Variant report

Variant	rs9476923
Chromosome Location	chr6:15785358-15785359
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:15784288..15786128-chr6:15797785..15800646,2	K562	blood:
2	chr6:15785339..15788012-chr6:15788868..15790666,2	MCF-7	breast:
3	chr6:15784886..15786712-chr6:15791467..15793235,2	K562	blood:

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs10949314	0.85[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.87[AFR][1000 genomes];0.90[AMR][1000 genomes];0.81[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10949315	0.99[ASN][1000 genomes]
rs12192181	0.82[CHB][hapmap];0.90[JPT][hapmap];0.82[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs12332848	0.94[ASN][1000 genomes]
rs12333139	0.93[ASN][1000 genomes]
rs1927575	0.87[AFR][1000 genomes];0.90[AMR][1000 genomes];0.81[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2149146	0.87[AFR][1000 genomes];0.90[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs220895	0.86[YRI][hapmap]
rs220897	0.83[YRI][hapmap]
rs220898	0.85[YRI][hapmap]
rs220899	0.83[YRI][hapmap]
rs220900	0.83[YRI][hapmap]
rs220917	0.81[AFR][1000 genomes]
rs220918	0.81[AFR][1000 genomes]
rs413080	0.85[YRI][hapmap]
rs4712256	0.91[AFR][1000 genomes];0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4715997	0.81[AFR][1000 genomes];0.91[AMR][1000 genomes];0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6911160	0.90[AMR][1000 genomes];0.81[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6925866	0.90[AMR][1000 genomes];0.81[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6935121	0.83[CHB][hapmap];0.90[JPT][hapmap];0.82[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs742386	0.83[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs742387	0.82[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs7739472	0.87[AFR][1000 genomes];0.91[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7739977	0.91[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7756956	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9476906	0.83[CHB][hapmap];0.90[JPT][hapmap];0.82[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs9476911	0.98[ASN][1000 genomes]
rs9476912	0.90[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs9476920	0.91[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs9476921	0.99[ASN][1000 genomes]
rs9476922	0.83[AFR][1000 genomes];0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:15782400-15789200	Weak transcription	Fetal Intestine Large	intestine
2	chr6:15783600-15785400	Enhancers	Pancreas	Pancrea
3	chr6:15784800-15785600	Enhancers	Gastric	stomach

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