Variant report

Variant	rs4759392
Chromosome Location	chr12:123285131-123285132
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	chr12:123277425..123279847-chr12:123284020..123285711,2	K562	blood:

Extended variants
information (count: 65 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:63)

rs_ID	r²[population]
rs10744434	0.81[AMR][1000 genomes]
rs10773627	0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10773657	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10847826	0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10847869	0.80[AFR][1000 genomes];0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11060064	0.95[ASN][1000 genomes]
rs11060065	0.95[ASN][1000 genomes]
rs12255	0.80[AMR][1000 genomes]
rs12297553	0.84[ASN][1000 genomes]
rs12298293	0.87[ASN][1000 genomes]
rs12298664	0.81[ASN][1000 genomes]
rs12313538	0.87[ASN][1000 genomes]
rs12313600	0.87[ASN][1000 genomes]
rs12314494	0.81[ASN][1000 genomes]
rs12314544	0.81[ASN][1000 genomes]
rs12315520	0.87[ASN][1000 genomes]
rs12318871	0.87[ASN][1000 genomes]
rs12319654	0.81[ASN][1000 genomes]
rs12321131	0.95[ASN][1000 genomes]
rs12426809	0.80[AFR][1000 genomes];0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1532835	0.82[EUR][1000 genomes]
rs1671685	0.81[ASN][1000 genomes]
rs1696326	0.81[ASN][1000 genomes]
rs1696349	0.81[ASN][1000 genomes]
rs1799618	0.81[ASN][1000 genomes]
rs1979236	0.81[ASN][1000 genomes]
rs1979237	0.81[ASN][1000 genomes]
rs2061098	0.80[AMR][1000 genomes]
rs2100500	0.81[ASN][1000 genomes]
rs2135014	0.82[EUR][1000 genomes]
rs2292131	0.81[ASN][1000 genomes]
rs2292134	0.82[EUR][1000 genomes]
rs2292135	0.82[EUR][1000 genomes]
rs2343108	0.81[EUR][1000 genomes]
rs2343109	0.81[AMR][1000 genomes]
rs2343685	0.82[AFR][1000 genomes];0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2649908	0.82[ASN][1000 genomes]
rs2649909	0.81[ASN][1000 genomes]
rs2880678	0.81[AFR][1000 genomes];0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs3825143	0.81[AMR][1000 genomes]
rs3852536	0.82[EUR][1000 genomes]
rs3852537	0.81[AMR][1000 genomes]
rs4759355	0.80[AFR][1000 genomes];0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4759389	0.81[AFR][1000 genomes];0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs56272219	0.81[ASN][1000 genomes]
rs58182048	0.95[ASN][1000 genomes]
rs59922385	0.81[ASN][1000 genomes]
rs7294991	0.85[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7303024	0.81[ASN][1000 genomes]
rs7309225	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs73421642	0.81[ASN][1000 genomes]
rs735378	0.81[ASN][1000 genomes]
rs754080	0.81[ASN][1000 genomes]
rs7959441	0.81[AMR][1000 genomes]
rs839360	0.84[ASN][1000 genomes]
rs897386	0.81[AMR][1000 genomes]
rs897391	0.80[AFR][1000 genomes];0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs897392	0.81[ASN][1000 genomes]
rs897393	0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs921808	0.80[AFR][1000 genomes];0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs937520	0.83[ASN][1000 genomes]
rs937766	0.82[EUR][1000 genomes]
rs9788290	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	nsv899571	chr12:123215734-123363562	Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
2	esv3388790	chr12:123275902-123655103	Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	55 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:123259400-123310600	Weak transcription	HSMMtube	muscle
2	chr12:123259800-123285800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr12:123259800-123310600	Weak transcription	Brain Substantia Nigra	brain
4	chr12:123260000-123303600	Weak transcription	Brain Inferior Temporal Lobe	brain
5	chr12:123264200-123290800	Weak transcription	Skeletal Muscle Female	skeletal muscle
6	chr12:123265600-123303600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr12:123266000-123303800	Weak transcription	Brain Hippocampus Middle	brain
8	chr12:123274600-123288800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr12:123278600-123305600	Weak transcription	Brain Cingulate Gyrus	brain
10	chr12:123284400-123297400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr12:123284600-123288800	Weak transcription	Gastric	stomach
12	chr12:123284600-123291000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr12:123284800-123285200	Enhancers	Primary neutrophils fromperipheralblood	blood
14	chr12:123284800-123293400	Weak transcription	Primary B cells from cord blood	blood
15	chr12:123284800-123297600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
16	chr12:123284800-123297600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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