2	K562	blood:

Variant related genes	Relation type
ENSG00000234611	Chromatin interaction

Extended variants
information (count: 31 )
Associated
traits (count: 16 )

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs10793112	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10899059	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs10899060	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs10899061	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10899064	0.87[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10899065	0.84[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs11236289	0.83[AFR][1000 genomes]
rs11236294	0.81[AFR][1000 genomes]
rs11236296	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs11236303	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11236304	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11236306	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11236307	0.87[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11236309	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11236310	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11236311	0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11236313	0.94[EUR][1000 genomes]
rs12223822	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12226763	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1371410	0.83[AFR][1000 genomes]
rs4456280	0.94[EUR][1000 genomes]
rs4531492	0.84[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs4554917	0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4944970	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4944971	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs56885894	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7106757	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7109716	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7482760	0.84[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs7483351	0.83[AFR][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	nsv897918	chr11:74757641-74798928	Enhancers Genic enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	inside rSNPs	diseases

mRNA abundance (count:16)

SNP	Gene	Cis/trans	Tissue	Source
rs11600328	XRRA1	cis	Thyroid	GTEx
rs11600328	XRRA1	cis	Artery Aorta	GTEx
rs11600328	XRRA1	cis	Whole Blood	GTEx
rs11600328	XRRA1	cis	lung	GTEx
rs11600328	XRRA1	cis	Adipose Subcutaneous	GTEx
rs11600328	XRRA1	cis	Artery Tibial	GTEx
rs11600328	XRRA1	cis	Skin Sun Exposed Lower leg	GTEx
rs11600328	XRRA1	cis	Stomach	GTEx
rs11600328	XRRA1	cis	Heart Left Ventricle	GTEx
rs11600328	XRRA1	cis	Esophagus Muscularis	GTEx
rs11600328	XRRA1	cis	Muscle Skeletal	GTEx
rs11600328	RP11-147I3.1	cis	Thyroid	GTEx
rs11600328	XRRA1	cis	Nerve Tibial	GTEx
rs11600328	XRRA1	Cis_1M	lymphoblastoid	RTeQTL
rs11600328	RP11-147I3.1	cis	Muscle Skeletal	GTEx
rs11600328	XRRA1	cis	Esophagus Mucosa	GTEx

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:74769600-74771400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr11:74771000-74771400	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr11:74771200-74771600	Enhancers	K562	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links