Variant report

Variant	rs10264765
Chromosome Location	chr7:137177213-137177214
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs10228926	1.00[CEU][hapmap];0.88[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs10235650	1.00[CEU][hapmap];0.93[YRI][hapmap];0.95[EUR][1000 genomes]
rs10236626	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10236885	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs10249961	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs10250999	1.00[CEU][hapmap];0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs10257221	1.00[CEU][hapmap];0.93[YRI][hapmap];0.86[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10268873	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10268889	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10276002	0.83[CEU][hapmap];1.00[EUR][1000 genomes]
rs10480523	1.00[CEU][hapmap];0.88[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs12707360	1.00[CEU][hapmap];0.83[YRI][hapmap];0.97[EUR][1000 genomes]
rs13242243	0.98[EUR][1000 genomes]
rs1406088	1.00[CEU][hapmap];0.96[YRI][hapmap];0.96[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1528099	1.00[CEU][hapmap];0.88[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1528100	1.00[CEU][hapmap];0.88[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1852641	1.00[CEU][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28434741	0.98[EUR][1000 genomes]
rs28491569	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs28573283	0.80[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs34395849	0.97[EUR][1000 genomes]
rs35080869	0.97[EUR][1000 genomes]
rs35470018	1.00[EUR][1000 genomes]
rs35481034	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs36125942	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6467704	1.00[CEU][hapmap];0.93[YRI][hapmap];0.97[EUR][1000 genomes]
rs6467705	1.00[CEU][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6467706	1.00[CEU][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6467707	0.91[CEU][hapmap];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs67112765	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs68124742	0.95[EUR][1000 genomes]
rs6950579	1.00[CEU][hapmap];0.88[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs6951059	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs6971080	1.00[CEU][hapmap];0.88[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7341469	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7341533	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7779526	1.00[CEU][hapmap];0.89[YRI][hapmap];0.95[EUR][1000 genomes]
rs7788161	1.00[CEU][hapmap];0.88[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7802865	1.00[CEU][hapmap];0.88[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7807425	1.00[CEU][hapmap];0.97[YRI][hapmap];0.94[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9655902	0.89[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869820	chr7:136990386-137347718	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
2	nsv1027868	chr7:137004690-137311653	Enhancers Flanking Active TSS Strong transcription Active TSS Weak transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
3	nsv539134	chr7:137004690-137311653	Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:137148600-137206400	Weak transcription	Aorta	Aorta
2	chr7:137152000-137179400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr7:137162000-137179000	Weak transcription	HSMM	muscle
4	chr7:137162000-137179000	Weak transcription	HSMMtube	muscle
5	chr7:137163600-137179000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr7:137166200-137177800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr7:137167800-137192800	Weak transcription	Osteobl	bone
8	chr7:137170200-137193000	Weak transcription	Muscle Satellite Cultured Cells	--
9	chr7:137176600-137177800	Enhancers	Brain Anterior Caudate	brain
10	chr7:137177200-137177800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links