Variant report

Variant	rs1374477
Chromosome Location	chr11:93007565-93007566
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:92971291..92974184-chr11:93005306..93007969,2	K562	blood:
2	chr11:93001767..93004260-chr11:93007086..93009805,2	K562	blood:

Variant related genes	Relation type
ENSG00000255233	Chromatin interaction

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs10741461	0.84[EUR][1000 genomes]
rs10765596	0.82[AFR][1000 genomes];0.80[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs10831010	0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10831011	0.89[ASN][1000 genomes]
rs10831016	0.97[ASN][1000 genomes]
rs10831017	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11020218	0.89[ASN][1000 genomes]
rs11020228	0.96[ASN][1000 genomes]
rs11020229	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11020230	0.93[ASN][1000 genomes]
rs11020233	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11020234	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11020235	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11020236	0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12099012	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12419806	0.96[ASN][1000 genomes]
rs12803876	0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12808030	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1446904	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1446905	0.89[ASN][1000 genomes]
rs1446907	0.89[ASN][1000 genomes]
rs1446908	0.89[ASN][1000 genomes]
rs1446918	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1446919	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1446920	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1446921	0.95[ASN][1000 genomes]
rs2121470	0.89[ASN][1000 genomes]
rs2399641	0.95[ASN][1000 genomes]
rs4313534	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4396248	0.96[ASN][1000 genomes]
rs4753082	0.94[ASN][1000 genomes]
rs6483228	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7482501	0.89[ASN][1000 genomes]
rs7930702	0.85[ASN][1000 genomes]
rs935450	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.97[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	nsv1039134	chr11:92790000-93219942	Strong transcription Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 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	chr11:93007400-93008600	Weak transcription	Fetal Stomach	stomach

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