Variant report

Variant	rs73750395
Chromosome Location	chr6:82049820-82049821
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 71 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:68)

rs_ID	r²[population]
rs1321763	1.00[EUR][1000 genomes]
rs1321764	1.00[EUR][1000 genomes]
rs16879669	1.00[EUR][1000 genomes]
rs16893157	1.00[EUR][1000 genomes]
rs1857302	1.00[EUR][1000 genomes]
rs1923151	1.00[EUR][1000 genomes]
rs1923152	1.00[EUR][1000 genomes]
rs1923153	1.00[EUR][1000 genomes]
rs1923154	1.00[EUR][1000 genomes]
rs4121081	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56139622	1.00[EUR][1000 genomes]
rs56166038	1.00[EUR][1000 genomes]
rs56347700	1.00[EUR][1000 genomes]
rs56354221	1.00[EUR][1000 genomes]
rs57049010	1.00[EUR][1000 genomes]
rs57540087	1.00[EUR][1000 genomes]
rs58348892	1.00[EUR][1000 genomes]
rs59561150	1.00[EUR][1000 genomes]
rs59828216	1.00[EUR][1000 genomes]
rs61279115	1.00[EUR][1000 genomes]
rs6903301	1.00[EUR][1000 genomes]
rs6903470	1.00[EUR][1000 genomes]
rs6903966	1.00[EUR][1000 genomes]
rs6904093	1.00[EUR][1000 genomes]
rs6904760	1.00[EUR][1000 genomes]
rs6905459	1.00[EUR][1000 genomes]
rs6909563	1.00[EUR][1000 genomes]
rs6923049	1.00[EUR][1000 genomes]
rs6923636	1.00[EUR][1000 genomes]
rs6926893	1.00[EUR][1000 genomes]
rs6931780	1.00[EUR][1000 genomes]
rs73480493	0.83[AMR][1000 genomes]
rs73748903	1.00[EUR][1000 genomes]
rs73748980	1.00[EUR][1000 genomes]
rs73749103	1.00[EUR][1000 genomes]
rs73749105	1.00[EUR][1000 genomes]
rs73749107	1.00[EUR][1000 genomes]
rs73749108	1.00[EUR][1000 genomes]
rs73749122	1.00[EUR][1000 genomes]
rs73749125	1.00[EUR][1000 genomes]
rs73749126	1.00[EUR][1000 genomes]
rs73749127	1.00[EUR][1000 genomes]
rs73749128	1.00[EUR][1000 genomes]
rs73749130	1.00[EUR][1000 genomes]
rs73749131	1.00[EUR][1000 genomes]
rs73749132	1.00[EUR][1000 genomes]
rs73749134	1.00[EUR][1000 genomes]
rs73749135	1.00[EUR][1000 genomes]
rs73749136	1.00[EUR][1000 genomes]
rs73749137	1.00[EUR][1000 genomes]
rs73749138	1.00[EUR][1000 genomes]
rs73749139	1.00[EUR][1000 genomes]
rs73749140	1.00[EUR][1000 genomes]
rs73749141	1.00[EUR][1000 genomes]
rs73749142	1.00[EUR][1000 genomes]
rs73750390	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73750394	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73750396	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73751152	1.00[EUR][1000 genomes]
rs73751432	1.00[EUR][1000 genomes]
rs73751433	1.00[EUR][1000 genomes]
rs73751439	1.00[EUR][1000 genomes]
rs73751440	1.00[EUR][1000 genomes]
rs73751441	1.00[EUR][1000 genomes]
rs73751443	1.00[EUR][1000 genomes]
rs73751445	1.00[EUR][1000 genomes]
rs9688608	1.00[EUR][1000 genomes]
rs9688618	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv604087	chr6:81792413-82326091	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv1032655	chr6:81942397-82225830	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
3	nsv886328	chr6:82036764-82120647	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	Chromatin interactive region	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	chr6:82047600-82059000	Weak transcription	ES-I3 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links