Variant report

Variant	rs61959367
Chromosome Location	chr13:67662064-67662065
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr13:67660306..67662402-chr13:67696166..67698306,2	K562	blood:

Extended variants
information (count: 85 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:74)

rs_ID	r²[population]
rs10492596	0.97[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10492597	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11148737	0.97[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11148738	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12184632	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12184736	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12372837	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1408171	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs149448	0.97[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs17195259	0.97[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs17195266	0.83[AFR][1000 genomes];0.97[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs17587572	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs17791056	0.97[EUR][1000 genomes]
rs260131	0.88[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs260140	0.96[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs260160	0.96[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs260162	0.97[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs260164	0.97[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs260165	0.82[AFR][1000 genomes];0.97[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs56226179	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs56309321	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56915128	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs61191692	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61959247	0.97[EUR][1000 genomes]
rs61959248	0.97[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs61959249	0.97[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs61959360	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs61959362	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs61959363	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61959407	0.80[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs61961771	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs61961774	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9317637	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9529163	0.84[EUR][1000 genomes]
rs9529166	0.94[EUR][1000 genomes]
rs9529167	0.94[EUR][1000 genomes]
rs9529169	0.94[EUR][1000 genomes]
rs9529174	0.97[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9529180	0.96[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9529182	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9529183	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9529185	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9529186	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs9529187	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9529188	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs9540964	0.84[EUR][1000 genomes]
rs9540967	0.84[EUR][1000 genomes]
rs9540968	0.93[EUR][1000 genomes]
rs9540969	0.94[EUR][1000 genomes]
rs9540971	0.94[EUR][1000 genomes]
rs9540980	0.97[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9540982	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9540983	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9540984	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9540987	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9540988	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9540989	0.92[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9540993	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9540994	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9540995	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9540996	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9540997	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9540998	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9540999	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9541000	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9541001	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9541002	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9541003	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9541004	0.93[EUR][1000 genomes]
rs9541006	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs9541007	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs9541008	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs9645951	0.84[EUR][1000 genomes]
rs972419	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530605	chr13:67126136-67697306	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	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
3	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
4	nsv900414	chr13:67515590-67701341	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv1045093	chr13:67517932-67693875	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv541821	chr13:67517932-67693875	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	nsv430581	chr13:67572850-67762288	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
8	nsv430582	chr13:67589898-67762299	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
9	nsv1037217	chr13:67589937-67728156	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
10	nsv1039600	chr13:67593961-67726047	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
11	nsv541823	chr13:67593961-67726047	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:67658800-67662800	Weak transcription	Brain Substantia Nigra	brain
2	chr13:67659600-67662400	Enhancers	Cortex derived primary cultured neurospheres	brain
3	chr13:67659800-67662400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr13:67660400-67663200	Enhancers	Brain Angular Gyrus	brain
5	chr13:67661000-67662200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr13:67661000-67665400	Weak transcription	Fetal Heart	heart
7	chr13:67661400-67662200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr13:67661400-67665000	Weak transcription	Brain Hippocampus Middle	brain
9	chr13:67661800-67662200	Flanking Active TSS	Brain Cingulate Gyrus	brain
10	chr13:67661800-67662200	Active TSS	Brain Inferior Temporal Lobe	brain
11	chr13:67661800-67662200	Enhancers	Colon Smooth Muscle	Colon
12	chr13:67661800-67662200	Flanking Active TSS	A549	lung
13	chr13:67662000-67662200	Enhancers	Brain Anterior Caudate	brain
14	chr13:67662000-67663000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain

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