Variant report

Variant	rs2791832
Chromosome Location	chr6:102295947-102295948
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 100 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:98)

rs_ID	r²[population]
rs10485276	0.80[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.91[AMR][1000 genomes];0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11156157	0.81[CHB][hapmap];0.91[JPT][hapmap]
rs11962789	0.81[CHB][hapmap];0.95[JPT][hapmap];0.90[ASN][1000 genomes]
rs1325060	0.88[CEU][hapmap];0.91[JPT][hapmap]
rs1340266	0.80[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1361444	0.80[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.91[AMR][1000 genomes];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1361445	0.80[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap]
rs1361446	0.80[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap]
rs1408767	0.82[ASN][1000 genomes]
rs1408768	0.80[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1555775	0.82[CHB][hapmap];0.91[JPT][hapmap]
rs1556993	0.80[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap]
rs1965603	0.81[CHB][hapmap];0.91[JPT][hapmap]
rs2038842	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2039853	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2147714	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2246394	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2399635	0.80[CEU][hapmap];0.86[CHB][hapmap];0.87[JPT][hapmap]
rs2399636	1.00[CHB][hapmap];0.95[JPT][hapmap];0.83[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs2518191	0.81[CHB][hapmap];0.91[JPT][hapmap];0.82[ASN][1000 genomes]
rs2518193	1.00[CHB][hapmap];0.95[JPT][hapmap];0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2518198	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs2518200	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs2518201	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs2518202	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs2518203	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs2518206	0.82[CHB][hapmap];0.91[JPT][hapmap];0.82[ASN][1000 genomes]
rs2518264	1.00[CEU][hapmap]
rs2518266	0.89[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap]
rs2518267	0.82[CHB][hapmap];0.91[JPT][hapmap];0.82[ASN][1000 genomes]
rs2518268	0.82[CHB][hapmap];0.91[JPT][hapmap];0.82[ASN][1000 genomes]
rs2518270	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2764218	0.89[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2764220	0.80[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2764222	0.80[CEU][hapmap];0.86[CHB][hapmap];0.87[JPT][hapmap];0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2764223	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2764224	0.82[JPT][hapmap]
rs2764225	0.81[CHB][hapmap];0.91[JPT][hapmap];0.82[ASN][1000 genomes]
rs2764226	0.80[CEU][hapmap];0.90[CHB][hapmap];0.86[JPT][hapmap];0.85[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2764228	1.00[CHB][hapmap];0.95[JPT][hapmap];0.85[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2764229	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2764230	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2764231	0.82[CHB][hapmap];0.91[JPT][hapmap]
rs2764233	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs2764236	0.89[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap]
rs2791812	0.80[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap]
rs2791813	1.00[CEU][hapmap]
rs2791817	0.95[JPT][hapmap]
rs2791818	0.80[CEU][hapmap];0.86[JPT][hapmap]
rs2791819	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2791821	0.81[CHB][hapmap];0.95[JPT][hapmap]
rs2791823	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2791826	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2791827	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2791834	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2791837	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs2852573	0.82[JPT][hapmap]
rs2852574	0.80[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap]
rs2852576	0.81[CHB][hapmap];0.91[JPT][hapmap]
rs4839802	0.82[CHB][hapmap];0.91[JPT][hapmap];0.82[ASN][1000 genomes]
rs4839803	0.81[CHB][hapmap];0.95[JPT][hapmap]
rs4839804	0.82[CHB][hapmap];0.95[JPT][hapmap]
rs4840195	0.89[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.82[AMR][1000 genomes];0.84[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4840196	0.89[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.82[AMR][1000 genomes];0.84[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4840197	0.90[JPT][hapmap]
rs4840198	0.82[CHB][hapmap];0.95[JPT][hapmap]
rs4840199	0.82[CHB][hapmap];0.95[JPT][hapmap]
rs6922753	0.89[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap]
rs7749469	0.86[JPT][hapmap]
rs7754022	0.86[JPT][hapmap]
rs7775876	0.80[ASN][1000 genomes]
rs9322609	0.91[JPT][hapmap]
rs9322611	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs9322613	0.82[CHB][hapmap];0.95[JPT][hapmap]
rs9377306	0.80[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9377307	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9377308	0.81[CHB][hapmap];0.91[JPT][hapmap];0.82[ASN][1000 genomes]
rs9377314	0.82[CHB][hapmap];0.95[JPT][hapmap]
rs9386291	0.86[JPT][hapmap]
rs9386293	0.85[AMR][1000 genomes];0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9386294	0.81[CHB][hapmap];0.95[JPT][hapmap];0.90[ASN][1000 genomes]
rs9390779	0.81[CHB][hapmap]
rs9390785	0.82[ASN][1000 genomes]
rs9390788	0.81[CHB][hapmap];0.95[JPT][hapmap];0.90[ASN][1000 genomes]
rs9399728	0.91[JPT][hapmap]
rs9399732	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9399733	0.90[JPT][hapmap];0.81[ASN][1000 genomes]
rs9404145	0.82[CHB][hapmap];0.91[JPT][hapmap]
rs9404148	0.80[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.91[AMR][1000 genomes];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9404152	0.82[CHB][hapmap];0.95[JPT][hapmap]
rs9404153	0.81[CHB][hapmap];0.95[JPT][hapmap]
rs9498691	0.81[CHB][hapmap];0.91[JPT][hapmap]
rs9498693	0.87[JPT][hapmap]
rs9498695	0.86[JPT][hapmap]
rs9498701	0.89[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.84[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs9498702	0.84[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs9498713	0.81[CHB][hapmap];0.91[JPT][hapmap]
rs9498727	0.82[CHB][hapmap];0.95[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1032499	chr6:102069885-102720998	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv830743	chr6:102284082-102459192	Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:102293800-102297400	Enhancers	iPS-15b Cell Line	embryonic stem cell
2	chr6:102293800-102297600	Enhancers	HUES64 Cell Line	embryonic stem cell
3	chr6:102294200-102297400	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr6:102294200-102297400	Enhancers	iPS-18 Cell Line	embryonic stem cell
5	chr6:102294400-102297400	Enhancers	HUES6 Cell Line	embryonic stem cell
6	chr6:102295200-102296400	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr6:102295400-102296000	Enhancers	H1 Cell Line	embryonic stem cell
8	chr6:102295400-102296000	Enhancers	H9 Cell Line	embryonic stem cell
9	chr6:102295400-102296200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr6:102295400-102296400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
11	chr6:102295800-102296200	Enhancers	iPS-20b Cell Line	embryonic stem cell

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