Variant report

Variant	rs10187168
Chromosome Location	chr2:151948747-151948748
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	chr2:151943398..151945542-chr2:151945977..151948805,2	K562	blood:

Extended variants
information (count: 39 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10174574	0.84[AMR][1000 genomes]
rs10176186	0.83[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10188675	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10193451	0.86[AMR][1000 genomes]
rs10205429	0.98[ASN][1000 genomes]
rs1074149	0.93[ASN][1000 genomes]
rs10930435	0.83[AMR][1000 genomes]
rs1115140	0.84[AMR][1000 genomes]
rs11883593	0.84[AMR][1000 genomes]
rs11883594	0.84[AMR][1000 genomes]
rs11889216	0.82[AMR][1000 genomes]
rs11890910	0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12992820	0.83[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1351930	0.84[AMR][1000 genomes]
rs1485097	0.84[AMR][1000 genomes]
rs1485099	0.81[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1485112	0.84[AMR][1000 genomes]
rs1485113	0.84[AMR][1000 genomes]
rs1485117	0.82[AMR][1000 genomes]
rs1601359	0.97[ASN][1000 genomes]
rs17197940	0.98[ASN][1000 genomes]
rs1843269	0.98[ASN][1000 genomes]
rs1843271	0.82[AMR][1000 genomes]
rs1905742	0.97[ASN][1000 genomes]
rs2062364	0.97[ASN][1000 genomes]
rs2086914	0.84[AMR][1000 genomes]
rs3940993	0.84[AMR][1000 genomes]
rs4374368	0.97[ASN][1000 genomes]
rs4606923	0.84[AMR][1000 genomes]
rs4664951	0.84[AMR][1000 genomes]
rs4664952	0.84[AMR][1000 genomes]
rs56317281	0.98[ASN][1000 genomes]
rs62169068	0.97[ASN][1000 genomes]
rs749691	0.98[ASN][1000 genomes]
rs936766	0.81[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]

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	nsv525350	chr2:151711700-152044794	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv523849	chr2:151718133-152143524	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
3	esv3693426	chr2:151725792-152295862	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
4	nsv1002140	chr2:151833257-152054910	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	9 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	chr2:151942400-151958800	Weak transcription	Fetal Brain Female	brain
2	chr2:151947000-151951400	Weak transcription	Fetal Lung	lung

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