Variant report

Variant	rs11684050
Chromosome Location	chr2:212996467-212996468
allele	A/T
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: 58 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:54)

rs_ID	r²[population]
rs10184407	0.86[ASN][1000 genomes]
rs10204324	0.89[ASN][1000 genomes]
rs10932423	0.82[CHB][hapmap];0.86[JPT][hapmap];0.91[ASN][1000 genomes]
rs11677987	0.81[ASN][1000 genomes]
rs11680307	0.88[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11689043	0.81[ASN][1000 genomes]
rs11689133	0.81[ASN][1000 genomes]
rs11690618	0.90[CHB][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs11695227	0.81[ASN][1000 genomes]
rs11887531	1.00[JPT][hapmap];0.80[ASN][1000 genomes]
rs11902372	0.81[ASN][1000 genomes]
rs12151841	0.92[ASN][1000 genomes]
rs12465933	0.91[ASN][1000 genomes]
rs12468336	1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs12469791	0.91[ASN][1000 genomes]
rs12473715	0.90[CHB][hapmap];0.93[JPT][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];0.83[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs13384295	0.95[ASN][1000 genomes]
rs1402768	0.83[ASN][1000 genomes]
rs1464451	0.87[ASN][1000 genomes]
rs1521655	0.89[CHB][hapmap];0.93[JPT][hapmap];0.88[ASN][1000 genomes]
rs1521656	0.91[CHB][hapmap];0.94[JPT][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];0.83[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs1521658	0.90[CHB][hapmap];0.86[JPT][hapmap];1.00[YRI][hapmap];0.81[AFR][1000 genomes];0.81[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs1568520	0.80[CHB][hapmap];0.85[ASN][1000 genomes]
rs17344266	0.94[JPT][hapmap];0.85[ASN][1000 genomes]
rs17344385	1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs17416263	0.80[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs17416297	1.00[CHB][hapmap];0.94[JPT][hapmap]
rs1829675	0.86[ASN][1000 genomes]
rs2371442	0.94[JPT][hapmap]
rs2371475	1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs2371476	0.94[JPT][hapmap];0.84[ASN][1000 genomes]
rs2888042	0.80[ASN][1000 genomes]
rs2888051	0.80[CHB][hapmap];0.94[JPT][hapmap];0.89[YRI][hapmap]
rs4571009	0.89[ASN][1000 genomes]
rs56242159	0.89[ASN][1000 genomes]
rs56351822	0.98[ASN][1000 genomes]
rs62183999	0.80[ASN][1000 genomes]
rs62184037	0.80[ASN][1000 genomes]
rs62184038	0.88[ASN][1000 genomes]
rs62184039	0.81[ASN][1000 genomes]
rs62184046	0.89[ASN][1000 genomes]
rs6435689	1.00[JPT][hapmap]
rs6435690	1.00[JPT][hapmap]
rs6715314	1.00[CHB][hapmap];0.93[JPT][hapmap];0.89[ASN][1000 genomes]
rs6738304	0.90[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs7426206	1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs7562352	0.92[ASN][1000 genomes]
rs7576561	0.82[ASN][1000 genomes]
rs7577530	0.90[CHB][hapmap];0.93[JPT][hapmap]
rs7579502	0.87[ASN][1000 genomes]
rs7579631	0.92[ASN][1000 genomes]
rs7583813	0.93[JPT][hapmap]
rs954553	1.00[JPT][hapmap]
rs9678442	0.93[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:0 , 50 per page) page:

No data

Quick Search:

Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links