Variant report

Variant	rs6958059
Chromosome Location	chr7:96722041-96722042
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 26 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs1014341	0.95[CHB][hapmap];0.83[JPT][hapmap];0.90[YRI][hapmap]
rs10229181	0.95[CHB][hapmap]
rs10231916	0.81[CEU][hapmap];0.95[CHB][hapmap];0.83[JPT][hapmap];0.85[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs10235199	0.95[CHB][hapmap]
rs10246622	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10260298	0.95[CHB][hapmap];0.83[JPT][hapmap];0.90[YRI][hapmap]
rs10275135	0.85[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs11972232	0.82[CEU][hapmap];0.96[CHB][hapmap];0.83[JPT][hapmap];0.90[YRI][hapmap]
rs11980904	0.94[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1199289	0.96[CHB][hapmap]
rs1199292	0.95[CHB][hapmap];0.83[JPT][hapmap]
rs12056091	0.80[CEU][hapmap];0.95[CHB][hapmap]
rs12669915	0.82[CEU][hapmap];0.96[CHB][hapmap];0.83[JPT][hapmap]
rs13475	0.92[CHB][hapmap];0.83[JPT][hapmap]
rs1534370	0.95[CHB][hapmap];0.83[JPT][hapmap];0.90[YRI][hapmap]
rs2140954	0.82[CHB][hapmap];0.91[AMR][1000 genomes];0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs28825121	0.85[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs4729330	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6465571	0.95[CHB][hapmap];0.83[JPT][hapmap];0.90[YRI][hapmap]
rs6973369	0.85[CEU][hapmap];0.95[CHB][hapmap];0.83[JPT][hapmap];0.89[AMR][1000 genomes];0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs73233819	0.91[AMR][1000 genomes];0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7787376	0.84[CEU][hapmap];0.91[CHB][hapmap];0.82[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7794886	0.81[CEU][hapmap];0.95[CHB][hapmap];0.83[JPT][hapmap];0.85[AMR][1000 genomes];0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7803945	0.82[CEU][hapmap]
rs7810432	0.81[CEU][hapmap];0.95[CHB][hapmap];0.83[JPT][hapmap];0.90[YRI][hapmap]
rs7811797	0.91[AFR][1000 genomes];0.88[AMR][1000 genomes];0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:96720600-96722400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr7:96722000-96722800	Enhancers	HepG2	liver

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