Variant report

Variant	rs9317650
Chromosome Location	chr13:67774520-67774521
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs12857493	1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs1983871	0.86[ASN][1000 genomes]
rs1983949	0.91[CHB][hapmap];0.82[JPT][hapmap];0.91[ASN][1000 genomes]
rs2147998	0.91[CHB][hapmap];0.82[JPT][hapmap];0.86[ASN][1000 genomes]
rs2182229	0.85[ASN][1000 genomes]
rs2325025	0.91[CHB][hapmap];0.88[CHD][hapmap];0.81[GIH][hapmap];0.83[ASN][1000 genomes]
rs2325027	0.91[CHB][hapmap];0.90[CHD][hapmap];0.81[GIH][hapmap];0.83[ASN][1000 genomes]
rs2985931	0.80[GIH][hapmap]
rs3812859	0.80[ASN][1000 genomes]
rs3812860	0.91[CHB][hapmap];0.88[CHD][hapmap];0.83[GIH][hapmap];0.81[ASN][1000 genomes]
rs4884719	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[YRI][hapmap];0.83[AFR][1000 genomes];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4884720	0.91[CHB][hapmap];0.82[JPT][hapmap];0.89[ASN][1000 genomes]
rs700329	0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs71427643	0.85[ASN][1000 genomes]
rs7489531	0.86[ASN][1000 genomes]
rs7992750	0.87[ASN][1000 genomes]
rs8002263	0.80[ASN][1000 genomes]
rs9317651	0.91[CHB][hapmap];0.91[CHD][hapmap];0.81[GIH][hapmap];0.82[JPT][hapmap];0.87[ASN][1000 genomes]
rs9317655	0.92[AFR][1000 genomes];0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9529199	0.91[CHB][hapmap];0.82[JPT][hapmap];0.89[ASN][1000 genomes]
rs9529206	0.83[ASN][1000 genomes]
rs9541034	0.83[ASN][1000 genomes]
rs9541035	0.91[CHB][hapmap];0.91[CHD][hapmap];0.81[GIH][hapmap];0.83[ASN][1000 genomes]
rs9571740	0.91[CHB][hapmap];0.91[CHD][hapmap];0.81[GIH][hapmap];0.83[MEX][hapmap];0.83[ASN][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	nsv1035741	chr13:67212973-68077950	Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv541817	chr13:67212973-68077950	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Active TSS Genic enhancers Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv1053514	chr13:67687520-67775011	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:67731400-67795400	Weak transcription	Primary B cells from cord blood	blood
2	chr13:67750600-67780800	Weak transcription	Brain Inferior Temporal Lobe	brain
3	chr13:67756200-67795800	Weak transcription	Left Ventricle	heart
4	chr13:67767000-67783000	Weak transcription	HSMM	muscle
5	chr13:67772200-67797200	Weak transcription	Fetal Kidney	kidney
6	chr13:67773600-67775200	Active TSS	A549	lung
7	chr13:67773800-67775000	Enhancers	Brain Anterior Caudate	brain
8	chr13:67773800-67775000	Enhancers	Brain Cingulate Gyrus	brain
9	chr13:67773800-67775000	Enhancers	Brain Substantia Nigra	brain
10	chr13:67774000-67775000	Enhancers	Brain Hippocampus Middle	brain
11	chr13:67774000-67775000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
12	chr13:67774400-67775000	Enhancers	Brain Angular Gyrus	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links