Variant report

Variant	rs12042276
Chromosome Location	chr1:58643305-58643306
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 51 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs10493244	0.87[CEU][hapmap]
rs1106367	0.81[CEU][hapmap]
rs11207170	0.81[CEU][hapmap]
rs11799299	0.87[CEU][hapmap]
rs11802821	0.84[CEU][hapmap]
rs12025945	0.99[ASN][1000 genomes]
rs12034198	0.84[AFR][1000 genomes];0.94[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12040062	1.00[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12048970	0.84[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs12058945	0.81[CEU][hapmap]
rs1213764	0.81[CEU][hapmap]
rs1213771	0.80[CEU][hapmap]
rs12565597	0.83[AFR][1000 genomes];0.94[AMR][1000 genomes];0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13374932	0.84[CEU][hapmap]
rs1342875	0.84[CEU][hapmap]
rs1359495	0.81[CEU][hapmap]
rs1416341	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[YRI][hapmap];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1416343	0.81[CEU][hapmap];0.91[JPT][hapmap];0.84[ASN][1000 genomes]
rs1416346	0.84[CEU][hapmap]
rs1418765	0.99[ASN][1000 genomes]
rs17116867	0.81[CEU][hapmap]
rs17116869	0.81[CEU][hapmap]
rs17116983	0.84[CEU][hapmap]
rs17116988	0.84[CEU][hapmap]
rs17117013	0.84[CEU][hapmap]
rs17117039	0.87[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.98[ASN][1000 genomes]
rs17117101	0.84[CEU][hapmap]
rs17117119	0.81[CEU][hapmap]
rs1776192	0.86[CEU][hapmap]
rs1832488	0.85[CEU][hapmap]
rs1832489	0.84[CEU][hapmap]
rs1953811	0.84[CEU][hapmap]
rs2225949	1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap]
rs2406591	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap];0.84[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2797608	0.84[CEU][hapmap]
rs3850534	1.00[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3850535	0.84[CEU][hapmap]
rs3905539	0.84[CEU][hapmap]
rs4320799	0.81[CEU][hapmap]
rs6667829	1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs6701275	0.84[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs74074998	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7522031	0.81[CEU][hapmap]
rs7551611	0.87[CEU][hapmap]
rs821528	0.80[CEU][hapmap]
rs9782935	0.81[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1015057	chr1:57976993-58793962	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv530017	chr1:58002290-58669736	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
3	nsv431379	chr1:58224212-58802608	Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
4	nsv1008968	chr1:58582159-58982440	Enhancers Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
5	nsv534974	chr1:58582159-58982440	Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 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