Variant report

Variant	rs12344899
Chromosome Location	chr9:103934475-103934476
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs10119316	0.86[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs1019873	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10512278	0.85[ASN][1000 genomes]
rs10989419	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12341807	0.93[ASN][1000 genomes]
rs12344900	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12352148	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1367754	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1431472	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17829436	0.85[ASN][1000 genomes]
rs17829926	0.93[ASN][1000 genomes]
rs1987400	0.95[ASN][1000 genomes]
rs4278208	0.93[ASN][1000 genomes]
rs4342669	0.90[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4742806	0.85[ASN][1000 genomes]
rs4743445	0.93[ASN][1000 genomes]
rs4743446	0.93[ASN][1000 genomes]
rs4743449	0.93[ASN][1000 genomes]
rs4743450	0.93[ASN][1000 genomes]
rs55672230	0.85[ASN][1000 genomes]
rs55903434	0.91[ASN][1000 genomes]
rs56156225	0.93[ASN][1000 genomes]
rs57097151	0.93[ASN][1000 genomes]
rs57409431	0.85[ASN][1000 genomes]
rs58088765	0.85[ASN][1000 genomes]
rs58422308	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs60195477	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs60390009	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs61489062	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61647398	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs72741430	0.85[ASN][1000 genomes]
rs72741437	0.85[ASN][1000 genomes]
rs72741438	0.85[ASN][1000 genomes]
rs72741439	0.93[ASN][1000 genomes]
rs72741444	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs72741445	0.93[ASN][1000 genomes]
rs72741449	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs72741452	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7852006	0.93[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv831671	chr9:103858107-104020816	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv948791	chr9:103893030-103964650	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:103930600-103936600	Weak transcription	Brain Hippocampus Middle	brain
2	chr9:103930800-103934800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
3	chr9:103930800-103936600	Weak transcription	Brain Anterior Caudate	brain
4	chr9:103931200-103936200	Weak transcription	HepG2	liver
5	chr9:103934400-103937000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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