Variant report

Variant	rs73204613
Chromosome Location	chr13:55490631-55490632
allele	A/C
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:54)

rs_ID	r²[population]
rs11839135	0.80[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs12184758	0.82[EUR][1000 genomes]
rs1462189	0.96[EUR][1000 genomes]
rs1462191	0.83[EUR][1000 genomes]
rs1462202	0.96[EUR][1000 genomes]
rs1531450	0.98[EUR][1000 genomes]
rs1531451	0.98[EUR][1000 genomes]
rs1551834	0.94[EUR][1000 genomes]
rs1599559	0.96[EUR][1000 genomes]
rs2126418	0.96[EUR][1000 genomes]
rs2126419	0.84[EUR][1000 genomes]
rs2409555	0.82[EUR][1000 genomes]
rs2409556	0.82[EUR][1000 genomes]
rs263809	0.81[EUR][1000 genomes]
rs263810	0.96[EUR][1000 genomes]
rs263824	0.96[EUR][1000 genomes]
rs263825	0.84[EUR][1000 genomes]
rs263831	0.96[EUR][1000 genomes]
rs263832	0.96[EUR][1000 genomes]
rs263833	0.84[EUR][1000 genomes]
rs2800657	0.84[EUR][1000 genomes]
rs420371	0.84[EUR][1000 genomes]
rs6561803	0.96[EUR][1000 genomes]
rs6561804	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs6561805	0.80[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7317573	0.98[EUR][1000 genomes]
rs7320026	0.80[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs73202867	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs73202894	0.96[EUR][1000 genomes]
rs73204603	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs73204607	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs73204610	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs73204611	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs73204615	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs73204619	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs73204620	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs73204623	0.80[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs73204626	0.80[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs73204627	0.98[EUR][1000 genomes]
rs73204628	0.98[EUR][1000 genomes]
rs73204633	0.98[EUR][1000 genomes]
rs73204637	0.81[AFR][1000 genomes];0.83[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs73204639	0.89[AFR][1000 genomes];0.83[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7321772	0.94[EUR][1000 genomes]
rs7989867	0.96[EUR][1000 genomes]
rs8000832	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9316755	0.84[EUR][1000 genomes]
rs9527289	0.96[EUR][1000 genomes]
rs9536881	0.94[EUR][1000 genomes]
rs9536893	0.96[EUR][1000 genomes]
rs9536917	0.87[EUR][1000 genomes]
rs9536926	0.96[EUR][1000 genomes]
rs9536927	0.84[EUR][1000 genomes]
rs9805429	0.94[EUR][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	nsv561702	chr13:55086271-55808127	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
2	nsv900096	chr13:55363417-55508485	Enhancers ZNF genes & repeats Weak transcription	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv561704	chr13:55395253-55764633	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	1 gene(s)	inside rSNPs	diseases
4	nsv528493	chr13:55438905-55602402	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
5	nsv1051	chr13:55466546-55511292	Weak transcription Enhancers ZNF genes & repeats Active TSS	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:55485800-55491400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr13:55490600-55491800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links