Variant report

Variant	rs61353392
Chromosome Location	chr2:168417394-168417395
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs10497325	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1113988	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11904438	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12104575	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1228656	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16841779	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16853635	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16853707	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16853726	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16853738	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16853749	0.87[AFR][1000 genomes];0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17564763	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17565731	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17622284	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17622965	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17623447	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2195790	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61010982	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73024082	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73024087	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73024093	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73026007	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73026011	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73026021	0.90[EUR][1000 genomes]
rs7572056	0.87[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7572439	0.87[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv491872	chr2:168220323-168737986	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	esv3388045	chr2:168289403-168424317	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
3	nsv834449	chr2:168340043-168511856	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv583592	chr2:168356232-168721539	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv1008206	chr2:168401249-168452887	ZNF genes & repeats Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
6	nsv528466	chr2:168402224-168447851	Enhancers Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
7	nsv583593	chr2:168402224-168452630	Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Active TSS Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
8	nsv1004326	chr2:168403386-168452887	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:168415000-168420800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr2:168415600-168419400	Weak transcription	H1 Cell Line	embryonic stem cell
3	chr2:168415800-168420800	Weak transcription	HUES48 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links