Variant report

Variant	rs73312787
Chromosome Location	chr8:91373772-91373773
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10956588	0.93[EUR][1000 genomes]
rs10956606	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11991337	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11996534	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12541215	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12542044	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12543683	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12543750	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12546505	0.93[EUR][1000 genomes]
rs12677080	0.83[AFR][1000 genomes];0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2205153	0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4422814	0.93[EUR][1000 genomes]
rs4551412	0.93[EUR][1000 genomes]
rs4560835	0.89[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57808255	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs59229746	0.86[ASN][1000 genomes]
rs6984328	0.81[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6989642	0.81[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7003176	0.97[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7004083	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs73312729	0.81[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs73312731	0.81[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs73312758	0.93[EUR][1000 genomes]
rs7822920	0.86[ASN][1000 genomes]
rs7825634	0.89[AFR][1000 genomes];0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7830901	0.92[AFR][1000 genomes];0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7840137	1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1018991	chr8:91336887-91374274	Strong transcription Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:91365200-91375800	Weak transcription	K562	blood
2	chr8:91373400-91374800	Enhancers	Fetal Brain Male	brain
3	chr8:91373400-91374800	Enhancers	Fetal Brain Female	brain
4	chr8:91373600-91374600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr8:91373600-91374800	Enhancers	Cortex derived primary cultured neurospheres	brain
6	chr8:91373600-91375000	Enhancers	Brain Germinal Matrix	brain

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