Variant report

Variant	rs4693317
Chromosome Location	chr4:94347094-94347095
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 57 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs10006372	0.88[ASN][1000 genomes]
rs10012463	0.84[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs10018947	0.90[ASN][1000 genomes]
rs10019885	0.83[ASN][1000 genomes]
rs10022753	0.90[ASN][1000 genomes]
rs10026391	1.00[ASN][1000 genomes]
rs10029321	0.90[ASN][1000 genomes]
rs1032125	0.98[ASN][1000 genomes]
rs1032126	0.88[ASN][1000 genomes]
rs10516919	0.88[ASN][1000 genomes]
rs11097362	0.82[AFR][1000 genomes];0.81[AMR][1000 genomes];0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11097363	0.94[ASN][1000 genomes]
rs11097364	0.91[ASN][1000 genomes]
rs1154861	0.88[ASN][1000 genomes]
rs11727464	0.82[ASN][1000 genomes]
rs1368715	0.82[ASN][1000 genomes]
rs1385410	0.86[ASN][1000 genomes]
rs1433659	0.82[ASN][1000 genomes]
rs1485023	0.83[ASN][1000 genomes]
rs1485033	0.86[ASN][1000 genomes]
rs1583337	0.81[ASN][1000 genomes]
rs17330509	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1816432	0.83[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs1872383	0.90[ASN][1000 genomes]
rs1905710	0.80[ASN][1000 genomes]
rs1905723	0.81[ASN][1000 genomes]
rs1905725	0.81[ASN][1000 genomes]
rs1905729	0.83[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs1905730	0.88[ASN][1000 genomes]
rs1905732	0.87[ASN][1000 genomes]
rs2046418	0.84[ASN][1000 genomes]
rs2200376	0.83[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs2220179	0.86[ASN][1000 genomes]
rs28404006	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs28446769	0.83[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs2870703	0.81[ASN][1000 genomes]
rs2870704	0.86[ASN][1000 genomes]
rs2870706	0.87[ASN][1000 genomes]
rs2904483	0.86[ASN][1000 genomes]
rs3913651	0.90[ASN][1000 genomes]
rs4693318	0.87[ASN][1000 genomes]
rs4693319	0.88[ASN][1000 genomes]
rs6836194	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6851479	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7661436	0.83[ASN][1000 genomes]
rs7668090	0.99[ASN][1000 genomes]
rs7670441	0.88[ASN][1000 genomes]
rs9790436	1.00[ASN][1000 genomes]
rs9994126	0.88[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs9996912	0.86[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1013255	chr4:94027129-94462345	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	esv2830401	chr4:94141655-94450106	Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	esv3584808	chr4:94156602-94559327	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv1008055	chr4:94169131-95030074	Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv533846	chr4:94264488-94462921	Enhancers Flanking Bivalent TSS/Enh Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv931979	chr4:94289958-95121723	Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
7	esv3336442	chr4:94344229-94348727	Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:94338000-94353600	Weak transcription	HUES48 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links