Variant report

Variant	rs186384
Chromosome Location	chr6:15813845-15813846
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs1041249	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1267672	0.81[EUR][1000 genomes]
rs170229	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs178331	0.89[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1883450	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs220892	0.89[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs220902	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs220906	0.91[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs220909	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs220910	0.91[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs220912	0.91[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs220915	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs220916	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs220921	0.98[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2327912	0.91[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2619511	0.83[EUR][1000 genomes]
rs2619513	0.82[EUR][1000 genomes]
rs2619554	0.85[EUR][1000 genomes]
rs391939	0.91[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs400487	0.91[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs4715994	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4715996	0.91[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs6459412	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs6908120	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs6926431	0.80[CHB][hapmap];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6942242	0.89[ASN][1000 genomes]
rs942088	0.91[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs942089	0.91[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs943726	0.82[EUR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:15800400-15816200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr6:15809800-15814800	Enhancers	Fetal Brain Male	brain
3	chr6:15813000-15817200	Weak transcription	K562	blood
4	chr6:15813800-15814400	Enhancers	Primary B cells from peripheral blood	blood

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