Variant report

Variant	rs2508029
Chromosome Location	chr6:30146733-30146734
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 65 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:64)

rs_ID	r²[population]
rs1573295	0.86[ASN][1000 genomes]
rs2021366	0.82[ASN][1000 genomes]
rs2074472	0.95[AFR][1000 genomes];0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2074473	0.89[ASN][1000 genomes]
rs2097772	0.84[ASN][1000 genomes]
rs2106070	0.87[ASN][1000 genomes]
rs2106071	0.83[ASN][1000 genomes]
rs2107196	0.94[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2158283	0.83[ASN][1000 genomes]
rs2253163	0.82[ASN][1000 genomes]
rs2253164	0.82[ASN][1000 genomes]
rs2284164	0.90[ASN][1000 genomes]
rs2285801	0.80[ASN][1000 genomes]
rs2394737	0.92[ASN][1000 genomes]
rs28441239	0.85[ASN][1000 genomes]
rs2844782	0.94[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2844786	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3094131	0.86[ASN][1000 genomes]
rs3094132	0.86[ASN][1000 genomes]
rs3094139	0.90[ASN][1000 genomes]
rs3094140	0.86[ASN][1000 genomes]
rs3094614	0.87[ASN][1000 genomes]
rs3094615	0.84[ASN][1000 genomes]
rs3129694	0.81[ASN][1000 genomes]
rs3130381	0.86[ASN][1000 genomes]
rs3130382	0.87[ASN][1000 genomes]
rs3130383	0.87[ASN][1000 genomes]
rs3130384	0.87[ASN][1000 genomes]
rs3130386	0.87[ASN][1000 genomes]
rs3130387	0.83[ASN][1000 genomes]
rs3130388	0.86[ASN][1000 genomes]
rs3130389	0.90[ASN][1000 genomes]
rs3130391	0.86[ASN][1000 genomes]
rs3130393	0.85[ASN][1000 genomes]
rs3130394	0.85[ASN][1000 genomes]
rs3132665	0.84[ASN][1000 genomes]
rs3132668	0.85[ASN][1000 genomes]
rs3132669	0.86[ASN][1000 genomes]
rs3132671	0.87[ASN][1000 genomes]
rs3132672	0.87[ASN][1000 genomes]
rs3132673	0.89[ASN][1000 genomes]
rs3132674	0.89[ASN][1000 genomes]
rs35848695	0.81[ASN][1000 genomes]
rs4959046	0.82[ASN][1000 genomes]
rs6457164	0.92[ASN][1000 genomes]
rs6457165	0.92[ASN][1000 genomes]
rs6457167	0.92[ASN][1000 genomes]
rs718254	0.91[ASN][1000 genomes]
rs7382110	0.83[ASN][1000 genomes]
rs7383511	0.91[ASN][1000 genomes]
rs757257	0.96[ASN][1000 genomes]
rs765977	0.91[ASN][1000 genomes]
rs7763162	0.96[ASN][1000 genomes]
rs7764012	0.94[ASN][1000 genomes]
rs7774730	0.92[ASN][1000 genomes]
rs885914	0.80[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs885915	0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs916568	0.86[ASN][1000 genomes]
rs916571	0.90[ASN][1000 genomes]
rs916572	0.90[ASN][1000 genomes]
rs9261539	0.92[ASN][1000 genomes]
rs9261543	0.92[ASN][1000 genomes]
rs9261546	0.96[ASN][1000 genomes]
rs9261548	0.80[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv884057	chr6:30140540-30149251	ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Active TSS Bivalent Enhancer Enhancers Strong transcription Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:30139000-30152000	Weak transcription	Liver	Liver
2	chr6:30142000-30149200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr6:30145000-30173800	Weak transcription	Right Atrium	heart
4	chr6:30146200-30147600	Enhancers	HepG2	liver

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