Variant report

Variant	rs7426206
Chromosome Location	chr2:212984455-212984456
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	chr2:212982925..212985652-chr2:212994637..212996884,2	K562	blood:

Extended variants
information (count: 57 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:53)

rs_ID	r²[population]
rs10184407	0.81[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs10204324	0.98[ASN][1000 genomes]
rs10932423	0.86[JPT][hapmap];0.82[ASN][1000 genomes]
rs11677987	0.87[ASN][1000 genomes]
rs11680307	1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs11684050	1.00[JPT][hapmap]
rs11689043	0.87[ASN][1000 genomes]
rs11689133	0.87[ASN][1000 genomes]
rs11690618	1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs11695227	0.87[ASN][1000 genomes]
rs11887531	0.90[CHB][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs11902372	0.84[ASN][1000 genomes]
rs12151841	0.92[ASN][1000 genomes]
rs12465933	0.97[ASN][1000 genomes]
rs12468336	0.81[CHB][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs12469791	0.94[ASN][1000 genomes]
rs12473715	0.93[JPT][hapmap];0.85[ASN][1000 genomes]
rs13384295	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1402768	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1521655	0.93[JPT][hapmap];0.87[ASN][1000 genomes]
rs1521656	0.94[JPT][hapmap];0.85[ASN][1000 genomes]
rs1521658	0.86[JPT][hapmap];0.83[ASN][1000 genomes]
rs1568520	0.88[CEU][hapmap];0.80[JPT][hapmap];0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs17344266	0.94[JPT][hapmap];0.88[ASN][1000 genomes]
rs17344385	1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs17416263	1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs17416297	0.93[JPT][hapmap]
rs2371442	0.94[JPT][hapmap];0.81[ASN][1000 genomes]
rs2371475	0.90[CHB][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs2371476	0.81[CHB][hapmap];0.94[JPT][hapmap];0.84[ASN][1000 genomes]
rs2888042	0.83[ASN][1000 genomes]
rs2888051	0.94[JPT][hapmap]
rs4571009	0.95[ASN][1000 genomes]
rs56242159	0.86[ASN][1000 genomes]
rs56351822	0.89[ASN][1000 genomes]
rs62183999	0.83[ASN][1000 genomes]
rs62184037	0.83[ASN][1000 genomes]
rs62184038	0.91[ASN][1000 genomes]
rs62184039	0.84[ASN][1000 genomes]
rs62184046	0.80[ASN][1000 genomes]
rs6435689	0.90[CHB][hapmap];1.00[JPT][hapmap];0.80[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6435690	1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs6715314	0.93[JPT][hapmap];0.80[ASN][1000 genomes]
rs6719517	0.82[ASN][1000 genomes]
rs6738304	1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs7562352	0.92[ASN][1000 genomes]
rs7576561	0.82[ASN][1000 genomes]
rs7577530	0.93[JPT][hapmap];0.82[EUR][1000 genomes]
rs7579502	0.86[ASN][1000 genomes]
rs7579631	0.92[ASN][1000 genomes]
rs7583813	0.93[JPT][hapmap]
rs954553	1.00[JPT][hapmap]
rs9678442	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1011572	chr2:212840066-213152279	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
2	nsv875802	chr2:212867291-213004603	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
3	nsv875804	chr2:212891401-212997024	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	nsv875805	chr2:212891401-213164837	Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:212975400-212984800	Weak transcription	Aorta	Aorta
2	chr2:212982200-212985000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr2:212982400-212984800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr2:212982400-212984800	Enhancers	Cortex derived primary cultured neurospheres	brain
5	chr2:212982600-212984600	Enhancers	HUES64 Cell Line	embryonic stem cell
6	chr2:212983200-212989200	Weak transcription	Fetal Heart	heart
7	chr2:212983400-212984600	Weak transcription	Brain Inferior Temporal Lobe	brain
8	chr2:212983400-212984600	Weak transcription	Brain Substantia Nigra	brain
9	chr2:212984000-212984600	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr2:212984000-212984600	Enhancers	iPS-20b Cell Line	embryonic stem cell
11	chr2:212984200-212984600	Enhancers	Brain Angular Gyrus	brain
12	chr2:212984400-212984600	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr2:212984400-212985000	Enhancers	Brain Anterior Caudate	brain
14	chr2:212984400-212985000	Enhancers	Brain Hippocampus Middle	brain

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