Variant report

Variant	rs377467
Chromosome Location	chr10:55296171-55296172
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 98 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:89)

rs_ID	r²[population]
rs10508996	0.86[ASN][1000 genomes]
rs10762989	0.97[ASN][1000 genomes]
rs10762990	0.94[ASN][1000 genomes]
rs10762992	0.94[ASN][1000 genomes]
rs10825032	0.81[ASN][1000 genomes]
rs10825036	0.84[ASN][1000 genomes]
rs10825037	0.86[ASN][1000 genomes]
rs10825039	0.87[ASN][1000 genomes]
rs10825040	0.90[ASN][1000 genomes]
rs10825044	0.88[ASN][1000 genomes]
rs10825045	0.87[ASN][1000 genomes]
rs10825046	0.87[ASN][1000 genomes]
rs10825048	0.87[ASN][1000 genomes]
rs10825049	0.85[ASN][1000 genomes]
rs10825050	0.85[ASN][1000 genomes]
rs10825051	0.90[ASN][1000 genomes]
rs10825054	0.94[ASN][1000 genomes]
rs10825056	0.93[ASN][1000 genomes]
rs10825057	0.97[ASN][1000 genomes]
rs10825058	0.96[ASN][1000 genomes]
rs10825059	0.92[ASN][1000 genomes]
rs10825060	0.92[ASN][1000 genomes]
rs10825061	0.93[ASN][1000 genomes]
rs10825062	0.97[ASN][1000 genomes]
rs11003648	0.81[ASN][1000 genomes]
rs11003652	0.81[ASN][1000 genomes]
rs11003660	0.87[ASN][1000 genomes]
rs11003662	0.85[ASN][1000 genomes]
rs11003663	0.97[ASN][1000 genomes]
rs11003667	0.97[ASN][1000 genomes]
rs11003673	0.89[ASN][1000 genomes]
rs1157254	0.87[ASN][1000 genomes]
rs12355148	0.83[ASN][1000 genomes]
rs12355167	0.83[ASN][1000 genomes]
rs12358302	0.82[ASN][1000 genomes]
rs1814085	0.87[ASN][1000 genomes]
rs28841706	0.83[ASN][1000 genomes]
rs34965206	0.87[ASN][1000 genomes]
rs351821	0.86[ASN][1000 genomes]
rs365441	0.88[ASN][1000 genomes]
rs367119	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs367719	0.88[ASN][1000 genomes]
rs369462	0.88[ASN][1000 genomes]
rs369979	0.89[ASN][1000 genomes]
rs371048	0.97[ASN][1000 genomes]
rs372884	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs373544	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs374406	0.87[ASN][1000 genomes]
rs374873	0.89[ASN][1000 genomes]
rs379770	0.92[ASN][1000 genomes]
rs379828	0.89[ASN][1000 genomes]
rs380479	0.89[ASN][1000 genomes]
rs381474	0.88[ASN][1000 genomes]
rs383932	0.88[ASN][1000 genomes]
rs387908	0.88[ASN][1000 genomes]
rs390597	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs399626	0.91[ASN][1000 genomes]
rs402461	0.91[ASN][1000 genomes]
rs403436	0.92[ASN][1000 genomes]
rs405136	0.86[ASN][1000 genomes]
rs405138	0.86[ASN][1000 genomes]
rs407008	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs408049	0.95[ASN][1000 genomes]
rs414705	0.91[ASN][1000 genomes]
rs414874	0.91[ASN][1000 genomes]
rs416975	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs417046	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs421811	0.94[ASN][1000 genomes]
rs422296	0.95[ASN][1000 genomes]
rs426610	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs428019	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs445739	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs447188	0.97[ASN][1000 genomes]
rs447399	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs452339	0.95[ASN][1000 genomes]
rs595633	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs612779	0.83[ASN][1000 genomes]
rs612813	0.86[ASN][1000 genomes]
rs61862612	0.90[ASN][1000 genomes]
rs7072272	0.87[ASN][1000 genomes]
rs7072928	0.88[ASN][1000 genomes]
rs7080156	0.86[ASN][1000 genomes]
rs7083928	0.90[ASN][1000 genomes]
rs7084959	0.90[ASN][1000 genomes]
rs7097071	0.90[ASN][1000 genomes]
rs7097292	0.86[ASN][1000 genomes]
rs7098611	0.88[ASN][1000 genomes]
rs7903691	0.90[ASN][1000 genomes]
rs996212	0.97[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2752952	chr10:54900994-55497594	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv1048399	chr10:55151470-55313737	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv1044282	chr10:55186501-55516392	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv540631	chr10:55186501-55516392	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv1043501	chr10:55186701-55516253	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	nsv540632	chr10:55186701-55516253	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	nsv1050323	chr10:55190079-55546575	Weak transcription ZNF genes & repeats Enhancers Active TSS Strong transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
8	esv3390330	chr10:55281995-55298396	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
9	esv19178	chr10:55294558-55296490	Enhancers Weak transcription	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	chr10:55289000-55315600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr10:55295800-55296400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr10:55296000-55296600	Enhancers	Fetal Adrenal Gland	Adrenal Gland

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links