Variant report

Variant	rs2821108
Chromosome Location	chr1:197342686-197342687
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	chr1:197334679..197337077-chr1:197341690..197343719,2	K562	blood:
2	chr1:197335577..197340315-chr1:197341690..197345883,4	K562	blood:

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs10754222	1.00[CEU][hapmap];0.88[CHB][hapmap];0.81[JPT][hapmap];0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10801604	1.00[CEU][hapmap];0.88[CHB][hapmap];0.81[JPT][hapmap];0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10801605	1.00[CEU][hapmap]
rs10922213	0.82[CEU][hapmap];0.88[CHB][hapmap];1.00[JPT][hapmap]
rs10922215	1.00[CEU][hapmap];0.91[EUR][1000 genomes]
rs10922216	1.00[CEU][hapmap]
rs10922221	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs10922223	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs10922225	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs11799515	1.00[CEU][hapmap]
rs11802794	1.00[CEU][hapmap]
rs12083773	1.00[CEU][hapmap];0.88[CHB][hapmap];0.81[JPT][hapmap];0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12128912	1.00[CEU][hapmap];0.82[JPT][hapmap]
rs12142127	0.80[CEU][hapmap]
rs2476020	1.00[CEU][hapmap];0.90[EUR][1000 genomes]
rs2494268	1.00[CEU][hapmap]
rs2494271	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2759655	0.91[EUR][1000 genomes]
rs2759656	0.85[YRI][hapmap]
rs2759662	0.95[CEU][hapmap];0.89[EUR][1000 genomes]
rs2759665	0.87[EUR][1000 genomes]
rs2821102	1.00[CEU][hapmap];0.90[EUR][1000 genomes]
rs2821121	1.00[CEU][hapmap]
rs34241991	0.96[EUR][1000 genomes]
rs35367258	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4262574	0.82[JPT][hapmap]
rs66619347	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs72740550	0.86[ASN][1000 genomes]
rs7522325	1.00[CEU][hapmap];0.88[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv528460	chr1:196542567-197446702	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
2	nsv1014039	chr1:197311285-197529212	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 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	chr1:197324000-197347000	Weak transcription	Cortex derived primary cultured neurospheres	brain

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