Variant report

Variant	rs1906216
Chromosome Location	chr8:122377649-122377650
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 63 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:56)

rs_ID	r²[population]
rs10094084	0.94[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs10102395	0.85[ASN][1000 genomes]
rs10107573	0.96[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs10481070	0.92[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs10481147	0.94[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs10505401	0.80[ASN][1000 genomes]
rs10956033	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10956035	0.96[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs10956038	0.94[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs10956039	0.94[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs10956040	0.94[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs11993674	0.81[ASN][1000 genomes]
rs12545486	0.94[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs13265234	0.94[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs13265478	0.94[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs13267289	0.81[ASN][1000 genomes]
rs13269889	0.81[ASN][1000 genomes]
rs13274258	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1386442	0.81[ASN][1000 genomes]
rs1487158	0.81[ASN][1000 genomes]
rs1487162	0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1487168	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1487169	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1487170	0.94[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs1565035	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs16892957	0.87[ASN][1000 genomes]
rs1843789	0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1843790	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2046570	0.87[ASN][1000 genomes]
rs2385927	0.90[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs2386122	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2891939	0.94[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs4144692	0.87[ASN][1000 genomes]
rs4282581	0.80[ASN][1000 genomes]
rs4460379	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4871187	1.00[CEU][hapmap];1.00[CHB][hapmap];0.84[CHD][hapmap];1.00[JPT][hapmap]
rs6469998	0.96[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs6470000	0.81[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs6985415	0.96[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs6988724	0.96[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs7000174	0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7004666	0.90[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs7006642	0.92[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs7006650	0.90[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs7008446	0.94[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs7008769	0.96[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs7015873	0.96[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs7017097	0.94[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs73332335	0.80[ASN][1000 genomes]
rs7824421	0.82[CEU][hapmap];0.87[CHB][hapmap];0.84[CHD][hapmap];0.90[JPT][hapmap];0.96[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs7824450	0.94[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs7829217	0.94[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs7838314	0.96[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs7846340	0.81[ASN][1000 genomes]
rs9643156	0.81[ASN][1000 genomes]
rs982818	0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv891424	chr8:121873345-122393258	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	esv3330574	chr8:122039099-122386130	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv891426	chr8:122078334-122393258	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv1025365	chr8:122323246-122394774	Weak transcription Flanking Active TSS Enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv465792	chr8:122329373-122398867	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv612131	chr8:122329373-122398867	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv831445	chr8:122336877-122509300	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:122375600-122377800	Weak transcription	Osteobl	bone
2	chr8:122377000-122379200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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