Variant report

Variant	rs7636316
Chromosome Location	chr3:144274117-144274118
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 59 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs1036439	0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10490827	1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10935507	0.86[ASN][1000 genomes]
rs12631899	0.84[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12632855	1.00[ASN][1000 genomes]
rs12638468	0.92[ASN][1000 genomes]
rs12638544	0.95[ASN][1000 genomes]
rs12639461	0.98[ASN][1000 genomes]
rs13081974	0.91[ASN][1000 genomes]
rs1815189	0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4290842	0.92[ASN][1000 genomes]
rs4388021	0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4681126	0.89[ASN][1000 genomes]
rs56096828	1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs56178175	0.94[ASN][1000 genomes]
rs56191622	1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs56228220	1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs57393618	0.87[ASN][1000 genomes]
rs59900584	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61641065	1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6783056	0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs73009099	0.92[ASN][1000 genomes]
rs73871205	0.94[ASN][1000 genomes]
rs73871207	0.94[ASN][1000 genomes]
rs73871211	0.98[ASN][1000 genomes]
rs73871221	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs73871228	0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs73871240	0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs73871243	0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs73871244	0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs73871245	0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs73871248	0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs73871252	0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs73875119	0.92[ASN][1000 genomes]
rs73875127	0.92[ASN][1000 genomes]
rs73875134	0.92[ASN][1000 genomes]
rs73875140	0.94[ASN][1000 genomes]
rs7614253	0.83[ASN][1000 genomes]
rs7630402	0.85[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs7637942	0.88[ASN][1000 genomes]
rs920146	0.93[ASN][1000 genomes]
rs9844730	0.86[ASN][1000 genomes]
rs9866198	0.88[ASN][1000 genomes]
rs9866442	0.89[ASN][1000 genomes]
rs9873732	0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv532633	chr3:143802417-144440646	Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv591928	chr3:144050897-144822081	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	esv2756108	chr3:144177836-144301659	Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv877571	chr3:144188561-144291254	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	esv3379740	chr3:144225847-144433818	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv1010388	chr3:144236022-144326640	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
7	esv2757895	chr3:144236202-144391387	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
8	esv2759185	chr3:144236202-144391387	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
9	nsv1013350	chr3:144239415-144326640	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
10	nsv536754	chr3:144239415-144326640	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
11	nsv877572	chr3:144244265-144312402	Weak transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
12	nsv1012719	chr3:144264442-144283362	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
13	nsv877573	chr3:144265840-144323993	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
14	nsv1014395	chr3:144268563-144283849	Weak transcription Enhancers	n/a	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	chr3:144271800-144275200	Weak transcription	Fetal Intestine Small	intestine
2	chr3:144274000-144274200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr3:144274000-144277000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links