Variant report

Variant	rs16829613
Chromosome Location	chr2:152008379-152008380
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	chr2:151997273..151999659-chr2:152006906..152009074,2	K562	blood:
2	chr2:151998007..151999659-chr2:152006655..152009074,2	K562	blood:

Extended variants
information (count: 49 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs10490524	1.00[EUR][1000 genomes]
rs1073614	1.00[EUR][1000 genomes]
rs12990096	1.00[AFR][1000 genomes]
rs12997492	1.00[AFR][1000 genomes]
rs13009048	1.00[AFR][1000 genomes]
rs13010851	1.00[AFR][1000 genomes]
rs13013474	1.00[AFR][1000 genomes]
rs13014189	1.00[AFR][1000 genomes]
rs13026983	1.00[AFR][1000 genomes]
rs13035255	1.00[AFR][1000 genomes]
rs16823204	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs16829612	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16829615	1.00[EUR][1000 genomes]
rs16829662	1.00[EUR][1000 genomes]
rs16829668	1.00[EUR][1000 genomes]
rs16829671	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16829674	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16829680	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs16829682	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs16829715	1.00[CHB][hapmap];0.91[JPT][hapmap];1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs16829723	0.84[CHB][hapmap];1.00[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs16829752	1.00[AFR][1000 genomes]
rs289929	0.97[ASN][1000 genomes]
rs34221803	1.00[AFR][1000 genomes]
rs34238735	1.00[AFR][1000 genomes]
rs34557584	1.00[AFR][1000 genomes]
rs34573599	1.00[AFR][1000 genomes]
rs34677748	1.00[AFR][1000 genomes]
rs34873254	1.00[AFR][1000 genomes]
rs35052859	1.00[AFR][1000 genomes]
rs35110064	1.00[AFR][1000 genomes]
rs35451836	1.00[AFR][1000 genomes]
rs35555169	1.00[AFR][1000 genomes]
rs35691151	1.00[AFR][1000 genomes]
rs35758708	1.00[AFR][1000 genomes]
rs35868647	1.00[AFR][1000 genomes]
rs36104725	1.00[AFR][1000 genomes]
rs61637122	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs71208329	1.00[AFR][1000 genomes]
rs71415117	1.00[AFR][1000 genomes]
rs71415118	1.00[AFR][1000 genomes]
rs71415119	1.00[AFR][1000 genomes]
rs71415121	1.00[AFR][1000 genomes]
rs71415122	1.00[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 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
5	nsv834417	chr2:151980473-152154950	Enhancers Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:152006000-152008400	Enhancers	Fetal Lung	lung
2	chr2:152007200-152018000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr2:152007600-152010200	Weak transcription	Fetal Stomach	stomach

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