Variant report

Variant	rs10490338
Chromosome Location	chr2:40181783-40181784
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 124 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:99)

rs_ID	r²[population]
rs1013954	0.84[ASN][1000 genomes]
rs10169489	0.95[EUR][1000 genomes]
rs10181331	0.94[ASN][1000 genomes]
rs10191782	0.83[ASN][1000 genomes]
rs10200630	0.96[ASN][1000 genomes]
rs10865160	0.96[ASN][1000 genomes]
rs11124713	0.87[ASN][1000 genomes]
rs11124723	0.81[ASN][1000 genomes]
rs11685420	0.87[ASN][1000 genomes]
rs11888334	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11889689	0.94[ASN][1000 genomes]
rs11893312	0.94[ASN][1000 genomes]
rs11902593	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12463415	0.82[ASN][1000 genomes]
rs12464341	0.89[ASN][1000 genomes]
rs12474732	0.84[ASN][1000 genomes]
rs12622032	0.82[ASN][1000 genomes]
rs12712668	0.94[ASN][1000 genomes]
rs12712669	0.94[ASN][1000 genomes]
rs12988439	0.86[ASN][1000 genomes]
rs13015010	0.87[ASN][1000 genomes]
rs13015269	0.87[ASN][1000 genomes]
rs13390026	0.81[ASN][1000 genomes]
rs13418507	0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1476989	0.96[ASN][1000 genomes]
rs1476990	0.95[ASN][1000 genomes]
rs1541561	0.96[ASN][1000 genomes]
rs1548876	0.84[ASN][1000 genomes]
rs17024636	0.87[ASN][1000 genomes]
rs17024711	0.81[ASN][1000 genomes]
rs17024746	0.81[ASN][1000 genomes]
rs1861250	0.83[ASN][1000 genomes]
rs1861251	0.83[ASN][1000 genomes]
rs2058627	0.94[EUR][1000 genomes]
rs2058636	0.96[ASN][1000 genomes]
rs2058637	0.96[ASN][1000 genomes]
rs2058638	0.97[ASN][1000 genomes]
rs2058639	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2080298	0.96[ASN][1000 genomes]
rs2215967	0.85[ASN][1000 genomes]
rs2373705	0.98[ASN][1000 genomes]
rs2373707	0.85[ASN][1000 genomes]
rs2373708	0.96[ASN][1000 genomes]
rs2373709	0.96[ASN][1000 genomes]
rs2373710	0.84[ASN][1000 genomes]
rs2373787	0.83[MEX][hapmap]
rs2888639	0.96[ASN][1000 genomes]
rs4321345	0.86[ASN][1000 genomes]
rs4519500	0.84[ASN][1000 genomes]
rs4670299	0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4670994	0.90[ASN][1000 genomes]
rs4670995	0.90[ASN][1000 genomes]
rs56118530	0.98[ASN][1000 genomes]
rs57091596	0.88[ASN][1000 genomes]
rs57677588	0.84[ASN][1000 genomes]
rs58570175	0.84[ASN][1000 genomes]
rs58969983	0.98[ASN][1000 genomes]
rs59034193	0.98[ASN][1000 genomes]
rs59957738	0.84[ASN][1000 genomes]
rs60613668	0.84[ASN][1000 genomes]
rs61481161	0.84[ASN][1000 genomes]
rs61604673	0.81[ASN][1000 genomes]
rs62136383	0.87[ASN][1000 genomes]
rs62137255	0.98[ASN][1000 genomes]
rs62150227	0.86[ASN][1000 genomes]
rs62150228	0.83[ASN][1000 genomes]
rs62150232	0.82[ASN][1000 genomes]
rs62150235	0.81[ASN][1000 genomes]
rs6544273	0.94[ASN][1000 genomes]
rs6544274	0.94[ASN][1000 genomes]
rs6544275	0.93[ASN][1000 genomes]
rs6544277	0.95[ASN][1000 genomes]
rs6544280	0.83[ASN][1000 genomes]
rs6544282	0.83[ASN][1000 genomes]
rs6544296	0.82[ASN][1000 genomes]
rs6725817	0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6735955	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs725374	0.90[ASN][1000 genomes]
rs733958	0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs737589	0.90[ASN][1000 genomes]
rs741270	0.84[ASN][1000 genomes]
rs7564447	0.81[ASN][1000 genomes]
rs7572755	0.89[ASN][1000 genomes]
rs7584288	0.98[ASN][1000 genomes]
rs759353	0.84[ASN][1000 genomes]
rs759356	0.81[ASN][1000 genomes]
rs759357	0.81[ASN][1000 genomes]
rs7599493	0.82[ASN][1000 genomes]
rs7600580	0.84[ASN][1000 genomes]
rs7607499	0.81[ASN][1000 genomes]
rs768271	0.87[ASN][1000 genomes]
rs8179517	0.81[ASN][1000 genomes]
rs917970	0.84[ASN][1000 genomes]
rs917971	0.85[ASN][1000 genomes]
rs917974	0.81[ASN][1000 genomes]
rs957117	0.88[ASN][1000 genomes]
rs9749783	0.82[ASN][1000 genomes]
rs979716	0.91[ASN][1000 genomes]
rs985455	0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:25 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv916300	chr2:40079899-40339019	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv1003896	chr2:40094081-40231585	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv1010609	chr2:40107234-40231674	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv535652	chr2:40107234-40231674	Weak transcription Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv998885	chr2:40123904-40182851	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	nsv873893	chr2:40137942-40222206	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
7	nsv873894	chr2:40139250-40198380	Enhancers Flanking Active TSS Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
8	nsv873895	chr2:40139250-40207338	Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
9	nsv873896	chr2:40139250-40208665	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
10	nsv873897	chr2:40139250-40225253	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
11	nsv869668	chr2:40141079-40249854	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
12	nsv1003920	chr2:40141776-40245464	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
13	nsv1000423	chr2:40143646-40245464	Enhancers Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
14	nsv456385	chr2:40151882-40195548	Enhancers Genic enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
15	nsv581497	chr2:40151882-40195548	Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
16	nsv456396	chr2:40154844-40231282	Enhancers Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
17	nsv581498	chr2:40154844-40231282	Enhancers Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
18	nsv581499	chr2:40154844-40241868	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
19	nsv873898	chr2:40156882-40246716	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
20	nsv456407	chr2:40158363-40208665	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
21	nsv581500	chr2:40158363-40208665	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
22	nsv873899	chr2:40161168-40281964	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
23	nsv1006550	chr2:40164769-40209936	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
24	nsv1009532	chr2:40165606-40291224	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
25	nsv535653	chr2:40165606-40291224	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:40176200-40195200	Weak transcription	HSMM	muscle
2	chr2:40176400-40181800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr2:40181200-40182000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr2:40181200-40182000	Enhancers	Muscle Satellite Cultured Cells	--
5	chr2:40181200-40182000	Enhancers	Osteobl	bone
6	chr2:40181400-40182000	Enhancers	NH-A	brain
7	chr2:40181600-40182000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr2:40181600-40182000	Enhancers	HMEC	breast

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links